| geneid | 7982 |
|---|---|
| ensemblid | ENSG00000004866.22 |
| hgncid | 11351 |
| symbol | ST7 |
| name | suppression of tumorigenicity 7 |
| refseq_nuc | NM_001369598.1 |
| refseq_prot | NP_001356527.1 |
| ensembl_nuc | ENST00000323984.8 |
| ensembl_prot | ENSP00000325673.3 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 116953501 |
| end | 117230176 |
| strand | + |
| ver | v1.2 |
| region | chr7:116953501-117230176 |
| region5000 | chr7:116948501-117235176 |
| regionname0 | ST7_chr7_116953501_117230176 |
| regionname5000 | ST7_chr7_116948501_117235176 |
| 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 | 1/1 | 577 | 188 | 70 | 36 | 58 | 10 | 12 | 40 | ST7_chr7_116948501_117235176 | ST7 | copy fasta | chr7 | 116948501 | 117235176 |
| 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 | 1/1 | 1734 | 187 | 69 | 36 | 58 | 10 | 12 | ST7_chr7_116948501_117235176 | ST7 | copy fasta | chr7 | 116948501 | 117235176 |
| c0002 | 0/0 | 1734 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | copy fasta | chr7 | 116948501 | 117235176 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 360 | 188 | 70 | 36 | 58 | 10 | 12 | ST7_chr7_116948501_117235176 | ST7 | copy fasta | chr7 | 116948501 | 117235176 |
| 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 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0060 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0116 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| 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 | 1/1 | 1734 | 187 | 69 | 36 | 58 | 10 | 12 | ST7_chr7_116948501_117235176 | ST7 | copy fasta | chr7 | 116948501 | 117235176 |
| a0001c0002 | 0/0 | 1734 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | copy fasta | chr7 | 116948501 | 117235176 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2093 | 187 | 69 | 36 | 58 | 10 | 12 | ST7_chr7_116948501_117235176 | ST7 | copy fasta | chr7 | 116948501 | 117235176 |
| a0001c0002t0001 | 0/0 | 2093 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | copy fasta | chr7 | 116948501 | 117235176 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0060 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0116 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0002t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0105 | EUR | GBR | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0074 | EUR | GBR | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0076 | EUR | FIN | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0104 | EUR | FIN | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0164 | EUR | FIN | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0110 | EUR | FIN | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | CHS | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | CHS | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | CHS | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | CHS | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | CLM | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | CLM | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | CLM | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | CLM | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PEL | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PEL | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PEL | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ACB | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | ACB | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PEL | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PEL | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | ACB | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | ESN | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | ESN | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | ESN | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | ESN | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ESN | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0044 | AFR | ESN | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | ESN | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | ESN | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | MSL | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ESN | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | ESN | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | ESN | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ESN | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ESN | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | ESN | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | MSL | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | MSL | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | MSL | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | MSL | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | MSL | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | ESN | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | MSL | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | MSL | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | BEB | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | BEB | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | STU | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | STU | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | CHB | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | CHB | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | YRI | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | YRI | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | LWK | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | LWK | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | YRI | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | YRI | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | ASW | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ASW | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | TSI | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0120 | EUR | TSI | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0108 | EUR | TSI | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0126 | EUR | TSI | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | GIH | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | GIH | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ACB | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | ACB | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | LWK | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | LWK | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0116 | REF | REF | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0060 | REF | REF | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:117099823
|
A | G | 1 | a0001c0002 | 1 | HG02970.hp2 | synonymous_variant | LOW | c.213A>G | p.Ser71Ser | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/16 | 253/2093 | 213/1734 | 71/577 | chr7 | 117099823 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:116953749
|
T | G | 3 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003 | 3 | HG02717.hp1 HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.151+58T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116953749 | ||||||
| chr7:116953758
|
C | A | 1 | a0001c0001t0001g0004 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.151+67C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116953758 | ||||||
| chr7:116953887
|
G | C | 41 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(38): Show | 41 | HG00408.hp1 HG00642.hp1 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.151+196G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116953887 | ||||||
| chr7:116954326
|
G | C | 15 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(12): Show | 15 | HG02055.hp2 HG02258.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.151+635G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116954326 | ||||||
| chr7:116954344
|
T | C | 1 | a0001c0001t0001g0043 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.151+653T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116954344 | ||||||
| chr7:116954699
|
GTTTTAAA | G | 3 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG01943.hp1 HG02004.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.151+1015_151+1021d others(9): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116954699 | |||||
| chr7:116954768
|
A | G | 2 | a0001c0001t0001g0038a0001c0001t0001g0039 | 2 | NA18960.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.151+1077A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116954768 | ||||||
| chr7:116955076
|
G | A | 10 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(7): Show | 10 | HG02040.hp2 HG02273.hp1 NA18960.hp2 others(7): Show |
intron_variant | MODIFIER | c.151+1385G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116955076 | ||||||
| chr7:116955383
|
C | G | 1 | a0001c0001t0001g0188 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.151+1692C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116955383 | ||||||
| chr7:116956643
|
A | G | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 182 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.151+2952A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116956643 | ||||||
| chr7:116956751
|
T | A | 4 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG01496.hp2 HG02572.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+3060T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116956751 | ||||||
| chr7:116956758
|
G | T | 3 | a0001c0001t0001g0043a0001c0001t0001g0056a0001c0001t0001g0057 | 3 | HG02486.hp2 HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.151+3067G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116956758 | ||||||
| chr7:116956825
|
T | C | 2 | a0001c0001t0001g0013a0001c0001t0001g0014 | 2 | HG02257.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.151+3134T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116956825 | ||||||
| chr7:116956857
|
C | G | 42 | a0001c0001t0001g0004a0001c0001t0001g0147a0001c0001t0001g0148others(39): Show | 42 | HG00323.hp1 HG00438.hp1 HG01192.hp1 others(39): Show |
intron_variant | MODIFIER | c.151+3166C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116956857 | ||||||
| chr7:116957069
|
C | A | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.151+3378C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116957069 | ||||||
| chr7:116957087
|
C | T | 17 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(14): Show | 17 | HG00408.hp1 HG00673.hp1 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.151+3396C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116957087 | ||||||
| chr7:116957175
|
C | T | 4 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG01496.hp2 HG02572.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+3484C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116957175 | ||||||
| chr7:116957369
|
T | G | 15 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(12): Show | 15 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.151+3678T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116957369 | ||||||
| chr7:116957644
|
A | G | 22 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127others(19): Show | 22 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.151+3953A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116957644 | ||||||
| chr7:116958021
|
C | T | 10 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(7): Show | 10 | HG00408.hp1 HG00673.hp1 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.151+4330C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116958021 | ||||||
| chr7:116958162
|
A | AT | 157 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(154): Show | 157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.151+4495dupT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116958162 | |||||
| chr7:116958162
|
A | ATT | 19 | a0001c0001t0001g0021a0001c0001t0001g0028a0001c0001t0001g0043others(16): Show | 19 | HG00673.hp2 HG01358.hp2 HG01978.hp1 others(16): Show |
intron_variant | MODIFIER | c.151+4494_151+4495d others(4): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116958162 | |||||
| chr7:116958670
|
C | T | 22 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127others(19): Show | 22 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.151+4979C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116958670 | ||||||
| chr7:116958681
|
A | G | 126 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(123): Show | 126 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.151+4990A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116958681 | ||||||
| chr7:116958730
|
A | G | 13 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(10): Show | 13 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.151+5039A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116958730 | ||||||
| chr7:116958789
|
T | C | 1 | a0001c0001t0001g0022 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.151+5098T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116958789 | ||||||
| chr7:116959010
|
A | G | 1 | a0001c0001t0001g0124 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.151+5319A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116959010 | ||||||
| chr7:116959089
|
C | T | 1 | a0001c0001t0001g0121 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.151+5398C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116959089 | ||||||
| chr7:116959097
|
C | T | 2 | a0001c0001t0001g0070a0001c0001t0001g0071 | 2 | HG02922.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.151+5406C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116959097 | ||||||
| chr7:116959359
|
T | C | 1 | a0001c0001t0001g0099 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.151+5668T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116959359 | ||||||
| chr7:116959995
|
A | T | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 182 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.151+6304A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116959995 | ||||||
| chr7:116960169
|
G | A | 22 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127others(19): Show | 22 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.151+6478G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116960169 | ||||||
| chr7:116960184
|
T | G | 1 | a0001c0001t0001g0148 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.151+6493T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116960184 | ||||||
| chr7:116960309
|
C | A | 1 | a0001c0001t0001g0100 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.151+6618C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116960309 | ||||||
| chr7:116960490
|
A | C | 1 | a0001c0001t0001g0180 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.151+6799A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116960490 | ||||||
| chr7:116960509
|
C | T | 15 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(12): Show | 15 | HG02055.hp2 HG02258.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.151+6818C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116960509 | ||||||
| chr7:116961256
|
C | T | 2 | a0001c0001t0001g0143a0001c0001t0001g0144 | 2 | NA18747.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.151+7565C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116961256 | ||||||
| chr7:116961395
|
A | G | 3 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0187 | 3 | NA19000.hp1 NA19004.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.151+7704A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116961395 | ||||||
| chr7:116961428
|
T | C | 13 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(10): Show | 13 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.151+7737T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116961428 | ||||||
| chr7:116961555
|
C | CGT | 15 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0022others(12): Show | 15 | HG00408.hp1 HG01192.hp2 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.151+7902_151+7903d others(4): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116961555 | |||||
| chr7:116961555
|
C | CGTGT | 23 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(20): Show | 23 | HG00673.hp1 HG00673.hp2 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.151+7900_151+7903d others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116961555 | |||||
| chr7:116961555
|
C | CGTGTGT | 10 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0019others(7): Show | 10 | HG00642.hp1 HG01071.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.151+7898_151+7903d others(8): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116961555 | |||||
| chr7:116961555
|
C | CGTGTGTG others(1): Show |
6 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(3): Show | 6 | HG00408.hp2 HG01358.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.151+7896_151+7903d others(10): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116961555 | |||||
| chr7:116961555
|
C | CGTGTGTG others(3): Show |
4 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(1): Show | 4 | HG00438.hp2 HG02040.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.151+7894_151+7903d others(12): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116961555 | |||||
| chr7:116961555
|
C | CGTGTGTG others(5): Show |
3 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138 | 3 | HG00738.hp2 NA18951.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.151+7892_151+7903d others(14): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116961555 | |||||
| chr7:116961555
|
C | CGTGTGTG others(7): Show |
2 | a0001c0001t0001g0139a0001c0001t0001g0140 | 2 | HG02717.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.151+7890_151+7903d others(16): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116961555 | |||||
| chr7:116961555
|
C | CGTGTGTG others(9): Show |
2 | a0001c0001t0001g0141a0001c0001t0001g0142 | 2 | HG02572.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.151+7888_151+7903d others(18): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116961555 | |||||
| chr7:116961555
|
C | CGTGTGTG others(11): Show |
1 | a0001c0001t0001g0146 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.151+7886_151+7903d others(20): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116961555 | |||||
| chr7:116961555
|
CGT | C | 70 | a0001c0001t0001g0004a0001c0001t0001g0023a0001c0001t0001g0043others(67): Show | 70 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.151+7902_151+7903d others(4): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116961555 | |||||
| chr7:116961555
|
CGTGT | C | 7 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0090others(4): Show | 7 | HG00738.hp1 HG02280.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.151+7900_151+7903d others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116961555 | |||||
| chr7:116961555
|
CGTGTGT | C | 7 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(4): Show | 7 | HG02451.hp1 HG02647.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.151+7898_151+7903d others(8): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116961555 | |||||
| chr7:116961555
|
CGTGTGTG others(3): Show |
C | 1 | a0001c0001t0001g0085 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.151+7894_151+7903d others(12): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116961555 | |||||
| chr7:116961767
|
T | C | 1 | a0001c0001t0001g0072 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.151+8076T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116961767 | ||||||
| chr7:116961785
|
A | G | 1 | a0001c0001t0001g0083 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.151+8094A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116961785 | ||||||
| chr7:116961810
|
A | G | 72 | a0001c0001t0001g0004a0001c0001t0001g0064a0001c0001t0001g0065others(69): Show | 72 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.151+8119A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116961810 | ||||||
| chr7:116962139
|
G | A | 172 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(169): Show | 172 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.151+8448G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116962139 | ||||||
| chr7:116962397
|
C | G | 1 | a0001c0001t0001g0059 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.151+8706C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116962397 | ||||||
| chr7:116962416
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.151+8725C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116962416 | ||||||
| chr7:116963411
|
A | C | 1 | a0001c0001t0001g0062 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.151+9720A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116963411 | ||||||
| chr7:116963632
|
C | CT | 6 | a0001c0001t0001g0062a0001c0001t0001g0112a0001c0001t0001g0120others(3): Show | 6 | HG02717.hp2 HG03209.hp2 NA19030.hp1 others(3): Show |
intron_variant | MODIFIER | c.151+9957dupT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116963632 | |||||
| chr7:116963632
|
CT | C | 10 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087others(7): Show | 10 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.151+9957delT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116963632 | |||||
| chr7:116963654
|
C | T | 1 | a0001c0001t0001g0120 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.151+9963C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116963654 | ||||||
| chr7:116963891
|
A | G | 1 | a0001c0001t0001g0132 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.151+10200A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116963891 | ||||||
| chr7:116963950
|
A | G | 10 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087others(7): Show | 10 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.151+10259A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116963950 | ||||||
| chr7:116964131
|
C | A | 1 | a0001c0001t0001g0085 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.151+10440C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116964131 | ||||||
| chr7:116964140
|
T | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 182 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.151+10449T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116964140 | ||||||
| chr7:116964322
|
T | G | 2 | a0001c0001t0001g0070a0001c0001t0001g0071 | 2 | HG02922.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.151+10631T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116964322 | ||||||
| chr7:116964716
|
A | G | 10 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087others(7): Show | 10 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.151+11025A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116964716 | ||||||
| chr7:116965339
|
C | CA | 42 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0023others(39): Show | 42 | HG00408.hp1 HG00673.hp1 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.151+11669dupA | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116965339 | |||||
| chr7:116965339
|
C | CAA | 8 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0061others(5): Show | 8 | HG01433.hp2 HG02109.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.151+11668_151+1166 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116965339 | |||||
| chr7:116965339
|
CA | C | 6 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(3): Show | 6 | HG02040.hp1 HG02280.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.151+11669delA | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116965339 | |||||
| chr7:116965481
|
C | G | 10 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087others(7): Show | 10 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.151+11790C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116965481 | ||||||
| chr7:116965565
|
C | G | 10 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087others(7): Show | 10 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.151+11874C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116965565 | ||||||
| chr7:116965763
|
G | GAAAAAGA others(321): Show |
1 | a0001c0001t0001g0071 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.151+12085_151+1208 others(332): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116965763 | |||||
| chr7:116965763
|
G | GAAAAAGA others(327): Show |
1 | a0001c0001t0001g0070 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.151+12085_151+1208 others(338): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116965763 | |||||
| chr7:116966037
|
A | ATACCCAA others(6): Show |
1 | a0001c0001t0001g0179 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.151+12348_151+1236 others(17): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116966037 | |||||
| chr7:116966187
|
C | T | 22 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127others(19): Show | 22 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.151+12496C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116966187 | ||||||
| chr7:116966232
|
TTTTCTTT others(4): Show |
T | 2 | a0001c0001t0001g0143a0001c0001t0001g0144 | 2 | NA18747.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.151+12552_151+1256 others(15): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116966232 | |||||
| chr7:116966247
|
C | CT | 7 | a0001c0001t0001g0015a0001c0001t0001g0110a0001c0001t0001g0111others(4): Show | 7 | HG00323.hp2 HG00642.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.151+12576dupT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116966247 | |||||
| chr7:116966247
|
CT | C | 12 | a0001c0001t0001g0033a0001c0001t0001g0058a0001c0001t0001g0059others(9): Show | 12 | HG00738.hp2 HG01081.hp2 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.151+12576delT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116966247 | |||||
| chr7:116966251
|
T | C | 2 | a0001c0001t0001g0029a0001c0001t0001g0102 | 2 | HG01978.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.151+12560T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116966251 | ||||||
| chr7:116966385
|
G | A | 19 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(16): Show | 19 | HG01433.hp1 HG02055.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.151+12694G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116966385 | ||||||
| chr7:116966542
|
C | T | 1 | a0001c0001t0001g0062 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.151+12851C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116966542 | ||||||
| chr7:116966742
|
T | A | 2 | a0001c0001t0001g0070a0001c0001t0001g0071 | 2 | HG02922.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.151+13051T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116966742 | ||||||
| chr7:116966762
|
C | A | 2 | a0001c0001t0001g0070a0001c0001t0001g0071 | 2 | HG02922.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.151+13071C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116966762 | ||||||
| chr7:116966782
|
C | A | 9 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(6): Show | 9 | HG02109.hp1 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.151+13091C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116966782 | ||||||
| chr7:116966782
|
C | T | 1 | a0001c0001t0001g0082 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.151+13091C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116966782 | ||||||
| chr7:116966783
|
A | G | 2 | a0001c0001t0001g0058a0001c0001t0001g0059 | 2 | HG02818.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.151+13092A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116966783 | ||||||
| chr7:116967118
|
C | CT | 6 | a0001c0001t0001g0062a0001c0001t0001g0133a0001c0001t0001g0134others(3): Show | 6 | HG00438.hp2 HG02040.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.151+13442dupT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116967118 | |||||
| chr7:116967118
|
C | CTT | 11 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(8): Show | 11 | HG00408.hp2 HG02109.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.151+13441_151+1344 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116967118 | |||||
| chr7:116967118
|
CT | C | 71 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0064others(68): Show | 71 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.151+13442delT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116967118 | |||||
| chr7:116967181
|
T | C | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.151+13490T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116967181 | ||||||
| chr7:116967293
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.151+13602G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116967293 | ||||||
| chr7:116967447
|
T | C | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(183): Show | 186 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.151+13756T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116967447 | ||||||
| chr7:116967488
|
C | T | 4 | a0001c0001t0001g0028a0001c0001t0001g0068a0001c0001t0001g0069others(1): Show | 4 | HG02280.hp1 HG02486.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+13797C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116967488 | ||||||
| chr7:116967559
|
T | C | 9 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(6): Show | 9 | HG02109.hp1 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.151+13868T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116967559 | ||||||
| chr7:116967560
|
A | G | 1 | a0001c0001t0001g0108 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.151+13869A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116967560 | ||||||
| chr7:116968127
|
A | C | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.151+14436A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116968127 | ||||||
| chr7:116968256
|
TCTCC | T | 9 | a0001c0001t0001g0061a0001c0001t0001g0086a0001c0001t0001g0087others(6): Show | 9 | HG01433.hp2 HG02109.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.151+14602_151+1460 others(8): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116968256 | |||||
| chr7:116968256
|
TCTCCCTC others(1): Show |
T | 2 | a0001c0001t0001g0085a0001c0001t0001g0097 | 2 | HG02109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.151+14598_151+1460 others(12): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116968256 | |||||
| chr7:116968256
|
TCTCCCTC others(5): Show |
T | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.151+14594_151+1460 others(16): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116968256 | |||||
| chr7:116968260
|
C | G | 1 | a0001c0001t0001g0024 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.151+14569C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116968260 | ||||||
| chr7:116968269
|
CTCCCTCC others(29): Show |
C | 1 | a0001c0001t0001g0132 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.151+14582_151+1461 others(40): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116968269 | |||||
| chr7:116968279
|
C | CCCTCCTT others(21): Show |
12 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(9): Show | 12 | HG02055.hp2 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.151+14593_151+1459 others(32): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116968279 | |||||
| chr7:116968281
|
CTCCCTCC others(17): Show |
C | 17 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0064others(14): Show | 17 | HG00738.hp1 HG01081.hp1 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.151+14594_151+1461 others(28): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116968281 | |||||
| chr7:116968285
|
C | T | 8 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(5): Show | 8 | HG02109.hp1 HG02451.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.151+14594C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116968285 | ||||||
| chr7:116968285
|
CTCCCTCC others(5): Show |
C | 3 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0062 | 3 | HG02818.hp1 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.151+14598_151+1460 others(16): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116968285 | |||||
| chr7:116968285
|
CTCCCTCC others(13): Show |
C | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.151+14598_151+1461 others(24): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116968285 | |||||
| chr7:116968285
|
CTCCCTCC others(17): Show |
C | 3 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0188 | 3 | HG02280.hp1 HG02486.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.151+14598_151+1462 others(28): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116968285 | |||||
| chr7:116968289
|
C | T | 9 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(6): Show | 9 | HG02109.hp1 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.151+14598C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116968289 | ||||||
| chr7:116968289
|
CTCCCTCC others(9): Show |
C | 3 | a0001c0001t0001g0013a0001c0001t0001g0034a0001c0001t0001g0133 | 3 | HG02257.hp2 HG02523.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.151+14602_151+1461 others(20): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116968289 | |||||
| chr7:116968293
|
C | T | 10 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087others(7): Show | 10 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.151+14602C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116968293 | ||||||
| chr7:116968297
|
T | C | 12 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(9): Show | 12 | HG02055.hp2 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.151+14606T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116968297 | ||||||
| chr7:116968301
|
T | C | 12 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(9): Show | 12 | HG02055.hp2 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.151+14610T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116968301 | ||||||
| chr7:116968305
|
T | C | 12 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(9): Show | 12 | HG02055.hp2 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.151+14614T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116968305 | ||||||
| chr7:116968417
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.151+14726G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116968417 | ||||||
| chr7:116968446
|
A | G | 15 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(12): Show | 15 | HG02055.hp2 HG02258.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.151+14755A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116968446 | ||||||
| chr7:116968447
|
A | G | 13 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(10): Show | 13 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.151+14756A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116968447 | ||||||
| chr7:116968566
|
G | T | 1 | a0001c0001t0001g0109 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.151+14875G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116968566 | ||||||
| chr7:116968580
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.151+14889G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116968580 | ||||||
| chr7:116968825
|
A | G | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 182 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.151+15134A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116968825 | ||||||
| chr7:116968975
|
T | C | 22 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127others(19): Show | 22 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.151+15284T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116968975 | ||||||
| chr7:116969309
|
T | C | 1 | a0001c0001t0001g0085 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.151+15618T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116969309 | ||||||
| chr7:116969481
|
T | C | 1 | a0001c0001t0001g0025 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.151+15790T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116969481 | ||||||
| chr7:116969740
|
A | G | 15 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(12): Show | 15 | HG02055.hp2 HG02258.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.151+16049A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116969740 | ||||||
| chr7:116969781
|
A | G | 1 | a0001c0001t0001g0188 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.151+16090A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116969781 | ||||||
| chr7:116970168
|
G | A | 1 | a0001c0001t0001g0135 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.151+16477G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116970168 | ||||||
| chr7:116970183
|
A | G | 40 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(37): Show | 40 | HG00408.hp1 HG00642.hp1 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.151+16492A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116970183 | ||||||
| chr7:116970445
|
G | C | 2 | a0001c0001t0001g0013a0001c0001t0001g0014 | 2 | HG02257.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.151+16754G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116970445 | ||||||
| chr7:116970510
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.151+16819C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116970510 | ||||||
| chr7:116970664
|
A | G | 1 | a0001c0001t0001g0127 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.151+16973A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116970664 | ||||||
| chr7:116971092
|
T | C | 1 | a0001c0001t0001g0133 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.151+17401T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116971092 | ||||||
| chr7:116971515
|
G | GA | 15 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(12): Show | 15 | HG02055.hp2 HG02258.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.151+17834dupA | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116971515 | |||||
| chr7:116971555
|
G | GTA | 3 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0123 | 3 | HG01358.hp2 HG01943.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.151+17868_151+1786 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116971555 | |||||
| chr7:116971724
|
G | A | 13 | a0001c0001t0001g0125a0001c0001t0001g0130a0001c0001t0001g0131others(10): Show | 13 | HG00408.hp2 HG00438.hp2 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.151+18033G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116971724 | ||||||
| chr7:116971784
|
CAAAAGTG others(3): Show |
C | 3 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0188 | 3 | HG02280.hp1 HG02486.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.151+18097_151+1810 others(14): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116971784 | |||||
| chr7:116971795
|
A | G | 1 | a0001c0001t0001g0016 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.151+18104A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116971795 | ||||||
| chr7:116971921
|
C | T | 1 | a0001c0001t0001g0042 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.151+18230C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116971921 | ||||||
| chr7:116972034
|
C | T | 3 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0188 | 3 | HG02280.hp1 HG02486.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.151+18343C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116972034 | ||||||
| chr7:116972316
|
C | G | 17 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(14): Show | 17 | HG00408.hp1 HG00673.hp1 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.151+18625C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116972316 | ||||||
| chr7:116972673
|
G | A | 22 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127others(19): Show | 22 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.151+18982G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116972673 | ||||||
| chr7:116973113
|
C | T | 15 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(12): Show | 15 | HG02055.hp2 HG02258.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.151+19422C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116973113 | ||||||
| chr7:116973132
|
C | T | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.151+19441C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116973132 | ||||||
| chr7:116973520
|
G | A | 1 | a0001c0001t0001g0103 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.151+19829G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116973520 | ||||||
| chr7:116973813
|
T | G | 1 | a0001c0001t0001g0085 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.151+20122T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116973813 | ||||||
| chr7:116974059
|
A | G | 4 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG01496.hp2 HG02572.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+20368A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116974059 | ||||||
| chr7:116974512
|
C | T | 4 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG01496.hp2 HG02572.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+20821C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116974512 | ||||||
| chr7:116974542
|
C | T | 172 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(169): Show | 172 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.151+20851C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116974542 | ||||||
| chr7:116974543
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.151+20852G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116974543 | ||||||
| chr7:116974736
|
C | G | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.151+21045C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116974736 | ||||||
| chr7:116974907
|
T | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 182 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.151+21216T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116974907 | ||||||
| chr7:116975065
|
C | T | 10 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087others(7): Show | 10 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.151+21374C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116975065 | ||||||
| chr7:116975142
|
T | C | 172 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(169): Show | 172 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.151+21451T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116975142 | ||||||
| chr7:116975179
|
A | G | 15 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(12): Show | 15 | HG02055.hp2 HG02258.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.151+21488A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116975179 | ||||||
| chr7:116975414
|
A | AT | 9 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(6): Show | 9 | HG02109.hp1 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.151+21734dupT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116975414 | |||||
| chr7:116975438
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.151+21747C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116975438 | ||||||
| chr7:116975510
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.151+21819C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116975510 | ||||||
| chr7:116975985
|
G | A | 41 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(38): Show | 41 | HG00408.hp1 HG00642.hp1 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.151+22294G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116975985 | ||||||
| chr7:116976137
|
A | G | 1 | a0001c0001t0001g0134 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.151+22446A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116976137 | ||||||
| chr7:116976145
|
A | G | 4 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0001g0076others(1): Show | 4 | HG00280.hp1 HG00741.hp1 HG01081.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+22454A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116976145 | ||||||
| chr7:116976644
|
A | G | 1 | a0001c0001t0001g0172 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.151+22953A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116976644 | ||||||
| chr7:116976659
|
C | T | 1 | a0001c0001t0001g0027 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.151+22968C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116976659 | ||||||
| chr7:116976775
|
C | T | 1 | a0001c0001t0001g0020 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.151+23084C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116976775 | ||||||
| chr7:116976782
|
G | A | 22 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127others(19): Show | 22 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.151+23091G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116976782 | ||||||
| chr7:116976783
|
TACCATTA others(11): Show |
T | 1 | a0001c0001t0001g0138 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.151+23094_151+2311 others(22): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116976783 | |||||
| chr7:116976795
|
C | T | 1 | a0001c0001t0001g0171 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.151+23104C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116976795 | ||||||
| chr7:116976847
|
GATGTTAC others(3): Show |
G | 1 | a0001c0001t0001g0082 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.151+23158_151+2316 others(14): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116976847 | |||||
| chr7:116977226
|
A | T | 1 | a0001c0001t0001g0107 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.151+23535A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116977226 | ||||||
| chr7:116977447
|
G | A | 1 | a0001c0001t0001g0040 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.151+23756G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116977447 | ||||||
| chr7:116977478
|
G | A | 14 | a0001c0001t0001g0100a0001c0001t0001g0102a0001c0001t0001g0103others(11): Show | 14 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(11): Show |
intron_variant | MODIFIER | c.151+23787G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116977478 | ||||||
| chr7:116977630
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.151+23939C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116977630 | ||||||
| chr7:116977761
|
T | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 182 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.151+24070T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116977761 | ||||||
| chr7:116977849
|
G | A | 17 | a0001c0001t0001g0004a0001c0001t0001g0147a0001c0001t0001g0148others(14): Show | 17 | HG01255.hp1 HG02004.hp2 HG02027.hp1 others(14): Show |
intron_variant | MODIFIER | c.151+24158G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116977849 | ||||||
| chr7:116977896
|
A | C | 2 | a0001c0001t0001g0106a0001c0001t0001g0122 | 2 | HG02615.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.151+24205A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116977896 | ||||||
| chr7:116978172
|
A | T | 1 | a0001c0001t0001g0180 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.151+24481A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116978172 | ||||||
| chr7:116978568
|
T | TTCTA | 10 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(7): Show | 10 | HG02109.hp1 HG02451.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.151+24898_151+2490 others(8): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116978568 | |||||
| chr7:116979094
|
G | A | 1 | a0001c0001t0001g0006 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.151+25403G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116979094 | ||||||
| chr7:116979161
|
A | G | 1 | a0001c0001t0001g0117 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.151+25470A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116979161 | ||||||
| chr7:116979196
|
T | C | 2 | a0001c0001t0001g0102a0001c0001t0001g0104 | 2 | HG00280.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.151+25505T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116979196 | ||||||
| chr7:116979222
|
G | A | 1 | a0001c0001t0001g0040 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.151+25531G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116979222 | ||||||
| chr7:116979328
|
CAA | C | 2 | a0001c0001t0001g0112a0001c0001t0001g0115 | 2 | HG02451.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.151+25638_151+2563 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116979328 | ||||||
| chr7:116979549
|
A | G | 15 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(12): Show | 15 | HG02055.hp2 HG02258.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.151+25858A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116979549 | ||||||
| chr7:116979564
|
T | C | 1 | a0001c0001t0001g0022 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.151+25873T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116979564 | ||||||
| chr7:116979720
|
C | A | 172 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(169): Show | 172 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.151+26029C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116979720 | ||||||
| chr7:116979868
|
C | T | 16 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(13): Show | 16 | HG02055.hp2 HG02258.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.151+26177C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116979868 | ||||||
| chr7:116979951
|
T | G | 6 | a0001c0001t0001g0100a0001c0001t0001g0103a0001c0001t0001g0105others(3): Show | 6 | HG00099.hp1 HG00741.hp2 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.151+26260T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116979951 | ||||||
| chr7:116979958
|
C | CT | 22 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127others(19): Show | 22 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.151+26284dupT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116979958 | |||||
| chr7:116979958
|
C | CTTTTTTT | 7 | a0001c0001t0001g0045a0001c0001t0001g0059a0001c0001t0001g0061others(4): Show | 7 | HG01433.hp2 HG02280.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.151+26278_151+2628 others(11): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116979958 | |||||
| chr7:116979958
|
C | CTTTTTTT others(1): Show |
128 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(125): Show | 128 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.151+26277_151+2628 others(12): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116979958 | |||||
| chr7:116979958
|
C | CTTTTTTT others(2): Show |
12 | a0001c0001t0001g0025a0001c0001t0001g0032a0001c0001t0001g0039others(9): Show | 12 | HG00280.hp2 HG01496.hp2 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.151+26276_151+2628 others(13): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116979958 | |||||
| chr7:116979958
|
C | CTTTTTTT others(3): Show |
4 | a0001c0001t0001g0067a0001c0001t0001g0070a0001c0001t0001g0071others(1): Show | 4 | HG01358.hp2 HG02572.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+26275_151+2628 others(14): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116979958 | |||||
| chr7:116979958
|
CTTTTTT | C | 9 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(6): Show | 9 | HG02109.hp1 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.151+26279_151+2628 others(10): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116979958 | |||||
| chr7:116979982
|
A | G | 2 | a0001c0001t0001g0169a0001c0001t0001g0178 | 2 | HG01192.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.151+26291A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116979982 | ||||||
| chr7:116980049
|
C | G | 19 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(16): Show | 19 | HG01433.hp1 HG02055.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.151+26358C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116980049 | ||||||
| chr7:116980169
|
G | A | 22 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127others(19): Show | 22 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.151+26478G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116980169 | ||||||
| chr7:116980752
|
C | G | 2 | a0001c0001t0001g0169a0001c0001t0001g0178 | 2 | HG01192.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.151+27061C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116980752 | ||||||
| chr7:116980753
|
A | C | 3 | a0001c0001t0001g0168a0001c0001t0001g0171a0001c0001t0001g0177 | 3 | HG00438.hp1 NA18945.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.151+27062A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116980753 | ||||||
| chr7:116980843
|
A | G | 2 | a0001c0001t0001g0009a0001c0001t0001g0010 | 2 | NA18973.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.151+27152A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116980843 | ||||||
| chr7:116980847
|
G | A | 172 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(169): Show | 172 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.151+27156G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116980847 | ||||||
| chr7:116981076
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.151+27385G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116981076 | ||||||
| chr7:116981222
|
C | G | 9 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0128others(6): Show | 9 | HG00738.hp2 HG01071.hp1 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.151+27531C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116981222 | ||||||
| chr7:116981497
|
A | G | 1 | a0001c0001t0001g0058 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.151+27806A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116981497 | ||||||
| chr7:116981806
|
A | G | 3 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0188 | 3 | HG02280.hp1 HG02486.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.151+28115A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116981806 | ||||||
| chr7:116982243
|
A | T | 9 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(6): Show | 9 | HG02109.hp1 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.151+28552A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116982243 | ||||||
| chr7:116982310
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.151+28619C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116982310 | ||||||
| chr7:116982398
|
A | G | 2 | a0001c0001t0001g0106a0001c0001t0001g0122 | 2 | HG02615.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.151+28707A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116982398 | ||||||
| chr7:116982494
|
T | C | 15 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(12): Show | 15 | HG02055.hp2 HG02258.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.151+28803T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116982494 | ||||||
| chr7:116982730
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.151+29039C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116982730 | ||||||
| chr7:116982812
|
G | C | 1 | a0001c0001t0001g0114 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.151+29121G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116982812 | ||||||
| chr7:116982903
|
A | T | 180 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(177): Show | 180 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.151+29212A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116982903 | ||||||
| chr7:116982984
|
C | T | 13 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(10): Show | 13 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.151+29293C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116982984 | ||||||
| chr7:116983249
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.151+29558G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116983249 | ||||||
| chr7:116983680
|
G | C | 3 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0062 | 3 | HG02818.hp1 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.151+29989G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116983680 | ||||||
| chr7:116983779
|
G | A | 10 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0001g0108others(7): Show | 10 | HG00738.hp1 HG01081.hp1 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.151+30088G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116983779 | ||||||
| chr7:116984010
|
A | G | 1 | a0001c0001t0001g0178 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.151+30319A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116984010 | ||||||
| chr7:116984113
|
C | CTG | 133 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.151+30452_151+3045 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116984113 | |||||
| chr7:116984113
|
C | CTGTG | 13 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0031others(10): Show | 13 | HG01192.hp2 HG01978.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.151+30450_151+3045 others(8): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116984113 | |||||
| chr7:116984113
|
C | CTGTGTG | 16 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0086others(13): Show | 16 | HG00323.hp1 HG00438.hp1 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.151+30448_151+3045 others(10): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116984113 | |||||
| chr7:116984113
|
C | CTGTGTGT others(1): Show |
3 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0184 | 3 | HG02965.hp1 HG02976.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.151+30446_151+3045 others(12): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116984113 | |||||
| chr7:116984113
|
CTG | C | 2 | a0001c0001t0001g0062a0001c0001t0001g0148 | 2 | NA19030.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.151+30452_151+3045 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116984113 | |||||
| chr7:116984113
|
CTGTG | C | 2 | a0001c0001t0001g0058a0001c0001t0001g0059 | 2 | HG02818.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.151+30450_151+3045 others(8): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116984113 | |||||
| chr7:116984143
|
GTC | G | 4 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG01496.hp2 HG02572.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+30454_151+3045 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116984143 | |||||
| chr7:116984145
|
C | G | 15 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(12): Show | 15 | HG02055.hp2 HG02258.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.151+30454C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116984145 | ||||||
| chr7:116984147
|
A | G | 4 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG01496.hp2 HG02572.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+30456A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116984147 | ||||||
| chr7:116984365
|
T | C | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.151+30674T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116984365 | ||||||
| chr7:116984973
|
A | G | 2 | a0001c0001t0001g0002a0001c0001t0001g0003 | 2 | HG02717.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.151+31282A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116984973 | ||||||
| chr7:116985032
|
A | G | 10 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087others(7): Show | 10 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.151+31341A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116985032 | ||||||
| chr7:116985061
|
A | G | 11 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(8): Show | 11 | HG02055.hp2 HG02258.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.151+31370A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116985061 | ||||||
| chr7:116985178
|
A | G | 17 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(14): Show | 17 | HG00408.hp1 HG00673.hp1 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.151+31487A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116985178 | ||||||
| chr7:116985531
|
AT | A | 19 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(16): Show | 19 | HG01433.hp1 HG02055.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.151+31845delT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116985531 | |||||
| chr7:116985793
|
T | C | 5 | a0001c0001t0001g0125a0001c0001t0001g0140a0001c0001t0001g0141others(2): Show | 5 | HG02055.hp1 HG02258.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.151+32102T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116985793 | ||||||
| chr7:116985956
|
G | T | 1 | a0001c0001t0001g0061 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.151+32265G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116985956 | ||||||
| chr7:116986102
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.151+32411G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116986102 | ||||||
| chr7:116986204
|
T | C | 2 | a0001c0001t0001g0153a0001c0001t0001g0159 | 2 | NA18965.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.151+32513T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116986204 | ||||||
| chr7:116986206
|
G | T | 19 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(16): Show | 19 | HG01433.hp1 HG02055.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.151+32515G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116986206 | ||||||
| chr7:116986321
|
A | G | 1 | a0001c0001t0001g0026 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.151+32630A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116986321 | ||||||
| chr7:116987031
|
C | A | 2 | a0001c0001t0001g0025a0001c0001t0001g0027 | 2 | HG01934.hp2 HG02071.hp2 |
intron_variant | MODIFIER | c.151+33340C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116987031 | ||||||
| chr7:116988364
|
G | A | 2 | a0001c0001t0001g0070a0001c0001t0001g0071 | 2 | HG02922.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.151+34673G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116988364 | ||||||
| chr7:116988656
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.151+34965G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116988656 | ||||||
| chr7:116989332
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.151+35641G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116989332 | ||||||
| chr7:116989514
|
T | G | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.151+35823T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116989514 | ||||||
| chr7:116989681
|
A | T | 1 | a0001c0001t0001g0041 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.151+35990A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116989681 | ||||||
| chr7:116989682
|
T | A | 31 | a0001c0001t0001g0004a0001c0001t0001g0147a0001c0001t0001g0148others(28): Show | 31 | HG00323.hp1 HG00438.hp1 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.151+35991T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116989682 | ||||||
| chr7:116990323
|
C | A | 4 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG01496.hp2 HG02572.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+36632C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116990323 | ||||||
| chr7:116990422
|
G | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 182 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.151+36731G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116990422 | ||||||
| chr7:116990959
|
C | T | 19 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(16): Show | 19 | HG01433.hp1 HG02055.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.151+37268C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116990959 | ||||||
| chr7:116991059
|
G | C | 58 | a0001c0001t0001g0004a0001c0001t0001g0100a0001c0001t0001g0102others(55): Show | 58 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.151+37368G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116991059 | ||||||
| chr7:116991069
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.151+37378G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116991069 | ||||||
| chr7:116991196
|
C | G | 4 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(1): Show | 4 | HG02055.hp1 HG02572.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+37505C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116991196 | ||||||
| chr7:116991233
|
