| geneid | 29886 |
|---|---|
| ensemblid | ENSG00000106266.11 |
| hgncid | 14972 |
| symbol | SNX8 |
| name | sorting nexin 8 |
| refseq_nuc | NM_013321.4 |
| refseq_prot | NP_037453.1 |
| ensembl_nuc | ENST00000222990.8 |
| ensembl_prot | ENSP00000222990.3 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 2251770 |
| end | 2314441 |
| strand | - |
| ver | v1.2 |
| region | chr7:2251770-2314441 |
| region5000 | chr7:2246770-2319441 |
| regionname0 | SNX8_chr7_2251770_2314441 |
| regionname5000 | SNX8_chr7_2246770_2319441 |
| 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 | 465 | 342 | 75 | 65 | 143 | 14 | 43 | 105 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0002 | 0/0 | 465 | 13 | 11 | 2 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0003 | 0/0 | 465 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0004 | 0/0 | 465 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0005 | 0/0 | 460 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0006 | 0/0 | 465 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0007 | 0/0 | 465 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0008 | 0/0 | 465 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0009 | 0/0 | 99 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0010 | 0/0 | 465 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 1398 | 254 | 49 | 58 | 100 | 13 | 33 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| c0002 | 1/0 | 1398 | 47 | 4 | 4 | 32 | 1 | 5 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| c0003 | 0/0 | 1398 | 23 | 21 | 1 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| c0004 | 0/0 | 1398 | 12 | 10 | 2 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| c0005 | 0/0 | 1398 | 9 | 0 | 0 | 8 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| c0006 | 0/0 | 1398 | 6 | 0 | 2 | 0 | 0 | 4 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| c0007 | 0/0 | 1398 | 5 | 5 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| c0008 | 0/0 | 1383 | 2 | 0 | 0 | 2 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| c0009 | 0/0 | 1398 | 2 | 2 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| c0010 | 0/0 | 1398 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| c0011 | 0/0 | 1398 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| c0012 | 0/0 | 1398 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| c0013 | 0/0 | 1398 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| c0014 | 0/0 | 1398 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| c0015 | 0/0 | 1398 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| c0016 | 0/0 | 1398 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| c0017 | 0/0 | 1427 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| c0018 | 0/0 | 1398 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| c0019 | 0/0 | 1398 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| 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 | 0/0 | 3307 | 90 | 2 | 17 | 57 | 5 | 9 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| t0002 | 0/0 | 3293 | 45 | 11 | 6 | 19 | 3 | 6 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| t0003 | 0/1 | 3309 | 38 | 5 | 13 | 8 | 2 | 9 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| t0004 | 1/0 | 3307 | 32 | 3 | 2 | 22 | 1 | 3 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| t0005 | 0/0 | 3294 | 25 | 22 | 3 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| t0006 | 0/0 | 3307 | 13 | 13 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| t0007 | 0/0 | 3295 | 12 | 0 | 1 | 9 | 0 | 2 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| t0008 | 0/0 | 3332 | 12 | 10 | 2 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| t0009 | 0/0 | 3290 | 9 | 0 | 0 | 9 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| t0010 | 0/0 | 3313 | 9 | 0 | 0 | 9 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| t0011 | 0/0 | 3309 | 8 | 0 | 6 | 0 | 0 | 2 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| t0012 | 0/0 | 3294 | 7 | 7 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| t0013 | 0/0 | 3309 | 6 | 0 | 3 | 0 | 0 | 3 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| t0014 | 0/0 | 3309 | 5 | 5 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| t0015 | 0/0 | 3308 | 4 | 0 | 0 | 4 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| t0016 | 0/0 | 3307 | 4 | 0 | 3 | 0 | 1 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| t0017 | 0/0 | 3254 | 4 | 1 | 0 | 0 | 0 | 3 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| t0018 | 0/0 | 3254 | 4 | 4 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| t0019 | 0/0 | 3293 | 3 | 0 | 1 | 0 | 0 | 2 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| t0020 | 0/0 | 3307 | 3 | 0 | 3 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| t0021 | 0/0 | 3294 | 3 | 3 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| t0022 | 0/0 | 3301 | 2 | 1 | 0 | 0 | 1 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| t0023 | 0/0 | 3301 | 2 | 2 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| t0024 | 0/0 | 3307 | 2 | 0 | 1 | 0 | 1 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| t0025 | 0/0 | 3295 | 2 | 0 | 0 | 2 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| t0026 | 0/0 | 3293 | 2 | 0 | 1 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| t0027 | 0/0 | 3313 | 2 | 0 | 2 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| t0028 | 0/0 | 3294 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| t0029 | 0/0 | 3307 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| t0030 | 0/0 | 3307 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| t0031 | 0/0 | 3282 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| t0032 | 0/0 | 3307 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| t0033 | 0/0 | 3321 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| t0034 | 0/0 | 3309 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| t0035 | 0/0 | 3301 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| t0036 | 0/0 | 3296 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| t0037 | 0/0 | 3293 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| t0038 | 0/0 | 3294 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| t0039 | 0/0 | 3310 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| t0040 | 0/0 | 3301 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| t0041 | 0/0 | 3301 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| t0042 | 0/0 | 3309 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| t0043 | 0/0 | 3293 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| t0044 | 0/0 | 3293 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| t0045 | 0/0 | 3301 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| t0046 | 0/0 | 3307 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| t0047 | 0/0 | 3308 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| t0048 | 0/0 | 3305 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| t0049 | 0/0 | 3307 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0070 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0317 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1398 | 254 | 49 | 58 | 100 | 13 | 33 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0001c0002 | 1/0 | 1398 | 47 | 4 | 4 | 32 | 1 | 5 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0001c0003 | 0/0 | 1398 | 23 | 21 | 1 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0001c0005 | 0/0 | 1398 | 9 | 0 | 0 | 8 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0001c0006 | 0/0 | 