| geneid | 101060226 |
|---|---|
| ensemblid | ENSG00000271383.9 |
| hgncid | 31999 |
| symbol | NBPF19 |
| name | NBPF member 19 |
| refseq_nuc | NM_001351365.2 |
| refseq_prot | NP_001338294.1 |
| ensembl_nuc | ENST00000651566.2 |
| ensembl_prot | ENSP00000498781.1 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 149475045 |
| end | 149556361 |
| strand | + |
| ver | v1.2 |
| region | chr1:149475045-149556361 |
| region5000 | chr1:149470045-149561361 |
| regionname0 | NBPF19_chr1_149475045_149556361 |
| regionname5000 | NBPF19_chr1_149470045_149561361 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 3843 | 7 | 1 | 4 | 1 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0002 | 0/0 | 3843 | 6 | 0 | 0 | 6 | 0 | 0 | 6 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0003 | 0/0 | 3843 | 5 | 0 | 0 | 4 | 0 | 1 | 2 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0004 | 0/0 | 3843 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0005 | 0/0 | 3599 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0006 | 0/0 | 416 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0007 | 0/0 | 1403 | 3 | 0 | 0 | 3 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0008 | 0/0 | 3843 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0009 | 0/0 | 3843 | 3 | 0 | 2 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0010 | 0/0 | 3599 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0011 | 0/0 | 3843 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0012 | 0/0 | 3345 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0013 | 0/0 | 3843 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0014 | 0/0 | 3843 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0015 | 0/0 | 3843 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0016 | 0/0 | 3355 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0017 | 0/0 | 3843 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0018 | 0/0 | 3843 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0019 | 1/0 | 3843 | 2 | 0 | 0 | 0 | 0 | 1 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0020 | 0/0 | 3355 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0021 | 0/0 | 3599 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0022 | 0/0 | 3843 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0023 | 0/0 | 3843 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0024 | 0/0 | 3843 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0025 | 0/1 | 3599 | 2 | 0 | 0 | 0 | 0 | 1 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0026 | 0/0 | 3355 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0027 | 0/0 | 3599 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0028 | 0/0 | 3843 | 2 | 1 | 0 | 0 | 0 | 1 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0029 | 0/0 | 3843 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0030 | 0/0 | 3355 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0031 | 0/0 | 3843 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0032 | 0/0 | 3843 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0033 | 0/0 | 3843 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0034 | 0/0 | 3843 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0035 | 0/0 | 3843 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0036 | 0/0 | 3843 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0037 | 0/0 | 3843 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0038 | 0/0 | 3843 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0039 | 0/0 | 3843 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0040 | 0/0 | 3843 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0041 | 0/0 | 103 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0042 | 0/0 | 3843 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0043 | 0/0 | 3843 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0044 | 0/0 | 3843 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0045 | 0/0 | 3843 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0046 | 0/0 | 3843 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0047 | 0/0 | 3355 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0048 | 0/0 | 3843 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0049 | 0/0 | 3599 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0050 | 0/0 | 3843 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0051 | 0/0 | 3843 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0052 | 0/0 | 3843 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0053 | 0/0 | 593 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0054 | 0/0 | 3599 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0055 | 0/0 | 3843 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0056 | 0/0 | 3843 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0057 | 0/0 | 3843 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0058 | 0/0 | 3599 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0059 | 0/0 | 3843 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0060 | 0/0 | 3843 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0061 | 0/0 | 3843 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0062 | 0/0 | 3111 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0063 | 0/0 | 3843 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0064 | 0/0 | 3355 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0065 | 0/0 | 3599 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0066 | 0/0 | 3599 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0067 | 0/0 | 3355 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0068 | 0/0 | 2867 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0069 | 0/0 | 3843 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0070 | 0/0 | 3843 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0071 | 0/0 | 3599 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0072 | 0/0 | 3843 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0073 | 0/0 | 3843 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0074 | 0/0 | 3843 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0075 | 0/0 | 3843 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0076 | 0/0 | 3843 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0077 | 0/0 | 3843 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0078 | 0/0 | 3599 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0079 | 0/0 | 3355 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0080 | 0/0 | 3843 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0081 | 0/0 | 3843 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0082 | 0/0 | 3843 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0083 | 0/0 | 3843 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0084 | 0/0 | 3843 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0085 | 0/0 | 3843 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0086 | 0/0 | 3843 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0087 | 0/0 | 3843 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0088 | 0/0 | 3355 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0089 | 0/0 | 3599 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0090 | 0/0 | 3355 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0091 | 0/0 | 3843 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0092 | 0/0 | 3599 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0093 | 0/0 | 3843 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0094 | 0/0 | 3843 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0095 | 0/0 | 3843 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0096 | 0/0 | 3843 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0097 | 0/0 | 3843 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0098 | 0/0 | 3599 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0099 | 0/0 | 3843 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0100 | 0/0 | 3355 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0101 | 0/0 | 3843 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0102 | 0/0 | 3843 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0103 | 0/0 | 3843 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0104 | 0/0 | 3674 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0105 | 0/0 | 3599 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0106 | 0/0 | 3599 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0107 | 0/0 | 3843 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0108 | 0/0 | 3355 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0109 | 0/0 | 3843 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0110 | 0/0 | 3843 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0111 | 0/0 | 3843 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0112 | 0/0 | 3843 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0113 | 0/0 | 3355 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0114 | 0/0 | 3599 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0115 | 0/0 | 3599 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0116 | 0/0 | 3599 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0117 | 0/0 | 3843 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0118 | 0/0 | 3843 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0119 | 0/0 | 3843 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0120 | 0/0 | 3599 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0121 | 0/0 | 3843 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0122 | 0/0 | 3599 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0123 | 0/0 | 3843 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0124 | 0/0 | 3843 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0125 | 0/0 | 3843 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0126 | 0/0 | 3355 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0127 | 0/0 | 3843 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0128 | 0/0 | 3843 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0129 | 0/0 | 3843 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0130 | 0/0 | 3843 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0131 | 0/0 | 3843 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0132 | 0/0 | 3843 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0133 | 0/0 | 3599 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0134 | 0/0 | 3843 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0135 | 0/0 | 3843 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0136 | 0/0 | 3843 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0137 | 0/0 | 3843 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0138 | 0/0 | 3843 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0139 | 0/0 | 3843 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0140 | 0/0 | 3345 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0141 | 0/0 | 3345 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0142 | 0/0 | 3843 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0143 | 0/0 | 3843 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0144 | 0/0 | 3843 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0145 | 0/0 | 3843 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0146 | 0/0 | 3843 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0147 | 0/0 | 3843 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0148 | 0/0 | 3843 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0149 | 0/0 | 3843 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0150 | 0/0 | 3355 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0151 | 0/0 | 3843 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0152 | 0/0 | 3843 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0153 | 0/0 | 3843 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0154 | 0/0 | 3843 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0155 | 0/0 | 3843 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0156 | 0/0 | 2135 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0157 | 0/0 | 2379 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0158 | 0/0 | 3355 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0159 | 0/0 | 3843 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0160 | 0/0 | 3843 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0161 | 0/0 | 3599 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0162 | 0/0 | 3599 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0163 | 0/0 | 3843 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0164 | 0/0 | 3843 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0165 | 0/0 | 3843 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0166 | 0/0 | 2867 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0167 | 0/0 | 2124 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0168 | 0/0 | 3843 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0169 | 0/0 | 3843 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0170 | 0/0 | 3843 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0171 | 0/0 | 3843 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0172 | 0/0 | 3843 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0173 | 0/0 | 3843 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0174 | 0/0 | 3843 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0175 | 0/0 | 3599 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0176 | 0/0 | 3599 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0177 | 0/0 | 3111 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0178 | 0/0 | 3843 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0179 | 0/0 | 3843 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0180 | 0/0 | 3843 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0181 | 0/0 | 3843 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0182 | 0/0 | 3843 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0183 | 0/0 | 3599 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0184 | 0/0 | 3599 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0185 | 0/0 | 3355 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0186 | 0/0 | 3843 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0187 | 0/0 | 3355 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0188 | 0/0 | 3599 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0189 | 0/0 | 3599 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0190 | 0/0 | 3599 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0191 | 0/0 | 3843 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0192 | 0/0 | 3843 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0193 | 0/0 | 3843 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0194 | 0/0 | 3843 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0195 | 0/0 | 3843 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0196 | 0/0 | 3843 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0197 | 0/0 | 1717 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0198 | 0/0 | 3843 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0199 | 0/0 | 3843 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0200 | 0/0 | 3843 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0201 | 0/0 | 3599 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0202 | 0/0 | 3843 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0203 | 0/0 | 3843 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0204 | 0/0 | 3843 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0205 | 0/0 | 3843 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0206 | 0/0 | 3599 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0207 | 0/0 | 1717 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0208 | 0/0 | 1717 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0209 | 0/0 | 3843 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0210 | 0/0 | 3599 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0211 | 0/0 | 3843 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0212 | 0/0 | 3599 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 11532 | 7 | 1 | 4 | 1 | 1 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0002 | 0/0 | 11532 | 6 | 0 | 0 | 6 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0003 | 0/0 | 11532 | 4 | 0 | 0 | 4 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0004 | 0/0 | 10800 | 4 | 0 | 0 | 4 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0005 | 0/0 | 4212 | 3 | 0 | 0 | 3 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0006 | 0/0 | 11532 | 3 | 0 | 2 | 0 | 1 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0007 | 0/0 | 10800 | 3 | 0 | 3 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0008 | 0/0 | 11532 | 3 | 0 | 3 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0009 | 0/0 | 10038 | 3 | 0 | 0 | 3 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0010 | 0/0 | 11532 | 3 | 0 | 0 | 3 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0011 | 0/0 | 11532 | 2 | 0 | 0 | 2 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0012 | 0/0 | 11532 | 2 | 0 | 2 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0013 | 0/0 | 11532 | 2 | 0 | 0 | 2 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0014 | 0/0 | 11532 | 2 | 0 | 0 | 2 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0015 | 0/0 | 11532 | 2 | 0 | 0 | 0 | 0 | 2 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0016 | 0/0 | 11532 | 2 | 0 | 2 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0017 | 0/0 | 10068 | 2 | 0 | 0 | 0 | 0 | 2 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0018 | 0/0 | 11532 | 2 | 2 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0019 | 0/0 | 11532 | 2 | 2 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0020 | 0/0 | 10068 | 2 | 0 | 1 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0021 | 1/0 | 11532 | 2 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0022 | 0/0 | 10800 | 2 | 2 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0023 | 0/0 | 11532 | 2 | 2 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0024 | 0/0 | 11532 | 2 | 2 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0025 | 0/0 | 11532 | 2 | 2 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0026 | 0/0 | 11532 | 2 | 2 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0027 | 0/0 | 11532 | 2 | 2 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0028 | 0/0 | 11532 | 2 | 0 | 0 | 2 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0029 | 0/0 | 10800 | 2 | 0 | 0 | 2 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0030 | 0/0 | 10068 | 2 | 0 | 2 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0031 | 0/1 | 10800 | 2 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0032 | 0/0 | 11532 | 2 | 1 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0033 | 0/0 | 11532 | 2 | 2 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0034 | 0/0 | 10068 | 2 | 2 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0035 | 0/0 | 11532 | 2 | 2 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0036 | 0/0 | 11532 | 2 | 2 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0037 | 0/0 | 11532 | 2 | 0 | 2 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0038 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0039 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0040 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0041 | 0/0 | 10800 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0042 | 0/0 | 10800 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0043 | 0/0 | 10068 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0044 | 0/0 | 11532 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0045 | 0/0 | 11532 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0046 | 0/0 | 35325 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0047 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0048 | 0/0 | 30568 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0049 | 0/0 | 10800 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0050 | 0/0 | 10068 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0051 | 0/0 | 10800 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0052 | 0/0 | 10800 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0053 | 0/0 | 10800 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0054 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0055 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0056 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0057 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0058 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0059 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0060 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0061 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0062 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0063 | 0/0 | 10800 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0064 | 0/0 | 11532 | 1 | 0 | 0 | 0 | 1 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0065 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0066 | 0/0 | 25795 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0067 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0068 | 0/0 | 10800 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0069 | 0/0 | 10800 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0070 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0071 | 0/0 | 11532 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0072 | 0/0 | 11532 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0073 | 0/0 | 11532 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0074 | 0/0 | 11532 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0075 | 0/0 | 9336 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0076 | 0/0 | 11532 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0077 | 0/0 | 11532 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0078 | 0/0 | 11532 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0079 | 0/0 | 11532 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0080 | 0/0 | 11532 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0081 | 0/0 | 11532 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0082 | 0/0 | 10800 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0083 | 0/0 | 11532 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0084 | 0/0 | 10068 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0085 | 0/0 | 10800 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0086 | 0/0 | 11532 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0087 | 0/0 | 10800 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0088 | 0/0 | 11532 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0089 | 0/0 | 11532 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0090 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0091 | 0/0 | 11532 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0092 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0093 | 0/0 | 9336 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0094 | 0/0 | 10068 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0095 | 0/0 | 10068 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0096 | 0/0 | 8604 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0097 | 0/0 | 10800 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0098 | 0/0 | 10800 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0099 | 0/0 | 6408 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0100 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0101 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0102 | 0/0 | 10800 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0103 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0104 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0105 | 0/0 | 10068 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0106 | 0/0 | 11532 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0107 | 0/0 | 10068 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0108 | 0/0 | 11532 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0109 | 0/0 | 11532 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0110 | 0/0 | 11532 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0111 | 0/0 | 10800 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0112 | 0/0 | 11532 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0113 | 0/0 | 11532 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0114 | 0/0 | 11532 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0115 | 0/0 | 11532 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0116 | 0/0 | 11532 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0117 | 0/0 | 11532 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0118 | 0/0 | 11532 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0119 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0120 | 0/0 | 10800 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0121 | 0/0 | 10068 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0122 | 0/0 | 11532 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0123 | 0/0 | 10800 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0124 | 0/0 | 11532 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0125 | 0/0 | 11532 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0126 | 0/0 | 11532 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0127 | 0/0 | 11532 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0128 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0129 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0130 | 0/0 | 10068 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0131 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0132 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0133 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0134 | 0/0 | 10068 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0135 | 0/0 | 11532 | 1 | 0 | 0 | 0 | 1 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0136 | 0/0 | 11532 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0137 | 0/0 | 10800 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0138 | 0/0 | 11532 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0139 | 0/0 | 10800 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0140 | 0/0 | 10800 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0141 | 0/0 | 11025 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0142 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0143 | 0/0 | 10068 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0144 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0145 | 0/0 | 10068 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0146 | 0/0 | 11532 | 1 | 0 | 0 | 0 | 1 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0147 | 0/0 | 10800 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0148 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0149 | 0/0 | 10800 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0150 | 0/0 | 10800 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0151 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0152 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0153 | 0/0 | 11532 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0154 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0155 | 0/0 | 10800 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0156 | 0/0 | 10800 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0157 | 0/0 | 11532 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0158 | 0/0 | 11532 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0159 | 0/0 | 11532 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0160 | 0/0 | 10068 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0161 | 0/0 | 11532 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0162 | 0/0 | 11532 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0163 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0164 | 0/0 | 11532 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0165 | 0/0 | 10800 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0166 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0167 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0168 | 0/0 | 11532 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0169 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0170 | 0/0 | 11532 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0171 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0172 | 0/0 | 11532 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0173 | 0/0 | 11532 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0174 | 0/0 | 11532 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0175 | 0/0 | 10038 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0176 | 0/0 | 11532 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0177 | 0/0 | 11532 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0178 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0179 | 0/0 | 11532 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0180 | 0/0 | 11532 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0181 | 0/0 | 11532 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0182 | 0/0 | 10038 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0183 | 0/0 | 11532 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0184 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0185 | 0/0 | 11532 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0186 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0187 | 0/0 | 11532 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0188 | 0/0 | 7140 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0189 | 0/0 | 11532 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0190 | 0/0 | 11518 | 1 | 0 | 0 | 0 | 1 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0191 | 0/0 | 11532 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0192 | 0/0 | 11532 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0193 | 0/0 | 10800 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0194 | 0/0 | 10800 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0195 | 0/0 | 11532 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0196 | 0/0 | 10800 | 1 | 0 | 0 | 0 | 1 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0197 | 0/0 | 10800 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0198 | 0/0 | 8604 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0199 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0200 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0201 | 0/0 | 11532 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0202 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0203 | 0/0 | 25786 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0204 | 0/0 | 11532 | 1 | 0 | 0 | 0 | 1 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0205 | 0/0 | 11532 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0206 | 0/0 | 11532 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0207 | 0/0 | 11532 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0208 | 0/0 | 11532 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0209 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0210 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0211 | 0/0 | 25796 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0212 | 0/0 | 35277 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0213 | 0/0 | 16283 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0214 | 0/0 | 21046 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0215 | 0/0 | 11532 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0216 | 0/0 | 10068 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0217 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0218 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0219 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| c0220 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 2410 | 170 | 57 | 29 | 54 | 5 | 23 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| t0002 | 0/0 | 2410 | 45 | 3 | 6 | 31 | 1 | 4 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| t0003 | 0/0 | 2410 | 14 | 0 | 3 | 10 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| t0004 | 0/0 | 2407 | 8 | 1 | 2 | 2 | 1 | 2 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| t0005 | 0/0 | 2410 | 5 | 0 | 1 | 2 | 1 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| t0006 | 0/0 | 2410 | 4 | 4 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| t0007 | 0/0 | 2410 | 3 | 0 | 0 | 3 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| t0008 | 0/0 | 2410 | 3 | 3 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| t0009 | 0/0 | 2410 | 2 | 0 | 0 | 2 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| t0010 | 0/0 | 2410 | 2 | 0 | 2 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| t0011 | 0/0 | 2410 | 2 | 0 | 1 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| t0012 | 0/0 | 2410 | 2 | 0 | 0 | 2 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| t0013 | 0/0 | 2407 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| t0014 | 0/0 | 2410 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| t0015 | 0/0 | 2410 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| t0016 | 0/0 | 2410 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| t0017 | 0/0 | 2410 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| t0018 | 0/0 | 2410 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| t0019 | 0/0 | 2410 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| t0020 | 0/0 | 2410 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| t0021 | 0/0 | 2410 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| t0022 | 0/0 | 2410 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| t0023 | 0/0 | 2410 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| t0024 | 0/0 | 2410 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| t0025 | 0/0 | 2410 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| t0026 | 0/0 | 2410 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| t0027 | 0/0 | 2410 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| t0028 | 0/0 | 2410 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0033 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0046 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 11532 | 7 | 1 | 4 | 1 | 1 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0002c0002 | 0/0 | 11532 | 6 | 0 | 0 | 6 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0003c0003 | 0/0 | 11532 | 4 | 0 | 0 | 4 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0003c0136 | 0/0 | 11532 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0004c0026 | 0/0 | 11532 | 2 | 2 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0004c0027 | 0/0 | 11532 | 2 | 2 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0005c0004 | 0/0 | 10800 | 4 | 0 | 0 | 4 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0006c0211 | 0/0 | 25796 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0006c0212 | 0/0 | 35277 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0006c0213 | 0/0 | 16283 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0006c0214 | 0/0 | 21046 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0007c0005 | 0/0 | 4212 | 3 | 0 | 0 | 3 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0008c0037 | 0/0 | 11532 | 2 | 0 | 2 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0008c0215 | 0/0 | 11532 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0009c0006 | 0/0 | 11532 | 3 | 0 | 2 | 0 | 1 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0010c0007 | 0/0 | 10800 | 3 | 0 | 3 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0011c0010 | 0/0 | 11532 | 3 | 0 | 0 | 3 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0012c0009 | 0/0 | 10038 | 3 | 0 | 0 | 3 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0013c0035 | 0/0 | 11532 | 2 | 2 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0013c0162 | 0/0 | 11532 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0014c0008 | 0/0 | 11532 | 3 | 0 | 3 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0015c0036 | 0/0 | 11532 | 2 | 2 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0015c0192 | 0/0 | 11532 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0016c0017 | 0/0 | 10068 | 2 | 0 | 0 | 0 | 0 | 2 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0017c0019 | 0/0 | 11532 | 2 | 2 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0018c0018 | 0/0 | 11532 | 2 | 2 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0019c0021 | 1/0 | 11532 | 2 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0020c0020 | 0/0 | 10068 | 2 | 0 | 1 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0021c0022 | 0/0 | 10800 | 2 | 2 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0022c0023 | 0/0 | 11532 | 2 | 2 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0023c0024 | 0/0 | 11532 | 2 | 2 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0024c0025 | 0/0 | 11532 | 2 | 2 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0025c0031 | 0/1 | 10800 | 2 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0026c0030 | 0/0 | 10068 | 2 | 0 | 2 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0027c0029 | 0/0 | 10800 | 2 | 0 | 0 | 2 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0028c0032 | 0/0 | 11532 | 2 | 1 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0029c0033 | 0/0 | 11532 | 2 | 2 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0030c0034 | 0/0 | 10068 | 2 | 2 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0031c0028 | 0/0 | 11532 | 2 | 0 | 0 | 2 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0032c0012 | 0/0 | 11532 | 2 | 0 | 2 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0033c0011 | 0/0 | 11532 | 2 | 0 | 0 | 2 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0034c0013 | 0/0 | 11532 | 2 | 0 | 0 | 2 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0035c0015 | 0/0 | 11532 | 2 | 0 | 0 | 0 | 0 | 2 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0036c0014 | 0/0 | 11532 | 2 | 0 | 0 | 2 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0037c0016 | 0/0 | 11532 | 2 | 0 | 2 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0038c0038 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0039c0219 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0040c0218 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0041c0217 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0042c0195 | 0/0 | 11532 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0043c0209 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0044c0210 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0045c0078 | 0/0 | 11532 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0046c0077 | 0/0 | 11532 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0047c0216 | 0/0 | 10068 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0048c0081 | 0/0 | 11532 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0049c0082 | 0/0 | 10800 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0050c0080 | 0/0 | 11532 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0051c0083 | 0/0 | 11532 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0052c0079 | 0/0 | 11532 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0053c0190 | 0/0 | 11518 | 1 | 0 | 0 | 0 | 1 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0054c0085 | 0/0 | 10800 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0055c0086 | 0/0 | 11532 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0056c0089 | 0/0 | 11532 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0057c0088 | 0/0 | 11532 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0058c0087 | 0/0 | 10800 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0059c0091 | 0/0 | 11532 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0060c0092 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0061c0187 | 0/0 | 11532 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0062c0093 | 0/0 | 9336 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0063c0090 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0064c0094 | 0/0 | 10068 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0065c0098 | 0/0 | 10800 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0066c0097 | 0/0 | 10800 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0067c0095 | 0/0 | 10068 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0068c0096 | 0/0 | 8604 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0069c0100 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0070c0101 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0071c0102 | 0/0 | 10800 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0072c0104 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0073c0103 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0074c0112 | 0/0 | 11532 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0075c0108 | 0/0 | 11532 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0076c0109 | 0/0 | 11532 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0077c0110 | 0/0 | 11532 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0078c0111 | 0/0 | 10800 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0079c0107 | 0/0 | 10068 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0080c0106 | 0/0 | 11532 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0081c0113 | 0/0 | 11532 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0082c0117 | 0/0 | 11532 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0083c0116 | 0/0 | 11532 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0084c0115 | 0/0 | 11532 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0085c0114 | 0/0 | 11532 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0086c0119 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0087c0118 | 0/0 | 11532 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0088c0105 | 0/0 | 10068 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0089c0123 | 0/0 | 10800 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0090c0121 | 0/0 | 10068 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0091c0122 | 0/0 | 11532 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0092c0120 | 0/0 | 10800 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0093c0124 | 0/0 | 11532 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0094c0125 | 0/0 | 11532 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0095c0126 | 0/0 | 11532 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0096c0127 | 0/0 | 11532 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0097c0148 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0098c0147 | 0/0 | 10800 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0099c0146 | 0/0 | 11532 | 1 | 0 | 0 | 0 | 1 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0100c0145 | 0/0 | 10068 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0101c0039 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0102c0144 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0103c0142 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0104c0141 | 0/0 | 11025 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0105c0140 | 0/0 | 10800 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0106c0139 | 0/0 | 10800 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0107c0138 | 0/0 | 11532 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0108c0143 | 0/0 | 10068 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0109c0135 | 0/0 | 11532 | 1 | 0 | 0 | 0 | 1 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0110c0133 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0111c0132 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0112c0131 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0113c0134 | 0/0 | 10068 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0114c0137 | 0/0 | 10800 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0115c0149 | 0/0 | 10800 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0116c0150 | 0/0 | 10800 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0117c0152 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0118c0151 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0119c0153 | 0/0 | 11532 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0120c0155 | 0/0 | 10800 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0121c0154 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0122c0156 | 0/0 | 10800 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0123c0157 | 0/0 | 11532 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0124c0158 | 0/0 | 11532 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0125c0159 | 0/0 | 11532 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0126c0130 | 0/0 | 10068 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0127c0169 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0128c0168 | 0/0 | 11532 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0129c0167 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0130c0170 | 0/0 | 11532 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0131c0171 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0132c0166 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0133c0165 | 0/0 | 10800 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0134c0164 | 0/0 | 11532 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0135c0161 | 0/0 | 11532 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0136c0163 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0137c0173 | 0/0 | 11532 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0138c0174 | 0/0 | 11532 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0139c0172 | 0/0 | 11532 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0140c0175 | 0/0 | 10038 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0141c0182 | 0/0 | 10038 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0142c0180 | 0/0 | 11532 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0143c0179 | 0/0 | 11532 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0144c0178 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0145c0177 | 0/0 | 11532 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0146c0176 | 0/0 | 11532 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0147c0220 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0148c0181 | 0/0 | 11532 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0149c0183 | 0/0 | 11532 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0150c0160 | 0/0 | 10068 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0151c0184 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0152c0129 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0153c0128 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0154c0185 | 0/0 | 11532 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0155c0186 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0156c0099 | 0/0 | 6408 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0157c0188 | 0/0 | 7140 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0158c0084 | 0/0 | 10068 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0159c0189 | 0/0 | 11532 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0160c0076 | 0/0 | 11532 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0161c0197 | 0/0 | 10800 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0162c0196 | 0/0 | 10800 | 1 | 0 | 0 | 0 | 1 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0163c0199 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0164c0201 | 0/0 | 11532 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0165c0200 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0166c0198 | 0/0 | 8604 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0167c0203 | 0/0 | 25786 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0168c0206 | 0/0 | 11532 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0169c0205 | 0/0 | 11532 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0170c0208 | 0/0 | 11532 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0171c0207 | 0/0 | 11532 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0172c0204 | 0/0 | 11532 | 1 | 0 | 0 | 0 | 1 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0173c0191 | 0/0 | 11532 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0174c0202 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0175c0193 | 0/0 | 10800 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0176c0194 | 0/0 | 10800 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0177c0075 | 0/0 | 9336 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0178c0070 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0179c0071 | 0/0 | 11532 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0180c0072 | 0/0 | 11532 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0181c0073 | 0/0 | 11532 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0182c0074 | 0/0 | 11532 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0183c0041 | 0/0 | 10800 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0184c0042 | 0/0 | 10800 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0185c0043 | 0/0 | 10068 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0186c0044 | 0/0 | 11532 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0187c0050 | 0/0 | 10068 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0188c0051 | 0/0 | 10800 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0189c0052 | 0/0 | 10800 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0190c0049 | 0/0 | 10800 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0191c0054 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0192c0055 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0193c0057 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0194c0058 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0195c0060 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0196c0045 | 0/0 | 11532 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0197c0066 | 0/0 | 25795 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0198c0059 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0199c0061 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0200c0062 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0201c0063 | 0/0 | 10800 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0202c0064 | 0/0 | 11532 | 1 | 0 | 0 | 0 | 1 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0203c0065 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0204c0067 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0205c0056 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0206c0053 | 0/0 | 10800 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0207c0046 | 0/0 | 35325 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0208c0048 | 0/0 | 30568 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0209c0047 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0210c0068 | 0/0 | 10800 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0211c0040 | 0/0 | 11532 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0212c0069 | 0/0 | 10800 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 13941 | 7 | 1 | 4 | 1 | 1 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0002c0002t0003 | 0/0 | 13941 | 4 | 0 | 0 | 4 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0002c0002t0007 | 0/0 | 13941 | 2 | 0 | 0 | 2 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0003c0003t0001 | 0/0 | 13941 | 4 | 0 | 0 | 4 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0003c0136t0001 | 0/0 | 13941 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0004c0026t0001 | 0/0 | 13941 | 2 | 2 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0004c0027t0001 | 0/0 | 13941 | 2 | 2 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0005c0004t0001 | 0/0 | 13209 | 3 | 0 | 0 | 3 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0005c0004t0025 | 0/0 | 13209 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0006c0211t0019 | 0/0 | 28205 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0006c0212t0002 | 0/0 | 37686 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0006c0213t0002 | 0/0 | 18692 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0006c0214t0002 | 0/0 | 23455 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0007c0005t0001 | 0/0 | 6621 | 3 | 0 | 0 | 3 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0008c0037t0001 | 0/0 | 13941 | 2 | 0 | 2 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0008c0215t0001 | 0/0 | 13941 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0009c0006t0001 | 0/0 | 13941 | 3 | 0 | 2 | 0 | 1 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0010c0007t0001 | 0/0 | 13209 | 3 | 0 | 3 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0011c0010t0001 | 0/0 | 13941 | 3 | 0 | 0 | 3 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0012c0009t0001 | 0/0 | 12447 | 3 | 0 | 0 | 3 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0013c0035t0001 | 0/0 | 13941 | 2 | 2 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0013c0162t0001 | 0/0 | 13941 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0014c0008t0003 | 0/0 | 13941 | 2 | 0 | 2 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0014c0008t0020 | 0/0 | 13941 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0015c0036t0006 | 0/0 | 13941 | 2 | 2 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0015c0192t0006 | 0/0 | 13941 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0016c0017t0001 | 0/0 | 12477 | 2 | 0 | 0 | 0 | 0 | 2 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0017c0019t0001 | 0/0 | 13941 | 2 | 2 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0018c0018t0001 | 0/0 | 13941 | 2 | 2 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0019c0021t0001 | 1/0 | 13941 | 2 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0020c0020t0001 | 0/0 | 12477 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0020c0020t0010 | 0/0 | 12477 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0021c0022t0001 | 0/0 | 13209 | 2 | 2 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0022c0023t0001 | 0/0 | 13941 | 2 | 2 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0023c0024t0001 | 0/0 | 13941 | 2 | 2 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0024c0025t0001 | 0/0 | 13941 | 2 | 2 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0025c0031t0001 | 0/1 | 13209 | 2 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0026c0030t0001 | 0/0 | 12477 | 2 | 0 | 2 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0027c0029t0001 | 0/0 | 13209 | 2 | 0 | 0 | 2 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0028c0032t0001 | 0/0 | 13941 | 2 | 1 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0029c0033t0001 | 0/0 | 13941 | 2 | 2 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0030c0034t0001 | 0/0 | 12477 | 2 | 2 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0031c0028t0003 | 0/0 | 13941 | 2 | 0 | 0 | 2 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0032c0012t0002 | 0/0 | 13941 | 2 | 0 | 2 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0033c0011t0002 | 0/0 | 13941 | 2 | 0 | 0 | 2 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0034c0013t0002 | 0/0 | 13941 | 2 | 0 | 0 | 2 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0035c0015t0002 | 0/0 | 13941 | 2 | 0 | 0 | 0 | 0 | 2 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0036c0014t0009 | 0/0 | 13941 | 2 | 0 | 0 | 2 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0037c0016t0002 | 0/0 | 13941 | 2 | 0 | 2 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0038c0038t0001 | 0/0 | 13941 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0039c0219t0002 | 0/0 | 13941 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0040c0218t0002 | 0/0 | 13941 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0041c0217t0003 | 0/0 | 13941 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0042c0195t0001 | 0/0 | 13941 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0043c0209t0004 | 0/0 | 13938 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0044c0210t0004 | 0/0 | 13938 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0045c0078t0001 | 0/0 | 13941 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0046c0077t0001 | 0/0 | 13941 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0047c0216t0001 | 0/0 | 12477 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0048c0081t0011 | 0/0 | 13941 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0049c0082t0011 | 0/0 | 13209 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0050c0080t0001 | 0/0 | 13941 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0051c0083t0001 | 0/0 | 13941 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0052c0079t0021 | 0/0 | 13941 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0053c0190t0001 | 0/0 | 13927 | 1 | 0 | 0 | 0 | 1 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0054c0085t0001 | 0/0 | 13209 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0055c0086t0001 | 0/0 | 13941 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0056c0089t0001 | 0/0 | 13941 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0057c0088t0001 | 0/0 | 13941 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0058c0087t0001 | 0/0 | 13209 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0059c0091t0001 | 0/0 | 13941 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0060c0092t0001 | 0/0 | 13941 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0061c0187t0001 | 0/0 | 13941 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0062c0093t0001 | 0/0 | 11745 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0063c0090t0003 | 0/0 | 13941 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0064c0094t0001 | 0/0 | 12477 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0065c0098t0001 | 0/0 | 13209 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0066c0097t0001 | 0/0 | 13209 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0067c0095t0001 | 0/0 | 12477 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0068c0096t0010 | 0/0 | 11013 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0069c0100t0001 | 0/0 | 13941 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0070c0101t0001 | 0/0 | 13941 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0071c0102t0001 | 0/0 | 13209 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0072c0104t0001 | 0/0 | 13941 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0073c0103t0001 | 0/0 | 13941 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0074c0112t0001 | 0/0 | 13941 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0075c0108t0001 | 0/0 | 13941 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0076c0109t0001 | 0/0 | 13941 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0077c0110t0001 | 0/0 | 13941 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0078c0111t0001 | 0/0 | 13209 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0079c0107t0001 | 0/0 | 12477 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0080c0106t0001 | 0/0 | 13941 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0081c0113t0001 | 0/0 | 13941 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0082c0117t0001 | 0/0 | 13941 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0083c0116t0023 | 0/0 | 13941 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0084c0115t0001 | 0/0 | 13941 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0085c0114t0001 | 0/0 | 13941 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0086c0119t0001 | 0/0 | 13941 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0087c0118t0001 | 0/0 | 13941 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0088c0105t0008 | 0/0 | 12477 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0089c0123t0001 | 0/0 | 13209 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0090c0121t0008 | 0/0 | 12477 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0091c0122t0008 | 0/0 | 13941 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0092c0120t0001 | 0/0 | 13209 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0093c0124t0001 | 0/0 | 13941 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0094c0125t0001 | 0/0 | 13941 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0095c0126t0001 | 0/0 | 13941 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0096c0127t0001 | 0/0 | 13941 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0097c0148t0001 | 0/0 | 13941 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0098c0147t0001 | 0/0 | 13209 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0099c0146t0001 | 0/0 | 13941 | 1 | 0 | 0 | 0 | 1 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0100c0145t0001 | 0/0 | 12477 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0101c0039t0001 | 0/0 | 13941 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0102c0144t0001 | 0/0 | 13941 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0103c0142t0001 | 0/0 | 13941 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0104c0141t0001 | 0/0 | 13434 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0105c0140t0001 | 0/0 | 13209 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0106c0139t0001 | 0/0 | 13209 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0107c0138t0001 | 0/0 | 13941 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0108c0143t0001 | 0/0 | 12477 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0109c0135t0001 | 0/0 | 13941 | 1 | 0 | 0 | 0 | 1 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0110c0133t0001 | 0/0 | 13941 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0111c0132t0001 | 0/0 | 13941 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0112c0131t0001 | 0/0 | 13941 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0113c0134t0001 | 0/0 | 12477 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0114c0137t0001 | 0/0 | 13209 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0115c0149t0026 | 0/0 | 13209 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0116c0150t0001 | 0/0 | 13209 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0117c0152t0001 | 0/0 | 13941 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0118c0151t0001 | 0/0 | 13941 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0119c0153t0001 | 0/0 | 13941 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0120c0155t0001 | 0/0 | 13209 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0121c0154t0024 | 0/0 | 13941 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0122c0156t0001 | 0/0 | 13209 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0123c0157t0001 | 0/0 | 13941 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0124c0158t0001 | 0/0 | 13941 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0125c0159t0001 | 0/0 | 13941 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0126c0130t0001 | 0/0 | 12477 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0127c0169t0001 | 0/0 | 13941 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0128c0168t0001 | 0/0 | 13941 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0129c0167t0012 | 0/0 | 13941 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0130c0170t0001 | 0/0 | 13941 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0131c0171t0001 | 0/0 | 13941 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0132c0166t0012 | 0/0 | 13941 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0133c0165t0022 | 0/0 | 13209 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0134c0164t0001 | 0/0 | 13941 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0135c0161t0001 | 0/0 | 13941 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0136c0163t0001 | 0/0 | 13941 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0137c0173t0001 | 0/0 | 13941 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0138c0174t0001 | 0/0 | 13941 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0139c0172t0001 | 0/0 | 13941 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0140c0175t0001 | 0/0 | 12447 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0141c0182t0001 | 0/0 | 12447 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0142c0180t0001 | 0/0 | 13941 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0143c0179t0001 | 0/0 | 13941 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0144c0178t0001 | 0/0 | 13941 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0145c0177t0001 | 0/0 | 13941 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0146c0176t0003 | 0/0 | 13941 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0147c0220t0001 | 0/0 | 13941 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0148c0181t0001 | 0/0 | 13941 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0149c0183t0001 | 0/0 | 13941 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0150c0160t0001 | 0/0 | 12477 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0151c0184t0001 | 0/0 | 13941 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0152c0129t0003 | 0/0 | 13941 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0153c0128t0003 | 0/0 | 13941 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0154c0185t0001 | 0/0 | 13941 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0155c0186t0007 | 0/0 | 13941 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0156c0099t0001 | 0/0 | 8817 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0157c0188t0001 | 0/0 | 9549 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0158c0084t0001 | 0/0 | 12477 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0159c0189t0003 | 0/0 | 13941 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0160c0076t0014 | 0/0 | 13941 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0161c0197t0005 | 0/0 | 13209 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0162c0196t0005 | 0/0 | 13209 | 1 | 0 | 0 | 0 | 1 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0163c0199t0005 | 0/0 | 13941 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0164c0201t0004 | 0/0 | 13938 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0165c0200t0005 | 0/0 | 13941 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0166c0198t0005 | 0/0 | 11013 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0167c0203t0028 | 0/0 | 28195 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0168c0206t0004 | 0/0 | 13938 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0169c0205t0004 | 0/0 | 13938 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0170c0208t0004 | 0/0 | 13938 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0171c0207t0004 | 0/0 | 13938 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0172c0204t0004 | 0/0 | 13938 | 1 | 0 | 0 | 0 | 1 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0173c0191t0006 | 0/0 | 13941 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0174c0202t0013 | 0/0 | 13938 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0175c0193t0001 | 0/0 | 13209 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0176c0194t0001 | 0/0 | 13209 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0177c0075t0001 | 0/0 | 11745 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0178c0070t0002 | 0/0 | 13941 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0179c0071t0002 | 0/0 | 13941 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0180c0072t0002 | 0/0 | 13941 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0181c0073t0002 | 0/0 | 13941 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0182c0074t0002 | 0/0 | 13941 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0183c0041t0002 | 0/0 | 13209 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0184c0042t0002 | 0/0 | 13209 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0185c0043t0002 | 0/0 | 12477 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0186c0044t0017 | 0/0 | 13941 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0187c0050t0002 | 0/0 | 12477 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0188c0051t0002 | 0/0 | 13209 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0189c0052t0027 | 0/0 | 13209 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0190c0049t0002 | 0/0 | 13209 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0191c0054t0002 | 0/0 | 13941 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0192c0055t0002 | 0/0 | 13941 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0193c0057t0002 | 0/0 | 13941 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0194c0058t0002 | 0/0 | 13941 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0195c0060t0002 | 0/0 | 13941 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0196c0045t0018 | 0/0 | 13941 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0197c0066t0002 | 0/0 | 28204 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0198c0059t0002 | 0/0 | 13941 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0199c0061t0002 | 0/0 | 13941 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0200c0062t0002 | 0/0 | 13941 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0201c0063t0002 | 0/0 | 13209 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0202c0064t0002 | 0/0 | 13941 | 1 | 0 | 0 | 0 | 1 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0203c0065t0002 | 0/0 | 13941 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0204c0067t0002 | 0/0 | 13941 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0205c0056t0015 | 0/0 | 13941 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0206c0053t0002 | 0/0 | 13209 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0207c0046t0002 | 0/0 | 37734 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0208c0048t0002 | 0/0 | 32977 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0209c0047t0002 | 0/0 | 13941 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0210c0068t0016 | 0/0 | 13209 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0211c0040t0002 | 0/0 | 13941 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| a0212c0069t0002 | 0/0 | 13209 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | copy fasta | chr1 | 149470045 | 149561361 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0002c0002t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0002c0002t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0002c0002t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0002c0002t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0002c0002t0007g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0002c0002t0007g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0003c0003t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0003c0003t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0003c0003t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0003c0003t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0003c0136t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0004c0026t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0004c0026t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0004c0027t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0005c0004t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0005c0004t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0005c0004t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0005c0004t0025g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0006c0211t0019g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0006c0212t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0006c0213t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0006c0214t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0007c0005t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0007c0005t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0007c0005t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0008c0037t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0008c0037t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0008c0215t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0009c0006t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0009c0006t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0009c0006t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0010c0007t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0010c0007t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0011c0010t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0011c0010t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0011c0010t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0012c0009t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0012c0009t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0012c0009t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0013c0035t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0013c0035t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0013c0162t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0014c0008t0003g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0014c0008t0003g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0014c0008t0020g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0015c0036t0006g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0015c0192t0006g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0016c0017t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0016c0017t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0017c0019t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0017c0019t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0018c0018t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0018c0018t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0019c0021t0001g0046 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0019c0021t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0020c0020t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0020c0020t0010g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0021c0022t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0021c0022t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0022c0023t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0022c0023t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0023c0024t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0024c0025t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0024c0025t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0025c0031t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0025c0031t0001g0033 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0026c0030t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0026c0030t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0027c0029t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0027c0029t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0028c0032t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0028c0032t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0029c0033t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0029c0033t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0030c0034t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0030c0034t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0031c0028t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0031c0028t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0032c0012t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0032c0012t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0033c0011t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0033c0011t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0034c0013t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0034c0013t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0035c0015t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0035c0015t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0036c0014t0009g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0036c0014t0009g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0037c0016t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0037c0016t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0038c0038t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0039c0219t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0040c0218t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0041c0217t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0042c0195t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0043c0209t0004g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0044c0210t0004g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0045c0078t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0046c0077t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0047c0216t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0048c0081t0011g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0049c0082t0011g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0050c0080t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0051c0083t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0052c0079t0021g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0053c0190t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0054c0085t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0055c0086t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0056c0089t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0057c0088t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0058c0087t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0059c0091t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0060c0092t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0061c0187t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0062c0093t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0063c0090t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0064c0094t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0065c0098t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0066c0097t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0067c0095t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0068c0096t0010g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0069c0100t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0070c0101t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0071c0102t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0072c0104t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0073c0103t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0074c0112t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0075c0108t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0076c0109t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0077c0110t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0078c0111t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0079c0107t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0080c0106t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0081c0113t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0082c0117t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0083c0116t0023g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0084c0115t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0085c0114t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0086c0119t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0087c0118t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0088c0105t0008g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0089c0123t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0090c0121t0008g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0091c0122t0008g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0092c0120t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0093c0124t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0094c0125t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0095c0126t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0096c0127t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0097c0148t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0098c0147t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0099c0146t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0100c0145t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0101c0039t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0102c0144t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0103c0142t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0104c0141t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0105c0140t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0106c0139t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0107c0138t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0108c0143t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0109c0135t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0110c0133t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0111c0132t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0112c0131t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0113c0134t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0114c0137t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0115c0149t0026g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0116c0150t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0117c0152t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0118c0151t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0119c0153t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0120c0155t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0121c0154t0024g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0122c0156t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0123c0157t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0124c0158t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0125c0159t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0126c0130t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0127c0169t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0128c0168t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0129c0167t0012g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0130c0170t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0131c0171t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0132c0166t0012g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0133c0165t0022g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0134c0164t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0135c0161t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0136c0163t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0137c0173t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0138c0174t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0139c0172t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0140c0175t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0141c0182t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0142c0180t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0143c0179t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0144c0178t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0145c0177t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0146c0176t0003g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0147c0220t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0148c0181t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0149c0183t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0150c0160t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0151c0184t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0152c0129t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0153c0128t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0154c0185t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0155c0186t0007g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0156c0099t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0157c0188t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0158c0084t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0159c0189t0003g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0160c0076t0014g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0161c0197t0005g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0162c0196t0005g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0163c0199t0005g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0164c0201t0004g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0165c0200t0005g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0166c0198t0005g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0167c0203t0028g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0168c0206t0004g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0169c0205t0004g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0170c0208t0004g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0171c0207t0004g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0172c0204t0004g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0173c0191t0006g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0174c0202t0013g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0175c0193t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0176c0194t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0177c0075t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0178c0070t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0179c0071t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0180c0072t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0181c0073t0002g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0182c0074t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0183c0041t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0184c0042t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0185c0043t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0186c0044t0017g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0187c0050t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0188c0051t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0189c0052t0027g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0190c0049t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0191c0054t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0192c0055t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0193c0057t0002g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0194c0058t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0195c0060t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0196c0045t0018g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0197c0066t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0198c0059t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0199c0061t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0200c0062t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0201c0063t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0202c0064t0002g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0203c0065t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0204c0067t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0205c0056t0015g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0206c0053t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0207c0046t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0208c0048t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0209c0047t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0210c0068t0016g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0211c0040t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| a0212c0069t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0009 | c0006 | t0001 | g0081 | EUR | GBR | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0077 | EUR | GBR | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG00408 | hp1 | a0101 | c0039 | t0001 | g0079 | EAS | CHS | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG00408 | hp2 | a0007 | c0005 | t0001 | g0155 | EAS | CHS | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG00423 | hp1 | a0102 | c0144 | t0001 | g0127 | EAS | CHS | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG00423 | hp2 | a0086 | c0119 | t0001 | g0085 | EAS | CHS | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG00438 | hp1 | a0012 | c0009 | t0001 | g0172 | EAS | CHS | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG00438 | hp2 | a0203 | c0065 | t0002 | g0240 | EAS | CHS | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG00544 | hp1 | a0003 | c0003 | t0001 | g0170 | EAS | CHS | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG00544 | hp2 | a0165 | c0200 | t0005 | g0212 | EAS | CHS | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG00558 | hp1 | a0141 | c0182 | t0001 | g0122 | EAS | CHS | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG00558 | hp2 | a0163 | c0199 | t0005 | g0215 | EAS | CHS | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG00609 | hp1 | a0007 | c0005 | t0001 | g0154 | EAS | CHS | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG00609 | hp2 | a0071 | c0102 | t0001 | g0143 | EAS | CHS | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG00621 | hp1 | a0194 | c0058 | t0002 | g0235 | EAS | CHS | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG00621 | hp2 | a0205 | c0056 | t0015 | g0258 | EAS | CHS | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG00642 | hp1 | a0037 | c0016 | t0002 | g0256 | AMR | PUR | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG00642 | hp2 | a0159 | c0189 | t0003 | g0191 | AMR | PUR | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG00733 | hp1 | a0135 | c0161 | t0001 | g0057 | AMR | PUR | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG00733 | hp2 | a0107 | c0138 | t0001 | g0072 | AMR | PUR | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG00735 | hp1 | a0164 | c0201 | t0004 | g0205 | AMR | PUR | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG00735 | hp2 | a0161 | c0197 | t0005 | g0214 | AMR | PUR | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG00738 | hp1 | a0179 | c0071 | t0002 | g0260 | AMR | PUR | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG00738 | hp2 | a0098 | c0147 | t0001 | g0031 | AMR | PUR | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG00741 | hp1 | a0008 | c0037 | t0001 | g0135 | AMR | PUR | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG00741 | hp2 | a0009 | c0006 | t0001 | g0082 | AMR | PUR | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG01069 | hp1 | a0010 | c0007 | t0001 | g0002 | AMR | PUR | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG01069 | hp2 | a0037 | c0016 | t0002 | g0257 | AMR | PUR | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG01071 | hp1 | a0014 | c0008 | t0003 | g0186 | AMR | PUR | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG01071 | hp2 | a0010 | c0007 | t0001 | g0002 | AMR | PUR | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG01074 | hp1 | a0130 | c0170 | t0001 | g0120 | AMR | PUR | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG01074 | hp2 | a0020 | c0020 | t0010 | g0043 | AMR | PUR | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG01081 | hp1 | a0032 | c0012 | t0002 | g0232 | AMR | PUR | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG01081 | hp2 | a0138 | c0174 | t0001 | g0109 | AMR | PUR | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG01099 | hp1 | a0168 | c0206 | t0004 | g0203 | AMR | PUR | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG01109 | hp1 | a0048 | c0081 | t0011 | g0151 | AMR | PUR | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG01109 | hp2 | a0089 | c0123 | t0001 | g0164 | AMR | PUR | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG01168 | hp1 | a0026 | c0030 | t0001 | g0030 | AMR | PUR | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG01168 | hp2 | a0142 | c0180 | t0001 | g0108 | AMR | PUR | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG01257 | hp1 | a0010 | c0007 | t0001 | g0045 | AMR | CLM | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG01257 | hp2 | a0150 | c0160 | t0001 | g0107 | AMR | CLM | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG01346 | hp2 | a0182 | c0074 | t0002 | g0261 | AMR | CLM | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG01358 | hp1 | a0128 | c0168 | t0001 | g0106 | AMR | CLM | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG01358 | hp2 | a0189 | c0052 | t0027 | g0231 | AMR | CLM | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG01496 | hp1 | a0008 | c0215 | t0001 | g0067 | AMR | CLM | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG01496 | hp2 | a0026 | c0030 | t0001 | g0035 | AMR | CLM | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG01516 | hp1 | a0162 | c0196 | t0005 | g0213 | EUR | IBS | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG01516 | hp2 | a0053 | c0190 | t0001 | g0064 | EUR | IBS | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG01517 | hp1 | a0109 | c0135 | t0001 | g0063 | EUR | IBS | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG01517 | hp2 | a0099 | c0146 | t0001 | g0034 | EUR | IBS | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG01891 | hp1 | a0006 | c0212 | t0002 | g0223 | AFR | ACB | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG01891 | hp2 | a0004 | c0026 | t0001 | g0008 | AFR | ACB | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG01928 | hp1 | a0077 | c0110 | t0001 | g0178 | AMR | PEL | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG01928 | hp2 | a0008 | c0037 | t0001 | g0075 | AMR | PEL | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG01934 | hp1 | a0009 | c0006 | t0001 | g0139 | AMR | PEL | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG01934 | hp2 | a0047 | c0216 | t0001 | g0068 | AMR | PEL | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG01952 | hp1 | a0068 | c0096 | t0010 | g0090 | AMR | PEL | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG01952 | hp2 | a0210 | c0068 | t0016 | g0233 | AMR | PEL | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG01975 | hp1 | a0014 | c0008 | t0020 | g0184 | AMR | PEL | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PEL | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG01978 | hp1 | a0050 | c0080 | t0001 | g0177 | AMR | PEL | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG01978 | hp2 | a0059 | c0091 | t0001 | g0130 | AMR | PEL | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG02027 | hp2 | a0117 | c0152 | t0001 | g0087 | EAS | KHV | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG02040 | hp1 | a0121 | c0154 | t0024 | g0091 | EAS | KHV | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG02040 | hp2 | a0193 | c0057 | t0002 | g0006 | EAS | KHV | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG02055 | hp1 | a0123 | c0157 | t0001 | g0015 | AFR | ACB | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG02055 | hp2 | a0024 | c0025 | t0001 | g0026 | AFR | ACB | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG02080 | hp1 | a0120 | c0155 | t0001 | g0126 | EAS | KHV | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG02080 | hp2 | a0208 | c0048 | t0002 | g0251 | EAS | KHV | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG02083 | hp1 | a0197 | c0066 | t0002 | g0238 | EAS | KHV | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG02083 | hp2 | a0073 | c0103 | t0001 | g0018 | EAS | KHV | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG02129 | hp1 | a0144 | c0178 | t0001 | g0119 | EAS | KHV | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG02129 | hp2 | a0204 | c0067 | t0002 | g0248 | EAS | KHV | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG02135 | hp1 | a0132 | c0166 | t0012 | g0179 | EAS | KHV | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG02135 | hp2 | a0157 | c0188 | t0001 | g0201 | EAS | KHV | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG02145 | hp1 | a0173 | c0191 | t0006 | g0271 | AFR | ACB | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG02145 | hp2 | a0061 | c0187 | t0001 | g0173 | AFR | ACB | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG02148 | hp1 | a0014 | c0008 | t0003 | g0181 | AMR | PEL | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG02148 | hp2 | a0032 | c0012 | t0002 | g0266 | AMR | PEL | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG02155 | hp1 | a0200 | c0062 | t0002 | g0237 | EAS | CDX | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG02155 | hp2 | a0054 | c0085 | t0001 | g0150 | EAS | CDX | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG02165 | hp1 | a0043 | c0209 | t0004 | g0207 | EAS | CDX | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG02165 | hp2 | a0041 | c0217 | t0003 | g0185 | EAS | CDX | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG02257 | hp1 | a0018 | c0018 | t0001 | g0166 | AFR | ACB | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG02257 | hp2 | a0076 | c0109 | t0001 | g0137 | AFR | ACB | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG02258 | hp1 | a0062 | c0093 | t0001 | g0267 | AFR | ACB | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG02258 | hp2 | a0013 | c0035 | t0001 | g0038 | AFR | ACB | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG02280 | hp1 | a0013 | c0035 | t0001 | g0084 | AFR | ACB | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG02280 | hp2 | a0021 | c0022 | t0001 | g0080 | AFR | ACB | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG02300 | hp1 | a0052 | c0079 | t0021 | g0176 | AMR | PEL | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG02300 | hp2 | a0066 | c0097 | t0001 | g0175 | AMR | PEL | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG02572 | hp1 | a0093 | c0124 | t0001 | g0153 | AFR | GWD | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG02572 | hp2 | a0022 | c0023 | t0001 | g0160 | AFR | GWD | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG02602 | hp1 | a0145 | c0177 | t0001 | g0165 | SAS | PJL | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG02602 | hp2 | a0186 | c0044 | t0017 | g0239 | SAS | PJL | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG02622 | hp1 | a0133 | c0165 | t0022 | g0020 | AFR | GWD | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG02622 | hp2 | a0160 | c0076 | t0014 | g0225 | AFR | GWD | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG02630 | hp1 | a0022 | c0023 | t0001 | g0156 | AFR | GWD | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG02630 | hp2 | a0023 | c0024 | t0001 | g0003 | AFR | GWD | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG02647 | hp2 | a0092 | c0120 | t0001 | g0141 | AFR | GWD | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG02683 | hp1 | a0051 | c0083 | t0001 | g0162 | SAS | PJL | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG02683 | hp2 | a0126 | c0130 | t0001 | g0134 | SAS | PJL | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG02698 | hp1 | a0171 | c0207 | t0004 | g0208 | SAS | PJL | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG02698 | hp2 | a0143 | c0179 | t0001 | g0021 | SAS | PJL | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG02717 | hp1 | a0096 | c0127 | t0001 | g0111 | AFR | GWD | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG02717 | hp2 | a0023 | c0024 | t0001 | g0003 | AFR | GWD | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG02738 | hp1 | a0049 | c0082 | t0011 | g0096 | SAS | PJL | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG02738 | hp2 | a0019 | c0021 | t0001 | g0098 | SAS | PJL | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG02809 | hp1 | a0095 | c0126 | t0001 | g0140 | AFR | GWD | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG02809 | hp2 | a0028 | c0032 | t0001 | g0161 | AFR | GWD | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG02895 | hp1 | a0006 | c0211 | t0019 | g0211 | AFR | GWD | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG02895 | hp2 | a0004 | c0027 | t0001 | g0001 | AFR | GWD | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG02896 | hp1 | a0015 | c0036 | t0006 | g0004 | AFR | GWD | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG02896 | hp2 | a0088 | c0105 | t0008 | g0100 | AFR | GWD | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG02897 | hp1 | a0015 | c0036 | t0006 | g0004 | AFR | GWD | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG02897 | hp2 | a0004 | c0027 | t0001 | g0001 | AFR | GWD | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG02922 | hp1 | a0125 | c0159 | t0001 | g0147 | AFR | ESN | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG02922 | hp2 | a0084 | c0115 | t0001 | g0114 | AFR | ESN | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG02965 | hp1 | a0158 | c0084 | t0001 | g0049 | AFR | ESN | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG02965 | hp2 | a0013 | c0162 | t0001 | g0040 | AFR | ESN | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG02976 | hp1 | a0082 | c0117 | t0001 | g0009 | AFR | ESN | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG02976 | hp2 | a0154 | c0185 | t0001 | g0152 | AFR | ESN | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG03017 | hp1 | a0124 | c0158 | t0001 | g0095 | SAS | PJL | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG03017 | hp2 | a0035 | c0015 | t0002 | g0216 | SAS | PJL | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG03041 | hp1 | a0119 | c0153 | t0001 | g0097 | AFR | GWD | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG03041 | hp2 | a0046 | c0077 | t0001 | g0083 | AFR | GWD | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG03098 | hp1 | a0029 | c0033 | t0001 | g0198 | AFR | MSL | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG03098 | hp2 | a0116 | c0150 | t0001 | g0014 | AFR | MSL | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG03130 | hp1 | a0134 | c0164 | t0001 | g0039 | AFR | ESN | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG03130 | hp2 | a0015 | c0192 | t0006 | g0270 | AFR | ESN | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG03139 | hp1 | a0074 | c0112 | t0001 | g0104 | AFR | ESN | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG03139 | hp2 | a0045 | c0078 | t0001 | g0099 | AFR | ESN | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG03195 | hp1 | a0004 | c0026 | t0001 | g0007 | AFR | ESN | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG03195 | hp2 | a0030 | c0034 | t0001 | g0093 | AFR | ESN | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG03209 | hp1 | a0021 | c0022 | t0001 | g0169 | AFR | MSL | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG03209 | hp2 | a0091 | c0122 | t0008 | g0157 | AFR | MSL | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG03225 | hp1 | a0029 | c0033 | t0001 | g0197 | AFR | MSL | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG03225 | hp2 | a0137 | c0173 | t0001 | g0159 | AFR | MSL | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG03239 | hp1 | a0105 | c0140 | t0001 | g0037 | SAS | PJL | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG03239 | hp2 | a0016 | c0017 | t0001 | g0028 | SAS | PJL | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG03486 | hp1 | a0080 | c0106 | t0001 | g0019 | AFR | MSL | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG03486 | hp2 | a0058 | c0087 | t0001 | g0048 | AFR | MSL | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG03516 | hp1 | a0055 | c0086 | t0001 | g0168 | AFR | ESN | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG03516 | hp2 | a0081 | c0113 | t0001 | g0148 | AFR | ESN | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG03654 | hp1 | a0122 | c0156 | t0001 | g0086 | SAS | PJL | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG03654 | hp2 | a0065 | c0098 | t0001 | g0101 | SAS | PJL | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG03669 | hp1 | a0025 | c0031 | t0001 | g0032 | SAS | PJL | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG03669 | hp2 | a0056 | c0089 | t0001 | g0060 | SAS | PJL | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG03688 | hp1 | a0003 | c0136 | t0001 | g0005 | SAS | STU | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG03688 | hp2 | a0057 | c0088 | t0001 | g0089 | SAS | STU | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG03704 | hp1 | a0028 | c0032 | t0001 | g0036 | SAS | PJL | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG03704 | hp2 | a0035 | c0015 | t0002 | g0217 | SAS | PJL | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG03710 | hp1 | a0064 | c0094 | t0001 | g0047 | SAS | PJL | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG03710 | hp2 | a0146 | c0176 | t0003 | g0110 | SAS | PJL | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG03831 | hp1 | a0181 | c0073 | t0002 | g0272 | SAS | BEB | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG03831 | hp2 | a0020 | c0020 | t0001 | g0041 | SAS | BEB | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG03942 | hp1 | a0196 | c0045 | t0018 | g0226 | SAS | BEB | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG03942 | hp2 | a0166 | c0198 | t0005 | g0210 | SAS | BEB | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG04115 | hp1 | a0169 | c0205 | t0004 | g0209 | SAS | STU | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG04115 | hp2 | a0176 | c0194 | t0001 | g0129 | SAS | STU | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG04184 | hp1 | a0148 | c0181 | t0001 | g0124 | SAS | BEB | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG04184 | hp2 | a0175 | c0193 | t0001 | g0128 | SAS | BEB | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG04199 | hp1 | a0149 | c0183 | t0001 | g0022 | SAS | STU | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG04199 | hp2 | a0016 | c0017 | t0001 | g0029 | SAS | STU | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG04204 | hp1 | a0180 | c0072 | t0002 | g0218 | SAS | STU | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG04204 | hp2 | a0067 | c0095 | t0001 | g0042 | SAS | STU | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA18522 | hp1 | a0087 | c0118 | t0001 | g0054 | AFR | YRI | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA18522 | hp2 | a0024 | c0025 | t0001 | g0024 | AFR | YRI | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA18612 | hp1 | a0003 | c0003 | t0001 | g0115 | EAS | CHB | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA18612 | hp2 | a0187 | c0050 | t0002 | g0250 | EAS | CHB | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA18747 | hp1 | a0072 | c0104 | t0001 | g0017 | EAS | CHB | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA18747 | hp2 | a0184 | c0042 | t0002 | g0236 | EAS | CHB | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA18906 | hp1 | a0083 | c0116 | t0023 | g0103 | AFR | YRI | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA18906 | hp2 | a0030 | c0034 | t0001 | g0092 | AFR | YRI | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA18939 | hp1 | a0027 | c0029 | t0001 | g0061 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA18939 | hp2 | a0209 | c0047 | t0002 | g0242 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA18942 | hp1 | a0002 | c0002 | t0007 | g0193 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA18942 | hp2 | a0111 | c0132 | t0001 | g0199 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA18946 | hp1 | a0152 | c0129 | t0003 | g0192 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA18946 | hp2 | a0211 | c0040 | t0002 | g0243 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA18947 | hp1 | a0106 | c0139 | t0001 | g0055 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA18947 | hp2 | a0033 | c0011 | t0002 | g0254 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA18954 | hp1 | a0070 | c0101 | t0001 | g0044 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA18954 | hp2 | a0206 | c0053 | t0002 | g0249 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA18957 | hp1 | a0103 | c0142 | t0001 | g0074 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA18957 | hp2 | a0198 | c0059 | t0002 | g0259 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA18959 | hp1 | a0191 | c0054 | t0002 | g0264 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA18959 | hp2 | a0060 | c0092 | t0001 | g0069 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA18960 | hp1 | a0036 | c0014 | t0009 | g0230 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA18960 | hp2 | a0002 | c0002 | t0007 | g0190 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA18961 | hp1 | a0034 | c0013 | t0002 | g0221 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA18961 | hp2 | a0002 | c0002 | t0003 | g0189 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA18962 | hp1 | a0174 | c0202 | t0013 | g0204 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA18962 | hp2 | a0190 | c0049 | t0002 | g0244 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA18963 | hp1 | a0100 | c0145 | t0001 | g0076 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA18963 | hp2 | a0188 | c0051 | t0002 | g0252 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA18967 | hp1 | a0002 | c0002 | t0003 | g0196 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA18967 | hp2 | a0151 | c0184 | t0001 | g0174 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA18969 | hp1 | a0131 | c0171 | t0001 | g0145 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA18969 | hp2 | a0155 | c0186 | t0007 | g0183 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA18972 | hp1 | a0044 | c0210 | t0004 | g0206 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA18972 | hp2 | a0031 | c0028 | t0003 | g0180 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA18977 | hp1 | a0005 | c0004 | t0001 | g0131 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA18977 | hp2 | a0147 | c0220 | t0001 | g0094 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA18980 | hp1 | a0012 | c0009 | t0001 | g0195 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA18980 | hp2 | a0153 | c0128 | t0003 | g0125 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA18981 | hp1 | a0039 | c0219 | t0002 | g0227 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA18981 | hp2 | a0011 | c0010 | t0001 | g0012 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA18982 | hp1 | a0212 | c0069 | t0002 | g0245 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA18982 | hp2 | a0113 | c0134 | t0001 | g0065 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA18983 | hp1 | a0207 | c0046 | t0002 | g0241 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA18983 | hp2 | a0118 | c0151 | t0001 | g0053 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA18984 | hp1 | a0079 | c0107 | t0001 | g0059 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA18984 | hp2 | a0104 | c0141 | t0001 | g0123 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA18985 | hp1 | a0005 | c0004 | t0001 | g0132 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA18985 | hp2 | a0036 | c0014 | t0009 | g0228 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA18990 | hp1 | a0040 | c0218 | t0002 | g0234 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA18990 | hp2 | a0005 | c0004 | t0025 | g0073 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA18994 | hp1 | a0114 | c0137 | t0001 | g0133 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA18994 | hp2 | a0192 | c0055 | t0002 | g0263 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA18998 | hp1 | a0185 | c0043 | t0002 | g0247 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA18998 | hp2 | a0112 | c0131 | t0001 | g0118 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA19005 | hp1 | a0002 | c0002 | t0003 | g0188 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA19005 | hp2 | a0183 | c0041 | t0002 | g0246 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA19011 | hp1 | a0199 | c0061 | t0002 | g0219 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA19011 | hp2 | a0069 | c0100 | t0001 | g0016 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA19012 | hp1 | a0034 | c0013 | t0002 | g0220 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA19012 | hp2 | a0027 | c0029 | t0001 | g0062 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA19030 | hp1 | a0075 | c0108 | t0001 | g0163 | AFR | LWK | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA19030 | hp2 | a0090 | c0121 | t0008 | g0149 | AFR | LWK | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA19043 | hp1 | a0115 | c0149 | t0026 | g0142 | AFR | LWK | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA19043 | hp2 | a0177 | c0075 | t0001 | g0146 | AFR | LWK | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA19062 | hp1 | a0201 | c0063 | t0002 | g0222 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA19062 | hp2 | a0156 | c0099 | t0001 | g0013 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA19065 | hp1 | a0011 | c0010 | t0001 | g0010 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA19065 | hp2 | a0003 | c0003 | t0001 | g0117 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA19066 | hp1 | a0038 | c0038 | t0001 | g0171 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA19066 | hp2 | a0012 | c0009 | t0001 | g0050 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA19068 | hp1 | a0129 | c0167 | t0012 | g0088 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA19068 | hp2 | a0003 | c0003 | t0001 | g0116 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA19074 | hp1 | a0140 | c0175 | t0001 | g0051 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA19074 | hp2 | a0110 | c0133 | t0001 | g0058 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA19079 | hp1 | a0127 | c0169 | t0001 | g0052 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA19079 | hp2 | a0005 | c0004 | t0001 | g0056 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA19082 | hp1 | a0178 | c0070 | t0002 | g0253 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA19082 | hp2 | a0002 | c0002 | t0003 | g0182 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA19084 | hp1 | a0033 | c0011 | t0002 | g0255 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA19084 | hp2 | a0007 | c0005 | t0001 | g0144 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA19087 | hp1 | a0195 | c0060 | t0002 | g0229 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA19087 | hp2 | a0063 | c0090 | t0003 | g0187 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA19088 | hp1 | a0011 | c0010 | t0001 | g0011 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA19088 | hp2 | a0031 | c0028 | t0003 | g0194 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA19240 | hp1 | a0017 | c0019 | t0001 | g0112 | AFR | YRI | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA19240 | hp2 | a0006 | c0213 | t0002 | g0224 | AFR | YRI | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA20129 | hp1 | a0170 | c0208 | t0004 | g0202 | AFR | ASW | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA20129 | hp2 | a0006 | c0214 | t0002 | g0265 | AFR | ASW | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA20752 | hp1 | a0202 | c0064 | t0002 | g0262 | EUR | TSI | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA20752 | hp2 | a0172 | c0204 | t0004 | g0268 | EUR | TSI | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG01123 | hp1 | a0108 | c0143 | t0001 | g0027 | AMR | CLM | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG02109 | hp1 | a0018 | c0018 | t0001 | g0113 | AFR | ACB | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG02109 | hp2 | a0167 | c0203 | t0028 | g0269 | AFR | ACB | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG02486 | hp1 | a0042 | c0195 | t0001 | g0023 | AFR | ACB | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG02486 | hp2 | a0017 | c0019 | t0001 | g0167 | AFR | ACB | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG02559 | hp1 | a0139 | c0172 | t0001 | g0105 | AFR | ACB | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG02559 | hp2 | a0085 | c0114 | t0001 | g0025 | AFR | ACB | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG03471 | hp1 | a0094 | c0125 | t0001 | g0138 | AFR | MSL | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| HG03471 | hp2 | a0078 | c0111 | t0001 | g0102 | AFR | MSL | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA18955 | hp1 | a0097 | c0148 | t0001 | g0066 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| NA18955 | hp2 | a0136 | c0163 | t0001 | g0200 | EAS | JPT | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| homoSapiens_chm13v2 | hp1 | a0025 | c0031 | t0001 | g0033 | REF | REF | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| homoSapiens_grch38 | hp1 | a0019 | c0021 | t0001 | g0046 | REF | REF | NBPF19_chr1_149470045_149561361 | NBPF19 | chr1 | 149470045 | 149561361 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:149477947
