Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 4892 |
|---|---|
| ensemblid | ENSG00000197893.14 |
| hgncid | 7988 |
| symbol | NRAP |
| name | nebulin related anchoring protein |
| refseq_nuc | NM_198060.4 |
| refseq_prot | NP_932326.2 |
| ensembl_nuc | ENST00000359988.4 |
| ensembl_prot | ENSP00000353078.3 |
| mane_status | MANE Select |
| chr | chr10 |
| start | 113588714 |
| end | 113664041 |
| strand | - |
| ver | v1.2 |
| region | chr10:113588714-113664041 |
| region5000 | chr10:113583714-113669041 |
| regionname0 | NRAP_chr10_113588714_113664041 |
| regionname5000 | NRAP_chr10_113583714_113669041 |
| 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 | 1730 | 56 | 4 | 11 | 34 | 4 | 3 | 27 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0002 | 0/0 | 1730 | 28 | 3 | 1 | 18 | 0 | 6 | 13 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0003 | 0/0 | 1730 | 24 | 8 | 0 | 10 | 1 | 5 | 9 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0004 | 0/0 | 1730 | 20 | 4 | 2 | 10 | 0 | 4 | 5 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0005 | 0/0 | 1730 | 20 | 0 | 4 | 13 | 1 | 2 | 11 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0006 | 0/0 | 1730 | 14 | 1 | 8 | 5 | 0 | 0 | 2 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0007 | 0/0 | 1730 | 14 | 5 | 4 | 4 | 1 | 0 | 2 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0008 | 0/0 | 1730 | 14 | 0 | 4 | 7 | 2 | 1 | 6 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0009 | 1/0 | 1730 | 13 | 5 | 5 | 2 | 0 | 0 | 2 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0010 | 0/0 | 1730 | 12 | 1 | 9 | 1 | 0 | 1 | 1 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0011 | 0/0 | 1730 | 11 | 7 | 0 | 3 | 0 | 1 | 1 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0012 | 0/0 | 1730 | 10 | 0 | 3 | 5 | 0 | 2 | 5 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0013 | 0/0 | 1730 | 8 | 0 | 0 | 7 | 1 | 0 | 7 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0014 | 0/1 | 1730 | 8 | 2 | 2 | 0 | 0 | 3 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0015 | 0/0 | 1730 | 8 | 0 | 0 | 8 | 0 | 0 | 3 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0016 | 0/0 | 1730 | 8 | 3 | 2 | 3 | 0 | 0 | 2 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0017 | 0/0 | 1730 | 7 | 0 | 5 | 0 | 1 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0018 | 0/0 | 1730 | 7 | 3 | 0 | 3 | 0 | 1 | 2 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0019 | 0/0 | 1730 | 6 | 3 | 0 | 0 | 0 | 3 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0020 | 0/0 | 1730 | 6 | 1 | 4 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0021 | 0/0 | 155 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0022 | 0/0 | 1730 | 5 | 0 | 0 | 4 | 1 | 0 | 2 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0023 | 0/0 | 1730 | 4 | 0 | 1 | 2 | 0 | 1 | 2 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0024 | 0/0 | 1730 | 4 | 0 | 0 | 4 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0025 | 0/0 | 1730 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0026 | 0/0 | 1730 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0027 | 0/0 | 1730 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0028 | 0/0 | 1730 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0029 | 0/0 | 1730 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0030 | 0/0 | 1730 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0031 | 0/0 | 1730 | 3 | 0 | 0 | 2 | 1 | 0 | 2 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0032 | 0/0 | 1730 | 3 | 2 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0033 | 0/0 | 1730 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0034 | 0/0 | 1730 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0035 | 0/0 | 1730 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0036 | 0/0 | 1730 | 2 | 0 | 0 | 1 | 1 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0037 | 0/0 | 1730 | 2 | 0 | 0 | 1 | 1 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0038 | 0/0 | 1730 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0039 | 0/0 | 1730 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0040 | 0/0 | 1730 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0041 | 0/0 | 1730 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0042 | 0/0 | 1730 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0043 | 0/0 | 1730 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0044 | 0/0 | 1730 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0045 | 0/0 | 1730 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0046 | 0/0 | 1730 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0047 | 0/0 | 1730 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0048 | 0/0 | 1730 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0049 | 0/0 | 1730 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0050 | 0/0 | 1730 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0051 | 0/0 | 1730 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0052 | 0/0 | 1730 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0053 | 0/0 | 1730 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0054 | 0/0 | 1730 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0055 | 0/0 | 1730 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0056 | 0/0 | 1730 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0057 | 0/0 | 1730 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0058 | 0/0 | 1730 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0059 | 0/0 | 1730 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0060 | 0/0 | 1730 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0061 | 0/0 | 1730 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0062 | 0/0 | 1730 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0063 | 0/0 | 1730 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0064 | 0/0 | 1730 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0065 | 0/0 | 1730 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0066 | 0/0 | 1730 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0067 | 0/0 | 1730 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0068 | 0/0 | 1730 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0069 | 0/0 | 1730 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0070 | 0/0 | 1730 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0071 | 0/0 | 1730 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0072 | 0/0 | 1730 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0073 | 0/0 | 1730 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0074 | 0/0 | 1730 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0075 | 0/0 | 1730 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0076 | 0/0 | 1730 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0077 | 0/0 | 1730 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0078 | 0/0 | 1730 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0079 | 0/0 | 1730 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0080 | 0/0 | 1730 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| 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 | 5193 | 53 | 3 | 11 | 32 | 4 | 3 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0002 | 0/0 | 5193 | 26 | 3 | 1 | 18 | 0 | 4 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0003 | 0/0 | 5193 | 20 | 8 | 0 | 7 | 0 | 5 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0004 | 0/0 | 5193 | 19 | 0 | 4 | 12 | 1 | 2 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0005 | 0/0 | 5193 | 14 | 3 | 1 | 6 | 0 | 4 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0006 | 0/0 | 5193 | 13 | 1 | 8 | 4 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0007 | 0/0 | 5193 | 13 | 0 | 3 | 7 | 2 | 1 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0008 | 0/0 | 5193 | 12 | 1 | 9 | 1 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0009 | 1/0 | 5193 | 12 | 5 | 5 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0010 | 0/0 | 5193 | 11 | 4 | 3 | 3 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0011 | 0/0 | 5193 | 10 | 0 | 3 | 5 | 0 | 2 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0012 | 0/0 | 5193 | 8 | 0 | 0 | 8 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0013 | 0/0 | 5193 | 7 | 2 | 2 | 3 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0014 | 0/0 | 5193 | 7 | 0 | 5 | 0 | 1 | 1 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0015 | 0/0 | 5193 | 6 | 3 | 0 | 3 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0016 | 0/0 | 5193 | 6 | 4 | 0 | 1 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0017 | 0/0 | 5193 | 6 | 1 | 4 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0018 | 0/0 | 5193 | 6 | 3 | 0 | 0 | 0 | 3 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0019 | 0/0 | 5193 | 6 | 0 | 0 | 6 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0020 | 0/0 | 5193 | 5 | 1 | 2 | 0 | 0 | 2 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0021 | 0/0 | 5193 | 5 | 0 | 1 | 4 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0022 | 0/0 | 5193 | 4 | 0 | 0 | 4 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0023 | 0/0 | 5193 | 4 | 0 | 0 | 3 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0024 | 0/0 | 5193 | 4 | 0 | 0 | 4 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0025 | 0/0 | 5193 | 3 | 0 | 0 | 2 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0026 | 0/0 | 5193 | 3 | 1 | 0 | 2 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0027 | 0/0 | 5193 | 3 | 0 | 0 | 3 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0028 | 0/0 | 5193 | 3 | 3 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0029 | 0/0 | 5193 | 3 | 3 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0030 | 0/0 | 5193 | 3 | 0 | 0 | 2 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0031 | 0/0 | 5193 | 3 | 0 | 0 | 3 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0032 | 0/0 | 5193 | 2 | 2 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0033 | 0/0 | 5193 | 2 | 2 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0034 | 0/0 | 5193 | 2 | 2 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0035 | 0/0 | 5193 | 2 | 0 | 1 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0036 | 0/0 | 5193 | 2 | 1 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0037 | 0/0 | 5193 | 2 | 0 | 0 | 0 | 0 | 2 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0038 | 0/0 | 5193 | 2 | 2 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0039 | 0/0 | 5193 | 2 | 0 | 0 | 2 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0040 | 0/0 | 5193 | 2 | 0 | 0 | 0 | 0 | 2 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0041 | 0/0 | 5193 | 2 | 2 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0042 | 0/0 | 5193 | 2 | 2 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0043 | 0/0 | 5193 | 2 | 2 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0044 | 0/0 | 5193 | 2 | 0 | 0 | 1 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0045 | 0/0 | 5193 | 2 | 0 | 0 | 1 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0046 | 0/0 | 5193 | 2 | 0 | 0 | 2 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0047 | 0/0 | 5193 | 2 | 2 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0048 | 0/0 | 5193 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0049 | 0/0 | 5193 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0050 | 0/0 | 5193 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0051 | 0/0 | 5193 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0052 | 0/0 | 5193 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0053 | 0/0 | 5193 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0054 | 0/0 | 5193 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0055 | 0/0 | 5193 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0056 | 0/0 | 5193 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0057 | 0/0 | 5193 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0058 | 0/0 | 5193 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0059 | 0/0 | 5193 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0060 | 0/0 | 5193 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0061 | 0/0 | 5193 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0062 | 0/0 | 5193 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0063 | 0/0 | 5193 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0064 | 0/0 | 5193 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0065 | 0/0 | 5193 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0066 | 0/0 | 5193 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0067 | 0/0 | 5193 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0068 | 0/0 | 5193 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0069 | 0/0 | 5193 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0070 | 0/0 | 5193 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0071 | 0/0 | 5176 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0072 | 0/0 | 5176 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0073 | 0/0 | 5176 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0074 | 0/0 | 5193 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0075 | 0/0 | 5193 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0076 | 0/0 | 5193 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0077 | 0/0 | 5193 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0078 | 0/0 | 5193 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0079 | 0/0 | 5193 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0080 | 0/0 | 5193 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0081 | 0/0 | 5193 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0082 | 0/0 | 5193 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0083 | 0/0 | 5193 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0084 | 0/0 | 5193 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0085 | 0/0 | 5193 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0086 | 0/0 | 5193 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0087 | 0/0 | 5193 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0088 | 0/0 | 5193 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0089 | 0/0 | 5193 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0090 | 0/0 | 5193 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0091 | 0/0 | 5193 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0092 | 0/0 | 5193 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0093 | 0/0 | 5193 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0094 | 0/1 | 5193 | 1 | 0 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0095 | 0/0 | 5193 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0096 | 0/0 | 5193 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0097 | 0/0 | 5193 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0098 | 0/0 | 5193 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0099 | 0/0 | 5193 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0100 | 0/0 | 5193 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0101 | 0/0 | 5193 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0102 | 0/0 | 5193 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0103 | 0/0 | 5193 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0104 | 0/0 | 5193 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0105 | 0/0 | 5193 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0106 | 0/0 | 5193 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0107 | 0/0 | 5193 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0108 | 0/0 | 5193 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0109 | 0/0 | 5193 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0110 | 0/0 | 5193 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0111 | 0/0 | 5193 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0112 | 0/0 | 5193 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0113 | 0/0 | 5193 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0114 | 0/0 | 5176 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| c0115 | 0/0 | 5176 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| 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 | 1/0 | 421 | 139 | 30 | 25 | 64 | 6 | 13 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| t0002 | 0/0 | 420 | 77 | 20 | 20 | 25 | 8 | 4 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| t0003 | 0/1 | 421 | 64 | 18 | 8 | 27 | 2 | 8 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| t0004 | 0/0 | 420 | 54 | 14 | 3 | 30 | 0 | 7 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| t0005 | 0/0 | 421 | 38 | 4 | 10 | 16 | 2 | 6 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| t0006 | 0/0 | 420 | 17 | 1 | 8 | 7 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| t0007 | 0/0 | 420 | 2 | 0 | 0 | 0 | 0 | 2 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| t0008 | 0/0 | 420 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| t0009 | 0/0 | 420 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| t0010 | 0/0 | 420 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| t0011 | 0/0 | 421 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| t0012 | 0/0 | 421 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| t0013 | 0/0 | 421 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| t0014 | 0/0 | 421 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| 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 | 4 | 0 | 3 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0005 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0067 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0288 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0369 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0371 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0375 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0376 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0382 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0383 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0384 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0385 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0386 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| g0387 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| 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 | 5193 | 53 | 3 | 11 | 32 | 4 | 3 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0001c0109 | 0/0 | 5193 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0001c0110 | 0/0 | 5193 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0001c0112 | 0/0 | 5193 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0002c0002 | 0/0 | 5193 | 26 | 3 | 1 | 18 | 0 | 4 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0002c0037 | 0/0 | 5193 | 2 | 0 | 0 | 0 | 0 | 2 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0003c0003 | 0/0 | 5193 | 20 | 8 | 0 | 7 | 0 | 5 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0003c0023 | 0/0 | 5193 | 4 | 0 | 0 | 3 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0004c0005 | 0/0 | 5193 | 14 | 3 | 1 | 6 | 0 | 4 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0004c0021 | 0/0 | 5193 | 5 | 0 | 1 | 4 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0004c0075 | 0/0 | 5193 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0005c0004 | 0/0 | 5193 | 19 | 0 | 4 | 12 | 1 | 2 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0005c0065 | 0/0 | 5193 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0006c0006 | 0/0 | 5193 | 13 | 1 | 8 | 4 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0006c0064 | 0/0 | 5193 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0007c0010 | 0/0 | 5193 | 11 | 4 | 3 | 3 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0007c0083 | 0/0 | 5193 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0007c0084 | 0/0 | 5193 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0007c0087 | 0/0 | 5193 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0008c0007 | 0/0 | 5193 | 13 | 0 | 3 | 7 | 2 | 1 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0008c0078 | 0/0 | 5193 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0009c0009 | 1/0 | 5193 | 12 | 5 | 5 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0009c0079 | 0/0 | 5193 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0010c0008 | 0/0 | 5193 | 12 | 1 | 9 | 1 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0011c0016 | 0/0 | 5193 | 6 | 4 | 0 | 1 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0011c0026 | 0/0 | 5193 | 3 | 1 | 0 | 2 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0011c0042 | 0/0 | 5193 | 2 | 2 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0012c0011 | 0/0 | 5193 | 10 | 0 | 3 | 5 | 0 | 2 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0013c0019 | 0/0 | 5193 | 6 | 0 | 0 | 6 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0013c0044 | 0/0 | 5193 | 2 | 0 | 0 | 1 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0014c0020 | 0/0 | 5193 | 5 | 1 | 2 | 0 | 0 | 2 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0014c0060 | 0/0 | 5193 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0014c0062 | 0/0 | 5193 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0014c0094 | 0/1 | 5193 | 1 | 0 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0015c0012 | 0/0 | 5193 | 8 | 0 | 0 | 8 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0016c0013 | 0/0 | 5193 | 7 | 2 | 2 | 3 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0016c0077 | 0/0 | 5193 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0017c0014 | 0/0 | 5193 | 7 | 0 | 5 | 0 | 1 | 1 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0018c0015 | 0/0 | 5193 | 6 | 3 | 0 | 3 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0018c0076 | 0/0 | 5193 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0019c0018 | 0/0 | 5193 | 6 | 3 | 0 | 0 | 0 | 3 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0020c0017 | 0/0 | 5193 | 6 | 1 | 4 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0021c0071 | 0/0 | 5176 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0021c0072 | 0/0 | 5176 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0021c0073 | 0/0 | 5176 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0021c0114 | 0/0 | 5176 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0021c0115 | 0/0 | 5176 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0022c0022 | 0/0 | 5193 | 4 | 0 | 0 | 4 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0022c0055 | 0/0 | 5193 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0023c0030 | 0/0 | 5193 | 3 | 0 | 0 | 2 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0023c0101 | 0/0 | 5193 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0024c0024 | 0/0 | 5193 | 4 | 0 | 0 | 4 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0025c0031 | 0/0 | 5193 | 3 | 0 | 0 | 3 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0026c0034 | 0/0 | 5193 | 2 | 2 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0026c0050 | 0/0 | 5193 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0027c0032 | 0/0 | 5193 | 2 | 2 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0027c0049 | 0/0 | 5193 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0028c0033 | 0/0 | 5193 | 2 | 2 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0028c0048 | 0/0 | 5193 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0029c0029 | 0/0 | 5193 | 3 | 3 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0030c0027 | 0/0 | 5193 | 3 | 0 | 0 | 3 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0031c0025 | 0/0 | 5193 | 3 | 0 | 0 | 2 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0032c0038 | 0/0 | 5193 | 2 | 2 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0032c0053 | 0/0 | 5193 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0033c0028 | 0/0 | 5193 | 3 | 3 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0034c0047 | 0/0 | 5193 | 2 | 2 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0035c0040 | 0/0 | 5193 | 2 | 0 | 0 | 0 | 0 | 2 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0036c0103 | 0/0 | 5193 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0036c0104 | 0/0 | 5193 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0037c0045 | 0/0 | 5193 | 2 | 0 | 0 | 1 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0038c0046 | 0/0 | 5193 | 2 | 0 | 0 | 2 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0039c0096 | 0/0 | 5193 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0039c0098 | 0/0 | 5193 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0040c0043 | 0/0 | 5193 | 2 | 2 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0041c0041 | 0/0 | 5193 | 2 | 2 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0042c0035 | 0/0 | 5193 | 2 | 0 | 1 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0043c0070 | 0/0 | 5193 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0043c0085 | 0/0 | 5193 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0044c0039 | 0/0 | 5193 | 2 | 0 | 0 | 2 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0045c0036 | 0/0 | 5193 | 2 | 1 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0046c0113 | 0/0 | 5193 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0047c0111 | 0/0 | 5193 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0048c0102 | 0/0 | 5193 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0049c0105 | 0/0 | 5193 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0050c0107 | 0/0 | 5193 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0051c0106 | 0/0 | 5193 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0052c0108 | 0/0 | 5193 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0053c0069 | 0/0 | 5193 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0054c0051 | 0/0 | 5193 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0055c0100 | 0/0 | 5193 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0056c0099 | 0/0 | 5193 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0057c0097 | 0/0 | 5193 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0058c0092 | 0/0 | 5193 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0059c0058 | 0/0 | 5193 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0060c0067 | 0/0 | 5193 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0061c0061 | 0/0 | 5193 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0062c0063 | 0/0 | 5193 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0063c0066 | 0/0 | 5193 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0064c0093 | 0/0 | 5193 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0065c0059 | 0/0 | 5193 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0066c0095 | 0/0 | 5193 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0067c0057 | 0/0 | 5193 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0068c0068 | 0/0 | 5193 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0069c0056 | 0/0 | 5193 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0070c0086 | 0/0 | 5193 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0071c0089 | 0/0 | 5193 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0072c0088 | 0/0 | 5193 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0073c0090 | 0/0 | 5193 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0074c0091 | 0/0 | 5193 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0075c0082 | 0/0 | 5193 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0076c0052 | 0/0 | 5193 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0077c0054 | 0/0 | 5193 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0078c0081 | 0/0 | 5193 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0079c0080 | 0/0 | 5193 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0080c0074 | 0/0 | 5193 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5613 | 52 | 3 | 10 | 32 | 4 | 3 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0001c0001t0013 | 0/0 | 5613 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0001c0109t0001 | 0/0 | 5613 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0001c0110t0001 | 0/0 | 5613 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0001c0112t0001 | 0/0 | 5613 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0002c0002t0004 | 0/0 | 5612 | 26 | 3 | 1 | 18 | 0 | 4 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0002c0037t0007 | 0/0 | 5612 | 2 | 0 | 0 | 0 | 0 | 2 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0003c0003t0003 | 0/0 | 5613 | 20 | 8 | 0 | 7 | 0 | 5 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0003c0023t0003 | 0/0 | 5613 | 4 | 0 | 0 | 3 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0004c0005t0001 | 0/0 | 5613 | 13 | 3 | 1 | 6 | 0 | 3 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0004c0005t0011 | 0/0 | 5613 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0004c0021t0001 | 0/0 | 5613 | 4 | 0 | 0 | 4 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0004c0021t0003 | 0/0 | 5613 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0004c0075t0001 | 0/0 | 5613 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0005c0004t0005 | 0/0 | 5613 | 19 | 0 | 4 | 12 | 1 | 2 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0005c0065t0005 | 0/0 | 5613 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0006c0006t0006 | 0/0 | 5612 | 13 | 1 | 8 | 4 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0006c0064t0006 | 0/0 | 5612 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0007c0010t0003 | 0/0 | 5613 | 10 | 3 | 3 | 3 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0007c0010t0014 | 0/0 | 5613 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0007c0083t0003 | 0/0 | 5613 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0007c0084t0003 | 0/0 | 5613 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0007c0087t0003 | 0/0 | 5613 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0008c0007t0002 | 0/0 | 5612 | 12 | 0 | 2 | 7 | 2 | 1 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0008c0007t0009 | 0/0 | 5612 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0008c0078t0002 | 0/0 | 5612 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0009c0009t0001 | 1/0 | 5613 | 12 | 5 | 5 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0009c0079t0001 | 0/0 | 5613 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0010c0008t0002 | 0/0 | 5612 | 11 | 1 | 8 | 1 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0010c0008t0010 | 0/0 | 5612 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0011c0016t0004 | 0/0 | 5612 | 6 | 4 | 0 | 1 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0011c0026t0002 | 0/0 | 5612 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0011c0026t0006 | 0/0 | 5612 | 2 | 0 | 0 | 2 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0011c0042t0004 | 0/0 | 5612 | 2 | 2 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0012c0011t0003 | 0/0 | 5613 | 10 | 0 | 3 | 5 | 0 | 2 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0013c0019t0002 | 0/0 | 5612 | 6 | 0 | 0 | 6 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0013c0044t0002 | 0/0 | 5612 | 2 | 0 | 0 | 1 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0014c0020t0005 | 0/0 | 5613 | 5 | 1 | 2 | 0 | 0 | 2 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0014c0060t0005 | 0/0 | 5613 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0014c0062t0005 | 0/0 | 5613 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0014c0094t0003 | 0/1 | 5613 | 1 | 0 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0015c0012t0004 | 0/0 | 5612 | 8 | 0 | 0 | 8 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0016c0013t0002 | 0/0 | 5612 | 7 | 2 | 2 | 3 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0016c0077t0002 | 0/0 | 5612 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0017c0014t0001 | 0/0 | 5613 | 7 | 0 | 5 | 0 | 1 | 1 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0018c0015t0001 | 0/0 | 5613 | 6 | 3 | 0 | 3 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0018c0076t0001 | 0/0 | 5613 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0019c0018t0001 | 0/0 | 5613 | 6 | 3 | 0 | 0 | 0 | 3 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0020c0017t0002 | 0/0 | 5612 | 6 | 1 | 4 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0021c0071t0002 | 0/0 | 5595 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0021c0072t0001 | 0/0 | 5596 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0021c0073t0001 | 0/0 | 5596 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0021c0114t0004 | 0/0 | 5595 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0021c0115t0004 | 0/0 | 5595 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0022c0022t0001 | 0/0 | 5613 | 3 | 0 | 0 | 3 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0022c0022t0012 | 0/0 | 5613 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0022c0055t0001 | 0/0 | 5613 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0023c0030t0001 | 0/0 | 5613 | 3 | 0 | 0 | 2 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0023c0101t0001 | 0/0 | 5613 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0024c0024t0003 | 0/0 | 5613 | 4 | 0 | 0 | 4 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0025c0031t0001 | 0/0 | 5613 | 3 | 0 | 0 | 3 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0026c0034t0002 | 0/0 | 5612 | 2 | 2 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0026c0050t0002 | 0/0 | 5612 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0027c0032t0002 | 0/0 | 5612 | 2 | 2 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0027c0049t0002 | 0/0 | 5612 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0028c0033t0001 | 0/0 | 5613 | 2 | 2 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0028c0048t0001 | 0/0 | 5613 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0029c0029t0002 | 0/0 | 5612 | 3 | 3 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0030c0027t0005 | 0/0 | 5613 | 3 | 0 | 0 | 3 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0031c0025t0002 | 0/0 | 5612 | 3 | 0 | 0 | 2 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0032c0038t0004 | 0/0 | 5612 | 2 | 2 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0032c0053t0002 | 0/0 | 5612 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0033c0028t0002 | 0/0 | 5612 | 3 | 3 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0034c0047t0003 | 0/0 | 5613 | 2 | 2 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0035c0040t0004 | 0/0 | 5612 | 2 | 0 | 0 | 0 | 0 | 2 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0036c0103t0002 | 0/0 | 5612 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0036c0104t0002 | 0/0 | 5612 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0037c0045t0002 | 0/0 | 5612 | 2 | 0 | 0 | 1 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0038c0046t0001 | 0/0 | 5613 | 2 | 0 | 0 | 2 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0039c0096t0002 | 0/0 | 5612 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0039c0098t0002 | 0/0 | 5612 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0040c0043t0001 | 0/0 | 5613 | 2 | 2 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0041c0041t0003 | 0/0 | 5613 | 2 | 2 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0042c0035t0002 | 0/0 | 5612 | 2 | 0 | 1 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0043c0070t0005 | 0/0 | 5613 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0043c0085t0003 | 0/0 | 5613 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0044c0039t0004 | 0/0 | 5612 | 2 | 0 | 0 | 2 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0045c0036t0002 | 0/0 | 5612 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0045c0036t0008 | 0/0 | 5612 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0046c0113t0004 | 0/0 | 5612 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0047c0111t0001 | 0/0 | 5613 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0048c0102t0001 | 0/0 | 5613 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0049c0105t0001 | 0/0 | 5613 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0050c0107t0001 | 0/0 | 5613 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0051c0106t0002 | 0/0 | 5612 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0052c0108t0001 | 0/0 | 5613 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0053c0069t0006 | 0/0 | 5612 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0054c0051t0001 | 0/0 | 5613 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0055c0100t0001 | 0/0 | 5613 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0056c0099t0002 | 0/0 | 5612 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0057c0097t0001 | 0/0 | 5613 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0058c0092t0003 | 0/0 | 5613 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0059c0058t0002 | 0/0 | 5612 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0060c0067t0005 | 0/0 | 5613 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0061c0061t0005 | 0/0 | 5613 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0062c0063t0005 | 0/0 | 5613 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0063c0066t0005 | 0/0 | 5613 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0064c0093t0004 | 0/0 | 5612 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0065c0059t0005 | 0/0 | 5613 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0066c0095t0003 | 0/0 | 5613 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0067c0057t0005 | 0/0 | 5613 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0068c0068t0005 | 0/0 | 5613 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0069c0056t0001 | 0/0 | 5613 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0070c0086t0003 | 0/0 | 5613 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0071c0089t0004 | 0/0 | 5612 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0072c0088t0003 | 0/0 | 5613 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0073c0090t0004 | 0/0 | 5612 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0074c0091t0003 | 0/0 | 5613 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0075c0082t0003 | 0/0 | 5613 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0076c0052t0001 | 0/0 | 5613 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0077c0054t0001 | 0/0 | 5613 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0078c0081t0001 | 0/0 | 5613 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0079c0080t0002 | 0/0 | 5612 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| a0080c0074t0001 | 0/0 | 5613 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | copy fasta | chr10 | 113583714 | 113669041 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0001c0001t0013g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0001c0109t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0001c0110t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0001c0112t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0002c0002t0004g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0002c0002t0004g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0002c0002t0004g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0002c0002t0004g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0002c0002t0004g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0002c0002t0004g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0002c0002t0004g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0002c0002t0004g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0002c0002t0004g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0002c0002t0004g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0002c0002t0004g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0002c0002t0004g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0002c0002t0004g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0002c0002t0004g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0002c0002t0004g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0002c0002t0004g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0002c0002t0004g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0002c0002t0004g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0002c0002t0004g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0002c0002t0004g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0002c0002t0004g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0002c0002t0004g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0002c0002t0004g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0002c0002t0004g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0002c0002t0004g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0002c0002t0004g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0002c0037t0007g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0002c0037t0007g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0003c0003t0003g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0003c0003t0003g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0003c0003t0003g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0003c0003t0003g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0003c0003t0003g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0003c0003t0003g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0003c0003t0003g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0003c0003t0003g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0003c0003t0003g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0003c0003t0003g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0003c0003t0003g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0003c0003t0003g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0003c0003t0003g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0003c0003t0003g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0003c0003t0003g0369 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0003c0003t0003g0371 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0003c0003t0003g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0003c0003t0003g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0003c0003t0003g0383 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0003c0003t0003g0386 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0003c0023t0003g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0003c0023t0003g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0003c0023t0003g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0003c0023t0003g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0004c0005t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0004c0005t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0004c0005t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0004c0005t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0004c0005t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0004c0005t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0004c0005t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0004c0005t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0004c0005t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0004c0005t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0004c0005t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0004c0005t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0004c0005t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0004c0005t0011g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0004c0021t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0004c0021t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0004c0021t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0004c0021t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0004c0021t0003g0387 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0004c0075t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0005c0004t0005g0001 