1398 | 6 | 0 | 2 | 0 | 0 | 4 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0001c0010 | 0/0 | 1398 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0001c0015 | 0/0 | 1398 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0001c0016 | 0/0 | 1398 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0002c0004 | 0/0 | 1398 | 12 | 10 | 2 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0002c0019 | 0/0 | 1398 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0003c0007 | 0/0 | 1398 | 5 | 5 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0004c0012 | 0/0 | 1398 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0004c0013 | 0/0 | 1398 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0005c0008 | 0/0 | 1383 | 2 | 0 | 0 | 2 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0006c0009 | 0/0 | 1398 | 2 | 2 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0007c0011 | 0/0 | 1398 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0008c0014 | 0/0 | 1398 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0009c0017 | 0/0 | 1427 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0010c0018 | 0/0 | 1398 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4704 | 79 | 1 | 17 | 49 | 5 | 7 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0001c0001t0002 | 0/0 | 4690 | 43 | 11 | 5 | 18 | 3 | 6 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0001c0001t0003 | 0/1 | 4706 | 36 | 3 | 13 | 8 | 2 | 9 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0001c0001t0005 | 0/0 | 4691 | 11 | 10 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0001c0001t0007 | 0/0 | 4692 | 11 | 0 | 1 | 8 | 0 | 2 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0001c0001t0008 | 0/0 | 4729 | 10 | 8 | 2 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0001c0001t0009 | 0/0 | 4687 | 9 | 0 | 0 | 9 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0001c0001t0011 | 0/0 | 4706 | 8 | 0 | 6 | 0 | 0 | 2 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0001c0001t0013 | 0/0 | 4706 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0001c0001t0014 | 0/0 | 4706 | 5 | 5 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0001c0001t0016 | 0/0 | 4704 | 4 | 0 | 3 | 0 | 1 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0001c0001t0017 | 0/0 | 4651 | 4 | 1 | 0 | 0 | 0 | 3 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0001c0001t0019 | 0/0 | 4690 | 3 | 0 | 1 | 0 | 0 | 2 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0001c0001t0020 | 0/0 | 4704 | 3 | 0 | 3 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0001c0001t0021 | 0/0 | 4691 | 3 | 3 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0001c0001t0022 | 0/0 | 4698 | 2 | 1 | 0 | 0 | 1 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0001c0001t0023 | 0/0 | 4698 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0001c0001t0024 | 0/0 | 4704 | 2 | 0 | 1 | 0 | 1 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0001c0001t0025 | 0/0 | 4692 | 2 | 0 | 0 | 2 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0001c0001t0026 | 0/0 | 4690 | 2 | 0 | 1 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0001c0001t0030 | 0/0 | 4704 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0001c0001t0031 | 0/0 | 4679 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0001c0001t0032 | 0/0 | 4704 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0001c0001t0033 | 0/0 | 4718 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0001c0001t0034 | 0/0 | 4706 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0001c0001t0035 | 0/0 | 4698 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0001c0001t0036 | 0/0 | 4693 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0001c0001t0037 | 0/0 | 4690 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0001c0001t0040 | 0/0 | 4698 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0001c0001t0041 | 0/0 | 4698 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0001c0001t0042 | 0/0 | 4706 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0001c0001t0043 | 0/0 | 4690 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0001c0001t0044 | 0/0 | 4690 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0001c0001t0045 | 0/0 | 4698 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0001c0001t0049 | 0/0 | 4704 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0001c0002t0004 | 1/0 | 4704 | 32 | 3 | 2 | 22 | 1 | 3 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0001c0002t0010 | 0/0 | 4710 | 9 | 0 | 0 | 9 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0001c0002t0027 | 0/0 | 4710 | 2 | 0 | 2 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0001c0002t0029 | 0/0 | 4704 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0001c0002t0046 | 0/0 | 4704 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0001c0002t0047 | 0/0 | 4705 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0001c0002t0048 | 0/0 | 4702 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0001c0003t0002 | 0/0 | 4690 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0001c0003t0005 | 0/0 | 4691 | 10 | 9 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0001c0003t0006 | 0/0 | 4704 | 11 | 11 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0001c0003t0028 | 0/0 | 4691 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0001c0005t0001 | 0/0 | 4704 | 5 | 0 | 0 | 4 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0001c0005t0015 | 0/0 | 4705 | 4 | 0 | 0 | 4 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0001c0006t0013 | 0/0 | 4706 | 5 | 0 | 2 | 0 | 0 | 3 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0001c0006t0039 | 0/0 | 4707 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0001c0010t0001 | 0/0 | 4704 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0001c0015t0007 | 0/0 | 4692 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0001c0016t0003 | 0/0 | 4706 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0002c0004t0005 | 0/0 | 4691 | 4 | 3 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0002c0004t0008 | 0/0 | 4729 | 2 | 2 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0002c0004t0018 | 0/0 | 4651 | 4 | 4 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0002c0004t0023 | 0/0 | 4698 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0002c0004t0038 | 0/0 | 4691 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0002c0019t0006 | 0/0 | 4704 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0003c0007t0012 | 0/0 | 4691 | 5 | 5 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0004c0012t0006 | 0/0 | 4704 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0004c0013t0003 | 0/0 | 4706 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0005c0008t0001 | 0/0 | 4689 | 2 | 0 | 0 | 2 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0006c0009t0012 | 0/0 | 4691 | 2 | 2 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0007c0011t0001 | 0/0 | 4704 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0008c0014t0001 | 0/0 | 4704 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0009c0017t0002 | 0/0 | 4719 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| a0010c0018t0001 | 0/0 | 4704 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | copy fasta | chr7 | 2246770 | 2319441 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0003g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0003g0070 