|
T | C | 1 | a0038 | 1 | NA19066.hp1 | missense_variant&splice_region_variant | MODERATE | c.178T>C | p.Tyr60His | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 3/94 | 964/13941 | 178/11532 | 60/3843 | chr1 | 149477947 | ||
| chr1:149478042
|
G | T | 2 | a0039a0040 | 2 | NA18981.hp1 NA18990.hp1 |
missense_variant | MODERATE | c.273G>T | p.Glu91Asp | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 3/94 | 1059/13941 | 273/11532 | 91/3843 | chr1 | 149478042 | ||
| chr1:149478911
|
C | T | 1 | a0041 | 1 | HG02165.hp2 | stop_gained | HIGH | c.310C>T | p.Arg104* | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 4/94 | 1096/13941 | 310/11532 | 104/3843 | chr1 | 149478911 | ||
| chr1:149486155
|
G | A | 43 | a0032a0033a0034others(40): Show | 49 | HG00438.hp2 HG00621.hp1 HG00621.hp2 others(46): Show |
missense_variant | MODERATE | c.850G>A | p.Glu284Lys | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 8/94 | 1636/13941 | 850/11532 | 284/3843 | chr1 | 149486155 | ||
| chr1:149488070
|
T | G | 1 | a0177 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.1098T>G | p.Asp366Glu | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 10/94 | 1884/13941 | 1098/11532 | 366/3843 | chr1 | 149488070 | ||
| chr1:149488158
|
C | T | 1 | a0042 | 1 | HG02486.hp1 | missense_variant | MODERATE | c.1186C>T | p.Arg396Cys | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 10/94 | 1972/13941 | 1186/11532 | 396/3843 | chr1 | 149488158 | ||
| chr1:149488173
|
A | G | 1 | a0042 | 1 | HG02486.hp1 | missense_variant | MODERATE | c.1201A>G | p.Ile401Val | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 10/94 | 1987/13941 | 1201/11532 | 401/3843 | chr1 | 149488173 | ||
| chr1:149488177
|
A | T | 2 | a0175a0176 | 2 | HG04115.hp2 HG04184.hp2 |
missense_variant | MODERATE | c.1205A>T | p.Asp402Val | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 10/94 | 1991/13941 | 1205/11532 | 402/3843 | chr1 | 149488177 | ||
| chr1:149489581
|
A | C | 2 | a0043a0044 | 2 | HG02165.hp1 NA18972.hp1 |
missense_variant | MODERATE | c.1286A>C | p.Asp429Ala | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 12/94 | 2072/13941 | 1286/11532 | 429/3843 | chr1 | 149489581 | ||
| chr1:149489610
|
T | C | 2 | a0043a0044 | 2 | HG02165.hp1 NA18972.hp1 |
missense_variant | MODERATE | c.1315T>C | p.Ser439Pro | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 12/94 | 2101/13941 | 1315/11532 | 439/3843 | chr1 | 149489610 | ||
| chr1:149489623
|
G | T | 10 | a0006a0015a0167others(7): Show | 12 | HG01099.hp1 HG02109.hp2 HG02145.hp1 others(9): Show |
missense_variant | MODERATE | c.1328G>T | p.Cys443Phe | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 12/94 | 2114/13941 | 1328/11532 | 443/3843 | chr1 | 149489623 | ||
| chr1:149489632
|
T | C | 56 | a0006a0015a0032others(53): Show | 65 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(62): Show |
missense_variant | MODERATE | c.1337T>C | p.Ile446Thr | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 12/94 | 2123/13941 | 1337/11532 | 446/3843 | chr1 | 149489632 | ||
| chr1:149490479
|
A | G | 4 | a0006a0043a0044others(1): Show | 4 | HG01891.hp1 HG02165.hp1 NA18972.hp1 others(1): Show |
missense_variant | MODERATE | c.1475A>G | p.Asp492Gly | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 13/94 | 2261/13941 | 1475/11532 | 492/3843 | chr1 | 149490479 | ||
| chr1:149490900
|
GTGTGTGT others(9503): Show |
G | 1 | a0062 | 1 | HG02258.hp1 | exon_loss_variant | HIGH | c.1491-218_2955-227d others(2): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 14/94 | INFO_REALIGN_3_PRIME | chr1 | 149490900 | |||||
| chr1:149491155
|
G | C | 14 | a0006a0007a0008others(11): Show | 19 | HG00408.hp2 HG00609.hp1 HG00741.hp1 others(16): Show |
missense_variant | MODERATE | c.1507G>C | p.Val503Leu | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 14/94 | 2293/13941 | 1507/11532 | 503/3843 | chr1 | 149491155 | ||
| chr1:149491265
|
T | G | 1 | a0174 | 1 | NA18962.hp1 | missense_variant | MODERATE | c.1617T>G | p.Phe539Leu | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 14/94 | 2403/13941 | 1617/11532 | 539/3843 | chr1 | 149491265 | ||
| chr1:149492041
|
GGAAGGGG others(7): Show |
G | 1 | a0053 | 1 | HG01516.hp2 | frameshift_variant | HIGH | c.1692_1705delAAGAAG others(8): Show |
p.Arg565fs | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 15/94 | 2478/13941 | 1692/11532 | 564/3843 | INFO_REALIGN_3_PRIME | chr1 | 149492041 | |
| chr1:149492125
|
C | G | 1 | a0159 | 1 | HG00642.hp2 | missense_variant | MODERATE | c.1763C>G | p.Pro588Arg | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 15/94 | 2549/13941 | 1763/11532 | 588/3843 | chr1 | 149492125 | ||
| chr1:149492561
|
CTCTCTCT others(4750): Show |
C | 2 | a0092a0177 | 2 | HG02647.hp2 NA19043.hp2 |
exon_loss_variant | HIGH | c.1773-136_2505-137d others(2): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 16/94 | INFO_REALIGN_3_PRIME | chr1 | 149492561 | |||||
| chr1:149492809
|
T | C | 1 | a0211 | 1 | NA18946.hp2 | missense_variant | MODERATE | c.1814T>C | p.Leu605Ser | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 16/94 | 2600/13941 | 1814/11532 | 605/3843 | chr1 | 149492809 | ||
| chr1:149492920
|
G | C | 1 | a0167 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.1925G>C | p.Gly642Ala | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 16/94 | 2711/13941 | 1925/11532 | 642/3843 | chr1 | 149492920 | ||
| chr1:149494380
|
G | T | 3 | a0006a0015a0173 | 6 | HG02145.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
missense_variant | MODERATE | c.2060G>T | p.Cys687Phe | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 18/94 | 2846/13941 | 2060/11532 | 687/3843 | chr1 | 149494380 | ||
| chr1:149494389
|
T | C | 5 | a0006a0015a0158others(2): Show | 8 | HG02145.hp1 HG02896.hp1 HG02897.hp1 others(5): Show |
missense_variant | MODERATE | c.2069T>C | p.Ile690Thr | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 18/94 | 2855/13941 | 2069/11532 | 690/3843 | chr1 | 149494389 | ||
| chr1:149494470
|
G | A | 1 | a0054 | 1 | HG02155.hp2 | missense_variant | MODERATE | c.2150G>A | p.Gly717Asp | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 18/94 | 2936/13941 | 2150/11532 | 717/3843 | chr1 | 149494470 | ||
| chr1:149495236
|
A | G | 2 | a0157a0174 | 2 | HG02135.hp2 NA18962.hp1 |
missense_variant | MODERATE | c.2207A>G | p.Asp736Gly | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 19/94 | 2993/13941 | 2207/11532 | 736/3843 | chr1 | 149495236 | ||
| chr1:149495918
|
G | C | 22 | a0006a0009a0017others(19): Show | 27 | HG00099.hp1 HG00741.hp2 HG01891.hp1 others(24): Show |
missense_variant | MODERATE | c.2239G>C | p.Val747Leu | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 20/94 | 3025/13941 | 2239/11532 | 747/3843 | chr1 | 149495918 | ||
| chr1:149495918
|
G | T | 1 | a0061 | 1 | HG02145.hp2 | missense_variant | MODERATE | c.2239G>T | p.Val747Leu | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 20/94 | 3025/13941 | 2239/11532 | 747/3843 | chr1 | 149495918 | ||
| chr1:149496028
|
T | G | 1 | a0174 | 1 | NA18962.hp1 | missense_variant | MODERATE | c.2349T>G | p.Phe783Leu | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 20/94 | 3135/13941 | 2349/11532 | 783/3843 | chr1 | 149496028 | ||
| chr1:149497322
|
CTCTCTCT others(47500): Show |
C | 1 | a0007 | 3 | HG00408.hp2 HG00609.hp1 NA19084.hp2 |
exon_loss_variant | HIGH | c.2505-191_9825-198d others(2): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 22/94 | INFO_REALIGN_3_PRIME | chr1 | 149497322 | |||||
| chr1:149497685
|
A | G | 202 | a0001a0002a0003others(199): Show | 260 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(257): Show |
missense_variant | MODERATE | c.2665A>G | p.Ile889Val | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 22/94 | 3451/13941 | 2665/11532 | 889/3843 | chr1 | 149497685 | ||
| chr1:149499093
|
A | C | 1 | a0167 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.2750A>C | p.Asp917Ala | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 24/94 | 3536/13941 | 2750/11532 | 917/3843 | chr1 | 149499093 | ||
| chr1:149499133
|
A | T | 1 | a0210 | 1 | HG01952.hp2 | missense_variant | MODERATE | c.2790A>T | p.Arg930Ser | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 24/94 | 3576/13941 | 2790/11532 | 930/3843 | chr1 | 149499133 | ||
| chr1:149499135
|
G | T | 1 | a0006 | 2 | NA19240.hp2 NA20129.hp2 |
missense_variant | MODERATE | c.2792G>T | p.Cys931Phe | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 24/94 | 3578/13941 | 2792/11532 | 931/3843 | chr1 | 149499135 | ||
| chr1:149499144
|
T | C | 7 | a0006a0156a0157others(4): Show | 9 | HG01891.hp1 HG02080.hp2 HG02135.hp2 others(6): Show |
missense_variant | MODERATE | c.2801T>C | p.Ile934Thr | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 24/94 | 3587/13941 | 2801/11532 | 934/3843 | chr1 | 149499144 | ||
| chr1:149499225
|
G | A | 5 | a0069a0070a0071others(2): Show | 5 | HG00609.hp2 HG02083.hp2 NA18747.hp1 others(2): Show |
missense_variant | MODERATE | c.2882G>A | p.Gly961Asp | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 24/94 | 3668/13941 | 2882/11532 | 961/3843 | chr1 | 149499225 | ||
| chr1:149499991
|
A | G | 9 | a0006a0044a0154others(6): Show | 9 | HG01891.hp1 HG02080.hp2 HG02976.hp2 others(6): Show |
missense_variant | MODERATE | c.2939A>G | p.Asp980Gly | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 25/94 | 3725/13941 | 2939/11532 | 980/3843 | chr1 | 149499991 | ||
| chr1:149500408
|
CTCTGTGT others(4762): Show |
C | 1 | a0090 | 1 | NA19030.hp2 | exon_loss_variant | HIGH | c.2955-247_3687-240d others(2): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 26/94 | INFO_REALIGN_3_PRIME | chr1 | 149500408 | |||||
| chr1:149500408
|
CTCTGTGT others(9523): Show |
C | 1 | a0088 | 1 | HG02896.hp2 | exon_loss_variant | HIGH | c.2955-247_4419-240d others(2): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 26/94 | INFO_REALIGN_3_PRIME | chr1 | 149500408 | |||||
| chr1:149500412
|
GTGTGTGT others(4752): Show |
G | 1 | a0126 | 1 | HG02683.hp2 | exon_loss_variant | HIGH | c.2955-222_3687-225d others(2): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 26/94 | INFO_REALIGN_3_PRIME | chr1 | 149500412 | |||||
| chr1:149500673
|
G | C | 58 | a0004a0006a0017others(55): Show | 69 | HG00423.hp2 HG00609.hp2 HG00735.hp2 others(66): Show |
missense_variant | MODERATE | c.2971G>C | p.Val991Leu | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 26/94 | 3757/13941 | 2971/11532 | 991/3843 | chr1 | 149500673 | ||
| chr1:149500783
|
T | G | 4 | a0044a0161a0162others(1): Show | 4 | HG00735.hp2 HG01516.hp1 NA18962.hp1 others(1): Show |
missense_variant | MODERATE | c.3081T>G | p.Phe1027Leu | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 26/94 | 3867/13941 | 3081/11532 | 1027/3843 | chr1 | 149500783 | ||
| chr1:149502327
|
T | C | 3 | a0190a0206a0211 | 3 | NA18946.hp2 NA18954.hp2 NA18962.hp2 |
missense_variant | MODERATE | c.3278T>C | p.Leu1093Ser | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 28/94 | 4064/13941 | 3278/11532 | 1093/3843 | chr1 | 149502327 | ||
| chr1:149502458
|
G | A | 9 | a0002a0014a0031others(6): Show | 17 | HG00642.hp2 HG01071.hp1 HG01975.hp1 others(14): Show |
missense_variant&splice_region_variant | MODERATE | c.3409G>A | p.Glu1137Lys | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 28/94 | 4195/13941 | 3409/11532 | 1137/3843 | chr1 | 149502458 | ||
| chr1:149503199
|
T | A | 5 | a0179a0180a0181others(2): Show | 5 | HG00738.hp1 HG03831.hp1 HG04204.hp1 others(2): Show |
missense_variant | MODERATE | c.3431T>A | p.Val1144Glu | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 29/94 | 4217/13941 | 3431/11532 | 1144/3843 | chr1 | 149503199 | ||
| chr1:149503854
|
A | C | 1 | a0167 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.3482A>C | p.Asp1161Ala | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 30/94 | 4268/13941 | 3482/11532 | 1161/3843 | chr1 | 149503854 | ||
| chr1:149503896
|
G | T | 1 | a0006 | 1 | NA19240.hp2 | missense_variant | MODERATE | c.3524G>T | p.Cys1175Phe | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 30/94 | 4310/13941 | 3524/11532 | 1175/3843 | chr1 | 149503896 | ||
| chr1:149503905
|
T | C | 6 | a0006a0044a0156others(3): Show | 6 | HG00621.hp2 HG03942.hp2 NA18972.hp1 others(3): Show |
missense_variant | MODERATE | c.3533T>C | p.Ile1178Thr | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 30/94 | 4319/13941 | 3533/11532 | 1178/3843 | chr1 | 149503905 | ||
| chr1:149503986
|
G | A | 1 | a0069 | 1 | NA19011.hp2 | missense_variant | MODERATE | c.3614G>A | p.Gly1205Asp | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 30/94 | 4400/13941 | 3614/11532 | 1205/3843 | chr1 | 149503986 | ||
| chr1:149504752
|
A | G | 13 | a0006a0044a0048others(10): Show | 13 | HG00621.hp2 HG01109.hp1 HG01978.hp1 others(10): Show |
missense_variant | MODERATE | c.3671A>G | p.Asp1224Gly | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 31/94 | 4457/13941 | 3671/11532 | 1224/3843 | chr1 | 149504752 | ||
| chr1:149505222
|
CATCTGTC others(28500): Show |
C | 1 | a0157 | 1 | HG02135.hp2 | exon_loss_variant | HIGH | c.3687-100_8079-101d others(2): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 32/94 | INFO_REALIGN_3_PRIME | chr1 | 149505222 | |||||
| chr1:149505318
|
C | CTTTCTTA others(4754): Show |
1 | a0095 | 1 | HG02809.hp1 | stop_gained&conservative_inframe_insertion | HIGH | c.3702_3703insCTGGAG others(4755): Show |
p.Leu1234_Val1235ins others(4761): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 32/94 | 4489/13941 | 3703/11532 | 1235/3843 | INFO_REALIGN_3_PRIME | chr1 | 149505318 | |
| chr1:149505344
|
CCATGAAA others(4754): Show |
C | 1 | a0079 | 1 | NA18984.hp1 | exon_loss_variant | HIGH | c.3968+73_4700+72del | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 34/94 | INFO_REALIGN_3_PRIME | chr1 | 149505344 | |||||
| chr1:149505434
|
G | C | 110 | a0001a0003a0004others(107): Show | 142 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(139): Show |
missense_variant | MODERATE | c.3703G>C | p.Val1235Leu | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 32/94 | 4489/13941 | 3703/11532 | 1235/3843 | chr1 | 149505434 | ||
| chr1:149505544
|
T | G | 6 | a0043a0044a0163others(3): Show | 6 | HG00544.hp2 HG00558.hp2 HG02165.hp1 others(3): Show |
missense_variant | MODERATE | c.3813T>G | p.Phe1271Leu | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 32/94 | 4599/13941 | 3813/11532 | 1271/3843 | chr1 | 149505544 | ||
| chr1:149505554
|
G | A | 1 | a0178 | 1 | NA19082.hp1 | missense_variant | MODERATE | c.3823G>A | p.Glu1275Lys | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 32/94 | 4609/13941 | 3823/11532 | 1275/3843 | chr1 | 149505554 | ||
| chr1:149505573
|
T | C | 1 | a0150 | 1 | HG01257.hp2 | missense_variant | MODERATE | c.3842T>C | p.Phe1281Ser | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 32/94 | 4628/13941 | 3842/11532 | 1281/3843 | chr1 | 149505573 | ||
| chr1:149507186
|
C | A | 1 | a0166 | 1 | HG03942.hp2 | missense_variant | MODERATE | c.4108C>A | p.Gln1370Lys | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 34/94 | 4894/13941 | 4108/11532 | 1370/3843 | chr1 | 149507186 | ||
| chr1:149507199
|
G | C | 1 | a0166 | 1 | HG03942.hp2 | missense_variant | MODERATE | c.4121G>C | p.Gly1374Ala | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 34/94 | 4907/13941 | 4121/11532 | 1374/3843 | chr1 | 149507199 | ||
| chr1:149507960
|
T | A | 4 | a0186a0193a0195others(1): Show | 4 | HG02040.hp2 HG02602.hp2 HG03942.hp1 others(1): Show |
missense_variant | MODERATE | c.4163T>A | p.Val1388Glu | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 35/94 | 4949/13941 | 4163/11532 | 1388/3843 | chr1 | 149507960 | ||
| chr1:149508424
|
CTCTACCT others(9508): Show |
C | 1 | a0030 | 2 | HG03195.hp2 NA18906.hp2 |
exon_loss_variant | HIGH | c.4265_5728del | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 37/94 | 5051/13941 | INFO_REALIGN_3_PRIME | chr1 | 149508424 | ||||
| chr1:149508615
|
A | C | 1 | a0167 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.4214A>C | p.Asp1405Ala | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 36/94 | 5000/13941 | 4214/11532 | 1405/3843 | chr1 | 149508615 | ||
| chr1:149508666
|
T | C | 3 | a0044a0166a0172 | 3 | HG03942.hp2 NA18972.hp1 NA20752.hp2 |
missense_variant | MODERATE | c.4265T>C | p.Ile1422Thr | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 36/94 | 5051/13941 | 4265/11532 | 1422/3843 | chr1 | 149508666 | ||
| chr1:149509513
|
A | G | 5 | a0006a0044a0156others(2): Show | 6 | HG01891.hp1 HG03942.hp2 NA18972.hp1 others(3): Show |
missense_variant | MODERATE | c.4403A>G | p.Asp1468Gly | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 37/94 | 5189/13941 | 4403/11532 | 1468/3843 | chr1 | 149509513 | ||
| chr1:149510195
|
G | C | 121 | a0001a0002a0003others(118): Show | 161 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(158): Show |
missense_variant | MODERATE | c.4435G>C | p.Val1479Leu | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 38/94 | 5221/13941 | 4435/11532 | 1479/3843 | chr1 | 149510195 | ||
| chr1:149510225
|
G | T | 1 | a0093 | 1 | HG02572.hp1 | missense_variant | MODERATE | c.4465G>T | p.Asp1489Tyr | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 38/94 | 5251/13941 | 4465/11532 | 1489/3843 | chr1 | 149510225 | ||
| chr1:149510305
|
T | G | 4 | a0006a0044a0166others(1): Show | 4 | HG02895.hp1 HG03942.hp2 NA18972.hp1 others(1): Show |
missense_variant | MODERATE | c.4545T>G | p.Phe1515Leu | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 38/94 | 5331/13941 | 4545/11532 | 1515/3843 | chr1 | 149510305 | ||
| chr1:149510306
|
T | C | 1 | a0166 | 1 | HG03942.hp2 | missense_variant | MODERATE | c.4546T>C | p.Tyr1516His | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 38/94 | 5332/13941 | 4546/11532 | 1516/3843 | chr1 | 149510306 | ||
| chr1:149510315
|
G | A | 1 | a0033 | 2 | NA18947.hp2 NA19084.hp1 |
missense_variant | MODERATE | c.4555G>A | p.Glu1519Lys | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 38/94 | 5341/13941 | 4555/11532 | 1519/3843 | chr1 | 149510315 | ||
| chr1:149511080
|
G | C | 1 | a0165 | 1 | HG00544.hp2 | missense_variant | MODERATE | c.4606G>C | p.Gly1536Arg | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 39/94 | 5392/13941 | 4606/11532 | 1536/3843 | chr1 | 149511080 | ||
| chr1:149511896
|
G | C | 1 | a0052 | 1 | HG02300.hp1 | missense_variant | MODERATE | c.4789G>C | p.Glu1597Gln | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 40/94 | 5575/13941 | 4789/11532 | 1597/3843 | chr1 | 149511896 | ||
| chr1:149511960
|
G | C | 1 | a0166 | 1 | HG03942.hp2 | missense_variant | MODERATE | c.4853G>C | p.Gly1618Ala | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 40/94 | 5639/13941 | 4853/11532 | 1618/3843 | chr1 | 149511960 | ||
| chr1:149511980
|
G | A | 3 | a0020a0067a0068 | 4 | HG01074.hp2 HG01952.hp1 HG03831.hp2 others(1): Show |
missense_variant&splice_region_variant | MODERATE | c.4873G>A | p.Glu1625Lys | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 40/94 | 5659/13941 | 4873/11532 | 1625/3843 | chr1 | 149511980 | ||
| chr1:149513376
|
A | C | 1 | a0167 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.4946A>C | p.Asp1649Ala | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 42/94 | 5732/13941 | 4946/11532 | 1649/3843 | chr1 | 149513376 | ||
| chr1:149513427
|
T | C | 20 | a0006a0044a0055others(17): Show | 20 | HG00735.hp1 HG00735.hp2 HG01516.hp1 others(17): Show |
missense_variant | MODERATE | c.4997T>C | p.Ile1666Thr | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 42/94 | 5783/13941 | 4997/11532 | 1666/3843 | chr1 | 149513427 | ||
| chr1:149513444
|
G | C | 1 | a0187 | 1 | NA18612.hp2 | missense_variant | MODERATE | c.5014G>C | p.Glu1672Gln | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 42/94 | 5800/13941 | 5014/11532 | 1672/3843 | chr1 | 149513444 | ||
| chr1:149513834
|
AGATTTCC others(4747): Show |
A | 1 | a0068 | 1 | HG01952.hp1 | exon_loss_variant | HIGH | c.5135_5866del | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 44/94 | 5921/13941 | INFO_REALIGN_3_PRIME | chr1 | 149513834 | ||||
| chr1:149514274
|
A | G | 20 | a0006a0043a0044others(17): Show | 21 | HG00735.hp1 HG00735.hp2 HG01516.hp1 others(18): Show |
missense_variant | MODERATE | c.5135A>G | p.Asp1712Gly | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 43/94 | 5921/13941 | 5135/11532 | 1712/3843 | chr1 | 149514274 | ||
| chr1:149514277
|
C | G | 1 | a0149 | 1 | HG04199.hp1 | missense_variant | MODERATE | c.5138C>G | p.Pro1713Arg | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 43/94 | 5924/13941 | 5138/11532 | 1713/3843 | chr1 | 149514277 | ||
| chr1:149514741
|
ATCTGTCT others(4745): Show |
A | 1 | a0064 | 1 | HG03710.hp1 | exon_loss_variant | HIGH | c.5323+31_6055+30del | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 45/94 | INFO_REALIGN_3_PRIME | chr1 | 149514741 | |||||
| chr1:149514836
|
G | GTTTCTTA others(14262): Show |
1 | a0193 | 1 | HG02040.hp2 | frameshift_variant&stop_gained | HIGH | c.5166_5167insGTGGAG others(14263): Show |
p.Leu1723fs | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 44/94 | 5953/13941 | 5167/11532 | 1723/3843 | INFO_REALIGN_3_PRIME | chr1 | 149514836 | |
| chr1:149514836
|
G | GTTTCTTA others(14262): Show |
1 | a0196 | 1 | HG03942.hp1 | frameshift_variant&stop_gained | HIGH | c.5166_5167insGTGGAG others(14263): Show |
p.Leu1723fs | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 44/94 | 5953/13941 | 5167/11532 | 1723/3843 | INFO_REALIGN_3_PRIME | chr1 | 149514836 | |
| chr1:149514836
|
G | GTTTCTTA others(14264): Show |
1 | a0036 | 1 | NA18960.hp1 | stop_gained&conservative_inframe_insertion | HIGH | c.5166_5167insGTGGAG others(14265): Show |
p.Leu1722_Leu1723ins others(14271): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 44/94 | 5953/13941 | 5167/11532 | 1723/3843 | INFO_REALIGN_3_PRIME | chr1 | 149514836 | |
| chr1:149514836
|
G | GTTTCTTA others(19035): Show |
1 | a0209 | 1 | NA18939.hp2 | frameshift_variant&stop_gained | HIGH | c.5166_5167insGTGGAG others(19036): Show |
p.Leu1723fs | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 44/94 | 5953/13941 | 5167/11532 | 1723/3843 | INFO_REALIGN_3_PRIME | chr1 | 149514836 | |
| chr1:149514952
|
C | G | 50 | a0006a0022a0028others(47): Show | 56 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(53): Show |
missense_variant | MODERATE | c.5167C>G | p.Leu1723Val | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 44/94 | 5953/13941 | 5167/11532 | 1723/3843 | chr1 | 149514952 | ||
| chr1:149515024
|
G | A | 1 | a0164 | 1 | HG00735.hp1 | missense_variant | MODERATE | c.5239G>A | p.Glu1747Lys | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 44/94 | 6025/13941 | 5239/11532 | 1747/3843 | chr1 | 149515024 | ||
| chr1:149515062
|
T | G | 8 | a0043a0044a0161others(5): Show | 8 | HG00735.hp1 HG00735.hp2 HG01516.hp1 others(5): Show |
missense_variant | MODERATE | c.5277T>G | p.Phe1759Leu | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 44/94 | 6063/13941 | 5277/11532 | 1759/3843 | chr1 | 149515062 | ||
| chr1:149515064
|
A | G | 1 | a0091 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.5279A>G | p.Tyr1760Cys | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 44/94 | 6065/13941 | 5279/11532 | 1760/3843 | chr1 | 149515064 | ||
| chr1:149515082
|
A | G | 1 | a0060 | 1 | NA18959.hp2 | missense_variant | MODERATE | c.5297A>G | p.His1766Arg | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 44/94 | 6083/13941 | 5297/11532 | 1766/3843 | chr1 | 149515082 | ||
| chr1:149515102
|
G | A | 1 | a0198 | 1 | NA18957.hp2 | missense_variant | MODERATE | c.5317G>A | p.Val1773Met | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 44/94 | 6103/13941 | 5317/11532 | 1773/3843 | chr1 | 149515102 | ||
| chr1:149515512
|
TAGAAATC others(33208): Show |
T | 1 | a0156 | 1 | NA19062.hp2 | exon_loss_variant | HIGH | c.5324-266_10448-267 others(3): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 45/94 | INFO_REALIGN_3_PRIME | chr1 | 149515512 | |||||
| chr1:149516716
|
G | C | 3 | a0161a0162a0166 | 3 | HG00735.hp2 HG01516.hp1 HG03942.hp2 |
missense_variant | MODERATE | c.5585G>C | p.Gly1862Ala | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 46/94 | 6371/13941 | 5585/11532 | 1862/3843 | chr1 | 149516716 | ||
| chr1:149518130
|
A | C | 1 | a0167 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.5678A>C | p.Asp1893Ala | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 48/94 | 6464/13941 | 5678/11532 | 1893/3843 | chr1 | 149518130 | ||
| chr1:149518140
|
G | T | 1 | a0097 | 1 | NA18955.hp1 | missense_variant | MODERATE | c.5688G>T | p.Glu1896Asp | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 48/94 | 6474/13941 | 5688/11532 | 1896/3843 | chr1 | 149518140 | ||
| chr1:149518181
|
C | T | 81 | a0001a0005a0006others(78): Show | 108 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(105): Show |
missense_variant | MODERATE | c.5729C>T | p.Thr1910Ile | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 48/94 | 6515/13941 | 5729/11532 | 1910/3843 | chr1 | 149518181 | ||
| chr1:149518198
|
G | C | 3 | a0036a0196a0205 | 4 | HG00621.hp2 HG03942.hp1 NA18960.hp1 others(1): Show |
missense_variant | MODERATE | c.5746G>C | p.Glu1916Gln | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 48/94 | 6532/13941 | 5746/11532 | 1916/3843 | chr1 | 149518198 | ||
| chr1:149519006
|
C | G | 1 | a0132 | 1 | HG02135.hp1 | missense_variant | MODERATE | c.5845C>G | p.Gln1949Glu | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 49/94 | 6631/13941 | 5845/11532 | 1949/3843 | chr1 | 149519006 | ||
| chr1:149519028
|
G | A | 83 | a0001a0002a0005others(80): Show | 114 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(111): Show |
missense_variant | MODERATE | c.5867G>A | p.Gly1956Asp | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 49/94 | 6653/13941 | 5867/11532 | 1956/3843 | chr1 | 149519028 | ||
| chr1:149519461
|
GTGTGTGT others(9477): Show |
G | 1 | a0187 | 1 | NA18612.hp2 | exon_loss_variant | HIGH | c.5883-195_7347-198d others(2): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 50/94 | INFO_REALIGN_3_PRIME | chr1 | 149519461 | |||||
| chr1:149519704
|
C | G | 20 | a0044a0064a0069others(17): Show | 20 | HG00621.hp1 HG00735.hp1 HG01099.hp1 others(17): Show |
missense_variant | MODERATE | c.5899C>G | p.Leu1967Val | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 50/94 | 6685/13941 | 5899/11532 | 1967/3843 | chr1 | 149519704 | ||
| chr1:149519814
|
T | G | 10 | a0006a0043a0161others(7): Show | 10 | HG00544.hp2 HG00735.hp1 HG00735.hp2 others(7): Show |
missense_variant | MODERATE | c.6009T>G | p.Phe2003Leu | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 50/94 | 6795/13941 | 6009/11532 | 2003/3843 | chr1 | 149519814 | ||
| chr1:149519816
|
A | G | 3 | a0088a0090a0133 | 3 | HG02622.hp1 HG02896.hp2 NA19030.hp2 |
missense_variant | MODERATE | c.6011A>G | p.Tyr2004Cys | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 50/94 | 6797/13941 | 6011/11532 | 2004/3843 | chr1 | 149519816 | ||
| chr1:149519834
|
A | T | 2 | a0021a0078 | 3 | HG02280.hp2 HG03209.hp1 HG03471.hp2 |
missense_variant | MODERATE | c.6029A>T | p.His2010Leu | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 50/94 | 6815/13941 | 6029/11532 | 2010/3843 | chr1 | 149519834 | ||
| chr1:149519845
|
T | C | 1 | a0122 | 1 | HG03654.hp1 | missense_variant | MODERATE | c.6040T>C | p.Ser2014Pro | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 50/94 | 6826/13941 | 6040/11532 | 2014/3843 | chr1 | 149519845 | ||
| chr1:149519854
|
G | A | 2 | a0081a0090 | 2 | HG03516.hp2 NA19030.hp2 |
missense_variant | MODERATE | c.6049G>A | p.Val2017Met | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 50/94 | 6835/13941 | 6049/11532 | 2017/3843 | chr1 | 149519854 | ||
| chr1:149520682
|
A | G | 2 | a0065a0066 | 2 | HG02300.hp2 HG03654.hp2 |
missense_variant&splice_region_variant | MODERATE | c.6163A>G | p.Arg2055Gly | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 51/94 | 6949/13941 | 6163/11532 | 2055/3843 | chr1 | 149520682 | ||
| chr1:149521269
|
CGGTTTCT others(4744): Show |
C | 4 | a0026a0113a0201others(1): Show | 5 | HG01168.hp1 HG01496.hp2 NA18982.hp1 others(2): Show |
exon_loss_variant | HIGH | c.6337+246_7069+245d others(2): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 53/94 | INFO_REALIGN_3_PRIME | chr1 | 149521269 | |||||
| chr1:149521458
|
C | A | 2 | a0161a0162 | 2 | HG00735.hp2 HG01516.hp1 |
missense_variant | MODERATE | c.6304C>A | p.Gln2102Lys | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 52/94 | 7090/13941 | 6304/11532 | 2102/3843 | chr1 | 149521458 | ||
| chr1:149521471
|
G | C | 4 | a0161a0162a0163others(1): Show | 4 | HG00544.hp2 HG00558.hp2 HG00735.hp2 others(1): Show |
missense_variant | MODERATE | c.6317G>C | p.Gly2106Ala | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 52/94 | 7103/13941 | 6317/11532 | 2106/3843 | chr1 | 149521471 | ||
| chr1:149522250
|
C | T | 2 | a0004a0082 | 5 | HG01891.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
missense_variant | MODERATE | c.6377C>T | p.Pro2126Leu | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 53/94 | 7163/13941 | 6377/11532 | 2126/3843 | chr1 | 149522250 | ||
| chr1:149522894
|
A | G | 1 | a0130 | 1 | HG01074.hp1 | missense_variant | MODERATE | c.6419A>G | p.Glu2140Gly | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 54/94 | 7205/13941 | 6419/11532 | 2140/3843 | chr1 | 149522894 | ||
| chr1:149522906
|
TGCAGGAC others(23): Show |
T | 3 | a0012a0140a0141 | 5 | HG00438.hp1 HG00558.hp1 NA18980.hp1 others(2): Show |
disruptive_inframe_deletion | MODERATE | c.6432_6461delGCAGGA others(24): Show |
p.Leu2144_Thr2154del others(6): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 54/94 | 7218/13941 | 6432/11532 | 2144/3843 | chr1 | 149522906 | ||
| chr1:149522933
|
C | T | 1 | a0098 | 1 | HG00738.hp2 | missense_variant | MODERATE | c.6458C>T | p.Ser2153Leu | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 54/94 | 7244/13941 | 6458/11532 | 2153/3843 | chr1 | 149522933 | ||
| chr1:149522936
|
C | T | 23 | a0006a0032a0033others(20): Show | 31 | HG00621.hp1 HG00642.hp1 HG00735.hp1 others(28): Show |
missense_variant | MODERATE | c.6461C>T | p.Thr2154Ile | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 54/94 | 7247/13941 | 6461/11532 | 2154/3843 | chr1 | 149522936 | ||
| chr1:149522938
|
C | T | 3 | a0012a0140a0141 | 5 | HG00438.hp1 HG00558.hp1 NA18980.hp1 others(2): Show |
missense_variant | MODERATE | c.6463C>T | p.Pro2155Ser | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 54/94 | 7249/13941 | 6463/11532 | 2155/3843 | chr1 | 149522938 | ||
| chr1:149522953
|
G | C | 1 | a0197 | 1 | HG02083.hp1 | missense_variant | MODERATE | c.6478G>C | p.Glu2160Gln | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 54/94 | 7264/13941 | 6478/11532 | 2160/3843 | chr1 | 149522953 | ||
| chr1:149523016
|
G | T | 1 | a0096 | 1 | HG02717.hp1 | missense_variant | MODERATE | c.6541G>T | p.Gly2181Cys | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 54/94 | 7327/13941 | 6541/11532 | 2181/3843 | chr1 | 149523016 | ||
| chr1:149523761
|
C | G | 1 | a0132 | 1 | HG02135.hp1 | missense_variant | MODERATE | c.6577C>G | p.Gln2193Glu | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 55/94 | 7363/13941 | 6577/11532 | 2193/3843 | chr1 | 149523761 | ||
| chr1:149523783
|
G | A | 25 | a0006a0014a0032others(22): Show | 33 | HG00621.hp1 HG00642.hp1 HG00642.hp2 others(30): Show |
missense_variant | MODERATE | c.6599G>A | p.Gly2200Asp | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 55/94 | 7385/13941 | 6599/11532 | 2200/3843 | chr1 | 149523783 | ||
| chr1:149524200
|
CTGTGTGT others(4740): Show |
C | 1 | a0133 | 1 | HG02622.hp1 | exon_loss_variant | HIGH | c.6615-215_7347-198d others(2): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 56/94 | INFO_REALIGN_3_PRIME | chr1 | 149524200 | |||||
| chr1:149524214
|
GTGTGTGT others(4724): Show |
G | 2 | a0049a0184 | 2 | HG02738.hp1 NA18747.hp2 |
exon_loss_variant | HIGH | c.6615-199_7347-198d others(2): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 56/94 | INFO_REALIGN_3_PRIME | chr1 | 149524214 | |||||
| chr1:149524216
|
GTGTGTGT others(4722): Show |
G | 4 | a0158a0183a0190others(1): Show | 4 | HG02965.hp1 NA18954.hp2 NA18962.hp2 others(1): Show |
exon_loss_variant | HIGH | c.6787+99_7519+98del | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 57/94 | INFO_REALIGN_3_PRIME | chr1 | 149524216 | |||||
| chr1:149524220
|
GTGTGTGT others(4718): Show |
G | 1 | a0188 | 1 | NA18963.hp2 | exon_loss_variant | HIGH | c.6615-197_7347-202d others(2): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 56/94 | INFO_REALIGN_3_PRIME | chr1 | 149524220 | |||||
| chr1:149524222
|
GTGTGTGT others(4716): Show |
G | 1 | a0100 | 1 | NA18963.hp1 | exon_loss_variant | HIGH | c.6615-197_7347-204d others(2): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 56/94 | INFO_REALIGN_3_PRIME | chr1 | 149524222 | |||||
| chr1:149524461
|
C | G | 16 | a0006a0032a0033others(13): Show | 20 | HG00621.hp1 HG00642.hp1 HG00738.hp1 others(17): Show |
missense_variant | MODERATE | c.6631C>G | p.Leu2211Val | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 56/94 | 7417/13941 | 6631/11532 | 2211/3843 | chr1 | 149524461 | ||
| chr1:149524470
|
G | A | 4 | a0186a0193a0204others(1): Show | 4 | HG02040.hp2 HG02129.hp2 HG02602.hp2 others(1): Show |
missense_variant | MODERATE | c.6640G>A | p.Val2214Ile | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 56/94 | 7426/13941 | 6640/11532 | 2214/3843 | chr1 | 149524470 | ||
| chr1:149524571
|
T | G | 12 | a0044a0161a0162others(9): Show | 12 | HG00544.hp2 HG00558.hp2 HG00735.hp2 others(9): Show |
missense_variant | MODERATE | c.6741T>G | p.Phe2247Leu | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 56/94 | 7527/13941 | 6741/11532 | 2247/3843 | chr1 | 149524571 | ||
| chr1:149524572
|
T | C | 2 | a0161a0162 | 2 | HG00735.hp2 HG01516.hp1 |
missense_variant | MODERATE | c.6742T>C | p.Tyr2248His | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 56/94 | 7528/13941 | 6742/11532 | 2248/3843 | chr1 | 149524572 | ||
| chr1:149525353
|
G | A | 8 | a0023a0076a0092others(5): Show | 9 | HG02055.hp1 HG02257.hp2 HG02630.hp2 others(6): Show |
missense_variant | MODERATE | c.6809G>A | p.Gly2270Glu | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 57/94 | 7595/13941 | 6809/11532 | 2270/3843 | chr1 | 149525353 | ||
| chr1:149526070
|
G | C | 1 | a0070 | 1 | NA18954.hp1 | missense_variant&splice_region_variant | MODERATE | c.6897G>C | p.Arg2299Ser | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 58/94 | 7683/13941 | 6897/11532 | 2299/3843 | chr1 | 149526070 | ||
| chr1:149526098
|
G | C | 1 | a0162 | 1 | HG01516.hp1 | missense_variant | MODERATE | c.6925G>C | p.Gly2309Arg | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 58/94 | 7711/13941 | 6925/11532 | 2309/3843 | chr1 | 149526098 | ||
| chr1:149526160
|
A | T | 1 | a0081 | 1 | HG03516.hp2 | missense_variant | MODERATE | c.6987A>T | p.Glu2329Asp | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 58/94 | 7773/13941 | 6987/11532 | 2329/3843 | chr1 | 149526160 | ||
| chr1:149526200
|
A | G | 1 | a0167 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.7027A>G | p.Ile2343Val | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 58/94 | 7813/13941 | 7027/11532 | 2343/3843 | chr1 | 149526200 | ||
| chr1:149526209
|
C | A | 1 | a0165 | 1 | HG00544.hp2 | missense_variant | MODERATE | c.7036C>A | p.Gln2346Lys | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 58/94 | 7822/13941 | 7036/11532 | 2346/3843 | chr1 | 149526209 | ||
| chr1:149526215
|
T | C | 1 | a0167 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.7042T>C | p.Cys2348Arg | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 58/94 | 7828/13941 | 7042/11532 | 2348/3843 | chr1 | 149526215 | ||
| chr1:149526222
|
G | C | 5 | a0006a0161a0162others(2): Show | 5 | HG00544.hp2 HG00558.hp2 HG00735.hp2 others(2): Show |
missense_variant | MODERATE | c.7049G>C | p.Gly2350Ala | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 58/94 | 7835/13941 | 7049/11532 | 2350/3843 | chr1 | 149526222 | ||
| chr1:149526230
|
G | A | 1 | a0167 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.7057G>A | p.Val2353Ile | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 58/94 | 7843/13941 | 7057/11532 | 2353/3843 | chr1 | 149526230 | ||
| chr1:149526982
|
G | A | 1 | a0077 | 1 | HG01928.hp1 | missense_variant | MODERATE | c.7090G>A | p.Val2364Met | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 59/94 | 7876/13941 | 7090/11532 | 2364/3843 | chr1 | 149526982 | ||
| chr1:149526991
|
G | A | 1 | a0202 | 1 | NA20752.hp1 | missense_variant | MODERATE | c.7099G>A | p.Asp2367Asn | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 59/94 | 7885/13941 | 7099/11532 | 2367/3843 | chr1 | 149526991 | ||
| chr1:149527634
|
A | C | 2 | a0125a0166 | 2 | HG02922.hp1 HG03942.hp2 |
missense_variant | MODERATE | c.7142A>C | p.Asp2381Ala | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 60/94 | 7928/13941 | 7142/11532 | 2381/3843 | chr1 | 149527634 | ||
| chr1:149527663
|
T | C | 2 | a0125a0166 | 2 | HG02922.hp1 HG03942.hp2 |
missense_variant | MODERATE | c.7171T>C | p.Ser2391Pro | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 60/94 | 7957/13941 | 7171/11532 | 2391/3843 | chr1 | 149527663 | ||
| chr1:149527685
|
C | T | 10 | a0006a0047a0083others(7): Show | 11 | HG00408.hp1 HG00423.hp1 HG00735.hp1 others(8): Show |
missense_variant | MODERATE | c.7193C>T | p.Thr2398Ile | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 60/94 | 7979/13941 | 7193/11532 | 2398/3843 | chr1 | 149527685 | ||
| chr1:149527702
|
G | C | 7 | a0186a0193a0197others(4): Show | 7 | HG00621.hp2 HG02040.hp2 HG02083.hp1 others(4): Show |
missense_variant | MODERATE | c.7210G>C | p.Glu2404Gln | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 60/94 | 7996/13941 | 7210/11532 | 2404/3843 | chr1 | 149527702 | ||
| chr1:149528532
|
G | A | 4 | a0047a0137a0164others(1): Show | 4 | HG00735.hp1 HG01934.hp2 HG03225.hp2 others(1): Show |
missense_variant | MODERATE | c.7331G>A | p.Gly2444Asp | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/94 | 8117/13941 | 7331/11532 | 2444/3843 | chr1 | 149528532 | ||
| chr1:149529190
|
C | G | 11 | a0045a0046a0051others(8): Show | 11 | HG01099.hp1 HG01123.hp1 HG02683.hp1 others(8): Show |
missense_variant | MODERATE | c.7363C>G | p.Leu2455Val | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 62/94 | 8149/13941 | 7363/11532 | 2455/3843 | chr1 | 149529190 | ||
| chr1:149529199
|
G | A | 7 | a0036a0185a0192others(4): Show | 8 | HG02080.hp2 HG03942.hp1 NA18939.hp2 others(5): Show |
missense_variant | MODERATE | c.7372G>A | p.Val2458Ile | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 62/94 | 8158/13941 | 7372/11532 | 2458/3843 | chr1 | 149529199 | ||
| chr1:149529244
|
A | C | 1 | a0168 | 1 | HG01099.hp1 | missense_variant | MODERATE | c.7417A>C | p.Thr2473Pro | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 62/94 | 8203/13941 | 7417/11532 | 2473/3843 | chr1 | 149529244 | ||
| chr1:149529300
|
T | G | 15 | a0006a0043a0044others(12): Show | 15 | HG00544.hp2 HG00558.hp2 HG00735.hp2 others(12): Show |
missense_variant | MODERATE | c.7473T>G | p.Phe2491Leu | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 62/94 | 8259/13941 | 7473/11532 | 2491/3843 | chr1 | 149529300 | ||
| chr1:149529301
|
T | C | 2 | a0165a0166 | 2 | HG00544.hp2 HG03942.hp2 |
missense_variant | MODERATE | c.7474T>C | p.Tyr2492His | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 62/94 | 8260/13941 | 7474/11532 | 2492/3843 | chr1 | 149529301 | ||
| chr1:149530082
|
G | A | 1 | a0116 | 1 | HG03098.hp2 | missense_variant | MODERATE | c.7541G>A | p.Gly2514Glu | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 63/94 | 8327/13941 | 7541/11532 | 2514/3843 | chr1 | 149530082 | ||
| chr1:149530903
|
G | T | 1 | a0148 | 1 | HG04184.hp1 | missense_variant | MODERATE | c.7733G>T | p.Cys2578Phe | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 64/94 | 8519/13941 | 7733/11532 | 2578/3843 | chr1 | 149530903 | ||
| chr1:149530951
|
G | C | 6 | a0006a0161a0162others(3): Show | 6 | HG00544.hp2 HG00558.hp2 HG00735.hp2 others(3): Show |
missense_variant | MODERATE | c.7781G>C | p.Gly2594Ala | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 64/94 | 8567/13941 | 7781/11532 | 2594/3843 | chr1 | 149530951 | ||
| chr1:149532365
|
A | C | 2 | a0089a0142 | 2 | HG01109.hp2 HG01168.hp2 |
missense_variant | MODERATE | c.7874A>C | p.Asp2625Ala | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 66/94 | 8660/13941 | 7874/11532 | 2625/3843 | chr1 | 149532365 | ||
| chr1:149532394
|
T | C | 2 | a0089a0142 | 2 | HG01109.hp2 HG01168.hp2 |
missense_variant | MODERATE | c.7903T>C | p.Ser2635Pro | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 66/94 | 8689/13941 | 7903/11532 | 2635/3843 | chr1 | 149532394 | ||
| chr1:149532416
|
C | T | 35 | a0003a0006a0012others(32): Show | 48 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(45): Show |
missense_variant | MODERATE | c.7925C>T | p.Thr2642Ile | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 66/94 | 8711/13941 | 7925/11532 | 2642/3843 | chr1 | 149532416 | ||
| chr1:149532433
|
G | C | 13 | a0036a0184a0185others(10): Show | 14 | HG00621.hp2 HG02040.hp2 HG02080.hp2 others(11): Show |
missense_variant | MODERATE | c.7942G>C | p.Glu2648Gln | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 66/94 | 8728/13941 | 7942/11532 | 2648/3843 | chr1 | 149532433 | ||
| chr1:149533019
|
ACCAGAAT others(18975): Show |
A | 1 | a0166 | 1 | HG03942.hp2 | exon_loss_variant | HIGH | c.8078+12_11006+11de others(1): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 68/94 | INFO_REALIGN_3_PRIME | chr1 | 149533019 | |||||
| chr1:149533263
|
G | A | 2 | a0164a0180 | 2 | HG00735.hp1 HG04204.hp1 |
missense_variant | MODERATE | c.8063G>A | p.Gly2688Asp | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 67/94 | 8849/13941 | 8063/11532 | 2688/3843 | chr1 | 149533263 | ||
| chr1:149533710
|
G | GTGTGTGT others(4722): Show |
1 | a0018 | 1 | HG02257.hp1 | frameshift_variant&stop_gained | HIGH | c.8241_8242insTACGTG others(4723): Show |
p.Asp2748fs | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 68/94 | 9028/13941 | 8242/11532 | 2748/3843 | INFO_REALIGN_3_PRIME | chr1 | 149533710 | |
| chr1:149533842
|
CTATGCTA others(9481): Show |
C | 1 | a0108 | 1 | HG01123.hp1 | exon_loss_variant | HIGH | c.8251+99_9715+98del | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 69/94 | INFO_REALIGN_3_PRIME | chr1 | 149533842 | |||||
| chr1:149533941
|
C | G | 8 | a0029a0044a0120others(5): Show | 9 | HG00735.hp1 HG02040.hp1 HG02080.hp1 others(6): Show |
missense_variant | MODERATE | c.8095C>G | p.Leu2699Val | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 68/94 | 8881/13941 | 8095/11532 | 2699/3843 | chr1 | 149533941 | ||
| chr1:149533950
|
G | A | 5 | a0186a0203a0204others(2): Show | 5 | HG00438.hp2 HG02129.hp2 HG02602.hp2 others(2): Show |
missense_variant | MODERATE | c.8104G>A | p.Val2702Ile | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 68/94 | 8890/13941 | 8104/11532 | 2702/3843 | chr1 | 149533950 | ||
| chr1:149534016
|
C | G | 1 | a0167 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.8170C>G | p.Gln2724Glu | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 68/94 | 8956/13941 | 8170/11532 | 2724/3843 | chr1 | 149534016 | ||
| chr1:149534034
|
C | A | 1 | a0022 | 2 | HG02572.hp2 HG02630.hp1 |
missense_variant | MODERATE | c.8188C>A | p.Pro2730Thr | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 68/94 | 8974/13941 | 8188/11532 | 2730/3843 | chr1 | 149534034 | ||
| chr1:149534051
|
T | G | 11 | a0006a0161a0162others(8): Show | 11 | HG00544.hp2 HG00558.hp2 HG00735.hp2 others(8): Show |
missense_variant | MODERATE | c.8205T>G | p.Phe2735Leu | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 68/94 | 8991/13941 | 8205/11532 | 2735/3843 | chr1 | 149534051 | ||
| chr1:149534082
|
T | G | 1 | a0125 | 1 | HG02922.hp1 | missense_variant | MODERATE | c.8236T>G | p.Ser2746Ala | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 68/94 | 9022/13941 | 8236/11532 | 2746/3843 | chr1 | 149534082 | ||
| chr1:149534502
|
TAGAAATC others(9481): Show |
T | 1 | a0150 | 1 | HG01257.hp2 | exon_loss_variant | HIGH | c.8361-306_9825-303d others(2): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 70/94 | INFO_REALIGN_3_PRIME | chr1 | 149534502 | |||||
| chr1:149535108
|
ACGTACCA others(14218): Show |
A | 1 | a0068 | 1 | HG01952.hp1 | exon_loss_variant | HIGH | c.8361-306_10557-303 others(3): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 70/94 | INFO_REALIGN_3_PRIME | chr1 | 149535108 | |||||
| chr1:149535669
|
A | G | 1 | a0043 | 1 | HG02165.hp1 | missense_variant | MODERATE | c.8476A>G | p.Arg2826Gly | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 70/94 | 9262/13941 | 8476/11532 | 2826/3843 | chr1 | 149535669 | ||
| chr1:149535700
|
G | A | 4 | a0050a0051a0052others(1): Show | 4 | HG01978.hp1 HG02300.hp1 HG02683.hp1 others(1): Show |
missense_variant | MODERATE | c.8507G>A | p.Cys2836Tyr | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 70/94 | 9293/13941 | 8507/11532 | 2836/3843 | chr1 | 149535700 | ||
| chr1:149535706
|
G | C | 6 | a0044a0163a0165others(3): Show | 6 | HG00544.hp2 HG00558.hp2 HG02109.hp2 others(3): Show |
missense_variant | MODERATE | c.8513G>C | p.Gly2838Ala | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 70/94 | 9299/13941 | 8513/11532 | 2838/3843 | chr1 | 149535706 | ||
| chr1:149536375
|
TTAGACAG others(9477): Show |
T | 2 | a0020a0067 | 3 | HG01074.hp2 HG03831.hp2 HG04204.hp2 |
exon_loss_variant | HIGH | c.8586-199_10050-206 others(3): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 72/94 | INFO_REALIGN_3_PRIME | chr1 | 149536375 | |||||
| chr1:149537120
|
A | C | 5 | a0082a0134a0167others(2): Show | 5 | HG02109.hp2 HG02698.hp1 HG02976.hp1 others(2): Show |
missense_variant | MODERATE | c.8606A>C | p.Asp2869Ala | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 72/94 | 9392/13941 | 8606/11532 | 2869/3843 | chr1 | 149537120 | ||
| chr1:149537149
|
T | C | 5 | a0082a0134a0167others(2): Show | 5 | HG02109.hp2 HG02698.hp1 HG02976.hp1 others(2): Show |
missense_variant | MODERATE | c.8635T>C | p.Ser2879Pro | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 72/94 | 9421/13941 | 8635/11532 | 2879/3843 | chr1 | 149537149 | ||
| chr1:149537171
|
C | T | 67 | a0001a0004a0005others(64): Show | 95 | HG00099.hp1 HG00099.hp2 HG00609.hp2 others(92): Show |
missense_variant | MODERATE | c.8657C>T | p.Thr2886Ile | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 72/94 | 9443/13941 | 8657/11532 | 2886/3843 | chr1 | 149537171 | ||
| chr1:149537188
|
G | C | 14 | a0036a0186a0187others(11): Show | 15 | HG00438.hp2 HG02040.hp2 HG02080.hp2 others(12): Show |
missense_variant | MODERATE | c.8674G>C | p.Glu2892Gln | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 72/94 | 9460/13941 | 8674/11532 | 2892/3843 | chr1 | 149537188 | ||
| chr1:149537197
|
G | A | 1 | a0178 | 1 | NA19082.hp1 | missense_variant | MODERATE | c.8683G>A | p.Asp2895Asn | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 72/94 | 9469/13941 | 8683/11532 | 2895/3843 | chr1 | 149537197 | ||
| chr1:149537774
|
ACCAGAAT others(4746): Show |
A | 1 | a0189 | 1 | HG01358.hp2 | exon_loss_variant | HIGH | c.8810+245_9542+244d others(2): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 74/94 | INFO_REALIGN_3_PRIME | chr1 | 149537774 | |||||
| chr1:149537774
|
ACCAGAAT others(9483): Show |
A | 1 | a0185 | 1 | NA18998.hp1 | exon_loss_variant | HIGH | c.8810+245_10274+244 others(3): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 74/94 | INFO_REALIGN_3_PRIME | chr1 | 149537774 | |||||
| chr1:149538018
|
G | A | 1 | a0078 | 1 | HG03471.hp2 | missense_variant | MODERATE | c.8795G>A | p.Gly2932Asp | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 73/94 | 9581/13941 | 8795/11532 | 2932/3843 | chr1 | 149538018 | ||
| chr1:149538290
|
GCACATTT others(9483): Show |
G | 1 | a0177 | 1 | NA19043.hp2 | exon_loss_variant | HIGH | c.8811-241_10275-226 others(3): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 74/94 | INFO_REALIGN_3_PRIME | chr1 | 149538290 | |||||
| chr1:149538465
|
GTGTGTGT others(4726): Show |
G | 1 | a0162 | 1 | HG01516.hp1 | exon_loss_variant | HIGH | c.8811-197_9543-202d others(2): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 74/94 | INFO_REALIGN_3_PRIME | chr1 | 149538465 | |||||
| chr1:149538467
|
GTGTGTGT others(4724): Show |
G | 1 | a0161 | 1 | HG00735.hp2 | exon_loss_variant | HIGH | c.8811-197_9543-204d others(2): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 74/94 | INFO_REALIGN_3_PRIME | chr1 | 149538467 | |||||
| chr1:149538593
|
C | CTATGCTA others(28559): Show |
1 | a0164 | 1 | HG00735.hp1 | stop_gained&disruptive_inframe_insertion | HIGH | c.8936_8937insGTATGC others(28560): Show |
p.Ser2978_Phe2979ins others(28566): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 74/94 | 9723/13941 | 8937/11532 | 2979/3843 | INFO_REALIGN_3_PRIME | chr1 | 149538593 | |
| chr1:149538593
|
C | CTATGCTA others(38074): Show |
1 | a0170 | 1 | NA20129.hp1 | frameshift_variant&stop_gained | HIGH | c.8826_8827insGTGGAG others(38075): Show |
p.Leu2943fs | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 74/94 | 9613/13941 | 8827/11532 | 2943/3843 | INFO_REALIGN_3_PRIME | chr1 | 149538593 | |
| chr1:149538593
|
CTATGCTA others(4730): Show |
C | 1 | a0210 | 1 | HG01952.hp2 | exon_loss_variant | HIGH | c.9092+62_9824+61del | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 76/94 | INFO_REALIGN_3_PRIME | chr1 | 149538593 | |||||
| chr1:149538593
|
CTATGCTA others(9467): Show |
C | 3 | a0012a0140a0141 | 5 | HG00438.hp1 HG00558.hp1 NA18980.hp1 others(2): Show |
exon_loss_variant | HIGH | c.8983+304_10447+303 others(3): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 75/94 | INFO_REALIGN_3_PRIME | chr1 | 149538593 | |||||
| chr1:149538692
|
C | G | 7 | a0044a0113a0147others(4): Show | 7 | HG01099.hp1 HG02698.hp1 HG04115.hp1 others(4): Show |
missense_variant | MODERATE | c.8827C>G | p.Leu2943Val | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 74/94 | 9613/13941 | 8827/11532 | 2943/3843 | chr1 | 149538692 | ||
| chr1:149538701
|
G | A | 15 | a0036a0183a0187others(12): Show | 16 | HG02040.hp2 HG02080.hp2 HG03942.hp1 others(13): Show |
missense_variant | MODERATE | c.8836G>A | p.Val2946Ile | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 74/94 | 9622/13941 | 8836/11532 | 2946/3843 | chr1 | 149538701 | ||
| chr1:149538755
|
A | T | 1 | a0144 | 1 | HG02129.hp1 | missense_variant | MODERATE | c.8890A>T | p.Ser2964Cys | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 74/94 | 9676/13941 | 8890/11532 | 2964/3843 | chr1 | 149538755 | ||
| chr1:149538773
|
G | A | 1 | a0135 | 1 | HG00733.hp1 | missense_variant | MODERATE | c.8908G>A | p.Asp2970Asn | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 74/94 | 9694/13941 | 8908/11532 | 2970/3843 | chr1 | 149538773 | ||
| chr1:149538802
|
T | G | 7 | a0006a0163a0165others(4): Show | 7 | HG00544.hp2 HG00558.hp2 HG01099.hp1 others(4): Show |
missense_variant | MODERATE | c.8937T>G | p.Phe2979Leu | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 74/94 | 9723/13941 | 8937/11532 | 2979/3843 | chr1 | 149538802 | ||
| chr1:149538803
|
T | C | 3 | a0006a0015a0173 | 5 | HG02145.hp1 HG02895.hp1 HG02896.hp1 others(2): Show |
missense_variant | MODERATE | c.8938T>C | p.Tyr2980His | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 74/94 | 9724/13941 | 8938/11532 | 2980/3843 | chr1 | 149538803 | ||
| chr1:149539999
|
CAGTGTCC others(9467): Show |
C | 2 | a0016a0047 | 3 | HG01934.hp2 HG03239.hp2 HG04199.hp2 |
exon_loss_variant | HIGH | c.9715+304_11179+303 others(3): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 81/94 | INFO_REALIGN_3_PRIME | chr1 | 149539999 | |||||
| chr1:149540330
|
G | A | 2 | a0175a0176 | 2 | HG04115.hp2 HG04184.hp2 |
missense_variant | MODERATE | c.9122G>A | p.Gly3041Glu | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 76/94 | 9908/13941 | 9122/11532 | 3041/3843 | chr1 | 149540330 | ||
| chr1:149540453
|
G | C | 2 | a0043a0044 | 2 | HG02165.hp1 NA18972.hp1 |
missense_variant | MODERATE | c.9245G>C | p.Gly3082Ala | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 76/94 | 10031/13941 | 9245/11532 | 3082/3843 | chr1 | 149540453 | ||
| chr1:149541873
|
C | A | 153 | a0001a0002a0004others(150): Show | 198 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(195): Show |
missense_variant | MODERATE | c.9338C>A | p.Ala3113Asp | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 78/94 | 10124/13941 | 9338/11532 | 3113/3843 | chr1 | 149541873 | ||
| chr1:149541898
|
G | C | 2 | a0053a0109 | 2 | HG01516.hp2 HG01517.hp1 |
missense_variant | MODERATE | c.9363G>C | p.Gln3121His | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 78/94 | 10149/13941 | 9363/11532 | 3121/3843 | chr1 | 149541898 | ||
| chr1:149541902
|
C | T | 152 | a0001a0002a0004others(149): Show | 197 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(194): Show |
missense_variant | MODERATE | c.9367C>T | p.Pro3123Ser | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 78/94 | 10153/13941 | 9367/11532 | 3123/3843 | chr1 | 149541902 | ||
| chr1:149541911
|
A | G | 1 | a0056 | 1 | HG03669.hp2 | missense_variant | MODERATE | c.9376A>G | p.Arg3126Gly | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 78/94 | 10162/13941 | 9376/11532 | 3126/3843 | chr1 | 149541911 | ||
| chr1:149541924
|
C | T | 19 | a0011a0017a0018others(16): Show | 24 | HG00423.hp2 HG01168.hp2 HG02027.hp2 others(21): Show |
missense_variant | MODERATE | c.9389C>T | p.Thr3130Ile | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 78/94 | 10175/13941 | 9389/11532 | 3130/3843 | chr1 | 149541924 | ||
| chr1:149541941
|
G | C | 30 | a0032a0033a0035others(27): Show | 35 | HG00438.hp2 HG00621.hp1 HG00642.hp1 others(32): Show |
missense_variant | MODERATE | c.9406G>C | p.Glu3136Gln | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 78/94 | 10192/13941 | 9406/11532 | 3136/3843 | chr1 | 149541941 | ||
| chr1:149543210
|
GTGTGTCT others(4706): Show |
G | 1 | a0116 | 1 | HG03098.hp2 | exon_loss_variant | HIGH | c.9543-197_10275-222 others(3): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 80/94 | INFO_REALIGN_3_PRIME | chr1 | 149543210 | |||||
| chr1:149543429
|
C | G | 4 | a0049a0167a0169others(1): Show | 4 | HG02109.hp2 HG02738.hp1 HG04115.hp1 others(1): Show |
missense_variant | MODERATE | c.9559C>G | p.Leu3187Val | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 80/94 | 10345/13941 | 9559/11532 | 3187/3843 | chr1 | 149543429 | ||
| chr1:149543438
|
G | A | 17 | a0036a0179a0180others(14): Show | 18 | HG00438.hp2 HG00738.hp1 HG02040.hp2 others(15): Show |
missense_variant | MODERATE | c.9568G>A | p.Val3190Ile | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 80/94 | 10354/13941 | 9568/11532 | 3190/3843 | chr1 | 149543438 | ||
| chr1:149543539
|
T | G | 1 | a0174 | 1 | NA18962.hp1 | missense_variant | MODERATE | c.9669T>G | p.Phe3223Leu | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 80/94 | 10455/13941 | 9669/11532 | 3223/3843 | chr1 | 149543539 | ||
| chr1:149544596
|
ACGTACCA others(4730): Show |
A | 29 | a0005a0010a0021others(26): Show | 38 | HG00609.hp2 HG00738.hp2 HG01069.hp1 others(35): Show |
exon_loss_variant | HIGH | c.9998-71_10730-72de others(1): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 83/94 | INFO_REALIGN_3_PRIME | chr1 | 149544596 | |||||
| chr1:149545190
|
G | C | 1 | a0174 | 1 | NA18962.hp1 | missense_variant | MODERATE | c.9977G>C | p.Gly3326Ala | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 82/94 | 10763/13941 | 9977/11532 | 3326/3843 | chr1 | 149545190 | ||
| chr1:149545859
|
CTAGACAG others(4730): Show |
C | 1 | a0158 | 1 | HG02965.hp1 | exon_loss_variant | HIGH | c.10557-215_11289-19 others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 88/94 | INFO_REALIGN_3_PRIME | chr1 | 149545859 | |||||
| chr1:149545960
|
A | C | 1 | a0133 | 1 | HG02622.hp1 | missense_variant | MODERATE | c.10028A>C | p.Asp3343Ala | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 83/94 | 10814/13941 | 10028/11532 | 3343/3843 | chr1 | 149545960 | ||
| chr1:149546610
|
C | A | 70 | a0006a0011a0015others(67): Show | 83 | HG00423.hp2 HG00438.hp2 HG00621.hp1 others(80): Show |
missense_variant | MODERATE | c.10070C>A | p.Ala3357Asp | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 84/94 | 10856/13941 | 10070/11532 | 3357/3843 | chr1 | 149546610 | ||
| chr1:149546639
|
C | T | 70 | a0006a0011a0015others(67): Show | 83 | HG00423.hp2 HG00438.hp2 HG00621.hp1 others(80): Show |
missense_variant | MODERATE | c.10099C>T | p.Pro3367Ser | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 84/94 | 10885/13941 | 10099/11532 | 3367/3843 | chr1 | 149546639 | ||
| chr1:149546653
|
T | G | 1 | a0009 | 3 | HG00099.hp1 HG00741.hp2 HG01934.hp1 |
missense_variant | MODERATE | c.10113T>G | p.Cys3371Trp | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 84/94 | 10899/13941 | 10113/11532 | 3371/3843 | chr1 | 149546653 | ||
| chr1:149546661
|
C | T | 2 | a0168a0170 | 2 | HG01099.hp1 NA20129.hp1 |
missense_variant | MODERATE | c.10121C>T | p.Thr3374Ile | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 84/94 | 10907/13941 | 10121/11532 | 3374/3843 | chr1 | 149546661 | ||
| chr1:149546678
|
G | C | 32 | a0034a0035a0036others(29): Show | 35 | HG00438.hp2 HG00621.hp1 HG00621.hp2 others(32): Show |
missense_variant | MODERATE | c.10138G>C | p.Glu3380Gln | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 84/94 | 10924/13941 | 10138/11532 | 3380/3843 | chr1 | 149546678 | ||
| chr1:149546706
|
G | A | 3 | a0101a0102a0127 | 3 | HG00408.hp1 HG00423.hp1 NA19079.hp1 |
missense_variant | MODERATE | c.10166G>A | p.Ser3389Asn | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 84/94 | 10952/13941 | 10166/11532 | 3389/3843 | chr1 | 149546706 | ||
| chr1:149547508
|
G | A | 1 | a0197 | 1 | HG02083.hp1 | missense_variant | MODERATE | c.10259G>A | p.Gly3420Asp | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 85/94 | 11045/13941 | 10259/11532 | 3420/3843 | chr1 | 149547508 | ||
| chr1:149547511
|
C | G | 1 | a0167 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.10262C>G | p.Pro3421Arg | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 85/94 | 11048/13941 | 10262/11532 | 3421/3843 | chr1 | 149547511 | ||
| chr1:149548163
|
C | G | 1 | a0006 | 1 | HG02895.hp1 | missense_variant | MODERATE | c.10288C>G | p.Leu3430Val | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 86/94 | 11074/13941 | 10288/11532 | 3430/3843 | chr1 | 149548163 | ||
| chr1:149548166
|
C | G | 10 | a0006a0011a0132others(7): Show | 12 | HG00544.hp2 HG00558.hp2 HG00735.hp2 others(9): Show |
missense_variant | MODERATE | c.10291C>G | p.Leu3431Val | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 86/94 | 11077/13941 | 10291/11532 | 3431/3843 | chr1 | 149548166 | ||
| chr1:149548175
|
G | A | 7 | a0185a0188a0190others(4): Show | 7 | NA18946.hp2 NA18954.hp2 NA18959.hp1 others(4): Show |
missense_variant | MODERATE | c.10300G>A | p.Val3434Ile | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 86/94 | 11086/13941 | 10300/11532 | 3434/3843 | chr1 | 149548175 | ||
| chr1:149548199
|
TCACTGGA others(3170): Show |
T | 1 | a0104 | 1 | NA18984.hp2 | exon_loss_variant | HIGH | c.10344_10850del | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 87/94 | 11130/13941 | INFO_REALIGN_3_PRIME | chr1 | 149548199 | ||||
| chr1:149548276
|
T | G | 4 | a0161a0162a0163others(1): Show | 4 | HG00544.hp2 HG00558.hp2 HG00735.hp2 others(1): Show |
missense_variant | MODERATE | c.10401T>G | p.Phe3467Leu | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 86/94 | 11187/13941 | 10401/11532 | 3467/3843 | chr1 | 149548276 | ||
| chr1:149548277
|
T | C | 5 | a0161a0162a0163others(2): Show | 5 | HG00544.hp2 HG00558.hp2 HG00735.hp2 others(2): Show |
missense_variant | MODERATE | c.10402T>C | p.Tyr3468His | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 86/94 | 11188/13941 | 10402/11532 | 3468/3843 | chr1 | 149548277 | ||
| chr1:149549051
|
G | A | 2 | a0024a0085 | 3 | HG02055.hp2 HG02559.hp2 NA18522.hp2 |
missense_variant | MODERATE | c.10462G>A | p.Gly3488Arg | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 87/94 | 11248/13941 | 10462/11532 | 3488/3843 | chr1 | 149549051 | ||
| chr1:149549919
|
G | T | 1 | a0067 | 1 | HG04204.hp2 | missense_variant | MODERATE | c.10701G>T | p.Gln3567His | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 88/94 | 11487/13941 | 10701/11532 | 3567/3843 | chr1 | 149549919 | ||
| chr1:149550673
|
A | G | 8 | a0043a0044a0164others(5): Show | 8 | HG00735.hp1 HG01099.hp1 HG02165.hp1 others(5): Show |
missense_variant | MODERATE | c.10736A>G | p.Glu3579Gly | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 89/94 | 11522/13941 | 10736/11532 | 3579/3843 | chr1 | 149550673 | ||
| chr1:149550697
|
A | C | 3 | a0088a0090a0091 | 3 | HG02896.hp2 HG03209.hp2 NA19030.hp2 |
missense_variant | MODERATE | c.10760A>C | p.Asp3587Ala | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 89/94 | 11546/13941 | 10760/11532 | 3587/3843 | chr1 | 149550697 | ||
| chr1:149551347
|
C | A | 53 | a0006a0013a0015others(50): Show | 66 | HG00438.hp2 HG00621.hp1 HG00621.hp2 others(63): Show |
missense_variant | MODERATE | c.10802C>A | p.Ala3601Asp | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 90/94 | 11588/13941 | 10802/11532 | 3601/3843 | chr1 | 149551347 | ||
| chr1:149551371
|
A | G | 1 | a0006 | 1 | HG02895.hp1 | missense_variant | MODERATE | c.10826A>G | p.Gln3609Arg | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 90/94 | 11612/13941 | 10826/11532 | 3609/3843 | chr1 | 149551371 | ||
| chr1:149551376
|
C | T | 52 | a0006a0013a0015others(49): Show | 65 | HG00438.hp2 HG00621.hp1 HG00621.hp2 others(62): Show |
missense_variant | MODERATE | c.10831C>T | p.Pro3611Ser | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 90/94 | 11617/13941 | 10831/11532 | 3611/3843 | chr1 | 149551376 | ||
| chr1:149551383
|
A | G | 1 | a0073 | 1 | HG02083.hp2 | missense_variant | MODERATE | c.10838A>G | p.Asp3613Gly | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 90/94 | 11624/13941 | 10838/11532 | 3613/3843 | chr1 | 149551383 | ||
| chr1:149551398
|
C | T | 1 | a0145 | 1 | HG02602.hp1 | missense_variant | MODERATE | c.10853C>T | p.Thr3618Ile | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 90/94 | 11639/13941 | 10853/11532 | 3618/3843 | chr1 | 149551398 | ||
| chr1:149551415
|
G | C | 3 | a0187a0204a0212 | 3 | HG02129.hp2 NA18612.hp2 NA18982.hp1 |
missense_variant | MODERATE | c.10870G>C | p.Glu3624Gln | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 90/94 | 11656/13941 | 10870/11532 | 3624/3843 | chr1 | 149551415 | ||
| chr1:149551490
|
G | C | 1 | a0006 | 3 | HG01891.hp1 NA19240.hp2 NA20129.hp2 |
missense_variant | MODERATE | c.10945G>C | p.Asp3649His | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 90/94 | 11731/13941 | 10945/11532 | 3649/3843 | chr1 | 149551490 | ||
| chr1:149552903
|
C | G | 2 | a0011a0156 | 4 | NA18981.hp2 NA19062.hp2 NA19065.hp1 others(1): Show |
missense_variant | MODERATE | c.11023C>G | p.Leu3675Val | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 92/94 | 11809/13941 | 11023/11532 | 3675/3843 | chr1 | 149552903 | ||
| chr1:149552912
|
G | A | 1 | a0183 | 1 | NA19005.hp2 | missense_variant | MODERATE | c.11032G>A | p.Val3678Ile | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 92/94 | 11818/13941 | 11032/11532 | 3678/3843 | chr1 | 149552912 | ||
| chr1:149553014
|
T | C | 2 | a0015a0173 | 4 | HG02145.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
missense_variant | MODERATE | c.11134T>C | p.Tyr3712His | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 92/94 | 11920/13941 | 11134/11532 | 3712/3843 | chr1 | 149553014 | ||
| chr1:149553047
|
C | G | 2 | a0074a0075 | 2 | HG03139.hp1 NA19030.hp1 |
missense_variant | MODERATE | c.11167C>G | p.Leu3723Val | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 92/94 | 11953/13941 | 11167/11532 | 3723/3843 | chr1 | 149553047 | ||
| chr1:149554508
|
C | G | 9 | a0043a0044a0164others(6): Show | 9 | HG00735.hp1 HG01099.hp1 HG02165.hp1 others(6): Show |
missense_variant | MODERATE | c.11302C>G | p.Leu3768Val | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 94/94 | 12088/13941 | 11302/11532 | 3768/3843 | chr1 | 149554508 | ||
| chr1:149554554
|
G | T | 2 | a0004a0082 | 5 | HG01891.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
missense_variant | MODERATE | c.11348G>T | p.Gly3783Val | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 94/94 | 12134/13941 | 11348/11532 | 3783/3843 | chr1 | 149554554 | ||
| chr1:149554569
|
C | A | 1 | a0098 | 1 | HG00738.hp2 | missense_variant | MODERATE | c.11363C>A | p.Pro3788Gln | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 94/94 | 12149/13941 | 11363/11532 | 3788/3843 | chr1 | 149554569 | ||
| chr1:149554594
|
C | G | 43 | a0032a0033a0034others(40): Show | 49 | HG00438.hp2 HG00621.hp1 HG00621.hp2 others(46): Show |
missense_variant | MODERATE | c.11388C>G | p.Asp3796Glu | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 94/94 | 12174/13941 | 11388/11532 | 3796/3843 | chr1 | 149554594 | ||
| chr1:149554661
|
T | G | 16 | a0006a0043a0044others(13): Show | 16 | HG00544.hp2 HG00558.hp2 HG00735.hp1 others(13): Show |
missense_variant | MODERATE | c.11455T>G | p.Leu3819Val | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 94/94 | 12241/13941 | 11455/11532 | 3819/3843 | chr1 | 149554661 | ||
| chr1:149554686
|
C | A | 1 | a0101 | 1 | HG00408.hp1 | missense_variant | MODERATE | c.11480C>A | p.Thr3827Lys | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 94/94 | 12266/13941 | 11480/11532 | 3827/3843 | chr1 | 149554686 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:149475947
|
C | T | 1 | a0147c0220 | 1 | NA18977.hp2 | synonymous_variant | LOW | c.15C>T | p.Ala5Ala | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 2/94 | 801/13941 | 15/11532 | 5/3843 | chr1 | 149475947 | ||
| chr1:149479024
|
G | A | 1 | a0101c0039 | 1 | HG00408.hp1 | synonymous_variant | LOW | c.423G>A | p.Gly141Gly | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 4/94 | 1209/13941 | 423/11532 | 141/3843 | chr1 | 149479024 | ||
| chr1:149480730
|
A | G | 3 | a0008c0037a0008c0215a0047c0216 | 4 | HG00741.hp1 HG01496.hp1 HG01928.hp2 others(1): Show |
synonymous_variant | LOW | c.618A>G | p.Glu206Glu | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 6/94 | 1404/13941 | 618/11532 | 206/3843 | chr1 | 149480730 | ||
| chr1:149487339
|
C | G | 19 | a0006c0211a0006c0212a0006c0213others(16): Show | 19 | HG00544.hp2 HG00558.hp2 HG00735.hp1 others(16): Show |
synonymous_variant | LOW | c.996C>G | p.Arg332Arg | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 9/94 | 1782/13941 | 996/11532 | 332/3843 | chr1 | 149487339 | ||
| chr1:149488049
|
A | G | 3 | a0006c0212a0006c0213a0006c0214 | 3 | HG01891.hp1 NA19240.hp2 NA20129.hp2 |
synonymous_variant | LOW | c.1077A>G | p.Glu359Glu | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 10/94 | 1863/13941 | 1077/11532 | 359/3843 | chr1 | 149488049 | ||
| chr1:149491139
|
G | A | 1 | a0008c0215 | 1 | HG01496.hp1 | splice_region_variant&synonymous_variant | LOW | c.1491G>A | p.Arg497Arg | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 14/94 | 2277/13941 | 1491/11532 | 497/3843 | chr1 | 149491139 | ||
| chr1:149491304
|
C | T | 2 | a0006c0212a0006c0214 | 2 | HG01891.hp1 NA20129.hp2 |
synonymous_variant | LOW | c.1656C>T | p.Asp552Asp | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 14/94 | 2442/13941 | 1656/11532 | 552/3843 | chr1 | 149491304 | ||
| chr1:149494387
|
G | A | 3 | a0015c0036a0015c0192a0173c0191 | 4 | HG02145.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
synonymous_variant | LOW | c.2067G>A | p.Ser689Ser | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 18/94 | 2853/13941 | 2067/11532 | 689/3843 | chr1 | 149494387 | ||
| chr1:149494408
|
A | G | 1 | a0015c0192 | 1 | HG03130.hp2 | synonymous_variant | LOW | c.2088A>G | p.Glu696Glu | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 18/94 | 2874/13941 | 2088/11532 | 696/3843 | chr1 | 149494408 | ||
| chr1:149496067
|
C | T | 1 | a0006c0213 | 1 | NA19240.hp2 | synonymous_variant | LOW | c.2388C>T | p.Asp796Asp | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 20/94 | 3174/13941 | 2388/11532 | 796/3843 | chr1 | 149496067 | ||
| chr1:149499139
|
T | C | 1 | a0196c0045 | 1 | HG03942.hp1 | synonymous_variant | LOW | c.2796T>C | p.Tyr932Tyr | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 24/94 | 3582/13941 | 2796/11532 | 932/3843 | chr1 | 149499139 | ||
| chr1:149505418
|
G | A | 1 | a0059c0091 | 1 | HG01978.hp2 | splice_region_variant&synonymous_variant | LOW | c.3687G>A | p.Arg1229Arg | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 32/94 | 4473/13941 | 3687/11532 | 1229/3843 | chr1 | 149505418 | ||
| chr1:149505583
|
C | T | 1 | a0006c0214 | 1 | NA20129.hp2 | synonymous_variant | LOW | c.3852C>T | p.Asp1284Asp | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 32/94 | 4638/13941 | 3852/11532 | 1284/3843 | chr1 | 149505583 | ||
| chr1:149506321
|
G | A | 1 | a0198c0059 | 1 | NA18957.hp2 | synonymous_variant | LOW | c.3876G>A | p.Gly1292Gly | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 33/94 | 4662/13941 | 3876/11532 | 1292/3843 | chr1 | 149506321 | ||
| chr1:149510344
|
C | T | 3 | a0006c0213a0185c0043a0187c0050 | 3 | NA18612.hp2 NA18998.hp1 NA19240.hp2 |
synonymous_variant | LOW | c.4584C>T | p.Asp1528Asp | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 38/94 | 5370/13941 | 4584/11532 | 1528/3843 | chr1 | 149510344 | ||
| chr1:149511919
|
C | T | 1 | a0154c0185 | 1 | HG02976.hp2 | synonymous_variant | LOW | c.4812C>T | p.Pro1604Pro | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 40/94 | 5598/13941 | 4812/11532 | 1604/3843 | chr1 | 149511919 | ||
| chr1:149515101
|
C | T | 11 | a0039c0219a0183c0041a0188c0051others(8): Show | 11 | HG00438.hp2 HG02129.hp2 NA18946.hp2 others(8): Show |
synonymous_variant | LOW | c.5316C>T | p.Asp1772Asp | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 44/94 | 6102/13941 | 5316/11532 | 1772/3843 | chr1 | 149515101 | ||
| chr1:149516582
|
G | T | 1 | a0039c0219 | 1 | NA18981.hp1 | synonymous_variant | LOW | c.5451G>T | p.Leu1817Leu | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 46/94 | 6237/13941 | 5451/11532 | 1817/3843 | chr1 | 149516582 | ||
| chr1:149519853
|
C | T | 6 | a0180c0072a0181c0073a0184c0042others(3): Show | 6 | HG03831.hp1 HG04204.hp1 NA18747.hp2 others(3): Show |
synonymous_variant | LOW | c.6048C>T | p.Asp2016Asp | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 50/94 | 6834/13941 | 6048/11532 | 2016/3843 | chr1 | 149519853 | ||
| chr1:149521337
|
G | T | 2 | a0184c0042a0202c0064 | 2 | NA18747.hp2 NA20752.hp1 |
synonymous_variant | LOW | c.6183G>T | p.Leu2061Leu | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 52/94 | 6969/13941 | 6183/11532 | 2061/3843 | chr1 | 149521337 | ||
| chr1:149522886
|
T | C | 1 | a0135c0161 | 1 | HG00733.hp1 | synonymous_variant | LOW | c.6411T>C | p.Asp2137Asp | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 54/94 | 7197/13941 | 6411/11532 | 2137/3843 | chr1 | 149522886 | ||
| chr1:149522937
|
T | A | 3 | a0012c0009a0140c0175a0141c0182 | 5 | HG00438.hp1 HG00558.hp1 NA18980.hp1 others(2): Show |
synonymous_variant | LOW | c.6462T>A | p.Thr2154Thr | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 54/94 | 7248/13941 | 6462/11532 | 2154/3843 | chr1 | 149522937 | ||
| chr1:149524610
|
C | T | 13 | a0032c0012a0033c0011a0034c0013others(10): Show | 17 | HG00621.hp1 HG00642.hp1 HG00738.hp1 others(14): Show |
synonymous_variant | LOW | c.6780C>T | p.Asp2260Asp | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 56/94 | 7566/13941 | 6780/11532 | 2260/3843 | chr1 | 149524610 | ||
| chr1:149526088
|
G | T | 14 | a0032c0012a0033c0011a0034c0013others(11): Show | 18 | HG00621.hp1 HG00642.hp1 HG00738.hp1 others(15): Show |
synonymous_variant | LOW | c.6915G>T | p.Leu2305Leu | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 58/94 | 7701/13941 | 6915/11532 | 2305/3843 | chr1 | 149526088 | ||
| chr1:149529339
|
C | T | 1 | a0201c0063 | 1 | NA19062.hp1 | synonymous_variant | LOW | c.7512C>T | p.Asp2504Asp | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 62/94 | 8298/13941 | 7512/11532 | 2504/3843 | chr1 | 149529339 | ||
| chr1:149530817
|
G | T | 1 | a0201c0063 | 1 | NA19062.hp1 | synonymous_variant | LOW | c.7647G>T | p.Leu2549Leu | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 64/94 | 8433/13941 | 7647/11532 | 2549/3843 | chr1 | 149530817 | ||
| chr1:149537136
|
A | G | 1 | a0149c0183 | 1 | HG04199.hp1 | synonymous_variant | LOW | c.8622A>G | p.Glu2874Glu | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 72/94 | 9408/13941 | 8622/11532 | 2874/3843 | chr1 | 149537136 | ||
| chr1:149538835
|
T | C | 3 | a0063c0090a0153c0128a0154c0185 | 3 | HG02976.hp2 NA18980.hp2 NA19087.hp2 |
synonymous_variant | LOW | c.8970T>C | p.Ser2990Ser | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 74/94 | 9756/13941 | 8970/11532 | 2990/3843 | chr1 | 149538835 | ||
| chr1:149541197
|
T | A | 1 | a0066c0097 | 1 | HG02300.hp2 | synonymous_variant | LOW | c.9270T>A | p.Ile3090Ile | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 77/94 | 10056/13941 | 9270/11532 | 3090/3843 | chr1 | 149541197 | ||
| chr1:149543521
|
G | A | 1 | a0013c0162 | 1 | HG02965.hp2 | synonymous_variant | LOW | c.9651G>A | p.Gln3217Gln | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 80/94 | 10437/13941 | 9651/11532 | 3217/3843 | chr1 | 149543521 | ||
| chr1:149543572
|
T | C | 14 | a0002c0002a0014c0008a0041c0217others(11): Show | 21 | HG00642.hp2 HG01071.hp1 HG01074.hp1 others(18): Show |
synonymous_variant | LOW | c.9702T>C | p.Ser3234Ser | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 80/94 | 10488/13941 | 9702/11532 | 3234/3843 | chr1 | 149543572 | ||
| chr1:149548309
|
T | C | 2 | a0031c0028a0152c0129 | 3 | NA18946.hp1 NA18972.hp2 NA19088.hp2 |
synonymous_variant | LOW | c.10434T>C | p.Ser3478Ser | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 86/94 | 11220/13941 | 10434/11532 | 3478/3843 | chr1 | 149548309 | ||
| chr1:149548315
|
C | T | 1 | a0004c0027 | 2 | HG02895.hp2 HG02897.hp2 |
synonymous_variant | LOW | c.10440C>T | p.Asp3480Asp | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 86/94 | 11226/13941 | 10440/11532 | 3480/3843 | chr1 | 149548315 | ||
| chr1:149549922
|
T | C | 1 | a0167c0203 | 1 | HG02109.hp2 | synonymous_variant | LOW | c.10704T>C | p.Cys3568Cys | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 88/94 | 11490/13941 | 10704/11532 | 3568/3843 | chr1 | 149549922 | ||
| chr1:149551405
|
A | C | 1 | a0104c0141 | 1 | NA18984.hp2 | synonymous_variant | LOW | c.10860A>C | p.Ser3620Ser | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 90/94 | 11646/13941 | 10860/11532 | 3620/3843 | chr1 | 149551405 | ||
| chr1:149553775
|
A | G | 3 | a0024c0025a0042c0195a0085c0114 | 4 | HG02055.hp2 HG02486.hp1 HG02559.hp2 others(1): Show |
splice_region_variant&synonymous_variant | LOW | c.11181A>G | p.Glu3727Glu | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 93/94 | 11967/13941 | 11181/11532 | 3727/3843 | chr1 | 149553775 | ||
| chr1:149554699
|
C | G | 2 | a0003c0003a0112c0131 | 5 | HG00544.hp1 NA18612.hp1 NA18998.hp2 others(2): Show |
synonymous_variant | LOW | c.11493C>G | p.Leu3831Leu | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 94/94 | 12279/13941 | 11493/11532 | 3831/3843 | chr1 | 149554699 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:149475062
|
G | A | 3 | a0015c0036t0006a0015c0192t0006a0173c0191t0006 | 4 | HG02145.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-769G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 1/94 | 871 | chr1 | 149475062 | |||||
| chr1:149475064
|
C | T | 1 | a0167c0203t0028 | 1 | HG02109.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-767C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 1/94 | chr1 | 149475064 | ||||||
| chr1:149475112
|
G | T | 1 | a0189c0052t0027 | 1 | HG01358.hp2 | 5_prime_UTR_variant | MODIFIER | c.-719G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 1/94 | 821 | chr1 | 149475112 | |||||
| chr1:149475128
|
G | A | 63 | a0006c0211t0019a0006c0212t0002a0006c0213t0002others(60): Show | 69 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(66): Show |
5_prime_UTR_variant | MODIFIER | c.-703G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 1/94 | 805 | chr1 | 149475128 | |||||
| chr1:149475138
|
C | T | 1 | a0167c0203t0028 | 1 | HG02109.hp2 | 5_prime_UTR_variant | MODIFIER | c.-693C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 1/94 | 795 | chr1 | 149475138 | |||||
| chr1:149475156
|
A | T | 1 | a0115c0149t0026 | 1 | NA19043.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-675A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 1/94 | chr1 | 149475156 | ||||||
| chr1:149475275
|
T | A | 3 | a0015c0036t0006a0015c0192t0006a0173c0191t0006 | 4 | HG02145.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-556T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 1/94 | 658 | chr1 | 149475275 | |||||
| chr1:149475393
|
ATGT | A | 9 | a0043c0209t0004a0044c0210t0004a0164c0201t0004others(6): Show | 9 | HG00735.hp1 HG01099.hp1 HG02165.hp1 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-434_-432delTGT | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 1/94 | 534 | INFO_REALIGN_3_PRIME | chr1 | 149475393 | ||||
| chr1:149475446
|
A | T | 1 | a0174c0202t0013 | 1 | NA18962.hp1 | 5_prime_UTR_variant | MODIFIER | c.-385A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 1/94 | 487 | chr1 | 149475446 | |||||
| chr1:149475539
|
A | G | 3 | a0088c0105t0008a0090c0121t0008a0091c0122t0008 | 3 | HG02896.hp2 HG03209.hp2 NA19030.hp2 |
5_prime_UTR_variant | MODIFIER | c.-292A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 1/94 | 394 | chr1 | 149475539 | |||||
| chr1:149475549
|
C | T | 2 | a0002c0002t0007a0155c0186t0007 | 3 | NA18942.hp1 NA18960.hp2 NA18969.hp2 |
5_prime_UTR_variant | MODIFIER | c.-282C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 1/94 | 384 | chr1 | 149475549 | |||||
| chr1:149475666
|
T | A | 1 | a0014c0008t0020 | 1 | HG01975.hp1 | 5_prime_UTR_variant | MODIFIER | c.-165T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 1/94 | 267 | chr1 | 149475666 | |||||
| chr1:149475670
|
G | A | 1 | a0014c0008t0020 | 1 | HG01975.hp1 | 5_prime_UTR_variant | MODIFIER | c.-161G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 1/94 | 263 | chr1 | 149475670 | |||||
| chr1:149475729
|
C | T | 1 | a0005c0004t0025 | 1 | NA18990.hp2 | 5_prime_UTR_variant | MODIFIER | c.-102C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 1/94 | 204 | chr1 | 149475729 | |||||
| chr1:149554793
|
G | A | 1 | a0160c0076t0014 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*55G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 94/94 | 55 | chr1 | 149554793 | |||||
| chr1:149554803
|
G | C | 1 | a0052c0079t0021 | 1 | HG02300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*65G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 94/94 | 65 | chr1 | 149554803 | |||||
| chr1:149554808
|
A | T | 16 | a0006c0211t0019a0043c0209t0004a0044c0210t0004others(13): Show | 16 | HG00544.hp2 HG00558.hp2 HG00735.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*70A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 94/94 | 70 | chr1 | 149554808 | |||||
| chr1:149554824
|
T | C | 1 | a0133c0165t0022 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*86T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 94/94 | 86 | chr1 | 149554824 | |||||
| chr1:149554919
|
A | T | 1 | a0121c0154t0024 | 1 | HG02040.hp1 | 3_prime_UTR_variant | MODIFIER | c.*181A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 94/94 | 181 | chr1 | 149554919 | |||||
| chr1:149554939
|
G | A | 2 | a0020c0020t0010a0068c0096t0010 | 2 | HG01074.hp2 HG01952.hp1 |
3_prime_UTR_variant | MODIFIER | c.*201G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 94/94 | 201 | chr1 | 149554939 | |||||
| chr1:149554993
|
G | C | 1 | a0205c0056t0015 | 1 | HG00621.hp2 | 3_prime_UTR_variant | MODIFIER | c.*255G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 94/94 | 255 | chr1 | 149554993 | |||||
| chr1:149555004
|
C | G | 12 | a0002c0002t0003a0002c0002t0007a0014c0008t0003others(9): Show | 18 | HG00642.hp2 HG01071.hp1 HG01975.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*266C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 94/94 | 266 | chr1 | 149555004 | |||||
| chr1:149555006
|
T | C | 1 | a0160c0076t0014 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*268T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 94/94 | 268 | chr1 | 149555006 | |||||
| chr1:149555021
|
A | G | 1 | a0160c0076t0014 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*283A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 94/94 | 283 | chr1 | 149555021 | |||||
| chr1:149555068
|
C | T | 1 | a0189c0052t0027 | 1 | HG01358.hp2 | 3_prime_UTR_variant | MODIFIER | c.*330C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 94/94 | 330 | chr1 | 149555068 | |||||
| chr1:149555100
|
C | T | 9 | a0043c0209t0004a0044c0210t0004a0164c0201t0004others(6): Show | 9 | HG00735.hp1 HG01099.hp1 HG02165.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*362C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 94/94 | 362 | chr1 | 149555100 | |||||
| chr1:149555186
|
G | A | 1 | a0160c0076t0014 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*448G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 94/94 | 448 | chr1 | 149555186 | |||||
| chr1:149555255
|
C | A | 1 | a0210c0068t0016 | 1 | HG01952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*517C>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 94/94 | 517 | chr1 | 149555255 | |||||
| chr1:149555258
|
G | A | 3 | a0048c0081t0011a0049c0082t0011a0167c0203t0028 | 3 | HG01109.hp1 HG02109.hp2 HG02738.hp1 |
3_prime_UTR_variant | MODIFIER | c.*520G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 94/94 | 520 | chr1 | 149555258 | |||||
| chr1:149555376
|
A | G | 1 | a0196c0045t0018 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*638A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 94/94 | 638 | chr1 | 149555376 | |||||
| chr1:149555613
|
T | G | 17 | a0006c0211t0019a0043c0209t0004a0044c0210t0004others(14): Show | 17 | HG00544.hp2 HG00558.hp2 HG00735.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*875T>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 94/94 | 875 | chr1 | 149555613 | |||||
| chr1:149555626
|
C | G | 1 | a0083c0116t0023 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*888C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 94/94 | 888 | chr1 | 149555626 | |||||
| chr1:149555653
|
G | A | 2 | a0129c0167t0012a0132c0166t0012 | 2 | HG02135.hp1 NA19068.hp1 |
3_prime_UTR_variant | MODIFIER | c.*915G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 94/94 | 915 | chr1 | 149555653 | |||||
| chr1:149556003
|
C | T | 9 | a0043c0209t0004a0044c0210t0004a0164c0201t0004others(6): Show | 9 | HG00735.hp1 HG01099.hp1 HG02165.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1265C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 94/94 | 1265 | chr1 | 149556003 | |||||
| chr1:149556004
|
G | A | 6 | a0036c0014t0009a0161c0197t0005a0162c0196t0005others(3): Show | 7 | HG00544.hp2 HG00558.hp2 HG00735.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1266G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 94/94 | 1266 | chr1 | 149556004 | |||||
| chr1:149556082
|
G | C | 1 | a0186c0044t0017 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1344G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 94/94 | 1344 | chr1 | 149556082 | |||||
| chr1:149556118
|
A | T | 66 | a0006c0211t0019a0006c0212t0002a0006c0213t0002others(63): Show | 73 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*1380A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 94/94 | 1380 | chr1 | 149556118 | |||||
| chr1:149556321
|
G | T | 6 | a0006c0211t0019a0161c0197t0005a0162c0196t0005others(3): Show | 6 | HG00544.hp2 HG00558.hp2 HG00735.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1583G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 94/94 | 1583 | chr1 | 149556321 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:149476308
|
A | G | 1 | a0181c0073t0002g0272 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.175+201A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 2/93 | chr1 | 149476308 | ||||||
| chr1:149476726
|
G | T | 3 | a0015c0036t0006g0004a0015c0192t0006g0270a0173c0191t0006g0271 | 4 | HG02145.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.175+619G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 2/93 | chr1 | 149476726 | ||||||
| chr1:149476796
|
A | G | 1 | a0167c0203t0028g0269 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.175+689A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 2/93 | chr1 | 149476796 | ||||||
| chr1:149476806
|
G | T | 3 | a0015c0036t0006g0004a0015c0192t0006g0270a0173c0191t0006g0271 | 4 | HG02145.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.175+699G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 2/93 | chr1 | 149476806 | ||||||
| chr1:149476827
|
C | T | 1 | a0167c0203t0028g0269 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.175+720C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 2/93 | chr1 | 149476827 | ||||||
| chr1:149476832
|
G | A | 1 | a0003c0136t0001g0005 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.175+725G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 2/93 | chr1 | 149476832 | ||||||
| chr1:149476928
|
C | T | 1 | a0172c0204t0004g0268 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.175+821C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 2/93 | chr1 | 149476928 | ||||||
| chr1:149477059
|
G | C | 1 | a0193c0057t0002g0006 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.176-886G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 2/93 | chr1 | 149477059 | ||||||
| chr1:149477075
|
C | G | 1 | a0062c0093t0001g0267 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.176-870C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 2/93 | chr1 | 149477075 | ||||||
| chr1:149477176
|
G | A | 4 | a0004c0026t0001g0007a0004c0026t0001g0008a0004c0027t0001g0001others(1): Show | 5 | HG01891.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.176-769G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 2/93 | chr1 | 149477176 | ||||||
| chr1:149477267
|
G | T | 69 | a0006c0211t0019g0211a0006c0212t0002g0223a0006c0213t0002g0224others(66): Show | 69 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.176-678G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 2/93 | chr1 | 149477267 | ||||||
| chr1:149477568
|
C | G | 1 | a0032c0012t0002g0266 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.176-377C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 2/93 | chr1 | 149477568 | ||||||
| chr1:149477569
|
C | T | 1 | a0006c0214t0002g0265 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.176-376C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 2/93 | chr1 | 149477569 | ||||||
| chr1:149477635
|
G | T | 1 | a0191c0054t0002g0264 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.176-310G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 2/93 | chr1 | 149477635 | ||||||
| chr1:149477695
|
G | A | 3 | a0015c0036t0006g0004a0015c0192t0006g0270a0173c0191t0006g0271 | 4 | HG02145.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.176-250G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 2/93 | chr1 | 149477695 | ||||||
| chr1:149477697
|
T | G | 6 | a0011c0010t0001g0010a0011c0010t0001g0011a0011c0010t0001g0012others(3): Show | 6 | HG01099.hp1 NA18981.hp2 NA19062.hp2 others(3): Show |
intron_variant | MODIFIER | c.176-248T>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 2/93 | chr1 | 149477697 | ||||||
| chr1:149477752
|
C | T | 1 | a0192c0055t0002g0263 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.176-193C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 2/93 | chr1 | 149477752 | ||||||
| chr1:149478061
|
G | A | 16 | a0006c0211t0019g0211a0043c0209t0004g0207a0044c0210t0004g0206others(13): Show | 16 | HG00544.hp2 HG00558.hp2 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.278+14G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 3/93 | chr1 | 149478061 | ||||||
| chr1:149478063
|
G | A | 2 | a0116c0150t0001g0014a0123c0157t0001g0015 | 2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.278+16G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 3/93 | chr1 | 149478063 | ||||||
| chr1:149478167
|
A | G | 16 | a0006c0211t0019g0211a0043c0209t0004g0207a0044c0210t0004g0206others(13): Show | 16 | HG00544.hp2 HG00558.hp2 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.278+120A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 3/93 | chr1 | 149478167 | ||||||
| chr1:149478197
|
T | A | 2 | a0035c0015t0002g0216a0035c0015t0002g0217 | 2 | HG03017.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.278+150T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 3/93 | chr1 | 149478197 | ||||||
| chr1:149478277
|
A | C | 1 | a0202c0064t0002g0262 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.278+230A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 3/93 | chr1 | 149478277 | ||||||
| chr1:149478284
|
A | C | 1 | a0172c0204t0004g0268 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.278+237A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 3/93 | chr1 | 149478284 | ||||||
| chr1:149478358
|
A | C | 2 | a0111c0132t0001g0199a0136c0163t0001g0200 | 2 | NA18942.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.278+311A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 3/93 | chr1 | 149478358 | ||||||
| chr1:149478358
|
A | G | 1 | a0157c0188t0001g0201 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.278+311A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 3/93 | chr1 | 149478358 | ||||||
| chr1:149478482
|
G | A | 1 | a0062c0093t0001g0267 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.279-398G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 3/93 | chr1 | 149478482 | ||||||
| chr1:149478611
|
C | T | 1 | a0015c0036t0006g0004 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.279-269C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 3/93 | chr1 | 149478611 | ||||||
| chr1:149479177
|
A | G | 16 | a0006c0211t0019g0211a0043c0209t0004g0207a0044c0210t0004g0206others(13): Show | 16 | HG00544.hp2 HG00558.hp2 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.493+83A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 4/93 | chr1 | 149479177 | ||||||
| chr1:149479197
|
T | C | 1 | a0180c0072t0002g0218 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.493+103T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 4/93 | chr1 | 149479197 | ||||||
| chr1:149479276
|
A | C | 2 | a0029c0033t0001g0197a0029c0033t0001g0198 | 2 | HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.493+182A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 4/93 | chr1 | 149479276 | ||||||