A | G | 15 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(12): Show | 15 | HG02055.hp2 HG02258.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.151+37542A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116991233 | ||||||
| chr7:116991240
|
C | A | 1 | a0001c0001t0001g0188 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.151+37549C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116991240 | ||||||
| chr7:116991442
|
T | C | 1 | a0001c0001t0001g0128 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.151+37751T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116991442 | ||||||
| chr7:116991483
|
A | T | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.151+37792A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116991483 | ||||||
| chr7:116991534
|
C | T | 19 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(16): Show | 19 | HG01433.hp1 HG02055.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.151+37843C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116991534 | ||||||
| chr7:116991550
|
G | A | 3 | a0001c0001t0001g0168a0001c0001t0001g0171a0001c0001t0001g0177 | 3 | HG00438.hp1 NA18945.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.151+37859G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116991550 | ||||||
| chr7:116991595
|
C | T | 41 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(38): Show | 41 | HG00408.hp1 HG00642.hp1 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.151+37904C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116991595 | ||||||
| chr7:116991655
|
A | G | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.151+37964A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116991655 | ||||||
| chr7:116991871
|
T | A | 1 | a0001c0001t0001g0116 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.151+38180T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116991871 | ||||||
| chr7:116992000
|
C | A | 1 | a0001c0001t0001g0120 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.151+38309C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116992000 | ||||||
| chr7:116992598
|
G | T | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.151+38907G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116992598 | ||||||
| chr7:116992609
|
G | A | 5 | a0001c0001t0001g0015a0001c0001t0001g0140a0001c0001t0001g0141others(2): Show | 5 | HG02055.hp1 HG02572.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.151+38918G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116992609 | ||||||
| chr7:116992646
|
A | G | 1 | a0001c0001t0001g0138 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.151+38955A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116992646 | ||||||
| chr7:116992683
|
A | C | 1 | a0001c0001t0001g0095 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.151+38992A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116992683 | ||||||
| chr7:116992932
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.151+39241C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116992932 | ||||||
| chr7:116993307
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.151+39616G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116993307 | ||||||
| chr7:116993322
|
T | C | 1 | a0001c0001t0001g0001 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.151+39631T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116993322 | ||||||
| chr7:116993466
|
G | A | 1 | a0001c0001t0001g0017 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.151+39775G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116993466 | ||||||
| chr7:116993644
|
T | A | 19 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(16): Show | 19 | HG01433.hp1 HG02055.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.151+39953T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116993644 | ||||||
| chr7:116994019
|
T | C | 1 | a0001c0001t0001g0121 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.151+40328T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116994019 | ||||||
| chr7:116994053
|
G | A | 19 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(16): Show | 19 | HG01433.hp1 HG02055.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.151+40362G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116994053 | ||||||
| chr7:116994475
|
G | T | 13 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(10): Show | 13 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.151+40784G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116994475 | ||||||
| chr7:116994680
|
T | G | 4 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(1): Show | 4 | HG02055.hp1 HG02572.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+40989T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116994680 | ||||||
| chr7:116994791
|
C | A | 22 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127others(19): Show | 22 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.151+41100C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116994791 | ||||||
| chr7:116994812
|
A | G | 1 | a0001c0001t0001g0148 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.151+41121A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116994812 | ||||||
| chr7:116994836
|
G | T | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 182 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.151+41145G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116994836 | ||||||
| chr7:116994929
|
C | T | 3 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0002t0001g0044 | 3 | HG02970.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.151+41238C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116994929 | ||||||
| chr7:116994994
|
T | C | 13 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(10): Show | 13 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.151+41303T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116994994 | ||||||
| chr7:116995145
|
T | G | 3 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0062 | 3 | HG02818.hp1 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.151+41454T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116995145 | ||||||
| chr7:116995651
|
C | T | 72 | a0001c0001t0001g0004a0001c0001t0001g0064a0001c0001t0001g0065others(69): Show | 72 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.151+41960C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116995651 | ||||||
| chr7:116995818
|
C | A | 19 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(16): Show | 19 | HG01433.hp1 HG02055.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.151+42127C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116995818 | ||||||
| chr7:116996082
|
G | GT | 46 | a0001c0001t0001g0025a0001c0001t0001g0062a0001c0001t0001g0063others(43): Show | 46 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.151+42408dupT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116996082 | |||||
| chr7:116996082
|
G | GTTT | 12 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(9): Show | 12 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.151+42406_151+4240 others(7): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116996082 | |||||
| chr7:116996167
|
C | T | 1 | a0001c0001t0001g0120 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.151+42476C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116996167 | ||||||
| chr7:116996169
|
C | T | 72 | a0001c0001t0001g0004a0001c0001t0001g0064a0001c0001t0001g0065others(69): Show | 72 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.151+42478C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116996169 | ||||||
| chr7:116996391
|
T | C | 1 | a0001c0001t0001g0084 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.151+42700T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116996391 | ||||||
| chr7:116996566
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.151+42875C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116996566 | ||||||
| chr7:116996600
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.151+42909C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116996600 | ||||||
| chr7:116996655
|
A | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 182 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.151+42964A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116996655 | ||||||
| chr7:116996911
|
T | C | 4 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(1): Show | 4 | HG01433.hp1 HG02723.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+43220T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116996911 | ||||||
| chr7:116996976
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.151+43285G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116996976 | ||||||
| chr7:116997038
|
G | A | 3 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0188 | 3 | HG02280.hp1 HG02486.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.151+43347G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116997038 | ||||||
| chr7:116997039
|
T | C | 3 | a0001c0001t0001g0168a0001c0001t0001g0171a0001c0001t0001g0177 | 3 | HG00438.hp1 NA18945.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.151+43348T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116997039 | ||||||
| chr7:116997246
|
G | A | 3 | a0001c0001t0001g0107a0001c0001t0001g0110a0001c0001t0001g0111 | 3 | HG00323.hp2 HG00642.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.151+43555G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116997246 | ||||||
| chr7:116997268
|
C | T | 1 | a0001c0001t0001g0061 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.151+43577C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116997268 | ||||||
| chr7:116997338
|
G | T | 9 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(6): Show | 9 | HG02109.hp1 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.151+43647G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116997338 | ||||||
| chr7:116997383
|
G | A | 1 | a0001c0001t0001g0062 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.151+43692G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116997383 | ||||||
| chr7:116997535
|
T | C | 41 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(38): Show | 41 | HG00408.hp1 HG00642.hp1 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.151+43844T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116997535 | ||||||
| chr7:116997635
|
G | T | 41 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(38): Show | 41 | HG00408.hp1 HG00642.hp1 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.151+43944G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116997635 | ||||||
| chr7:116997695
|
T | C | 9 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(6): Show | 9 | HG02109.hp1 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.151+44004T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116997695 | ||||||
| chr7:116997777
|
C | T | 1 | a0001c0001t0001g0121 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.151+44086C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116997777 | ||||||
| chr7:116997945
|
C | T | 172 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(169): Show | 172 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.151+44254C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116997945 | ||||||
| chr7:116997987
|
G | A | 1 | a0001c0001t0001g0020 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.151+44296G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116997987 | ||||||
| chr7:116997997
|
G | A | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.151+44306G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116997997 | ||||||
| chr7:116998014
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.151+44323C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116998014 | ||||||
| chr7:116998106
|
C | T | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.151+44415C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116998106 | ||||||
| chr7:116998194
|
G | A | 2 | a0001c0001t0001g0149a0001c0001t0001g0150 | 2 | NA18974.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.151+44503G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116998194 | ||||||
| chr7:116998238
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.151+44547G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116998238 | ||||||
| chr7:116998251
|
C | T | 2 | a0001c0001t0001g0070a0001c0001t0001g0071 | 2 | HG02922.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.151+44560C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116998251 | ||||||
| chr7:116998273
|
G | A | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.151+44582G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116998273 | ||||||
| chr7:116998304
|
C | T | 2 | a0001c0001t0001g0112a0001c0001t0001g0115 | 2 | HG02451.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.151+44613C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116998304 | ||||||
| chr7:116998373
|
C | T | 3 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0062 | 3 | HG02818.hp1 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.151+44682C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116998373 | ||||||
| chr7:116998502
|
C | T | 1 | a0001c0001t0001g0008 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.151+44811C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116998502 | ||||||
| chr7:116998655
|
C | G | 14 | a0001c0001t0001g0100a0001c0001t0001g0102a0001c0001t0001g0103others(11): Show | 14 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(11): Show |
intron_variant | MODIFIER | c.151+44964C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116998655 | ||||||
| chr7:116998699
|
C | T | 1 | a0001c0001t0001g0118 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.151+45008C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116998699 | ||||||
| chr7:116999367
|
G | T | 3 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0188 | 3 | HG02280.hp1 HG02486.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.151+45676G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116999367 | ||||||
| chr7:116999370
|
A | T | 3 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0188 | 3 | HG02280.hp1 HG02486.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.151+45679A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116999370 | ||||||
| chr7:116999519
|
C | A | 2 | a0001c0001t0001g0153a0001c0001t0001g0159 | 2 | NA18965.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.151+45828C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116999519 | ||||||
| chr7:116999808
|
C | CT | 102 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(99): Show | 102 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.151+46137dupT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116999808 | |||||
| chr7:116999808
|
C | CTT | 66 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0020others(63): Show | 66 | HG00280.hp2 HG00323.hp1 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.151+46136_151+4613 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116999808 | |||||
| chr7:116999808
|
C | CTTT | 10 | a0001c0001t0001g0102a0001c0001t0001g0158a0001c0001t0001g0160others(7): Show | 10 | HG01192.hp1 HG01978.hp2 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.151+46135_151+4613 others(7): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116999808 | |||||
| chr7:116999813
|
T | TC | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.151+46122_151+4612 others(5): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116999813 | ||||||
| chr7:116999817
|
T | C | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.151+46126T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116999817 | ||||||
| chr7:117000091
|
G | A | 2 | a0001c0001t0001g0070a0001c0001t0001g0071 | 2 | HG02922.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.151+46400G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117000091 | ||||||
| chr7:117000203
|
T | G | 1 | a0001c0001t0001g0046 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.151+46512T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117000203 | ||||||
| chr7:117000266
|
G | C | 17 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(14): Show | 17 | HG00408.hp1 HG00673.hp1 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.151+46575G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117000266 | ||||||
| chr7:117000487
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.151+46796G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117000487 | ||||||
| chr7:117000628
|
G | A | 3 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0188 | 3 | HG02280.hp1 HG02486.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.151+46937G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117000628 | ||||||
| chr7:117000836
|
C | T | 4 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(1): Show | 4 | HG01433.hp1 HG02723.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+47145C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117000836 | ||||||
| chr7:117001205
|
A | G | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.151+47514A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117001205 | ||||||
| chr7:117001279
|
A | G | 1 | a0001c0001t0001g0128 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.151+47588A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117001279 | ||||||
| chr7:117001331
|
GA | G | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(183): Show | 186 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.151+47647delA | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117001331 | |||||
| chr7:117001341
|
T | C | 3 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0188 | 3 | HG02280.hp1 HG02486.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.151+47650T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117001341 | ||||||
| chr7:117001406
|
C | A | 2 | a0001c0001t0001g0179a0001c0001t0001g0187 | 2 | NA19000.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.151+47715C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117001406 | ||||||
| chr7:117001474
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.151+47783G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117001474 | ||||||
| chr7:117001494
|
C | A | 3 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0097 | 3 | HG02109.hp1 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.151+47803C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117001494 | ||||||
| chr7:117002184
|
C | T | 172 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(169): Show | 172 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.151+48493C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117002184 | ||||||
| chr7:117002404
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.151+48713C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117002404 | ||||||
| chr7:117002420
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.151+48729C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117002420 | ||||||
| chr7:117002433
|
A | G | 13 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(10): Show | 13 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.151+48742A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117002433 | ||||||
| chr7:117002639
|
C | CTG | 5 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0081others(2): Show | 5 | HG02109.hp2 HG02280.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.151+48974_151+4897 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117002639 | |||||
| chr7:117002639
|
C | CTGTG | 67 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(64): Show | 67 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(64): Show |
intron_variant | MODIFIER | c.151+48972_151+4897 others(8): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117002639 | |||||
| chr7:117002639
|
C | CTGTGTG | 97 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0014others(94): Show | 97 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.151+48970_151+4897 others(10): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117002639 | |||||
| chr7:117002639
|
C | CTGTGTGT others(1): Show |
12 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(9): Show | 12 | HG01192.hp1 HG02027.hp1 HG02071.hp1 others(9): Show |
intron_variant | MODIFIER | c.151+48968_151+4897 others(12): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117002639 | |||||
| chr7:117002639
|
CTGTGTGT others(9): Show |
C | 1 | a0001c0001t0001g0120 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.151+48960_151+4897 others(20): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117002639 | |||||
| chr7:117002813
|
C | CT | 121 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(118): Show | 121 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.151+49148dupT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117002813 | |||||
| chr7:117002813
|
C | CTT | 35 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0011others(32): Show | 35 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.151+49147_151+4914 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117002813 | |||||
| chr7:117002813
|
CTTTTTTT | C | 5 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(2): Show | 5 | HG01433.hp1 HG02723.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.151+49142_151+4914 others(11): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117002813 | |||||
| chr7:117003016
|
T | G | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 182 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.151+49325T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117003016 | ||||||
| chr7:117003161
|
T | A | 3 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0188 | 3 | HG02280.hp1 HG02486.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.151+49470T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117003161 | ||||||
| chr7:117003189
|
C | T | 14 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(11): Show | 14 | HG00738.hp1 HG01081.hp1 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.151+49498C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117003189 | ||||||
| chr7:117003656
|
C | T | 22 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127others(19): Show | 22 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.151+49965C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117003656 | ||||||
| chr7:117004096
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.151+50405G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117004096 | ||||||
| chr7:117004296
|
C | A | 22 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127others(19): Show | 22 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.151+50605C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117004296 | ||||||
| chr7:117004343
|
T | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 182 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.151+50652T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117004343 | ||||||
| chr7:117004430
|
G | T | 1 | a0001c0001t0001g0148 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.151+50739G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117004430 | ||||||
| chr7:117004619
|
C | T | 1 | a0001c0001t0001g0001 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.151+50928C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117004619 | ||||||
| chr7:117004905
|
T | A | 4 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG01496.hp2 HG02572.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+51214T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117004905 | ||||||
| chr7:117005286
|
T | A | 2 | a0001c0001t0001g0086a0001c0001t0001g0089 | 2 | HG02647.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.151+51595T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117005286 | ||||||
| chr7:117005325
|
T | A | 1 | a0001c0001t0001g0154 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.151+51634T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117005325 | ||||||
| chr7:117005420
|
T | C | 1 | a0001c0001t0001g0139 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.151+51729T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117005420 | ||||||
| chr7:117005572
|
G | A | 10 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087others(7): Show | 10 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.151+51881G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117005572 | ||||||
| chr7:117005715
|
C | G | 1 | a0001c0001t0001g0152 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.151+52024C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117005715 | ||||||
| chr7:117005782
|
C | T | 1 | a0001c0001t0001g0019 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.151+52091C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117005782 | ||||||
| chr7:117005825
|
A | G | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.151+52134A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117005825 | ||||||
| chr7:117005826
|
T | C | 72 | a0001c0001t0001g0004a0001c0001t0001g0064a0001c0001t0001g0065others(69): Show | 72 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.151+52135T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117005826 | ||||||
| chr7:117006085
|
G | A | 1 | a0001c0001t0001g0076 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.151+52394G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117006085 | ||||||
| chr7:117006473
|
C | T | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 182 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.151+52782C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117006473 | ||||||
| chr7:117006748
|
A | G | 9 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0162others(6): Show | 9 | HG02630.hp1 HG02818.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.151+53057A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117006748 | ||||||
| chr7:117007890
|
C | A | 1 | a0001c0001t0001g0072 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.151+54199C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117007890 | ||||||
| chr7:117008004
|
T | C | 10 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(7): Show | 10 | HG02040.hp2 HG02273.hp1 NA18960.hp2 others(7): Show |
intron_variant | MODIFIER | c.151+54313T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117008004 | ||||||
| chr7:117009012
|
T | C | 1 | a0001c0001t0001g0045 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.151+55321T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117009012 | ||||||
| chr7:117009253
|
TTTTGTTT others(11): Show |
T | 10 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087others(7): Show | 10 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.151+55566_151+5558 others(22): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117009253 | |||||
| chr7:117009262
|
T | G | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.151+55571T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117009262 | ||||||
| chr7:117009264
|
T | G | 12 | a0001c0001t0001g0022a0001c0001t0001g0028a0001c0001t0001g0029others(9): Show | 12 | HG00408.hp1 HG00673.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.151+55573T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117009264 | ||||||
| chr7:117009266
|
T | G | 1 | a0001c0001t0001g0054 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.151+55575T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117009266 | ||||||
| chr7:117009269
|
TTG | T | 22 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127others(19): Show | 22 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.151+55580_151+5558 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117009269 | |||||
| chr7:117009270
|
TG | T | 149 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(146): Show | 149 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.151+55580delG | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117009270 | ||||||
| chr7:117009271
|
G | T | 6 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0061others(3): Show | 6 | HG01433.hp2 HG02071.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.151+55580G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117009271 | ||||||
| chr7:117009784
|
G | A | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 182 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.151+56093G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117009784 | ||||||
| chr7:117010520
|
G | A | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 182 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.151+56829G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117010520 | ||||||
| chr7:117010790
|
T | C | 3 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0187 | 3 | NA19000.hp1 NA19004.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.151+57099T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117010790 | ||||||
| chr7:117010873
|
G | A | 1 | a0001c0001t0001g0138 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.151+57182G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117010873 | ||||||
| chr7:117011134
|
T | TTG | 8 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0093others(5): Show | 8 | HG01433.hp1 HG02280.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.151+57461_151+5746 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117011134 | |||||
| chr7:117011247
|
C | G | 6 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0162others(3): Show | 6 | HG02630.hp1 HG02818.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.151+57556C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117011247 | ||||||
| chr7:117011278
|
C | A | 2 | a0001c0001t0001g0016a0001c0001t0001g0018 | 2 | HG03492.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.151+57587C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117011278 | ||||||
| chr7:117011355
|
C | T | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 182 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.151+57664C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117011355 | ||||||
| chr7:117011761
|
C | G | 1 | a0001c0001t0001g0078 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.151+58070C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117011761 | ||||||
| chr7:117011762
|
T | A | 1 | a0001c0001t0001g0047 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.151+58071T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117011762 | ||||||
| chr7:117011778
|
C | T | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 182 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.151+58087C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117011778 | ||||||
| chr7:117011908
|
A | G | 1 | a0001c0001t0001g0085 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.151+58217A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117011908 | ||||||
| chr7:117012189
|
T | A | 185 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(182): Show | 185 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.151+58498T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117012189 | ||||||
| chr7:117012220
|
C | T | 3 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0084 | 3 | NA18990.hp1 NA19004.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.151+58529C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117012220 | ||||||
| chr7:117012283
|
A | AT | 39 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(36): Show | 39 | HG00408.hp1 HG00642.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.151+58608dupT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117012283 | |||||
| chr7:117012413
|
G | A | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 182 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.151+58722G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117012413 | ||||||
| chr7:117012480
|
G | A | 3 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0084 | 3 | NA18990.hp1 NA19004.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.151+58789G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117012480 | ||||||
| chr7:117012716
|
T | A | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 182 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.151+59025T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117012716 | ||||||
| chr7:117013432
|
T | G | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.151+59741T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117013432 | ||||||
| chr7:117013510
|
G | GTACTTTC | 2 | a0001c0001t0001g0113a0001c0001t0001g0183 | 2 | HG04184.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.151+59821_151+5982 others(11): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117013510 | |||||
| chr7:117013512
|
A | C | 9 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(6): Show | 9 | HG02109.hp1 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.151+59821A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117013512 | ||||||
| chr7:117013782
|
G | A | 1 | a0001c0001t0001g0181 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.151+60091G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117013782 | ||||||
| chr7:117013801
|
C | G | 1 | a0001c0001t0001g0180 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.151+60110C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117013801 | ||||||
| chr7:117013902
|
CTAGAATT others(2): Show |
C | 3 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0097 | 3 | HG02109.hp1 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.151+60223_151+6023 others(13): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117013902 | |||||
| chr7:117014147
|
A | G | 72 | a0001c0001t0001g0004a0001c0001t0001g0064a0001c0001t0001g0065others(69): Show | 72 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.151+60456A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117014147 | ||||||
| chr7:117014155
|
G | T | 17 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(14): Show | 17 | HG00408.hp1 HG00673.hp1 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.151+60464G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117014155 | ||||||
| chr7:117014287
|
G | GATTGAAA others(2): Show |
182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 182 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.151+60600_151+6060 others(13): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117014287 | |||||
| chr7:117015804
|
G | A | 22 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127others(19): Show | 22 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.151+62113G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117015804 | ||||||
| chr7:117016010
|
A | T | 1 | a0001c0001t0001g0085 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.151+62319A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117016010 | ||||||
| chr7:117016384
|
G | A | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 182 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.151+62693G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117016384 | ||||||
| chr7:117016410
|
A | G | 9 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(6): Show | 9 | HG02109.hp1 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.151+62719A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117016410 | ||||||
| chr7:117016504
|
TTAAG | T | 172 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(169): Show | 172 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.151+62817_151+6282 others(8): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117016504 | |||||
| chr7:117017057
|
A | G | 4 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(1): Show | 4 | HG02055.hp1 HG02572.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+63366A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117017057 | ||||||
| chr7:117017060
|
C | T | 15 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(12): Show | 15 | HG02055.hp2 HG02258.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.151+63369C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117017060 | ||||||
| chr7:117017410
|
C | T | 22 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127others(19): Show | 22 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.151+63719C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117017410 | ||||||
| chr7:117017597
|
C | T | 3 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0188 | 3 | HG02280.hp1 HG02486.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.151+63906C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117017597 | ||||||
| chr7:117017612
|
T | C | 1 | a0001c0001t0001g0047 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.151+63921T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117017612 | ||||||
| chr7:117017627
|
T | G | 2 | a0001c0001t0001g0169a0001c0001t0001g0178 | 2 | HG01192.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.151+63936T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117017627 | ||||||
| chr7:117017677
|
C | T | 1 | a0001c0001t0001g0021 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.151+63986C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117017677 | ||||||
| chr7:117017859
|
A | C | 10 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087others(7): Show | 10 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.151+64168A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117017859 | ||||||
| chr7:117018112
|
G | A | 2 | a0001c0001t0001g0031a0001c0001t0001g0042 | 2 | HG01192.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.151+64421G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117018112 | ||||||
| chr7:117018505
|
A | G | 1 | a0001c0001t0001g0119 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.151+64814A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117018505 | ||||||
| chr7:117019163
|
G | C | 3 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003 | 3 | HG02717.hp1 HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.151+65472G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117019163 | ||||||
| chr7:117019210
|
A | G | 1 | a0001c0001t0001g0142 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.151+65519A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117019210 | ||||||
| chr7:117020119
|
G | A | 4 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(1): Show | 4 | HG01433.hp1 HG02723.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+66428G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117020119 | ||||||
| chr7:117020139
|
G | A | 2 | a0001c0001t0001g0016a0001c0001t0001g0018 | 2 | HG03492.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.151+66448G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117020139 | ||||||
| chr7:117020410
|
AC | A | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 182 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.151+66721delC | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117020410 | |||||
| chr7:117020481
|
T | G | 1 | a0001c0001t0001g0120 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.151+66790T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117020481 | ||||||
| chr7:117020560
|
T | C | 13 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(10): Show | 13 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.151+66869T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117020560 | ||||||
| chr7:117020646
|
C | T | 3 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0184 | 3 | HG02965.hp1 HG02976.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.151+66955C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117020646 | ||||||
| chr7:117020749
|
A | G | 72 | a0001c0001t0001g0004a0001c0001t0001g0064a0001c0001t0001g0065others(69): Show | 72 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.151+67058A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117020749 | ||||||
| chr7:117020796
|
T | C | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.151+67105T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117020796 | ||||||
| chr7:117020797
|
A | T | 1 | a0001c0001t0001g0062 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.151+67106A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117020797 | ||||||
| chr7:117020856
|
G | A | 12 | a0001c0001t0001g0022a0001c0001t0001g0028a0001c0001t0001g0029others(9): Show | 12 | HG00408.hp1 HG00673.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.151+67165G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117020856 | ||||||
| chr7:117021109
|
G | A | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(183): Show | 186 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.151+67418G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117021109 | ||||||
| chr7:117021113
|
G | A | 1 | a0001c0001t0001g0139 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.151+67422G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117021113 | ||||||
| chr7:117021468
|
A | G | 1 | a0001c0001t0001g0137 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.151+67777A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117021468 | ||||||
| chr7:117021795
|
T | A | 1 | a0001c0001t0001g0124 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.151+68104T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117021795 | ||||||
| chr7:117021952
|
T | A | 22 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127others(19): Show | 22 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.151+68261T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117021952 | ||||||
| chr7:117022054
|
CT | C | 72 | a0001c0001t0001g0004a0001c0001t0001g0064a0001c0001t0001g0065others(69): Show | 72 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.151+68366delT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117022054 | |||||
| chr7:117022290
|
G | A | 4 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(1): Show | 4 | HG02055.hp1 HG02572.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+68599G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117022290 | ||||||
| chr7:117022336
|
C | T | 1 | a0001c0001t0001g0136 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.151+68645C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117022336 | ||||||
| chr7:117022458
|
T | A | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 182 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.151+68767T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117022458 | ||||||
| chr7:117022538
|
A | G | 1 | a0001c0001t0001g0020 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.151+68847A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117022538 | ||||||
| chr7:117022975
|
T | C | 13 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(10): Show | 13 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.151+69284T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117022975 | ||||||
| chr7:117023097
|
G | GGAAATGT others(33): Show |
1 | a0001c0001t0001g0129 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.151+69407_151+6944 others(44): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117023097 | |||||
| chr7:117023777
|
T | TTA | 163 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(160): Show | 163 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.151+70102_151+7010 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117023777 | |||||
| chr7:117023777
|
T | TTATA | 8 | a0001c0001t0001g0059a0001c0001t0001g0062a0001c0001t0001g0070others(5): Show | 8 | HG00438.hp2 HG01192.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.151+70100_151+7010 others(8): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117023777 | |||||
| chr7:117023805
|
C | CGT | 2 | a0001c0001t0001g0061a0001c0001t0001g0129 | 2 | HG01358.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.151+70130_151+7013 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117023805 | |||||
| chr7:117023934
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.151+70243C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117023934 | ||||||
| chr7:117023941
|
C | G | 1 | a0001c0001t0001g0072 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.151+70250C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117023941 | ||||||
| chr7:117024067
|
A | G | 1 | a0001c0001t0001g0152 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.151+70376A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117024067 | ||||||
| chr7:117024092
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.151+70401G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117024092 | ||||||
| chr7:117024673
|
C | G | 13 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(10): Show | 13 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.151+70982C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117024673 | ||||||
| chr7:117024723
|
A | G | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.151+71032A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117024723 | ||||||
| chr7:117024816
|
A | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 182 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.151+71125A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117024816 | ||||||
| chr7:117024964
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.151+71273A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117024964 | ||||||
| chr7:117025000
|
A | G | 1 | a0001c0001t0001g0133 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.151+71309A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117025000 | ||||||
| chr7:117025536
|
G | T | 1 | a0001c0001t0001g0188 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.151+71845G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117025536 | ||||||
| chr7:117025537
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.151+71846C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117025537 | ||||||
| chr7:117025732
|
C | T | 1 | a0001c0001t0001g0061 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.151+72041C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117025732 | ||||||
| chr7:117026649
|
A | G | 1 | a0001c0001t0001g0132 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.151+72958A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117026649 | ||||||
| chr7:117027121
|
T | C | 1 | a0001c0001t0001g0027 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.152-72641T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117027121 | ||||||
| chr7:117027132
|
A | G | 172 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(169): Show | 172 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.152-72630A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117027132 | ||||||
| chr7:117027355
|
G | A | 126 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(123): Show | 126 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.152-72407G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117027355 | ||||||
| chr7:117027446
|
G | A | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 182 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.152-72316G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117027446 | ||||||
| chr7:117027462
|
T | TAAAAGTA others(120): Show |
2 | a0001c0001t0001g0093a0001c0001t0001g0095 | 2 | HG01433.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.152-72291_152-7229 others(131): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117027462 | |||||
| chr7:117027462
|
T | TAAAAGTA others(115): Show |
1 | a0001c0001t0001g0094 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.152-72291_152-7229 others(126): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117027462 | |||||
| chr7:117027462
|
T | TAAAAGTA others(110): Show |
1 | a0001c0001t0001g0098 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.152-72291_152-7229 others(121): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117027462 | |||||
| chr7:117027463
|
A | AAAAATTA others(24): Show |
1 | a0001c0001t0001g0048 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.152-72296_152-7229 others(35): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117027463 | |||||
| chr7:117027463
|
A | AAAAATTA others(29): Show |
4 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0055others(1): Show | 4 | HG02622.hp2 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-72296_152-7229 others(40): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117027463 | |||||
| chr7:117027463
|
A | AAAAATTA others(34): Show |
9 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(6): Show | 9 | HG02258.hp2 HG02280.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.152-72296_152-7229 others(45): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117027463 | |||||
| chr7:117027463
|
A | AAAAATTA others(44): Show |
1 | a0001c0001t0001g0054 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.152-72296_152-7229 others(55): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117027463 | |||||
| chr7:117027463
|
A | AAAAGT | 32 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(29): Show | 32 | HG00408.hp1 HG00642.hp1 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.152-72266_152-7226 others(9): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117027463 | |||||
| chr7:117027463
|
A | AAAAGTAA others(28): Show |
3 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0097 | 3 | HG02109.hp1 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.152-72291_152-7229 others(39): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117027463 | |||||
| chr7:117027463
|
A | AAAAGTAA others(37): Show |
3 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088 | 3 | HG02451.hp1 NA19240.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.152-72291_152-7229 others(48): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117027463 | |||||
| chr7:117027463
|
A | AAAAGTAA others(42): Show |
2 | a0001c0001t0001g0089a0001c0001t0001g0092 | 2 | HG02647.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.152-72291_152-7229 others(53): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117027463 | |||||
| chr7:117027463
|
A | AAAAGTAA others(47): Show |
1 | a0001c0001t0001g0096 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.152-72291_152-7229 others(58): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117027463 | |||||
| chr7:117027463
|
A | AAAAGTAA others(27): Show |
1 | a0001c0001t0001g0085 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.152-72291_152-7229 others(38): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117027463 | |||||
| chr7:117027463
|
A | AAAAGTAA others(25): Show |
1 | a0001c0001t0001g0069 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.152-72291_152-7229 others(36): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117027463 | |||||
| chr7:117027463
|
A | AAAAGTAA others(40): Show |
1 | a0001c0001t0001g0068 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.152-72291_152-7229 others(51): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117027463 | |||||
| chr7:117027463
|
A | AAAAGTAA others(80): Show |
1 | a0001c0001t0001g0188 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.152-72291_152-7229 others(91): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117027463 | |||||
| chr7:117027463
|
A | AAAAGTAA others(3): Show |
16 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0016others(13): Show | 16 | HG00408.hp2 HG00438.hp2 HG02040.hp1 others(13): Show |
intron_variant | MODIFIER | c.152-72271_152-7226 others(14): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117027463 | |||||
| chr7:117027463
|
A | AAAAGTAA others(8): Show |
10 | a0001c0001t0001g0015a0001c0001t0001g0072a0001c0001t0001g0154others(7): Show | 10 | HG01255.hp1 HG01934.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.152-72276_152-7226 others(19): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117027463 | |||||
| chr7:117027463
|
A | AAAAGTAA others(13): Show |
28 | a0001c0001t0001g0012a0001c0001t0001g0062a0001c0001t0001g0073others(25): Show | 28 | HG00323.hp2 HG00741.hp1 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.152-72281_152-7226 others(24): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117027463 | |||||
| chr7:117027463
|
A | AAAAGTAA others(18): Show |
33 | a0001c0001t0001g0004a0001c0001t0001g0064a0001c0001t0001g0065others(30): Show | 33 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(30): Show |
intron_variant | MODIFIER | c.152-72286_152-7226 others(29): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117027463 | |||||
| chr7:117027463
|
A | AAAAGTAA others(23): Show |
19 | a0001c0001t0001g0074a0001c0001t0001g0103a0001c0001t0001g0105others(16): Show | 19 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(16): Show |
intron_variant | MODIFIER | c.152-72291_152-7226 others(34): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117027463 | |||||
| chr7:117027463
|
A | AAAAGTAA others(28): Show |
7 | a0001c0001t0001g0071a0001c0001t0001g0101a0001c0001t0001g0107others(4): Show | 7 | HG00738.hp1 HG00738.hp2 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.152-72296_152-7226 others(39): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117027463 | |||||
| chr7:117027463
|
A | AAAAGTAA others(33): Show |
1 | a0001c0001t0001g0151 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.152-72262_152-7226 others(44): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117027463 | |||||
| chr7:117027473
|
T | TAA | 15 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(12): Show | 15 | HG02055.hp2 HG02258.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.152-72287_152-7228 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117027473 | |||||
| chr7:117027767
|
G | T | 172 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(169): Show | 172 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.152-71995G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117027767 | ||||||
| chr7:117027930
|
A | G | 9 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(6): Show | 9 | HG02109.hp1 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.152-71832A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117027930 | ||||||
| chr7:117028608
|
T | C | 169 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(166): Show | 169 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.152-71154T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117028608 | ||||||
| chr7:117028958
|
C | T | 185 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(182): Show | 185 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.152-70804C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117028958 | ||||||
| chr7:117029234
|
T | C | 1 | a0001c0001t0001g0047 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.152-70528T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117029234 | ||||||
| chr7:117029239
|
C | T | 15 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(12): Show | 15 | HG02055.hp2 HG02258.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.152-70523C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117029239 | ||||||
| chr7:117029241
|
A | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 182 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.152-70521A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117029241 | ||||||
| chr7:117029641
|
C | T | 13 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(10): Show | 13 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.152-70121C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117029641 | ||||||
| chr7:117029756
|
A | AT | 76 | a0001c0001t0001g0004a0001c0001t0001g0061a0001c0001t0001g0064others(73): Show | 76 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.152-69994dupT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117029756 | |||||
| chr7:117029861
|
C | T | 172 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(169): Show | 172 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.152-69901C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117029861 | ||||||
| chr7:117029889
|
G | T | 1 | a0001c0001t0001g0032 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.152-69873G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117029889 | ||||||
| chr7:117030605
|
A | G | 40 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(37): Show | 40 | HG00408.hp1 HG00642.hp1 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.152-69157A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117030605 | ||||||
| chr7:117030620
|
A | G | 1 | a0001c0001t0001g0005 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.152-69142A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117030620 | ||||||
| chr7:117030637
|
A | T | 1 | a0001c0001t0001g0008 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.152-69125A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117030637 | ||||||
| chr7:117030719
|
C | T | 1 | a0001c0001t0001g0101 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.152-69043C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117030719 | ||||||
| chr7:117030787
|
G | A | 1 | a0001c0001t0001g0018 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.152-68975G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117030787 | ||||||
| chr7:117030907
|
T | C | 1 | a0001c0001t0001g0085 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.152-68855T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117030907 | ||||||
| chr7:117031128
|
G | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 182 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.152-68634G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031128 | ||||||
| chr7:117031311
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.152-68451C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031311 | ||||||
| chr7:117031364
|
G | GTGTGTAT others(27): Show |
8 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0085others(5): Show | 8 | HG01071.hp1 HG02109.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.152-68383_152-6838 others(38): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031364 | |||||
| chr7:117031368
|
G | A | 2 | a0001c0001t0001g0079a0001c0001t0001g0112 | 2 | HG03209.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.152-68394G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031368 | ||||||
| chr7:117031372
|
A | G | 2 | a0001c0001t0001g0079a0001c0001t0001g0112 | 2 | HG03209.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.152-68390A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031372 | ||||||
| chr7:117031376
|
G | GTGTGTAT others(7): Show |
1 | a0001c0001t0001g0128 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(18): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031376 | |||||
| chr7:117031379
|
T | TATATATA others(325): Show |
1 | a0001c0001t0001g0112 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.152-68377_152-6837 others(336): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031379 | |||||
| chr7:117031379
|
T | TATATATA others(653): Show |
1 | a0001c0001t0001g0079 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.152-68377_152-6837 others(664): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031379 | |||||
| chr7:117031379
|
T | TGTATATA others(177): Show |
1 | a0001c0001t0001g0045 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(188): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(237): Show |
1 | a0001c0001t0001g0054 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(248): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(505): Show |
1 | a0001c0001t0001g0188 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.152-68383_152-6838 others(516): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(207): Show |
1 | a0001c0001t0001g0055 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(218): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(267): Show |
4 | a0001c0001t0001g0043a0001c0001t0001g0050a0001c0001t0001g0051others(1): Show | 4 | HG02258.hp2 HG02647.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-68383_152-6838 others(278): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(297): Show |
1 | a0001c0001t0001g0046 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.152-68383_152-6838 others(308): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(297): Show |
1 | a0001c0001t0001g0056 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(308): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(87): Show |
2 | a0001c0001t0001g0129a0001c0001t0001g0144 | 2 | HG01358.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.152-68383_152-6838 others(98): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(117): Show |
1 | a0001c0001t0001g0182 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(128): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(327): Show |
1 | a0001c0001t0001g0173 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(338): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(137): Show |
1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.152-68383_152-6838 others(148): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(117): Show |
3 | a0001c0001t0001g0126a0001c0001t0001g0136a0001c0001t0001g0139 | 3 | HG00738.hp2 NA18971.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.152-68383_152-6838 others(128): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(387): Show |
1 | a0001c0001t0001g0157 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(398): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(147): Show |
1 | a0001c0001t0001g0004 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.152-68383_152-6838 others(158): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(267): Show |
3 | a0001c0001t0001g0168a0001c0001t0001g0171a0001c0001t0001g0177 | 3 | HG00438.hp1 NA18945.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.152-68383_152-6838 others(278): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(297): Show |
2 | a0001c0001t0001g0154a0001c0001t0001g0174 | 2 | HG01934.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.152-68383_152-6838 others(308): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(327): Show |
3 | a0001c0001t0001g0163a0001c0001t0001g0172a0001c0001t0001g0176 | 3 | NA18960.hp1 NA18988.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.152-68383_152-6838 others(338): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(357): Show |
2 | a0001c0001t0001g0110a0001c0001t0001g0159 | 2 | HG00323.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.152-68383_152-6838 others(368): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(297): Show |
1 | a0001c0001t0001g0162 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.152-68383_152-6838 others(308): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(327): Show |
1 | a0001c0001t0001g0160 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(338): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(237): Show |
3 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0184 | 3 | HG02965.hp1 HG02976.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.152-68383_152-6838 others(248): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(267): Show |
1 | a0001c0001t0001g0148 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.152-68383_152-6838 others(278): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(297): Show |
2 | a0001c0001t0001g0147a0001c0001t0001g0152 | 2 | HG02004.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.152-68383_152-6838 others(308): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(417): Show |
1 | a0001c0001t0001g0123 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(428): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(327): Show |
5 | a0001c0001t0001g0155a0001c0001t0001g0161a0001c0001t0001g0167others(2): Show | 5 | HG01255.hp1 HG03041.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.152-68383_152-6838 others(338): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(357): Show |
4 | a0001c0001t0001g0105a0001c0001t0001g0111a0001c0001t0001g0122others(1): Show | 4 | HG00099.hp1 HG00642.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-68383_152-6838 others(368): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(387): Show |