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0005c0004t0005g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0005c0004t0005g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0005c0004t0005g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0005c0004t0005g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0005c0004t0005g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0005c0004t0005g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0005c0004t0005g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0005c0004t0005g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0005c0004t0005g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0005c0004t0005g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0005c0004t0005g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0005c0004t0005g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0005c0004t0005g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0005c0004t0005g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0005c0004t0005g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0005c0065t0005g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0006c0006t0006g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0006c0006t0006g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0006c0006t0006g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0006c0006t0006g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0006c0006t0006g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0006c0006t0006g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0006c0006t0006g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0006c0006t0006g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0006c0006t0006g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0006c0006t0006g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0006c0006t0006g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0006c0006t0006g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0006c0006t0006g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0006c0064t0006g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0007c0010t0003g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0007c0010t0003g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0007c0010t0003g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0007c0010t0003g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0007c0010t0003g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0007c0010t0003g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0007c0010t0003g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0007c0010t0003g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0007c0010t0003g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0007c0010t0003g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0007c0010t0014g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0007c0083t0003g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0007c0084t0003g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0007c0087t0003g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0008c0007t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0008c0007t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0008c0007t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0008c0007t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0008c0007t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0008c0007t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0008c0007t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0008c0007t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0008c0007t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0008c0007t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0008c0007t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0008c0007t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0008c0007t0009g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0008c0078t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0009c0009t0001g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0009c0009t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0009c0009t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0009c0009t0001g0067 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0009c0009t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0009c0009t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0009c0009t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0009c0009t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0009c0009t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0009c0009t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0009c0079t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0010c0008t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0010c0008t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0010c0008t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0010c0008t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0010c0008t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0010c0008t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0010c0008t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0010c0008t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0010c0008t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0010c0008t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0010c0008t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0010c0008t0010g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0011c0016t0004g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0011c0016t0004g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0011c0016t0004g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0011c0016t0004g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0011c0016t0004g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0011c0016t0004g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0011c0026t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0011c0026t0006g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0011c0026t0006g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0011c0042t0004g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0011c0042t0004g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0012c0011t0003g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0012c0011t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0012c0011t0003g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0012c0011t0003g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0012c0011t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0012c0011t0003g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0012c0011t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0012c0011t0003g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0012c0011t0003g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0013c0019t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0013c0019t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0013c0019t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0013c0019t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0013c0019t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0013c0019t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0013c0044t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0013c0044t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0014c0020t0005g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0014c0020t0005g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0014c0020t0005g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0014c0020t0005g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0014c0020t0005g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0014c0060t0005g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0014c0062t0005g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0014c0094t0003g0288 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0015c0012t0004g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0015c0012t0004g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0015c0012t0004g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0015c0012t0004g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0015c0012t0004g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0015c0012t0004g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0016c0013t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0016c0013t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0016c0013t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0016c0013t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0016c0013t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0016c0013t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0016c0013t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0016c0077t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0017c0014t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0017c0014t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0017c0014t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0017c0014t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0017c0014t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0017c0014t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0017c0014t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0018c0015t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0018c0015t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0018c0015t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0018c0015t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0018c0015t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0018c0015t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0018c0076t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0019c0018t0001g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0019c0018t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0019c0018t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0019c0018t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0019c0018t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0020c0017t0002g0005 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0020c0017t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0020c0017t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0020c0017t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0020c0017t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0021c0071t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0021c0072t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0021c0073t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0021c0114t0004g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0021c0115t0004g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0022c0022t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0022c0022t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0022c0022t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0022c0022t0012g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0022c0055t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0023c0030t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0023c0030t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0023c0030t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0023c0101t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0024c0024t0003g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0024c0024t0003g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0024c0024t0003g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0024c0024t0003g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0025c0031t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0025c0031t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0025c0031t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0026c0034t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0026c0034t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0026c0050t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0027c0032t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0027c0032t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0027c0049t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0028c0033t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0028c0033t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0028c0048t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0029c0029t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0029c0029t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0029c0029t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0030c0027t0005g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0030c0027t0005g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0031c0025t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0031c0025t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0031c0025t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0032c0038t0004g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0032c0038t0004g0382 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0032c0053t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0033c0028t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0033c0028t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0033c0028t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0034c0047t0003g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0034c0047t0003g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0035c0040t0004g0375 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0035c0040t0004g0376 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0036c0103t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0036c0104t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0037c0045t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0037c0045t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0038c0046t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0038c0046t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0039c0096t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0039c0098t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0040c0043t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0040c0043t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0041c0041t0003g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0041c0041t0003g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0042c0035t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0042c0035t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0043c0070t0005g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0043c0085t0003g0384 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0044c0039t0004g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0044c0039t0004g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0045c0036t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0045c0036t0008g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0046c0113t0004g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0047c0111t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0048c0102t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0049c0105t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0050c0107t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0051c0106t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0052c0108t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0053c0069t0006g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0054c0051t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0055c0100t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0056c0099t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0057c0097t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0058c0092t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0059c0058t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0060c0067t0005g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0061c0061t0005g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0062c0063t0005g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0063c0066t0005g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0064c0093t0004g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0065c0059t0005g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0066c0095t0003g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0067c0057t0005g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0068c0068t0005g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0069c0056t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0070c0086t0003g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0071c0089t0004g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0072c0088t0003g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0073c0090t0004g0385 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0074c0091t0003g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0075c0082t0003g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0076c0052t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0077c0054t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0078c0081t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0079c0080t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| a0080c0074t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0200 | EUR | GBR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG00099 | hp2 | a0013 | c0044 | t0002 | g0188 | EUR | GBR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0195 | EUR | GBR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG00140 | hp2 | a0042 | c0035 | t0002 | g0252 | EUR | GBR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG00280 | hp1 | a0007 | c0010 | t0003 | g0317 | EUR | FIN | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG00280 | hp2 | a0022 | c0055 | t0001 | g0250 | EUR | FIN | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG00323 | hp1 | a0031 | c0025 | t0002 | g0248 | EUR | FIN | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG00323 | hp2 | a0003 | c0023 | t0003 | g0314 | EUR | FIN | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG00408 | hp1 | a0002 | c0002 | t0004 | g0339 | EAS | CHS | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG00408 | hp2 | a0015 | c0012 | t0004 | g0003 | EAS | CHS | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG00423 | hp1 | a0006 | c0006 | t0006 | g0011 | EAS | CHS | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | CHS | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG00438 | hp1 | a0070 | c0086 | t0003 | g0327 | EAS | CHS | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | CHS | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG00544 | hp1 | a0015 | c0012 | t0004 | g0003 | EAS | CHS | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG00544 | hp2 | a0039 | c0098 | t0002 | g0129 | EAS | CHS | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG00558 | hp1 | a0002 | c0002 | t0004 | g0361 | EAS | CHS | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG00558 | hp2 | a0008 | c0007 | t0002 | g0095 | EAS | CHS | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG00597 | hp1 | a0022 | c0022 | t0001 | g0262 | EAS | CHS | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG00597 | hp2 | a0002 | c0002 | t0004 | g0374 | EAS | CHS | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG00609 | hp1 | a0044 | c0039 | t0004 | g0331 | EAS | CHS | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG00609 | hp2 | a0071 | c0089 | t0004 | g0305 | EAS | CHS | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG00621 | hp1 | a0006 | c0006 | t0006 | g0013 | EAS | CHS | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG00621 | hp2 | a0007 | c0087 | t0003 | g0310 | EAS | CHS | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG00639 | hp2 | a0005 | c0004 | t0005 | g0001 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG00642 | hp1 | a0009 | c0009 | t0001 | g0002 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG00642 | hp2 | a0010 | c0008 | t0002 | g0240 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG00733 | hp1 | a0042 | c0035 | t0002 | g0263 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG00733 | hp2 | a0005 | c0004 | t0005 | g0043 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG00735 | hp1 | a0001 | c0001 | t0013 | g0204 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG00735 | hp2 | a0010 | c0008 | t0002 | g0241 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG00738 | hp1 | a0007 | c0010 | t0003 | g0347 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG00738 | hp2 | a0010 | c0008 | t0002 | g0265 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG00741 | hp1 | a0006 | c0006 | t0006 | g0029 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG00741 | hp2 | a0002 | c0002 | t0004 | g0322 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG01069 | hp1 | a0007 | c0010 | t0003 | g0315 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG01069 | hp2 | a0016 | c0013 | t0002 | g0086 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG01070 | hp1 | a0017 | c0014 | t0001 | g0184 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG01070 | hp2 | a0010 | c0008 | t0002 | g0243 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG01071 | hp1 | a0017 | c0014 | t0001 | g0187 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG01071 | hp2 | a0016 | c0013 | t0002 | g0087 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG01081 | hp1 | a0017 | c0014 | t0001 | g0199 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG01081 | hp2 | a0045 | c0036 | t0008 | g0057 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG01099 | hp1 | a0047 | c0111 | t0001 | g0209 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG01099 | hp2 | a0014 | c0020 | t0005 | g0037 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG01106 | hp1 | a0009 | c0009 | t0001 | g0002 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG01106 | hp2 | a0064 | c0093 | t0004 | g0281 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG01109 | hp1 | a0004 | c0021 | t0003 | g0387 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG01109 | hp2 | a0059 | c0058 | t0002 | g0239 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG01167 | hp1 | a0020 | c0017 | t0002 | g0119 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG01168 | hp1 | a0009 | c0009 | t0001 | g0091 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG01168 | hp2 | a0017 | c0014 | t0001 | g0181 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG01169 | hp1 | a0009 | c0009 | t0001 | g0093 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG01169 | hp2 | a0020 | c0017 | t0002 | g0117 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG01175 | hp1 | a0073 | c0090 | t0004 | g0385 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG01175 | hp2 | a0008 | c0007 | t0002 | g0082 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG01192 | hp1 | a0012 | c0011 | t0003 | g0292 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG01192 | hp2 | a0020 | c0017 | t0002 | g0133 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG01243 | hp1 | a0009 | c0009 | t0001 | g0002 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG01243 | hp2 | a0007 | c0010 | t0003 | g0348 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG01255 | hp1 | a0023 | c0101 | t0001 | g0182 | AMR | CLM | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG01255 | hp2 | a0004 | c0005 | t0001 | g0122 | AMR | CLM | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG01256 | hp1 | a0005 | c0004 | t0005 | g0001 | AMR | CLM | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG01257 | hp1 | a0012 | c0011 | t0003 | g0007 | AMR | CLM | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG01257 | hp2 | a0049 | c0105 | t0001 | g0215 | AMR | CLM | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG01258 | hp1 | a0012 | c0011 | t0003 | g0007 | AMR | CLM | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG01258 | hp2 | a0005 | c0004 | t0005 | g0001 | AMR | CLM | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG01261 | hp1 | a0010 | c0008 | t0002 | g0244 | AMR | CLM | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG01261 | hp2 | a0008 | c0007 | t0009 | g0094 | AMR | CLM | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG01346 | hp1 | a0014 | c0020 | t0005 | g0027 | AMR | CLM | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG01346 | hp2 | a0008 | c0078 | t0002 | g0063 | AMR | CLM | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG01358 | hp1 | a0067 | c0057 | t0005 | g0017 | AMR | CLM | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG01358 | hp2 | a0007 | c0083 | t0003 | g0346 | AMR | CLM | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | CLM | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG01361 | hp2 | a0006 | c0006 | t0006 | g0031 | AMR | CLM | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG01433 | hp1 | a0017 | c0014 | t0001 | g0194 | AMR | CLM | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG01433 | hp2 | a0051 | c0106 | t0002 | g0151 | AMR | CLM | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG01496 | hp1 | a0020 | c0017 | t0002 | g0005 | AMR | CLM | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG01496 | hp2 | a0010 | c0008 | t0010 | g0249 | AMR | CLM | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG01515 | hp1 | a0008 | c0007 | t0002 | g0078 | EUR | IBS | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0186 | EUR | IBS | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG01516 | hp1 | a0036 | c0103 | t0002 | g0192 | EUR | IBS | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG01516 | hp2 | a0056 | c0099 | t0002 | g0110 | EUR | IBS | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG01517 | hp1 | a0037 | c0045 | t0002 | g0162 | EUR | IBS | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG01517 | hp2 | a0008 | c0007 | t0002 | g0077 | EUR | IBS | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG01884 | hp1 | a0041 | c0041 | t0003 | g0279 | AFR | ACB | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG01884 | hp2 | a0029 | c0029 | t0002 | g0114 | AFR | ACB | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG01891 | hp1 | a0026 | c0050 | t0002 | g0229 | AFR | ACB | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG01891 | hp2 | a0021 | c0071 | t0002 | g0269 | AFR | ACB | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG01928 | hp1 | a0006 | c0006 | t0006 | g0033 | AMR | PEL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PEL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG01943 | hp1 | a0063 | c0066 | t0005 | g0051 | AMR | PEL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG01943 | hp2 | a0050 | c0107 | t0001 | g0206 | AMR | PEL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG01975 | hp1 | a0006 | c0006 | t0006 | g0009 | AMR | PEL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PEL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG01978 | hp1 | a0061 | c0061 | t0005 | g0038 | AMR | PEL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG01978 | hp2 | a0006 | c0006 | t0006 | g0039 | AMR | PEL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG01981 | hp1 | a0068 | c0068 | t0005 | g0023 | AMR | PEL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02004 | hp1 | a0006 | c0006 | t0006 | g0041 | AMR | PEL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02015 | hp2 | a0015 | c0012 | t0004 | g0295 | EAS | KHV | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02027 | hp2 | a0024 | c0024 | t0003 | g0321 | EAS | KHV | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02040 | hp2 | a0024 | c0024 | t0003 | g0330 | EAS | KHV | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | ACB | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02055 | hp2 | a0003 | c0003 | t0003 | g0340 | AFR | ACB | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02056 | hp1 | a0004 | c0021 | t0001 | g0132 | EAS | KHV | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02056 | hp2 | a0011 | c0016 | t0004 | g0294 | EAS | KHV | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02071 | hp1 | a0006 | c0064 | t0006 | g0012 | EAS | KHV | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02071 | hp2 | a0074 | c0091 | t0003 | g0323 | EAS | KHV | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02074 | hp1 | a0039 | c0096 | t0002 | g0130 | EAS | KHV | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02074 | hp2 | a0003 | c0023 | t0003 | g0329 | EAS | KHV | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02080 | hp1 | a0005 | c0004 | t0005 | g0032 | EAS | KHV | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02080 | hp2 | a0004 | c0021 | t0001 | g0120 | EAS | KHV | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02083 | hp1 | a0024 | c0024 | t0003 | g0324 | EAS | KHV | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02083 | hp2 | a0032 | c0053 | t0002 | g0253 | EAS | KHV | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02129 | hp1 | a0011 | c0026 | t0006 | g0015 | EAS | KHV | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02129 | hp2 | a0018 | c0015 | t0001 | g0084 | EAS | KHV | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02132 | hp1 | a0004 | c0021 | t0001 | g0125 | EAS | KHV | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02132 | hp2 | a0002 | c0002 | t0004 | g0303 | EAS | KHV | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02135 | hp1 | a0069 | c0056 | t0001 | g0245 | EAS | KHV | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | KHV | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02145 | hp1 | a0011 | c0016 | t0004 | g0297 | AFR | ACB | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02145 | hp2 | a0007 | c0084 | t0003 | g0345 | AFR | ACB | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02148 | hp1 | a0010 | c0008 | t0002 | g0247 | AMR | PEL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02148 | hp2 | a0006 | c0006 | t0006 | g0030 | AMR | PEL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02155 | hp1 | a0004 | c0005 | t0001 | g0111 | EAS | CDX | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02155 | hp2 | a0015 | c0012 | t0004 | g0286 | EAS | CDX | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02165 | hp1 | a0004 | c0005 | t0001 | g0126 | EAS | CDX | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02165 | hp2 | a0007 | c0010 | t0003 | g0378 | EAS | CDX | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | ACB | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02257 | hp2 | a0018 | c0015 | t0001 | g0070 | AFR | ACB | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02258 | hp1 | a0062 | c0063 | t0005 | g0054 | AFR | ACB | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02258 | hp2 | a0046 | c0113 | t0004 | g0275 | AFR | ACB | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02273 | hp1 | a0010 | c0008 | t0002 | g0251 | AMR | PEL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02293 | hp1 | a0010 | c0008 | t0002 | g0246 | AMR | PEL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02293 | hp2 | a0006 | c0006 | t0006 | g0020 | AMR | PEL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02451 | hp1 | a0032 | c0038 | t0004 | g0379 | AFR | ACB | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02451 | hp2 | a0021 | c0072 | t0001 | g0271 | AFR | ACB | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02523 | hp1 | a0015 | c0012 | t0004 | g0293 | EAS | KHV | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02523 | hp2 | a0005 | c0004 | t0005 | g0045 | EAS | KHV | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02572 | hp1 | a0004 | c0005 | t0001 | g0104 | AFR | GWD | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02572 | hp2 | a0028 | c0033 | t0001 | g0060 | AFR | GWD | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02602 | hp1 | a0060 | c0067 | t0005 | g0046 | SAS | PJL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02602 | hp2 | a0002 | c0002 | t0004 | g0333 | SAS | PJL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02615 | hp1 | a0004 | c0005 | t0001 | g0106 | AFR | GWD | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02615 | hp2 | a0029 | c0029 | t0002 | g0118 | AFR | GWD | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02622 | hp1 | a0026 | c0034 | t0002 | g0238 | AFR | GWD | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02622 | hp2 | a0057 | c0097 | t0001 | g0105 | AFR | GWD | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02630 | hp1 | a0045 | c0036 | t0002 | g0267 | AFR | GWD | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02630 | hp2 | a0041 | c0041 | t0003 | g0343 | AFR | GWD | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02698 | hp1 | a0012 | c0011 | t0003 | g0282 | SAS | PJL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02698 | hp2 | a0004 | c0005 | t0011 | g0116 | SAS | PJL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02717 | hp1 | a0033 | c0028 | t0002 | g0232 | AFR | GWD | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02717 | hp2 | a0018 | c0015 | t0001 | g0100 | AFR | GWD | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02735 | hp1 | a0019 | c0018 | t0001 | g0131 | SAS | PJL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02735 | hp2 | a0004 | c0005 | t0001 | g0108 | SAS | PJL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02809 | hp1 | a0004 | c0005 | t0001 | g0166 | AFR | GWD | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02809 | hp2 | a0019 | c0018 | t0001 | g0112 | AFR | GWD | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02886 | hp1 | a0043 | c0085 | t0003 | g0384 | AFR | GWD | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02886 | hp2 | a0028 | c0033 | t0001 | g0059 | AFR | GWD | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02895 | hp1 | a0014 | c0062 | t0005 | g0055 | AFR | GWD | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02895 | hp2 | a0011 | c0042 | t0004 | g0342 | AFR | GWD | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02896 | hp1 | a0003 | c0003 | t0003 | g0381 | AFR | GWD | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02896 | hp2 | a0034 | c0047 | t0003 | g0277 | AFR | GWD | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02897 | hp1 | a0034 | c0047 | t0003 | g0276 | AFR | GWD | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02897 | hp2 | a0011 | c0042 | t0004 | g0341 | AFR | GWD | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02922 | hp1 | a0009 | c0009 | t0001 | g0101 | AFR | ESN | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02922 | hp2 | a0016 | c0013 | t0002 | g0098 | AFR | ESN | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02965 | hp1 | a0007 | c0010 | t0014 | g0351 | AFR | ESN | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02965 | hp2 | a0040 | c0043 | t0001 | g0103 | AFR | ESN | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02970 | hp1 | a0009 | c0009 | t0001 | g0065 | AFR | ESN | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02970 | hp2 | a0029 | c0029 | t0002 | g0123 | AFR | ESN | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02976 | hp1 | a0027 | c0049 | t0002 | g0266 | AFR | ESN | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02976 | hp2 | a0040 | c0043 | t0001 | g0102 | AFR | ESN | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG03041 | hp1 | a0016 | c0013 | t0002 | g0079 | AFR | GWD | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG03041 | hp2 | a0007 | c0010 | t0003 | g0354 | AFR | GWD | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG03098 | hp1 | a0019 | c0018 | t0001 | g0163 | AFR | MSL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG03098 | hp2 | a0080 | c0074 | t0001 | g0268 | AFR | MSL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG03130 | hp1 | a0009 | c0009 | t0001 | g0073 | AFR | ESN | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG03130 | hp2 | a0020 | c0017 | t0002 | g0107 | AFR | ESN | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG03139 | hp1 | a0003 | c0003 | t0003 | g0380 | AFR | ESN | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG03139 | hp2 | a0016 | c0077 | t0002 | g0064 | AFR | ESN | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG03195 | hp1 | a0054 | c0051 | t0001 | g0235 | AFR | ESN | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG03195 | hp2 | a0011 | c0016 | t0004 | g0278 | AFR | ESN | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG03239 | hp1 | a0014 | c0020 | t0005 | g0036 | SAS | PJL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG03239 | hp2 | a0003 | c0003 | t0003 | g0325 | SAS | PJL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG03453 | hp1 | a0011 | c0016 | t0004 | g0298 | AFR | MSL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG03453 | hp2 | a0055 | c0100 | t0001 | g0164 | AFR | MSL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG03486 | hp1 | a0011 | c0026 | t0002 | g0237 | AFR | MSL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG03486 | hp2 | a0003 | c0003 | t0003 | g0383 | AFR | MSL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG03490 | hp1 | a0005 | c0004 | t0005 | g0001 | SAS | PJL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG03490 | hp2 | a0019 | c0018 | t0001 | g0006 | SAS | PJL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG03491 | hp1 | a0035 | c0040 | t0004 | g0376 | SAS | PJL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG03492 | hp1 | a0019 | c0018 | t0001 | g0006 | SAS | PJL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG03492 | hp2 | a0035 | c0040 | t0004 | g0375 | SAS | PJL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG03516 | hp1 | a0011 | c0016 | t0004 | g0299 | AFR | ESN | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG03516 | hp2 | a0021 | c0073 | t0001 | g0270 | AFR | ESN | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG03540 | hp1 | a0002 | c0002 | t0004 | g0335 | AFR | GWD | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG03540 | hp2 | a0009 | c0009 | t0001 | g0071 | AFR | GWD | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG03579 | hp1 | a0004 | c0075 | t0001 | g0160 | AFR | MSL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG03579 | hp2 | a0003 | c0003 | t0003 | g0386 | AFR | MSL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG03654 | hp1 | a0014 | c0020 | t0005 | g0042 | SAS | PJL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG03654 | hp2 | a0008 | c0007 | t0002 | g0090 | SAS | PJL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG03669 | hp1 | a0002 | c0002 | t0004 | g0300 | SAS | PJL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG03669 | hp2 | a0012 | c0011 | t0003 | g0287 | SAS | PJL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | STU | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG03688 | hp2 | a0053 | c0069 | t0006 | g0048 | SAS | STU | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG03704 | hp1 | a0018 | c0076 | t0001 | g0099 | SAS | PJL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG03704 | hp2 | a0002 | c0002 | t0004 | g0332 | SAS | PJL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG03710 | hp1 | a0010 | c0008 | t0002 | g0242 | SAS | PJL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG03710 | hp2 | a0004 | c0005 | t0001 | g0115 | SAS | PJL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG03831 | hp1 | a0003 | c0003 | t0003 | g0334 | SAS | BEB | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | BEB | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG03834 | hp1 | a0020 | c0017 | t0002 | g0005 | SAS | BEB | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG03834 | hp2 | a0002 | c0002 | t0004 | g0328 | SAS | BEB | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG03927 | hp1 | a0003 | c0003 | t0003 | g0313 | SAS | BEB | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG03927 | hp2 | a0014 | c0060 | t0005 | g0021 | SAS | BEB | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG03942 | hp1 | a0078 | c0081 | t0001 | g0076 | SAS | BEB | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG03942 | hp2 | a0075 | c0082 | t0003 | g0355 | SAS | BEB | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG04115 | hp1 | a0017 | c0014 | t0001 | g0172 | SAS | STU | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG04115 | hp2 | a0003 | c0003 | t0003 | g0371 | SAS | STU | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG04184 | hp1 | a0004 | c0005 | t0001 | g0113 | SAS | BEB | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG04184 | hp2 | a0002 | c0037 | t0007 | g0357 | SAS | BEB | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG04199 | hp1 | a0079 | c0080 | t0002 | g0081 | SAS | STU | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG04199 | hp2 | a0011 | c0016 | t0004 | g0280 | SAS | STU | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG04228 | hp1 | a0002 | c0037 | t0007 | g0356 | SAS | STU | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG04228 | hp2 | a0003 | c0003 | t0003 | g0369 | SAS | STU | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18522 | hp1 | a0002 | c0002 | t0004 | g0344 | AFR | YRI | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18522 | hp2 | a0007 | c0010 | t0003 | g0352 | AFR | YRI | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18612 | hp1 | a0016 | c0013 | t0002 | g0072 | EAS | CHB | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18612 | hp2 | a0022 | c0022 | t0001 | g0258 | EAS | CHB | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18747 | hp1 | a0002 | c0002 | t0004 | g0309 | EAS | CHB | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | CHB | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18906 | hp1 | a0027 | c0032 | t0002 | g0231 | AFR | YRI | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18906 | hp2 | a0032 | c0038 | t0004 | g0382 | AFR | YRI | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18939 | hp1 | a0037 | c0045 | t0002 | g0221 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18939 | hp2 | a0038 | c0046 | t0001 | g0168 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18940 | hp1 | a0002 | c0002 | t0004 | g0307 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18940 | hp2 | a0015 | c0012 | t0004 | g0296 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18942 | hp2 | a0048 | c0102 | t0001 | g0136 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18944 | hp1 | a0052 | c0108 | t0001 | g0134 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18944 | hp2 | a0018 | c0015 | t0001 | g0088 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18948 | hp1 | a0044 | c0039 | t0004 | g0319 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18948 | hp2 | a0012 | c0011 | t0003 | g0290 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18950 | hp1 | a0002 | c0002 | t0004 | g0362 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18950 | hp2 | a0002 | c0002 | t0004 | g0377 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18951 | hp1 | a0003 | c0023 | t0003 | g0318 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18952 | hp1 | a0005 | c0004 | t0005 | g0049 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18952 | hp2 | a0030 | c0027 | t0005 | g0014 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18954 | hp1 | a0058 | c0092 | t0003 | g0291 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18954 | hp2 | a0003 | c0023 | t0003 | g0320 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18956 | hp2 | a0005 | c0004 | t0005 | g0025 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18959 | hp1 | a0002 | c0002 | t0004 | g0359 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18959 | hp2 | a0016 | c0013 | t0002 | g0061 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18960 | hp1 | a0005 | c0004 | t0005 | g0024 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18960 | hp2 | a0008 | c0007 | t0002 | g0080 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18962 | hp1 | a0025 | c0031 | t0001 | g0226 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18962 | hp2 | a0002 | c0002 | t0004 | g0304 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18963 | hp1 | a0005 | c0004 | t0005 | g0035 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18964 | hp1 | a0025 | c0031 | t0001 | g0227 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18964 | hp2 | a0009 | c0079 | t0001 | g0069 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18968 | hp1 | a0025 | c0031 | t0001 | g0228 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18968 | hp2 | a0003 | c0003 | t0003 | g0358 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18970 | hp1 | a0077 | c0054 | t0001 | g0255 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18970 | hp2 | a0005 | c0004 | t0005 | g0047 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18971 | hp1 | a0003 | c0003 | t0003 | g0365 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18971 | hp2 | a0031 | c0025 | t0002 | g0257 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18972 | hp1 | a0004 | c0005 | t0001 | g0167 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18972 | hp2 | a0016 | c0013 | t0002 | g0062 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18973 | hp1 | a0013 | c0044 | t0002 | g0214 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18973 | hp2 | a0003 | c0003 | t0003 | g0366 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18974 | hp1 | a0005 | c0004 | t0005 | g0040 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18974 | hp2 | a0024 | c0024 | t0003 | g0326 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18975 | hp1 | a0006 | c0006 | t0006 | g0018 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18975 | hp2 | a0005 | c0004 | t0005 | g0008 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18981 | hp1 | a0008 | c0007 | t0002 | g0068 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18981 | hp2 | a0072 | c0088 | t0003 | g0311 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18983 | hp1 | a0023 | c0030 | t0001 | g0158 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18983 | hp2 | a0013 | c0019 | t0002 | g0159 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18984 | hp2 | a0002 | c0002 | t0004 | g0368 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18986 | hp1 | a0008 | c0007 | t0002 | g0092 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18988 | hp1 | a0030 | c0027 | t0005 | g0004 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18988 | hp2 | a0002 | c0002 | t0004 | g0373 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18989 | hp2 | a0012 | c0011 | t0003 | g0272 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18990 | hp1 | a0002 | c0002 | t0004 | g0338 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18990 | hp2 | a0008 | c0007 | t0002 | g0096 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18992 | hp2 | a0002 | c0002 | t0004 | g0364 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18993 | hp1 | a0013 | c0019 | t0002 | g0224 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18993 | hp2 | a0076 | c0052 | t0001 | g0254 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18998 | hp1 | a0004 | c0005 | t0001 | g0127 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18998 | hp2 | a0011 | c0026 | t0006 | g0026 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18999 | hp1 | a0006 | c0006 | t0006 | g0010 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA18999 | hp2 | a0013 | c0019 | t0002 | g0197 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA19000 | hp1 | a0007 | c0010 | t0003 | g0312 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA19000 | hp2 | a0031 | c0025 | t0002 | g0260 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA19003 | hp1 | a0002 | c0002 | t0004 | g0337 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA19003 | hp2 | a0012 | c0011 | t0003 | g0289 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA19004 | hp2 | a0003 | c0003 | t0003 | g0363 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA19005 | hp1 | a0001 | c0110 | t0001 | g0202 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA19007 | hp1 | a0012 | c0011 | t0003 | g0285 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA19007 | hp2 | a0008 | c0007 | t0002 | g0074 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA19009 | hp1 | a0003 | c0003 | t0003 | g0367 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA19011 | hp1 | a0013 | c0019 | t0002 | g0176 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA19012 | hp1 | a0008 | c0007 | t0002 | g0083 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA19012 | hp2 | a0005 | c0004 | t0005 | g0028 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA19030 | hp1 | a0003 | c0003 | t0003 | g0350 | AFR | LWK | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA19030 | hp2 | a0027 | c0032 | t0002 | g0230 | AFR | LWK | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA19043 | hp1 | a0021 | c0115 | t0004 | g0274 | AFR | LWK | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA19043 | hp2 | a0033 | c0028 | t0002 | g0234 | AFR | LWK | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA19056 | hp2 | a0003 | c0003 | t0003 | g0301 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA19057 | hp1 | a0023 | c0030 | t0001 | g0175 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA19057 | hp2 | a0015 | c0012 | t0004 | g0003 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA19062 | hp1 | a0007 | c0010 | t0003 | g0308 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA19062 | hp2 | a0005 | c0065 | t0005 | g0050 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA19064 | hp1 | a0012 | c0011 | t0003 | g0283 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA19064 | hp2 | a0002 | c0002 | t0004 | g0360 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA19065 | hp1 | a0003 | c0003 | t0003 | g0306 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA19067 | hp1 | a0004 | c0005 | t0001 | g0121 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA19067 | hp2 | a0005 | c0004 | t0005 | g0019 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA19068 | hp1 | a0013 | c0019 | t0002 | g0203 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA19068 | hp2 | a0004 | c0021 | t0001 | g0124 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA19072 | hp2 | a0010 | c0008 | t0002 | g0256 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA19078 | hp1 | a0015 | c0012 | t0004 | g0284 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA19079 | hp1 | a0022 | c0022 | t0001 | g0259 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA19080 | hp1 | a0018 | c0015 | t0001 | g0097 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA19083 | hp2 | a0002 | c0002 | t0004 | g0370 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA19084 | hp2 | a0002 | c0002 | t0004 | g0372 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA19085 | hp1 | a0030 | c0027 | t0005 | g0004 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA19087 | hp1 | a0001 | c0109 | t0001 | g0155 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA19088 | hp1 | a0038 | c0046 | t0001 | g0177 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA19088 | hp2 | a0005 | c0004 | t0005 | g0016 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA19089 | hp1 | a0009 | c0009 | t0001 | g0085 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA19089 | hp2 | a0036 | c0104 | t0002 | g0190 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA19090 | hp1 | a0022 | c0022 | t0012 | g0261 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA19091 | hp1 | a0004 | c0005 | t0001 | g0128 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA19091 | hp2 | a0013 | c0019 | t0002 | g0109 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA19240 | hp1 | a0028 | c0048 | t0001 | g0058 | AFR | YRI | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA19240 | hp2 | a0002 | c0002 | t0004 | g0336 | AFR | YRI | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA20129 | hp1 | a0006 | c0006 | t0006 | g0053 | AFR | ASW | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA20129 | hp2 | a0003 | c0003 | t0003 | g0316 | AFR | ASW | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0207 | EUR | TSI | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA20752 | hp2 | a0005 | c0004 | t0005 | g0052 | EUR | TSI | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA20805 | hp1 | a0017 | c0014 | t0001 | g0179 | EUR | TSI | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA20805 | hp2 | a0065 | c0059 | t0005 | g0044 | EUR | TSI | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA20905 | hp1 | a0005 | c0004 | t0005 | g0022 | SAS | GIH | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA20905 | hp2 | a0023 | c0030 | t0001 | g0174 | SAS | GIH | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | CLM | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG01123 | hp2 | a0008 | c0007 | t0002 | g0089 | AMR | CLM | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02109 | hp1 | a0007 | c0010 | t0003 | g0349 | AFR | ACB | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02109 | hp2 | a0019 | c0018 | t0001 | g0165 | AFR | ACB | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02486 | hp1 | a0014 | c0020 | t0005 | g0034 | AFR | ACB | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02486 | hp2 | a0026 | c0034 | t0002 | g0236 | AFR | ACB | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02559 | hp1 | a0043 | c0070 | t0005 | g0056 | AFR | ACB | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG02559 | hp2 | a0033 | c0028 | t0002 | g0233 | AFR | ACB | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG03471 | hp1 | a0018 | c0015 | t0001 | g0075 | AFR | MSL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG03471 | hp2 | a0021 | c0114 | t0004 | g0273 | AFR | MSL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG06807 | hp1 | a0009 | c0009 | t0001 | g0066 | AFR | USA | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| HG06807 | hp2 | a0001 | c0112 | t0001 | g0180 | AFR | USA | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA20300 | hp1 | a0010 | c0008 | t0002 | g0264 | AFR | USA | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | USA | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA21309 | hp1 | a0003 | c0003 | t0003 | g0353 | AFR | LWK | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| NA21309 | hp2 | a0066 | c0095 | t0003 | g0302 | AFR | LWK | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| homoSapiens_chm13v2 | hp1 | a0014 | c0094 | t0003 | g0288 | REF | REF | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| homoSapiens_grch38 | hp1 | a0009 | c0009 | t0001 | g0067 | REF | REF | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:113588715
|
C | T | 1 | a0010 | 1 | HG01496.hp2 | splice_region_variant | LOW | c.*260G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 42/42 | chr10 | 113588715 | ||||||
| chr10:113589718
|
C | G | 1 | a0050 | 1 | HG01943.hp2 | missense_variant | MODERATE | c.5036G>C | p.Arg1679Pro | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 41/42 | 5195/5613 | 5036/5193 | 1679/1730 | chr10 | 113589718 | ||
| chr10:113590607
|
C | A | 1 | a0027 | 3 | HG02976.hp1 NA18906.hp1 NA19030.hp2 |
missense_variant | MODERATE | c.4927G>T | p.Ala1643Ser | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 40/42 | 5086/5613 | 4927/5193 | 1643/1730 | chr10 | 113590607 | ||
| chr10:113590838
|
G | A | 34 | a0002a0006a0008others(31): Show | 158 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(155): Show |
missense_variant | MODERATE | c.4696C>T | p.Arg1566Cys | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 40/42 | 4855/5613 | 4696/5193 | 1566/1730 | chr10 | 113590838 | ||
| chr10:113592246
|
A | G | 11 | a0008a0015a0020others(8): Show | 40 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(37): Show |
missense_variant | MODERATE | c.4592T>C | p.Leu1531Pro | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 39/42 | 4751/5613 | 4592/5193 | 1531/1730 | chr10 | 113592246 | ||
| chr10:113595639
|
G | A | 1 | a0057 | 1 | HG02622.hp2 | missense_variant | MODERATE | c.4520C>T | p.Ala1507Val | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/42 | 4679/5613 | 4520/5193 | 1507/1730 | chr10 | 113595639 | ||
| chr10:113595726
|
C | T | 1 | a0070 | 1 | HG00438.hp1 | missense_variant&splice_region_variant | MODERATE | c.4433G>A | p.Arg1478His | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/42 | 4592/5613 | 4433/5193 | 1478/1730 | chr10 | 113595726 | ||
| chr10:113597971
|
C | T | 1 | a0034 | 2 | HG02896.hp2 HG02897.hp1 |
missense_variant&splice_region_variant | MODERATE | c.4330G>A | p.Glu1444Lys | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 36/42 | 4489/5613 | 4330/5193 | 1444/1730 | chr10 | 113597971 | ||
| chr10:113604826
|
A | G | 1 | a0061 | 1 | HG01978.hp1 | missense_variant | MODERATE | c.4010T>C | p.Met1337Thr | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/42 | 4169/5613 | 4010/5193 | 1337/1730 | chr10 | 113604826 | ||
| chr10:113604847
|
C | T | 1 | a0049 | 1 | HG01257.hp2 | missense_variant | MODERATE | c.3989G>A | p.Arg1330Gln | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/42 | 4148/5613 | 3989/5193 | 1330/1730 | chr10 | 113604847 | ||
| chr10:113606247
|
G | T | 3 | a0030a0048a0072 | 5 | NA18942.hp2 NA18952.hp2 NA18981.hp2 others(2): Show |
missense_variant | MODERATE | c.3738C>A | p.His1246Gln | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 33/42 | 3897/5613 | 3738/5193 | 1246/1730 | chr10 | 113606247 | ||
| chr10:113606257
|
T | A | 2 | a0043a0080 | 3 | HG02559.hp1 HG02886.hp1 HG03098.hp2 |
missense_variant | MODERATE | c.3728A>T | p.Asp1243Val | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 33/42 | 3887/5613 | 3728/5193 | 1243/1730 | chr10 | 113606257 | ||
| chr10:113610515
|
T | C | 39 | a0001a0003a0004others(36): Show | 190 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(187): Show |
missense_variant | MODERATE | c.3547A>G | p.Ile1183Val | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 31/42 | 3706/5613 | 3547/5193 | 1183/1730 | chr10 | 113610515 | ||
| chr10:113612397
|
G | A | 1 | a0017 | 7 | HG01070.hp1 HG01071.hp1 HG01081.hp1 others(4): Show |
missense_variant | MODERATE | c.3335C>T | p.Ala1112Val | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 30/42 | 3494/5613 | 3335/5193 | 1112/1730 | chr10 | 113612397 | ||
| chr10:113614241
|
C | T | 1 | a0021 | 1 | HG03471.hp2 | missense_variant | MODERATE | c.3242G>A | p.Ser1081Asn | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 29/42 | 3401/5613 | 3242/5193 | 1081/1730 | chr10 | 113614241 | ||
| chr10:113614244
|
C | T | 1 | a0070 | 1 | HG00438.hp1 | missense_variant | MODERATE | c.3239G>A | p.Arg1080Gln | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 29/42 | 3398/5613 | 3239/5193 | 1080/1730 | chr10 | 113614244 | ||
| chr10:113614862
|
C | T | 1 | a0042 | 2 | HG00140.hp2 HG00733.hp1 |
missense_variant | MODERATE | c.3163G>A | p.Ala1055Thr | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 28/42 | 3322/5613 | 3163/5193 | 1055/1730 | chr10 | 113614862 | ||
| chr10:113615726
|
T | C | 1 | a0028 | 3 | HG02572.hp2 HG02886.hp2 NA19240.hp1 |
missense_variant | MODERATE | c.3064A>G | p.Met1022Val | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 27/42 | 3223/5613 | 3064/5193 | 1022/1730 | chr10 | 113615726 | ||
| chr10:113615783
|
G | A | 1 | a0063 | 1 | HG01943.hp1 | missense_variant | MODERATE | c.3007C>T | p.His1003Tyr | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 27/42 | 3166/5613 | 3007/5193 | 1003/1730 | chr10 | 113615783 | ||
| chr10:113617531
|
T | C | 11 | a0005a0024a0044others(8): Show | 34 | HG00609.hp1 HG00639.hp2 HG00733.hp2 others(31): Show |
missense_variant | MODERATE | c.2897A>G | p.Asp966Gly | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 26/42 | 3056/5613 | 2897/5193 | 966/1730 | chr10 | 113617531 | ||
| chr10:113621937
|
G | A | 1 | a0079 | 1 | HG04199.hp1 | missense_variant | MODERATE | c.2701C>T | p.His901Tyr | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 24/42 | 2860/5613 | 2701/5193 | 901/1730 | chr10 | 113621937 | ||
| chr10:113621954
|
T | C | 1 | a0060 | 1 | HG02602.hp1 | missense_variant | MODERATE | c.2684A>G | p.Tyr895Cys | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 24/42 | 2843/5613 | 2684/5193 | 895/1730 | chr10 | 113621954 | ||
| chr10:113621988
|
G | A | 16 | a0005a0006a0010others(13): Show | 77 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(74): Show |
missense_variant | MODERATE | c.2650C>T | p.Arg884Cys | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 24/42 | 2809/5613 | 2650/5193 | 884/1730 | chr10 | 113621988 | ||
| chr10:113622070
|
A | T | 1 | a0059 | 1 | HG01109.hp2 | missense_variant | MODERATE | c.2568T>A | p.Ser856Arg | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 24/42 | 2727/5613 | 2568/5193 | 856/1730 | chr10 | 113622070 | ||
| chr10:113623569
|
G | C | 1 | a0055 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.2417C>G | p.Thr806Ser | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 23/42 | 2576/5613 | 2417/5193 | 806/1730 | chr10 | 113623569 | ||
| chr10:113629607
|
G | A | 21 | a0005a0006a0011others(18): Show | 92 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(89): Show |
missense_variant | MODERATE | c.2021C>T | p.Ala674Val | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 19/42 | 2180/5613 | 2021/5193 | 674/1730 | chr10 | 113629607 | ||
| chr10:113629689
|
C | A | 1 | a0038 | 2 | NA18939.hp2 NA19088.hp1 |
missense_variant | MODERATE | c.1939G>T | p.Ala647Ser | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 19/42 | 2098/5613 | 1939/5193 | 647/1730 | chr10 | 113629689 | ||
| chr10:113629731
|
C | A | 1 | a0066 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.1897G>T | p.Asp633Tyr | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 19/42 | 2056/5613 | 1897/5193 | 633/1730 | chr10 | 113629731 | ||
| chr10:113631886
|
C | T | 1 | a0067 | 1 | HG01358.hp1 | missense_variant | MODERATE | c.1711G>A | p.Ala571Thr | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 17/42 | 1870/5613 | 1711/5193 | 571/1730 | chr10 | 113631886 | ||
| chr10:113631927
|
T | C | 1 | a0068 | 1 | HG01981.hp1 | missense_variant | MODERATE | c.1670A>G | p.Lys557Arg | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 17/42 | 1829/5613 | 1670/5193 | 557/1730 | chr10 | 113631927 | ||
| chr10:113633160
|
T | A | 20 | a0002a0003a0007others(17): Show | 109 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(106): Show |
missense_variant | MODERATE | c.1556A>T | p.Asn519Ile | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 16/42 | 1715/5613 | 1556/5193 | 519/1730 | chr10 | 113633160 | ||
| chr10:113634170
|
G | A | 26 | a0001a0004a0013others(23): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
missense_variant | MODERATE | c.1469C>T | p.Ser490Leu | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 15/42 | 1628/5613 | 1469/5193 | 490/1730 | chr10 | 113634170 | ||
| chr10:113634189
|
C | T | 16 | a0002a0003a0007others(13): Show | 87 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(84): Show |
missense_variant | MODERATE | c.1450G>A | p.Asp484Asn | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 15/42 | 1609/5613 | 1450/5193 | 484/1730 | chr10 | 113634189 | ||
| chr10:113641423
|
C | T | 1 | a0021 | 3 | HG01891.hp2 HG02451.hp2 HG03516.hp2 |
missense_variant | MODERATE | c.1265G>A | p.Gly422Glu | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 13/42 | 1424/5613 | 1265/5193 | 422/1730 | chr10 | 113641423 | ||
| chr10:113645856
|
T | C | 48 | a0001a0004a0005others(45): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
missense_variant | MODERATE | c.1079A>G | p.Gln360Arg | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/42 | 1238/5613 | 1079/5193 | 360/1730 | chr10 | 113645856 | ||
| chr10:113645889
|
G | A | 1 | a0047 | 1 | HG01099.hp1 | missense_variant | MODERATE | c.1046C>T | p.Ser349Leu | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/42 | 1205/5613 | 1046/5193 | 349/1730 | chr10 | 113645889 | ||
| chr10:113645905
|
C | T | 48 | a0001a0004a0005others(45): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
missense_variant | MODERATE | c.1030G>A | p.Ala344Thr | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/42 | 1189/5613 | 1030/5193 | 344/1730 | chr10 | 113645905 | ||
| chr10:113647020
|
G | A | 1 | a0078 | 1 | HG03942.hp1 | missense_variant | MODERATE | c.896C>T | p.Pro299Leu | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 10/42 | 1055/5613 | 896/5193 | 299/1730 | chr10 | 113647020 | ||
| chr10:113650081
|
C | T | 24 | a0002a0003a0007others(21): Show | 115 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(112): Show |
missense_variant | MODERATE | c.844G>A | p.Ala282Thr | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/42 | 1003/5613 | 844/5193 | 282/1730 | chr10 | 113650081 | ||
| chr10:113650475
|
T | C | 14 | a0001a0013a0017others(11): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(87): Show |
missense_variant | MODERATE | c.746A>G | p.Tyr249Cys | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 8/42 | 905/5613 | 746/5193 | 249/1730 | chr10 | 113650475 | ||
| chr10:113650479
|
C | T | 1 | a0021 | 1 | HG01891.hp2 | missense_variant | MODERATE | c.742G>A | p.Ala248Thr | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 8/42 | 901/5613 | 742/5193 | 248/1730 | chr10 | 113650479 | ||
| chr10:113651855
|
A | G | 74 | a0001a0002a0003others(71): Show | 354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
missense_variant | MODERATE | c.623T>C | p.Val208Ala | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 7/42 | 782/5613 | 623/5193 | 208/1730 | chr10 | 113651855 | ||
| chr10:113651879
|
C | A | 1 | a0035 | 2 | HG03491.hp1 HG03492.hp2 |
missense_variant | MODERATE | c.599G>T | p.Arg200Leu | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 7/42 | 758/5613 | 599/5193 | 200/1730 | chr10 | 113651879 | ||
| chr10:113652949
|
G | C | 2 | a0034a0046 | 3 | HG02258.hp2 HG02896.hp2 HG02897.hp1 |
missense_variant | MODERATE | c.556C>G | p.Gln186Glu | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 6/42 | 715/5613 | 556/5193 | 186/1730 | chr10 | 113652949 | ||
| chr10:113653022
|
ATAGTCTT others(121): Show |
A | 1 | a0021 | 5 | HG01891.hp2 HG02451.hp2 HG03471.hp2 others(2): Show |
frameshift_variant&splice_acceptor_variant&splice_region_variant&intron_variant | HIGH | c.466-111_482del | p.Glu156fs | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 6/42 | 641/5613 | 466/5193 | 156/1730 | chr10 | 113653022 | ||
| chr10:113654092
|
C | A | 1 | a0033 | 3 | HG02559.hp2 HG02717.hp1 NA19043.hp2 |
missense_variant | MODERATE | c.394G>T | p.Ala132Ser | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 5/42 | 553/5613 | 394/5193 | 132/1730 | chr10 | 113654092 | ||
| chr10:113662689
|
G | A | 2 | a0045a0080 | 3 | HG01081.hp2 HG02630.hp1 HG03098.hp2 |
missense_variant | MODERATE | c.245C>T | p.Ala82Val | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/42 | 404/5613 | 245/5193 | 82/1730 | chr10 | 113662689 | ||
| chr10:113663383
|
C | A | 1 | a0025 | 3 | NA18962.hp1 NA18964.hp1 NA18968.hp1 |
missense_variant | MODERATE | c.136G>T | p.Val46Leu | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 2/42 | 295/5613 | 136/5193 | 46/1730 | chr10 | 113663383 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:113589708
|
C | T | 1 | a0062c0063 | 1 | HG02258.hp1 | synonymous_variant | LOW | c.5046G>A | p.Ala1682Ala | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 41/42 | 5205/5613 | 5046/5193 | 1682/1730 | chr10 | 113589708 | ||
| chr10:113590629
|
C | T | 2 | a0014c0020a0014c0060 | 6 | HG01099.hp2 HG01346.hp1 HG02486.hp1 others(3): Show |
synonymous_variant | LOW | c.4905G>A | p.Pro1635Pro | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 40/42 | 5064/5613 | 4905/5193 | 1635/1730 | chr10 | 113590629 | ||
| chr10:113610495
|
A | G | 49 | a0001c0001a0001c0109a0001c0110others(46): Show | 192 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(189): Show |
synonymous_variant | LOW | c.3567T>C | p.Ile1189Ile | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 31/42 | 3726/5613 | 3567/5193 | 1189/1730 | chr10 | 113610495 | ||
| chr10:113614201
|
C | G | 1 | a0014c0060 | 1 | HG03927.hp2 | synonymous_variant | LOW | c.3282G>C | p.Ala1094Ala | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 29/42 | 3441/5613 | 3282/5193 | 1094/1730 | chr10 | 113614201 | ||
| chr10:113614911
|
A | G | 14 | a0010c0008a0014c0020a0014c0060others(11): Show | 38 | HG00140.hp2 HG00323.hp1 HG00597.hp1 others(35): Show |
synonymous_variant | LOW | c.3114T>C | p.Asp1038Asp | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 28/42 | 3273/5613 | 3114/5193 | 1038/1730 | chr10 | 113614911 | ||
| chr10:113615769
|
C | A | 29 | a0001c0001a0001c0110a0001c0112others(26): Show | 107 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(104): Show |
synonymous_variant | LOW | c.3021G>T | p.Pro1007Pro | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 27/42 | 3180/5613 | 3021/5193 | 1007/1730 | chr10 | 113615769 | ||
| chr10:113626050
|
G | A | 2 | a0001c0109a0001c0110 | 2 | NA19005.hp1 NA19087.hp1 |
synonymous_variant | LOW | c.2241C>T | p.Ser747Ser | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 21/42 | 2400/5613 | 2241/5193 | 747/1730 | chr10 | 113626050 | ||
| chr10:113629597
|
G | A | 28 | a0005c0004a0005c0065a0006c0006others(25): Show | 92 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(89): Show |
synonymous_variant | LOW | c.2031C>T | p.Leu677Leu | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 19/42 | 2190/5613 | 2031/5193 | 677/1730 | chr10 | 113629597 | ||
| chr10:113633138
|
G | T | 1 | a0007c0084 | 1 | HG02145.hp2 | synonymous_variant | LOW | c.1578C>A | p.Pro526Pro | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 16/42 | 1737/5613 | 1578/5193 | 526/1730 | chr10 | 113633138 | ||
| chr10:113633141
|
C | T | 1 | a0007c0083 | 1 | HG01358.hp2 | synonymous_variant | LOW | c.1575G>A | p.Leu525Leu | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 16/42 | 1734/5613 | 1575/5193 | 525/1730 | chr10 | 113633141 | ||
| chr10:113634169
|
C | T | 4 | a0021c0071a0021c0072a0021c0073others(1): Show | 4 | HG01891.hp2 HG02451.hp2 HG02976.hp1 others(1): Show |
synonymous_variant | LOW | c.1470G>A | p.Ser490Ser | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 15/42 | 1629/5613 | 1470/5193 | 490/1730 | chr10 | 113634169 | ||
| chr10:113640317
|
A | G | 1 | a0018c0076 | 1 | HG03704.hp1 | synonymous_variant | LOW | c.1338T>C | p.Ala446Ala | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/42 | 1497/5613 | 1338/5193 | 446/1730 | chr10 | 113640317 | ||
| chr10:113646932
|
G | A | 1 | a0001c0112 | 1 | HG06807.hp2 | synonymous_variant | LOW | c.984C>T | p.Leu328Leu | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 10/42 | 1143/5613 | 984/5193 | 328/1730 | chr10 | 113646932 | ||
| chr10:113651839
|
C | A | 31 | a0002c0002a0002c0037a0003c0003others(28): Show | 113 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(110): Show |
synonymous_variant | LOW | c.639G>T | p.Leu213Leu | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 7/42 | 798/5613 | 639/5193 | 213/1730 | chr10 | 113651839 | ||
| chr10:113651905
|
C | T | 1 | a0002c0037 | 2 | HG04184.hp2 HG04228.hp1 |
splice_region_variant&synonymous_variant | LOW | c.573G>A | p.Val191Val | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 7/42 | 732/5613 | 573/5193 | 191/1730 | chr10 | 113651905 | ||
| chr10:113653034
|
A | G | 37 | a0002c0002a0002c0037a0003c0003others(34): Show | 122 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(119): Show |
synonymous_variant | LOW | c.471T>C | p.Tyr157Tyr | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 6/42 | 630/5613 | 471/5193 | 157/1730 | chr10 | 113653034 | ||
| chr10:113657530
|
G | A | 104 | a0001c0001a0001c0109a0001c0110others(101): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
synonymous_variant | LOW | c.300C>T | p.His100His | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/42 | 459/5613 | 300/5193 | 100/1730 | chr10 | 113657530 | ||
| chr10:113662715
|
A | G | 41 | a0005c0004a0005c0065a0006c0006others(38): Show | 102 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(99): Show |
synonymous_variant | LOW | c.219T>C | p.Asn73Asn | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/42 | 378/5613 | 219/5193 | 73/1730 | chr10 | 113662715 | ||
| chr10:113663363
|
C | T | 1 | a0028c0048 | 1 | NA19240.hp1 | synonymous_variant | LOW | c.156G>A | p.Pro52Pro | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 2/42 | 315/5613 | 156/5193 | 52/1730 | chr10 | 113663363 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:113588734
|
A | G | 1 | a0008c0007t0009 | 1 | HG01261.hp2 | 3_prime_UTR_variant | MODIFIER | c.*241T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 42/42 | 241 | chr10 | 113588734 | |||||
| chr10:113588787
|
C | T | 1 | a0004c0005t0011 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*188G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 42/42 | 188 | chr10 | 113588787 | |||||
| chr10:113588823
|
C | A | 1 | a0022c0022t0012 | 1 | NA19090.hp1 | 3_prime_UTR_variant | MODIFIER | c.*152G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 42/42 | 152 | chr10 | 113588823 | |||||
| chr10:113588844
|
T | C | 1 | a0001c0001t0013 | 1 | HG00735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*131A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 42/42 | 131 | chr10 | 113588844 | |||||
| chr10:113588883
|
C | T | 1 | a0002c0037t0007 | 2 | HG04184.hp2 HG04228.hp1 |
3_prime_UTR_variant | MODIFIER | c.*92G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 42/42 | 92 | chr10 | 113588883 | |||||
| chr10:113588934
|
A | G | 1 | a0007c0010t0014 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*41T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 42/42 | 41 | chr10 | 113588934 | |||||
| chr10:113588967
|
GA | G | 50 | a0002c0002t0004a0002c0037t0007a0006c0006t0006others(47): Show | 153 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(150): Show |
3_prime_UTR_variant | MODIFIER | c.*7delT | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 42/42 | 7 | chr10 | 113588967 | |||||
| chr10:113663891
|
C | T | 1 | a0045c0036t0008 | 1 | HG01081.hp2 | 5_prime_UTR_variant | MODIFIER | c.-9G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 1/42 | 9 | chr10 | 113663891 | |||||
| chr10:113663936
|
A | C | 18 | a0005c0004t0005a0005c0065t0005a0006c0006t0006others(15): Show | 55 | HG00423.hp1 HG00621.hp1 HG00639.hp2 others(52): Show |
5_prime_UTR_variant | MODIFIER | c.-54T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 1/42 | 54 | chr10 | 113663936 | |||||
| chr10:113663988
|
G | A | 34 | a0002c0002t0004a0002c0037t0007a0003c0003t0003others(31): Show | 121 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(118): Show |
5_prime_UTR_variant | MODIFIER | c.-106C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 1/42 | 106 | chr10 | 113663988 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:113589157
|
G | A | 34 | a0008c0007t0002g0068a0008c0007t0002g0074a0008c0007t0002g0077others(31): Show | 37 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.5089-78C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 41/41 | chr10 | 113589157 | ||||||
| chr10:113589238
|
T | G | 1 | a0039c0096t0002g0130 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.5089-159A>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 41/41 | chr10 | 113589238 | ||||||
| chr10:113589357
|
C | T | 1 | a0003c0003t0003g0340 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.5089-278G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 41/41 | chr10 | 113589357 | ||||||
| chr10:113589484
|
C | A | 2 | a0005c0004t0005g0052a0063c0066t0005g0051 | 2 | HG01943.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.5088+182G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 41/41 | chr10 | 113589484 | ||||||
| chr10:113589528
|
C | T | 1 | a0001c0001t0001g0216 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.5088+138G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 41/41 | chr10 | 113589528 | ||||||
| chr10:113589529
|
G | A | 3 | a0027c0032t0002g0230a0027c0032t0002g0231a0027c0049t0002g0266 | 3 | HG02976.hp1 NA18906.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.5088+137C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 41/41 | chr10 | 113589529 | ||||||
| chr10:113589638
|
AG | A | 382 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(379): Show | 393 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(390): Show |
intron_variant | MODIFIER | c.5088+27delC | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 41/41 | chr10 | 113589638 | ||||||
| chr10:113589922
|
A | C | 1 | a0021c0072t0001g0271 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4957-125T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 40/41 | chr10 | 113589922 | ||||||
| chr10:113589932
|
G | A | 3 | a0033c0028t0002g0232a0033c0028t0002g0233a0033c0028t0002g0234 | 3 | HG02559.hp2 HG02717.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.4957-135C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 40/41 | chr10 | 113589932 | ||||||
| chr10:113589976
|
A | C | 4 | a0014c0062t0005g0055a0021c0072t0001g0271a0062c0063t0005g0054others(1): Show | 4 | HG02258.hp1 HG02451.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.4957-179T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 40/41 | chr10 | 113589976 | ||||||
| chr10:113590010
|
T | G | 1 | a0001c0001t0001g0146 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.4957-213A>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 40/41 | chr10 | 113590010 | ||||||
| chr10:113590049
|
G | T | 2 | a0008c0007t0002g0090a0079c0080t0002g0081 | 2 | HG03654.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.4957-252C>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 40/41 | chr10 | 113590049 | ||||||
| chr10:113590174
|
T | C | 3 | a0014c0020t0005g0027a0014c0020t0005g0037a0014c0060t0005g0021 | 3 | HG01099.hp2 HG01346.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.4957-377A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 40/41 | chr10 | 113590174 | ||||||
| chr10:113590288
|
C | G | 1 | a0062c0063t0005g0054 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.4956+290G>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 40/41 | chr10 | 113590288 | ||||||
| chr10:113590341
|
A | G | 124 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(121): Show | 125 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.4956+237T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 40/41 | chr10 | 113590341 | ||||||
| chr10:113590384
|
G | A | 9 | a0011c0016t0004g0278a0011c0016t0004g0297a0011c0016t0004g0299others(6): Show | 9 | HG02145.hp1 HG02559.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.4956+194C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 40/41 | chr10 | 113590384 | ||||||
| chr10:113590410
|
AGTG | A | 3 | a0027c0032t0002g0230a0027c0032t0002g0231a0027c0049t0002g0266 | 3 | HG02976.hp1 NA18906.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.4956+165_4956+167d others(5): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 40/41 | chr10 | 113590410 | ||||||
| chr10:113590540
|
G | A | 1 | a0059c0058t0002g0239 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.4956+38C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 40/41 | chr10 | 113590540 | ||||||
| chr10:113590950
|
C | T | 1 | a0016c0013t0002g0079 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.4645-61G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 39/41 | chr10 | 113590950 | ||||||
| chr10:113591030
|
T | C | 4 | a0014c0062t0005g0055a0021c0072t0001g0271a0062c0063t0005g0054others(1): Show | 4 | HG02258.hp1 HG02451.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.4645-141A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 39/41 | chr10 | 113591030 | ||||||
| chr10:113591041
|
T | C | 283 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(280): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.4645-152A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 39/41 | chr10 | 113591041 | ||||||
| chr10:113591047
|
G | T | 4 | a0014c0062t0005g0055a0021c0072t0001g0271a0062c0063t0005g0054others(1): Show | 4 | HG02258.hp1 HG02451.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.4645-158C>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 39/41 | chr10 | 113591047 | ||||||
| chr10:113591096
|
T | C | 1 | a0066c0095t0003g0302 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4645-207A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 39/41 | chr10 | 113591096 | ||||||
| chr10:113591117
|
A | T | 2 | a0001c0001t0001g0195a0001c0001t0001g0201 | 2 | HG00140.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.4645-228T>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 39/41 | chr10 | 113591117 | ||||||
| chr10:113591170
|
C | A | 98 | a0002c0002t0004g0300a0002c0002t0004g0303a0002c0002t0004g0304others(95): Show | 98 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.4645-281G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 39/41 | chr10 | 113591170 | ||||||
| chr10:113591317
|
A | T | 1 | a0023c0101t0001g0182 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.4645-428T>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 39/41 | chr10 | 113591317 | ||||||
| chr10:113591346
|
T | C | 122 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(119): Show | 123 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.4645-457A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 39/41 | chr10 | 113591346 | ||||||
| chr10:113591667
|
C | T | 4 | a0022c0022t0001g0258a0022c0022t0001g0259a0022c0022t0001g0262others(1): Show | 4 | HG00597.hp1 NA18612.hp2 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.4644+527G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 39/41 | chr10 | 113591667 | ||||||
| chr10:113591740
|
G | A | 1 | a0014c0020t0005g0037 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.4644+454C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 39/41 | chr10 | 113591740 | ||||||
| chr10:113591810
|
A | G | 6 | a0014c0020t0005g0027a0014c0020t0005g0034a0014c0020t0005g0036others(3): Show | 6 | HG01099.hp2 HG01346.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.4644+384T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 39/41 | chr10 | 113591810 | ||||||
| chr10:113591857
|
T | G | 3 | a0033c0028t0002g0232a0033c0028t0002g0233a0033c0028t0002g0234 | 3 | HG02559.hp2 HG02717.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.4644+337A>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 39/41 | chr10 | 113591857 | ||||||
| chr10:113591933
|
T | G | 1 | a0066c0095t0003g0302 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4644+261A>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 39/41 | chr10 | 113591933 | ||||||
| chr10:113592141
|
A | G | 3 | a0027c0032t0002g0230a0027c0032t0002g0231a0027c0049t0002g0266 | 3 | HG02976.hp1 NA18906.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.4644+53T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 39/41 | chr10 | 113592141 | ||||||
| chr10:113592169
|
G | A | 1 | a0062c0063t0005g0054 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.4644+25C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 39/41 | chr10 | 113592169 | ||||||
| chr10:113592181
|
A | G | 4 | a0014c0062t0005g0055a0021c0072t0001g0271a0062c0063t0005g0054others(1): Show | 4 | HG02258.hp1 HG02451.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.4644+13T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 39/41 | chr10 | 113592181 | ||||||
| chr10:113592398
|
G | T | 1 | a0066c0095t0003g0302 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4537-97C>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113592398 | ||||||
| chr10:113592408
|
C | T | 40 | a0008c0007t0002g0068a0008c0007t0002g0074a0008c0007t0002g0077others(37): Show | 43 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.4537-107G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113592408 | ||||||
| chr10:113592428
|
T | C | 1 | a0059c0058t0002g0239 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.4537-127A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113592428 | ||||||
| chr10:113592499
|
C | T | 3 | a0006c0006t0006g0053a0011c0016t0004g0298a0011c0026t0002g0237 | 3 | HG03453.hp1 HG03486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.4537-198G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113592499 | ||||||
| chr10:113592504
|
C | T | 31 | a0001c0001t0001g0148a0001c0109t0001g0155a0003c0003t0003g0334others(28): Show | 31 | HG01884.hp1 HG02055.hp2 HG02129.hp2 others(28): Show |
intron_variant | MODIFIER | c.4537-203G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113592504 | ||||||
| chr10:113592704
|
T | C | 7 | a0001c0001t0001g0193a0001c0001t0001g0195a0001c0001t0001g0200others(4): Show | 7 | HG00099.hp1 HG00140.hp1 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.4537-403A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113592704 | ||||||
| chr10:113592750
|
C | T | 2 | a0014c0062t0005g0055a0021c0072t0001g0271 | 2 | HG02451.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.4537-449G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113592750 | ||||||
| chr10:113593202
|
G | A | 1 | a0024c0024t0003g0324 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.4537-901C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113593202 | ||||||
| chr10:113593213
|
C | T | 2 | a0005c0004t0005g0052a0063c0066t0005g0051 | 2 | HG01943.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.4537-912G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113593213 | ||||||
| chr10:113593214
|
G | A | 119 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(116): Show | 120 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.4537-913C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113593214 | ||||||
| chr10:113593254
|
G | A | 1 | a0018c0015t0001g0084 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.4537-953C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113593254 | ||||||
| chr10:113593493
|
C | T | 102 | a0002c0002t0004g0300a0002c0002t0004g0303a0002c0002t0004g0304others(99): Show | 102 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.4537-1192G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113593493 | ||||||
| chr10:113593552
|
C | T | 22 | a0001c0001t0001g0148a0001c0109t0001g0155a0003c0003t0003g0334others(19): Show | 22 | HG02129.hp2 HG02165.hp1 HG02523.hp2 others(19): Show |
intron_variant | MODIFIER | c.4537-1251G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113593552 | ||||||
| chr10:113593563
|
G | T | 4 | a0003c0003t0003g0306a0003c0003t0003g0363a0003c0003t0003g0365others(1): Show | 4 | NA18971.hp1 NA19004.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.4537-1262C>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113593563 | ||||||
| chr10:113593773
|
G | A | 80 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(77): Show | 80 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.4537-1472C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113593773 | ||||||
| chr10:113593828
|
G | C | 1 | a0046c0113t0004g0275 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4537-1527C>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113593828 | ||||||
| chr10:113593942
|
G | A | 48 | a0008c0007t0002g0068a0008c0007t0002g0074a0008c0007t0002g0077others(45): Show | 51 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.4537-1641C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113593942 | ||||||
| chr10:113593979
|
G | A | 8 | a0010c0008t0002g0241a0010c0008t0002g0242a0010c0008t0002g0243others(5): Show | 8 | HG00735.hp2 HG01070.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.4536+1644C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113593979 | ||||||
| chr10:113593988
|
C | T | 1 | a0018c0076t0001g0099 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.4536+1635G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113593988 | ||||||
| chr10:113594085
|
C | T | 1 | a0043c0070t0005g0056 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.4536+1538G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113594085 | ||||||
| chr10:113594147
|
A | G | 2 | a0034c0047t0003g0276a0034c0047t0003g0277 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.4536+1476T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113594147 | ||||||
| chr10:113594185
|
C | T | 1 | a0041c0041t0003g0343 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.4536+1438G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113594185 | ||||||
| chr10:113594270
|
T | C | 1 | a0008c0007t0002g0083 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.4536+1353A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113594270 | ||||||
| chr10:113594343
|
C | G | 1 | a0075c0082t0003g0355 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.4536+1280G>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113594343 | ||||||
| chr10:113594485
|
C | T | 1 | a0003c0003t0003g0363 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.4536+1138G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113594485 | ||||||
| chr10:113594500
|
C | T | 1 | a0004c0005t0001g0108 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.4536+1123G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113594500 | ||||||
| chr10:113594813
|
C | T | 25 | a0007c0010t0003g0315a0007c0010t0003g0317a0007c0010t0003g0378others(22): Show | 29 | HG00280.hp1 HG00280.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.4536+810G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113594813 | ||||||
| chr10:113594903
|
G | T | 1 | a0014c0020t0005g0037 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.4536+720C>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113594903 | ||||||
| chr10:113595119
|
C | T | 1 | a0008c0007t0002g0090 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.4536+504G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113595119 | ||||||
| chr10:113595158
|
G | A | 1 | a0057c0097t0001g0105 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.4536+465C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113595158 | ||||||
| chr10:113595187
|
T | C | 1 | a0079c0080t0002g0081 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.4536+436A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113595187 | ||||||
| chr10:113595284
|
G | C | 1 | a0004c0005t0001g0111 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.4536+339C>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113595284 | ||||||
| chr10:113595365
|
T | A | 1 | a0079c0080t0002g0081 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.4536+258A>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113595365 | ||||||
| chr10:113595412
|