| chr1:149479489
|
C | T | 6 | a0006c0211t0019g0211a0161c0197t0005g0214a0162c0196t0005g0213others(3): Show | 6 | HG00544.hp2 HG00558.hp2 HG00735.hp2 others(3): Show |
intron_variant | MODIFIER | c.493+395C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 4/93 | chr1 | 149479489 | ||||||
| chr1:149479592
|
C | A | 1 | a0174c0202t0013g0204 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.493+498C>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 4/93 | chr1 | 149479592 | ||||||
| chr1:149479628
|
G | A | 3 | a0069c0100t0001g0016a0072c0104t0001g0017a0073c0103t0001g0018 | 3 | HG02083.hp2 NA18747.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.494-514G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 4/93 | chr1 | 149479628 | ||||||
| chr1:149479647
|
G | A | 1 | a0080c0106t0001g0019 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.494-495G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 4/93 | chr1 | 149479647 | ||||||
| chr1:149479668
|
C | T | 3 | a0015c0036t0006g0004a0015c0192t0006g0270a0173c0191t0006g0271 | 4 | HG02145.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.494-474C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 4/93 | chr1 | 149479668 | ||||||
| chr1:149479865
|
C | A | 4 | a0034c0013t0002g0220a0034c0013t0002g0221a0199c0061t0002g0219others(1): Show | 4 | NA18961.hp1 NA19011.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.494-277C>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 4/93 | chr1 | 149479865 | ||||||
| chr1:149479911
|
A | T | 1 | a0182c0074t0002g0261 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.494-231A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 4/93 | chr1 | 149479911 | ||||||
| chr1:149479922
|
A | G | 1 | a0169c0205t0004g0209 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.494-220A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 4/93 | chr1 | 149479922 | ||||||
| chr1:149479999
|
A | T | 17 | a0002c0002t0003g0182a0002c0002t0003g0188a0002c0002t0003g0189others(14): Show | 17 | HG00642.hp2 HG01071.hp1 HG01975.hp1 others(14): Show |
intron_variant | MODIFIER | c.494-143A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 4/93 | chr1 | 149479999 | ||||||
| chr1:149480112
|
A | G | 1 | a0179c0071t0002g0260 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.494-30A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 4/93 | chr1 | 149480112 | ||||||
| chr1:149480227
|
A | T | 1 | a0132c0166t0012g0179 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.566+13A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 5/93 | chr1 | 149480227 | ||||||
| chr1:149480264
|
T | A | 1 | a0169c0205t0004g0209 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.566+50T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 5/93 | chr1 | 149480264 | ||||||
| chr1:149480292
|
C | G | 2 | a0077c0110t0001g0178a0163c0199t0005g0215 | 2 | HG00558.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.566+78C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 5/93 | chr1 | 149480292 | ||||||
| chr1:149480367
|
T | C | 1 | a0133c0165t0022g0020 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.566+153T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 5/93 | chr1 | 149480367 | ||||||
| chr1:149480370
|
C | G | 1 | a0133c0165t0022g0020 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.566+156C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 5/93 | chr1 | 149480370 | ||||||
| chr1:149480412
|
T | A | 1 | a0167c0203t0028g0269 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.566+198T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 5/93 | chr1 | 149480412 | ||||||
| chr1:149480412
|
T | G | 17 | a0006c0211t0019g0211a0043c0209t0004g0207a0044c0210t0004g0206others(14): Show | 17 | HG00544.hp2 HG00558.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.566+198T>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 5/93 | chr1 | 149480412 | ||||||
| chr1:149480647
|
T | G | 9 | a0043c0209t0004g0207a0044c0210t0004g0206a0164c0201t0004g0205others(6): Show | 9 | HG00735.hp1 HG01099.hp1 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.567-32T>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 5/93 | chr1 | 149480647 | ||||||
| chr1:149481019
|
T | G | 4 | a0024c0025t0001g0024a0024c0025t0001g0026a0042c0195t0001g0023others(1): Show | 4 | HG02055.hp2 HG02486.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.772+135T>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 6/93 | chr1 | 149481019 | ||||||
| chr1:149481133
|
G | A | 9 | a0016c0017t0001g0028a0016c0017t0001g0029a0025c0031t0001g0032others(6): Show | 9 | HG00738.hp2 HG01123.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.772+249G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 6/93 | chr1 | 149481133 | ||||||
| chr1:149481159
|
C | T | 49 | a0032c0012t0002g0232a0032c0012t0002g0266a0033c0011t0002g0254others(46): Show | 49 | HG00438.hp2 HG00621.hp1 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.772+275C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 6/93 | chr1 | 149481159 | ||||||
| chr1:149481272
|
T | C | 1 | a0196c0045t0018g0226 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.772+388T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 6/93 | chr1 | 149481272 | ||||||
| chr1:149481473
|
A | AT | 110 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(107): Show | 111 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.772+614dupT | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 6/93 | INFO_REALIGN_3_PRIME | chr1 | 149481473 | |||||
| chr1:149481473
|
A | ATT | 64 | a0001c0001t0001g0136a0001c0001t0001g0158a0003c0003t0001g0170others(61): Show | 64 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.772+613_772+614dup others(2): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 6/93 | INFO_REALIGN_3_PRIME | chr1 | 149481473 | |||||
| chr1:149481473
|
A | ATTT | 8 | a0012c0009t0001g0172a0023c0024t0001g0003a0024c0025t0001g0026others(5): Show | 9 | HG00438.hp1 HG02055.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.772+612_772+614dup others(3): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 6/93 | INFO_REALIGN_3_PRIME | chr1 | 149481473 | |||||
| chr1:149481473
|
A | ATTTT | 6 | a0043c0209t0004g0207a0050c0080t0001g0177a0168c0206t0004g0203others(3): Show | 6 | HG01099.hp1 HG01978.hp1 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.772+611_772+614dup others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 6/93 | INFO_REALIGN_3_PRIME | chr1 | 149481473 | |||||
| chr1:149481473
|
ATTTTTTT others(1): Show |
A | 49 | a0032c0012t0002g0232a0032c0012t0002g0266a0033c0011t0002g0254others(46): Show | 49 | HG00438.hp2 HG00621.hp1 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.772+607_772+614del others(8): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 6/93 | INFO_REALIGN_3_PRIME | chr1 | 149481473 | |||||
| chr1:149481473
|
ATTTTTTT others(4): Show |
A | 2 | a0028c0032t0001g0036a0169c0205t0004g0209 | 2 | HG03704.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.772+604_772+614del others(11): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 6/93 | INFO_REALIGN_3_PRIME | chr1 | 149481473 | |||||
| chr1:149481617
|
A | G | 1 | a0038c0038t0001g0171 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.773-558A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 6/93 | chr1 | 149481617 | ||||||
| chr1:149481774
|
A | C | 6 | a0024c0025t0001g0024a0024c0025t0001g0026a0042c0195t0001g0023others(3): Show | 6 | HG02055.hp2 HG02486.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.773-401A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 6/93 | chr1 | 149481774 | ||||||
| chr1:149481779
|
T | G | 17 | a0006c0211t0019g0211a0028c0032t0001g0036a0043c0209t0004g0207others(14): Show | 17 | HG00544.hp2 HG00558.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.773-396T>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 6/93 | chr1 | 149481779 | ||||||
| chr1:149481781
|
ATCTATCA others(1): Show |
A | 3 | a0006c0212t0002g0223a0006c0213t0002g0224a0006c0214t0002g0265 | 3 | HG01891.hp1 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.773-391_773-384del others(8): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 6/93 | INFO_REALIGN_3_PRIME | chr1 | 149481781 | |||||
| chr1:149481811
|
C | T | 3 | a0015c0036t0006g0004a0015c0192t0006g0270a0173c0191t0006g0271 | 4 | HG02145.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.773-364C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 6/93 | chr1 | 149481811 | ||||||
| chr1:149482035
|
A | G | 49 | a0032c0012t0002g0232a0032c0012t0002g0266a0033c0011t0002g0254others(46): Show | 49 | HG00438.hp2 HG00621.hp1 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.773-140A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 6/93 | chr1 | 149482035 | ||||||
| chr1:149482092
|
T | C | 6 | a0006c0211t0019g0211a0161c0197t0005g0214a0162c0196t0005g0213others(3): Show | 6 | HG00544.hp2 HG00558.hp2 HG00735.hp2 others(3): Show |
intron_variant | MODIFIER | c.773-83T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 6/93 | chr1 | 149482092 | ||||||
| chr1:149482118
|
T | G | 49 | a0032c0012t0002g0232a0032c0012t0002g0266a0033c0011t0002g0254others(46): Show | 49 | HG00438.hp2 HG00621.hp1 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.773-57T>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 6/93 | chr1 | 149482118 | ||||||
| chr1:149482136
|
A | G | 1 | a0141c0182t0001g0122 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.773-39A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 6/93 | chr1 | 149482136 | ||||||
| chr1:149482377
|
C | A | 1 | a0170c0208t0004g0202 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.824+151C>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 7/93 | chr1 | 149482377 | ||||||
| chr1:149482564
|
T | C | 1 | a0196c0045t0018g0226 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.824+338T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 7/93 | chr1 | 149482564 | ||||||
| chr1:149482761
|
C | T | 3 | a0015c0036t0006g0004a0015c0192t0006g0270a0173c0191t0006g0271 | 4 | HG02145.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.824+535C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 7/93 | chr1 | 149482761 | ||||||
| chr1:149482859
|
T | A | 1 | a0111c0132t0001g0199 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.824+633T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 7/93 | chr1 | 149482859 | ||||||
| chr1:149483066
|
G | A | 11 | a0011c0010t0001g0010a0011c0010t0001g0011a0011c0010t0001g0012others(8): Show | 11 | HG00438.hp1 HG00558.hp1 NA18942.hp2 others(8): Show |
intron_variant | MODIFIER | c.824+840G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 7/93 | chr1 | 149483066 | ||||||
| chr1:149483135
|
A | G | 1 | a0001c0001t0001g0121 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.824+909A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 7/93 | chr1 | 149483135 | ||||||
| chr1:149483200
|
G | C | 1 | a0120c0155t0001g0126 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.824+974G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 7/93 | chr1 | 149483200 | ||||||
| chr1:149483550
|
T | A | 1 | a0061c0187t0001g0173 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.824+1324T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 7/93 | chr1 | 149483550 | ||||||
| chr1:149483598
|
G | A | 1 | a0104c0141t0001g0123 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.824+1372G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 7/93 | chr1 | 149483598 | ||||||
| chr1:149483670
|
G | A | 1 | a0061c0187t0001g0173 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.824+1444G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 7/93 | chr1 | 149483670 | ||||||
| chr1:149483751
|
G | A | 1 | a0006c0213t0002g0224 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.824+1525G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 7/93 | chr1 | 149483751 | ||||||
| chr1:149483778
|
T | G | 2 | a0102c0144t0001g0127a0127c0169t0001g0052 | 2 | HG00423.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.824+1552T>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 7/93 | chr1 | 149483778 | ||||||
| chr1:149484060
|
C | T | 2 | a0198c0059t0002g0259a0205c0056t0015g0258 | 2 | HG00621.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.824+1834C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 7/93 | chr1 | 149484060 | ||||||
| chr1:149484249
|
A | G | 1 | a0130c0170t0001g0120 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.825-1881A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 7/93 | chr1 | 149484249 | ||||||
| chr1:149484263
|
C | T | 1 | a0182c0074t0002g0261 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.825-1867C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 7/93 | chr1 | 149484263 | ||||||
| chr1:149484395
|
C | T | 72 | a0006c0211t0019g0211a0006c0212t0002g0223a0006c0213t0002g0224others(69): Show | 73 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.825-1735C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 7/93 | chr1 | 149484395 | ||||||
| chr1:149484499
|
A | AAT | 5 | a0015c0036t0006g0004a0015c0192t0006g0270a0037c0016t0002g0256others(2): Show | 6 | HG00642.hp1 HG01069.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.825-1630_825-1629i others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 7/93 | INFO_REALIGN_3_PRIME | chr1 | 149484499 | |||||
| chr1:149484499
|
A | T | 9 | a0043c0209t0004g0207a0044c0210t0004g0206a0164c0201t0004g0205others(6): Show | 9 | HG00735.hp1 HG01099.hp1 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.825-1631A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 7/93 | chr1 | 149484499 | ||||||
| chr1:149484501
|
A | T | 86 | a0003c0003t0001g0115a0003c0003t0001g0116a0003c0003t0001g0117others(83): Show | 87 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.825-1629A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 7/93 | chr1 | 149484501 | ||||||
| chr1:149484503
|
T | A | 5 | a0087c0118t0001g0054a0118c0151t0001g0053a0143c0179t0001g0021others(2): Show | 5 | HG02698.hp2 HG04115.hp2 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.825-1627T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 7/93 | chr1 | 149484503 | ||||||
| chr1:149484530
|
A | T | 3 | a0033c0011t0002g0254a0033c0011t0002g0255a0178c0070t0002g0253 | 3 | NA18947.hp2 NA19082.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.825-1600A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 7/93 | chr1 | 149484530 | ||||||
| chr1:149484556
|
G | GA | 6 | a0006c0212t0002g0223a0006c0213t0002g0224a0006c0214t0002g0265others(3): Show | 7 | HG01891.hp1 HG02145.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.825-1564dupA | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 7/93 | INFO_REALIGN_3_PRIME | chr1 | 149484556 | |||||
| chr1:149484654
|
G | T | 1 | a0160c0076t0014g0225 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.825-1476G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 7/93 | chr1 | 149484654 | ||||||
| chr1:149484662
|
A | G | 72 | a0006c0211t0019g0211a0006c0212t0002g0223a0006c0213t0002g0224others(69): Show | 73 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.825-1468A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 7/93 | chr1 | 149484662 | ||||||
| chr1:149484719
|
T | C | 49 | a0032c0012t0002g0232a0032c0012t0002g0266a0033c0011t0002g0254others(46): Show | 49 | HG00438.hp2 HG00621.hp1 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.825-1411T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 7/93 | chr1 | 149484719 | ||||||
| chr1:149484724
|
A | G | 1 | a0002c0002t0007g0193 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.825-1406A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 7/93 | chr1 | 149484724 | ||||||
| chr1:149484728
|
C | T | 1 | a0167c0203t0028g0269 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.825-1402C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 7/93 | chr1 | 149484728 | ||||||
| chr1:149484809
|
C | T | 1 | a0021c0022t0001g0169 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.825-1321C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 7/93 | chr1 | 149484809 | ||||||
| chr1:149484812
|
G | T | 1 | a0188c0051t0002g0252 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.825-1318G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 7/93 | chr1 | 149484812 | ||||||
| chr1:149484819
|
G | T | 5 | a0161c0197t0005g0214a0162c0196t0005g0213a0163c0199t0005g0215others(2): Show | 5 | HG00544.hp2 HG00558.hp2 HG00735.hp2 others(2): Show |
intron_variant | MODIFIER | c.825-1311G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 7/93 | chr1 | 149484819 | ||||||
| chr1:149484876
|
G | A | 49 | a0032c0012t0002g0232a0032c0012t0002g0266a0033c0011t0002g0254others(46): Show | 49 | HG00438.hp2 HG00621.hp1 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.825-1254G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 7/93 | chr1 | 149484876 | ||||||
| chr1:149484915
|
T | C | 1 | a0043c0209t0004g0207 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.825-1215T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 7/93 | chr1 | 149484915 | ||||||
| chr1:149484985
|
T | A | 1 | a0160c0076t0014g0225 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.825-1145T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 7/93 | chr1 | 149484985 | ||||||
| chr1:149485025
|
G | A | 53 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(50): Show | 53 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.825-1105G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 7/93 | chr1 | 149485025 | ||||||
| chr1:149485108
|
C | G | 16 | a0006c0211t0019g0211a0043c0209t0004g0207a0044c0210t0004g0206others(13): Show | 16 | HG00544.hp2 HG00558.hp2 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.825-1022C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 7/93 | chr1 | 149485108 | ||||||
| chr1:149485235
|
G | A | 1 | a0199c0061t0002g0219 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.825-895G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 7/93 | chr1 | 149485235 | ||||||
| chr1:149485260
|
T | G | 68 | a0006c0211t0019g0211a0006c0212t0002g0223a0006c0213t0002g0224others(65): Show | 68 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.825-870T>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 7/93 | chr1 | 149485260 | ||||||
| chr1:149485264
|
A | G | 49 | a0032c0012t0002g0232a0032c0012t0002g0266a0033c0011t0002g0254others(46): Show | 49 | HG00438.hp2 HG00621.hp1 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.825-866A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 7/93 | chr1 | 149485264 | ||||||
| chr1:149485304
|
G | A | 1 | a0167c0203t0028g0269 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.825-826G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 7/93 | chr1 | 149485304 | ||||||
| chr1:149485420
|
C | T | 1 | a0084c0115t0001g0114 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.825-710C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 7/93 | chr1 | 149485420 | ||||||
| chr1:149485656
|
T | A | 3 | a0023c0024t0001g0003a0076c0109t0001g0137a0094c0125t0001g0138 | 4 | HG02257.hp2 HG02630.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.825-474T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 7/93 | chr1 | 149485656 | ||||||
| chr1:149485681
|
A | T | 8 | a0017c0019t0001g0112a0017c0019t0001g0167a0018c0018t0001g0113others(5): Show | 8 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.825-449A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 7/93 | chr1 | 149485681 | ||||||
| chr1:149485747
|
C | T | 1 | a0096c0127t0001g0111 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.825-383C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 7/93 | chr1 | 149485747 | ||||||
| chr1:149485762
|
G | A | 2 | a0031c0028t0003g0180a0031c0028t0003g0194 | 2 | NA18972.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.825-368G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 7/93 | chr1 | 149485762 | ||||||
| chr1:149486394
|
T | A | 1 | a0158c0084t0001g0049 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.988+101T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 8/93 | chr1 | 149486394 | ||||||
| chr1:149486399
|
G | A | 5 | a0161c0197t0005g0214a0162c0196t0005g0213a0163c0199t0005g0215others(2): Show | 5 | HG00544.hp2 HG00558.hp2 HG00735.hp2 others(2): Show |
intron_variant | MODIFIER | c.988+106G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 8/93 | chr1 | 149486399 | ||||||
| chr1:149486481
|
C | T | 40 | a0002c0002t0003g0182a0002c0002t0003g0188a0002c0002t0003g0189others(37): Show | 40 | HG00438.hp1 HG00558.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.988+188C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 8/93 | chr1 | 149486481 | ||||||
| chr1:149486504
|
G | A | 1 | a0021c0022t0001g0080 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.988+211G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 8/93 | chr1 | 149486504 | ||||||
| chr1:149486536
|
C | T | 2 | a0074c0112t0001g0104a0075c0108t0001g0163 | 2 | HG03139.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.988+243C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 8/93 | chr1 | 149486536 | ||||||
| chr1:149486826
|
G | A | 49 | a0032c0012t0002g0232a0032c0012t0002g0266a0033c0011t0002g0254others(46): Show | 49 | HG00438.hp2 HG00621.hp1 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.989-506G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 8/93 | chr1 | 149486826 | ||||||
| chr1:149486839
|
G | A | 4 | a0024c0025t0001g0024a0024c0025t0001g0026a0042c0195t0001g0023others(1): Show | 4 | HG02055.hp2 HG02486.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.989-493G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 8/93 | chr1 | 149486839 | ||||||
| chr1:149486985
|
G | C | 3 | a0009c0006t0001g0081a0009c0006t0001g0082a0009c0006t0001g0139 | 3 | HG00099.hp1 HG00741.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.989-347G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 8/93 | chr1 | 149486985 | ||||||
| chr1:149487014
|
A | C | 1 | a0146c0176t0003g0110 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.989-318A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 8/93 | chr1 | 149487014 | ||||||
| chr1:149487135
|
AT | A | 9 | a0043c0209t0004g0207a0044c0210t0004g0206a0164c0201t0004g0205others(6): Show | 9 | HG00735.hp1 HG01099.hp1 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.989-193delT | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 8/93 | INFO_REALIGN_3_PRIME | chr1 | 149487135 | |||||
| chr1:149487158
|
A | G | 3 | a0015c0036t0006g0004a0015c0192t0006g0270a0173c0191t0006g0271 | 4 | HG02145.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.989-174A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 8/93 | chr1 | 149487158 | ||||||
| chr1:149487199
|
G | A | 1 | a0160c0076t0014g0225 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.989-133G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 8/93 | chr1 | 149487199 | ||||||
| chr1:149487200
|
C | G | 1 | a0084c0115t0001g0114 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.989-132C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 8/93 | chr1 | 149487200 | ||||||
| chr1:149487216
|
G | C | 1 | a0167c0203t0028g0269 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.989-116G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 8/93 | chr1 | 149487216 | ||||||
| chr1:149487403
|
G | A | 1 | a0006c0214t0002g0265 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1040+20G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 9/93 | chr1 | 149487403 | ||||||
| chr1:149487460
|
C | T | 16 | a0006c0211t0019g0211a0043c0209t0004g0207a0044c0210t0004g0206others(13): Show | 16 | HG00544.hp2 HG00558.hp2 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.1040+77C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 9/93 | chr1 | 149487460 | ||||||
| chr1:149487479
|
C | T | 1 | a0003c0136t0001g0005 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1040+96C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 9/93 | chr1 | 149487479 | ||||||
| chr1:149487517
|
T | G | 1 | a0139c0172t0001g0105 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1040+134T>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 9/93 | chr1 | 149487517 | ||||||
| chr1:149487571
|
A | G | 1 | a0132c0166t0012g0179 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1040+188A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 9/93 | chr1 | 149487571 | ||||||
| chr1:149487626
|
C | T | 1 | a0208c0048t0002g0251 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1040+243C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 9/93 | chr1 | 149487626 | ||||||
| chr1:149487633
|
G | A | 1 | a0059c0091t0001g0130 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1040+250G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 9/93 | chr1 | 149487633 | ||||||
| chr1:149487638
|
T | G | 3 | a0015c0036t0006g0004a0015c0192t0006g0270a0173c0191t0006g0271 | 4 | HG02145.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1040+255T>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 9/93 | chr1 | 149487638 | ||||||
| chr1:149487661
|
A | G | 49 | a0032c0012t0002g0232a0032c0012t0002g0266a0033c0011t0002g0254others(46): Show | 49 | HG00438.hp2 HG00621.hp1 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.1040+278A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 9/93 | chr1 | 149487661 | ||||||
| chr1:149487668
|
A | C | 1 | a0139c0172t0001g0105 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1040+285A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 9/93 | chr1 | 149487668 | ||||||
| chr1:149487673
|
C | A | 1 | a0011c0010t0001g0010 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1040+290C>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 9/93 | chr1 | 149487673 | ||||||
| chr1:149487723
|
G | C | 19 | a0006c0211t0019g0211a0006c0212t0002g0223a0006c0213t0002g0224others(16): Show | 19 | HG00544.hp2 HG00558.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.1041-290G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 9/93 | chr1 | 149487723 | ||||||
| chr1:149487775
|
C | CTG | 13 | a0010c0007t0001g0002a0021c0022t0001g0080a0022c0023t0001g0160others(10): Show | 14 | HG00642.hp2 HG01069.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.1041-190_1041-189d others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 9/93 | INFO_REALIGN_3_PRIME | chr1 | 149487775 | |||||
| chr1:149487775
|
C | CTGTG | 11 | a0002c0002t0007g0193a0004c0027t0001g0001a0018c0018t0001g0166others(8): Show | 12 | HG01978.hp1 HG02257.hp1 HG02300.hp1 others(9): Show |
intron_variant | MODIFIER | c.1041-192_1041-189d others(6): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 9/93 | INFO_REALIGN_3_PRIME | chr1 | 149487775 | |||||
| chr1:149487775
|
C | CTGTGTG | 7 | a0006c0212t0002g0223a0006c0214t0002g0265a0017c0019t0001g0112others(4): Show | 7 | HG01891.hp1 HG02486.hp2 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.1041-194_1041-189d others(8): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 9/93 | INFO_REALIGN_3_PRIME | chr1 | 149487775 | |||||
| chr1:149487775
|
C | CTGTGTGT others(3): Show |
1 | a0018c0018t0001g0113 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1041-198_1041-189d others(12): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 9/93 | INFO_REALIGN_3_PRIME | chr1 | 149487775 | |||||
| chr1:149487775
|
CTG | C | 33 | a0001c0001t0001g0070a0001c0001t0001g0071a0002c0002t0003g0182others(30): Show | 33 | HG00733.hp2 HG00741.hp2 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.1041-190_1041-189d others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 9/93 | INFO_REALIGN_3_PRIME | chr1 | 149487775 | |||||
| chr1:149487775
|
CTGTG | C | 65 | a0001c0001t0001g0121a0003c0003t0001g0115a0003c0003t0001g0116others(62): Show | 66 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.1041-192_1041-189d others(6): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 9/93 | INFO_REALIGN_3_PRIME | chr1 | 149487775 | |||||
| chr1:149487775
|
CTGTGTG | C | 13 | a0024c0025t0001g0026a0028c0032t0001g0036a0035c0015t0002g0217others(10): Show | 13 | HG00438.hp2 HG02055.hp2 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.1041-194_1041-189d others(8): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 9/93 | INFO_REALIGN_3_PRIME | chr1 | 149487775 | |||||
| chr1:149487775
|
CTGTGTGT others(1): Show |
C | 37 | a0013c0035t0001g0038a0013c0035t0001g0084a0032c0012t0002g0232others(34): Show | 37 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.1041-196_1041-189d others(10): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 9/93 | INFO_REALIGN_3_PRIME | chr1 | 149487775 | |||||
| chr1:149487775
|
CTGTGTGT others(3): Show |
C | 3 | a0034c0013t0002g0220a0034c0013t0002g0221a0196c0045t0018g0226 | 3 | HG03942.hp1 NA18961.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.1041-198_1041-189d others(12): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 9/93 | INFO_REALIGN_3_PRIME | chr1 | 149487775 | |||||
| chr1:149487775
|
CTGTGTGT others(9): Show |
C | 1 | a0042c0195t0001g0023 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1041-204_1041-189d others(18): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 9/93 | INFO_REALIGN_3_PRIME | chr1 | 149487775 | |||||
| chr1:149487775
|
CTGTGTGT others(13): Show |
C | 3 | a0005c0004t0001g0056a0005c0004t0001g0131a0005c0004t0001g0132 | 3 | NA18977.hp1 NA18985.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1041-208_1041-189d others(22): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 9/93 | INFO_REALIGN_3_PRIME | chr1 | 149487775 | |||||
| chr1:149487782
|
T | G | 1 | a0106c0139t0001g0055 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1041-231T>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 9/93 | chr1 | 149487782 | ||||||
| chr1:149487805
|
G | GTGTGTGT others(3): Show |
5 | a0164c0201t0004g0205a0168c0206t0004g0203a0170c0208t0004g0202others(2): Show | 5 | HG00735.hp1 HG01099.hp1 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.1041-199_1041-198i others(12): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 9/93 | INFO_REALIGN_3_PRIME | chr1 | 149487805 | |||||
| chr1:149487805
|
G | GTGTGTT | 8 | a0043c0209t0004g0207a0044c0210t0004g0206a0161c0197t0005g0214others(5): Show | 8 | HG00544.hp2 HG00558.hp2 HG00735.hp2 others(5): Show |
intron_variant | MODIFIER | c.1041-203_1041-202i others(8): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 9/93 | INFO_REALIGN_3_PRIME | chr1 | 149487805 | |||||
| chr1:149487832
|
G | A | 15 | a0003c0136t0001g0005a0004c0026t0001g0007a0004c0026t0001g0008others(12): Show | 17 | HG01891.hp2 HG02055.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.1041-181G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 9/93 | chr1 | 149487832 | ||||||
| chr1:149487838
|
C | G | 49 | a0032c0012t0002g0232a0032c0012t0002g0266a0033c0011t0002g0254others(46): Show | 49 | HG00438.hp2 HG00621.hp1 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.1041-175C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 9/93 | chr1 | 149487838 | ||||||
| chr1:149487894
|
C | T | 69 | a0006c0211t0019g0211a0006c0212t0002g0223a0006c0213t0002g0224others(66): Show | 69 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.1041-119C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 9/93 | chr1 | 149487894 | ||||||
| chr1:149487905
|
C | G | 17 | a0006c0211t0019g0211a0043c0209t0004g0207a0044c0210t0004g0206others(14): Show | 17 | HG00544.hp2 HG00558.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.1041-108C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 9/93 | chr1 | 149487905 | ||||||
| chr1:149487963
|
T | TGGTTTCT others(4748): Show |
1 | a0060c0092t0001g0069 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1438+104_1438+105i others(4757): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 12/93 | INFO_REALIGN_3_PRIME | chr1 | 149487963 | |||||
| chr1:149487967
|
T | A | 5 | a0089c0123t0001g0164a0142c0180t0001g0108a0145c0177t0001g0165others(2): Show | 5 | HG01109.hp2 HG01168.hp2 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1041-46T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 9/93 | chr1 | 149487967 | ||||||
| chr1:149487992
|
T | C | 1 | a0160c0076t0014g0225 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1041-21T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 9/93 | chr1 | 149487992 | ||||||
| chr1:149488173
|
A | ATTGACAT others(23738): Show |
1 | a0006c0212t0002g0223 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1213+176_1213+177i others(23747): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 10/93 | INFO_REALIGN_3_PRIME | chr1 | 149488173 | |||||
| chr1:149488173
|
A | ATTGACAT others(4744): Show |
1 | a0006c0213t0002g0224 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1213+176_1213+177i others(4753): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 10/93 | INFO_REALIGN_3_PRIME | chr1 | 149488173 | |||||
| chr1:149488173
|
A | ATTGACAT others(9507): Show |
1 | a0006c0214t0002g0265 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1213+176_1213+177i others(9516): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 10/93 | INFO_REALIGN_3_PRIME | chr1 | 149488173 | |||||
| chr1:149488173
|
A | ATTGACAT others(14257): Show |
1 | a0006c0211t0019g0211 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1213+176_1213+177i others(14266): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 10/93 | INFO_REALIGN_3_PRIME | chr1 | 149488173 | |||||
| chr1:149488260
|
C | CCCTTACT others(14251): Show |
1 | a0182c0074t0002g0261 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1213+176_1213+177i others(14260): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 10/93 | INFO_REALIGN_3_PRIME | chr1 | 149488260 | |||||
| chr1:149488279
|
T | A | 1 | a0068c0096t0010g0090 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1213+94T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 10/93 | chr1 | 149488279 | ||||||
| chr1:149488362
|
T | G | 78 | a0004c0027t0001g0001a0006c0211t0019g0211a0006c0212t0002g0223others(75): Show | 80 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.1213+177T>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 10/93 | chr1 | 149488362 | ||||||
| chr1:149488382
|
T | C | 2 | a0116c0150t0001g0014a0123c0157t0001g0015 | 2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1213+197T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 10/93 | chr1 | 149488382 | ||||||
| chr1:149488399
|
A | G | 75 | a0006c0211t0019g0211a0006c0212t0002g0223a0006c0213t0002g0224others(72): Show | 76 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.1213+214A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 10/93 | chr1 | 149488399 | ||||||
| chr1:149488407
|
C | A | 2 | a0116c0150t0001g0014a0123c0157t0001g0015 | 2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1213+222C>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 10/93 | chr1 | 149488407 | ||||||
| chr1:149488426
|
T | A | 67 | a0015c0036t0006g0004a0015c0192t0006g0270a0032c0012t0002g0232others(64): Show | 68 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.1213+241T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 10/93 | chr1 | 149488426 | ||||||
| chr1:149488429
|
C | T | 67 | a0015c0036t0006g0004a0015c0192t0006g0270a0032c0012t0002g0232others(64): Show | 68 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.1213+244C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 10/93 | chr1 | 149488429 | ||||||
| chr1:149488430
|
G | A | 5 | a0006c0211t0019g0211a0042c0195t0001g0023a0116c0150t0001g0014others(2): Show | 5 | HG01346.hp2 HG02055.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1213+245G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 10/93 | chr1 | 149488430 | ||||||
| chr1:149488431
|
T | C | 2 | a0116c0150t0001g0014a0123c0157t0001g0015 | 2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1213+246T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 10/93 | chr1 | 149488431 | ||||||
| chr1:149488436
|
C | T | 67 | a0015c0036t0006g0004a0015c0192t0006g0270a0032c0012t0002g0232others(64): Show | 68 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.1213+251C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 10/93 | chr1 | 149488436 | ||||||
| chr1:149488437
|
C | G | 2 | a0035c0015t0002g0216a0035c0015t0002g0217 | 2 | HG03017.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.1213+252C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 10/93 | chr1 | 149488437 | ||||||
| chr1:149488460
|
A | G | 1 | a0042c0195t0001g0023 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1213+275A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 10/93 | chr1 | 149488460 | ||||||
| chr1:149488480
|
A | G | 1 | a0006c0213t0002g0224 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1213+295A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 10/93 | chr1 | 149488480 | ||||||
| chr1:149488537
|
G | A | 1 | a0171c0207t0004g0208 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1213+352G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 10/93 | chr1 | 149488537 | ||||||
| chr1:149488716
|
C | G | 1 | a0112c0131t0001g0118 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1214-189C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 10/93 | chr1 | 149488716 | ||||||
| chr1:149488822
|
T | C | 1 | a0156c0099t0001g0013 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1214-83T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 10/93 | chr1 | 149488822 | ||||||
| chr1:149488838
|
A | G | 2 | a0006c0212t0002g0223a0006c0214t0002g0265 | 2 | HG01891.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1214-67A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 10/93 | chr1 | 149488838 | ||||||
| chr1:149488878
|
G | A | 1 | a0042c0195t0001g0023 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1214-27G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 10/93 | chr1 | 149488878 | ||||||
| chr1:149488893
|
A | G | 1 | a0100c0145t0001g0076 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1214-12A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 10/93 | chr1 | 149488893 | ||||||
| chr1:149489029
|
G | T | 1 | a0073c0103t0001g0018 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1265+73G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 11/93 | chr1 | 149489029 | ||||||
| chr1:149489035
|
T | C | 1 | a0006c0212t0002g0223 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1265+79T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 11/93 | chr1 | 149489035 | ||||||
| chr1:149489051
|
A | C | 1 | a0156c0099t0001g0013 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1265+95A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 11/93 | chr1 | 149489051 | ||||||
| chr1:149489123
|
T | G | 1 | a0203c0065t0002g0240 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1265+167T>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 11/93 | chr1 | 149489123 | ||||||
| chr1:149489130
|
C | T | 2 | a0144c0178t0001g0119a0147c0220t0001g0094 | 2 | HG02129.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.1265+174C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 11/93 | chr1 | 149489130 | ||||||
| chr1:149489135
|
T | A | 4 | a0006c0213t0002g0224a0043c0209t0004g0207a0044c0210t0004g0206others(1): Show | 4 | HG02165.hp1 HG02622.hp2 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.1265+179T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 11/93 | chr1 | 149489135 | ||||||
| chr1:149489135
|
T | TCATTTAC others(4729): Show |
2 | a0179c0071t0002g0260a0180c0072t0002g0218 | 2 | HG00738.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1265+216_1265+217i others(4738): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 11/93 | INFO_REALIGN_3_PRIME | chr1 | 149489135 | |||||
| chr1:149489135
|
T | TCATTTAC others(4729): Show |
1 | a0181c0073t0002g0272 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1265+216_1265+217i others(4738): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 11/93 | INFO_REALIGN_3_PRIME | chr1 | 149489135 | |||||
| chr1:149489135
|
T | TCATTTAC others(4729): Show |
2 | a0039c0219t0002g0227a0178c0070t0002g0253 | 2 | NA18981.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.1265+216_1265+217i others(4738): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 11/93 | INFO_REALIGN_3_PRIME | chr1 | 149489135 | |||||
| chr1:149489167
|
C | T | 1 | a0186c0044t0017g0239 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1265+211C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 11/93 | chr1 | 149489167 | ||||||
| chr1:149489173
|
G | A | 60 | a0006c0214t0002g0265a0015c0036t0006g0004a0015c0192t0006g0270others(57): Show | 61 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.1265+217G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 11/93 | chr1 | 149489173 | ||||||
| chr1:149489190
|
A | G | 1 | a0006c0212t0002g0223 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1265+234A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 11/93 | chr1 | 149489190 | ||||||
| chr1:149489195
|
A | G | 1 | a0006c0213t0002g0224 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1265+239A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 11/93 | chr1 | 149489195 | ||||||
| chr1:149489227
|
C | A | 5 | a0161c0197t0005g0214a0162c0196t0005g0213a0163c0199t0005g0215others(2): Show | 5 | HG00544.hp2 HG00558.hp2 HG00735.hp2 others(2): Show |
intron_variant | MODIFIER | c.1265+271C>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 11/93 | chr1 | 149489227 | ||||||
| chr1:149489294
|
C | A | 3 | a0015c0036t0006g0004a0015c0192t0006g0270a0173c0191t0006g0271 | 4 | HG02145.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1266-267C>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 11/93 | chr1 | 149489294 | ||||||
| chr1:149489313
|
G | A | 1 | a0009c0006t0001g0082 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1266-248G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 11/93 | chr1 | 149489313 | ||||||
| chr1:149489322
|
G | A | 1 | a0114c0137t0001g0133 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1266-239G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 11/93 | chr1 | 149489322 | ||||||
| chr1:149489338
|
CCT | C | 62 | a0006c0214t0002g0265a0015c0036t0006g0004a0015c0192t0006g0270others(59): Show | 63 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.1266-201_1266-200d others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 11/93 | INFO_REALIGN_3_PRIME | chr1 | 149489338 | |||||
| chr1:149489338
|
CCTCT | C | 3 | a0006c0213t0002g0224a0125c0159t0001g0147a0135c0161t0001g0057 | 3 | HG00733.hp1 HG02922.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1266-203_1266-200d others(6): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 11/93 | INFO_REALIGN_3_PRIME | chr1 | 149489338 | |||||
| chr1:149489338
|
CCTCTCTC others(5): Show |
C | 1 | a0179c0071t0002g0260 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1266-211_1266-200d others(14): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 11/93 | INFO_REALIGN_3_PRIME | chr1 | 149489338 | |||||
| chr1:149489390
|
C | T | 64 | a0006c0213t0002g0224a0006c0214t0002g0265a0015c0036t0006g0004others(61): Show | 65 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.1266-171C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 11/93 | chr1 | 149489390 | ||||||
| chr1:149489459
|
T | C | 1 | a0006c0214t0002g0265 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1266-102T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 11/93 | chr1 | 149489459 | ||||||
| chr1:149489496
|
C | G | 2 | a0006c0211t0019g0211a0167c0203t0028g0269 | 2 | HG02109.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1266-65C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 11/93 | chr1 | 149489496 | ||||||
| chr1:149489543
|
T | A | 3 | a0021c0022t0001g0080a0021c0022t0001g0169a0078c0111t0001g0102 | 3 | HG02280.hp2 HG03209.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1266-18T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 11/93 | chr1 | 149489543 | ||||||
| chr1:149489827
|
A | G | 3 | a0009c0006t0001g0081a0009c0006t0001g0082a0009c0006t0001g0139 | 3 | HG00099.hp1 HG00741.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.1438+94A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 12/93 | chr1 | 149489827 | ||||||
| chr1:149489838
|
G | A | 157 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(154): Show | 157 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.1438+105G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 12/93 | chr1 | 149489838 | ||||||
| chr1:149489851
|
A | G | 15 | a0001c0001t0001g0158a0002c0002t0007g0190a0021c0022t0001g0169others(12): Show | 15 | HG02055.hp2 HG02135.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1438+118A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 12/93 | chr1 | 149489851 | ||||||
| chr1:149489952
|
T | C | 53 | a0006c0213t0002g0224a0015c0036t0006g0004a0015c0192t0006g0270others(50): Show | 54 | HG00438.hp2 HG00621.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.1438+219T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 12/93 | chr1 | 149489952 | ||||||
| chr1:149489969
|
G | A | 1 | a0199c0061t0002g0219 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1438+236G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 12/93 | chr1 | 149489969 | ||||||
| chr1:149489974
|
C | G | 2 | a0043c0209t0004g0207a0044c0210t0004g0206 | 2 | HG02165.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.1438+241C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 12/93 | chr1 | 149489974 | ||||||
| chr1:149489998
|
C | T | 64 | a0006c0213t0002g0224a0006c0214t0002g0265a0015c0036t0006g0004others(61): Show | 65 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.1438+265C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 12/93 | chr1 | 149489998 | ||||||
| chr1:149490032
|
G | T | 2 | a0043c0209t0004g0207a0044c0210t0004g0206 | 2 | HG02165.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.1438+299G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 12/93 | chr1 | 149490032 | ||||||
| chr1:149490039
|
A | G | 2 | a0043c0209t0004g0207a0044c0210t0004g0206 | 2 | HG02165.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.1438+306A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 12/93 | chr1 | 149490039 | ||||||
| chr1:149490099
|
G | A | 7 | a0164c0201t0004g0205a0168c0206t0004g0203a0169c0205t0004g0209others(4): Show | 7 | HG00735.hp1 HG01099.hp1 HG02698.hp1 others(4): Show |
intron_variant | MODIFIER | c.1439-344G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 12/93 | chr1 | 149490099 | ||||||
| chr1:149490172
|
T | C | 43 | a0032c0012t0002g0232a0032c0012t0002g0266a0033c0011t0002g0254others(40): Show | 43 | HG00438.hp2 HG00621.hp1 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.1439-271T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 12/93 | chr1 | 149490172 | ||||||
| chr1:149490213
|
A | G | 1 | a0198c0059t0002g0259 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1439-230A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 12/93 | chr1 | 149490213 | ||||||
| chr1:149490235
|
A | T | 2 | a0043c0209t0004g0207a0044c0210t0004g0206 | 2 | HG02165.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.1439-208A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 12/93 | chr1 | 149490235 | ||||||
| chr1:149490314
|
T | A | 1 | a0006c0214t0002g0265 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1439-129T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 12/93 | chr1 | 149490314 | ||||||
| chr1:149490361
|
CT | C | 59 | a0015c0036t0006g0004a0015c0192t0006g0270a0032c0012t0002g0232others(56): Show | 60 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.1439-81delT | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 12/93 | chr1 | 149490361 | ||||||
| chr1:149490544
|
C | A | 9 | a0028c0032t0001g0161a0029c0033t0001g0197a0029c0033t0001g0198others(6): Show | 9 | HG02155.hp2 HG02809.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1490+50C>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 13/93 | chr1 | 149490544 | ||||||
| chr1:149490611
|
TCCTACTA others(6): Show |
T | 1 | a0004c0027t0001g0001 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1490+119_1490+131d others(15): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 13/93 | INFO_REALIGN_3_PRIME | chr1 | 149490611 | |||||
| chr1:149490621
|
A | G | 2 | a0043c0209t0004g0207a0044c0210t0004g0206 | 2 | HG02165.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.1490+127A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 13/93 | chr1 | 149490621 | ||||||
| chr1:149490714
|
A | C | 2 | a0143c0179t0001g0021a0149c0183t0001g0022 | 2 | HG02698.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1490+220A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 13/93 | chr1 | 149490714 | ||||||
| chr1:149490739
|
A | G | 1 | a0160c0076t0014g0225 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1490+245A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 13/93 | chr1 | 149490739 | ||||||
| chr1:149490834
|
C | G | 1 | a0106c0139t0001g0055 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1491-305C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 13/93 | chr1 | 149490834 | ||||||
| chr1:149490844
|
C | G | 22 | a0032c0012t0002g0232a0032c0012t0002g0266a0033c0011t0002g0254others(19): Show | 22 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.1491-295C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 13/93 | chr1 | 149490844 | ||||||
| chr1:149490852
|
G | C | 1 | a0009c0006t0001g0081 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1491-287G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 13/93 | chr1 | 149490852 | ||||||
| chr1:149490882
|
TTC | T | 5 | a0006c0211t0019g0211a0161c0197t0005g0214a0162c0196t0005g0213others(2): Show | 5 | HG00558.hp2 HG00735.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1491-241_1491-240d others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 13/93 | INFO_REALIGN_3_PRIME | chr1 | 149490882 | |||||
| chr1:149490892
|
CTCTCTCT others(3): Show |
C | 1 | a0006c0214t0002g0265 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1491-245_1491-236d others(12): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 13/93 | INFO_REALIGN_3_PRIME | chr1 | 149490892 | |||||
| chr1:149490892
|
CTCTCTCT others(9): Show |
C | 47 | a0015c0036t0006g0004a0015c0192t0006g0270a0032c0012t0002g0232others(44): Show | 48 | HG00438.hp2 HG00621.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.1491-245_1491-230d others(18): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 13/93 | INFO_REALIGN_3_PRIME | chr1 | 149490892 | |||||
| chr1:149490896
|
CTCTGTGT others(19): Show |
C | 1 | a0091c0122t0008g0157 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1491-241_1491-216d others(28): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 13/93 | INFO_REALIGN_3_PRIME | chr1 | 149490896 | |||||
| chr1:149490898
|
C | CTG | 26 | a0002c0002t0003g0182a0002c0002t0003g0188a0002c0002t0003g0189others(23): Show | 26 | HG01071.hp1 HG01975.hp1 HG02148.hp1 others(23): Show |
intron_variant | MODIFIER | c.1491-220_1491-219d others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 13/93 | INFO_REALIGN_3_PRIME | chr1 | 149490898 | |||||
| chr1:149490898
|
C | G | 9 | a0006c0211t0019g0211a0042c0195t0001g0023a0057c0088t0001g0089others(6): Show | 9 | HG00558.hp2 HG00735.hp2 HG01516.hp1 others(6): Show |
intron_variant | MODIFIER | c.1491-241C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 13/93 | chr1 | 149490898 | ||||||
| chr1:149490898
|
CTGTG | C | 11 | a0065c0098t0001g0101a0066c0097t0001g0175a0164c0201t0004g0205others(8): Show | 11 | HG00735.hp1 HG01099.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1491-222_1491-219d others(6): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 13/93 | INFO_REALIGN_3_PRIME | chr1 | 149490898 | |||||
| chr1:149490900
|
G | C | 7 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(4): Show | 7 | HG00099.hp2 HG01099.hp2 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.1491-239G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 13/93 | chr1 | 149490900 | ||||||
| chr1:149490901
|
T | A | 5 | a0006c0211t0019g0211a0161c0197t0005g0214a0162c0196t0005g0213others(2): Show | 5 | HG00558.hp2 HG00735.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1491-238T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 13/93 | chr1 | 149490901 | ||||||
| chr1:149490903
|
T | A | 1 | a0165c0200t0005g0212 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1491-236T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 13/93 | chr1 | 149490903 | ||||||
| chr1:149490914
|
G | C | 1 | a0160c0076t0014g0225 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1491-225G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 13/93 | chr1 | 149490914 | ||||||
| chr1:149490915
|
T | TGC | 3 | a0043c0209t0004g0207a0044c0210t0004g0206a0182c0074t0002g0261 | 3 | HG01346.hp2 HG02165.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.1491-223_1491-222i others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 13/93 | INFO_REALIGN_3_PRIME | chr1 | 149490915 | |||||
| chr1:149490917
|
T | C | 2 | a0039c0219t0002g0227a0178c0070t0002g0253 | 2 | NA18981.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.1491-222T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 13/93 | chr1 | 149490917 | ||||||
| chr1:149490919
|
T | C | 2 | a0083c0116t0023g0103a0110c0133t0001g0058 | 2 | NA18906.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.1491-220T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 13/93 | chr1 | 149490919 | ||||||
| chr1:149490921
|
C | CGT | 3 | a0029c0033t0001g0197a0029c0033t0001g0198a0131c0171t0001g0145 | 3 | HG03098.hp1 HG03225.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.1491-195_1491-194d others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 13/93 | INFO_REALIGN_3_PRIME | chr1 | 149490921 | |||||
| chr1:149490921
|
C | T | 56 | a0006c0212t0002g0223a0006c0213t0002g0224a0015c0036t0006g0004others(53): Show | 57 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.1491-218C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 13/93 | chr1 | 149490921 | ||||||
| chr1:149490922
|
G | C | 47 | a0015c0036t0006g0004a0015c0192t0006g0270a0032c0012t0002g0232others(44): Show | 48 | HG00438.hp2 HG00621.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.1491-217G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 13/93 | chr1 | 149490922 | ||||||
| chr1:149490923
|
T | C | 2 | a0006c0212t0002g0223a0165c0200t0005g0212 | 2 | HG00544.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.1491-216T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 13/93 | chr1 | 149490923 | ||||||
| chr1:149490942
|
G | C | 51 | a0006c0211t0019g0211a0006c0214t0002g0265a0015c0036t0006g0004others(48): Show | 52 | HG00438.hp2 HG00621.hp1 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.1491-197G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 13/93 | chr1 | 149490942 | ||||||
| chr1:149490943
|
T | C | 2 | a0006c0211t0019g0211a0006c0214t0002g0265 | 2 | HG02895.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1491-196T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 13/93 | chr1 | 149490943 | ||||||
| chr1:149490944
|
G | A | 51 | a0006c0211t0019g0211a0006c0214t0002g0265a0015c0036t0006g0004others(48): Show | 52 | HG00438.hp2 HG00621.hp1 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.1491-195G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 13/93 | chr1 | 149490944 | ||||||
| chr1:149490947
|
C | T | 52 | a0006c0211t0019g0211a0006c0213t0002g0224a0006c0214t0002g0265others(49): Show | 53 | HG00438.hp2 HG00621.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.1491-192C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 13/93 | chr1 | 149490947 | ||||||
| chr1:149490948
|
A | G | 51 | a0006c0211t0019g0211a0006c0214t0002g0265a0015c0036t0006g0004others(48): Show | 52 | HG00438.hp2 HG00621.hp1 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.1491-191A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 13/93 | chr1 | 149490948 | ||||||
| chr1:149490952
|
G | GTCTT | 32 | a0006c0212t0002g0223a0006c0213t0002g0224a0022c0023t0001g0156others(29): Show | 32 | HG00544.hp2 HG00558.hp2 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.1491-184_1491-183i others(6): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 13/93 | INFO_REALIGN_3_PRIME | chr1 | 149490952 | |||||
| chr1:149490952
|
G | T | 51 | a0006c0211t0019g0211a0006c0214t0002g0265a0015c0036t0006g0004others(48): Show | 52 | HG00438.hp2 HG00621.hp1 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.1491-187G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 13/93 | chr1 | 149490952 | ||||||
| chr1:149491039
|
C | G | 30 | a0004c0027t0001g0001a0006c0211t0019g0211a0006c0212t0002g0223others(27): Show | 31 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.1491-100C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 13/93 | chr1 | 149491039 | ||||||
| chr1:149491056
|
C | T | 47 | a0015c0036t0006g0004a0015c0192t0006g0270a0032c0012t0002g0232others(44): Show | 48 | HG00438.hp2 HG00621.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.1491-83C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 13/93 | chr1 | 149491056 | ||||||
| chr1:149491058
|
A | G | 1 | a0179c0071t0002g0260 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1491-81A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 13/93 | chr1 | 149491058 | ||||||
| chr1:149491082
|
G | T | 1 | a0160c0076t0014g0225 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1491-57G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 13/93 | chr1 | 149491082 | ||||||
| chr1:149491339
|
G | A | 2 | a0043c0209t0004g0207a0044c0210t0004g0206 | 2 | HG02165.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.1663+28G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 14/93 | chr1 | 149491339 | ||||||
| chr1:149491410
|
G | A | 1 | a0079c0107t0001g0059 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1663+99G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 14/93 | chr1 | 149491410 | ||||||
| chr1:149491514
|
G | C | 3 | a0023c0024t0001g0003a0076c0109t0001g0137a0094c0125t0001g0138 | 4 | HG02257.hp2 HG02630.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1663+203G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 14/93 | chr1 | 149491514 | ||||||
| chr1:149491534
|
C | T | 1 | a0072c0104t0001g0017 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1663+223C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 14/93 | chr1 | 149491534 | ||||||
| chr1:149491646
|
C | G | 1 | a0160c0076t0014g0225 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1663+335C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 14/93 | chr1 | 149491646 | ||||||
| chr1:149491692
|
G | A | 5 | a0161c0197t0005g0214a0162c0196t0005g0213a0163c0199t0005g0215others(2): Show | 5 | HG00544.hp2 HG00558.hp2 HG00735.hp2 others(2): Show |
intron_variant | MODIFIER | c.1664-334G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 14/93 | chr1 | 149491692 | ||||||
| chr1:149491699
|
T | G | 3 | a0186c0044t0017g0239a0207c0046t0002g0241a0209c0047t0002g0242 | 3 | HG02602.hp2 NA18939.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.1664-327T>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 14/93 | chr1 | 149491699 | ||||||
| chr1:149491716
|
T | C | 3 | a0015c0036t0006g0004a0015c0192t0006g0270a0173c0191t0006g0271 | 4 | HG02145.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1664-310T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 14/93 | chr1 | 149491716 | ||||||
| chr1:149491739
|
C | T | 1 | a0029c0033t0001g0197 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1664-287C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 14/93 | chr1 | 149491739 | ||||||
| chr1:149491826
|
C | T | 1 | a0185c0043t0002g0247 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1664-200C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 14/93 | chr1 | 149491826 | ||||||
| chr1:149491857
|
G | A | 1 | a0006c0212t0002g0223 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1664-169G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 14/93 | chr1 | 149491857 | ||||||
| chr1:149491886
|
G | C | 38 | a0032c0012t0002g0232a0032c0012t0002g0266a0033c0011t0002g0254others(35): Show | 38 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1664-140G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 14/93 | chr1 | 149491886 | ||||||
| chr1:149491887
|
C | T | 5 | a0161c0197t0005g0214a0162c0196t0005g0213a0163c0199t0005g0215others(2): Show | 5 | HG00544.hp2 HG00558.hp2 HG00735.hp2 others(2): Show |
intron_variant | MODIFIER | c.1664-139C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 14/93 | chr1 | 149491887 | ||||||
| chr1:149491974
|
G | A | 2 | a0031c0028t0003g0180a0031c0028t0003g0194 | 2 | NA18972.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1664-52G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 14/93 | chr1 | 149491974 | ||||||
| chr1:149492207
|
C | T | 78 | a0006c0211t0019g0211a0006c0212t0002g0223a0006c0213t0002g0224others(75): Show | 80 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.1772+73C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 15/93 | chr1 | 149492207 | ||||||
| chr1:149492210
|
G | C | 4 | a0162c0196t0005g0213a0163c0199t0005g0215a0165c0200t0005g0212others(1): Show | 4 | HG00544.hp2 HG00558.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1772+76G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 15/93 | chr1 | 149492210 | ||||||
| chr1:149492286
|
T | C | 13 | a0006c0211t0019g0211a0043c0209t0004g0207a0044c0210t0004g0206others(10): Show | 13 | HG00735.hp1 HG00735.hp2 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.1772+152T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 15/93 | chr1 | 149492286 | ||||||
| chr1:149492318
|
C | A | 245 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(242): Show | 247 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.1772+184C>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 15/93 | chr1 | 149492318 | ||||||
| chr1:149492322
|
A | G | 3 | a0006c0212t0002g0223a0006c0213t0002g0224a0006c0214t0002g0265 | 3 | HG01891.hp1 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1772+188A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 15/93 | chr1 | 149492322 | ||||||
| chr1:149492324
|
G | A | 2 | a0056c0089t0001g0060a0107c0138t0001g0072 | 2 | HG00733.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1772+190G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 15/93 | chr1 | 149492324 | ||||||
| chr1:149492361
|
C | T | 1 | a0006c0211t0019g0211 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1772+227C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 15/93 | chr1 | 149492361 | ||||||
| chr1:149492395
|
T | C | 1 | a0155c0186t0007g0183 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1772+261T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 15/93 | chr1 | 149492395 | ||||||
| chr1:149492445
|
A | G | 9 | a0043c0209t0004g0207a0044c0210t0004g0206a0164c0201t0004g0205others(6): Show | 9 | HG00735.hp1 HG01099.hp1 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.1772+311A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 15/93 | chr1 | 149492445 | ||||||
| chr1:149492502
|
A | G | 2 | a0143c0179t0001g0021a0149c0183t0001g0022 | 2 | HG02698.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1773-266A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 15/93 | chr1 | 149492502 | ||||||
| chr1:149492543
|
C | G | 1 | a0006c0212t0002g0223 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1773-225C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 15/93 | chr1 | 149492543 | ||||||
| chr1:149492545
|
CTCTGTCT others(3): Show |
C | 1 | a0006c0212t0002g0223 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1773-219_1773-210d others(12): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 15/93 | INFO_REALIGN_3_PRIME | chr1 | 149492545 | |||||
| chr1:149492555
|
G | GTC | 13 | a0001c0001t0001g0121a0043c0209t0004g0207a0044c0210t0004g0206others(10): Show | 13 | HG01099.hp1 HG01346.hp2 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.1773-193_1773-192d others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 15/93 | INFO_REALIGN_3_PRIME | chr1 | 149492555 | |||||
| chr1:149492555
|
G | GTCTC | 5 | a0039c0219t0002g0227a0178c0070t0002g0253a0179c0071t0002g0260others(2): Show | 5 | HG00738.hp1 HG03831.hp1 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.1773-195_1773-192d others(6): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 15/93 | INFO_REALIGN_3_PRIME | chr1 | 149492555 | |||||
| chr1:149492555
|
G | GTCTCTGT others(3): Show |
1 | a0006c0214t0002g0265 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1773-208_1773-207i others(12): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 15/93 | INFO_REALIGN_3_PRIME | chr1 | 149492555 | |||||
| chr1:149492555
|
GTCTC | G | 3 | a0015c0036t0006g0004a0015c0192t0006g0270a0173c0191t0006g0271 | 4 | HG02145.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1773-195_1773-192d others(6): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 15/93 | INFO_REALIGN_3_PRIME | chr1 | 149492555 | |||||
| chr1:149492627
|
A | G | 3 | a0163c0199t0005g0215a0165c0200t0005g0212a0166c0198t0005g0210 | 3 | HG00544.hp2 HG00558.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1773-141A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 15/93 | chr1 | 149492627 | ||||||
| chr1:149492632
|
G | A | 90 | a0006c0211t0019g0211a0006c0212t0002g0223a0006c0213t0002g0224others(87): Show | 92 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.1773-136G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 15/93 | chr1 | 149492632 | ||||||
| chr1:149492683
|
C | G | 3 | a0101c0039t0001g0079a0102c0144t0001g0127a0127c0169t0001g0052 | 3 | HG00408.hp1 HG00423.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.1773-85C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 15/93 | chr1 | 149492683 | ||||||
| chr1:149492701
|
A | G | 1 | a0086c0119t0001g0085 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1773-67A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 15/93 | chr1 | 149492701 | ||||||
| chr1:149492718
|
C | T | 21 | a0017c0019t0001g0112a0017c0019t0001g0167a0018c0018t0001g0113others(18): Show | 22 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(19): Show |
intron_variant | MODIFIER | c.1773-50C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 15/93 | chr1 | 149492718 | ||||||
| chr1:149492971
|
T | A | 1 | a0160c0076t0014g0225 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1945+31T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 16/93 | chr1 | 149492971 | ||||||
| chr1:149492987
|
G | C | 1 | a0019c0021t0001g0098 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1945+47G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 16/93 | chr1 | 149492987 | ||||||
| chr1:149493117
|
G | T | 1 | a0160c0076t0014g0225 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1945+177G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 16/93 | chr1 | 149493117 | ||||||
| chr1:149493136
|
T | G | 1 | a0211c0040t0002g0243 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1945+196T>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 16/93 | chr1 | 149493136 | ||||||
| chr1:149493137
|
T | C | 62 | a0017c0019t0001g0112a0017c0019t0001g0167a0018c0018t0001g0113others(59): Show | 63 | HG00423.hp2 HG00438.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.1945+197T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 16/93 | chr1 | 149493137 | ||||||
| chr1:149493147
|
A | C | 2 | a0191c0054t0002g0264a0195c0060t0002g0229 | 2 | NA18959.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.1945+207A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 16/93 | chr1 | 149493147 | ||||||
| chr1:149493162
|
C | A | 18 | a0017c0019t0001g0112a0017c0019t0001g0167a0018c0018t0001g0113others(15): Show | 19 | HG00423.hp2 HG02055.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1945+222C>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 16/93 | chr1 | 149493162 | ||||||
| chr1:149493163
|
G | A | 4 | a0015c0036t0006g0004a0015c0192t0006g0270a0173c0191t0006g0271others(1): Show | 5 | HG02040.hp2 HG02145.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1945+223G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 16/93 | chr1 | 149493163 | ||||||
| chr1:149493182
|
G | A | 1 | a0014c0008t0020g0184 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1945+242G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 16/93 | chr1 | 149493182 | ||||||
| chr1:149493185
|
A | G | 4 | a0006c0212t0002g0223a0006c0213t0002g0224a0006c0214t0002g0265others(1): Show | 4 | HG01891.hp1 HG03688.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.1945+245A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 16/93 | chr1 | 149493185 | ||||||
| chr1:149493186
|
T | C | 20 | a0017c0019t0001g0112a0017c0019t0001g0167a0018c0018t0001g0113others(17): Show | 21 | HG00423.hp2 HG02055.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.1945+246T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 16/93 | chr1 | 149493186 | ||||||
| chr1:149493215
|
A | G | 11 | a0039c0219t0002g0227a0119c0153t0001g0097a0125c0159t0001g0147others(8): Show | 11 | HG00738.hp1 HG02080.hp2 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.1945+275A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 16/93 | chr1 | 149493215 | ||||||
| chr1:149493218
|
ACT | A | 9 | a0016c0017t0001g0028a0016c0017t0001g0029a0025c0031t0001g0032others(6): Show | 9 | HG00738.hp2 HG01123.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.1945+281_1945+282d others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 16/93 | INFO_REALIGN_3_PRIME | chr1 | 149493218 | |||||
| chr1:149493261
|
C | T | 2 | a0031c0028t0003g0180a0031c0028t0003g0194 | 2 | NA18972.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1945+321C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 16/93 | chr1 | 149493261 | ||||||
| chr1:149493283
|
A | G | 1 | a0056c0089t0001g0060 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1945+343A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 16/93 | chr1 | 149493283 | ||||||
| chr1:149493292
|
G | A | 12 | a0043c0209t0004g0207a0044c0210t0004g0206a0163c0199t0005g0215others(9): Show | 12 | HG00544.hp2 HG00558.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.1945+352G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 16/93 | chr1 | 149493292 | ||||||
| chr1:149493300
|
G | T | 3 | a0163c0199t0005g0215a0165c0200t0005g0212a0166c0198t0005g0210 | 3 | HG00544.hp2 HG00558.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1945+360G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 16/93 | chr1 | 149493300 | ||||||
| chr1:149493476
|
T | G | 1 | a0174c0202t0013g0204 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1946-184T>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 16/93 | chr1 | 149493476 | ||||||
| chr1:149493543
|
A | G | 1 | a0164c0201t0004g0205 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1946-117A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 16/93 | chr1 | 149493543 | ||||||
| chr1:149493563
|
A | T | 3 | a0207c0046t0002g0241a0208c0048t0002g0251a0209c0047t0002g0242 | 3 | HG02080.hp2 NA18939.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.1946-97A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 16/93 | chr1 | 149493563 | ||||||
| chr1:149493577
|
T | C | 43 | a0032c0012t0002g0232a0032c0012t0002g0266a0033c0011t0002g0254others(40): Show | 43 | HG00438.hp2 HG00621.hp1 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.1946-83T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 16/93 | chr1 | 149493577 | ||||||
| chr1:149493593
|
A | G | 3 | a0006c0212t0002g0223a0006c0213t0002g0224a0006c0214t0002g0265 | 3 | HG01891.hp1 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1946-67A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 16/93 | chr1 | 149493593 | ||||||
| chr1:149493633
|
G | A | 16 | a0017c0019t0001g0112a0017c0019t0001g0167a0018c0018t0001g0113others(13): Show | 17 | HG00423.hp2 HG02109.hp1 HG02135.hp2 others(14): Show |
intron_variant | MODIFIER | c.1946-27G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 16/93 | chr1 | 149493633 | ||||||
| chr1:149493765
|
A | G | 6 | a0039c0219t0002g0227a0178c0070t0002g0253a0179c0071t0002g0260others(3): Show | 6 | HG00738.hp1 HG03831.hp1 HG04204.hp1 others(3): Show |
intron_variant | MODIFIER | c.1997+54A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 17/93 | chr1 | 149493765 | ||||||
| chr1:149493890
|
T | A | 48 | a0032c0012t0002g0232a0032c0012t0002g0266a0033c0011t0002g0254others(45): Show | 48 | HG00438.hp2 HG00621.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.1997+179T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 17/93 | chr1 | 149493890 | ||||||
| chr1:149493901
|
C | T | 1 | a0133c0165t0022g0020 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1997+190C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 17/93 | chr1 | 149493901 | ||||||
| chr1:149493928
|
G | A | 2 | a0006c0213t0002g0224a0006c0214t0002g0265 | 2 | NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1997+217G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 17/93 | chr1 | 149493928 | ||||||
| chr1:149493943
|
G | T | 1 | a0211c0040t0002g0243 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1997+232G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 17/93 | chr1 | 149493943 | ||||||
| chr1:149493945
|
A | G | 1 | a0006c0212t0002g0223 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1997+234A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 17/93 | chr1 | 149493945 | ||||||
| chr1:149493963
|
T | A | 1 | a0211c0040t0002g0243 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1997+252T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 17/93 | chr1 | 149493963 | ||||||
| chr1:149494006
|
G | A | 2 | a0119c0153t0001g0097a0125c0159t0001g0147 | 2 | HG02922.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1997+295G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 17/93 | chr1 | 149494006 | ||||||
| chr1:149494011
|
G | C | 3 | a0015c0036t0006g0004a0015c0192t0006g0270a0173c0191t0006g0271 | 4 | HG02145.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1997+300G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 17/93 | chr1 | 149494011 | ||||||
| chr1:149494093
|
C | CCT | 3 | a0029c0033t0001g0197a0029c0033t0001g0198a0146c0176t0003g0110 | 3 | HG03098.hp1 HG03225.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1998-201_1998-200d others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 17/93 | INFO_REALIGN_3_PRIME | chr1 | 149494093 | |||||
| chr1:149494093
|
CCT | C | 77 | a0004c0026t0001g0007a0006c0212t0002g0223a0015c0036t0006g0004others(74): Show | 79 | HG00423.hp2 HG00438.hp2 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.1998-201_1998-200d others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 17/93 | INFO_REALIGN_3_PRIME | chr1 | 149494093 | |||||
| chr1:149494095
|
T | TCTCTCTC others(9503): Show |
1 | a0111c0132t0001g0199 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1998-202_1998-201i others(9512): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 17/93 | INFO_REALIGN_3_PRIME | chr1 | 149494095 | |||||
| chr1:149494115
|
T | C | 4 | a0023c0024t0001g0003a0076c0109t0001g0137a0094c0125t0001g0138others(1): Show | 5 | HG02257.hp2 HG02630.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1998-203T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 17/93 | chr1 | 149494115 | ||||||
| chr1:149494119
|
C | T | 2 | a0126c0130t0001g0134a0166c0198t0005g0210 | 2 | HG02683.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1998-199C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 17/93 | chr1 | 149494119 | ||||||
| chr1:149494147
|
C | CTCTACCT others(1539): Show |
3 | a0015c0036t0006g0004a0015c0192t0006g0270a0173c0191t0006g0271 | 4 | HG02145.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1998-12_1998-11ins others(1546): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 17/93 | INFO_REALIGN_3_PRIME | chr1 | 149494147 | |||||
| chr1:149494147
|
C | T | 3 | a0006c0213t0002g0224a0006c0214t0002g0265a0167c0203t0028g0269 | 3 | HG02109.hp2 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1998-171C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 17/93 | chr1 | 149494147 | ||||||
| chr1:149494181
|
C | A | 3 | a0013c0035t0001g0038a0013c0035t0001g0084a0013c0162t0001g0040 | 3 | HG02258.hp2 HG02280.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1998-137C>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 17/93 | chr1 | 149494181 | ||||||
| chr1:149494216
|
T | C | 2 | a0006c0213t0002g0224a0006c0214t0002g0265 | 2 | NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1998-102T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 17/93 | chr1 | 149494216 | ||||||
| chr1:149494246
|
A | C | 1 | a0006c0212t0002g0223 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1998-72A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 17/93 | chr1 | 149494246 | ||||||
| chr1:149494253
|
C | G | 16 | a0006c0211t0019g0211a0043c0209t0004g0207a0044c0210t0004g0206others(13): Show | 16 | HG00544.hp2 HG00558.hp2 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.1998-65C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 17/93 | chr1 | 149494253 | ||||||
| chr1:149494531
|
C | G | 1 | a0149c0183t0001g0022 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2170+41C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 18/93 | chr1 | 149494531 | ||||||
| chr1:149494595
|
G | A | 51 | a0032c0012t0002g0232a0032c0012t0002g0266a0033c0011t0002g0254others(48): Show | 51 | HG00438.hp2 HG00621.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.2170+105G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 18/93 | chr1 | 149494595 | ||||||
| chr1:149494608
|
G | A | 77 | a0006c0211t0019g0211a0006c0212t0002g0223a0006c0213t0002g0224others(74): Show | 78 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.2170+118G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 18/93 | chr1 | 149494608 | ||||||
| chr1:149494674
|
T | C | 3 | a0015c0036t0006g0004a0015c0192t0006g0270a0173c0191t0006g0271 | 4 | HG02145.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.2170+184T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 18/93 | chr1 | 149494674 | ||||||
| chr1:149494709
|
T | C | 45 | a0015c0036t0006g0004a0015c0192t0006g0270a0032c0012t0002g0232others(42): Show | 46 | HG00438.hp2 HG00621.hp1 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.2170+219T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 18/93 | chr1 | 149494709 | ||||||
| chr1:149494755
|
C | T | 5 | a0006c0213t0002g0224a0006c0214t0002g0265a0015c0036t0006g0004others(2): Show | 6 | HG02145.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.2170+265C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 18/93 | chr1 | 149494755 | ||||||
| chr1:149494834
|
C | G | 1 | a0164c0201t0004g0205 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2170+344C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 18/93 | chr1 | 149494834 | ||||||
| chr1:149494948
|
C | A | 2 | a0043c0209t0004g0207a0044c0210t0004g0206 | 2 | HG02165.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.2171-252C>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 18/93 | chr1 | 149494948 | ||||||
| chr1:149494971
|
G | A | 1 | a0003c0003t0001g0115 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2171-229G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 18/93 | chr1 | 149494971 | ||||||
| chr1:149495052
|
G | C | 3 | a0017c0019t0001g0112a0017c0019t0001g0167a0055c0086t0001g0168 | 3 | HG02486.hp2 HG03516.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2171-148G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 18/93 | chr1 | 149495052 | ||||||
| chr1:149495071
|
T | A | 1 | a0006c0213t0002g0224 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2171-129T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 18/93 | chr1 | 149495071 | ||||||
| chr1:149495118
|
CT | C | 3 | a0015c0036t0006g0004a0015c0192t0006g0270a0173c0191t0006g0271 | 4 | HG02145.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.2171-81delT | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 18/93 | chr1 | 149495118 | ||||||
| chr1:149495258
|
G | C | 3 | a0013c0035t0001g0038a0013c0035t0001g0084a0134c0164t0001g0039 | 3 | HG02258.hp2 HG02280.hp1 HG03130.hp1 |
splice_region_variant&intron_variant | LOW | c.2222+7G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 19/93 | chr1 | 149495258 | ||||||
| chr1:149495301
|
A | C | 89 | a0006c0211t0019g0211a0006c0212t0002g0223a0006c0213t0002g0224others(86): Show | 91 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.2222+50A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 19/93 | chr1 | 149495301 | ||||||
| chr1:149495353
|
G | C | 1 | a0185c0043t0002g0247 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.2222+102G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 19/93 | chr1 | 149495353 | ||||||
| chr1:149495355
|
A | C | 1 | a0139c0172t0001g0105 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2222+104A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 19/93 | chr1 | 149495355 | ||||||
| chr1:149495362
|
A | T | 1 | a0099c0146t0001g0034 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.2222+111A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 19/93 | chr1 | 149495362 | ||||||
| chr1:149495496
|
A | ATGGAAAC others(4748): Show |
1 | a0097c0148t0001g0066 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2223-225_2223-224i others(4757): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 19/93 | INFO_REALIGN_3_PRIME | chr1 | 149495496 | |||||
| chr1:149495496
|
A | G | 7 | a0038c0038t0001g0171a0053c0190t0001g0064a0077c0110t0001g0178others(4): Show | 7 | HG01516.hp2 HG01517.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.2222+245A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 19/93 | chr1 | 149495496 | ||||||
| chr1:149495508
|
G | A | 1 | a0059c0091t0001g0130 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2222+257G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 19/93 | chr1 | 149495508 | ||||||
| chr1:149495563
|
G | A | 7 | a0043c0209t0004g0207a0164c0201t0004g0205a0168c0206t0004g0203others(4): Show | 7 | HG00735.hp1 HG01099.hp1 HG02165.hp1 others(4): Show |
intron_variant | MODIFIER | c.2222+312G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 19/93 | chr1 | 149495563 | ||||||
| chr1:149495608
|
A | G | 1 | a0158c0084t0001g0049 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2223-294A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 19/93 | chr1 | 149495608 | ||||||
| chr1:149495649
|
CTCTCTCT others(5): Show |
C | 3 | a0006c0212t0002g0223a0006c0213t0002g0224a0006c0214t0002g0265 | 3 | HG01891.hp1 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2223-251_2223-240d others(14): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 19/93 | INFO_REALIGN_3_PRIME | chr1 | 149495649 | |||||
| chr1:149495649
|
CTCTCTCT others(15): Show |
C | 3 | a0015c0036t0006g0004a0015c0192t0006g0270a0173c0191t0006g0271 | 4 | HG02145.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.2223-251_2223-230d others(24): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 19/93 | INFO_REALIGN_3_PRIME | chr1 | 149495649 | |||||
| chr1:149495655
|
C | CTG | 3 | a0030c0034t0001g0092a0030c0034t0001g0093a0148c0181t0001g0124 | 3 | HG03195.hp2 HG04184.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2223-224_2223-223d others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 19/93 | INFO_REALIGN_3_PRIME | chr1 | 149495655 | |||||
| chr1:149495655
|
C | G | 9 | a0021c0022t0001g0080a0021c0022t0001g0169a0024c0025t0001g0024others(6): Show | 9 | HG02055.hp2 HG02280.hp2 HG02300.hp2 others(6): Show |
intron_variant | MODIFIER | c.2223-247C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 19/93 | chr1 | 149495655 | ||||||
| chr1:149495655
|
CTG | C | 8 | a0001c0001t0001g0121a0013c0035t0001g0038a0013c0035t0001g0084others(5): Show | 8 | HG02027.hp1 HG02055.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.2223-224_2223-223d others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 19/93 | INFO_REALIGN_3_PRIME | chr1 | 149495655 | |||||
| chr1:149495655
|
CTGTG | C | 3 | a0088c0105t0008g0100a0090c0121t0008g0149a0091c0122t0008g0157 | 3 | HG02896.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2223-226_2223-223d others(6): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 19/93 | INFO_REALIGN_3_PRIME | chr1 | 149495655 | |||||
| chr1:149495657
|
G | C | 1 | a0006c0211t0019g0211 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2223-245G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 19/93 | chr1 | 149495657 | ||||||
| chr1:149495668
|
TGTGTGTG others(5): Show |
T | 1 | a0174c0202t0013g0204 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2223-222_2223-211d others(14): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 19/93 | INFO_REALIGN_3_PRIME | chr1 | 149495668 | |||||
| chr1:149495674
|
T | C | 58 | a0032c0012t0002g0232a0032c0012t0002g0266a0033c0011t0002g0254others(55): Show | 58 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.2223-228T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 19/93 | chr1 | 149495674 | ||||||
| chr1:149495676
|
T | C | 2 | a0202c0064t0002g0262a0209c0047t0002g0242 | 2 | NA18939.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.2223-226T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 19/93 | chr1 | 149495676 | ||||||
| chr1:149495678
|
TGC | T | 42 | a0032c0012t0002g0232a0032c0012t0002g0266a0033c0011t0002g0254others(39): Show | 42 | HG00438.hp2 HG00621.hp1 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.2223-222_2223-221d others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 19/93 | INFO_REALIGN_3_PRIME | chr1 | 149495678 | |||||
| chr1:149495680
|
C | CGTGT | 6 | a0004c0026t0001g0007a0004c0026t0001g0008a0004c0027t0001g0001others(3): Show | 7 | HG01891.hp2 HG02145.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.2223-201_2223-198d others(6): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 19/93 | INFO_REALIGN_3_PRIME | chr1 | 149495680 | |||||
| chr1:149495680
|
C | T | 22 | a0015c0036t0006g0004a0015c0192t0006g0270a0039c0219t0002g0227others(19): Show | 23 | HG00544.hp2 HG00558.hp2 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.2223-222C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 19/93 | chr1 | 149495680 | ||||||
| chr1:149495684
|
T | C | 1 | a0006c0211t0019g0211 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2223-218T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 19/93 | chr1 | 149495684 | ||||||
| chr1:149495685
|
G | C | 3 | a0015c0036t0006g0004a0015c0192t0006g0270a0173c0191t0006g0271 | 4 | HG02145.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.2223-217G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 19/93 | chr1 | 149495685 | ||||||
| chr1:149495697
|
G | T | 1 | a0044c0210t0004g0206 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.2223-205G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 19/93 | chr1 | 149495697 | ||||||
| chr1:149495706
|
C | T | 4 | a0015c0036t0006g0004a0015c0192t0006g0270a0173c0191t0006g0271others(1): Show | 5 | HG02145.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.2223-196C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 19/93 | chr1 | 149495706 | ||||||
| chr1:149495711
|
GTCTT | G | 4 | a0114c0137t0001g0133a0115c0149t0026g0142a0116c0150t0001g0014others(1): Show | 4 | HG02055.hp1 HG03098.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.2223-187_2223-184d others(6): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 19/93 | INFO_REALIGN_3_PRIME | chr1 | 149495711 | |||||
| chr1:149495712
|
T | C | 3 | a0015c0036t0006g0004a0015c0192t0006g0270a0173c0191t0006g0271 | 4 | HG02145.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.2223-190T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 19/93 | chr1 | 149495712 | ||||||
| chr1:149495802
|
C | G | 89 | a0006c0211t0019g0211a0006c0212t0002g0223a0006c0213t0002g0224others(86): Show | 90 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.2223-100C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 19/93 | chr1 | 149495802 | ||||||
| chr1:149495819
|
C | T | 3 | a0015c0036t0006g0004a0015c0192t0006g0270a0173c0191t0006g0271 | 4 | HG02145.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.2223-83C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 19/93 | chr1 | 149495819 | ||||||
| chr1:149495865
|
C | T | 1 | a0093c0124t0001g0153 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2223-37C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 19/93 | chr1 | 149495865 | ||||||
| chr1:149495875
|
A | T | 1 | a0093c0124t0001g0153 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2223-27A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 19/93 | chr1 | 149495875 | ||||||
| chr1:149496120
|
A | G | 1 | a0112c0131t0001g0118 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.2395+46A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 20/93 | chr1 | 149496120 | ||||||
| chr1:149496173
|
G | A | 5 | a0161c0197t0005g0214a0162c0196t0005g0213a0163c0199t0005g0215others(2): Show | 5 | HG00544.hp2 HG00558.hp2 HG00735.hp2 others(2): Show |
intron_variant | MODIFIER | c.2395+99G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 20/93 | chr1 | 149496173 | ||||||
| chr1:149496193
|
T | C | 1 | a0006c0211t0019g0211 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2395+119T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 20/93 | chr1 | 149496193 | ||||||
| chr1:149496317
|
G | C | 3 | a0017c0019t0001g0112a0017c0019t0001g0167a0055c0086t0001g0168 | 3 | HG02486.hp2 HG03516.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2395+243G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 20/93 | chr1 | 149496317 | ||||||
| chr1:149496447
|
T | C | 5 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(2): Show | 5 | HG00099.hp2 HG01099.hp2 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.2396-342T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 20/93 | chr1 | 149496447 | ||||||
| chr1:149496462
|
T | G | 2 | a0186c0044t0017g0239a0193c0057t0002g0006 | 2 | HG02040.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.2396-327T>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 20/93 | chr1 | 149496462 | ||||||
| chr1:149496479
|
T | C | 5 | a0161c0197t0005g0214a0162c0196t0005g0213a0163c0199t0005g0215others(2): Show | 5 | HG00544.hp2 HG00558.hp2 HG00735.hp2 others(2): Show |
intron_variant | MODIFIER | c.2396-310T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 20/93 | chr1 | 149496479 | ||||||
| chr1:149496619
|
C | T | 5 | a0161c0197t0005g0214a0162c0196t0005g0213a0163c0199t0005g0215others(2): Show | 5 | HG00544.hp2 HG00558.hp2 HG00735.hp2 others(2): Show |
intron_variant | MODIFIER | c.2396-170C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 20/93 | chr1 | 149496619 | ||||||
| chr1:149496632
|
T | G | 1 | a0054c0085t0001g0150 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2396-157T>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 20/93 | chr1 | 149496632 | ||||||
| chr1:149496649
|
G | A | 5 | a0161c0197t0005g0214a0162c0196t0005g0213a0163c0199t0005g0215others(2): Show | 5 | HG00544.hp2 HG00558.hp2 HG00735.hp2 others(2): Show |
intron_variant | MODIFIER | c.2396-140G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 20/93 | chr1 | 149496649 | ||||||
| chr1:149496772
|
G | A | 1 | a0044c0210t0004g0206 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.2396-17G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 20/93 | chr1 | 149496772 | ||||||
| chr1:149496969
|
G | C | 1 | a0157c0188t0001g0201 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2504+72G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 21/93 | chr1 | 149496969 | ||||||
| chr1:149496970
|
T | C | 54 | a0021c0022t0001g0169a0022c0023t0001g0156a0022c0023t0001g0160others(51): Show | 54 | HG00438.hp2 HG00621.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.2504+73T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 21/93 | chr1 | 149496970 | ||||||
| chr1:149497041
|
T | C | 1 | a0139c0172t0001g0105 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2504+144T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 21/93 | chr1 | 149497041 | ||||||
| chr1:149497049
|
T | C | 2 | a0006c0211t0019g0211a0167c0203t0028g0269 | 2 | HG02109.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.2504+152T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 21/93 | chr1 | 149497049 | ||||||
| chr1:149497081
|
C | A | 121 | a0001c0001t0001g0121a0006c0211t0019g0211a0006c0212t0002g0223others(118): Show | 122 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.2504+184C>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 21/93 | chr1 | 149497081 | ||||||
| chr1:149497085
|
A | G | 4 | a0006c0212t0002g0223a0006c0213t0002g0224a0006c0214t0002g0265others(1): Show | 4 | HG01891.hp1 NA18962.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.2504+188A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 21/93 | chr1 | 149497085 | ||||||
| chr1:149497087
|
G | A | 2 | a0076c0109t0001g0137a0179c0071t0002g0260 | 2 | HG00738.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.2504+190G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 21/93 | chr1 | 149497087 | ||||||
| chr1:149497124
|
C | T | 1 | a0006c0211t0019g0211 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2504+227C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 21/93 | chr1 | 149497124 | ||||||
| chr1:149497152
|
A | C | 1 | a0001c0001t0001g0121 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2504+255A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 21/93 | chr1 | 149497152 | ||||||
| chr1:149497208
|
A | G | 9 | a0043c0209t0004g0207a0044c0210t0004g0206a0164c0201t0004g0205others(6): Show | 9 | HG00735.hp1 HG01099.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.2504+311A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 21/93 | chr1 | 149497208 | ||||||
| chr1:149497225
|
G | C | 2 | a0021c0022t0001g0080a0078c0111t0001g0102 | 2 | HG02280.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2505-300G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 21/93 | chr1 | 149497225 | ||||||
| chr1:149497257
|
C | T | 4 | a0013c0035t0001g0038a0013c0035t0001g0084a0013c0162t0001g0040others(1): Show | 4 | HG02258.hp2 HG02280.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.2505-268C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 21/93 | chr1 | 149497257 | ||||||
| chr1:149497276
|
C | A | 2 | a0016c0017t0001g0028a0016c0017t0001g0029 | 2 | HG03239.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.2505-249C>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 21/93 | chr1 | 149497276 | ||||||
| chr1:149497278
|
C | T | 1 | a0089c0123t0001g0164 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2505-247C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 21/93 | chr1 | 149497278 | ||||||
| chr1:149497282
|
C | CTCTCTG | 206 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(203): Show | 208 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.2505-231_2505-226d others(8): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 21/93 | INFO_REALIGN_3_PRIME | chr1 | 149497282 | |||||
| chr1:149497300
|
C | G | 51 | a0006c0212t0002g0223a0007c0005t0001g0144a0007c0005t0001g0154others(48): Show | 52 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.2505-225C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 21/93 | chr1 | 149497300 | ||||||
| chr1:149497306
|
G | C | 51 | a0006c0212t0002g0223a0007c0005t0001g0144a0007c0005t0001g0154others(48): Show | 52 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.2505-219G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 21/93 | chr1 | 149497306 | ||||||
| chr1:149497318
|
G | C | 216 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(213): Show | 219 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.2505-207G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 21/93 | chr1 | 149497318 | ||||||
| chr1:149497318
|
G | GTC | 4 | a0015c0036t0006g0004a0015c0192t0006g0270a0021c0022t0001g0169others(1): Show | 5 | HG02145.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.2505-193_2505-192d others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 21/93 | INFO_REALIGN_3_PRIME | chr1 | 149497318 | |||||
| chr1:149497318
|
G | GTCTCTCT others(1): Show |
12 | a0006c0212t0002g0223a0006c0213t0002g0224a0043c0209t0004g0207others(9): Show | 12 | HG00735.hp1 HG01099.hp1 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.2505-199_2505-192d others(10): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 21/93 | INFO_REALIGN_3_PRIME | chr1 | 149497318 | |||||
| chr1:149497318
|
G | GTCTCTCT others(3): Show |
30 | a0032c0012t0002g0232a0032c0012t0002g0266a0033c0011t0002g0254others(27): Show | 30 | HG00438.hp2 HG00621.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.2505-201_2505-192d others(12): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 21/93 | INFO_REALIGN_3_PRIME | chr1 | 149497318 | |||||
| chr1:149497318
|
G | GTCTCTCT others(5): Show |
1 | a0191c0054t0002g0264 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2505-203_2505-192d others(14): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 21/93 | INFO_REALIGN_3_PRIME | chr1 | 149497318 | |||||
| chr1:149497389
|
A | G | 1 | a0135c0161t0001g0057 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2505-136A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 21/93 | chr1 | 149497389 | ||||||
| chr1:149497399
|
A | C | 5 | a0030c0034t0001g0092a0030c0034t0001g0093a0180c0072t0002g0218others(2): Show | 5 | HG03195.hp2 HG03831.hp1 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.2505-126A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 21/93 | chr1 | 149497399 | ||||||
| chr1:149497407
|
A | C | 1 | a0174c0202t0013g0204 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2505-118A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 21/93 | chr1 | 149497407 | ||||||
| chr1:149497430
|
C | T | 3 | a0088c0105t0008g0100a0090c0121t0008g0149a0091c0122t0008g0157 | 3 | HG02896.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2505-95C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 21/93 | chr1 | 149497430 | ||||||
| chr1:149497435
|
T | A | 3 | a0088c0105t0008g0100a0090c0121t0008g0149a0091c0122t0008g0157 | 3 | HG02896.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2505-90T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 21/93 | chr1 | 149497435 | ||||||
| chr1:149497436
|
C | G | 3 | a0088c0105t0008g0100a0090c0121t0008g0149a0091c0122t0008g0157 | 3 | HG02896.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2505-89C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 21/93 | chr1 | 149497436 | ||||||
| chr1:149497442
|
TA | T | 3 | a0088c0105t0008g0100a0090c0121t0008g0149a0091c0122t0008g0157 | 3 | HG02896.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2505-81delA | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 21/93 | INFO_REALIGN_3_PRIME | chr1 | 149497442 | |||||
| chr1:149497445
|
C | T | 3 | a0088c0105t0008g0100a0090c0121t0008g0149a0091c0122t0008g0157 | 3 | HG02896.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2505-80C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 21/93 | chr1 | 149497445 | ||||||
| chr1:149497468
|
G | C | 1 | a0093c0124t0001g0153 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2505-57G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 21/93 | chr1 | 149497468 | ||||||
| chr1:149497475
|
T | A | 2 | a0161c0197t0005g0214a0162c0196t0005g0213 | 2 | HG00735.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.2505-50T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 21/93 | chr1 | 149497475 | ||||||
| chr1:149497475
|
T | C | 79 | a0006c0211t0019g0211a0006c0212t0002g0223a0006c0213t0002g0224others(76): Show | 81 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.2505-50T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 21/93 | chr1 | 149497475 | ||||||
| chr1:149497755
|
A | G | 1 | a0160c0076t0014g0225 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2677+58A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 22/93 | chr1 | 149497755 | ||||||
| chr1:149497772
|
C | T | 12 | a0039c0219t0002g0227a0178c0070t0002g0253a0179c0071t0002g0260others(9): Show | 12 | HG00738.hp1 HG03831.hp1 HG04204.hp1 others(9): Show |
intron_variant | MODIFIER | c.2677+75C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 22/93 | chr1 | 149497772 | ||||||
| chr1:149497892
|
C | T | 2 | a0143c0179t0001g0021a0149c0183t0001g0022 | 2 | HG02698.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.2677+195C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 22/93 | chr1 | 149497892 | ||||||
| chr1:149497893
|
T | G | 1 | a0185c0043t0002g0247 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.2677+196T>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 22/93 | chr1 | 149497893 | ||||||
| chr1:149497894
|
C | T | 51 | a0006c0211t0019g0211a0006c0212t0002g0223a0006c0213t0002g0224others(48): Show | 53 | HG00544.hp2 HG00558.hp2 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.2677+197C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 22/93 | chr1 | 149497894 | ||||||
| chr1:149497908
|
C | T | 1 | a0080c0106t0001g0019 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2677+211C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 22/93 | chr1 | 149497908 | ||||||
| chr1:149497919
|
A | C | 89 | a0006c0211t0019g0211a0006c0212t0002g0223a0006c0213t0002g0224others(86): Show | 91 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.2677+222A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 22/93 | chr1 | 149497919 | ||||||
| chr1:149497920
|
G | A | 6 | a0015c0036t0006g0004a0015c0192t0006g0270a0173c0191t0006g0271others(3): Show | 7 | HG02080.hp2 HG02145.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.2677+223G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 22/93 | chr1 | 149497920 | ||||||
| chr1:149497926
|
A | C | 1 | a0204c0067t0002g0248 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2677+229A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 22/93 | chr1 | 149497926 | ||||||
| chr1:149497934
|
C | G | 1 | a0130c0170t0001g0120 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2677+237C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 22/93 | chr1 | 149497934 | ||||||
| chr1:149497935
|
T | C | 1 | a0204c0067t0002g0248 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2677+238T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 22/93 | chr1 | 149497935 | ||||||
| chr1:149497942
|
A | G | 3 | a0006c0212t0002g0223a0006c0213t0002g0224a0006c0214t0002g0265 | 3 | HG01891.hp1 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2677+245A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 22/93 | chr1 | 149497942 | ||||||
| chr1:149497943
|
C | T | 75 | a0006c0211t0019g0211a0006c0212t0002g0223a0006c0213t0002g0224others(72): Show | 76 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.2677+246C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 22/93 | chr1 | 149497943 | ||||||
| chr1:149497956
|