5 | a0001c0001t0001g0107a0001c0001t0001g0151a0001c0001t0001g0164others(2): Show | 5 | HG00323.hp1 HG01256.hp2 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.152-68383_152-6838 others(398): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(417): Show |
5 | a0001c0001t0001g0106a0001c0001t0001g0116a0001c0001t0001g0156others(2): Show | 5 | HG02027.hp1 HG02083.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.152-68383_152-6838 others(428): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(447): Show |
3 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0158 | 3 | HG02071.hp1 HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.152-68383_152-6838 others(458): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(417): Show |
1 | a0001c0001t0001g0100 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(428): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(297): Show |
1 | a0001c0001t0001g0150 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(308): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(327): Show |
1 | a0001c0001t0001g0149 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(338): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(447): Show |
1 | a0001c0001t0001g0102 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(458): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(347): Show |
1 | a0001c0001t0001g0178 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.152-68383_152-6838 others(358): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(347): Show |
1 | a0001c0001t0001g0169 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.152-68383_152-6838 others(358): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(175): Show |
1 | a0001c0001t0001g0131 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.152-68383_152-6838 others(186): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(357): Show |
1 | a0001c0001t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(368): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(507): Show |
1 | a0001c0001t0001g0104 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(518): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(327): Show |
1 | a0001c0001t0001g0153 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(338): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(177): Show |
11 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(8): Show | 11 | HG00408.hp2 HG00438.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.152-68383_152-6838 others(188): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(447): Show |
1 | a0001c0001t0001g0183 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.152-68383_152-6838 others(458): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(387): Show |
1 | a0001c0001t0001g0117 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(398): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(297): Show |
3 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0002t0001g0044 | 3 | HG02970.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.152-68383_152-6838 others(308): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(327): Show |
1 | a0001c0001t0001g0047 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.152-68383_152-6838 others(338): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(387): Show |
1 | a0001c0001t0001g0071 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(398): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(567): Show |
1 | a0001c0001t0001g0070 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(578): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(117): Show |
1 | a0001c0001t0001g0143 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(128): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(55): Show |
1 | a0001c0001t0001g0073 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(66): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(505): Show |
1 | a0001c0001t0001g0074 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(516): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(535): Show |
1 | a0001c0001t0001g0078 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(546): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(355): Show |
2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02027.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.152-68383_152-6838 others(366): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(535): Show |
1 | a0001c0001t0001g0080 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.152-68383_152-6838 others(546): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(625): Show |
1 | a0001c0001t0001g0084 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.152-68383_152-6838 others(636): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(595): Show |
1 | a0001c0001t0001g0072 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.152-68383_152-6838 others(606): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(625): Show |
1 | a0001c0001t0001g0077 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(636): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(625): Show |
1 | a0001c0001t0001g0076 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.152-68383_152-6838 others(636): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(625): Show |
1 | a0001c0001t0001g0081 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(636): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(625): Show |
1 | a0001c0001t0001g0075 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.152-68383_152-6838 others(636): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(385): Show |
1 | a0001c0001t0001g0069 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.152-68383_152-6838 others(396): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(145): Show |
1 | a0001c0001t0001g0065 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(156): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(265): Show |
1 | a0001c0001t0001g0064 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(276): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(325): Show |
1 | a0001c0001t0001g0067 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(336): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(355): Show |
1 | a0001c0001t0001g0066 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(366): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(445): Show |
1 | a0001c0001t0001g0103 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(456): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(265): Show |
1 | a0001c0001t0001g0124 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.152-68383_152-6838 others(276): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(325): Show |
1 | a0001c0001t0001g0120 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(336): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(355): Show |
1 | a0001c0001t0001g0108 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.152-68383_152-6838 others(366): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(385): Show |
4 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0001g0109others(1): Show | 4 | HG00738.hp1 HG01081.hp1 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-68383_152-6838 others(396): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(415): Show |
2 | a0001c0001t0001g0113a0001c0001t0001g0119 | 2 | HG04184.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.152-68383_152-6838 others(426): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(325): Show |
1 | a0001c0001t0001g0121 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.152-68383_152-6838 others(336): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(295): Show |
1 | a0001c0001t0001g0068 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(306): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(235): Show |
1 | a0001c0001t0001g0012 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(246): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(145): Show |
1 | a0001c0001t0001g0013 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(156): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(175): Show |
1 | a0001c0001t0001g0027 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(186): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(205): Show |
1 | a0001c0001t0001g0032 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.152-68383_152-6838 others(216): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(295): Show |
1 | a0001c0001t0001g0028 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.152-68383_152-6838 others(306): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(235): Show |
7 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0023others(4): Show | 7 | HG01256.hp1 HG02071.hp2 HG02683.hp2 others(4): Show |
intron_variant | MODIFIER | c.152-68383_152-6838 others(246): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(265): Show |
9 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0029others(6): Show | 9 | HG00408.hp1 HG00673.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.152-68383_152-6838 others(276): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(295): Show |
1 | a0001c0001t0001g0031 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(306): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(175): Show |
2 | a0001c0001t0001g0007a0001c0001t0001g0017 | 2 | HG01255.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.152-68383_152-6838 others(186): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(205): Show |
6 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0019others(3): Show | 6 | HG00673.hp2 HG01943.hp1 HG02273.hp1 others(3): Show |
intron_variant | MODIFIER | c.152-68383_152-6838 others(216): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(385): Show |
1 | a0001c0001t0001g0180 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.152-68383_152-6838 others(396): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(235): Show |
7 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(4): Show | 7 | HG00642.hp1 HG02040.hp2 NA18960.hp2 others(4): Show |
intron_variant | MODIFIER | c.152-68383_152-6838 others(246): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(263): Show |
1 | a0001c0001t0001g0022 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.152-68383_152-6838 others(274): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031379
|
T | TGTATATA others(233): Show |
2 | a0001c0001t0001g0016a0001c0001t0001g0018 | 2 | HG03492.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.152-68383_152-6838 others(244): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | ||||||
| chr7:117031380
|
A | G | 9 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(6): Show | 9 | HG02109.hp1 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.152-68382A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031380 | ||||||
| chr7:117031383
|
TATGTGTA others(49): Show |
T | 1 | a0001c0001t0001g0091 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.152-68376_152-6832 others(60): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031383 | |||||
| chr7:117031384
|
ATGTG | A | 8 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(5): Show | 8 | HG02451.hp1 HG02622.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.152-68376_152-6837 others(8): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031384 | |||||
| chr7:117031386
|
G | A | 9 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0085others(6): Show | 9 | HG01071.hp1 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.152-68376G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031386 | ||||||
| chr7:117031387
|
T | C | 1 | a0001c0001t0001g0073 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.152-68375T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031387 | ||||||
| chr7:117031389
|
T | A | 1 | a0001c0001t0001g0027 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.152-68373T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031389 | ||||||
| chr7:117031390
|
A | G | 162 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(159): Show | 162 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.152-68372A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031390 | ||||||
| chr7:117031391
|
T | C | 1 | a0001c0001t0001g0076 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.152-68371T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031391 | ||||||
| chr7:117031392
|
A | G | 2 | a0001c0001t0001g0136a0001c0001t0001g0143 | 2 | HG00738.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.152-68370A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031392 | ||||||
| chr7:117031394
|
A | G | 1 | a0001c0001t0001g0128 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.152-68368A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031394 | ||||||
| chr7:117031397
|
T | C | 10 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(7): Show | 10 | HG01081.hp2 HG02055.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.152-68365T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031397 | ||||||
| chr7:117031397
|
TGCATATA others(5): Show |
T | 8 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(5): Show | 8 | HG02451.hp1 HG02622.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.152-68364_152-6835 others(16): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031397 | ||||||
| chr7:117031399
|
C | T | 6 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0061others(3): Show | 6 | HG01433.hp2 HG02055.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.152-68363C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031399 | ||||||
| chr7:117031400
|
A | G | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.152-68362A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031400 | ||||||
| chr7:117031404
|
A | G | 1 | a0001c0001t0001g0146 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.152-68358A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031404 | ||||||
| chr7:117031406
|
A | G | 1 | a0001c0001t0001g0146 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.152-68356A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031406 | ||||||
| chr7:117031407
|
C | CGCATATA others(143): Show |
1 | a0001c0001t0001g0061 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.152-68263_152-6811 others(154): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031407 | |||||
| chr7:117031407
|
C | CGCATATA others(171): Show |
1 | a0001c0001t0001g0059 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.152-68354_152-6817 others(182): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031407 | |||||
| chr7:117031407
|
C | CGCATATA others(231): Show |
1 | a0001c0001t0001g0062 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.152-68177_152-6817 others(242): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031407 | |||||
| chr7:117031407
|
C | CGCATATA others(171): Show |
1 | a0001c0001t0001g0058 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.152-68207_152-6820 others(182): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031407 | |||||
| chr7:117031407
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.152-68355C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031407 | ||||||
| chr7:117031409
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.152-68353C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031409 | ||||||
| chr7:117031416
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.152-68346G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031416 | ||||||
| chr7:117031417
|
T | C | 2 | a0001c0001t0001g0048a0001c0001t0001g0073 | 2 | HG01081.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.152-68345T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031417 | ||||||
| chr7:117031419
|
T | A | 2 | a0001c0001t0001g0013a0001c0001t0001g0073 | 2 | HG01081.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.152-68343T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031419 | ||||||
| chr7:117031420
|
G | A | 9 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(6): Show | 9 | HG02055.hp1 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.152-68342G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031420 | ||||||
| chr7:117031421
|
T | C | 1 | a0001c0001t0001g0076 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.152-68341T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031421 | ||||||
| chr7:117031422
|
A | G | 5 | a0001c0001t0001g0126a0001c0001t0001g0136a0001c0001t0001g0139others(2): Show | 5 | HG00738.hp2 NA18747.hp2 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.152-68340A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031422 | ||||||
| chr7:117031424
|
A | G | 8 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(5): Show | 8 | HG02451.hp1 HG02622.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.152-68338A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031424 | ||||||
| chr7:117031427
|
T | C | 12 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(9): Show | 12 | HG01081.hp2 HG02055.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.152-68335T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031427 | ||||||
| chr7:117031428
|
GCATATAT others(5): Show |
G | 8 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(5): Show | 8 | HG02451.hp1 HG02622.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.152-68333_152-6832 others(16): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031428 | ||||||
| chr7:117031430
|
A | G | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.152-68332A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031430 | ||||||
| chr7:117031437
|
T | C | 172 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(169): Show | 172 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.152-68325T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031437 | ||||||
| chr7:117031437
|
T | TATGCGCA others(7): Show |
1 | a0001c0001t0001g0073 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.152-68325_152-6832 others(18): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031437 | ||||||
| chr7:117031446
|
G | A | 9 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(6): Show | 9 | HG02109.hp1 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.152-68316G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031446 | ||||||
| chr7:117031447
|
T | C | 2 | a0001c0001t0001g0048a0001c0001t0001g0073 | 2 | HG01081.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.152-68315T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031447 | ||||||
| chr7:117031449
|
T | A | 3 | a0001c0001t0001g0004a0001c0001t0001g0065a0001c0001t0001g0182 | 3 | HG02293.hp2 HG02300.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.152-68313T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031449 | ||||||
| chr7:117031450
|
G | A | 9 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(6): Show | 9 | HG02109.hp1 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.152-68312G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031450 | ||||||
| chr7:117031451
|
T | C | 1 | a0001c0001t0001g0076 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.152-68311T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031451 | ||||||
| chr7:117031452
|
A | G | 6 | a0001c0001t0001g0126a0001c0001t0001g0129a0001c0001t0001g0136others(3): Show | 6 | HG00738.hp2 HG01358.hp1 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.152-68310A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031452 | ||||||
| chr7:117031457
|
T | C | 10 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0048others(7): Show | 10 | HG01081.hp2 HG02055.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.152-68305T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031457 | ||||||
| chr7:117031460
|
A | G | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.152-68302A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031460 | ||||||
| chr7:117031465
|
T | C | 1 | a0001c0001t0001g0073 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.152-68297T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031465 | ||||||
| chr7:117031466
|
A | G | 1 | a0001c0001t0001g0091 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.152-68296A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031466 | ||||||
| chr7:117031467
|
T | C | 181 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(178): Show | 181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.152-68295T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031467 | ||||||
| chr7:117031469
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.152-68293C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031469 | ||||||
| chr7:117031470
|
A | G | 1 | a0001c0001t0001g0091 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.152-68292A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031470 | ||||||
| chr7:117031476
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.152-68286G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031476 | ||||||
| chr7:117031477
|
T | C | 2 | a0001c0001t0001g0048a0001c0001t0001g0073 | 2 | HG01081.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.152-68285T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031477 | ||||||
| chr7:117031480
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.152-68282G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031480 | ||||||
| chr7:117031482
|
A | G | 7 | a0001c0001t0001g0126a0001c0001t0001g0128a0001c0001t0001g0129others(4): Show | 7 | HG00738.hp2 HG01358.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.152-68280A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031482 | ||||||
| chr7:117031487
|
T | C | 9 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0048others(6): Show | 9 | HG02055.hp2 HG02258.hp2 HG02273.hp2 others(6): Show |
intron_variant | MODIFIER | c.152-68275T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031487 | ||||||
| chr7:117031490
|
A | G | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.152-68272A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031490 | ||||||
| chr7:117031495
|
T | C | 1 | a0001c0001t0001g0089 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.152-68267T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031495 | ||||||
| chr7:117031497
|
T | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 182 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.152-68265T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031497 | ||||||
| chr7:117031507
|
T | C | 2 | a0001c0001t0001g0048a0001c0001t0001g0073 | 2 | HG01081.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.152-68255T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031507 | ||||||
| chr7:117031512
|
A | G | 9 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0128others(6): Show | 9 | HG00738.hp2 HG01071.hp1 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.152-68250A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031512 | ||||||
| chr7:117031517
|
T | C | 9 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0048others(6): Show | 9 | HG02055.hp2 HG02258.hp2 HG02273.hp2 others(6): Show |
intron_variant | MODIFIER | c.152-68245T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031517 | ||||||
| chr7:117031520
|
A | G | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.152-68242A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031520 | ||||||
| chr7:117031525
|
T | C | 2 | a0001c0001t0001g0068a0001c0001t0001g0089 | 2 | HG02647.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.152-68237T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031525 | ||||||
| chr7:117031527
|
T | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 182 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.152-68235T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031527 | ||||||
| chr7:117031537
|
T | C | 2 | a0001c0001t0001g0048a0001c0001t0001g0073 | 2 | HG01081.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.152-68225T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031537 | ||||||
| chr7:117031542
|
A | G | 9 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0128others(6): Show | 9 | HG00738.hp2 HG01071.hp1 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.152-68220A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031542 | ||||||
| chr7:117031547
|
T | C | 8 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0048others(5): Show | 8 | HG02055.hp2 HG02258.hp2 HG02273.hp2 others(5): Show |
intron_variant | MODIFIER | c.152-68215T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031547 | ||||||
| chr7:117031550
|
A | G | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.152-68212A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031550 | ||||||
| chr7:117031555
|
T | C | 6 | a0001c0001t0001g0068a0001c0001t0001g0086a0001c0001t0001g0087others(3): Show | 6 | HG02451.hp1 HG02647.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.152-68207T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031555 | ||||||
| chr7:117031557
|
T | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 182 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.152-68205T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031557 | ||||||
| chr7:117031567
|
T | C | 2 | a0001c0001t0001g0048a0001c0001t0001g0073 | 2 | HG01081.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.152-68195T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031567 | ||||||
| chr7:117031572
|
A | G | 9 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0128others(6): Show | 9 | HG00738.hp2 HG01071.hp1 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.152-68190A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031572 | ||||||
| chr7:117031577
|
T | C | 8 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0048others(5): Show | 8 | HG02055.hp2 HG02258.hp2 HG02273.hp2 others(5): Show |
intron_variant | MODIFIER | c.152-68185T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031577 | ||||||
| chr7:117031580
|
A | G | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.152-68182A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031580 | ||||||
| chr7:117031585
|
T | C | 1 | a0001c0001t0001g0068 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.152-68177T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031585 | ||||||
| chr7:117031587
|
T | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 182 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.152-68175T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031587 | ||||||
| chr7:117031597
|
T | C | 2 | a0001c0001t0001g0048a0001c0001t0001g0073 | 2 | HG01081.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.152-68165T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031597 | ||||||
| chr7:117031602
|
A | G | 7 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(4): Show | 7 | HG00738.hp2 HG01071.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.152-68160A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031602 | ||||||
| chr7:117031607
|
T | C | 7 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0048others(4): Show | 7 | HG02055.hp2 HG02258.hp2 HG02273.hp2 others(4): Show |
intron_variant | MODIFIER | c.152-68155T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031607 | ||||||
| chr7:117031610
|
A | G | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.152-68152A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031610 | ||||||
| chr7:117031615
|
T | C | 1 | a0001c0001t0001g0068 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.152-68147T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031615 | ||||||
| chr7:117031617
|
T | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 182 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.152-68145T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031617 | ||||||
| chr7:117031619
|
C | T | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.152-68143C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031619 | ||||||
| chr7:117031627
|
T | C | 1 | a0001c0001t0001g0048 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.152-68135T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031627 | ||||||
| chr7:117031632
|
A | G | 4 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(1): Show | 4 | HG01071.hp1 HG01358.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.152-68130A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031632 | ||||||
| chr7:117031637
|
T | C | 6 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0048others(3): Show | 6 | HG02055.hp2 HG02258.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.152-68125T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031637 | ||||||
| chr7:117031640
|
A | G | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.152-68122A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031640 | ||||||
| chr7:117031645
|
T | C | 1 | a0001c0001t0001g0068 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.152-68117T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031645 | ||||||
| chr7:117031647
|
T | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 182 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.152-68115T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031647 | ||||||
| chr7:117031649
|
T | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 182 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.152-68113T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031649 | ||||||
| chr7:117031654
|
ATGTGTGT others(7): Show |
A | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.152-68107_152-6809 others(18): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031654 | ||||||
| chr7:117031657
|
T | C | 1 | a0001c0001t0001g0048 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.152-68105T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031657 | ||||||
| chr7:117031662
|
A | G | 3 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0132 | 3 | HG01071.hp1 HG02683.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.152-68100A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031662 | ||||||
| chr7:117031667
|
T | C | 3 | a0001c0001t0001g0045a0001c0001t0001g0048a0001c0001t0001g0049 | 3 | HG02280.hp2 HG02895.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.152-68095T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031667 | ||||||
| chr7:117031670
|
A | G | 2 | a0001c0001t0001g0043a0001c0001t0001g0051 | 2 | HG02647.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.152-68092A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031670 | ||||||
| chr7:117031671
|
T | C | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.152-68091T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031671 | ||||||
| chr7:117031672
|
A | ATACACGC others(11): Show |
1 | a0001c0001t0001g0068 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.152-68088_152-6808 others(22): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031672 | |||||
| chr7:117031673
|
T | C | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.152-68089T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031673 | ||||||
| chr7:117031676
|
A | ACGCATAT others(5): Show |
77 | a0001c0001t0001g0004a0001c0001t0001g0045a0001c0001t0001g0051others(74): Show | 77 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.152-68086_152-6808 others(16): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031676 | ||||||
| chr7:117031676
|
A | ACGCATAT others(97): Show |
1 | a0001c0001t0001g0128 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.152-68086_152-6808 others(108): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031676 | ||||||
| chr7:117031677
|
T | C | 31 | a0001c0001t0001g0043a0001c0001t0001g0046a0001c0001t0001g0047others(28): Show | 31 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.152-68085T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031677 | ||||||
| chr7:117031678
|
G | GCATATAT others(195): Show |
1 | a0001c0001t0001g0049 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.152-68084_152-6808 others(206): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031678 | ||||||
| chr7:117031679
|
T | C | 40 | a0001c0001t0001g0043a0001c0001t0001g0046a0001c0001t0001g0047others(37): Show | 40 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.152-68083T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031679 | ||||||
| chr7:117031682
|
A | G | 1 | a0001c0001t0001g0128 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.152-68080A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031682 | ||||||
| chr7:117031683
|
TACAC | T | 4 | a0001c0001t0001g0043a0001c0001t0001g0046a0001c0001t0001g0056others(1): Show | 4 | HG02486.hp2 HG02965.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.152-68075_152-6807 others(8): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031683 | |||||
| chr7:117031683
|
TACACAC | T | 8 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0050others(5): Show | 8 | HG02109.hp2 HG02258.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.152-68077_152-6807 others(10): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031683 | |||||
| chr7:117031684
|
A | ATGTGTGT others(7): Show |
12 | a0001c0001t0001g0126a0001c0001t0001g0130a0001c0001t0001g0131others(9): Show | 12 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.152-68078_152-6807 others(18): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031684 | ||||||
| chr7:117031684
|
A | ATGTGTGT others(97): Show |
1 | a0001c0001t0001g0141 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.152-68078_152-6807 others(108): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031684 | ||||||
| chr7:117031684
|
A | ATGTGTGT others(127): Show |
2 | a0001c0001t0001g0140a0001c0001t0001g0142 | 2 | HG02717.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.152-68078_152-6807 others(138): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031684 | ||||||
| chr7:117031684
|
A | ATGTGTGT others(125): Show |
1 | a0001c0001t0001g0152 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.152-68078_152-6807 others(136): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031684 | ||||||
| chr7:117031684
|
A | ATGTGTGT others(97): Show |
1 | a0001c0001t0001g0132 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.152-68078_152-6807 others(108): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031684 | ||||||
| chr7:117031684
|
A | ATGTGTGT others(97): Show |
1 | a0001c0001t0001g0127 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.152-68078_152-6807 others(108): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031684 | ||||||
| chr7:117031684
|
A | G | 78 | a0001c0001t0001g0004a0001c0001t0001g0045a0001c0001t0001g0051others(75): Show | 78 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.152-68078A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031684 | ||||||
| chr7:117031685
|
C | T | 78 | a0001c0001t0001g0004a0001c0001t0001g0045a0001c0001t0001g0051others(75): Show | 78 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.152-68077C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031685 | ||||||
| chr7:117031686
|
A | G | 79 | a0001c0001t0001g0004a0001c0001t0001g0045a0001c0001t0001g0049others(76): Show | 79 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.152-68076A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031686 | ||||||
| chr7:117031687
|
C | T | 20 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127others(17): Show | 20 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.152-68075C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031687 | ||||||
| chr7:117031688
|
A | G | 3 | a0001c0001t0001g0051a0001c0001t0001g0068a0001c0001t0001g0125 | 3 | HG02258.hp1 HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.152-68074A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031688 | ||||||
| chr7:117031689
|
C | T | 102 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0045others(99): Show | 102 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.152-68073C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031689 | ||||||
| chr7:117031690
|
A | G | 5 | a0001c0001t0001g0043a0001c0001t0001g0046a0001c0001t0001g0056others(2): Show | 5 | HG02258.hp1 HG02486.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.152-68072A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031690 | ||||||
| chr7:117031692
|
A | G | 12 | a0001c0001t0001g0043a0001c0001t0001g0046a0001c0001t0001g0047others(9): Show | 12 | HG02109.hp2 HG02258.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.152-68070A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031692 | ||||||
| chr7:117031693
|
T | C | 19 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0128others(16): Show | 19 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.152-68069T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031693 | ||||||
| chr7:117031693
|
T | TACGC | 77 | a0001c0001t0001g0004a0001c0001t0001g0045a0001c0001t0001g0051others(74): Show | 77 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.152-68069_152-6806 others(8): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031693 | ||||||
| chr7:117031694
|
G | A | 77 | a0001c0001t0001g0004a0001c0001t0001g0045a0001c0001t0001g0051others(74): Show | 77 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.152-68068G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031694 | ||||||
| chr7:117031695
|
T | C | 18 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0128others(15): Show | 18 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.152-68067T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031695 | ||||||
| chr7:117031696
|
A | G | 8 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0049others(5): Show | 8 | HG02109.hp2 HG02258.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.152-68066A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031696 | ||||||
| chr7:117031700
|
A | ATG | 40 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(37): Show | 40 | HG00408.hp1 HG00642.hp1 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.152-68058_152-6805 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031700 | |||||
| chr7:117031700
|
A | G | 83 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0045others(80): Show | 83 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.152-68062A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031700 | ||||||
| chr7:117031703
|
T | C | 5 | a0001c0001t0001g0043a0001c0001t0001g0046a0001c0001t0001g0050others(2): Show | 5 | HG02258.hp1 HG02258.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.152-68059T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031703 | ||||||
| chr7:117031704
|
G | A | 2 | a0001c0001t0001g0063a0001c0001t0001g0125 | 2 | HG02258.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.152-68058G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031704 | ||||||
| chr7:117031704
|
G | GCA | 8 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0049others(5): Show | 8 | HG02109.hp2 HG02258.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.152-68058_152-6805 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031704 | ||||||
| chr7:117031704
|
G | GTATATAT others(3): Show |
4 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0061others(1): Show | 4 | HG01433.hp2 HG02818.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.152-68032_152-6802 others(14): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031704 | |||||
| chr7:117031705
|
TATATATG others(1): Show |
T | 32 | a0001c0001t0001g0015a0001c0001t0001g0065a0001c0001t0001g0069others(29): Show | 32 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.152-68050_152-6804 others(12): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031705 | |||||
| chr7:117031706
|
A | G | 18 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0128others(15): Show | 18 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.152-68056A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031706 | ||||||
| chr7:117031710
|
A | G | 137 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(134): Show | 137 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.152-68052A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031710 | ||||||
| chr7:117031711
|
T | C | 11 | a0001c0001t0001g0043a0001c0001t0001g0046a0001c0001t0001g0047others(8): Show | 11 | HG02258.hp2 HG02486.hp2 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.152-68051T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031711 | ||||||
| chr7:117031713
|
C | T | 2 | a0001c0001t0001g0051a0001c0001t0001g0125 | 2 | HG02258.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.152-68049C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031713 | ||||||
| chr7:117031714
|
A | ATATATGT others(3): Show |
8 | a0001c0001t0001g0043a0001c0001t0001g0046a0001c0001t0001g0047others(5): Show | 8 | HG02486.hp2 HG02965.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.152-68043_152-6804 others(14): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031714 | |||||
| chr7:117031714
|
A | G | 33 | a0001c0001t0001g0015a0001c0001t0001g0051a0001c0001t0001g0065others(30): Show | 33 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.152-68048A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031714 | ||||||
| chr7:117031719
|
T | C | 1 | a0001c0001t0001g0068 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.152-68043T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031719 | ||||||
| chr7:117031720
|
A | G | 12 | a0001c0001t0001g0043a0001c0001t0001g0046a0001c0001t0001g0047others(9): Show | 12 | HG02258.hp1 HG02258.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.152-68042A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031720 | ||||||
| chr7:117031721
|
T | C | 11 | a0001c0001t0001g0045a0001c0001t0001g0054a0001c0001t0001g0055others(8): Show | 11 | HG01358.hp1 HG01433.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.152-68041T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031721 | ||||||
| chr7:117031723
|
C | T | 80 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0046others(77): Show | 80 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.152-68039C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031723 | ||||||
| chr7:117031724
|
A | ATATATGT others(3): Show |
1 | a0001c0001t0001g0085 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.152-68033_152-6803 others(14): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031724 | |||||
| chr7:117031724
|
A | G | 12 | a0001c0001t0001g0043a0001c0001t0001g0046a0001c0001t0001g0047others(9): Show | 12 | HG02258.hp1 HG02258.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.152-68038A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031724 | ||||||
| chr7:117031727
|
T | TACACAC | 91 | a0001c0001t0001g0004a0001c0001t0001g0064a0001c0001t0001g0066others(88): Show | 91 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.152-68034_152-6803 others(10): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031727 | |||||
| chr7:117031730
|
A | G | 8 | a0001c0001t0001g0045a0001c0001t0001g0048a0001c0001t0001g0050others(5): Show | 8 | HG01358.hp1 HG02055.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.152-68032A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031730 | ||||||
| chr7:117031731
|
T | C | 1 | a0001c0001t0001g0043 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.152-68031T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031731 | ||||||
| chr7:117031733
|
C | T | 94 | a0001c0001t0001g0004a0001c0001t0001g0054a0001c0001t0001g0055others(91): Show | 94 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.152-68029C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031733 | ||||||
| chr7:117031733
|
CATATATG others(3): Show |
C | 33 | a0001c0001t0001g0015a0001c0001t0001g0051a0001c0001t0001g0065others(30): Show | 33 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.152-68022_152-6801 others(14): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031733 | |||||
| chr7:117031734
|
A | G | 44 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(41): Show | 44 | HG00408.hp1 HG00642.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.152-68028A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031734 | ||||||
| chr7:117031740
|
G | A | 14 | a0001c0001t0001g0043a0001c0001t0001g0046a0001c0001t0001g0047others(11): Show | 14 | HG01358.hp1 HG02109.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.152-68022G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031740 | ||||||
| chr7:117031743
|
T | C | 16 | a0001c0001t0001g0043a0001c0001t0001g0046a0001c0001t0001g0047others(13): Show | 16 | HG01358.hp1 HG02109.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.152-68019T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031743 | ||||||
| chr7:117031744
|
A | G | 106 | a0001c0001t0001g0004a0001c0001t0001g0042a0001c0001t0001g0043others(103): Show | 106 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.152-68018A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031744 | ||||||
| chr7:117031751
|
T | C | 2 | a0001c0001t0001g0055a0001c0001t0001g0068 | 2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.152-68011T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031751 | ||||||
| chr7:117031754
|
A | G | 47 | a0001c0001t0001g0015a0001c0001t0001g0043a0001c0001t0001g0046others(44): Show | 47 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.152-68008A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031754 | ||||||
| chr7:117031758
|
A | ATG | 3 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0062 | 3 | HG02818.hp1 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.152-68000_152-6799 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031758 | |||||
| chr7:117031760
|
G | A | 93 | a0001c0001t0001g0004a0001c0001t0001g0045a0001c0001t0001g0054others(90): Show | 93 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.152-68002G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031760 | ||||||
| chr7:117031763
|
T | C | 93 | a0001c0001t0001g0004a0001c0001t0001g0045a0001c0001t0001g0054others(90): Show | 93 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.152-67999T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031763 | ||||||
| chr7:117031764
|
A | G | 4 | a0001c0001t0001g0045a0001c0001t0001g0054a0001c0001t0001g0055others(1): Show | 4 | HG02055.hp2 HG02280.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-67998A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031764 | ||||||
| chr7:117031770
|
A | G | 2 | a0001c0001t0001g0055a0001c0001t0001g0068 | 2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.152-67992A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031770 | ||||||
| chr7:117031774
|
A | G | 96 | a0001c0001t0001g0004a0001c0001t0001g0045a0001c0001t0001g0048others(93): Show | 96 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.152-67988A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031774 | ||||||
| chr7:117031778
|
A | ATG | 39 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(36): Show | 39 | HG00408.hp1 HG00642.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.152-67980_152-6797 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031778 | |||||
| chr7:117031780
|
G | A | 2 | a0001c0001t0001g0055a0001c0001t0001g0068 | 2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.152-67982G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031780 | ||||||
| chr7:117031781
|
T | C | 2 | a0001c0001t0001g0055a0001c0001t0001g0068 | 2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.152-67981T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031781 | ||||||
| chr7:117031783
|
T | C | 3 | a0001c0001t0001g0015a0001c0001t0001g0055a0001c0001t0001g0068 | 3 | HG02622.hp2 HG02630.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.152-67979T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031783 | ||||||
| chr7:117031784
|
A | G | 4 | a0001c0001t0001g0065a0001c0001t0001g0106a0001c0001t0001g0113others(1): Show | 4 | HG02615.hp2 HG02976.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.152-67978A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031784 | ||||||
| chr7:117031790
|
A | G | 2 | a0001c0001t0001g0055a0001c0001t0001g0068 | 2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.152-67972A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031790 | ||||||
| chr7:117031793
|
C | T | 1 | a0001c0001t0001g0055 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.152-67969C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031793 | ||||||
| chr7:117031794
|
A | G | 2 | a0001c0001t0001g0045a0001c0001t0001g0055 | 2 | HG02280.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.152-67968A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031794 | ||||||
| chr7:117031796
|
A | G | 1 | a0001c0001t0001g0068 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.152-67966A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031796 | ||||||
| chr7:117031798
|
ATG | A | 64 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(61): Show | 64 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.152-67958_152-6795 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031798 | |||||
| chr7:117031800
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.152-67962G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031800 | ||||||
| chr7:117031803
|
T | C | 1 | a0001c0001t0001g0055 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.152-67959T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031803 | ||||||
| chr7:117031804
|
G | A | 1 | a0001c0001t0001g0055 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.152-67958G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031804 | ||||||
| chr7:117031804
|
GTA | G | 35 | a0001c0001t0001g0004a0001c0001t0001g0110a0001c0001t0001g0122others(32): Show | 35 | HG00323.hp2 HG00438.hp1 HG01255.hp1 others(32): Show |
intron_variant | MODIFIER | c.152-67950_152-6794 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031804 | |||||
| chr7:117031805
|
T | C | 1 | a0001c0001t0001g0068 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.152-67957T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031805 | ||||||
| chr7:117031806
|
A | G | 1 | a0001c0001t0001g0114 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.152-67956A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031806 | ||||||
| chr7:117031807
|
T | TATATGC | 33 | a0001c0001t0001g0064a0001c0001t0001g0066a0001c0001t0001g0067others(30): Show | 33 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.152-67951_152-6795 others(10): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031807 | |||||
| chr7:117031810
|
A | G | 1 | a0001c0001t0001g0096 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.152-67952A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031810 | ||||||
| chr7:117031813
|
T | C | 1 | a0001c0001t0001g0068 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.152-67949T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031813 | ||||||
| chr7:117031815
|
C | T | 34 | a0001c0001t0001g0055a0001c0001t0001g0064a0001c0001t0001g0066others(31): Show | 34 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(31): Show |
intron_variant | MODIFIER | c.152-67947C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031815 | ||||||
| chr7:117031816
|
A | G | 34 | a0001c0001t0001g0055a0001c0001t0001g0064a0001c0001t0001g0066others(31): Show | 34 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(31): Show |
intron_variant | MODIFIER | c.152-67946A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031816 | ||||||
| chr7:117031816
|
ATATATC | A | 3 | a0001c0001t0001g0061a0001c0001t0001g0085a0001c0001t0001g0113 | 3 | HG01433.hp2 HG02109.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.152-67906_152-6790 others(10): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031816 | |||||
| chr7:117031816
|
ATATATCT others(5): Show |
A | 32 | a0001c0001t0001g0015a0001c0001t0001g0043a0001c0001t0001g0046others(29): Show | 32 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.152-67912_152-6790 others(16): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031816 | |||||
| chr7:117031818
|
A | ATATGTGT others(1): Show |
21 | a0001c0001t0001g0045a0001c0001t0001g0054a0001c0001t0001g0126others(18): Show | 21 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.152-67941_152-6794 others(12): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031818 | |||||
| chr7:117031818
|
A | G | 33 | a0001c0001t0001g0064a0001c0001t0001g0066a0001c0001t0001g0067others(30): Show | 33 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.152-67944A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031818 | ||||||
| chr7:117031820
|
A | ATGTG | 66 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(63): Show | 66 | HG00323.hp2 HG00438.hp1 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.152-67941_152-6794 others(8): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031820 | |||||
| chr7:117031820
|
ATC | A | 13 | a0001c0001t0001g0022a0001c0001t0001g0025a0001c0001t0001g0027others(10): Show | 13 | HG00408.hp1 HG00673.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.152-67940_152-6793 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031820 | |||||
| chr7:117031822
|
C | A | 55 | a0001c0001t0001g0045a0001c0001t0001g0054a0001c0001t0001g0055others(52): Show | 55 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.152-67940C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031822 | ||||||
| chr7:117031822
|
C | G | 66 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(63): Show | 66 | HG00323.hp2 HG00438.hp1 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.152-67940C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031822 | ||||||
| chr7:117031824
|
A | G | 13 | a0001c0001t0001g0022a0001c0001t0001g0025a0001c0001t0001g0027others(10): Show | 13 | HG00408.hp1 HG00673.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.152-67938A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031824 | ||||||
| chr7:117031826
|
A | G | 14 | a0001c0001t0001g0022a0001c0001t0001g0025a0001c0001t0001g0027others(11): Show | 14 | HG00408.hp1 HG00673.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.152-67936A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031826 | ||||||
| chr7:117031827
|
T | C | 1 | a0001c0001t0001g0055 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.152-67935T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031827 | ||||||
| chr7:117031827
|
T | TGC | 54 | a0001c0001t0001g0045a0001c0001t0001g0054a0001c0001t0001g0064others(51): Show | 54 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.152-67935_152-6793 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031827 | ||||||
| chr7:117031828
|
C | A | 121 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(118): Show | 121 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.152-67934C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031828 | ||||||
| chr7:117031828
|
C | G | 13 | a0001c0001t0001g0022a0001c0001t0001g0025a0001c0001t0001g0027others(10): Show | 13 | HG00408.hp1 HG00673.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.152-67934C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031828 | ||||||
| chr7:117031830
|
ATATCTAT others(21): Show |
A | 1 | a0001c0001t0001g0034 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.152-67924_152-6789 others(32): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031830 | |||||
| chr7:117031832
|
A | G | 65 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(62): Show | 65 | HG00323.hp2 HG00438.hp1 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.152-67930A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031832 | ||||||
| chr7:117031833
|
T | C | 65 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(62): Show | 65 | HG00323.hp2 HG00438.hp1 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.152-67929T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031833 | ||||||
| chr7:117031834
|
C | A | 78 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(75): Show | 78 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.152-67928C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031834 | ||||||
| chr7:117031838
|
A | G | 13 | a0001c0001t0001g0022a0001c0001t0001g0025a0001c0001t0001g0027others(10): Show | 13 | HG00408.hp1 HG00673.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.152-67924A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031838 | ||||||
| chr7:117031839
|
T | C | 13 | a0001c0001t0001g0022a0001c0001t0001g0025a0001c0001t0001g0027others(10): Show | 13 | HG00408.hp1 HG00673.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.152-67923T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031839 | ||||||
| chr7:117031840
|
C | A | 13 | a0001c0001t0001g0022a0001c0001t0001g0025a0001c0001t0001g0027others(10): Show | 13 | HG00408.hp1 HG00673.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.152-67922C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031840 | ||||||
| chr7:117031846
|
CTATATCT others(1): Show |
C | 7 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0106others(4): Show | 7 | HG01358.hp1 HG02055.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.152-67912_152-6790 others(12): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031846 | |||||
| chr7:117031852
|
CTA | C | 6 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(3): Show | 6 | HG02451.hp1 HG02622.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.152-67906_152-6790 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031852 | |||||
| chr7:117031854
|
ATATC | A | 13 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0027others(10): Show | 13 | HG00408.hp1 HG00673.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.152-67892_152-6788 others(8): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031854 | |||||
| chr7:117031858
|
C | CTA | 28 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(25): Show | 28 | HG00642.hp1 HG00673.hp2 HG01255.hp2 others(25): Show |
intron_variant | MODIFIER | c.152-67902_152-6790 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031858 | |||||
| chr7:117031868
|
ATC | A | 2 | a0001c0001t0001g0106a0001c0001t0001g0114 | 2 | HG02615.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.152-67892_152-6789 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031868 | |||||
| chr7:117031870
|
C | A | 16 | a0001c0001t0001g0025a0001c0001t0001g0058a0001c0001t0001g0059others(13): Show | 16 | HG01358.hp1 HG02055.hp1 HG02071.hp2 others(13): Show |
intron_variant | MODIFIER | c.152-67892C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031870 | ||||||
| chr7:117031880
|
ATAT | A | 8 | a0001c0001t0001g0025a0001c0001t0001g0086a0001c0001t0001g0087others(5): Show | 8 | HG01358.hp1 HG02071.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.152-67880_152-6787 others(7): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031880 | |||||
| chr7:117031882
|
ATTT | A | 5 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0085others(2): Show | 5 | HG02055.hp1 HG02109.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.152-67866_152-6786 others(7): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031882 | |||||
| chr7:117031883
|
T | TA | 22 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0097others(19): Show | 22 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.152-67879_152-6787 others(5): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031883 | ||||||
| chr7:117031884
|
T | A | 130 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.152-67878T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031884 | ||||||
| chr7:117031885
|
T | A | 12 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0133others(9): Show | 12 | HG00408.hp2 HG00438.hp2 HG02040.hp1 others(9): Show |
intron_variant | MODIFIER | c.152-67877T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031885 | ||||||
| chr7:117031886
|
T | A | 40 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0068others(37): Show | 40 | HG00099.hp2 HG00738.hp1 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.152-67876T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031886 | ||||||
| chr7:117031887
|
T | A | 3 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0125 | 3 | HG02258.hp1 HG02922.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.152-67875T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031887 | ||||||
| chr7:117031888
|
T | A | 2 | a0001c0001t0001g0024a0001c0001t0001g0026 | 2 | HG02683.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.152-67874T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031888 | ||||||
| chr7:117032140
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.152-67622C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117032140 | ||||||
| chr7:117032386
|
G | T | 1 | a0001c0001t0001g0093 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.152-67376G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117032386 | ||||||
| chr7:117032533
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.152-67229C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117032533 | ||||||
| chr7:117032710
|
G | A | 126 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(123): Show | 126 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.152-67052G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117032710 | ||||||
| chr7:117032776
|
A | C | 4 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG01496.hp2 HG02572.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-66986A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117032776 | ||||||
| chr7:117033296
|
G | A | 3 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0184 | 3 | HG02965.hp1 HG02976.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.152-66466G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117033296 | ||||||
| chr7:117033419
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.152-66343G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117033419 | ||||||
| chr7:117033420
|
CT | C | 5 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0062others(2): Show | 5 | HG02280.hp1 HG02451.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.152-66328delT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117033420 | |||||
| chr7:117033441
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.152-66321G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117033441 | ||||||
| chr7:117033480
|
G | C | 72 | a0001c0001t0001g0004a0001c0001t0001g0064a0001c0001t0001g0065others(69): Show | 72 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.152-66282G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117033480 | ||||||
| chr7:117033577
|
C | T | 3 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0002t0001g0044 | 3 | HG02970.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.152-66185C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117033577 | ||||||
| chr7:117033635
|
T | G | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 182 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.152-66127T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117033635 | ||||||
| chr7:117033689
|
G | A | 1 | a0001c0001t0001g0116 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.152-66073G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117033689 | ||||||
| chr7:117033815
|
A | C | 1 | a0001c0001t0001g0066 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.152-65947A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117033815 | ||||||
| chr7:117033838
|
G | A | 1 | a0001c0001t0001g0008 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.152-65924G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117033838 | ||||||
| chr7:117033848
|
A | G | 13 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(10): Show | 13 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.152-65914A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117033848 | ||||||
| chr7:117034182
|
T | C | 3 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0062 | 3 | HG02818.hp1 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.152-65580T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117034182 | ||||||