G | GC | 277 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(274): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.4536+210dupG | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113595412 | ||||||
| chr10:113595436
|
A | G | 41 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0154others(38): Show | 41 | HG01884.hp1 HG01981.hp2 HG02004.hp2 others(38): Show |
intron_variant | MODIFIER | c.4536+187T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113595436 | ||||||
| chr10:113595544
|
T | A | 1 | a0062c0063t0005g0054 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.4536+79A>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113595544 | ||||||
| chr10:113595566
|
G | T | 3 | a0027c0032t0002g0230a0027c0032t0002g0231a0027c0049t0002g0266 | 3 | HG02976.hp1 NA18906.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.4536+57C>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113595566 | ||||||
| chr10:113595569
|
A | G | 18 | a0010c0008t0002g0240a0010c0008t0002g0241a0010c0008t0002g0242others(15): Show | 18 | HG00642.hp2 HG00735.hp2 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.4536+54T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113595569 | ||||||
| chr10:113595901
|
C | A | 1 | a0026c0034t0002g0238 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4432-174G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 37/41 | chr10 | 113595901 | ||||||
| chr10:113595991
|
A | G | 1 | a0007c0010t0003g0317 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.4432-264T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 37/41 | chr10 | 113595991 | ||||||
| chr10:113596148
|
T | C | 1 | a0004c0021t0001g0124 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.4432-421A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 37/41 | chr10 | 113596148 | ||||||
| chr10:113596165
|
C | A | 1 | a0007c0084t0003g0345 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.4432-438G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 37/41 | chr10 | 113596165 | ||||||
| chr10:113596407
|
C | T | 5 | a0001c0001t0001g0152a0001c0001t0001g0207a0001c0001t0001g0208others(2): Show | 5 | HG01928.hp2 HG01943.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.4431+679G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 37/41 | chr10 | 113596407 | ||||||
| chr10:113596595
|
T | C | 2 | a0011c0016t0004g0278a0011c0016t0004g0297 | 2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.4431+491A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 37/41 | chr10 | 113596595 | ||||||
| chr10:113596705
|
C | G | 7 | a0011c0042t0004g0341a0011c0042t0004g0342a0014c0062t0005g0055others(4): Show | 7 | HG01891.hp1 HG02451.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.4431+381G>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 37/41 | chr10 | 113596705 | ||||||
| chr10:113596829
|
T | A | 1 | a0004c0005t0001g0128 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.4431+257A>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 37/41 | chr10 | 113596829 | ||||||
| chr10:113596917
|
A | C | 8 | a0002c0002t0004g0335a0002c0002t0004g0336a0016c0013t0002g0079others(5): Show | 8 | HG01891.hp2 HG02486.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.4431+169T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 37/41 | chr10 | 113596917 | ||||||
| chr10:113596930
|
T | C | 8 | a0011c0042t0004g0341a0011c0042t0004g0342a0014c0062t0005g0055others(5): Show | 8 | HG01891.hp1 HG02258.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.4431+156A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 37/41 | chr10 | 113596930 | ||||||
| chr10:113596988
|
T | G | 1 | a0021c0114t0004g0273 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.4431+98A>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 37/41 | chr10 | 113596988 | ||||||
| chr10:113597287
|
T | C | 1 | a0002c0002t0004g0344 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4333-103A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 36/41 | chr10 | 113597287 | ||||||
| chr10:113597319
|
G | A | 115 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(112): Show | 115 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.4333-135C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 36/41 | chr10 | 113597319 | ||||||
| chr10:113597367
|
T | C | 1 | a0018c0015t0001g0070 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.4333-183A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 36/41 | chr10 | 113597367 | ||||||
| chr10:113597372
|
CA | C | 115 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(112): Show | 115 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.4333-189delT | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 36/41 | chr10 | 113597372 | ||||||
| chr10:113597420
|
C | T | 115 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(112): Show | 115 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.4333-236G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 36/41 | chr10 | 113597420 | ||||||
| chr10:113597563
|
C | A | 1 | a0002c0002t0004g0328 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.4333-379G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 36/41 | chr10 | 113597563 | ||||||
| chr10:113597705
|
A | G | 1 | a0041c0041t0003g0343 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.4332+264T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 36/41 | chr10 | 113597705 | ||||||
| chr10:113597732
|
A | G | 8 | a0011c0042t0004g0341a0011c0042t0004g0342a0014c0062t0005g0055others(5): Show | 8 | HG01891.hp1 HG02258.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.4332+237T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 36/41 | chr10 | 113597732 | ||||||
| chr10:113597815
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.4332+154C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 36/41 | chr10 | 113597815 | ||||||
| chr10:113597928
|
G | T | 7 | a0001c0001t0001g0150a0004c0021t0001g0124a0004c0021t0001g0132others(4): Show | 7 | HG02040.hp2 HG02056.hp1 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.4332+41C>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 36/41 | chr10 | 113597928 | ||||||
| chr10:113598217
|
T | C | 1 | a0026c0034t0002g0238 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4228-144A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113598217 | ||||||
| chr10:113598325
|
G | A | 1 | a0021c0114t0004g0273 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.4228-252C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113598325 | ||||||
| chr10:113598338
|
T | C | 3 | a0011c0016t0004g0278a0011c0016t0004g0297a0011c0016t0004g0299 | 3 | HG02145.hp1 HG03195.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.4228-265A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113598338 | ||||||
| chr10:113598483
|
CT | C | 278 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(275): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.4228-411delA | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113598483 | ||||||
| chr10:113598725
|
C | T | 1 | a0079c0080t0002g0081 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.4228-652G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113598725 | ||||||
| chr10:113598769
|
C | T | 3 | a0010c0008t0002g0241a0037c0045t0002g0162a0056c0099t0002g0110 | 3 | HG00735.hp2 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.4228-696G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113598769 | ||||||
| chr10:113598817
|
T | C | 2 | a0044c0039t0004g0319a0044c0039t0004g0331 | 2 | HG00609.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.4228-744A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113598817 | ||||||
| chr10:113599036
|
C | T | 1 | a0046c0113t0004g0275 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4228-963G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113599036 | ||||||
| chr10:113599061
|
C | G | 63 | a0008c0007t0002g0068a0008c0007t0002g0074a0008c0007t0002g0077others(60): Show | 66 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.4228-988G>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113599061 | ||||||
| chr10:113599138
|
G | A | 1 | a0007c0010t0003g0315 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.4228-1065C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113599138 | ||||||
| chr10:113599163
|
C | T | 1 | a0004c0005t0011g0116 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.4228-1090G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113599163 | ||||||
| chr10:113599376
|
T | G | 2 | a0021c0073t0001g0270a0059c0058t0002g0239 | 2 | HG01109.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.4228-1303A>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113599376 | ||||||
| chr10:113599778
|
CGAA | C | 3 | a0028c0033t0001g0059a0028c0033t0001g0060a0028c0048t0001g0058 | 3 | HG02572.hp2 HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.4228-1708_4228-170 others(7): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113599778 | ||||||
| chr10:113599806
|
C | T | 1 | a0013c0019t0002g0109 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.4228-1733G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113599806 | ||||||
| chr10:113599807
|
CT | C | 35 | a0001c0001t0001g0148a0001c0109t0001g0155a0003c0003t0003g0334others(32): Show | 35 | HG01884.hp1 HG02055.hp2 HG02129.hp2 others(32): Show |
intron_variant | MODIFIER | c.4228-1735delA | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113599807 | ||||||
| chr10:113599858
|
T | C | 1 | a0069c0056t0001g0245 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.4228-1785A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113599858 | ||||||
| chr10:113599898
|
G | C | 1 | a0014c0020t0005g0042 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.4228-1825C>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113599898 | ||||||
| chr10:113600155
|
T | TTC | 40 | a0001c0001t0001g0138a0001c0001t0001g0144a0001c0001t0001g0170others(37): Show | 41 | HG00597.hp1 HG01081.hp2 HG01099.hp2 others(38): Show |
intron_variant | MODIFIER | c.4228-2084_4228-208 others(6): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113600155 | ||||||
| chr10:113600155
|
T | TTCTC | 76 | a0002c0002t0004g0300a0002c0002t0004g0303a0002c0002t0004g0304others(73): Show | 76 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.4228-2086_4228-208 others(8): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113600155 | ||||||
| chr10:113600155
|
T | TTCTCTC | 14 | a0002c0002t0004g0337a0006c0006t0006g0018a0007c0010t0003g0312others(11): Show | 14 | HG01069.hp2 HG01071.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.4228-2088_4228-208 others(10): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113600155 | ||||||
| chr10:113600155
|
T | TTCTCTCT others(1): Show |
3 | a0011c0042t0004g0341a0011c0042t0004g0342a0021c0073t0001g0270 | 3 | HG02895.hp2 HG02897.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.4228-2090_4228-208 others(12): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113600155 | ||||||
| chr10:113600155
|
T | TTCTCTCT others(3): Show |
14 | a0001c0001t0001g0208a0007c0010t0003g0315a0009c0009t0001g0002others(11): Show | 16 | HG00642.hp1 HG01069.hp1 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.4228-2092_4228-208 others(14): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113600155 | ||||||
| chr10:113600155
|
T | TTCTCTCT others(5): Show |
8 | a0007c0010t0003g0317a0007c0010t0003g0347a0010c0008t0002g0242others(5): Show | 8 | HG00280.hp1 HG00738.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.4228-2094_4228-208 others(16): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113600155 | ||||||
| chr10:113600155
|
T | TTCTCTCT others(7): Show |
13 | a0007c0010t0003g0378a0007c0084t0003g0345a0010c0008t0002g0247others(10): Show | 14 | HG00280.hp2 HG00738.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.4228-2096_4228-208 others(18): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113600155 | ||||||
| chr10:113600155
|
T | TTCTCTCT others(9): Show |
5 | a0010c0008t0002g0240a0010c0008t0002g0256a0012c0011t0003g0007others(2): Show | 6 | HG00642.hp2 HG01192.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.4228-2098_4228-208 others(20): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113600155 | ||||||
| chr10:113600155
|
T | TTCTCTCT others(11): Show |
2 | a0061c0061t0005g0038a0075c0082t0003g0355 | 2 | HG01978.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.4228-2100_4228-208 others(22): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113600155 | ||||||
| chr10:113600155
|
T | TTCTCTCT others(13): Show |
4 | a0007c0010t0003g0348a0007c0010t0003g0352a0009c0009t0001g0091others(1): Show | 4 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.4228-2102_4228-208 others(24): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113600155 | ||||||
| chr10:113600155
|
T | TTCTCTCT others(17): Show |
1 | a0007c0010t0003g0354 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.4228-2106_4228-208 others(28): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113600155 | ||||||
| chr10:113600155
|
T | TTCTCTCT others(19): Show |
1 | a0007c0010t0014g0351 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.4228-2108_4228-208 others(30): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113600155 | ||||||
| chr10:113600155
|
TTCTC | T | 8 | a0004c0005t0001g0104a0004c0005t0001g0106a0004c0005t0001g0166others(5): Show | 8 | HG02572.hp1 HG02615.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.4228-2086_4228-208 others(8): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113600155 | ||||||
| chr10:113600155
|
TTCTCTC | T | 111 | a0001c0001t0001g0140a0001c0001t0001g0148a0001c0001t0001g0153others(108): Show | 117 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.4228-2088_4228-208 others(10): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113600155 | ||||||
| chr10:113600155
|
TTCTCTCT others(3): Show |
T | 1 | a0049c0105t0001g0215 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.4228-2092_4228-208 others(14): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113600155 | ||||||
| chr10:113600159
|
C | CTCTCTCT others(3): Show |
1 | a0010c0008t0002g0241 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.4228-2087_4228-208 others(14): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113600159 | ||||||
| chr10:113600338
|
A | AT | 115 | a0001c0001t0001g0140a0001c0001t0001g0148a0001c0001t0001g0153others(112): Show | 121 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.4228-2266dupA | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113600338 | ||||||
| chr10:113600378
|
C | G | 1 | a0066c0095t0003g0302 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4228-2305G>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113600378 | ||||||
| chr10:113600380
|
A | T | 8 | a0011c0042t0004g0341a0011c0042t0004g0342a0014c0062t0005g0055others(5): Show | 8 | HG01109.hp2 HG01891.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.4228-2307T>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113600380 | ||||||
| chr10:113600607
|
G | C | 1 | a0073c0090t0004g0385 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.4228-2534C>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113600607 | ||||||
| chr10:113600784
|
C | T | 1 | a0004c0005t0001g0106 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.4228-2711G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113600784 | ||||||
| chr10:113600928
|
A | G | 220 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(217): Show | 226 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.4228-2855T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113600928 | ||||||
| chr10:113601037
|
A | G | 220 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(217): Show | 226 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.4228-2964T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113601037 | ||||||
| chr10:113601196
|
C | T | 1 | a0027c0032t0002g0230 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.4228-3123G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113601196 | ||||||
| chr10:113601266
|
T | C | 1 | a0018c0015t0001g0070 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.4228-3193A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113601266 | ||||||
| chr10:113601301
|
A | G | 220 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(217): Show | 226 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.4228-3228T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113601301 | ||||||
| chr10:113601302
|
G | C | 3 | a0028c0033t0001g0059a0028c0033t0001g0060a0028c0048t0001g0058 | 3 | HG02572.hp2 HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.4228-3229C>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113601302 | ||||||
| chr10:113601558
|
G | A | 324 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(321): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.4227+3051C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113601558 | ||||||
| chr10:113601606
|
G | A | 1 | a0011c0016t0004g0294 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.4227+3003C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113601606 | ||||||
| chr10:113601846
|
TG | T | 81 | a0001c0001t0001g0140a0001c0001t0001g0148a0001c0001t0001g0153others(78): Show | 84 | HG00438.hp1 HG00639.hp2 HG00733.hp2 others(81): Show |
intron_variant | MODIFIER | c.4227+2762delC | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113601846 | ||||||
| chr10:113601935
|
A | C | 1 | a0006c0006t0006g0029 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.4227+2674T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113601935 | ||||||
| chr10:113602006
|
C | T | 2 | a0005c0004t0005g0043a0065c0059t0005g0044 | 2 | HG00733.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.4227+2603G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113602006 | ||||||
| chr10:113602042
|
C | T | 1 | a0062c0063t0005g0054 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.4227+2567G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113602042 | ||||||
| chr10:113602092
|
A | G | 324 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(321): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.4227+2517T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113602092 | ||||||
| chr10:113602331
|
G | A | 1 | a0002c0002t0004g0344 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4227+2278C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113602331 | ||||||
| chr10:113602427
|
G | A | 2 | a0034c0047t0003g0276a0034c0047t0003g0277 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.4227+2182C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113602427 | ||||||
| chr10:113602637
|
A | T | 1 | a0008c0007t0009g0094 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.4227+1972T>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113602637 | ||||||
| chr10:113602831
|
T | C | 1 | a0066c0095t0003g0302 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4227+1778A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113602831 | ||||||
| chr10:113603037
|
C | T | 1 | a0019c0018t0001g0112 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4227+1572G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113603037 | ||||||
| chr10:113603319
|
A | G | 85 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(82): Show | 85 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.4227+1290T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113603319 | ||||||
| chr10:113603369
|
T | G | 1 | a0021c0072t0001g0271 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4227+1240A>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113603369 | ||||||
| chr10:113603432
|
C | G | 1 | a0041c0041t0003g0343 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.4227+1177G>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113603432 | ||||||
| chr10:113603432
|
C | T | 3 | a0033c0028t0002g0232a0033c0028t0002g0233a0033c0028t0002g0234 | 3 | HG02559.hp2 HG02717.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.4227+1177G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113603432 | ||||||
| chr10:113603504
|
C | T | 14 | a0011c0016t0004g0278a0011c0016t0004g0297a0011c0016t0004g0299others(11): Show | 14 | HG01109.hp2 HG01891.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.4227+1105G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113603504 | ||||||
| chr10:113603585
|
G | A | 83 | a0002c0002t0004g0300a0002c0002t0004g0303a0002c0002t0004g0304others(80): Show | 83 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.4227+1024C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113603585 | ||||||
| chr10:113603620
|
G | A | 200 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(197): Show | 206 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(203): Show |
intron_variant | MODIFIER | c.4227+989C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113603620 | ||||||
| chr10:113603785
|
G | C | 1 | a0001c0109t0001g0155 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.4227+824C>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113603785 | ||||||
| chr10:113603809
|
C | T | 14 | a0011c0016t0004g0278a0011c0016t0004g0297a0011c0016t0004g0299others(11): Show | 14 | HG01109.hp2 HG01891.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.4227+800G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113603809 | ||||||
| chr10:113603879
|
C | T | 386 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(383): Show | 397 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(394): Show |
intron_variant | MODIFIER | c.4227+730G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113603879 | ||||||
| chr10:113603890
|
A | G | 219 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(216): Show | 225 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(222): Show |
intron_variant | MODIFIER | c.4227+719T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113603890 | ||||||
| chr10:113603905
|
C | T | 99 | a0001c0001t0001g0140a0001c0001t0001g0148a0001c0001t0001g0153others(96): Show | 103 | HG00438.hp1 HG00597.hp1 HG00639.hp2 others(100): Show |
intron_variant | MODIFIER | c.4227+704G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113603905 | ||||||
| chr10:113604122
|
C | T | 219 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(216): Show | 225 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(222): Show |
intron_variant | MODIFIER | c.4227+487G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113604122 | ||||||
| chr10:113604177
|
C | G | 1 | a0046c0113t0004g0275 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4227+432G>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113604177 | ||||||
| chr10:113604179
|
C | T | 1 | a0004c0005t0011g0116 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.4227+430G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113604179 | ||||||
| chr10:113604358
|
G | A | 2 | a0034c0047t0003g0276a0034c0047t0003g0277 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.4227+251C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113604358 | ||||||
| chr10:113604549
|
C | T | 1 | a0004c0021t0001g0132 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.4227+60G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113604549 | ||||||
| chr10:113604959
|
G | A | 1 | a0015c0012t0004g0286 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.3916-39C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 34/41 | chr10 | 113604959 | ||||||
| chr10:113604993
|
C | T | 1 | a0014c0020t0005g0037 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.3916-73G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 34/41 | chr10 | 113604993 | ||||||
| chr10:113605039
|
G | A | 2 | a0002c0037t0007g0356a0002c0037t0007g0357 | 2 | HG04184.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.3916-119C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 34/41 | chr10 | 113605039 | ||||||
| chr10:113605381
|
C | T | 1 | a0060c0067t0005g0046 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3915+381G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 34/41 | chr10 | 113605381 | ||||||
| chr10:113605577
|
T | G | 1 | a0002c0002t0004g0344 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3915+185A>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 34/41 | chr10 | 113605577 | ||||||
| chr10:113605905
|
A | C | 3 | a0005c0004t0005g0028a0005c0004t0005g0040a0005c0004t0005g0049 | 3 | NA18952.hp1 NA18974.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.3808-36T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 33/41 | chr10 | 113605905 | ||||||
| chr10:113605927
|
G | C | 1 | a0007c0083t0003g0346 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.3808-58C>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 33/41 | chr10 | 113605927 | ||||||
| chr10:113605951
|
A | G | 1 | a0013c0019t0002g0176 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.3808-82T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 33/41 | chr10 | 113605951 | ||||||
| chr10:113605968
|
T | C | 5 | a0002c0002t0004g0370a0011c0026t0006g0015a0011c0026t0006g0026others(2): Show | 5 | HG02129.hp1 NA18983.hp2 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.3808-99A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 33/41 | chr10 | 113605968 | ||||||
| chr10:113606755
|
A | C | 1 | a0001c0001t0001g0193 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.3703-473T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113606755 | ||||||
| chr10:113606850
|
C | G | 221 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(218): Show | 227 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(224): Show |
intron_variant | MODIFIER | c.3703-568G>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113606850 | ||||||
| chr10:113606894
|
C | T | 1 | a0046c0113t0004g0275 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3703-612G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113606894 | ||||||
| chr10:113606928
|
C | T | 6 | a0005c0004t0005g0052a0033c0028t0002g0232a0033c0028t0002g0233others(3): Show | 6 | HG01943.hp1 HG02135.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.3703-646G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113606928 | ||||||
| chr10:113607134
|
G | A | 3 | a0027c0032t0002g0230a0027c0032t0002g0231a0027c0049t0002g0266 | 3 | HG02976.hp1 NA18906.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.3703-852C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607134 | ||||||
| chr10:113607199
|
T | TCAAA | 67 | a0001c0001t0001g0140a0001c0001t0001g0148a0001c0001t0001g0153others(64): Show | 70 | HG00438.hp1 HG00639.hp2 HG00733.hp2 others(67): Show |
intron_variant | MODIFIER | c.3703-921_3703-918d others(6): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607199 | ||||||
| chr10:113607199
|
TCAAACAA others(1): Show |
T | 23 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(20): Show | 23 | HG00438.hp2 HG01981.hp2 HG02004.hp2 others(20): Show |
intron_variant | MODIFIER | c.3703-925_3703-918d others(10): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607199 | ||||||
| chr10:113607201
|
A | T | 1 | a0016c0013t0002g0072 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3703-919T>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607201 | ||||||
| chr10:113607243
|
C | CA | 44 | a0008c0007t0002g0068a0008c0007t0002g0074a0008c0007t0002g0077others(41): Show | 47 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.3703-962dupT | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607243 | ||||||
| chr10:113607373
|
G | A | 1 | a0021c0071t0002g0269 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3702+1041C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607373 | ||||||
| chr10:113607388
|
C | T | 82 | a0001c0001t0001g0140a0001c0001t0001g0148a0001c0001t0001g0153others(79): Show | 85 | HG00438.hp1 HG00639.hp2 HG00733.hp2 others(82): Show |
intron_variant | MODIFIER | c.3702+1026G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607388 | ||||||
| chr10:113607396
|
C | T | 2 | a0014c0062t0005g0055a0021c0072t0001g0271 | 2 | HG02451.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.3702+1018G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607396 | ||||||
| chr10:113607399
|
C | CA | 15 | a0007c0010t0003g0315a0007c0010t0003g0317a0007c0010t0003g0349others(12): Show | 16 | HG00280.hp1 HG00280.hp2 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.3702+1014dupT | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607399 | ||||||
| chr10:113607399
|
C | CAA | 6 | a0007c0010t0003g0348a0007c0083t0003g0346a0007c0084t0003g0345others(3): Show | 8 | HG00642.hp1 HG01106.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.3702+1013_3702+101 others(6): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607399 | ||||||
| chr10:113607399
|
C | CAAAAAAA others(3): Show |
5 | a0009c0079t0001g0069a0014c0020t0005g0036a0023c0030t0001g0175others(2): Show | 5 | HG02886.hp1 HG03239.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.3702+1005_3702+101 others(14): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607399 | ||||||
| chr10:113607399
|
C | CAAAAAAA others(4): Show |
2 | a0014c0020t0005g0037a0014c0020t0005g0042 | 2 | HG01099.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.3702+1004_3702+101 others(15): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607399 | ||||||
| chr10:113607399
|
C | CAAAAAAA others(6): Show |
2 | a0014c0020t0005g0027a0043c0070t0005g0056 | 2 | HG01346.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.3702+1002_3702+101 others(17): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607399 | ||||||
| chr10:113607399
|
C | CAAAAAAA others(8): Show |
1 | a0080c0074t0001g0268 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3702+1000_3702+101 others(19): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607399 | ||||||
| chr10:113607399
|
CAAAAAAA | C | 13 | a0006c0006t0006g0031a0007c0010t0003g0312a0010c0008t0002g0240others(10): Show | 13 | HG00642.hp2 HG00738.hp2 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.3702+1008_3702+101 others(11): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607399 | ||||||
| chr10:113607399
|
CAAAAAAA others(1): Show |
C | 15 | a0002c0002t0004g0360a0006c0006t0006g0011a0006c0006t0006g0013others(12): Show | 15 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(12): Show |
intron_variant | MODIFIER | c.3702+1007_3702+101 others(12): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607399 | ||||||
| chr10:113607399
|
CAAAAAAA others(2): Show |
C | 61 | a0002c0002t0004g0300a0002c0002t0004g0303a0002c0002t0004g0307others(58): Show | 61 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.3702+1006_3702+101 others(13): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607399 | ||||||
| chr10:113607399
|
CAAAAAAA others(3): Show |
C | 7 | a0002c0002t0004g0304a0002c0002t0004g0328a0002c0002t0004g0372others(4): Show | 7 | HG00140.hp2 HG02896.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.3702+1005_3702+101 others(14): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607399 | ||||||
| chr10:113607399
|
CAAAAAAA others(4): Show |
C | 1 | a0003c0003t0003g0334 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.3702+1004_3702+101 others(15): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607399 | ||||||
| chr10:113607399
|
CAAAAAAA others(5): Show |
C | 23 | a0003c0003t0003g0386a0004c0005t0001g0104a0004c0005t0001g0115others(20): Show | 23 | HG00558.hp2 HG00733.hp2 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.3702+1003_3702+101 others(16): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607399 | ||||||
| chr10:113607399
|
CAAAAAAA others(6): Show |
C | 92 | a0001c0001t0001g0140a0001c0001t0001g0148a0001c0001t0001g0153others(89): Show | 98 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.3702+1002_3702+101 others(17): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607399 | ||||||
| chr10:113607399
|
CAAAAAAA others(7): Show |
C | 6 | a0003c0003t0003g0325a0008c0007t0002g0089a0011c0016t0004g0299others(3): Show | 6 | HG01123.hp2 HG01943.hp1 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.3702+1001_3702+101 others(18): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607399 | ||||||
| chr10:113607399
|
CAAAAAAA others(8): Show |
C | 14 | a0011c0016t0004g0278a0011c0016t0004g0297a0011c0042t0004g0342others(11): Show | 14 | HG01109.hp2 HG01891.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.3702+1000_3702+101 others(19): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607399 | ||||||
| chr10:113607399
|
CAAAAAAA others(9): Show |
C | 5 | a0004c0021t0001g0124a0011c0042t0004g0341a0024c0024t0003g0324others(2): Show | 5 | HG02040.hp2 HG02083.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.3702+999_3702+1014 others(19): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607399 | ||||||
| chr10:113607399
|
CAAAAAAA others(10): Show |
C | 16 | a0001c0001t0001g0144a0001c0001t0001g0150a0001c0001t0001g0170others(13): Show | 16 | HG00639.hp1 HG02027.hp1 HG02056.hp1 others(13): Show |
intron_variant | MODIFIER | c.3702+998_3702+1014 others(20): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607399 | ||||||
| chr10:113607399
|
CAAAAAAA others(11): Show |
C | 62 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(59): Show | 62 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.3702+997_3702+1014 others(21): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607399 | ||||||
| chr10:113607399
|
CAAAAAAA others(12): Show |
C | 4 | a0010c0008t0002g0242a0045c0036t0002g0267a0045c0036t0008g0057others(1): Show | 4 | HG01081.hp2 HG02258.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.3702+996_3702+1014 others(22): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607399 | ||||||
| chr10:113607399
|
CAAAAAAA others(17): Show |
C | 3 | a0028c0033t0001g0059a0028c0033t0001g0060a0028c0048t0001g0058 | 3 | HG02572.hp2 HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.3702+991_3702+1014 others(27): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607399 | ||||||
| chr10:113607414
|
A | C | 2 | a0011c0016t0004g0299a0021c0073t0001g0270 | 2 | HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3702+1000T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607414 | ||||||
| chr10:113607415
|
A | C | 12 | a0011c0016t0004g0278a0011c0016t0004g0297a0011c0042t0004g0342others(9): Show | 12 | HG01109.hp2 HG01891.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.3702+999T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607415 | ||||||
| chr10:113607416
|
A | C | 1 | a0011c0042t0004g0341 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.3702+998T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607416 | ||||||
| chr10:113607419
|
AAAAAAAA others(11): Show |
A | 1 | a0053c0069t0006g0048 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.3702+977_3702+994d others(20): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607419 | ||||||
| chr10:113607424
|
A | C | 3 | a0028c0033t0001g0059a0028c0033t0001g0060a0028c0048t0001g0058 | 3 | HG02572.hp2 HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.3702+990T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607424 | ||||||
| chr10:113607432
|
A | G | 2 | a0027c0032t0002g0230a0027c0032t0002g0231 | 2 | NA18906.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.3702+982T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607432 | ||||||
| chr10:113607433
|
A | G | 8 | a0016c0013t0002g0062a0016c0013t0002g0079a0016c0013t0002g0098others(5): Show | 8 | HG02451.hp1 HG02486.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.3702+981T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607433 | ||||||
| chr10:113607437
|
G | A | 1 | a0016c0013t0002g0062 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.3702+977C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607437 | ||||||
| chr10:113607438
|
A | G | 1 | a0016c0013t0002g0062 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.3702+976T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607438 | ||||||
| chr10:113607624
|
A | T | 221 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(218): Show | 227 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(224): Show |
intron_variant | MODIFIER | c.3702+790T>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607624 | ||||||
| chr10:113608054
|
T | A | 1 | a0053c0069t0006g0048 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.3702+360A>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113608054 | ||||||
| chr10:113608213
|
A | C | 1 | a0002c0002t0004g0368 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.3702+201T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113608213 | ||||||
| chr10:113608304
|
A | C | 1 | a0024c0024t0003g0321 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.3702+110T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113608304 | ||||||
| chr10:113608542
|
C | T | 2 | a0001c0001t0001g0152a0001c0001t0001g0223 | 2 | NA19087.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.3604-30G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 31/41 | chr10 | 113608542 | ||||||
| chr10:113608575
|
C | T | 1 | a0001c0110t0001g0202 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.3604-63G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 31/41 | chr10 | 113608575 | ||||||
| chr10:113608761
|
G | A | 1 | a0046c0113t0004g0275 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3604-249C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 31/41 | chr10 | 113608761 | ||||||
| chr10:113608987
|
T | C | 1 | a0004c0021t0001g0124 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.3604-475A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 31/41 | chr10 | 113608987 | ||||||
| chr10:113609043
|
C | T | 3 | a0027c0032t0002g0230a0027c0032t0002g0231a0027c0049t0002g0266 | 3 | HG02976.hp1 NA18906.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.3604-531G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 31/41 | chr10 | 113609043 | ||||||
| chr10:113609114
|
C | T | 1 | a0026c0050t0002g0229 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3604-602G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 31/41 | chr10 | 113609114 | ||||||
| chr10:113609328
|
T | A | 3 | a0027c0032t0002g0230a0027c0032t0002g0231a0027c0049t0002g0266 | 3 | HG02976.hp1 NA18906.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.3604-816A>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 31/41 | chr10 | 113609328 | ||||||
| chr10:113609335
|
G | C | 16 | a0010c0008t0002g0240a0010c0008t0002g0241a0010c0008t0002g0242others(13): Show | 16 | HG00642.hp2 HG00735.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.3604-823C>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 31/41 | chr10 | 113609335 | ||||||
| chr10:113609479
|
A | G | 35 | a0008c0007t0002g0068a0008c0007t0002g0074a0008c0007t0002g0077others(32): Show | 38 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.3604-967T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 31/41 | chr10 | 113609479 | ||||||
| chr10:113609544
|
T | C | 2 | a0027c0032t0002g0230a0027c0032t0002g0231 | 2 | NA18906.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.3603+915A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 31/41 | chr10 | 113609544 | ||||||
| chr10:113609966
|
GA | G | 33 | a0002c0002t0004g0307a0008c0007t0002g0068a0008c0007t0002g0074others(30): Show | 36 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.3603+492delT | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 31/41 | chr10 | 113609966 | ||||||
| chr10:113610042
|
C | T | 1 | a0013c0019t0002g0109 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.3603+417G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 31/41 | chr10 | 113610042 | ||||||
| chr10:113610069
|
G | A | 1 | a0016c0077t0002g0064 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3603+390C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 31/41 | chr10 | 113610069 | ||||||
| chr10:113610162
|
C | A | 69 | a0001c0001t0001g0140a0001c0001t0001g0148a0001c0001t0001g0153others(66): Show | 72 | HG00438.hp1 HG00639.hp2 HG00733.hp2 others(69): Show |
intron_variant | MODIFIER | c.3603+297G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 31/41 | chr10 | 113610162 | ||||||
| chr10:113610176
|
C | A | 1 | a0008c0007t0009g0094 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.3603+283G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 31/41 | chr10 | 113610176 | ||||||
| chr10:113610252
|
AG | A | 32 | a0008c0007t0002g0068a0008c0007t0002g0074a0008c0007t0002g0077others(29): Show | 35 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.3603+206delC | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 31/41 | chr10 | 113610252 | ||||||
| chr10:113610265
|
G | A | 2 | a0003c0003t0003g0381a0007c0010t0003g0312 | 2 | HG02896.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.3603+194C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 31/41 | chr10 | 113610265 | ||||||
| chr10:113610282
|
G | A | 1 | a0019c0018t0001g0165 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3603+177C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 31/41 | chr10 | 113610282 | ||||||
| chr10:113610354
|
T | TA | 34 | a0002c0002t0004g0307a0008c0007t0002g0068a0008c0007t0002g0074others(31): Show | 37 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.3603+104dupT | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 31/41 | chr10 | 113610354 | ||||||
| chr10:113610354
|
TA | T | 28 | a0001c0001t0001g0135a0001c0001t0001g0191a0001c0001t0001g0193others(25): Show | 28 | HG00099.hp1 HG00140.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.3603+104delT | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 31/41 | chr10 | 113610354 | ||||||
| chr10:113610825
|
G | A | 1 | a0003c0003t0003g0381 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.3499-262C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 30/41 | chr10 | 113610825 | ||||||
| chr10:113611026
|
G | A | 1 | a0055c0100t0001g0164 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3499-463C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 30/41 | chr10 | 113611026 | ||||||
| chr10:113611216
|
G | A | 1 | a0019c0018t0001g0112 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3499-653C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 30/41 | chr10 | 113611216 | ||||||
| chr10:113611231
|
C | G | 7 | a0001c0001t0001g0193a0001c0001t0001g0195a0001c0001t0001g0200others(4): Show | 7 | HG00099.hp1 HG00140.hp1 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.3499-668G>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 30/41 | chr10 | 113611231 | ||||||
| chr10:113611260
|
G | A | 4 | a0003c0003t0003g0340a0018c0015t0001g0075a0018c0015t0001g0100others(1): Show | 4 | HG02055.hp2 HG02717.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.3499-697C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 30/41 | chr10 | 113611260 | ||||||
| chr10:113611355
|
T | C | 2 | a0037c0045t0002g0162a0056c0099t0002g0110 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.3499-792A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 30/41 | chr10 | 113611355 | ||||||
| chr10:113611378
|
G | A | 1 | a0061c0061t0005g0038 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.3499-815C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 30/41 | chr10 | 113611378 | ||||||
| chr10:113611521
|
G | T | 1 | a0027c0049t0002g0266 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3498+713C>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 30/41 | chr10 | 113611521 | ||||||
| chr10:113611676
|
G | A | 1 | a0001c0001t0001g0178 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.3498+558C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 30/41 | chr10 | 113611676 | ||||||
| chr10:113611736
|
G | A | 1 | a0004c0005t0001g0108 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.3498+498C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 30/41 | chr10 | 113611736 | ||||||
| chr10:113611799
|
A | T | 1 | a0016c0077t0002g0064 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3498+435T>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 30/41 | chr10 | 113611799 | ||||||
| chr10:113612062
|
G | A | 2 | a0034c0047t0003g0276a0034c0047t0003g0277 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.3498+172C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 30/41 | chr10 | 113612062 | ||||||
| chr10:113612096
|
GA | G | 3 | a0027c0032t0002g0230a0027c0032t0002g0231a0027c0049t0002g0266 | 3 | HG02976.hp1 NA18906.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.3498+137delT | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 30/41 | chr10 | 113612096 | ||||||
| chr10:113612114
|
G | T | 85 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(82): Show | 85 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.3498+120C>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 30/41 | chr10 | 113612114 | ||||||