G | C | 1 | a0172c0204t0004g0268 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2677+259G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 22/93 | chr1 | 149497956 | ||||||
| chr1:149497972
|
A | G | 44 | a0023c0024t0001g0003a0024c0025t0001g0024a0024c0025t0001g0026others(41): Show | 45 | HG00438.hp2 HG00621.hp1 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.2677+275A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 22/93 | chr1 | 149497972 | ||||||
| chr1:149497972
|
A | T | 1 | a0156c0099t0001g0013 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2677+275A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 22/93 | chr1 | 149497972 | ||||||
| chr1:149497997
|
G | T | 1 | a0081c0113t0001g0148 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2677+300G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 22/93 | chr1 | 149497997 | ||||||
| chr1:149498049
|
G | A | 7 | a0043c0209t0004g0207a0044c0210t0004g0206a0164c0201t0004g0205others(4): Show | 7 | HG00735.hp1 HG01099.hp1 HG02165.hp1 others(4): Show |
intron_variant | MODIFIER | c.2677+352G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 22/93 | chr1 | 149498049 | ||||||
| chr1:149498066
|
G | C | 2 | a0037c0016t0002g0256a0037c0016t0002g0257 | 2 | HG00642.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.2678-351G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 22/93 | chr1 | 149498066 | ||||||
| chr1:149498161
|
C | A | 2 | a0004c0026t0001g0007a0004c0026t0001g0008 | 2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2678-256C>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 22/93 | chr1 | 149498161 | ||||||
| chr1:149498161
|
C | G | 1 | a0174c0202t0013g0204 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2678-256C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 22/93 | chr1 | 149498161 | ||||||
| chr1:149498320
|
A | T | 1 | a0211c0040t0002g0243 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2678-97A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 22/93 | chr1 | 149498320 | ||||||
| chr1:149498333
|
C | T | 1 | a0103c0142t0001g0074 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.2678-84C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 22/93 | chr1 | 149498333 | ||||||
| chr1:149498334
|
T | C | 34 | a0006c0212t0002g0223a0032c0012t0002g0232a0032c0012t0002g0266others(31): Show | 34 | HG00438.hp2 HG00621.hp1 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.2678-83T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 22/93 | chr1 | 149498334 | ||||||
| chr1:149498350
|
A | G | 3 | a0006c0212t0002g0223a0006c0213t0002g0224a0006c0214t0002g0265 | 3 | HG01891.hp1 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2678-67A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 22/93 | chr1 | 149498350 | ||||||
| chr1:149498365
|
G | T | 3 | a0207c0046t0002g0241a0208c0048t0002g0251a0209c0047t0002g0242 | 3 | HG02080.hp2 NA18939.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.2678-52G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 22/93 | chr1 | 149498365 | ||||||
| chr1:149498376
|
A | T | 3 | a0008c0037t0001g0075a0008c0215t0001g0067a0047c0216t0001g0068 | 3 | HG01496.hp1 HG01928.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.2678-41A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 22/93 | chr1 | 149498376 | ||||||
| chr1:149498390
|
A | G | 79 | a0001c0001t0001g0158a0006c0211t0019g0211a0006c0212t0002g0223others(76): Show | 80 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.2678-27A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 22/93 | chr1 | 149498390 | ||||||
| chr1:149498486
|
T | C | 2 | a0043c0209t0004g0207a0044c0210t0004g0206 | 2 | HG02165.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.2729+18T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 23/93 | chr1 | 149498486 | ||||||
| chr1:149498522
|
A | G | 31 | a0032c0012t0002g0232a0032c0012t0002g0266a0033c0011t0002g0254others(28): Show | 31 | HG00438.hp2 HG00621.hp1 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.2729+54A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 23/93 | chr1 | 149498522 | ||||||
| chr1:149498641
|
C | T | 2 | a0043c0209t0004g0207a0044c0210t0004g0206 | 2 | HG02165.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.2729+173C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 23/93 | chr1 | 149498641 | ||||||
| chr1:149498647
|
T | A | 38 | a0006c0212t0002g0223a0032c0012t0002g0232a0032c0012t0002g0266others(35): Show | 38 | HG00438.hp2 HG00621.hp1 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.2729+179T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 23/93 | chr1 | 149498647 | ||||||
| chr1:149498672
|
A | T | 3 | a0207c0046t0002g0241a0208c0048t0002g0251a0209c0047t0002g0242 | 3 | HG02080.hp2 NA18939.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.2729+204A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 23/93 | chr1 | 149498672 | ||||||
| chr1:149498685
|
G | A | 2 | a0006c0213t0002g0224a0006c0214t0002g0265 | 2 | NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2729+217G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 23/93 | chr1 | 149498685 | ||||||
| chr1:149498700
|
G | T | 3 | a0182c0074t0002g0261a0185c0043t0002g0247a0211c0040t0002g0243 | 3 | HG01346.hp2 NA18946.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.2729+232G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 23/93 | chr1 | 149498700 | ||||||
| chr1:149498707
|
A | G | 4 | a0006c0212t0002g0223a0207c0046t0002g0241a0208c0048t0002g0251others(1): Show | 4 | HG01891.hp1 HG02080.hp2 NA18939.hp2 others(1): Show |
intron_variant | MODIFIER | c.2729+239A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 23/93 | chr1 | 149498707 | ||||||
| chr1:149498720
|
T | A | 3 | a0182c0074t0002g0261a0185c0043t0002g0247a0211c0040t0002g0243 | 3 | HG01346.hp2 NA18946.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.2729+252T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 23/93 | chr1 | 149498720 | ||||||
| chr1:149498762
|
C | T | 1 | a0199c0061t0002g0219 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2729+294C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 23/93 | chr1 | 149498762 | ||||||
| chr1:149498766
|
G | T | 1 | a0164c0201t0004g0205 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2729+298G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 23/93 | chr1 | 149498766 | ||||||
| chr1:149498813
|
A | T | 1 | a0147c0220t0001g0094 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2730-260A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 23/93 | chr1 | 149498813 | ||||||
| chr1:149498850
|
C | CCT | 13 | a0009c0006t0001g0081a0009c0006t0001g0082a0009c0006t0001g0139others(10): Show | 13 | HG00099.hp1 HG00544.hp2 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.2730-201_2730-200d others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 23/93 | INFO_REALIGN_3_PRIME | chr1 | 149498850 | |||||
| chr1:149498850
|
CCT | C | 4 | a0006c0213t0002g0224a0006c0214t0002g0265a0044c0210t0004g0206others(1): Show | 4 | HG02135.hp2 NA18972.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.2730-201_2730-200d others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 23/93 | INFO_REALIGN_3_PRIME | chr1 | 149498850 | |||||
| chr1:149498850
|
CCTCT | C | 5 | a0156c0099t0001g0013a0174c0202t0013g0204a0207c0046t0002g0241others(2): Show | 5 | HG02080.hp2 NA18939.hp2 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.2730-203_2730-200d others(6): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 23/93 | INFO_REALIGN_3_PRIME | chr1 | 149498850 | |||||
| chr1:149498870
|
T | C | 10 | a0004c0026t0001g0007a0004c0026t0001g0008a0004c0027t0001g0001others(7): Show | 11 | HG01891.hp2 HG02055.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.2730-203T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 23/93 | chr1 | 149498870 | ||||||
| chr1:149498902
|
C | T | 7 | a0006c0213t0002g0224a0006c0214t0002g0265a0156c0099t0001g0013others(4): Show | 7 | HG02080.hp2 HG02135.hp2 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.2730-171C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 23/93 | chr1 | 149498902 | ||||||
| chr1:149498971
|
T | C | 2 | a0006c0213t0002g0224a0006c0214t0002g0265 | 2 | NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2730-102T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 23/93 | chr1 | 149498971 | ||||||
| chr1:149499008
|
C | G | 16 | a0006c0211t0019g0211a0043c0209t0004g0207a0044c0210t0004g0206others(13): Show | 16 | HG00544.hp2 HG00558.hp2 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.2730-65C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 23/93 | chr1 | 149499008 | ||||||
| chr1:149499350
|
G | A | 33 | a0032c0012t0002g0232a0032c0012t0002g0266a0033c0011t0002g0254others(30): Show | 33 | HG00438.hp2 HG00621.hp1 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.2902+105G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 24/93 | chr1 | 149499350 | ||||||
| chr1:149499363
|
G | A | 100 | a0006c0211t0019g0211a0006c0212t0002g0223a0006c0213t0002g0224others(97): Show | 102 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.2902+118G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 24/93 | chr1 | 149499363 | ||||||
| chr1:149499363
|
G | GTGGGCGC others(22180): Show |
1 | a0051c0083t0001g0162 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2954+49_2954+50ins others(22187): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 25/93 | INFO_REALIGN_3_PRIME | chr1 | 149499363 | |||||
| chr1:149499368
|
C | T | 1 | a0081c0113t0001g0148 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2902+123C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 24/93 | chr1 | 149499368 | ||||||
| chr1:149499369
|
G | A | 1 | a0019c0021t0001g0098 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2902+124G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 24/93 | chr1 | 149499369 | ||||||
| chr1:149499442
|
A | T | 1 | a0211c0040t0002g0243 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2902+197A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 24/93 | chr1 | 149499442 | ||||||
| chr1:149499464
|
T | C | 9 | a0044c0210t0004g0206a0172c0204t0004g0268a0174c0202t0013g0204others(6): Show | 9 | HG02080.hp2 NA18939.hp2 NA18962.hp1 others(6): Show |
intron_variant | MODIFIER | c.2902+219T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 24/93 | chr1 | 149499464 | ||||||
| chr1:149499476
|
A | G | 1 | a0102c0144t0001g0127 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2902+231A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 24/93 | chr1 | 149499476 | ||||||
| chr1:149499498
|
C | T | 13 | a0023c0024t0001g0003a0045c0078t0001g0099a0046c0077t0001g0083others(10): Show | 14 | HG00423.hp2 HG01928.hp1 HG02155.hp2 others(11): Show |
intron_variant | MODIFIER | c.2902+253C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 24/93 | chr1 | 149499498 | ||||||
| chr1:149499510
|
C | T | 7 | a0006c0213t0002g0224a0006c0214t0002g0265a0157c0188t0001g0201others(4): Show | 7 | HG02080.hp2 HG02135.hp2 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.2902+265C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 24/93 | chr1 | 149499510 | ||||||
| chr1:149499551
|
A | G | 2 | a0156c0099t0001g0013a0157c0188t0001g0201 | 2 | HG02135.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.2902+306A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 24/93 | chr1 | 149499551 | ||||||
| chr1:149499757
|
G | A | 1 | a0160c0076t0014g0225 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2903-198G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 24/93 | chr1 | 149499757 | ||||||
| chr1:149500013
|
G | C | 4 | a0013c0035t0001g0038a0013c0035t0001g0084a0013c0162t0001g0040others(1): Show | 4 | HG02258.hp2 HG02280.hp1 HG02965.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.2954+7G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 25/93 | chr1 | 149500013 | ||||||
| chr1:149500056
|
C | A | 137 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(134): Show | 137 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.2954+50C>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 25/93 | chr1 | 149500056 | ||||||
| chr1:149500065
|
G | A | 1 | a0153c0128t0003g0125 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2954+59G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 25/93 | chr1 | 149500065 | ||||||
| chr1:149500108
|
G | C | 9 | a0180c0072t0002g0218a0181c0073t0002g0272a0183c0041t0002g0246others(6): Show | 9 | HG03831.hp1 HG04204.hp1 NA18612.hp2 others(6): Show |
intron_variant | MODIFIER | c.2954+102G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 25/93 | chr1 | 149500108 | ||||||
| chr1:149500113
|
C | G | 1 | a0061c0187t0001g0173 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2954+107C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 25/93 | chr1 | 149500113 | ||||||
| chr1:149500163
|
T | G | 1 | a0131c0171t0001g0145 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.2954+157T>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 25/93 | chr1 | 149500163 | ||||||
| chr1:149500210
|
G | C | 1 | a0156c0099t0001g0013 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2954+204G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 25/93 | chr1 | 149500210 | ||||||
| chr1:149500217
|
C | G | 1 | a0192c0055t0002g0263 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.2954+211C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 25/93 | chr1 | 149500217 | ||||||
| chr1:149500245
|
G | A | 1 | a0079c0107t0001g0059 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2954+239G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 25/93 | chr1 | 149500245 | ||||||
| chr1:149500251
|
A | G | 53 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(50): Show | 53 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.2954+245A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 25/93 | chr1 | 149500251 | ||||||
| chr1:149500280
|
T | C | 1 | a0160c0076t0014g0225 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2954+274T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 25/93 | chr1 | 149500280 | ||||||
| chr1:149500318
|
G | A | 5 | a0164c0201t0004g0205a0168c0206t0004g0203a0169c0205t0004g0209others(2): Show | 5 | HG00735.hp1 HG01099.hp1 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.2954+312G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 25/93 | chr1 | 149500318 | ||||||
| chr1:149500336
|
C | T | 1 | a0211c0040t0002g0243 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2955-321C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 25/93 | chr1 | 149500336 | ||||||
| chr1:149500392
|
C | T | 1 | a0156c0099t0001g0013 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2955-265C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 25/93 | chr1 | 149500392 | ||||||
| chr1:149500394
|
TTC | T | 2 | a0193c0057t0002g0006a0202c0064t0002g0262 | 2 | HG02040.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.2955-247_2955-246d others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 25/93 | INFO_REALIGN_3_PRIME | chr1 | 149500394 | |||||
| chr1:149500394
|
TTCTC | T | 5 | a0030c0034t0001g0092a0030c0034t0001g0093a0161c0197t0005g0214others(2): Show | 5 | HG00735.hp2 HG01516.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.2955-249_2955-246d others(6): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 25/93 | INFO_REALIGN_3_PRIME | chr1 | 149500394 | |||||
| chr1:149500404
|
CTCTCTCT others(5): Show |
C | 2 | a0006c0213t0002g0224a0006c0214t0002g0265 | 2 | NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2955-251_2955-240d others(14): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 25/93 | INFO_REALIGN_3_PRIME | chr1 | 149500404 | |||||
| chr1:149500404
|
CTCTCTCT others(15): Show |
C | 3 | a0207c0046t0002g0241a0208c0048t0002g0251a0209c0047t0002g0242 | 3 | HG02080.hp2 NA18939.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.2955-251_2955-230d others(24): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 25/93 | INFO_REALIGN_3_PRIME | chr1 | 149500404 | |||||
| chr1:149500404
|
CTCTCTCT others(17): Show |
C | 1 | a0156c0099t0001g0013 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2955-251_2955-228d others(26): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 25/93 | INFO_REALIGN_3_PRIME | chr1 | 149500404 | |||||
| chr1:149500410
|
C | CTG | 8 | a0013c0035t0001g0038a0013c0035t0001g0084a0013c0162t0001g0040others(5): Show | 8 | HG02258.hp2 HG02280.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.2955-224_2955-223d others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 25/93 | INFO_REALIGN_3_PRIME | chr1 | 149500410 | |||||
| chr1:149500410
|
C | G | 5 | a0008c0037t0001g0075a0008c0037t0001g0135a0008c0215t0001g0067others(2): Show | 5 | HG00741.hp1 HG01496.hp1 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.2955-247C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 25/93 | chr1 | 149500410 | ||||||
| chr1:149500410
|
CTG | C | 4 | a0031c0028t0003g0180a0133c0165t0022g0020a0157c0188t0001g0201others(1): Show | 4 | HG02135.hp2 HG02622.hp1 NA18946.hp2 others(1): Show |
intron_variant | MODIFIER | c.2955-224_2955-223d others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 25/93 | INFO_REALIGN_3_PRIME | chr1 | 149500410 | |||||
| chr1:149500410
|
CTGTGTG | C | 9 | a0006c0211t0019g0211a0015c0036t0006g0004a0015c0192t0006g0270others(6): Show | 10 | HG00544.hp2 HG00558.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.2955-228_2955-223d others(8): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 25/93 | INFO_REALIGN_3_PRIME | chr1 | 149500410 | |||||
| chr1:149500410
|
CTGTGTGT others(19): Show |
C | 4 | a0017c0019t0001g0112a0017c0019t0001g0167a0055c0086t0001g0168others(1): Show | 4 | HG02486.hp2 HG03516.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.2955-223_2955-198d others(28): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 25/93 | INFO_REALIGN_3_PRIME | chr1 | 149500410 | |||||
| chr1:149500410
|
CTGTGTGT others(25): Show |
C | 1 | a0009c0006t0001g0139 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2955-229_2955-198d others(34): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 25/93 | INFO_REALIGN_3_PRIME | chr1 | 149500410 | |||||
| chr1:149500412
|
G | C | 5 | a0024c0025t0001g0024a0026c0030t0001g0030a0026c0030t0001g0035others(2): Show | 5 | HG01168.hp1 HG01496.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.2955-245G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 25/93 | chr1 | 149500412 | ||||||
| chr1:149500415
|
T | A | 2 | a0161c0197t0005g0214a0162c0196t0005g0213 | 2 | HG00735.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.2955-242T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 25/93 | chr1 | 149500415 | ||||||
| chr1:149500421
|
TGTGTGTG others(7): Show |
T | 1 | a0006c0212t0002g0223 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2955-222_2955-209d others(16): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 25/93 | INFO_REALIGN_3_PRIME | chr1 | 149500421 | |||||
| chr1:149500427
|
T | C | 1 | a0195c0060t0002g0229 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.2955-230T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 25/93 | chr1 | 149500427 | ||||||
| chr1:149500429
|
T | C | 44 | a0032c0012t0002g0232a0032c0012t0002g0266a0033c0011t0002g0254others(41): Show | 44 | HG00438.hp2 HG00621.hp1 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.2955-228T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 25/93 | chr1 | 149500429 | ||||||
| chr1:149500431
|
T | C | 3 | a0181c0073t0002g0272a0193c0057t0002g0006a0202c0064t0002g0262 | 3 | HG02040.hp2 HG03831.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.2955-226T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 25/93 | chr1 | 149500431 | ||||||
| chr1:149500431
|
TGTGC | T | 5 | a0024c0025t0001g0024a0024c0025t0001g0026a0042c0195t0001g0023others(2): Show | 5 | HG02055.hp2 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.2955-222_2955-219d others(6): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 25/93 | INFO_REALIGN_3_PRIME | chr1 | 149500431 | |||||
| chr1:149500433
|
T | C | 1 | a0062c0093t0001g0267 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2955-224T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 25/93 | chr1 | 149500433 | ||||||
| chr1:149500433
|
TGC | T | 29 | a0032c0012t0002g0232a0032c0012t0002g0266a0033c0011t0002g0254others(26): Show | 29 | HG00438.hp2 HG00621.hp1 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.2955-222_2955-221d others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 25/93 | INFO_REALIGN_3_PRIME | chr1 | 149500433 | |||||
| chr1:149500435
|
C | T | 27 | a0039c0219t0002g0227a0044c0210t0004g0206a0062c0093t0001g0267others(24): Show | 27 | HG00735.hp1 HG00738.hp1 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.2955-222C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 25/93 | chr1 | 149500435 | ||||||
| chr1:149500436
|
G | A | 4 | a0006c0211t0019g0211a0163c0199t0005g0215a0165c0200t0005g0212others(1): Show | 4 | HG00544.hp2 HG00558.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2955-221G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 25/93 | chr1 | 149500436 | ||||||
| chr1:149500440
|
G | C | 3 | a0207c0046t0002g0241a0208c0048t0002g0251a0209c0047t0002g0242 | 3 | HG02080.hp2 NA18939.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.2955-217G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 25/93 | chr1 | 149500440 | ||||||
| chr1:149500442
|
G | C | 1 | a0156c0099t0001g0013 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2955-215G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 25/93 | chr1 | 149500442 | ||||||
| chr1:149500452
|
G | T | 1 | a0043c0209t0004g0207 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2955-205G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 25/93 | chr1 | 149500452 | ||||||
| chr1:149500458
|
G | C | 1 | a0006c0211t0019g0211 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2955-199G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 25/93 | chr1 | 149500458 | ||||||
| chr1:149500461
|
C | T | 13 | a0006c0212t0002g0223a0024c0025t0001g0024a0024c0025t0001g0026others(10): Show | 13 | HG01891.hp1 HG02055.hp2 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.2955-196C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 25/93 | chr1 | 149500461 | ||||||
| chr1:149500557
|
C | G | 99 | a0006c0211t0019g0211a0006c0212t0002g0223a0006c0213t0002g0224others(96): Show | 100 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.2955-100C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 25/93 | chr1 | 149500557 | ||||||
| chr1:149500574
|
C | T | 3 | a0207c0046t0002g0241a0208c0048t0002g0251a0209c0047t0002g0242 | 3 | HG02080.hp2 NA18939.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.2955-83C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 25/93 | chr1 | 149500574 | ||||||
| chr1:149500878
|
T | G | 4 | a0006c0211t0019g0211a0163c0199t0005g0215a0165c0200t0005g0212others(1): Show | 4 | HG00544.hp2 HG00558.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.3127+49T>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 26/93 | chr1 | 149500878 | ||||||
| chr1:149500948
|
T | C | 1 | a0172c0204t0004g0268 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.3127+119T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 26/93 | chr1 | 149500948 | ||||||
| chr1:149501004
|
T | A | 2 | a0012c0009t0001g0195a0140c0175t0001g0051 | 2 | NA18980.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.3127+175T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 26/93 | chr1 | 149501004 | ||||||
| chr1:149501127
|
G | C | 1 | a0107c0138t0001g0072 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.3127+298G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 26/93 | chr1 | 149501127 | ||||||
| chr1:149501140
|
C | A | 2 | a0015c0036t0006g0004a0173c0191t0006g0271 | 3 | HG02145.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3127+311C>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 26/93 | chr1 | 149501140 | ||||||
| chr1:149501149
|
C | T | 2 | a0161c0197t0005g0214a0162c0196t0005g0213 | 2 | HG00735.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.3127+320C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 26/93 | chr1 | 149501149 | ||||||
| chr1:149501217
|
T | G | 2 | a0185c0043t0002g0247a0187c0050t0002g0250 | 2 | NA18612.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.3128-327T>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 26/93 | chr1 | 149501217 | ||||||
| chr1:149501374
|
C | T | 1 | a0006c0214t0002g0265 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3128-170C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 26/93 | chr1 | 149501374 | ||||||
| chr1:149501404
|
G | C | 3 | a0207c0046t0002g0241a0208c0048t0002g0251a0209c0047t0002g0242 | 3 | HG02080.hp2 NA18939.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.3128-140G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 26/93 | chr1 | 149501404 | ||||||
| chr1:149501724
|
G | C | 5 | a0024c0025t0001g0024a0024c0025t0001g0026a0042c0195t0001g0023others(2): Show | 5 | HG00733.hp2 HG02055.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.3236+72G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 27/93 | chr1 | 149501724 | ||||||
| chr1:149501725
|
T | C | 45 | a0015c0036t0006g0004a0015c0192t0006g0270a0021c0022t0001g0080others(42): Show | 46 | HG00438.hp2 HG00621.hp1 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.3236+73T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 27/93 | chr1 | 149501725 | ||||||
| chr1:149501751
|
A | C | 1 | a0205c0056t0015g0258 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.3236+99A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 27/93 | chr1 | 149501751 | ||||||
| chr1:149501804
|
T | C | 6 | a0006c0211t0019g0211a0044c0210t0004g0206a0163c0199t0005g0215others(3): Show | 6 | HG00544.hp2 HG00558.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.3236+152T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 27/93 | chr1 | 149501804 | ||||||
| chr1:149501836
|
C | A | 173 | a0001c0001t0001g0121a0003c0003t0001g0115a0003c0003t0001g0116others(170): Show | 175 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(172): Show |
intron_variant | MODIFIER | c.3236+184C>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 27/93 | chr1 | 149501836 | ||||||
| chr1:149501840
|
A | ACGTACCA others(9519): Show |
1 | a0171c0207t0004g0208 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.3236+310_3236+311i others(9528): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 27/93 | INFO_REALIGN_3_PRIME | chr1 | 149501840 | |||||
| chr1:149501840
|
A | G | 7 | a0006c0212t0002g0223a0006c0213t0002g0224a0006c0214t0002g0265others(4): Show | 8 | HG00735.hp1 HG01891.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.3236+188A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 27/93 | chr1 | 149501840 | ||||||
| chr1:149501841
|
C | T | 1 | a0081c0113t0001g0148 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3236+189C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 27/93 | chr1 | 149501841 | ||||||
| chr1:149501879
|
C | T | 3 | a0006c0211t0019g0211a0165c0200t0005g0212a0166c0198t0005g0210 | 3 | HG00544.hp2 HG02895.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.3236+227C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 27/93 | chr1 | 149501879 | ||||||
| chr1:149501963
|
A | G | 8 | a0043c0209t0004g0207a0161c0197t0005g0214a0162c0196t0005g0213others(5): Show | 8 | HG00735.hp2 HG01099.hp1 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.3236+311A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 27/93 | chr1 | 149501963 | ||||||
| chr1:149502037
|
C | CTCTCTG | 4 | a0006c0211t0019g0211a0163c0199t0005g0215a0165c0200t0005g0212others(1): Show | 4 | HG00544.hp2 HG00558.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.3237-231_3237-226d others(8): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 27/93 | INFO_REALIGN_3_PRIME | chr1 | 149502037 | |||||
| chr1:149502073
|
G | GTC | 24 | a0043c0209t0004g0207a0045c0078t0001g0099a0046c0077t0001g0083others(21): Show | 24 | HG00735.hp1 HG00735.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.3237-193_3237-192d others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 27/93 | INFO_REALIGN_3_PRIME | chr1 | 149502073 | |||||
| chr1:149502073
|
G | GTCTC | 3 | a0179c0071t0002g0260a0199c0061t0002g0219a0202c0064t0002g0262 | 3 | HG00738.hp1 NA19011.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.3237-195_3237-192d others(6): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 27/93 | INFO_REALIGN_3_PRIME | chr1 | 149502073 | |||||
| chr1:149502073
|
GTC | G | 9 | a0011c0010t0001g0010a0011c0010t0001g0011a0011c0010t0001g0012others(6): Show | 9 | HG00438.hp1 HG03831.hp1 NA18955.hp2 others(6): Show |
intron_variant | MODIFIER | c.3237-193_3237-192d others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 27/93 | INFO_REALIGN_3_PRIME | chr1 | 149502073 | |||||
| chr1:149502083
|
C | A | 1 | a0205c0056t0015g0258 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.3237-203C>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 27/93 | chr1 | 149502083 | ||||||
| chr1:149502095
|
G | A | 3 | a0015c0036t0006g0004a0015c0192t0006g0270a0173c0191t0006g0271 | 4 | HG02145.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.3237-191G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 27/93 | chr1 | 149502095 | ||||||
| chr1:149502150
|
A | G | 6 | a0021c0022t0001g0080a0079c0107t0001g0059a0080c0106t0001g0019others(3): Show | 6 | HG02135.hp2 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.3237-136A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 27/93 | chr1 | 149502150 | ||||||
| chr1:149502160
|
A | C | 5 | a0015c0036t0006g0004a0015c0192t0006g0270a0077c0110t0001g0178others(2): Show | 6 | HG01928.hp1 HG02145.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.3237-126A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 27/93 | chr1 | 149502160 | ||||||
| chr1:149502168
|
A | C | 2 | a0164c0201t0004g0205a0171c0207t0004g0208 | 2 | HG00735.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.3237-118A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 27/93 | chr1 | 149502168 | ||||||
| chr1:149502236
|
C | T | 137 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(134): Show | 137 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.3237-50C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 27/93 | chr1 | 149502236 | ||||||
| chr1:149502266
|
A | T | 1 | a0205c0056t0015g0258 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.3237-20A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 27/93 | chr1 | 149502266 | ||||||
| chr1:149502492
|
A | G | 1 | a0110c0133t0001g0058 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.3409+34A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 28/93 | chr1 | 149502492 | ||||||
| chr1:149502516
|
A | G | 1 | a0160c0076t0014g0225 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3409+58A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 28/93 | chr1 | 149502516 | ||||||
| chr1:149502533
|
C | T | 24 | a0032c0012t0002g0232a0032c0012t0002g0266a0033c0011t0002g0254others(21): Show | 24 | HG00438.hp2 HG00621.hp1 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.3409+75C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 28/93 | chr1 | 149502533 | ||||||
| chr1:149502546
|
G | A | 9 | a0005c0004t0001g0056a0005c0004t0001g0131a0005c0004t0001g0132others(6): Show | 9 | NA18939.hp1 NA18947.hp1 NA18957.hp1 others(6): Show |
intron_variant | MODIFIER | c.3409+88G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 28/93 | chr1 | 149502546 | ||||||
| chr1:149502553
|
G | A | 1 | a0205c0056t0015g0258 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.3409+95G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 28/93 | chr1 | 149502553 | ||||||
| chr1:149502564
|
A | G | 1 | a0205c0056t0015g0258 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.3409+106A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 28/93 | chr1 | 149502564 | ||||||
| chr1:149502569
|
G | C | 1 | a0138c0174t0001g0109 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.3409+111G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 28/93 | chr1 | 149502569 | ||||||
| chr1:149502582
|
C | T | 2 | a0163c0199t0005g0215a0165c0200t0005g0212 | 2 | HG00544.hp2 HG00558.hp2 |
intron_variant | MODIFIER | c.3409+124C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 28/93 | chr1 | 149502582 | ||||||
| chr1:149502635
|
G | T | 2 | a0161c0197t0005g0214a0162c0196t0005g0213 | 2 | HG00735.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.3409+177G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 28/93 | chr1 | 149502635 | ||||||
| chr1:149502654
|
T | G | 6 | a0183c0041t0002g0246a0188c0051t0002g0252a0190c0049t0002g0244others(3): Show | 6 | NA18946.hp2 NA18954.hp2 NA18962.hp2 others(3): Show |
intron_variant | MODIFIER | c.3409+196T>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 28/93 | chr1 | 149502654 | ||||||
| chr1:149502655
|
T | C | 145 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(142): Show | 145 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.3409+197T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 28/93 | chr1 | 149502655 | ||||||
| chr1:149502673
|
C | T | 1 | a0086c0119t0001g0085 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.3409+215C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 28/93 | chr1 | 149502673 | ||||||
| chr1:149502680
|
C | A | 137 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(134): Show | 137 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.3409+222C>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 28/93 | chr1 | 149502680 | ||||||
| chr1:149502681
|
G | A | 1 | a0006c0212t0002g0223 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3409+223G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 28/93 | chr1 | 149502681 | ||||||
| chr1:149502687
|
A | C | 1 | a0211c0040t0002g0243 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.3409+229A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 28/93 | chr1 | 149502687 | ||||||
| chr1:149502696
|
T | C | 1 | a0211c0040t0002g0243 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.3409+238T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 28/93 | chr1 | 149502696 | ||||||
| chr1:149502703
|
A | G | 2 | a0006c0213t0002g0224a0006c0214t0002g0265 | 2 | NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.3409+245A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 28/93 | chr1 | 149502703 | ||||||
| chr1:149502704
|
C | T | 99 | a0006c0211t0019g0211a0006c0212t0002g0223a0006c0213t0002g0224others(96): Show | 100 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.3409+246C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 28/93 | chr1 | 149502704 | ||||||
| chr1:149502717
|
G | C | 1 | a0172c0204t0004g0268 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.3409+259G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 28/93 | chr1 | 149502717 | ||||||
| chr1:149502733
|
G | A | 202 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(199): Show | 204 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.3409+275G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 28/93 | chr1 | 149502733 | ||||||
| chr1:149502810
|
G | A | 5 | a0043c0209t0004g0207a0168c0206t0004g0203a0169c0205t0004g0209others(2): Show | 5 | HG01099.hp1 HG02165.hp1 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.3409+352G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 28/93 | chr1 | 149502810 | ||||||
| chr1:149503081
|
A | T | 2 | a0185c0043t0002g0247a0187c0050t0002g0250 | 2 | NA18612.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.3410-97A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 28/93 | chr1 | 149503081 | ||||||
| chr1:149503095
|
T | C | 9 | a0036c0014t0009g0228a0036c0014t0009g0230a0156c0099t0001g0013others(6): Show | 9 | HG00621.hp2 HG02080.hp2 NA18939.hp2 others(6): Show |
intron_variant | MODIFIER | c.3410-83T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 28/93 | chr1 | 149503095 | ||||||
| chr1:149503111
|
A | G | 2 | a0006c0213t0002g0224a0006c0214t0002g0265 | 2 | NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.3410-67A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 28/93 | chr1 | 149503111 | ||||||
| chr1:149503151
|
A | G | 81 | a0001c0001t0001g0158a0006c0211t0019g0211a0006c0212t0002g0223others(78): Show | 82 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.3410-27A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 28/93 | chr1 | 149503151 | ||||||
| chr1:149503283
|
A | G | 2 | a0199c0061t0002g0219a0202c0064t0002g0262 | 2 | NA19011.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.3461+54A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 29/93 | chr1 | 149503283 | ||||||
| chr1:149503308
|
T | C | 1 | a0006c0214t0002g0265 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3461+79T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 29/93 | chr1 | 149503308 | ||||||
| chr1:149503318
|
G | T | 2 | a0030c0034t0001g0092a0030c0034t0001g0093 | 2 | HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.3461+89G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 29/93 | chr1 | 149503318 | ||||||
| chr1:149503340
|
C | T | 1 | a0001c0001t0001g0136 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.3461+111C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 29/93 | chr1 | 149503340 | ||||||
| chr1:149503408
|
T | A | 11 | a0036c0014t0009g0228a0036c0014t0009g0230a0044c0210t0004g0206others(8): Show | 11 | HG00621.hp2 HG02080.hp2 NA18939.hp2 others(8): Show |
intron_variant | MODIFIER | c.3461+179T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 29/93 | chr1 | 149503408 | ||||||
| chr1:149503446
|
G | A | 1 | a0006c0213t0002g0224 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3461+217G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 29/93 | chr1 | 149503446 | ||||||
| chr1:149503461
|
G | T | 10 | a0039c0219t0002g0227a0182c0074t0002g0261a0183c0041t0002g0246others(7): Show | 10 | HG01346.hp2 NA18612.hp2 NA18946.hp2 others(7): Show |
intron_variant | MODIFIER | c.3461+232G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 29/93 | chr1 | 149503461 | ||||||
| chr1:149503463
|
A | G | 1 | a0006c0214t0002g0265 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3461+234A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 29/93 | chr1 | 149503463 | ||||||
| chr1:149503481
|
T | A | 10 | a0039c0219t0002g0227a0182c0074t0002g0261a0183c0041t0002g0246others(7): Show | 10 | HG01346.hp2 NA18612.hp2 NA18946.hp2 others(7): Show |
intron_variant | MODIFIER | c.3461+252T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 29/93 | chr1 | 149503481 | ||||||
| chr1:149503524
|
G | A | 2 | a0079c0107t0001g0059a0093c0124t0001g0153 | 2 | HG02572.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.3461+295G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 29/93 | chr1 | 149503524 | ||||||
| chr1:149503546
|
A | T | 1 | a0008c0215t0001g0067 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.3462-288A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 29/93 | chr1 | 149503546 | ||||||
| chr1:149503611
|
C | CCT | 15 | a0008c0037t0001g0135a0011c0010t0001g0012a0030c0034t0001g0092others(12): Show | 15 | HG00621.hp2 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.3462-201_3462-200d others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 29/93 | INFO_REALIGN_3_PRIME | chr1 | 149503611 | |||||
| chr1:149503611
|
C | CCTCT | 3 | a0015c0036t0006g0004a0015c0192t0006g0270a0173c0191t0006g0271 | 4 | HG02145.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.3462-203_3462-200d others(6): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 29/93 | INFO_REALIGN_3_PRIME | chr1 | 149503611 | |||||
| chr1:149503611
|
CCTCT | C | 3 | a0044c0210t0004g0206a0061c0187t0001g0173a0172c0204t0004g0268 | 3 | HG02145.hp2 NA18972.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.3462-203_3462-200d others(6): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 29/93 | INFO_REALIGN_3_PRIME | chr1 | 149503611 | |||||
| chr1:149503646
|
C | G | 3 | a0015c0036t0006g0004a0015c0192t0006g0270a0173c0191t0006g0271 | 4 | HG02145.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.3462-188C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 29/93 | chr1 | 149503646 | ||||||
| chr1:149503663
|
C | T | 5 | a0006c0213t0002g0224a0044c0210t0004g0206a0156c0099t0001g0013others(2): Show | 5 | HG00621.hp2 NA18972.hp1 NA19062.hp2 others(2): Show |
intron_variant | MODIFIER | c.3462-171C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 29/93 | chr1 | 149503663 | ||||||
| chr1:149503732
|
T | C | 1 | a0006c0213t0002g0224 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3462-102T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 29/93 | chr1 | 149503732 | ||||||
| chr1:149503762
|
A | C | 1 | a0006c0212t0002g0223 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3462-72A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 29/93 | chr1 | 149503762 | ||||||
| chr1:149503769
|
C | G | 14 | a0006c0211t0019g0211a0043c0209t0004g0207a0161c0197t0005g0214others(11): Show | 14 | HG00544.hp2 HG00558.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.3462-65C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 29/93 | chr1 | 149503769 | ||||||
| chr1:149503786
|
G | C | 1 | a0114c0137t0001g0133 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.3462-48G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 29/93 | chr1 | 149503786 | ||||||
| chr1:149504071
|
G | C | 1 | a0003c0003t0001g0115 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3634+65G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 30/93 | chr1 | 149504071 | ||||||
| chr1:149504111
|
G | A | 13 | a0003c0003t0001g0115a0003c0003t0001g0116a0003c0003t0001g0117others(10): Show | 13 | HG00544.hp1 HG02080.hp2 HG03225.hp2 others(10): Show |
intron_variant | MODIFIER | c.3634+105G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 30/93 | chr1 | 149504111 | ||||||
| chr1:149504124
|
G | A | 242 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(239): Show | 245 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(242): Show |
intron_variant | MODIFIER | c.3634+118G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 30/93 | chr1 | 149504124 | ||||||
| chr1:149504203
|
A | T | 3 | a0185c0043t0002g0247a0187c0050t0002g0250a0211c0040t0002g0243 | 3 | NA18612.hp2 NA18946.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.3634+197A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 30/93 | chr1 | 149504203 | ||||||
| chr1:149504204
|
T | C | 1 | a0166c0198t0005g0210 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3634+198T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 30/93 | chr1 | 149504204 | ||||||
| chr1:149504225
|
T | C | 19 | a0036c0014t0009g0228a0036c0014t0009g0230a0044c0210t0004g0206others(16): Show | 19 | HG00735.hp1 HG02080.hp2 HG02572.hp1 others(16): Show |
intron_variant | MODIFIER | c.3634+219T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 30/93 | chr1 | 149504225 | ||||||
| chr1:149504230
|
C | T | 1 | a0086c0119t0001g0085 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.3634+224C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 30/93 | chr1 | 149504230 | ||||||
| chr1:149504259
|
C | T | 130 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(127): Show | 132 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.3634+253C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 30/93 | chr1 | 149504259 | ||||||
| chr1:149504271
|
C | T | 6 | a0006c0213t0002g0224a0044c0210t0004g0206a0156c0099t0001g0013others(3): Show | 6 | HG00621.hp2 HG03942.hp2 NA18972.hp1 others(3): Show |
intron_variant | MODIFIER | c.3634+265C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 30/93 | chr1 | 149504271 | ||||||
| chr1:149504277
|
A | T | 3 | a0002c0002t0007g0190a0002c0002t0007g0193a0155c0186t0007g0183 | 3 | NA18942.hp1 NA18960.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.3634+271A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 30/93 | chr1 | 149504277 | ||||||
| chr1:149504284
|
G | A | 1 | a0156c0099t0001g0013 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.3634+278G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 30/93 | chr1 | 149504284 | ||||||
| chr1:149504312
|
A | G | 1 | a0205c0056t0015g0258 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.3634+306A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 30/93 | chr1 | 149504312 | ||||||
| chr1:149504535
|
T | A | 1 | a0160c0076t0014g0225 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3635-181T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 30/93 | chr1 | 149504535 | ||||||
| chr1:149504592
|
C | G | 1 | a0202c0064t0002g0262 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.3635-124C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 30/93 | chr1 | 149504592 | ||||||
| chr1:149504774
|
G | C | 1 | a0134c0164t0001g0039 | 1 | HG03130.hp1 | splice_region_variant&intron_variant | LOW | c.3686+7G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 31/93 | chr1 | 149504774 | ||||||
| chr1:149504779
|
A | G | 6 | a0048c0081t0011g0151a0049c0082t0011g0096a0050c0080t0001g0177others(3): Show | 6 | HG01109.hp1 HG01978.hp1 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.3686+12A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 31/93 | chr1 | 149504779 | ||||||
| chr1:149504817
|
C | A | 14 | a0001c0001t0001g0158a0028c0032t0001g0161a0029c0033t0001g0197others(11): Show | 14 | HG00558.hp1 HG00733.hp1 HG02135.hp2 others(11): Show |
intron_variant | MODIFIER | c.3686+50C>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 31/93 | chr1 | 149504817 | ||||||
| chr1:149504817
|
C | CCTGGTTC others(4746): Show |
1 | a0096c0127t0001g0111 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3687-248_3687-247i others(4755): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 31/93 | INFO_REALIGN_3_PRIME | chr1 | 149504817 | |||||
| chr1:149504869
|
G | C | 6 | a0186c0044t0017g0239a0193c0057t0002g0006a0195c0060t0002g0229others(3): Show | 6 | HG00438.hp2 HG02040.hp2 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.3686+102G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 31/93 | chr1 | 149504869 | ||||||
| chr1:149504998
|
C | A | 1 | a0039c0219t0002g0227 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.3686+231C>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 31/93 | chr1 | 149504998 | ||||||
| chr1:149505012
|
A | G | 3 | a0135c0161t0001g0057a0156c0099t0001g0013a0157c0188t0001g0201 | 3 | HG00733.hp1 HG02135.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.3686+245A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 31/93 | chr1 | 149505012 | ||||||
| chr1:149505015
|
G | C | 4 | a0020c0020t0001g0041a0020c0020t0010g0043a0067c0095t0001g0042others(1): Show | 4 | HG01074.hp2 HG01952.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.3686+248G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 31/93 | chr1 | 149505015 | ||||||
| chr1:149505079
|
G | A | 1 | a0174c0202t0013g0204 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.3686+312G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 31/93 | chr1 | 149505079 | ||||||
| chr1:149505097
|
C | T | 2 | a0185c0043t0002g0247a0187c0050t0002g0250 | 2 | NA18612.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.3687-321C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 31/93 | chr1 | 149505097 | ||||||
| chr1:149505104
|
T | C | 5 | a0089c0123t0001g0164a0142c0180t0001g0108a0145c0177t0001g0165others(2): Show | 5 | HG01109.hp2 HG01168.hp2 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.3687-314T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 31/93 | chr1 | 149505104 | ||||||
| chr1:149505155
|
TTC | T | 3 | a0111c0132t0001g0199a0158c0084t0001g0049a0166c0198t0005g0210 | 3 | HG02965.hp1 HG03942.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.3687-247_3687-246d others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 31/93 | INFO_REALIGN_3_PRIME | chr1 | 149505155 | |||||
| chr1:149505155
|
TTCTC | T | 2 | a0163c0199t0005g0215a0165c0200t0005g0212 | 2 | HG00544.hp2 HG00558.hp2 |
intron_variant | MODIFIER | c.3687-249_3687-246d others(6): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 31/93 | INFO_REALIGN_3_PRIME | chr1 | 149505155 | |||||
| chr1:149505165
|
C | T | 1 | a0100c0145t0001g0076 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.3687-253C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 31/93 | chr1 | 149505165 | ||||||
| chr1:149505165
|
CTCTCTCT others(5): Show |
C | 1 | a0006c0213t0002g0224 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3687-251_3687-240d others(14): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 31/93 | INFO_REALIGN_3_PRIME | chr1 | 149505165 | |||||
| chr1:149505169
|
CTCTG | C | 6 | a0050c0080t0001g0177a0051c0083t0001g0162a0052c0079t0021g0176others(3): Show | 6 | HG01928.hp1 HG01978.hp1 HG02155.hp2 others(3): Show |
intron_variant | MODIFIER | c.3687-247_3687-244d others(6): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 31/93 | INFO_REALIGN_3_PRIME | chr1 | 149505169 | |||||
| chr1:149505169
|
CTCTGTGT others(3): Show |
C | 3 | a0045c0078t0001g0099a0046c0077t0001g0083a0049c0082t0011g0096 | 3 | HG02738.hp1 HG03041.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.3687-247_3687-238d others(12): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 31/93 | INFO_REALIGN_3_PRIME | chr1 | 149505169 | |||||
| chr1:149505169
|
CTCTGTGT others(5): Show |
C | 1 | a0057c0088t0001g0089 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.3687-247_3687-236d others(14): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 31/93 | INFO_REALIGN_3_PRIME | chr1 | 149505169 | |||||
| chr1:149505171
|
C | CTG | 3 | a0134c0164t0001g0039a0152c0129t0003g0192a0174c0202t0013g0204 | 3 | HG03130.hp1 NA18946.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.3687-224_3687-223d others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 31/93 | INFO_REALIGN_3_PRIME | chr1 | 149505171 | |||||
| chr1:149505171
|
C | G | 11 | a0002c0002t0003g0182a0002c0002t0003g0188a0002c0002t0003g0189others(8): Show | 11 | HG01952.hp1 HG02258.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.3687-247C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 31/93 | chr1 | 149505171 | ||||||
| chr1:149505171
|
CTG | C | 10 | a0009c0006t0001g0081a0009c0006t0001g0082a0009c0006t0001g0139others(7): Show | 11 | HG00099.hp1 HG00741.hp2 HG01346.hp2 others(8): Show |
intron_variant | MODIFIER | c.3687-224_3687-223d others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 31/93 | INFO_REALIGN_3_PRIME | chr1 | 149505171 | |||||
| chr1:149505171
|
CTGTGTG | C | 5 | a0006c0211t0019g0211a0164c0201t0004g0205a0167c0203t0028g0269others(2): Show | 5 | HG00735.hp1 HG01099.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.3687-228_3687-223d others(8): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 31/93 | INFO_REALIGN_3_PRIME | chr1 | 149505171 | |||||
| chr1:149505173
|
G | C | 2 | a0006c0212t0002g0223a0006c0214t0002g0265 | 2 | HG01891.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3687-245G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 31/93 | chr1 | 149505173 | ||||||
| chr1:149505176
|
T | A | 2 | a0163c0199t0005g0215a0165c0200t0005g0212 | 2 | HG00544.hp2 HG00558.hp2 |
intron_variant | MODIFIER | c.3687-242T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 31/93 | chr1 | 149505176 | ||||||
| chr1:149505180
|
T | C | 1 | a0044c0210t0004g0206 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.3687-238T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 31/93 | chr1 | 149505180 | ||||||
| chr1:149505188
|
T | C | 1 | a0171c0207t0004g0208 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.3687-230T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 31/93 | chr1 | 149505188 | ||||||
| chr1:149505188
|
T | TGC | 4 | a0034c0013t0002g0220a0034c0013t0002g0221a0161c0197t0005g0214others(1): Show | 4 | HG00735.hp2 HG01516.hp1 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.3687-229_3687-228i others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 31/93 | INFO_REALIGN_3_PRIME | chr1 | 149505188 | |||||
| chr1:149505188
|
TGTGTGTG others(1): Show |
T | 6 | a0017c0019t0001g0112a0017c0019t0001g0167a0018c0018t0001g0113others(3): Show | 6 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.3687-222_3687-215d others(10): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 31/93 | INFO_REALIGN_3_PRIME | chr1 | 149505188 | |||||
| chr1:149505190
|
T | C | 44 | a0032c0012t0002g0232a0032c0012t0002g0266a0033c0011t0002g0254others(41): Show | 44 | HG00438.hp2 HG00621.hp1 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.3687-228T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 31/93 | chr1 | 149505190 | ||||||
| chr1:149505194
|
T | C | 2 | a0074c0112t0001g0104a0075c0108t0001g0163 | 2 | HG03139.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.3687-224T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 31/93 | chr1 | 149505194 | ||||||
| chr1:149505194
|
TGC | T | 16 | a0032c0012t0002g0232a0033c0011t0002g0254a0033c0011t0002g0255others(13): Show | 16 | HG00438.hp2 HG00642.hp1 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.3687-222_3687-221d others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 31/93 | INFO_REALIGN_3_PRIME | chr1 | 149505194 | |||||
| chr1:149505196
|
C | CGT | 5 | a0022c0023t0001g0156a0022c0023t0001g0160a0027c0029t0001g0062others(2): Show | 5 | HG02572.hp2 HG02630.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.3687-199_3687-198d others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 31/93 | INFO_REALIGN_3_PRIME | chr1 | 149505196 | |||||
| chr1:149505196
|
C | T | 53 | a0032c0012t0002g0266a0034c0013t0002g0220a0034c0013t0002g0221others(50): Show | 53 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.3687-222C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 31/93 | chr1 | 149505196 | ||||||
| chr1:149505196
|
CGT | C | 6 | a0006c0212t0002g0223a0089c0123t0001g0164a0142c0180t0001g0108others(3): Show | 6 | HG01109.hp2 HG01168.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.3687-199_3687-198d others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 31/93 | INFO_REALIGN_3_PRIME | chr1 | 149505196 | |||||
| chr1:149505196
|
CGTGTGTG others(3): Show |
C | 5 | a0026c0030t0001g0030a0026c0030t0001g0035a0098c0147t0001g0031others(2): Show | 5 | HG00738.hp2 HG01123.hp1 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.3687-207_3687-198d others(12): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 31/93 | INFO_REALIGN_3_PRIME | chr1 | 149505196 | |||||
| chr1:149505197
|
G | A | 1 | a0006c0211t0019g0211 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.3687-221G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 31/93 | chr1 | 149505197 | ||||||
| chr1:149505213
|
G | T | 3 | a0043c0209t0004g0207a0169c0205t0004g0209a0174c0202t0013g0204 | 3 | HG02165.hp1 HG04115.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.3687-205G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 31/93 | chr1 | 149505213 | ||||||
| chr1:149505222
|
C | T | 27 | a0017c0019t0001g0112a0017c0019t0001g0167a0018c0018t0001g0113others(24): Show | 27 | HG00423.hp2 HG01109.hp1 HG01928.hp1 others(24): Show |
intron_variant | MODIFIER | c.3687-196C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 31/93 | chr1 | 149505222 | ||||||
| chr1:149505286
|
T | A | 1 | a0118c0151t0001g0053 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.3687-132T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 31/93 | chr1 | 149505286 | ||||||
| chr1:149505318
|
C | G | 112 | a0002c0002t0003g0189a0006c0211t0019g0211a0006c0212t0002g0223others(109): Show | 113 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.3687-100C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 31/93 | chr1 | 149505318 | ||||||
| chr1:149505382
|
C | G | 1 | a0166c0198t0005g0210 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3687-36C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 31/93 | chr1 | 149505382 | ||||||
| chr1:149505631
|
C | G | 2 | a0043c0209t0004g0207a0044c0210t0004g0206 | 2 | HG02165.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.3859+41C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 32/93 | chr1 | 149505631 | ||||||
| chr1:149505639
|
T | G | 1 | a0006c0211t0019g0211 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.3859+49T>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 32/93 | chr1 | 149505639 | ||||||
| chr1:149505689
|
G | A | 1 | a0167c0203t0028g0269 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3859+99G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 32/93 | chr1 | 149505689 | ||||||
| chr1:149505695
|
G | T | 1 | a0083c0116t0023g0103 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3859+105G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 32/93 | chr1 | 149505695 | ||||||
| chr1:149505709
|
T | C | 4 | a0161c0197t0005g0214a0162c0196t0005g0213a0164c0201t0004g0205others(1): Show | 4 | HG00735.hp1 HG00735.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.3859+119T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 32/93 | chr1 | 149505709 | ||||||
| chr1:149505761
|
G | T | 1 | a0166c0198t0005g0210 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3859+171G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 32/93 | chr1 | 149505761 | ||||||
| chr1:149505817
|
C | G | 1 | a0166c0198t0005g0210 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3859+227C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 32/93 | chr1 | 149505817 | ||||||
| chr1:149505860
|
A | T | 1 | a0167c0203t0028g0269 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3859+270A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 32/93 | chr1 | 149505860 | ||||||
| chr1:149505910
|
C | T | 2 | a0163c0199t0005g0215a0165c0200t0005g0212 | 2 | HG00544.hp2 HG00558.hp2 |
intron_variant | MODIFIER | c.3859+320C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 32/93 | chr1 | 149505910 | ||||||
| chr1:149505978
|
T | G | 13 | a0183c0041t0002g0246a0185c0043t0002g0247a0187c0050t0002g0250others(10): Show | 13 | HG00438.hp2 HG00621.hp1 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.3860-327T>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 32/93 | chr1 | 149505978 | ||||||
| chr1:149505990
|
T | TCTCCTAG others(4760): Show |
1 | a0036c0014t0009g0228 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.3968+72_3968+73ins others(4767): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 33/93 | INFO_REALIGN_3_PRIME | chr1 | 149505990 | |||||
| chr1:149505995
|
T | C | 8 | a0004c0026t0001g0007a0004c0026t0001g0008a0004c0027t0001g0001others(5): Show | 10 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.3860-310T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 32/93 | chr1 | 149505995 | ||||||
| chr1:149506085
|
A | G | 1 | a0044c0210t0004g0206 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.3860-220A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 32/93 | chr1 | 149506085 | ||||||
| chr1:149506136
|
G | A | 1 | a0006c0214t0002g0265 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3860-169G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 32/93 | chr1 | 149506136 | ||||||
| chr1:149506175
|
A | T | 2 | a0003c0003t0001g0115a0003c0003t0001g0116 | 2 | NA18612.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.3860-130A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 32/93 | chr1 | 149506175 | ||||||
| chr1:149506196
|
ATTC | A | 2 | a0164c0201t0004g0205a0171c0207t0004g0208 | 2 | HG00735.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.3860-106_3860-104d others(5): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 32/93 | INFO_REALIGN_3_PRIME | chr1 | 149506196 | |||||
| chr1:149506253
|
G | A | 9 | a0002c0002t0003g0182a0002c0002t0003g0188a0002c0002t0003g0189others(6): Show | 9 | NA18942.hp1 NA18960.hp2 NA18961.hp2 others(6): Show |
intron_variant | MODIFIER | c.3860-52G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 32/93 | chr1 | 149506253 | ||||||
| chr1:149506288
|
G | A | 4 | a0168c0206t0004g0203a0169c0205t0004g0209a0170c0208t0004g0202others(1): Show | 4 | HG01099.hp1 HG04115.hp1 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.3860-17G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 32/93 | chr1 | 149506288 | ||||||
| chr1:149506463
|
C | G | 2 | a0161c0197t0005g0214a0162c0196t0005g0213 | 2 | HG00735.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.3968+50C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 33/93 | chr1 | 149506463 | ||||||
| chr1:149506486
|
T | C | 88 | a0002c0002t0003g0182a0002c0002t0003g0188a0002c0002t0003g0189others(85): Show | 89 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.3968+73T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 33/93 | chr1 | 149506486 | ||||||
| chr1:149506565
|
T | C | 7 | a0006c0211t0019g0211a0044c0210t0004g0206a0161c0197t0005g0214others(4): Show | 7 | HG00735.hp1 HG00735.hp2 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.3968+152T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 33/93 | chr1 | 149506565 | ||||||
| chr1:149506597
|
C | A | 226 | a0001c0001t0001g0121a0002c0002t0003g0182a0002c0002t0003g0188others(223): Show | 229 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(226): Show |
intron_variant | MODIFIER | c.3968+184C>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 33/93 | chr1 | 149506597 | ||||||
| chr1:149506601
|
A | ACGTACCA others(4752): Show |
1 | a0170c0208t0004g0202 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3968+310_3968+311i others(4761): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 33/93 | INFO_REALIGN_3_PRIME | chr1 | 149506601 | |||||
| chr1:149506601
|
A | G | 6 | a0006c0213t0002g0224a0006c0214t0002g0265a0015c0036t0006g0004others(3): Show | 7 | HG02145.hp1 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.3968+188A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 33/93 | chr1 | 149506601 | ||||||
| chr1:149506624
|
T | G | 1 | a0093c0124t0001g0153 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3968+211T>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 33/93 | chr1 | 149506624 | ||||||
| chr1:149506640
|
C | T | 1 | a0006c0211t0019g0211 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.3968+227C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 33/93 | chr1 | 149506640 | ||||||
| chr1:149506724
|
A | G | 6 | a0043c0209t0004g0207a0163c0199t0005g0215a0165c0200t0005g0212others(3): Show | 6 | HG00544.hp2 HG00558.hp2 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.3968+311A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 33/93 | chr1 | 149506724 | ||||||
| chr1:149506778
|
C | G | 1 | a0172c0204t0004g0268 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.3969-269C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 33/93 | chr1 | 149506778 | ||||||
| chr1:149506816
|
G | C | 3 | a0168c0206t0004g0203a0169c0205t0004g0209a0174c0202t0013g0204 | 3 | HG01099.hp1 HG04115.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.3969-231G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 33/93 | chr1 | 149506816 | ||||||
| chr1:149506822
|
C | G | 4 | a0006c0214t0002g0265a0168c0206t0004g0203a0169c0205t0004g0209others(1): Show | 4 | HG01099.hp1 HG04115.hp1 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.3969-225C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 33/93 | chr1 | 149506822 | ||||||
| chr1:149506824
|
CTCTGTCT others(3): Show |
C | 1 | a0006c0214t0002g0265 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3969-219_3969-210d others(12): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 33/93 | INFO_REALIGN_3_PRIME | chr1 | 149506824 | |||||
| chr1:149506830
|
CTCTG | C | 3 | a0168c0206t0004g0203a0169c0205t0004g0209a0174c0202t0013g0204 | 3 | HG01099.hp1 HG04115.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.3969-213_3969-210d others(6): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 33/93 | INFO_REALIGN_3_PRIME | chr1 | 149506830 | |||||
| chr1:149506834
|
G | GTC | 39 | a0006c0212t0002g0223a0032c0012t0002g0232a0032c0012t0002g0266others(36): Show | 39 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.3969-193_3969-192d others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 33/93 | INFO_REALIGN_3_PRIME | chr1 | 149506834 | |||||
| chr1:149506834
|
G | GTCTC | 8 | a0005c0004t0001g0056a0005c0004t0001g0131a0005c0004t0001g0132others(5): Show | 8 | HG00621.hp2 HG02080.hp2 NA18939.hp2 others(5): Show |
intron_variant | MODIFIER | c.3969-195_3969-192d others(6): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 33/93 | INFO_REALIGN_3_PRIME | chr1 | 149506834 | |||||
| chr1:149506834
|
GTCTC | G | 4 | a0161c0197t0005g0214a0162c0196t0005g0213a0164c0201t0004g0205others(1): Show | 4 | HG00735.hp1 HG00735.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.3969-195_3969-192d others(6): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 33/93 | INFO_REALIGN_3_PRIME | chr1 | 149506834 | |||||
| chr1:149506856
|
G | A | 3 | a0015c0036t0006g0004a0015c0192t0006g0270a0173c0191t0006g0271 | 4 | HG02145.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.3969-191G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 33/93 | chr1 | 149506856 | ||||||
| chr1:149506911
|
A | G | 46 | a0002c0002t0003g0182a0002c0002t0003g0188a0002c0002t0003g0189others(43): Show | 46 | HG00423.hp2 HG00544.hp1 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.3969-136A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 33/93 | chr1 | 149506911 | ||||||
| chr1:149506921
|
A | C | 10 | a0015c0036t0006g0004a0015c0192t0006g0270a0089c0123t0001g0164others(7): Show | 11 | HG01109.hp2 HG01168.hp2 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.3969-126A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 33/93 | chr1 | 149506921 | ||||||
| chr1:149506929
|
A | C | 1 | a0170c0208t0004g0202 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3969-118A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 33/93 | chr1 | 149506929 | ||||||
| chr1:149506997
|
C | T | 12 | a0001c0001t0001g0078a0001c0001t0001g0158a0013c0035t0001g0038others(9): Show | 12 | HG00558.hp1 HG00733.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.3969-50C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 33/93 | chr1 | 149506997 | ||||||
| chr1:149507234
|
A | G | 2 | a0161c0197t0005g0214a0162c0196t0005g0213 | 2 | HG00735.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.4141+15A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 34/93 | chr1 | 149507234 | ||||||
| chr1:149507253
|
A | G | 1 | a0110c0133t0001g0058 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.4141+34A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 34/93 | chr1 | 149507253 | ||||||
| chr1:149507265
|
G | A | 1 | a0158c0084t0001g0049 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.4141+46G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 34/93 | chr1 | 149507265 | ||||||
| chr1:149507277
|
A | G | 1 | a0160c0076t0014g0225 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.4141+58A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 34/93 | chr1 | 149507277 | ||||||
| chr1:149507294
|
C | T | 1 | a0036c0014t0009g0228 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.4141+75C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 34/93 | chr1 | 149507294 | ||||||
| chr1:149507396
|
G | T | 2 | a0163c0199t0005g0215a0165c0200t0005g0212 | 2 | HG00544.hp2 HG00558.hp2 |
intron_variant | MODIFIER | c.4141+177G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 34/93 | chr1 | 149507396 | ||||||
| chr1:149507415
|
T | G | 4 | a0179c0071t0002g0260a0180c0072t0002g0218a0181c0073t0002g0272others(1): Show | 4 | HG00738.hp1 HG03831.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.4141+196T>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 34/93 | chr1 | 149507415 | ||||||
| chr1:149507416
|
T | C | 16 | a0001c0001t0001g0121a0001c0001t0001g0158a0036c0014t0009g0230others(13): Show | 16 | HG00558.hp1 HG00733.hp1 HG02027.hp1 others(13): Show |
intron_variant | MODIFIER | c.4141+197T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 34/93 | chr1 | 149507416 | ||||||
| chr1:149507441
|
C | A | 7 | a0001c0001t0001g0158a0069c0100t0001g0016a0083c0116t0023g0103others(4): Show | 7 | HG00558.hp1 HG00733.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.4141+222C>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 34/93 | chr1 | 149507441 | ||||||
| chr1:149507448
|
A | C | 2 | a0185c0043t0002g0247a0187c0050t0002g0250 | 2 | NA18612.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.4141+229A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 34/93 | chr1 | 149507448 | ||||||
| chr1:149507457
|
T | C | 2 | a0185c0043t0002g0247a0187c0050t0002g0250 | 2 | NA18612.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.4141+238T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 34/93 | chr1 | 149507457 | ||||||
| chr1:149507464
|
A | G | 3 | a0006c0212t0002g0223a0006c0213t0002g0224a0006c0214t0002g0265 | 3 | HG01891.hp1 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.4141+245A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 34/93 | chr1 | 149507464 | ||||||
| chr1:149507465
|
C | G | 1 | a0166c0198t0005g0210 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.4141+246C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 34/93 | chr1 | 149507465 | ||||||
| chr1:149507465
|
C | T | 235 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(232): Show | 237 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(234): Show |
intron_variant | MODIFIER | c.4141+246C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 34/93 | chr1 | 149507465 | ||||||
| chr1:149507478
|
G | C | 2 | a0164c0201t0004g0205a0171c0207t0004g0208 | 2 | HG00735.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.4141+259G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 34/93 | chr1 | 149507478 | ||||||
| chr1:149507493
|
C | G | 1 | a0098c0147t0001g0031 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.4141+274C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 34/93 | chr1 | 149507493 | ||||||
| chr1:149507493
|
C | T | 1 | a0025c0031t0001g0033 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.4141+274C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 34/93 | chr1 | 149507493 | ||||||
| chr1:149507494
|
G | A | 56 | a0001c0001t0001g0121a0001c0001t0001g0158a0006c0211t0019g0211others(53): Show | 57 | HG00544.hp2 HG00558.hp2 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.4141+275G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 34/93 | chr1 | 149507494 | ||||||
| chr1:149507494
|
G | GCAACTCT others(4749): Show |
4 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0078others(1): Show | 4 | HG01099.hp2 HG01123.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.4366+252_4366+253i others(4758): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 36/93 | INFO_REALIGN_3_PRIME | chr1 | 149507494 | |||||
| chr1:149507494
|
G | GCAACTCT others(4751): Show |
1 | a0001c0001t0001g0077 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.4366+252_4366+253i others(4760): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 36/93 | INFO_REALIGN_3_PRIME | chr1 | 149507494 | |||||
| chr1:149507558
|
G | A | 2 | a0050c0080t0001g0177a0052c0079t0021g0176 | 2 | HG01978.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.4141+339G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 34/93 | chr1 | 149507558 | ||||||
| chr1:149507571
|
G | A | 4 | a0043c0209t0004g0207a0168c0206t0004g0203a0169c0205t0004g0209others(1): Show | 4 | HG01099.hp1 HG02165.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.4141+352G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 34/93 | chr1 | 149507571 | ||||||
| chr1:149507625
|
T | C | 1 | a0006c0211t0019g0211 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.4142-314T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 34/93 | chr1 | 149507625 | ||||||
| chr1:149507695
|
A | C | 2 | a0050c0080t0001g0177a0052c0079t0021g0176 | 2 | HG01978.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.4142-244A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 34/93 | chr1 | 149507695 | ||||||
| chr1:149507842
|
A | T | 10 | a0039c0219t0002g0227a0183c0041t0002g0246a0188c0051t0002g0252others(7): Show | 10 | HG00438.hp2 HG02129.hp2 NA18946.hp2 others(7): Show |
intron_variant | MODIFIER | c.4142-97A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 34/93 | chr1 | 149507842 | ||||||
| chr1:149507856
|
T | C | 4 | a0036c0014t0009g0230a0207c0046t0002g0241a0208c0048t0002g0251others(1): Show | 4 | HG02080.hp2 NA18939.hp2 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.4142-83T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 34/93 | chr1 | 149507856 | ||||||
| chr1:149507872
|
A | G | 3 | a0006c0212t0002g0223a0006c0213t0002g0224a0006c0214t0002g0265 | 3 | HG01891.hp1 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.4142-67A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 34/93 | chr1 | 149507872 | ||||||
| chr1:149507912
|
A | G | 130 | a0001c0001t0001g0158a0002c0002t0003g0182a0002c0002t0003g0188others(127): Show | 131 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.4142-27A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 34/93 | chr1 | 149507912 | ||||||
| chr1:149508008
|
T | C | 3 | a0168c0206t0004g0203a0169c0205t0004g0209a0174c0202t0013g0204 | 3 | HG01099.hp1 HG04115.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.4193+18T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 35/93 | chr1 | 149508008 | ||||||
| chr1:149508044
|
A | G | 4 | a0036c0014t0009g0230a0207c0046t0002g0241a0208c0048t0002g0251others(1): Show | 4 | HG02080.hp2 NA18939.hp2 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.4193+54A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 35/93 | chr1 | 149508044 | ||||||
| chr1:149508069
|
T | C | 2 | a0006c0212t0002g0223a0006c0213t0002g0224 | 2 | HG01891.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.4193+79T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 35/93 | chr1 | 149508069 | ||||||
| chr1:149508163
|
C | T | 3 | a0168c0206t0004g0203a0169c0205t0004g0209a0174c0202t0013g0204 | 3 | HG01099.hp1 HG04115.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.4193+173C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 35/93 | chr1 | 149508163 | ||||||
| chr1:149508169
|
T | A | 10 | a0025c0031t0001g0032a0036c0014t0009g0230a0166c0198t0005g0210others(7): Show | 10 | HG02080.hp2 HG02155.hp1 HG03669.hp1 others(7): Show |
intron_variant | MODIFIER | c.4193+179T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 35/93 | chr1 | 149508169 | ||||||
| chr1:149508194
|
A | T | 3 | a0185c0043t0002g0247a0187c0050t0002g0250a0200c0062t0002g0237 | 3 | HG02155.hp1 NA18612.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.4193+204A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 35/93 | chr1 | 149508194 | ||||||
| chr1:149508222
|
G | T | 17 | a0039c0219t0002g0227a0178c0070t0002g0253a0179c0071t0002g0260others(14): Show | 17 | HG00438.hp2 HG00738.hp1 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.4193+232G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 35/93 | chr1 | 149508222 | ||||||
| chr1:149508224
|
A | G | 2 | a0006c0213t0002g0224a0006c0214t0002g0265 | 2 | NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.4193+234A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 35/93 | chr1 | 149508224 | ||||||
| chr1:149508229
|
A | G | 3 | a0185c0043t0002g0247a0187c0050t0002g0250a0200c0062t0002g0237 | 3 | HG02155.hp1 NA18612.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.4193+239A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 35/93 | chr1 | 149508229 | ||||||
| chr1:149508242
|
T | A | 17 | a0039c0219t0002g0227a0178c0070t0002g0253a0179c0071t0002g0260others(14): Show | 17 | HG00438.hp2 HG00738.hp1 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.4193+252T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 35/93 | chr1 | 149508242 | ||||||
| chr1:149508285
|
G | A | 31 | a0002c0002t0003g0182a0002c0002t0003g0188a0002c0002t0003g0189others(28): Show | 31 | HG00423.hp2 HG00544.hp1 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.4193+295G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 35/93 | chr1 | 149508285 | ||||||
| chr1:149508335
|
A | T | 1 | a0006c0212t0002g0223 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.4194-260A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 35/93 | chr1 | 149508335 | ||||||
| chr1:149508346
|
C | T | 1 | a0006c0212t0002g0223 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.4194-249C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 35/93 | chr1 | 149508346 | ||||||
| chr1:149508347
|
G | A | 3 | a0009c0006t0001g0081a0009c0006t0001g0082a0009c0006t0001g0139 | 3 | HG00099.hp1 HG00741.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.4194-248G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 35/93 | chr1 | 149508347 | ||||||
| chr1:149508364
|
C | T | 1 | a0156c0099t0001g0013 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.4194-231C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 35/93 | chr1 | 149508364 | ||||||
| chr1:149508372
|
C | CCT | 10 | a0043c0209t0004g0207a0048c0081t0011g0151a0049c0082t0011g0096others(7): Show | 10 | HG00621.hp2 HG01099.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.4194-201_4194-200d others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 35/93 | INFO_REALIGN_3_PRIME | chr1 | 149508372 | |||||
| chr1:149508372
|
C | CCTCT | 3 | a0015c0036t0006g0004a0015c0192t0006g0270a0173c0191t0006g0271 | 4 | HG02145.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.4194-203_4194-200d others(6): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 35/93 | INFO_REALIGN_3_PRIME | chr1 | 149508372 | |||||
| chr1:149508372
|
CCTCT | C | 3 | a0061c0187t0001g0173a0166c0198t0005g0210a0172c0204t0004g0268 | 3 | HG02145.hp2 HG03942.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.4194-203_4194-200d others(6): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 35/93 | INFO_REALIGN_3_PRIME | chr1 | 149508372 | |||||
| chr1:149508407
|
C | G | 3 | a0015c0036t0006g0004a0015c0192t0006g0270a0173c0191t0006g0271 | 4 | HG02145.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.4194-188C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 35/93 | chr1 | 149508407 | ||||||
| chr1:149508424
|
C | T | 2 | a0166c0198t0005g0210a0172c0204t0004g0268 | 2 | HG03942.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.4194-171C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 35/93 | chr1 | 149508424 | ||||||
| chr1:149508471
|
C | A | 1 | a0003c0136t0001g0005 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.4194-124C>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 35/93 | chr1 | 149508471 | ||||||
| chr1:149508483
|
A | T | 1 | a0009c0006t0001g0082 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.4194-112A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 35/93 | chr1 | 149508483 | ||||||
| chr1:149508487
|
G | C | 1 | a0174c0202t0013g0204 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.4194-108G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 35/93 | chr1 | 149508487 | ||||||
| chr1:149508514
|
A | T | 1 | a0006c0211t0019g0211 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.4194-81A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 35/93 | chr1 | 149508514 | ||||||
| chr1:149508523
|
A | C | 2 | a0006c0212t0002g0223a0006c0214t0002g0265 | 2 | HG01891.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.4194-72A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 35/93 | chr1 | 149508523 | ||||||
| chr1:149508530
|
C | G | 15 | a0006c0211t0019g0211a0043c0209t0004g0207a0044c0210t0004g0206others(12): Show | 15 | HG00544.hp2 HG00558.hp2 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.4194-65C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 35/93 | chr1 | 149508530 | ||||||
| chr1:149508580
|
T | G | 1 | a0151c0184t0001g0174 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.4194-15T>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 35/93 | chr1 | 149508580 | ||||||
| chr1:149508855
|
C | T | 1 | a0170c0208t0004g0202 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.4366+88C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 36/93 | chr1 | 149508855 | ||||||
| chr1:149508872
|
G | A | 38 | a0002c0002t0003g0182a0002c0002t0003g0188a0002c0002t0003g0189others(35): Show | 38 | HG00423.hp2 HG00544.hp1 HG01928.hp1 others(35): Show |
intron_variant | MODIFIER | c.4366+105G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 36/93 | chr1 | 149508872 | ||||||
| chr1:149508872
|
G | GCAGGCAG others(4748): Show |
1 | a0085c0114t0001g0025 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.4366+252_4366+253i others(4757): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 36/93 | INFO_REALIGN_3_PRIME | chr1 | 149508872 | |||||
| chr1:149508872
|
G | GCAGGCAG others(4748): Show |
2 | a0024c0025t0001g0024a0042c0195t0001g0023 | 2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.4366+252_4366+253i others(4757): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 36/93 | INFO_REALIGN_3_PRIME | chr1 | 149508872 | |||||
| chr1:149508872
|
G | GCAGGCAG others(4750): Show |
1 | a0024c0025t0001g0026 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4366+252_4366+253i others(4759): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 36/93 | INFO_REALIGN_3_PRIME | chr1 | 149508872 | |||||
| chr1:149508872
|
G | GCAGGCAG others(4750): Show |
1 | a0013c0035t0001g0084 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.4366+252_4366+253i others(4759): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 36/93 | INFO_REALIGN_3_PRIME | chr1 | 149508872 | |||||
| chr1:149508885
|
A | G | 5 | a0001c0001t0001g0158a0048c0081t0011g0151a0049c0082t0011g0096others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.4366+118A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 36/93 | chr1 | 149508885 | ||||||
| chr1:149508920
|
C | T | 1 | a0043c0209t0004g0207 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.4366+153C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 36/93 | chr1 | 149508920 | ||||||
| chr1:149508964
|
A | T | 12 | a0039c0219t0002g0227a0183c0041t0002g0246a0185c0043t0002g0247others(9): Show | 12 | HG00438.hp2 HG02129.hp2 NA18612.hp2 others(9): Show |
intron_variant | MODIFIER | c.4366+197A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 36/93 | chr1 | 149508964 | ||||||
| chr1:149508975
|
C | G | 1 | a0006c0211t0019g0211 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.4366+208C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 36/93 | chr1 | 149508975 | ||||||
| chr1:149508986
|
T | C | 11 | a0044c0210t0004g0206a0164c0201t0004g0205a0166c0198t0005g0210others(8): Show | 11 | HG00735.hp1 HG00738.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.4366+219T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 36/93 | chr1 | 149508986 | ||||||
| chr1:149509020
|
T | C | 235 | a0001c0001t0001g0121a0001c0001t0001g0158a0002c0002t0003g0182others(232): Show | 238 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(235): Show |
intron_variant | MODIFIER | c.4366+253T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 36/93 | chr1 | 149509020 | ||||||
| chr1:149509032
|
C | T | 2 | a0166c0198t0005g0210a0172c0204t0004g0268 | 2 | HG03942.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.4366+265C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 36/93 | chr1 | 149509032 | ||||||
| chr1:149509038
|
A | G | 1 | a0036c0014t0009g0228 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.4366+271A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 36/93 | chr1 | 149509038 | ||||||
| chr1:149509073
|
A | G | 1 | a0027c0029t0001g0061 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.4366+306A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 36/93 | chr1 | 149509073 | ||||||
| chr1:149509111
|
C | G | 3 | a0168c0206t0004g0203a0169c0205t0004g0209a0174c0202t0013g0204 | 3 | HG01099.hp1 HG04115.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.4366+344C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 36/93 | chr1 | 149509111 | ||||||
| chr1:149509225
|
C | A | 1 | a0043c0209t0004g0207 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.4367-252C>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 36/93 | chr1 | 149509225 | ||||||
| chr1:149509269
|
A | T | 1 | a0166c0198t0005g0210 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.4367-208A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 36/93 | chr1 | 149509269 | ||||||
| chr1:149509279
|
G | A | 1 | a0160c0076t0014g0225 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.4367-198G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 36/93 | chr1 | 149509279 | ||||||
| chr1:149509371
|
C | T | 1 | a0164c0201t0004g0205 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.4367-106C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 36/93 | chr1 | 149509371 | ||||||
| chr1:149509554
|
C | G | 1 | a0064c0094t0001g0047 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.4418+26C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 37/93 | chr1 | 149509554 | ||||||
| chr1:149509565
|
A | G | 1 | a0091c0122t0008g0157 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4418+37A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 37/93 | chr1 | 149509565 | ||||||
| chr1:149509578
|
C | A | 48 | a0001c0001t0001g0158a0002c0002t0003g0182a0002c0002t0003g0188others(45): Show | 48 | HG00423.hp2 HG00544.hp1 HG01109.hp1 others(45): Show |
intron_variant | MODIFIER | c.4418+50C>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 37/93 | chr1 | 149509578 | ||||||
| chr1:149509578
|
C | CCTGGTTC others(4754): Show |
1 | a0081c0113t0001g0148 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.4418+301_4418+302i others(4763): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 37/93 | INFO_REALIGN_3_PRIME | chr1 | 149509578 | |||||
| chr1:149509578
|
C | CCTGGTTC others(4754): Show |
1 | a0003c0136t0001g0005 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.4419-101_4419-100i others(4763): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 37/93 | INFO_REALIGN_3_PRIME | chr1 | 149509578 | |||||
| chr1:149509578
|
C | CCTGGTTC others(9511): Show |
1 | a0135c0161t0001g0057 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.4419-101_4419-100i others(9520): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 37/93 | INFO_REALIGN_3_PRIME | chr1 | 149509578 | |||||
| chr1:149509578
|
C | CCTGGTTC others(4756): Show |
3 | a0142c0180t0001g0108a0145c0177t0001g0165a0148c0181t0001g0124 | 3 | HG01168.hp2 HG02602.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.4419-198_4419-197i others(4765): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 37/93 | INFO_REALIGN_3_PRIME | chr1 | 149509578 | |||||
| chr1:149509578
|
C | CCTGGTTC others(4746): Show |
1 | a0084c0115t0001g0114 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.4419-223_4419-222i others(4755): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 37/93 | INFO_REALIGN_3_PRIME | chr1 | 149509578 | |||||
| chr1:149509578
|
C | CCTGGTTC others(4750): Show |
1 | a0004c0026t0001g0007 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.4419-223_4419-222i others(4759): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 37/93 | INFO_REALIGN_3_PRIME | chr1 | 149509578 | |||||
| chr1:149509578
|
C | CCTGGTTC others(4750): Show |
1 | a0146c0176t0003g0110 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.4419-223_4419-222i others(4759): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 37/93 | INFO_REALIGN_3_PRIME | chr1 | 149509578 | |||||
| chr1:149509578
|
C | CCTGGTTC others(4752): Show |
1 | a0004c0027t0001g0001 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.4419-223_4419-222i others(4761): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 37/93 | INFO_REALIGN_3_PRIME | chr1 | 149509578 | |||||
| chr1:149509578
|
C | CCTGGTTC others(4754): Show |
1 | a0004c0026t0001g0008 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.4419-223_4419-222i others(4763): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 37/93 | INFO_REALIGN_3_PRIME | chr1 | 149509578 | |||||
| chr1:149509578
|
C | CCTGGTTC others(4750): Show |
1 | a0041c0217t0003g0185 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.4419-248_4419-247i others(4759): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 37/93 | INFO_REALIGN_3_PRIME | chr1 | 149509578 | |||||
| chr1:149509578
|
C | CCTGGTTC others(4750): Show |
2 | a0123c0157t0001g0015a0136c0163t0001g0200 | 2 | HG02055.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.4419-248_4419-247i others(4759): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 37/93 | INFO_REALIGN_3_PRIME | chr1 | 149509578 | |||||
| chr1:149509578
|
C | CCTGGTTC others(4750): Show |
1 | a0109c0135t0001g0063 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.4419-248_4419-247i others(4759): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 37/93 | INFO_REALIGN_3_PRIME | chr1 | 149509578 | |||||
| chr1:149509578
|
C | CCTGGTTC others(4752): Show |
2 | a0076c0109t0001g0137a0094c0125t0001g0138 | 2 | HG02257.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.4419-248_4419-247i others(4761): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 37/93 | INFO_REALIGN_3_PRIME | chr1 | 149509578 | |||||
| chr1:149509578
|
C | CCTGGTTC others(4752): Show |
1 | a0053c0190t0001g0064 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.4419-248_4419-247i others(4761): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 37/93 | INFO_REALIGN_3_PRIME | chr1 | 149509578 | |||||
| chr1:149509578
|
C | CCTGGTTC others(4754): Show |
1 | a0023c0024t0001g0003 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.4419-248_4419-247i others(4763): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 37/93 | INFO_REALIGN_3_PRIME | chr1 | 149509578 | |||||
| chr1:149509578
|
C | CCTGGTTC others(4754): Show |
1 | a0149c0183t0001g0022 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.4419-248_4419-247i others(4763): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 37/93 | INFO_REALIGN_3_PRIME | chr1 | 149509578 | |||||
| chr1:149509578
|
C | CCTGGTTC others(4756): Show |
1 | a0143c0179t0001g0021 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.4419-248_4419-247i others(4765): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 37/93 | INFO_REALIGN_3_PRIME | chr1 | 149509578 | |||||
| chr1:149509630
|
G | C | 1 | a0036c0014t0009g0228 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.4418+102G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 37/93 | chr1 | 149509630 | ||||||
| chr1:149509678
|
T | C | 1 | a0166c0198t0005g0210 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.4418+150T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 37/93 | chr1 | 149509678 | ||||||
| chr1:149509731
|
A | T | 1 | a0022c0023t0001g0156 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.4418+203A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 37/93 | chr1 | 149509731 | ||||||
| chr1:149509757
|
T | C | 1 | a0181c0073t0002g0272 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.4418+229T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 37/93 | chr1 | 149509757 | ||||||
| chr1:149509759
|
C | A | 2 | a0178c0070t0002g0253a0201c0063t0002g0222 | 2 | NA19062.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.4418+231C>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 37/93 | chr1 | 149509759 | ||||||
| chr1:149509773
|
A | G | 1 | a0156c0099t0001g0013 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.4418+245A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 37/93 | chr1 | 149509773 | ||||||
| chr1:149509858
|
C | T | 10 | a0039c0219t0002g0227a0183c0041t0002g0246a0188c0051t0002g0252others(7): Show | 10 | HG00438.hp2 HG02129.hp2 NA18946.hp2 others(7): Show |
intron_variant | MODIFIER | c.4419-321C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 37/93 | chr1 | 149509858 | ||||||
| chr1:149509862
|
G | GAGTGTCC others(4744): Show |
1 | a0125c0159t0001g0147 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.4419-248_4419-247i others(4753): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 37/93 | INFO_REALIGN_3_PRIME | chr1 | 149509862 | |||||
| chr1:149509915
|
G | T | 1 | a0203c0065t0002g0240 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.4419-264G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 37/93 | chr1 | 149509915 | ||||||
| chr1:149509916
|
TTC | T | 12 | a0011c0010t0001g0010a0011c0010t0001g0011a0011c0010t0001g0012others(9): Show | 12 | HG00438.hp1 HG00642.hp2 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.4419-247_4419-246d others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 37/93 | INFO_REALIGN_3_PRIME | chr1 | 149509916 | |||||
| chr1:149509918
|
C | CTCTCTCT others(4748): Show |
2 | a0013c0035t0001g0038a0013c0162t0001g0040 | 2 | HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.4419-248_4419-247i others(4757): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 37/93 | INFO_REALIGN_3_PRIME | chr1 | 149509918 | |||||
| chr1:149509926
|
CTCTCTCT others(5): Show |
C | 1 | a0006c0214t0002g0265 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.4419-251_4419-240d others(14): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 37/93 | INFO_REALIGN_3_PRIME | chr1 | 149509926 | |||||
| chr1:149509930
|
C | CTG | 4 | a0087c0118t0001g0054a0101c0039t0001g0079a0107c0138t0001g0072others(1): Show | 4 | HG00408.hp1 HG00733.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.4419-248_4419-247i others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 37/93 | INFO_REALIGN_3_PRIME | chr1 | 149509930 | |||||
| chr1:149509930
|
C | CTGTG | 3 | a0015c0036t0006g0004a0015c0192t0006g0270a0173c0191t0006g0271 | 4 | HG02145.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.4419-248_4419-247i others(6): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 37/93 | INFO_REALIGN_3_PRIME | chr1 | 149509930 | |||||
| chr1:149509930
|
CTCTG | C | 29 | a0008c0037t0001g0075a0008c0037t0001g0135a0008c0215t0001g0067others(26): Show | 29 | HG00423.hp1 HG00738.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.4419-247_4419-244d others(6): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 37/93 | INFO_REALIGN_3_PRIME | chr1 | 149509930 | |||||
| chr1:149509930
|
CTCTGTG | C | 3 | a0005c0004t0025g0073a0070c0101t0001g0044a0114c0137t0001g0133 | 3 | NA18954.hp1 NA18990.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.4419-247_4419-242d others(8): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 37/93 | INFO_REALIGN_3_PRIME | chr1 | 149509930 | |||||
| chr1:149509930
|
CTCTGTGT others(1): Show |
C | 14 | a0001c0001t0001g0121a0005c0004t0001g0056a0005c0004t0001g0131others(11): Show | 14 | HG01978.hp2 HG02027.hp1 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.4419-247_4419-240d others(10): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 37/93 | INFO_REALIGN_3_PRIME | chr1 | 149509930 | |||||
| chr1:149509930
|
CTCTGTGT others(3): Show |
C | 3 | a0021c0022t0001g0080a0021c0022t0001g0169a0129c0167t0012g0088 | 3 | HG02280.hp2 HG03209.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.4419-247_4419-238d others(12): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 37/93 | INFO_REALIGN_3_PRIME | chr1 | 149509930 | |||||
| chr1:149509930
|
CTCTGTGT others(5): Show |
C | 3 | a0119c0153t0001g0097a0120c0155t0001g0126a0130c0170t0001g0120 | 3 | HG01074.hp1 HG02080.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.4419-247_4419-236d others(14): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 37/93 | INFO_REALIGN_3_PRIME | chr1 | 149509930 | |||||
| chr1:149509932
|
C | G | 23 | a0006c0211t0019g0211a0009c0006t0001g0081a0009c0006t0001g0082others(20): Show | 24 | HG00099.hp1 HG00408.hp1 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.4419-247C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 37/93 | chr1 | 149509932 | ||||||
| chr1:149509932
|
CTG | C | 13 | a0013c0035t0001g0084a0056c0089t0001g0060a0178c0070t0002g0253others(10): Show | 13 | HG00438.hp2 HG01346.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.4419-224_4419-223d others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 37/93 | INFO_REALIGN_3_PRIME | chr1 | 149509932 | |||||
| chr1:149509932
|
CTGTGTG | C | 5 | a0164c0201t0004g0205a0167c0203t0028g0269a0171c0207t0004g0208others(2): Show | 5 | HG00735.hp1 HG02109.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.4419-228_4419-223d others(8): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 37/93 | INFO_REALIGN_3_PRIME | chr1 | 149509932 | |||||
| chr1:149509934
|
G | C | 10 | a0003c0003t0001g0115a0003c0003t0001g0116a0003c0003t0001g0117others(7): Show | 10 | HG00544.hp1 HG01891.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.4419-245G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 37/93 | chr1 | 149509934 | ||||||
| chr1:149509935
|
T | A | 1 | a0006c0211t0019g0211 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.4419-244T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 37/93 | chr1 | 149509935 | ||||||
| chr1:149509936
|
G | GTGTGTGT others(9491): Show |
1 | a0160c0076t0014g0225 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.4419-223_4419-222i others(9500): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 37/93 | INFO_REALIGN_3_PRIME | chr1 | 149509936 | |||||
| chr1:149509949
|
T | C | 1 | a0170c0208t0004g0202 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.4419-230T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 37/93 | chr1 | 149509949 | ||||||
| chr1:149509949
|
T | TGC | 4 | a0161c0197t0005g0214a0162c0196t0005g0213a0163c0199t0005g0215others(1): Show | 4 | HG00544.hp2 HG00558.hp2 HG00735.hp2 others(1): Show |
intron_variant | MODIFIER | c.4419-229_4419-228i others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 37/93 | INFO_REALIGN_3_PRIME | chr1 | 149509949 | |||||
| chr1:149509951
|
T | C | 33 | a0032c0012t0002g0232a0032c0012t0002g0266a0033c0011t0002g0254others(30): Show | 33 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.4419-228T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 37/93 | chr1 | 149509951 | ||||||
| chr1:149509953
|
TGTGC | T | 4 | a0091c0122t0008g0157a0093c0124t0001g0153a0170c0208t0004g0202others(1): Show | 4 | HG02572.hp1 HG03209.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.4419-222_4419-219d others(6): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 37/93 | INFO_REALIGN_3_PRIME | chr1 | 149509953 | |||||
| chr1:149509955
|
T | C | 3 | a0006c0211t0019g0211a0039c0219t0002g0227a0075c0108t0001g0163 | 3 | HG02895.hp1 NA18981.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.4419-224T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 37/93 | chr1 | 149509955 | ||||||
| chr1:149509955
|
TGC | T | 8 | a0036c0014t0009g0228a0036c0014t0009g0230a0044c0210t0004g0206others(5): Show | 8 | HG02080.hp2 HG02976.hp2 HG03486.hp1 others(5): Show |
intron_variant | MODIFIER | c.4419-222_4419-221d others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 37/93 | INFO_REALIGN_3_PRIME | chr1 | 149509955 | |||||
| chr1:149509957
|
C | CGTGTGTG others(14278): Show |
1 | a0083c0116t0023g0103 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.4419-101_4419-100i others(14287): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 37/93 | INFO_REALIGN_3_PRIME | chr1 | 149509957 | |||||
| chr1:149509957
|
C | T | 121 | a0001c0001t0001g0121a0005c0004t0001g0056a0005c0004t0001g0131others(118): Show | 121 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.4419-222C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 37/93 | chr1 | 149509957 | ||||||
| chr1:149509957
|
CGT | C | 9 | a0006c0212t0002g0223a0006c0213t0002g0224a0054c0085t0001g0150others(6): Show | 9 | HG00423.hp2 HG01891.hp1 HG02155.hp2 others(6): Show |
intron_variant | MODIFIER | c.4419-199_4419-198d others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 37/93 | INFO_REALIGN_3_PRIME | chr1 | 149509957 | |||||
| chr1:149509959
|
T | TGTGTGTG others(4742): Show |
1 | a0132c0166t0012g0179 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.4419-208_4419-207i others(4751): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 37/93 | INFO_REALIGN_3_PRIME | chr1 | 149509959 | |||||
| chr1:149509959
|
T | TGTGTGTG others(4748): Show |
3 | a0009c0006t0001g0081a0009c0006t0001g0082a0009c0006t0001g0139 | 3 | HG00099.hp1 HG00741.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.4419-206_4419-205i others(4757): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 37/93 | INFO_REALIGN_3_PRIME | chr1 | 149509959 | |||||
| chr1:149509959
|
T | TGTGTGTG others(4744): Show |
3 | a0072c0104t0001g0017a0124c0158t0001g0095a0147c0220t0001g0094 | 3 | HG03017.hp1 NA18747.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.4419-206_4419-205i others(4753): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 37/93 | INFO_REALIGN_3_PRIME | chr1 | 149509959 | |||||
| chr1:149509959
|
T | TGTGTGTG others(4740): Show |
1 | a0144c0178t0001g0119 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.4419-206_4419-205i others(4749): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 37/93 | INFO_REALIGN_3_PRIME | chr1 | 149509959 | |||||
| chr1:149509959
|
T | TGTGTGTG others(9505): Show |
1 | a0061c0187t0001g0173 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.4419-101_4419-100i others(9514): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 37/93 | INFO_REALIGN_3_PRIME | chr1 | 149509959 | |||||
| chr1:149509959
|
T | TGTGTGTG others(9505): Show |
1 | a0073c0103t0001g0018 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.4419-101_4419-100i others(9514): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 37/93 | INFO_REALIGN_3_PRIME | chr1 | 149509959 | |||||
| chr1:149509961
|
T | C | 2 | a0185c0043t0002g0247a0187c0050t0002g0250 | 2 | NA18612.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.4419-218T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 37/93 | chr1 | 149509961 | ||||||
| chr1:149509974
|
G | C | 1 | a0006c0211t0019g0211 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.4419-205G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 37/93 | chr1 | 149509974 | ||||||
| chr1:149509974
|
G | T | 4 | a0043c0209t0004g0207a0168c0206t0004g0203a0169c0205t0004g0209others(1): Show | 4 | HG01099.hp1 HG02165.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.4419-205G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 37/93 | chr1 | 149509974 | ||||||
| chr1:149509983
|
C | T | 84 | a0001c0001t0001g0121a0005c0004t0001g0056a0005c0004t0001g0131others(81): Show | 84 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.4419-196C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 37/93 | chr1 | 149509983 | ||||||
| chr1:149510001
|
A | G | 1 | a0019c0021t0001g0098 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.4419-178A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 37/93 | chr1 | 149510001 | ||||||
| chr1:149510055
|
C | T | 1 | a0006c0211t0019g0211 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.4419-124C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 37/93 | chr1 | 149510055 | ||||||
| chr1:149510057
|
C | A | 1 | a0168c0206t0004g0203 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.4419-122C>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 37/93 | chr1 | 149510057 | ||||||