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0003g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0003g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0003g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0003g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0003g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0003g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0003g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0003g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0003g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0003g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0003g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0005g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0005g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0005g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0005g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0005g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0005g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0005g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0005g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0005g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0005g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0005g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0007g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0007g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0007g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0007g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0007g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0007g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0007g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0007g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0007g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0007g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0007g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0008g0001 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0008g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0008g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0008g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0008g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0008g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0008g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0008g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0008g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0009g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0009g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0009g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0009g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0009g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0009g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0009g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0009g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0009g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0011g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0011g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0011g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0011g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0011g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0011g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0011g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0011g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0013g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0014g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0014g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0014g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0014g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0014g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0016g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0016g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0016g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0016g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0017g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0017g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0017g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0017g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0019g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0019g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0019g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0020g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0020g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0020g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0021g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0021g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0021g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0022g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0022g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0023g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0024g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0024g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0025g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0025g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0026g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0026g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0030g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0031g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0032g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0033g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0034g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0035g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0036g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0037g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0040g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0041g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0042g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0043g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0044g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0045g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0049g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0004g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0004g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0004g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0004g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0004g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0004g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0004g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0004g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0004g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0004g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0004g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0004g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0004g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0004g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0004g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0004g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0004g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0004g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0004g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0004g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0004g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0004g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0004g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0004g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0004g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0004g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0004g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0004g0317 