| chr10:113612651
|
T | C | 1 | a0003c0003t0003g0340 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3301-220A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 29/41 | chr10 | 113612651 | ||||||
| chr10:113612697
|
A | G | 1 | a0072c0088t0003g0311 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.3301-266T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 29/41 | chr10 | 113612697 | ||||||
| chr10:113612700
|
G | A | 1 | a0007c0010t0003g0315 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.3301-269C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 29/41 | chr10 | 113612700 | ||||||
| chr10:113612776
|
C | T | 1 | a0013c0019t0002g0224 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.3301-345G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 29/41 | chr10 | 113612776 | ||||||
| chr10:113612806
|
G | A | 1 | a0046c0113t0004g0275 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3301-375C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 29/41 | chr10 | 113612806 | ||||||
| chr10:113612811
|
C | T | 17 | a0010c0008t0002g0240a0010c0008t0002g0241a0010c0008t0002g0242others(14): Show | 17 | HG00323.hp1 HG00642.hp2 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.3301-380G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 29/41 | chr10 | 113612811 | ||||||
| chr10:113612826
|
G | A | 96 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(93): Show | 96 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.3301-395C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 29/41 | chr10 | 113612826 | ||||||
| chr10:113612841
|
C | T | 1 | a0002c0002t0004g0333 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.3301-410G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 29/41 | chr10 | 113612841 | ||||||
| chr10:113612911
|
G | C | 3 | a0028c0033t0001g0059a0028c0033t0001g0060a0028c0048t0001g0058 | 3 | HG02572.hp2 HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.3301-480C>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 29/41 | chr10 | 113612911 | ||||||
| chr10:113613518
|
C | T | 39 | a0010c0008t0002g0240a0010c0008t0002g0241a0010c0008t0002g0242others(36): Show | 39 | HG00140.hp2 HG00323.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.3300+665G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 29/41 | chr10 | 113613518 | ||||||
| chr10:113613640
|
C | G | 2 | a0011c0016t0004g0278a0011c0016t0004g0297 | 2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.3300+543G>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 29/41 | chr10 | 113613640 | ||||||
| chr10:113613666
|
G | T | 1 | a0012c0011t0003g0292 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.3300+517C>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 29/41 | chr10 | 113613666 | ||||||
| chr10:113613773
|
T | A | 1 | a0003c0003t0003g0313 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.3300+410A>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 29/41 | chr10 | 113613773 | ||||||
| chr10:113613851
|
T | C | 1 | a0002c0002t0004g0372 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.3300+332A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 29/41 | chr10 | 113613851 | ||||||
| chr10:113613874
|
C | T | 2 | a0012c0011t0003g0282a0019c0018t0001g0131 | 2 | HG02698.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.3300+309G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 29/41 | chr10 | 113613874 | ||||||
| chr10:113613921
|
A | C | 144 | a0002c0002t0004g0300a0002c0002t0004g0303a0002c0002t0004g0304others(141): Show | 152 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.3300+262T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 29/41 | chr10 | 113613921 | ||||||
| chr10:113613999
|
C | T | 31 | a0010c0008t0002g0240a0010c0008t0002g0241a0010c0008t0002g0242others(28): Show | 31 | HG00140.hp2 HG00323.hp1 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.3300+184G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 29/41 | chr10 | 113613999 | ||||||
| chr10:113614062
|
G | A | 8 | a0001c0001t0001g0144a0001c0001t0001g0170a0001c0001t0001g0171others(5): Show | 8 | HG02027.hp1 NA18939.hp2 NA18994.hp2 others(5): Show |
intron_variant | MODIFIER | c.3300+121C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 29/41 | chr10 | 113614062 | ||||||
| chr10:113614092
|
T | C | 345 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(342): Show | 356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.3300+91A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 29/41 | chr10 | 113614092 | ||||||
| chr10:113614313
|
C | T | 1 | a0005c0004t0005g0028 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.3187-17G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 28/41 | chr10 | 113614313 | ||||||
| chr10:113614409
|
TAAAAG | T | 4 | a0009c0079t0001g0069a0023c0030t0001g0158a0023c0030t0001g0175others(1): Show | 4 | NA18964.hp2 NA18983.hp1 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.3187-118_3187-114d others(7): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 28/41 | chr10 | 113614409 | ||||||
| chr10:113614467
|
A | G | 1 | a0024c0024t0003g0321 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.3187-171T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 28/41 | chr10 | 113614467 | ||||||
| chr10:113614523
|
G | A | 1 | a0027c0049t0002g0266 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3187-227C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 28/41 | chr10 | 113614523 | ||||||
| chr10:113614564
|
A | G | 1 | a0013c0019t0002g0224 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.3187-268T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 28/41 | chr10 | 113614564 | ||||||
| chr10:113614976
|
C | T | 1 | a0037c0045t0002g0221 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.3079-30G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 27/41 | chr10 | 113614976 | ||||||
| chr10:113615472
|
G | A | 1 | a0001c0001t0001g0169 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.3078+240C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 27/41 | chr10 | 113615472 | ||||||
| chr10:113615524
|
A | G | 1 | a0010c0008t0002g0256 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.3078+188T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 27/41 | chr10 | 113615524 | ||||||
| chr10:113615567
|
G | T | 1 | a0016c0077t0002g0064 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3078+145C>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 27/41 | chr10 | 113615567 | ||||||
| chr10:113615668
|
C | T | 1 | a0001c0001t0001g0223 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.3078+44G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 27/41 | chr10 | 113615668 | ||||||
| chr10:113615669
|
G | A | 3 | a0028c0033t0001g0059a0028c0033t0001g0060a0028c0048t0001g0058 | 3 | HG02572.hp2 HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.3078+43C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 27/41 | chr10 | 113615669 | ||||||
| chr10:113616188
|
T | C | 6 | a0014c0020t0005g0027a0014c0020t0005g0034a0014c0020t0005g0036others(3): Show | 6 | HG01099.hp2 HG01346.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2974-372A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 26/41 | chr10 | 113616188 | ||||||
| chr10:113616229
|
C | T | 2 | a0005c0004t0005g0052a0063c0066t0005g0051 | 2 | HG01943.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.2974-413G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 26/41 | chr10 | 113616229 | ||||||
| chr10:113616359
|
A | G | 341 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(338): Show | 352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.2974-543T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 26/41 | chr10 | 113616359 | ||||||
| chr10:113616402
|
T | G | 2 | a0004c0005t0001g0126a0004c0005t0001g0128 | 2 | HG02165.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.2974-586A>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 26/41 | chr10 | 113616402 | ||||||
| chr10:113616428
|
C | T | 14 | a0011c0016t0004g0278a0011c0016t0004g0297a0011c0016t0004g0299others(11): Show | 14 | HG01081.hp2 HG01884.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.2974-612G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 26/41 | chr10 | 113616428 | ||||||
| chr10:113616497
|
A | C | 1 | a0026c0050t0002g0229 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2974-681T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 26/41 | chr10 | 113616497 | ||||||
| chr10:113616892
|
G | A | 172 | a0001c0001t0001g0205a0002c0002t0004g0300a0002c0002t0004g0303others(169): Show | 180 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.2973+563C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 26/41 | chr10 | 113616892 | ||||||
| chr10:113616939
|
G | C | 2 | a0006c0006t0006g0053a0062c0063t0005g0054 | 2 | HG02258.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2973+516C>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 26/41 | chr10 | 113616939 | ||||||
| chr10:113616965
|
A | C | 2 | a0002c0002t0004g0338a0002c0002t0004g0339 | 2 | HG00408.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.2973+490T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 26/41 | chr10 | 113616965 | ||||||
| chr10:113617432
|
A | G | 3 | a0001c0001t0001g0139a0001c0001t0001g0141a0001c0001t0001g0149 | 3 | NA18963.hp2 NA19078.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.2973+23T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 26/41 | chr10 | 113617432 | ||||||
| chr10:113617614
|
A | G | 1 | a0002c0037t0007g0357 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2875-61T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 25/41 | chr10 | 113617614 | ||||||
| chr10:113617744
|
A | C | 103 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(100): Show | 103 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.2875-191T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 25/41 | chr10 | 113617744 | ||||||
| chr10:113617957
|
C | T | 4 | a0003c0003t0003g0313a0003c0003t0003g0316a0007c0010t0003g0315others(1): Show | 4 | HG00280.hp1 HG01069.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.2875-404G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 25/41 | chr10 | 113617957 | ||||||
| chr10:113618013
|
G | C | 1 | a0014c0062t0005g0055 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2875-460C>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 25/41 | chr10 | 113618013 | ||||||
| chr10:113618018
|
C | T | 341 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(338): Show | 352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.2875-465G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 25/41 | chr10 | 113618018 | ||||||
| chr10:113618024
|
C | G | 1 | a0003c0003t0003g0383 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2875-471G>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 25/41 | chr10 | 113618024 | ||||||
| chr10:113618105
|
T | C | 4 | a0021c0071t0002g0269a0021c0072t0001g0271a0021c0073t0001g0270others(1): Show | 4 | HG01109.hp2 HG01891.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.2875-552A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 25/41 | chr10 | 113618105 | ||||||
| chr10:113618148
|
C | CA | 48 | a0001c0001t0001g0137a0001c0001t0001g0161a0002c0002t0004g0307others(45): Show | 55 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.2875-596dupT | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 25/41 | chr10 | 113618148 | ||||||
| chr10:113618341
|
C | A | 1 | a0002c0002t0004g0344 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2875-788G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 25/41 | chr10 | 113618341 | ||||||
| chr10:113618481
|
C | T | 4 | a0016c0077t0002g0064a0034c0047t0003g0276a0034c0047t0003g0277others(1): Show | 4 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.2875-928G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 25/41 | chr10 | 113618481 | ||||||
| chr10:113618549
|
C | G | 1 | a0001c0001t0001g0161 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.2875-996G>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 25/41 | chr10 | 113618549 | ||||||
| chr10:113618592
|
G | A | 4 | a0001c0001t0001g0178a0001c0001t0001g0183a0001c0001t0001g0196others(1): Show | 4 | HG00639.hp1 HG01123.hp1 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.2875-1039C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 25/41 | chr10 | 113618592 | ||||||
| chr10:113618605
|
T | C | 109 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(106): Show | 109 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.2875-1052A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 25/41 | chr10 | 113618605 | ||||||
| chr10:113618878
|
G | A | 2 | a0006c0006t0006g0010a0006c0006t0006g0018 | 2 | NA18975.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.2875-1325C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 25/41 | chr10 | 113618878 | ||||||
| chr10:113619009
|
C | T | 5 | a0001c0001t0001g0147a0001c0001t0001g0152a0001c0001t0001g0154others(2): Show | 5 | HG01433.hp2 HG01981.hp2 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.2875-1456G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 25/41 | chr10 | 113619009 | ||||||
| chr10:113619357
|
G | A | 1 | a0027c0049t0002g0266 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2874+1247C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 25/41 | chr10 | 113619357 | ||||||
| chr10:113619619
|
CA | C | 225 | a0001c0001t0001g0135a0001c0001t0001g0138a0001c0001t0001g0140others(222): Show | 232 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.2874+984delT | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 25/41 | chr10 | 113619619 | ||||||
| chr10:113619619
|
CAA | C | 120 | a0001c0001t0001g0205a0002c0002t0004g0300a0002c0002t0004g0303others(117): Show | 122 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.2874+983_2874+984d others(4): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 25/41 | chr10 | 113619619 | ||||||
| chr10:113619801
|
G | A | 4 | a0021c0071t0002g0269a0021c0072t0001g0271a0021c0073t0001g0270others(1): Show | 4 | HG01109.hp2 HG01891.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.2874+803C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 25/41 | chr10 | 113619801 | ||||||
| chr10:113619838
|
G | C | 7 | a0003c0003t0003g0380a0003c0003t0003g0381a0003c0003t0003g0383others(4): Show | 7 | HG02559.hp1 HG02886.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.2874+766C>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 25/41 | chr10 | 113619838 | ||||||
| chr10:113619933
|
C | T | 1 | a0005c0065t0005g0050 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2874+671G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 25/41 | chr10 | 113619933 | ||||||
| chr10:113620033
|
C | T | 4 | a0021c0071t0002g0269a0021c0072t0001g0271a0021c0073t0001g0270others(1): Show | 4 | HG01109.hp2 HG01891.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.2874+571G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 25/41 | chr10 | 113620033 | ||||||
| chr10:113620170
|
A | G | 3 | a0034c0047t0003g0276a0034c0047t0003g0277a0046c0113t0004g0275 | 3 | HG02258.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2874+434T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 25/41 | chr10 | 113620170 | ||||||
| chr10:113620303
|
A | T | 6 | a0011c0042t0004g0341a0011c0042t0004g0342a0026c0034t0002g0236others(3): Show | 6 | HG01891.hp1 HG02486.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.2874+301T>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 25/41 | chr10 | 113620303 | ||||||
| chr10:113620433
|
G | C | 1 | a0001c0109t0001g0155 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.2874+171C>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 25/41 | chr10 | 113620433 | ||||||
| chr10:113620552
|
C | T | 8 | a0008c0007t0002g0082a0008c0007t0002g0089a0008c0007t0009g0094others(5): Show | 8 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.2874+52G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 25/41 | chr10 | 113620552 | ||||||
| chr10:113620849
|
A | C | 346 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(343): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.2770-141T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 24/41 | chr10 | 113620849 | ||||||
| chr10:113620948
|
T | C | 11 | a0027c0032t0002g0230a0027c0032t0002g0231a0028c0033t0001g0059others(8): Show | 11 | HG01081.hp2 HG02559.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.2770-240A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 24/41 | chr10 | 113620948 | ||||||
| chr10:113621058
|
C | T | 4 | a0033c0028t0002g0232a0033c0028t0002g0233a0033c0028t0002g0234others(1): Show | 4 | HG01884.hp1 HG02559.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2770-350G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 24/41 | chr10 | 113621058 | ||||||
| chr10:113621301
|
G | C | 1 | a0006c0006t0006g0053 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2769+568C>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 24/41 | chr10 | 113621301 | ||||||
| chr10:113621314
|
T | TAC | 5 | a0011c0016t0004g0278a0011c0016t0004g0297a0011c0016t0004g0299others(2): Show | 5 | HG02145.hp1 HG03041.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.2769+553_2769+554d others(4): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 24/41 | chr10 | 113621314 | ||||||
| chr10:113621314
|
T | TACAC | 40 | a0003c0003t0003g0350a0007c0010t0003g0347a0007c0010t0003g0348others(37): Show | 43 | HG00408.hp2 HG00544.hp1 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.2769+551_2769+554d others(6): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 24/41 | chr10 | 113621314 | ||||||
| chr10:113621314
|
T | TACACAC | 55 | a0002c0002t0004g0300a0002c0002t0004g0303a0002c0002t0004g0304others(52): Show | 55 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(52): Show |
intron_variant | MODIFIER | c.2769+549_2769+554d others(8): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 24/41 | chr10 | 113621314 | ||||||
| chr10:113621314
|
T | TACACACA others(1): Show |
6 | a0002c0002t0004g0309a0002c0002t0004g0368a0002c0002t0004g0370others(3): Show | 6 | HG02165.hp2 NA18747.hp1 NA18984.hp2 others(3): Show |
intron_variant | MODIFIER | c.2769+547_2769+554d others(10): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 24/41 | chr10 | 113621314 | ||||||
| chr10:113621314
|
TAC | T | 100 | a0001c0001t0001g0146a0001c0001t0001g0195a0001c0001t0001g0201others(97): Show | 104 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.2769+553_2769+554d others(4): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 24/41 | chr10 | 113621314 | ||||||
| chr10:113621314
|
TACAC | T | 127 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(124): Show | 129 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.2769+551_2769+554d others(6): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 24/41 | chr10 | 113621314 | ||||||
| chr10:113621350
|
G | T | 1 | a0053c0069t0006g0048 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2769+519C>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 24/41 | chr10 | 113621350 | ||||||
| chr10:113621486
|
C | G | 1 | a0066c0095t0003g0302 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2769+383G>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 24/41 | chr10 | 113621486 | ||||||
| chr10:113621583
|
C | A | 43 | a0005c0004t0005g0001a0005c0004t0005g0008a0005c0004t0005g0016others(40): Show | 47 | HG00423.hp1 HG00621.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.2769+286G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 24/41 | chr10 | 113621583 | ||||||
| chr10:113621587
|
C | A | 1 | a0008c0007t0002g0080 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2769+282G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 24/41 | chr10 | 113621587 | ||||||
| chr10:113621690
|
C | T | 2 | a0045c0036t0002g0267a0045c0036t0008g0057 | 2 | HG01081.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.2769+179G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 24/41 | chr10 | 113621690 | ||||||
| chr10:113621719
|
T | C | 1 | a0027c0049t0002g0266 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2769+150A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 24/41 | chr10 | 113621719 | ||||||
| chr10:113621776
|
T | C | 1 | a0016c0077t0002g0064 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2769+93A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 24/41 | chr10 | 113621776 | ||||||
| chr10:113622305
|
T | C | 2 | a0021c0114t0004g0273a0021c0115t0004g0274 | 2 | HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2458-125A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 23/41 | chr10 | 113622305 | ||||||
| chr10:113622354
|
A | G | 1 | a0045c0036t0002g0267 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2458-174T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 23/41 | chr10 | 113622354 | ||||||
| chr10:113622486
|
G | C | 345 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(342): Show | 354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.2458-306C>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 23/41 | chr10 | 113622486 | ||||||
| chr10:113622832
|
CAACT | C | 4 | a0026c0034t0002g0236a0026c0034t0002g0238a0026c0050t0002g0229others(1): Show | 4 | HG01891.hp1 HG02486.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.2458-656_2458-653d others(6): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 23/41 | chr10 | 113622832 | ||||||
| chr10:113622882
|
C | A | 1 | a0001c0001t0001g0140 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.2457+647G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 23/41 | chr10 | 113622882 | ||||||
| chr10:113622940
|
A | G | 129 | a0002c0002t0004g0300a0002c0002t0004g0303a0002c0002t0004g0304others(126): Show | 132 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.2457+589T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 23/41 | chr10 | 113622940 | ||||||
| chr10:113623110
|
T | C | 1 | a0001c0001t0001g0225 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2457+419A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 23/41 | chr10 | 113623110 | ||||||
| chr10:113623210
|
C | A | 1 | a0027c0049t0002g0266 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2457+319G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 23/41 | chr10 | 113623210 | ||||||
| chr10:113623387
|
G | A | 87 | a0002c0002t0004g0300a0002c0002t0004g0303a0002c0002t0004g0304others(84): Show | 87 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.2457+142C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 23/41 | chr10 | 113623387 | ||||||
| chr10:113623475
|
G | A | 1 | a0006c0064t0006g0012 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2457+54C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 23/41 | chr10 | 113623475 | ||||||
| chr10:113623724
|
C | A | 1 | a0010c0008t0002g0241 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2350-88G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 22/41 | chr10 | 113623724 | ||||||
| chr10:113623893
|
G | A | 2 | a0010c0008t0002g0242a0010c0008t0002g0264 | 2 | HG03710.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2350-257C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 22/41 | chr10 | 113623893 | ||||||
| chr10:113624000
|
G | T | 1 | a0061c0061t0005g0038 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2350-364C>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 22/41 | chr10 | 113624000 | ||||||
| chr10:113624112
|
G | T | 3 | a0027c0032t0002g0230a0027c0032t0002g0231a0041c0041t0003g0343 | 3 | HG02630.hp2 NA18906.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2350-476C>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 22/41 | chr10 | 113624112 | ||||||
| chr10:113624115
|
G | A | 344 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(341): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.2350-479C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 22/41 | chr10 | 113624115 | ||||||
| chr10:113624315
|
T | G | 1 | a0010c0008t0010g0249 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2349+511A>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 22/41 | chr10 | 113624315 | ||||||
| chr10:113624354
|
G | A | 29 | a0010c0008t0002g0240a0010c0008t0002g0241a0010c0008t0002g0242others(26): Show | 29 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.2349+472C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 22/41 | chr10 | 113624354 | ||||||
| chr10:113624378
|
T | A | 1 | a0048c0102t0001g0136 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2349+448A>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 22/41 | chr10 | 113624378 | ||||||
| chr10:113624520
|
T | A | 1 | a0011c0026t0002g0237 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2349+306A>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 22/41 | chr10 | 113624520 | ||||||
| chr10:113624538
|
C | T | 1 | a0043c0070t0005g0056 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2349+288G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 22/41 | chr10 | 113624538 | ||||||
| chr10:113624704
|
C | T | 1 | a0014c0062t0005g0055 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2349+122G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 22/41 | chr10 | 113624704 | ||||||
| chr10:113624708
|
C | A | 48 | a0005c0004t0005g0001a0005c0004t0005g0008a0005c0004t0005g0016others(45): Show | 52 | HG00423.hp1 HG00621.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.2349+118G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 22/41 | chr10 | 113624708 | ||||||
| chr10:113625000
|
G | A | 1 | a0009c0009t0001g0071 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2245-70C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 21/41 | chr10 | 113625000 | ||||||
| chr10:113625116
|
A | G | 1 | a0026c0034t0002g0238 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2245-186T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 21/41 | chr10 | 113625116 | ||||||
| chr10:113625148
|
G | A | 1 | a0011c0016t0004g0299 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2245-218C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 21/41 | chr10 | 113625148 | ||||||
| chr10:113625250
|
A | T | 89 | a0003c0023t0003g0320a0005c0004t0005g0001a0005c0004t0005g0008others(86): Show | 96 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.2245-320T>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 21/41 | chr10 | 113625250 | ||||||
| chr10:113625261
|
C | A | 1 | a0014c0062t0005g0055 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2245-331G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 21/41 | chr10 | 113625261 | ||||||
| chr10:113625521
|
A | G | 3 | a0012c0011t0003g0272a0012c0011t0003g0285a0012c0011t0003g0289 | 3 | NA18989.hp2 NA19003.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.2244+526T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 21/41 | chr10 | 113625521 | ||||||
| chr10:113625891
|
C | T | 19 | a0011c0016t0004g0280a0011c0016t0004g0294a0012c0011t0003g0007others(16): Show | 22 | HG00408.hp2 HG00544.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.2244+156G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 21/41 | chr10 | 113625891 | ||||||
| chr10:113625968
|
G | A | 7 | a0026c0034t0002g0236a0026c0034t0002g0238a0026c0050t0002g0229others(4): Show | 7 | HG01891.hp1 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2244+79C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 21/41 | chr10 | 113625968 | ||||||
| chr10:113626217
|
A | C | 90 | a0001c0001t0001g0219a0002c0002t0004g0300a0002c0002t0004g0303others(87): Show | 90 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.2146-72T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 20/41 | chr10 | 113626217 | ||||||
| chr10:113626219
|
A | C | 2 | a0002c0037t0007g0356a0070c0086t0003g0327 | 2 | HG00438.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.2146-74T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 20/41 | chr10 | 113626219 | ||||||
| chr10:113626220
|
C | T | 1 | a0007c0084t0003g0345 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2146-75G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 20/41 | chr10 | 113626220 | ||||||
| chr10:113626329
|
C | G | 87 | a0005c0004t0005g0001a0005c0004t0005g0008a0005c0004t0005g0016others(84): Show | 94 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.2146-184G>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 20/41 | chr10 | 113626329 | ||||||
| chr10:113626344
|
A | T | 1 | a0016c0077t0002g0064 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2146-199T>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 20/41 | chr10 | 113626344 | ||||||
| chr10:113626528
|
T | C | 1 | a0051c0106t0002g0151 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2146-383A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 20/41 | chr10 | 113626528 | ||||||
| chr10:113626760
|
C | T | 7 | a0026c0034t0002g0236a0026c0034t0002g0238a0026c0050t0002g0229others(4): Show | 7 | HG01891.hp1 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2146-615G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 20/41 | chr10 | 113626760 | ||||||
| chr10:113626821
|
C | A | 87 | a0005c0004t0005g0001a0005c0004t0005g0008a0005c0004t0005g0016others(84): Show | 94 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.2146-676G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 20/41 | chr10 | 113626821 | ||||||
| chr10:113626945
|
C | T | 87 | a0005c0004t0005g0001a0005c0004t0005g0008a0005c0004t0005g0016others(84): Show | 94 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.2146-800G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 20/41 | chr10 | 113626945 | ||||||
| chr10:113626985
|
G | A | 2 | a0008c0007t0002g0092a0009c0079t0001g0069 | 2 | NA18964.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.2146-840C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 20/41 | chr10 | 113626985 | ||||||
| chr10:113627123
|
A | G | 6 | a0021c0071t0002g0269a0021c0072t0001g0271a0021c0073t0001g0270others(3): Show | 6 | HG01891.hp2 HG02258.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.2146-978T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 20/41 | chr10 | 113627123 | ||||||
| chr10:113627172
|
T | A | 87 | a0005c0004t0005g0001a0005c0004t0005g0008a0005c0004t0005g0016others(84): Show | 94 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.2146-1027A>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 20/41 | chr10 | 113627172 | ||||||
| chr10:113627211
|
GA | G | 3 | a0021c0071t0002g0269a0021c0072t0001g0271a0021c0073t0001g0270 | 3 | HG01891.hp2 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2146-1067delT | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 20/41 | chr10 | 113627211 | ||||||
| chr10:113627253
|
C | T | 87 | a0005c0004t0005g0001a0005c0004t0005g0008a0005c0004t0005g0016others(84): Show | 94 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.2146-1108G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 20/41 | chr10 | 113627253 | ||||||
| chr10:113627349
|
G | A | 1 | a0027c0049t0002g0266 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2146-1204C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 20/41 | chr10 | 113627349 | ||||||
| chr10:113627840
|
T | C | 3 | a0028c0033t0001g0059a0028c0033t0001g0060a0028c0048t0001g0058 | 3 | HG02572.hp2 HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2145+1077A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 20/41 | chr10 | 113627840 | ||||||
| chr10:113627979
|
G | A | 83 | a0002c0002t0004g0300a0002c0002t0004g0303a0002c0002t0004g0304others(80): Show | 83 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.2145+938C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 20/41 | chr10 | 113627979 | ||||||
| chr10:113628200
|
C | T | 87 | a0005c0004t0005g0001a0005c0004t0005g0008a0005c0004t0005g0016others(84): Show | 94 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.2145+717G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 20/41 | chr10 | 113628200 | ||||||
| chr10:113628240
|
A | T | 87 | a0005c0004t0005g0001a0005c0004t0005g0008a0005c0004t0005g0016others(84): Show | 94 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.2145+677T>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 20/41 | chr10 | 113628240 | ||||||
| chr10:113628257
|
G | A | 1 | a0059c0058t0002g0239 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2145+660C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 20/41 | chr10 | 113628257 | ||||||
| chr10:113628378
|
C | T | 3 | a0034c0047t0003g0276a0034c0047t0003g0277a0046c0113t0004g0275 | 3 | HG02258.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2145+539G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 20/41 | chr10 | 113628378 | ||||||
| chr10:113628379
|
G | A | 22 | a0011c0016t0004g0280a0011c0016t0004g0294a0011c0026t0002g0237others(19): Show | 25 | HG00408.hp2 HG00544.hp1 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.2145+538C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 20/41 | chr10 | 113628379 | ||||||
| chr10:113628463
|
C | A | 3 | a0021c0071t0002g0269a0021c0072t0001g0271a0021c0073t0001g0270 | 3 | HG01891.hp2 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2145+454G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 20/41 | chr10 | 113628463 | ||||||
| chr10:113628487
|
C | T | 87 | a0005c0004t0005g0001a0005c0004t0005g0008a0005c0004t0005g0016others(84): Show | 94 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.2145+430G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 20/41 | chr10 | 113628487 | ||||||
| chr10:113628521
|
T | G | 87 | a0005c0004t0005g0001a0005c0004t0005g0008a0005c0004t0005g0016others(84): Show | 94 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.2145+396A>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 20/41 | chr10 | 113628521 | ||||||
| chr10:113628609
|
A | C | 87 | a0005c0004t0005g0001a0005c0004t0005g0008a0005c0004t0005g0016others(84): Show | 94 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.2145+308T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 20/41 | chr10 | 113628609 | ||||||
| chr10:113628639
|
A | G | 1 | a0006c0006t0006g0020 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2145+278T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 20/41 | chr10 | 113628639 | ||||||
| chr10:113628707
|
A | G | 3 | a0034c0047t0003g0276a0034c0047t0003g0277a0046c0113t0004g0275 | 3 | HG02258.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2145+210T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 20/41 | chr10 | 113628707 | ||||||
| chr10:113628791
|
T | C | 1 | a0022c0055t0001g0250 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2145+126A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 20/41 | chr10 | 113628791 | ||||||
| chr10:113628829
|
A | G | 87 | a0005c0004t0005g0001a0005c0004t0005g0008a0005c0004t0005g0016others(84): Show | 94 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.2145+88T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 20/41 | chr10 | 113628829 | ||||||
| chr10:113628862
|
T | C | 1 | a0002c0037t0007g0357 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2145+55A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 20/41 | chr10 | 113628862 | ||||||
| chr10:113629062
|
A | G | 1 | a0014c0062t0005g0055 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2041-41T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 19/41 | chr10 | 113629062 | ||||||
| chr10:113629098
|
G | A | 2 | a0009c0009t0001g0091a0009c0009t0001g0093 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.2041-77C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 19/41 | chr10 | 113629098 | ||||||
| chr10:113629123
|
T | C | 1 | a0066c0095t0003g0302 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2041-102A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 19/41 | chr10 | 113629123 | ||||||
| chr10:113629185
|
C | T | 88 | a0005c0004t0005g0001a0005c0004t0005g0008a0005c0004t0005g0016others(85): Show | 95 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.2041-164G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 19/41 | chr10 | 113629185 | ||||||
| chr10:113629283
|
CT | C | 49 | a0005c0004t0005g0001a0005c0004t0005g0008a0005c0004t0005g0016others(46): Show | 53 | HG00423.hp1 HG00621.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.2041-263delA | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 19/41 | chr10 | 113629283 | ||||||
| chr10:113629370
|
A | T | 4 | a0008c0007t0002g0077a0008c0007t0002g0078a0008c0078t0002g0063others(1): Show | 6 | HG00642.hp1 HG01106.hp1 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.2040+218T>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 19/41 | chr10 | 113629370 | ||||||
| chr10:113629421
|
A | C | 88 | a0005c0004t0005g0001a0005c0004t0005g0008a0005c0004t0005g0016others(85): Show | 95 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.2040+167T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 19/41 | chr10 | 113629421 | ||||||
| chr10:113629455
|
C | T | 88 | a0005c0004t0005g0001a0005c0004t0005g0008a0005c0004t0005g0016others(85): Show | 95 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.2040+133G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 19/41 | chr10 | 113629455 | ||||||
| chr10:113629508
|
G | A | 88 | a0005c0004t0005g0001a0005c0004t0005g0008a0005c0004t0005g0016others(85): Show | 95 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.2040+80C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 19/41 | chr10 | 113629508 | ||||||
| chr10:113629809
|
C | T | 2 | a0015c0012t0004g0284a0015c0012t0004g0293 | 2 | HG02523.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.1843-24G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 18/41 | chr10 | 113629809 | ||||||
| chr10:113629877
|
C | T | 2 | a0001c0001t0001g0142a0001c0001t0001g0143 | 2 | NA18956.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.1843-92G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 18/41 | chr10 | 113629877 | ||||||
| chr10:113629892
|
C | T | 1 | a0006c0006t0006g0053 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1843-107G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 18/41 | chr10 | 113629892 | ||||||
| chr10:113630291
|
G | A | 1 | a0001c0001t0001g0225 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1843-506C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 18/41 | chr10 | 113630291 | ||||||
| chr10:113630332
|
T | C | 114 | a0002c0002t0004g0300a0002c0002t0004g0303a0002c0002t0004g0304others(111): Show | 114 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.1843-547A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 18/41 | chr10 | 113630332 | ||||||
| chr10:113630423
|
T | C | 114 | a0002c0002t0004g0300a0002c0002t0004g0303a0002c0002t0004g0304others(111): Show | 114 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.1843-638A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 18/41 | chr10 | 113630423 | ||||||
| chr10:113630508
|
A | G | 85 | a0005c0004t0005g0001a0005c0004t0005g0008a0005c0004t0005g0016others(82): Show | 92 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.1843-723T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 18/41 | chr10 | 113630508 | ||||||
| chr10:113630526
|
T | C | 3 | a0033c0028t0002g0232a0033c0028t0002g0233a0033c0028t0002g0234 | 3 | HG02559.hp2 HG02717.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1843-741A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 18/41 | chr10 | 113630526 | ||||||
| chr10:113630569
|
C | T | 1 | a0070c0086t0003g0327 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1843-784G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 18/41 | chr10 | 113630569 | ||||||
| chr10:113630594
|
C | T | 226 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(223): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.1843-809G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 18/41 | chr10 | 113630594 | ||||||
| chr10:113630605
|
G | A | 2 | a0004c0021t0003g0387a0004c0075t0001g0160 | 2 | HG01109.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1843-820C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 18/41 | chr10 | 113630605 | ||||||
| chr10:113630857
|
C | G | 19 | a0011c0016t0004g0280a0011c0016t0004g0294a0012c0011t0003g0007others(16): Show | 22 | HG00408.hp2 HG00544.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.1842+652G>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 18/41 | chr10 | 113630857 | ||||||
| chr10:113630927
|
A | G | 85 | a0005c0004t0005g0001a0005c0004t0005g0008a0005c0004t0005g0016others(82): Show | 92 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.1842+582T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 18/41 | chr10 | 113630927 | ||||||
| chr10:113631221
|
A | T | 1 | a0003c0003t0003g0358 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1842+288T>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 18/41 | chr10 | 113631221 | ||||||
| chr10:113631382
|
C | A | 1 | a0021c0071t0002g0269 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1842+127G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 18/41 | chr10 | 113631382 | ||||||
| chr10:113631663
|
A | G | 1 | a0007c0010t0003g0352 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1741-53T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 17/41 | chr10 | 113631663 | ||||||
| chr10:113631703
|
G | C | 1 | a0008c0007t0002g0068 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1741-93C>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 17/41 | chr10 | 113631703 | ||||||
| chr10:113631853
|
G | A | 4 | a0001c0001t0001g0178a0001c0001t0001g0183a0001c0001t0001g0196others(1): Show | 4 | HG00639.hp1 HG01123.hp1 HG01255.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.1740+4C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 17/41 | chr10 | 113631853 | ||||||
| chr10:113632076
|
C | T | 1 | a0066c0095t0003g0302 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1633-112G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 16/41 | chr10 | 113632076 | ||||||
| chr10:113632121
|
A | G | 4 | a0021c0071t0002g0269a0021c0072t0001g0271a0021c0073t0001g0270others(1): Show | 4 | HG01891.hp2 HG02451.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1633-157T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 16/41 | chr10 | 113632121 | ||||||
| chr10:113632237
|
C | A | 1 | a0005c0004t0005g0016 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1633-273G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 16/41 | chr10 | 113632237 | ||||||
| chr10:113632246
|
G | A | 1 | a0018c0015t0001g0097 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1633-282C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 16/41 | chr10 | 113632246 | ||||||
| chr10:113632352
|
A | G | 86 | a0005c0004t0005g0001a0005c0004t0005g0008a0005c0004t0005g0016others(83): Show | 93 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.1633-388T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 16/41 | chr10 | 113632352 | ||||||
| chr10:113632431
|
T | G | 2 | a0005c0004t0005g0052a0063c0066t0005g0051 | 2 | HG01943.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1633-467A>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 16/41 | chr10 | 113632431 | ||||||
| chr10:113632497
|
A | C | 1 | a0027c0049t0002g0266 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1633-533T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 16/41 | chr10 | 113632497 | ||||||
| chr10:113632569
|
GTGTCCCT others(41): Show |
G | 6 | a0003c0003t0003g0353a0007c0010t0003g0348a0007c0010t0003g0349others(3): Show | 6 | HG01243.hp2 HG02109.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1632+467_1632+514d others(50): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 16/41 | chr10 | 113632569 | ||||||
| chr10:113632620
|
C | A | 6 | a0003c0003t0003g0353a0007c0010t0003g0348a0007c0010t0003g0349others(3): Show | 6 | HG01243.hp2 HG02109.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1632+464G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 16/41 | chr10 | 113632620 | ||||||
| chr10:113632622
|
G | GT | 6 | a0003c0003t0003g0353a0007c0010t0003g0348a0007c0010t0003g0349others(3): Show | 6 | HG01243.hp2 HG02109.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1632+461_1632+462i others(3): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 16/41 | chr10 | 113632622 | ||||||
| chr10:113632631
|
T | C | 1 | a0016c0077t0002g0064 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1632+453A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 16/41 | chr10 | 113632631 | ||||||
| chr10:113632720
|
C | A | 1 | a0003c0003t0003g0371 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1632+364G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 16/41 | chr10 | 113632720 | ||||||