| chr7:117034794
|
T | G | 3 | a0001c0001t0001g0021a0001c0001t0001g0040a0001c0001t0001g0041 | 3 | HG00673.hp2 HG01943.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.152-64968T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117034794 | ||||||
| chr7:117034821
|
C | G | 1 | a0001c0001t0001g0148 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.152-64941C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117034821 | ||||||
| chr7:117034969
|
C | A | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 182 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.152-64793C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117034969 | ||||||
| chr7:117035041
|
A | G | 1 | a0001c0001t0001g0074 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.152-64721A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117035041 | ||||||
| chr7:117035119
|
GTTT | G | 181 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(178): Show | 181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.152-64623_152-6462 others(7): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117035119 | |||||
| chr7:117035215
|
C | G | 1 | a0001c0001t0001g0033 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.152-64547C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117035215 | ||||||
| chr7:117035296
|
T | C | 1 | a0001c0001t0001g0148 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.152-64466T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117035296 | ||||||
| chr7:117035441
|
G | T | 3 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0062 | 3 | HG02818.hp1 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.152-64321G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117035441 | ||||||
| chr7:117035587
|
C | T | 13 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(10): Show | 13 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.152-64175C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117035587 | ||||||
| chr7:117035819
|
CT | C | 72 | a0001c0001t0001g0004a0001c0001t0001g0064a0001c0001t0001g0065others(69): Show | 72 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.152-63932delT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117035819 | |||||
| chr7:117036025
|
G | A | 1 | a0001c0001t0001g0086 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.152-63737G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117036025 | ||||||
| chr7:117036042
|
A | G | 1 | a0001c0001t0001g0059 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.152-63720A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117036042 | ||||||
| chr7:117036059
|
T | C | 9 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(6): Show | 9 | HG02109.hp1 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.152-63703T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117036059 | ||||||
| chr7:117036256
|
C | T | 2 | a0001c0001t0001g0106a0001c0001t0001g0122 | 2 | HG02615.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.152-63506C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117036256 | ||||||
| chr7:117036315
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.152-63447C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117036315 | ||||||
| chr7:117036375
|
T | C | 5 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0061others(2): Show | 5 | HG01433.hp2 HG02818.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.152-63387T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117036375 | ||||||
| chr7:117036825
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.152-62937C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117036825 | ||||||
| chr7:117036922
|
G | A | 1 | a0001c0001t0001g0023 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.152-62840G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117036922 | ||||||
| chr7:117037051
|
G | T | 1 | a0001c0001t0001g0090 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.152-62711G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117037051 | ||||||
| chr7:117037123
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.152-62639A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117037123 | ||||||
| chr7:117037124
|
C | T | 5 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0061others(2): Show | 5 | HG01433.hp2 HG02818.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.152-62638C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117037124 | ||||||
| chr7:117037472
|
C | G | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.152-62290C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117037472 | ||||||
| chr7:117037495
|
C | T | 1 | a0001c0001t0001g0118 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.152-62267C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117037495 | ||||||
| chr7:117037643
|
C | T | 5 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(2): Show | 5 | HG02257.hp2 HG02717.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.152-62119C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117037643 | ||||||
| chr7:117037651
|
T | A | 3 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0097 | 3 | HG02109.hp1 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.152-62111T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117037651 | ||||||
| chr7:117038056
|
T | C | 2 | a0001c0001t0001g0061a0001c0001t0001g0063 | 2 | HG01433.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.152-61706T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117038056 | ||||||
| chr7:117038202
|
G | A | 3 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0062 | 3 | HG02818.hp1 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.152-61560G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117038202 | ||||||
| chr7:117038276
|
C | T | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.152-61486C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117038276 | ||||||
| chr7:117038542
|
A | T | 5 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0061others(2): Show | 5 | HG01433.hp2 HG02818.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.152-61220A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117038542 | ||||||
| chr7:117038585
|
G | A | 22 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127others(19): Show | 22 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.152-61177G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117038585 | ||||||
| chr7:117038683
|
T | C | 1 | a0001c0001t0001g0140 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.152-61079T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117038683 | ||||||
| chr7:117039033
|
T | A | 1 | a0001c0001t0001g0188 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.152-60729T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117039033 | ||||||
| chr7:117039246
|
C | T | 1 | a0001c0001t0001g0139 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.152-60516C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117039246 | ||||||
| chr7:117039580
|
CA | C | 5 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0061others(2): Show | 5 | HG01433.hp2 HG02818.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.152-60166delA | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117039580 | |||||
| chr7:117039638
|
A | G | 5 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0061others(2): Show | 5 | HG01433.hp2 HG02818.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.152-60124A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117039638 | ||||||
| chr7:117039957
|
A | G | 1 | a0001c0001t0001g0173 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.152-59805A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117039957 | ||||||
| chr7:117040244
|
C | T | 5 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0061others(2): Show | 5 | HG01433.hp2 HG02818.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.152-59518C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117040244 | ||||||
| chr7:117040388
|
A | G | 22 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127others(19): Show | 22 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.152-59374A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117040388 | ||||||
| chr7:117040625
|
G | A | 115 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(112): Show | 115 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.152-59137G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117040625 | ||||||
| chr7:117040777
|
A | G | 1 | a0001c0001t0001g0004 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.152-58985A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117040777 | ||||||
| chr7:117041073
|
G | C | 15 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0061others(12): Show | 15 | HG01433.hp2 HG02109.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.152-58689G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117041073 | ||||||
| chr7:117041554
|
G | A | 1 | a0001c0001t0001g0012 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.152-58208G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117041554 | ||||||
| chr7:117041677
|
C | T | 1 | a0001c0001t0001g0138 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.152-58085C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117041677 | ||||||
| chr7:117041849
|
T | C | 1 | a0001c0001t0001g0164 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.152-57913T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117041849 | ||||||
| chr7:117041966
|
G | A | 3 | a0001c0001t0001g0133a0001c0001t0001g0135a0001c0001t0001g0137 | 3 | HG02040.hp1 HG02523.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.152-57796G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117041966 | ||||||
| chr7:117042030
|
A | C | 3 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0062 | 3 | HG02818.hp1 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.152-57732A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117042030 | ||||||
| chr7:117042047
|
T | A | 10 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087others(7): Show | 10 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.152-57715T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117042047 | ||||||
| chr7:117042128
|
A | G | 1 | a0001c0001t0001g0109 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.152-57634A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117042128 | ||||||
| chr7:117043370
|
T | A | 4 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG01496.hp2 HG02572.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-56392T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117043370 | ||||||
| chr7:117043587
|
A | G | 1 | a0001c0001t0001g0138 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.152-56175A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117043587 | ||||||
| chr7:117044142
|
T | A | 22 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127others(19): Show | 22 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.152-55620T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117044142 | ||||||
| chr7:117044321
|
C | T | 2 | a0001c0001t0001g0070a0001c0001t0001g0071 | 2 | HG02922.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.152-55441C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117044321 | ||||||
| chr7:117044323
|
G | A | 5 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0061others(2): Show | 5 | HG01433.hp2 HG02818.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.152-55439G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117044323 | ||||||
| chr7:117044343
|
A | G | 2 | a0001c0001t0001g0102a0001c0001t0001g0104 | 2 | HG00280.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.152-55419A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117044343 | ||||||
| chr7:117044380
|
C | T | 74 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(71): Show | 74 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.152-55382C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117044380 | ||||||
| chr7:117044608
|
CT | C | 22 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127others(19): Show | 22 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.152-55153delT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117044608 | ||||||
| chr7:117044968
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.152-54794C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117044968 | ||||||
| chr7:117045567
|
G | T | 61 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(58): Show | 61 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(58): Show |
intron_variant | MODIFIER | c.152-54195G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117045567 | ||||||
| chr7:117046239
|
G | A | 42 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(39): Show | 42 | HG00323.hp1 HG00408.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.152-53523G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117046239 | ||||||
| chr7:117046401
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.152-53361C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117046401 | ||||||
| chr7:117046574
|
C | T | 5 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0061others(2): Show | 5 | HG01433.hp2 HG02818.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.152-53188C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117046574 | ||||||
| chr7:117046798
|
T | C | 1 | a0001c0001t0001g0013 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.152-52964T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117046798 | ||||||
| chr7:117046940
|
A | G | 6 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0162others(3): Show | 6 | HG02630.hp1 HG02818.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.152-52822A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117046940 | ||||||
| chr7:117046980
|
C | T | 1 | a0001c0001t0001g0103 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.152-52782C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117046980 | ||||||
| chr7:117047047
|
A | T | 1 | a0001c0001t0001g0173 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.152-52715A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117047047 | ||||||
| chr7:117047107
|
C | G | 3 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0188 | 3 | HG02280.hp1 HG02486.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.152-52655C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117047107 | ||||||
| chr7:117047136
|
C | T | 3 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0062 | 3 | HG02818.hp1 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.152-52626C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117047136 | ||||||
| chr7:117047277
|
G | T | 5 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(2): Show | 5 | HG02451.hp1 HG02647.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.152-52485G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117047277 | ||||||
| chr7:117047744
|
C | A | 3 | a0001c0001t0001g0106a0001c0001t0001g0114a0001c0001t0001g0122 | 3 | HG02615.hp2 HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.152-52018C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117047744 | ||||||
| chr7:117048540
|
G | C | 1 | a0001c0001t0001g0061 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.152-51222G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117048540 | ||||||
| chr7:117048926
|
T | A | 3 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0184 | 3 | HG02965.hp1 HG02976.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.152-50836T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117048926 | ||||||
| chr7:117048966
|
G | A | 1 | a0001c0001t0001g0128 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.152-50796G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117048966 | ||||||
| chr7:117049274
|
A | G | 10 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087others(7): Show | 10 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.152-50488A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117049274 | ||||||
| chr7:117049287
|
G | A | 2 | a0001c0001t0001g0111a0001c0001t0001g0152 | 2 | HG00642.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.152-50475G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117049287 | ||||||
| chr7:117049977
|
C | A | 2 | a0001c0001t0001g0070a0001c0001t0001g0071 | 2 | HG02922.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.152-49785C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117049977 | ||||||
| chr7:117050023
|
G | A | 31 | a0001c0001t0001g0004a0001c0001t0001g0110a0001c0001t0001g0147others(28): Show | 31 | HG00323.hp2 HG00438.hp1 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.152-49739G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117050023 | ||||||
| chr7:117050047
|
A | G | 10 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087others(7): Show | 10 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.152-49715A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117050047 | ||||||
| chr7:117050050
|
C | CA | 9 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0058others(6): Show | 9 | HG00323.hp1 HG01433.hp1 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.152-49696dupA | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117050050 | |||||
| chr7:117050050
|
CA | C | 71 | a0001c0001t0001g0004a0001c0001t0001g0048a0001c0001t0001g0064others(68): Show | 71 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.152-49696delA | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117050050 | |||||
| chr7:117050070
|
C | G | 15 | a0001c0001t0001g0100a0001c0001t0001g0102a0001c0001t0001g0103others(12): Show | 15 | HG00099.hp1 HG00280.hp2 HG00642.hp2 others(12): Show |
intron_variant | MODIFIER | c.152-49692C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117050070 | ||||||
| chr7:117050139
|
C | T | 1 | a0001c0001t0001g0049 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.152-49623C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117050139 | ||||||
| chr7:117050214
|
C | CA | 40 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(37): Show | 40 | HG00408.hp1 HG00642.hp1 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.152-49534dupA | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117050214 | |||||
| chr7:117050632
|
T | C | 1 | a0001c0001t0001g0072 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.152-49130T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117050632 | ||||||
| chr7:117050772
|
T | G | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.152-48990T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117050772 | ||||||
| chr7:117050928
|
C | CA | 5 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0062others(2): Show | 5 | HG02818.hp1 HG02922.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.152-48817dupA | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117050928 | |||||
| chr7:117050928
|
CA | C | 179 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(176): Show | 179 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.152-48817delA | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117050928 | |||||
| chr7:117051041
|
C | T | 2 | a0001c0001t0001g0040a0001c0001t0001g0041 | 2 | HG01943.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.152-48721C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117051041 | ||||||
| chr7:117051528
|
G | T | 1 | a0001c0001t0001g0070 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.152-48234G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117051528 | ||||||
| chr7:117051954
|
C | T | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.152-47808C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117051954 | ||||||
| chr7:117052600
|
C | T | 6 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0061others(3): Show | 6 | HG01433.hp2 HG02109.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.152-47162C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117052600 | ||||||
| chr7:117052872
|
C | T | 2 | a0001c0001t0001g0058a0001c0001t0001g0059 | 2 | HG02818.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.152-46890C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117052872 | ||||||
| chr7:117052904
|
A | C | 12 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(9): Show | 12 | HG02055.hp2 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.152-46858A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117052904 | ||||||
| chr7:117052912
|
C | T | 2 | a0001c0001t0001g0040a0001c0001t0001g0041 | 2 | HG01943.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.152-46850C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117052912 | ||||||
| chr7:117052920
|
C | T | 1 | a0001c0001t0001g0012 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.152-46842C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117052920 | ||||||
| chr7:117053041
|
A | G | 1 | a0001c0001t0001g0151 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.152-46721A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117053041 | ||||||
| chr7:117053105
|
GTTGT | G | 3 | a0001c0001t0001g0118a0001c0001t0001g0120a0001c0001t0001g0121 | 3 | HG01081.hp1 HG02257.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.152-46651_152-4664 others(8): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117053105 | |||||
| chr7:117053266
|
C | G | 1 | a0001c0001t0001g0120 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.152-46496C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117053266 | ||||||
| chr7:117053328
|
A | G | 19 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(16): Show | 19 | HG01433.hp1 HG02055.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.152-46434A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117053328 | ||||||
| chr7:117053377
|
G | A | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.152-46385G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117053377 | ||||||
| chr7:117053431
|
C | G | 5 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0061others(2): Show | 5 | HG01433.hp2 HG02818.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.152-46331C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117053431 | ||||||
| chr7:117053607
|
C | T | 1 | a0001c0001t0001g0084 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.152-46155C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117053607 | ||||||
| chr7:117053688
|
G | T | 9 | a0001c0001t0001g0017a0001c0001t0001g0126a0001c0001t0001g0127others(6): Show | 9 | HG00738.hp2 HG01071.hp1 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.152-46074G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117053688 | ||||||
| chr7:117053736
|
A | G | 9 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(6): Show | 9 | HG02109.hp1 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.152-46026A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117053736 | ||||||
| chr7:117053756
|
T | G | 12 | a0001c0001t0001g0072a0001c0001t0001g0074a0001c0001t0001g0075others(9): Show | 12 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.152-46006T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117053756 | ||||||
| chr7:117053848
|
C | T | 15 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(12): Show | 15 | HG02055.hp2 HG02258.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.152-45914C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117053848 | ||||||
| chr7:117053850
|
GT | G | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(162): Show | 165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.152-45899delT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117053850 | |||||
| chr7:117053886
|
C | T | 13 | a0001c0001t0001g0100a0001c0001t0001g0102a0001c0001t0001g0103others(10): Show | 13 | HG00099.hp1 HG00280.hp2 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.152-45876C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117053886 | ||||||
| chr7:117053928
|
C | T | 12 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0086others(9): Show | 12 | HG02109.hp1 HG02280.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.152-45834C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117053928 | ||||||
| chr7:117054214
|
G | A | 1 | a0001c0001t0001g0026 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.152-45548G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117054214 | ||||||
| chr7:117054682
|
G | A | 2 | a0001c0001t0001g0085a0001c0001t0001g0166 | 2 | HG02109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.152-45080G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117054682 | ||||||
| chr7:117054874
|
A | G | 1 | a0001c0001t0001g0154 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.152-44888A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117054874 | ||||||
| chr7:117055227
|
G | T | 19 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(16): Show | 19 | HG01433.hp1 HG02055.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.152-44535G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117055227 | ||||||
| chr7:117055235
|
C | G | 5 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0061others(2): Show | 5 | HG01433.hp2 HG02818.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.152-44527C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117055235 | ||||||
| chr7:117055440
|
G | T | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.152-44322G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117055440 | ||||||
| chr7:117055588
|
A | G | 1 | a0001c0001t0001g0085 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.152-44174A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117055588 | ||||||
| chr7:117055590
|
C | A | 1 | a0001c0001t0001g0085 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.152-44172C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117055590 | ||||||
| chr7:117056343
|
A | T | 2 | a0001c0001t0001g0143a0001c0001t0001g0144 | 2 | NA18747.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.152-43419A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117056343 | ||||||
| chr7:117056366
|
G | A | 23 | a0001c0001t0001g0017a0001c0001t0001g0125a0001c0001t0001g0126others(20): Show | 23 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.152-43396G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117056366 | ||||||
| chr7:117056367
|
G | T | 1 | a0001c0001t0001g0025 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.152-43395G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117056367 | ||||||
| chr7:117056372
|
T | C | 5 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0061others(2): Show | 5 | HG01433.hp2 HG02818.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.152-43390T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117056372 | ||||||
| chr7:117056527
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.152-43235C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117056527 | ||||||
| chr7:117056621
|
C | T | 1 | a0001c0001t0001g0178 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.152-43141C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117056621 | ||||||
| chr7:117056867
|
G | A | 18 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(15): Show | 18 | HG00323.hp1 HG00408.hp1 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.152-42895G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117056867 | ||||||
| chr7:117057028
|
A | G | 1 | a0001c0001t0001g0034 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.152-42734A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117057028 | ||||||
| chr7:117057034
|
G | A | 1 | a0001c0001t0001g0020 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.152-42728G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117057034 | ||||||
| chr7:117057473
|
A | G | 11 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087others(8): Show | 11 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.152-42289A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117057473 | ||||||
| chr7:117058071
|
T | A | 1 | a0001c0001t0001g0119 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.152-41691T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117058071 | ||||||
| chr7:117058413
|
A | G | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.152-41349A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117058413 | ||||||
| chr7:117058872
|
A | G | 5 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0061others(2): Show | 5 | HG01433.hp2 HG02818.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.152-40890A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117058872 | ||||||
| chr7:117059033
|
T | A | 2 | a0001c0001t0001g0093a0001c0001t0001g0098 | 2 | HG01433.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.152-40729T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117059033 | ||||||
| chr7:117059408
|
G | A | 1 | a0001c0001t0001g0029 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.152-40354G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117059408 | ||||||
| chr7:117059807
|
C | CA | 62 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(59): Show | 62 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.152-39929dupA | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117059807 | |||||
| chr7:117059898
|
G | A | 1 | a0001c0001t0001g0155 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.152-39864G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117059898 | ||||||
| chr7:117059944
|
C | T | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.152-39818C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117059944 | ||||||
| chr7:117060137
|
G | T | 1 | a0001c0001t0001g0101 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.152-39625G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117060137 | ||||||
| chr7:117060207
|
G | A | 2 | a0001c0001t0001g0061a0001c0001t0001g0063 | 2 | HG01433.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.152-39555G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117060207 | ||||||
| chr7:117060793
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.152-38969G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117060793 | ||||||
| chr7:117060875
|
G | A | 12 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(9): Show | 12 | HG02055.hp2 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.152-38887G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117060875 | ||||||
| chr7:117061303
|
T | G | 12 | a0001c0001t0001g0072a0001c0001t0001g0074a0001c0001t0001g0075others(9): Show | 12 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.152-38459T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117061303 | ||||||
| chr7:117061706
|
T | C | 8 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(5): Show | 8 | HG02040.hp2 HG02273.hp1 NA18960.hp2 others(5): Show |
intron_variant | MODIFIER | c.152-38056T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117061706 | ||||||
| chr7:117061754
|
G | A | 25 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(22): Show | 25 | HG00323.hp1 HG00408.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.152-38008G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117061754 | ||||||
| chr7:117061767
|
C | G | 1 | a0001c0001t0001g0131 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.152-37995C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117061767 | ||||||
| chr7:117062126
|
A | G | 6 | a0001c0001t0001g0085a0001c0001t0001g0090a0001c0001t0001g0091others(3): Show | 6 | HG02109.hp1 HG02109.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.152-37636A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117062126 | ||||||
| chr7:117062673
|
T | C | 1 | a0001c0001t0001g0111 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.152-37089T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117062673 | ||||||
| chr7:117062696
|
A | G | 2 | a0001c0001t0001g0031a0001c0001t0001g0042 | 2 | HG01192.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.152-37066A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117062696 | ||||||
| chr7:117063506
|
C | G | 1 | a0001c0001t0001g0058 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.152-36256C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117063506 | ||||||
| chr7:117063511
|
C | T | 12 | a0001c0001t0001g0072a0001c0001t0001g0074a0001c0001t0001g0075others(9): Show | 12 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.152-36251C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117063511 | ||||||
| chr7:117063596
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.152-36166C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117063596 | ||||||
| chr7:117063965
|
C | T | 1 | a0001c0001t0001g0144 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.152-35797C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117063965 | ||||||
| chr7:117064171
|
C | A | 2 | a0001c0001t0001g0058a0001c0001t0001g0059 | 2 | HG02818.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.152-35591C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117064171 | ||||||
| chr7:117064188
|
GT | G | 13 | a0001c0001t0001g0100a0001c0001t0001g0102a0001c0001t0001g0103others(10): Show | 13 | HG00099.hp1 HG00280.hp2 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.152-35566delT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117064188 | |||||
| chr7:117064428
|
C | G | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.152-35334C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117064428 | ||||||
| chr7:117064630
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.152-35132C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117064630 | ||||||
| chr7:117065164
|
A | G | 63 | a0001c0001t0001g0017a0001c0001t0001g0043a0001c0001t0001g0045others(60): Show | 63 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(60): Show |
intron_variant | MODIFIER | c.152-34598A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117065164 | ||||||
| chr7:117065176
|
A | G | 4 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(1): Show | 4 | HG01433.hp1 HG02723.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-34586A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117065176 | ||||||
| chr7:117065204
|
C | CT | 5 | a0001c0001t0001g0061a0001c0001t0001g0063a0001c0001t0001g0112others(2): Show | 5 | HG00438.hp2 HG01433.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.152-34535dupT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117065204 | |||||
| chr7:117065204
|
CT | C | 114 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(111): Show | 114 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.152-34535delT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117065204 | |||||
| chr7:117065489
|
G | T | 1 | a0001c0001t0001g0144 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.152-34273G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117065489 | ||||||
| chr7:117065790
|
T | C | 1 | a0001c0001t0001g0145 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.152-33972T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117065790 | ||||||
| chr7:117065799
|
C | T | 23 | a0001c0001t0001g0017a0001c0001t0001g0125a0001c0001t0001g0126others(20): Show | 23 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.152-33963C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117065799 | ||||||
| chr7:117066486
|
G | T | 3 | a0001c0001t0001g0064a0001c0001t0001g0066a0001c0001t0001g0067 | 3 | HG01496.hp2 HG02572.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.152-33276G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117066486 | ||||||
| chr7:117066653
|
C | T | 1 | a0001c0001t0001g0116 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.152-33109C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117066653 | ||||||
| chr7:117066685
|
T | C | 2 | a0001c0001t0001g0063a0001c0001t0001g0112 | 2 | HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.152-33077T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117066685 | ||||||
| chr7:117066709
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.152-33053C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117066709 | ||||||
| chr7:117066764
|
C | CA | 46 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(43): Show | 46 | HG00323.hp1 HG00408.hp1 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.152-32975dupA | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117066764 | |||||
| chr7:117066764
|
CA | C | 16 | a0001c0001t0001g0057a0001c0001t0001g0064a0001c0001t0001g0065others(13): Show | 16 | HG00099.hp2 HG00738.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.152-32975delA | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117066764 | |||||
| chr7:117066866
|
C | T | 1 | a0001c0001t0001g0023 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.152-32896C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117066866 | ||||||
| chr7:117067041
|
G | C | 2 | a0001c0001t0001g0038a0001c0001t0001g0039 | 2 | NA18960.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.152-32721G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117067041 | ||||||
| chr7:117067082
|
C | T | 12 | a0001c0001t0001g0072a0001c0001t0001g0074a0001c0001t0001g0075others(9): Show | 12 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.152-32680C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117067082 | ||||||
| chr7:117067701
|
A | G | 1 | a0001c0001t0001g0024 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.152-32061A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117067701 | ||||||
| chr7:117067857
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.152-31905C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117067857 | ||||||
| chr7:117067972
|
G | A | 56 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0011others(53): Show | 56 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.152-31790G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117067972 | ||||||
| chr7:117068103
|
A | G | 4 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(1): Show | 4 | HG02055.hp1 HG02572.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-31659A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117068103 | ||||||
| chr7:117069464
|
C | G | 2 | a0001c0001t0001g0153a0001c0001t0001g0159 | 2 | NA18965.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.152-30298C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117069464 | ||||||
| chr7:117069516
|
C | T | 40 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(37): Show | 40 | HG00323.hp1 HG00408.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.152-30246C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117069516 | ||||||
| chr7:117069685
|
A | T | 1 | a0001c0001t0001g0139 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.152-30077A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117069685 | ||||||
| chr7:117069704
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.152-30058C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117069704 | ||||||
| chr7:117070336
|
G | A | 4 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(1): Show | 4 | HG01433.hp1 HG02723.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-29426G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117070336 | ||||||
| chr7:117070403
|
C | T | 2 | a0001c0001t0001g0009a0001c0001t0001g0010 | 2 | NA18973.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.152-29359C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117070403 | ||||||
| chr7:117070531
|
T | TTTTG | 5 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0026others(2): Show | 5 | HG02280.hp1 HG02683.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152-29207_152-2920 others(8): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117070531 | |||||
| chr7:117070531
|
TTTTG | T | 13 | a0001c0001t0001g0015a0001c0001t0001g0072a0001c0001t0001g0074others(10): Show | 13 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.152-29207_152-2920 others(8): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117070531 | |||||
| chr7:117070580
|
C | A | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.152-29182C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117070580 | ||||||
| chr7:117070702
|
T | G | 177 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(174): Show | 177 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.152-29060T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117070702 | ||||||
| chr7:117071111
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.152-28651C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117071111 | ||||||
| chr7:117071123
|
A | G | 3 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0187 | 3 | NA19000.hp1 NA19004.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.152-28639A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117071123 | ||||||
| chr7:117071180
|
C | G | 9 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(6): Show | 9 | HG02109.hp1 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.152-28582C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117071180 | ||||||
| chr7:117072214
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.152-27548C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117072214 | ||||||
| chr7:117072586
|
A | G | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.152-27176A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117072586 | ||||||
| chr7:117072637
|
G | A | 1 | a0001c0001t0001g0163 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.152-27125G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117072637 | ||||||
| chr7:117072833
|
G | A | 18 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(15): Show | 18 | HG00323.hp1 HG00408.hp1 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.152-26929G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117072833 | ||||||
| chr7:117072841
|
T | A | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.152-26921T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117072841 | ||||||
| chr7:117073595
|
T | A | 1 | a0001c0001t0001g0130 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.152-26167T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117073595 | ||||||
| chr7:117073631
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.152-26131C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117073631 | ||||||
| chr7:117073731
|
A | G | 1 | a0001c0001t0001g0019 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.152-26031A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117073731 | ||||||
| chr7:117074260
|
G | A | 19 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(16): Show | 19 | HG01433.hp1 HG02055.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.152-25502G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117074260 | ||||||
| chr7:117074489
|
C | T | 6 | a0001c0001t0001g0008a0001c0001t0001g0149a0001c0001t0001g0150others(3): Show | 6 | HG02273.hp1 HG02615.hp1 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.152-25273C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117074489 | ||||||
| chr7:117074792
|
T | C | 3 | a0001c0001t0001g0043a0001c0001t0001g0056a0001c0001t0001g0057 | 3 | HG02486.hp2 HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.152-24970T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117074792 | ||||||
| chr7:117075262
|
G | C | 1 | a0001c0001t0001g0025 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.152-24500G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117075262 | ||||||
| chr7:117075814
|
A | G | 23 | a0001c0001t0001g0017a0001c0001t0001g0125a0001c0001t0001g0126others(20): Show | 23 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.152-23948A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117075814 | ||||||
| chr7:117075953
|
C | G | 1 | a0001c0001t0001g0070 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.152-23809C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117075953 | ||||||
| chr7:117076389
|
T | C | 1 | a0001c0001t0001g0188 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.152-23373T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117076389 | ||||||
| chr7:117076544
|
G | A | 34 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0011others(31): Show | 34 | HG00323.hp2 HG00438.hp1 HG01255.hp1 others(31): Show |
intron_variant | MODIFIER | c.152-23218G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117076544 | ||||||
| chr7:117076663
|
C | T | 2 | a0001c0001t0001g0100a0001c0001t0001g0103 | 2 | HG00741.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.152-23099C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117076663 | ||||||
| chr7:117076746
|
C | T | 12 | a0001c0001t0001g0072a0001c0001t0001g0074a0001c0001t0001g0075others(9): Show | 12 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.152-23016C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117076746 | ||||||
| chr7:117076854
|
C | T | 3 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0085 | 3 | HG02109.hp2 HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.152-22908C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117076854 | ||||||
| chr7:117076894
|
A | C | 34 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0011others(31): Show | 34 | HG00323.hp2 HG00438.hp1 HG01255.hp1 others(31): Show |
intron_variant | MODIFIER | c.152-22868A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117076894 | ||||||
| chr7:117077110
|
G | A | 19 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(16): Show | 19 | HG01433.hp1 HG02055.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.152-22652G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117077110 | ||||||
| chr7:117077242
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.152-22520A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117077242 | ||||||
| chr7:117077495
|
G | A | 2 | a0001c0001t0001g0085a0001c0001t0001g0166 | 2 | HG02109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.152-22267G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117077495 | ||||||
| chr7:117077563
|
T | C | 1 | a0001c0001t0001g0004 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.152-22199T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117077563 | ||||||
| chr7:117077844
|
C | CT | 5 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0015others(2): Show | 5 | HG02630.hp2 HG03139.hp1 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.152-21899dupT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117077844 | |||||
| chr7:117077844
|
CT | C | 46 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0043others(43): Show | 46 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.152-21899delT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117077844 | |||||
| chr7:117077858
|
T | C | 11 | a0001c0001t0001g0022a0001c0001t0001g0028a0001c0001t0001g0029others(8): Show | 11 | HG00408.hp1 HG00673.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.152-21904T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117077858 | ||||||
| chr7:117077912
|
C | T | 19 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(16): Show | 19 | HG01433.hp1 HG02055.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.152-21850C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117077912 | ||||||
| chr7:117078422
|
T | C | 3 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0062 | 3 | HG02818.hp1 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.152-21340T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117078422 | ||||||
| chr7:117078681
|
A | T | 2 | a0001c0001t0001g0085a0001c0001t0001g0166 | 2 | HG02109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.152-21081A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117078681 | ||||||
| chr7:117078904
|
C | T | 35 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(32): Show | 35 | HG00323.hp1 HG00408.hp1 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.152-20858C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117078904 | ||||||
| chr7:117079196
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.152-20566C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117079196 | ||||||
| chr7:117079235
|
G | A | 1 | a0001c0001t0001g0004 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.152-20527G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117079235 | ||||||
| chr7:117079968
|
C | CT | 39 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(36): Show | 39 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.152-19764dupT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117079968 | |||||
| chr7:117079968
|
C | CTT | 8 | a0001c0001t0001g0070a0001c0001t0001g0078a0001c0001t0001g0079others(5): Show | 8 | HG00741.hp1 HG02027.hp2 HG02083.hp2 others(5): Show |
intron_variant | MODIFIER | c.152-19765_152-1976 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117079968 | |||||
| chr7:117079968
|
C | CTTTTTTT others(3): Show |
2 | a0001c0001t0001g0058a0001c0001t0001g0059 | 2 | HG02818.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.152-19773_152-1976 others(14): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117079968 | |||||
| chr7:117079968
|
CT | C | 39 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0028others(36): Show | 39 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(36): Show |
intron_variant | MODIFIER | c.152-19764delT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117079968 | |||||
| chr7:117079968
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0077 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.152-19773_152-1976 others(14): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117079968 | |||||
| chr7:117079968
|
CTTTTTTT others(9): Show |
C | 6 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(3): Show | 6 | HG02451.hp1 HG02622.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.152-19779_152-1976 others(20): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117079968 | |||||
| chr7:117080019
|
C | T | 15 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(12): Show | 15 | HG00642.hp1 HG00673.hp2 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.152-19743C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117080019 | ||||||
| chr7:117080129
|
C | T | 35 | a0001c0001t0001g0017a0001c0001t0001g0100a0001c0001t0001g0102others(32): Show | 35 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.152-19633C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117080129 | ||||||
| chr7:117080330
|
C | T | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.152-19432C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117080330 | ||||||
| chr7:117080403
|
G | C | 4 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(1): Show | 4 | HG02055.hp1 HG02572.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-19359G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117080403 | ||||||
| chr7:117080973
|
A | T | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.152-18789A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117080973 | ||||||
| chr7:117080976
|
C | T | 12 | a0001c0001t0001g0072a0001c0001t0001g0074a0001c0001t0001g0075others(9): Show | 12 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.152-18786C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117080976 | ||||||
| chr7:117081135
|
T | C | 2 | a0001c0001t0001g0085a0001c0001t0001g0166 | 2 | HG02109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.152-18627T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117081135 | ||||||
| chr7:117081150
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.152-18612G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117081150 | ||||||
| chr7:117081892
|
T | TGA | 7 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0109others(4): Show | 7 | HG02293.hp2 HG02300.hp1 NA19000.hp1 others(4): Show |
intron_variant | MODIFIER | c.152-17850_152-1784 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117081892 | |||||
| chr7:117081892
|
T | TGAGAGA | 26 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(23): Show | 26 | HG00323.hp1 HG00408.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.152-17854_152-1784 others(10): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117081892 | |||||
| chr7:117082104
|
C | T | 1 | a0001c0001t0001g0073 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.152-17658C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117082104 | ||||||
| chr7:117082118
|
A | G | 1 | a0001c0001t0001g0069 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.152-17644A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117082118 | ||||||
| chr7:117082521
|
T | C | 2 | a0001c0001t0001g0085a0001c0001t0001g0166 | 2 | HG02109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.152-17241T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117082521 | ||||||
| chr7:117082530
|
T | C | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.152-17232T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117082530 | ||||||
| chr7:117082532
|
A | G | 3 | a0001c0001t0001g0147a0001c0001t0001g0155a0001c0001t0001g0157 | 3 | HG01255.hp1 HG02004.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.152-17230A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117082532 | ||||||
| chr7:117082590
|
C | T | 2 | a0001c0001t0001g0016a0001c0001t0001g0018 | 2 | HG03492.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.152-17172C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117082590 | ||||||
| chr7:117082635
|
A | G | 1 | a0001c0001t0001g0020 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.152-17127A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117082635 | ||||||
| chr7:117083116
|
A | G | 15 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(12): Show | 15 | HG00642.hp1 HG00673.hp2 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.152-16646A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117083116 | ||||||
| chr7:117083162
|
C | T | 3 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0062 | 3 | HG02818.hp1 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.152-16600C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117083162 | ||||||
| chr7:117083167
|
C | T | 7 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0133others(4): Show | 7 | HG00408.hp2 HG00438.hp2 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.152-16595C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117083167 | ||||||
| chr7:117083450
|
G | A | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.152-16312G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117083450 | ||||||
| chr7:117083649
|
A | G | 1 | a0001c0001t0001g0087 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.152-16113A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117083649 | ||||||
| chr7:117083661
|
T | C | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.152-16101T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117083661 | ||||||
| chr7:117083829
|
T | C | 1 | a0001c0001t0001g0151 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.152-15933T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117083829 | ||||||
| chr7:117083842
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.152-15920G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117083842 | ||||||
| chr7:117083851
|
C | CTG | 31 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(28): Show | 31 | HG00323.hp1 HG00408.hp1 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.152-15910_152-1590 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117083851 | |||||
| chr7:117083992
|
G | A | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.152-15770G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117083992 | ||||||
| chr7:117084134
|
T | C | 1 | a0001c0001t0001g0070 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.152-15628T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117084134 | ||||||
| chr7:117084218
|
T | C | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.152-15544T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117084218 | ||||||
| chr7:117084405
|
G | C | 27 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(24): Show | 27 | HG00323.hp1 HG00408.hp1 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.152-15357G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117084405 | ||||||
| chr7:117084689
|
G | A | 4 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0036others(1): Show | 4 | HG00673.hp1 HG01071.hp2 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.152-15073G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117084689 | ||||||
| chr7:117084724
|
CATT | C | 2 | a0001c0001t0001g0085a0001c0001t0001g0166 | 2 | HG02109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.152-15028_152-1502 others(7): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117084724 | |||||
| chr7:117084811
|
T | C | 1 | a0001c0001t0001g0174 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.152-14951T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117084811 | ||||||
| chr7:117084893
|
T | C | 13 | a0001c0001t0001g0125a0001c0001t0001g0130a0001c0001t0001g0131others(10): Show | 13 | HG00408.hp2 HG00438.hp2 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.152-14869T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117084893 | ||||||
| chr7:117085281
|
A | G | 1 | a0001c0001t0001g0019 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.152-14481A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117085281 | ||||||
| chr7:117085345
|
C | T | 4 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0036others(1): Show | 4 | HG00673.hp1 HG01071.hp2 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.152-14417C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117085345 | ||||||
| chr7:117085522
|
A | G | 1 | a0001c0001t0001g0069 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.152-14240A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117085522 | ||||||
| chr7:117085940
|
G | A | 1 | a0001c0001t0001g0019 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.152-13822G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117085940 | ||||||
| chr7:117086778
|
C | T | 3 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0184 | 3 | HG02965.hp1 HG02976.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.152-12984C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117086778 | ||||||
| chr7:117087319
|
G | T | 1 | a0001c0001t0001g0099 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.152-12443G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117087319 | ||||||
| chr7:117087636
|
A | G | 2 | a0001c0001t0001g0102a0001c0001t0001g0104 | 2 | HG00280.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.152-12126A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117087636 | ||||||
| chr7:117088047
|
C | T | 1 | a0001c0001t0001g0055 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.152-11715C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117088047 | ||||||
| chr7:117088238
|
T | G | 2 | a0001c0001t0001g0153a0001c0001t0001g0159 | 2 | NA18965.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.152-11524T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117088238 | ||||||
| chr7:117088442
|
T | C | 2 | a0001c0001t0001g0013a0001c0001t0001g0014 | 2 | HG02257.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.152-11320T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117088442 | ||||||
| chr7:117088543
|
G | A | 1 | a0001c0001t0001g0105 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.152-11219G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117088543 | ||||||
| chr7:117088897
|
T | C | 3 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0097 | 3 | HG02109.hp1 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.152-10865T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117088897 | ||||||
| chr7:117088998
|
G | A | 3 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0002t0001g0044 | 3 | HG02970.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.152-10764G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117088998 | ||||||
| chr7:117089062
|
C | T | 14 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(11): Show | 14 | HG00642.hp1 HG00673.hp2 HG01943.hp1 others(11): Show |
intron_variant | MODIFIER | c.152-10700C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117089062 | ||||||
| chr7:117089119
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.152-10643C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117089119 | ||||||
| chr7:117089270
|
T | A | 1 | a0001c0001t0001g0099 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.152-10492T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117089270 | ||||||
| chr7:117089499
|
A | C | 82 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(79): Show | 82 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.152-10263A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117089499 | ||||||
| chr7:117089566
|
G | T | 1 | a0001c0001t0001g0169 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.152-10196G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117089566 | ||||||
| chr7:117089574
|
G | GT | 14 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0028others(11): Show | 14 | HG00738.hp1 HG01255.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.152-10173dupT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117089574 | |||||
| chr7:117089602
|
C | T | 1 | a0001c0001t0001g0019 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.152-10160C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117089602 | ||||||
| chr7:117089650
|
C | A | 1 | a0001c0001t0001g0062 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.152-10112C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117089650 | ||||||
| chr7:117089657
|
T | C | 172 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(169): Show | 172 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.152-10105T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117089657 | ||||||
| chr7:117089835
|
G | T | 11 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(8): Show | 11 | HG00673.hp2 HG01943.hp1 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.152-9927G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117089835 | ||||||
| chr7:117089904
|
AC | A | 3 | a0001c0001t0001g0147a0001c0001t0001g0155a0001c0001t0001g0157 | 3 | HG01255.hp1 HG02004.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.152-9857delC | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117089904 | ||||||
| chr7:117090236
|
A | AAC | 2 | a0001c0001t0001g0143a0001c0001t0001g0144 | 2 | NA18747.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.152-9510_152-9509d others(4): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117090236 | |||||
| chr7:117090240
|
C | A | 1 | a0001c0001t0001g0085 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.152-9522C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117090240 | ||||||
| chr7:117090254
|
GAC | G | 82 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(79): Show | 82 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.152-9485_152-9484d others(4): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117090254 | |||||
| chr7:117090254
|
GACAC | G | 2 | a0001c0001t0001g0040a0001c0001t0001g0041 | 2 | HG01943.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.152-9487_152-9484d others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117090254 | |||||
| chr7:117090254
|
GACACACA others(7): Show |
G | 1 | a0001c0001t0001g0075 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.152-9497_152-9484d others(16): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117090254 | |||||
| chr7:117090266
|
C | A | 1 | a0001c0001t0001g0118 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.152-9496C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117090266 | ||||||
| chr7:117090413
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.152-9349G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117090413 | ||||||
| chr7:117091092
|