| chr1:149510079
|
G | C | 15 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(12): Show | 15 | HG00099.hp2 HG00558.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.4419-100G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 37/93 | chr1 | 149510079 | ||||||
| chr1:149510105
|
G | C | 254 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(251): Show | 257 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(254): Show |
intron_variant | MODIFIER | c.4419-74G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 37/93 | chr1 | 149510105 | ||||||
| chr1:149510105
|
G | GCATGAAA others(4748): Show |
1 | a0019c0021t0001g0098 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.5151-221_5151-220i others(4757): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 43/93 | INFO_REALIGN_3_PRIME | chr1 | 149510105 | |||||
| chr1:149510381
|
AT | A | 5 | a0055c0086t0001g0168a0080c0106t0001g0019a0091c0122t0008g0157others(2): Show | 5 | HG02572.hp1 HG02976.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.4591+31delT | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 38/93 | chr1 | 149510381 | ||||||
| chr1:149510395
|
C | T | 1 | a0166c0198t0005g0210 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.4591+44C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 38/93 | chr1 | 149510395 | ||||||
| chr1:149510400
|
T | G | 1 | a0165c0200t0005g0212 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.4591+49T>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 38/93 | chr1 | 149510400 | ||||||
| chr1:149510427
|
C | A | 1 | a0002c0002t0003g0196 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.4591+76C>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 38/93 | chr1 | 149510427 | ||||||
| chr1:149510430
|
T | C | 1 | a0002c0002t0003g0196 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.4591+79T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 38/93 | chr1 | 149510430 | ||||||
| chr1:149510433
|
C | G | 1 | a0002c0002t0003g0196 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.4591+82C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 38/93 | chr1 | 149510433 | ||||||
| chr1:149510434
|
T | A | 1 | a0002c0002t0003g0196 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.4591+83T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 38/93 | chr1 | 149510434 | ||||||
| chr1:149510435
|
G | T | 1 | a0002c0002t0003g0196 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.4591+84G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 38/93 | chr1 | 149510435 | ||||||
| chr1:149510436
|
A | C | 1 | a0002c0002t0003g0196 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.4591+85A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 38/93 | chr1 | 149510436 | ||||||
| chr1:149510440
|
G | T | 1 | a0002c0002t0003g0196 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.4591+89G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 38/93 | chr1 | 149510440 | ||||||
| chr1:149510470
|
T | C | 6 | a0161c0197t0005g0214a0162c0196t0005g0213a0163c0199t0005g0215others(3): Show | 6 | HG00544.hp2 HG00558.hp2 HG00735.hp1 others(3): Show |
intron_variant | MODIFIER | c.4591+119T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 38/93 | chr1 | 149510470 | ||||||
| chr1:149510574
|
C | A | 1 | a0177c0075t0001g0146 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4591+223C>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 38/93 | chr1 | 149510574 | ||||||
| chr1:149510664
|
T | C | 1 | a0017c0019t0001g0112 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.4591+313T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 38/93 | chr1 | 149510664 | ||||||
| chr1:149510671
|
C | T | 1 | a0006c0211t0019g0211 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.4591+320C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 38/93 | chr1 | 149510671 | ||||||
| chr1:149510739
|
T | G | 19 | a0036c0014t0009g0228a0180c0072t0002g0218a0181c0073t0002g0272others(16): Show | 19 | HG00438.hp2 HG00621.hp2 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.4592-327T>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 38/93 | chr1 | 149510739 | ||||||
| chr1:149510756
|
T | C | 4 | a0015c0036t0006g0004a0015c0192t0006g0270a0126c0130t0001g0134others(1): Show | 5 | HG02145.hp1 HG02683.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.4592-310T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 38/93 | chr1 | 149510756 | ||||||
| chr1:149510856
|
A | C | 1 | a0002c0002t0003g0196 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.4592-210A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 38/93 | chr1 | 149510856 | ||||||
| chr1:149510897
|
G | A | 1 | a0006c0213t0002g0224 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.4592-169G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 38/93 | chr1 | 149510897 | ||||||
| chr1:149510957
|
ATTC | A | 3 | a0164c0201t0004g0205a0170c0208t0004g0202a0171c0207t0004g0208 | 3 | HG00735.hp1 HG02698.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.4592-106_4592-104d others(5): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 38/93 | INFO_REALIGN_3_PRIME | chr1 | 149510957 | |||||
| chr1:149510971
|
G | A | 2 | a0037c0016t0002g0256a0037c0016t0002g0257 | 2 | HG00642.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.4592-95G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 38/93 | chr1 | 149510971 | ||||||
| chr1:149511014
|
G | A | 6 | a0014c0008t0003g0181a0014c0008t0003g0186a0014c0008t0020g0184others(3): Show | 6 | HG00642.hp2 HG01071.hp1 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.4592-52G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 38/93 | chr1 | 149511014 | ||||||
| chr1:149511049
|
G | A | 1 | a0043c0209t0004g0207 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.4592-17G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 38/93 | chr1 | 149511049 | ||||||
| chr1:149511246
|
G | C | 2 | a0093c0124t0001g0153a0156c0099t0001g0013 | 2 | HG02572.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.4700+72G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 39/93 | chr1 | 149511246 | ||||||
| chr1:149511247
|
C | T | 78 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(75): Show | 78 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.4700+73C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 39/93 | chr1 | 149511247 | ||||||
| chr1:149511326
|
T | C | 8 | a0161c0197t0005g0214a0162c0196t0005g0213a0163c0199t0005g0215others(5): Show | 8 | HG00544.hp2 HG00558.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.4700+152T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 39/93 | chr1 | 149511326 | ||||||
| chr1:149511329
|
G | A | 2 | a0053c0190t0001g0064a0109c0135t0001g0063 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.4700+155G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 39/93 | chr1 | 149511329 | ||||||
| chr1:149511358
|
C | A | 172 | a0001c0001t0001g0121a0001c0001t0001g0158a0003c0136t0001g0005others(169): Show | 173 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.4700+184C>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 39/93 | chr1 | 149511358 | ||||||
| chr1:149511362
|
A | G | 15 | a0006c0212t0002g0223a0006c0213t0002g0224a0006c0214t0002g0265others(12): Show | 15 | HG01099.hp1 HG01891.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.4700+188A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 39/93 | chr1 | 149511362 | ||||||
| chr1:149511480
|
G | C | 1 | a0103c0142t0001g0074 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.4700+306G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 39/93 | chr1 | 149511480 | ||||||
| chr1:149511482
|
G | T | 2 | a0185c0043t0002g0247a0187c0050t0002g0250 | 2 | NA18612.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.4700+308G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 39/93 | chr1 | 149511482 | ||||||
| chr1:149511485
|
A | G | 3 | a0006c0211t0019g0211a0043c0209t0004g0207a0167c0203t0028g0269 | 3 | HG02109.hp2 HG02165.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.4700+311A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 39/93 | chr1 | 149511485 | ||||||
| chr1:149511537
|
G | A | 1 | a0132c0166t0012g0179 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.4701-271G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 39/93 | chr1 | 149511537 | ||||||
| chr1:149511577
|
G | C | 1 | a0043c0209t0004g0207 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.4701-231G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 39/93 | chr1 | 149511577 | ||||||
| chr1:149511583
|
C | G | 2 | a0006c0213t0002g0224a0043c0209t0004g0207 | 2 | HG02165.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.4701-225C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 39/93 | chr1 | 149511583 | ||||||
| chr1:149511585
|
CTCTGTCT others(3): Show |
C | 1 | a0006c0213t0002g0224 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.4701-219_4701-210d others(12): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 39/93 | INFO_REALIGN_3_PRIME | chr1 | 149511585 | |||||
| chr1:149511595
|
G | GTC | 20 | a0006c0211t0019g0211a0006c0214t0002g0265a0035c0015t0002g0216others(17): Show | 20 | HG01099.hp1 HG01346.hp2 HG02622.hp2 others(17): Show |
intron_variant | MODIFIER | c.4701-193_4701-192d others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 39/93 | INFO_REALIGN_3_PRIME | chr1 | 149511595 | |||||
| chr1:149511595
|
GTCTC | G | 6 | a0156c0099t0001g0013a0163c0199t0005g0215a0164c0201t0004g0205others(3): Show | 6 | HG00544.hp2 HG00558.hp2 HG00735.hp1 others(3): Show |
intron_variant | MODIFIER | c.4701-195_4701-192d others(6): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 39/93 | INFO_REALIGN_3_PRIME | chr1 | 149511595 | |||||
| chr1:149511597
|
C | A | 1 | a0083c0116t0023g0103 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.4701-211C>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 39/93 | chr1 | 149511597 | ||||||
| chr1:149511672
|
A | G | 77 | a0001c0001t0001g0121a0001c0001t0001g0158a0005c0004t0001g0056others(74): Show | 77 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.4701-136A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 39/93 | chr1 | 149511672 | ||||||
| chr1:149511682
|
A | C | 12 | a0015c0036t0006g0004a0015c0192t0006g0270a0055c0086t0001g0168others(9): Show | 13 | HG01952.hp1 HG02145.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.4701-126A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 39/93 | chr1 | 149511682 | ||||||
| chr1:149511690
|
A | C | 3 | a0044c0210t0004g0206a0168c0206t0004g0203a0174c0202t0013g0204 | 3 | HG01099.hp1 NA18962.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.4701-118A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 39/93 | chr1 | 149511690 | ||||||
| chr1:149511723
|
C | G | 3 | a0101c0039t0001g0079a0102c0144t0001g0127a0127c0169t0001g0052 | 3 | HG00408.hp1 HG00423.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.4701-85C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 39/93 | chr1 | 149511723 | ||||||
| chr1:149511758
|
C | T | 3 | a0093c0124t0001g0153a0137c0173t0001g0159a0156c0099t0001g0013 | 3 | HG02572.hp1 HG03225.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.4701-50C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 39/93 | chr1 | 149511758 | ||||||
| chr1:149511995
|
A | G | 3 | a0163c0199t0005g0215a0165c0200t0005g0212a0167c0203t0028g0269 | 3 | HG00544.hp2 HG00558.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.4873+15A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 40/93 | chr1 | 149511995 | ||||||
| chr1:149512055
|
C | T | 4 | a0036c0014t0009g0230a0207c0046t0002g0241a0208c0048t0002g0251others(1): Show | 4 | HG02080.hp2 NA18939.hp2 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.4873+75C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 40/93 | chr1 | 149512055 | ||||||
| chr1:149512072
|
G | C | 2 | a0062c0093t0001g0267a0087c0118t0001g0054 | 2 | HG02258.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.4873+92G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 40/93 | chr1 | 149512072 | ||||||
| chr1:149512075
|
G | A | 1 | a0200c0062t0002g0237 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.4873+95G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 40/93 | chr1 | 149512075 | ||||||
| chr1:149512157
|
G | T | 1 | a0006c0211t0019g0211 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.4873+177G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 40/93 | chr1 | 149512157 | ||||||
| chr1:149512176
|
T | G | 3 | a0186c0044t0017g0239a0193c0057t0002g0006a0196c0045t0018g0226 | 3 | HG02040.hp2 HG02602.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.4873+196T>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 40/93 | chr1 | 149512176 | ||||||
| chr1:149512177
|
T | C | 14 | a0024c0025t0001g0024a0024c0025t0001g0026a0042c0195t0001g0023others(11): Show | 14 | HG02055.hp2 HG02155.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.4873+197T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 40/93 | chr1 | 149512177 | ||||||
| chr1:149512200
|
G | T | 1 | a0154c0185t0001g0152 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4873+220G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 40/93 | chr1 | 149512200 | ||||||
| chr1:149512202
|
C | A | 2 | a0137c0173t0001g0159a0156c0099t0001g0013 | 2 | HG03225.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.4873+222C>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 40/93 | chr1 | 149512202 | ||||||
| chr1:149512203
|
G | A | 3 | a0006c0212t0002g0223a0185c0043t0002g0247a0187c0050t0002g0250 | 3 | HG01891.hp1 NA18612.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.4873+223G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 40/93 | chr1 | 149512203 | ||||||
| chr1:149512209
|
A | C | 9 | a0183c0041t0002g0246a0188c0051t0002g0252a0190c0049t0002g0244others(6): Show | 9 | HG00438.hp2 HG02129.hp2 NA18946.hp2 others(6): Show |
intron_variant | MODIFIER | c.4873+229A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 40/93 | chr1 | 149512209 | ||||||
| chr1:149512218
|
T | C | 9 | a0183c0041t0002g0246a0188c0051t0002g0252a0190c0049t0002g0244others(6): Show | 9 | HG00438.hp2 HG02129.hp2 NA18946.hp2 others(6): Show |
intron_variant | MODIFIER | c.4873+238T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 40/93 | chr1 | 149512218 | ||||||
| chr1:149512225
|
A | G | 2 | a0006c0213t0002g0224a0006c0214t0002g0265 | 2 | NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.4873+245A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 40/93 | chr1 | 149512225 | ||||||
| chr1:149512226
|
T | C | 3 | a0137c0173t0001g0159a0156c0099t0001g0013a0160c0076t0014g0225 | 3 | HG02622.hp2 HG03225.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.4873+246T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 40/93 | chr1 | 149512226 | ||||||
| chr1:149512226
|
T | G | 1 | a0166c0198t0005g0210 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.4873+246T>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 40/93 | chr1 | 149512226 | ||||||
| chr1:149512239
|
G | C | 3 | a0164c0201t0004g0205a0170c0208t0004g0202a0171c0207t0004g0208 | 3 | HG00735.hp1 HG02698.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.4873+259G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 40/93 | chr1 | 149512239 | ||||||
| chr1:149512255
|
G | A | 37 | a0006c0211t0019g0211a0006c0212t0002g0223a0006c0213t0002g0224others(34): Show | 38 | HG00544.hp2 HG00558.hp2 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.4873+275G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 40/93 | chr1 | 149512255 | ||||||
| chr1:149512301
|
C | A | 1 | a0118c0151t0001g0053 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.4873+321C>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 40/93 | chr1 | 149512301 | ||||||
| chr1:149512319
|
G | A | 1 | a0181c0073t0002g0272 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.4873+339G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 40/93 | chr1 | 149512319 | ||||||
| chr1:149512332
|
G | A | 2 | a0043c0209t0004g0207a0174c0202t0013g0204 | 2 | HG02165.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.4873+352G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 40/93 | chr1 | 149512332 | ||||||
| chr1:149512444
|
C | G | 2 | a0165c0200t0005g0212a0172c0204t0004g0268 | 2 | HG00544.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.4874-256C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 40/93 | chr1 | 149512444 | ||||||
| chr1:149512509
|
C | T | 1 | a0137c0173t0001g0159 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.4874-191C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 40/93 | chr1 | 149512509 | ||||||
| chr1:149512603
|
A | T | 9 | a0036c0014t0009g0228a0178c0070t0002g0253a0179c0071t0002g0260others(6): Show | 9 | HG00738.hp1 HG01346.hp2 HG03831.hp1 others(6): Show |
intron_variant | MODIFIER | c.4874-97A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 40/93 | chr1 | 149512603 | ||||||
| chr1:149512616
|
C | T | 6 | a0055c0086t0001g0168a0080c0106t0001g0019a0091c0122t0008g0157others(3): Show | 6 | HG02572.hp1 HG02683.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.4874-84C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 40/93 | chr1 | 149512616 | ||||||
| chr1:149512617
|
T | C | 12 | a0006c0214t0002g0265a0008c0037t0001g0075a0008c0037t0001g0135others(9): Show | 12 | HG00741.hp1 HG01496.hp1 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.4874-83T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 40/93 | chr1 | 149512617 | ||||||
| chr1:149512633
|
A | G | 2 | a0006c0213t0002g0224a0006c0214t0002g0265 | 2 | NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.4874-67A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 40/93 | chr1 | 149512633 | ||||||
| chr1:149512648
|
G | T | 2 | a0185c0043t0002g0247a0187c0050t0002g0250 | 2 | NA18612.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.4874-52G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 40/93 | chr1 | 149512648 | ||||||
| chr1:149512673
|
G | A | 11 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(8): Show | 11 | HG00099.hp2 HG00558.hp1 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.4874-27G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 40/93 | chr1 | 149512673 | ||||||
| chr1:149512769
|
T | C | 1 | a0043c0209t0004g0207 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.4925+18T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 41/93 | chr1 | 149512769 | ||||||
| chr1:149512770
|
G | A | 1 | a0166c0198t0005g0210 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.4925+19G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 41/93 | chr1 | 149512770 | ||||||
| chr1:149512800
|
A | T | 2 | a0055c0086t0001g0168a0080c0106t0001g0019 | 2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.4925+49A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 41/93 | chr1 | 149512800 | ||||||
| chr1:149512924
|
C | T | 1 | a0043c0209t0004g0207 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.4925+173C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 41/93 | chr1 | 149512924 | ||||||
| chr1:149512930
|
T | A | 30 | a0006c0214t0002g0265a0044c0210t0004g0206a0055c0086t0001g0168others(27): Show | 30 | HG00438.hp2 HG00735.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.4925+179T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 41/93 | chr1 | 149512930 | ||||||
| chr1:149512955
|
A | T | 11 | a0183c0041t0002g0246a0185c0043t0002g0247a0187c0050t0002g0250others(8): Show | 11 | HG00438.hp2 HG02129.hp2 NA18612.hp2 others(8): Show |
intron_variant | MODIFIER | c.4925+204A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 41/93 | chr1 | 149512955 | ||||||
| chr1:149512983
|
G | T | 31 | a0032c0012t0002g0232a0032c0012t0002g0266a0033c0011t0002g0254others(28): Show | 31 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.4925+232G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 41/93 | chr1 | 149512983 | ||||||
| chr1:149512985
|
A | G | 1 | a0006c0213t0002g0224 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.4925+234A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 41/93 | chr1 | 149512985 | ||||||
| chr1:149512990
|
A | G | 12 | a0006c0214t0002g0265a0183c0041t0002g0246a0185c0043t0002g0247others(9): Show | 12 | HG00438.hp2 HG02129.hp2 NA18612.hp2 others(9): Show |
intron_variant | MODIFIER | c.4925+239A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 41/93 | chr1 | 149512990 | ||||||
| chr1:149513003
|
T | A | 31 | a0032c0012t0002g0232a0032c0012t0002g0266a0033c0011t0002g0254others(28): Show | 31 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.4925+252T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 41/93 | chr1 | 149513003 | ||||||
| chr1:149513046
|
G | A | 64 | a0001c0001t0001g0121a0005c0004t0001g0056a0005c0004t0001g0131others(61): Show | 64 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.4925+295G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 41/93 | chr1 | 149513046 | ||||||
| chr1:149513096
|
A | T | 1 | a0006c0212t0002g0223 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.4926-260A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 41/93 | chr1 | 149513096 | ||||||
| chr1:149513107
|
C | T | 1 | a0006c0212t0002g0223 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.4926-249C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 41/93 | chr1 | 149513107 | ||||||
| chr1:149513114
|
C | G | 1 | a0040c0218t0002g0234 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.4926-242C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 41/93 | chr1 | 149513114 | ||||||
| chr1:149513133
|
CCT | C | 8 | a0055c0086t0001g0168a0080c0106t0001g0019a0091c0122t0008g0157others(5): Show | 8 | HG02572.hp1 HG02683.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.4926-201_4926-200d others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 41/93 | INFO_REALIGN_3_PRIME | chr1 | 149513133 | |||||
| chr1:149513133
|
CCTCT | C | 10 | a0130c0170t0001g0120a0131c0171t0001g0145a0160c0076t0014g0225others(7): Show | 10 | HG00735.hp1 HG00735.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.4926-203_4926-200d others(6): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 41/93 | INFO_REALIGN_3_PRIME | chr1 | 149513133 | |||||
| chr1:149513155
|
T | C | 1 | a0083c0116t0023g0103 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.4926-201T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 41/93 | chr1 | 149513155 | ||||||
| chr1:149513185
|
C | T | 17 | a0044c0210t0004g0206a0055c0086t0001g0168a0080c0106t0001g0019others(14): Show | 17 | HG00735.hp1 HG00735.hp2 HG01516.hp1 others(14): Show |
intron_variant | MODIFIER | c.4926-171C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 41/93 | chr1 | 149513185 | ||||||
| chr1:149513232
|
C | A | 9 | a0003c0136t0001g0005a0026c0030t0001g0030a0026c0030t0001g0035others(6): Show | 9 | HG00733.hp1 HG01168.hp1 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.4926-124C>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 41/93 | chr1 | 149513232 | ||||||
| chr1:149513250
|
C | A | 1 | a0064c0094t0001g0047 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.4926-106C>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 41/93 | chr1 | 149513250 | ||||||
| chr1:149513284
|
A | C | 2 | a0006c0212t0002g0223a0006c0213t0002g0224 | 2 | HG01891.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.4926-72A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 41/93 | chr1 | 149513284 | ||||||
| chr1:149513291
|
C | G | 12 | a0006c0211t0019g0211a0043c0209t0004g0207a0161c0197t0005g0214others(9): Show | 12 | HG00544.hp2 HG00558.hp2 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.4926-65C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 41/93 | chr1 | 149513291 | ||||||
| chr1:149513314
|
G | C | 1 | a0156c0099t0001g0013 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.4926-42G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 41/93 | chr1 | 149513314 | ||||||
| chr1:149513612
|
G | A | 1 | a0179c0071t0002g0260 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.5098+84G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 42/93 | chr1 | 149513612 | ||||||
| chr1:149513616
|
C | T | 1 | a0168c0206t0004g0203 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.5098+88C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 42/93 | chr1 | 149513616 | ||||||
| chr1:149513633
|
G | A | 76 | a0001c0001t0001g0121a0005c0004t0001g0056a0005c0004t0001g0131others(73): Show | 76 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.5098+105G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 42/93 | chr1 | 149513633 | ||||||
| chr1:149513646
|
A | G | 2 | a0125c0159t0001g0147a0175c0193t0001g0128 | 2 | HG02922.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.5098+118A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 42/93 | chr1 | 149513646 | ||||||
| chr1:149513725
|
A | T | 18 | a0036c0014t0009g0228a0039c0219t0002g0227a0178c0070t0002g0253others(15): Show | 18 | HG00438.hp2 HG00738.hp1 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.5098+197A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 42/93 | chr1 | 149513725 | ||||||
| chr1:149513726
|
T | C | 2 | a0161c0197t0005g0214a0162c0196t0005g0213 | 2 | HG00735.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.5098+198T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 42/93 | chr1 | 149513726 | ||||||
| chr1:149513747
|
T | C | 19 | a0033c0011t0002g0254a0043c0209t0004g0207a0044c0210t0004g0206others(16): Show | 19 | HG00735.hp1 HG00735.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.5098+219T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 42/93 | chr1 | 149513747 | ||||||
| chr1:149513750
|
G | A | 2 | a0163c0199t0005g0215a0165c0200t0005g0212 | 2 | HG00544.hp2 HG00558.hp2 |
intron_variant | MODIFIER | c.5098+222G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 42/93 | chr1 | 149513750 | ||||||
| chr1:149513781
|
C | T | 1 | a0137c0173t0001g0159 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.5098+253C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 42/93 | chr1 | 149513781 | ||||||
| chr1:149513782
|
C | T | 1 | a0166c0198t0005g0210 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.5098+254C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 42/93 | chr1 | 149513782 | ||||||
| chr1:149513793
|
C | T | 16 | a0044c0210t0004g0206a0055c0086t0001g0168a0080c0106t0001g0019others(13): Show | 16 | HG00735.hp1 HG00735.hp2 HG01516.hp1 others(13): Show |
intron_variant | MODIFIER | c.5098+265C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 42/93 | chr1 | 149513793 | ||||||
| chr1:149513799
|
A | G | 1 | a0036c0014t0009g0230 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.5098+271A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 42/93 | chr1 | 149513799 | ||||||
| chr1:149513806
|
G | A | 1 | a0156c0099t0001g0013 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.5098+278G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 42/93 | chr1 | 149513806 | ||||||
| chr1:149513827
|
G | T | 1 | a0166c0198t0005g0210 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.5098+299G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 42/93 | chr1 | 149513827 | ||||||
| chr1:149513834
|
A | AGATTTCC others(9506): Show |
1 | a0031c0028t0003g0194 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.5150+49_5150+50ins others(9513): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 43/93 | INFO_REALIGN_3_PRIME | chr1 | 149513834 | |||||
| chr1:149513834
|
A | AGATTTCC others(9503): Show |
1 | a0031c0028t0003g0180 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.5150+49_5150+50ins others(9510): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 43/93 | INFO_REALIGN_3_PRIME | chr1 | 149513834 | |||||
| chr1:149513834
|
A | G | 10 | a0021c0022t0001g0080a0021c0022t0001g0169a0055c0086t0001g0168others(7): Show | 10 | HG02280.hp2 HG02572.hp1 HG02683.hp2 others(7): Show |
intron_variant | MODIFIER | c.5098+306A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 42/93 | chr1 | 149513834 | ||||||
| chr1:149513848
|
A | T | 1 | a0166c0198t0005g0210 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.5098+320A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 42/93 | chr1 | 149513848 | ||||||
| chr1:149514030
|
A | T | 1 | a0166c0198t0005g0210 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.5099-208A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 42/93 | chr1 | 149514030 | ||||||
| chr1:149514045
|
T | C | 1 | a0131c0171t0001g0145 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.5099-193T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 42/93 | chr1 | 149514045 | ||||||
| chr1:149514274
|
A | ACCCACCA others(19029): Show |
1 | a0208c0048t0002g0251 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.5150+101_5150+102i others(19038): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 43/93 | INFO_REALIGN_3_PRIME | chr1 | 149514274 | |||||
| chr1:149514274
|
A | ACCCACCA others(23786): Show |
1 | a0207c0046t0002g0241 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.5150+101_5150+102i others(23795): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 43/93 | INFO_REALIGN_3_PRIME | chr1 | 149514274 | |||||
| chr1:149514274
|
A | ACCCACCA others(14256): Show |
1 | a0197c0066t0002g0238 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.5150+230_5150+231i others(14265): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 43/93 | INFO_REALIGN_3_PRIME | chr1 | 149514274 | |||||
| chr1:149514301
|
A | G | 1 | a0126c0130t0001g0134 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.5150+12A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 43/93 | chr1 | 149514301 | ||||||
| chr1:149514339
|
C | A | 73 | a0001c0001t0001g0121a0005c0004t0001g0056a0005c0004t0001g0131others(70): Show | 74 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.5150+50C>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 43/93 | chr1 | 149514339 | ||||||
| chr1:149514353
|
A | C | 1 | a0085c0114t0001g0025 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.5150+64A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 43/93 | chr1 | 149514353 | ||||||
| chr1:149514359
|
G | C | 1 | a0126c0130t0001g0134 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.5150+70G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 43/93 | chr1 | 149514359 | ||||||
| chr1:149514391
|
G | C | 1 | a0036c0014t0009g0230 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.5150+102G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 43/93 | chr1 | 149514391 | ||||||
| chr1:149514408
|
C | T | 1 | a0184c0042t0002g0236 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.5150+119C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 43/93 | chr1 | 149514408 | ||||||
| chr1:149514416
|
A | G | 1 | a0166c0198t0005g0210 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.5150+127A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 43/93 | chr1 | 149514416 | ||||||
| chr1:149514520
|
C | A | 16 | a0032c0012t0002g0232a0032c0012t0002g0266a0033c0011t0002g0254others(13): Show | 16 | HG00621.hp1 HG00642.hp1 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.5150+231C>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 43/93 | chr1 | 149514520 | ||||||
| chr1:149514527
|
C | T | 1 | a0027c0029t0001g0061 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.5150+238C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 43/93 | chr1 | 149514527 | ||||||
| chr1:149514534
|
A | G | 9 | a0008c0037t0001g0075a0008c0037t0001g0135a0008c0215t0001g0067others(6): Show | 9 | HG00741.hp1 HG01496.hp1 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.5150+245A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 43/93 | chr1 | 149514534 | ||||||
| chr1:149514619
|
C | T | 8 | a0036c0014t0009g0228a0179c0071t0002g0260a0180c0072t0002g0218others(5): Show | 8 | HG00621.hp2 HG00738.hp1 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.5151-317C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 43/93 | chr1 | 149514619 | ||||||
| chr1:149514677
|
TTC | T | 4 | a0041c0217t0003g0185a0099c0146t0001g0034a0124c0158t0001g0095others(1): Show | 4 | HG01517.hp2 HG02165.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.5151-243_5151-242d others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 43/93 | INFO_REALIGN_3_PRIME | chr1 | 149514677 | |||||
| chr1:149514677
|
TTCTC | T | 2 | a0062c0093t0001g0267a0087c0118t0001g0054 | 2 | HG02258.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.5151-245_5151-242d others(6): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 43/93 | INFO_REALIGN_3_PRIME | chr1 | 149514677 | |||||
| chr1:149514681
|
C | CTCTCTCT others(19006): Show |
1 | a0008c0215t0001g0067 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.5151-244_5151-243i others(19015): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 43/93 | INFO_REALIGN_3_PRIME | chr1 | 149514681 | |||||
| chr1:149514687
|
CTCTCTCT others(13): Show |
C | 1 | a0074c0112t0001g0104 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.5151-247_5151-228d others(22): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 43/93 | INFO_REALIGN_3_PRIME | chr1 | 149514687 | |||||
| chr1:149514689
|
C | CTGTGTGT others(3): Show |
1 | a0187c0050t0002g0250 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.5151-246_5151-245i others(12): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 43/93 | INFO_REALIGN_3_PRIME | chr1 | 149514689 | |||||
| chr1:149514691
|
C | CTG | 5 | a0001c0001t0001g0158a0015c0036t0006g0004a0111c0132t0001g0199others(2): Show | 6 | HG02145.hp1 HG02647.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.5151-244_5151-243i others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 43/93 | INFO_REALIGN_3_PRIME | chr1 | 149514691 | |||||
| chr1:149514691
|
C | G | 5 | a0075c0108t0001g0163a0187c0050t0002g0250a0197c0066t0002g0238others(2): Show | 5 | HG02080.hp2 HG02083.hp1 NA18612.hp2 others(2): Show |
intron_variant | MODIFIER | c.5151-245C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 43/93 | chr1 | 149514691 | ||||||
| chr1:149514693
|
C | CTG | 10 | a0009c0006t0001g0081a0009c0006t0001g0082a0066c0097t0001g0175others(7): Show | 10 | HG00099.hp1 HG00741.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.5151-199_5151-198d others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 43/93 | INFO_REALIGN_3_PRIME | chr1 | 149514693 | |||||
| chr1:149514693
|
C | CTGTG | 17 | a0002c0002t0003g0182a0009c0006t0001g0139a0010c0007t0001g0002others(14): Show | 18 | HG00733.hp1 HG00735.hp1 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.5151-201_5151-198d others(6): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 43/93 | INFO_REALIGN_3_PRIME | chr1 | 149514693 | |||||
| chr1:149514693
|
C | CTGTGTGT others(1): Show |
6 | a0018c0018t0001g0113a0049c0082t0011g0096a0050c0080t0001g0177others(3): Show | 6 | HG00735.hp2 HG01516.hp1 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.5151-205_5151-198d others(10): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 43/93 | INFO_REALIGN_3_PRIME | chr1 | 149514693 | |||||
| chr1:149514693
|
C | CTGTGTGT others(3): Show |
4 | a0052c0079t0021g0176a0055c0086t0001g0168a0151c0184t0001g0174others(1): Show | 4 | HG02300.hp1 HG02622.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.5151-207_5151-198d others(12): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 43/93 | INFO_REALIGN_3_PRIME | chr1 | 149514693 | |||||
| chr1:149514693
|
C | CTGTGTGT others(5): Show |
4 | a0048c0081t0011g0151a0051c0083t0001g0162a0080c0106t0001g0019others(1): Show | 4 | HG01109.hp1 HG02572.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.5151-209_5151-198d others(14): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 43/93 | INFO_REALIGN_3_PRIME | chr1 | 149514693 | |||||
| chr1:149514693
|
C | CTGTGTGT others(7): Show |
1 | a0154c0185t0001g0152 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.5151-211_5151-198d others(16): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 43/93 | INFO_REALIGN_3_PRIME | chr1 | 149514693 | |||||
| chr1:149514693
|
C | CTGTGTGT others(19020): Show |
1 | a0186c0044t0017g0239 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.5151-225_5151-224i others(19029): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 43/93 | INFO_REALIGN_3_PRIME | chr1 | 149514693 | |||||
| chr1:149514693
|
C | G | 25 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(22): Show | 26 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(23): Show |
intron_variant | MODIFIER | c.5151-243C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 43/93 | chr1 | 149514693 | ||||||
| chr1:149514693
|
CTG | C | 34 | a0002c0002t0003g0189a0002c0002t0007g0190a0002c0002t0007g0193others(31): Show | 35 | HG00438.hp2 HG01168.hp2 HG01891.hp2 others(32): Show |
intron_variant | MODIFIER | c.5151-199_5151-198d others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 43/93 | INFO_REALIGN_3_PRIME | chr1 | 149514693 | |||||
| chr1:149514693
|
CTGTG | C | 9 | a0004c0027t0001g0001a0006c0211t0019g0211a0069c0100t0001g0016others(6): Show | 10 | HG02083.hp2 HG02895.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.5151-201_5151-198d others(6): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 43/93 | INFO_REALIGN_3_PRIME | chr1 | 149514693 | |||||
| chr1:149514693
|
CTGTGTG | C | 8 | a0003c0003t0001g0115a0003c0003t0001g0116a0003c0003t0001g0170others(5): Show | 8 | HG00544.hp1 HG02145.hp2 NA18612.hp1 others(5): Show |
intron_variant | MODIFIER | c.5151-203_5151-198d others(8): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 43/93 | INFO_REALIGN_3_PRIME | chr1 | 149514693 | |||||
| chr1:149514693
|
CTGTGTGT others(3): Show |
C | 2 | a0006c0214t0002g0265a0176c0194t0001g0129 | 2 | HG04115.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.5151-207_5151-198d others(12): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 43/93 | INFO_REALIGN_3_PRIME | chr1 | 149514693 | |||||
| chr1:149514693
|
CTGTGTGT others(9): Show |
C | 1 | a0004c0026t0001g0007 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.5151-213_5151-198d others(18): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 43/93 | INFO_REALIGN_3_PRIME | chr1 | 149514693 | |||||
| chr1:149514695
|
G | C | 4 | a0006c0212t0002g0223a0008c0215t0001g0067a0024c0025t0001g0024others(1): Show | 4 | HG01496.hp1 HG01891.hp1 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.5151-241G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 43/93 | chr1 | 149514695 | ||||||
| chr1:149514697
|
G | C | 1 | a0085c0114t0001g0025 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.5151-239G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 43/93 | chr1 | 149514697 | ||||||
| chr1:149514697
|
G | GTGTGTGT others(19000): Show |
1 | a0008c0037t0001g0135 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.5151-219_5151-218i others(19009): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 43/93 | INFO_REALIGN_3_PRIME | chr1 | 149514697 | |||||
| chr1:149514697
|
G | GTGTGTGT others(19000): Show |
1 | a0008c0037t0001g0075 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.5151-219_5151-218i others(19009): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 43/93 | INFO_REALIGN_3_PRIME | chr1 | 149514697 | |||||
| chr1:149514707
|
G | GTGTGTGT others(19000): Show |
1 | a0110c0133t0001g0058 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.5151-219_5151-218i others(19009): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 43/93 | INFO_REALIGN_3_PRIME | chr1 | 149514707 | |||||
| chr1:149514708
|
T | C | 1 | a0190c0049t0002g0244 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.5151-228T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 43/93 | chr1 | 149514708 | ||||||
| chr1:149514708
|
T | TGTGC | 7 | a0035c0015t0002g0216a0035c0015t0002g0217a0166c0198t0005g0210others(4): Show | 7 | HG02040.hp2 HG03017.hp2 HG03704.hp2 others(4): Show |
intron_variant | MODIFIER | c.5151-225_5151-224i others(6): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 43/93 | INFO_REALIGN_3_PRIME | chr1 | 149514708 | |||||
| chr1:149514710
|
T | C | 2 | a0168c0206t0004g0203a0174c0202t0013g0204 | 2 | HG01099.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.5151-226T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 43/93 | chr1 | 149514710 | ||||||
| chr1:149514712
|
T | TGTGC | 3 | a0182c0074t0002g0261a0184c0042t0002g0236a0205c0056t0015g0258 | 3 | HG00621.hp2 HG01346.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.5151-221_5151-220i others(6): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 43/93 | INFO_REALIGN_3_PRIME | chr1 | 149514712 | |||||
| chr1:149514714
|
T | C | 16 | a0006c0213t0002g0224a0039c0219t0002g0227a0062c0093t0001g0267others(13): Show | 16 | HG00438.hp2 HG00642.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.5151-222T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 43/93 | chr1 | 149514714 | ||||||
| chr1:149514714
|
T | TGC | 19 | a0032c0012t0002g0232a0032c0012t0002g0266a0033c0011t0002g0254others(16): Show | 19 | HG00621.hp1 HG00642.hp1 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.5151-221_5151-220i others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 43/93 | INFO_REALIGN_3_PRIME | chr1 | 149514714 | |||||
| chr1:149514714
|
T | TGTGC | 56 | a0005c0004t0001g0056a0005c0004t0001g0131a0005c0004t0001g0132others(53): Show | 56 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.5151-219_5151-218i others(6): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 43/93 | INFO_REALIGN_3_PRIME | chr1 | 149514714 | |||||
| chr1:149514716
|
T | C | 3 | a0006c0211t0019g0211a0006c0212t0002g0223a0120c0155t0001g0126 | 3 | HG01891.hp1 HG02080.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.5151-220T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 43/93 | chr1 | 149514716 | ||||||
| chr1:149514716
|
T | TGC | 8 | a0001c0001t0001g0121a0028c0032t0001g0036a0071c0102t0001g0143others(5): Show | 8 | HG00423.hp2 HG00609.hp2 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.5151-219_5151-218i others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 43/93 | INFO_REALIGN_3_PRIME | chr1 | 149514716 | |||||
| chr1:149514718
|
T | C | 10 | a0039c0219t0002g0227a0047c0216t0001g0068a0183c0041t0002g0246others(7): Show | 10 | HG00438.hp2 HG01934.hp2 HG02129.hp2 others(7): Show |
intron_variant | MODIFIER | c.5151-218T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 43/93 | chr1 | 149514718 | ||||||
| chr1:149514721
|
G | A | 2 | a0035c0015t0002g0216a0035c0015t0002g0217 | 2 | HG03017.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.5151-215G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 43/93 | chr1 | 149514721 | ||||||
| chr1:149514721
|
G | C | 2 | a0074c0112t0001g0104a0110c0133t0001g0058 | 2 | HG03139.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.5151-215G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 43/93 | chr1 | 149514721 | ||||||
| chr1:149514725
|
G | A | 1 | a0166c0198t0005g0210 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.5151-211G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 43/93 | chr1 | 149514725 | ||||||
| chr1:149514740
|
T | C | 124 | a0001c0001t0001g0121a0005c0004t0001g0056a0005c0004t0001g0131others(121): Show | 124 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.5151-196T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 43/93 | chr1 | 149514740 | ||||||
| chr1:149514741
|
A | G | 1 | a0091c0122t0008g0157 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.5151-195A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 43/93 | chr1 | 149514741 | ||||||
| chr1:149514790
|
C | A | 1 | a0187c0050t0002g0250 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.5151-146C>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 43/93 | chr1 | 149514790 | ||||||
| chr1:149514811
|
C | A | 1 | a0198c0059t0002g0259 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.5151-125C>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 43/93 | chr1 | 149514811 | ||||||
| chr1:149514815
|
A | G | 1 | a0065c0098t0001g0101 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.5151-121A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 43/93 | chr1 | 149514815 | ||||||
| chr1:149514825
|
C | G | 6 | a0185c0043t0002g0247a0186c0044t0017g0239a0187c0050t0002g0250others(3): Show | 6 | HG02080.hp2 HG02083.hp1 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.5151-111C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 43/93 | chr1 | 149514825 | ||||||
| chr1:149514836
|
G | C | 11 | a0015c0036t0006g0004a0015c0192t0006g0270a0047c0216t0001g0068others(8): Show | 12 | HG01934.hp2 HG02080.hp2 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.5151-100G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 43/93 | chr1 | 149514836 | ||||||
| chr1:149515116
|
C | A | 1 | a0076c0109t0001g0137 | 1 | HG02257.hp2 | splice_region_variant&intron_variant | LOW | c.5323+8C>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 44/93 | chr1 | 149515116 | ||||||
| chr1:149515138
|
A | AT | 164 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(161): Show | 165 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.5323+30_5323+31ins others(1): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 44/93 | chr1 | 149515138 | ||||||
| chr1:149515138
|
A | ATCCACTG others(4735): Show |
1 | a0195c0060t0002g0229 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.5323+30_5323+31ins others(4742): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 44/93 | chr1 | 149515138 | ||||||
| chr1:149515138
|
A | ATCCACTG others(9490): Show |
1 | a0075c0108t0001g0163 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.5323+30_5323+31ins others(9497): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 44/93 | chr1 | 149515138 | ||||||
| chr1:149515205
|
C | T | 1 | a0079c0107t0001g0059 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.5323+97C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 44/93 | chr1 | 149515205 | ||||||
| chr1:149515211
|
C | A | 1 | a0005c0004t0001g0131 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.5323+103C>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 44/93 | chr1 | 149515211 | ||||||
| chr1:149515226
|
T | C | 7 | a0006c0211t0019g0211a0163c0199t0005g0215a0165c0200t0005g0212others(4): Show | 7 | HG00544.hp2 HG00558.hp2 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.5323+118T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 44/93 | chr1 | 149515226 | ||||||
| chr1:149515227
|
A | T | 1 | a0005c0004t0001g0131 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.5323+119A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 44/93 | chr1 | 149515227 | ||||||
| chr1:149515242
|
G | A | 1 | a0082c0117t0001g0009 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.5323+134G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 44/93 | chr1 | 149515242 | ||||||
| chr1:149515330
|
C | T | 2 | a0072c0104t0001g0017a0073c0103t0001g0018 | 2 | HG02083.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.5323+222C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 44/93 | chr1 | 149515330 | ||||||
| chr1:149515350
|
G | T | 3 | a0101c0039t0001g0079a0102c0144t0001g0127a0127c0169t0001g0052 | 3 | HG00408.hp1 HG00423.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.5323+242G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 44/93 | chr1 | 149515350 | ||||||
| chr1:149515405
|
G | C | 1 | a0107c0138t0001g0072 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.5323+297G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 44/93 | chr1 | 149515405 | ||||||
| chr1:149515495
|
T | G | 14 | a0039c0219t0002g0227a0180c0072t0002g0218a0181c0073t0002g0272others(11): Show | 14 | HG00438.hp2 HG02129.hp2 HG03831.hp1 others(11): Show |
intron_variant | MODIFIER | c.5324-327T>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 44/93 | chr1 | 149515495 | ||||||
| chr1:149515512
|
T | C | 6 | a0055c0086t0001g0168a0080c0106t0001g0019a0091c0122t0008g0157others(3): Show | 6 | HG02572.hp1 HG02683.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.5324-310T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 44/93 | chr1 | 149515512 | ||||||
| chr1:149515556
|
G | A | 254 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(251): Show | 257 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(254): Show |
intron_variant | MODIFIER | c.5324-266G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 44/93 | chr1 | 149515556 | ||||||
| chr1:149515713
|
ATTC | A | 4 | a0168c0206t0004g0203a0169c0205t0004g0209a0170c0208t0004g0202others(1): Show | 4 | HG01099.hp1 HG04115.hp1 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.5324-106_5324-104d others(5): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 44/93 | INFO_REALIGN_3_PRIME | chr1 | 149515713 | |||||
| chr1:149515759
|
T | C | 2 | a0096c0127t0001g0111a0125c0159t0001g0147 | 2 | HG02717.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.5324-63T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 44/93 | chr1 | 149515759 | ||||||
| chr1:149515805
|
G | A | 1 | a0169c0205t0004g0209 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.5324-17G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 44/93 | chr1 | 149515805 | ||||||
| chr1:149516002
|
G | C | 1 | a0080c0106t0001g0019 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.5432+72G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 45/93 | chr1 | 149516002 | ||||||
| chr1:149516003
|
C | T | 74 | a0006c0211t0019g0211a0006c0212t0002g0223a0006c0213t0002g0224others(71): Show | 75 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.5432+73C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 45/93 | chr1 | 149516003 | ||||||
| chr1:149516004
|
GTGTTTGA others(5): Show |
G | 1 | a0060c0092t0001g0069 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.5432+80_5432+91del others(12): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 45/93 | INFO_REALIGN_3_PRIME | chr1 | 149516004 | |||||
| chr1:149516073
|
G | A | 2 | a0120c0155t0001g0126a0121c0154t0024g0091 | 2 | HG02040.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.5432+143G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 45/93 | chr1 | 149516073 | ||||||
| chr1:149516082
|
T | C | 12 | a0043c0209t0004g0207a0044c0210t0004g0206a0161c0197t0005g0214others(9): Show | 12 | HG00544.hp2 HG00558.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.5432+152T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 45/93 | chr1 | 149516082 | ||||||
| chr1:149516114
|
A | C | 70 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(67): Show | 70 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.5432+184A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 45/93 | chr1 | 149516114 | ||||||
| chr1:149516118
|
G | A | 128 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(125): Show | 128 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.5432+188G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 45/93 | chr1 | 149516118 | ||||||
| chr1:149516119
|
C | T | 9 | a0036c0014t0009g0230a0185c0043t0002g0247a0187c0050t0002g0250others(6): Show | 9 | HG02040.hp2 HG02080.hp2 HG02129.hp2 others(6): Show |
intron_variant | MODIFIER | c.5432+189C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 45/93 | chr1 | 149516119 | ||||||
| chr1:149516238
|
G | T | 8 | a0039c0219t0002g0227a0183c0041t0002g0246a0188c0051t0002g0252others(5): Show | 8 | HG00438.hp2 NA18946.hp2 NA18954.hp2 others(5): Show |
intron_variant | MODIFIER | c.5432+308G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 45/93 | chr1 | 149516238 | ||||||
| chr1:149516293
|
G | A | 1 | a0129c0167t0012g0088 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.5433-271G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 45/93 | chr1 | 149516293 | ||||||
| chr1:149516295
|
C | G | 2 | a0164c0201t0004g0205a0171c0207t0004g0208 | 2 | HG00735.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.5433-269C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 45/93 | chr1 | 149516295 | ||||||
| chr1:149516351
|
G | C | 1 | a0131c0171t0001g0145 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.5433-213G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 45/93 | chr1 | 149516351 | ||||||
| chr1:149516351
|
G | GTC | 36 | a0006c0211t0019g0211a0006c0213t0002g0224a0015c0036t0006g0004others(33): Show | 37 | HG00642.hp1 HG01069.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.5433-193_5433-192d others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 45/93 | INFO_REALIGN_3_PRIME | chr1 | 149516351 | |||||
| chr1:149516351
|
G | GTCTC | 3 | a0036c0014t0009g0228a0172c0204t0004g0268a0194c0058t0002g0235 | 3 | HG00621.hp1 NA18985.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.5433-195_5433-192d others(6): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 45/93 | INFO_REALIGN_3_PRIME | chr1 | 149516351 | |||||
| chr1:149516351
|
GTCTC | G | 5 | a0110c0133t0001g0058a0168c0206t0004g0203a0169c0205t0004g0209others(2): Show | 5 | HG01099.hp1 HG04115.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.5433-195_5433-192d others(6): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 45/93 | INFO_REALIGN_3_PRIME | chr1 | 149516351 | |||||
| chr1:149516353
|
C | CTCTCTCT others(19026): Show |
1 | a0134c0164t0001g0039 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.5433-137_5433-136i others(19035): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 45/93 | INFO_REALIGN_3_PRIME | chr1 | 149516353 | |||||
| chr1:149516401
|
G | A | 1 | a0180c0072t0002g0218 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.5433-163G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 45/93 | chr1 | 149516401 | ||||||
| chr1:149516417
|
A | C | 1 | a0091c0122t0008g0157 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.5433-147A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 45/93 | chr1 | 149516417 | ||||||
| chr1:149516428
|
A | G | 6 | a0001c0001t0001g0158a0028c0032t0001g0036a0069c0100t0001g0016others(3): Show | 6 | HG00558.hp1 HG01517.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.5433-136A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 45/93 | chr1 | 149516428 | ||||||
| chr1:149516438
|
C | A | 153 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(150): Show | 154 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.5433-126C>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 45/93 | chr1 | 149516438 | ||||||
| chr1:149516446
|
A | C | 1 | a0172c0204t0004g0268 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.5433-118A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 45/93 | chr1 | 149516446 | ||||||
| chr1:149516514
|
C | T | 34 | a0009c0006t0001g0081a0009c0006t0001g0082a0009c0006t0001g0139others(31): Show | 35 | HG00099.hp1 HG00741.hp2 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.5433-50C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 45/93 | chr1 | 149516514 | ||||||
| chr1:149516751
|
A | G | 2 | a0006c0211t0019g0211a0167c0203t0028g0269 | 2 | HG02109.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.5605+15A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 46/93 | chr1 | 149516751 | ||||||
| chr1:149516913
|
G | T | 1 | a0207c0046t0002g0241 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.5605+177G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 46/93 | chr1 | 149516913 | ||||||
| chr1:149516924
|
A | G | 4 | a0024c0025t0001g0024a0024c0025t0001g0026a0042c0195t0001g0023others(1): Show | 4 | HG02055.hp2 HG02486.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.5605+188A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 46/93 | chr1 | 149516924 | ||||||
| chr1:149516933
|
C | T | 142 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(139): Show | 142 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.5605+197C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 46/93 | chr1 | 149516933 | ||||||
| chr1:149516958
|
C | A | 6 | a0015c0036t0006g0004a0015c0192t0006g0270a0110c0133t0001g0058others(3): Show | 7 | HG02145.hp1 HG02683.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.5605+222C>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 46/93 | chr1 | 149516958 | ||||||
| chr1:149516958
|
C | T | 1 | a0166c0198t0005g0210 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.5605+222C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 46/93 | chr1 | 149516958 | ||||||
| chr1:149516959
|
G | A | 11 | a0006c0212t0002g0223a0006c0214t0002g0265a0039c0219t0002g0227others(8): Show | 11 | HG00438.hp2 HG01891.hp1 NA18946.hp2 others(8): Show |
intron_variant | MODIFIER | c.5605+223G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 46/93 | chr1 | 149516959 | ||||||
| chr1:149516965
|
A | C | 6 | a0036c0014t0009g0228a0179c0071t0002g0260a0180c0072t0002g0218others(3): Show | 6 | HG00738.hp1 HG03831.hp1 HG04204.hp1 others(3): Show |
intron_variant | MODIFIER | c.5605+229A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 46/93 | chr1 | 149516965 | ||||||
| chr1:149516974
|
T | C | 6 | a0036c0014t0009g0228a0179c0071t0002g0260a0180c0072t0002g0218others(3): Show | 6 | HG00738.hp1 HG03831.hp1 HG04204.hp1 others(3): Show |
intron_variant | MODIFIER | c.5605+238T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 46/93 | chr1 | 149516974 | ||||||
| chr1:149516981
|
A | G | 1 | a0006c0213t0002g0224 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.5605+245A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 46/93 | chr1 | 149516981 | ||||||
| chr1:149516982
|
T | C | 13 | a0015c0036t0006g0004a0015c0192t0006g0270a0055c0086t0001g0168others(10): Show | 14 | HG02145.hp1 HG02572.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.5605+246T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 46/93 | chr1 | 149516982 | ||||||
| chr1:149516982
|
T | G | 1 | a0166c0198t0005g0210 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.5605+246T>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 46/93 | chr1 | 149516982 | ||||||
| chr1:149516982
|
T | TTGGACCT others(28505): Show |
1 | a0205c0056t0015g0258 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.5605+274_5605+275i others(28514): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 46/93 | INFO_REALIGN_3_PRIME | chr1 | 149516982 | |||||
| chr1:149516991
|
G | C | 1 | a0042c0195t0001g0023 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.5605+255G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 46/93 | chr1 | 149516991 | ||||||
| chr1:149516995
|
G | C | 5 | a0168c0206t0004g0203a0169c0205t0004g0209a0170c0208t0004g0202others(2): Show | 5 | HG01099.hp1 HG02698.hp1 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.5605+259G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 46/93 | chr1 | 149516995 | ||||||
| chr1:149517011
|
A | G | 99 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(96): Show | 99 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.5605+275A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 46/93 | chr1 | 149517011 | ||||||
| chr1:149517087
|
C | T | 1 | a0100c0145t0001g0076 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.5605+351C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 46/93 | chr1 | 149517087 | ||||||
| chr1:149517288
|
A | G | 1 | a0154c0185t0001g0152 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.5606-168A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 46/93 | chr1 | 149517288 | ||||||
| chr1:149517359
|
A | T | 17 | a0032c0012t0002g0232a0032c0012t0002g0266a0033c0011t0002g0254others(14): Show | 17 | HG00621.hp1 HG00642.hp1 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.5606-97A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 46/93 | chr1 | 149517359 | ||||||
| chr1:149517370
|
G | T | 1 | a0205c0056t0015g0258 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.5606-86G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 46/93 | chr1 | 149517370 | ||||||
| chr1:149517372
|
T | C | 163 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(160): Show | 165 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.5606-84T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 46/93 | chr1 | 149517372 | ||||||
| chr1:149517373
|
C | T | 141 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(138): Show | 141 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.5606-83C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 46/93 | chr1 | 149517373 | ||||||
| chr1:149517387
|
A | T | 3 | a0013c0035t0001g0038a0013c0035t0001g0084a0013c0162t0001g0040 | 3 | HG02258.hp2 HG02280.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.5606-69A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 46/93 | chr1 | 149517387 | ||||||
| chr1:149517388
|
G | C | 1 | a0076c0109t0001g0137 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.5606-68G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 46/93 | chr1 | 149517388 | ||||||
| chr1:149517389
|
A | G | 1 | a0006c0213t0002g0224 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.5606-67A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 46/93 | chr1 | 149517389 | ||||||
| chr1:149517396
|
A | G | 1 | a0210c0068t0016g0233 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.5606-60A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 46/93 | chr1 | 149517396 | ||||||
| chr1:149517404
|
G | T | 9 | a0039c0219t0002g0227a0183c0041t0002g0246a0184c0042t0002g0236others(6): Show | 9 | HG00438.hp2 NA18747.hp2 NA18946.hp2 others(6): Show |
intron_variant | MODIFIER | c.5606-52G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 46/93 | chr1 | 149517404 | ||||||
| chr1:149517429
|
G | A | 2 | a0047c0216t0001g0068a0137c0173t0001g0159 | 2 | HG01934.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.5606-27G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 46/93 | chr1 | 149517429 | ||||||
| chr1:149517526
|
G | A | 1 | a0166c0198t0005g0210 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.5657+19G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 47/93 | chr1 | 149517526 | ||||||
| chr1:149517538
|
C | T | 1 | a0205c0056t0015g0258 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.5657+31C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 47/93 | chr1 | 149517538 | ||||||
| chr1:149517556
|
A | T | 6 | a0017c0019t0001g0112a0017c0019t0001g0167a0018c0018t0001g0113others(3): Show | 6 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.5657+49A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 47/93 | chr1 | 149517556 | ||||||
| chr1:149517561
|
A | G | 1 | a0180c0072t0002g0218 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.5657+54A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 47/93 | chr1 | 149517561 | ||||||
| chr1:149517581
|
T | C | 1 | a0038c0038t0001g0171 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.5657+74T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 47/93 | chr1 | 149517581 | ||||||
| chr1:149517622
|
T | C | 1 | a0158c0084t0001g0049 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.5657+115T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 47/93 | chr1 | 149517622 | ||||||
| chr1:149517682
|
C | T | 1 | a0166c0198t0005g0210 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.5657+175C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 47/93 | chr1 | 149517682 | ||||||
| chr1:149517686
|
A | T | 106 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(103): Show | 106 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.5657+179A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 47/93 | chr1 | 149517686 | ||||||
| chr1:149517711
|
A | T | 21 | a0036c0014t0009g0228a0036c0014t0009g0230a0039c0219t0002g0227others(18): Show | 21 | HG00438.hp2 HG02040.hp2 HG02080.hp2 others(18): Show |
intron_variant | MODIFIER | c.5657+204A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 47/93 | chr1 | 149517711 | ||||||
| chr1:149517739
|
G | T | 22 | a0032c0012t0002g0232a0032c0012t0002g0266a0033c0011t0002g0254others(19): Show | 22 | HG00621.hp1 HG00642.hp1 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.5657+232G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 47/93 | chr1 | 149517739 | ||||||
| chr1:149517746
|
A | G | 23 | a0006c0213t0002g0224a0036c0014t0009g0228a0036c0014t0009g0230others(20): Show | 23 | HG00438.hp2 HG02040.hp2 HG02080.hp2 others(20): Show |
intron_variant | MODIFIER | c.5657+239A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 47/93 | chr1 | 149517746 | ||||||
| chr1:149517759
|
T | A | 22 | a0032c0012t0002g0232a0032c0012t0002g0266a0033c0011t0002g0254others(19): Show | 22 | HG00621.hp1 HG00642.hp1 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.5657+252T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 47/93 | chr1 | 149517759 | ||||||
| chr1:149517802
|
G | A | 2 | a0069c0100t0001g0016a0099c0146t0001g0034 | 2 | HG01517.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.5657+295G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 47/93 | chr1 | 149517802 | ||||||
| chr1:149517876
|
G | T | 2 | a0034c0013t0002g0220a0034c0013t0002g0221 | 2 | NA18961.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.5658-234G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 47/93 | chr1 | 149517876 | ||||||
| chr1:149517889
|
C | CCT | 108 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(105): Show | 108 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.5658-201_5658-200d others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 47/93 | INFO_REALIGN_3_PRIME | chr1 | 149517889 | |||||
| chr1:149517889
|
C | CCTCT | 3 | a0034c0013t0002g0221a0174c0202t0013g0204a0186c0044t0017g0239 | 3 | HG02602.hp2 NA18961.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.5658-203_5658-200d others(6): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 47/93 | INFO_REALIGN_3_PRIME | chr1 | 149517889 | |||||
| chr1:149517889
|
CCT | C | 37 | a0008c0037t0001g0075a0008c0037t0001g0135a0008c0215t0001g0067others(34): Show | 38 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.5658-201_5658-200d others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 47/93 | INFO_REALIGN_3_PRIME | chr1 | 149517889 | |||||
| chr1:149517939
|
T | C | 109 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(106): Show | 109 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.5658-171T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 47/93 | chr1 | 149517939 | ||||||
| chr1:149517959
|
T | C | 2 | a0161c0197t0005g0214a0162c0196t0005g0213 | 2 | HG00735.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.5658-151T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 47/93 | chr1 | 149517959 | ||||||
| chr1:149517986
|
C | A | 26 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(23): Show | 26 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(23): Show |
intron_variant | MODIFIER | c.5658-124C>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 47/93 | chr1 | 149517986 | ||||||
| chr1:149517990
|
A | G | 2 | a0035c0015t0002g0216a0035c0015t0002g0217 | 2 | HG03017.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.5658-120A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 47/93 | chr1 | 149517990 | ||||||
| chr1:149518029
|
A | T | 1 | a0006c0211t0019g0211 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.5658-81A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 47/93 | chr1 | 149518029 | ||||||
| chr1:149518038
|
A | C | 2 | a0006c0212t0002g0223a0006c0214t0002g0265 | 2 | HG01891.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.5658-72A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 47/93 | chr1 | 149518038 | ||||||
| chr1:149518045
|
C | G | 11 | a0006c0211t0019g0211a0161c0197t0005g0214a0162c0196t0005g0213others(8): Show | 11 | HG00544.hp2 HG00558.hp2 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.5658-65C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 47/93 | chr1 | 149518045 | ||||||
| chr1:149518106
|
C | T | 2 | a0186c0044t0017g0239a0207c0046t0002g0241 | 2 | HG02602.hp2 NA18983.hp1 |
splice_region_variant&intron_variant | LOW | c.5658-4C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 47/93 | chr1 | 149518106 | ||||||
| chr1:149518387
|
G | A | 7 | a0022c0023t0001g0156a0022c0023t0001g0160a0069c0100t0001g0016others(4): Show | 7 | HG01517.hp2 HG02572.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.5830+105G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 48/93 | chr1 | 149518387 | ||||||
| chr1:149518400
|
A | G | 2 | a0111c0132t0001g0199a0136c0163t0001g0200 | 2 | NA18942.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.5830+118A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 48/93 | chr1 | 149518400 | ||||||
| chr1:149518406
|
G | A | 1 | a0205c0056t0015g0258 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.5830+124G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 48/93 | chr1 | 149518406 | ||||||
| chr1:149518473
|
G | T | 1 | a0186c0044t0017g0239 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.5830+191G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 48/93 | chr1 | 149518473 | ||||||
| chr1:149518479
|
A | T | 24 | a0032c0012t0002g0232a0032c0012t0002g0266a0033c0011t0002g0254others(21): Show | 24 | HG00621.hp1 HG00642.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.5830+197A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 48/93 | chr1 | 149518479 | ||||||
| chr1:149518480
|
T | C | 5 | a0044c0210t0004g0206a0161c0197t0005g0214a0162c0196t0005g0213others(2): Show | 5 | HG00544.hp2 HG00558.hp2 HG00735.hp2 others(2): Show |
intron_variant | MODIFIER | c.5830+198T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 48/93 | chr1 | 149518480 | ||||||
| chr1:149518490
|
C | G | 1 | a0006c0211t0019g0211 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.5830+208C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 48/93 | chr1 | 149518490 | ||||||
| chr1:149518501
|
T | A | 1 | a0202c0064t0002g0262 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.5830+219T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 48/93 | chr1 | 149518501 | ||||||
| chr1:149518501
|
T | C | 38 | a0015c0036t0006g0004a0015c0192t0006g0270a0036c0014t0009g0228others(35): Show | 39 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.5830+219T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 48/93 | chr1 | 149518501 | ||||||
| chr1:149518547
|
T | C | 112 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(109): Show | 112 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.5830+265T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 48/93 | chr1 | 149518547 | ||||||
| chr1:149518555
|
T | G | 1 | a0171c0207t0004g0208 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.5830+273T>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 48/93 | chr1 | 149518555 | ||||||
| chr1:149518581
|
G | T | 1 | a0166c0198t0005g0210 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.5830+299G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 48/93 | chr1 | 149518581 | ||||||
| chr1:149518588
|
G | A | 139 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(136): Show | 140 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.5830+306G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 48/93 | chr1 | 149518588 | ||||||
| chr1:149518591
|
T | A | 1 | a0160c0076t0014g0225 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.5830+309T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 48/93 | chr1 | 149518591 | ||||||
| chr1:149518602
|
A | T | 1 | a0166c0198t0005g0210 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.5830+320A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 48/93 | chr1 | 149518602 | ||||||
| chr1:149518784
|
A | T | 1 | a0166c0198t0005g0210 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.5831-208A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 48/93 | chr1 | 149518784 | ||||||
| chr1:149519055
|
A | G | 23 | a0003c0003t0001g0115a0003c0003t0001g0116a0003c0003t0001g0117others(20): Show | 23 | HG00544.hp1 HG00733.hp1 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.5882+12A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 49/93 | chr1 | 149519055 | ||||||
| chr1:149519069
|
C | G | 1 | a0091c0122t0008g0157 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.5882+26C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 49/93 | chr1 | 149519069 | ||||||
| chr1:149519076
|
G | T | 2 | a0096c0127t0001g0111a0125c0159t0001g0147 | 2 | HG02717.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.5882+33G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 49/93 | chr1 | 149519076 | ||||||
| chr1:149519093
|
C | A | 8 | a0022c0023t0001g0156a0022c0023t0001g0160a0069c0100t0001g0016others(5): Show | 8 | HG01517.hp2 HG02572.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.5882+50C>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 49/93 | chr1 | 149519093 | ||||||
| chr1:149519113
|
G | C | 17 | a0003c0003t0001g0115a0003c0003t0001g0116a0003c0003t0001g0117others(14): Show | 17 | HG00544.hp1 HG00733.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.5882+70G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 49/93 | chr1 | 149519113 | ||||||
| chr1:149519142
|
C | T | 1 | a0086c0119t0001g0085 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.5882+99C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 49/93 | chr1 | 149519142 | ||||||
| chr1:149519170
|
A | G | 1 | a0166c0198t0005g0210 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.5882+127A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 49/93 | chr1 | 149519170 | ||||||
| chr1:149519211
|
T | A | 3 | a0015c0036t0006g0004a0015c0192t0006g0270a0173c0191t0006g0271 | 4 | HG02145.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.5882+168T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 49/93 | chr1 | 149519211 | ||||||
| chr1:149519226
|
A | G | 1 | a0001c0001t0001g0121 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.5882+183A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 49/93 | chr1 | 149519226 | ||||||
| chr1:149519247
|
G | C | 3 | a0110c0133t0001g0058a0126c0130t0001g0134a0158c0084t0001g0049 | 3 | HG02683.hp2 HG02965.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.5882+204G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 49/93 | chr1 | 149519247 | ||||||
| chr1:149519274
|
C | A | 2 | a0035c0015t0002g0216a0035c0015t0002g0217 | 2 | HG03017.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.5882+231C>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 49/93 | chr1 | 149519274 | ||||||
| chr1:149519281
|
C | T | 3 | a0142c0180t0001g0108a0186c0044t0017g0239a0207c0046t0002g0241 | 3 | HG01168.hp2 HG02602.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.5882+238C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 49/93 | chr1 | 149519281 | ||||||
| chr1:149519288
|
A | G | 31 | a0003c0003t0001g0115a0003c0003t0001g0116a0003c0003t0001g0117others(28): Show | 31 | HG00544.hp1 HG00733.hp1 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.5882+245A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 49/93 | chr1 | 149519288 | ||||||
| chr1:149519296
|
T | A | 3 | a0028c0032t0001g0161a0029c0033t0001g0197a0029c0033t0001g0198 | 3 | HG02809.hp2 HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.5882+253T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 49/93 | chr1 | 149519296 | ||||||
| chr1:149519327
|
C | T | 1 | a0135c0161t0001g0057 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.5882+284C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 49/93 | chr1 | 149519327 | ||||||
| chr1:149519373
|
C | T | 19 | a0032c0012t0002g0232a0032c0012t0002g0266a0033c0011t0002g0254others(16): Show | 19 | HG00621.hp1 HG00642.hp1 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.5883-315C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 49/93 | chr1 | 149519373 | ||||||
| chr1:149519406
|
T | C | 3 | a0015c0036t0006g0004a0015c0192t0006g0270a0173c0191t0006g0271 | 4 | HG02145.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.5883-282T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 49/93 | chr1 | 149519406 | ||||||
| chr1:149519431
|
T | TTC | 33 | a0001c0001t0001g0121a0005c0004t0001g0056a0005c0004t0001g0131others(30): Show | 33 | HG00423.hp2 HG00609.hp2 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.5883-243_5883-242d others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 49/93 | INFO_REALIGN_3_PRIME | chr1 | 149519431 | |||||
| chr1:149519431
|
T | TTCTCTCT others(5): Show |
2 | a0015c0036t0006g0004a0015c0192t0006g0270 | 3 | HG02896.hp1 HG02897.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.5883-253_5883-242d others(14): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 49/93 | INFO_REALIGN_3_PRIME | chr1 | 149519431 | |||||
| chr1:149519431
|
T | TTCTCTCT others(7): Show |
1 | a0173c0191t0006g0271 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.5883-255_5883-242d others(16): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 49/93 | INFO_REALIGN_3_PRIME | chr1 | 149519431 | |||||
| chr1:149519441
|
CTCTCTGT others(11): Show |
C | 8 | a0008c0037t0001g0075a0008c0037t0001g0135a0008c0215t0001g0067others(5): Show | 8 | HG00741.hp1 HG01496.hp1 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.5883-245_5883-228d others(20): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 49/93 | INFO_REALIGN_3_PRIME | chr1 | 149519441 | |||||
| chr1:149519443
|
CTCTGTGT others(3): Show |
C | 1 | a0026c0030t0001g0030 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.5883-243_5883-234d others(12): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 49/93 | INFO_REALIGN_3_PRIME | chr1 | 149519443 | |||||
| chr1:149519443
|
CTCTGTGT others(11): Show |
C | 1 | a0126c0130t0001g0134 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.5883-243_5883-226d others(20): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 49/93 | INFO_REALIGN_3_PRIME | chr1 | 149519443 | |||||
| chr1:149519445
|
C | CTCTCTGT others(3): Show |
1 | a0030c0034t0001g0092 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.5883-242_5883-241i others(12): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 49/93 | INFO_REALIGN_3_PRIME | chr1 | 149519445 | |||||
| chr1:149519445
|
C | CTCTCTGT others(5): Show |
2 | a0018c0018t0001g0113a0030c0034t0001g0093 | 2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.5883-242_5883-241i others(14): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 49/93 | INFO_REALIGN_3_PRIME | chr1 | 149519445 | |||||
| chr1:149519445
|
C | G | 22 | a0022c0023t0001g0156a0022c0023t0001g0160a0036c0014t0009g0228others(19): Show | 22 | HG00438.hp2 HG00621.hp2 HG02040.hp2 others(19): Show |
intron_variant | MODIFIER | c.5883-243C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 49/93 | chr1 | 149519445 | ||||||
| chr1:149519445
|
CTG | C | 10 | a0019c0021t0001g0098a0027c0029t0001g0062a0028c0032t0001g0036others(7): Show | 10 | HG01952.hp1 HG02486.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.5883-195_5883-194d others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 49/93 | INFO_REALIGN_3_PRIME | chr1 | 149519445 | |||||
| chr1:149519445
|
CTGTG | C | 13 | a0003c0003t0001g0115a0003c0003t0001g0116a0003c0003t0001g0117others(10): Show | 14 | HG00733.hp1 HG01069.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.5883-197_5883-194d others(6): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 49/93 | INFO_REALIGN_3_PRIME | chr1 | 149519445 | |||||
| chr1:149519445
|
CTGTGTGT others(9): Show |
C | 1 | a0038c0038t0001g0171 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.5883-209_5883-194d others(18): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 49/93 | INFO_REALIGN_3_PRIME | chr1 | 149519445 | |||||
| chr1:149519445
|
CTGTGTGT others(11): Show |
C | 1 | a0027c0029t0001g0061 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.5883-211_5883-194d others(20): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 49/93 | INFO_REALIGN_3_PRIME | chr1 | 149519445 | |||||
| chr1:149519447
|
G | C | 135 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(132): Show | 137 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.5883-241G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 49/93 | chr1 | 149519447 | ||||||
| chr1:149519449
|
G | C | 8 | a0001c0001t0001g0136a0006c0214t0002g0265a0042c0195t0001g0023others(5): Show | 8 | HG01099.hp2 HG01952.hp1 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.5883-239G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 49/93 | chr1 | 149519449 | ||||||
| chr1:149519450
|
T | A | 1 | a0006c0211t0019g0211 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.5883-238T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 49/93 | chr1 | 149519450 | ||||||
| chr1:149519451
|
G | C | 2 | a0024c0025t0001g0026a0090c0121t0008g0149 | 2 | HG02055.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.5883-237G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 49/93 | chr1 | 149519451 | ||||||
| chr1:149519455
|
G | C | 1 | a0006c0213t0002g0224 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.5883-233G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 49/93 | chr1 | 149519455 | ||||||
| chr1:149519463
|
G | C | 1 | a0038c0038t0001g0171 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.5883-225G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 49/93 | chr1 | 149519463 | ||||||
| chr1:149519466
|
T | C | 13 | a0044c0210t0004g0206a0165c0200t0005g0212a0166c0198t0005g0210others(10): Show | 13 | HG00544.hp2 HG01099.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.5883-222T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 49/93 | chr1 | 149519466 | ||||||
| chr1:149519468
|
T | C | 5 | a0006c0212t0002g0223a0022c0023t0001g0156a0022c0023t0001g0160others(2): Show | 5 | HG01891.hp1 HG02572.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.5883-220T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 49/93 | chr1 | 149519468 | ||||||
| chr1:149519470
|
T | C | 29 | a0006c0211t0019g0211a0032c0012t0002g0232a0032c0012t0002g0266others(26): Show | 29 | HG00621.hp1 HG00642.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.5883-218T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 49/93 | chr1 | 149519470 | ||||||
| chr1:149519472
|
T | C | 5 | a0006c0214t0002g0265a0069c0100t0001g0016a0099c0146t0001g0034others(2): Show | 5 | HG01517.hp2 HG03041.hp1 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.5883-216T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 49/93 | chr1 | 149519472 | ||||||
| chr1:149519473
|
G | C | 9 | a0008c0037t0001g0075a0008c0037t0001g0135a0008c0215t0001g0067others(6): Show | 9 | HG00741.hp1 HG01496.hp1 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.5883-215G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 49/93 | chr1 | 149519473 | ||||||
| chr1:149519475
|
G | C | 2 | a0008c0037t0001g0075a0008c0037t0001g0135 | 2 | HG00741.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.5883-213G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 49/93 | chr1 | 149519475 | ||||||
| chr1:149519483
|
G | A | 1 | a0166c0198t0005g0210 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.5883-205G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 49/93 | chr1 | 149519483 | ||||||
| chr1:149519489
|
G | C | 1 | a0006c0211t0019g0211 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.5883-199G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 49/93 | chr1 | 149519489 | ||||||
| chr1:149519491
|
G | C | 103 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(100): Show | 104 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.5883-197G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 49/93 | chr1 | 149519491 | ||||||
| chr1:149519491
|
G | GTC | 14 | a0001c0001t0001g0158a0011c0010t0001g0010a0011c0010t0001g0011others(11): Show | 14 | HG00735.hp2 HG01516.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.5883-196_5883-195i others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 49/93 | INFO_REALIGN_3_PRIME | chr1 | 149519491 | |||||
| chr1:149519491
|
G | GTCTATCT others(4724): Show |
1 | a0080c0106t0001g0019 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.5883-196_5883-195i others(4733): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 49/93 | INFO_REALIGN_3_PRIME | chr1 | 149519491 | |||||
| chr1:149519492
|
T | C | 10 | a0006c0212t0002g0223a0167c0203t0028g0269a0168c0206t0004g0203others(7): Show | 10 | HG01099.hp1 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.5883-196T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 49/93 | chr1 | 149519492 | ||||||
| chr1:149519492
|
T | TCC | 5 | a0022c0023t0001g0156a0022c0023t0001g0160a0074c0112t0001g0104others(2): Show | 5 | HG02572.hp2 HG02630.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.5883-196_5883-195i others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 49/93 | chr1 | 149519492 | ||||||
| chr1:149519493
|
G | A | 123 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(120): Show | 124 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.5883-195G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 49/93 | chr1 | 149519493 | ||||||
| chr1:149519493
|
G | GTCCA | 7 | a0006c0214t0002g0265a0035c0015t0002g0216a0035c0015t0002g0217others(4): Show | 7 | HG00738.hp1 HG03017.hp2 HG03704.hp2 others(4): Show |
intron_variant | MODIFIER | c.5883-193_5883-192i others(6): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 49/93 | INFO_REALIGN_3_PRIME | chr1 | 149519493 | |||||
| chr1:149519493
|
G | GTCTA | 29 | a0005c0004t0025g0073a0012c0009t0001g0172a0013c0035t0001g0038others(26): Show | 29 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(26): Show |
intron_variant | MODIFIER | c.5883-192_5883-191i others(6): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 49/93 | INFO_REALIGN_3_PRIME | chr1 | 149519493 | |||||
| chr1:149519493
|
G | GTGTCCA | 22 | a0006c0211t0019g0211a0032c0012t0002g0232a0032c0012t0002g0266others(19): Show | 22 | HG00621.hp1 HG00642.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.5883-194_5883-193i others(8): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 49/93 | INFO_REALIGN_3_PRIME | chr1 | 149519493 | |||||
| chr1:149519493
|
G | GTGTCTA | 9 | a0012c0009t0001g0195a0025c0031t0001g0033a0029c0033t0001g0198others(6): Show | 9 | HG00738.hp2 HG02559.hp1 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.5883-194_5883-193i others(8): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 49/93 | INFO_REALIGN_3_PRIME | chr1 | 149519493 | |||||
| chr1:149519493
|
G | GTGTGTCT others(1): Show |
10 | a0012c0009t0001g0050a0031c0028t0003g0194a0047c0216t0001g0068others(7): Show | 10 | HG01081.hp2 HG01934.hp2 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.5883-194_5883-193i others(10): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 49/93 | INFO_REALIGN_3_PRIME | chr1 | 149519493 | |||||
| chr1:149519493
|
G | GTGTGTGT others(3): Show |
12 | a0018c0018t0001g0166a0021c0022t0001g0080a0021c0022t0001g0169others(9): Show | 12 | HG02083.hp2 HG02129.hp1 HG02155.hp2 others(9): Show |
intron_variant | MODIFIER | c.5883-194_5883-193i others(12): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 49/93 | INFO_REALIGN_3_PRIME | chr1 | 149519493 | |||||
| chr1:149519493
|
G | GTGTGTGT others(5): Show |
11 | a0017c0019t0001g0112a0017c0019t0001g0167a0023c0024t0001g0003others(8): Show | 12 | HG00558.hp2 HG02055.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.5883-194_5883-193i others(14): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 49/93 | INFO_REALIGN_3_PRIME | chr1 | 149519493 | |||||
| chr1:149519493
|
G | GTGTGTGT others(7): Show |
16 | a0004c0026t0001g0008a0004c0027t0001g0001a0009c0006t0001g0082others(13): Show | 17 | HG00544.hp2 HG00741.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.5883-194_5883-193i others(16): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 49/93 | INFO_REALIGN_3_PRIME | chr1 | 149519493 | |||||
| chr1:149519493
|
G | GTGTGTGT others(9): Show |
7 | a0004c0026t0001g0007a0009c0006t0001g0081a0009c0006t0001g0139others(4): Show | 7 | HG00099.hp1 HG01934.hp1 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.5883-194_5883-193i others(18): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 49/93 | INFO_REALIGN_3_PRIME | chr1 | 149519493 | |||||
| chr1:149519542
|
C | A | 2 | a0203c0065t0002g0240a0204c0067t0002g0248 | 2 | HG00438.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.5883-146C>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 49/93 | chr1 | 149519542 | ||||||
| chr1:149519564
|
C | T | 1 | a0006c0211t0019g0211 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.5883-124C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 49/93 | chr1 | 149519564 | ||||||
| chr1:149519577
|
C | G | 17 | a0036c0014t0009g0228a0036c0014t0009g0230a0183c0041t0002g0246others(14): Show | 17 | HG00438.hp2 HG00621.hp2 HG02040.hp2 others(14): Show |
intron_variant | MODIFIER | c.5883-111C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 49/93 | chr1 | 149519577 | ||||||
| chr1:149519579
|
A | G | 3 | a0015c0036t0006g0004a0015c0192t0006g0270a0173c0191t0006g0271 | 4 | HG02145.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.5883-109A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 49/93 | chr1 | 149519579 | ||||||
| chr1:149519588
|
G | C | 25 | a0008c0037t0001g0075a0008c0037t0001g0135a0008c0215t0001g0067others(22): Show | 25 | HG00438.hp2 HG00621.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.5883-100G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 49/93 | chr1 | 149519588 | ||||||
| chr1:149519605
|
C | T | 3 | a0186c0044t0017g0239a0197c0066t0002g0238a0207c0046t0002g0241 | 3 | HG02083.hp1 HG02602.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.5883-83C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 49/93 | chr1 | 149519605 | ||||||
| chr1:149519652
|
C | G | 2 | a0161c0197t0005g0214a0162c0196t0005g0213 | 2 | HG00735.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.5883-36C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 49/93 | chr1 | 149519652 | ||||||
| chr1:149519670
|
T | G | 3 | a0186c0044t0017g0239a0197c0066t0002g0238a0207c0046t0002g0241 | 3 | HG02083.hp1 HG02602.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.5883-18T>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 49/93 | chr1 | 149519670 | ||||||
| chr1:149519890
|
AT | A | 66 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(63): Show | 66 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.6055+31delT | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 50/93 | chr1 | 149519890 | ||||||
| chr1:149519944
|
G | T | 1 | a0183c0041t0002g0246 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.6055+84G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 50/93 | chr1 | 149519944 | ||||||
| chr1:149519946
|
G | A | 1 | a0083c0116t0023g0103 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.6055+86G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 50/93 | chr1 | 149519946 | ||||||
| chr1:149519959
|
G | A | 7 | a0083c0116t0023g0103a0091c0122t0008g0157a0093c0124t0001g0153others(4): Show | 7 | HG02083.hp1 HG02572.hp1 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.6055+99G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 50/93 | chr1 | 149519959 | ||||||
| chr1:149519979
|
T | C | 3 | a0168c0206t0004g0203a0169c0205t0004g0209a0174c0202t0013g0204 | 3 | HG01099.hp1 HG04115.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.6055+119T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 50/93 | chr1 | 149519979 | ||||||
| chr1:149519995
|
G | C | 1 | a0091c0122t0008g0157 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.6055+135G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 50/93 | chr1 | 149519995 | ||||||
| chr1:149520030
|
A | T | 7 | a0083c0116t0023g0103a0091c0122t0008g0157a0093c0124t0001g0153others(4): Show | 7 | HG02083.hp1 HG02572.hp1 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.6055+170A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 50/93 | chr1 | 149520030 | ||||||
| chr1:149520031
|
G | T | 2 | a0161c0197t0005g0214a0162c0196t0005g0213 | 2 | HG00735.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.6055+171G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 50/93 | chr1 | 149520031 | ||||||
| chr1:149520049
|
A | T | 7 | a0083c0116t0023g0103a0091c0122t0008g0157a0093c0124t0001g0153others(4): Show | 7 | HG02083.hp1 HG02572.hp1 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.6055+189A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 50/93 | chr1 | 149520049 | ||||||
| chr1:149520051
|
A | G | 7 | a0083c0116t0023g0103a0091c0122t0008g0157a0093c0124t0001g0153others(4): Show | 7 | HG02083.hp1 HG02572.hp1 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.6055+191A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 50/93 | chr1 | 149520051 | ||||||
| chr1:149520084
|
G | A | 7 | a0083c0116t0023g0103a0091c0122t0008g0157a0093c0124t0001g0153others(4): Show | 7 | HG02083.hp1 HG02572.hp1 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.6055+224G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 50/93 | chr1 | 149520084 | ||||||
| chr1:149520086
|
C | T | 7 | a0083c0116t0023g0103a0091c0122t0008g0157a0093c0124t0001g0153others(4): Show | 7 | HG02083.hp1 HG02572.hp1 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.6055+226C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 50/93 | chr1 | 149520086 | ||||||
| chr1:149520087
|
C | G | 2 | a0161c0197t0005g0214a0162c0196t0005g0213 | 2 | HG00735.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.6055+227C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 50/93 | chr1 | 149520087 | ||||||
| chr1:149520092
|
C | T | 7 | a0083c0116t0023g0103a0091c0122t0008g0157a0093c0124t0001g0153others(4): Show | 7 | HG02083.hp1 HG02572.hp1 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.6055+232C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 50/93 | chr1 | 149520092 | ||||||
| chr1:149520096
|
T | C | 7 | a0083c0116t0023g0103a0091c0122t0008g0157a0093c0124t0001g0153others(4): Show | 7 | HG02083.hp1 HG02572.hp1 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.6055+236T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 50/93 | chr1 | 149520096 | ||||||
| chr1:149520164
|
T | C | 13 | a0009c0006t0001g0081a0009c0006t0001g0082a0009c0006t0001g0139others(10): Show | 13 | HG00099.hp1 HG00741.hp2 HG01934.hp1 others(10): Show |
intron_variant | MODIFIER | c.6055+304T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 50/93 | chr1 | 149520164 | ||||||
| chr1:149520164
|
T | TAGATTTC others(9485): Show |
1 | a0204c0067t0002g0248 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.6056-311_6056-310i others(9494): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 50/93 | INFO_REALIGN_3_PRIME | chr1 | 149520164 | |||||
| chr1:149520214
|
G | A | 1 | a0160c0076t0014g0225 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.6055+354G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 50/93 | chr1 | 149520214 | ||||||
| chr1:149520248
|
T | G | 9 | a0035c0015t0002g0216a0036c0014t0009g0228a0036c0014t0009g0230others(6): Show | 9 | HG03017.hp2 HG03831.hp1 HG04204.hp1 others(6): Show |
intron_variant | MODIFIER | c.6056-327T>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 50/93 | chr1 | 149520248 | ||||||
| chr1:149520265
|
C | T | 158 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(155): Show | 159 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.6056-310C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 50/93 | chr1 | 149520265 | ||||||
| chr1:149520280
|
G | A | 1 | a0185c0043t0002g0247 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.6056-295G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 50/93 | chr1 | 149520280 | ||||||
| chr1:149520466
|
ATTC | A | 3 | a0168c0206t0004g0203a0169c0205t0004g0209a0174c0202t0013g0204 | 3 | HG01099.hp1 HG04115.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.6056-106_6056-104d others(5): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 50/93 | INFO_REALIGN_3_PRIME | chr1 | 149520466 | |||||
| chr1:149520700
|
G | A | 4 | a0003c0136t0001g0005a0053c0190t0001g0064a0077c0110t0001g0178others(1): Show | 4 | HG01516.hp2 HG01517.hp1 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.6164+17G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 51/93 | chr1 | 149520700 | ||||||
| chr1:149520755
|
G | C | 4 | a0065c0098t0001g0101a0066c0097t0001g0175a0138c0174t0001g0109others(1): Show | 4 | HG01081.hp2 HG02300.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.6164+72G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 51/93 | chr1 | 149520755 | ||||||
| chr1:149520756
|
T | C | 83 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(80): Show | 83 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.6164+73T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 51/93 | chr1 | 149520756 | ||||||
| chr1:149520829
|
G | C | 1 | a0060c0092t0001g0069 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.6164+146G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 51/93 | chr1 | 149520829 | ||||||
| chr1:149520835
|
T | C | 9 | a0163c0199t0005g0215a0164c0201t0004g0205a0165c0200t0005g0212others(6): Show | 9 | HG00544.hp2 HG00558.hp2 HG00735.hp1 others(6): Show |
intron_variant | MODIFIER | c.6164+152T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 51/93 | chr1 | 149520835 | ||||||
| chr1:149520867
|
A | C | 12 | a0024c0025t0001g0024a0024c0025t0001g0026a0042c0195t0001g0023others(9): Show | 12 | HG01517.hp2 HG02055.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.6164+184A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 51/93 | chr1 | 149520867 | ||||||
| chr1:149520871
|
A | G | 103 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(100): Show | 104 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.6164+188A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 51/93 | chr1 | 149520871 | ||||||
| chr1:149520872
|
C | T | 7 | a0183c0041t0002g0246a0188c0051t0002g0252a0190c0049t0002g0244others(4): Show | 7 | HG00438.hp2 NA18946.hp2 NA18954.hp2 others(4): Show |
intron_variant | MODIFIER | c.6164+189C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 51/93 | chr1 | 149520872 | ||||||
| chr1:149520991
|
G | T | 6 | a0180c0072t0002g0218a0181c0073t0002g0272a0184c0042t0002g0236others(3): Show | 6 | HG03831.hp1 HG04204.hp1 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.6164+308G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 51/93 | chr1 | 149520991 | ||||||
| chr1:149520994
|
A | G | 2 | a0006c0211t0019g0211a0044c0210t0004g0206 | 2 | HG02895.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.6164+311A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 51/93 | chr1 | 149520994 | ||||||
| chr1:149521011
|
G | C | 2 | a0049c0082t0011g0096a0080c0106t0001g0019 | 2 | HG02738.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.6165-308G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 51/93 | chr1 | 149521011 | ||||||
| chr1:149521043
|
C | T | 1 | a0134c0164t0001g0039 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.6165-276C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 51/93 | chr1 | 149521043 | ||||||
| chr1:149521048
|
C | G | 2 | a0170c0208t0004g0202a0171c0207t0004g0208 | 2 | HG02698.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.6165-271C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 51/93 | chr1 | 149521048 | ||||||
| chr1:149521104
|
GTC | G | 204 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(201): Show | 207 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.6165-193_6165-192d others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 51/93 | INFO_REALIGN_3_PRIME | chr1 | 149521104 | |||||
| chr1:149521104
|
GTCTCTC | G | 17 | a0008c0037t0001g0075a0008c0037t0001g0135a0008c0215t0001g0067others(14): Show | 17 | HG00741.hp1 HG01099.hp1 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.6165-197_6165-192d others(8): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 51/93 | INFO_REALIGN_3_PRIME | chr1 | 149521104 | |||||
| chr1:149521110
|
C | CTCTCTCT others(19024): Show |
1 | a0172c0204t0004g0268 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.6165-194_6165-193i others(19033): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 51/93 | INFO_REALIGN_3_PRIME | chr1 | 149521110 | |||||
| chr1:149521110
|
C | CTCTCTCT others(14236): Show |
1 | a0017c0019t0001g0112 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.6165-194_6165-193i others(14245): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 51/93 | INFO_REALIGN_3_PRIME | chr1 | 149521110 | |||||
| chr1:149521110
|
C | CTCTCTCT others(14238): Show |
1 | a0017c0019t0001g0167 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.6165-194_6165-193i others(14247): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 51/93 | INFO_REALIGN_3_PRIME | chr1 | 149521110 | |||||
| chr1:149521154
|
T | A | 1 | a0020c0020t0010g0043 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.6165-165T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 51/93 | chr1 | 149521154 | ||||||
| chr1:149521156
|
G | A | 2 | a0050c0080t0001g0177a0052c0079t0021g0176 | 2 | HG01978.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.6165-163G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 51/93 | chr1 | 149521156 | ||||||
| chr1:149521172
|
A | C | 14 | a0019c0021t0001g0098a0020c0020t0001g0041a0020c0020t0010g0043others(11): Show | 14 | HG01074.hp2 HG01952.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.6165-147A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 51/93 | chr1 | 149521172 | ||||||
| chr1:149521183
|
A | G | 3 | a0028c0032t0001g0036a0047c0216t0001g0068a0137c0173t0001g0159 | 3 | HG01934.hp2 HG03225.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.6165-136A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 51/93 | chr1 | 149521183 | ||||||
| chr1:149521193
|
A | C | 78 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(75): Show | 79 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.6165-126A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 51/93 | chr1 | 149521193 | ||||||
| chr1:149521201
|
A | C | 1 | a0043c0209t0004g0207 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.6165-118A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 51/93 | chr1 | 149521201 | ||||||
| chr1:149521240
|
G | A | 2 | a0119c0153t0001g0097a0186c0044t0017g0239 | 2 | HG02602.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.6165-79G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 51/93 | chr1 | 149521240 | ||||||
| chr1:149521269
|
C | CGGTTTCT others(9510): Show |
1 | a0028c0032t0001g0036 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.6337+196_6337+197i others(9519): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 52/93 | INFO_REALIGN_3_PRIME | chr1 | 149521269 | |||||
| chr1:149521269
|
C | CGGTTTCT others(4745): Show |
1 | a0069c0100t0001g0016 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.6337+196_6337+197i others(4754): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 52/93 | INFO_REALIGN_3_PRIME | chr1 | 149521269 | |||||
| chr1:149521269
|
C | CGGTTTCT others(4751): Show |
1 | a0131c0171t0001g0145 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.6337+196_6337+197i others(4760): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 52/93 | INFO_REALIGN_3_PRIME | chr1 | 149521269 | |||||
| chr1:149521269
|
C | T | 37 | a0001c0001t0001g0121a0008c0037t0001g0075a0008c0037t0001g0135others(34): Show | 37 | HG00423.hp2 HG00609.hp2 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.6165-50C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 51/93 | chr1 | 149521269 | ||||||