| chr10:113632735
|
G | A | 2 | a0002c0002t0004g0344a0003c0003t0003g0340 | 2 | HG02055.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1632+349C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 16/41 | chr10 | 113632735 | ||||||
| chr10:113632834
|
G | T | 89 | a0001c0001t0001g0178a0001c0001t0001g0183a0001c0001t0001g0196others(86): Show | 96 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.1632+250C>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 16/41 | chr10 | 113632834 | ||||||
| chr10:113632925
|
G | A | 88 | a0002c0002t0004g0300a0002c0002t0004g0303a0002c0002t0004g0304others(85): Show | 88 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.1632+159C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 16/41 | chr10 | 113632925 | ||||||
| chr10:113632930
|
A | C | 135 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(132): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.1632+154T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 16/41 | chr10 | 113632930 | ||||||
| chr10:113633446
|
C | T | 1 | a0004c0005t0001g0122 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1528-258G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 15/41 | chr10 | 113633446 | ||||||
| chr10:113633458
|
T | C | 1 | a0059c0058t0002g0239 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1528-270A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 15/41 | chr10 | 113633458 | ||||||
| chr10:113633470
|
A | G | 3 | a0034c0047t0003g0276a0034c0047t0003g0277a0046c0113t0004g0275 | 3 | HG02258.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1528-282T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 15/41 | chr10 | 113633470 | ||||||
| chr10:113633499
|
G | A | 2 | a0009c0009t0001g0091a0009c0009t0001g0093 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1528-311C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 15/41 | chr10 | 113633499 | ||||||
| chr10:113633618
|
G | A | 1 | a0002c0002t0004g0344 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1528-430C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 15/41 | chr10 | 113633618 | ||||||
| chr10:113633627
|
C | T | 23 | a0010c0008t0002g0240a0010c0008t0002g0241a0010c0008t0002g0242others(20): Show | 23 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(20): Show |
intron_variant | MODIFIER | c.1528-439G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 15/41 | chr10 | 113633627 | ||||||
| chr10:113633732
|
GTT | G | 4 | a0021c0071t0002g0269a0021c0072t0001g0271a0021c0073t0001g0270others(1): Show | 4 | HG01891.hp2 HG02451.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1527+378_1527+379d others(4): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 15/41 | chr10 | 113633732 | ||||||
| chr10:113633766
|
G | C | 3 | a0034c0047t0003g0276a0034c0047t0003g0277a0046c0113t0004g0275 | 3 | HG02258.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1527+346C>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 15/41 | chr10 | 113633766 | ||||||
| chr10:113633820
|
G | A | 220 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(217): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1527+292C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 15/41 | chr10 | 113633820 | ||||||
| chr10:113633865
|
T | C | 1 | a0002c0002t0004g0328 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1527+247A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 15/41 | chr10 | 113633865 | ||||||
| chr10:113633889
|
G | C | 18 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0140others(15): Show | 18 | HG00438.hp2 HG01433.hp2 HG01981.hp2 others(15): Show |
intron_variant | MODIFIER | c.1527+223C>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 15/41 | chr10 | 113633889 | ||||||
| chr10:113634103
|
G | T | 1 | a0016c0013t0002g0098 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1527+9C>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 15/41 | chr10 | 113634103 | ||||||
| chr10:113634287
|
A | G | 6 | a0010c0008t0002g0240a0010c0008t0002g0246a0010c0008t0002g0247others(3): Show | 6 | HG00323.hp1 HG00642.hp2 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.1429-77T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113634287 | ||||||
| chr10:113634309
|
G | A | 1 | a0014c0062t0005g0055 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1429-99C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113634309 | ||||||
| chr10:113634310
|
C | T | 1 | a0014c0062t0005g0055 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1429-100G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113634310 | ||||||
| chr10:113634508
|
C | A | 1 | a0015c0012t0004g0295 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1429-298G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113634508 | ||||||
| chr10:113634545
|
C | G | 3 | a0011c0016t0004g0294a0015c0012t0004g0295a0015c0012t0004g0296 | 3 | HG02015.hp2 HG02056.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.1429-335G>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113634545 | ||||||
| chr10:113634766
|
G | C | 1 | a0005c0004t0005g0047 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1429-556C>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113634766 | ||||||
| chr10:113634792
|
C | T | 87 | a0002c0002t0004g0300a0002c0002t0004g0303a0002c0002t0004g0304others(84): Show | 87 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.1429-582G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113634792 | ||||||
| chr10:113634930
|
C | T | 1 | a0027c0049t0002g0266 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1429-720G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113634930 | ||||||
| chr10:113634931
|
G | A | 110 | a0002c0002t0004g0300a0002c0002t0004g0303a0002c0002t0004g0304others(107): Show | 110 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.1429-721C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113634931 | ||||||
| chr10:113635096
|
A | G | 221 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(218): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.1429-886T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113635096 | ||||||
| chr10:113635139
|
G | A | 86 | a0002c0002t0004g0300a0002c0002t0004g0303a0002c0002t0004g0304others(83): Show | 86 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.1429-929C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113635139 | ||||||
| chr10:113635572
|
C | T | 9 | a0026c0034t0002g0236a0026c0034t0002g0238a0026c0050t0002g0229others(6): Show | 9 | HG01891.hp1 HG02486.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1429-1362G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113635572 | ||||||
| chr10:113635642
|
G | T | 2 | a0002c0002t0004g0304a0071c0089t0004g0305 | 2 | HG00609.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.1429-1432C>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113635642 | ||||||
| chr10:113635877
|
G | C | 221 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(218): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.1429-1667C>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113635877 | ||||||
| chr10:113636147
|
C | T | 1 | a0027c0049t0002g0266 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1429-1937G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113636147 | ||||||
| chr10:113636304
|
G | T | 221 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(218): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.1429-2094C>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113636304 | ||||||
| chr10:113636446
|
C | T | 110 | a0002c0002t0004g0300a0002c0002t0004g0303a0002c0002t0004g0304others(107): Show | 110 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.1429-2236G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113636446 | ||||||
| chr10:113636493
|
T | A | 9 | a0003c0003t0003g0350a0003c0003t0003g0353a0007c0010t0003g0347others(6): Show | 9 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1429-2283A>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113636493 | ||||||
| chr10:113636537
|
G | A | 1 | a0009c0009t0001g0101 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1429-2327C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113636537 | ||||||
| chr10:113636623
|
T | C | 2 | a0035c0040t0004g0375a0035c0040t0004g0376 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1429-2413A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113636623 | ||||||
| chr10:113636756
|
C | T | 1 | a0022c0055t0001g0250 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1429-2546G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113636756 | ||||||
| chr10:113636864
|
G | A | 1 | a0061c0061t0005g0038 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1429-2654C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113636864 | ||||||
| chr10:113636891
|
G | A | 4 | a0021c0071t0002g0269a0021c0072t0001g0271a0021c0073t0001g0270others(1): Show | 4 | HG01891.hp2 HG02451.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1429-2681C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113636891 | ||||||
| chr10:113636922
|
G | A | 20 | a0011c0016t0004g0280a0011c0016t0004g0294a0012c0011t0003g0007others(17): Show | 23 | HG00408.hp2 HG00544.hp1 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.1429-2712C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113636922 | ||||||
| chr10:113636957
|
C | A | 344 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(341): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.1429-2747G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113636957 | ||||||
| chr10:113637006
|
CA | C | 157 | a0002c0002t0004g0300a0002c0002t0004g0303a0002c0002t0004g0304others(154): Show | 162 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.1429-2797delT | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113637006 | ||||||
| chr10:113637006
|
CAA | C | 34 | a0001c0001t0001g0195a0001c0001t0001g0200a0001c0001t0001g0201others(31): Show | 37 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.1429-2798_1429-279 others(6): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113637006 | ||||||
| chr10:113637006
|
CAAA | C | 164 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(161): Show | 167 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.1429-2799_1429-279 others(7): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113637006 | ||||||
| chr10:113637039
|
C | G | 1 | a0009c0009t0001g0066 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1429-2829G>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113637039 | ||||||
| chr10:113637121
|
G | A | 5 | a0011c0026t0002g0237a0011c0042t0004g0341a0011c0042t0004g0342others(2): Show | 5 | HG02630.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1429-2911C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113637121 | ||||||
| chr10:113637132
|
A | C | 1 | a0011c0016t0004g0298 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1429-2922T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113637132 | ||||||
| chr10:113637262
|
C | T | 4 | a0026c0034t0002g0236a0026c0034t0002g0238a0026c0050t0002g0229others(1): Show | 4 | HG01891.hp1 HG02486.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1428+2965G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113637262 | ||||||
| chr10:113637320
|
T | C | 1 | a0019c0018t0001g0006 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1428+2907A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113637320 | ||||||
| chr10:113637374
|
G | A | 221 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(218): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.1428+2853C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113637374 | ||||||
| chr10:113637416
|
T | C | 7 | a0002c0002t0004g0307a0002c0002t0004g0309a0003c0003t0003g0306others(4): Show | 7 | HG00621.hp2 NA18747.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.1428+2811A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113637416 | ||||||
| chr10:113637445
|
G | A | 7 | a0022c0022t0001g0258a0022c0022t0001g0259a0022c0022t0001g0262others(4): Show | 7 | HG00597.hp1 HG02135.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.1428+2782C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113637445 | ||||||
| chr10:113637464
|
G | A | 221 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(218): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.1428+2763C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113637464 | ||||||
| chr10:113637600
|
G | A | 1 | a0014c0062t0005g0055 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1428+2627C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113637600 | ||||||
| chr10:113637605
|
G | A | 221 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(218): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.1428+2622C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113637605 | ||||||
| chr10:113637779
|
G | T | 16 | a0002c0002t0004g0335a0002c0002t0004g0336a0002c0002t0004g0344others(13): Show | 16 | HG00738.hp1 HG01243.hp2 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.1428+2448C>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113637779 | ||||||
| chr10:113637826
|
G | A | 2 | a0005c0004t0005g0052a0063c0066t0005g0051 | 2 | HG01943.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1428+2401C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113637826 | ||||||
| chr10:113637863
|
T | C | 221 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(218): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.1428+2364A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113637863 | ||||||
| chr10:113637917
|
T | C | 344 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(341): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.1428+2310A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113637917 | ||||||
| chr10:113637922
|
CA | C | 322 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(319): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.1428+2304delT | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113637922 | ||||||
| chr10:113638015
|
A | G | 1 | a0004c0005t0001g0108 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1428+2212T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113638015 | ||||||
| chr10:113638167
|
T | A | 221 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(218): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.1428+2060A>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113638167 | ||||||
| chr10:113638231
|
A | G | 3 | a0028c0033t0001g0059a0028c0033t0001g0060a0028c0048t0001g0058 | 3 | HG02572.hp2 HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1428+1996T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113638231 | ||||||
| chr10:113638825
|
G | A | 87 | a0002c0002t0004g0300a0002c0002t0004g0303a0002c0002t0004g0304others(84): Show | 87 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.1428+1402C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113638825 | ||||||
| chr10:113638833
|
C | T | 1 | a0003c0003t0003g0350 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1428+1394G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113638833 | ||||||
| chr10:113638835
|
C | G | 6 | a0026c0034t0002g0236a0026c0034t0002g0238a0026c0050t0002g0229others(3): Show | 6 | HG01891.hp1 HG02486.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1428+1392G>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113638835 | ||||||
| chr10:113638972
|
C | T | 62 | a0002c0002t0004g0300a0002c0002t0004g0303a0002c0002t0004g0304others(59): Show | 62 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.1428+1255G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113638972 | ||||||
| chr10:113639066
|
C | T | 1 | a0019c0018t0001g0131 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1428+1161G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113639066 | ||||||
| chr10:113639091
|
C | CA | 26 | a0002c0002t0004g0300a0002c0002t0004g0337a0002c0002t0004g0338others(23): Show | 26 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(23): Show |
intron_variant | MODIFIER | c.1428+1135dupT | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113639091 | ||||||
| chr10:113639091
|
CA | C | 29 | a0002c0002t0004g0370a0007c0010t0003g0347a0007c0084t0003g0345others(26): Show | 29 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.1428+1135delT | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113639091 | ||||||
| chr10:113639091
|
CAAAAAA | C | 13 | a0001c0001t0001g0143a0001c0001t0013g0204a0004c0005t0001g0167others(10): Show | 13 | HG00735.hp1 HG02056.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1428+1130_1428+113 others(10): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113639091 | ||||||
| chr10:113639091
|
CAAAAAAA | C | 209 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(206): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.1428+1129_1428+113 others(11): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113639091 | ||||||
| chr10:113639091
|
CAAAAAAA others(2): Show |
C | 6 | a0026c0034t0002g0236a0026c0034t0002g0238a0026c0050t0002g0229others(3): Show | 6 | HG01891.hp1 HG02486.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1428+1127_1428+113 others(13): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113639091 | ||||||
| chr10:113639103
|
A | T | 4 | a0003c0003t0003g0380a0003c0003t0003g0381a0003c0003t0003g0383others(1): Show | 4 | HG02896.hp1 HG03139.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1428+1124T>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113639103 | ||||||
| chr10:113639158
|
T | TAAGTC | 221 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(218): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.1428+1064_1428+106 others(9): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113639158 | ||||||
| chr10:113639234
|
C | T | 1 | a0001c0001t0001g0191 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1428+993G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113639234 | ||||||
| chr10:113639350
|
T | C | 1 | a0008c0007t0002g0090 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1428+877A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113639350 | ||||||
| chr10:113639440
|
T | C | 135 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(132): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.1428+787A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113639440 | ||||||
| chr10:113639477
|
T | A | 221 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(218): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.1428+750A>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113639477 | ||||||
| chr10:113639481
|
A | G | 221 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(218): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.1428+746T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113639481 | ||||||
| chr10:113639535
|
T | G | 344 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(341): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.1428+692A>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113639535 | ||||||
| chr10:113639613
|
T | G | 29 | a0005c0004t0005g0008a0005c0004t0005g0016a0005c0004t0005g0019others(26): Show | 30 | HG00423.hp1 HG00621.hp1 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.1428+614A>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113639613 | ||||||
| chr10:113639625
|
C | T | 1 | a0028c0033t0001g0059 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1428+602G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113639625 | ||||||
| chr10:113639666
|
C | A | 5 | a0011c0016t0004g0278a0011c0016t0004g0297a0011c0016t0004g0298others(2): Show | 5 | HG01884.hp1 HG02145.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1428+561G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113639666 | ||||||
| chr10:113639700
|
C | T | 221 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(218): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.1428+527G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113639700 | ||||||
| chr10:113639770
|
C | A | 221 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(218): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.1428+457G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113639770 | ||||||
| chr10:113639936
|
T | C | 1 | a0064c0093t0004g0281 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1428+291A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113639936 | ||||||
| chr10:113639953
|
G | T | 1 | a0066c0095t0003g0302 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1428+274C>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113639953 | ||||||
| chr10:113639973
|
A | G | 1 | a0003c0003t0003g0369 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1428+254T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113639973 | ||||||
| chr10:113640029
|
T | C | 1 | a0014c0062t0005g0055 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1428+198A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113640029 | ||||||
| chr10:113640212
|
TG | T | 4 | a0021c0071t0002g0269a0021c0072t0001g0271a0021c0073t0001g0270others(1): Show | 4 | HG01891.hp2 HG02451.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1428+14delC | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113640212 | ||||||
| chr10:113640387
|
C | T | 1 | a0001c0001t0001g0200 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1324-56G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 13/41 | chr10 | 113640387 | ||||||
| chr10:113640505
|
C | A | 221 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(218): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.1324-174G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 13/41 | chr10 | 113640505 | ||||||
| chr10:113640541
|
G | A | 1 | a0009c0009t0001g0101 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1324-210C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 13/41 | chr10 | 113640541 | ||||||
| chr10:113640626
|
G | GAAGA | 20 | a0011c0016t0004g0280a0011c0016t0004g0294a0012c0011t0003g0007others(17): Show | 23 | HG00408.hp2 HG00544.hp1 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.1324-299_1324-296d others(6): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 13/41 | chr10 | 113640626 | ||||||
| chr10:113640735
|
C | G | 1 | a0014c0062t0005g0055 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1324-404G>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 13/41 | chr10 | 113640735 | ||||||
| chr10:113640933
|
AG | A | 221 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(218): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.1323+431delC | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 13/41 | chr10 | 113640933 | ||||||
| chr10:113640996
|
C | A | 2 | a0002c0002t0004g0335a0002c0002t0004g0336 | 2 | HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1323+369G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 13/41 | chr10 | 113640996 | ||||||
| chr10:113641000
|
C | T | 221 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(218): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.1323+365G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 13/41 | chr10 | 113641000 | ||||||
| chr10:113641003
|
T | C | 6 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0210others(3): Show | 6 | HG01099.hp1 HG01928.hp2 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.1323+362A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 13/41 | chr10 | 113641003 | ||||||
| chr10:113641123
|
T | A | 3 | a0011c0016t0004g0278a0011c0016t0004g0297a0041c0041t0003g0279 | 3 | HG01884.hp1 HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1323+242A>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 13/41 | chr10 | 113641123 | ||||||
| chr10:113641123
|
T | C | 23 | a0010c0008t0002g0240a0010c0008t0002g0241a0010c0008t0002g0242others(20): Show | 23 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(20): Show |
intron_variant | MODIFIER | c.1323+242A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 13/41 | chr10 | 113641123 | ||||||
| chr10:113641199
|
C | T | 221 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(218): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.1323+166G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 13/41 | chr10 | 113641199 | ||||||
| chr10:113641213
|
G | A | 221 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(218): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.1323+152C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 13/41 | chr10 | 113641213 | ||||||
| chr10:113641272
|
AT | A | 344 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(341): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.1323+92delA | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 13/41 | chr10 | 113641272 | ||||||
| chr10:113641284
|
G | A | 1 | a0008c0007t0002g0095 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1323+81C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 13/41 | chr10 | 113641284 | ||||||
| chr10:113641322
|
T | C | 221 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(218): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.1323+43A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 13/41 | chr10 | 113641322 | ||||||
| chr10:113641327
|
C | G | 1 | a0007c0083t0003g0346 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1323+38G>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 13/41 | chr10 | 113641327 | ||||||
| chr10:113641505
|
A | G | 221 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(218): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.1216-33T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 12/41 | chr10 | 113641505 | ||||||
| chr10:113641570
|
A | T | 1 | a0066c0095t0003g0302 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1216-98T>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 12/41 | chr10 | 113641570 | ||||||
| chr10:113641592
|
A | G | 1 | a0005c0004t0005g0008 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1216-120T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 12/41 | chr10 | 113641592 | ||||||
| chr10:113641598
|
C | T | 1 | a0001c0001t0001g0138 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1216-126G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 12/41 | chr10 | 113641598 | ||||||
| chr10:113641606
|
A | G | 344 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(341): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.1216-134T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 12/41 | chr10 | 113641606 | ||||||
| chr10:113641608
|
A | G | 4 | a0002c0002t0004g0328a0002c0002t0004g0332a0002c0002t0004g0333others(1): Show | 4 | HG02602.hp2 HG03704.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.1216-136T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 12/41 | chr10 | 113641608 | ||||||
| chr10:113641666
|
T | C | 3 | a0034c0047t0003g0276a0034c0047t0003g0277a0046c0113t0004g0275 | 3 | HG02258.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1216-194A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 12/41 | chr10 | 113641666 | ||||||
| chr10:113641695
|
T | C | 1 | a0021c0073t0001g0270 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1216-223A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 12/41 | chr10 | 113641695 | ||||||
| chr10:113641708
|
G | A | 221 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(218): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.1216-236C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 12/41 | chr10 | 113641708 | ||||||
| chr10:113641805
|
G | A | 1 | a0011c0016t0004g0298 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1216-333C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 12/41 | chr10 | 113641805 | ||||||
| chr10:113641807
|
C | T | 220 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(217): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1216-335G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 12/41 | chr10 | 113641807 | ||||||
| chr10:113641808
|
A | G | 221 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(218): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.1216-336T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 12/41 | chr10 | 113641808 | ||||||
| chr10:113641833
|
G | A | 25 | a0011c0016t0004g0278a0011c0016t0004g0280a0011c0016t0004g0294others(22): Show | 28 | HG00408.hp2 HG00544.hp1 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.1216-361C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 12/41 | chr10 | 113641833 | ||||||
| chr10:113641960
|
C | T | 221 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(218): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.1216-488G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 12/41 | chr10 | 113641960 | ||||||
| chr10:113642002
|
T | C | 221 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(218): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.1216-530A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 12/41 | chr10 | 113642002 | ||||||
| chr10:113642028
|
A | T | 1 | a0001c0001t0001g0189 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1216-556T>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 12/41 | chr10 | 113642028 | ||||||
| chr10:113642054
|
T | C | 135 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(132): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.1216-582A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 12/41 | chr10 | 113642054 | ||||||
| chr10:113642125
|
C | T | 4 | a0021c0071t0002g0269a0021c0072t0001g0271a0021c0073t0001g0270others(1): Show | 4 | HG01891.hp2 HG02451.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1216-653G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 12/41 | chr10 | 113642125 | ||||||
| chr10:113642212
|
C | T | 1 | a0004c0005t0001g0115 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1215+722G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 12/41 | chr10 | 113642212 | ||||||
| chr10:113642243
|
G | T | 1 | a0019c0018t0001g0131 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1215+691C>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 12/41 | chr10 | 113642243 | ||||||
| chr10:113642316
|
G | A | 221 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(218): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.1215+618C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 12/41 | chr10 | 113642316 | ||||||
| chr10:113642385
|
T | A | 3 | a0034c0047t0003g0276a0034c0047t0003g0277a0046c0113t0004g0275 | 3 | HG02258.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1215+549A>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 12/41 | chr10 | 113642385 | ||||||
| chr10:113642393
|
G | A | 25 | a0011c0016t0004g0278a0011c0016t0004g0280a0011c0016t0004g0294others(22): Show | 28 | HG00408.hp2 HG00544.hp1 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.1215+541C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 12/41 | chr10 | 113642393 | ||||||
| chr10:113642488
|
G | A | 221 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(218): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.1215+446C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 12/41 | chr10 | 113642488 | ||||||
| chr10:113642721
|
G | A | 1 | a0045c0036t0008g0057 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1215+213C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 12/41 | chr10 | 113642721 | ||||||
| chr10:113642763
|
A | G | 2 | a0036c0103t0002g0192a0037c0045t0002g0162 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1215+171T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 12/41 | chr10 | 113642763 | ||||||
| chr10:113642772
|
A | G | 1 | a0078c0081t0001g0076 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1215+162T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 12/41 | chr10 | 113642772 | ||||||
| chr10:113642856
|
T | A | 3 | a0034c0047t0003g0276a0034c0047t0003g0277a0046c0113t0004g0275 | 3 | HG02258.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1215+78A>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 12/41 | chr10 | 113642856 | ||||||
| chr10:113642921
|
G | T | 2 | a0036c0103t0002g0192a0037c0045t0002g0162 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1215+13C>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 12/41 | chr10 | 113642921 | ||||||
| chr10:113643263
|
G | A | 1 | a0010c0008t0002g0247 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1111-225C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113643263 | ||||||
| chr10:113643428
|
C | T | 1 | a0079c0080t0002g0081 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1111-390G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113643428 | ||||||
| chr10:113643522
|
C | A | 2 | a0006c0006t0006g0053a0062c0063t0005g0054 | 2 | HG02258.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1111-484G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113643522 | ||||||
| chr10:113643534
|
G | T | 1 | a0026c0034t0002g0238 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1111-496C>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113643534 | ||||||
| chr10:113643569
|
C | G | 87 | a0002c0002t0004g0300a0002c0002t0004g0303a0002c0002t0004g0304others(84): Show | 87 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.1111-531G>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113643569 | ||||||
| chr10:113643612
|
T | C | 5 | a0010c0008t0002g0240a0010c0008t0002g0246a0010c0008t0002g0247others(2): Show | 5 | HG00642.hp2 HG01496.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.1111-574A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113643612 | ||||||
| chr10:113643828
|
C | T | 1 | a0059c0058t0002g0239 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1111-790G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113643828 | ||||||
| chr10:113644062
|
C | A | 1 | a0001c0001t0001g0185 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1111-1024G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113644062 | ||||||
| chr10:113644062
|
C | T | 1 | a0006c0006t0006g0041 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1111-1024G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113644062 | ||||||
| chr10:113644147
|
C | CAAAAA | 76 | a0002c0002t0004g0300a0002c0002t0004g0303a0002c0002t0004g0309others(73): Show | 76 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.1111-1114_1111-111 others(9): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113644147 | ||||||
| chr10:113644147
|
C | CAAAAAA | 37 | a0001c0001t0001g0135a0002c0002t0004g0307a0002c0002t0004g0372others(34): Show | 37 | HG00280.hp2 HG00438.hp1 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.1111-1115_1111-111 others(10): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113644147 | ||||||
| chr10:113644147
|
C | CAAAAAAA | 89 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(86): Show | 92 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(89): Show |
intron_variant | MODIFIER | c.1111-1116_1111-111 others(11): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113644147 | ||||||
| chr10:113644147
|
C | CAAAAAAA others(1): Show |
65 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0144others(62): Show | 67 | HG01071.hp1 HG01106.hp2 HG01109.hp1 others(64): Show |
intron_variant | MODIFIER | c.1111-1117_1111-111 others(12): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113644147 | ||||||
| chr10:113644147
|
C | CAAAAAAA others(2): Show |
46 | a0004c0005t0001g0104a0004c0005t0001g0106a0004c0005t0001g0167others(43): Show | 50 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.1111-1118_1111-111 others(13): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113644147 | ||||||
| chr10:113644147
|
C | CAAAAAAA others(3): Show |
15 | a0005c0004t0005g0025a0005c0004t0005g0028a0005c0004t0005g0035others(12): Show | 15 | HG00423.hp1 HG01109.hp2 HG01346.hp1 others(12): Show |
intron_variant | MODIFIER | c.1111-1119_1111-111 others(14): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113644147 | ||||||
| chr10:113644147
|
C | CAAAAAAA others(4): Show |
3 | a0014c0020t0005g0034a0028c0033t0001g0059a0060c0067t0005g0046 | 3 | HG02486.hp1 HG02602.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1111-1120_1111-111 others(15): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113644147 | ||||||
| chr10:113644147
|
C | CAAAAAAA others(5): Show |
1 | a0006c0006t0006g0018 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1111-1121_1111-111 others(16): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113644147 | ||||||
| chr10:113644147
|
C | CAAAAAAA others(6): Show |
1 | a0005c0004t0005g0019 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1111-1122_1111-111 others(17): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113644147 | ||||||
| chr10:113644233
|
G | C | 1 | a0009c0009t0001g0071 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1111-1195C>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113644233 | ||||||
| chr10:113644259
|
C | T | 49 | a0005c0004t0005g0001a0005c0004t0005g0008a0005c0004t0005g0016others(46): Show | 53 | HG00423.hp1 HG00621.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.1111-1221G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113644259 | ||||||
| chr10:113644288
|
G | A | 2 | a0002c0002t0004g0335a0002c0002t0004g0336 | 2 | HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1111-1250C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113644288 | ||||||
| chr10:113644463
|
C | T | 1 | a0016c0077t0002g0064 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1110+1362G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113644463 | ||||||
| chr10:113644486
|
G | A | 344 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(341): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.1110+1339C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113644486 | ||||||
| chr10:113644562
|
T | C | 1 | a0041c0041t0003g0279 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1110+1263A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113644562 | ||||||
| chr10:113644670
|
C | T | 1 | a0050c0107t0001g0206 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1110+1155G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113644670 | ||||||
| chr10:113644872
|
C | T | 3 | a0005c0004t0005g0028a0005c0004t0005g0040a0030c0027t0005g0014 | 3 | NA18952.hp2 NA18974.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.1110+953G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113644872 | ||||||
| chr10:113644960
|
A | G | 344 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(341): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.1110+865T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113644960 | ||||||
| chr10:113645186
|
A | T | 1 | a0066c0095t0003g0302 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1110+639T>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113645186 | ||||||
| chr10:113645190
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1110+635C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113645190 | ||||||
| chr10:113645191
|
T | G | 221 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(218): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.1110+634A>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113645191 | ||||||
| chr10:113645296
|
A | C | 221 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(218): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.1110+529T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113645296 | ||||||
| chr10:113645335
|
T | C | 2 | a0005c0004t0005g0045a0006c0064t0006g0012 | 2 | HG02071.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.1110+490A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113645335 | ||||||
| chr10:113645415
|
GTTGT | G | 221 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(218): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.1110+406_1110+409d others(6): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113645415 | ||||||
| chr10:113645494
|
C | T | 9 | a0026c0034t0002g0236a0026c0034t0002g0238a0026c0050t0002g0229others(6): Show | 9 | HG01891.hp1 HG02486.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1110+331G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113645494 | ||||||
| chr10:113645495
|
G | A | 3 | a0033c0028t0002g0232a0033c0028t0002g0233a0033c0028t0002g0234 | 3 | HG02559.hp2 HG02717.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1110+330C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113645495 | ||||||
| chr10:113645496
|
C | A | 1 | a0015c0012t0004g0284 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1110+329G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113645496 | ||||||
| chr10:113645497
|
G | A | 1 | a0009c0009t0001g0066 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1110+328C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113645497 | ||||||
| chr10:113645530
|
G | A | 135 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(132): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.1110+295C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113645530 | ||||||
| chr10:113645650
|
C | G | 9 | a0026c0034t0002g0236a0026c0034t0002g0238a0026c0050t0002g0229others(6): Show | 9 | HG01891.hp1 HG02486.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1110+175G>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113645650 | ||||||
| chr10:113645665
|
C | T | 1 | a0009c0009t0001g0066 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1110+160G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113645665 | ||||||
| chr10:113645707
|
G | A | 221 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(218): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.1110+118C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113645707 | ||||||
| chr10:113645710
|
C | A | 1 | a0026c0034t0002g0236 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1110+115G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113645710 | ||||||
| chr10:113645809
|
C | T | 2 | a0005c0004t0005g0043a0065c0059t0005g0044 | 2 | HG00733.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1110+16G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113645809 | ||||||
| chr10:113645818
|
T | TACGC | 3 | a0028c0033t0001g0059a0028c0033t0001g0060a0028c0048t0001g0058 | 3 | HG02572.hp2 HG02886.hp2 NA19240.hp1 |
splice_region_variant&intron_variant | LOW | c.1110+3_1110+6dupGC others(2): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113645818 | ||||||
| chr10:113645944
|
G | GAA | 215 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(212): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
splice_region_variant&intron_variant | LOW | c.994-5_994-4dupTT | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 10/41 | chr10 | 113645944 | ||||||
| chr10:113645944
|
G | GAAA | 6 | a0004c0005t0001g0113a0006c0006t0006g0053a0014c0062t0005g0055others(3): Show | 6 | HG02258.hp2 HG02895.hp1 HG02896.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.994-6_994-4dupTTT | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 10/41 | chr10 | 113645944 | ||||||
| chr10:113646009
|
A | C | 1 | a0009c0009t0001g0071 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.994-68T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 10/41 | chr10 | 113646009 | ||||||
| chr10:113646032
|
A | T | 221 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(218): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.994-91T>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 10/41 | chr10 | 113646032 | ||||||
| chr10:113646091
|
T | C | 2 | a0001c0001t0001g0142a0001c0001t0001g0143 | 2 | NA18956.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.994-150A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 10/41 | chr10 | 113646091 | ||||||
| chr10:113646159
|
A | C | 1 | a0033c0028t0002g0232 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.994-218T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 10/41 | chr10 | 113646159 | ||||||
| chr10:113646164
|
A | G | 2 | a0038c0046t0001g0168a0038c0046t0001g0177 | 2 | NA18939.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.994-223T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 10/41 | chr10 | 113646164 | ||||||
| chr10:113646179
|
G | A | 344 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(341): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.994-238C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 10/41 | chr10 | 113646179 | ||||||
| chr10:113646301
|
C | T | 4 | a0011c0026t0002g0237a0011c0042t0004g0341a0011c0042t0004g0342others(1): Show | 4 | HG02630.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.994-360G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 10/41 | chr10 | 113646301 | ||||||
| chr10:113646414
|