G | A | 2 | a0001c0001t0001g0063a0001c0001t0001g0112 | 2 | HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.152-8670G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117091092 | ||||||
| chr7:117091228
|
G | T | 1 | a0001c0001t0001g0014 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.152-8534G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117091228 | ||||||
| chr7:117091334
|
G | A | 7 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0132others(4): Show | 7 | HG00738.hp2 HG01358.hp1 HG02683.hp1 others(4): Show |
intron_variant | MODIFIER | c.152-8428G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117091334 | ||||||
| chr7:117092201
|
C | G | 1 | a0001c0001t0001g0128 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.152-7561C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117092201 | ||||||
| chr7:117092278
|
C | CA | 25 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(22): Show | 25 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(22): Show |
intron_variant | MODIFIER | c.152-7458dupA | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117092278 | |||||
| chr7:117092278
|
CA | C | 21 | a0001c0001t0001g0038a0001c0001t0001g0041a0001c0001t0001g0052others(18): Show | 21 | HG00323.hp2 HG01433.hp1 HG01943.hp1 others(18): Show |
intron_variant | MODIFIER | c.152-7458delA | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117092278 | |||||
| chr7:117092278
|
CAAAAAA | C | 6 | a0001c0001t0001g0022a0001c0001t0001g0090a0001c0001t0001g0091others(3): Show | 6 | HG00323.hp1 HG02109.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.152-7463_152-7458d others(8): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117092278 | |||||
| chr7:117092278
|
CAAAAAAA | C | 22 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(19): Show | 22 | HG00408.hp1 HG00673.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.152-7464_152-7458d others(9): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117092278 | |||||
| chr7:117092294
|
AAAAAAAA others(22): Show |
A | 2 | a0001c0001t0001g0158a0001c0001t0001g0183 | 2 | HG02071.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.152-7457_152-7429d others(31): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117092294 | |||||
| chr7:117092323
|
C | CA | 34 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(31): Show | 34 | HG00323.hp1 HG00408.hp1 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.152-7425dupA | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117092323 | |||||
| chr7:117092323
|
CA | C | 13 | a0001c0001t0001g0125a0001c0001t0001g0130a0001c0001t0001g0131others(10): Show | 13 | HG00408.hp2 HG00438.hp2 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.152-7425delA | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117092323 | |||||
| chr7:117092797
|
C | T | 1 | a0001c0001t0001g0047 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.152-6965C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117092797 | ||||||
| chr7:117093152
|
G | T | 13 | a0001c0001t0001g0125a0001c0001t0001g0130a0001c0001t0001g0131others(10): Show | 13 | HG00408.hp2 HG00438.hp2 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.152-6610G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117093152 | ||||||
| chr7:117093478
|
G | A | 1 | a0001c0001t0001g0006 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.152-6284G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117093478 | ||||||
| chr7:117093529
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.152-6233G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117093529 | ||||||
| chr7:117093705
|
A | C | 20 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0093others(17): Show | 20 | HG00408.hp2 HG00438.hp2 HG01433.hp1 others(17): Show |
intron_variant | MODIFIER | c.152-6057A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117093705 | ||||||
| chr7:117093720
|
C | A | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02027.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.152-6042C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117093720 | ||||||
| chr7:117093778
|
G | A | 14 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(11): Show | 14 | HG00642.hp1 HG00673.hp2 HG01943.hp1 others(11): Show |
intron_variant | MODIFIER | c.152-5984G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117093778 | ||||||
| chr7:117093856
|
A | C | 3 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0002t0001g0044 | 3 | HG02970.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.152-5906A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117093856 | ||||||
| chr7:117093883
|
C | T | 1 | a0001c0001t0001g0005 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.152-5879C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117093883 | ||||||
| chr7:117094586
|
C | T | 1 | a0001c0001t0001g0077 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.152-5176C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117094586 | ||||||
| chr7:117094677
|
C | T | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.152-5085C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117094677 | ||||||
| chr7:117094935
|
G | A | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.152-4827G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117094935 | ||||||
| chr7:117094942
|
A | G | 2 | a0001c0001t0001g0161a0001c0001t0001g0181 | 2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.152-4820A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117094942 | ||||||
| chr7:117095138
|
A | G | 1 | a0001c0001t0001g0143 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.152-4624A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117095138 | ||||||
| chr7:117095540
|
A | G | 2 | a0001c0001t0001g0085a0001c0001t0001g0166 | 2 | HG02109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.152-4222A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117095540 | ||||||
| chr7:117095654
|
A | G | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.152-4108A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117095654 | ||||||
| chr7:117095962
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.152-3800G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117095962 | ||||||
| chr7:117096054
|
C | T | 1 | a0001c0001t0001g0143 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.152-3708C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117096054 | ||||||
| chr7:117096067
|
C | CA | 22 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0028others(19): Show | 22 | HG00642.hp2 HG00738.hp2 HG01358.hp1 others(19): Show |
intron_variant | MODIFIER | c.152-3664dupA | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117096067 | |||||
| chr7:117096067
|
C | CAA | 6 | a0001c0001t0001g0055a0001c0001t0001g0090a0001c0001t0001g0121others(3): Show | 6 | HG02257.hp1 HG02622.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.152-3665_152-3664d others(4): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117096067 | |||||
| chr7:117096067
|
CA | C | 38 | a0001c0001t0001g0006a0001c0001t0001g0023a0001c0001t0001g0024others(35): Show | 38 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(35): Show |
intron_variant | MODIFIER | c.152-3664delA | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117096067 | |||||
| chr7:117096067
|
CAA | C | 29 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(26): Show | 29 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.152-3665_152-3664d others(4): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117096067 | |||||
| chr7:117096067
|
CAAA | C | 6 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0093others(3): Show | 6 | HG01433.hp1 HG02040.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.152-3666_152-3664d others(5): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117096067 | |||||
| chr7:117096067
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0188 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.152-3674_152-3664d others(13): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117096067 | |||||
| chr7:117096067
|
CAAAAAAA others(5): Show |
C | 3 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0062 | 3 | HG02818.hp1 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.152-3675_152-3664d others(14): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117096067 | |||||
| chr7:117096178
|
G | T | 1 | a0001c0001t0001g0109 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.152-3584G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117096178 | ||||||
| chr7:117096281
|
C | A | 177 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(174): Show | 177 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.152-3481C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117096281 | ||||||
| chr7:117096315
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.152-3447C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117096315 | ||||||
| chr7:117096328
|
G | A | 3 | a0001c0001t0001g0168a0001c0001t0001g0171a0001c0001t0001g0177 | 3 | HG00438.hp1 NA18945.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.152-3434G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117096328 | ||||||
| chr7:117096332
|
TCTGCCTT others(12): Show |
T | 1 | a0001c0001t0001g0153 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.152-3427_152-3409d others(21): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117096332 | |||||
| chr7:117096537
|
C | T | 1 | a0001c0001t0001g0103 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.152-3225C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117096537 | ||||||
| chr7:117096628
|
G | A | 19 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(16): Show | 19 | HG00738.hp2 HG01358.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.152-3134G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117096628 | ||||||
| chr7:117096734
|
G | C | 2 | a0001c0001t0001g0160a0001c0001t0001g0162 | 2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.152-3028G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117096734 | ||||||
| chr7:117097060
|
A | G | 3 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0026 | 3 | HG02683.hp2 HG04228.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.152-2702A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117097060 | ||||||
| chr7:117097093
|
A | G | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.152-2669A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117097093 | ||||||
| chr7:117097250
|
C | T | 1 | a0001c0001t0001g0136 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.152-2512C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117097250 | ||||||
| chr7:117097326
|
G | C | 27 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(24): Show | 27 | HG00323.hp1 HG00408.hp1 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.152-2436G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117097326 | ||||||
| chr7:117097327
|
C | CT | 5 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0153others(2): Show | 5 | HG02293.hp2 HG02486.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.152-2420dupT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097327 | |||||
| chr7:117097422
|
T | C | 1 | a0001c0001t0001g0047 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.152-2340T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117097422 | ||||||
| chr7:117097599
|
C | T | 7 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0093others(4): Show | 7 | HG01433.hp1 HG02723.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.152-2163C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117097599 | ||||||
| chr7:117097767
|
T | G | 1 | a0001c0001t0001g0007 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.152-1995T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117097767 | ||||||
| chr7:117097822
|
C | CTA | 42 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0001t0001g0023others(39): Show | 42 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(39): Show |
intron_variant | MODIFIER | c.152-1920_152-1919d others(4): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097822 | |||||
| chr7:117097822
|
C | CTATA | 17 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(14): Show | 17 | HG00642.hp1 HG00673.hp2 HG01934.hp2 others(14): Show |
intron_variant | MODIFIER | c.152-1922_152-1919d others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097822 | |||||
| chr7:117097822
|
C | CTATATA | 3 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0062 | 3 | HG02818.hp1 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.152-1924_152-1919d others(8): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097822 | |||||
| chr7:117097822
|
C | CTATATAT others(3): Show |
1 | a0001c0001t0001g0112 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.152-1928_152-1919d others(12): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097822 | |||||
| chr7:117097880
|
C | CTATATA | 4 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0021others(1): Show | 4 | HG00642.hp1 HG00673.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.152-1858_152-1853d others(8): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097880 | |||||
| chr7:117097880
|
C | CTATATAT others(1): Show |
4 | a0001c0001t0001g0018a0001c0001t0001g0040a0001c0001t0001g0045others(1): Show | 4 | HG00280.hp2 HG02280.hp2 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-1860_152-1853d others(10): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097880 | |||||
| chr7:117097880
|
C | CTATATAT others(3): Show |
4 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0015others(1): Show | 4 | HG02630.hp2 NA18988.hp2 NA19086.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-1862_152-1853d others(12): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097880 | |||||
| chr7:117097880
|
C | CTATATAT others(5): Show |
6 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0100others(3): Show | 6 | HG00738.hp1 HG00741.hp2 HG02273.hp1 others(3): Show |
intron_variant | MODIFIER | c.152-1864_152-1853d others(14): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097880 | |||||
| chr7:117097880
|
C | CTATATAT others(7): Show |
8 | a0001c0001t0001g0003a0001c0001t0001g0102a0001c0001t0001g0106others(5): Show | 8 | HG01978.hp2 HG02615.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.152-1866_152-1853d others(16): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097880 | |||||
| chr7:117097880
|
C | CTATATAT others(9): Show |
6 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0049others(3): Show | 6 | HG01358.hp2 HG03195.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.152-1868_152-1853d others(18): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097880 | |||||
| chr7:117097880
|
C | CTATATAT others(11): Show |
7 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0055others(4): Show | 7 | HG00642.hp2 HG01978.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.152-1870_152-1853d others(20): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097880 | |||||
| chr7:117097880
|
C | CTATATAT others(13): Show |
4 | a0001c0001t0001g0048a0001c0001t0001g0057a0001c0001t0001g0105others(1): Show | 4 | HG00099.hp1 HG01256.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.152-1872_152-1853d others(22): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097880 | |||||
| chr7:117097880
|
C | CTATATAT others(15): Show |
2 | a0001c0001t0001g0067a0001c0001t0001g0118 | 2 | HG01081.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.152-1874_152-1853d others(24): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097880 | |||||
| chr7:117097880
|
C | CTATATAT others(17): Show |
4 | a0001c0001t0001g0050a0001c0001t0001g0113a0001c0001t0001g0120others(1): Show | 4 | HG00738.hp2 HG02258.hp2 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-1876_152-1853d others(26): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097880 | |||||
| chr7:117097880
|
C | CTATATAT others(19): Show |
1 | a0001c0001t0001g0119 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.152-1878_152-1853d others(28): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097880 | |||||
| chr7:117097880
|
C | CTATATAT others(21): Show |
2 | a0001c0001t0001g0103a0001c0001t0001g0139 | 2 | NA18971.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.152-1880_152-1853d others(30): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097880 | |||||
| chr7:117097880
|
C | CTATATAT others(23): Show |
1 | a0001c0001t0001g0129 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.152-1853_152-1852i others(32): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097880 | |||||
| chr7:117097880
|
CTATATAT others(1): Show |
C | 4 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0068others(1): Show | 4 | HG02280.hp1 HG02723.hp2 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-1860_152-1853d others(10): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097880 | |||||
| chr7:117097884
|
A | ATATATAT others(12): Show |
3 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0002t0001g0044 | 3 | HG02970.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.152-1869_152-1868i others(21): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097884 | |||||
| chr7:117097888
|
A | ATATATGA others(8): Show |
5 | a0001c0001t0001g0062a0001c0001t0001g0093a0001c0001t0001g0094others(2): Show | 5 | HG01433.hp1 HG02723.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.152-1869_152-1868i others(17): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097888 | |||||
| chr7:117097904
|
ATATATTT others(2): Show |
A | 5 | a0001c0001t0001g0086a0001c0001t0001g0089a0001c0001t0001g0091others(2): Show | 5 | HG02109.hp1 HG02622.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.152-1856_152-1848d others(11): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097904 | |||||
| chr7:117097906
|
A | T | 3 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0080 | 3 | HG00741.hp1 HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.152-1856A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117097906 | ||||||
| chr7:117097908
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0001g0152 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.152-1853_152-1852i others(15): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | |||||
| chr7:117097908
|
A | ATATATAT others(8): Show |
2 | a0001c0001t0001g0148a0001c0001t0001g0150 | 2 | NA18981.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.152-1853_152-1852i others(17): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | |||||
| chr7:117097908
|
A | ATATATAT others(10): Show |
4 | a0001c0001t0001g0071a0001c0001t0001g0153a0001c0001t0001g0176others(1): Show | 4 | HG03041.hp2 HG04184.hp1 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.152-1853_152-1852i others(19): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | |||||
| chr7:117097908
|
A | ATATATAT others(20): Show |
1 | a0001c0001t0001g0155 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.152-1853_152-1852i others(29): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | |||||
| chr7:117097908
|
A | ATATATAT others(17): Show |
1 | a0001c0001t0001g0017 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.152-1853_152-1852i others(26): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | |||||
| chr7:117097908
|
A | ATATATAT others(13): Show |
1 | a0001c0001t0001g0151 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.152-1853_152-1852i others(22): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | |||||
| chr7:117097908
|
A | ATATATAT others(14): Show |
1 | a0001c0001t0001g0126 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.152-1853_152-1852i others(23): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | |||||
| chr7:117097908
|
A | ATATATAT others(11): Show |
1 | a0001c0001t0001g0173 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.152-1853_152-1852i others(20): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | |||||
| chr7:117097908
|
A | ATATATAT others(12): Show |
1 | a0001c0001t0001g0157 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.152-1853_152-1852i others(21): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | |||||
| chr7:117097908
|
A | ATATATAT others(15): Show |
1 | a0001c0001t0001g0019 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.152-1853_152-1852i others(24): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | |||||
| chr7:117097908
|
A | ATATATAT others(9): Show |
1 | a0001c0001t0001g0186 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.152-1853_152-1852i others(18): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | |||||
| chr7:117097908
|
A | ATATATAT others(10): Show |
3 | a0001c0001t0001g0168a0001c0001t0001g0171a0001c0001t0001g0177 | 3 | HG00438.hp1 NA18945.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.152-1853_152-1852i others(19): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | |||||
| chr7:117097908
|
A | ATATATAT others(11): Show |
1 | a0001c0001t0001g0185 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.152-1853_152-1852i others(20): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | |||||
| chr7:117097908
|
A | ATATATAT others(13): Show |
1 | a0001c0001t0001g0163 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.152-1853_152-1852i others(22): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | |||||
| chr7:117097908
|
A | ATATATAT others(15): Show |
2 | a0001c0001t0001g0082a0001c0001t0001g0127 | 2 | HG01071.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.152-1853_152-1852i others(24): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | |||||
| chr7:117097908
|
A | ATATATAT others(17): Show |
2 | a0001c0001t0001g0074a0001c0001t0001g0076 | 2 | HG00099.hp2 HG00280.hp1 |
intron_variant | MODIFIER | c.152-1853_152-1852i others(26): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | |||||
| chr7:117097908
|
A | ATATATAT others(7): Show |
1 | a0001c0001t0001g0149 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.152-1853_152-1852i others(16): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | |||||
| chr7:117097908
|
A | ATATATAT others(9): Show |
3 | a0001c0001t0001g0004a0001c0001t0001g0154a0001c0001t0001g0158 | 3 | HG01934.hp1 HG02071.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.152-1853_152-1852i others(18): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | |||||
| chr7:117097908
|
A | ATATATAT others(11): Show |
1 | a0001c0001t0001g0179 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.152-1853_152-1852i others(20): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | |||||
| chr7:117097908
|
A | ATATATAT others(12): Show |
2 | a0001c0001t0001g0011a0001c0001t0001g0187 | 2 | NA19000.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.152-1853_152-1852i others(21): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | |||||
| chr7:117097908
|
A | ATATATAT others(17): Show |
1 | a0001c0001t0001g0075 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.152-1853_152-1852i others(26): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | |||||
| chr7:117097908
|
A | ATATATAT others(19): Show |
1 | a0001c0001t0001g0072 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.152-1853_152-1852i others(28): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | |||||
| chr7:117097908
|
A | ATATATAT others(5): Show |
3 | a0001c0001t0001g0109a0001c0001t0001g0156a0001c0001t0001g0165 | 3 | HG02965.hp1 NA18747.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.152-1853_152-1852i others(14): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | |||||
| chr7:117097908
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0001g0174 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.152-1853_152-1852i others(15): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | |||||
| chr7:117097908
|
A | ATATATAT others(7): Show |
2 | a0001c0001t0001g0078a0001c0001t0001g0175 | 2 | HG02083.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.152-1853_152-1852i others(16): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | |||||
| chr7:117097908
|
A | ATATATAT others(8): Show |
1 | a0001c0001t0001g0172 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.152-1853_152-1852i others(17): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | |||||
| chr7:117097908
|
A | ATATATAT others(9): Show |
1 | a0001c0001t0001g0182 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.152-1853_152-1852i others(18): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | |||||
| chr7:117097908
|
A | ATATATAT others(16): Show |
1 | a0001c0001t0001g0180 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.152-1853_152-1852i others(25): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | |||||
| chr7:117097908
|
A | ATATATAT others(17): Show |
2 | a0001c0001t0001g0077a0001c0001t0001g0079 | 2 | HG02523.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.152-1853_152-1852i others(26): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | |||||
| chr7:117097908
|
A | ATATATAT others(3): Show |
2 | a0001c0001t0001g0009a0001c0001t0001g0010 | 2 | NA18973.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.152-1853_152-1852i others(12): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | |||||
| chr7:117097908
|
A | ATATATAT others(4): Show |
3 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0146 | 3 | HG02055.hp1 HG02572.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.152-1853_152-1852i others(13): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | |||||
| chr7:117097908
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0001g0135 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.152-1853_152-1852i others(15): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | |||||
| chr7:117097908
|
A | ATATATAT others(13): Show |
1 | a0001c0001t0001g0083 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.152-1853_152-1852i others(22): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | |||||
| chr7:117097908
|
A | ATATATAT others(24): Show |
1 | a0001c0001t0001g0081 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.152-1853_152-1852i others(33): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | |||||
| chr7:117097908
|
A | ATATATAT others(4): Show |
1 | a0001c0001t0001g0131 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.152-1853_152-1852i others(13): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | |||||
| chr7:117097908
|
A | ATATATAT others(5): Show |
1 | a0001c0001t0001g0134 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.152-1853_152-1852i others(14): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | |||||
| chr7:117097908
|
A | ATATATAT others(14): Show |
1 | a0001c0001t0001g0084 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.152-1853_152-1852i others(23): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | |||||
| chr7:117097908
|
A | ATATATTT others(4): Show |
1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.152-1853_152-1852i others(13): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | |||||
| chr7:117097908
|
A | ATATATTT others(5): Show |
1 | a0001c0001t0001g0133 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.152-1853_152-1852i others(14): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | |||||
| chr7:117097908
|
A | ATATATTT others(7): Show |
1 | a0001c0001t0001g0145 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.152-1853_152-1852i others(16): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | |||||
| chr7:117097908
|
A | ATATTTTT others(3): Show |
1 | a0001c0001t0001g0130 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.152-1853_152-1852i others(12): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | |||||
| chr7:117097908
|
A | T | 3 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0080 | 3 | HG00741.hp1 HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.152-1854A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117097908 | ||||||
| chr7:117097908
|
ATTTTTTT | A | 14 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0026others(11): Show | 14 | HG00323.hp1 HG00408.hp1 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.152-1840_152-1834d others(9): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | |||||
| chr7:117097909
|
T | TATATATA | 2 | a0001c0001t0001g0041a0001c0001t0001g0188 | 2 | HG01943.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.152-1853_152-1852i others(9): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117097909 | ||||||
| chr7:117097909
|
T | TATATATA others(2): Show |
3 | a0001c0001t0001g0005a0001c0001t0001g0170a0001c0001t0001g0181 | 3 | HG02040.hp2 HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.152-1853_152-1852i others(11): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117097909 | ||||||
| chr7:117097909
|
T | TATATATA others(4): Show |
1 | a0001c0001t0001g0054 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.152-1853_152-1852i others(13): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117097909 | ||||||
| chr7:117097909
|
T | TATATATA others(6): Show |
3 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117 | 3 | HG01943.hp2 HG02451.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.152-1853_152-1852i others(15): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117097909 | ||||||
| chr7:117097909
|
T | TATATATA others(8): Show |
3 | a0001c0001t0001g0002a0001c0001t0001g0110a0001c0001t0001g0160 | 3 | HG00323.hp2 HG02818.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.152-1853_152-1852i others(17): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117097909 | ||||||
| chr7:117097909
|
T | TATATATA others(10): Show |
4 | a0001c0001t0001g0043a0001c0001t0001g0051a0001c0001t0001g0065others(1): Show | 4 | HG02647.hp1 HG02976.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-1853_152-1852i others(19): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117097909 | ||||||
| chr7:117097909
|
T | TATATATA others(12): Show |
4 | a0001c0001t0001g0056a0001c0001t0001g0064a0001c0001t0001g0073others(1): Show | 4 | HG01081.hp2 HG01496.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-1853_152-1852i others(21): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117097909 | ||||||
| chr7:117097909
|
T | TATATATA others(14): Show |
1 | a0001c0001t0001g0099 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.152-1853_152-1852i others(23): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117097909 | ||||||
| chr7:117097910
|
T | A | 44 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(41): Show | 44 | HG00099.hp1 HG00280.hp2 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.152-1852T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117097910 | ||||||
| chr7:117097911
|
T | A | 18 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0013others(15): Show | 18 | HG00323.hp2 HG01081.hp2 HG01943.hp1 others(15): Show |
intron_variant | MODIFIER | c.152-1851T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117097911 | ||||||
| chr7:117097912
|
T | A | 16 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0015others(13): Show | 16 | HG00099.hp1 HG00280.hp2 HG00673.hp2 others(13): Show |
intron_variant | MODIFIER | c.152-1850T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117097912 | ||||||
| chr7:117097913
|
T | A | 5 | a0001c0001t0001g0013a0001c0001t0001g0022a0001c0001t0001g0051others(2): Show | 5 | HG01081.hp2 HG02257.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.152-1849T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117097913 | ||||||
| chr7:117097914
|
T | A | 4 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0102others(1): Show | 4 | HG00280.hp2 HG01978.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.152-1848T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117097914 | ||||||
| chr7:117097915
|
T | A | 3 | a0001c0001t0001g0013a0001c0001t0001g0022a0001c0001t0001g0116 | 3 | HG02257.hp2 NA18981.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.152-1847T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117097915 | ||||||
| chr7:117097916
|
T | A | 1 | a0001c0001t0001g0112 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.152-1846T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117097916 | ||||||
| chr7:117097917
|
T | A | 1 | a0001c0001t0001g0028 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.152-1845T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117097917 | ||||||
| chr7:117097970
|
C | T | 3 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0002t0001g0044 | 3 | HG02970.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.152-1792C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117097970 | ||||||
| chr7:117098008
|
C | T | 2 | a0001c0001t0001g0061a0001c0001t0001g0070 | 2 | HG01433.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.152-1754C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117098008 | ||||||
| chr7:117098102
|
G | A | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.152-1660G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117098102 | ||||||
| chr7:117098186
|
G | A | 3 | a0001c0001t0001g0017a0001c0001t0001g0126a0001c0001t0001g0127 | 3 | HG01071.hp1 HG01255.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.152-1576G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117098186 | ||||||
| chr7:117098524
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.152-1238G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117098524 | ||||||
| chr7:117098534
|
T | A | 1 | a0001c0001t0001g0107 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.152-1228T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117098534 | ||||||
| chr7:117098589
|
A | G | 1 | a0001c0001t0001g0185 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.152-1173A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117098589 | ||||||
| chr7:117098765
|
T | C | 2 | a0001c0001t0001g0025a0001c0001t0001g0032 | 2 | HG02071.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.152-997T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117098765 | ||||||
| chr7:117099046
|
C | CA | 20 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0099others(17): Show | 20 | HG00099.hp1 HG00280.hp2 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.152-697dupA | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117099046 | |||||
| chr7:117099046
|
C | CAA | 11 | a0001c0001t0001g0048a0001c0001t0001g0052a0001c0001t0001g0057others(8): Show | 11 | HG01192.hp1 HG01358.hp1 HG01978.hp2 others(8): Show |
intron_variant | MODIFIER | c.152-698_152-697dup others(2): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117099046 | |||||
| chr7:117099046
|
C | CAAA | 33 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0043others(30): Show | 33 | HG00438.hp1 HG01255.hp1 HG01358.hp2 others(30): Show |
intron_variant | MODIFIER | c.152-699_152-697dup others(3): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117099046 | |||||
| chr7:117099046
|
C | CAAAA | 11 | a0001c0001t0001g0007a0001c0001t0001g0055a0001c0001t0001g0091others(8): Show | 11 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(8): Show |
intron_variant | MODIFIER | c.152-700_152-697dup others(4): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117099046 | |||||
| chr7:117099046
|
C | CAAAAA | 18 | a0001c0001t0001g0022a0001c0001t0001g0028a0001c0001t0001g0029others(15): Show | 18 | HG00408.hp1 HG01192.hp2 HG02004.hp1 others(15): Show |
intron_variant | MODIFIER | c.152-701_152-697dup others(5): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117099046 | |||||
| chr7:117099046
|
C | CAAAAAAA | 6 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0037others(3): Show | 6 | HG00673.hp1 HG01071.hp2 HG02071.hp1 others(3): Show |
intron_variant | MODIFIER | c.152-703_152-697dup others(7): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117099046 | |||||
| chr7:117099046
|
C | CAAAAAAA others(4): Show |
2 | a0001c0001t0001g0125a0001c0001t0001g0145 | 2 | HG02258.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.152-707_152-697dup others(11): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117099046 | |||||
| chr7:117099046
|
C | CAAAAAAA others(6): Show |
1 | a0001c0001t0001g0135 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.152-709_152-697dup others(13): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117099046 | |||||
| chr7:117099046
|
C | CAAAAAAA others(7): Show |
3 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0142 | 3 | HG02717.hp2 HG02895.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.152-710_152-697dup others(14): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117099046 | |||||
| chr7:117099046
|
C | CAAAAAAA others(8): Show |
1 | a0001c0001t0001g0134 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.152-711_152-697dup others(15): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117099046 | |||||
| chr7:117099046
|
C | CAAAAAAA others(11): Show |
1 | a0001c0001t0001g0131 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.152-714_152-697dup others(18): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117099046 | |||||
| chr7:117099046
|
C | CAAAAAAA others(12): Show |
1 | a0001c0001t0001g0137 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.152-715_152-697dup others(19): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117099046 | |||||
| chr7:117099046
|
C | CAAAAAAA others(13): Show |
3 | a0001c0001t0001g0130a0001c0001t0001g0133a0001c0001t0001g0141 | 3 | HG00408.hp2 HG02523.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.152-697_152-696ins others(20): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117099046 | |||||
| chr7:117099052
|
AAAAAAAA others(7): Show |
A | 1 | a0001c0001t0001g0188 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.152-699_152-686del others(14): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117099052 | |||||
| chr7:117099055
|
AAAAAAAA others(4): Show |
A | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.152-696_152-686del others(11): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117099055 | |||||
| chr7:117099063
|
AAAC | A | 7 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(4): Show | 7 | HG02055.hp1 HG02615.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.152-696_152-694del others(3): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117099063 | |||||
| chr7:117099065
|
AC | A | 23 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(20): Show | 23 | HG00099.hp2 HG00642.hp1 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.152-696delC | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117099065 | ||||||
| chr7:117099066
|
C | A | 137 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(134): Show | 137 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.152-696C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117099066 | ||||||
| chr7:117099081
|
A | G | 1 | a0001c0001t0001g0089 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.152-681A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117099081 | ||||||
| chr7:117099315
|
T | G | 13 | a0001c0001t0001g0125a0001c0001t0001g0130a0001c0001t0001g0131others(10): Show | 13 | HG00408.hp2 HG00438.hp2 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.152-447T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117099315 | ||||||
| chr7:117099448
|
A | G | 1 | a0001c0001t0001g0070 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.152-314A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117099448 | ||||||
| chr7:117099571
|
A | G | 1 | a0001c0001t0001g0085 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.152-191A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117099571 | ||||||
| chr7:117099650
|
A | G | 5 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0062others(2): Show | 5 | HG02818.hp1 HG02922.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.152-112A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117099650 | ||||||
| chr7:117100284
|
C | T | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.234+440C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117100284 | ||||||
| chr7:117100606
|
T | C | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.234+762T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117100606 | ||||||
| chr7:117100758
|
G | C | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.234+914G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117100758 | ||||||
| chr7:117101025
|
G | A | 5 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(2): Show | 5 | HG01496.hp2 HG02572.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.234+1181G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117101025 | ||||||
| chr7:117101174
|
G | A | 1 | a0001c0001t0001g0028 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.234+1330G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117101174 | ||||||
| chr7:117101492
|
T | C | 1 | a0001c0001t0001g0086 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.234+1648T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117101492 | ||||||
| chr7:117101541
|
A | G | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.234+1697A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117101541 | ||||||
| chr7:117102033
|
T | G | 15 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(12): Show | 15 | HG00642.hp1 HG00673.hp2 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.234+2189T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117102033 | ||||||
| chr7:117102302
|
C | T | 2 | a0001c0001t0001g0063a0001c0001t0001g0112 | 2 | HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.234+2458C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117102302 | ||||||
| chr7:117102376
|
G | C | 1 | a0001c0001t0001g0105 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.234+2532G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117102376 | ||||||
| chr7:117102393
|
A | G | 2 | a0001c0001t0001g0099a0001c0001t0001g0108 | 2 | NA20805.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.234+2549A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117102393 | ||||||
| chr7:117102482
|
C | T | 1 | a0001c0001t0001g0001 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.234+2638C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117102482 | ||||||
| chr7:117102944
|
T | C | 2 | a0001c0001t0001g0085a0001c0001t0001g0166 | 2 | HG02109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.234+3100T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117102944 | ||||||
| chr7:117103243
|
G | GA | 6 | a0001c0001t0001g0125a0001c0001t0001g0139a0001c0001t0001g0149others(3): Show | 6 | HG02258.hp1 NA18965.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.234+3408dupA | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 117103243 | |||||
| chr7:117103293
|
A | G | 16 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0072others(13): Show | 16 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.234+3449A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117103293 | ||||||
| chr7:117103325
|
A | G | 1 | a0001c0001t0001g0110 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.234+3481A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117103325 | ||||||
| chr7:117103621
|
TCTAAGA | T | 16 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0072others(13): Show | 16 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.234+3779_234+3784d others(8): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 117103621 | |||||
| chr7:117103746
|
T | C | 13 | a0001c0001t0001g0125a0001c0001t0001g0130a0001c0001t0001g0131others(10): Show | 13 | HG00408.hp2 HG00438.hp2 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.234+3902T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117103746 | ||||||
| chr7:117104113
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.234+4269G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117104113 | ||||||
| chr7:117104372
|
G | A | 2 | a0001c0001t0001g0161a0001c0001t0001g0181 | 2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.234+4528G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117104372 | ||||||
| chr7:117104463
|
T | C | 177 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(174): Show | 177 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.234+4619T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117104463 | ||||||
| chr7:117104555
|
C | G | 1 | a0001c0001t0001g0103 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.234+4711C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117104555 | ||||||
| chr7:117104623
|
T | C | 14 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(11): Show | 14 | HG00642.hp1 HG00673.hp2 HG01943.hp1 others(11): Show |
intron_variant | MODIFIER | c.234+4779T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117104623 | ||||||
| chr7:117104686
|
G | A | 4 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0085others(1): Show | 4 | HG02109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.234+4842G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117104686 | ||||||
| chr7:117104793
|
T | A | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.234+4949T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117104793 | ||||||
| chr7:117105009
|
C | T | 1 | a0001c0001t0001g0080 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.234+5165C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117105009 | ||||||
| chr7:117105036
|
T | C | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.234+5192T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117105036 | ||||||
| chr7:117105175
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.234+5331G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117105175 | ||||||
| chr7:117105427
|
C | T | 7 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0093others(4): Show | 7 | HG01433.hp1 HG02723.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.234+5583C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117105427 | ||||||
| chr7:117105499
|
G | C | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.234+5655G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117105499 | ||||||
| chr7:117105505
|
T | C | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.234+5661T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117105505 | ||||||
| chr7:117105726
|
A | C | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.234+5882A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117105726 | ||||||
| chr7:117105925
|
G | A | 3 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0085 | 3 | HG02109.hp2 HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.234+6081G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117105925 | ||||||
| chr7:117105988
|
T | A | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.234+6144T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117105988 | ||||||
| chr7:117105998
|
G | GT | 6 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0010others(3): Show | 6 | HG02083.hp1 HG03098.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.234+6165dupT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 117105998 | |||||
| chr7:117105998
|
GT | G | 57 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(54): Show | 57 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.234+6165delT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 117105998 | |||||
| chr7:117106004
|
T | G | 1 | a0001c0001t0001g0169 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.234+6160T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117106004 | ||||||
| chr7:117106005
|
T | G | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.234+6161T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117106005 | ||||||
| chr7:117106046
|
C | T | 2 | a0001c0001t0001g0074a0001c0001t0001g0075 | 2 | HG00099.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.234+6202C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117106046 | ||||||
| chr7:117106047
|
G | A | 5 | a0001c0001t0001g0007a0001c0001t0001g0151a0001c0001t0001g0156others(2): Show | 5 | HG02027.hp1 HG02083.hp1 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.234+6203G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117106047 | ||||||
| chr7:117106150
|
C | T | 83 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(80): Show | 83 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.234+6306C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117106150 | ||||||
| chr7:117106159
|
G | C | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.234+6315G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117106159 | ||||||
| chr7:117106183
|
A | G | 3 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0002t0001g0044 | 3 | HG02970.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.234+6339A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117106183 | ||||||
| chr7:117106261
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.234+6417G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117106261 | ||||||
| chr7:117106409
|
A | G | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.234+6565A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117106409 | ||||||
| chr7:117106454
|
T | G | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.234+6610T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117106454 | ||||||
| chr7:117106616
|
C | CT | 7 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0100others(4): Show | 7 | HG00099.hp1 HG00642.hp2 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.234+6794dupT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 117106616 | |||||
| chr7:117106616
|
CT | C | 11 | a0001c0001t0001g0006a0001c0001t0001g0061a0001c0001t0001g0068others(8): Show | 11 | HG01433.hp2 HG01496.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.234+6794delT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 117106616 | |||||
| chr7:117106651
|
T | C | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.234+6807T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117106651 | ||||||
| chr7:117106781
|
C | T | 1 | a0001c0001t0001g0062 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.234+6937C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117106781 | ||||||
| chr7:117106810
|
C | T | 28 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(25): Show | 28 | HG00323.hp1 HG00408.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.234+6966C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117106810 | ||||||
| chr7:117106893
|
T | G | 2 | a0001c0001t0001g0085a0001c0001t0001g0166 | 2 | HG02109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.234+7049T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117106893 | ||||||
| chr7:117107123
|
A | G | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.234+7279A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117107123 | ||||||
| chr7:117107206
|
G | A | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.234+7362G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117107206 | ||||||
| chr7:117107603
|
C | CT | 21 | a0001c0001t0001g0008a0001c0001t0001g0023a0001c0001t0001g0033others(18): Show | 21 | HG00099.hp1 HG00741.hp1 HG01256.hp1 others(18): Show |
intron_variant | MODIFIER | c.234+7785dupT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 117107603 | |||||
| chr7:117107603
|
CT | C | 25 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0058others(22): Show | 25 | HG00408.hp2 HG00438.hp2 HG02040.hp1 others(22): Show |
intron_variant | MODIFIER | c.234+7785delT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 117107603 | |||||
| chr7:117107867
|
G | A | 1 | a0001c0001t0001g0034 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.234+8023G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117107867 | ||||||
| chr7:117107944
|
C | T | 89 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(86): Show | 89 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.234+8100C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117107944 | ||||||
| chr7:117108276
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.234+8432C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117108276 | ||||||
| chr7:117108843
|
T | A | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.234+8999T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117108843 | ||||||
| chr7:117109196
|
A | G | 3 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0002t0001g0044 | 3 | HG02970.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.234+9352A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117109196 | ||||||
| chr7:117109217
|
T | G | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.234+9373T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117109217 | ||||||
| chr7:117109330
|
GAGA | G | 16 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0072others(13): Show | 16 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.234+9493_234+9495d others(5): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 117109330 | |||||
| chr7:117109369
|
C | T | 1 | a0001c0001t0001g0186 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.234+9525C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117109369 | ||||||
| chr7:117109461
|
T | TAGA | 2 | a0001c0001t0001g0085a0001c0001t0001g0166 | 2 | HG02109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.234+9621_234+9623d others(5): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 117109461 | |||||
| chr7:117109475
|
G | A | 4 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0085others(1): Show | 4 | HG02109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.234+9631G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117109475 | ||||||
| chr7:117109673
|
C | T | 1 | a0001c0001t0001g0178 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.234+9829C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117109673 | ||||||
| chr7:117109767
|
A | C | 1 | a0001c0001t0001g0173 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.235-9794A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117109767 | ||||||
| chr7:117109773
|
G | A | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.235-9788G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117109773 | ||||||
| chr7:117110156
|
G | C | 1 | a0001c0001t0001g0012 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.235-9405G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117110156 | ||||||
| chr7:117110255
|
G | A | 3 | a0001c0001t0001g0147a0001c0001t0001g0155a0001c0001t0001g0157 | 3 | HG01255.hp1 HG02004.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.235-9306G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117110255 | ||||||
| chr7:117110440
|
G | A | 4 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0085others(1): Show | 4 | HG02109.hp2 HG02280.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.235-9121G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117110440 | ||||||
| chr7:117110649
|
G | A | 1 | a0001c0001t0001g0156 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.235-8912G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117110649 | ||||||
| chr7:117111072
|
GAGCTTGT others(10): Show |
G | 2 | a0001c0001t0001g0074a0001c0001t0001g0075 | 2 | HG00099.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.235-8485_235-8469d others(19): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 117111072 | |||||
| chr7:117111190
|
C | T | 2 | a0001c0001t0001g0079a0001c0001t0001g0081 | 2 | NA19004.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.235-8371C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117111190 | ||||||
| chr7:117111569
|
G | A | 7 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0093others(4): Show | 7 | HG01433.hp1 HG02723.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.235-7992G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117111569 | ||||||
| chr7:117111821
|
T | C | 3 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0085 | 3 | HG02109.hp2 HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.235-7740T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117111821 | ||||||
| chr7:117111860
|
G | A | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.235-7701G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117111860 | ||||||
| chr7:117111863
|
G | GT | 15 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(12): Show | 15 | HG00642.hp1 HG00673.hp2 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.235-7697dupT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 117111863 | |||||
| chr7:117111943
|
T | C | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.235-7618T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117111943 | ||||||
| chr7:117112108
|
G | GTGTGTGT others(17): Show |
2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.235-7452_235-7451i others(26): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 117112108 | |||||
| chr7:117112119
|
T | A | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.235-7442T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117112119 | ||||||
| chr7:117112129
|
G | A | 7 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0061others(4): Show | 7 | HG01433.hp2 HG02818.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.235-7432G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117112129 | ||||||
| chr7:117112238
|
A | G | 7 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0061others(4): Show | 7 | HG01433.hp2 HG02818.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.235-7323A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117112238 | ||||||
| chr7:117112365
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.235-7196A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117112365 | ||||||
| chr7:117112612
|
C | G | 1 | a0001c0001t0001g0072 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.235-6949C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117112612 | ||||||
| chr7:117112633
|
G | A | 2 | a0001c0001t0001g0063a0001c0001t0001g0112 | 2 | HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.235-6928G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117112633 | ||||||
| chr7:117113042
|
G | C | 1 | a0001c0001t0001g0085 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.235-6519G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117113042 | ||||||
| chr7:117113297
|
T | A | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.235-6264T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117113297 | ||||||
| chr7:117113444
|
GAA | G | 5 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0062others(2): Show | 5 | HG02818.hp1 HG02922.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.235-6115_235-6114d others(4): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 117113444 | |||||
| chr7:117113451
|
A | G | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.235-6110A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117113451 | ||||||
| chr7:117113766
|
G | T | 20 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0093others(17): Show | 20 | HG00408.hp2 HG00438.hp2 HG01433.hp1 others(17): Show |
intron_variant | MODIFIER | c.235-5795G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117113766 | ||||||
| chr7:117114099
|
A | G | 1 | a0001c0001t0001g0160 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.235-5462A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117114099 | ||||||
| chr7:117114340
|
G | A | 20 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0093others(17): Show | 20 | HG00408.hp2 HG00438.hp2 HG01433.hp1 others(17): Show |
intron_variant | MODIFIER | c.235-5221G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117114340 | ||||||
| chr7:117114634
|
G | A | 16 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0072others(13): Show | 16 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.235-4927G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117114634 | ||||||
| chr7:117114808
|
A | G | 14 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(11): Show | 14 | HG00642.hp1 HG00673.hp2 HG01943.hp1 others(11): Show |
intron_variant | MODIFIER | c.235-4753A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117114808 | ||||||
| chr7:117114921
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.235-4640G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117114921 | ||||||
| chr7:117114931
|
G | A | 12 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(9): Show | 12 | HG02055.hp2 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.235-4630G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117114931 | ||||||
| chr7:117115058
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.235-4503C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117115058 | ||||||
| chr7:117115281
|
A | G | 1 | a0001c0001t0001g0058 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.235-4280A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117115281 | ||||||
| chr7:117115474
|
C | A | 1 | a0001c0001t0001g0080 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.235-4087C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117115474 | ||||||
| chr7:117115624
|
G | A | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.235-3937G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117115624 | ||||||
| chr7:117116469
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.235-3092G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117116469 | ||||||
| chr7:117116481
|
C | T | 17 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0072others(14): Show | 17 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.235-3080C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117116481 | ||||||
| chr7:117116695
|
C | T | 5 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0062others(2): Show | 5 | HG02818.hp1 HG02922.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.235-2866C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117116695 | ||||||
| chr7:117116773
|
C | G | 1 | a0001c0001t0001g0188 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.235-2788C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117116773 | ||||||
| chr7:117116782
|
A | C | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.235-2779A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117116782 | ||||||
| chr7:117116842
|
A | G | 5 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0001g0167others(2): Show | 5 | HG02630.hp1 HG02818.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.235-2719A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117116842 | ||||||
| chr7:117117079
|
G | A | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.235-2482G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117117079 | ||||||
| chr7:117117342
|
G | A | 3 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0020 | 3 | HG00642.hp1 HG03492.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.235-2219G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117117342 | ||||||
| chr7:117117400
|
T | G | 1 | a0001c0001t0001g0070 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.235-2161T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117117400 | ||||||
| chr7:117117473
|
A | T | 1 | a0001c0001t0001g0126 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.235-2088A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117117473 | ||||||
| chr7:117117505
|
A | G | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.235-2056A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117117505 | ||||||
| chr7:117117702
|
G | C | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.235-1859G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117117702 | ||||||
| chr7:117117790
|
G | A | 3 | a0001c0001t0001g0021a0001c0001t0001g0040a0001c0001t0001g0041 | 3 | HG00673.hp2 HG01943.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.235-1771G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117117790 | ||||||
| chr7:117117805
|
C | T | 1 | a0001c0001t0001g0061 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.235-1756C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117117805 | ||||||
| chr7:117117937
|
T | G | 1 | a0001c0001t0001g0168 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.235-1624T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117117937 | ||||||