| chr1:149521479
|
G | GTTGACAT others(14247): Show |
1 | a0167c0203t0028g0269 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.6337+14_6337+15ins others(14254): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 52/93 | INFO_REALIGN_3_PRIME | chr1 | 149521479 | |||||
| chr1:149521506
|
A | G | 1 | a0166c0198t0005g0210 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.6337+15A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 52/93 | chr1 | 149521506 | ||||||
| chr1:149521668
|
G | A | 3 | a0015c0036t0006g0004a0015c0192t0006g0270a0173c0191t0006g0271 | 4 | HG02145.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.6337+177G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 52/93 | chr1 | 149521668 | ||||||
| chr1:149521668
|
G | T | 3 | a0006c0211t0019g0211a0208c0048t0002g0251a0209c0047t0002g0242 | 3 | HG02080.hp2 HG02895.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.6337+177G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 52/93 | chr1 | 149521668 | ||||||
| chr1:149521688
|
C | T | 68 | a0001c0001t0001g0158a0006c0211t0019g0211a0006c0212t0002g0223others(65): Show | 69 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.6337+197C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 52/93 | chr1 | 149521688 | ||||||
| chr1:149521713
|
C | A | 17 | a0008c0037t0001g0075a0008c0037t0001g0135a0008c0215t0001g0067others(14): Show | 17 | HG00741.hp1 HG01496.hp1 HG01928.hp2 others(14): Show |
intron_variant | MODIFIER | c.6337+222C>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 52/93 | chr1 | 149521713 | ||||||
| chr1:149521713
|
C | T | 1 | a0169c0205t0004g0209 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.6337+222C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 52/93 | chr1 | 149521713 | ||||||
| chr1:149521714
|
G | A | 12 | a0006c0212t0002g0223a0006c0213t0002g0224a0036c0014t0009g0228others(9): Show | 12 | HG01891.hp1 HG02080.hp2 HG03831.hp1 others(9): Show |
intron_variant | MODIFIER | c.6337+223G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 52/93 | chr1 | 149521714 | ||||||
| chr1:149521720
|
A | C | 1 | a0179c0071t0002g0260 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.6337+229A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 52/93 | chr1 | 149521720 | ||||||
| chr1:149521729
|
T | C | 1 | a0179c0071t0002g0260 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.6337+238T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 52/93 | chr1 | 149521729 | ||||||
| chr1:149521736
|
A | G | 1 | a0006c0214t0002g0265 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.6337+245A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 52/93 | chr1 | 149521736 | ||||||
| chr1:149521737
|
C | G | 2 | a0161c0197t0005g0214a0162c0196t0005g0213 | 2 | HG00735.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.6337+246C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 52/93 | chr1 | 149521737 | ||||||
| chr1:149521737
|
C | T | 158 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(155): Show | 159 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.6337+246C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 52/93 | chr1 | 149521737 | ||||||
| chr1:149521746
|
G | T | 1 | a0003c0136t0001g0005 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.6337+255G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 52/93 | chr1 | 149521746 | ||||||
| chr1:149521750
|
G | C | 4 | a0168c0206t0004g0203a0169c0205t0004g0209a0172c0204t0004g0268others(1): Show | 4 | HG01099.hp1 HG04115.hp1 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.6337+259G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 52/93 | chr1 | 149521750 | ||||||
| chr1:149521750
|
G | GATGTGAC others(38058): Show |
1 | a0171c0207t0004g0208 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.6338-84_6338-83ins others(38065): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 52/93 | INFO_REALIGN_3_PRIME | chr1 | 149521750 | |||||
| chr1:149521750
|
G | GATGTGAC others(14269): Show |
1 | a0044c0210t0004g0206 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.6338-84_6338-83ins others(14276): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 52/93 | INFO_REALIGN_3_PRIME | chr1 | 149521750 | |||||
| chr1:149521766
|
A | G | 28 | a0001c0001t0001g0158a0032c0012t0002g0232a0032c0012t0002g0266others(25): Show | 28 | HG00621.hp1 HG00642.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.6337+275A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 52/93 | chr1 | 149521766 | ||||||
| chr1:149521766
|
A | T | 1 | a0143c0179t0001g0021 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.6337+275A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 52/93 | chr1 | 149521766 | ||||||
| chr1:149521907
|
A | G | 1 | a0051c0083t0001g0162 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.6338-304A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 52/93 | chr1 | 149521907 | ||||||
| chr1:149521994
|
G | A | 1 | a0135c0161t0001g0057 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.6338-217G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 52/93 | chr1 | 149521994 | ||||||
| chr1:149522028
|
C | T | 1 | a0027c0029t0001g0061 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.6338-183C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 52/93 | chr1 | 149522028 | ||||||
| chr1:149522043
|
A | G | 14 | a0031c0028t0003g0180a0031c0028t0003g0194a0089c0123t0001g0164others(11): Show | 14 | HG01074.hp1 HG01081.hp2 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.6338-168A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 52/93 | chr1 | 149522043 | ||||||
| chr1:149522114
|
A | T | 5 | a0035c0015t0002g0216a0035c0015t0002g0217a0191c0054t0002g0264others(2): Show | 5 | HG02155.hp1 HG03017.hp2 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.6338-97A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 52/93 | chr1 | 149522114 | ||||||
| chr1:149522127
|
C | T | 69 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(66): Show | 69 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.6338-84C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 52/93 | chr1 | 149522127 | ||||||
| chr1:149522128
|
C | T | 69 | a0001c0001t0001g0158a0006c0211t0019g0211a0006c0212t0002g0223others(66): Show | 70 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.6338-83C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 52/93 | chr1 | 149522128 | ||||||
| chr1:149522144
|
A | G | 1 | a0006c0214t0002g0265 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.6338-67A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 52/93 | chr1 | 149522144 | ||||||
| chr1:149522159
|
G | T | 5 | a0180c0072t0002g0218a0181c0073t0002g0272a0184c0042t0002g0236others(2): Show | 5 | HG03831.hp1 HG04204.hp1 NA18747.hp2 others(2): Show |
intron_variant | MODIFIER | c.6338-52G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 52/93 | chr1 | 149522159 | ||||||
| chr1:149522194
|
G | T | 1 | a0166c0198t0005g0210 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.6338-17G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 52/93 | chr1 | 149522194 | ||||||
| chr1:149522270
|
T | A | 1 | a0004c0026t0001g0008 | 1 | HG01891.hp2 | splice_region_variant&intron_variant | LOW | c.6389+8T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 53/93 | chr1 | 149522270 | ||||||
| chr1:149522293
|
C | T | 1 | a0197c0066t0002g0238 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.6389+31C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 53/93 | chr1 | 149522293 | ||||||
| chr1:149522341
|
T | C | 1 | a0006c0214t0002g0265 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.6389+79T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 53/93 | chr1 | 149522341 | ||||||
| chr1:149522441
|
A | T | 33 | a0001c0001t0001g0158a0006c0211t0019g0211a0006c0212t0002g0223others(30): Show | 33 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.6389+179A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 53/93 | chr1 | 149522441 | ||||||
| chr1:149522466
|
A | T | 12 | a0180c0072t0002g0218a0181c0073t0002g0272a0183c0041t0002g0246others(9): Show | 12 | HG00438.hp2 HG03831.hp1 HG04204.hp1 others(9): Show |
intron_variant | MODIFIER | c.6389+204A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 53/93 | chr1 | 149522466 | ||||||
| chr1:149522494
|
G | T | 21 | a0032c0012t0002g0232a0032c0012t0002g0266a0033c0011t0002g0254others(18): Show | 21 | HG00621.hp1 HG00642.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.6389+232G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 53/93 | chr1 | 149522494 | ||||||
| chr1:149522501
|
A | G | 12 | a0180c0072t0002g0218a0181c0073t0002g0272a0183c0041t0002g0246others(9): Show | 12 | HG00438.hp2 HG03831.hp1 HG04204.hp1 others(9): Show |
intron_variant | MODIFIER | c.6389+239A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 53/93 | chr1 | 149522501 | ||||||
| chr1:149522514
|
T | A | 21 | a0032c0012t0002g0232a0032c0012t0002g0266a0033c0011t0002g0254others(18): Show | 21 | HG00621.hp1 HG00642.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.6389+252T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 53/93 | chr1 | 149522514 | ||||||
| chr1:149522556
|
C | T | 1 | a0011c0010t0001g0012 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.6389+294C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 53/93 | chr1 | 149522556 | ||||||
| chr1:149522557
|
G | A | 2 | a0047c0216t0001g0068a0137c0173t0001g0159 | 2 | HG01934.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.6389+295G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 53/93 | chr1 | 149522557 | ||||||
| chr1:149522607
|
A | T | 1 | a0006c0214t0002g0265 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.6390-258A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 53/93 | chr1 | 149522607 | ||||||
| chr1:149522618
|
C | T | 1 | a0006c0214t0002g0265 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.6390-247C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 53/93 | chr1 | 149522618 | ||||||
| chr1:149522644
|
C | CCT | 39 | a0006c0211t0019g0211a0006c0212t0002g0223a0006c0213t0002g0224others(36): Show | 39 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.6390-201_6390-200d others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 53/93 | INFO_REALIGN_3_PRIME | chr1 | 149522644 | |||||
| chr1:149522644
|
C | CCTCT | 8 | a0036c0014t0009g0228a0036c0014t0009g0230a0043c0209t0004g0207others(5): Show | 8 | HG00735.hp1 HG02040.hp2 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.6390-203_6390-200d others(6): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 53/93 | INFO_REALIGN_3_PRIME | chr1 | 149522644 | |||||
| chr1:149522644
|
C | CCTCTCTC others(3): Show |
1 | a0006c0214t0002g0265 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.6390-209_6390-200d others(12): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 53/93 | INFO_REALIGN_3_PRIME | chr1 | 149522644 | |||||
| chr1:149522644
|
C | CCTCTCTC others(4755): Show |
1 | a0001c0001t0001g0158 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.6390-200_6390-199i others(4764): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 53/93 | INFO_REALIGN_3_PRIME | chr1 | 149522644 | |||||
| chr1:149522644
|
CCT | C | 45 | a0003c0003t0001g0115a0003c0003t0001g0116a0003c0003t0001g0117others(42): Show | 45 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.6390-201_6390-200d others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 53/93 | INFO_REALIGN_3_PRIME | chr1 | 149522644 | |||||
| chr1:149522644
|
CCTCTCT | C | 3 | a0015c0036t0006g0004a0015c0192t0006g0270a0173c0191t0006g0271 | 4 | HG02145.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.6390-205_6390-200d others(8): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 53/93 | INFO_REALIGN_3_PRIME | chr1 | 149522644 | |||||
| chr1:149522694
|
T | C | 33 | a0001c0001t0001g0158a0006c0211t0019g0211a0006c0212t0002g0223others(30): Show | 33 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.6390-171T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 53/93 | chr1 | 149522694 | ||||||
| chr1:149522709
|
G | T | 2 | a0043c0209t0004g0207a0164c0201t0004g0205 | 2 | HG00735.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.6390-156G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 53/93 | chr1 | 149522709 | ||||||
| chr1:149522714
|
T | C | 2 | a0163c0199t0005g0215a0165c0200t0005g0212 | 2 | HG00544.hp2 HG00558.hp2 |
intron_variant | MODIFIER | c.6390-151T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 53/93 | chr1 | 149522714 | ||||||
| chr1:149522732
|
A | T | 1 | a0154c0185t0001g0152 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.6390-133A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 53/93 | chr1 | 149522732 | ||||||
| chr1:149522741
|
C | A | 1 | a0099c0146t0001g0034 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.6390-124C>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 53/93 | chr1 | 149522741 | ||||||
| chr1:149522754
|
T | C | 1 | a0198c0059t0002g0259 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.6390-111T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 53/93 | chr1 | 149522754 | ||||||
| chr1:149522793
|
A | C | 3 | a0006c0212t0002g0223a0006c0213t0002g0224a0006c0214t0002g0265 | 3 | HG01891.hp1 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.6390-72A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 53/93 | chr1 | 149522793 | ||||||
| chr1:149522800
|
C | G | 8 | a0006c0211t0019g0211a0043c0209t0004g0207a0161c0197t0005g0214others(5): Show | 8 | HG00544.hp2 HG00558.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.6390-65C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 53/93 | chr1 | 149522800 | ||||||
| chr1:149522861
|
C | T | 12 | a0036c0014t0009g0228a0036c0014t0009g0230a0185c0043t0002g0247others(9): Show | 12 | HG00621.hp2 HG02040.hp2 HG02080.hp2 others(9): Show |
splice_region_variant&intron_variant | LOW | c.6390-4C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 53/93 | chr1 | 149522861 | ||||||
| chr1:149523139
|
G | A | 2 | a0163c0199t0005g0215a0165c0200t0005g0212 | 2 | HG00544.hp2 HG00558.hp2 |
intron_variant | MODIFIER | c.6562+102G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 54/93 | chr1 | 149523139 | ||||||
| chr1:149523142
|
G | A | 2 | a0047c0216t0001g0068a0137c0173t0001g0159 | 2 | HG01934.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.6562+105G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 54/93 | chr1 | 149523142 | ||||||
| chr1:149523155
|
A | G | 1 | a0027c0029t0001g0061 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.6562+118A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 54/93 | chr1 | 149523155 | ||||||
| chr1:149523161
|
G | A | 1 | a0197c0066t0002g0238 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.6562+124G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 54/93 | chr1 | 149523161 | ||||||
| chr1:149523234
|
A | T | 21 | a0032c0012t0002g0232a0032c0012t0002g0266a0033c0011t0002g0254others(18): Show | 21 | HG00621.hp1 HG00642.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.6562+197A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 54/93 | chr1 | 149523234 | ||||||
| chr1:149523235
|
T | C | 2 | a0163c0199t0005g0215a0165c0200t0005g0212 | 2 | HG00544.hp2 HG00558.hp2 |
intron_variant | MODIFIER | c.6562+198T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 54/93 | chr1 | 149523235 | ||||||
| chr1:149523256
|
T | C | 38 | a0008c0037t0001g0075a0008c0037t0001g0135a0008c0215t0001g0067others(35): Show | 38 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.6562+219T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 54/93 | chr1 | 149523256 | ||||||
| chr1:149523264
|
C | T | 1 | a0170c0208t0004g0202 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.6562+227C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 54/93 | chr1 | 149523264 | ||||||
| chr1:149523294
|
G | A | 1 | a0077c0110t0001g0178 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.6562+257G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 54/93 | chr1 | 149523294 | ||||||
| chr1:149523302
|
T | C | 54 | a0003c0003t0001g0115a0003c0003t0001g0116a0003c0003t0001g0117others(51): Show | 55 | HG00544.hp1 HG00621.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.6562+265T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 54/93 | chr1 | 149523302 | ||||||
| chr1:149523313
|
C | G | 2 | a0102c0144t0001g0127a0127c0169t0001g0052 | 2 | HG00423.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.6562+276C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 54/93 | chr1 | 149523313 | ||||||
| chr1:149523343
|
G | A | 71 | a0006c0211t0019g0211a0006c0212t0002g0223a0006c0213t0002g0224others(68): Show | 72 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.6562+306G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 54/93 | chr1 | 149523343 | ||||||
| chr1:149523381
|
C | G | 2 | a0043c0209t0004g0207a0164c0201t0004g0205 | 2 | HG00735.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.6562+344C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 54/93 | chr1 | 149523381 | ||||||
| chr1:149523539
|
A | T | 4 | a0161c0197t0005g0214a0162c0196t0005g0213a0163c0199t0005g0215others(1): Show | 4 | HG00558.hp2 HG00735.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.6563-208A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 54/93 | chr1 | 149523539 | ||||||
| chr1:149523810
|
G | A | 148 | a0001c0001t0001g0121a0001c0001t0001g0158a0002c0002t0003g0182others(145): Show | 149 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(146): Show |
intron_variant | MODIFIER | c.6614+12G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 55/93 | chr1 | 149523810 | ||||||
| chr1:149523848
|
C | A | 2 | a0047c0216t0001g0068a0137c0173t0001g0159 | 2 | HG01934.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.6614+50C>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 55/93 | chr1 | 149523848 | ||||||
| chr1:149523868
|
G | C | 26 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(23): Show | 26 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(23): Show |
intron_variant | MODIFIER | c.6614+70G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 55/93 | chr1 | 149523868 | ||||||
| chr1:149523925
|
A | G | 1 | a0163c0199t0005g0215 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.6614+127A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 55/93 | chr1 | 149523925 | ||||||
| chr1:149523958
|
G | A | 3 | a0021c0022t0001g0080a0021c0022t0001g0169a0078c0111t0001g0102 | 3 | HG02280.hp2 HG03209.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.6614+160G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 55/93 | chr1 | 149523958 | ||||||
| chr1:149523959
|
G | C | 1 | a0166c0198t0005g0210 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.6614+161G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 55/93 | chr1 | 149523959 | ||||||
| chr1:149523984
|
A | C | 2 | a0036c0014t0009g0228a0036c0014t0009g0230 | 2 | NA18960.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.6614+186A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 55/93 | chr1 | 149523984 | ||||||
| chr1:149524002
|
G | C | 17 | a0003c0003t0001g0115a0003c0003t0001g0116a0003c0003t0001g0170others(14): Show | 17 | HG00544.hp1 HG00733.hp1 HG01516.hp2 others(14): Show |
intron_variant | MODIFIER | c.6614+204G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 55/93 | chr1 | 149524002 | ||||||
| chr1:149524036
|
C | T | 10 | a0036c0014t0009g0228a0036c0014t0009g0230a0063c0090t0003g0187others(7): Show | 10 | HG00621.hp1 HG01257.hp2 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.6614+238C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 55/93 | chr1 | 149524036 | ||||||
| chr1:149524043
|
G | A | 131 | a0001c0001t0001g0121a0001c0001t0001g0158a0002c0002t0003g0182others(128): Show | 132 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.6614+245G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 55/93 | chr1 | 149524043 | ||||||
| chr1:149524055
|
G | A | 1 | a0107c0138t0001g0072 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.6614+257G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 55/93 | chr1 | 149524055 | ||||||
| chr1:149524123
|
A | C | 1 | a0181c0073t0002g0272 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.6615-322A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 55/93 | chr1 | 149524123 | ||||||
| chr1:149524128
|
C | T | 5 | a0035c0015t0002g0216a0035c0015t0002g0217a0144c0178t0001g0119others(2): Show | 5 | HG02129.hp1 HG02155.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.6615-317C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 55/93 | chr1 | 149524128 | ||||||
| chr1:149524184
|
C | T | 1 | a0143c0179t0001g0021 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.6615-261C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 55/93 | chr1 | 149524184 | ||||||
| chr1:149524186
|
T | TTC | 5 | a0002c0002t0003g0196a0006c0213t0002g0224a0006c0214t0002g0265others(2): Show | 5 | HG02809.hp2 NA18962.hp1 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.6615-245_6615-244d others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 55/93 | INFO_REALIGN_3_PRIME | chr1 | 149524186 | |||||
| chr1:149524186
|
TTC | T | 3 | a0041c0217t0003g0185a0202c0064t0002g0262a0203c0065t0002g0240 | 3 | HG00438.hp2 HG02165.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.6615-245_6615-244d others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 55/93 | INFO_REALIGN_3_PRIME | chr1 | 149524186 | |||||
| chr1:149524192
|
CTCTCTCT others(3): Show |
C | 1 | a0006c0212t0002g0223 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.6615-251_6615-242d others(12): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 55/93 | INFO_REALIGN_3_PRIME | chr1 | 149524192 | |||||
| chr1:149524196
|
CTCTCTGT others(13): Show |
C | 34 | a0003c0003t0001g0115a0003c0003t0001g0116a0003c0003t0001g0117others(31): Show | 34 | HG00544.hp1 HG00621.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.6615-247_6615-228d others(22): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 55/93 | INFO_REALIGN_3_PRIME | chr1 | 149524196 | |||||
| chr1:149524198
|
C | G | 2 | a0180c0072t0002g0218a0181c0073t0002g0272 | 2 | HG03831.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.6615-247C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 55/93 | chr1 | 149524198 | ||||||
| chr1:149524200
|
C | CTCTCTGT others(3): Show |
1 | a0171c0207t0004g0208 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.6615-244_6615-243i others(12): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 55/93 | INFO_REALIGN_3_PRIME | chr1 | 149524200 | |||||
| chr1:149524200
|
C | CTCTCTGT others(5): Show |
4 | a0015c0036t0006g0004a0015c0192t0006g0270a0069c0100t0001g0016others(1): Show | 5 | HG02145.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.6615-244_6615-243i others(14): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 55/93 | INFO_REALIGN_3_PRIME | chr1 | 149524200 | |||||
| chr1:149524200
|
C | CTCTG | 9 | a0029c0033t0001g0197a0029c0033t0001g0198a0035c0015t0002g0216others(6): Show | 9 | HG00735.hp1 HG02155.hp1 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.6615-244_6615-243i others(6): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 55/93 | INFO_REALIGN_3_PRIME | chr1 | 149524200 | |||||
| chr1:149524200
|
C | CTCTGTG | 8 | a0002c0002t0007g0190a0002c0002t0007g0193a0006c0211t0019g0211others(5): Show | 8 | HG01934.hp2 HG02895.hp1 HG03209.hp2 others(5): Show |
intron_variant | MODIFIER | c.6615-244_6615-243i others(8): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 55/93 | INFO_REALIGN_3_PRIME | chr1 | 149524200 | |||||
| chr1:149524200
|
C | CTCTGTGT others(1): Show |
4 | a0002c0002t0003g0182a0002c0002t0003g0189a0063c0090t0003g0187others(1): Show | 4 | NA18961.hp2 NA18980.hp2 NA19082.hp2 others(1): Show |
intron_variant | MODIFIER | c.6615-244_6615-243i others(10): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 55/93 | INFO_REALIGN_3_PRIME | chr1 | 149524200 | |||||
| chr1:149524200
|
C | CTCTGTGT others(3): Show |
5 | a0002c0002t0003g0188a0012c0009t0001g0050a0071c0102t0001g0143others(2): Show | 5 | HG00609.hp2 HG03098.hp2 NA19005.hp1 others(2): Show |
intron_variant | MODIFIER | c.6615-244_6615-243i others(12): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 55/93 | INFO_REALIGN_3_PRIME | chr1 | 149524200 | |||||
| chr1:149524200
|
C | CTCTGTGT others(5): Show |
9 | a0008c0215t0001g0067a0011c0010t0001g0011a0012c0009t0001g0172others(6): Show | 9 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(6): Show |
intron_variant | MODIFIER | c.6615-244_6615-243i others(14): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 55/93 | INFO_REALIGN_3_PRIME | chr1 | 149524200 | |||||
| chr1:149524200
|
C | CTCTGTGT others(7): Show |
6 | a0008c0037t0001g0075a0008c0037t0001g0135a0011c0010t0001g0010others(3): Show | 6 | HG00741.hp1 HG01928.hp2 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.6615-244_6615-243i others(16): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 55/93 | INFO_REALIGN_3_PRIME | chr1 | 149524200 | |||||
| chr1:149524200
|
C | CTCTGTGT others(13): Show |
2 | a0022c0023t0001g0160a0118c0151t0001g0053 | 2 | HG02572.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.6615-244_6615-243i others(22): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 55/93 | INFO_REALIGN_3_PRIME | chr1 | 149524200 | |||||
| chr1:149524200
|
C | CTG | 26 | a0001c0001t0001g0071a0017c0019t0001g0112a0017c0019t0001g0167others(23): Show | 26 | HG00544.hp2 HG01074.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.6615-199_6615-198d others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 55/93 | INFO_REALIGN_3_PRIME | chr1 | 149524200 | |||||
| chr1:149524200
|
C | CTGTG | 6 | a0018c0018t0001g0166a0057c0088t0001g0089a0080c0106t0001g0019others(3): Show | 6 | HG02257.hp1 HG02809.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.6615-201_6615-198d others(6): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 55/93 | INFO_REALIGN_3_PRIME | chr1 | 149524200 | |||||
| chr1:149524200
|
C | CTGTGTG | 9 | a0023c0024t0001g0003a0076c0109t0001g0137a0092c0120t0001g0141others(6): Show | 10 | HG00735.hp2 HG01081.hp2 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.6615-203_6615-198d others(8): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 55/93 | INFO_REALIGN_3_PRIME | chr1 | 149524200 | |||||
| chr1:149524200
|
C | CTGTGTGT others(1): Show |
6 | a0009c0006t0001g0081a0054c0085t0001g0150a0073c0103t0001g0018others(3): Show | 6 | HG00099.hp1 HG02040.hp1 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.6615-205_6615-198d others(10): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 55/93 | INFO_REALIGN_3_PRIME | chr1 | 149524200 | |||||
| chr1:149524200
|
C | CTGTGTGT others(3): Show |
3 | a0131c0171t0001g0145a0132c0166t0012g0179a0144c0178t0001g0119 | 3 | HG02129.hp1 HG02135.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.6615-207_6615-198d others(12): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 55/93 | INFO_REALIGN_3_PRIME | chr1 | 149524200 | |||||
| chr1:149524200
|
C | CTGTGTGT others(5): Show |
2 | a0001c0001t0001g0121a0070c0101t0001g0044 | 2 | HG02027.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.6615-209_6615-198d others(14): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 55/93 | INFO_REALIGN_3_PRIME | chr1 | 149524200 | |||||
| chr1:149524200
|
C | CTGTGTGT others(4694): Show |
1 | a0139c0172t0001g0105 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.6615-198_6615-197i others(4703): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 55/93 | INFO_REALIGN_3_PRIME | chr1 | 149524200 | |||||
| chr1:149524200
|
C | CTGTGTGT others(9521): Show |
1 | a0009c0006t0001g0082 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.6615-198_6615-197i others(9530): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 55/93 | INFO_REALIGN_3_PRIME | chr1 | 149524200 | |||||
| chr1:149524200
|
C | CTGTGTGT others(9535): Show |
1 | a0009c0006t0001g0139 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.6615-198_6615-197i others(9544): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 55/93 | INFO_REALIGN_3_PRIME | chr1 | 149524200 | |||||
| chr1:149524200
|
C | G | 9 | a0115c0149t0026g0142a0180c0072t0002g0218a0181c0073t0002g0272others(6): Show | 9 | HG02083.hp1 HG03831.hp1 HG04204.hp1 others(6): Show |
intron_variant | MODIFIER | c.6615-245C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 55/93 | chr1 | 149524200 | ||||||
| chr1:149524200
|
CTG | C | 37 | a0001c0001t0001g0070a0001c0001t0001g0077a0001c0001t0001g0078others(34): Show | 37 | HG00099.hp2 HG00621.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.6615-199_6615-198d others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 55/93 | INFO_REALIGN_3_PRIME | chr1 | 149524200 | |||||
| chr1:149524200
|
CTGTG | C | 8 | a0005c0004t0025g0073a0025c0031t0001g0032a0056c0089t0001g0060others(5): Show | 8 | HG00408.hp1 HG03017.hp1 HG03669.hp1 others(5): Show |
intron_variant | MODIFIER | c.6615-201_6615-198d others(6): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 55/93 | INFO_REALIGN_3_PRIME | chr1 | 149524200 | |||||
| chr1:149524200
|
CTGTGTG | C | 11 | a0016c0017t0001g0028a0016c0017t0001g0029a0059c0091t0001g0130others(8): Show | 11 | HG00423.hp1 HG00733.hp2 HG01978.hp2 others(8): Show |
intron_variant | MODIFIER | c.6615-203_6615-198d others(8): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 55/93 | INFO_REALIGN_3_PRIME | chr1 | 149524200 | |||||
| chr1:149524200
|
CTGTGTGT others(1): Show |
C | 4 | a0005c0004t0001g0056a0005c0004t0001g0131a0005c0004t0001g0132others(1): Show | 4 | NA18977.hp1 NA18985.hp1 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.6615-205_6615-198d others(10): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 55/93 | INFO_REALIGN_3_PRIME | chr1 | 149524200 | |||||
| chr1:149524200
|
CTGTGTGT others(5): Show |
C | 2 | a0098c0147t0001g0031a0108c0143t0001g0027 | 2 | HG00738.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.6615-209_6615-198d others(14): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 55/93 | INFO_REALIGN_3_PRIME | chr1 | 149524200 | |||||
| chr1:149524200
|
CTGTGTGT others(7): Show |
C | 1 | a0167c0203t0028g0269 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.6615-211_6615-198d others(16): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 55/93 | INFO_REALIGN_3_PRIME | chr1 | 149524200 | |||||
| chr1:149524200
|
CTGTGTGT others(9): Show |
C | 1 | a0081c0113t0001g0148 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.6615-213_6615-198d others(18): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 55/93 | INFO_REALIGN_3_PRIME | chr1 | 149524200 | |||||
| chr1:149524202
|
G | C | 17 | a0001c0001t0001g0158a0004c0026t0001g0008a0004c0027t0001g0001others(14): Show | 18 | HG01099.hp1 HG01517.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.6615-243G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 55/93 | chr1 | 149524202 | ||||||
| chr1:149524204
|
G | C | 25 | a0004c0026t0001g0007a0013c0035t0001g0084a0014c0008t0003g0181others(22): Show | 25 | HG00621.hp1 HG00642.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.6615-241G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 55/93 | chr1 | 149524204 | ||||||
| chr1:149524205
|
T | A | 2 | a0029c0033t0001g0197a0029c0033t0001g0198 | 2 | HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.6615-240T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 55/93 | chr1 | 149524205 | ||||||
| chr1:149524207
|
T | A | 1 | a0028c0032t0001g0161 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.6615-238T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 55/93 | chr1 | 149524207 | ||||||
| chr1:149524209
|
T | A | 1 | a0001c0001t0001g0158 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.6615-236T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 55/93 | chr1 | 149524209 | ||||||
| chr1:149524215
|
T | C | 1 | a0006c0211t0019g0211 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.6615-230T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 55/93 | chr1 | 149524215 | ||||||
| chr1:149524216
|
G | C | 1 | a0167c0203t0028g0269 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.6615-229G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 55/93 | chr1 | 149524216 | ||||||
| chr1:149524218
|
G | C | 2 | a0081c0113t0001g0148a0167c0203t0028g0269 | 2 | HG02109.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.6615-227G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 55/93 | chr1 | 149524218 | ||||||
| chr1:149524219
|
T | C | 2 | a0199c0061t0002g0219a0200c0062t0002g0237 | 2 | HG02155.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.6615-226T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 55/93 | chr1 | 149524219 | ||||||
| chr1:149524221
|
T | C | 3 | a0035c0015t0002g0216a0035c0015t0002g0217a0047c0216t0001g0068 | 3 | HG01934.hp2 HG03017.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.6615-224T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 55/93 | chr1 | 149524221 | ||||||
| chr1:149524223
|
T | C | 20 | a0032c0012t0002g0232a0032c0012t0002g0266a0033c0011t0002g0254others(17): Show | 20 | HG00621.hp1 HG00642.hp1 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.6615-222T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 55/93 | chr1 | 149524223 | ||||||
| chr1:149524225
|
T | C | 3 | a0006c0212t0002g0223a0006c0213t0002g0224a0006c0214t0002g0265 | 3 | HG01891.hp1 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.6615-220T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 55/93 | chr1 | 149524225 | ||||||
| chr1:149524227
|
T | C | 17 | a0032c0012t0002g0232a0032c0012t0002g0266a0033c0011t0002g0254others(14): Show | 17 | HG00621.hp1 HG00642.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.6615-218T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 55/93 | chr1 | 149524227 | ||||||
| chr1:149524230
|
G | C | 33 | a0003c0003t0001g0115a0003c0003t0001g0116a0003c0003t0001g0117others(30): Show | 33 | HG00544.hp1 HG00621.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.6615-215G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 55/93 | chr1 | 149524230 | ||||||
| chr1:149524234
|
G | A | 1 | a0163c0199t0005g0215 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.6615-211G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 55/93 | chr1 | 149524234 | ||||||
| chr1:149524240
|
G | T | 2 | a0043c0209t0004g0207a0164c0201t0004g0205 | 2 | HG00735.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.6615-205G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 55/93 | chr1 | 149524240 | ||||||
| chr1:149524249
|
T | C | 30 | a0006c0211t0019g0211a0006c0212t0002g0223a0006c0213t0002g0224others(27): Show | 30 | HG00558.hp2 HG00621.hp1 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.6615-196T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 55/93 | chr1 | 149524249 | ||||||
| chr1:149524324
|
A | C | 4 | a0186c0044t0017g0239a0193c0057t0002g0006a0204c0067t0002g0248others(1): Show | 4 | HG02040.hp2 HG02129.hp2 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.6615-121A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 55/93 | chr1 | 149524324 | ||||||
| chr1:149524333
|
T | A | 1 | a0160c0076t0014g0225 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.6615-112T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 55/93 | chr1 | 149524333 | ||||||
| chr1:149524334
|
C | G | 6 | a0180c0072t0002g0218a0181c0073t0002g0272a0191c0054t0002g0264others(3): Show | 6 | HG00438.hp2 HG03831.hp1 HG04204.hp1 others(3): Show |
intron_variant | MODIFIER | c.6615-111C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 55/93 | chr1 | 149524334 | ||||||
| chr1:149524345
|
G | C | 20 | a0036c0014t0009g0228a0036c0014t0009g0230a0166c0198t0005g0210others(17): Show | 20 | HG00438.hp2 HG00621.hp2 HG02040.hp2 others(17): Show |
intron_variant | MODIFIER | c.6615-100G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 55/93 | chr1 | 149524345 | ||||||
| chr1:149524362
|
C | T | 14 | a0036c0014t0009g0228a0036c0014t0009g0230a0166c0198t0005g0210others(11): Show | 14 | HG00621.hp2 HG02040.hp2 HG02080.hp2 others(11): Show |
intron_variant | MODIFIER | c.6615-83C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 55/93 | chr1 | 149524362 | ||||||
| chr1:149524409
|
C | G | 1 | a0165c0200t0005g0212 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.6615-36C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 55/93 | chr1 | 149524409 | ||||||
| chr1:149524427
|
T | G | 13 | a0036c0014t0009g0228a0036c0014t0009g0230a0185c0043t0002g0247others(10): Show | 13 | HG00621.hp2 HG02040.hp2 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.6615-18T>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 55/93 | chr1 | 149524427 | ||||||
| chr1:149524647
|
AT | A | 6 | a0014c0008t0003g0181a0014c0008t0003g0186a0014c0008t0020g0184others(3): Show | 6 | HG00642.hp2 HG01071.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.6787+31delT | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 56/93 | chr1 | 149524647 | ||||||
| chr1:149524661
|
C | T | 2 | a0161c0197t0005g0214a0162c0196t0005g0213 | 2 | HG00735.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.6787+44C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 56/93 | chr1 | 149524661 | ||||||
| chr1:149524686
|
C | A | 3 | a0015c0036t0006g0004a0015c0192t0006g0270a0173c0191t0006g0271 | 4 | HG02145.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.6787+69C>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 56/93 | chr1 | 149524686 | ||||||
| chr1:149524716
|
A | G | 152 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(149): Show | 153 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.6787+99A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 56/93 | chr1 | 149524716 | ||||||
| chr1:149524736
|
T | C | 1 | a0006c0211t0019g0211 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.6787+119T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 56/93 | chr1 | 149524736 | ||||||
| chr1:149524787
|
T | A | 152 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(149): Show | 153 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.6787+170T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 56/93 | chr1 | 149524787 | ||||||
| chr1:149524788
|
G | T | 1 | a0165c0200t0005g0212 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.6787+171G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 56/93 | chr1 | 149524788 | ||||||
| chr1:149524806
|
T | A | 152 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(149): Show | 153 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.6787+189T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 56/93 | chr1 | 149524806 | ||||||
| chr1:149524808
|
G | A | 152 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(149): Show | 153 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.6787+191G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 56/93 | chr1 | 149524808 | ||||||
| chr1:149524840
|
C | T | 1 | a0160c0076t0014g0225 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.6787+223C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 56/93 | chr1 | 149524840 | ||||||
| chr1:149524841
|
A | G | 152 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(149): Show | 153 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.6787+224A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 56/93 | chr1 | 149524841 | ||||||
| chr1:149524843
|
T | C | 152 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(149): Show | 153 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.6787+226T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 56/93 | chr1 | 149524843 | ||||||
| chr1:149524844
|
C | G | 2 | a0165c0200t0005g0212a0167c0203t0028g0269 | 2 | HG00544.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.6787+227C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 56/93 | chr1 | 149524844 | ||||||
| chr1:149524846
|
G | C | 1 | a0101c0039t0001g0079 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.6787+229G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 56/93 | chr1 | 149524846 | ||||||
| chr1:149524849
|
T | C | 152 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(149): Show | 153 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.6787+232T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 56/93 | chr1 | 149524849 | ||||||
| chr1:149524853
|
C | T | 152 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(149): Show | 153 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.6787+236C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 56/93 | chr1 | 149524853 | ||||||
| chr1:149524921
|
C | T | 153 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(150): Show | 154 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.6787+304C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 56/93 | chr1 | 149524921 | ||||||
| chr1:149525005
|
T | G | 17 | a0032c0012t0002g0232a0032c0012t0002g0266a0033c0011t0002g0254others(14): Show | 17 | HG00621.hp1 HG00642.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.6788-327T>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 56/93 | chr1 | 149525005 | ||||||
| chr1:149525016
|
T | A | 5 | a0186c0044t0017g0239a0192c0055t0002g0263a0193c0057t0002g0006others(2): Show | 5 | HG02040.hp2 HG02129.hp2 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.6788-316T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 56/93 | chr1 | 149525016 | ||||||
| chr1:149525022
|
C | T | 88 | a0003c0003t0001g0115a0003c0003t0001g0116a0003c0003t0001g0117others(85): Show | 89 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.6788-310C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 56/93 | chr1 | 149525022 | ||||||
| chr1:149525125
|
A | T | 4 | a0031c0028t0003g0180a0031c0028t0003g0194a0041c0217t0003g0185others(1): Show | 4 | HG02165.hp2 NA18946.hp1 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.6788-207A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 56/93 | chr1 | 149525125 | ||||||
| chr1:149525185
|
C | G | 5 | a0018c0018t0001g0113a0018c0018t0001g0166a0055c0086t0001g0168others(2): Show | 5 | HG02109.hp1 HG02257.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.6788-147C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 56/93 | chr1 | 149525185 | ||||||
| chr1:149525226
|
C | CTTATGCT others(9510): Show |
1 | a0043c0209t0004g0207 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.6788-18_6788-17ins others(9517): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 56/93 | INFO_REALIGN_3_PRIME | chr1 | 149525226 | |||||
| chr1:149525457
|
G | A | 1 | a0105c0140t0001g0037 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.6896+17G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 57/93 | chr1 | 149525457 | ||||||
| chr1:149525510
|
G | A | 1 | a0194c0058t0002g0235 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.6896+70G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 57/93 | chr1 | 149525510 | ||||||
| chr1:149525511
|
A | T | 1 | a0194c0058t0002g0235 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.6896+71A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 57/93 | chr1 | 149525511 | ||||||
| chr1:149525512
|
G | C | 2 | a0042c0195t0001g0023a0144c0178t0001g0119 | 2 | HG02129.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.6896+72G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 57/93 | chr1 | 149525512 | ||||||
| chr1:149525513
|
T | C | 28 | a0014c0008t0003g0181a0014c0008t0003g0186a0014c0008t0020g0184others(25): Show | 28 | HG00621.hp1 HG00642.hp1 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.6896+73T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 57/93 | chr1 | 149525513 | ||||||
| chr1:149525592
|
T | C | 8 | a0043c0209t0004g0207a0044c0210t0004g0206a0168c0206t0004g0203others(5): Show | 8 | HG01099.hp1 HG02165.hp1 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.6896+152T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 57/93 | chr1 | 149525592 | ||||||
| chr1:149525624
|
A | C | 11 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(8): Show | 11 | HG00099.hp2 HG01099.hp2 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.6896+184A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 57/93 | chr1 | 149525624 | ||||||
| chr1:149525628
|
A | G | 47 | a0006c0211t0019g0211a0006c0212t0002g0223a0006c0214t0002g0265others(44): Show | 48 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.6896+188A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 57/93 | chr1 | 149525628 | ||||||
| chr1:149525629
|
C | T | 3 | a0180c0072t0002g0218a0181c0073t0002g0272a0191c0054t0002g0264 | 3 | HG03831.hp1 HG04204.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.6896+189C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 57/93 | chr1 | 149525629 | ||||||
| chr1:149525646
|
A | G | 1 | a0180c0072t0002g0218 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.6896+206A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 57/93 | chr1 | 149525646 | ||||||
| chr1:149525720
|
C | G | 1 | a0195c0060t0002g0229 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.6896+280C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 57/93 | chr1 | 149525720 | ||||||
| chr1:149525731
|
A | G | 1 | a0139c0172t0001g0105 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.6896+291A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 57/93 | chr1 | 149525731 | ||||||
| chr1:149525748
|
G | T | 18 | a0032c0012t0002g0232a0032c0012t0002g0266a0033c0011t0002g0254others(15): Show | 18 | HG00621.hp1 HG00642.hp1 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.6896+308G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 57/93 | chr1 | 149525748 | ||||||
| chr1:149525751
|
A | G | 1 | a0164c0201t0004g0205 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.6896+311A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 57/93 | chr1 | 149525751 | ||||||
| chr1:149525768
|
G | C | 1 | a0117c0152t0001g0087 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.6897-302G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 57/93 | chr1 | 149525768 | ||||||
| chr1:149525805
|
C | G | 2 | a0168c0206t0004g0203a0169c0205t0004g0209 | 2 | HG01099.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.6897-265C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 57/93 | chr1 | 149525805 | ||||||
| chr1:149525843
|
G | C | 2 | a0006c0211t0019g0211a0006c0212t0002g0223 | 2 | HG01891.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.6897-227G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 57/93 | chr1 | 149525843 | ||||||
| chr1:149525849
|
C | G | 2 | a0006c0211t0019g0211a0006c0212t0002g0223 | 2 | HG01891.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.6897-221C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 57/93 | chr1 | 149525849 | ||||||
| chr1:149525861
|
G | C | 1 | a0006c0212t0002g0223 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.6897-209G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 57/93 | chr1 | 149525861 | ||||||
| chr1:149525861
|
G | GTC | 4 | a0013c0035t0001g0038a0013c0035t0001g0084a0013c0162t0001g0040others(1): Show | 4 | HG02129.hp2 HG02258.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.6897-193_6897-192d others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 57/93 | INFO_REALIGN_3_PRIME | chr1 | 149525861 | |||||
| chr1:149525861
|
G | GTCTC | 116 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(113): Show | 117 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.6897-195_6897-192d others(6): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 57/93 | INFO_REALIGN_3_PRIME | chr1 | 149525861 | |||||
| chr1:149525861
|
G | GTCTCTC | 14 | a0006c0213t0002g0224a0019c0021t0001g0098a0036c0014t0009g0228others(11): Show | 14 | HG00735.hp1 HG02080.hp2 HG02738.hp2 others(11): Show |
intron_variant | MODIFIER | c.6897-197_6897-192d others(8): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 57/93 | INFO_REALIGN_3_PRIME | chr1 | 149525861 | |||||
| chr1:149525861
|
G | GTCTCTCT others(3): Show |
2 | a0163c0199t0005g0215a0165c0200t0005g0212 | 2 | HG00544.hp2 HG00558.hp2 |
intron_variant | MODIFIER | c.6897-201_6897-192d others(12): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 57/93 | INFO_REALIGN_3_PRIME | chr1 | 149525861 | |||||
| chr1:149525944
|
A | C | 23 | a0014c0008t0003g0181a0014c0008t0003g0186a0014c0008t0020g0184others(20): Show | 23 | HG00621.hp1 HG00642.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.6897-126A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 57/93 | chr1 | 149525944 | ||||||
| chr1:149526003
|
A | G | 2 | a0053c0190t0001g0064a0109c0135t0001g0063 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.6897-67A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 57/93 | chr1 | 149526003 | ||||||
| chr1:149526020
|
T | C | 132 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(129): Show | 133 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.6897-50T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 57/93 | chr1 | 149526020 | ||||||
| chr1:149526291
|
T | A | 1 | a0167c0203t0028g0269 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.7069+49T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 58/93 | chr1 | 149526291 | ||||||
| chr1:149526337
|
G | A | 1 | a0197c0066t0002g0238 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.7069+95G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 58/93 | chr1 | 149526337 | ||||||
| chr1:149526357
|
C | G | 1 | a0137c0173t0001g0159 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.7069+115C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 58/93 | chr1 | 149526357 | ||||||
| chr1:149526439
|
C | T | 47 | a0006c0212t0002g0223a0006c0213t0002g0224a0006c0214t0002g0265others(44): Show | 48 | HG00438.hp2 HG00621.hp1 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.7069+197C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 58/93 | chr1 | 149526439 | ||||||
| chr1:149526464
|
C | A | 40 | a0001c0001t0001g0158a0003c0003t0001g0115a0003c0003t0001g0116others(37): Show | 40 | HG00544.hp1 HG00621.hp2 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.7069+222C>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 58/93 | chr1 | 149526464 | ||||||
| chr1:149526465
|
G | A | 21 | a0006c0214t0002g0265a0032c0012t0002g0232a0032c0012t0002g0266others(18): Show | 21 | HG00438.hp2 HG00621.hp1 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.7069+223G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 58/93 | chr1 | 149526465 | ||||||
| chr1:149526465
|
G | GCCCTAAT others(4748): Show |
3 | a0035c0015t0002g0216a0035c0015t0002g0217a0199c0061t0002g0219 | 3 | HG03017.hp2 HG03704.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.7069+274_7069+275i others(4757): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 58/93 | INFO_REALIGN_3_PRIME | chr1 | 149526465 | |||||
| chr1:149526487
|
A | G | 2 | a0006c0212t0002g0223a0006c0213t0002g0224 | 2 | HG01891.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.7069+245A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 58/93 | chr1 | 149526487 | ||||||
| chr1:149526488
|
T | C | 86 | a0001c0001t0001g0121a0001c0001t0001g0158a0002c0002t0003g0182others(83): Show | 86 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.7069+246T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 58/93 | chr1 | 149526488 | ||||||
| chr1:149526488
|
T | G | 6 | a0006c0211t0019g0211a0161c0197t0005g0214a0162c0196t0005g0213others(3): Show | 6 | HG00544.hp2 HG00558.hp2 HG00735.hp2 others(3): Show |
intron_variant | MODIFIER | c.7069+246T>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 58/93 | chr1 | 149526488 | ||||||
| chr1:149526501
|
G | C | 1 | a0043c0209t0004g0207 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.7069+259G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 58/93 | chr1 | 149526501 | ||||||
| chr1:149526517
|
A | G | 3 | a0047c0216t0001g0068a0137c0173t0001g0159a0201c0063t0002g0222 | 3 | HG01934.hp2 HG03225.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.7069+275A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 58/93 | chr1 | 149526517 | ||||||
| chr1:149526517
|
A | T | 14 | a0031c0028t0003g0180a0031c0028t0003g0194a0089c0123t0001g0164others(11): Show | 14 | HG01074.hp1 HG01081.hp2 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.7069+275A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 58/93 | chr1 | 149526517 | ||||||
| chr1:149526594
|
G | A | 1 | a0164c0201t0004g0205 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.7069+352G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 58/93 | chr1 | 149526594 | ||||||
| chr1:149526684
|
C | T | 1 | a0169c0205t0004g0209 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.7070-278C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 58/93 | chr1 | 149526684 | ||||||
| chr1:149526794
|
A | G | 19 | a0002c0002t0003g0182a0002c0002t0003g0188a0002c0002t0003g0189others(16): Show | 19 | HG00438.hp1 HG00558.hp1 HG01257.hp2 others(16): Show |
intron_variant | MODIFIER | c.7070-168A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 58/93 | chr1 | 149526794 | ||||||
| chr1:149526829
|
G | A | 3 | a0015c0036t0006g0004a0015c0192t0006g0270a0173c0191t0006g0271 | 4 | HG02145.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.7070-133G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 58/93 | chr1 | 149526829 | ||||||
| chr1:149526876
|
G | T | 1 | a0205c0056t0015g0258 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.7070-86G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 58/93 | chr1 | 149526876 | ||||||
| chr1:149526878
|
C | T | 8 | a0009c0006t0001g0081a0014c0008t0003g0181a0014c0008t0003g0186others(5): Show | 8 | HG00099.hp1 HG00642.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.7070-84C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 58/93 | chr1 | 149526878 | ||||||
| chr1:149526879
|
C | T | 55 | a0006c0211t0019g0211a0006c0212t0002g0223a0006c0213t0002g0224others(52): Show | 56 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.7070-83C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 58/93 | chr1 | 149526879 | ||||||
| chr1:149526895
|
A | G | 1 | a0006c0213t0002g0224 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.7070-67A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 58/93 | chr1 | 149526895 | ||||||
| chr1:149526910
|
G | T | 21 | a0032c0012t0002g0232a0032c0012t0002g0266a0033c0011t0002g0254others(18): Show | 21 | HG00621.hp1 HG00642.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.7070-52G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 58/93 | chr1 | 149526910 | ||||||
| chr1:149526935
|
G | A | 2 | a0083c0116t0023g0103a0134c0164t0001g0039 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.7070-27G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 58/93 | chr1 | 149526935 | ||||||
| chr1:149526937
|
C | G | 1 | a0166c0198t0005g0210 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.7070-25C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 58/93 | chr1 | 149526937 | ||||||
| chr1:149527031
|
T | C | 1 | a0164c0201t0004g0205 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.7121+18T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 59/93 | chr1 | 149527031 | ||||||
| chr1:149527032
|
G | A | 2 | a0161c0197t0005g0214a0162c0196t0005g0213 | 2 | HG00735.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.7121+19G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 59/93 | chr1 | 149527032 | ||||||
| chr1:149527044
|
C | T | 5 | a0186c0044t0017g0239a0193c0057t0002g0006a0204c0067t0002g0248others(2): Show | 5 | HG00621.hp2 HG02040.hp2 HG02129.hp2 others(2): Show |
intron_variant | MODIFIER | c.7121+31C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 59/93 | chr1 | 149527044 | ||||||
| chr1:149527090
|
G | T | 1 | a0196c0045t0018g0226 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.7121+77G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 59/93 | chr1 | 149527090 | ||||||
| chr1:149527092
|
T | C | 1 | a0006c0213t0002g0224 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.7121+79T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 59/93 | chr1 | 149527092 | ||||||
| chr1:149527104
|
T | A | 1 | a0177c0075t0001g0146 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.7121+91T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 59/93 | chr1 | 149527104 | ||||||
| chr1:149527128
|
T | C | 4 | a0001c0001t0001g0158a0028c0032t0001g0161a0029c0033t0001g0197others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.7121+115T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 59/93 | chr1 | 149527128 | ||||||
| chr1:149527169
|
G | A | 6 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(3): Show | 6 | HG00099.hp2 HG01099.hp2 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.7121+156G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 59/93 | chr1 | 149527169 | ||||||
| chr1:149527186
|
C | T | 1 | a0164c0201t0004g0205 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.7121+173C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 59/93 | chr1 | 149527186 | ||||||
| chr1:149527192
|
A | T | 11 | a0006c0213t0002g0224a0006c0214t0002g0265a0008c0037t0001g0075others(8): Show | 11 | HG00735.hp1 HG01928.hp2 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.7121+179A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 59/93 | chr1 | 149527192 | ||||||
| chr1:149527217
|
A | T | 26 | a0032c0012t0002g0232a0032c0012t0002g0266a0033c0011t0002g0254others(23): Show | 26 | HG00621.hp1 HG00642.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.7121+204A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 59/93 | chr1 | 149527217 | ||||||
| chr1:149527234
|
G | T | 1 | a0164c0201t0004g0205 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.7121+221G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 59/93 | chr1 | 149527234 | ||||||
| chr1:149527245
|
G | T | 1 | a0201c0063t0002g0222 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.7121+232G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 59/93 | chr1 | 149527245 | ||||||
| chr1:149527252
|
A | G | 27 | a0006c0212t0002g0223a0032c0012t0002g0232a0032c0012t0002g0266others(24): Show | 27 | HG00621.hp1 HG00642.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.7121+239A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 59/93 | chr1 | 149527252 | ||||||
| chr1:149527265
|
T | A | 1 | a0201c0063t0002g0222 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.7121+252T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 59/93 | chr1 | 149527265 | ||||||
| chr1:149527320
|
G | A | 3 | a0132c0166t0012g0179a0144c0178t0001g0119a0147c0220t0001g0094 | 3 | HG02129.hp1 HG02135.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.7122-294G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 59/93 | chr1 | 149527320 | ||||||
| chr1:149527348
|
C | T | 1 | a0167c0203t0028g0269 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.7122-266C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 59/93 | chr1 | 149527348 | ||||||
| chr1:149527358
|
A | T | 2 | a0006c0213t0002g0224a0006c0214t0002g0265 | 2 | NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.7122-256A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 59/93 | chr1 | 149527358 | ||||||
| chr1:149527369
|
C | T | 2 | a0006c0213t0002g0224a0006c0214t0002g0265 | 2 | NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.7122-245C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 59/93 | chr1 | 149527369 | ||||||
| chr1:149527395
|
C | CCT | 85 | a0001c0001t0001g0121a0001c0001t0001g0158a0002c0002t0003g0182others(82): Show | 85 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.7122-201_7122-200d others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 59/93 | INFO_REALIGN_3_PRIME | chr1 | 149527395 | |||||
| chr1:149527395
|
C | CCTCT | 13 | a0036c0014t0009g0228a0036c0014t0009g0230a0047c0216t0001g0068others(10): Show | 13 | HG00438.hp2 HG01934.hp2 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.7122-203_7122-200d others(6): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 59/93 | INFO_REALIGN_3_PRIME | chr1 | 149527395 | |||||
| chr1:149527395
|
C | CCTCTCT | 4 | a0164c0201t0004g0205a0166c0198t0005g0210a0199c0061t0002g0219others(1): Show | 4 | HG00735.hp1 HG03942.hp2 NA18946.hp2 others(1): Show |
intron_variant | MODIFIER | c.7122-205_7122-200d others(8): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 59/93 | INFO_REALIGN_3_PRIME | chr1 | 149527395 | |||||
| chr1:149527395
|
C | CCTCTCTC others(5): Show |
2 | a0006c0213t0002g0224a0006c0214t0002g0265 | 2 | NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.7122-211_7122-200d others(14): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 59/93 | INFO_REALIGN_3_PRIME | chr1 | 149527395 | |||||
| chr1:149527443
|
T | C | 8 | a0006c0213t0002g0224a0006c0214t0002g0265a0047c0216t0001g0068others(5): Show | 8 | HG00735.hp1 HG01934.hp2 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.7122-171T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 59/93 | chr1 | 149527443 | ||||||
| chr1:149527458
|
G | T | 1 | a0164c0201t0004g0205 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.7122-156G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 59/93 | chr1 | 149527458 | ||||||
| chr1:149527463
|
T | C | 1 | a0163c0199t0005g0215 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.7122-151T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 59/93 | chr1 | 149527463 | ||||||
| chr1:149527469
|
C | A | 1 | a0126c0130t0001g0134 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.7122-145C>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 59/93 | chr1 | 149527469 | ||||||
| chr1:149527542
|
A | C | 2 | a0006c0213t0002g0224a0006c0214t0002g0265 | 2 | NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.7122-72A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 59/93 | chr1 | 149527542 | ||||||
| chr1:149527549
|
C | G | 6 | a0006c0211t0019g0211a0161c0197t0005g0214a0162c0196t0005g0213others(3): Show | 6 | HG00544.hp2 HG00558.hp2 HG00735.hp1 others(3): Show |
intron_variant | MODIFIER | c.7122-65C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 59/93 | chr1 | 149527549 | ||||||
| chr1:149527607
|
T | G | 1 | a0166c0198t0005g0210 | 1 | HG03942.hp2 | splice_region_variant&intron_variant | LOW | c.7122-7T>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 59/93 | chr1 | 149527607 | ||||||
| chr1:149527610
|
C | T | 10 | a0036c0014t0009g0228a0036c0014t0009g0230a0185c0043t0002g0247others(7): Show | 10 | HG00438.hp2 HG02080.hp2 HG03942.hp1 others(7): Show |
splice_region_variant&intron_variant | LOW | c.7122-4C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 59/93 | chr1 | 149527610 | ||||||
| chr1:149527904
|
A | G | 9 | a0005c0004t0001g0056a0005c0004t0001g0131a0005c0004t0001g0132others(6): Show | 9 | HG03130.hp1 NA18906.hp1 NA18947.hp1 others(6): Show |
intron_variant | MODIFIER | c.7294+118A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 60/93 | chr1 | 149527904 | ||||||
| chr1:149527910
|
G | A | 6 | a0186c0044t0017g0239a0193c0057t0002g0006a0197c0066t0002g0238others(3): Show | 6 | HG00621.hp2 HG02040.hp2 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.7294+124G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 60/93 | chr1 | 149527910 | ||||||
| chr1:149527914
|
A | G | 1 | a0211c0040t0002g0243 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.7294+128A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 60/93 | chr1 | 149527914 | ||||||
| chr1:149527953
|
G | C | 3 | a0031c0028t0003g0180a0031c0028t0003g0194a0152c0129t0003g0192 | 3 | NA18946.hp1 NA18972.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.7294+167G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 60/93 | chr1 | 149527953 | ||||||
| chr1:149527981
|
C | G | 1 | a0167c0203t0028g0269 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.7294+195C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 60/93 | chr1 | 149527981 | ||||||
| chr1:149527983
|
A | T | 1 | a0201c0063t0002g0222 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.7294+197A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 60/93 | chr1 | 149527983 | ||||||
| chr1:149527984
|
T | C | 3 | a0044c0210t0004g0206a0171c0207t0004g0208a0172c0204t0004g0268 | 3 | HG02698.hp1 NA18972.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.7294+198T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 60/93 | chr1 | 149527984 | ||||||
| chr1:149528005
|
T | C | 85 | a0003c0003t0001g0115a0003c0003t0001g0116a0003c0003t0001g0117others(82): Show | 86 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.7294+219T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 60/93 | chr1 | 149528005 | ||||||
| chr1:149528006
|
G | A | 3 | a0044c0210t0004g0206a0171c0207t0004g0208a0172c0204t0004g0268 | 3 | HG02698.hp1 NA18972.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.7294+220G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 60/93 | chr1 | 149528006 | ||||||
| chr1:149528012
|
A | G | 1 | a0106c0139t0001g0055 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.7294+226A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 60/93 | chr1 | 149528012 | ||||||
| chr1:149528040
|
C | T | 3 | a0161c0197t0005g0214a0162c0196t0005g0213a0163c0199t0005g0215 | 3 | HG00558.hp2 HG00735.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.7294+254C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 60/93 | chr1 | 149528040 | ||||||
| chr1:149528051
|
C | T | 139 | a0001c0001t0001g0121a0002c0002t0003g0182a0002c0002t0003g0188others(136): Show | 140 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.7294+265C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 60/93 | chr1 | 149528051 | ||||||
| chr1:149528064
|
G | A | 2 | a0143c0179t0001g0021a0154c0185t0001g0152 | 2 | HG02698.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.7294+278G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 60/93 | chr1 | 149528064 | ||||||
| chr1:149528085
|
G | T | 5 | a0161c0197t0005g0214a0162c0196t0005g0213a0163c0199t0005g0215others(2): Show | 5 | HG00558.hp2 HG00735.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.7294+299G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 60/93 | chr1 | 149528085 | ||||||
| chr1:149528092
|
G | A | 88 | a0003c0003t0001g0115a0003c0003t0001g0116a0003c0003t0001g0117others(85): Show | 89 | HG00544.hp1 HG00544.hp2 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.7294+306G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 60/93 | chr1 | 149528092 | ||||||
| chr1:149528106
|
A | T | 4 | a0161c0197t0005g0214a0162c0196t0005g0213a0163c0199t0005g0215others(1): Show | 4 | HG00558.hp2 HG00735.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.7294+320A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 60/93 | chr1 | 149528106 | ||||||
| chr1:149528115
|
T | A | 1 | a0043c0209t0004g0207 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.7294+329T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 60/93 | chr1 | 149528115 | ||||||
| chr1:149528117
|
A | T | 3 | a0015c0036t0006g0004a0015c0192t0006g0270a0173c0191t0006g0271 | 4 | HG02145.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.7294+331A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 60/93 | chr1 | 149528117 | ||||||
| chr1:149528130
|
C | G | 1 | a0164c0201t0004g0205 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.7294+344C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 60/93 | chr1 | 149528130 | ||||||
| chr1:149528152
|
G | A | 1 | a0192c0055t0002g0263 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.7295-344G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 60/93 | chr1 | 149528152 | ||||||
| chr1:149528152
|
G | T | 1 | a0029c0033t0001g0198 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.7295-344G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 60/93 | chr1 | 149528152 | ||||||
| chr1:149528288
|
A | T | 6 | a0161c0197t0005g0214a0162c0196t0005g0213a0163c0199t0005g0215others(3): Show | 6 | HG00544.hp2 HG00558.hp2 HG00735.hp2 others(3): Show |
intron_variant | MODIFIER | c.7295-208A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 60/93 | chr1 | 149528288 | ||||||
| chr1:149528490
|
T | C | 3 | a0015c0036t0006g0004a0015c0192t0006g0270a0173c0191t0006g0271 | 4 | HG02145.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.7295-6T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 60/93 | chr1 | 149528490 | ||||||
| chr1:149528559
|
A | G | 27 | a0001c0001t0001g0121a0011c0010t0001g0010a0011c0010t0001g0011others(24): Show | 27 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(24): Show |
intron_variant | MODIFIER | c.7346+12A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | chr1 | 149528559 | ||||||
| chr1:149528597
|
C | A | 5 | a0016c0017t0001g0028a0016c0017t0001g0029a0083c0116t0023g0103others(2): Show | 5 | HG03130.hp1 HG03239.hp2 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.7346+50C>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | chr1 | 149528597 | ||||||
| chr1:149528617
|
G | C | 1 | a0099c0146t0001g0034 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.7346+70G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | chr1 | 149528617 | ||||||
| chr1:149528674
|
A | G | 5 | a0161c0197t0005g0214a0162c0196t0005g0213a0163c0199t0005g0215others(2): Show | 5 | HG00558.hp2 HG00735.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.7346+127A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | chr1 | 149528674 | ||||||
| chr1:149528751
|
C | G | 146 | a0001c0001t0001g0121a0002c0002t0003g0182a0002c0002t0003g0188others(143): Show | 147 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.7346+204C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | chr1 | 149528751 | ||||||
| chr1:149528770
|
A | C | 1 | a0093c0124t0001g0153 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.7346+223A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | chr1 | 149528770 | ||||||
| chr1:149528785
|
C | T | 2 | a0203c0065t0002g0240a0211c0040t0002g0243 | 2 | HG00438.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.7346+238C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | chr1 | 149528785 | ||||||
| chr1:149528792
|
G | A | 95 | a0002c0002t0003g0182a0002c0002t0003g0188a0002c0002t0003g0189others(92): Show | 96 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.7346+245G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | chr1 | 149528792 | ||||||
| chr1:149528804
|
G | A | 1 | a0143c0179t0001g0021 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.7346+257G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | chr1 | 149528804 | ||||||
| chr1:149528933
|
C | T | 17 | a0015c0036t0006g0004a0015c0192t0006g0270a0031c0028t0003g0180others(14): Show | 18 | HG01074.hp1 HG01081.hp2 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.7347-241C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | chr1 | 149528933 | ||||||
| chr1:149528935
|
T | TTC | 2 | a0047c0216t0001g0068a0171c0207t0004g0208 | 2 | HG01934.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.7347-229_7347-228d others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | INFO_REALIGN_3_PRIME | chr1 | 149528935 | |||||
| chr1:149528945
|
C | CTCTCTCT others(11): Show |
3 | a0015c0036t0006g0004a0015c0192t0006g0270a0173c0191t0006g0271 | 4 | HG02145.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.7347-228_7347-227i others(20): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | INFO_REALIGN_3_PRIME | chr1 | 149528945 | |||||
| chr1:149528945
|
C | CTCTCTCT others(15): Show |
1 | a0006c0213t0002g0224 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.7347-228_7347-227i others(24): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | INFO_REALIGN_3_PRIME | chr1 | 149528945 | |||||
| chr1:149528945
|
C | CTCTCTCT others(17): Show |
1 | a0006c0214t0002g0265 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.7347-228_7347-227i others(26): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | INFO_REALIGN_3_PRIME | chr1 | 149528945 | |||||
| chr1:149528945
|
C | CTCTCTCT others(19): Show |
1 | a0043c0209t0004g0207 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.7347-228_7347-227i others(28): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | INFO_REALIGN_3_PRIME | chr1 | 149528945 | |||||
| chr1:149528945
|
C | CTCTCTCT others(5): Show |
1 | a0201c0063t0002g0222 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.7347-228_7347-227i others(14): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | INFO_REALIGN_3_PRIME | chr1 | 149528945 | |||||
| chr1:149528945
|
C | CTCTCTCT others(11): Show |
5 | a0061c0187t0001g0173a0114c0137t0001g0133a0159c0189t0003g0191others(2): Show | 5 | HG00642.hp2 HG02145.hp2 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.7347-228_7347-227i others(20): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | INFO_REALIGN_3_PRIME | chr1 | 149528945 | |||||
| chr1:149528945
|
C | CTCTCTCT others(13): Show |
6 | a0088c0105t0008g0100a0110c0133t0001g0058a0168c0206t0004g0203others(3): Show | 6 | HG01099.hp1 HG02896.hp2 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.7347-228_7347-227i others(22): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | INFO_REALIGN_3_PRIME | chr1 | 149528945 | |||||
| chr1:149528945
|
C | CTCTCTCT others(15): Show |
18 | a0003c0003t0001g0115a0003c0003t0001g0116a0003c0003t0001g0117others(15): Show | 18 | HG01516.hp2 HG01517.hp1 HG01928.hp1 others(15): Show |
intron_variant | MODIFIER | c.7347-228_7347-227i others(24): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | INFO_REALIGN_3_PRIME | chr1 | 149528945 | |||||
| chr1:149528945
|
C | CTCTCTCT others(17): Show |
9 | a0003c0003t0001g0170a0027c0029t0001g0061a0027c0029t0001g0062others(6): Show | 9 | HG00544.hp1 HG00735.hp1 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.7347-228_7347-227i others(26): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | INFO_REALIGN_3_PRIME | chr1 | 149528945 | |||||
| chr1:149528945
|
C | CTCTCTCT others(19): Show |
13 | a0002c0002t0007g0190a0002c0002t0007g0193a0014c0008t0003g0181others(10): Show | 13 | HG01975.hp1 HG02148.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.7347-228_7347-227i others(28): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | INFO_REALIGN_3_PRIME | chr1 | 149528945 | |||||
| chr1:149528945
|
C | CTCTCTCT others(21): Show |
7 | a0002c0002t0003g0182a0002c0002t0003g0188a0002c0002t0003g0196others(4): Show | 7 | HG02083.hp1 HG02976.hp2 NA18967.hp1 others(4): Show |
intron_variant | MODIFIER | c.7347-228_7347-227i others(30): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | INFO_REALIGN_3_PRIME | chr1 | 149528945 | |||||
| chr1:149528945
|
C | CTCTCTCT others(23): Show |
5 | a0002c0002t0003g0189a0009c0006t0001g0081a0014c0008t0003g0186others(2): Show | 5 | HG00099.hp1 HG00621.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.7347-228_7347-227i others(32): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | INFO_REALIGN_3_PRIME | chr1 | 149528945 | |||||
| chr1:149528945
|
C | CTCTCTCT others(25): Show |
2 | a0006c0212t0002g0223a0135c0161t0001g0057 | 2 | HG00733.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.7347-228_7347-227i others(34): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | INFO_REALIGN_3_PRIME | chr1 | 149528945 | |||||
| chr1:149528945
|
C | CTCTCTCT others(27): Show |
1 | a0006c0211t0019g0211 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.7347-228_7347-227i others(36): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | INFO_REALIGN_3_PRIME | chr1 | 149528945 | |||||
| chr1:149528945
|
C | CTCTCTGT others(9): Show |
1 | a0081c0113t0001g0148 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.7347-228_7347-227i others(18): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | INFO_REALIGN_3_PRIME | chr1 | 149528945 | |||||
| chr1:149528945
|
C | CTCTCTGT others(11): Show |
2 | a0019c0021t0001g0098a0071c0102t0001g0143 | 2 | HG00609.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.7347-228_7347-227i others(20): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | INFO_REALIGN_3_PRIME | chr1 | 149528945 | |||||
| chr1:149528945
|
C | CTCTCTGT others(13): Show |
1 | a0117c0152t0001g0087 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.7347-228_7347-227i others(22): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | INFO_REALIGN_3_PRIME | chr1 | 149528945 | |||||
| chr1:149528945
|
C | CTCTCTGT others(15): Show |
5 | a0011c0010t0001g0012a0048c0081t0011g0151a0116c0150t0001g0014others(2): Show | 5 | HG00558.hp1 HG01109.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.7347-228_7347-227i others(24): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | INFO_REALIGN_3_PRIME | chr1 | 149528945 | |||||
| chr1:149528945
|
C | CTCTCTGT others(17): Show |
3 | a0011c0010t0001g0011a0108c0143t0001g0027a0165c0200t0005g0212 | 3 | HG00544.hp2 HG01123.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.7347-228_7347-227i others(26): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | INFO_REALIGN_3_PRIME | chr1 | 149528945 | |||||
| chr1:149528945
|
C | CTCTCTGT others(19): Show |
4 | a0011c0010t0001g0010a0012c0009t0001g0050a0012c0009t0001g0172others(1): Show | 4 | HG00438.hp1 NA18983.hp2 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.7347-228_7347-227i others(28): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | INFO_REALIGN_3_PRIME | chr1 | 149528945 | |||||
| chr1:149528945
|
C | CTCTCTGT others(21): Show |
3 | a0001c0001t0001g0121a0086c0119t0001g0085a0091c0122t0008g0157 | 3 | HG00423.hp2 HG02027.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.7347-228_7347-227i others(30): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | INFO_REALIGN_3_PRIME | chr1 | 149528945 | |||||
| chr1:149528945
|
C | CTCTCTGT others(23): Show |
1 | a0129c0167t0012g0088 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.7347-228_7347-227i others(32): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | INFO_REALIGN_3_PRIME | chr1 | 149528945 | |||||
| chr1:149528945
|
C | CTCTGTGT others(3): Show |
1 | a0210c0068t0016g0233 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.7347-228_7347-227i others(12): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | INFO_REALIGN_3_PRIME | chr1 | 149528945 | |||||
| chr1:149528945
|
C | CTCTGTGT others(9): Show |
1 | a0199c0061t0002g0219 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.7347-228_7347-227i others(18): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | INFO_REALIGN_3_PRIME | chr1 | 149528945 | |||||
| chr1:149528945
|
C | CTCTGTGT others(11): Show |
9 | a0032c0012t0002g0232a0032c0012t0002g0266a0037c0016t0002g0256others(6): Show | 9 | HG00642.hp1 HG01069.hp2 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.7347-228_7347-227i others(20): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | INFO_REALIGN_3_PRIME | chr1 | 149528945 | |||||
| chr1:149528945
|
C | CTCTGTGT others(13): Show |
5 | a0039c0219t0002g0227a0041c0217t0003g0185a0191c0054t0002g0264others(2): Show | 5 | HG00621.hp1 HG02040.hp2 HG02165.hp2 others(2): Show |
intron_variant | MODIFIER | c.7347-228_7347-227i others(22): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | INFO_REALIGN_3_PRIME | chr1 | 149528945 | |||||
| chr1:149528945
|
C | CTCTGTGT others(15): Show |
5 | a0033c0011t0002g0255a0179c0071t0002g0260a0181c0073t0002g0272others(2): Show | 5 | HG00738.hp1 HG02129.hp2 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.7347-228_7347-227i others(24): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | INFO_REALIGN_3_PRIME | chr1 | 149528945 | |||||
| chr1:149528945
|
C | CTCTGTGT others(17): Show |
4 | a0034c0013t0002g0220a0034c0013t0002g0221a0180c0072t0002g0218others(1): Show | 4 | HG02155.hp1 HG04204.hp1 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.7347-228_7347-227i others(26): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | INFO_REALIGN_3_PRIME | chr1 | 149528945 | |||||
| chr1:149528945
|
C | CTCTGTGT others(19): Show |
4 | a0012c0009t0001g0195a0033c0011t0002g0254a0140c0175t0001g0051others(1): Show | 4 | NA18947.hp2 NA18980.hp1 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.7347-228_7347-227i others(28): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | INFO_REALIGN_3_PRIME | chr1 | 149528945 | |||||
| chr1:149528945
|
C | CTCTGTGT others(23): Show |
1 | a0150c0160t0001g0107 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.7347-228_7347-227i others(32): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | INFO_REALIGN_3_PRIME | chr1 | 149528945 | |||||
| chr1:149528945
|
C | CTGTGTGT others(11): Show |
1 | a0035c0015t0002g0216 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.7347-215_7347-198d others(20): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | INFO_REALIGN_3_PRIME | chr1 | 149528945 | |||||
| chr1:149528945
|
C | CTGTGTGT others(13): Show |
2 | a0035c0015t0002g0217a0212c0069t0002g0245 | 2 | HG03704.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.7347-217_7347-198d others(22): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | INFO_REALIGN_3_PRIME | chr1 | 149528945 | |||||
| chr1:149528945
|
C | G | 2 | a0092c0120t0001g0141a0185c0043t0002g0247 | 2 | HG02647.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.7347-229C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | chr1 | 149528945 | ||||||
| chr1:149528946
|
T | TCTCTCTC others(17): Show |
1 | a0167c0203t0028g0269 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.7347-228_7347-227i others(26): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | chr1 | 149528946 | ||||||
| chr1:149528946
|
T | TCTCTGTG others(17): Show |
3 | a0161c0197t0005g0214a0162c0196t0005g0213a0163c0199t0005g0215 | 3 | HG00558.hp2 HG00735.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.7347-228_7347-227i others(26): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | chr1 | 149528946 | ||||||
| chr1:149528947
|
G | C | 6 | a0045c0078t0001g0099a0046c0077t0001g0083a0047c0216t0001g0068others(3): Show | 6 | HG01934.hp2 HG02698.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.7347-227G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | chr1 | 149528947 | ||||||
| chr1:149528949
|
G | C | 3 | a0047c0216t0001g0068a0133c0165t0022g0020a0171c0207t0004g0208 | 3 | HG01934.hp2 HG02622.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.7347-225G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | chr1 | 149528949 | ||||||
| chr1:149528950
|
T | C | 2 | a0052c0079t0021g0176a0148c0181t0001g0124 | 2 | HG02300.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.7347-224T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | chr1 | 149528950 | ||||||
| chr1:149528952
|
T | C | 7 | a0050c0080t0001g0177a0083c0116t0023g0103a0108c0143t0001g0027others(4): Show | 7 | HG00735.hp1 HG01123.hp1 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.7347-222T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | chr1 | 149528952 | ||||||
| chr1:149528954
|
T | C | 2 | a0006c0213t0002g0224a0006c0214t0002g0265 | 2 | NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.7347-220T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | chr1 | 149528954 | ||||||
| chr1:149528959
|
G | C | 115 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(112): Show | 117 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.7347-215G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | chr1 | 149528959 | ||||||
| chr1:149528963
|
G | A | 3 | a0161c0197t0005g0214a0162c0196t0005g0213a0163c0199t0005g0215 | 3 | HG00558.hp2 HG00735.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.7347-211G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | chr1 | 149528963 | ||||||
| chr1:149528969
|
G | T | 1 | a0164c0201t0004g0205 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.7347-205G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | chr1 | 149528969 | ||||||
| chr1:149528977
|
C | G | 1 | a0019c0021t0001g0098 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.7347-197C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | chr1 | 149528977 | ||||||
| chr1:149528978
|
T | C | 16 | a0006c0213t0002g0224a0006c0214t0002g0265a0050c0080t0001g0177others(13): Show | 16 | HG00558.hp2 HG00735.hp1 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.7347-196T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | chr1 | 149528978 | ||||||
| chr1:149528979
|
A | G | 2 | a0019c0021t0001g0098a0051c0083t0001g0162 | 2 | HG02683.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.7347-195A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | chr1 | 149528979 | ||||||
| chr1:149529053
|
A | C | 8 | a0036c0014t0009g0228a0036c0014t0009g0230a0185c0043t0002g0247others(5): Show | 8 | HG02080.hp2 HG03942.hp1 NA18939.hp2 others(5): Show |
intron_variant | MODIFIER | c.7347-121A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | chr1 | 149529053 | ||||||
| chr1:149529057
|
A | G | 1 | a0196c0045t0018g0226 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.7347-117A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | chr1 | 149529057 | ||||||
| chr1:149529063
|
C | G | 32 | a0032c0012t0002g0232a0032c0012t0002g0266a0033c0011t0002g0254others(29): Show | 32 | HG00621.hp1 HG00642.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.7347-111C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | chr1 | 149529063 | ||||||
| chr1:149529074
|
G | C | 52 | a0008c0037t0001g0075a0008c0037t0001g0135a0008c0215t0001g0067others(49): Show | 52 | HG00438.hp2 HG00621.hp1 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.7347-100G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | chr1 | 149529074 | ||||||
| chr1:149529091
|
C | T | 10 | a0036c0014t0009g0228a0036c0014t0009g0230a0185c0043t0002g0247others(7): Show | 10 | HG00438.hp2 HG02080.hp2 HG03942.hp1 others(7): Show |
intron_variant | MODIFIER | c.7347-83C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | chr1 | 149529091 | ||||||
| chr1:149529156
|
T | G | 10 | a0036c0014t0009g0228a0036c0014t0009g0230a0185c0043t0002g0247others(7): Show | 10 | HG00438.hp2 HG02080.hp2 HG03942.hp1 others(7): Show |
intron_variant | MODIFIER | c.7347-18T>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | chr1 | 149529156 | ||||||
| chr1:149529357
|
T | C | 1 | a0019c0021t0001g0098 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.7519+11T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 62/93 | chr1 | 149529357 | ||||||
| chr1:149529361
|
A | G | 1 | a0006c0212t0002g0223 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.7519+15A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 62/93 | chr1 | 149529361 | ||||||
| chr1:149529376
|
AT | A | 3 | a0077c0110t0001g0178a0137c0173t0001g0159a0159c0189t0003g0191 | 3 | HG00642.hp2 HG01928.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.7519+31delT | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 62/93 | chr1 | 149529376 | ||||||
| chr1:149529390
|
C | T | 1 | a0165c0200t0005g0212 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.7519+44C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 62/93 | chr1 | 149529390 | ||||||
| chr1:149529445
|
G | A | 26 | a0001c0001t0001g0121a0011c0010t0001g0010a0011c0010t0001g0011others(23): Show | 26 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.7519+99G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 62/93 | chr1 | 149529445 | ||||||
| chr1:149529461
|
C | A | 1 | a0006c0212t0002g0223 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.7519+115C>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 62/93 | chr1 | 149529461 | ||||||
| chr1:149529477
|
G | A | 1 | a0142c0180t0001g0108 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.7519+131G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 62/93 | chr1 | 149529477 | ||||||
| chr1:149529516
|
A | T | 26 | a0001c0001t0001g0121a0011c0010t0001g0010a0011c0010t0001g0011others(23): Show | 26 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.7519+170A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 62/93 | chr1 | 149529516 | ||||||
| chr1:149529535
|
A | T | 26 | a0001c0001t0001g0121a0011c0010t0001g0010a0011c0010t0001g0011others(23): Show | 26 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.7519+189A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 62/93 | chr1 | 149529535 | ||||||
| chr1:149529537
|
A | G | 26 | a0001c0001t0001g0121a0011c0010t0001g0010a0011c0010t0001g0011others(23): Show | 26 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.7519+191A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 62/93 | chr1 | 149529537 | ||||||
| chr1:149529569
|
C | T | 3 | a0003c0003t0001g0115a0003c0003t0001g0117a0003c0003t0001g0170 | 3 | HG00544.hp1 NA18612.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.7519+223C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 62/93 | chr1 | 149529569 | ||||||
| chr1:149529570
|
G | A | 27 | a0001c0001t0001g0121a0011c0010t0001g0010a0011c0010t0001g0011others(24): Show | 27 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(24): Show |
intron_variant | MODIFIER | c.7519+224G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 62/93 | chr1 | 149529570 | ||||||
| chr1:149529572
|
C | T | 26 | a0001c0001t0001g0121a0011c0010t0001g0010a0011c0010t0001g0011others(23): Show | 26 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.7519+226C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 62/93 | chr1 | 149529572 | ||||||
| chr1:149529578
|
C | T | 26 | a0001c0001t0001g0121a0011c0010t0001g0010a0011c0010t0001g0011others(23): Show | 26 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.7519+232C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 62/93 | chr1 | 149529578 | ||||||
| chr1:149529582
|
T | C | 26 | a0001c0001t0001g0121a0011c0010t0001g0010a0011c0010t0001g0011others(23): Show | 26 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.7519+236T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 62/93 | chr1 | 149529582 | ||||||
| chr1:149529630
|
G | T | 1 | a0186c0044t0017g0239 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.7519+284G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 62/93 | chr1 | 149529630 | ||||||
| chr1:149529650
|
T | C | 26 | a0001c0001t0001g0121a0011c0010t0001g0010a0011c0010t0001g0011others(23): Show | 26 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.7519+304T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 62/93 | chr1 | 149529650 | ||||||
| chr1:149529734
|
T | G | 1 | a0201c0063t0002g0222 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.7520-327T>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 62/93 | chr1 | 149529734 | ||||||
| chr1:149529745
|
T | A | 8 | a0036c0014t0009g0228a0036c0014t0009g0230a0185c0043t0002g0247others(5): Show | 8 | HG02080.hp2 HG03942.hp1 NA18939.hp2 others(5): Show |
intron_variant | MODIFIER | c.7520-316T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 62/93 | chr1 | 149529745 | ||||||
| chr1:149529751
|
T | C | 49 | a0001c0001t0001g0121a0002c0002t0003g0182a0002c0002t0003g0188others(46): Show | 49 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.7520-310T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 62/93 | chr1 | 149529751 | ||||||
| chr1:149529761
|
T | A | 1 | a0129c0167t0012g0088 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.7520-300T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 62/93 | chr1 | 149529761 | ||||||
| chr1:149529766
|
G | A | 1 | a0183c0041t0002g0246 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.7520-295G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 62/93 | chr1 | 149529766 | ||||||
| chr1:149529854
|
A | T | 1 | a0041c0217t0003g0185 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.7520-207A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 62/93 | chr1 | 149529854 | ||||||
| chr1:149529873
|
A | C | 1 | a0072c0104t0001g0017 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.7520-188A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 62/93 | chr1 | 149529873 | ||||||
| chr1:149530211
|
C | T | 1 | a0200c0062t0002g0237 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.7628+42C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 63/93 | chr1 | 149530211 | ||||||
| chr1:149530241
|
G | C | 6 | a0061c0187t0001g0173a0086c0119t0001g0085a0089c0123t0001g0164others(3): Show | 6 | HG00408.hp1 HG00423.hp2 HG01109.hp2 others(3): Show |
intron_variant | MODIFIER | c.7628+72G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 63/93 | chr1 | 149530241 | ||||||
| chr1:149530241
|
G | GTGTGTTT others(9511): Show |
1 | a0093c0124t0001g0153 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.7628+183_7628+184i others(9520): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 63/93 | INFO_REALIGN_3_PRIME | chr1 | 149530241 | |||||
| chr1:149530242
|
T | C | 6 | a0050c0080t0001g0177a0052c0079t0021g0176a0137c0173t0001g0159others(3): Show | 6 | HG00642.hp2 HG01978.hp1 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.7628+73T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 63/93 | chr1 | 149530242 | ||||||
| chr1:149530268
|
A | C | 2 | a0186c0044t0017g0239a0205c0056t0015g0258 | 2 | HG00621.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.7628+99A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 63/93 | chr1 | 149530268 | ||||||
| chr1:149530321
|
T | C | 4 | a0043c0209t0004g0207a0168c0206t0004g0203a0169c0205t0004g0209others(1): Show | 4 | HG01099.hp1 HG02165.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.7628+152T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 63/93 | chr1 | 149530321 | ||||||
| chr1:149530353
|
A | C | 5 | a0013c0035t0001g0038a0013c0035t0001g0084a0013c0162t0001g0040others(2): Show | 5 | HG01168.hp1 HG02258.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.7628+184A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 63/93 | chr1 | 149530353 | ||||||
| chr1:149530357
|
A | G | 52 | a0006c0211t0019g0211a0006c0212t0002g0223a0006c0213t0002g0224others(49): Show | 53 | HG00544.hp2 HG00558.hp2 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.7628+188A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 63/93 | chr1 | 149530357 | ||||||
| chr1:149530358
|
C | T | 24 | a0032c0012t0002g0232a0032c0012t0002g0266a0033c0011t0002g0254others(21): Show | 24 | HG00621.hp1 HG00642.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.7628+189C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 63/93 | chr1 | 149530358 | ||||||
| chr1:149530359
|
G | A | 1 | a0164c0201t0004g0205 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.7628+190G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 63/93 | chr1 | 149530359 | ||||||
| chr1:149530477
|
G | T | 1 | a0201c0063t0002g0222 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.7628+308G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 63/93 | chr1 | 149530477 | ||||||
| chr1:149530486
|
G | A | 1 | a0046c0077t0001g0083 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.7629-313G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 63/93 | chr1 | 149530486 | ||||||
| chr1:149530497
|
G | C | 7 | a0020c0020t0001g0041a0020c0020t0010g0043a0062c0093t0001g0267others(4): Show | 7 | HG00408.hp1 HG00423.hp2 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.7629-302G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 63/93 | chr1 | 149530497 | ||||||
| chr1:149530511
|
T | C | 1 | a0186c0044t0017g0239 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.7629-288T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 63/93 | chr1 | 149530511 | ||||||
| chr1:149530529
|
C | T | 3 | a0013c0035t0001g0038a0013c0035t0001g0084a0013c0162t0001g0040 | 3 | HG02258.hp2 HG02280.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.7629-270C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 63/93 | chr1 | 149530529 | ||||||
| chr1:149530572
|
G | C | 1 | a0166c0198t0005g0210 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.7629-227G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 63/93 | chr1 | 149530572 | ||||||
| chr1:149530576
|
CTCTCTCT others(7): Show |
C | 1 | a0027c0029t0001g0062 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.7629-215_7629-202d others(16): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 63/93 | INFO_REALIGN_3_PRIME | chr1 | 149530576 | |||||
| chr1:149530578
|
C | G | 1 | a0166c0198t0005g0210 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.7629-221C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 63/93 | chr1 | 149530578 | ||||||
| chr1:149530590
|
G | GTC | 4 | a0013c0035t0001g0038a0013c0035t0001g0084a0013c0162t0001g0040others(1): Show | 4 | HG00735.hp1 HG02258.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.7629-193_7629-192d others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 63/93 | INFO_REALIGN_3_PRIME | chr1 | 149530590 | |||||
| chr1:149530590
|
G | GTCTC | 83 | a0002c0002t0003g0182a0002c0002t0003g0188a0002c0002t0003g0189others(80): Show | 83 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.7629-195_7629-192d others(6): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 63/93 | INFO_REALIGN_3_PRIME | chr1 | 149530590 | |||||
| chr1:149530590
|
G | GTCTCTC | 33 | a0015c0036t0006g0004a0015c0192t0006g0270a0019c0021t0001g0098others(30): Show | 34 | HG00438.hp2 HG00621.hp1 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.7629-197_7629-192d others(8): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 63/93 | INFO_REALIGN_3_PRIME | chr1 | 149530590 | |||||
| chr1:149530590
|
G | GTCTCTCT others(1): Show |
4 | a0044c0210t0004g0206a0170c0208t0004g0202a0171c0207t0004g0208others(1): Show | 4 | HG02698.hp1 NA18972.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.7629-199_7629-192d others(10): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 63/93 | INFO_REALIGN_3_PRIME | chr1 | 149530590 | |||||
| chr1:149530652
|
A | C | 1 | a0019c0021t0001g0098 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.7629-147A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 63/93 | chr1 | 149530652 | ||||||
| chr1:149530673
|
A | C | 6 | a0122c0156t0001g0086a0137c0173t0001g0159a0159c0189t0003g0191others(3): Show | 6 | HG00642.hp2 HG03225.hp2 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.7629-126A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 63/93 | chr1 | 149530673 | ||||||
| chr1:149530681
|
A | C | 2 | a0170c0208t0004g0202a0172c0204t0004g0268 | 2 | NA20129.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.7629-118A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 63/93 | chr1 | 149530681 | ||||||
| chr1:149530716
|
TA | T | 17 | a0009c0006t0001g0082a0009c0006t0001g0139a0028c0032t0001g0036others(14): Show | 17 | HG00741.hp2 HG01934.hp1 HG02040.hp1 others(14): Show |
intron_variant | MODIFIER | c.7629-81delA | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 63/93 | INFO_REALIGN_3_PRIME | chr1 | 149530716 | |||||
| chr1:149530720
|
G | A | 1 | a0006c0211t0019g0211 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.7629-79G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 63/93 | chr1 | 149530720 | ||||||
| chr1:149530749
|
T | C | 79 | a0002c0002t0003g0182a0002c0002t0003g0188a0002c0002t0003g0189others(76): Show | 80 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.7629-50T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 63/93 | chr1 | 149530749 | ||||||
| chr1:149530779
|
A | T | 2 | a0186c0044t0017g0239a0205c0056t0015g0258 | 2 | HG00621.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.7629-20A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 63/93 | chr1 | 149530779 | ||||||
| chr1:149530977
|
T | C | 1 | a0108c0143t0001g0027 | 1 | HG01123.hp1 | splice_region_variant&intron_variant | LOW | c.7801+6T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 64/93 | chr1 | 149530977 | ||||||
| chr1:149531066
|
G | A | 5 | a0186c0044t0017g0239a0197c0066t0002g0238a0204c0067t0002g0248others(2): Show | 5 | HG00621.hp2 HG02083.hp1 HG02129.hp2 others(2): Show |
intron_variant | MODIFIER | c.7801+95G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 64/93 | chr1 | 149531066 | ||||||
| chr1:149531077
|
A | G | 2 | a0186c0044t0017g0239a0205c0056t0015g0258 | 2 | HG00621.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.7801+106A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 64/93 | chr1 | 149531077 | ||||||
| chr1:149531119
|
T | C | 1 | a0063c0090t0003g0187 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.7801+148T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 64/93 | chr1 | 149531119 | ||||||
| chr1:149531168
|
C | T | 47 | a0006c0211t0019g0211a0006c0212t0002g0223a0006c0213t0002g0224others(44): Show | 48 | HG00621.hp1 HG00642.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.7801+197C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 64/93 | chr1 | 149531168 | ||||||
| chr1:149531173
|
G | C | 1 | a0179c0071t0002g0260 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.7801+202G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 64/93 | chr1 | 149531173 | ||||||
| chr1:149531193
|
A | C | 94 | a0001c0001t0001g0121a0002c0002t0003g0182a0002c0002t0003g0188others(91): Show | 95 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.7801+222A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 64/93 | chr1 | 149531193 | ||||||
| chr1:149531193
|
A | T | 3 | a0161c0197t0005g0214a0162c0196t0005g0213a0163c0199t0005g0215 | 3 | HG00558.hp2 HG00735.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.7801+222A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 64/93 | chr1 | 149531193 | ||||||
| chr1:149531194
|
G | A | 5 | a0006c0212t0002g0223a0006c0213t0002g0224a0006c0214t0002g0265others(2): Show | 5 | HG01891.hp1 NA18612.hp2 NA19062.hp1 others(2): Show |
intron_variant | MODIFIER | c.7801+223G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 64/93 | chr1 | 149531194 | ||||||
| chr1:149531217
|
C | G | 5 | a0161c0197t0005g0214a0162c0196t0005g0213a0163c0199t0005g0215others(2): Show | 5 | HG00544.hp2 HG00558.hp2 HG00735.hp2 others(2): Show |
intron_variant | MODIFIER | c.7801+246C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 64/93 | chr1 | 149531217 | ||||||
| chr1:149531217
|
C | T | 75 | a0001c0001t0001g0121a0006c0211t0019g0211a0006c0212t0002g0223others(72): Show | 76 | HG00609.hp2 HG00621.hp1 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.7801+246C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 64/93 | chr1 | 149531217 | ||||||
| chr1:149531230
|
G | C | 3 | a0044c0210t0004g0206a0171c0207t0004g0208a0172c0204t0004g0268 | 3 | HG02698.hp1 NA18972.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.7801+259G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 64/93 | chr1 | 149531230 | ||||||
| chr1:149531246
|
A | T | 5 | a0011c0010t0001g0010a0011c0010t0001g0011a0011c0010t0001g0012others(2): Show | 5 | HG01257.hp2 HG02165.hp2 NA18981.hp2 others(2): Show |
intron_variant | MODIFIER | c.7801+275A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 64/93 | chr1 | 149531246 | ||||||
| chr1:149531307
|
A | G | 1 | a0164c0201t0004g0205 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.7801+336A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 64/93 | chr1 | 149531307 | ||||||
| chr1:149531310
|
G | A | 1 | a0166c0198t0005g0210 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.7801+339G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 64/93 | chr1 | 149531310 | ||||||
| chr1:149531507
|
T | G | 1 | a0174c0202t0013g0204 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.7802-184T>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 64/93 | chr1 | 149531507 | ||||||
| chr1:149531523
|