G | A | 1 | a0061c0061t0005g0038 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.994-473C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 10/41 | chr10 | 113646414 | ||||||
| chr10:113646463
|
A | G | 221 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(218): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.993+460T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 10/41 | chr10 | 113646463 | ||||||
| chr10:113646499
|
A | G | 1 | a0002c0002t0004g0303 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.993+424T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 10/41 | chr10 | 113646499 | ||||||
| chr10:113646548
|
A | G | 226 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(223): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.993+375T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 10/41 | chr10 | 113646548 | ||||||
| chr10:113646565
|
C | T | 136 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(133): Show | 138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): Show |
intron_variant | MODIFIER | c.993+358G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 10/41 | chr10 | 113646565 | ||||||
| chr10:113646609
|
C | G | 4 | a0011c0026t0002g0237a0011c0042t0004g0341a0011c0042t0004g0342others(1): Show | 4 | HG02630.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.993+314G>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 10/41 | chr10 | 113646609 | ||||||
| chr10:113646702
|
A | G | 225 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(222): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.993+221T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 10/41 | chr10 | 113646702 | ||||||
| chr10:113646726
|
C | T | 221 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(218): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.993+197G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 10/41 | chr10 | 113646726 | ||||||
| chr10:113646731
|
C | T | 1 | a0003c0003t0003g0340 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.993+192G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 10/41 | chr10 | 113646731 | ||||||
| chr10:113647389
|
T | G | 1 | a0002c0002t0004g0373 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.889-362A>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647389 | ||||||
| chr10:113647451
|
C | T | 25 | a0011c0016t0004g0278a0011c0016t0004g0280a0011c0016t0004g0294others(22): Show | 28 | HG00408.hp2 HG00544.hp1 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.889-424G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647451 | ||||||
| chr10:113647498
|
C | T | 9 | a0005c0004t0005g0045a0005c0004t0005g0049a0006c0064t0006g0012others(6): Show | 10 | HG01891.hp2 HG02071.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.889-471G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647498 | ||||||
| chr10:113647498
|
CCTCCCCA others(11): Show |
C | 1 | a0029c0029t0002g0114 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.889-489_889-472del others(18): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647498 | ||||||
| chr10:113647505
|
A | C | 9 | a0005c0004t0005g0045a0005c0004t0005g0049a0006c0064t0006g0012others(6): Show | 10 | HG01891.hp2 HG02071.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.889-478T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647505 | ||||||
| chr10:113647506
|
A | G | 4 | a0021c0071t0002g0269a0021c0072t0001g0271a0021c0073t0001g0270others(1): Show | 4 | HG01891.hp2 HG02451.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.889-479T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647506 | ||||||
| chr10:113647516
|
T | C | 5 | a0005c0004t0005g0045a0005c0004t0005g0049a0006c0064t0006g0012others(2): Show | 6 | HG02071.hp1 HG02523.hp2 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.889-489A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647516 | ||||||
| chr10:113647516
|
T | TCTCCCCC others(336): Show |
1 | a0014c0062t0005g0055 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.889-490_889-489ins others(343): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647516 | ||||||
| chr10:113647523
|
C | CAGTGGTA others(29): Show |
1 | a0021c0071t0002g0269 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.889-497_889-496ins others(36): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647523 | ||||||
| chr10:113647524
|
G | A | 11 | a0005c0004t0005g0040a0005c0004t0005g0045a0005c0004t0005g0049others(8): Show | 12 | HG01884.hp2 HG01891.hp2 HG02071.hp1 others(9): Show |
intron_variant | MODIFIER | c.889-497C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647524 | ||||||
| chr10:113647534
|
T | C | 3 | a0021c0072t0001g0271a0021c0073t0001g0270a0027c0049t0002g0266 | 3 | HG02451.hp2 HG02976.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.889-507A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647534 | ||||||
| chr10:113647534
|
T | TCTCCCCC others(11): Show |
2 | a0038c0046t0001g0168a0038c0046t0001g0177 | 2 | NA18939.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.889-508_889-507ins others(18): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647534 | ||||||
| chr10:113647536
|
T | TCCCCCAG others(246): Show |
1 | a0033c0028t0002g0232 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.889-510_889-509ins others(253): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647536 | ||||||
| chr10:113647536
|
T | TCCCCTGG others(30): Show |
3 | a0021c0072t0001g0271a0021c0073t0001g0270a0027c0049t0002g0266 | 3 | HG02451.hp2 HG02976.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.889-510_889-509ins others(37): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647536 | ||||||
| chr10:113647537
|
C | T | 1 | a0003c0003t0003g0386 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.889-510G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647537 | ||||||
| chr10:113647541
|
C | CAGTGGTA others(173): Show |
1 | a0013c0044t0002g0188 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.889-515_889-514ins others(180): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647541 | ||||||
| chr10:113647541
|
C | T | 7 | a0005c0004t0005g0045a0005c0004t0005g0049a0006c0064t0006g0012others(4): Show | 8 | HG01884.hp2 HG02071.hp1 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.889-514G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647541 | ||||||
| chr10:113647542
|
G | A | 205 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(202): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.889-515C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647542 | ||||||
| chr10:113647542
|
G | GGTGGTAC others(29): Show |
1 | a0043c0070t0005g0056 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.889-516_889-515ins others(36): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647542 | ||||||
| chr10:113647542
|
G | GGTGGTAC others(155): Show |
2 | a0038c0046t0001g0168a0038c0046t0001g0177 | 2 | NA18939.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.889-516_889-515ins others(162): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647542 | ||||||
| chr10:113647552
|
T | C | 210 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(207): Show | 218 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(215): Show |
intron_variant | MODIFIER | c.889-525A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647552 | ||||||
| chr10:113647559
|
C | CAGTGGTA others(228): Show |
1 | a0033c0028t0002g0234 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.889-533_889-532ins others(235): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647559 | ||||||
| chr10:113647560
|
A | AGTGGTAC others(65): Show |
31 | a0001c0001t0001g0207a0004c0005t0001g0106a0004c0005t0001g0108others(28): Show | 33 | HG00544.hp2 HG01167.hp1 HG01169.hp2 others(30): Show |
intron_variant | MODIFIER | c.889-534_889-533ins others(72): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647560 | ||||||
| chr10:113647560
|
A | AGTGGTAC others(83): Show |
1 | a0059c0058t0002g0239 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.889-534_889-533ins others(90): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647560 | ||||||
| chr10:113647560
|
A | G | 9 | a0013c0044t0002g0188a0014c0062t0005g0055a0021c0071t0002g0269others(6): Show | 9 | HG00099.hp2 HG01891.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.889-533T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647560 | ||||||
| chr10:113647570
|
C | CCTCCCCC others(65): Show |
3 | a0034c0047t0003g0276a0034c0047t0003g0277a0046c0113t0004g0275 | 3 | HG02258.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.889-544_889-543ins others(72): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647570 | ||||||
| chr10:113647570
|
C | T | 172 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(169): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.889-543G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647570 | ||||||
| chr10:113647577
|
T | C | 12 | a0005c0004t0005g0045a0005c0004t0005g0049a0006c0064t0006g0012others(9): Show | 13 | HG00099.hp2 HG01884.hp2 HG02071.hp1 others(10): Show |
intron_variant | MODIFIER | c.889-550A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647577 | ||||||
| chr10:113647577
|
T | TGGTGGTA others(283): Show |
1 | a0004c0005t0001g0104 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.889-551_889-550ins others(290): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647577 | ||||||
| chr10:113647577
|
T | TGGTGGTA others(173): Show |
1 | a0013c0019t0002g0176 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.889-551_889-550ins others(180): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647577 | ||||||
| chr10:113647577
|
T | TGGTGGTA others(174): Show |
1 | a0004c0005t0001g0126 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.889-551_889-550ins others(181): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647577 | ||||||
| chr10:113647577
|
T | TGGTGGTA others(173): Show |
88 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(85): Show | 88 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.889-551_889-550ins others(180): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647577 | ||||||
| chr10:113647577
|
T | TGGTGGTA others(227): Show |
1 | a0017c0014t0001g0172 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.889-551_889-550ins others(234): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647577 | ||||||
| chr10:113647577
|
T | TGGTGGTA others(318): Show |
2 | a0011c0016t0004g0278a0041c0041t0003g0279 | 2 | HG01884.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.889-551_889-550ins others(325): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647577 | ||||||
| chr10:113647577
|
TGGTGGTA others(29): Show |
T | 7 | a0022c0022t0001g0258a0022c0022t0001g0259a0022c0022t0001g0262others(4): Show | 7 | HG00597.hp1 HG02135.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.889-586_889-551del others(36): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647577 | ||||||
| chr10:113647578
|
G | A | 6 | a0005c0004t0005g0045a0005c0004t0005g0049a0006c0064t0006g0012others(3): Show | 7 | HG01884.hp2 HG02071.hp1 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.889-551C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647578 | ||||||
| chr10:113647578
|
GGTGGTAC others(11): Show |
G | 1 | a0033c0028t0002g0234 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.889-569_889-552del others(18): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647578 | ||||||
| chr10:113647587
|
T | G | 87 | a0001c0001t0001g0210a0005c0004t0005g0001a0005c0004t0005g0008others(84): Show | 94 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.889-560A>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647587 | ||||||
| chr10:113647588
|
C | T | 75 | a0001c0001t0001g0210a0005c0004t0005g0001a0005c0004t0005g0008others(72): Show | 81 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.889-561G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647588 | ||||||
| chr10:113647595
|
T | C | 87 | a0001c0001t0001g0210a0005c0004t0005g0001a0005c0004t0005g0008others(84): Show | 94 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.889-568A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647595 | ||||||
| chr10:113647596
|
A | AGTGGTAC others(137): Show |
1 | a0006c0006t0006g0053 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.889-570_889-569ins others(144): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647596 | ||||||
| chr10:113647596
|
A | AGTGGTAC others(137): Show |
8 | a0001c0001t0001g0210a0011c0026t0002g0237a0011c0042t0004g0341others(5): Show | 8 | HG01975.hp2 HG02559.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.889-570_889-569ins others(144): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647596 | ||||||
| chr10:113647596
|
A | AGTGGTAC others(533): Show |
1 | a0066c0095t0003g0302 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.889-570_889-569ins others(540): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647596 | ||||||
| chr10:113647596
|
A | AGTGGTAC others(137): Show |
39 | a0005c0004t0005g0001a0005c0004t0005g0008a0005c0004t0005g0016others(36): Show | 42 | HG00423.hp1 HG00621.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.889-570_889-569ins others(144): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647596 | ||||||
| chr10:113647596
|
A | AGTGGTAC others(155): Show |
1 | a0006c0006t0006g0010 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.889-570_889-569ins others(162): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647596 | ||||||
| chr10:113647596
|
A | AGTGGTAC others(371): Show |
2 | a0005c0004t0005g0022a0068c0068t0005g0023 | 2 | HG01981.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.889-570_889-569ins others(378): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647596 | ||||||
| chr10:113647596
|
A | AGTGGTAC others(191): Show |
1 | a0011c0016t0004g0299 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.889-570_889-569ins others(198): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647596 | ||||||
| chr10:113647596
|
A | AGTGGTAC others(11): Show |
32 | a0001c0001t0001g0207a0004c0005t0001g0106a0004c0005t0001g0108others(29): Show | 34 | HG00544.hp2 HG01109.hp2 HG01167.hp1 others(31): Show |
intron_variant | MODIFIER | c.889-587_889-570dup others(18): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647596 | ||||||
| chr10:113647596
|
A | AGTGGTAC others(642): Show |
1 | a0062c0063t0005g0054 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.889-570_889-569ins others(649): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647596 | ||||||
| chr10:113647596
|
A | G | 12 | a0005c0004t0005g0045a0005c0004t0005g0049a0006c0064t0006g0012others(9): Show | 13 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.889-569T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647596 | ||||||
| chr10:113647602
|
A | G | 4 | a0021c0071t0002g0269a0021c0072t0001g0271a0021c0073t0001g0270others(1): Show | 4 | HG01891.hp2 HG02451.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.889-575T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647602 | ||||||
| chr10:113647606
|
T | C | 28 | a0005c0004t0005g0045a0005c0004t0005g0049a0006c0006t0006g0010others(25): Show | 32 | HG00408.hp2 HG00544.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.889-579A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647606 | ||||||
| chr10:113647608
|
T | TC | 99 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(96): Show | 99 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(96): Show |
intron_variant | MODIFIER | c.889-582dupG | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647608 | ||||||
| chr10:113647613
|
C | T | 5 | a0005c0004t0005g0045a0005c0004t0005g0049a0006c0064t0006g0012others(2): Show | 6 | HG01884.hp2 HG02071.hp1 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.889-586G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647613 | ||||||
| chr10:113647614
|
G | A | 22 | a0011c0016t0004g0280a0011c0016t0004g0294a0011c0016t0004g0297others(19): Show | 25 | HG00408.hp2 HG00544.hp1 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.889-587C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647614 | ||||||
| chr10:113647623
|
T | G | 130 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(127): Show | 133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.889-596A>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647623 | ||||||
| chr10:113647624
|
C | T | 26 | a0011c0016t0004g0280a0011c0016t0004g0294a0011c0016t0004g0297others(23): Show | 29 | HG00408.hp2 HG00544.hp1 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.889-597G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647624 | ||||||
| chr10:113647631
|
T | A | 1 | a0027c0032t0002g0231 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.889-604A>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647631 | ||||||
| chr10:113647631
|
T | C | 108 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(105): Show | 108 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(105): Show |
intron_variant | MODIFIER | c.889-604A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647631 | ||||||
| chr10:113647632
|
A | G | 130 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(127): Show | 133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.889-605T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647632 | ||||||
| chr10:113647644
|
TC | T | 109 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.889-618delG | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647644 | ||||||
| chr10:113647645
|
C | CCCCCAGT others(245): Show |
22 | a0011c0016t0004g0280a0011c0016t0004g0294a0011c0016t0004g0297others(19): Show | 25 | HG00408.hp2 HG00544.hp1 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.889-619_889-618ins others(252): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647645 | ||||||
| chr10:113647645
|
C | CCCCCCGG others(47): Show |
46 | a0005c0004t0005g0001a0005c0004t0005g0008a0005c0004t0005g0016others(43): Show | 49 | HG00423.hp1 HG00621.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.889-619_889-618ins others(54): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647645 | ||||||
| chr10:113647645
|
C | CCCCCCGG others(119): Show |
1 | a0011c0026t0002g0237 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.889-619_889-618ins others(126): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647645 | ||||||
| chr10:113647645
|
C | CCCCCCGG others(65): Show |
1 | a0033c0028t0002g0233 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.889-619_889-618ins others(72): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647645 | ||||||
| chr10:113647645
|
C | CCCCCCGG others(29): Show |
31 | a0001c0001t0001g0207a0004c0005t0001g0106a0004c0005t0001g0108others(28): Show | 33 | HG00544.hp2 HG01167.hp1 HG01169.hp2 others(30): Show |
intron_variant | MODIFIER | c.889-619_889-618ins others(36): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647645 | ||||||
| chr10:113647645
|
C | CCCCCGGT others(10): Show |
1 | a0027c0049t0002g0266 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.889-619_889-618ins others(17): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647645 | ||||||
| chr10:113647645
|
C | CCCCCGGT others(28): Show |
1 | a0027c0032t0002g0231 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.889-619_889-618ins others(35): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647645 | ||||||
| chr10:113647645
|
C | CCCCCGGT others(83): Show |
1 | a0029c0029t0002g0114 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.889-619_889-618ins others(90): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647645 | ||||||
| chr10:113647645
|
C | CCCCCGGT others(155): Show |
4 | a0005c0004t0005g0045a0005c0004t0005g0049a0006c0064t0006g0012others(1): Show | 5 | HG02071.hp1 HG02523.hp2 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.889-619_889-618ins others(162): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647645 | ||||||
| chr10:113647645
|
C | CCCCCGGT others(64): Show |
9 | a0007c0010t0003g0349a0026c0034t0002g0236a0026c0034t0002g0238others(6): Show | 9 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.889-619_889-618ins others(71): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647645 | ||||||
| chr10:113647645
|
CCCCCCGG others(11): Show |
C | 1 | a0003c0003t0003g0316 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.889-636_889-619del others(18): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647645 | ||||||
| chr10:113647650
|
C | CGGTGGTA others(47): Show |
1 | a0011c0016t0004g0299 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.889-624_889-623ins others(54): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647650 | ||||||
| chr10:113647675
|
G | A | 215 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(212): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.889-648C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647675 | ||||||
| chr10:113647678
|
G | A | 1 | a0026c0034t0002g0238 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.889-651C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647678 | ||||||
| chr10:113647696
|
G | GCCTCCCC others(29): Show |
1 | a0001c0001t0001g0210 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.889-670_889-669ins others(36): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647696 | ||||||
| chr10:113647700
|
C | A | 4 | a0026c0034t0002g0236a0026c0034t0002g0238a0026c0050t0002g0229others(1): Show | 4 | HG01891.hp1 HG02486.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.889-673G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647700 | ||||||
| chr10:113647822
|
A | C | 4 | a0021c0071t0002g0269a0021c0072t0001g0271a0021c0073t0001g0270others(1): Show | 4 | HG01891.hp2 HG02451.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.889-795T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647822 | ||||||
| chr10:113647890
|
C | A | 1 | a0059c0058t0002g0239 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.889-863G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647890 | ||||||
| chr10:113648006
|
G | A | 128 | a0002c0002t0004g0300a0002c0002t0004g0303a0002c0002t0004g0304others(125): Show | 128 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.889-979C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648006 | ||||||
| chr10:113648071
|
C | T | 4 | a0002c0002t0004g0328a0002c0002t0004g0332a0002c0002t0004g0333others(1): Show | 4 | HG02602.hp2 HG03704.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.889-1044G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648071 | ||||||
| chr10:113648136
|
T | C | 1 | a0010c0008t0002g0256 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.889-1109A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648136 | ||||||
| chr10:113648155
|
G | T | 74 | a0005c0004t0005g0001a0005c0004t0005g0008a0005c0004t0005g0016others(71): Show | 81 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.889-1128C>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648155 | ||||||
| chr10:113648249
|
C | T | 26 | a0010c0008t0002g0240a0010c0008t0002g0241a0010c0008t0002g0242others(23): Show | 26 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(23): Show |
intron_variant | MODIFIER | c.889-1222G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648249 | ||||||
| chr10:113648279
|
G | A | 1 | a0017c0014t0001g0181 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.889-1252C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648279 | ||||||
| chr10:113648309
|
G | T | 1 | a0013c0044t0002g0214 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.889-1282C>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648309 | ||||||
| chr10:113648437
|
T | TCTCTCTC others(4): Show |
2 | a0001c0001t0001g0211a0048c0102t0001g0136 | 2 | HG01928.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.889-1411_889-1410i others(13): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648437 | ||||||
| chr10:113648437
|
T | TCTCTCTC others(6): Show |
1 | a0020c0017t0002g0119 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.889-1411_889-1410i others(15): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648437 | ||||||
| chr10:113648437
|
T | TTC | 26 | a0001c0001t0001g0161a0002c0002t0004g0304a0002c0002t0004g0335others(23): Show | 29 | HG00323.hp2 HG00408.hp2 HG00544.hp1 others(26): Show |
intron_variant | MODIFIER | c.889-1412_889-1411d others(4): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648437 | ||||||
| chr10:113648437
|
T | TTCCCTCT others(7): Show |
1 | a0001c0001t0001g0205 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.889-1411_889-1410i others(16): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648437 | ||||||
| chr10:113648437
|
T | TTCTC | 52 | a0001c0001t0001g0191a0002c0002t0004g0309a0002c0002t0004g0328others(49): Show | 52 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.889-1414_889-1411d others(6): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648437 | ||||||
| chr10:113648437
|
T | TTCTCTC | 33 | a0001c0001t0001g0139a0001c0001t0001g0141a0001c0001t0001g0142others(30): Show | 33 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.889-1416_889-1411d others(8): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648437 | ||||||
| chr10:113648437
|
T | TTCTCTCT others(1): Show |
18 | a0001c0001t0001g0137a0001c0001t0001g0144a0001c0001t0001g0157others(15): Show | 18 | HG01069.hp2 HG01071.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.889-1418_889-1411d others(10): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648437 | ||||||
| chr10:113648437
|
T | TTCTCTCT others(3): Show |
35 | a0001c0001t0001g0138a0001c0001t0001g0145a0001c0001t0001g0146others(32): Show | 35 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.889-1420_889-1411d others(12): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648437 | ||||||
| chr10:113648437
|
T | TTCTCTCT others(5): Show |
19 | a0001c0001t0001g0147a0001c0001t0001g0152a0001c0001t0001g0156others(16): Show | 22 | HG00423.hp1 HG00438.hp2 HG00621.hp1 others(19): Show |
intron_variant | MODIFIER | c.889-1422_889-1411d others(14): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648437 | ||||||
| chr10:113648437
|
T | TTCTCTCT others(7): Show |
2 | a0001c0001t0001g0135a0001c0001t0001g0198 | 2 | NA18986.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.889-1424_889-1411d others(16): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648437 | ||||||
| chr10:113648437
|
T | TTCTCTCT others(9): Show |
3 | a0019c0018t0001g0163a0019c0018t0001g0165a0062c0063t0005g0054 | 3 | HG02109.hp2 HG02258.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.889-1426_889-1411d others(18): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648437 | ||||||
| chr10:113648437
|
T | TTCTCTCT others(15): Show |
1 | a0006c0006t0006g0053 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.889-1432_889-1411d others(24): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648437 | ||||||
| chr10:113648437
|
TTC | T | 4 | a0007c0010t0003g0312a0018c0076t0001g0099a0028c0033t0001g0059others(1): Show | 4 | HG02572.hp2 HG02886.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.889-1412_889-1411d others(4): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648437 | ||||||
| chr10:113648461
|
CTCTCTCT others(1): Show |
C | 3 | a0034c0047t0003g0276a0034c0047t0003g0277a0046c0113t0004g0275 | 3 | HG02258.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.889-1442_889-1435d others(10): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648461 | ||||||
| chr10:113648463
|
C | A | 1 | a0033c0028t0002g0234 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.889-1436G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648463 | ||||||
| chr10:113648465
|
C | A | 3 | a0033c0028t0002g0232a0033c0028t0002g0233a0033c0028t0002g0234 | 3 | HG02559.hp2 HG02717.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.889-1438G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648465 | ||||||
| chr10:113648465
|
CTCTA | C | 3 | a0011c0016t0004g0278a0011c0016t0004g0297a0041c0041t0003g0279 | 3 | HG01884.hp1 HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.889-1442_889-1439d others(6): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648465 | ||||||
| chr10:113648467
|
C | A | 7 | a0003c0003t0003g0369a0007c0084t0003g0345a0026c0034t0002g0238others(4): Show | 7 | HG02145.hp2 HG02559.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.889-1440G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648467 | ||||||
| chr10:113648467
|
C | CTA | 4 | a0011c0016t0004g0280a0012c0011t0003g0289a0012c0011t0003g0290others(1): Show | 4 | HG04199.hp2 NA18948.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.889-1442_889-1441d others(4): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648467 | ||||||
| chr10:113648467
|
C | CTATA | 4 | a0001c0109t0001g0155a0002c0002t0004g0336a0003c0003t0003g0371others(1): Show | 4 | HG04115.hp2 NA18970.hp1 NA19087.hp1 others(1): Show |
intron_variant | MODIFIER | c.889-1444_889-1441d others(6): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648467 | ||||||
| chr10:113648467
|
C | CTATATA | 8 | a0003c0003t0003g0353a0003c0023t0003g0318a0004c0021t0001g0124others(5): Show | 8 | HG00597.hp1 HG02273.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.889-1446_889-1441d others(8): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648467 | ||||||
| chr10:113648467
|
C | CTATATAT others(1): Show |
3 | a0004c0005t0001g0128a0039c0096t0002g0130a0039c0098t0002g0129 | 3 | HG00544.hp2 HG02074.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.889-1448_889-1441d others(10): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648467 | ||||||
| chr10:113648467
|
C | CTCTA | 14 | a0002c0002t0004g0333a0002c0002t0004g0344a0002c0002t0004g0370others(11): Show | 14 | HG00621.hp2 HG01243.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.889-1441_889-1440i others(6): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648467 | ||||||
| chr10:113648467
|
C | CTCTATA | 11 | a0003c0003t0003g0350a0007c0010t0014g0351a0010c0008t0002g0241others(8): Show | 11 | HG00733.hp1 HG00735.hp2 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.889-1441_889-1440i others(8): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648467 | ||||||
| chr10:113648467
|
C | CTCTATAT others(1): Show |
5 | a0004c0005t0001g0126a0004c0021t0001g0125a0005c0004t0005g0035others(2): Show | 5 | HG02132.hp1 HG02165.hp1 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.889-1441_889-1440i others(10): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648467 | ||||||
| chr10:113648467
|
C | CTCTATAT others(3): Show |
1 | a0004c0021t0001g0132 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.889-1441_889-1440i others(12): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648467 | ||||||
| chr10:113648467
|
C | CTCTATAT others(5): Show |
2 | a0016c0013t0002g0062a0057c0097t0001g0105 | 2 | HG02622.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.889-1441_889-1440i others(14): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648467 | ||||||
| chr10:113648467
|
C | CTCTCTA | 14 | a0003c0003t0003g0381a0007c0010t0003g0349a0007c0010t0003g0378others(11): Show | 14 | HG00280.hp2 HG00323.hp1 HG01123.hp2 others(11): Show |
intron_variant | MODIFIER | c.889-1441_889-1440i others(8): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648467 | ||||||
| chr10:113648467
|
C | CTCTCTAT others(1): Show |
7 | a0004c0075t0001g0160a0005c0004t0005g0022a0005c0004t0005g0024others(4): Show | 8 | HG01981.hp1 HG03579.hp1 NA18956.hp2 others(5): Show |
intron_variant | MODIFIER | c.889-1441_889-1440i others(10): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648467 | ||||||
| chr10:113648467
|
C | CTCTCTAT others(3): Show |
4 | a0008c0007t0009g0094a0014c0020t0005g0036a0016c0013t0002g0061others(1): Show | 4 | HG01261.hp2 HG03239.hp1 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.889-1441_889-1440i others(12): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648467 | ||||||
| chr10:113648467
|
C | CTCTCTAT others(5): Show |
6 | a0004c0005t0001g0104a0004c0005t0001g0167a0006c0006t0006g0041others(3): Show | 7 | HG02004.hp1 HG02572.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.889-1441_889-1440i others(14): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648467 | ||||||
| chr10:113648467
|
C | CTCTCTCT others(1): Show |
10 | a0004c0005t0001g0111a0004c0021t0001g0120a0004c0021t0003g0387others(7): Show | 10 | HG01081.hp1 HG01109.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.889-1441_889-1440i others(10): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648467 | ||||||
| chr10:113648467
|
C | CTCTCTCT others(3): Show |
6 | a0001c0001t0001g0201a0001c0001t0001g0222a0011c0026t0006g0026others(3): Show | 6 | HG01346.hp1 HG02055.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.889-1441_889-1440i others(12): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648467 | ||||||
| chr10:113648467
|
C | CTCTCTCT others(5): Show |
6 | a0001c0001t0001g0154a0003c0003t0003g0340a0004c0005t0001g0127others(3): Show | 6 | HG01099.hp2 HG01978.hp1 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.889-1441_889-1440i others(14): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648467 | ||||||
| chr10:113648467
|
C | CTCTCTCT others(9): Show |
4 | a0004c0005t0001g0106a0005c0004t0005g0043a0005c0065t0005g0050others(1): Show | 4 | HG00733.hp2 HG02615.hp1 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.889-1441_889-1440i others(18): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648467 | ||||||
| chr10:113648467
|
C | CTCTCTCT others(3): Show |
7 | a0001c0001t0001g0200a0001c0001t0001g0212a0001c0001t0001g0213others(4): Show | 7 | HG00099.hp1 HG01361.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.889-1441_889-1440i others(12): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648467 | ||||||
| chr10:113648467
|
C | CTCTCTCT others(5): Show |
14 | a0001c0001t0001g0218a0001c0110t0001g0202a0004c0005t0001g0166others(11): Show | 14 | HG00423.hp2 HG00741.hp1 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.889-1441_889-1440i others(14): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648467 | ||||||
| chr10:113648467
|
C | CTCTCTCT others(7): Show |
2 | a0001c0001t0001g0220a0006c0006t0006g0039 | 2 | HG01978.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.889-1441_889-1440i others(16): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648467 | ||||||
| chr10:113648467
|
C | CTCTCTCT others(11): Show |
1 | a0027c0032t0002g0231 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.889-1441_889-1440i others(20): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648467 | ||||||
| chr10:113648467
|
C | CTCTCTCT others(5): Show |
7 | a0001c0001t0001g0153a0001c0001t0001g0216a0001c0001t0001g0217others(4): Show | 8 | HG01257.hp2 HG01496.hp1 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.889-1441_889-1440i others(14): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648467 | ||||||
| chr10:113648467
|
C | CTCTCTCT others(7): Show |
3 | a0001c0001t0001g0223a0006c0006t0006g0009a0014c0062t0005g0055 | 3 | HG01975.hp1 HG02895.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.889-1441_889-1440i others(16): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648467 | ||||||
| chr10:113648467
|
C | CTCTCTCT others(9): Show |
1 | a0005c0004t0005g0040 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.889-1441_889-1440i others(18): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648467 | ||||||
| chr10:113648467
|
C | CTCTCTCT others(11): Show |
1 | a0027c0032t0002g0230 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.889-1441_889-1440i others(20): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648467 | ||||||
| chr10:113648467
|
C | CTCTCTCT others(7): Show |
2 | a0004c0005t0001g0122a0014c0060t0005g0021 | 2 | HG01255.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.889-1441_889-1440i others(16): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648467 | ||||||
| chr10:113648467
|
C | CTCTCTCT others(9): Show |
2 | a0001c0001t0001g0219a0020c0017t0002g0133 | 2 | HG01192.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.889-1441_889-1440i others(18): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648467 | ||||||
| chr10:113648467
|
CTA | C | 5 | a0001c0001t0001g0140a0009c0009t0001g0002a0011c0026t0002g0237others(2): Show | 7 | HG00642.hp1 HG01106.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.889-1442_889-1441d others(4): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648467 | ||||||
| chr10:113648469
|
A | C | 130 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(127): Show | 131 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.889-1442T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648469 | ||||||
| chr10:113648471
|
A | C | 53 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(50): Show | 55 | HG00558.hp1 HG00642.hp1 HG01106.hp1 others(52): Show |
intron_variant | MODIFIER | c.889-1444T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648471 | ||||||
| chr10:113648473
|
A | C | 21 | a0001c0001t0001g0135a0001c0001t0001g0138a0001c0001t0001g0169others(18): Show | 21 | HG02015.hp2 HG02056.hp2 HG02523.hp1 others(18): Show |
intron_variant | MODIFIER | c.889-1446T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648473 | ||||||
| chr10:113648475
|
A | C | 5 | a0001c0001t0001g0169a0011c0042t0004g0341a0011c0042t0004g0342others(2): Show | 5 | HG02630.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.889-1448T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648475 | ||||||
| chr10:113648477
|
A | C | 1 | a0041c0041t0003g0343 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.889-1450T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648477 | ||||||
| chr10:113648479
|
A | C | 1 | a0041c0041t0003g0343 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.889-1452T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648479 | ||||||
| chr10:113648649
|
G | A | 128 | a0002c0002t0004g0300a0002c0002t0004g0303a0002c0002t0004g0304others(125): Show | 128 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.888+1388C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648649 | ||||||
| chr10:113648808
|
G | A | 2 | a0002c0002t0004g0372a0002c0002t0004g0373 | 2 | NA18988.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.888+1229C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648808 | ||||||
| chr10:113648877
|
G | A | 6 | a0026c0034t0002g0236a0026c0034t0002g0238a0026c0050t0002g0229others(3): Show | 6 | HG01891.hp1 HG02486.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.888+1160C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648877 | ||||||
| chr10:113648920
|
G | T | 216 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(213): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.888+1117C>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648920 | ||||||
| chr10:113648935
|
A | G | 1 | a0009c0009t0001g0071 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.888+1102T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648935 | ||||||
| chr10:113649114
|
C | A | 1 | a0062c0063t0005g0054 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.888+923G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113649114 | ||||||
| chr10:113649258
|
T | C | 3 | a0008c0007t0002g0095a0008c0007t0002g0096a0018c0015t0001g0097 | 3 | HG00558.hp2 NA18990.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.888+779A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113649258 | ||||||
| chr10:113649278
|
T | C | 1 | a0014c0062t0005g0055 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.888+759A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113649278 | ||||||
| chr10:113649310
|
A | T | 216 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(213): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.888+727T>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113649310 | ||||||
| chr10:113649318
|
A | C | 2 | a0028c0033t0001g0059a0028c0033t0001g0060 | 2 | HG02572.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.888+719T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113649318 | ||||||
| chr10:113649474
|
T | A | 1 | a0005c0004t0005g0045 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.888+563A>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113649474 | ||||||
| chr10:113649640
|
A | C | 345 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(342): Show | 354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.888+397T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113649640 | ||||||
| chr10:113649709
|
A | T | 130 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(127): Show | 132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.888+328T>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113649709 | ||||||
| chr10:113649775
|
T | C | 4 | a0021c0071t0002g0269a0021c0072t0001g0271a0021c0073t0001g0270others(1): Show | 4 | HG01891.hp2 HG02451.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.888+262A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113649775 | ||||||
| chr10:113649798
|
G | A | 9 | a0026c0034t0002g0236a0026c0034t0002g0238a0026c0050t0002g0229others(6): Show | 9 | HG01891.hp1 HG02486.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.888+239C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113649798 | ||||||
| chr10:113649855
|
G | A | 1 | a0013c0019t0002g0203 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.888+182C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113649855 | ||||||
| chr10:113649915
|
T | C | 3 | a0028c0033t0001g0059a0028c0033t0001g0060a0028c0048t0001g0058 | 3 | HG02572.hp2 HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.888+122A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113649915 | ||||||
| chr10:113649927
|
G | A | 1 | a0002c0002t0004g0300 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.888+110C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113649927 | ||||||
| chr10:113650166
|
C | G | 3 | a0011c0016t0004g0278a0011c0016t0004g0297a0041c0041t0003g0279 | 3 | HG01884.hp1 HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.784-25G>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 8/41 | chr10 | 113650166 | ||||||
| chr10:113650166
|
C | T | 4 | a0021c0071t0002g0269a0021c0072t0001g0271a0021c0073t0001g0270others(1): Show | 4 | HG01891.hp2 HG02451.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.784-25G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 8/41 | chr10 | 113650166 | ||||||
| chr10:113650167
|
G | A | 2 | a0027c0032t0002g0230a0027c0032t0002g0231 | 2 | NA18906.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.784-26C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 8/41 | chr10 | 113650167 | ||||||
| chr10:113650285
|
C | T | 1 | a0014c0062t0005g0055 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.784-144G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 8/41 | chr10 | 113650285 | ||||||
| chr10:113650812
|
G | A | 1 | a0001c0001t0001g0220 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.676-267C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 7/41 | chr10 | 113650812 | ||||||
| chr10:113650899
|
A | G | 216 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(213): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.676-354T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 7/41 | chr10 | 113650899 | ||||||
| chr10:113650948
|
T | A | 1 | a0010c0008t0002g0256 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.676-403A>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 7/41 | chr10 | 113650948 | ||||||
| chr10:113651069
|
A | T | 216 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(213): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.676-524T>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 7/41 | chr10 | 113651069 | ||||||
| chr10:113651080
|
A | C | 9 | a0026c0034t0002g0236a0026c0034t0002g0238a0026c0050t0002g0229others(6): Show | 9 | HG01891.hp1 HG02486.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.676-535T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 7/41 | chr10 | 113651080 | ||||||
| chr10:113651304
|
T | C | 3 | a0011c0016t0004g0278a0011c0016t0004g0297a0041c0041t0003g0279 | 3 | HG01884.hp1 HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.675+499A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 7/41 | chr10 | 113651304 | ||||||
| chr10:113651318
|
T | G | 1 | a0020c0017t0002g0107 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.675+485A>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 7/41 | chr10 | 113651318 | ||||||
| chr10:113651386
|
G | T | 6 | a0026c0034t0002g0236a0026c0034t0002g0238a0026c0050t0002g0229others(3): Show | 6 | HG01891.hp1 HG02486.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.675+417C>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 7/41 | chr10 | 113651386 | ||||||