| chr7:117118003
|
C | T | 27 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(24): Show | 27 | HG00323.hp1 HG00408.hp1 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.235-1558C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117118003 | ||||||
| chr7:117118116
|
A | C | 5 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0001g0167others(2): Show | 5 | HG02630.hp1 HG02818.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.235-1445A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117118116 | ||||||
| chr7:117118613
|
T | C | 13 | a0001c0001t0001g0125a0001c0001t0001g0130a0001c0001t0001g0131others(10): Show | 13 | HG00408.hp2 HG00438.hp2 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.235-948T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117118613 | ||||||
| chr7:117118707
|
G | A | 58 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(55): Show | 58 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.235-854G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117118707 | ||||||
| chr7:117119109
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.235-452G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117119109 | ||||||
| chr7:117119280
|
T | C | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.235-281T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117119280 | ||||||
| chr7:117119361
|
C | T | 3 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0062 | 3 | HG02818.hp1 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.235-200C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117119361 | ||||||
| chr7:117119796
|
T | G | 4 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0085others(1): Show | 4 | HG02109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.394+76T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117119796 | ||||||
| chr7:117119880
|
G | A | 2 | a0001c0001t0001g0063a0001c0001t0001g0112 | 2 | HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.394+160G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117119880 | ||||||
| chr7:117119935
|
C | CT | 36 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0011others(33): Show | 36 | HG00323.hp2 HG00438.hp1 HG01192.hp1 others(33): Show |
intron_variant | MODIFIER | c.394+226dupT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr7 | 117119935 | |||||
| chr7:117120006
|
G | A | 1 | a0001c0001t0001g0004 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.394+286G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117120006 | ||||||
| chr7:117120411
|
G | A | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.394+691G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117120411 | ||||||
| chr7:117120478
|
G | A | 1 | a0001c0001t0001g0105 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.394+758G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117120478 | ||||||
| chr7:117120586
|
C | T | 1 | a0001c0001t0001g0069 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.394+866C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117120586 | ||||||
| chr7:117120981
|
G | A | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.394+1261G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117120981 | ||||||
| chr7:117121589
|
A | G | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.394+1869A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117121589 | ||||||
| chr7:117121659
|
A | G | 15 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0072others(12): Show | 15 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.394+1939A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117121659 | ||||||
| chr7:117121782
|
A | G | 6 | a0001c0001t0001g0123a0001c0001t0001g0132a0001c0001t0001g0136others(3): Show | 6 | HG00738.hp2 HG01358.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.394+2062A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117121782 | ||||||
| chr7:117121887
|
T | TAAGAGGA others(263): Show |
1 | a0001c0001t0001g0038 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.394+2176_394+2177i others(272): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr7 | 117121887 | |||||
| chr7:117121887
|
T | TAAGAGGA others(269): Show |
3 | a0001c0001t0001g0018a0001c0001t0001g0040a0001c0001t0001g0041 | 3 | HG01943.hp1 HG02300.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.394+2176_394+2177i others(278): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr7 | 117121887 | |||||
| chr7:117121887
|
T | TAAGAGGA others(270): Show |
1 | a0001c0001t0001g0021 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.394+2176_394+2177i others(279): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr7 | 117121887 | |||||
| chr7:117121887
|
T | TAAGAGGA others(271): Show |
5 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0010others(2): Show | 5 | HG02040.hp2 HG02273.hp1 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.394+2176_394+2177i others(280): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr7 | 117121887 | |||||
| chr7:117121887
|
T | TAAGAGGA others(276): Show |
2 | a0001c0001t0001g0006a0001c0001t0001g0039 | 2 | NA18990.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.394+2176_394+2177i others(285): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr7 | 117121887 | |||||
| chr7:117121887
|
T | TAAGAGGA others(277): Show |
2 | a0001c0001t0001g0009a0001c0001t0001g0020 | 2 | HG00642.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.394+2176_394+2177i others(286): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr7 | 117121887 | |||||
| chr7:117121992
|
T | C | 18 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(15): Show | 18 | HG00738.hp2 HG01358.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.394+2272T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117121992 | ||||||
| chr7:117122098
|
T | A | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.394+2378T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117122098 | ||||||
| chr7:117122246
|
A | G | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.394+2526A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117122246 | ||||||
| chr7:117122267
|
T | C | 2 | a0001c0001t0001g0038a0001c0001t0001g0039 | 2 | NA18960.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.394+2547T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117122267 | ||||||
| chr7:117122355
|
G | A | 1 | a0001c0001t0001g0012 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.394+2635G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117122355 | ||||||
| chr7:117122536
|
A | G | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.394+2816A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117122536 | ||||||
| chr7:117122858
|
G | A | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.394+3138G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117122858 | ||||||
| chr7:117123206
|
G | A | 1 | a0001c0001t0001g0073 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.394+3486G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117123206 | ||||||
| chr7:117123282
|
A | G | 27 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(24): Show | 27 | HG00323.hp1 HG00408.hp1 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.394+3562A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117123282 | ||||||
| chr7:117123522
|
G | A | 1 | a0001c0001t0001g0024 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.394+3802G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117123522 | ||||||
| chr7:117123891
|
A | C | 1 | a0001c0001t0001g0088 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.394+4171A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117123891 | ||||||
| chr7:117123983
|
A | T | 1 | a0001c0001t0001g0108 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.394+4263A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117123983 | ||||||
| chr7:117124036
|
A | G | 1 | a0001c0001t0001g0026 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.394+4316A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117124036 | ||||||
| chr7:117124129
|
C | T | 5 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0001g0167others(2): Show | 5 | HG02630.hp1 HG02818.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.394+4409C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117124129 | ||||||
| chr7:117124295
|
C | T | 15 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(12): Show | 15 | HG00642.hp1 HG00673.hp2 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.394+4575C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117124295 | ||||||
| chr7:117125045
|
T | C | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.395-4748T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117125045 | ||||||
| chr7:117125215
|
C | G | 1 | a0001c0001t0001g0124 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.395-4578C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117125215 | ||||||
| chr7:117125225
|
G | T | 2 | a0001c0001t0001g0077a0001c0001t0001g0078 | 2 | HG02083.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.395-4568G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117125225 | ||||||
| chr7:117126261
|
C | CT | 5 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(2): Show | 5 | HG01496.hp2 HG02572.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.395-3524dupT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr7 | 117126261 | |||||
| chr7:117126835
|
T | C | 3 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0062 | 3 | HG02818.hp1 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.395-2958T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117126835 | ||||||
| chr7:117126863
|
C | T | 2 | a0001c0001t0001g0038a0001c0001t0001g0039 | 2 | NA18960.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.395-2930C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117126863 | ||||||
| chr7:117126867
|
G | C | 3 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0062 | 3 | HG02818.hp1 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.395-2926G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117126867 | ||||||
| chr7:117126981
|
A | G | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.395-2812A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117126981 | ||||||
| chr7:117126996
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.395-2797G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117126996 | ||||||
| chr7:117127500
|
T | G | 8 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0085others(5): Show | 8 | HG02109.hp2 HG02280.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.395-2293T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117127500 | ||||||
| chr7:117127910
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.395-1883G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117127910 | ||||||
| chr7:117128161
|
G | A | 3 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0085 | 3 | HG02109.hp2 HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.395-1632G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117128161 | ||||||
| chr7:117128341
|
C | A | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.395-1452C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117128341 | ||||||
| chr7:117128533
|
T | C | 4 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0085others(1): Show | 4 | HG02109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.395-1260T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117128533 | ||||||
| chr7:117128820
|
A | G | 8 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(5): Show | 8 | HG02257.hp2 HG02486.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.395-973A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117128820 | ||||||
| chr7:117128898
|
G | A | 1 | a0001c0001t0001g0045 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.395-895G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117128898 | ||||||
| chr7:117129168
|
A | G | 1 | a0001c0001t0001g0061 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.395-625A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117129168 | ||||||
| chr7:117129448
|
C | T | 1 | a0001c0001t0001g0151 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.395-345C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117129448 | ||||||
| chr7:117129516
|
A | C | 1 | a0001c0001t0001g0061 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.395-277A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117129516 | ||||||
| chr7:117130351
|
A | T | 3 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0002t0001g0044 | 3 | HG02970.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.450-140A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 4/15 | chr7 | 117130351 | ||||||
| chr7:117130661
|
A | C | 15 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0072others(12): Show | 15 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.565+55A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 5/15 | chr7 | 117130661 | ||||||
| chr7:117132075
|
G | C | 1 | a0001c0001t0001g0148 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.641+115G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 6/15 | chr7 | 117132075 | ||||||
| chr7:117132252
|
T | C | 1 | a0001c0001t0001g0099 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.641+292T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 6/15 | chr7 | 117132252 | ||||||
| chr7:117132273
|
A | C | 3 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0129 | 3 | HG01358.hp1 HG01943.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.641+313A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 6/15 | chr7 | 117132273 | ||||||
| chr7:117132343
|
A | G | 4 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(1): Show | 4 | HG00438.hp2 HG02040.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.641+383A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 6/15 | chr7 | 117132343 | ||||||
| chr7:117132798
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.641+838C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 6/15 | chr7 | 117132798 | ||||||
| chr7:117133089
|
A | T | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.642-1035A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 6/15 | chr7 | 117133089 | ||||||
| chr7:117133106
|
C | T | 1 | a0001c0001t0001g0101 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.642-1018C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 6/15 | chr7 | 117133106 | ||||||
| chr7:117133180
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.642-944G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 6/15 | chr7 | 117133180 | ||||||
| chr7:117133650
|
G | A | 5 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0062others(2): Show | 5 | HG02818.hp1 HG02922.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.642-474G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 6/15 | chr7 | 117133650 | ||||||
| chr7:117133791
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.642-333C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 6/15 | chr7 | 117133791 | ||||||
| chr7:117133835
|
G | A | 1 | a0001c0001t0001g0080 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.642-289G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 6/15 | chr7 | 117133835 | ||||||
| chr7:117133910
|
T | G | 1 | a0001c0001t0001g0115 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.642-214T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 6/15 | chr7 | 117133910 | ||||||
| chr7:117134208
|
G | T | 1 | a0001c0001t0001g0070 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.710+16G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 7/15 | chr7 | 117134208 | ||||||
| chr7:117134447
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.710+255G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 7/15 | chr7 | 117134447 | ||||||
| chr7:117134447
|
G | T | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.710+255G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 7/15 | chr7 | 117134447 | ||||||
| chr7:117134959
|
C | T | 1 | a0001c0001t0001g0161 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.710+767C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 7/15 | chr7 | 117134959 | ||||||
| chr7:117134992
|
A | T | 17 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0072others(14): Show | 17 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.710+800A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 7/15 | chr7 | 117134992 | ||||||
| chr7:117134993
|
T | A | 17 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0072others(14): Show | 17 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.710+801T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 7/15 | chr7 | 117134993 | ||||||
| chr7:117135546
|
T | G | 1 | a0001c0001t0001g0061 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.711-535T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 7/15 | chr7 | 117135546 | ||||||
| chr7:117135593
|
A | C | 1 | a0001c0001t0001g0077 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.711-488A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 7/15 | chr7 | 117135593 | ||||||
| chr7:117136047
|
T | C | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.711-34T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 7/15 | chr7 | 117136047 | ||||||
| chr7:117136386
|
A | G | 1 | a0001c0001t0001g0082 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.865+151A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 8/15 | chr7 | 117136386 | ||||||
| chr7:117136543
|
G | C | 1 | a0001c0001t0001g0035 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.865+308G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 8/15 | chr7 | 117136543 | ||||||
| chr7:117136562
|
T | G | 1 | a0001c0001t0001g0148 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.865+327T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 8/15 | chr7 | 117136562 | ||||||
| chr7:117136672
|
T | C | 25 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0052others(22): Show | 25 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.865+437T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 8/15 | chr7 | 117136672 | ||||||
| chr7:117136817
|
A | G | 1 | a0001c0001t0001g0139 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.865+582A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 8/15 | chr7 | 117136817 | ||||||
| chr7:117136947
|
G | A | 1 | a0001c0001t0001g0164 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.865+712G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 8/15 | chr7 | 117136947 | ||||||
| chr7:117137268
|
C | T | 1 | a0001c0001t0001g0061 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.865+1033C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 8/15 | chr7 | 117137268 | ||||||
| chr7:117137441
|
A | G | 5 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0001g0167others(2): Show | 5 | HG02630.hp1 HG02818.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.866-994A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 8/15 | chr7 | 117137441 | ||||||
| chr7:117137448
|
A | T | 1 | a0001c0001t0001g0062 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.866-987A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 8/15 | chr7 | 117137448 | ||||||
| chr7:117137577
|
A | G | 27 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(24): Show | 27 | HG00323.hp1 HG00408.hp1 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.866-858A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 8/15 | chr7 | 117137577 | ||||||
| chr7:117137755
|
T | C | 1 | a0001c0001t0001g0034 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.866-680T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 8/15 | chr7 | 117137755 | ||||||
| chr7:117137852
|
A | G | 1 | a0001c0001t0001g0027 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.866-583A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 8/15 | chr7 | 117137852 | ||||||
| chr7:117137853
|
C | T | 1 | a0001c0001t0001g0027 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.866-582C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 8/15 | chr7 | 117137853 | ||||||
| chr7:117137868
|
A | G | 1 | a0001c0001t0001g0128 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.866-567A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 8/15 | chr7 | 117137868 | ||||||
| chr7:117138385
|
C | T | 4 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0153others(1): Show | 4 | NA18965.hp2 NA18971.hp2 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.866-50C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 8/15 | chr7 | 117138385 | ||||||
| chr7:117138404
|
A | T | 4 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(1): Show | 4 | HG00408.hp1 HG01192.hp2 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.866-31A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 8/15 | chr7 | 117138404 | ||||||
| chr7:117138704
|
A | G | 2 | a0001c0001t0001g0110a0001c0001t0001g0176 | 2 | HG00323.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.963+172A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117138704 | ||||||
| chr7:117138792
|
T | G | 25 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0061others(22): Show | 25 | HG00408.hp2 HG00438.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.963+260T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117138792 | ||||||
| chr7:117139021
|
A | G | 14 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(11): Show | 14 | HG00642.hp1 HG00673.hp2 HG01943.hp1 others(11): Show |
intron_variant | MODIFIER | c.963+489A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117139021 | ||||||
| chr7:117139540
|
C | T | 47 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(44): Show | 47 | HG00323.hp1 HG00408.hp1 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.963+1008C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117139540 | ||||||
| chr7:117139631
|
A | G | 4 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(1): Show | 4 | HG02055.hp1 HG02572.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.963+1099A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117139631 | ||||||
| chr7:117139914
|
G | A | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.963+1382G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117139914 | ||||||
| chr7:117139992
|
C | A | 2 | a0001c0001t0001g0102a0001c0001t0001g0104 | 2 | HG00280.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.963+1460C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117139992 | ||||||
| chr7:117140055
|
T | C | 5 | a0001c0001t0001g0125a0001c0001t0001g0160a0001c0001t0001g0162others(2): Show | 5 | HG02258.hp1 HG02630.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.963+1523T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117140055 | ||||||
| chr7:117140129
|
A | G | 4 | a0001c0001t0001g0043a0001c0001t0001g0056a0001c0001t0001g0057others(1): Show | 4 | HG02109.hp2 HG02486.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.963+1597A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117140129 | ||||||
| chr7:117140134
|
A | G | 4 | a0001c0001t0001g0053a0001c0001t0001g0085a0001c0001t0001g0125others(1): Show | 4 | HG02109.hp2 HG02258.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.963+1602A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117140134 | ||||||
| chr7:117140329
|
T | C | 12 | a0001c0001t0001g0045a0001c0001t0001g0088a0001c0001t0001g0090others(9): Show | 12 | HG02055.hp1 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.963+1797T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117140329 | ||||||
| chr7:117140445
|
A | G | 35 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0048others(32): Show | 35 | HG01433.hp1 HG01496.hp2 HG02055.hp1 others(32): Show |
intron_variant | MODIFIER | c.963+1913A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117140445 | ||||||
| chr7:117140520
|
G | A | 1 | a0001c0001t0001g0152 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.963+1988G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117140520 | ||||||
| chr7:117140564
|
A | G | 5 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(2): Show | 5 | HG01496.hp2 HG02572.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.963+2032A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117140564 | ||||||
| chr7:117140572
|
C | T | 2 | a0001c0001t0001g0088a0001c0001t0001g0092 | 2 | HG02970.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.963+2040C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117140572 | ||||||
| chr7:117140686
|
A | G | 19 | a0001c0001t0001g0013a0001c0001t0001g0054a0001c0001t0001g0088others(16): Show | 19 | HG00408.hp2 HG00438.hp2 HG02040.hp1 others(16): Show |
intron_variant | MODIFIER | c.963+2154A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117140686 | ||||||
| chr7:117140801
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.963+2269G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117140801 | ||||||
| chr7:117140813
|
T | C | 1 | a0001c0001t0001g0112 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.963+2281T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117140813 | ||||||
| chr7:117140882
|
A | G | 1 | a0001c0001t0001g0019 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.963+2350A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117140882 | ||||||
| chr7:117140912
|
A | G | 17 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0012others(14): Show | 17 | HG00673.hp2 HG01192.hp2 HG01943.hp1 others(14): Show |
intron_variant | MODIFIER | c.963+2380A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117140912 | ||||||
| chr7:117141076
|
G | A | 2 | a0001c0001t0001g0076a0001c0001t0001g0117 | 2 | HG00280.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.963+2544G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117141076 | ||||||
| chr7:117141112
|
A | T | 1 | a0001c0001t0001g0006 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.963+2580A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117141112 | ||||||
| chr7:117141190
|
C | A | 12 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(9): Show | 12 | HG02615.hp2 HG02622.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.963+2658C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117141190 | ||||||
| chr7:117141224
|
C | T | 35 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0012others(32): Show | 35 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.963+2692C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117141224 | ||||||
| chr7:117141381
|
G | A | 3 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0002t0001g0044 | 3 | HG02970.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.963+2849G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117141381 | ||||||
| chr7:117141503
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.963+2971G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117141503 | ||||||
| chr7:117141748
|
C | T | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.963+3216C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117141748 | ||||||
| chr7:117141809
|
G | A | 13 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(10): Show | 13 | HG02615.hp2 HG02622.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.963+3277G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117141809 | ||||||
| chr7:117141815
|
G | T | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.963+3283G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117141815 | ||||||
| chr7:117141858
|
C | T | 2 | a0001c0001t0001g0128a0001c0001t0001g0188 | 2 | HG02486.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.963+3326C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117141858 | ||||||
| chr7:117141921
|
C | T | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.963+3389C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117141921 | ||||||
| chr7:117142172
|
G | A | 35 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0012others(32): Show | 35 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.963+3640G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117142172 | ||||||
| chr7:117142293
|
A | G | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.963+3761A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117142293 | ||||||
| chr7:117142352
|
C | T | 1 | a0001c0001t0001g0062 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.963+3820C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117142352 | ||||||
| chr7:117142381
|
T | A | 1 | a0001c0001t0001g0102 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.963+3849T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117142381 | ||||||
| chr7:117142427
|
G | A | 50 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(47): Show | 50 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.963+3895G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117142427 | ||||||
| chr7:117142481
|
GA | G | 49 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(46): Show | 49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.963+3959delA | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117142481 | |||||
| chr7:117142811
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.963+4279C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117142811 | ||||||
| chr7:117142847
|
T | C | 1 | a0001c0001t0001g0100 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.963+4315T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117142847 | ||||||
| chr7:117142862
|
G | A | 14 | a0001c0001t0001g0047a0001c0001t0001g0061a0001c0001t0001g0095others(11): Show | 14 | HG00323.hp1 HG00642.hp2 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.963+4330G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117142862 | ||||||
| chr7:117142935
|
T | C | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.963+4403T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117142935 | ||||||
| chr7:117143429
|
C | A | 8 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0133others(5): Show | 8 | HG00408.hp2 HG00438.hp2 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.963+4897C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117143429 | ||||||
| chr7:117143593
|
C | G | 4 | a0001c0001t0001g0070a0001c0001t0001g0112a0001c0001t0001g0142others(1): Show | 4 | HG02895.hp2 HG02922.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.963+5061C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117143593 | ||||||
| chr7:117143621
|
C | T | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.963+5089C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117143621 | ||||||
| chr7:117143962
|
A | G | 3 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0002t0001g0044 | 3 | HG02970.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.963+5430A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117143962 | ||||||
| chr7:117144401
|
G | T | 4 | a0001c0001t0001g0070a0001c0001t0001g0112a0001c0001t0001g0142others(1): Show | 4 | HG02895.hp2 HG02922.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.963+5869G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117144401 | ||||||
| chr7:117144523
|
C | A | 1 | a0001c0001t0001g0058 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.963+5991C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117144523 | ||||||
| chr7:117144584
|
A | G | 74 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(71): Show | 74 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.963+6052A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117144584 | ||||||
| chr7:117144633
|
C | CA | 49 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0012others(46): Show | 49 | HG00408.hp2 HG00438.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.963+6117dupA | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117144633 | |||||
| chr7:117144633
|
C | CAAA | 17 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(14): Show | 17 | HG02615.hp2 HG02622.hp1 HG02630.hp2 others(14): Show |
intron_variant | MODIFIER | c.963+6115_963+6117d others(5): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117144633 | |||||
| chr7:117144691
|
C | G | 2 | a0001c0001t0001g0073a0001c0001t0001g0116 | 2 | HG01081.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.963+6159C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117144691 | ||||||
| chr7:117144850
|
A | T | 1 | a0001c0001t0001g0115 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.963+6318A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117144850 | ||||||
| chr7:117144853
|
T | G | 4 | a0001c0001t0001g0070a0001c0001t0001g0112a0001c0001t0001g0142others(1): Show | 4 | HG02895.hp2 HG02922.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.963+6321T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117144853 | ||||||
| chr7:117145014
|
A | G | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.963+6482A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117145014 | ||||||
| chr7:117145057
|
A | G | 14 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(11): Show | 14 | HG02615.hp2 HG02622.hp1 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.963+6525A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117145057 | ||||||
| chr7:117145113
|
A | G | 1 | a0001c0001t0001g0032 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.963+6581A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117145113 | ||||||
| chr7:117145157
|
A | G | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.963+6625A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117145157 | ||||||
| chr7:117145204
|
CA | C | 72 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(69): Show | 72 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.963+6681delA | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117145204 | |||||
| chr7:117145234
|
A | G | 2 | a0001c0001t0001g0128a0001c0001t0001g0188 | 2 | HG02486.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.963+6702A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117145234 | ||||||
| chr7:117145320
|
A | G | 14 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(11): Show | 14 | HG02615.hp2 HG02622.hp1 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.963+6788A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117145320 | ||||||
| chr7:117145524
|
T | C | 53 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(50): Show | 53 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.963+6992T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117145524 | ||||||
| chr7:117145633
|
G | A | 35 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0012others(32): Show | 35 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.963+7101G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117145633 | ||||||
| chr7:117145973
|
C | G | 163 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(160): Show | 163 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.963+7441C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117145973 | ||||||
| chr7:117146068
|
A | G | 73 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(70): Show | 73 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.963+7536A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117146068 | ||||||
| chr7:117146133
|
A | C | 1 | a0001c0001t0001g0062 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.963+7601A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117146133 | ||||||
| chr7:117146369
|
G | A | 1 | a0001c0001t0001g0081 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.963+7837G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117146369 | ||||||
| chr7:117146491
|
A | C | 1 | a0001c0001t0001g0123 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.963+7959A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117146491 | ||||||
| chr7:117146580
|
G | A | 12 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(9): Show | 12 | HG02615.hp2 HG02622.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.963+8048G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117146580 | ||||||
| chr7:117146696
|
G | A | 73 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(70): Show | 73 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.963+8164G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117146696 | ||||||
| chr7:117147122
|
A | G | 49 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(46): Show | 49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.963+8590A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117147122 | ||||||
| chr7:117147280
|
G | A | 1 | a0001c0001t0001g0062 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.963+8748G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117147280 | ||||||
| chr7:117147382
|
C | T | 49 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(46): Show | 49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.963+8850C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117147382 | ||||||
| chr7:117147455
|
C | T | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.963+8923C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117147455 | ||||||
| chr7:117147755
|
C | A | 1 | a0001c0001t0001g0058 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.963+9223C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117147755 | ||||||
| chr7:117147890
|
AAGCATAC | A | 11 | a0001c0001t0001g0047a0001c0001t0001g0061a0001c0001t0001g0095others(8): Show | 11 | HG00323.hp1 HG00642.hp2 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.963+9360_963+9366d others(9): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117147890 | |||||
| chr7:117147899
|
T | A | 11 | a0001c0001t0001g0047a0001c0001t0001g0061a0001c0001t0001g0095others(8): Show | 11 | HG00323.hp1 HG00642.hp2 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.963+9367T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117147899 | ||||||
| chr7:117147991
|
G | A | 49 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(46): Show | 49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.963+9459G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117147991 | ||||||
| chr7:117148031
|
T | A | 1 | a0001c0001t0001g0058 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.963+9499T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117148031 | ||||||
| chr7:117148153
|
C | T | 12 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(9): Show | 12 | HG02615.hp2 HG02622.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.963+9621C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117148153 | ||||||
| chr7:117148231
|
A | G | 1 | a0001c0001t0001g0123 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.963+9699A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117148231 | ||||||
| chr7:117148363
|
T | C | 35 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0012others(32): Show | 35 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.963+9831T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117148363 | ||||||
| chr7:117148386
|
A | G | 1 | a0001c0001t0001g0062 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.963+9854A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117148386 | ||||||
| chr7:117148675
|
G | A | 1 | a0001c0001t0001g0022 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.963+10143G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117148675 | ||||||
| chr7:117148756
|
G | A | 1 | a0001c0001t0001g0145 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.963+10224G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117148756 | ||||||
| chr7:117148994
|
T | C | 11 | a0001c0001t0001g0047a0001c0001t0001g0061a0001c0001t0001g0095others(8): Show | 11 | HG00323.hp1 HG00642.hp2 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.963+10462T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117148994 | ||||||
| chr7:117149173
|
C | G | 12 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(9): Show | 12 | HG02615.hp2 HG02622.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.963+10641C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117149173 | ||||||
| chr7:117149217
|
A | T | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.963+10685A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117149217 | ||||||
| chr7:117149222
|
G | A | 2 | a0001c0001t0001g0128a0001c0001t0001g0188 | 2 | HG02486.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.963+10690G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117149222 | ||||||
| chr7:117149302
|
A | G | 12 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(9): Show | 12 | HG02615.hp2 HG02622.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.963+10770A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117149302 | ||||||
| chr7:117149461
|
A | G | 1 | a0001c0001t0001g0136 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.963+10929A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117149461 | ||||||
| chr7:117149592
|
C | CT | 12 | a0001c0001t0001g0011a0001c0001t0001g0036a0001c0001t0001g0082others(9): Show | 12 | HG00280.hp2 HG01071.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.963+11083dupT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117149592 | |||||
| chr7:117149592
|
CT | C | 23 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0052others(20): Show | 23 | HG01433.hp2 HG01496.hp2 HG01934.hp1 others(20): Show |
intron_variant | MODIFIER | c.963+11083delT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117149592 | |||||
| chr7:117149592
|
CTT | C | 11 | a0001c0001t0001g0001a0001c0001t0001g0039a0001c0001t0001g0047others(8): Show | 11 | HG00408.hp2 HG00438.hp2 HG02040.hp1 others(8): Show |
intron_variant | MODIFIER | c.963+11082_963+1108 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117149592 | |||||
| chr7:117149592
|
CTTT | C | 40 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(37): Show | 40 | HG00673.hp2 HG01192.hp2 HG01943.hp1 others(37): Show |
intron_variant | MODIFIER | c.963+11081_963+1108 others(7): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117149592 | |||||
| chr7:117149592
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.963+11073_963+1108 others(15): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117149592 | |||||
| chr7:117149714
|
C | T | 72 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(69): Show | 72 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.963+11182C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117149714 | ||||||
| chr7:117149880
|
G | A | 69 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(66): Show | 69 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.963+11348G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117149880 | ||||||
| chr7:117149889
|
G | A | 35 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0012others(32): Show | 35 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.963+11357G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117149889 | ||||||
| chr7:117149918
|
A | G | 1 | a0001c0001t0001g0031 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.963+11386A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117149918 | ||||||
| chr7:117149975
|
G | A | 2 | a0001c0001t0001g0016a0001c0001t0001g0119 | 2 | HG03492.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.963+11443G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117149975 | ||||||
| chr7:117150138
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.963+11606C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117150138 | ||||||
| chr7:117150205
|
G | A | 17 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0012others(14): Show | 17 | HG00673.hp2 HG01192.hp2 HG01943.hp1 others(14): Show |
intron_variant | MODIFIER | c.963+11673G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117150205 | ||||||
| chr7:117150439
|
G | A | 72 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(69): Show | 72 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.963+11907G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117150439 | ||||||
| chr7:117150558
|
C | T | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.963+12026C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117150558 | ||||||
| chr7:117151048
|
G | A | 49 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(46): Show | 49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.963+12516G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117151048 | ||||||
| chr7:117151085
|
G | A | 2 | a0001c0001t0001g0103a0001c0001t0001g0105 | 2 | HG00099.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.963+12553G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117151085 | ||||||
| chr7:117151117
|
G | T | 49 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(46): Show | 49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.963+12585G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117151117 | ||||||
| chr7:117151470
|
A | C | 1 | a0001c0001t0001g0095 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.963+12938A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117151470 | ||||||
| chr7:117151530
|
T | G | 53 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(50): Show | 53 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.963+12998T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117151530 | ||||||
| chr7:117151544
|
A | AT | 53 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(50): Show | 53 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.963+13019dupT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117151544 | |||||
| chr7:117151706
|
A | G | 1 | a0001c0001t0001g0118 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.963+13174A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117151706 | ||||||
| chr7:117151717
|
T | C | 1 | a0001c0001t0001g0115 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.963+13185T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117151717 | ||||||
| chr7:117151839
|
G | T | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.963+13307G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117151839 | ||||||
| chr7:117152083
|
C | T | 2 | a0001c0001t0001g0115a0001c0001t0001g0166 | 2 | HG02451.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.963+13551C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117152083 | ||||||
| chr7:117152118
|
C | CAA | 52 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(49): Show | 52 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.963+13594_963+1359 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117152118 | |||||
| chr7:117152128
|
T | A | 2 | a0001c0001t0001g0015a0001c0001t0001g0059 | 2 | HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.963+13596T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117152128 | ||||||
| chr7:117152162
|
TTATATAT others(12): Show |
T | 1 | a0001c0001t0001g0169 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.963+13641_963+1365 others(23): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117152162 | |||||
| chr7:117152173
|
A | T | 1 | a0001c0001t0001g0082 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.963+13641A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117152173 | ||||||
| chr7:117152177
|
C | CTA | 23 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(20): Show | 23 | HG00099.hp1 HG01071.hp2 HG02004.hp1 others(20): Show |
intron_variant | MODIFIER | c.963+13690_963+1369 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117152177 | |||||
| chr7:117152177
|
C | CTATA | 12 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0025others(9): Show | 12 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(9): Show |
intron_variant | MODIFIER | c.963+13688_963+1369 others(8): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117152177 | |||||
| chr7:117152177
|
C | CTATATA | 4 | a0001c0001t0001g0030a0001c0001t0001g0078a0001c0001t0001g0110others(1): Show | 4 | HG00323.hp2 HG00408.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.963+13686_963+1369 others(10): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117152177 | |||||
| chr7:117152177
|
C | CTATATAT others(1): Show |
6 | a0001c0001t0001g0007a0001c0001t0001g0037a0001c0001t0001g0077others(3): Show | 6 | HG00673.hp1 HG01071.hp1 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.963+13684_963+1369 others(12): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117152177 | |||||
| chr7:117152177
|
C | CTATATAT others(3): Show |
2 | a0001c0001t0001g0011a0001c0001t0001g0144 | 2 | NA18747.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.963+13682_963+1369 others(14): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117152177 | |||||
| chr7:117152177
|
CTA | C | 11 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0032others(8): Show | 11 | HG01081.hp2 HG01358.hp1 HG01358.hp2 others(8): Show |
intron_variant | MODIFIER | c.963+13690_963+1369 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117152177 | |||||
| chr7:117152177
|
CTATA | C | 4 | a0001c0001t0001g0017a0001c0001t0001g0063a0001c0001t0001g0080others(1): Show | 4 | HG00741.hp1 HG01255.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.963+13688_963+1369 others(8): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117152177 | |||||
| chr7:117152177
|
CTATATA | C | 3 | a0001c0001t0001g0057a0001c0001t0001g0136a0001c0001t0001g0156 | 3 | HG00738.hp2 HG02965.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.963+13686_963+1369 others(10): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117152177 | |||||
| chr7:117152177
|
CTATATAT others(1): Show |
C | 3 | a0001c0001t0001g0108a0001c0001t0001g0115a0001c0001t0001g0166 | 3 | HG02451.hp2 HG02976.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.963+13684_963+1369 others(12): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117152177 | |||||
| chr7:117152177
|
CTATATAT others(3): Show |
C | 3 | a0001c0001t0001g0024a0001c0001t0001g0153a0001c0001t0001g0159 | 3 | HG02683.hp2 NA18965.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.963+13682_963+1369 others(14): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117152177 | |||||
| chr7:117152177
|
CTATATAT others(5): Show |
C | 1 | a0001c0001t0001g0051 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.963+13680_963+1369 others(16): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117152177 | |||||
| chr7:117152177
|
CTATATAT others(9): Show |
C | 1 | a0001c0001t0001g0101 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.963+13676_963+1369 others(20): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117152177 | |||||
| chr7:117152177
|
CTATATAT others(11): Show |
C | 11 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(8): Show | 11 | HG02109.hp2 HG02258.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.963+13674_963+1369 others(22): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117152177 | |||||
| chr7:117152177
|
CTATATAT others(21): Show |
C | 13 | a0001c0001t0001g0047a0001c0001t0001g0061a0001c0001t0001g0095others(10): Show | 13 | HG00323.hp1 HG00642.hp2 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.963+13664_963+1369 others(32): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117152177 | |||||
| chr7:117152177
|
CTATATAT others(25): Show |
C | 3 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0002t0001g0044 | 3 | HG02970.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.963+13660_963+1369 others(36): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117152177 | |||||
| chr7:117152177
|
CTATATAT others(27): Show |
C | 1 | a0001c0001t0001g0028 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.963+13658_963+1369 others(38): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117152177 | |||||
| chr7:117152177
|
CTATATAT others(29): Show |
C | 1 | a0001c0001t0001g0059 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.963+13656_963+1369 others(40): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117152177 | |||||
| chr7:117152184
|
TATA | T | 11 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(8): Show | 11 | HG02615.hp2 HG02622.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.963+13653_963+1365 others(7): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117152184 | ||||||
| chr7:117152184
|
TATATATA others(8): Show |
T | 1 | a0001c0001t0001g0012 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.963+13653_963+1366 others(19): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117152184 | ||||||
| chr7:117152184
|
TATATATA others(10): Show |
T | 38 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(35): Show | 38 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.963+13653_963+1366 others(21): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117152184 | ||||||
| chr7:117152185
|
A | T | 1 | a0001c0001t0001g0170 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.963+13653A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117152185 | ||||||
| chr7:117152189
|
A | T | 11 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(8): Show | 11 | HG02615.hp2 HG02622.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.963+13657A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117152189 | ||||||
| chr7:117152202
|
T | TATATATA others(7): Show |
1 | a0001c0001t0001g0014 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.963+13683_963+1368 others(18): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117152202 | |||||
| chr7:117152203
|
A | G | 1 | a0001c0001t0001g0024 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.963+13671A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117152203 | ||||||
| chr7:117152222
|
T | A | 53 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(50): Show | 53 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.963+13690T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117152222 | ||||||
| chr7:117152250
|
G | C | 1 | a0001c0001t0001g0082 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.963+13718G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117152250 | ||||||
| chr7:117152283
|
A | G | 1 | a0001c0001t0001g0002 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.963+13751A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117152283 | ||||||
| chr7:117152754
|
A | T | 12 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(9): Show | 12 | HG02615.hp2 HG02622.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.963+14222A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117152754 | ||||||
| chr7:117152771
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.963+14239G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117152771 | ||||||
| chr7:117152859
|
T | G | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.963+14327T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117152859 | ||||||
| chr7:117152949
|
C | T | 2 | a0001c0001t0001g0128a0001c0001t0001g0188 | 2 | HG02486.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.963+14417C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117152949 | ||||||
| chr7:117153033
|
A | G | 1 | a0001c0001t0001g0062 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.963+14501A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117153033 | ||||||
| chr7:117153374
|
T | C | 1 | a0001c0001t0001g0053 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.963+14842T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117153374 | ||||||
| chr7:117153376
|
G | A | 4 | a0001c0001t0001g0070a0001c0001t0001g0112a0001c0001t0001g0142others(1): Show | 4 | HG02895.hp2 HG02922.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.963+14844G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117153376 | ||||||
| chr7:117153388
|
A | C | 4 | a0001c0001t0001g0070a0001c0001t0001g0112a0001c0001t0001g0142others(1): Show | 4 | HG02895.hp2 HG02922.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.963+14856A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117153388 | ||||||
| chr7:117153456
|
A | T | 4 | a0001c0001t0001g0070a0001c0001t0001g0112a0001c0001t0001g0142others(1): Show | 4 | HG02895.hp2 HG02922.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.963+14924A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117153456 | ||||||
| chr7:117153546
|
T | A | 2 | a0001c0001t0001g0045a0001c0001t0001g0087 | 2 | HG02280.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.963+15014T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117153546 | ||||||
| chr7:117153694
|
A | C | 1 | a0001c0001t0001g0041 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.963+15162A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117153694 | ||||||
| chr7:117154068
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.963+15536C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117154068 | ||||||
| chr7:117154230
|
G | A | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.963+15698G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117154230 | ||||||
| chr7:117154380
|
A | C | 1 | a0001c0001t0001g0128 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.963+15848A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117154380 | ||||||
| chr7:117154941
|
A | G | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.964-15921A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117154941 | ||||||
| chr7:117155576
|
G | A | 47 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(44): Show | 47 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.964-15286G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117155576 | ||||||
| chr7:117155804
|
A | G | 47 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(44): Show | 47 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.964-15058A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117155804 | ||||||
| chr7:117155815
|
A | G | 1 | a0001c0001t0001g0112 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.964-15047A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117155815 | ||||||
| chr7:117156029
|
A | G | 73 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(70): Show | 73 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.964-14833A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117156029 | ||||||
| chr7:117156050
|
C | T | 1 | a0001c0001t0001g0062 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.964-14812C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117156050 | ||||||
| chr7:117156094
|
A | T | 2 | a0001c0001t0001g0128a0001c0001t0001g0188 | 2 | HG02486.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.964-14768A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117156094 | ||||||
| chr7:117156222
|
C | T | 4 | a0001c0001t0001g0015a0001c0001t0001g0070a0001c0001t0001g0142others(1): Show | 4 | HG02630.hp2 HG02895.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.964-14640C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117156222 | ||||||
| chr7:117156442
|
T | A | 35 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0012others(32): Show | 35 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.964-14420T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117156442 | ||||||
| chr7:117156584
|
A | G | 47 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(44): Show | 47 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.964-14278A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117156584 | ||||||
| chr7:117156599
|
T | G | 5 | a0001c0001t0001g0015a0001c0001t0001g0070a0001c0001t0001g0112others(2): Show | 5 | HG02630.hp2 HG02895.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.964-14263T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117156599 | ||||||
| chr7:117156904
|
T | C | 1 | a0001c0001t0001g0185 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.964-13958T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117156904 | ||||||
| chr7:117156955
|
A | T | 3 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0002t0001g0044 | 3 | HG02970.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.964-13907A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117156955 | ||||||
| chr7:117157025
|
C | G | 47 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(44): Show | 47 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.964-13837C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117157025 | ||||||
| chr7:117157085
|
A | G | 47 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(44): Show | 47 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.964-13777A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117157085 | ||||||
| chr7:117157216
|
T | C | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.964-13646T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117157216 | ||||||
| chr7:117157625
|
A | G | 1 | a0001c0001t0001g0080 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.964-13237A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117157625 | ||||||
| chr7:117157888
|
C | T | 3 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0138 | 3 | NA19000.hp2 NA19009.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.964-12974C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117157888 | ||||||
| chr7:117157985
|
A | T | 4 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0036others(1): Show | 4 | HG00673.hp1 HG01071.hp2 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.964-12877A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117157985 | ||||||
| chr7:117158372
|
A | G | 12 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0086others(9): Show | 12 | HG02615.hp2 HG02622.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.964-12490A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117158372 | ||||||
| chr7:117158659
|
A | G | 13 | a0001c0001t0001g0047a0001c0001t0001g0061a0001c0001t0001g0095others(10): Show | 13 | HG00323.hp1 HG00642.hp2 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.964-12203A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117158659 | ||||||
| chr7:117158835
|
C | G | 1 | a0001c0001t0001g0058 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.964-12027C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117158835 | ||||||
| chr7:117159118
|
G | C | 47 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(44): Show | 47 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.964-11744G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117159118 | ||||||
| chr7:117159352
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.964-11510C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117159352 | ||||||
| chr7:117159358
|
T | C | 12 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0062others(9): Show | 12 | HG02615.hp2 HG02622.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.964-11504T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117159358 | ||||||
| chr7:117159386
|
C | T | 47 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(44): Show | 47 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.964-11476C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117159386 | ||||||
| chr7:117159396
|
A | T | 47 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(44): Show | 47 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.964-11466A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117159396 | ||||||
| chr7:117159399
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.964-11463G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117159399 | ||||||
| chr7:117159412
|
T | G | 47 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(44): Show | 47 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.964-11450T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117159412 | ||||||
| chr7:117159521
|
A | G | 35 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0012others(32): Show | 35 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.964-11341A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117159521 | ||||||
| chr7:117159533
|
T | C | 52 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(49): Show | 52 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.964-11329T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117159533 | ||||||
| chr7:117159582
|