A | G | 12 | a0002c0002t0003g0182a0002c0002t0003g0188a0002c0002t0003g0189others(9): Show | 12 | HG01071.hp1 HG01975.hp1 HG02148.hp1 others(9): Show |
intron_variant | MODIFIER | c.7802-168A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 64/93 | chr1 | 149531523 | ||||||
| chr1:149531607
|
C | T | 2 | a0137c0173t0001g0159a0159c0189t0003g0191 | 2 | HG00642.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.7802-84C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 64/93 | chr1 | 149531607 | ||||||
| chr1:149531608
|
C | T | 93 | a0003c0003t0001g0115a0003c0003t0001g0116a0003c0003t0001g0117others(90): Show | 94 | HG00438.hp1 HG00544.hp1 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.7802-83C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 64/93 | chr1 | 149531608 | ||||||
| chr1:149531620
|
T | G | 1 | a0160c0076t0014g0225 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.7802-71T>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 64/93 | chr1 | 149531620 | ||||||
| chr1:149531636
|
T | C | 1 | a0137c0173t0001g0159 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.7802-55T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 64/93 | chr1 | 149531636 | ||||||
| chr1:149531639
|
G | T | 1 | a0201c0063t0002g0222 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.7802-52G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 64/93 | chr1 | 149531639 | ||||||
| chr1:149531646
|
G | A | 1 | a0006c0211t0019g0211 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.7802-45G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 64/93 | chr1 | 149531646 | ||||||
| chr1:149531664
|
G | A | 33 | a0003c0003t0001g0115a0003c0003t0001g0116a0003c0003t0001g0117others(30): Show | 33 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.7802-27G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 64/93 | chr1 | 149531664 | ||||||
| chr1:149531761
|
G | A | 4 | a0161c0197t0005g0214a0162c0196t0005g0213a0163c0199t0005g0215others(1): Show | 4 | HG00544.hp2 HG00558.hp2 HG00735.hp2 others(1): Show |
intron_variant | MODIFIER | c.7853+19G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 65/93 | chr1 | 149531761 | ||||||
| chr1:149531773
|
C | T | 11 | a0036c0014t0009g0228a0036c0014t0009g0230a0185c0043t0002g0247others(8): Show | 11 | HG02040.hp2 HG02080.hp2 HG02129.hp2 others(8): Show |
intron_variant | MODIFIER | c.7853+31C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 65/93 | chr1 | 149531773 | ||||||
| chr1:149531839
|
C | T | 1 | a0124c0158t0001g0095 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.7853+97C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 65/93 | chr1 | 149531839 | ||||||
| chr1:149531917
|
C | T | 3 | a0161c0197t0005g0214a0162c0196t0005g0213a0163c0199t0005g0215 | 3 | HG00558.hp2 HG00735.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.7853+175C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 65/93 | chr1 | 149531917 | ||||||
| chr1:149531921
|
A | T | 44 | a0003c0003t0001g0115a0003c0003t0001g0116a0003c0003t0001g0117others(41): Show | 44 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.7853+179A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 65/93 | chr1 | 149531921 | ||||||
| chr1:149531946
|
A | T | 27 | a0032c0012t0002g0232a0032c0012t0002g0266a0033c0011t0002g0254others(24): Show | 27 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.7853+204A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 65/93 | chr1 | 149531946 | ||||||
| chr1:149531981
|
A | G | 27 | a0032c0012t0002g0232a0032c0012t0002g0266a0033c0011t0002g0254others(24): Show | 27 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.7853+239A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 65/93 | chr1 | 149531981 | ||||||
| chr1:149532049
|
G | A | 2 | a0118c0151t0001g0053a0129c0167t0012g0088 | 2 | NA18983.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.7854-296G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 65/93 | chr1 | 149532049 | ||||||
| chr1:149532061
|
T | A | 1 | a0154c0185t0001g0152 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.7854-284T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 65/93 | chr1 | 149532061 | ||||||
| chr1:149532077
|
C | T | 1 | a0167c0203t0028g0269 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.7854-268C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 65/93 | chr1 | 149532077 | ||||||
| chr1:149532087
|
A | T | 1 | a0006c0213t0002g0224 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.7854-258A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 65/93 | chr1 | 149532087 | ||||||
| chr1:149532098
|
C | T | 1 | a0006c0213t0002g0224 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.7854-247C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 65/93 | chr1 | 149532098 | ||||||
| chr1:149532116
|
C | T | 6 | a0012c0009t0001g0050a0012c0009t0001g0172a0012c0009t0001g0195others(3): Show | 6 | HG00438.hp1 HG00558.hp1 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.7854-229C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 65/93 | chr1 | 149532116 | ||||||
| chr1:149532124
|
C | CCT | 46 | a0003c0003t0001g0115a0003c0003t0001g0116a0003c0003t0001g0117others(43): Show | 46 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.7854-201_7854-200d others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 65/93 | INFO_REALIGN_3_PRIME | chr1 | 149532124 | |||||
| chr1:149532124
|
C | CCTCT | 9 | a0126c0130t0001g0134a0183c0041t0002g0246a0186c0044t0017g0239others(6): Show | 9 | HG02602.hp2 HG02683.hp2 NA18612.hp2 others(6): Show |
intron_variant | MODIFIER | c.7854-203_7854-200d others(6): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 65/93 | INFO_REALIGN_3_PRIME | chr1 | 149532124 | |||||
| chr1:149532124
|
C | CCTCTCT | 5 | a0010c0007t0001g0002a0010c0007t0001g0045a0089c0123t0001g0164others(2): Show | 6 | HG01069.hp1 HG01071.hp2 HG01109.hp2 others(3): Show |
intron_variant | MODIFIER | c.7854-205_7854-200d others(8): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 65/93 | INFO_REALIGN_3_PRIME | chr1 | 149532124 | |||||
| chr1:149532124
|
C | CCTCTCTC others(3): Show |
1 | a0006c0213t0002g0224 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.7854-209_7854-200d others(12): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 65/93 | INFO_REALIGN_3_PRIME | chr1 | 149532124 | |||||
| chr1:149532124
|
CCT | C | 69 | a0001c0001t0001g0121a0006c0211t0019g0211a0011c0010t0001g0010others(66): Show | 70 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.7854-201_7854-200d others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 65/93 | INFO_REALIGN_3_PRIME | chr1 | 149532124 | |||||
| chr1:149532142
|
T | C | 1 | a0087c0118t0001g0054 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.7854-203T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 65/93 | chr1 | 149532142 | ||||||
| chr1:149532174
|
T | C | 50 | a0003c0003t0001g0115a0003c0003t0001g0116a0003c0003t0001g0117others(47): Show | 50 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.7854-171T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 65/93 | chr1 | 149532174 | ||||||
| chr1:149532194
|
T | C | 1 | a0006c0211t0019g0211 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.7854-151T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 65/93 | chr1 | 149532194 | ||||||
| chr1:149532242
|
T | C | 1 | a0138c0174t0001g0109 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.7854-103T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 65/93 | chr1 | 149532242 | ||||||
| chr1:149532273
|
A | C | 3 | a0006c0212t0002g0223a0006c0213t0002g0224a0006c0214t0002g0265 | 3 | HG01891.hp1 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.7854-72A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 65/93 | chr1 | 149532273 | ||||||
| chr1:149532280
|
C | G | 8 | a0006c0211t0019g0211a0043c0209t0004g0207a0163c0199t0005g0215others(5): Show | 8 | HG00544.hp2 HG00558.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.7854-65C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 65/93 | chr1 | 149532280 | ||||||
| chr1:149532341
|
C | T | 9 | a0183c0041t0002g0246a0187c0050t0002g0250a0188c0051t0002g0252others(6): Show | 9 | HG00438.hp2 NA18612.hp2 NA18946.hp2 others(6): Show |
splice_region_variant&intron_variant | LOW | c.7854-4C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 65/93 | chr1 | 149532341 | ||||||
| chr1:149532538
|
G | A | 1 | a0022c0023t0001g0156 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.8026+21G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 66/93 | chr1 | 149532538 | ||||||
| chr1:149532619
|
G | A | 1 | a0143c0179t0001g0021 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.8026+102G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 66/93 | chr1 | 149532619 | ||||||
| chr1:149532635
|
A | ATGGGCGC others(4752): Show |
1 | a0096c0127t0001g0111 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.8026+218_8026+219i others(4761): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 66/93 | INFO_REALIGN_3_PRIME | chr1 | 149532635 | |||||
| chr1:149532635
|
A | G | 51 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(48): Show | 51 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.8026+118A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 66/93 | chr1 | 149532635 | ||||||
| chr1:149532641
|
G | A | 14 | a0036c0014t0009g0228a0036c0014t0009g0230a0185c0043t0002g0247others(11): Show | 14 | HG00621.hp2 HG02040.hp2 HG02080.hp2 others(11): Show |
intron_variant | MODIFIER | c.8026+124G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 66/93 | chr1 | 149532641 | ||||||
| chr1:149532645
|
A | G | 2 | a0190c0049t0002g0244a0206c0053t0002g0249 | 2 | NA18954.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.8026+128A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 66/93 | chr1 | 149532645 | ||||||
| chr1:149532686
|
C | T | 1 | a0091c0122t0008g0157 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.8026+169C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 66/93 | chr1 | 149532686 | ||||||
| chr1:149532708
|
G | T | 1 | a0183c0041t0002g0246 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.8026+191G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 66/93 | chr1 | 149532708 | ||||||
| chr1:149532712
|
C | G | 1 | a0167c0203t0028g0269 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.8026+195C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 66/93 | chr1 | 149532712 | ||||||
| chr1:149532715
|
T | C | 4 | a0006c0211t0019g0211a0043c0209t0004g0207a0166c0198t0005g0210others(1): Show | 4 | HG02165.hp1 HG02895.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.8026+198T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 66/93 | chr1 | 149532715 | ||||||
| chr1:149532718
|
C | T | 1 | a0082c0117t0001g0009 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.8026+201C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 66/93 | chr1 | 149532718 | ||||||
| chr1:149532736
|
T | C | 153 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(150): Show | 156 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.8026+219T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 66/93 | chr1 | 149532736 | ||||||
| chr1:149532737
|
G | A | 2 | a0043c0209t0004g0207a0169c0205t0004g0209 | 2 | HG02165.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.8026+220G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 66/93 | chr1 | 149532737 | ||||||
| chr1:149532771
|
C | T | 1 | a0165c0200t0005g0212 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.8026+254C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 66/93 | chr1 | 149532771 | ||||||
| chr1:149532782
|
T | C | 77 | a0001c0001t0001g0121a0003c0003t0001g0115a0003c0003t0001g0116others(74): Show | 77 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.8026+265T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 66/93 | chr1 | 149532782 | ||||||
| chr1:149532795
|
G | A | 13 | a0031c0028t0003g0180a0031c0028t0003g0194a0111c0132t0001g0199others(10): Show | 13 | HG01074.hp1 HG01081.hp2 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.8026+278G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 66/93 | chr1 | 149532795 | ||||||
| chr1:149532812
|
C | G | 1 | a0146c0176t0003g0110 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.8026+295C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 66/93 | chr1 | 149532812 | ||||||
| chr1:149532816
|
G | T | 5 | a0161c0197t0005g0214a0162c0196t0005g0213a0163c0199t0005g0215others(2): Show | 5 | HG00544.hp2 HG00558.hp2 HG00735.hp2 others(2): Show |
intron_variant | MODIFIER | c.8026+299G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 66/93 | chr1 | 149532816 | ||||||
| chr1:149532823
|
G | A | 201 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(198): Show | 204 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(201): Show |
intron_variant | MODIFIER | c.8026+306G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 66/93 | chr1 | 149532823 | ||||||
| chr1:149532837
|
A | T | 5 | a0161c0197t0005g0214a0162c0196t0005g0213a0163c0199t0005g0215others(2): Show | 5 | HG00544.hp2 HG00558.hp2 HG00735.hp2 others(2): Show |
intron_variant | MODIFIER | c.8026+320A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 66/93 | chr1 | 149532837 | ||||||
| chr1:149532875
|
C | T | 1 | a0080c0106t0001g0019 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.8027-352C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 66/93 | chr1 | 149532875 | ||||||
| chr1:149532936
|
G | T | 1 | a0008c0037t0001g0075 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.8027-291G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 66/93 | chr1 | 149532936 | ||||||
| chr1:149532975
|
C | T | 1 | a0170c0208t0004g0202 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.8027-252C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 66/93 | chr1 | 149532975 | ||||||
| chr1:149532979
|
T | C | 1 | a0164c0201t0004g0205 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.8027-248T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 66/93 | chr1 | 149532979 | ||||||
| chr1:149533019
|
A | T | 8 | a0044c0210t0004g0206a0161c0197t0005g0214a0162c0196t0005g0213others(5): Show | 8 | HG00544.hp2 HG00558.hp2 HG00735.hp2 others(5): Show |
intron_variant | MODIFIER | c.8027-208A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 66/93 | chr1 | 149533019 | ||||||
| chr1:149533020
|
C | T | 1 | a0108c0143t0001g0027 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.8027-207C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 66/93 | chr1 | 149533020 | ||||||
| chr1:149533045
|
G | T | 1 | a0163c0199t0005g0215 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.8027-182G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 66/93 | chr1 | 149533045 | ||||||
| chr1:149533145
|
C | T | 1 | a0120c0155t0001g0126 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.8027-82C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 66/93 | chr1 | 149533145 | ||||||
| chr1:149533156
|
T | C | 1 | a0135c0161t0001g0057 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.8027-71T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 66/93 | chr1 | 149533156 | ||||||
| chr1:149533290
|
G | A | 241 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(238): Show | 244 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(241): Show |
intron_variant | MODIFIER | c.8078+12G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 67/93 | chr1 | 149533290 | ||||||
| chr1:149533328
|
C | A | 44 | a0003c0003t0001g0115a0003c0003t0001g0116a0003c0003t0001g0117others(41): Show | 44 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.8078+50C>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 67/93 | chr1 | 149533328 | ||||||
| chr1:149533328
|
C | CCTGGTTC others(23754): Show |
1 | a0153c0128t0003g0125 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.8078+244_8078+245i others(23763): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 67/93 | INFO_REALIGN_3_PRIME | chr1 | 149533328 | |||||
| chr1:149533328
|
C | CCTGGTTC others(23758): Show |
1 | a0063c0090t0003g0187 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.8078+244_8078+245i others(23767): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 67/93 | INFO_REALIGN_3_PRIME | chr1 | 149533328 | |||||
| chr1:149533348
|
G | C | 2 | a0016c0017t0001g0028a0016c0017t0001g0029 | 2 | HG03239.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.8078+70G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 67/93 | chr1 | 149533348 | ||||||
| chr1:149533349
|
C | T | 1 | a0081c0113t0001g0148 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.8078+71C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 67/93 | chr1 | 149533349 | ||||||
| chr1:149533380
|
G | C | 1 | a0180c0072t0002g0218 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.8078+102G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 67/93 | chr1 | 149533380 | ||||||
| chr1:149533405
|
A | G | 4 | a0161c0197t0005g0214a0162c0196t0005g0213a0163c0199t0005g0215others(1): Show | 4 | HG00544.hp2 HG00558.hp2 HG00735.hp2 others(1): Show |
intron_variant | MODIFIER | c.8078+127A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 67/93 | chr1 | 149533405 | ||||||
| chr1:149533439
|
G | A | 1 | a0202c0064t0002g0262 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.8078+161G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 67/93 | chr1 | 149533439 | ||||||
| chr1:149533482
|
G | C | 15 | a0001c0001t0001g0121a0011c0010t0001g0010a0011c0010t0001g0011others(12): Show | 15 | HG00423.hp2 HG00609.hp2 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.8078+204G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 67/93 | chr1 | 149533482 | ||||||
| chr1:149533501
|
A | C | 1 | a0093c0124t0001g0153 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.8078+223A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 67/93 | chr1 | 149533501 | ||||||
| chr1:149533516
|
C | T | 6 | a0183c0041t0002g0246a0188c0051t0002g0252a0190c0049t0002g0244others(3): Show | 6 | NA18954.hp2 NA18959.hp1 NA18962.hp2 others(3): Show |
intron_variant | MODIFIER | c.8078+238C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 67/93 | chr1 | 149533516 | ||||||
| chr1:149533523
|
G | A | 80 | a0002c0002t0003g0182a0002c0002t0003g0188a0002c0002t0003g0189others(77): Show | 81 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.8078+245G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 67/93 | chr1 | 149533523 | ||||||
| chr1:149533661
|
G | C | 3 | a0043c0209t0004g0207a0044c0210t0004g0206a0172c0204t0004g0268 | 3 | HG02165.hp1 NA18972.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.8079-264G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 67/93 | chr1 | 149533661 | ||||||
| chr1:149533664
|
C | T | 5 | a0011c0010t0001g0010a0011c0010t0001g0011a0011c0010t0001g0012others(2): Show | 5 | HG01257.hp2 HG02165.hp2 NA18981.hp2 others(2): Show |
intron_variant | MODIFIER | c.8079-261C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 67/93 | chr1 | 149533664 | ||||||
| chr1:149533666
|
T | TTC | 36 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(33): Show | 37 | HG00099.hp2 HG00733.hp2 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.8079-245_8079-244d others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 67/93 | INFO_REALIGN_3_PRIME | chr1 | 149533666 | |||||
| chr1:149533666
|
T | TTCTC | 2 | a0015c0036t0006g0004a0015c0192t0006g0270 | 3 | HG02896.hp1 HG02897.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.8079-247_8079-244d others(6): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 67/93 | INFO_REALIGN_3_PRIME | chr1 | 149533666 | |||||
| chr1:149533666
|
T | TTCTCTCT others(9477): Show |
1 | a0055c0086t0001g0168 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.8079-198_8079-197i others(9486): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 67/93 | INFO_REALIGN_3_PRIME | chr1 | 149533666 | |||||
| chr1:149533666
|
T | TTCTCTCT others(4754): Show |
1 | a0009c0006t0001g0081 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.8079-198_8079-197i others(4763): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 67/93 | INFO_REALIGN_3_PRIME | chr1 | 149533666 | |||||
| chr1:149533666
|
TTC | T | 5 | a0179c0071t0002g0260a0184c0042t0002g0236a0187c0050t0002g0250others(2): Show | 5 | HG00738.hp1 HG03942.hp1 NA18612.hp2 others(2): Show |
intron_variant | MODIFIER | c.8079-245_8079-244d others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 67/93 | INFO_REALIGN_3_PRIME | chr1 | 149533666 | |||||
| chr1:149533672
|
CTCTCTCT others(3): Show |
C | 2 | a0006c0212t0002g0223a0006c0214t0002g0265 | 2 | HG01891.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.8079-251_8079-242d others(12): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 67/93 | INFO_REALIGN_3_PRIME | chr1 | 149533672 | |||||
| chr1:149533672
|
CTCTCTCT others(7): Show |
C | 1 | a0006c0213t0002g0224 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.8079-251_8079-238d others(16): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 67/93 | INFO_REALIGN_3_PRIME | chr1 | 149533672 | |||||
| chr1:149533674
|
CTCTCTCT others(13): Show |
C | 2 | a0204c0067t0002g0248a0207c0046t0002g0241 | 2 | HG02129.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.8079-249_8079-230d others(22): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 67/93 | INFO_REALIGN_3_PRIME | chr1 | 149533674 | |||||
| chr1:149533676
|
CTCTCTGT others(13): Show |
C | 25 | a0001c0001t0001g0121a0011c0010t0001g0010a0011c0010t0001g0011others(22): Show | 25 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(22): Show |
intron_variant | MODIFIER | c.8079-247_8079-228d others(22): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 67/93 | INFO_REALIGN_3_PRIME | chr1 | 149533676 | |||||
| chr1:149533678
|
C | CTG | 6 | a0034c0013t0002g0220a0034c0013t0002g0221a0181c0073t0002g0272others(3): Show | 6 | HG00621.hp1 HG03831.hp1 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.8079-246_8079-245i others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 67/93 | INFO_REALIGN_3_PRIME | chr1 | 149533678 | |||||
| chr1:149533678
|
CTCTGTGT others(3): Show |
C | 8 | a0032c0012t0002g0232a0032c0012t0002g0266a0033c0011t0002g0254others(5): Show | 8 | HG01081.hp1 HG01358.hp2 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.8079-245_8079-236d others(12): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 67/93 | INFO_REALIGN_3_PRIME | chr1 | 149533678 | |||||
| chr1:149533678
|
CTCTGTGT others(13): Show |
C | 1 | a0119c0153t0001g0097 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.8079-245_8079-226d others(22): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 67/93 | INFO_REALIGN_3_PRIME | chr1 | 149533678 | |||||
| chr1:149533680
|
C | CTCTCTCT others(3): Show |
1 | a0172c0204t0004g0268 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.8079-244_8079-243i others(12): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 67/93 | INFO_REALIGN_3_PRIME | chr1 | 149533680 | |||||
| chr1:149533680
|
C | CTCTG | 55 | a0003c0003t0001g0115a0003c0003t0001g0116a0003c0003t0001g0117others(52): Show | 55 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.8079-244_8079-243i others(6): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 67/93 | INFO_REALIGN_3_PRIME | chr1 | 149533680 | |||||
| chr1:149533680
|
C | CTCTGTG | 20 | a0004c0026t0001g0008a0020c0020t0001g0041a0021c0022t0001g0169others(17): Show | 20 | HG01891.hp2 HG01978.hp1 HG01978.hp2 others(17): Show |
intron_variant | MODIFIER | c.8079-244_8079-243i others(8): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 67/93 | INFO_REALIGN_3_PRIME | chr1 | 149533680 | |||||
| chr1:149533680
|
C | CTCTGTGT others(1): Show |
5 | a0052c0079t0021g0176a0068c0096t0010g0090a0088c0105t0008g0100others(2): Show | 5 | HG00423.hp1 HG01109.hp2 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.8079-244_8079-243i others(10): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 67/93 | INFO_REALIGN_3_PRIME | chr1 | 149533680 | |||||
| chr1:149533680
|
C | CTCTGTGT others(3): Show |
9 | a0005c0004t0001g0056a0005c0004t0001g0131a0005c0004t0001g0132others(6): Show | 9 | HG00408.hp1 HG00621.hp2 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.8079-244_8079-243i others(12): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 67/93 | INFO_REALIGN_3_PRIME | chr1 | 149533680 | |||||
| chr1:149533680
|
C | CTCTGTGT others(5): Show |
3 | a0008c0037t0001g0075a0127c0169t0001g0052a0142c0180t0001g0108 | 3 | HG01168.hp2 HG01928.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.8079-244_8079-243i others(14): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 67/93 | INFO_REALIGN_3_PRIME | chr1 | 149533680 | |||||
| chr1:149533680
|
C | CTCTGTGT others(7): Show |
1 | a0078c0111t0001g0102 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.8079-244_8079-243i others(16): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 67/93 | INFO_REALIGN_3_PRIME | chr1 | 149533680 | |||||
| chr1:149533680
|
C | CTCTGTGT others(9): Show |
2 | a0008c0215t0001g0067a0197c0066t0002g0238 | 2 | HG01496.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.8079-244_8079-243i others(18): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 67/93 | INFO_REALIGN_3_PRIME | chr1 | 149533680 | |||||
| chr1:149533680
|
C | CTG | 12 | a0002c0002t0003g0182a0002c0002t0003g0188a0002c0002t0003g0189others(9): Show | 12 | HG01071.hp1 HG01975.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.8079-199_8079-198d others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 67/93 | INFO_REALIGN_3_PRIME | chr1 | 149533680 | |||||
| chr1:149533680
|
C | CTGTG | 3 | a0018c0018t0001g0166a0108c0143t0001g0027a0148c0181t0001g0124 | 3 | HG01123.hp1 HG02257.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.8079-201_8079-198d others(6): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 67/93 | INFO_REALIGN_3_PRIME | chr1 | 149533680 | |||||
| chr1:149533680
|
C | G | 17 | a0006c0211t0019g0211a0034c0013t0002g0220a0034c0013t0002g0221others(14): Show | 17 | HG00621.hp1 HG00738.hp1 HG02040.hp2 others(14): Show |
intron_variant | MODIFIER | c.8079-245C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 67/93 | chr1 | 149533680 | ||||||
| chr1:149533680
|
CTG | C | 8 | a0043c0209t0004g0207a0044c0210t0004g0206a0131c0171t0001g0145others(5): Show | 8 | HG00735.hp1 HG02129.hp1 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.8079-199_8079-198d others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 67/93 | INFO_REALIGN_3_PRIME | chr1 | 149533680 | |||||
| chr1:149533680
|
CTGTG | C | 3 | a0001c0001t0001g0158a0048c0081t0011g0151a0082c0117t0001g0009 | 3 | HG01109.hp1 HG02647.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.8079-201_8079-198d others(6): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 67/93 | INFO_REALIGN_3_PRIME | chr1 | 149533680 | |||||
| chr1:149533680
|
CTGTGTG | C | 3 | a0042c0195t0001g0023a0064c0094t0001g0047a0103c0142t0001g0074 | 3 | HG02486.hp1 HG03710.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.8079-203_8079-198d others(8): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 67/93 | INFO_REALIGN_3_PRIME | chr1 | 149533680 | |||||
| chr1:149533680
|
CTGTGTGT others(3): Show |
C | 3 | a0037c0016t0002g0256a0037c0016t0002g0257a0130c0170t0001g0120 | 3 | HG00642.hp1 HG01069.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.8079-207_8079-198d others(12): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 67/93 | INFO_REALIGN_3_PRIME | chr1 | 149533680 | |||||
| chr1:149533680
|
CTGTGTGT others(7): Show |
C | 2 | a0002c0002t0007g0190a0005c0004t0025g0073 | 2 | NA18960.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.8079-211_8079-198d others(16): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 67/93 | INFO_REALIGN_3_PRIME | chr1 | 149533680 | |||||
| chr1:149533680
|
CTGTGTGT others(11): Show |
C | 1 | a0004c0027t0001g0001 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.8079-215_8079-198d others(20): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 67/93 | INFO_REALIGN_3_PRIME | chr1 | 149533680 | |||||
| chr1:149533680
|
CTGTGTGT others(15): Show |
C | 1 | a0180c0072t0002g0218 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.8079-219_8079-198d others(24): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 67/93 | INFO_REALIGN_3_PRIME | chr1 | 149533680 | |||||
| chr1:149533682
|
G | C | 12 | a0001c0001t0001g0136a0022c0023t0001g0156a0022c0023t0001g0160others(9): Show | 12 | HG01099.hp1 HG01099.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.8079-243G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 67/93 | chr1 | 149533682 | ||||||
| chr1:149533684
|
G | C | 7 | a0043c0209t0004g0207a0044c0210t0004g0206a0131c0171t0001g0145others(4): Show | 7 | HG00735.hp1 HG02129.hp1 HG02165.hp1 others(4): Show |
intron_variant | MODIFIER | c.8079-241G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 67/93 | chr1 | 149533684 | ||||||
| chr1:149533686
|
G | C | 4 | a0001c0001t0001g0158a0043c0209t0004g0207a0044c0210t0004g0206others(1): Show | 4 | HG02165.hp1 HG02647.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.8079-239G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 67/93 | chr1 | 149533686 | ||||||
| chr1:149533688
|
G | C | 3 | a0043c0209t0004g0207a0044c0210t0004g0206a0103c0142t0001g0074 | 3 | HG02165.hp1 NA18957.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.8079-237G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 67/93 | chr1 | 149533688 | ||||||
| chr1:149533692
|
G | C | 1 | a0130c0170t0001g0120 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.8079-233G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 67/93 | chr1 | 149533692 | ||||||
| chr1:149533696
|
G | C | 1 | a0005c0004t0025g0073 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.8079-229G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 67/93 | chr1 | 149533696 | ||||||
| chr1:149533696
|
G | GTGTGTGT others(28488): Show |
1 | a0080c0106t0001g0019 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.8079-219_8079-218i others(28497): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 67/93 | INFO_REALIGN_3_PRIME | chr1 | 149533696 | |||||
| chr1:149533697
|
T | TGTGC | 4 | a0161c0197t0005g0214a0162c0196t0005g0213a0163c0199t0005g0215others(1): Show | 4 | HG00544.hp2 HG00558.hp2 HG00735.hp2 others(1): Show |
intron_variant | MODIFIER | c.8079-225_8079-224i others(6): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 67/93 | INFO_REALIGN_3_PRIME | chr1 | 149533697 | |||||
| chr1:149533700
|
G | C | 1 | a0004c0027t0001g0001 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.8079-225G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 67/93 | chr1 | 149533700 | ||||||
| chr1:149533701
|
T | C | 2 | a0006c0211t0019g0211a0066c0097t0001g0175 | 2 | HG02300.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.8079-224T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 67/93 | chr1 | 149533701 | ||||||
| chr1:149533703
|
T | C | 39 | a0003c0003t0001g0115a0003c0003t0001g0116a0003c0003t0001g0117others(36): Show | 39 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.8079-222T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 67/93 | chr1 | 149533703 | ||||||
| chr1:149533703
|
T | TGTGC | 5 | a0027c0029t0001g0062a0047c0216t0001g0068a0065c0098t0001g0101others(2): Show | 5 | HG01934.hp2 HG03209.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.8079-219_8079-218i others(6): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 67/93 | INFO_REALIGN_3_PRIME | chr1 | 149533703 | |||||
| chr1:149533704
|
G | C | 1 | a0180c0072t0002g0218 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.8079-221G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 67/93 | chr1 | 149533704 | ||||||
| chr1:149533705
|
T | C | 3 | a0006c0212t0002g0223a0006c0213t0002g0224a0006c0214t0002g0265 | 3 | HG01891.hp1 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.8079-220T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 67/93 | chr1 | 149533705 | ||||||
| chr1:149533710
|
G | C | 29 | a0001c0001t0001g0121a0011c0010t0001g0010a0011c0010t0001g0011others(26): Show | 29 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.8079-215G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 67/93 | chr1 | 149533710 | ||||||
| chr1:149533710
|
G | GTGTGTGT others(4722): Show |
1 | a0084c0115t0001g0114 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.8251+98_8251+99ins others(4729): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 68/93 | INFO_REALIGN_3_PRIME | chr1 | 149533710 | |||||
| chr1:149533714
|
G | A | 4 | a0161c0197t0005g0214a0162c0196t0005g0213a0163c0199t0005g0215others(1): Show | 4 | HG00544.hp2 HG00558.hp2 HG00735.hp2 others(1): Show |
intron_variant | MODIFIER | c.8079-211G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 67/93 | chr1 | 149533714 | ||||||
| chr1:149533729
|
T | C | 54 | a0003c0003t0001g0115a0003c0003t0001g0116a0003c0003t0001g0117others(51): Show | 54 | HG00438.hp1 HG00544.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.8079-196T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 67/93 | chr1 | 149533729 | ||||||
| chr1:149533729
|
T | TATCTGTC others(18971): Show |
1 | a0048c0081t0011g0151 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.8251+98_8251+99ins others(18978): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 68/93 | INFO_REALIGN_3_PRIME | chr1 | 149533729 | |||||
| chr1:149533729
|
T | TATCTGTC others(14248): Show |
1 | a0019c0021t0001g0098 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.8251+98_8251+99ins others(14255): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 68/93 | INFO_REALIGN_3_PRIME | chr1 | 149533729 | |||||
| chr1:149533729
|
T | TATCTGTC others(14280): Show |
1 | a0101c0039t0001g0079 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.8361-307_8361-306i others(14289): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 69/93 | INFO_REALIGN_3_PRIME | chr1 | 149533729 | |||||
| chr1:149533729
|
T | TATCTGTC others(4752): Show |
1 | a0046c0077t0001g0083 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.8360+71_8360+72ins others(4759): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 69/93 | INFO_REALIGN_3_PRIME | chr1 | 149533729 | |||||
| chr1:149533729
|
T | TATCTGTC others(14268): Show |
1 | a0004c0026t0001g0008 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.8360+71_8360+72ins others(14275): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 69/93 | INFO_REALIGN_3_PRIME | chr1 | 149533729 | |||||
| chr1:149533729
|
T | TATCTGTC others(4754): Show |
1 | a0149c0183t0001g0022 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.8360+71_8360+72ins others(4761): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 69/93 | INFO_REALIGN_3_PRIME | chr1 | 149533729 | |||||
| chr1:149533729
|
T | TATCTGTC others(4750): Show |
1 | a0087c0118t0001g0054 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.8360+71_8360+72ins others(4757): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 69/93 | INFO_REALIGN_3_PRIME | chr1 | 149533729 | |||||
| chr1:149533729
|
T | TATCTGTC others(4754): Show |
1 | a0112c0131t0001g0118 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.8251+222_8251+223i others(4763): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 68/93 | INFO_REALIGN_3_PRIME | chr1 | 149533729 | |||||
| chr1:149533789
|
A | G | 7 | a0002c0002t0003g0182a0002c0002t0003g0188a0002c0002t0003g0189others(4): Show | 7 | NA18942.hp1 NA18960.hp2 NA18961.hp2 others(4): Show |
intron_variant | MODIFIER | c.8079-136A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 67/93 | chr1 | 149533789 | ||||||
| chr1:149533804
|
A | C | 5 | a0186c0044t0017g0239a0203c0065t0002g0240a0204c0067t0002g0248others(2): Show | 5 | HG00438.hp2 HG02129.hp2 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.8079-121A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 67/93 | chr1 | 149533804 | ||||||
| chr1:149533814
|
C | G | 25 | a0032c0012t0002g0232a0032c0012t0002g0266a0033c0011t0002g0254others(22): Show | 25 | HG00621.hp1 HG00642.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.8079-111C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 67/93 | chr1 | 149533814 | ||||||
| chr1:149533825
|
G | C | 39 | a0032c0012t0002g0232a0032c0012t0002g0266a0033c0011t0002g0254others(36): Show | 39 | HG00438.hp2 HG00621.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.8079-100G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 67/93 | chr1 | 149533825 | ||||||
| chr1:149533842
|
C | T | 11 | a0183c0041t0002g0246a0186c0044t0017g0239a0188c0051t0002g0252others(8): Show | 11 | HG00438.hp2 HG02129.hp2 HG02602.hp2 others(8): Show |
intron_variant | MODIFIER | c.8079-83C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 67/93 | chr1 | 149533842 | ||||||
| chr1:149533907
|
T | G | 11 | a0183c0041t0002g0246a0186c0044t0017g0239a0188c0051t0002g0252others(8): Show | 11 | HG00438.hp2 HG02129.hp2 HG02602.hp2 others(8): Show |
intron_variant | MODIFIER | c.8079-18T>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 67/93 | chr1 | 149533907 | ||||||
| chr1:149534142
|
C | T | 1 | a0164c0201t0004g0205 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.8251+45C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 68/93 | chr1 | 149534142 | ||||||
| chr1:149534196
|
G | A | 27 | a0002c0002t0003g0182a0002c0002t0003g0188a0002c0002t0003g0189others(24): Show | 27 | HG00438.hp2 HG01071.hp1 HG01975.hp1 others(24): Show |
intron_variant | MODIFIER | c.8251+99G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 68/93 | chr1 | 149534196 | ||||||
| chr1:149534216
|
T | C | 1 | a0164c0201t0004g0205 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.8251+119T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 68/93 | chr1 | 149534216 | ||||||
| chr1:149534267
|
A | T | 27 | a0002c0002t0003g0182a0002c0002t0003g0188a0002c0002t0003g0189others(24): Show | 27 | HG00438.hp2 HG01071.hp1 HG01975.hp1 others(24): Show |
intron_variant | MODIFIER | c.8251+170A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 68/93 | chr1 | 149534267 | ||||||
| chr1:149534286
|
A | T | 27 | a0002c0002t0003g0182a0002c0002t0003g0188a0002c0002t0003g0189others(24): Show | 27 | HG00438.hp2 HG01071.hp1 HG01975.hp1 others(24): Show |
intron_variant | MODIFIER | c.8251+189A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 68/93 | chr1 | 149534286 | ||||||
| chr1:149534288
|
A | G | 27 | a0002c0002t0003g0182a0002c0002t0003g0188a0002c0002t0003g0189others(24): Show | 27 | HG00438.hp2 HG01071.hp1 HG01975.hp1 others(24): Show |
intron_variant | MODIFIER | c.8251+191A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 68/93 | chr1 | 149534288 | ||||||
| chr1:149534313
|
C | A | 3 | a0015c0036t0006g0004a0015c0192t0006g0270a0173c0191t0006g0271 | 4 | HG02145.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.8251+216C>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 68/93 | chr1 | 149534313 | ||||||
| chr1:149534320
|
C | T | 2 | a0102c0144t0001g0127a0127c0169t0001g0052 | 2 | HG00423.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.8251+223C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 68/93 | chr1 | 149534320 | ||||||
| chr1:149534321
|
G | A | 27 | a0002c0002t0003g0182a0002c0002t0003g0188a0002c0002t0003g0189others(24): Show | 27 | HG00438.hp2 HG01071.hp1 HG01975.hp1 others(24): Show |
intron_variant | MODIFIER | c.8251+224G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 68/93 | chr1 | 149534321 | ||||||
| chr1:149534323
|
C | T | 27 | a0002c0002t0003g0182a0002c0002t0003g0188a0002c0002t0003g0189others(24): Show | 27 | HG00438.hp2 HG01071.hp1 HG01975.hp1 others(24): Show |
intron_variant | MODIFIER | c.8251+226C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 68/93 | chr1 | 149534323 | ||||||
| chr1:149534324
|
C | G | 1 | a0006c0211t0019g0211 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.8251+227C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 68/93 | chr1 | 149534324 | ||||||
| chr1:149534329
|
C | T | 27 | a0002c0002t0003g0182a0002c0002t0003g0188a0002c0002t0003g0189others(24): Show | 27 | HG00438.hp2 HG01071.hp1 HG01975.hp1 others(24): Show |
intron_variant | MODIFIER | c.8251+232C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 68/93 | chr1 | 149534329 | ||||||
| chr1:149534333
|
T | C | 27 | a0002c0002t0003g0182a0002c0002t0003g0188a0002c0002t0003g0189others(24): Show | 27 | HG00438.hp2 HG01071.hp1 HG01975.hp1 others(24): Show |
intron_variant | MODIFIER | c.8251+236T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 68/93 | chr1 | 149534333 | ||||||
| chr1:149534350
|
C | A | 2 | a0024c0025t0001g0024a0024c0025t0001g0026 | 2 | HG02055.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.8251+253C>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 68/93 | chr1 | 149534350 | ||||||
| chr1:149534381
|
G | T | 1 | a0197c0066t0002g0238 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.8251+284G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 68/93 | chr1 | 149534381 | ||||||
| chr1:149534401
|
T | C | 27 | a0002c0002t0003g0182a0002c0002t0003g0188a0002c0002t0003g0189others(24): Show | 27 | HG00438.hp2 HG01071.hp1 HG01975.hp1 others(24): Show |
intron_variant | MODIFIER | c.8251+304T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 68/93 | chr1 | 149534401 | ||||||
| chr1:149534485
|
T | G | 3 | a0035c0015t0002g0216a0036c0014t0009g0228a0036c0014t0009g0230 | 3 | HG03017.hp2 NA18960.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.8252-327T>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 68/93 | chr1 | 149534485 | ||||||
| chr1:149534496
|
T | A | 5 | a0186c0044t0017g0239a0203c0065t0002g0240a0204c0067t0002g0248others(2): Show | 5 | HG00438.hp2 HG02129.hp2 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.8252-316T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 68/93 | chr1 | 149534496 | ||||||
| chr1:149534502
|
T | C | 32 | a0002c0002t0003g0182a0002c0002t0003g0188a0002c0002t0003g0189others(29): Show | 33 | HG00438.hp2 HG00642.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.8252-310T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 68/93 | chr1 | 149534502 | ||||||
| chr1:149534502
|
T | TAGAAATC others(23782): Show |
1 | a0082c0117t0001g0009 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.8360+71_8360+72ins others(23789): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 69/93 | INFO_REALIGN_3_PRIME | chr1 | 149534502 | |||||
| chr1:149534557
|
G | T | 1 | a0190c0049t0002g0244 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.8252-255G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 68/93 | chr1 | 149534557 | ||||||
| chr1:149534605
|
A | T | 10 | a0002c0002t0003g0182a0002c0002t0003g0188a0002c0002t0003g0189others(7): Show | 10 | HG01071.hp1 HG01975.hp1 HG02148.hp1 others(7): Show |
intron_variant | MODIFIER | c.8252-207A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 68/93 | chr1 | 149534605 | ||||||
| chr1:149534992
|
C | G | 208 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(205): Show | 211 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(208): Show |
intron_variant | MODIFIER | c.8360+72C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 69/93 | chr1 | 149534992 | ||||||
| chr1:149534993
|
T | C | 3 | a0036c0014t0009g0228a0036c0014t0009g0230a0139c0172t0001g0105 | 3 | HG02559.hp1 NA18960.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.8360+73T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 69/93 | chr1 | 149534993 | ||||||
| chr1:149535019
|
A | C | 1 | a0205c0056t0015g0258 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.8360+99A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 69/93 | chr1 | 149535019 | ||||||
| chr1:149535072
|
T | C | 2 | a0164c0201t0004g0205a0170c0208t0004g0202 | 2 | HG00735.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.8360+152T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 69/93 | chr1 | 149535072 | ||||||
| chr1:149535072
|
T | TAGGTTTC others(23791): Show |
1 | a0174c0202t0013g0204 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.8360+187_8360+188i others(23800): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 69/93 | INFO_REALIGN_3_PRIME | chr1 | 149535072 | |||||
| chr1:149535104
|
A | C | 9 | a0013c0035t0001g0038a0013c0035t0001g0084a0013c0162t0001g0040others(6): Show | 9 | HG00642.hp2 HG01071.hp1 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.8360+184A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 69/93 | chr1 | 149535104 | ||||||
| chr1:149535108
|
A | G | 39 | a0006c0211t0019g0211a0006c0212t0002g0223a0006c0213t0002g0224others(36): Show | 40 | HG00544.hp2 HG00558.hp2 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.8360+188A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 69/93 | chr1 | 149535108 | ||||||
| chr1:149535161
|
C | T | 1 | a0006c0211t0019g0211 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.8360+241C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 69/93 | chr1 | 149535161 | ||||||
| chr1:149535179
|
T | C | 1 | a0154c0185t0001g0152 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.8360+259T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 69/93 | chr1 | 149535179 | ||||||
| chr1:149535200
|
C | G | 1 | a0191c0054t0002g0264 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.8360+280C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 69/93 | chr1 | 149535200 | ||||||
| chr1:149535248
|
C | G | 251 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(248): Show | 255 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(252): Show |
intron_variant | MODIFIER | c.8361-306C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 69/93 | chr1 | 149535248 | ||||||
| chr1:149535341
|
G | A | 1 | a0172c0204t0004g0268 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.8361-213G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 69/93 | chr1 | 149535341 | ||||||
| chr1:149535341
|
G | GTC | 9 | a0160c0076t0014g0225a0161c0197t0005g0214a0162c0196t0005g0213others(6): Show | 9 | HG00735.hp2 HG01516.hp1 HG02080.hp2 others(6): Show |
intron_variant | MODIFIER | c.8361-193_8361-192d others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 69/93 | INFO_REALIGN_3_PRIME | chr1 | 149535341 | |||||
| chr1:149535341
|
G | GTCTC | 9 | a0015c0036t0006g0004a0015c0192t0006g0270a0043c0209t0004g0207others(6): Show | 10 | HG01099.hp1 HG02145.hp1 HG02165.hp1 others(7): Show |
intron_variant | MODIFIER | c.8361-195_8361-192d others(6): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 69/93 | INFO_REALIGN_3_PRIME | chr1 | 149535341 | |||||
| chr1:149535341
|
GTCTC | G | 89 | a0001c0001t0001g0121a0001c0001t0001g0158a0002c0002t0003g0182others(86): Show | 89 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.8361-195_8361-192d others(6): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 69/93 | INFO_REALIGN_3_PRIME | chr1 | 149535341 | |||||
| chr1:149535436
|
A | C | 5 | a0044c0210t0004g0206a0168c0206t0004g0203a0169c0205t0004g0209others(2): Show | 5 | HG01099.hp1 HG02698.hp1 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.8361-118A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 69/93 | chr1 | 149535436 | ||||||
| chr1:149535471
|
TA | T | 6 | a0069c0100t0001g0016a0086c0119t0001g0085a0117c0152t0001g0087others(3): Show | 6 | HG00423.hp2 HG02027.hp2 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.8361-81delA | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 69/93 | INFO_REALIGN_3_PRIME | chr1 | 149535471 | |||||
| chr1:149535501
|
G | A | 1 | a0112c0131t0001g0118 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.8361-53G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 69/93 | chr1 | 149535501 | ||||||
| chr1:149535504
|
T | C | 69 | a0006c0211t0019g0211a0006c0212t0002g0223a0006c0213t0002g0224others(66): Show | 70 | HG00544.hp2 HG00558.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.8361-50T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 69/93 | chr1 | 149535504 | ||||||
| chr1:149535534
|
A | T | 2 | a0193c0057t0002g0006a0205c0056t0015g0258 | 2 | HG00621.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.8361-20A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 69/93 | chr1 | 149535534 | ||||||
| chr1:149535550
|
C | G | 4 | a0001c0001t0001g0158a0028c0032t0001g0161a0029c0033t0001g0197others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG03098.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.8361-4C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 69/93 | chr1 | 149535550 | ||||||
| chr1:149535741
|
A | G | 2 | a0161c0197t0005g0214a0162c0196t0005g0213 | 2 | HG00735.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.8533+15A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 70/93 | chr1 | 149535741 | ||||||
| chr1:149535821
|
G | A | 12 | a0036c0014t0009g0228a0036c0014t0009g0230a0185c0043t0002g0247others(9): Show | 12 | HG00621.hp2 HG02040.hp2 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.8533+95G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 70/93 | chr1 | 149535821 | ||||||
| chr1:149535832
|
A | G | 1 | a0205c0056t0015g0258 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.8533+106A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 70/93 | chr1 | 149535832 | ||||||
| chr1:149535882
|
G | C | 2 | a0171c0207t0004g0208a0172c0204t0004g0268 | 2 | HG02698.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.8533+156G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 70/93 | chr1 | 149535882 | ||||||
| chr1:149535923
|
C | T | 40 | a0006c0212t0002g0223a0006c0213t0002g0224a0006c0214t0002g0265others(37): Show | 41 | HG00621.hp1 HG00642.hp1 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.8533+197C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 70/93 | chr1 | 149535923 | ||||||
| chr1:149535948
|
A | C | 70 | a0006c0211t0019g0211a0006c0212t0002g0223a0006c0213t0002g0224others(67): Show | 71 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.8533+222A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 70/93 | chr1 | 149535948 | ||||||
| chr1:149535948
|
A | T | 2 | a0163c0199t0005g0215a0165c0200t0005g0212 | 2 | HG00544.hp2 HG00558.hp2 |
intron_variant | MODIFIER | c.8533+222A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 70/93 | chr1 | 149535948 | ||||||
| chr1:149535949
|
G | A | 3 | a0006c0212t0002g0223a0006c0213t0002g0224a0006c0214t0002g0265 | 3 | HG01891.hp1 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.8533+223G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 70/93 | chr1 | 149535949 | ||||||
| chr1:149535972
|
C | G | 4 | a0163c0199t0005g0215a0165c0200t0005g0212a0171c0207t0004g0208others(1): Show | 4 | HG00544.hp2 HG00558.hp2 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.8533+246C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 70/93 | chr1 | 149535972 | ||||||
| chr1:149535972
|
C | T | 60 | a0006c0211t0019g0211a0006c0212t0002g0223a0006c0213t0002g0224others(57): Show | 61 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.8533+246C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 70/93 | chr1 | 149535972 | ||||||
| chr1:149535985
|
G | C | 2 | a0043c0209t0004g0207a0174c0202t0013g0204 | 2 | HG02165.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.8533+259G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 70/93 | chr1 | 149535985 | ||||||
| chr1:149536026
|
G | T | 1 | a0081c0113t0001g0148 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.8533+300G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 70/93 | chr1 | 149536026 | ||||||
| chr1:149536035
|
G | A | 1 | a0197c0066t0002g0238 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.8533+309G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 70/93 | chr1 | 149536035 | ||||||
| chr1:149536091
|
A | G | 2 | a0045c0078t0001g0099a0062c0093t0001g0267 | 2 | HG02258.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.8534-355A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 70/93 | chr1 | 149536091 | ||||||
| chr1:149536117
|
G | C | 1 | a0212c0069t0002g0245 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.8534-329G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 70/93 | chr1 | 149536117 | ||||||
| chr1:149536278
|
A | G | 11 | a0002c0002t0003g0182a0002c0002t0003g0188a0002c0002t0003g0189others(8): Show | 11 | HG00642.hp2 HG01071.hp1 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.8534-168A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 70/93 | chr1 | 149536278 | ||||||
| chr1:149536319
|
T | C | 1 | a0154c0185t0001g0152 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.8534-127T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 70/93 | chr1 | 149536319 | ||||||
| chr1:149536363
|
C | T | 134 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(131): Show | 136 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(133): Show |
intron_variant | MODIFIER | c.8534-83C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 70/93 | chr1 | 149536363 | ||||||
| chr1:149536366
|
G | C | 2 | a0004c0026t0001g0008a0059c0091t0001g0130 | 2 | HG01891.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.8534-80G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 70/93 | chr1 | 149536366 | ||||||
| chr1:149536405
|
A | T | 1 | a0008c0037t0001g0075 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.8534-41A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 70/93 | chr1 | 149536405 | ||||||
| chr1:149536419
|
G | A | 90 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(87): Show | 92 | HG00099.hp1 HG00099.hp2 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.8534-27G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 70/93 | chr1 | 149536419 | ||||||
| chr1:149536426
|
C | T | 1 | a0081c0113t0001g0148 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.8534-20C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 70/93 | chr1 | 149536426 | ||||||
| chr1:149536429
|
G | T | 2 | a0161c0197t0005g0214a0162c0196t0005g0213 | 2 | HG00735.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.8534-17G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 70/93 | chr1 | 149536429 | ||||||
| chr1:149536516
|
G | A | 2 | a0163c0199t0005g0215a0165c0200t0005g0212 | 2 | HG00544.hp2 HG00558.hp2 |
intron_variant | MODIFIER | c.8585+19G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 71/93 | chr1 | 149536516 | ||||||
| chr1:149536528
|
C | T | 16 | a0036c0014t0009g0228a0036c0014t0009g0230a0185c0043t0002g0247others(13): Show | 16 | HG00438.hp2 HG02040.hp2 HG02080.hp2 others(13): Show |
intron_variant | MODIFIER | c.8585+31C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 71/93 | chr1 | 149536528 | ||||||
| chr1:149536567
|
A | G | 1 | a0188c0051t0002g0252 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.8585+70A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 71/93 | chr1 | 149536567 | ||||||
| chr1:149536672
|
C | T | 2 | a0163c0199t0005g0215a0165c0200t0005g0212 | 2 | HG00544.hp2 HG00558.hp2 |
intron_variant | MODIFIER | c.8585+175C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 71/93 | chr1 | 149536672 | ||||||
| chr1:149536676
|
A | T | 122 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(119): Show | 124 | HG00099.hp1 HG00099.hp2 HG00609.hp2 others(121): Show |
intron_variant | MODIFIER | c.8585+179A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 71/93 | chr1 | 149536676 | ||||||
| chr1:149536691
|
C | G | 1 | a0188c0051t0002g0252 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.8585+194C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 71/93 | chr1 | 149536691 | ||||||
| chr1:149536701
|
A | T | 1 | a0205c0056t0015g0258 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.8585+204A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 71/93 | chr1 | 149536701 | ||||||
| chr1:149536736
|
A | G | 1 | a0205c0056t0015g0258 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.8585+239A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 71/93 | chr1 | 149536736 | ||||||
| chr1:149536792
|
G | A | 1 | a0032c0012t0002g0232 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.8585+295G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 71/93 | chr1 | 149536792 | ||||||
| chr1:149536854
|
G | A | 1 | a0112c0131t0001g0118 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.8586-246G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 71/93 | chr1 | 149536854 | ||||||
| chr1:149536871
|
C | T | 13 | a0031c0028t0003g0180a0031c0028t0003g0194a0089c0123t0001g0164others(10): Show | 13 | HG01074.hp1 HG01081.hp2 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.8586-229C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 71/93 | chr1 | 149536871 | ||||||
| chr1:149536879
|
C | CCT | 125 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(122): Show | 127 | HG00099.hp1 HG00099.hp2 HG00609.hp2 others(124): Show |
intron_variant | MODIFIER | c.8586-201_8586-200d others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 71/93 | INFO_REALIGN_3_PRIME | chr1 | 149536879 | |||||
| chr1:149536879
|
CCT | C | 36 | a0006c0211t0019g0211a0006c0214t0002g0265a0015c0036t0006g0004others(33): Show | 37 | HG00438.hp2 HG00621.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.8586-201_8586-200d others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 71/93 | INFO_REALIGN_3_PRIME | chr1 | 149536879 | |||||
| chr1:149536926
|
C | T | 3 | a0033c0011t0002g0254a0033c0011t0002g0255a0178c0070t0002g0253 | 3 | NA18947.hp2 NA19082.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.8586-174C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 71/93 | chr1 | 149536926 | ||||||
| chr1:149536929
|
T | C | 121 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(118): Show | 123 | HG00099.hp1 HG00099.hp2 HG00609.hp2 others(120): Show |
intron_variant | MODIFIER | c.8586-171T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 71/93 | chr1 | 149536929 | ||||||
| chr1:149537028
|
A | C | 3 | a0006c0212t0002g0223a0006c0213t0002g0224a0006c0214t0002g0265 | 3 | HG01891.hp1 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.8586-72A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 71/93 | chr1 | 149537028 | ||||||
| chr1:149537035
|
C | G | 5 | a0006c0211t0019g0211a0161c0197t0005g0214a0162c0196t0005g0213others(2): Show | 5 | HG00558.hp2 HG00735.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.8586-65C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 71/93 | chr1 | 149537035 | ||||||
| chr1:149537096
|
C | T | 31 | a0032c0012t0002g0232a0032c0012t0002g0266a0033c0011t0002g0254others(28): Show | 31 | HG00642.hp1 HG00738.hp1 HG01069.hp2 others(28): Show |
splice_region_variant&intron_variant | LOW | c.8586-4C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 71/93 | chr1 | 149537096 | ||||||
| chr1:149537390
|
A | G | 90 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(87): Show | 91 | HG00099.hp1 HG00099.hp2 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.8758+118A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 72/93 | chr1 | 149537390 | ||||||
| chr1:149537396
|
G | A | 14 | a0036c0014t0009g0228a0036c0014t0009g0230a0186c0044t0017g0239others(11): Show | 14 | HG00438.hp2 HG02040.hp2 HG02080.hp2 others(11): Show |
intron_variant | MODIFIER | c.8758+124G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 72/93 | chr1 | 149537396 | ||||||
| chr1:149537463
|
G | T | 2 | a0180c0072t0002g0218a0181c0073t0002g0272 | 2 | HG03831.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.8758+191G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 72/93 | chr1 | 149537463 | ||||||
| chr1:149537470
|
T | C | 1 | a0170c0208t0004g0202 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.8758+198T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 72/93 | chr1 | 149537470 | ||||||
| chr1:149537491
|
T | C | 60 | a0006c0211t0019g0211a0011c0010t0001g0010a0011c0010t0001g0011others(57): Show | 61 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.8758+219T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 72/93 | chr1 | 149537491 | ||||||
| chr1:149537513
|
C | G | 2 | a0171c0207t0004g0208a0172c0204t0004g0268 | 2 | HG02698.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.8758+241C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 72/93 | chr1 | 149537513 | ||||||
| chr1:149537537
|
T | C | 102 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(99): Show | 104 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.8758+265T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 72/93 | chr1 | 149537537 | ||||||
| chr1:149537550
|
G | A | 10 | a0011c0010t0001g0010a0011c0010t0001g0011a0011c0010t0001g0012others(7): Show | 10 | HG00438.hp1 HG00558.hp1 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.8758+278G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 72/93 | chr1 | 149537550 | ||||||
| chr1:149537553
|
C | G | 1 | a0196c0045t0018g0226 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.8758+281C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 72/93 | chr1 | 149537553 | ||||||
| chr1:149537567
|
C | G | 1 | a0044c0210t0004g0206 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.8758+295C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 72/93 | chr1 | 149537567 | ||||||
| chr1:149537571
|
G | T | 4 | a0163c0199t0005g0215a0165c0200t0005g0212a0171c0207t0004g0208others(1): Show | 4 | HG00544.hp2 HG00558.hp2 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.8758+299G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 72/93 | chr1 | 149537571 | ||||||
| chr1:149537578
|
G | A | 155 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(152): Show | 157 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.8758+306G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 72/93 | chr1 | 149537578 | ||||||
| chr1:149537578
|
G | GGATTTCC others(19003): Show |
1 | a0002c0002t0007g0190 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.8810+11_8810+12ins others(19010): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 73/93 | INFO_REALIGN_3_PRIME | chr1 | 149537578 | |||||
| chr1:149537578
|
G | GGATTTCC others(19007): Show |
2 | a0002c0002t0007g0193a0155c0186t0007g0183 | 2 | NA18942.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.8810+11_8810+12ins others(19014): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 73/93 | INFO_REALIGN_3_PRIME | chr1 | 149537578 | |||||
| chr1:149537592
|
A | T | 2 | a0163c0199t0005g0215a0165c0200t0005g0212 | 2 | HG00544.hp2 HG00558.hp2 |
intron_variant | MODIFIER | c.8758+320A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 72/93 | chr1 | 149537592 | ||||||
| chr1:149537603
|
A | T | 3 | a0015c0036t0006g0004a0015c0192t0006g0270a0173c0191t0006g0271 | 4 | HG02145.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.8758+331A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 72/93 | chr1 | 149537603 | ||||||
| chr1:149537619
|
G | A | 2 | a0082c0117t0001g0009a0134c0164t0001g0039 | 2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.8758+347G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 72/93 | chr1 | 149537619 | ||||||
| chr1:149537625
|
A | G | 1 | a0044c0210t0004g0206 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.8758+353A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 72/93 | chr1 | 149537625 | ||||||
| chr1:149537630
|
C | T | 1 | a0080c0106t0001g0019 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.8759-352C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 72/93 | chr1 | 149537630 | ||||||
| chr1:149537719
|
A | G | 1 | a0197c0066t0002g0238 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.8759-263A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 72/93 | chr1 | 149537719 | ||||||
| chr1:149537774
|
A | T | 9 | a0006c0211t0019g0211a0043c0209t0004g0207a0044c0210t0004g0206others(6): Show | 9 | HG00544.hp2 HG00558.hp2 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.8759-208A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 72/93 | chr1 | 149537774 | ||||||
| chr1:149537800
|
G | T | 1 | a0163c0199t0005g0215 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.8759-182G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 72/93 | chr1 | 149537800 | ||||||
| chr1:149537900
|
C | T | 1 | a0131c0171t0001g0145 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.8759-82C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 72/93 | chr1 | 149537900 | ||||||
| chr1:149537938
|
G | T | 1 | a0106c0139t0001g0055 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.8759-44G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 72/93 | chr1 | 149537938 | ||||||
| chr1:149538045
|
A | G | 8 | a0002c0002t0003g0182a0002c0002t0003g0188a0002c0002t0003g0189others(5): Show | 8 | HG00642.hp2 HG01071.hp1 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.8810+12A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 73/93 | chr1 | 149538045 | ||||||
| chr1:149538083
|
C | A | 91 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(88): Show | 92 | HG00099.hp1 HG00099.hp2 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.8810+50C>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 73/93 | chr1 | 149538083 | ||||||
| chr1:149538104
|
C | T | 1 | a0126c0130t0001g0134 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.8810+71C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 73/93 | chr1 | 149538104 | ||||||
| chr1:149538155
|
C | T | 1 | a0164c0201t0004g0205 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.8810+122C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 73/93 | chr1 | 149538155 | ||||||
| chr1:149538160
|
A | G | 4 | a0163c0199t0005g0215a0165c0200t0005g0212a0171c0207t0004g0208others(1): Show | 4 | HG00544.hp2 HG00558.hp2 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.8810+127A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 73/93 | chr1 | 149538160 | ||||||
| chr1:149538174
|
T | G | 3 | a0033c0011t0002g0254a0033c0011t0002g0255a0178c0070t0002g0253 | 3 | NA18947.hp2 NA19082.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.8810+141T>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 73/93 | chr1 | 149538174 | ||||||
| chr1:149538194
|
G | C | 2 | a0161c0197t0005g0214a0162c0196t0005g0213 | 2 | HG00735.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.8810+161G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 73/93 | chr1 | 149538194 | ||||||
| chr1:149538237
|
G | C | 6 | a0018c0018t0001g0113a0023c0024t0001g0003a0058c0087t0001g0048others(3): Show | 7 | HG02109.hp1 HG02257.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.8810+204G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 73/93 | chr1 | 149538237 | ||||||
| chr1:149538271
|
C | T | 2 | a0180c0072t0002g0218a0181c0073t0002g0272 | 2 | HG03831.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.8810+238C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 73/93 | chr1 | 149538271 | ||||||
| chr1:149538278
|
G | A | 79 | a0002c0002t0003g0182a0002c0002t0003g0188a0002c0002t0003g0189others(76): Show | 80 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.8810+245G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 73/93 | chr1 | 149538278 | ||||||
| chr1:149538290
|
G | A | 2 | a0082c0117t0001g0009a0134c0164t0001g0039 | 2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.8810+257G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 73/93 | chr1 | 149538290 | ||||||
| chr1:149538321
|
C | T | 1 | a0018c0018t0001g0166 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.8810+288C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 73/93 | chr1 | 149538321 | ||||||
| chr1:149538367
|
G | A | 3 | a0015c0036t0006g0004a0015c0192t0006g0270a0173c0191t0006g0271 | 4 | HG02145.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.8811-309G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 73/93 | chr1 | 149538367 | ||||||
| chr1:149538386
|
C | A | 2 | a0034c0013t0002g0220a0034c0013t0002g0221 | 2 | NA18961.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.8811-290C>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 73/93 | chr1 | 149538386 | ||||||
| chr1:149538416
|
G | C | 2 | a0043c0209t0004g0207a0044c0210t0004g0206 | 2 | HG02165.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.8811-260G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 73/93 | chr1 | 149538416 | ||||||
| chr1:149538421
|
T | TTC | 8 | a0011c0010t0001g0010a0011c0010t0001g0011a0011c0010t0001g0012others(5): Show | 8 | HG01099.hp1 HG02027.hp2 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.8811-241_8811-240d others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 73/93 | INFO_REALIGN_3_PRIME | chr1 | 149538421 | |||||
| chr1:149538421
|
TTCTCTC | T | 3 | a0006c0212t0002g0223a0006c0213t0002g0224a0006c0214t0002g0265 | 3 | HG01891.hp1 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.8811-245_8811-240d others(8): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 73/93 | INFO_REALIGN_3_PRIME | chr1 | 149538421 | |||||
| chr1:149538429
|
CTCTCTCT others(9): Show |
C | 9 | a0036c0014t0009g0228a0036c0014t0009g0230a0183c0041t0002g0246others(6): Show | 9 | HG02080.hp2 NA18612.hp2 NA18939.hp2 others(6): Show |
intron_variant | MODIFIER | c.8811-245_8811-230d others(18): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 73/93 | INFO_REALIGN_3_PRIME | chr1 | 149538429 | |||||
| chr1:149538431
|
CTCTCTGT others(9): Show |
C | 38 | a0018c0018t0001g0113a0023c0024t0001g0003a0028c0032t0001g0036others(35): Show | 39 | HG00621.hp1 HG00642.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.8811-243_8811-228d others(18): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 73/93 | INFO_REALIGN_3_PRIME | chr1 | 149538431 | |||||
| chr1:149538433
|
C | CTGTGTGT others(7): Show |
1 | a0203c0065t0002g0240 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.8811-242_8811-241i others(16): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 73/93 | INFO_REALIGN_3_PRIME | chr1 | 149538433 | |||||
| chr1:149538433
|
CTCTGTGT others(9): Show |
C | 2 | a0082c0117t0001g0009a0131c0171t0001g0145 | 2 | HG02976.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.8811-241_8811-226d others(18): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 73/93 | INFO_REALIGN_3_PRIME | chr1 | 149538433 | |||||
| chr1:149538435
|
C | CTCTCTGT others(3): Show |
3 | a0045c0078t0001g0099a0164c0201t0004g0205a0174c0202t0013g0204 | 3 | HG00735.hp1 HG03139.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.8811-240_8811-239i others(12): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 73/93 | INFO_REALIGN_3_PRIME | chr1 | 149538435 | |||||
| chr1:149538435
|
C | CTCTG | 4 | a0071c0102t0001g0143a0080c0106t0001g0019a0107c0138t0001g0072others(1): Show | 4 | HG00558.hp1 HG00609.hp2 HG00733.hp2 others(1): Show |
intron_variant | MODIFIER | c.8811-240_8811-239i others(6): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 73/93 | INFO_REALIGN_3_PRIME | chr1 | 149538435 | |||||
| chr1:149538435
|
C | CTCTGTG | 8 | a0012c0009t0001g0172a0050c0080t0001g0177a0081c0113t0001g0148others(5): Show | 8 | HG00423.hp2 HG00438.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.8811-240_8811-239i others(8): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 73/93 | INFO_REALIGN_3_PRIME | chr1 | 149538435 | |||||
| chr1:149538435
|
C | CTCTGTGT others(1): Show |
77 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(74): Show | 78 | HG00099.hp1 HG00099.hp2 HG00741.hp2 others(75): Show |
intron_variant | MODIFIER | c.8811-240_8811-239i others(10): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 73/93 | INFO_REALIGN_3_PRIME | chr1 | 149538435 | |||||
| chr1:149538435
|
C | CTCTGTGT others(3): Show |
19 | a0012c0009t0001g0050a0012c0009t0001g0195a0013c0035t0001g0038others(16): Show | 19 | HG01109.hp2 HG01168.hp2 HG02165.hp2 others(16): Show |
intron_variant | MODIFIER | c.8811-240_8811-239i others(12): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 73/93 | INFO_REALIGN_3_PRIME | chr1 | 149538435 | |||||
| chr1:149538435
|
C | CTCTGTGT others(5): Show |
3 | a0084c0115t0001g0114a0102c0144t0001g0127a0127c0169t0001g0052 | 3 | HG00423.hp1 HG02922.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.8811-240_8811-239i others(14): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 73/93 | INFO_REALIGN_3_PRIME | chr1 | 149538435 | |||||
| chr1:149538435
|
C | CTCTGTGT others(7): Show |
2 | a0171c0207t0004g0208a0172c0204t0004g0268 | 2 | HG02698.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.8811-240_8811-239i others(16): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 73/93 | INFO_REALIGN_3_PRIME | chr1 | 149538435 | |||||
| chr1:149538435
|
C | CTCTGTGT others(9): Show |
2 | a0004c0026t0001g0008a0197c0066t0002g0238 | 2 | HG01891.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.8811-240_8811-239i others(18): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 73/93 | INFO_REALIGN_3_PRIME | chr1 | 149538435 | |||||
| chr1:149538435
|
C | CTCTGTGT others(9515): Show |
1 | a0056c0089t0001g0060 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.8811-240_8811-239i others(9524): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 73/93 | INFO_REALIGN_3_PRIME | chr1 | 149538435 | |||||
| chr1:149538435
|
C | CTG | 15 | a0003c0003t0001g0115a0003c0003t0001g0117a0010c0007t0001g0002others(12): Show | 16 | HG00733.hp1 HG01069.hp1 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.8811-199_8811-198d others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 73/93 | INFO_REALIGN_3_PRIME | chr1 | 149538435 | |||||
| chr1:149538435
|
C | CTGTG | 7 | a0002c0002t0003g0196a0003c0136t0001g0005a0027c0029t0001g0061others(4): Show | 7 | HG01516.hp2 HG01517.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.8811-201_8811-198d others(6): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 73/93 | INFO_REALIGN_3_PRIME | chr1 | 149538435 | |||||
| chr1:149538435
|
C | CTGTGTG | 15 | a0002c0002t0003g0182a0002c0002t0003g0188a0002c0002t0003g0189others(12): Show | 15 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(12): Show |
intron_variant | MODIFIER | c.8811-203_8811-198d others(8): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 73/93 | INFO_REALIGN_3_PRIME | chr1 | 149538435 | |||||
| chr1:149538435
|
C | CTGTGTGT others(1): Show |
9 | a0014c0008t0003g0181a0025c0031t0001g0032a0025c0031t0001g0033others(6): Show | 9 | HG00738.hp2 HG01168.hp1 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.8811-205_8811-198d others(10): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 73/93 | INFO_REALIGN_3_PRIME | chr1 | 149538435 | |||||
| chr1:149538435
|
C | CTGTGTGT others(9): Show |
1 | a0016c0017t0001g0028 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.8811-213_8811-198d others(18): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 73/93 | INFO_REALIGN_3_PRIME | chr1 | 149538435 | |||||
| chr1:149538435
|
C | CTGTGTGT others(11): Show |
1 | a0016c0017t0001g0029 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.8811-215_8811-198d others(20): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 73/93 | INFO_REALIGN_3_PRIME | chr1 | 149538435 | |||||
| chr1:149538435
|
C | G | 8 | a0006c0212t0002g0223a0006c0213t0002g0224a0006c0214t0002g0265others(5): Show | 8 | HG00438.hp2 HG00621.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.8811-241C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 73/93 | chr1 | 149538435 | ||||||
| chr1:149538437
|
G | C | 6 | a0015c0036t0006g0004a0015c0192t0006g0270a0043c0209t0004g0207others(3): Show | 7 | HG02145.hp1 HG02165.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.8811-239G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 73/93 | chr1 | 149538437 | ||||||
| chr1:149538439
|
G | C | 4 | a0006c0211t0019g0211a0043c0209t0004g0207a0044c0210t0004g0206others(1): Show | 4 | HG02165.hp1 HG02622.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.8811-237G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 73/93 | chr1 | 149538439 | ||||||
| chr1:149538441
|
G | C | 1 | a0006c0211t0019g0211 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.8811-235G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 73/93 | chr1 | 149538441 | ||||||
| chr1:149538442
|
T | C | 2 | a0171c0207t0004g0208a0172c0204t0004g0268 | 2 | HG02698.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.8811-234T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 73/93 | chr1 | 149538442 | ||||||
| chr1:149538443
|
G | C | 1 | a0006c0211t0019g0211 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.8811-233G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 73/93 | chr1 | 149538443 | ||||||
| chr1:149538445
|
G | C | 2 | a0030c0034t0001g0092a0030c0034t0001g0093 | 2 | HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.8811-231G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 73/93 | chr1 | 149538445 | ||||||
| chr1:149538446
|
T | TGTGTGTG others(3): Show |
1 | a0167c0203t0028g0269 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.8811-221_8811-220i others(12): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 73/93 | INFO_REALIGN_3_PRIME | chr1 | 149538446 | |||||
| chr1:149538448
|
T | C | 1 | a0170c0208t0004g0202 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.8811-228T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 73/93 | chr1 | 149538448 | ||||||
| chr1:149538452
|
T | C | 5 | a0089c0123t0001g0164a0142c0180t0001g0108a0145c0177t0001g0165others(2): Show | 5 | HG01109.hp2 HG01168.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.8811-224T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 73/93 | chr1 | 149538452 | ||||||
| chr1:149538454
|
T | C | 78 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(75): Show | 79 | HG00099.hp1 HG00099.hp2 HG00741.hp2 others(76): Show |
intron_variant | MODIFIER | c.8811-222T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 73/93 | chr1 | 149538454 | ||||||
| chr1:149538454
|
T | TGTGTGTG others(1): Show |
6 | a0008c0037t0001g0075a0008c0037t0001g0135a0008c0215t0001g0067others(3): Show | 6 | HG00741.hp1 HG01496.hp1 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.8811-215_8811-214i others(10): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 73/93 | INFO_REALIGN_3_PRIME | chr1 | 149538454 | |||||
| chr1:149538455
|
G | T | 1 | a0107c0138t0001g0072 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.8811-221G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 73/93 | chr1 | 149538455 | ||||||
| chr1:149538456
|
T | C | 5 | a0006c0212t0002g0223a0006c0213t0002g0224a0006c0214t0002g0265others(2): Show | 5 | HG01891.hp1 HG01978.hp1 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.8811-220T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 73/93 | chr1 | 149538456 | ||||||
| chr1:149538458
|
T | C | 1 | a0071c0102t0001g0143 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.8811-218T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 73/93 | chr1 | 149538458 | ||||||
| chr1:149538461
|
G | C | 52 | a0015c0036t0006g0004a0015c0192t0006g0270a0018c0018t0001g0113others(49): Show | 54 | HG00621.hp1 HG00642.hp1 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.8811-215G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 73/93 | chr1 | 149538461 | ||||||
| chr1:149538465
|
G | A | 2 | a0163c0199t0005g0215a0165c0200t0005g0212 | 2 | HG00544.hp2 HG00558.hp2 |
intron_variant | MODIFIER | c.8811-211G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 73/93 | chr1 | 149538465 | ||||||
| chr1:149538480
|
T | C | 101 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(98): Show | 102 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.8811-196T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 73/93 | chr1 | 149538480 | ||||||
| chr1:149538480
|
T | TATCTGTC others(4754): Show |
1 | a0085c0114t0001g0025 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.8983+98_8983+99ins others(4761): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 74/93 | INFO_REALIGN_3_PRIME | chr1 | 149538480 | |||||
| chr1:149538480
|
T | TATCTGTC others(4754): Show |
1 | a0042c0195t0001g0023 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.8983+98_8983+99ins others(4761): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 74/93 | INFO_REALIGN_3_PRIME | chr1 | 149538480 | |||||
| chr1:149538480
|
T | TATCTGTC others(9515): Show |
2 | a0102c0144t0001g0127a0127c0169t0001g0052 | 2 | HG00423.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.8983+98_8983+99ins others(9522): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 74/93 | INFO_REALIGN_3_PRIME | chr1 | 149538480 | |||||
| chr1:149538480
|
T | TATCTGTC others(9515): Show |
1 | a0041c0217t0003g0185 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.8983+98_8983+99ins others(9522): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 74/93 | INFO_REALIGN_3_PRIME | chr1 | 149538480 | |||||
| chr1:149538480
|
T | TATCTGTC others(4750): Show |
1 | a0121c0154t0024g0091 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.8983+98_8983+99ins others(4757): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 74/93 | INFO_REALIGN_3_PRIME | chr1 | 149538480 | |||||
| chr1:149538555
|
A | C | 16 | a0036c0014t0009g0228a0036c0014t0009g0230a0183c0041t0002g0246others(13): Show | 16 | HG02040.hp2 HG02080.hp2 HG03942.hp1 others(13): Show |
intron_variant | MODIFIER | c.8811-121A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 73/93 | chr1 | 149538555 | ||||||
| chr1:149538565
|
C | G | 1 | a0205c0056t0015g0258 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.8811-111C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 73/93 | chr1 | 149538565 | ||||||
| chr1:149538576
|
G | C | 50 | a0001c0001t0001g0158a0008c0037t0001g0135a0015c0036t0006g0004others(47): Show | 51 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.8811-100G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 73/93 | chr1 | 149538576 | ||||||
| chr1:149538593
|
C | CTATGCTA others(4730): Show |
1 | a0003c0003t0001g0116 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.9092+61_9092+62ins others(4737): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 75/93 | INFO_REALIGN_3_PRIME | chr1 | 149538593 | |||||
| chr1:149538593
|
C | T | 43 | a0015c0036t0006g0004a0015c0192t0006g0270a0032c0012t0002g0232others(40): Show | 44 | HG00621.hp1 HG00642.hp1 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.8811-83C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 73/93 | chr1 | 149538593 | ||||||
| chr1:149538620
|
G | A | 1 | a0082c0117t0001g0009 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.8811-56G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 73/93 | chr1 | 149538620 | ||||||
| chr1:149538657
|
C | T | 1 | a0195c0060t0002g0229 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.8811-19C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 73/93 | chr1 | 149538657 | ||||||
| chr1:149538658
|
T | G | 40 | a0032c0012t0002g0232a0032c0012t0002g0266a0033c0011t0002g0254others(37): Show | 40 | HG00621.hp1 HG00642.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.8811-18T>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 73/93 | chr1 | 149538658 | ||||||
| chr1:149538871
|
G | A | 5 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(2): Show | 5 | HG00099.hp2 HG01099.hp2 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.8983+23G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 74/93 | chr1 | 149538871 | ||||||
| chr1:149538892
|
C | T | 1 | a0006c0211t0019g0211 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.8983+44C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 74/93 | chr1 | 149538892 | ||||||
| chr1:149538947
|
A | G | 143 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(140): Show | 145 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.8983+99A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 74/93 | chr1 | 149538947 | ||||||
| chr1:149539014
|
G | A | 1 | a0014c0008t0020g0184 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.8983+166G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 74/93 | chr1 | 149539014 | ||||||
| chr1:149539018
|
T | A | 140 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(137): Show | 142 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.8983+170T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 74/93 | chr1 | 149539018 | ||||||
| chr1:149539037
|
T | A | 140 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(137): Show | 142 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.8983+189T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 74/93 | chr1 | 149539037 | ||||||
| chr1:149539039
|
G | A | 140 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(137): Show | 142 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.8983+191G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 74/93 | chr1 | 149539039 | ||||||
| chr1:149539071
|
C | T | 1 | a0160c0076t0014g0225 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.8983+223C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 74/93 | chr1 | 149539071 | ||||||
| chr1:149539072
|
A | G | 140 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(137): Show | 142 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.8983+224A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 74/93 | chr1 | 149539072 | ||||||
| chr1:149539074
|
T | C | 142 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(139): Show | 144 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.8983+226T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 74/93 | chr1 | 149539074 | ||||||
| chr1:149539080
|
T | C | 140 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(137): Show | 142 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.8983+232T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 74/93 | chr1 | 149539080 | ||||||
| chr1:149539084
|
C | T | 140 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(137): Show | 142 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.8983+236C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 74/93 | chr1 | 149539084 | ||||||
| chr1:149539124
|
A | G | 2 | a0164c0201t0004g0205a0170c0208t0004g0202 | 2 | HG00735.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.8983+276A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 74/93 | chr1 | 149539124 | ||||||
| chr1:149539132
|
G | T | 2 | a0186c0044t0017g0239a0197c0066t0002g0238 | 2 | HG02083.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.8983+284G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 74/93 | chr1 | 149539132 | ||||||
| chr1:149539152
|
C | T | 140 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(137): Show | 142 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.8983+304C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 74/93 | chr1 | 149539152 | ||||||
| chr1:149539211
|
G | C | 1 | a0171c0207t0004g0208 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.8984-352G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 74/93 | chr1 | 149539211 | ||||||
| chr1:149539247
|
T | A | 16 | a0036c0014t0009g0228a0036c0014t0009g0230a0183c0041t0002g0246others(13): Show | 16 | HG02040.hp2 HG02080.hp2 HG03942.hp1 others(13): Show |
intron_variant | MODIFIER | c.8984-316T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 74/93 | chr1 | 149539247 | ||||||
| chr1:149539253
|
C | CAGAAATC others(19001): Show |
2 | a0014c0008t0003g0181a0014c0008t0003g0186 | 2 | HG01071.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.8984-208_8984-207i others(19010): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 74/93 | INFO_REALIGN_3_PRIME | chr1 | 149539253 | |||||
| chr1:149539253
|
C | CAGAAATC others(19003): Show |
1 | a0002c0002t0003g0196 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.8984-208_8984-207i others(19012): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 74/93 | INFO_REALIGN_3_PRIME | chr1 | 149539253 | |||||
| chr1:149539253
|
C | CAGAAATC others(19003): Show |
1 | a0002c0002t0003g0182 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.8984-208_8984-207i others(19012): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 74/93 | INFO_REALIGN_3_PRIME | chr1 | 149539253 | |||||
| chr1:149539253
|
C | CAGAAATC others(18999): Show |
1 | a0002c0002t0003g0188 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.8984-208_8984-207i others(19008): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 74/93 | INFO_REALIGN_3_PRIME | chr1 | 149539253 | |||||
| chr1:149539253
|
C | CAGAAATC others(19003): Show |
1 | a0014c0008t0020g0184 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.8984-208_8984-207i others(19012): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 74/93 | INFO_REALIGN_3_PRIME | chr1 | 149539253 | |||||
| chr1:149539253
|
C | CAGAAATC others(19003): Show |
1 | a0002c0002t0003g0189 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.8984-208_8984-207i others(19012): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 74/93 | INFO_REALIGN_3_PRIME | chr1 | 149539253 | |||||
| chr1:149539253
|
C | CAGAAATC others(23754): Show |
1 | a0159c0189t0003g0191 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.8984-208_8984-207i others(23763): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 74/93 | INFO_REALIGN_3_PRIME | chr1 | 149539253 | |||||
| chr1:149539253
|
C | T | 134 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(131): Show | 136 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.8984-310C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 74/93 | chr1 | 149539253 | ||||||
| chr1:149539268
|
G | T | 2 | a0090c0121t0008g0149a0133c0165t0022g0020 | 2 | HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.8984-295G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 74/93 | chr1 | 149539268 | ||||||
| chr1:149539344
|
C | T | 1 | a0120c0155t0001g0126 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.8984-219C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 74/93 | chr1 | 149539344 | ||||||
| chr1:149539521
|
G | C | 1 | a0120c0155t0001g0126 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.8984-42G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 74/93 | chr1 | 149539521 | ||||||
| chr1:149539732
|
G | A | 1 | a0119c0153t0001g0097 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.9092+61G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 75/93 | chr1 | 149539732 | ||||||
| chr1:149539733
|
A | G | 244 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(241): Show | 247 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.9092+62A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 75/93 | chr1 | 149539733 | ||||||
| chr1:149539743
|
C | G | 103 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(100): Show | 105 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.9092+72C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 75/93 | chr1 | 149539743 | ||||||
| chr1:149539744
|
T | C | 3 | a0061c0187t0001g0173a0082c0117t0001g0009a0160c0076t0014g0225 | 3 | HG02145.hp2 HG02622.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.9092+73T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 75/93 | chr1 | 149539744 | ||||||
| chr1:149539770
|
A | C | 1 | a0186c0044t0017g0239 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.9092+99A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 75/93 | chr1 | 149539770 | ||||||
| chr1:149539823
|
T | C | 3 | a0168c0206t0004g0203a0169c0205t0004g0209a0174c0202t0013g0204 | 3 | HG01099.hp1 HG04115.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.9092+152T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 75/93 | chr1 | 149539823 | ||||||
| chr1:149539855
|
A | C | 4 | a0028c0032t0001g0161a0029c0033t0001g0197a0029c0033t0001g0198others(1): Show | 4 | HG02809.hp2 HG03098.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.9092+184A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 75/93 | chr1 | 149539855 | ||||||
| chr1:149539859
|
A | G | 13 | a0006c0211t0019g0211a0006c0212t0002g0223a0006c0213t0002g0224others(10): Show | 14 | HG00544.hp2 HG00558.hp2 HG00621.hp2 others(11): Show |
intron_variant | MODIFIER | c.9092+188A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 75/93 | chr1 | 149539859 | ||||||
| chr1:149539902
|
G | A | 3 | a0028c0032t0001g0161a0029c0033t0001g0197a0029c0033t0001g0198 | 3 | HG02809.hp2 HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.9092+231G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 75/93 | chr1 | 149539902 | ||||||
| chr1:149539999
|
C | G | 180 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(177): Show | 183 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.9093-302C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 75/93 | chr1 | 149539999 | ||||||
| chr1:149540010
|
T | G | 2 | a0143c0179t0001g0021a0149c0183t0001g0022 | 2 | HG02698.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.9093-291T>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 75/93 | chr1 | 149540010 | ||||||
| chr1:149540013
|
T | C | 1 | a0186c0044t0017g0239 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.9093-288T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 75/93 | chr1 | 149540013 | ||||||
| chr1:149540074
|
G | C | 3 | a0006c0212t0002g0223a0006c0213t0002g0224a0006c0214t0002g0265 | 3 | HG01891.hp1 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.9093-227G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 75/93 | chr1 | 149540074 | ||||||
| chr1:149540080
|
C | A | 1 | a0093c0124t0001g0153 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.9093-221C>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 75/93 | chr1 | 149540080 | ||||||
| chr1:149540080
|
C | G | 3 | a0006c0212t0002g0223a0006c0213t0002g0224a0006c0214t0002g0265 | 3 | HG01891.hp1 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.9093-221C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 75/93 | chr1 | 149540080 | ||||||
| chr1:149540086
|
G | C | 1 | a0063c0090t0003g0187 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.9093-215G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 75/93 | chr1 | 149540086 | ||||||
| chr1:149540092
|
G | C | 3 | a0006c0212t0002g0223a0006c0213t0002g0224a0006c0214t0002g0265 | 3 | HG01891.hp1 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.9093-209G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 75/93 | chr1 | 149540092 | ||||||
| chr1:149540092
|
G | GTCTC | 133 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(130): Show | 135 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.9093-195_9093-192d others(6): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 75/93 | INFO_REALIGN_3_PRIME | chr1 | 149540092 | |||||
| chr1:149540092
|
G | GTCTCTC | 6 | a0006c0211t0019g0211a0163c0199t0005g0215a0165c0200t0005g0212others(3): Show | 6 | HG00544.hp2 HG00558.hp2 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.9093-197_9093-192d others(8): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 75/93 | INFO_REALIGN_3_PRIME | chr1 | 149540092 | |||||
| chr1:149540092
|
G | GTCTCTCT others(1): Show |
6 | a0043c0209t0004g0207a0044c0210t0004g0206a0106c0139t0001g0055others(3): Show | 6 | HG00735.hp1 HG02165.hp1 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.9093-199_9093-192d others(10): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 75/93 | INFO_REALIGN_3_PRIME | chr1 | 149540092 | |||||
| chr1:149540092
|
G | GTCTCTCT others(5): Show |
1 | a0170c0208t0004g0202 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.9093-203_9093-192d others(14): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 75/93 | INFO_REALIGN_3_PRIME | chr1 | 149540092 | |||||
| chr1:149540175
|
A | C | 1 | a0054c0085t0001g0150 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.9093-126A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 75/93 | chr1 | 149540175 | ||||||
| chr1:149540183
|
A | C | 2 | a0043c0209t0004g0207a0044c0210t0004g0206 | 2 | HG02165.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.9093-118A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 75/93 | chr1 | 149540183 | ||||||
| chr1:149540222
|
G | A | 2 | a0180c0072t0002g0218a0181c0073t0002g0272 | 2 | HG03831.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.9093-79G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 75/93 | chr1 | 149540222 | ||||||
| chr1:149540251
|
T | C | 33 | a0006c0211t0019g0211a0006c0212t0002g0223a0006c0213t0002g0224others(30): Show | 34 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.9093-50T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 75/93 | chr1 | 149540251 | ||||||
| chr1:149540281
|
A | T | 5 | a0034c0013t0002g0220a0034c0013t0002g0221a0186c0044t0017g0239others(2): Show | 5 | HG02602.hp2 NA18961.hp1 NA19011.hp1 others(2): Show |
intron_variant | MODIFIER | c.9093-20A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 75/93 | chr1 | 149540281 | ||||||
| chr1:149540488
|
A | G | 3 | a0006c0211t0019g0211a0163c0199t0005g0215a0165c0200t0005g0212 | 3 | HG00544.hp2 HG00558.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.9265+15A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 76/93 | chr1 | 149540488 | ||||||
| chr1:149540568
|
G | A | 9 | a0034c0013t0002g0220a0034c0013t0002g0221a0186c0044t0017g0239others(6): Show | 9 | HG00438.hp2 HG02083.hp1 HG02129.hp2 others(6): Show |
intron_variant | MODIFIER | c.9265+95G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 76/93 | chr1 | 149540568 | ||||||
| chr1:149540579
|
A | G | 5 | a0034c0013t0002g0220a0034c0013t0002g0221a0186c0044t0017g0239others(2): Show | 5 | HG02602.hp2 NA18961.hp1 NA19011.hp1 others(2): Show |
intron_variant | MODIFIER | c.9265+106A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 76/93 | chr1 | 149540579 | ||||||
| chr1:149540593
|
G | A | 1 | a0196c0045t0018g0226 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.9265+120G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 76/93 | chr1 | 149540593 | ||||||
| chr1:149540629
|
G | T | 2 | a0028c0032t0001g0036a0124c0158t0001g0095 | 2 | HG03017.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.9265+156G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 76/93 | chr1 | 149540629 | ||||||
| chr1:149540650
|
G | A | 3 | a0015c0036t0006g0004a0015c0192t0006g0270a0173c0191t0006g0271 | 4 | HG02145.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.9265+177G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 76/93 | chr1 | 149540650 | ||||||
| chr1:149540670
|
C | T | 20 | a0006c0211t0019g0211a0006c0212t0002g0223a0006c0213t0002g0224others(17): Show | 21 | HG00544.hp2 HG00558.hp2 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.9265+197C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 76/93 | chr1 | 149540670 | ||||||
| chr1:149540695
|
A | C | 35 | a0006c0211t0019g0211a0006c0212t0002g0223a0006c0213t0002g0224others(32): Show | 36 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.9265+222A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 76/93 | chr1 | 149540695 | ||||||
| chr1:149540718
|
A | G | 3 | a0006c0212t0002g0223a0006c0213t0002g0224a0006c0214t0002g0265 | 3 | HG01891.hp1 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.9265+245A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 76/93 | chr1 | 149540718 | ||||||
| chr1:149540719
|
C | T | 31 | a0006c0211t0019g0211a0006c0212t0002g0223a0006c0213t0002g0224others(28): Show | 32 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.9265+246C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 76/93 | chr1 | 149540719 | ||||||
| chr1:149540773
|
G | T | 1 | a0081c0113t0001g0148 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.9265+300G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 76/93 | chr1 | 149540773 | ||||||
| chr1:149540812
|
G | A | 1 | a0009c0006t0001g0139 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.9265+339G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 76/93 | chr1 | 149540812 | ||||||
| chr1:149540825
|
G | A | 1 | a0062c0093t0001g0267 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.9265+352G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 76/93 | chr1 | 149540825 | ||||||
| chr1:149541110
|
C | T | 42 | a0006c0212t0002g0223a0006c0213t0002g0224a0006c0214t0002g0265others(39): Show | 43 | HG00423.hp2 HG00621.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.9266-83C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 76/93 | chr1 | 149541110 | ||||||
| chr1:149541166
|
G | A | 18 | a0011c0010t0001g0010a0011c0010t0001g0011a0011c0010t0001g0012others(15): Show | 18 | HG00423.hp2 HG01168.hp2 HG02027.hp2 others(15): Show |
intron_variant | MODIFIER | c.9266-27G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 76/93 | chr1 | 149541166 | ||||||
| chr1:149541176
|
G | T | 2 | a0163c0199t0005g0215a0165c0200t0005g0212 | 2 | HG00544.hp2 HG00558.hp2 |
intron_variant | MODIFIER | c.9266-17G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 76/93 | chr1 | 149541176 | ||||||
| chr1:149541275
|
C | T | 36 | a0032c0012t0002g0232a0032c0012t0002g0266a0033c0011t0002g0254others(33): Show | 36 | HG00438.hp2 HG00621.hp1 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.9317+31C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 77/93 | chr1 | 149541275 | ||||||
| chr1:149541284
|
C | T | 1 | a0032c0012t0002g0266 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.9317+40C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 77/93 | chr1 | 149541284 | ||||||
| chr1:149541293
|
A | T | 1 | a0084c0115t0001g0114 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.9317+49A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 77/93 | chr1 | 149541293 | ||||||
| chr1:149541423
|
A | T | 34 | a0011c0010t0001g0010a0011c0010t0001g0011a0011c0010t0001g0012others(31): Show | 34 | HG00423.hp2 HG00621.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.9317+179A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 77/93 | chr1 | 149541423 | ||||||
| chr1:149541483
|
A | G | 3 | a0006c0212t0002g0223a0006c0213t0002g0224a0006c0214t0002g0265 | 3 | HG01891.hp1 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.9317+239A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 77/93 | chr1 | 149541483 | ||||||
| chr1:149541511
|
G | A | 1 | a0143c0179t0001g0021 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.9317+267G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 77/93 | chr1 | 149541511 | ||||||
| chr1:149541582
|
C | T | 1 | a0164c0201t0004g0205 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.9318-271C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 77/93 | chr1 | 149541582 | ||||||
| chr1:149541602
|
G | T | 1 | a0179c0071t0002g0260 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.9318-251G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 77/93 | chr1 | 149541602 | ||||||
| chr1:149541618
|
C | T | 9 | a0011c0010t0001g0010a0011c0010t0001g0011a0011c0010t0001g0012others(6): Show | 9 | HG01168.hp2 HG02602.hp1 HG04184.hp1 others(6): Show |
intron_variant | MODIFIER | c.9318-235C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 77/93 | chr1 | 149541618 | ||||||
| chr1:149541626
|
CCT | C | 5 | a0034c0013t0002g0220a0034c0013t0002g0221a0186c0044t0017g0239others(2): Show | 5 | HG02602.hp2 NA18961.hp1 NA19011.hp1 others(2): Show |
intron_variant | MODIFIER | c.9318-201_9318-200d others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 77/93 | INFO_REALIGN_3_PRIME | chr1 | 149541626 | |||||
| chr1:149541626
|
CCTCT | C | 29 | a0011c0010t0001g0010a0011c0010t0001g0011a0011c0010t0001g0012others(26): Show | 29 | HG00423.hp2 HG00621.hp2 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.9318-203_9318-200d others(6): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 77/93 | INFO_REALIGN_3_PRIME | chr1 | 149541626 | |||||
| chr1:149541626
|