| chr10:113651404
|
T | C | 1 | a0027c0049t0002g0266 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.675+399A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 7/41 | chr10 | 113651404 | ||||||
| chr10:113651483
|
T | C | 131 | a0002c0002t0004g0300a0002c0002t0004g0303a0002c0002t0004g0304others(128): Show | 131 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.675+320A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 7/41 | chr10 | 113651483 | ||||||
| chr10:113651507
|
G | C | 89 | a0002c0002t0004g0300a0002c0002t0004g0303a0002c0002t0004g0304others(86): Show | 89 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.675+296C>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 7/41 | chr10 | 113651507 | ||||||
| chr10:113651546
|
G | C | 1 | a0002c0002t0004g0374 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.675+257C>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 7/41 | chr10 | 113651546 | ||||||
| chr10:113651609
|
G | A | 1 | a0012c0011t0003g0292 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.675+194C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 7/41 | chr10 | 113651609 | ||||||
| chr10:113651670
|
C | T | 3 | a0034c0047t0003g0276a0034c0047t0003g0277a0046c0113t0004g0275 | 3 | HG02258.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.675+133G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 7/41 | chr10 | 113651670 | ||||||
| chr10:113651721
|
T | C | 1 | a0011c0016t0004g0298 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.675+82A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 7/41 | chr10 | 113651721 | ||||||
| chr10:113651914
|
A | G | 1 | a0001c0001t0001g0137 | 1 | NA19009.hp2 | splice_region_variant&intron_variant | LOW | c.571-7T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 6/41 | chr10 | 113651914 | ||||||
| chr10:113651951
|
C | A | 1 | a0001c0001t0013g0204 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.571-44G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 6/41 | chr10 | 113651951 | ||||||
| chr10:113652029
|
T | G | 3 | a0028c0033t0001g0059a0028c0033t0001g0060a0028c0048t0001g0058 | 3 | HG02572.hp2 HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.571-122A>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 6/41 | chr10 | 113652029 | ||||||
| chr10:113652073
|
C | A | 6 | a0026c0034t0002g0236a0026c0034t0002g0238a0026c0050t0002g0229others(3): Show | 6 | HG01891.hp1 HG02486.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.571-166G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 6/41 | chr10 | 113652073 | ||||||
| chr10:113652168
|
ATGTTT | A | 218 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(215): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.571-266_571-262del others(5): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 6/41 | chr10 | 113652168 | ||||||
| chr10:113652201
|
A | G | 345 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(342): Show | 354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.571-294T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 6/41 | chr10 | 113652201 | ||||||
| chr10:113652438
|
A | G | 347 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(344): Show | 356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.570+497T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 6/41 | chr10 | 113652438 | ||||||
| chr10:113652455
|
C | A | 4 | a0002c0002t0004g0309a0007c0010t0003g0308a0007c0010t0003g0312others(1): Show | 4 | HG00621.hp2 NA18747.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.570+480G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 6/41 | chr10 | 113652455 | ||||||
| chr10:113652517
|
T | TGCCTGTA others(30): Show |
1 | a0001c0109t0001g0155 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.570+381_570+417dup others(37): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 6/41 | chr10 | 113652517 | ||||||
| chr10:113652668
|
G | A | 127 | a0002c0002t0004g0300a0002c0002t0004g0303a0002c0002t0004g0304others(124): Show | 127 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.570+267C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 6/41 | chr10 | 113652668 | ||||||
| chr10:113652768
|
G | A | 1 | a0018c0015t0001g0097 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.570+167C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 6/41 | chr10 | 113652768 | ||||||
| chr10:113652793
|
G | A | 1 | a0013c0019t0002g0224 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.570+142C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 6/41 | chr10 | 113652793 | ||||||
| chr10:113652927
|
G | A | 345 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(342): Show | 354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
splice_region_variant&intron_variant | LOW | c.570+8C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 6/41 | chr10 | 113652927 | ||||||
| chr10:113652928
|
C | T | 47 | a0005c0004t0005g0001a0005c0004t0005g0008a0005c0004t0005g0016others(44): Show | 51 | HG00423.hp1 HG00621.hp1 HG00639.hp2 others(48): Show |
splice_region_variant&intron_variant | LOW | c.570+7G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 6/41 | chr10 | 113652928 | ||||||
| chr10:113653082
|
T | C | 1 | a0008c0007t0002g0068 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.466-43A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 5/41 | chr10 | 113653082 | ||||||
| chr10:113653104
|
G | A | 2 | a0027c0032t0002g0230a0027c0032t0002g0231 | 2 | NA18906.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.466-65C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 5/41 | chr10 | 113653104 | ||||||
| chr10:113653194
|
T | C | 1 | a0015c0012t0004g0293 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.466-155A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 5/41 | chr10 | 113653194 | ||||||
| chr10:113653326
|
C | T | 127 | a0002c0002t0004g0300a0002c0002t0004g0303a0002c0002t0004g0304others(124): Show | 127 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.466-287G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 5/41 | chr10 | 113653326 | ||||||
| chr10:113653359
|
C | T | 127 | a0002c0002t0004g0300a0002c0002t0004g0303a0002c0002t0004g0304others(124): Show | 127 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.466-320G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 5/41 | chr10 | 113653359 | ||||||
| chr10:113653408
|
C | G | 1 | a0018c0015t0001g0070 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.466-369G>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 5/41 | chr10 | 113653408 | ||||||
| chr10:113653461
|
A | C | 4 | a0011c0026t0002g0237a0011c0042t0004g0341a0011c0042t0004g0342others(1): Show | 4 | HG02630.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.466-422T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 5/41 | chr10 | 113653461 | ||||||
| chr10:113653566
|
G | C | 127 | a0002c0002t0004g0300a0002c0002t0004g0303a0002c0002t0004g0304others(124): Show | 127 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.465+455C>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 5/41 | chr10 | 113653566 | ||||||
| chr10:113653728
|
T | C | 345 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(342): Show | 354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.465+293A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 5/41 | chr10 | 113653728 | ||||||
| chr10:113653798
|
A | C | 345 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(342): Show | 354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.465+223T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 5/41 | chr10 | 113653798 | ||||||
| chr10:113653799
|
C | T | 218 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(215): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.465+222G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 5/41 | chr10 | 113653799 | ||||||
| chr10:113653903
|
T | G | 1 | a0001c0001t0001g0205 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.465+118A>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 5/41 | chr10 | 113653903 | ||||||
| chr10:113653941
|
T | C | 1 | a0026c0034t0002g0238 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.465+80A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 5/41 | chr10 | 113653941 | ||||||
| chr10:113654142
|
T | C | 127 | a0002c0002t0004g0300a0002c0002t0004g0303a0002c0002t0004g0304others(124): Show | 127 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.361-17A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113654142 | ||||||
| chr10:113654198
|
A | AAGAAGAT others(335): Show |
1 | a0028c0033t0001g0060 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.361-74_361-73insGG others(340): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113654198 | ||||||
| chr10:113654198
|
A | AAGAAGAT others(336): Show |
1 | a0028c0048t0001g0058 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.361-74_361-73insGG others(341): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113654198 | ||||||
| chr10:113654198
|
A | AAGAAGAT others(337): Show |
1 | a0028c0033t0001g0059 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.361-74_361-73insGG others(342): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113654198 | ||||||
| chr10:113654241
|
T | C | 20 | a0011c0016t0004g0280a0011c0016t0004g0294a0012c0011t0003g0007others(17): Show | 23 | HG00408.hp2 HG00544.hp1 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.361-116A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113654241 | ||||||
| chr10:113654391
|
G | A | 127 | a0002c0002t0004g0300a0002c0002t0004g0303a0002c0002t0004g0304others(124): Show | 127 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.361-266C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113654391 | ||||||
| chr10:113654408
|
A | T | 218 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(215): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.361-283T>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113654408 | ||||||
| chr10:113654412
|
T | C | 1 | a0011c0016t0004g0298 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.361-287A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113654412 | ||||||
| chr10:113654507
|
C | CA | 93 | a0002c0002t0004g0303a0002c0002t0004g0304a0002c0002t0004g0307others(90): Show | 93 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.361-383dupT | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113654507 | ||||||
| chr10:113654507
|
C | CAA | 30 | a0010c0008t0002g0240a0010c0008t0002g0241a0010c0008t0002g0242others(27): Show | 30 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.361-384_361-383dup others(2): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113654507 | ||||||
| chr10:113654507
|
CA | C | 20 | a0011c0016t0004g0280a0012c0011t0003g0007a0012c0011t0003g0272others(17): Show | 23 | HG00408.hp2 HG00544.hp1 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.361-383delT | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113654507 | ||||||
| chr10:113654507
|
CAAA | C | 185 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(182): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.361-385_361-383del others(3): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113654507 | ||||||
| chr10:113654520
|
A | G | 3 | a0033c0028t0002g0232a0033c0028t0002g0233a0033c0028t0002g0234 | 3 | HG02559.hp2 HG02717.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.361-395T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113654520 | ||||||
| chr10:113654607
|
G | A | 1 | a0060c0067t0005g0046 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.361-482C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113654607 | ||||||
| chr10:113654632
|
T | C | 2 | a0002c0002t0004g0377a0026c0050t0002g0229 | 2 | HG01891.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.361-507A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113654632 | ||||||
| chr10:113654751
|
G | A | 6 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0210others(3): Show | 6 | HG01099.hp1 HG01928.hp2 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.361-626C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113654751 | ||||||
| chr10:113654779
|
T | C | 127 | a0002c0002t0004g0300a0002c0002t0004g0303a0002c0002t0004g0304others(124): Show | 127 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.361-654A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113654779 | ||||||
| chr10:113654780
|
T | A | 1 | a0001c0001t0001g0156 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.361-655A>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113654780 | ||||||
| chr10:113654832
|
A | T | 1 | a0064c0093t0004g0281 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.361-707T>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113654832 | ||||||
| chr10:113654919
|
TA | T | 14 | a0002c0002t0004g0335a0002c0002t0004g0336a0002c0002t0004g0344others(11): Show | 14 | HG00738.hp1 HG01243.hp2 HG01358.hp2 others(11): Show |
intron_variant | MODIFIER | c.361-795delT | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113654919 | ||||||
| chr10:113654925
|
C | T | 12 | a0010c0008t0002g0240a0010c0008t0002g0241a0010c0008t0002g0242others(9): Show | 12 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.361-800G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113654925 | ||||||
| chr10:113655081
|
A | C | 127 | a0002c0002t0004g0300a0002c0002t0004g0303a0002c0002t0004g0304others(124): Show | 127 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.361-956T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113655081 | ||||||
| chr10:113655152
|
A | G | 129 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(126): Show | 131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.361-1027T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113655152 | ||||||
| chr10:113655215
|
G | T | 7 | a0022c0022t0001g0258a0022c0022t0001g0259a0022c0022t0001g0262others(4): Show | 7 | HG00597.hp1 HG02135.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.361-1090C>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113655215 | ||||||
| chr10:113655234
|
G | A | 1 | a0026c0050t0002g0229 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.361-1109C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113655234 | ||||||
| chr10:113655242
|
A | G | 1 | a0066c0095t0003g0302 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.361-1117T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113655242 | ||||||
| chr10:113655448
|
A | ATCCATTC others(1): Show |
6 | a0021c0071t0002g0269a0021c0072t0001g0271a0021c0073t0001g0270others(3): Show | 6 | HG01891.hp2 HG02451.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.361-1324_361-1323i others(10): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113655448 | ||||||
| chr10:113655452
|
A | ATTC | 210 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(207): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.361-1328_361-1327i others(5): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113655452 | ||||||
| chr10:113655452
|
AT | A | 88 | a0002c0002t0004g0300a0002c0002t0004g0303a0002c0002t0004g0304others(85): Show | 90 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.361-1328delA | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113655452 | ||||||
| chr10:113655453
|
T | TTC | 8 | a0001c0001t0001g0212a0005c0004t0005g0047a0011c0026t0002g0237others(5): Show | 8 | HG01361.hp1 HG02630.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.361-1329_361-1328i others(4): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113655453 | ||||||
| chr10:113655455
|
T | C | 42 | a0007c0084t0003g0345a0010c0008t0002g0240a0010c0008t0002g0241others(39): Show | 42 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.361-1330A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113655455 | ||||||
| chr10:113655456
|
T | C | 84 | a0002c0002t0004g0300a0002c0002t0004g0303a0002c0002t0004g0304others(81): Show | 84 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.361-1331A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113655456 | ||||||
| chr10:113655457
|
T | C | 1 | a0007c0010t0003g0378 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.361-1332A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113655457 | ||||||
| chr10:113655468
|
T | C | 1 | a0019c0018t0001g0131 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.361-1343A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113655468 | ||||||
| chr10:113655505
|
G | A | 127 | a0002c0002t0004g0300a0002c0002t0004g0303a0002c0002t0004g0304others(124): Show | 127 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.361-1380C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113655505 | ||||||
| chr10:113655790
|
T | A | 218 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(215): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.361-1665A>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113655790 | ||||||
| chr10:113655794
|
C | T | 128 | a0002c0002t0004g0300a0002c0002t0004g0303a0002c0002t0004g0304others(125): Show | 128 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.361-1669G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113655794 | ||||||
| chr10:113656044
|
TCTCATTA others(7): Show |
T | 128 | a0002c0002t0004g0300a0002c0002t0004g0303a0002c0002t0004g0304others(125): Show | 128 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.360+1412_360+1425d others(16): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113656044 | ||||||
| chr10:113656230
|
C | CT | 128 | a0002c0002t0004g0300a0002c0002t0004g0303a0002c0002t0004g0304others(125): Show | 128 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.360+1239dupA | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113656230 | ||||||
| chr10:113656324
|
C | T | 1 | a0059c0058t0002g0239 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.360+1146G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113656324 | ||||||
| chr10:113656347
|
G | A | 1 | a0003c0003t0003g0383 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.360+1123C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113656347 | ||||||
| chr10:113656414
|
C | T | 2 | a0011c0042t0004g0341a0011c0042t0004g0342 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.360+1056G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113656414 | ||||||
| chr10:113656463
|
T | C | 1 | a0001c0001t0001g0213 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.360+1007A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113656463 | ||||||
| chr10:113656465
|
G | A | 1 | a0022c0022t0001g0262 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.360+1005C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113656465 | ||||||
| chr10:113656559
|
T | C | 112 | a0002c0002t0004g0300a0002c0002t0004g0303a0002c0002t0004g0304others(109): Show | 112 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.360+911A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113656559 | ||||||
| chr10:113656575
|
G | A | 128 | a0002c0002t0004g0300a0002c0002t0004g0303a0002c0002t0004g0304others(125): Show | 128 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.360+895C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113656575 | ||||||
| chr10:113656638
|
C | G | 3 | a0034c0047t0003g0276a0034c0047t0003g0277a0046c0113t0004g0275 | 3 | HG02258.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.360+832G>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113656638 | ||||||
| chr10:113656659
|
T | C | 1 | a0018c0076t0001g0099 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.360+811A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113656659 | ||||||
| chr10:113656687
|
G | A | 3 | a0021c0071t0002g0269a0021c0072t0001g0271a0021c0073t0001g0270 | 3 | HG01891.hp2 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.360+783C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113656687 | ||||||
| chr10:113656698
|
T | C | 128 | a0002c0002t0004g0300a0002c0002t0004g0303a0002c0002t0004g0304others(125): Show | 128 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.360+772A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113656698 | ||||||
| chr10:113656809
|
C | T | 1 | a0003c0023t0003g0318 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.360+661G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113656809 | ||||||
| chr10:113656841
|
T | C | 1 | a0001c0001t0001g0157 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.360+629A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113656841 | ||||||
| chr10:113656925
|
A | T | 1 | a0002c0002t0004g0344 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.360+545T>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113656925 | ||||||
| chr10:113656939
|
T | C | 3 | a0034c0047t0003g0276a0034c0047t0003g0277a0046c0113t0004g0275 | 3 | HG02258.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.360+531A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113656939 | ||||||
| chr10:113657001
|
C | T | 128 | a0002c0002t0004g0300a0002c0002t0004g0303a0002c0002t0004g0304others(125): Show | 128 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.360+469G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113657001 | ||||||
| chr10:113657060
|
T | C | 128 | a0002c0002t0004g0300a0002c0002t0004g0303a0002c0002t0004g0304others(125): Show | 128 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.360+410A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113657060 | ||||||
| chr10:113657073
|
G | C | 2 | a0045c0036t0002g0267a0045c0036t0008g0057 | 2 | HG01081.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.360+397C>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113657073 | ||||||
| chr10:113657078
|
G | A | 1 | a0009c0009t0001g0065 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.360+392C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113657078 | ||||||
| chr10:113657096
|
G | A | 1 | a0003c0003t0003g0301 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.360+374C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113657096 | ||||||
| chr10:113657162
|
G | T | 1 | a0019c0018t0001g0112 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.360+308C>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113657162 | ||||||
| chr10:113657318
|
G | C | 7 | a0001c0001t0001g0216a0001c0001t0001g0217a0001c0001t0001g0218others(4): Show | 7 | HG00423.hp2 HG01257.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.360+152C>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113657318 | ||||||
| chr10:113657469
|
C | T | 1 | a0003c0003t0003g0340 | 1 | HG02055.hp2 | splice_donor_variant&intron_variant | HIGH | c.360+1G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113657469 | ||||||
| chr10:113657678
|
T | C | 6 | a0003c0003t0003g0380a0003c0003t0003g0381a0003c0003t0003g0383others(3): Show | 6 | HG02451.hp1 HG02896.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.256-104A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113657678 | ||||||
| chr10:113657891
|
T | C | 3 | a0028c0033t0001g0059a0028c0033t0001g0060a0028c0048t0001g0058 | 3 | HG02572.hp2 HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.256-317A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113657891 | ||||||
| chr10:113658034
|
C | T | 48 | a0010c0008t0002g0240a0010c0008t0002g0241a0010c0008t0002g0242others(45): Show | 48 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.256-460G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113658034 | ||||||
| chr10:113658035
|
A | G | 345 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(342): Show | 354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.256-461T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113658035 | ||||||
| chr10:113658127
|
T | C | 5 | a0011c0026t0002g0237a0026c0034t0002g0236a0026c0034t0002g0238others(2): Show | 5 | HG01891.hp1 HG02486.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.256-553A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113658127 | ||||||
| chr10:113658163
|
T | C | 6 | a0022c0022t0001g0258a0022c0022t0001g0259a0022c0022t0001g0262others(3): Show | 6 | HG00597.hp1 NA18612.hp2 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.256-589A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113658163 | ||||||
| chr10:113658190
|
T | C | 2 | a0005c0004t0005g0049a0030c0027t0005g0004 | 3 | NA18952.hp1 NA18988.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.256-616A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113658190 | ||||||
| chr10:113658214
|
T | G | 1 | a0037c0045t0002g0221 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.256-640A>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113658214 | ||||||
| chr10:113658222
|
T | C | 2 | a0002c0002t0004g0332a0002c0002t0004g0333 | 2 | HG02602.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.256-648A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113658222 | ||||||
| chr10:113658255
|
T | A | 85 | a0002c0002t0004g0300a0002c0002t0004g0303a0002c0002t0004g0304others(82): Show | 85 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.256-681A>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113658255 | ||||||
| chr10:113658352
|
G | A | 3 | a0034c0047t0003g0276a0034c0047t0003g0277a0046c0113t0004g0275 | 3 | HG02258.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.256-778C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113658352 | ||||||
| chr10:113658429
|
T | C | 48 | a0010c0008t0002g0240a0010c0008t0002g0241a0010c0008t0002g0242others(45): Show | 48 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.256-855A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113658429 | ||||||
| chr10:113658570
|
G | A | 2 | a0021c0114t0004g0273a0021c0115t0004g0274 | 2 | HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.256-996C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113658570 | ||||||
| chr10:113658607
|
G | A | 86 | a0002c0002t0004g0300a0002c0002t0004g0303a0002c0002t0004g0304others(83): Show | 86 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.256-1033C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113658607 | ||||||
| chr10:113658618
|
C | T | 52 | a0004c0005t0001g0111a0005c0004t0005g0001a0005c0004t0005g0008others(49): Show | 56 | HG00423.hp1 HG00621.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.256-1044G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113658618 | ||||||
| chr10:113658704
|
A | T | 48 | a0010c0008t0002g0240a0010c0008t0002g0241a0010c0008t0002g0242others(45): Show | 48 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.256-1130T>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113658704 | ||||||
| chr10:113658706
|
T | C | 48 | a0010c0008t0002g0240a0010c0008t0002g0241a0010c0008t0002g0242others(45): Show | 48 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.256-1132A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113658706 | ||||||
| chr10:113658800
|
T | C | 1 | a0004c0021t0001g0132 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.256-1226A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113658800 | ||||||
| chr10:113658881
|
C | CA | 11 | a0001c0001t0001g0222a0001c0001t0001g0223a0003c0003t0003g0334others(8): Show | 11 | HG02258.hp2 HG02559.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.256-1308dupT | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113658881 | ||||||
| chr10:113658881
|
CA | C | 55 | a0001c0001t0001g0135a0001c0001t0001g0161a0002c0002t0004g0337others(52): Show | 55 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.256-1308delT | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113658881 | ||||||
| chr10:113658896
|
A | G | 3 | a0006c0006t0006g0053a0026c0050t0002g0229a0062c0063t0005g0054 | 3 | HG01891.hp1 HG02258.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.256-1322T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113658896 | ||||||
| chr10:113658960
|
A | G | 51 | a0005c0004t0005g0001a0005c0004t0005g0008a0005c0004t0005g0016others(48): Show | 55 | HG00423.hp1 HG00621.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.256-1386T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113658960 | ||||||
| chr10:113659156
|
C | T | 1 | a0059c0058t0002g0239 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.256-1582G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113659156 | ||||||
| chr10:113659290
|
C | T | 48 | a0010c0008t0002g0240a0010c0008t0002g0241a0010c0008t0002g0242others(45): Show | 48 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.256-1716G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113659290 | ||||||
| chr10:113659377
|
C | G | 3 | a0021c0071t0002g0269a0021c0072t0001g0271a0021c0073t0001g0270 | 3 | HG01891.hp2 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.256-1803G>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113659377 | ||||||
| chr10:113659821
|
C | G | 2 | a0021c0114t0004g0273a0021c0115t0004g0274 | 2 | HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.256-2247G>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113659821 | ||||||
| chr10:113659833
|
C | T | 26 | a0010c0008t0002g0240a0010c0008t0002g0241a0010c0008t0002g0242others(23): Show | 26 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(23): Show |
intron_variant | MODIFIER | c.256-2259G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113659833 | ||||||
| chr10:113659947
|
A | G | 10 | a0011c0026t0002g0237a0026c0034t0002g0236a0026c0034t0002g0238others(7): Show | 10 | HG01891.hp1 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.256-2373T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113659947 | ||||||
| chr10:113660001
|
G | A | 48 | a0010c0008t0002g0240a0010c0008t0002g0241a0010c0008t0002g0242others(45): Show | 48 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.256-2427C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113660001 | ||||||
| chr10:113660028
|
A | G | 2 | a0002c0002t0004g0335a0002c0002t0004g0336 | 2 | HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.256-2454T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113660028 | ||||||
| chr10:113660051
|
A | AAC | 8 | a0003c0003t0003g0301a0013c0019t0002g0159a0014c0062t0005g0055others(5): Show | 8 | HG01109.hp2 HG02559.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.256-2479_256-2478d others(4): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113660051 | ||||||
| chr10:113660051
|
A | AACAC | 35 | a0002c0002t0004g0303a0002c0002t0004g0304a0002c0002t0004g0307others(32): Show | 35 | HG00438.hp1 HG00609.hp1 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.256-2481_256-2478d others(6): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113660051 | ||||||
| chr10:113660051
|
A | AACACAC | 50 | a0003c0003t0003g0316a0005c0004t0005g0001a0005c0004t0005g0008others(47): Show | 54 | HG00280.hp1 HG00423.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.256-2483_256-2478d others(8): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113660051 | ||||||
| chr10:113660051
|
A | AACACACA others(1): Show |
31 | a0003c0003t0003g0313a0003c0023t0003g0314a0006c0006t0006g0009others(28): Show | 31 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(28): Show |
intron_variant | MODIFIER | c.256-2485_256-2478d others(10): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113660051 | ||||||
| chr10:113660051
|
A | AACACACA others(3): Show |
5 | a0010c0008t0002g0240a0010c0008t0002g0241a0010c0008t0002g0242others(2): Show | 5 | HG00642.hp2 HG00735.hp2 HG01070.hp2 others(2): Show |
intron_variant | MODIFIER | c.256-2487_256-2478d others(12): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113660051 | ||||||
| chr10:113660051
|
A | C | 1 | a0001c0001t0001g0225 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.256-2477T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113660051 | ||||||
| chr10:113660051
|
AAC | A | 56 | a0008c0007t0002g0068a0008c0007t0002g0074a0008c0007t0002g0077others(53): Show | 60 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.256-2479_256-2478d others(4): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113660051 | ||||||
| chr10:113660051
|
AACAC | A | 12 | a0003c0003t0003g0386a0004c0021t0003g0387a0011c0016t0004g0278others(9): Show | 13 | HG01109.hp1 HG01192.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.256-2481_256-2478d others(6): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113660051 | ||||||
| chr10:113660100
|
T | C | 3 | a0045c0036t0002g0267a0045c0036t0008g0057a0080c0074t0001g0268 | 3 | HG01081.hp2 HG02630.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.256-2526A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113660100 | ||||||
| chr10:113660100
|
TATAC | T | 129 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(126): Show | 131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.256-2530_256-2527d others(6): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113660100 | ||||||
| chr10:113660126
|
A | T | 1 | a0001c0001t0001g0225 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.256-2552T>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113660126 | ||||||
| chr10:113660154
|
C | T | 10 | a0002c0002t0004g0303a0002c0002t0004g0304a0002c0002t0004g0307others(7): Show | 10 | HG00609.hp2 HG00621.hp2 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.255+2525G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113660154 | ||||||
| chr10:113660196
|
C | T | 86 | a0002c0002t0004g0300a0002c0002t0004g0303a0002c0002t0004g0304others(83): Show | 86 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.255+2483G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113660196 | ||||||
| chr10:113660222
|
A | C | 1 | a0066c0095t0003g0302 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.255+2457T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113660222 | ||||||
| chr10:113660360
|
C | T | 2 | a0021c0114t0004g0273a0021c0115t0004g0274 | 2 | HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.255+2319G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113660360 | ||||||
| chr10:113660376
|
T | A | 1 | a0010c0008t0002g0265 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.255+2303A>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113660376 | ||||||
| chr10:113660407
|
G | T | 26 | a0010c0008t0002g0240a0010c0008t0002g0241a0010c0008t0002g0242others(23): Show | 26 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(23): Show |
intron_variant | MODIFIER | c.255+2272C>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113660407 | ||||||
| chr10:113660498
|
C | T | 2 | a0021c0114t0004g0273a0021c0115t0004g0274 | 2 | HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.255+2181G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113660498 | ||||||
| chr10:113660562
|
C | T | 1 | a0059c0058t0002g0239 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.255+2117G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113660562 | ||||||
| chr10:113660669
|
A | C | 29 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(26): Show | 29 | HG00438.hp2 HG01433.hp2 HG01981.hp2 others(26): Show |
intron_variant | MODIFIER | c.255+2010T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113660669 | ||||||
| chr10:113660688
|
C | G | 47 | a0005c0004t0005g0001a0005c0004t0005g0008a0005c0004t0005g0016others(44): Show | 51 | HG00423.hp1 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.255+1991G>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113660688 | ||||||
| chr10:113660739
|
G | T | 1 | a0008c0078t0002g0063 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.255+1940C>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113660739 | ||||||
| chr10:113660793
|
G | T | 1 | a0003c0003t0003g0301 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.255+1886C>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113660793 | ||||||
| chr10:113660898
|
C | T | 2 | a0021c0114t0004g0273a0021c0115t0004g0274 | 2 | HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.255+1781G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113660898 | ||||||
| chr10:113660976
|
G | T | 33 | a0004c0005t0001g0104a0004c0005t0001g0106a0004c0005t0001g0108others(30): Show | 35 | HG00544.hp2 HG01167.hp1 HG01169.hp2 others(32): Show |
intron_variant | MODIFIER | c.255+1703C>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113660976 | ||||||
| chr10:113661017
|
T | C | 98 | a0005c0004t0005g0001a0005c0004t0005g0008a0005c0004t0005g0016others(95): Show | 102 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.255+1662A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113661017 | ||||||
| chr10:113661032
|
A | C | 1 | a0001c0001t0001g0225 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.255+1647T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113661032 | ||||||
| chr10:113661301
|
T | A | 1 | a0001c0001t0001g0225 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.255+1378A>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113661301 | ||||||
| chr10:113661704
|
T | G | 1 | a0027c0049t0002g0266 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.255+975A>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113661704 | ||||||
| chr10:113661724
|
T | C | 25 | a0011c0016t0004g0278a0011c0016t0004g0280a0011c0016t0004g0294others(22): Show | 28 | HG00408.hp2 HG00544.hp1 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.255+955A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113661724 | ||||||
| chr10:113661749
|
C | T | 1 | a0002c0002t0004g0300 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.255+930G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113661749 | ||||||
| chr10:113661785
|
C | A | 2 | a0005c0004t0005g0052a0063c0066t0005g0051 | 2 | HG01943.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.255+894G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113661785 | ||||||
| chr10:113662033
|
C | T | 1 | a0013c0019t0002g0109 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.255+646G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113662033 | ||||||
| chr10:113662059
|
A | G | 1 | a0026c0050t0002g0229 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.255+620T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113662059 | ||||||
| chr10:113662130
|
T | C | 47 | a0010c0008t0002g0240a0010c0008t0002g0241a0010c0008t0002g0242others(44): Show | 47 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.255+549A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113662130 | ||||||
| chr10:113662149
|
C | T | 47 | a0005c0004t0005g0001a0005c0004t0005g0008a0005c0004t0005g0016others(44): Show | 51 | HG00423.hp1 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.255+530G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113662149 | ||||||
| chr10:113662183
|
C | T | 7 | a0004c0005t0001g0104a0004c0005t0001g0106a0004c0005t0001g0108others(4): Show | 7 | HG02572.hp1 HG02615.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.255+496G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113662183 | ||||||
| chr10:113662202
|
T | G | 3 | a0028c0033t0001g0059a0028c0033t0001g0060a0028c0048t0001g0058 | 3 | HG02572.hp2 HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.255+477A>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113662202 | ||||||
| chr10:113662227
|
T | G | 1 | a0027c0049t0002g0266 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.255+452A>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113662227 | ||||||
| chr10:113662237
|
G | A | 216 | a0002c0002t0004g0300a0002c0002t0004g0303a0002c0002t0004g0304others(213): Show | 223 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.255+442C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113662237 | ||||||
| chr10:113662337
|
C | T | 2 | a0011c0016t0004g0278a0041c0041t0003g0279 | 2 | HG01884.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.255+342G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113662337 | ||||||
| chr10:113662338
|
G | C | 3 | a0028c0033t0001g0059a0028c0033t0001g0060a0028c0048t0001g0058 | 3 | HG02572.hp2 HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.255+341C>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113662338 | ||||||
| chr10:113662408
|
CTCTG | C | 47 | a0010c0008t0002g0240a0010c0008t0002g0241a0010c0008t0002g0242others(44): Show | 47 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.255+267_255+270del others(4): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113662408 | ||||||
| chr10:113662419
|
A | T | 47 | a0010c0008t0002g0240a0010c0008t0002g0241a0010c0008t0002g0242others(44): Show | 47 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.255+260T>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113662419 | ||||||
| chr10:113662439
|
C | T | 1 | a0005c0004t0005g0008 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.255+240G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113662439 | ||||||
| chr10:113662500
|
C | G | 13 | a0011c0026t0002g0237a0026c0034t0002g0236a0026c0034t0002g0238others(10): Show | 13 | HG01891.hp1 HG02486.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.255+179G>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113662500 | ||||||
| chr10:113662518
|
G | A | 47 | a0010c0008t0002g0240a0010c0008t0002g0241a0010c0008t0002g0242others(44): Show | 47 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.255+161C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113662518 | ||||||
| chr10:113662533
|
C | A | 2 | a0009c0009t0001g0101a0018c0015t0001g0100 | 2 | HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.255+146G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113662533 | ||||||
| chr10:113662866
|
A | T | 3 | a0034c0047t0003g0276a0034c0047t0003g0277a0046c0113t0004g0275 | 3 | HG02258.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.168-100T>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 2/41 | chr10 | 113662866 | ||||||
| chr10:113662902
|
C | A | 47 | a0010c0008t0002g0240a0010c0008t0002g0241a0010c0008t0002g0242others(44): Show | 47 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.168-136G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 2/41 | chr10 | 113662902 | ||||||
| chr10:113663129
|
T | C | 47 | a0010c0008t0002g0240a0010c0008t0002g0241a0010c0008t0002g0242others(44): Show | 47 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.167+223A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 2/41 | chr10 | 113663129 | ||||||
| chr10:113663227
|
G | T | 25 | a0011c0016t0004g0278a0011c0016t0004g0280a0011c0016t0004g0294others(22): Show | 28 | HG00408.hp2 HG00544.hp1 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.167+125C>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 2/41 | chr10 | 113663227 | ||||||
| chr10:113663255
|
A | T | 2 | a0016c0013t0002g0061a0016c0013t0002g0062 | 2 | NA18959.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.167+97T>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 2/41 | chr10 | 113663255 | ||||||
| chr10:113663283
|
G | A | 3 | a0045c0036t0002g0267a0045c0036t0008g0057a0080c0074t0001g0268 | 3 | HG01081.hp2 HG02630.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.167+69C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 2/41 | chr10 | 113663283 | ||||||
| chr10:113663335
|
G | C | 132 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(129): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.167+17C>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 2/41 | chr10 | 113663335 | ||||||
| chr10:113663501
|
G | A | 1 | a0004c0021t0003g0387 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.73-55C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 1/41 | chr10 | 113663501 | ||||||
| chr10:113663536
|
G | A | 3 | a0021c0071t0002g0269a0021c0072t0001g0271a0021c0073t0001g0270 | 3 | HG01891.hp2 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.73-90C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 1/41 | chr10 | 113663536 | ||||||
| chr10:113663576
|
A | G | 47 | a0010c0008t0002g0240a0010c0008t0002g0241a0010c0008t0002g0242others(44): Show | 47 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.73-130T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 1/41 | chr10 | 113663576 | ||||||
| chr10:113663616
|
CT | C | 159 | a0002c0002t0004g0300a0002c0002t0004g0303a0002c0002t0004g0304others(156): Show | 162 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.73-171delA | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 1/41 | chr10 | 113663616 | ||||||
| chr10:113663632
|
C | T | 51 | a0005c0004t0005g0001a0005c0004t0005g0008a0005c0004t0005g0016others(48): Show | 55 | HG00423.hp1 HG00621.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.72+179G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 1/41 | chr10 | 113663632 | ||||||
| chr10:113663793
|
C | T | 3 | a0028c0033t0001g0059a0028c0033t0001g0060a0028c0048t0001g0058 | 3 | HG02572.hp2 HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.72+18G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 1/41 | chr10 | 113663793 |