A | G | 1 | a0001c0001t0001g0034 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.964-11280A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117159582 | ||||||
| chr7:117159635
|
G | C | 1 | a0001c0001t0001g0034 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.964-11227G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117159635 | ||||||
| chr7:117159815
|
C | G | 11 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0086others(8): Show | 11 | HG02615.hp2 HG02622.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.964-11047C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117159815 | ||||||
| chr7:117159871
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.964-10991C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117159871 | ||||||
| chr7:117159872
|
G | A | 7 | a0001c0001t0001g0020a0001c0001t0001g0151a0001c0001t0001g0156others(4): Show | 7 | HG00438.hp1 HG00642.hp1 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.964-10990G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117159872 | ||||||
| chr7:117159929
|
C | T | 3 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0002t0001g0044 | 3 | HG02970.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.964-10933C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117159929 | ||||||
| chr7:117159958
|
T | C | 1 | a0001c0001t0001g0022 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.964-10904T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117159958 | ||||||
| chr7:117160043
|
A | G | 2 | a0001c0001t0001g0128a0001c0001t0001g0188 | 2 | HG02486.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.964-10819A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117160043 | ||||||
| chr7:117160182
|
A | G | 47 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(44): Show | 47 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.964-10680A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117160182 | ||||||
| chr7:117160243
|
A | G | 3 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0002t0001g0044 | 3 | HG02970.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.964-10619A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117160243 | ||||||
| chr7:117160246
|
AG | A | 45 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(42): Show | 45 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.964-10615delG | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117160246 | ||||||
| chr7:117160284
|
A | G | 1 | a0001c0001t0001g0124 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.964-10578A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117160284 | ||||||
| chr7:117160542
|
ATC | A | 47 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(44): Show | 47 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.964-10308_964-1030 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117160542 | |||||
| chr7:117160618
|
A | G | 11 | a0001c0001t0001g0047a0001c0001t0001g0061a0001c0001t0001g0095others(8): Show | 11 | HG00323.hp1 HG00642.hp2 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.964-10244A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117160618 | ||||||
| chr7:117160653
|
G | GTA | 2 | a0001c0001t0001g0058a0001c0001t0001g0064 | 2 | HG01496.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.964-10194_964-1019 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117160653 | |||||
| chr7:117160653
|
G | GTGTATAT others(3): Show |
33 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0012others(30): Show | 33 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.964-10208_964-1020 others(14): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117160653 | |||||
| chr7:117160653
|
G | GTGTATAT others(5): Show |
12 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0023others(9): Show | 12 | HG02615.hp2 HG02622.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.964-10208_964-1020 others(16): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117160653 | |||||
| chr7:117160653
|
G | GTGTATAT others(7): Show |
2 | a0001c0001t0001g0062a0001c0001t0001g0162 | 2 | HG02630.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.964-10208_964-1020 others(18): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117160653 | |||||
| chr7:117160655
|
A | G | 1 | a0001c0001t0001g0105 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.964-10207A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117160655 | ||||||
| chr7:117160661
|
A | G | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.964-10201A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117160661 | ||||||
| chr7:117161075
|
A | G | 1 | a0001c0001t0001g0090 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.964-9787A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117161075 | ||||||
| chr7:117161090
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.964-9772G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117161090 | ||||||
| chr7:117161100
|
GT | G | 36 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0012others(33): Show | 36 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.964-9749delT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117161100 | |||||
| chr7:117161100
|
GTT | G | 12 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0062others(9): Show | 12 | HG02615.hp2 HG02622.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.964-9750_964-9749d others(4): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117161100 | |||||
| chr7:117161113
|
T | A | 19 | a0001c0001t0001g0013a0001c0001t0001g0054a0001c0001t0001g0088others(16): Show | 19 | HG00408.hp2 HG00438.hp2 HG02040.hp1 others(16): Show |
intron_variant | MODIFIER | c.964-9749T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117161113 | ||||||
| chr7:117161223
|
A | T | 35 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0012others(32): Show | 35 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.964-9639A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117161223 | ||||||
| chr7:117161269
|
G | C | 47 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(44): Show | 47 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.964-9593G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117161269 | ||||||
| chr7:117161317
|
G | A | 20 | a0001c0001t0001g0015a0001c0001t0001g0047a0001c0001t0001g0061others(17): Show | 20 | HG00323.hp1 HG00642.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.964-9545G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117161317 | ||||||
| chr7:117161506
|
G | A | 6 | a0001c0001t0001g0015a0001c0001t0001g0070a0001c0001t0001g0115others(3): Show | 6 | HG02451.hp2 HG02630.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.964-9356G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117161506 | ||||||
| chr7:117161591
|
C | CT | 114 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(111): Show | 114 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.964-9251dupT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117161591 | |||||
| chr7:117161591
|
C | CTT | 13 | a0001c0001t0001g0047a0001c0001t0001g0061a0001c0001t0001g0063others(10): Show | 13 | HG00323.hp1 HG00741.hp2 HG01256.hp2 others(10): Show |
intron_variant | MODIFIER | c.964-9252_964-9251d others(4): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117161591 | |||||
| chr7:117161591
|
CT | C | 14 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0038others(11): Show | 14 | HG02615.hp2 HG02622.hp1 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.964-9251delT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117161591 | |||||
| chr7:117161596
|
T | C | 1 | a0001c0001t0001g0140 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.964-9266T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117161596 | ||||||
| chr7:117161600
|
T | C | 3 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0002t0001g0044 | 3 | HG02970.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.964-9262T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117161600 | ||||||
| chr7:117161703
|
G | A | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.964-9159G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117161703 | ||||||
| chr7:117161739
|
A | G | 1 | a0001c0001t0001g0115 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.964-9123A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117161739 | ||||||
| chr7:117161779
|
T | C | 1 | a0001c0001t0001g0148 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.964-9083T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117161779 | ||||||
| chr7:117161798
|
T | C | 72 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(69): Show | 72 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.964-9064T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117161798 | ||||||
| chr7:117161955
|
G | T | 11 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0086others(8): Show | 11 | HG02615.hp2 HG02622.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.964-8907G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117161955 | ||||||
| chr7:117162037
|
G | A | 5 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0034others(2): Show | 5 | HG00408.hp1 HG02004.hp1 HG02027.hp1 others(2): Show |
intron_variant | MODIFIER | c.964-8825G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117162037 | ||||||
| chr7:117162119
|
T | A | 2 | a0001c0001t0001g0093a0001c0001t0001g0098 | 2 | HG01433.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.964-8743T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117162119 | ||||||
| chr7:117162218
|
T | G | 47 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(44): Show | 47 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.964-8644T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117162218 | ||||||
| chr7:117162254
|
A | AT | 3 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0148 | 3 | NA18960.hp2 NA18990.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.964-8607dupT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117162254 | |||||
| chr7:117162258
|
G | A | 47 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(44): Show | 47 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.964-8604G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117162258 | ||||||
| chr7:117162336
|
G | A | 35 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0012others(32): Show | 35 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.964-8526G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117162336 | ||||||
| chr7:117162728
|
A | C | 1 | a0001c0001t0001g0050 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.964-8134A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117162728 | ||||||
| chr7:117162744
|
A | G | 3 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0042 | 3 | HG00408.hp1 HG02004.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.964-8118A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117162744 | ||||||
| chr7:117162792
|
A | G | 1 | a0001c0001t0001g0099 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.964-8070A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117162792 | ||||||
| chr7:117163037
|
G | A | 1 | a0001c0001t0001g0062 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.964-7825G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117163037 | ||||||
| chr7:117163258
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.964-7604C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117163258 | ||||||
| chr7:117163333
|
G | A | 72 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(69): Show | 72 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.964-7529G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117163333 | ||||||
| chr7:117163741
|
C | T | 35 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0012others(32): Show | 35 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.964-7121C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117163741 | ||||||
| chr7:117163774
|
G | A | 50 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(47): Show | 50 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.964-7088G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117163774 | ||||||
| chr7:117163948
|
A | G | 11 | a0001c0001t0001g0047a0001c0001t0001g0061a0001c0001t0001g0095others(8): Show | 11 | HG00323.hp1 HG00642.hp2 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.964-6914A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117163948 | ||||||
| chr7:117163962
|
T | C | 3 | a0001c0001t0001g0018a0001c0001t0001g0023a0001c0001t0001g0113 | 3 | HG04184.hp2 HG04228.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.964-6900T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117163962 | ||||||
| chr7:117164269
|
G | C | 2 | a0001c0001t0001g0046a0001c0001t0001g0051 | 2 | HG02647.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.964-6593G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117164269 | ||||||
| chr7:117164313
|
A | AC | 35 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0012others(32): Show | 35 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.964-6542dupC | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117164313 | |||||
| chr7:117164551
|
A | G | 11 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0086others(8): Show | 11 | HG02615.hp2 HG02622.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.964-6311A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117164551 | ||||||
| chr7:117164627
|
C | T | 1 | a0001c0001t0001g0062 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.964-6235C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117164627 | ||||||
| chr7:117164876
|
A | G | 77 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(74): Show | 77 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.964-5986A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117164876 | ||||||
| chr7:117164880
|
G | A | 3 | a0001c0001t0001g0018a0001c0001t0001g0023a0001c0001t0001g0113 | 3 | HG04184.hp2 HG04228.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.964-5982G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117164880 | ||||||
| chr7:117164983
|
G | C | 1 | a0001c0001t0001g0003 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.964-5879G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117164983 | ||||||
| chr7:117165064
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.964-5798G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117165064 | ||||||
| chr7:117165087
|
A | G | 3 | a0001c0001t0001g0031a0001c0001t0001g0040a0001c0001t0001g0041 | 3 | HG01192.hp2 HG01943.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.964-5775A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117165087 | ||||||
| chr7:117165155
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.964-5707G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117165155 | ||||||
| chr7:117165393
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.964-5469G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117165393 | ||||||
| chr7:117165437
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.964-5425G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117165437 | ||||||
| chr7:117165454
|
G | A | 73 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(70): Show | 73 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.964-5408G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117165454 | ||||||
| chr7:117165458
|
C | T | 49 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(46): Show | 49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.964-5404C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117165458 | ||||||
| chr7:117165814
|
G | A | 49 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(46): Show | 49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.964-5048G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117165814 | ||||||
| chr7:117165868
|
G | A | 2 | a0001c0001t0001g0059a0001c0001t0001g0128 | 2 | HG02922.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.964-4994G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117165868 | ||||||
| chr7:117166049
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.964-4813C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117166049 | ||||||
| chr7:117166097
|
A | G | 1 | a0001c0001t0001g0166 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.964-4765A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117166097 | ||||||
| chr7:117166280
|
T | A | 3 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0002t0001g0044 | 3 | HG02970.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.964-4582T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117166280 | ||||||
| chr7:117166450
|
AT | A | 71 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(68): Show | 71 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.964-4398delT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117166450 | |||||
| chr7:117166655
|
T | C | 50 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(47): Show | 50 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.964-4207T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117166655 | ||||||
| chr7:117166655
|
T | G | 1 | a0001c0001t0001g0061 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.964-4207T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117166655 | ||||||
| chr7:117166761
|
C | T | 3 | a0001c0001t0001g0024a0001c0001t0001g0076a0001c0001t0001g0117 | 3 | HG00280.hp1 HG01943.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.964-4101C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117166761 | ||||||
| chr7:117166762
|
G | A | 5 | a0001c0001t0001g0015a0001c0001t0001g0070a0001c0001t0001g0112others(2): Show | 5 | HG02630.hp2 HG02895.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.964-4100G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117166762 | ||||||
| chr7:117166839
|
A | C | 21 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0047others(18): Show | 21 | HG00323.hp1 HG00642.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.964-4023A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117166839 | ||||||
| chr7:117166890
|
C | CA | 41 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0012others(38): Show | 41 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.964-3960dupA | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117166890 | |||||
| chr7:117166890
|
C | CAA | 8 | a0001c0001t0001g0003a0001c0001t0001g0062a0001c0001t0001g0086others(5): Show | 8 | HG02615.hp2 HG02622.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.964-3961_964-3960d others(4): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117166890 | |||||
| chr7:117166908
|
T | C | 1 | a0001c0001t0001g0080 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.964-3954T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117166908 | ||||||
| chr7:117167053
|
C | CTT | 49 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(46): Show | 49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.964-3798_964-3797d others(4): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117167053 | |||||
| chr7:117167070
|
TG | T | 2 | a0001c0001t0001g0139a0001c0001t0001g0159 | 2 | NA18971.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.964-3791delG | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117167070 | ||||||
| chr7:117167071
|
G | GT | 49 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(46): Show | 49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.964-3783dupT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117167071 | |||||
| chr7:117167103
|
G | T | 13 | a0001c0001t0001g0016a0001c0001t0001g0047a0001c0001t0001g0061others(10): Show | 13 | HG00323.hp1 HG00642.hp2 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.964-3759G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117167103 | ||||||
| chr7:117167173
|
A | G | 1 | a0001c0001t0001g0099 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.964-3689A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117167173 | ||||||
| chr7:117167225
|
C | T | 40 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0012others(37): Show | 40 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.964-3637C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117167225 | ||||||
| chr7:117167319
|
C | T | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.964-3543C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117167319 | ||||||
| chr7:117168024
|
T | C | 1 | a0001c0001t0001g0072 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.964-2838T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117168024 | ||||||
| chr7:117168272
|
G | A | 40 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0012others(37): Show | 40 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.964-2590G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117168272 | ||||||
| chr7:117168436
|
G | C | 8 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0086others(5): Show | 8 | HG02615.hp2 HG02622.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.964-2426G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117168436 | ||||||
| chr7:117168613
|
C | T | 49 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(46): Show | 49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.964-2249C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117168613 | ||||||
| chr7:117168719
|
T | C | 20 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0047others(17): Show | 20 | HG00323.hp1 HG00642.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.964-2143T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117168719 | ||||||
| chr7:117168966
|
A | G | 3 | a0001c0001t0001g0086a0001c0001t0001g0089a0001c0001t0001g0140 | 3 | HG02647.hp2 HG02717.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.964-1896A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117168966 | ||||||
| chr7:117168976
|
G | A | 40 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0012others(37): Show | 40 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.964-1886G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117168976 | ||||||
| chr7:117169104
|
A | G | 40 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0012others(37): Show | 40 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.964-1758A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117169104 | ||||||
| chr7:117169119
|
C | T | 52 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(49): Show | 52 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.964-1743C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117169119 | ||||||
| chr7:117169127
|
A | C | 49 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(46): Show | 49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.964-1735A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117169127 | ||||||
| chr7:117169128
|
A | T | 49 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(46): Show | 49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.964-1734A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117169128 | ||||||
| chr7:117169135
|
TC | T | 48 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(45): Show | 48 | HG00408.hp2 HG00438.hp2 HG01192.hp2 others(45): Show |
intron_variant | MODIFIER | c.964-1725delC | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117169135 | |||||
| chr7:117169137
|
C | T | 1 | a0001c0001t0001g0021 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.964-1725C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117169137 | ||||||
| chr7:117169137
|
CT | C | 23 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0047others(20): Show | 23 | HG00323.hp1 HG00642.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.964-1709delT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117169137 | |||||
| chr7:117169282
|
C | T | 3 | a0001c0001t0001g0017a0001c0001t0001g0073a0001c0001t0001g0116 | 3 | HG01081.hp2 HG01255.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.964-1580C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117169282 | ||||||
| chr7:117169286
|
T | C | 49 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(46): Show | 49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.964-1576T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117169286 | ||||||
| chr7:117169456
|
A | G | 49 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(46): Show | 49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.964-1406A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117169456 | ||||||
| chr7:117169568
|
G | A | 8 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0086others(5): Show | 8 | HG02615.hp2 HG02622.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.964-1294G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117169568 | ||||||
| chr7:117169704
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.964-1158C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117169704 | ||||||
| chr7:117169820
|
TTTTG | T | 40 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0012others(37): Show | 40 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.964-1040_964-1037d others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117169820 | |||||
| chr7:117169821
|
TTTG | T | 9 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0062others(6): Show | 9 | HG02615.hp2 HG02622.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.964-1039_964-1037d others(5): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117169821 | |||||
| chr7:117169824
|
G | T | 26 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0047others(23): Show | 26 | HG00323.hp1 HG00642.hp2 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.964-1038G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117169824 | ||||||
| chr7:117169921
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.964-941G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117169921 | ||||||
| chr7:117170079
|
G | A | 49 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(46): Show | 49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.964-783G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117170079 | ||||||
| chr7:117170680
|
C | CAAAT | 3 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0002t0001g0044 | 3 | HG02970.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.964-167_964-164dup others(4): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117170680 | |||||
| chr7:117170758
|
TC | T | 49 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(46): Show | 49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.964-102delC | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117170758 | |||||
| chr7:117170764
|
C | A | 49 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(46): Show | 49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.964-98C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117170764 | ||||||
| chr7:117170766
|
G | T | 3 | a0001c0001t0001g0161a0001c0001t0001g0169a0001c0001t0001g0178 | 3 | HG01192.hp1 HG02615.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.964-96G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117170766 | ||||||
| chr7:117170983
|
T | C | 73 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(70): Show | 73 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(70): Show |
splice_region_variant&intron_variant | LOW | c.1078+7T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117170983 | ||||||
| chr7:117171085
|
T | C | 49 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(46): Show | 49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.1078+109T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117171085 | ||||||
| chr7:117171255
|
A | G | 49 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(46): Show | 49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.1078+279A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117171255 | ||||||
| chr7:117171303
|
T | A | 49 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(46): Show | 49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.1078+327T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117171303 | ||||||
| chr7:117171400
|
A | T | 7 | a0001c0001t0001g0015a0001c0001t0001g0070a0001c0001t0001g0112others(4): Show | 7 | HG02451.hp2 HG02630.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1078+424A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117171400 | ||||||
| chr7:117171609
|
C | T | 49 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(46): Show | 49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.1078+633C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117171609 | ||||||
| chr7:117171946
|
C | CTTT | 24 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0054others(21): Show | 24 | HG00408.hp2 HG00438.hp2 HG02040.hp1 others(21): Show |
intron_variant | MODIFIER | c.1078+984_1078+986d others(5): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr7 | 117171946 | |||||
| chr7:117171946
|
C | CTTTT | 21 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(18): Show | 21 | HG00673.hp2 HG01192.hp2 HG01943.hp1 others(18): Show |
intron_variant | MODIFIER | c.1078+983_1078+986d others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr7 | 117171946 | |||||
| chr7:117171946
|
CT | C | 7 | a0001c0001t0001g0068a0001c0001t0001g0086a0001c0001t0001g0089others(4): Show | 7 | HG01256.hp2 HG02647.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1078+986delT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr7 | 117171946 | |||||
| chr7:117172012
|
A | G | 2 | a0001c0001t0001g0070a0001c0001t0001g0142 | 2 | HG02895.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1078+1036A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117172012 | ||||||
| chr7:117172037
|
A | G | 4 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0106others(1): Show | 4 | HG02615.hp2 HG02717.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1078+1061A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117172037 | ||||||
| chr7:117172084
|
A | G | 3 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0002t0001g0044 | 3 | HG02970.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1078+1108A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117172084 | ||||||
| chr7:117172347
|
T | G | 1 | a0001c0001t0001g0135 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1078+1371T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117172347 | ||||||
| chr7:117172685
|
C | A | 49 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(46): Show | 49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.1078+1709C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117172685 | ||||||
| chr7:117172730
|
A | G | 49 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(46): Show | 49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.1078+1754A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117172730 | ||||||
| chr7:117172761
|
G | A | 1 | a0001c0001t0001g0062 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1078+1785G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117172761 | ||||||
| chr7:117172786
|
A | G | 1 | a0001c0001t0001g0062 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1078+1810A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117172786 | ||||||
| chr7:117172920
|
G | A | 22 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0047others(19): Show | 22 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.1078+1944G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117172920 | ||||||
| chr7:117173186
|
A | G | 1 | a0001c0001t0001g0054 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1078+2210A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117173186 | ||||||
| chr7:117173225
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1078+2249C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117173225 | ||||||
| chr7:117174041
|
C | A | 1 | a0001c0001t0001g0142 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1078+3065C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117174041 | ||||||
| chr7:117174180
|
T | G | 21 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0047others(18): Show | 21 | HG00323.hp1 HG00642.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.1078+3204T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117174180 | ||||||
| chr7:117174273
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1078+3297G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117174273 | ||||||
| chr7:117174511
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1078+3535C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117174511 | ||||||
| chr7:117174721
|
T | A | 3 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0002t0001g0044 | 3 | HG02970.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1078+3745T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117174721 | ||||||
| chr7:117175017
|
G | A | 1 | a0001c0001t0001g0027 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1078+4041G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117175017 | ||||||
| chr7:117175101
|
T | C | 1 | a0001c0001t0001g0062 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1078+4125T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117175101 | ||||||
| chr7:117175103
|
C | A | 49 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(46): Show | 49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.1078+4127C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117175103 | ||||||
| chr7:117175205
|
C | T | 49 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(46): Show | 49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.1078+4229C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117175205 | ||||||
| chr7:117175445
|
C | G | 49 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(46): Show | 49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.1078+4469C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117175445 | ||||||
| chr7:117175457
|
A | G | 49 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(46): Show | 49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.1078+4481A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117175457 | ||||||
| chr7:117175543
|
T | C | 14 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0012others(11): Show | 14 | HG00673.hp2 HG01192.hp2 HG01943.hp1 others(11): Show |
intron_variant | MODIFIER | c.1078+4567T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117175543 | ||||||
| chr7:117175934
|
G | A | 20 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0047others(17): Show | 20 | HG00323.hp1 HG00642.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.1078+4958G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117175934 | ||||||
| chr7:117175934
|
GA | G | 11 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0062others(8): Show | 11 | HG02615.hp2 HG02622.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.1078+4959delA | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117175934 | ||||||
| chr7:117176230
|
C | A | 49 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(46): Show | 49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.1078+5254C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117176230 | ||||||
| chr7:117176412
|
G | A | 49 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(46): Show | 49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.1078+5436G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117176412 | ||||||
| chr7:117176552
|
T | G | 2 | a0001c0001t0001g0057a0001c0001t0001g0184 | 2 | HG02965.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1078+5576T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117176552 | ||||||
| chr7:117176883
|
T | C | 2 | a0001c0001t0001g0153a0001c0001t0001g0159 | 2 | NA18965.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.1078+5907T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117176883 | ||||||
| chr7:117177078
|
T | C | 49 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(46): Show | 49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.1078+6102T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117177078 | ||||||
| chr7:117177378
|
C | T | 14 | a0001c0001t0001g0016a0001c0001t0001g0047a0001c0001t0001g0061others(11): Show | 14 | HG00323.hp1 HG00642.hp2 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.1078+6402C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117177378 | ||||||
| chr7:117177408
|
T | C | 10 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0086others(7): Show | 10 | HG02615.hp2 HG02622.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1078+6432T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117177408 | ||||||
| chr7:117177584
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1078+6608G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117177584 | ||||||
| chr7:117177738
|
C | G | 50 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(47): Show | 50 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.1078+6762C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117177738 | ||||||
| chr7:117177760
|
G | A | 2 | a0001c0001t0001g0115a0001c0001t0001g0166 | 2 | HG02451.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1078+6784G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117177760 | ||||||
| chr7:117177982
|
A | C | 1 | a0001c0001t0001g0005 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1078+7006A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117177982 | ||||||
| chr7:117178239
|
T | C | 49 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(46): Show | 49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.1078+7263T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117178239 | ||||||
| chr7:117178275
|
A | G | 1 | a0001c0001t0001g0107 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1078+7299A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117178275 | ||||||
| chr7:117178327
|
A | G | 49 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(46): Show | 49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.1078+7351A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117178327 | ||||||
| chr7:117178464
|
T | C | 49 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(46): Show | 49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.1078+7488T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117178464 | ||||||
| chr7:117178534
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1078+7558G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117178534 | ||||||
| chr7:117178774
|
C | T | 6 | a0001c0001t0001g0015a0001c0001t0001g0070a0001c0001t0001g0115others(3): Show | 6 | HG02451.hp2 HG02630.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1078+7798C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117178774 | ||||||
| chr7:117179081
|
C | T | 49 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(46): Show | 49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.1078+8105C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117179081 | ||||||
| chr7:117179098
|
C | T | 49 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(46): Show | 49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.1078+8122C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117179098 | ||||||
| chr7:117179456
|
T | C | 55 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(52): Show | 55 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.1078+8480T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117179456 | ||||||
| chr7:117179621
|
T | C | 1 | a0001c0001t0001g0062 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1078+8645T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117179621 | ||||||
| chr7:117179854
|
A | T | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1078+8878A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117179854 | ||||||
| chr7:117179876
|
G | A | 1 | a0001c0001t0001g0062 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1078+8900G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117179876 | ||||||
| chr7:117180115
|
T | A | 2 | a0001c0001t0001g0073a0001c0001t0001g0116 | 2 | HG01081.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1078+9139T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117180115 | ||||||
| chr7:117180126
|
C | T | 49 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(46): Show | 49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.1078+9150C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117180126 | ||||||
| chr7:117180127
|
C | T | 3 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0002t0001g0044 | 3 | HG02970.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1078+9151C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117180127 | ||||||
| chr7:117180130
|
G | A | 3 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0002t0001g0044 | 3 | HG02970.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1078+9154G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117180130 | ||||||
| chr7:117180233
|
T | C | 49 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(46): Show | 49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.1079-9088T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117180233 | ||||||
| chr7:117180378
|
C | T | 38 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0012others(35): Show | 38 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.1079-8943C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117180378 | ||||||
| chr7:117180562
|
T | A | 1 | a0001c0001t0001g0188 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1079-8759T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117180562 | ||||||
| chr7:117180785
|
G | A | 49 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(46): Show | 49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.1079-8536G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117180785 | ||||||
| chr7:117180899
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1079-8422G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117180899 | ||||||
| chr7:117181201
|
A | G | 3 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0002t0001g0044 | 3 | HG02970.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1079-8120A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117181201 | ||||||
| chr7:117181277
|
C | T | 2 | a0001c0001t0001g0153a0001c0001t0001g0159 | 2 | NA18965.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.1079-8044C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117181277 | ||||||
| chr7:117181586
|
A | G | 1 | a0001c0001t0001g0146 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1079-7735A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117181586 | ||||||
| chr7:117181592
|
T | A | 1 | a0001c0001t0001g0091 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1079-7729T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117181592 | ||||||
| chr7:117181692
|
A | G | 71 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(68): Show | 71 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.1079-7629A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117181692 | ||||||
| chr7:117181723
|
A | G | 75 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(72): Show | 75 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.1079-7598A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117181723 | ||||||
| chr7:117181738
|
C | A | 10 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0086others(7): Show | 10 | HG02615.hp2 HG02622.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1079-7583C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117181738 | ||||||
| chr7:117182206
|
C | T | 38 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0012others(35): Show | 38 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.1079-7115C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117182206 | ||||||
| chr7:117182271
|
G | A | 38 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0012others(35): Show | 38 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.1079-7050G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117182271 | ||||||
| chr7:117182339
|
T | C | 1 | a0001c0001t0001g0144 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1079-6982T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117182339 | ||||||
| chr7:117182368
|
G | A | 3 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0002t0001g0044 | 3 | HG02970.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1079-6953G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117182368 | ||||||
| chr7:117182441
|
A | G | 2 | a0001c0001t0001g0057a0001c0001t0001g0184 | 2 | HG02965.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1079-6880A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117182441 | ||||||
| chr7:117182446
|
G | T | 6 | a0001c0001t0001g0015a0001c0001t0001g0070a0001c0001t0001g0115others(3): Show | 6 | HG02451.hp2 HG02630.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1079-6875G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117182446 | ||||||
| chr7:117182606
|
G | C | 1 | a0001c0001t0001g0108 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1079-6715G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117182606 | ||||||
| chr7:117182614
|
T | G | 1 | a0001c0001t0001g0108 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1079-6707T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117182614 | ||||||
| chr7:117182615
|
A | G | 50 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(47): Show | 50 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.1079-6706A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117182615 | ||||||
| chr7:117182801
|
T | C | 1 | a0001c0001t0001g0188 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1079-6520T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117182801 | ||||||
| chr7:117182938
|
C | A | 1 | a0001c0001t0001g0145 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1079-6383C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117182938 | ||||||
| chr7:117183100
|
TTTTGTTT others(1): Show |
T | 10 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0086others(7): Show | 10 | HG02615.hp2 HG02622.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1079-6197_1079-619 others(12): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr7 | 117183100 | |||||
| chr7:117183100
|
TTTTGTTT others(5): Show |
T | 2 | a0001c0001t0001g0076a0001c0001t0001g0104 | 2 | HG00280.hp1 HG00280.hp2 |
intron_variant | MODIFIER | c.1079-6201_1079-619 others(16): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr7 | 117183100 | |||||
| chr7:117183214
|
A | T | 50 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(47): Show | 50 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.1079-6107A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117183214 | ||||||
| chr7:117183280
|
T | A | 1 | a0001c0001t0001g0140 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1079-6041T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117183280 | ||||||
| chr7:117183287
|
G | A | 1 | a0001c0001t0001g0099 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1079-6034G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117183287 | ||||||
| chr7:117183350
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1079-5971C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117183350 | ||||||
| chr7:117183755
|
A | G | 7 | a0001c0001t0001g0015a0001c0001t0001g0070a0001c0001t0001g0112others(4): Show | 7 | HG02451.hp2 HG02630.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1079-5566A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117183755 | ||||||
| chr7:117183907
|
A | T | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1079-5414A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117183907 | ||||||
| chr7:117183992
|
GACAAAAA others(5): Show |
G | 14 | a0001c0001t0001g0016a0001c0001t0001g0047a0001c0001t0001g0061others(11): Show | 14 | HG00323.hp1 HG00642.hp2 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.1079-5316_1079-530 others(16): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr7 | 117183992 | |||||
| chr7:117184063
|
G | A | 13 | a0001c0001t0001g0016a0001c0001t0001g0047a0001c0001t0001g0061others(10): Show | 13 | HG00323.hp1 HG00642.hp2 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.1079-5258G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117184063 | ||||||
| chr7:117184284
|
TG | T | 77 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0009others(74): Show | 77 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.1079-5036delG | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117184284 | ||||||
| chr7:117184541
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1079-4780G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117184541 | ||||||
| chr7:117184582
|
G | A | 38 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0012others(35): Show | 38 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.1079-4739G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117184582 | ||||||
| chr7:117184660
|
A | G | 1 | a0001c0001t0001g0163 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1079-4661A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117184660 | ||||||
| chr7:117184704
|
G | A | 1 | a0001c0001t0001g0174 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1079-4617G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117184704 | ||||||
| chr7:117184868
|
G | A | 1 | a0001c0001t0001g0062 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1079-4453G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117184868 | ||||||
| chr7:117184876
|
A | G | 21 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0047others(18): Show | 21 | HG00323.hp1 HG00642.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.1079-4445A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117184876 | ||||||
| chr7:117184921
|
T | G | 2 | a0001c0001t0001g0062a0001c0001t0001g0125 | 2 | HG02258.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1079-4400T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117184921 | ||||||
| chr7:117184924
|
T | C | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1079-4397T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117184924 | ||||||
| chr7:117184943
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1079-4378C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117184943 | ||||||
| chr7:117184969
|
T | C | 1 | a0001c0001t0001g0096 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1079-4352T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117184969 | ||||||
| chr7:117185046
|
A | C | 1 | a0001c0001t0001g0161 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1079-4275A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117185046 | ||||||
| chr7:117185237
|
A | C | 1 | a0001c0001t0001g0047 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1079-4084A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117185237 | ||||||
| chr7:117185467
|
C | T | 1 | a0001c0001t0001g0062 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1079-3854C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117185467 | ||||||
| chr7:117185571
|
C | T | 1 | a0001c0001t0001g0139 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1079-3750C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117185571 | ||||||
| chr7:117185596
|
A | G | 1 | a0001c0001t0001g0034 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1079-3725A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117185596 | ||||||
| chr7:117185647
|
C | T | 10 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0086others(7): Show | 10 | HG02615.hp2 HG02622.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1079-3674C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117185647 | ||||||
| chr7:117185794
|
A | G | 74 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(71): Show | 74 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.1079-3527A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117185794 | ||||||
| chr7:117186176
|
G | C | 1 | a0001c0001t0001g0186 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1079-3145G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117186176 | ||||||
| chr7:117186435
|
C | T | 14 | a0001c0001t0001g0016a0001c0001t0001g0047a0001c0001t0001g0061others(11): Show | 14 | HG00323.hp1 HG00642.hp2 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.1079-2886C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117186435 | ||||||
| chr7:117186735
|
C | T | 1 | a0001c0001t0001g0002 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1079-2586C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117186735 | ||||||
| chr7:117187088
|
T | A | 49 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(46): Show | 49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.1079-2233T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117187088 | ||||||
| chr7:117187106
|
T | C | 38 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0012others(35): Show | 38 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.1079-2215T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117187106 | ||||||
| chr7:117187138
|
T | C | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1079-2183T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117187138 | ||||||
| chr7:117187527
|
T | C | 1 | a0001c0001t0001g0112 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1079-1794T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117187527 | ||||||
| chr7:117187684
|
T | A | 1 | a0001c0001t0001g0121 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1079-1637T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117187684 | ||||||
| chr7:117187866
|
C | T | 1 | a0001c0001t0001g0118 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1079-1455C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117187866 | ||||||
| chr7:117188007
|
G | A | 49 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(46): Show | 49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.1079-1314G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117188007 | ||||||
| chr7:117188103
|
A | G | 38 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0012others(35): Show | 38 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.1079-1218A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117188103 | ||||||
| chr7:117188326
|
G | C | 2 | a0001c0001t0001g0002a0001c0001t0001g0014 | 2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1079-995G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117188326 | ||||||
| chr7:117188773
|
T | TATATATA others(41): Show |
1 | a0001c0001t0001g0062 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1079-547_1079-546i others(50): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr7 | 117188773 | |||||
| chr7:117188773
|
T | TATATATA others(17): Show |
1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1079-547_1079-546i others(26): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr7 | 117188773 | |||||
| chr7:117188773
|
T | TATATATA others(15): Show |
10 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0086others(7): Show | 10 | HG02615.hp2 HG02622.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1079-547_1079-546i others(24): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr7 | 117188773 | |||||
| chr7:117188773
|
T | TATATATC others(3): Show |
38 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0012others(35): Show | 38 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.1079-547_1079-546i others(12): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr7 | 117188773 | |||||
| chr7:117189013
|
G | T | 49 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(46): Show | 49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.1079-308G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117189013 | ||||||
| chr7:117189409
|
T | C | 50 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(47): Show | 50 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.1151+16T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 11/15 | chr7 | 117189409 | ||||||
| chr7:117189569
|
C | T | 1 | a0001c0001t0001g0021 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1151+176C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 11/15 | chr7 | 117189569 | ||||||
| chr7:117189685
|
TA | T | 50 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(47): Show | 50 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.1151+294delA | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr7 | 117189685 | |||||
| chr7:117190018
|
G | A | 1 | a0001c0001t0001g0145 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1151+625G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 11/15 | chr7 | 117190018 | ||||||
| chr7:117190049
|
C | T | 1 | a0001c0001t0001g0081 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1151+656C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 11/15 | chr7 | 117190049 | ||||||
| chr7:117190351
|
C | G | 50 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(47): Show | 50 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.1152-483C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 11/15 | chr7 | 117190351 | ||||||
| chr7:117190356
|
G | A | 3 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0002t0001g0044 | 3 | HG02970.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1152-478G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 11/15 | chr7 | 117190356 | ||||||
| chr7:117190423
|
C | T | 4 | a0001c0001t0001g0015a0001c0001t0001g0070a0001c0001t0001g0142others(1): Show | 4 | HG02630.hp2 HG02895.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1152-411C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 11/15 | chr7 | 117190423 | ||||||
| chr7:117190680
|
C | T | 3 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0002t0001g0044 | 3 | HG02970.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1152-154C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 11/15 | chr7 | 117190680 | ||||||
| chr7:117190726
|
A | G | 1 | a0001c0001t0001g0088 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1152-108A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 11/15 | chr7 | 117190726 | ||||||
| chr7:117191014
|
G | C | 10 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0086others(7): Show | 10 | HG02615.hp2 HG02622.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1254+78G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117191014 | ||||||
| chr7:117191448
|
G | C | 1 | a0001c0001t0001g0186 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1254+512G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117191448 | ||||||
| chr7:117191449
|
A | G | 5 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(2): Show | 5 | HG01496.hp2 HG02572.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1254+513A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117191449 | ||||||
| chr7:117191511
|
A | AT | 187 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(184): Show | 187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.1254+583dupT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117191511 | |||||
| chr7:117191887
|
A | C | 1 | a0001c0001t0001g0115 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1254+951A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117191887 | ||||||
| chr7:117191961
|
T | TATC | 75 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(72): Show | 75 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.1254+1027_1254+102 others(7): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117191961 | |||||
| chr7:117192626
|
C | T | 5 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0079others(2): Show | 5 | HG01934.hp2 HG02071.hp2 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.1254+1690C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117192626 | ||||||
| chr7:117192866
|
G | T | 2 | a0001c0001t0001g0045a0001c0001t0001g0087 | 2 | HG02280.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1254+1930G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117192866 | ||||||
| chr7:117192869
|
T | C | 3 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0002t0001g0044 | 3 | HG02970.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1254+1933T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117192869 | ||||||
| chr7:117192880
|
G | C | 50 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(47): Show | 50 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.1254+1944G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117192880 | ||||||
| chr7:117192905
|
G | T | 1 | a0001c0001t0001g0174 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1254+1969G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117192905 | ||||||
| chr7:117192906
|
C | T | 1 | a0001c0001t0001g0174 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1254+1970C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117192906 | ||||||
| chr7:117193124
|
T | C | 2 | a0001c0001t0001g0022a0001c0001t0001g0180 | 2 | NA18981.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1254+2188T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117193124 | ||||||
| chr7:117193150
|
T | TAC | 6 | a0001c0001t0001g0057a0001c0001t0001g0082a0001c0001t0001g0108others(3): Show | 6 | HG02965.hp2 HG03209.hp2 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.1254+2245_1254+224 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117193150 | |||||
| chr7:117193150
|
T | TACACACA others(3): Show |
2 | a0001c0001t0001g0018a0001c0001t0001g0113 | 2 | HG04184.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1254+2237_1254+224 others(14): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117193150 | |||||
| chr7:117193150
|
T | TACACACA others(5): Show |
11 | a0001c0001t0001g0023a0001c0001t0001g0099a0001c0001t0001g0125others(8): Show | 11 | HG00408.hp2 HG00438.hp2 HG02040.hp1 others(8): Show |
intron_variant | MODIFIER | c.1254+2235_1254+224 others(16): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117193150 | |||||
| chr7:117193150
|
T | TACACACA others(7): Show |
16 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0012others(13): Show | 16 | HG01192.hp2 HG01943.hp1 HG02040.hp2 others(13): Show |
intron_variant | MODIFIER | c.1254+2233_1254+224 others(18): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117193150 | |||||
| chr7:117193150
|
T | TACACACA others(9): Show |
12 | a0001c0001t0001g0021a0001c0001t0001g0038a0001c0001t0001g0088others(9): Show | 12 | HG00673.hp2 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1254+2231_1254+224 others(20): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117193150 | |||||
| chr7:117193150
|
T | TACACACA others(11): Show |
7 | a0001c0001t0001g0003a0001c0001t0001g0054a0001c0001t0001g0059others(4): Show | 7 | HG02055.hp2 HG02647.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1254+2229_1254+224 others(22): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117193150 | |||||
| chr7:117193150
|
TACAC | T | 15 | a0001c0001t0001g0016a0001c0001t0001g0046a0001c0001t0001g0051others(12): Show | 15 | HG00323.hp1 HG00642.hp2 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.1254+2243_1254+224 others(8): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117193150 | |||||
| chr7:117193150
|
TACACAC | T | 6 | a0001c0001t0001g0015a0001c0001t0001g0070a0001c0001t0001g0115others(3): Show | 6 | HG02451.hp2 HG02630.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1254+2241_1254+224 others(10): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117193150 | |||||
| chr7:117193230
|
G | A | 5 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(2): Show | 5 | HG01496.hp2 HG02572.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1254+2294G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117193230 | ||||||
| chr7:117193401
|
T | C | 50 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(47): Show | 50 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.1254+2465T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117193401 | ||||||
| chr7:117193430
|
A | G | 76 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(73): Show | 76 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.1254+2494A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117193430 | ||||||