CCTCTCT | C | 103 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(100): Show | 104 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.9318-205_9318-200d others(8): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 77/93 | INFO_REALIGN_3_PRIME | chr1 | 149541626 | |||||
| chr1:149541626
|
CCTCTCTC others(1): Show |
C | 55 | a0006c0211t0019g0211a0006c0212t0002g0223a0006c0213t0002g0224others(52): Show | 56 | HG00438.hp2 HG00621.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.9318-207_9318-200d others(10): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 77/93 | INFO_REALIGN_3_PRIME | chr1 | 149541626 | |||||
| chr1:149541632
|
T | TCTCTCTC others(9501): Show |
1 | a0076c0109t0001g0137 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.9318-206_9318-205i others(9510): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 77/93 | INFO_REALIGN_3_PRIME | chr1 | 149541632 | |||||
| chr1:149541632
|
T | TCTCTCTC others(14262): Show |
1 | a0004c0026t0001g0007 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.9318-206_9318-205i others(14271): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 77/93 | INFO_REALIGN_3_PRIME | chr1 | 149541632 | |||||
| chr1:149541632
|
T | TCTCTCTC others(14262): Show |
1 | a0004c0027t0001g0001 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.9318-206_9318-205i others(14271): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 77/93 | INFO_REALIGN_3_PRIME | chr1 | 149541632 | |||||
| chr1:149541682
|
T | C | 27 | a0001c0001t0001g0121a0011c0010t0001g0010a0011c0010t0001g0011others(24): Show | 27 | HG00423.hp2 HG00621.hp2 HG01168.hp2 others(24): Show |
intron_variant | MODIFIER | c.9318-171T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 77/93 | chr1 | 149541682 | ||||||
| chr1:149541788
|
C | G | 4 | a0006c0211t0019g0211a0163c0199t0005g0215a0165c0200t0005g0212others(1): Show | 4 | HG00544.hp2 HG00558.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.9318-65C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 77/93 | chr1 | 149541788 | ||||||
| chr1:149541849
|
C | T | 4 | a0179c0071t0002g0260a0180c0072t0002g0218a0181c0073t0002g0272others(1): Show | 4 | HG00621.hp2 HG00738.hp1 HG03831.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.9318-4C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 77/93 | chr1 | 149541849 | ||||||
| chr1:149542076
|
G | A | 2 | a0096c0127t0001g0111a0125c0159t0001g0147 | 2 | HG02717.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.9490+51G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 78/93 | chr1 | 149542076 | ||||||
| chr1:149542088
|
C | A | 1 | a0106c0139t0001g0055 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.9490+63C>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 78/93 | chr1 | 149542088 | ||||||
| chr1:149542143
|
A | G | 24 | a0011c0010t0001g0010a0011c0010t0001g0011a0011c0010t0001g0012others(21): Show | 24 | HG00423.hp2 HG01168.hp2 HG02027.hp2 others(21): Show |
intron_variant | MODIFIER | c.9490+118A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 78/93 | chr1 | 149542143 | ||||||
| chr1:149542149
|
G | A | 37 | a0032c0012t0002g0232a0032c0012t0002g0266a0033c0011t0002g0254others(34): Show | 37 | HG00438.hp2 HG00621.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.9490+124G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 78/93 | chr1 | 149542149 | ||||||
| chr1:149542223
|
T | C | 9 | a0043c0209t0004g0207a0044c0210t0004g0206a0164c0201t0004g0205others(6): Show | 9 | HG00735.hp1 HG01099.hp1 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.9490+198T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 78/93 | chr1 | 149542223 | ||||||
| chr1:149542244
|
T | C | 64 | a0006c0211t0019g0211a0006c0212t0002g0223a0006c0213t0002g0224others(61): Show | 66 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.9490+219T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 78/93 | chr1 | 149542244 | ||||||
| chr1:149542260
|
C | CGCTCTCA others(4748): Show |
3 | a0015c0036t0006g0004a0015c0192t0006g0270a0173c0191t0006g0271 | 4 | HG02145.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.9490+346_9490+347i others(4757): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 78/93 | INFO_REALIGN_3_PRIME | chr1 | 149542260 | |||||
| chr1:149542290
|
T | C | 26 | a0011c0010t0001g0010a0011c0010t0001g0011a0011c0010t0001g0012others(23): Show | 26 | HG00423.hp2 HG01168.hp2 HG02027.hp2 others(23): Show |
intron_variant | MODIFIER | c.9490+265T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 78/93 | chr1 | 149542290 | ||||||
| chr1:149542303
|
G | A | 2 | a0111c0132t0001g0199a0136c0163t0001g0200 | 2 | NA18942.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.9490+278G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 78/93 | chr1 | 149542303 | ||||||
| chr1:149542320
|
C | G | 4 | a0043c0209t0004g0207a0044c0210t0004g0206a0171c0207t0004g0208others(1): Show | 4 | HG02165.hp1 HG02698.hp1 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.9490+295C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 78/93 | chr1 | 149542320 | ||||||
| chr1:149542331
|
A | G | 111 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(108): Show | 112 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.9490+306A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 78/93 | chr1 | 149542331 | ||||||
| chr1:149542372
|
A | G | 195 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(192): Show | 198 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.9490+347A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 78/93 | chr1 | 149542372 | ||||||
| chr1:149542378
|
A | G | 4 | a0043c0209t0004g0207a0044c0210t0004g0206a0171c0207t0004g0208others(1): Show | 4 | HG02165.hp1 HG02698.hp1 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.9490+353A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 78/93 | chr1 | 149542378 | ||||||
| chr1:149542464
|
T | C | 1 | a0192c0055t0002g0263 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.9491-271T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 78/93 | chr1 | 149542464 | ||||||
| chr1:149542472
|
A | G | 1 | a0197c0066t0002g0238 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.9491-263A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 78/93 | chr1 | 149542472 | ||||||
| chr1:149542489
|
G | C | 1 | a0071c0102t0001g0143 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.9491-246G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 78/93 | chr1 | 149542489 | ||||||
| chr1:149542527
|
T | A | 195 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(192): Show | 198 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.9491-208T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 78/93 | chr1 | 149542527 | ||||||
| chr1:149542640
|
G | A | 1 | a0079c0107t0001g0059 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.9491-95G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 78/93 | chr1 | 149542640 | ||||||
| chr1:149542653
|
C | T | 2 | a0086c0119t0001g0085a0117c0152t0001g0087 | 2 | HG00423.hp2 HG02027.hp2 |
intron_variant | MODIFIER | c.9491-82C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 78/93 | chr1 | 149542653 | ||||||
| chr1:149542691
|
G | T | 1 | a0106c0139t0001g0055 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.9491-44G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 78/93 | chr1 | 149542691 | ||||||
| chr1:149542798
|
A | G | 1 | a0157c0188t0001g0201 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.9542+12A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 79/93 | chr1 | 149542798 | ||||||
| chr1:149542836
|
C | A | 21 | a0011c0010t0001g0010a0011c0010t0001g0011a0011c0010t0001g0012others(18): Show | 21 | HG00423.hp2 HG02027.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.9542+50C>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 79/93 | chr1 | 149542836 | ||||||
| chr1:149542836
|
C | T | 26 | a0003c0003t0001g0115a0003c0003t0001g0117a0003c0003t0001g0170others(23): Show | 26 | HG00544.hp1 HG00733.hp1 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.9542+50C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 79/93 | chr1 | 149542836 | ||||||
| chr1:149542878
|
A | T | 1 | a0184c0042t0002g0236 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.9542+92A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 79/93 | chr1 | 149542878 | ||||||
| chr1:149542881
|
T | C | 1 | a0057c0088t0001g0089 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.9542+95T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 79/93 | chr1 | 149542881 | ||||||
| chr1:149542911
|
A | ACATTGCT others(1609): Show |
1 | a0077c0110t0001g0178 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.9542+155_9824+148d others(1618): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 81/93 | INFO_REALIGN_3_PRIME | chr1 | 149542911 | |||||
| chr1:149542913
|
A | G | 1 | a0174c0202t0013g0204 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.9542+127A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 79/93 | chr1 | 149542913 | ||||||
| chr1:149542947
|
G | C | 2 | a0163c0199t0005g0215a0165c0200t0005g0212 | 2 | HG00544.hp2 HG00558.hp2 |
intron_variant | MODIFIER | c.9542+161G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 79/93 | chr1 | 149542947 | ||||||
| chr1:149542990
|
G | C | 1 | a0049c0082t0011g0096 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.9542+204G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 79/93 | chr1 | 149542990 | ||||||
| chr1:149543012
|
G | C | 1 | a0017c0019t0001g0167 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.9542+226G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 79/93 | chr1 | 149543012 | ||||||
| chr1:149543031
|
A | G | 131 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(128): Show | 133 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.9542+245A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 79/93 | chr1 | 149543031 | ||||||
| chr1:149543043
|
A | G | 192 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(189): Show | 195 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.9542+257A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 79/93 | chr1 | 149543043 | ||||||
| chr1:149543070
|
C | T | 1 | a0135c0161t0001g0057 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.9542+284C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 79/93 | chr1 | 149543070 | ||||||
| chr1:149543101
|
T | A | 1 | a0170c0208t0004g0202 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.9543-312T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 79/93 | chr1 | 149543101 | ||||||
| chr1:149543169
|
G | C | 1 | a0174c0202t0013g0204 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.9543-244G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 79/93 | chr1 | 149543169 | ||||||
| chr1:149543184
|
C | G | 3 | a0183c0041t0002g0246a0203c0065t0002g0240a0204c0067t0002g0248 | 3 | HG00438.hp2 HG02129.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.9543-229C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 79/93 | chr1 | 149543184 | ||||||
| chr1:149543186
|
C | CTCTCTCT others(7): Show |
1 | a0174c0202t0013g0204 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.9543-226_9543-225i others(16): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 79/93 | INFO_REALIGN_3_PRIME | chr1 | 149543186 | |||||
| chr1:149543186
|
C | CTCTCTCT others(21): Show |
1 | a0015c0192t0006g0270 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.9543-226_9543-225i others(30): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 79/93 | INFO_REALIGN_3_PRIME | chr1 | 149543186 | |||||
| chr1:149543186
|
C | CTCTCTCT others(23): Show |
2 | a0015c0036t0006g0004a0173c0191t0006g0271 | 3 | HG02145.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.9543-226_9543-225i others(32): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 79/93 | INFO_REALIGN_3_PRIME | chr1 | 149543186 | |||||
| chr1:149543186
|
C | CTCTCTCT others(17): Show |
1 | a0167c0203t0028g0269 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.9543-226_9543-225i others(26): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 79/93 | INFO_REALIGN_3_PRIME | chr1 | 149543186 | |||||
| chr1:149543186
|
C | CTCTCTCT others(21): Show |
1 | a0006c0213t0002g0224 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.9543-226_9543-225i others(30): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 79/93 | INFO_REALIGN_3_PRIME | chr1 | 149543186 | |||||
| chr1:149543186
|
C | CTCTCTCT others(15): Show |
1 | a0160c0076t0014g0225 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.9543-226_9543-225i others(24): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 79/93 | INFO_REALIGN_3_PRIME | chr1 | 149543186 | |||||
| chr1:149543186
|
C | CTCTCTGT others(11): Show |
2 | a0050c0080t0001g0177a0052c0079t0021g0176 | 2 | HG01978.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.9543-226_9543-225i others(20): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 79/93 | INFO_REALIGN_3_PRIME | chr1 | 149543186 | |||||
| chr1:149543186
|
C | CTCTCTGT others(13): Show |
10 | a0004c0026t0001g0007a0004c0026t0001g0008a0004c0027t0001g0001others(7): Show | 11 | HG01891.hp2 HG02135.hp1 HG02165.hp2 others(8): Show |
intron_variant | MODIFIER | c.9543-226_9543-225i others(22): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 79/93 | INFO_REALIGN_3_PRIME | chr1 | 149543186 | |||||
| chr1:149543186
|
C | CTCTCTGT others(15): Show |
12 | a0002c0002t0003g0188a0013c0035t0001g0038a0013c0035t0001g0084others(9): Show | 12 | HG02165.hp1 HG02257.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.9543-226_9543-225i others(24): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 79/93 | INFO_REALIGN_3_PRIME | chr1 | 149543186 | |||||
| chr1:149543186
|
C | CTCTCTGT others(17): Show |
1 | a0169c0205t0004g0209 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.9543-226_9543-225i others(26): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 79/93 | INFO_REALIGN_3_PRIME | chr1 | 149543186 | |||||
| chr1:149543186
|
C | CTCTCTGT others(38092): Show |
1 | a0168c0206t0004g0203 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.9543-226_9543-225i others(38101): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 79/93 | INFO_REALIGN_3_PRIME | chr1 | 149543186 | |||||
| chr1:149543186
|
C | CTCTCTGT others(17): Show |
30 | a0002c0002t0003g0182a0002c0002t0003g0189a0002c0002t0003g0196others(27): Show | 30 | HG00423.hp2 HG00642.hp2 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.9543-226_9543-225i others(26): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 79/93 | INFO_REALIGN_3_PRIME | chr1 | 149543186 | |||||
| chr1:149543186
|
C | CTCTCTGT others(19): Show |
7 | a0006c0211t0019g0211a0006c0214t0002g0265a0014c0008t0020g0184others(4): Show | 7 | HG01168.hp2 HG01975.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.9543-226_9543-225i others(28): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 79/93 | INFO_REALIGN_3_PRIME | chr1 | 149543186 | |||||
| chr1:149543186
|
C | CTCTCTGT others(21): Show |
1 | a0006c0212t0002g0223 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.9543-226_9543-225i others(30): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 79/93 | INFO_REALIGN_3_PRIME | chr1 | 149543186 | |||||
| chr1:149543186
|
C | CTCTCTGT others(27): Show |
1 | a0197c0066t0002g0238 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.9543-226_9543-225i others(36): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 79/93 | INFO_REALIGN_3_PRIME | chr1 | 149543186 | |||||
| chr1:149543186
|
C | CTCTCTGT others(9531): Show |
1 | a0094c0125t0001g0138 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.9543-226_9543-225i others(9540): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 79/93 | INFO_REALIGN_3_PRIME | chr1 | 149543186 | |||||
| chr1:149543186
|
C | CTCTCTGT others(9533): Show |
1 | a0023c0024t0001g0003 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.9543-226_9543-225i others(9542): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 79/93 | INFO_REALIGN_3_PRIME | chr1 | 149543186 | |||||
| chr1:149543186
|
C | CTCTGTGT others(7): Show |
6 | a0024c0025t0001g0024a0024c0025t0001g0026a0042c0195t0001g0023others(3): Show | 6 | HG02055.hp2 HG02486.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.9543-226_9543-225i others(16): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 79/93 | INFO_REALIGN_3_PRIME | chr1 | 149543186 | |||||
| chr1:149543186
|
C | CTCTGTGT others(9): Show |
4 | a0061c0187t0001g0173a0088c0105t0008g0100a0123c0157t0001g0015others(1): Show | 4 | HG02055.hp1 HG02145.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.9543-226_9543-225i others(18): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 79/93 | INFO_REALIGN_3_PRIME | chr1 | 149543186 | |||||
| chr1:149543186
|
C | CTCTGTGT others(11): Show |
13 | a0001c0001t0001g0158a0009c0006t0001g0081a0009c0006t0001g0082others(10): Show | 13 | HG00099.hp1 HG00609.hp2 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.9543-226_9543-225i others(20): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 79/93 | INFO_REALIGN_3_PRIME | chr1 | 149543186 | |||||
| chr1:149543186
|
C | CTCTGTGT others(13): Show |
25 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(22): Show | 25 | HG00099.hp2 HG00741.hp1 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.9543-226_9543-225i others(22): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 79/93 | INFO_REALIGN_3_PRIME | chr1 | 149543186 | |||||
| chr1:149543186
|
C | CTCTGTGT others(15): Show |
16 | a0022c0023t0001g0156a0051c0083t0001g0162a0072c0104t0001g0017others(13): Show | 16 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(13): Show |
intron_variant | MODIFIER | c.9543-226_9543-225i others(24): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 79/93 | INFO_REALIGN_3_PRIME | chr1 | 149543186 | |||||
| chr1:149543186
|
C | CTCTGTGT others(17): Show |
7 | a0028c0032t0001g0036a0059c0091t0001g0130a0095c0126t0001g0140others(4): Show | 7 | HG00733.hp2 HG01978.hp2 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.9543-226_9543-225i others(26): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 79/93 | INFO_REALIGN_3_PRIME | chr1 | 149543186 | |||||
| chr1:149543186
|
C | CTCTGTGT others(19): Show |
1 | a0110c0133t0001g0058 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.9543-226_9543-225i others(28): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 79/93 | INFO_REALIGN_3_PRIME | chr1 | 149543186 | |||||
| chr1:149543186
|
C | CTCTGTGT others(21): Show |
1 | a0138c0174t0001g0109 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.9543-226_9543-225i others(30): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 79/93 | INFO_REALIGN_3_PRIME | chr1 | 149543186 | |||||
| chr1:149543186
|
C | CTCTGTGT others(23): Show |
1 | a0146c0176t0003g0110 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.9543-226_9543-225i others(32): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 79/93 | INFO_REALIGN_3_PRIME | chr1 | 149543186 | |||||
| chr1:149543186
|
C | CTGTGTGT others(9): Show |
1 | a0045c0078t0001g0099 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.9543-216_9543-215i others(18): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 79/93 | INFO_REALIGN_3_PRIME | chr1 | 149543186 | |||||
| chr1:149543186
|
C | CTGTGTGT others(11): Show |
2 | a0037c0016t0002g0256a0037c0016t0002g0257 | 2 | HG00642.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.9543-216_9543-215i others(20): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 79/93 | INFO_REALIGN_3_PRIME | chr1 | 149543186 | |||||
| chr1:149543186
|
C | CTGTGTGT others(13): Show |
6 | a0033c0011t0002g0254a0035c0015t0002g0216a0035c0015t0002g0217others(3): Show | 6 | HG00621.hp1 HG03017.hp2 HG03704.hp2 others(3): Show |
intron_variant | MODIFIER | c.9543-216_9543-215i others(22): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 79/93 | INFO_REALIGN_3_PRIME | chr1 | 149543186 | |||||
| chr1:149543186
|
C | CTGTGTGT others(15): Show |
12 | a0032c0012t0002g0232a0032c0012t0002g0266a0033c0011t0002g0255others(9): Show | 12 | HG01081.hp1 HG01346.hp2 HG02148.hp2 others(9): Show |
intron_variant | MODIFIER | c.9543-216_9543-215i others(24): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 79/93 | INFO_REALIGN_3_PRIME | chr1 | 149543186 | |||||
| chr1:149543186
|
C | CTGTGTGT others(17): Show |
2 | a0039c0219t0002g0227a0178c0070t0002g0253 | 2 | NA18981.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.9543-216_9543-215i others(26): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 79/93 | INFO_REALIGN_3_PRIME | chr1 | 149543186 | |||||
| chr1:149543186
|
C | G | 26 | a0034c0013t0002g0220a0034c0013t0002g0221a0036c0014t0009g0228others(23): Show | 26 | HG00438.hp2 HG00621.hp2 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.9543-227C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 79/93 | chr1 | 149543186 | ||||||
| chr1:149543188
|
G | C | 1 | a0116c0150t0001g0014 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.9543-225G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 79/93 | chr1 | 149543188 | ||||||
| chr1:149543189
|
T | C | 3 | a0142c0180t0001g0108a0145c0177t0001g0165a0148c0181t0001g0124 | 3 | HG01168.hp2 HG02602.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.9543-224T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 79/93 | chr1 | 149543189 | ||||||
| chr1:149543190
|
G | C | 1 | a0116c0150t0001g0014 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.9543-223G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 79/93 | chr1 | 149543190 | ||||||
| chr1:149543191
|
T | C | 21 | a0011c0010t0001g0010a0011c0010t0001g0011a0011c0010t0001g0012others(18): Show | 21 | HG00423.hp2 HG02027.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.9543-222T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 79/93 | chr1 | 149543191 | ||||||
| chr1:149543194
|
G | C | 1 | a0171c0207t0004g0208 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.9543-219G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 79/93 | chr1 | 149543194 | ||||||
| chr1:149543195
|
T | C | 1 | a0081c0113t0001g0148 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.9543-218T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 79/93 | chr1 | 149543195 | ||||||
| chr1:149543198
|
C | CTG | 5 | a0043c0209t0004g0207a0044c0210t0004g0206a0168c0206t0004g0203others(2): Show | 5 | HG01099.hp1 HG02165.hp1 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.9543-199_9543-198d others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 79/93 | INFO_REALIGN_3_PRIME | chr1 | 149543198 | |||||
| chr1:149543198
|
C | G | 167 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(164): Show | 170 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.9543-215C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 79/93 | chr1 | 149543198 | ||||||
| chr1:149543217
|
T | C | 26 | a0011c0010t0001g0010a0011c0010t0001g0011a0011c0010t0001g0012others(23): Show | 26 | HG00423.hp2 HG01168.hp2 HG02027.hp2 others(23): Show |
intron_variant | MODIFIER | c.9543-196T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 79/93 | chr1 | 149543217 | ||||||
| chr1:149543284
|
G | T | 1 | a0086c0119t0001g0085 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.9543-129G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 79/93 | chr1 | 149543284 | ||||||
| chr1:149543292
|
A | C | 18 | a0036c0014t0009g0228a0036c0014t0009g0230a0179c0071t0002g0260others(15): Show | 18 | HG00438.hp2 HG00738.hp1 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.9543-121A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 79/93 | chr1 | 149543292 | ||||||
| chr1:149543304
|
A | T | 2 | a0010c0007t0001g0002a0010c0007t0001g0045 | 3 | HG01069.hp1 HG01071.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.9543-109A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 79/93 | chr1 | 149543304 | ||||||
| chr1:149543313
|
C | G | 159 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(156): Show | 162 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.9543-100C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 79/93 | chr1 | 149543313 | ||||||
| chr1:149543323
|
C | T | 1 | a0158c0084t0001g0049 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.9543-90C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 79/93 | chr1 | 149543323 | ||||||
| chr1:149543330
|
T | C | 163 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(160): Show | 166 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.9543-83T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 79/93 | chr1 | 149543330 | ||||||
| chr1:149543365
|
G | T | 1 | a0009c0006t0001g0082 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.9543-48G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 79/93 | chr1 | 149543365 | ||||||
| chr1:149543395
|
T | G | 24 | a0034c0013t0002g0220a0034c0013t0002g0221a0036c0014t0009g0228others(21): Show | 24 | HG00438.hp2 HG00621.hp2 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.9543-18T>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 79/93 | chr1 | 149543395 | ||||||
| chr1:149543593
|
C | T | 1 | a0164c0201t0004g0205 | 1 | HG00735.hp1 | splice_region_variant&intron_variant | LOW | c.9715+8C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 80/93 | chr1 | 149543593 | ||||||
| chr1:149543600
|
A | G | 3 | a0006c0212t0002g0223a0006c0213t0002g0224a0006c0214t0002g0265 | 3 | HG01891.hp1 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.9715+15A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 80/93 | chr1 | 149543600 | ||||||
| chr1:149543619
|
A | T | 1 | a0149c0183t0001g0022 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.9715+34A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 80/93 | chr1 | 149543619 | ||||||
| chr1:149543684
|
A | G | 69 | a0006c0212t0002g0223a0006c0213t0002g0224a0006c0214t0002g0265others(66): Show | 70 | HG00423.hp2 HG00621.hp1 HG00642.hp1 others(67): Show |
intron_variant | MODIFIER | c.9715+99A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 80/93 | chr1 | 149543684 | ||||||
| chr1:149543700
|
C | A | 3 | a0006c0212t0002g0223a0006c0213t0002g0224a0006c0214t0002g0265 | 3 | HG01891.hp1 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.9715+115C>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 80/93 | chr1 | 149543700 | ||||||
| chr1:149543755
|
T | A | 62 | a0006c0212t0002g0223a0006c0213t0002g0224a0006c0214t0002g0265others(59): Show | 63 | HG00423.hp2 HG00621.hp1 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.9715+170T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 80/93 | chr1 | 149543755 | ||||||
| chr1:149543774
|
T | A | 63 | a0006c0212t0002g0223a0006c0213t0002g0224a0006c0214t0002g0265others(60): Show | 64 | HG00423.hp2 HG00621.hp1 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.9715+189T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 80/93 | chr1 | 149543774 | ||||||
| chr1:149543776
|
G | A | 63 | a0006c0212t0002g0223a0006c0213t0002g0224a0006c0214t0002g0265others(60): Show | 64 | HG00423.hp2 HG00621.hp1 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.9715+191G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 80/93 | chr1 | 149543776 | ||||||
| chr1:149543808
|
C | T | 1 | a0160c0076t0014g0225 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.9715+223C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 80/93 | chr1 | 149543808 | ||||||
| chr1:149543809
|
A | G | 63 | a0006c0212t0002g0223a0006c0213t0002g0224a0006c0214t0002g0265others(60): Show | 64 | HG00423.hp2 HG00621.hp1 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.9715+224A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 80/93 | chr1 | 149543809 | ||||||
| chr1:149543811
|
T | C | 64 | a0006c0212t0002g0223a0006c0213t0002g0224a0006c0214t0002g0265others(61): Show | 65 | HG00423.hp2 HG00621.hp1 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.9715+226T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 80/93 | chr1 | 149543811 | ||||||
| chr1:149543812
|
C | G | 1 | a0167c0203t0028g0269 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.9715+227C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 80/93 | chr1 | 149543812 | ||||||
| chr1:149543817
|
T | C | 63 | a0006c0212t0002g0223a0006c0213t0002g0224a0006c0214t0002g0265others(60): Show | 64 | HG00423.hp2 HG00621.hp1 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.9715+232T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 80/93 | chr1 | 149543817 | ||||||
| chr1:149543821
|
C | T | 63 | a0006c0212t0002g0223a0006c0213t0002g0224a0006c0214t0002g0265others(60): Show | 64 | HG00423.hp2 HG00621.hp1 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.9715+236C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 80/93 | chr1 | 149543821 | ||||||
| chr1:149543861
|
A | G | 6 | a0043c0209t0004g0207a0044c0210t0004g0206a0168c0206t0004g0203others(3): Show | 6 | HG01099.hp1 HG02165.hp1 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.9715+276A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 80/93 | chr1 | 149543861 | ||||||
| chr1:149543868
|
T | A | 3 | a0122c0156t0001g0086a0175c0193t0001g0128a0176c0194t0001g0129 | 3 | HG03654.hp1 HG04115.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.9715+283T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 80/93 | chr1 | 149543868 | ||||||
| chr1:149543869
|
G | T | 1 | a0197c0066t0002g0238 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.9715+284G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 80/93 | chr1 | 149543869 | ||||||
| chr1:149543889
|
C | T | 68 | a0006c0211t0019g0211a0006c0212t0002g0223a0006c0213t0002g0224others(65): Show | 69 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.9715+304C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 80/93 | chr1 | 149543889 | ||||||
| chr1:149543984
|
T | A | 18 | a0036c0014t0009g0228a0036c0014t0009g0230a0179c0071t0002g0260others(15): Show | 18 | HG00438.hp2 HG00738.hp1 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.9716-316T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 80/93 | chr1 | 149543984 | ||||||
| chr1:149543990
|
C | T | 61 | a0006c0212t0002g0223a0006c0213t0002g0224a0006c0214t0002g0265others(58): Show | 62 | HG00423.hp2 HG00621.hp1 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.9716-310C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 80/93 | chr1 | 149543990 | ||||||
| chr1:149544005
|
G | T | 2 | a0088c0105t0008g0100a0091c0122t0008g0157 | 2 | HG02896.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.9716-295G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 80/93 | chr1 | 149544005 | ||||||
| chr1:149544045
|
G | C | 1 | a0074c0112t0001g0104 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.9716-255G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 80/93 | chr1 | 149544045 | ||||||
| chr1:149544150
|
C | G | 1 | a0115c0149t0026g0142 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.9716-150C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 80/93 | chr1 | 149544150 | ||||||
| chr1:149544183
|
A | C | 1 | a0172c0204t0004g0268 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.9716-117A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 80/93 | chr1 | 149544183 | ||||||
| chr1:149544248
|
G | T | 1 | a0126c0130t0001g0134 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.9716-52G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 80/93 | chr1 | 149544248 | ||||||
| chr1:149544258
|
G | C | 1 | a0121c0154t0024g0091 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.9716-42G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 80/93 | chr1 | 149544258 | ||||||
| chr1:149544420
|
C | G | 1 | a0133c0165t0022g0020 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.9824+12C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 81/93 | chr1 | 149544420 | ||||||
| chr1:149544480
|
C | G | 86 | a0006c0211t0019g0211a0006c0212t0002g0223a0006c0213t0002g0224others(83): Show | 88 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.9824+72C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 81/93 | chr1 | 149544480 | ||||||
| chr1:149544481
|
T | G | 1 | a0160c0076t0014g0225 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.9824+73T>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 81/93 | chr1 | 149544481 | ||||||
| chr1:149544482
|
G | C | 1 | a0048c0081t0011g0151 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.9824+74G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 81/93 | chr1 | 149544482 | ||||||
| chr1:149544596
|
A | G | 18 | a0006c0211t0019g0211a0006c0212t0002g0223a0006c0213t0002g0224others(15): Show | 18 | HG00544.hp2 HG00558.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.9824+188A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 81/93 | chr1 | 149544596 | ||||||
| chr1:149544663
|
A | G | 1 | a0022c0023t0001g0156 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.9824+255A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 81/93 | chr1 | 149544663 | ||||||
| chr1:149544719
|
A | G | 1 | a0169c0205t0004g0209 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.9824+311A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 81/93 | chr1 | 149544719 | ||||||
| chr1:149544736
|
G | C | 108 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(105): Show | 110 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.9825-302G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 81/93 | chr1 | 149544736 | ||||||
| chr1:149544747
|
T | G | 2 | a0143c0179t0001g0021a0149c0183t0001g0022 | 2 | HG02698.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.9825-291T>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 81/93 | chr1 | 149544747 | ||||||
| chr1:149544829
|
G | C | 1 | a0174c0202t0013g0204 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.9825-209G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 81/93 | chr1 | 149544829 | ||||||
| chr1:149544829
|
G | GTC | 6 | a0004c0026t0001g0007a0004c0026t0001g0008a0004c0027t0001g0001others(3): Show | 7 | HG00735.hp2 HG01516.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.9825-193_9825-192d others(4): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 81/93 | INFO_REALIGN_3_PRIME | chr1 | 149544829 | |||||
| chr1:149544829
|
G | GTCTC | 53 | a0006c0212t0002g0223a0006c0213t0002g0224a0006c0214t0002g0265others(50): Show | 54 | HG00423.hp2 HG00621.hp1 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.9825-195_9825-192d others(6): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 81/93 | INFO_REALIGN_3_PRIME | chr1 | 149544829 | |||||
| chr1:149544829
|
G | GTCTCTC | 3 | a0160c0076t0014g0225a0167c0203t0028g0269a0169c0205t0004g0209 | 3 | HG02109.hp2 HG02622.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.9825-197_9825-192d others(8): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 81/93 | INFO_REALIGN_3_PRIME | chr1 | 149544829 | |||||
| chr1:149544829
|
G | GTCTCTCT others(1): Show |
5 | a0043c0209t0004g0207a0044c0210t0004g0206a0164c0201t0004g0205others(2): Show | 5 | HG00735.hp1 HG02165.hp1 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.9825-199_9825-192d others(10): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 81/93 | INFO_REALIGN_3_PRIME | chr1 | 149544829 | |||||
| chr1:149544829
|
G | GTCTCTCT others(5): Show |
2 | a0168c0206t0004g0203a0170c0208t0004g0202 | 2 | HG01099.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.9825-203_9825-192d others(14): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 81/93 | INFO_REALIGN_3_PRIME | chr1 | 149544829 | |||||
| chr1:149544871
|
C | T | 2 | a0053c0190t0001g0064a0109c0135t0001g0063 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.9825-167C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 81/93 | chr1 | 149544871 | ||||||
| chr1:149544920
|
A | C | 1 | a0174c0202t0013g0204 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.9825-118A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 81/93 | chr1 | 149544920 | ||||||
| chr1:149544940
|
T | C | 2 | a0036c0014t0009g0228a0036c0014t0009g0230 | 2 | NA18960.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.9825-98T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 81/93 | chr1 | 149544940 | ||||||
| chr1:149544988
|
T | C | 47 | a0006c0212t0002g0223a0006c0213t0002g0224a0006c0214t0002g0265others(44): Show | 48 | HG00438.hp2 HG00621.hp1 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.9825-50T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 81/93 | chr1 | 149544988 | ||||||
| chr1:149545218
|
C | A | 1 | a0167c0203t0028g0269 | 1 | HG02109.hp2 | splice_region_variant&intron_variant | LOW | c.9997+8C>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 82/93 | chr1 | 149545218 | ||||||
| chr1:149545305
|
G | A | 27 | a0032c0012t0002g0232a0032c0012t0002g0266a0033c0011t0002g0254others(24): Show | 27 | HG00621.hp1 HG00642.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.9997+95G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 82/93 | chr1 | 149545305 | ||||||
| chr1:149545366
|
G | C | 1 | a0174c0202t0013g0204 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.9997+156G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 82/93 | chr1 | 149545366 | ||||||
| chr1:149545407
|
C | T | 17 | a0006c0211t0019g0211a0006c0212t0002g0223a0006c0213t0002g0224others(14): Show | 17 | HG00544.hp2 HG00558.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.9997+197C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 82/93 | chr1 | 149545407 | ||||||
| chr1:149545432
|
A | C | 49 | a0006c0211t0019g0211a0006c0212t0002g0223a0006c0213t0002g0224others(46): Show | 50 | HG00544.hp2 HG00558.hp2 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.9997+222A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 82/93 | chr1 | 149545432 | ||||||
| chr1:149545433
|
G | A | 4 | a0006c0212t0002g0223a0006c0213t0002g0224a0006c0214t0002g0265others(1): Show | 4 | HG01891.hp1 HG04115.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.9997+223G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 82/93 | chr1 | 149545433 | ||||||
| chr1:149545447
|
C | G | 1 | a0130c0170t0001g0120 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.9997+237C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 82/93 | chr1 | 149545447 | ||||||
| chr1:149545456
|
C | G | 1 | a0174c0202t0013g0204 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.9997+246C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 82/93 | chr1 | 149545456 | ||||||
| chr1:149545456
|
C | T | 43 | a0006c0212t0002g0223a0006c0213t0002g0224a0006c0214t0002g0265others(40): Show | 44 | HG00621.hp1 HG00642.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.9997+246C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 82/93 | chr1 | 149545456 | ||||||
| chr1:149545461
|
C | T | 1 | a0014c0008t0003g0181 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.9997+251C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 82/93 | chr1 | 149545461 | ||||||
| chr1:149545469
|
G | GATGTGAC others(23778): Show |
1 | a0169c0205t0004g0209 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.9998-84_9998-83ins others(23785): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 82/93 | INFO_REALIGN_3_PRIME | chr1 | 149545469 | |||||
| chr1:149545599
|
C | T | 1 | a0158c0084t0001g0049 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.9998-331C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 82/93 | chr1 | 149545599 | ||||||
| chr1:149545844
|
G | T | 1 | a0205c0056t0015g0258 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.9998-86G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 82/93 | chr1 | 149545844 | ||||||
| chr1:149545847
|
C | T | 20 | a0006c0212t0002g0223a0006c0213t0002g0224a0006c0214t0002g0265others(17): Show | 20 | HG00735.hp1 HG01099.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.9998-83C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 82/93 | chr1 | 149545847 | ||||||
| chr1:149545859
|
C | T | 216 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(213): Show | 219 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.9998-71C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 82/93 | chr1 | 149545859 | ||||||
| chr1:149545905
|
C | G | 5 | a0006c0211t0019g0211a0161c0197t0005g0214a0162c0196t0005g0213others(2): Show | 5 | HG00544.hp2 HG00558.hp2 HG00735.hp2 others(2): Show |
intron_variant | MODIFIER | c.9998-25C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 82/93 | chr1 | 149545905 | ||||||
| chr1:149546012
|
C | T | 46 | a0032c0012t0002g0232a0032c0012t0002g0266a0033c0011t0002g0254others(43): Show | 46 | HG00438.hp2 HG00621.hp1 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.10049+31C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 83/93 | chr1 | 149546012 | ||||||
| chr1:149546160
|
A | T | 8 | a0043c0209t0004g0207a0044c0210t0004g0206a0164c0201t0004g0205others(5): Show | 8 | HG00735.hp1 HG01099.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.10049+179A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 83/93 | chr1 | 149546160 | ||||||
| chr1:149546220
|
A | G | 3 | a0006c0212t0002g0223a0006c0213t0002g0224a0006c0214t0002g0265 | 3 | HG01891.hp1 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.10049+239A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 83/93 | chr1 | 149546220 | ||||||
| chr1:149546319
|
C | T | 4 | a0043c0209t0004g0207a0044c0210t0004g0206a0164c0201t0004g0205others(1): Show | 4 | HG00735.hp1 HG02165.hp1 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.10050-271C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 83/93 | chr1 | 149546319 | ||||||
| chr1:149546363
|
C | CCT | 9 | a0007c0005t0001g0144a0007c0005t0001g0154a0007c0005t0001g0155others(6): Show | 9 | HG00408.hp2 HG00609.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.10050-201_10050-20 others(6): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 83/93 | INFO_REALIGN_3_PRIME | chr1 | 149546363 | |||||
| chr1:149546363
|
CCTCT | C | 7 | a0013c0035t0001g0038a0013c0035t0001g0084a0013c0162t0001g0040others(4): Show | 7 | HG02135.hp2 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.10050-203_10050-20 others(8): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 83/93 | INFO_REALIGN_3_PRIME | chr1 | 149546363 | |||||
| chr1:149546363
|
CCTCTCT | C | 24 | a0011c0010t0001g0010a0011c0010t0001g0011a0011c0010t0001g0012others(21): Show | 25 | HG00423.hp2 HG00733.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.10050-205_10050-20 others(10): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 83/93 | INFO_REALIGN_3_PRIME | chr1 | 149546363 | |||||
| chr1:149546363
|
CCTCTCTC others(1): Show |
C | 61 | a0006c0212t0002g0223a0006c0213t0002g0224a0006c0214t0002g0265others(58): Show | 61 | HG00438.hp2 HG00621.hp1 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.10050-207_10050-20 others(12): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 83/93 | INFO_REALIGN_3_PRIME | chr1 | 149546363 | |||||
| chr1:149546389
|
T | TCC | 4 | a0024c0025t0001g0024a0024c0025t0001g0026a0042c0195t0001g0023others(1): Show | 4 | HG02055.hp2 HG02486.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.10050-199_10050-19 others(6): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 83/93 | INFO_REALIGN_3_PRIME | chr1 | 149546389 | |||||
| chr1:149546447
|
T | A | 1 | a0171c0207t0004g0208 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.10050-143T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 83/93 | chr1 | 149546447 | ||||||
| chr1:149546474
|
A | G | 1 | a0020c0020t0010g0043 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.10050-116A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 83/93 | chr1 | 149546474 | ||||||
| chr1:149546525
|
C | G | 1 | a0167c0203t0028g0269 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.10050-65C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 83/93 | chr1 | 149546525 | ||||||
| chr1:149546548
|
G | C | 3 | a0011c0010t0001g0010a0011c0010t0001g0011a0011c0010t0001g0012 | 3 | NA18981.hp2 NA19065.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.10050-42G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 83/93 | chr1 | 149546548 | ||||||
| chr1:149546557
|
T | C | 1 | a0007c0005t0001g0154 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.10050-33T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 83/93 | chr1 | 149546557 | ||||||
| chr1:149546583
|
T | G | 4 | a0161c0197t0005g0214a0162c0196t0005g0213a0163c0199t0005g0215others(1): Show | 4 | HG00544.hp2 HG00558.hp2 HG00735.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.10050-7T>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 83/93 | chr1 | 149546583 | ||||||
| chr1:149546765
|
G | A | 1 | a0192c0055t0002g0263 | 1 | NA18994.hp2 | splice_region_variant&intron_variant | LOW | c.10222+3G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 84/93 | chr1 | 149546765 | ||||||
| chr1:149546809
|
G | C | 2 | a0035c0015t0002g0216a0035c0015t0002g0217 | 2 | HG03017.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.10222+47G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 84/93 | chr1 | 149546809 | ||||||
| chr1:149546813
|
G | A | 2 | a0096c0127t0001g0111a0125c0159t0001g0147 | 2 | HG02717.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.10222+51G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 84/93 | chr1 | 149546813 | ||||||
| chr1:149546867
|
G | A | 1 | a0093c0124t0001g0153 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.10222+105G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 84/93 | chr1 | 149546867 | ||||||
| chr1:149546886
|
G | A | 47 | a0032c0012t0002g0232a0032c0012t0002g0266a0033c0011t0002g0254others(44): Show | 47 | HG00438.hp2 HG00621.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.10222+124G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 84/93 | chr1 | 149546886 | ||||||
| chr1:149546929
|
G | C | 1 | a0015c0036t0006g0004 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.10222+167G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 84/93 | chr1 | 149546929 | ||||||
| chr1:149546960
|
T | C | 9 | a0043c0209t0004g0207a0044c0210t0004g0206a0164c0201t0004g0205others(6): Show | 9 | HG00735.hp1 HG01099.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.10222+198T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 84/93 | chr1 | 149546960 | ||||||
| chr1:149546981
|
T | C | 72 | a0006c0211t0019g0211a0006c0212t0002g0223a0006c0213t0002g0224others(69): Show | 72 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.10222+219T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 84/93 | chr1 | 149546981 | ||||||
| chr1:149547033
|
A | T | 2 | a0035c0015t0002g0216a0035c0015t0002g0217 | 2 | HG03017.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.10222+271A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 84/93 | chr1 | 149547033 | ||||||
| chr1:149547040
|
G | A | 2 | a0111c0132t0001g0199a0136c0163t0001g0200 | 2 | NA18942.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.10222+278G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 84/93 | chr1 | 149547040 | ||||||
| chr1:149547061
|
G | T | 5 | a0006c0211t0019g0211a0161c0197t0005g0214a0162c0196t0005g0213others(2): Show | 5 | HG00544.hp2 HG00558.hp2 HG00735.hp2 others(2): Show |
intron_variant | MODIFIER | c.10222+299G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 84/93 | chr1 | 149547061 | ||||||
| chr1:149547068
|
A | G | 58 | a0006c0211t0019g0211a0015c0036t0006g0004a0015c0192t0006g0270others(55): Show | 59 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.10222+306A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 84/93 | chr1 | 149547068 | ||||||
| chr1:149547106
|
C | G | 1 | a0172c0204t0004g0268 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.10222+344C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 84/93 | chr1 | 149547106 | ||||||
| chr1:149547109
|
A | G | 88 | a0006c0211t0019g0211a0006c0212t0002g0223a0006c0213t0002g0224others(85): Show | 89 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.10222+347A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 84/93 | chr1 | 149547109 | ||||||
| chr1:149547229
|
C | G | 1 | a0003c0003t0001g0117 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.10223-243C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 84/93 | chr1 | 149547229 | ||||||
| chr1:149547264
|
T | A | 83 | a0006c0212t0002g0223a0006c0213t0002g0224a0006c0214t0002g0265others(80): Show | 84 | HG00423.hp2 HG00438.hp2 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.10223-208T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 84/93 | chr1 | 149547264 | ||||||
| chr1:149547298
|
A | T | 1 | a0121c0154t0024g0091 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.10223-174A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 84/93 | chr1 | 149547298 | ||||||
| chr1:149547355
|
A | T | 1 | a0165c0200t0005g0212 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.10223-117A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 84/93 | chr1 | 149547355 | ||||||
| chr1:149547386
|
A | G | 3 | a0015c0036t0006g0004a0015c0192t0006g0270a0173c0191t0006g0271 | 4 | HG02145.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.10223-86A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 84/93 | chr1 | 149547386 | ||||||
| chr1:149547535
|
A | G | 1 | a0157c0188t0001g0201 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.10274+12A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 85/93 | chr1 | 149547535 | ||||||
| chr1:149547573
|
C | A | 1 | a0086c0119t0001g0085 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.10274+50C>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 85/93 | chr1 | 149547573 | ||||||
| chr1:149547573
|
C | T | 19 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(16): Show | 19 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(16): Show |
intron_variant | MODIFIER | c.10274+50C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 85/93 | chr1 | 149547573 | ||||||
| chr1:149547650
|
A | G | 6 | a0006c0211t0019g0211a0161c0197t0005g0214a0162c0196t0005g0213others(3): Show | 6 | HG00544.hp2 HG00558.hp2 HG00735.hp2 others(3): Show |
intron_variant | MODIFIER | c.10274+127A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 85/93 | chr1 | 149547650 | ||||||
| chr1:149547768
|
A | G | 22 | a0011c0010t0001g0010a0011c0010t0001g0011a0011c0010t0001g0012others(19): Show | 23 | HG00423.hp2 HG00733.hp2 HG02027.hp2 others(20): Show |
intron_variant | MODIFIER | c.10274+245A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 85/93 | chr1 | 149547768 | ||||||
| chr1:149547780
|
A | G | 90 | a0006c0211t0019g0211a0006c0212t0002g0223a0006c0213t0002g0224others(87): Show | 91 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.10274+257A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 85/93 | chr1 | 149547780 | ||||||
| chr1:149547819
|
G | T | 1 | a0093c0124t0001g0153 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.10274+296G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 85/93 | chr1 | 149547819 | ||||||
| chr1:149547823
|
A | C | 3 | a0009c0006t0001g0081a0009c0006t0001g0082a0009c0006t0001g0139 | 3 | HG00099.hp1 HG00741.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.10274+300A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 85/93 | chr1 | 149547823 | ||||||
| chr1:149547915
|
C | T | 1 | a0006c0211t0019g0211 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.10275-235C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 85/93 | chr1 | 149547915 | ||||||
| chr1:149547921
|
C | G | 6 | a0185c0043t0002g0247a0188c0051t0002g0252a0190c0049t0002g0244others(3): Show | 6 | NA18946.hp2 NA18954.hp2 NA18962.hp2 others(3): Show |
intron_variant | MODIFIER | c.10275-229C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 85/93 | chr1 | 149547921 | ||||||
| chr1:149547923
|
C | CTCTCTCT others(15): Show |
1 | a0160c0076t0014g0225 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.10275-226_10275-22 others(26): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 85/93 | INFO_REALIGN_3_PRIME | chr1 | 149547923 | |||||
| chr1:149547923
|
C | CTCTCTCT others(19): Show |
1 | a0208c0048t0002g0251 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.10275-226_10275-22 others(30): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 85/93 | INFO_REALIGN_3_PRIME | chr1 | 149547923 | |||||
| chr1:149547923
|
C | CTCTCTGT others(15): Show |
7 | a0011c0010t0001g0010a0011c0010t0001g0011a0011c0010t0001g0012others(4): Show | 7 | HG00642.hp1 NA18942.hp2 NA18946.hp1 others(4): Show |
intron_variant | MODIFIER | c.10275-226_10275-22 others(26): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 85/93 | INFO_REALIGN_3_PRIME | chr1 | 149547923 | |||||
| chr1:149547923
|
C | CTCTCTGT others(21): Show |
5 | a0006c0211t0019g0211a0161c0197t0005g0214a0162c0196t0005g0213others(2): Show | 5 | HG00544.hp2 HG00558.hp2 HG00735.hp2 others(2): Show |
intron_variant | MODIFIER | c.10275-226_10275-22 others(32): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 85/93 | INFO_REALIGN_3_PRIME | chr1 | 149547923 | |||||
| chr1:149547923
|
C | CTCTCTGT others(23): Show |
1 | a0174c0202t0013g0204 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.10275-226_10275-22 others(34): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 85/93 | INFO_REALIGN_3_PRIME | chr1 | 149547923 | |||||
| chr1:149547923
|
C | CTCTCTGT others(17): Show |
3 | a0031c0028t0003g0180a0031c0028t0003g0194a0210c0068t0016g0233 | 3 | HG01952.hp2 NA18972.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.10275-226_10275-22 others(28): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 85/93 | INFO_REALIGN_3_PRIME | chr1 | 149547923 | |||||
| chr1:149547923
|
C | CTCTCTGT others(19): Show |
4 | a0037c0016t0002g0257a0186c0044t0017g0239a0202c0064t0002g0262others(1): Show | 4 | HG01069.hp2 HG02602.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.10275-226_10275-22 others(30): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 85/93 | INFO_REALIGN_3_PRIME | chr1 | 149547923 | |||||
| chr1:149547923
|
C | CTCTCTGT others(21): Show |
9 | a0034c0013t0002g0220a0034c0013t0002g0221a0036c0014t0009g0228others(6): Show | 9 | HG00438.hp2 HG03942.hp1 NA18612.hp2 others(6): Show |
intron_variant | MODIFIER | c.10275-226_10275-22 others(32): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 85/93 | INFO_REALIGN_3_PRIME | chr1 | 149547923 | |||||
| chr1:149547923
|
C | CTCTCTGT others(23): Show |
12 | a0006c0213t0002g0224a0006c0214t0002g0265a0032c0012t0002g0232others(9): Show | 12 | HG01081.hp1 HG01346.hp2 HG02129.hp2 others(9): Show |
intron_variant | MODIFIER | c.10275-226_10275-22 others(34): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 85/93 | INFO_REALIGN_3_PRIME | chr1 | 149547923 | |||||
| chr1:149547923
|
C | CTCTCTGT others(25): Show |
12 | a0006c0212t0002g0223a0033c0011t0002g0254a0033c0011t0002g0255others(9): Show | 12 | HG00621.hp2 HG01891.hp1 HG02040.hp2 others(9): Show |
intron_variant | MODIFIER | c.10275-226_10275-22 others(36): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 85/93 | INFO_REALIGN_3_PRIME | chr1 | 149547923 | |||||
| chr1:149547923
|
C | CTCTCTGT others(29): Show |
1 | a0194c0058t0002g0235 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.10275-226_10275-22 others(40): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 85/93 | INFO_REALIGN_3_PRIME | chr1 | 149547923 | |||||
| chr1:149547923
|
C | CTCTCTGT others(41): Show |
1 | a0192c0055t0002g0263 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.10275-226_10275-22 others(52): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 85/93 | INFO_REALIGN_3_PRIME | chr1 | 149547923 | |||||
| chr1:149547923
|
C | CTCTGTGT others(9): Show |
2 | a0049c0082t0011g0096a0119c0153t0001g0097 | 2 | HG02738.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.10275-226_10275-22 others(20): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 85/93 | INFO_REALIGN_3_PRIME | chr1 | 149547923 | |||||
| chr1:149547923
|
C | CTCTGTGT others(11): Show |
4 | a0167c0203t0028g0269a0169c0205t0004g0209a0170c0208t0004g0202others(1): Show | 4 | HG02109.hp2 HG04115.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.10275-226_10275-22 others(22): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 85/93 | INFO_REALIGN_3_PRIME | chr1 | 149547923 | |||||
| chr1:149547923
|
C | CTCTGTGT others(13): Show |
7 | a0073c0103t0001g0018a0081c0113t0001g0148a0086c0119t0001g0085others(4): Show | 7 | HG00423.hp2 HG01099.hp1 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.10275-226_10275-22 others(24): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 85/93 | INFO_REALIGN_3_PRIME | chr1 | 149547923 | |||||
| chr1:149547923
|
C | CTCTGTGT others(15): Show |
2 | a0043c0209t0004g0207a0044c0210t0004g0206 | 2 | HG02165.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.10275-226_10275-22 others(26): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 85/93 | INFO_REALIGN_3_PRIME | chr1 | 149547923 | |||||
| chr1:149547923
|
C | CTCTGTGT others(17): Show |
3 | a0107c0138t0001g0072a0137c0173t0001g0159a0164c0201t0004g0205 | 3 | HG00733.hp2 HG00735.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.10275-226_10275-22 others(28): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 85/93 | INFO_REALIGN_3_PRIME | chr1 | 149547923 | |||||
| chr1:149547923
|
C | CTCTGTGT others(21): Show |
2 | a0118c0151t0001g0053a0157c0188t0001g0201 | 2 | HG02135.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.10275-226_10275-22 others(32): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 85/93 | INFO_REALIGN_3_PRIME | chr1 | 149547923 | |||||
| chr1:149547923
|
C | CTGTGTGT others(11): Show |
1 | a0183c0041t0002g0246 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.10275-216_10275-21 others(22): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 85/93 | INFO_REALIGN_3_PRIME | chr1 | 149547923 | |||||
| chr1:149547923
|
C | CTGTGTGT others(13): Show |
1 | a0179c0071t0002g0260 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.10275-216_10275-21 others(24): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 85/93 | INFO_REALIGN_3_PRIME | chr1 | 149547923 | |||||
| chr1:149547923
|
C | CTGTGTGT others(19): Show |
1 | a0189c0052t0027g0231 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.10275-216_10275-21 others(30): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 85/93 | INFO_REALIGN_3_PRIME | chr1 | 149547923 | |||||
| chr1:149547923
|
C | G | 14 | a0015c0036t0006g0004a0015c0192t0006g0270a0060c0092t0001g0069others(11): Show | 15 | HG02145.hp1 HG02896.hp1 HG02896.hp2 others(12): Show |
intron_variant | MODIFIER | c.10275-227C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 85/93 | chr1 | 149547923 | ||||||
| chr1:149547928
|
T | C | 1 | a0116c0150t0001g0014 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.10275-222T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 85/93 | chr1 | 149547928 | ||||||
| chr1:149547935
|
C | G | 81 | a0006c0211t0019g0211a0006c0212t0002g0223a0006c0213t0002g0224others(78): Show | 81 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.10275-215C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 85/93 | chr1 | 149547935 | ||||||
| chr1:149547947
|
G | T | 4 | a0024c0025t0001g0024a0024c0025t0001g0026a0042c0195t0001g0023others(1): Show | 4 | HG02055.hp2 HG02486.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.10275-203G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 85/93 | chr1 | 149547947 | ||||||
| chr1:149547954
|
T | C | 7 | a0006c0211t0019g0211a0116c0150t0001g0014a0161c0197t0005g0214others(4): Show | 7 | HG00544.hp2 HG00558.hp2 HG00735.hp2 others(4): Show |
intron_variant | MODIFIER | c.10275-196T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 85/93 | chr1 | 149547954 | ||||||
| chr1:149548021
|
G | C | 2 | a0036c0014t0009g0228a0036c0014t0009g0230 | 2 | NA18960.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.10275-129G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 85/93 | chr1 | 149548021 | ||||||
| chr1:149548029
|
A | C | 7 | a0185c0043t0002g0247a0188c0051t0002g0252a0190c0049t0002g0244others(4): Show | 7 | NA18946.hp2 NA18954.hp2 NA18959.hp1 others(4): Show |
intron_variant | MODIFIER | c.10275-121A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 85/93 | chr1 | 149548029 | ||||||
| chr1:149548038
|
T | A | 1 | a0160c0076t0014g0225 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.10275-112T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 85/93 | chr1 | 149548038 | ||||||
| chr1:149548050
|
C | G | 71 | a0006c0211t0019g0211a0006c0212t0002g0223a0006c0213t0002g0224others(68): Show | 71 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.10275-100C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 85/93 | chr1 | 149548050 | ||||||
| chr1:149548067
|
T | C | 71 | a0006c0211t0019g0211a0006c0212t0002g0223a0006c0213t0002g0224others(68): Show | 71 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.10275-83T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 85/93 | chr1 | 149548067 | ||||||
| chr1:149548094
|
G | A | 4 | a0004c0026t0001g0007a0004c0026t0001g0008a0004c0027t0001g0001others(1): Show | 5 | HG01891.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.10275-56G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 85/93 | chr1 | 149548094 | ||||||
| chr1:149548132
|
T | G | 7 | a0185c0043t0002g0247a0188c0051t0002g0252a0190c0049t0002g0244others(4): Show | 7 | NA18946.hp2 NA18954.hp2 NA18959.hp1 others(4): Show |
intron_variant | MODIFIER | c.10275-18T>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 85/93 | chr1 | 149548132 | ||||||
| chr1:149548146
|
C | A | 1 | a0167c0203t0028g0269 | 1 | HG02109.hp2 | splice_region_variant&intron_variant | LOW | c.10275-4C>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 85/93 | chr1 | 149548146 | ||||||
| chr1:149548330
|
C | T | 8 | a0043c0209t0004g0207a0044c0210t0004g0206a0164c0201t0004g0205others(5): Show | 8 | HG00735.hp1 HG01099.hp1 HG02165.hp1 others(5): Show |
splice_region_variant&intron_variant | LOW | c.10447+8C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 86/93 | chr1 | 149548330 | ||||||
| chr1:149548337
|
A | G | 3 | a0006c0212t0002g0223a0006c0213t0002g0224a0006c0214t0002g0265 | 3 | HG01891.hp1 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.10447+15A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 86/93 | chr1 | 149548337 | ||||||
| chr1:149548378
|
C | G | 1 | a0007c0005t0001g0154 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.10447+56C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 86/93 | chr1 | 149548378 | ||||||
| chr1:149548394
|
G | A | 1 | a0041c0217t0003g0185 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.10447+72G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 86/93 | chr1 | 149548394 | ||||||
| chr1:149548421
|
A | G | 64 | a0001c0001t0001g0136a0006c0211t0019g0211a0006c0212t0002g0223others(61): Show | 64 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.10447+99A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 86/93 | chr1 | 149548421 | ||||||
| chr1:149548426
|
C | T | 1 | a0125c0159t0001g0147 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.10447+104C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 86/93 | chr1 | 149548426 | ||||||
| chr1:149548430
|
G | T | 1 | a0169c0205t0004g0209 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.10447+108G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 86/93 | chr1 | 149548430 | ||||||
| chr1:149548437
|
C | A | 3 | a0006c0212t0002g0223a0006c0213t0002g0224a0006c0214t0002g0265 | 3 | HG01891.hp1 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.10447+115C>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 86/93 | chr1 | 149548437 | ||||||
| chr1:149548492
|
T | A | 63 | a0006c0211t0019g0211a0006c0212t0002g0223a0006c0213t0002g0224others(60): Show | 63 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.10447+170T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 86/93 | chr1 | 149548492 | ||||||
| chr1:149548511
|
T | A | 63 | a0006c0211t0019g0211a0006c0212t0002g0223a0006c0213t0002g0224others(60): Show | 63 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.10447+189T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 86/93 | chr1 | 149548511 | ||||||
| chr1:149548513
|
G | A | 63 | a0006c0211t0019g0211a0006c0212t0002g0223a0006c0213t0002g0224others(60): Show | 63 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.10447+191G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 86/93 | chr1 | 149548513 | ||||||
| chr1:149548535
|
A | C | 1 | a0093c0124t0001g0153 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.10447+213A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 86/93 | chr1 | 149548535 | ||||||
| chr1:149548545
|
C | T | 1 | a0160c0076t0014g0225 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.10447+223C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 86/93 | chr1 | 149548545 | ||||||
| chr1:149548546
|
A | G | 63 | a0006c0211t0019g0211a0006c0212t0002g0223a0006c0213t0002g0224others(60): Show | 63 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.10447+224A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 86/93 | chr1 | 149548546 | ||||||
| chr1:149548548
|
T | C | 63 | a0006c0211t0019g0211a0006c0212t0002g0223a0006c0213t0002g0224others(60): Show | 63 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.10447+226T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 86/93 | chr1 | 149548548 | ||||||
| chr1:149548554
|
T | C | 63 | a0006c0211t0019g0211a0006c0212t0002g0223a0006c0213t0002g0224others(60): Show | 63 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.10447+232T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 86/93 | chr1 | 149548554 | ||||||
| chr1:149548558
|
C | T | 63 | a0006c0211t0019g0211a0006c0212t0002g0223a0006c0213t0002g0224others(60): Show | 63 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.10447+236C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 86/93 | chr1 | 149548558 | ||||||
| chr1:149548606
|
G | T | 22 | a0034c0013t0002g0220a0034c0013t0002g0221a0035c0015t0002g0216others(19): Show | 22 | HG00438.hp2 HG00621.hp1 HG02040.hp2 others(19): Show |
intron_variant | MODIFIER | c.10447+284G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 86/93 | chr1 | 149548606 | ||||||
| chr1:149548626
|
T | C | 157 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(154): Show | 160 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.10447+304T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 86/93 | chr1 | 149548626 | ||||||
| chr1:149548721
|
T | A | 7 | a0185c0043t0002g0247a0188c0051t0002g0252a0190c0049t0002g0244others(4): Show | 7 | NA18946.hp2 NA18954.hp2 NA18959.hp1 others(4): Show |
intron_variant | MODIFIER | c.10448-316T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 86/93 | chr1 | 149548721 | ||||||
| chr1:149548727
|
C | T | 48 | a0006c0211t0019g0211a0006c0212t0002g0223a0006c0213t0002g0224others(45): Show | 48 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.10448-310C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 86/93 | chr1 | 149548727 | ||||||
| chr1:149548881
|
C | T | 1 | a0204c0067t0002g0248 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.10448-156C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 86/93 | chr1 | 149548881 | ||||||
| chr1:149548937
|
C | T | 1 | a0059c0091t0001g0130 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.10448-100C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 86/93 | chr1 | 149548937 | ||||||
| chr1:149548975
|
G | A | 10 | a0032c0012t0002g0232a0032c0012t0002g0266a0033c0011t0002g0254others(7): Show | 10 | HG00642.hp1 HG01069.hp2 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.10448-62G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 86/93 | chr1 | 149548975 | ||||||
| chr1:149548983
|
A | G | 4 | a0203c0065t0002g0240a0207c0046t0002g0241a0208c0048t0002g0251others(1): Show | 4 | HG00438.hp2 HG02080.hp2 NA18939.hp2 others(1): Show |
intron_variant | MODIFIER | c.10448-54A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 86/93 | chr1 | 149548983 | ||||||
| chr1:149549217
|
G | C | 130 | a0001c0001t0001g0121a0001c0001t0001g0158a0002c0002t0003g0182others(127): Show | 131 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.10556+72G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 87/93 | chr1 | 149549217 | ||||||
| chr1:149549218
|
T | C | 4 | a0004c0026t0001g0008a0004c0027t0001g0001a0061c0187t0001g0173others(1): Show | 5 | HG01891.hp2 HG02145.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.10556+73T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 87/93 | chr1 | 149549218 | ||||||
| chr1:149549219
|
G | C | 1 | a0048c0081t0011g0151 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.10556+74G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 87/93 | chr1 | 149549219 | ||||||
| chr1:149549227
|
T | C | 1 | a0181c0073t0002g0272 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.10556+82T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 87/93 | chr1 | 149549227 | ||||||
| chr1:149549244
|
A | C | 37 | a0032c0012t0002g0232a0032c0012t0002g0266a0033c0011t0002g0254others(34): Show | 37 | HG00438.hp2 HG00621.hp2 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.10556+99A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 87/93 | chr1 | 149549244 | ||||||
| chr1:149549297
|
T | C | 1 | a0174c0202t0013g0204 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.10556+152T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 87/93 | chr1 | 149549297 | ||||||
| chr1:149549329
|
A | C | 1 | a0011c0010t0001g0012 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.10556+184A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 87/93 | chr1 | 149549329 | ||||||
| chr1:149549333
|
G | A | 215 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(212): Show | 217 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.10556+188G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 87/93 | chr1 | 149549333 | ||||||
| chr1:149549388
|
A | T | 1 | a0122c0156t0001g0086 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.10556+243A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 87/93 | chr1 | 149549388 | ||||||
| chr1:149549464
|
A | G | 1 | a0027c0029t0001g0062 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.10557-311A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 87/93 | chr1 | 149549464 | ||||||
| chr1:149549473
|
G | C | 155 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0077others(152): Show | 155 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.10557-302G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 87/93 | chr1 | 149549473 | ||||||
| chr1:149549473
|
G | GAGTGTCC others(4730): Show |
1 | a0031c0028t0003g0194 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.11179+303_11179+30 others(4741): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 92/93 | INFO_REALIGN_3_PRIME | chr1 | 149549473 | |||||
| chr1:149549484
|
T | G | 1 | a0056c0089t0001g0060 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.10557-291T>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 87/93 | chr1 | 149549484 | ||||||
| chr1:149549487
|
T | C | 1 | a0186c0044t0017g0239 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.10557-288T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 87/93 | chr1 | 149549487 | ||||||
| chr1:149549522
|
G | C | 1 | a0056c0089t0001g0060 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.10557-253G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 87/93 | chr1 | 149549522 | ||||||
| chr1:149549548
|
G | C | 4 | a0161c0197t0005g0214a0162c0196t0005g0213a0163c0199t0005g0215others(1): Show | 4 | HG00544.hp2 HG00558.hp2 HG00735.hp2 others(1): Show |
intron_variant | MODIFIER | c.10557-227G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 87/93 | chr1 | 149549548 | ||||||
| chr1:149549554
|
C | G | 5 | a0056c0089t0001g0060a0161c0197t0005g0214a0162c0196t0005g0213others(2): Show | 5 | HG00544.hp2 HG00558.hp2 HG00735.hp2 others(2): Show |
intron_variant | MODIFIER | c.10557-221C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 87/93 | chr1 | 149549554 | ||||||
| chr1:149549564
|
CTG | C | 4 | a0161c0197t0005g0214a0162c0196t0005g0213a0163c0199t0005g0215others(1): Show | 4 | HG00544.hp2 HG00558.hp2 HG00735.hp2 others(1): Show |
intron_variant | MODIFIER | c.10557-209_10557-20 others(6): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 87/93 | INFO_REALIGN_3_PRIME | chr1 | 149549564 | |||||
| chr1:149549566
|
G | C | 3 | a0035c0015t0002g0216a0035c0015t0002g0217a0181c0073t0002g0272 | 3 | HG03017.hp2 HG03704.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.10557-209G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 87/93 | chr1 | 149549566 | ||||||
| chr1:149549566
|
G | GTCTC | 45 | a0006c0212t0002g0223a0006c0213t0002g0224a0006c0214t0002g0265others(42): Show | 45 | HG00438.hp2 HG00621.hp1 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.10557-195_10557-19 others(8): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 87/93 | INFO_REALIGN_3_PRIME | chr1 | 149549566 | |||||
| chr1:149549578
|
C | T | 11 | a0011c0010t0001g0010a0011c0010t0001g0011a0011c0010t0001g0012others(8): Show | 11 | HG00438.hp1 HG00558.hp1 NA18942.hp2 others(8): Show |
intron_variant | MODIFIER | c.10557-197C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 87/93 | chr1 | 149549578 | ||||||
| chr1:149549649
|
A | C | 1 | a0200c0062t0002g0237 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.10557-126A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 87/93 | chr1 | 149549649 | ||||||
| chr1:149549710
|
C | A | 1 | a0006c0211t0019g0211 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.10557-65C>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 87/93 | chr1 | 149549710 | ||||||
| chr1:149549725
|
T | C | 51 | a0006c0211t0019g0211a0006c0212t0002g0223a0006c0213t0002g0224others(48): Show | 51 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.10557-50T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 87/93 | chr1 | 149549725 | ||||||
| chr1:149549737
|
C | CCCCCTGG others(4729): Show |
1 | a0031c0028t0003g0180 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.11179+303_11179+30 others(4740): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 92/93 | INFO_REALIGN_3_PRIME | chr1 | 149549737 | |||||
| chr1:149549755
|
A | T | 37 | a0032c0012t0002g0232a0032c0012t0002g0266a0033c0011t0002g0254others(34): Show | 37 | HG00438.hp2 HG00621.hp2 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.10557-20A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 87/93 | chr1 | 149549755 | ||||||
| chr1:149549771
|
C | G | 4 | a0001c0001t0001g0158a0028c0032t0001g0161a0029c0033t0001g0197others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG03098.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.10557-4C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 87/93 | chr1 | 149549771 | ||||||
| chr1:149550042
|
G | A | 42 | a0032c0012t0002g0232a0032c0012t0002g0266a0033c0011t0002g0254others(39): Show | 42 | HG00438.hp2 HG00621.hp1 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.10729+95G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 88/93 | chr1 | 149550042 | ||||||
| chr1:149550053
|
A | AGGGAGGA others(4760): Show |
1 | a0194c0058t0002g0235 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.10729+221_10729+22 others(4771): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 88/93 | INFO_REALIGN_3_PRIME | chr1 | 149550053 | |||||
| chr1:149550053
|
A | AGGGAGGA others(4756): Show |
1 | a0040c0218t0002g0234 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.10729+221_10729+22 others(4767): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 88/93 | INFO_REALIGN_3_PRIME | chr1 | 149550053 | |||||
| chr1:149550053
|
A | G | 37 | a0032c0012t0002g0232a0032c0012t0002g0266a0033c0011t0002g0254others(34): Show | 37 | HG00438.hp2 HG00621.hp2 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.10729+106A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 88/93 | chr1 | 149550053 | ||||||
| chr1:149550144
|
C | T | 18 | a0006c0211t0019g0211a0006c0212t0002g0223a0006c0213t0002g0224others(15): Show | 18 | HG00544.hp2 HG00558.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.10729+197C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 88/93 | chr1 | 149550144 | ||||||
| chr1:149550169
|
A | C | 61 | a0006c0211t0019g0211a0006c0212t0002g0223a0006c0213t0002g0224others(58): Show | 61 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.10729+222A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 88/93 | chr1 | 149550169 | ||||||
| chr1:149550192
|
A | G | 3 | a0006c0212t0002g0223a0006c0213t0002g0224a0006c0214t0002g0265 | 3 | HG01891.hp1 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.10729+245A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 88/93 | chr1 | 149550192 | ||||||
| chr1:149550193
|
C | CTGGACCT others(4758): Show |
1 | a0191c0054t0002g0264 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.10781+30_10781+31i others(4767): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 89/93 | INFO_REALIGN_3_PRIME | chr1 | 149550193 | |||||
| chr1:149550193
|
C | T | 62 | a0006c0211t0019g0211a0006c0212t0002g0223a0006c0213t0002g0224others(59): Show | 63 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.10729+246C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 88/93 | chr1 | 149550193 | ||||||
| chr1:149550206
|
G | C | 1 | a0057c0088t0001g0089 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.10729+259G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 88/93 | chr1 | 149550206 | ||||||
| chr1:149550216
|
A | T | 1 | a0192c0055t0002g0263 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.10729+269A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 88/93 | chr1 | 149550216 | ||||||
| chr1:149550286
|
G | A | 4 | a0161c0197t0005g0214a0162c0196t0005g0213a0163c0199t0005g0215others(1): Show | 4 | HG00544.hp2 HG00558.hp2 HG00735.hp2 others(1): Show |
intron_variant | MODIFIER | c.10729+339G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 88/93 | chr1 | 149550286 | ||||||
| chr1:149550299
|
G | A | 8 | a0043c0209t0004g0207a0044c0210t0004g0206a0164c0201t0004g0205others(5): Show | 8 | HG00735.hp1 HG01099.hp1 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.10729+352G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 88/93 | chr1 | 149550299 | ||||||
| chr1:149550360
|
G | A | 1 | a0084c0115t0001g0114 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.10730-307G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 88/93 | chr1 | 149550360 | ||||||
| chr1:149550411
|
C | G | 1 | a0174c0202t0013g0204 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.10730-256C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 88/93 | chr1 | 149550411 | ||||||
| chr1:149550431
|
C | G | 1 | a0198c0059t0002g0259 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.10730-236C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 88/93 | chr1 | 149550431 | ||||||
| chr1:149550584
|
C | T | 7 | a0006c0211t0019g0211a0145c0177t0001g0165a0161c0197t0005g0214others(4): Show | 7 | HG00544.hp2 HG00558.hp2 HG00735.hp2 others(4): Show |
intron_variant | MODIFIER | c.10730-83C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 88/93 | chr1 | 149550584 | ||||||
| chr1:149550640
|
G | A | 1 | a0145c0177t0001g0165 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.10730-27G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 88/93 | chr1 | 149550640 | ||||||
| chr1:149550652
|
C | CTGAACTT others(14214): Show |
1 | a0192c0055t0002g0263 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.10781+30_10781+31i others(14223): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 89/93 | INFO_REALIGN_3_PRIME | chr1 | 149550652 | |||||
| chr1:149550749
|
C | T | 6 | a0183c0041t0002g0246a0185c0043t0002g0247a0188c0051t0002g0252others(3): Show | 6 | NA18946.hp2 NA18954.hp2 NA18962.hp2 others(3): Show |
intron_variant | MODIFIER | c.10781+31C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 89/93 | chr1 | 149550749 | ||||||
| chr1:149550773
|
G | T | 1 | a0006c0211t0019g0211 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.10781+55G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 89/93 | chr1 | 149550773 | ||||||
| chr1:149550897
|
A | T | 7 | a0006c0211t0019g0211a0145c0177t0001g0165a0161c0197t0005g0214others(4): Show | 7 | HG00544.hp2 HG00558.hp2 HG00735.hp2 others(4): Show |
intron_variant | MODIFIER | c.10781+179A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 89/93 | chr1 | 149550897 | ||||||
| chr1:149550901
|
T | C | 1 | a0154c0185t0001g0152 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.10781+183T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 89/93 | chr1 | 149550901 | ||||||
| chr1:149550925
|
A | G | 1 | a0006c0211t0019g0211 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.10781+207A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 89/93 | chr1 | 149550925 | ||||||
| chr1:149550957
|
A | G | 3 | a0006c0212t0002g0223a0006c0213t0002g0224a0006c0214t0002g0265 | 3 | HG01891.hp1 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.10781+239A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 89/93 | chr1 | 149550957 | ||||||
| chr1:149550988
|
C | T | 2 | a0036c0014t0009g0228a0036c0014t0009g0230 | 2 | NA18960.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.10781+270C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 89/93 | chr1 | 149550988 | ||||||
| chr1:149551100
|
C | CCT | 17 | a0007c0005t0001g0144a0007c0005t0001g0154a0007c0005t0001g0155others(14): Show | 17 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(14): Show |
intron_variant | MODIFIER | c.10782-201_10782-20 others(6): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 89/93 | INFO_REALIGN_3_PRIME | chr1 | 149551100 | |||||
| chr1:149551100
|
CCT | C | 54 | a0032c0012t0002g0232a0032c0012t0002g0266a0033c0011t0002g0254others(51): Show | 54 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.10782-201_10782-20 others(6): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 89/93 | INFO_REALIGN_3_PRIME | chr1 | 149551100 | |||||
| chr1:149551100
|
CCTCT | C | 27 | a0001c0001t0001g0121a0009c0006t0001g0081a0009c0006t0001g0082others(24): Show | 28 | HG00099.hp1 HG00741.hp2 HG01934.hp1 others(25): Show |
intron_variant | MODIFIER | c.10782-203_10782-20 others(8): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 89/93 | INFO_REALIGN_3_PRIME | chr1 | 149551100 | |||||
| chr1:149551100
|
CCTCTCT | C | 4 | a0013c0035t0001g0038a0013c0035t0001g0084a0013c0162t0001g0040others(1): Show | 4 | HG02258.hp2 HG02280.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.10782-205_10782-20 others(10): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 89/93 | INFO_REALIGN_3_PRIME | chr1 | 149551100 | |||||
| chr1:149551100
|
CCTCTCTC others(1): Show |
C | 17 | a0006c0211t0019g0211a0006c0212t0002g0223a0006c0213t0002g0224others(14): Show | 17 | HG00735.hp2 HG01074.hp2 HG01516.hp1 others(14): Show |
intron_variant | MODIFIER | c.10782-207_10782-20 others(12): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 89/93 | INFO_REALIGN_3_PRIME | chr1 | 149551100 | |||||
| chr1:149551156
|
T | C | 2 | a0145c0177t0001g0165a0195c0060t0002g0229 | 2 | HG02602.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.10782-171T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 89/93 | chr1 | 149551156 | ||||||
| chr1:149551237
|
C | T | 1 | a0006c0211t0019g0211 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.10782-90C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 89/93 | chr1 | 149551237 | ||||||
| chr1:149551262
|
C | G | 3 | a0161c0197t0005g0214a0162c0196t0005g0213a0167c0203t0028g0269 | 3 | HG00735.hp2 HG01516.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.10782-65C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 89/93 | chr1 | 149551262 | ||||||
| chr1:149551320
|
T | G | 2 | a0163c0199t0005g0215a0165c0200t0005g0212 | 2 | HG00544.hp2 HG00558.hp2 |
splice_region_variant&intron_variant | LOW | c.10782-7T>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 89/93 | chr1 | 149551320 | ||||||
| chr1:149551534
|
C | T | 3 | a0032c0012t0002g0266a0135c0161t0001g0057a0182c0074t0002g0261 | 3 | HG00733.hp1 HG01346.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.10954+35C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 90/93 | chr1 | 149551534 | ||||||
| chr1:149551550
|
G | A | 3 | a0096c0127t0001g0111a0119c0153t0001g0097a0125c0159t0001g0147 | 3 | HG02717.hp1 HG02922.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.10954+51G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 90/93 | chr1 | 149551550 | ||||||
| chr1:149551609
|
C | T | 3 | a0009c0006t0001g0081a0009c0006t0001g0082a0009c0006t0001g0139 | 3 | HG00099.hp1 HG00741.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.10954+110C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 90/93 | chr1 | 149551609 | ||||||
| chr1:149551623
|
G | A | 6 | a0185c0043t0002g0247a0188c0051t0002g0252a0190c0049t0002g0244others(3): Show | 6 | NA18946.hp2 NA18954.hp2 NA18962.hp2 others(3): Show |
intron_variant | MODIFIER | c.10954+124G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 90/93 | chr1 | 149551623 | ||||||
| chr1:149551697
|
T | C | 4 | a0006c0211t0019g0211a0161c0197t0005g0214a0162c0196t0005g0213others(1): Show | 4 | HG00735.hp2 HG01516.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.10954+198T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 90/93 | chr1 | 149551697 | ||||||
| chr1:149551697
|
T | TTCCTAGT others(4748): Show |
1 | a0165c0200t0005g0212 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.10954+218_10954+21 others(4759): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 90/93 | INFO_REALIGN_3_PRIME | chr1 | 149551697 | |||||
| chr1:149551718
|
T | C | 24 | a0006c0211t0019g0211a0006c0212t0002g0223a0006c0213t0002g0224others(21): Show | 25 | HG00544.hp2 HG00558.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.10954+219T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 90/93 | chr1 | 149551718 | ||||||
| chr1:149551734
|
C | T | 1 | a0160c0076t0014g0225 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.10954+235C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 90/93 | chr1 | 149551734 | ||||||
| chr1:149551741
|
A | AGCACATT others(9509): Show |
1 | a0163c0199t0005g0215 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.10954+298_10954+29 others(9520): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 90/93 | INFO_REALIGN_3_PRIME | chr1 | 149551741 | |||||
| chr1:149551747
|
T | C | 1 | a0064c0094t0001g0047 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.10954+248T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 90/93 | chr1 | 149551747 | ||||||
| chr1:149551794
|
C | G | 1 | a0174c0202t0013g0204 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.10954+295C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 90/93 | chr1 | 149551794 | ||||||
| chr1:149551805
|
A | G | 42 | a0032c0012t0002g0232a0032c0012t0002g0266a0033c0011t0002g0254others(39): Show | 42 | HG00438.hp2 HG00621.hp1 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.10954+306A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 90/93 | chr1 | 149551805 | ||||||
| chr1:149551810
|
T | A | 3 | a0015c0036t0006g0004a0015c0192t0006g0270a0173c0191t0006g0271 | 4 | HG02145.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.10954+311T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 90/93 | chr1 | 149551810 | ||||||
| chr1:149551846
|
A | G | 75 | a0006c0211t0019g0211a0006c0212t0002g0223a0006c0213t0002g0224others(72): Show | 76 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.10954+347A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 90/93 | chr1 | 149551846 | ||||||
| chr1:149551852
|
A | G | 10 | a0043c0209t0004g0207a0044c0210t0004g0206a0164c0201t0004g0205others(7): Show | 10 | HG00735.hp1 HG01099.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.10954+353A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 90/93 | chr1 | 149551852 | ||||||
| chr1:149551858
|
G | A | 1 | a0077c0110t0001g0178 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.10955-351G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 90/93 | chr1 | 149551858 | ||||||
| chr1:149551946
|
A | G | 3 | a0015c0036t0006g0004a0015c0192t0006g0270a0173c0191t0006g0271 | 4 | HG02145.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.10955-263A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 90/93 | chr1 | 149551946 | ||||||
| chr1:149552001
|
T | A | 58 | a0006c0211t0019g0211a0015c0036t0006g0004a0015c0192t0006g0270others(55): Show | 59 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.10955-208T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 90/93 | chr1 | 149552001 | ||||||
| chr1:149552152
|
G | A | 3 | a0006c0212t0002g0223a0006c0213t0002g0224a0006c0214t0002g0265 | 3 | HG01891.hp1 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.10955-57G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 90/93 | chr1 | 149552152 | ||||||
| chr1:149552193
|
T | C | 1 | a0137c0173t0001g0159 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.10955-16T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 90/93 | chr1 | 149552193 | ||||||
| chr1:149552354
|
C | G | 1 | a0196c0045t0018g0226 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.11006+94C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 91/93 | chr1 | 149552354 | ||||||
| chr1:149552498
|
C | T | 8 | a0007c0005t0001g0144a0007c0005t0001g0154a0007c0005t0001g0155others(5): Show | 8 | HG00408.hp2 HG00609.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.11006+238C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 91/93 | chr1 | 149552498 | ||||||
| chr1:149552505
|
A | G | 51 | a0015c0036t0006g0004a0015c0192t0006g0270a0032c0012t0002g0232others(48): Show | 52 | HG00438.hp2 HG00621.hp1 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.11006+245A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 91/93 | chr1 | 149552505 | ||||||
| chr1:149552517
|
A | G | 62 | a0006c0211t0019g0211a0015c0036t0006g0004a0015c0192t0006g0270others(59): Show | 63 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.11006+257A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 91/93 | chr1 | 149552517 | ||||||
| chr1:149552618
|
G | A | 9 | a0043c0209t0004g0207a0044c0210t0004g0206a0164c0201t0004g0205others(6): Show | 9 | HG00735.hp1 HG01099.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.11007-269G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 91/93 | chr1 | 149552618 | ||||||
| chr1:149552658
|
C | G | 1 | a0183c0041t0002g0246 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.11007-229C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 91/93 | chr1 | 149552658 | ||||||
| chr1:149552660
|
C | CTCTCTCT others(21): Show |
1 | a0184c0042t0002g0236 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.11007-226_11007-22 others(32): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 91/93 | INFO_REALIGN_3_PRIME | chr1 | 149552660 | |||||
| chr1:149552660
|
C | CTCTCTGT others(7): Show |
1 | a0112c0131t0001g0118 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.11007-226_11007-22 others(18): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 91/93 | INFO_REALIGN_3_PRIME | chr1 | 149552660 | |||||
| chr1:149552660
|
C | CTCTCTGT others(11): Show |
4 | a0161c0197t0005g0214a0162c0196t0005g0213a0165c0200t0005g0212others(1): Show | 4 | HG00544.hp2 HG00735.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.11007-226_11007-22 others(22): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 91/93 | INFO_REALIGN_3_PRIME | chr1 | 149552660 | |||||
| chr1:149552660
|
C | CTCTCTGT others(13): Show |
1 | a0163c0199t0005g0215 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.11007-226_11007-22 others(24): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 91/93 | INFO_REALIGN_3_PRIME | chr1 | 149552660 | |||||
| chr1:149552660
|
C | CTCTCTGT others(15): Show |
2 | a0006c0211t0019g0211a0174c0202t0013g0204 | 2 | HG02895.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.11007-226_11007-22 others(26): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 91/93 | INFO_REALIGN_3_PRIME | chr1 | 149552660 | |||||
| chr1:149552660
|
C | G | 64 | a0015c0036t0006g0004a0015c0192t0006g0270a0024c0025t0001g0024others(61): Show | 65 | HG00438.hp2 HG00621.hp1 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.11007-227C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 91/93 | chr1 | 149552660 | ||||||
| chr1:149552672
|
C | CTG | 12 | a0015c0036t0006g0004a0015c0192t0006g0270a0043c0209t0004g0207others(9): Show | 13 | HG00735.hp1 HG01099.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.11007-199_11007-19 others(6): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 91/93 | INFO_REALIGN_3_PRIME | chr1 | 149552672 | |||||
| chr1:149552672
|
C | G | 9 | a0006c0211t0019g0211a0112c0131t0001g0118a0128c0168t0001g0106others(6): Show | 9 | HG00544.hp2 HG00558.hp2 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.11007-215C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 91/93 | chr1 | 149552672 | ||||||
| chr1:149552696
|
G | T | 1 | a0195c0060t0002g0229 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.11007-191G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 91/93 | chr1 | 149552696 | ||||||
| chr1:149552726
|
C | T | 47 | a0032c0012t0002g0232a0032c0012t0002g0266a0033c0011t0002g0254others(44): Show | 47 | HG00438.hp2 HG00621.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.11007-161C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 91/93 | chr1 | 149552726 | ||||||
| chr1:149552766
|
A | C | 1 | a0183c0041t0002g0246 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.11007-121A>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 91/93 | chr1 | 149552766 | ||||||
| chr1:149552773
|
G | T | 2 | a0194c0058t0002g0235a0197c0066t0002g0238 | 2 | HG00621.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.11007-114G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 91/93 | chr1 | 149552773 | ||||||
| chr1:149552787
|
C | G | 48 | a0032c0012t0002g0232a0032c0012t0002g0266a0033c0011t0002g0254others(45): Show | 48 | HG00438.hp2 HG00621.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.11007-100C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 91/93 | chr1 | 149552787 | ||||||
| chr1:149552796
|
C | T | 1 | a0032c0012t0002g0232 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.11007-91C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 91/93 | chr1 | 149552796 | ||||||
| chr1:149552804
|
T | C | 5 | a0024c0025t0001g0024a0024c0025t0001g0026a0042c0195t0001g0023others(2): Show | 5 | HG02055.hp2 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.11007-83T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 91/93 | chr1 | 149552804 | ||||||
| chr1:149552869
|
T | G | 1 | a0183c0041t0002g0246 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.11007-18T>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 91/93 | chr1 | 149552869 | ||||||
| chr1:149553062
|
G | T | 1 | a0198c0059t0002g0259 | 1 | NA18957.hp2 | splice_region_variant&intron_variant | LOW | c.11179+3G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 92/93 | chr1 | 149553062 | ||||||
| chr1:149553158
|
A | G | 1 | a0001c0001t0001g0158 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.11179+99A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 92/93 | chr1 | 149553158 | ||||||
| chr1:149553247
|
A | T | 1 | a0160c0076t0014g0225 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.11179+188A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 92/93 | chr1 | 149553247 | ||||||
| chr1:149553309
|
G | A | 1 | a0131c0171t0001g0145 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.11179+250G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 92/93 | chr1 | 149553309 | ||||||
| chr1:149553335
|
A | G | 10 | a0043c0209t0004g0207a0044c0210t0004g0206a0164c0201t0004g0205others(7): Show | 10 | HG00735.hp1 HG01099.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.11179+276A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 92/93 | chr1 | 149553335 | ||||||
| chr1:149553343
|
G | T | 1 | a0167c0203t0028g0269 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.11179+284G>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 92/93 | chr1 | 149553343 | ||||||
| chr1:149553352
|
T | C | 1 | a0044c0210t0004g0206 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.11179+293T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 92/93 | chr1 | 149553352 | ||||||
| chr1:149553363
|
T | C | 77 | a0006c0211t0019g0211a0006c0212t0002g0223a0006c0213t0002g0224others(74): Show | 78 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.11179+304T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 92/93 | chr1 | 149553363 | ||||||
| chr1:149553363
|
T | G | 2 | a0022c0023t0001g0156a0022c0023t0001g0160 | 2 | HG02572.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.11179+304T>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 92/93 | chr1 | 149553363 | ||||||
| chr1:149553371
|
C | G | 48 | a0032c0012t0002g0232a0032c0012t0002g0266a0033c0011t0002g0254others(45): Show | 48 | HG00438.hp2 HG00621.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.11179+312C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 92/93 | chr1 | 149553371 | ||||||
| chr1:149553399
|
G | C | 2 | a0028c0032t0001g0036a0124c0158t0001g0095 | 2 | HG03017.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.11179+340G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 92/93 | chr1 | 149553399 | ||||||
| chr1:149553436
|
A | G | 3 | a0006c0212t0002g0223a0006c0213t0002g0224a0006c0214t0002g0265 | 3 | HG01891.hp1 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.11180-338A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 92/93 | chr1 | 149553436 | ||||||
| chr1:149553458
|
T | A | 1 | a0183c0041t0002g0246 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.11180-316T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 92/93 | chr1 | 149553458 | ||||||
| chr1:149553493
|
A | T | 3 | a0006c0212t0002g0223a0006c0213t0002g0224a0006c0214t0002g0265 | 3 | HG01891.hp1 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.11180-281A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 92/93 | chr1 | 149553493 | ||||||
| chr1:149553509
|
T | A | 3 | a0023c0024t0001g0003a0076c0109t0001g0137a0094c0125t0001g0138 | 4 | HG02257.hp2 HG02630.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.11180-265T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 92/93 | chr1 | 149553509 | ||||||
| chr1:149553557
|
A | G | 1 | a0146c0176t0003g0110 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.11180-217A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 92/93 | chr1 | 149553557 | ||||||
| chr1:149553732
|
GA | G | 49 | a0032c0012t0002g0232a0032c0012t0002g0266a0033c0011t0002g0254others(46): Show | 49 | HG00438.hp2 HG00621.hp1 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.11180-40delA | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 92/93 | INFO_REALIGN_3_PRIME | chr1 | 149553732 | |||||
| chr1:149553915
|
G | C | 2 | a0144c0178t0001g0119a0147c0220t0001g0094 | 2 | HG02129.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.11288+33G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 93/93 | chr1 | 149553915 | ||||||
| chr1:149553929
|
A | T | 9 | a0043c0209t0004g0207a0044c0210t0004g0206a0164c0201t0004g0205others(6): Show | 9 | HG00735.hp1 HG01099.hp1 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.11288+47A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 93/93 | chr1 | 149553929 | ||||||
| chr1:149553946
|
A | G | 1 | a0149c0183t0001g0022 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.11288+64A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 93/93 | chr1 | 149553946 | ||||||
| chr1:149553954
|
G | C | 8 | a0019c0021t0001g0098a0030c0034t0001g0092a0030c0034t0001g0093others(5): Show | 8 | HG00609.hp2 HG01074.hp1 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.11288+72G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 93/93 | chr1 | 149553954 | ||||||
| chr1:149553955
|
T | C | 1 | a0150c0160t0001g0107 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.11288+73T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 93/93 | chr1 | 149553955 | ||||||
| chr1:149554008
|
T | C | 6 | a0001c0001t0001g0158a0028c0032t0001g0161a0029c0033t0001g0197others(3): Show | 6 | HG02572.hp1 HG02647.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.11288+126T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 93/93 | chr1 | 149554008 | ||||||
| chr1:149554070
|
G | A | 15 | a0043c0209t0004g0207a0044c0210t0004g0206a0071c0102t0001g0143others(12): Show | 15 | HG00544.hp2 HG00558.hp2 HG00609.hp2 others(12): Show |
intron_variant | MODIFIER | c.11288+188G>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 93/93 | chr1 | 149554070 | ||||||
| chr1:149554193
|
A | G | 1 | a0167c0203t0028g0269 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.11289-302A>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 93/93 | chr1 | 149554193 | ||||||
| chr1:149554210
|
G | C | 1 | a0071c0102t0001g0143 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.11289-285G>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 93/93 | chr1 | 149554210 | ||||||
| chr1:149554239
|
T | C | 16 | a0006c0211t0019g0211a0043c0209t0004g0207a0044c0210t0004g0206others(13): Show | 16 | HG00544.hp2 HG00558.hp2 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.11289-256T>C | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 93/93 | chr1 | 149554239 | ||||||
| chr1:149554250
|
A | T | 6 | a0006c0211t0019g0211a0161c0197t0005g0214a0162c0196t0005g0213others(3): Show | 6 | HG00544.hp2 HG00558.hp2 HG00735.hp2 others(3): Show |
intron_variant | MODIFIER | c.11289-245A>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 93/93 | chr1 | 149554250 | ||||||
| chr1:149554263
|
C | A | 5 | a0045c0078t0001g0099a0046c0077t0001g0083a0096c0127t0001g0111others(2): Show | 5 | HG02717.hp1 HG02922.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.11289-232C>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 93/93 | chr1 | 149554263 | ||||||
| chr1:149554310
|
T | A | 16 | a0006c0211t0019g0211a0043c0209t0004g0207a0044c0210t0004g0206others(13): Show | 16 | HG00544.hp2 HG00558.hp2 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.11289-185T>A | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 93/93 | chr1 | 149554310 | ||||||
| chr1:149554324
|
C | G | 1 | a0021c0022t0001g0080 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.11289-171C>G | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 93/93 | chr1 | 149554324 | ||||||
| chr1:149554358
|
A | AT | 9 | a0043c0209t0004g0207a0044c0210t0004g0206a0164c0201t0004g0205others(6): Show | 9 | HG00735.hp1 HG01099.hp1 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.11289-126dupT | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 93/93 | INFO_REALIGN_3_PRIME | chr1 | 149554358 | |||||
| chr1:149554358
|
AT | A | 13 | a0002c0002t0003g0182a0002c0002t0003g0188a0002c0002t0003g0189others(10): Show | 13 | HG00642.hp2 HG01071.hp1 HG01975.hp1 others(10): Show |
intron_variant | MODIFIER | c.11289-126delT | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 93/93 | INFO_REALIGN_3_PRIME | chr1 | 149554358 | |||||
| chr1:149554406
|
C | T | 16 | a0006c0211t0019g0211a0043c0209t0004g0207a0044c0210t0004g0206others(13): Show | 16 | HG00544.hp2 HG00558.hp2 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.11289-89C>T | NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 93/93 | chr1 | 149554406 |