| chr7:117193484
|
C | T | 2 | a0001c0001t0001g0077a0001c0001t0001g0078 | 2 | HG02083.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.1254+2548C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117193484 | ||||||
| chr7:117193614
|
C | T | 38 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0012others(35): Show | 38 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.1254+2678C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117193614 | ||||||
| chr7:117193881
|
G | A | 1 | a0001c0001t0001g0087 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1254+2945G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117193881 | ||||||
| chr7:117194118
|
C | T | 14 | a0001c0001t0001g0016a0001c0001t0001g0047a0001c0001t0001g0061others(11): Show | 14 | HG00323.hp1 HG00642.hp2 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.1254+3182C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117194118 | ||||||
| chr7:117194294
|
A | T | 4 | a0001c0001t0001g0043a0001c0001t0001g0056a0001c0001t0001g0085others(1): Show | 4 | HG02109.hp2 HG02486.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1254+3358A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117194294 | ||||||
| chr7:117194537
|
T | A | 4 | a0001c0001t0001g0070a0001c0001t0001g0115a0001c0001t0001g0142others(1): Show | 4 | HG02451.hp2 HG02895.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1254+3601T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117194537 | ||||||
| chr7:117194719
|
T | C | 18 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0015others(15): Show | 18 | HG01496.hp2 HG02572.hp2 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.1254+3783T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117194719 | ||||||
| chr7:117194809
|
C | T | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(98): Show | 101 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.1254+3873C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117194809 | ||||||
| chr7:117195074
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1254+4138G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117195074 | ||||||
| chr7:117195086
|
A | T | 1 | a0001c0001t0001g0114 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1254+4150A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117195086 | ||||||
| chr7:117195154
|
TA | T | 48 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0013others(45): Show | 48 | HG00408.hp2 HG00438.hp2 HG02055.hp2 others(45): Show |
intron_variant | MODIFIER | c.1254+4227delA | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117195154 | |||||
| chr7:117195169
|
A | G | 11 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0062others(8): Show | 11 | HG02572.hp2 HG02615.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.1254+4233A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117195169 | ||||||
| chr7:117195170
|
T | C | 1 | a0001c0001t0001g0114 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1254+4234T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117195170 | ||||||
| chr7:117195349
|
T | C | 4 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0069others(1): Show | 4 | HG02280.hp1 HG03098.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1254+4413T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117195349 | ||||||
| chr7:117195680
|
C | T | 98 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(95): Show | 98 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.1254+4744C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117195680 | ||||||
| chr7:117195817
|
C | A | 1 | a0001c0001t0001g0034 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1254+4881C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117195817 | ||||||
| chr7:117195838
|
C | T | 9 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0053others(6): Show | 9 | HG02280.hp1 HG02895.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.1254+4902C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117195838 | ||||||
| chr7:117196386
|
CCAACA | C | 103 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 103 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.1254+5451_1254+545 others(9): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117196386 | ||||||
| chr7:117196514
|
G | A | 3 | a0001c0001t0001g0057a0001c0001t0001g0064a0001c0001t0001g0184 | 3 | HG01496.hp2 HG02965.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1254+5578G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117196514 | ||||||
| chr7:117196619
|
T | G | 1 | a0001c0001t0001g0145 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1254+5683T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117196619 | ||||||
| chr7:117196624
|
C | CT | 11 | a0001c0001t0001g0043a0001c0001t0001g0048a0001c0001t0001g0049others(8): Show | 11 | HG01433.hp2 HG02622.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.1254+5715dupT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117196624 | |||||
| chr7:117196624
|
C | CTTT | 6 | a0001c0001t0001g0001a0001c0001t0001g0065a0001c0001t0001g0066others(3): Show | 6 | HG02615.hp2 HG02970.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1254+5713_1254+571 others(7): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117196624 | |||||
| chr7:117196624
|
CT | C | 7 | a0001c0001t0001g0070a0001c0001t0001g0086a0001c0001t0001g0089others(4): Show | 7 | HG02451.hp2 HG02647.hp2 HG02683.hp1 others(4): Show |
intron_variant | MODIFIER | c.1254+5715delT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117196624 | |||||
| chr7:117196624
|
CTTTT | C | 5 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0139others(2): Show | 5 | HG03098.hp2 HG03492.hp1 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.1254+5712_1254+571 others(8): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117196624 | |||||
| chr7:117196624
|
CTTTTT | C | 97 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(94): Show | 97 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.1254+5711_1254+571 others(9): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117196624 | |||||
| chr7:117196624
|
CTTTTTTT others(3): Show |
C | 19 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0054others(16): Show | 19 | HG00408.hp2 HG00438.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.1254+5706_1254+571 others(14): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117196624 | |||||
| chr7:117196680
|
G | GTTTTCAA | 140 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(137): Show | 140 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.1254+5746_1254+575 others(11): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117196680 | |||||
| chr7:117196852
|
T | C | 3 | a0001c0001t0001g0100a0001c0001t0001g0107a0001c0001t0001g0126 | 3 | HG00741.hp2 HG01256.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1254+5916T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117196852 | ||||||
| chr7:117196940
|
A | G | 3 | a0001c0001t0001g0001a0001c0001t0001g0106a0001c0001t0001g0122 | 3 | HG02615.hp2 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1254+6004A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117196940 | ||||||
| chr7:117197556
|
T | G | 141 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(138): Show | 141 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.1254+6620T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117197556 | ||||||
| chr7:117197738
|
A | G | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1254+6802A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117197738 | ||||||
| chr7:117198257
|
G | A | 127 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(124): Show | 127 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.1254+7321G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117198257 | ||||||
| chr7:117198316
|
G | T | 1 | a0001c0001t0001g0102 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1254+7380G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117198316 | ||||||
| chr7:117198592
|
T | C | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1254+7656T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117198592 | ||||||
| chr7:117198700
|
CA | C | 9 | a0001c0001t0001g0001a0001c0001t0001g0065a0001c0001t0001g0066others(6): Show | 9 | HG02572.hp2 HG02615.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1254+7765delA | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117198700 | ||||||
| chr7:117198978
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1254+8042C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117198978 | ||||||
| chr7:117199184
|
T | A | 127 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(124): Show | 127 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.1254+8248T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117199184 | ||||||
| chr7:117199368
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1254+8432A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117199368 | ||||||
| chr7:117199539
|
A | G | 140 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(137): Show | 140 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.1254+8603A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117199539 | ||||||
| chr7:117199583
|
T | C | 140 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(137): Show | 140 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.1254+8647T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117199583 | ||||||
| chr7:117199612
|
A | G | 4 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0069others(1): Show | 4 | HG02280.hp1 HG03098.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1254+8676A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117199612 | ||||||
| chr7:117199666
|
T | C | 140 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(137): Show | 140 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.1254+8730T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117199666 | ||||||
| chr7:117199685
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1254+8749C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117199685 | ||||||
| chr7:117199691
|
C | T | 103 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 103 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.1254+8755C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117199691 | ||||||
| chr7:117199811
|
A | G | 140 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(137): Show | 140 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.1254+8875A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117199811 | ||||||
| chr7:117199896
|
C | T | 99 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(96): Show | 99 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.1254+8960C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117199896 | ||||||
| chr7:117200026
|
C | T | 2 | a0001c0001t0001g0070a0001c0001t0001g0142 | 2 | HG02895.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1254+9090C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117200026 | ||||||
| chr7:117200154
|
T | C | 1 | a0001c0001t0001g0166 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1254+9218T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117200154 | ||||||
| chr7:117200438
|
C | A | 140 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(137): Show | 140 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.1255-9349C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117200438 | ||||||
| chr7:117200742
|
C | T | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1255-9045C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117200742 | ||||||
| chr7:117200779
|
A | G | 1 | a0001c0001t0001g0142 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1255-9008A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117200779 | ||||||
| chr7:117200818
|
CT | C | 112 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(109): Show | 112 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.1255-8953delT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117200818 | |||||
| chr7:117200818
|
CTT | C | 31 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0026others(28): Show | 31 | HG00323.hp2 HG00408.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.1255-8954_1255-895 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117200818 | |||||
| chr7:117200833
|
T | A | 54 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(51): Show | 54 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(51): Show |
intron_variant | MODIFIER | c.1255-8954T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117200833 | ||||||
| chr7:117200834
|
T | A | 121 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(118): Show | 121 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.1255-8953T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117200834 | ||||||
| chr7:117200834
|
TA | T | 17 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0053others(14): Show | 17 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.1255-8943delA | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117200834 | |||||
| chr7:117200834
|
TAA | T | 4 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0088others(1): Show | 4 | HG02976.hp2 HG03195.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1255-8944_1255-894 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117200834 | |||||
| chr7:117200836
|
A | T | 8 | a0001c0001t0001g0067a0001c0001t0001g0070a0001c0001t0001g0071others(5): Show | 8 | HG02572.hp2 HG02615.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1255-8951A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117200836 | ||||||
| chr7:117200889
|
A | T | 1 | a0001c0001t0001g0112 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1255-8898A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117200889 | ||||||
| chr7:117201060
|
A | G | 1 | a0001c0001t0001g0121 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1255-8727A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117201060 | ||||||
| chr7:117201112
|
G | A | 7 | a0001c0001t0001g0070a0001c0001t0001g0086a0001c0001t0001g0089others(4): Show | 7 | HG02647.hp2 HG02717.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1255-8675G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117201112 | ||||||
| chr7:117201197
|
A | T | 1 | a0001c0001t0001g0134 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1255-8590A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117201197 | ||||||
| chr7:117201310
|
C | A | 36 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0043others(33): Show | 36 | HG00408.hp2 HG00438.hp2 HG02055.hp2 others(33): Show |
intron_variant | MODIFIER | c.1255-8477C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117201310 | ||||||
| chr7:117201445
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1255-8342C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117201445 | ||||||
| chr7:117201560
|
G | GT | 47 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0043others(44): Show | 47 | HG00408.hp2 HG00438.hp2 HG02027.hp2 others(44): Show |
intron_variant | MODIFIER | c.1255-8215dupT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117201560 | |||||
| chr7:117201617
|
G | A | 19 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0054others(16): Show | 19 | HG00408.hp2 HG00438.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.1255-8170G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117201617 | ||||||
| chr7:117201644
|
G | A | 3 | a0001c0001t0001g0004a0001c0001t0001g0035a0001c0001t0001g0154 | 3 | HG01934.hp1 HG02293.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.1255-8143G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117201644 | ||||||
| chr7:117201820
|
C | T | 1 | a0001c0001t0001g0008 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1255-7967C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117201820 | ||||||
| chr7:117201894
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1255-7893G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117201894 | ||||||
| chr7:117201900
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1255-7887A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117201900 | ||||||
| chr7:117201949
|
GCTCGAAG others(304): Show |
G | 127 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(124): Show | 127 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.1255-7823_1255-751 others(4): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117201949 | |||||
| chr7:117201961
|
C | CT | 30 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0043others(27): Show | 30 | HG02109.hp2 HG02258.hp2 HG02280.hp2 others(27): Show |
intron_variant | MODIFIER | c.1255-7809dupT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117201961 | |||||
| chr7:117201963
|
T | TG | 2 | a0001c0001t0001g0114a0001c0001t0001g0115 | 2 | HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1255-7824_1255-782 others(5): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117201963 | ||||||
| chr7:117202587
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1255-7200C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117202587 | ||||||
| chr7:117202734
|
A | C | 20 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(17): Show | 20 | HG02109.hp2 HG02258.hp2 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1255-7053A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117202734 | ||||||
| chr7:117202792
|
G | A | 127 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(124): Show | 127 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.1255-6995G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117202792 | ||||||
| chr7:117202863
|
GT | G | 13 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(10): Show | 13 | HG02109.hp2 HG02258.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.1255-6917delT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117202863 | |||||
| chr7:117202870
|
T | C | 127 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(124): Show | 127 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.1255-6917T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117202870 | ||||||
| chr7:117202876
|
C | T | 127 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(124): Show | 127 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.1255-6911C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117202876 | ||||||
| chr7:117202894
|
A | T | 8 | a0001c0001t0001g0032a0001c0001t0001g0130a0001c0001t0001g0131others(5): Show | 8 | HG00408.hp2 HG00438.hp2 HG02523.hp1 others(5): Show |
intron_variant | MODIFIER | c.1255-6893A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117202894 | ||||||
| chr7:117202895
|
T | G | 1 | a0001c0001t0001g0028 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1255-6892T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117202895 | ||||||
| chr7:117203002
|
G | A | 19 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0054others(16): Show | 19 | HG00408.hp2 HG00438.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.1255-6785G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117203002 | ||||||
| chr7:117203030
|
A | G | 2 | a0001c0001t0001g0070a0001c0001t0001g0142 | 2 | HG02895.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1255-6757A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117203030 | ||||||
| chr7:117203046
|
G | A | 1 | a0001c0001t0001g0155 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1255-6741G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117203046 | ||||||
| chr7:117204074
|
G | A | 1 | a0001c0001t0001g0012 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1255-5713G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117204074 | ||||||
| chr7:117204297
|
T | C | 1 | a0001c0001t0001g0113 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1255-5490T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117204297 | ||||||
| chr7:117204566
|
T | A | 1 | a0001c0001t0001g0017 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1255-5221T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117204566 | ||||||
| chr7:117204571
|
T | G | 1 | a0001c0001t0001g0017 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1255-5216T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117204571 | ||||||
| chr7:117204705
|
A | G | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1255-5082A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117204705 | ||||||
| chr7:117204889
|
G | T | 14 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(11): Show | 14 | HG02109.hp2 HG02258.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.1255-4898G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117204889 | ||||||
| chr7:117204901
|
A | C | 1 | a0001c0001t0001g0037 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1255-4886A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117204901 | ||||||
| chr7:117204927
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1255-4860C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117204927 | ||||||
| chr7:117205197
|
CTACCTA | C | 4 | a0001c0001t0001g0024a0001c0001t0001g0098a0001c0001t0001g0104others(1): Show | 4 | HG00099.hp1 HG00280.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.1255-4584_1255-457 others(10): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117205197 | |||||
| chr7:117205203
|
A | G | 20 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(17): Show | 20 | HG02109.hp2 HG02258.hp2 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1255-4584A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117205203 | ||||||
| chr7:117205207
|
C | CT | 21 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(18): Show | 21 | HG02109.hp2 HG02258.hp1 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.1255-4573dupT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117205207 | |||||
| chr7:117205463
|
G | A | 147 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(144): Show | 147 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.1255-4324G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117205463 | ||||||
| chr7:117205536
|
T | G | 2 | a0001c0001t0001g0114a0001c0001t0001g0115 | 2 | HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1255-4251T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117205536 | ||||||
| chr7:117205657
|
A | G | 20 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(17): Show | 20 | HG02109.hp2 HG02258.hp2 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1255-4130A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117205657 | ||||||
| chr7:117205784
|
A | C | 1 | a0001c0001t0001g0119 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1255-4003A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117205784 | ||||||
| chr7:117205910
|
A | G | 9 | a0001c0001t0001g0001a0001c0001t0001g0065a0001c0001t0001g0066others(6): Show | 9 | HG02572.hp2 HG02615.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1255-3877A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117205910 | ||||||
| chr7:117206185
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1255-3602G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117206185 | ||||||
| chr7:117206225
|
G | T | 20 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(17): Show | 20 | HG02109.hp2 HG02258.hp2 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1255-3562G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117206225 | ||||||
| chr7:117206402
|
A | G | 21 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(18): Show | 21 | HG02109.hp2 HG02258.hp1 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.1255-3385A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117206402 | ||||||
| chr7:117206435
|
G | C | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1255-3352G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117206435 | ||||||
| chr7:117206803
|
A | G | 1 | a0001c0001t0001g0040 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1255-2984A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117206803 | ||||||
| chr7:117206846
|
A | G | 185 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(182): Show | 185 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.1255-2941A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117206846 | ||||||
| chr7:117206890
|
T | A | 3 | a0001c0001t0001g0053a0001c0001t0001g0166a0001c0002t0001g0044 | 3 | HG02970.hp2 HG02976.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1255-2897T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117206890 | ||||||
| chr7:117207149
|
A | AT | 12 | a0001c0001t0001g0053a0001c0001t0001g0070a0001c0001t0001g0086others(9): Show | 12 | HG00438.hp2 HG02647.hp2 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.1255-2624dupT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117207149 | |||||
| chr7:117207149
|
AT | A | 114 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(111): Show | 114 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.1255-2624delT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117207149 | |||||
| chr7:117207151
|
T | TG | 13 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(10): Show | 13 | HG02109.hp2 HG02258.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.1255-2636_1255-263 others(5): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117207151 | ||||||
| chr7:117207246
|
A | G | 20 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(17): Show | 20 | HG02109.hp2 HG02258.hp2 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1255-2541A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117207246 | ||||||
| chr7:117207431
|
C | T | 2 | a0001c0001t0001g0114a0001c0001t0001g0115 | 2 | HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1255-2356C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117207431 | ||||||
| chr7:117207497
|
C | A | 1 | a0001c0001t0001g0098 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1255-2290C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117207497 | ||||||
| chr7:117207503
|
C | T | 20 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(17): Show | 20 | HG02109.hp2 HG02258.hp2 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1255-2284C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117207503 | ||||||
| chr7:117207664
|
T | TA | 2 | a0001c0001t0001g0114a0001c0001t0001g0115 | 2 | HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1255-2122dupA | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117207664 | |||||
| chr7:117207701
|
T | G | 1 | a0001c0001t0001g0186 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1255-2086T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117207701 | ||||||
| chr7:117208140
|
T | G | 147 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(144): Show | 147 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.1255-1647T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117208140 | ||||||
| chr7:117208262
|
A | G | 4 | a0001c0001t0001g0086a0001c0001t0001g0089a0001c0001t0001g0097others(1): Show | 4 | HG02647.hp2 HG02717.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1255-1525A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117208262 | ||||||
| chr7:117208366
|
C | G | 2 | a0001c0001t0001g0114a0001c0001t0001g0115 | 2 | HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1255-1421C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117208366 | ||||||
| chr7:117208576
|
A | G | 1 | a0001c0001t0001g0048 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1255-1211A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117208576 | ||||||
| chr7:117208682
|
A | G | 1 | a0001c0001t0001g0058 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1255-1105A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117208682 | ||||||
| chr7:117208786
|
G | A | 20 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(17): Show | 20 | HG02109.hp2 HG02258.hp2 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1255-1001G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117208786 | ||||||
| chr7:117208902
|
G | GGTGT | 9 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(6): Show | 9 | HG02109.hp1 HG02572.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1255-846_1255-843d others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117208902 | |||||
| chr7:117208902
|
G | T | 1 | a0001c0001t0001g0151 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1255-885G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117208902 | ||||||
| chr7:117208902
|
GGT | G | 6 | a0001c0001t0001g0013a0001c0001t0001g0059a0001c0001t0001g0063others(3): Show | 6 | HG01978.hp2 HG02257.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.1255-844_1255-843d others(4): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117208902 | |||||
| chr7:117208902
|
GGTGT | G | 15 | a0001c0001t0001g0015a0001c0001t0001g0043a0001c0001t0001g0045others(12): Show | 15 | HG02109.hp2 HG02258.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1255-846_1255-843d others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117208902 | |||||
| chr7:117208902
|
GGTGTGT | G | 7 | a0001c0001t0001g0070a0001c0001t0001g0080a0001c0001t0001g0113others(4): Show | 7 | HG00741.hp1 HG02040.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1255-848_1255-843d others(8): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117208902 | |||||
| chr7:117208902
|
GGTGTGTG others(1): Show |
G | 98 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(95): Show | 98 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.1255-850_1255-843d others(10): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117208902 | |||||
| chr7:117208902
|
GGTGTGTG others(3): Show |
G | 1 | a0001c0001t0001g0114 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1255-852_1255-843d others(12): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117208902 | |||||
| chr7:117208902
|
GGTGTGTG others(5): Show |
G | 3 | a0001c0001t0001g0009a0001c0001t0001g0153a0001c0001t0001g0159 | 3 | NA18965.hp2 NA18971.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.1255-854_1255-843d others(14): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117208902 | |||||
| chr7:117208910
|
T | G | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1255-877T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117208910 | ||||||
| chr7:117209045
|
G | C | 1 | a0001c0001t0001g0139 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1255-742G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117209045 | ||||||
| chr7:117209056
|
G | T | 2 | a0001c0001t0001g0143a0001c0001t0001g0149 | 2 | NA18973.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.1255-731G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117209056 | ||||||
| chr7:117209273
|
G | A | 99 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(96): Show | 99 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.1255-514G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117209273 | ||||||
| chr7:117209401
|
A | G | 2 | a0001c0001t0001g0100a0001c0001t0001g0107 | 2 | HG00741.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.1255-386A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117209401 | ||||||
| chr7:117209519
|
T | C | 2 | a0001c0001t0001g0153a0001c0001t0001g0159 | 2 | NA18965.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.1255-268T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117209519 | ||||||
| chr7:117209671
|
G | C | 20 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(17): Show | 20 | HG02109.hp2 HG02258.hp2 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1255-116G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117209671 | ||||||
| chr7:117210306
|
G | T | 1 | a0001c0001t0001g0108 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1405+369G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117210306 | ||||||
| chr7:117210499
|
A | G | 2 | a0001c0001t0001g0093a0001c0001t0001g0103 | 2 | HG01433.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1405+562A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117210499 | ||||||
| chr7:117210528
|
T | C | 20 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(17): Show | 20 | HG02109.hp2 HG02258.hp2 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1405+591T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117210528 | ||||||
| chr7:117210716
|
C | G | 103 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 103 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.1405+779C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117210716 | ||||||
| chr7:117210776
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1405+839G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117210776 | ||||||
| chr7:117211043
|
T | C | 2 | a0001c0001t0001g0015a0001c0001t0001g0112 | 2 | HG02630.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1405+1106T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117211043 | ||||||
| chr7:117211103
|
G | A | 23 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0053others(20): Show | 23 | HG00408.hp2 HG00438.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.1405+1166G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117211103 | ||||||
| chr7:117211299
|
C | T | 1 | a0001c0001t0001g0024 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1405+1362C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117211299 | ||||||
| chr7:117211427
|
A | G | 2 | a0001c0001t0001g0076a0001c0001t0001g0164 | 2 | HG00280.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.1405+1490A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117211427 | ||||||
| chr7:117211438
|
T | G | 2 | a0001c0001t0001g0083a0001c0001t0001g0151 | 2 | HG02027.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.1405+1501T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117211438 | ||||||
| chr7:117211481
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1405+1544G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117211481 | ||||||
| chr7:117211526
|
A | G | 4 | a0001c0001t0001g0086a0001c0001t0001g0089a0001c0001t0001g0097others(1): Show | 4 | HG02647.hp2 HG02717.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1405+1589A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117211526 | ||||||
| chr7:117211685
|
G | A | 43 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0020others(40): Show | 43 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.1405+1748G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117211685 | ||||||
| chr7:117211921
|
G | A | 103 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 103 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.1405+1984G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117211921 | ||||||
| chr7:117212177
|
G | A | 14 | a0001c0001t0001g0012a0001c0001t0001g0026a0001c0001t0001g0027others(11): Show | 14 | HG00408.hp1 HG01934.hp2 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.1405+2240G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117212177 | ||||||
| chr7:117212347
|
C | G | 20 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(17): Show | 20 | HG02109.hp2 HG02258.hp2 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1405+2410C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117212347 | ||||||
| chr7:117212659
|
T | G | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1405+2722T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117212659 | ||||||
| chr7:117212702
|
T | A | 1 | a0001c0001t0001g0124 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1405+2765T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117212702 | ||||||
| chr7:117212758
|
A | G | 2 | a0001c0001t0001g0015a0001c0001t0001g0112 | 2 | HG02630.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1405+2821A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117212758 | ||||||
| chr7:117212886
|
A | C | 1 | a0001c0001t0001g0135 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1405+2949A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117212886 | ||||||
| chr7:117213079
|
C | T | 4 | a0001c0001t0001g0086a0001c0001t0001g0089a0001c0001t0001g0097others(1): Show | 4 | HG02647.hp2 HG02717.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1405+3142C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117213079 | ||||||
| chr7:117213226
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1405+3289G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117213226 | ||||||
| chr7:117213306
|
T | C | 9 | a0001c0001t0001g0001a0001c0001t0001g0065a0001c0001t0001g0066others(6): Show | 9 | HG02572.hp2 HG02615.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1405+3369T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117213306 | ||||||
| chr7:117213356
|
A | G | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1405+3419A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117213356 | ||||||
| chr7:117213636
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1405+3699G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117213636 | ||||||
| chr7:117213641
|
TA | T | 20 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(17): Show | 20 | HG02109.hp2 HG02258.hp2 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1405+3715delA | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr7 | 117213641 | |||||
| chr7:117213643
|
A | T | 13 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(10): Show | 13 | HG02109.hp2 HG02258.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.1405+3706A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117213643 | ||||||
| chr7:117213708
|
T | G | 1 | a0001c0001t0001g0022 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1405+3771T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117213708 | ||||||
| chr7:117213741
|
A | G | 2 | a0001c0001t0001g0002a0001c0001t0001g0014 | 2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1405+3804A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117213741 | ||||||
| chr7:117213876
|
G | A | 19 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0054others(16): Show | 19 | HG00408.hp2 HG00438.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.1405+3939G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117213876 | ||||||
| chr7:117213940
|
C | A | 13 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(10): Show | 13 | HG02109.hp2 HG02258.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.1405+4003C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117213940 | ||||||
| chr7:117213969
|
G | A | 20 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(17): Show | 20 | HG02109.hp2 HG02258.hp2 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1405+4032G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117213969 | ||||||
| chr7:117214151
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1405+4214C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117214151 | ||||||
| chr7:117214208
|
A | G | 1 | a0001c0001t0001g0022 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1405+4271A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117214208 | ||||||
| chr7:117214273
|
A | G | 1 | a0001c0001t0001g0101 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1405+4336A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117214273 | ||||||
| chr7:117214291
|
C | G | 2 | a0001c0001t0001g0179a0001c0001t0001g0187 | 2 | NA19000.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.1405+4354C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117214291 | ||||||
| chr7:117214375
|
G | A | 2 | a0001c0001t0001g0015a0001c0001t0001g0112 | 2 | HG02630.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1405+4438G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117214375 | ||||||
| chr7:117214725
|
C | T | 5 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0016others(2): Show | 5 | HG03492.hp2 HG04228.hp1 NA18747.hp2 others(2): Show |
intron_variant | MODIFIER | c.1406-4359C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117214725 | ||||||
| chr7:117214749
|
C | G | 1 | a0001c0001t0001g0166 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1406-4335C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117214749 | ||||||
| chr7:117214795
|
G | A | 4 | a0001c0001t0001g0063a0001c0001t0001g0114a0001c0001t0001g0115others(1): Show | 4 | HG02258.hp1 HG02451.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1406-4289G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117214795 | ||||||
| chr7:117214910
|
T | TTG | 4 | a0001c0001t0001g0016a0001c0001t0001g0101a0001c0001t0001g0117others(1): Show | 4 | HG00738.hp1 HG01943.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.1406-4130_1406-412 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr7 | 117214910 | |||||
| chr7:117214910
|
TTG | T | 10 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0010others(7): Show | 10 | HG01192.hp1 HG01358.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1406-4130_1406-412 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr7 | 117214910 | |||||
| chr7:117214910
|
TTGTG | T | 12 | a0001c0001t0001g0004a0001c0001t0001g0036a0001c0001t0001g0040others(9): Show | 12 | HG01071.hp2 HG02040.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1406-4132_1406-412 others(8): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr7 | 117214910 | |||||
| chr7:117214910
|
TTGTGTG | T | 86 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(83): Show | 86 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.1406-4134_1406-412 others(10): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr7 | 117214910 | |||||
| chr7:117214910
|
TTGTGTGT others(1): Show |
T | 9 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0088others(6): Show | 9 | HG00642.hp1 HG01081.hp1 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1406-4136_1406-412 others(12): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr7 | 117214910 | |||||
| chr7:117214910
|
TTGTGTGT others(3): Show |
T | 5 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(2): Show | 5 | HG00323.hp2 HG02572.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1406-4138_1406-412 others(14): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr7 | 117214910 | |||||
| chr7:117214910
|
TTGTGTGT others(15): Show |
T | 23 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0053others(20): Show | 23 | HG00408.hp2 HG00438.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.1406-4150_1406-412 others(26): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr7 | 117214910 | |||||
| chr7:117214910
|
TTGTGTGT others(17): Show |
T | 23 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(20): Show | 23 | HG02109.hp2 HG02258.hp2 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.1406-4152_1406-412 others(28): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr7 | 117214910 | |||||
| chr7:117214958
|
A | G | 1 | a0001c0001t0001g0070 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1406-4126A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117214958 | ||||||
| chr7:117214977
|
T | C | 27 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0053others(24): Show | 27 | HG00408.hp2 HG00438.hp2 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.1406-4107T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117214977 | ||||||
| chr7:117215037
|
G | A | 18 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(15): Show | 18 | HG02109.hp2 HG02258.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.1406-4047G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117215037 | ||||||
| chr7:117215059
|
A | G | 2 | a0001c0001t0001g0114a0001c0001t0001g0115 | 2 | HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1406-4025A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117215059 | ||||||
| chr7:117215326
|
G | A | 2 | a0001c0001t0001g0015a0001c0001t0001g0112 | 2 | HG02630.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1406-3758G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117215326 | ||||||
| chr7:117215355
|
T | C | 3 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0103 | 3 | HG01433.hp1 HG03130.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1406-3729T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117215355 | ||||||
| chr7:117215787
|
A | T | 1 | a0001c0001t0001g0003 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1406-3297A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117215787 | ||||||
| chr7:117216082
|
TC | T | 4 | a0001c0001t0001g0086a0001c0001t0001g0089a0001c0001t0001g0097others(1): Show | 4 | HG02647.hp2 HG02717.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1406-2996delC | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr7 | 117216082 | |||||
| chr7:117216129
|
A | T | 2 | a0001c0001t0001g0114a0001c0001t0001g0115 | 2 | HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1406-2955A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117216129 | ||||||
| chr7:117216146
|
T | C | 1 | a0001c0001t0001g0161 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1406-2938T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117216146 | ||||||
| chr7:117216590
|
G | C | 47 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0032others(44): Show | 47 | HG00408.hp2 HG00438.hp2 HG02055.hp2 others(44): Show |
intron_variant | MODIFIER | c.1406-2494G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117216590 | ||||||
| chr7:117216619
|
A | G | 2 | a0001c0001t0001g0114a0001c0001t0001g0115 | 2 | HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1406-2465A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117216619 | ||||||
| chr7:117217178
|
A | T | 1 | a0001c0001t0001g0172 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1406-1906A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117217178 | ||||||
| chr7:117217288
|
G | GA | 17 | a0001c0001t0001g0021a0001c0001t0001g0043a0001c0001t0001g0045others(14): Show | 17 | HG00673.hp2 HG02109.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.1406-1785dupA | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr7 | 117217288 | |||||
| chr7:117217296
|
A | C | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1406-1788A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117217296 | ||||||
| chr7:117217300
|
C | A | 23 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(20): Show | 23 | HG02109.hp2 HG02258.hp2 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.1406-1784C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117217300 | ||||||
| chr7:117217304
|
A | C | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1406-1780A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117217304 | ||||||
| chr7:117217319
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1406-1765C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117217319 | ||||||
| chr7:117217493
|
G | T | 19 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0054others(16): Show | 19 | HG00408.hp2 HG00438.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.1406-1591G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117217493 | ||||||
| chr7:117217622
|
C | A | 1 | a0001c0001t0001g0054 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1406-1462C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117217622 | ||||||
| chr7:117217686
|
A | G | 1 | a0001c0001t0001g0141 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1406-1398A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117217686 | ||||||
| chr7:117218187
|
A | C | 2 | a0001c0001t0001g0070a0001c0001t0001g0142 | 2 | HG02895.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1406-897A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117218187 | ||||||
| chr7:117218330
|
A | G | 103 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 103 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.1406-754A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117218330 | ||||||
| chr7:117218344
|
G | A | 103 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 103 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.1406-740G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117218344 | ||||||
| chr7:117218754
|
A | G | 3 | a0001c0001t0001g0053a0001c0001t0001g0166a0001c0002t0001g0044 | 3 | HG02970.hp2 HG02976.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1406-330A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117218754 | ||||||
| chr7:117218886
|
A | G | 1 | a0001c0001t0001g0064 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1406-198A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117218886 | ||||||
| chr7:117218900
|
A | ATG | 3 | a0001c0001t0001g0053a0001c0001t0001g0166a0001c0002t0001g0044 | 3 | HG02970.hp2 HG02976.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1406-179_1406-178d others(4): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr7 | 117218900 | |||||
| chr7:117219073
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1406-11C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117219073 | ||||||
| chr7:117219219
|
A | T | 1 | a0001c0001t0001g0014 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1498+43A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 14/15 | chr7 | 117219219 | ||||||
| chr7:117219638
|
T | C | 12 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0011others(9): Show | 12 | HG01081.hp1 HG01192.hp1 HG01358.hp2 others(9): Show |
intron_variant | MODIFIER | c.1498+462T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 14/15 | chr7 | 117219638 | ||||||
| chr7:117219728
|
C | T | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1498+552C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 14/15 | chr7 | 117219728 | ||||||
| chr7:117219801
|
G | A | 2 | a0001c0001t0001g0083a0001c0001t0001g0151 | 2 | HG02027.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.1498+625G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 14/15 | chr7 | 117219801 | ||||||
| chr7:117219806
|
C | T | 1 | a0001c0001t0001g0003 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1498+630C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 14/15 | chr7 | 117219806 | ||||||
| chr7:117219861
|
G | T | 103 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 103 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.1498+685G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 14/15 | chr7 | 117219861 | ||||||
| chr7:117219948
|
T | C | 1 | a0001c0001t0001g0025 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1498+772T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 14/15 | chr7 | 117219948 | ||||||
| chr7:117220075
|
A | G | 1 | a0001c0001t0001g0062 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1498+899A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 14/15 | chr7 | 117220075 | ||||||
| chr7:117220139
|
G | C | 20 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(17): Show | 20 | HG02109.hp2 HG02258.hp2 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1498+963G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 14/15 | chr7 | 117220139 | ||||||
| chr7:117220227
|
A | G | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1498+1051A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 14/15 | chr7 | 117220227 | ||||||
| chr7:117220247
|
G | T | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1498+1071G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 14/15 | chr7 | 117220247 | ||||||
| chr7:117220271
|
C | T | 1 | a0001c0001t0001g0020 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1498+1095C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 14/15 | chr7 | 117220271 | ||||||
| chr7:117220306
|
G | A | 3 | a0001c0001t0001g0053a0001c0001t0001g0166a0001c0002t0001g0044 | 3 | HG02970.hp2 HG02976.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1498+1130G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 14/15 | chr7 | 117220306 | ||||||
| chr7:117220771
|
C | T | 103 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 103 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.1499-1152C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 14/15 | chr7 | 117220771 | ||||||
| chr7:117221091
|
C | T | 103 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 103 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.1499-832C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 14/15 | chr7 | 117221091 | ||||||
| chr7:117221199
|
T | C | 1 | a0001c0001t0001g0145 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1499-724T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 14/15 | chr7 | 117221199 | ||||||
| chr7:117221492
|
A | G | 4 | a0001c0001t0001g0048a0001c0001t0001g0050a0001c0001t0001g0055others(1): Show | 4 | HG02258.hp2 HG02622.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1499-431A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 14/15 | chr7 | 117221492 | ||||||
| chr7:117221615
|
G | GA | 5 | a0001c0001t0001g0025a0001c0001t0001g0077a0001c0001t0001g0078others(2): Show | 5 | HG02071.hp2 HG02083.hp2 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.1499-301dupA | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr7 | 117221615 | |||||
| chr7:117221760
|
G | T | 3 | a0001c0001t0001g0070a0001c0001t0001g0142a0001c0001t0001g0145 | 3 | HG02895.hp2 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1499-163G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 14/15 | chr7 | 117221760 | ||||||
| chr7:117222204
|
T | C | 1 | a0001c0001t0001g0106 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1638+142T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117222204 | ||||||
| chr7:117222206
|
G | A | 141 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(138): Show | 141 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.1638+144G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117222206 | ||||||
| chr7:117222475
|
A | T | 8 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0030others(5): Show | 8 | HG00408.hp1 HG01934.hp2 HG02004.hp1 others(5): Show |
intron_variant | MODIFIER | c.1638+413A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117222475 | ||||||
| chr7:117222554
|
G | C | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1638+492G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117222554 | ||||||
| chr7:117222650
|
G | A | 4 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0069others(1): Show | 4 | HG02280.hp1 HG03098.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1638+588G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117222650 | ||||||
| chr7:117222862
|
T | C | 1 | a0001c0001t0001g0062 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1638+800T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117222862 | ||||||
| chr7:117222922
|
G | T | 1 | a0001c0001t0001g0076 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1638+860G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117222922 | ||||||
| chr7:117222950
|
G | A | 1 | a0001c0001t0001g0163 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1638+888G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117222950 | ||||||
| chr7:117223041
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1638+979G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117223041 | ||||||
| chr7:117223074
|
G | T | 1 | a0001c0001t0001g0130 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1638+1012G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117223074 | ||||||
| chr7:117223278
|
C | T | 14 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(11): Show | 14 | HG02109.hp2 HG02258.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.1638+1216C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117223278 | ||||||
| chr7:117223449
|
G | T | 1 | a0001c0001t0001g0166 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1638+1387G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117223449 | ||||||
| chr7:117223608
|
ACTGTCAC others(4): Show |
A | 3 | a0001c0001t0001g0070a0001c0001t0001g0142a0001c0001t0001g0145 | 3 | HG02895.hp2 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1638+1550_1638+156 others(15): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr7 | 117223608 | |||||
| chr7:117223735
|
G | A | 28 | a0001c0001t0001g0009a0001c0001t0001g0020a0001c0001t0001g0022others(25): Show | 28 | HG00323.hp2 HG00438.hp1 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.1638+1673G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117223735 | ||||||
| chr7:117224277
|
C | T | 41 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0020others(38): Show | 41 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.1638+2215C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117224277 | ||||||
| chr7:117224466
|
C | T | 2 | a0001c0001t0001g0109a0001c0001t0001g0180 | 2 | NA19004.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.1638+2404C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117224466 | ||||||
| chr7:117224836
|
C | T | 150 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(147): Show | 150 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.1638+2774C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117224836 | ||||||
| chr7:117224995
|
G | T | 1 | a0001c0001t0001g0142 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1638+2933G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117224995 | ||||||
| chr7:117225145
|
G | A | 13 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(10): Show | 13 | HG02109.hp2 HG02258.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.1638+3083G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117225145 | ||||||
| chr7:117225145
|
G | T | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1638+3083G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117225145 | ||||||
| chr7:117225251
|
T | G | 1 | a0001c0001t0001g0181 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1638+3189T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117225251 | ||||||
| chr7:117225355
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1638+3293C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117225355 | ||||||
| chr7:117225681
|
A | T | 3 | a0001c0001t0001g0057a0001c0001t0001g0064a0001c0001t0001g0184 | 3 | HG01496.hp2 HG02965.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1638+3619A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117225681 | ||||||
| chr7:117225831
|
C | T | 1 | a0001c0001t0001g0109 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1638+3769C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117225831 | ||||||
| chr7:117226143
|
A | G | 1 | a0001c0001t0001g0049 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1639-3619A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117226143 | ||||||
| chr7:117226262
|
A | T | 1 | a0001c0001t0001g0072 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1639-3500A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117226262 | ||||||
| chr7:117226719
|
C | G | 14 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(11): Show | 14 | HG02109.hp2 HG02258.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.1639-3043C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117226719 | ||||||
| chr7:117226757
|
C | A | 83 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0011others(80): Show | 83 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.1639-3005C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117226757 | ||||||
| chr7:117226822
|
T | C | 1 | a0001c0001t0001g0022 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1639-2940T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117226822 | ||||||
| chr7:117227030
|
C | T | 83 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0011others(80): Show | 83 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.1639-2732C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117227030 | ||||||
| chr7:117227212
|
G | C | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1639-2550G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117227212 | ||||||
| chr7:117227241
|
C | T | 35 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0011others(32): Show | 35 | HG00099.hp2 HG00738.hp1 HG01081.hp1 others(32): Show |
intron_variant | MODIFIER | c.1639-2521C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117227241 | ||||||
| chr7:117227242
|
G | A | 2 | a0001c0001t0001g0006a0001c0001t0001g0167 | 2 | HG03139.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.1639-2520G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117227242 | ||||||
| chr7:117227600
|
G | GT | 3 | a0001c0001t0001g0053a0001c0001t0001g0166a0001c0002t0001g0044 | 3 | HG02970.hp2 HG02976.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1639-2161dupT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr7 | 117227600 | |||||
| chr7:117227743
|
A | G | 5 | a0001c0001t0001g0033a0001c0001t0001g0129a0001c0001t0001g0147others(2): Show | 5 | HG01255.hp1 HG01256.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.1639-2019A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117227743 | ||||||
| chr7:117227802
|
C | T | 3 | a0001c0001t0001g0015a0001c0001t0001g0063a0001c0001t0001g0112 | 3 | HG02630.hp2 HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1639-1960C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117227802 | ||||||
| chr7:117227876
|
G | A | 13 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(10): Show | 13 | HG02109.hp2 HG02258.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.1639-1886G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117227876 | ||||||
| chr7:117228095
|
G | A | 3 | a0001c0001t0001g0015a0001c0001t0001g0063a0001c0001t0001g0112 | 3 | HG02630.hp2 HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1639-1667G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117228095 | ||||||
| chr7:117228133
|
C | T | 3 | a0001c0001t0001g0070a0001c0001t0001g0142a0001c0001t0001g0145 | 3 | HG02895.hp2 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1639-1629C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117228133 | ||||||
| chr7:117228357
|
T | C | 1 | a0001c0001t0001g0082 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1639-1405T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117228357 | ||||||
| chr7:117228518
|
T | A | 35 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0011others(32): Show | 35 | HG00099.hp2 HG00738.hp1 HG01081.hp1 others(32): Show |
intron_variant | MODIFIER | c.1639-1244T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117228518 | ||||||
| chr7:117228525
|
G | A | 1 | a0001c0001t0001g0137 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1639-1237G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117228525 | ||||||
| chr7:117228531
|
T | A | 83 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0011others(80): Show | 83 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.1639-1231T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117228531 | ||||||
| chr7:117228642
|
C | T | 35 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0011others(32): Show | 35 | HG00099.hp2 HG00738.hp1 HG01081.hp1 others(32): Show |
intron_variant | MODIFIER | c.1639-1120C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117228642 | ||||||
| chr7:117228763
|
G | A | 1 | a0001c0001t0001g0167 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1639-999G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117228763 | ||||||
| chr7:117228766
|
C | G | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1639-996C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117228766 | ||||||
| chr7:117228779
|
A | G | 1 | a0001c0001t0001g0039 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1639-983A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117228779 | ||||||
| chr7:117229183
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1639-579G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117229183 | ||||||
| chr7:117229425
|
A | T | 3 | a0001c0001t0001g0100a0001c0001t0001g0107a0001c0001t0001g0126 | 3 | HG00741.hp2 HG01256.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1639-337A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117229425 | ||||||
| chr7:117229687
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1639-75G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117229687 |