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0004g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0004g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0004g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0010g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0010g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0010g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0010g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0010g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0010g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0010g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0010g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0010g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0027g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0027g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0029g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0046g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0047g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0048g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0003t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0003t0005g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0003t0005g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0003t0005g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0003t0005g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0003t0005g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0003t0005g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0003t0005g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0003t0005g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0003t0005g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0003t0005g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0003t0006g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0003t0006g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0003t0006g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0003t0006g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0003t0006g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0003t0006g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0003t0006g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0003t0006g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0003t0006g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0003t0006g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0003t0006g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0003t0028g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0005t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0005t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0005t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0005t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0005t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0005t0015g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0005t0015g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0005t0015g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0005t0015g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0006t0013g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0006t0013g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0006t0013g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0006t0013g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0006t0013g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0006t0039g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0010t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0015t0007g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0016t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0002c0004t0005g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0002c0004t0005g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0002c0004t0005g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0002c0004t0008g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0002c0004t0008g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0002c0004t0018g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0002c0004t0018g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0002c0004t0018g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0002c0004t0018g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0002c0004t0023g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0002c0004t0038g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0002c0019t0006g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0003c0007t0012g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0003c0007t0012g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0003c0007t0012g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0003c0007t0012g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0003c0007t0012g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0004c0012t0006g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0004c0013t0003g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0005c0008t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0005c0008t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0006c0009t0012g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0006c0009t0012g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0007c0011t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0008c0014t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0009c0017t0002g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0010c0018t0001g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0231 | EUR | GBR | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0239 | EUR | GBR | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0240 | EUR | FIN | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0071 | EUR | FIN | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG00423 | hp1 | a0001 | c0005 | t0001 | g0057 | EAS | CHS | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | CHS | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | CHS | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | CHS | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0115 | EAS | CHS | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG00558 | hp1 | a0001 | c0002 | t0004 | g0308 | EAS | CHS | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG00558 | hp2 | a0001 | c0001 | t0009 | g0149 | EAS | CHS | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | CHS | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG00597 | hp2 | a0001 | c0002 | t0004 | g0167 | EAS | CHS | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | CHS | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | CHS | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG00639 | hp1 | a0001 | c0002 | t0027 | g0348 | AMR | PUR | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0038 | AMR | PUR | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG00642 | hp1 | a0001 | c0001 | t0013 | g0074 | AMR | PUR | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0180 | AMR | PUR | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG00673 | hp1 | a0001 | c0005 | t0001 | g0220 | EAS | CHS | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG00673 | hp2 | a0001 | c0001 | t0009 | g0108 | EAS | CHS | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG00733 | hp1 | a0009 | c0017 | t0002 | g0327 | AMR | PUR | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0274 | AMR | PUR | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG00735 | hp2 | a0001 | c0006 | t0013 | g0234 | AMR | PUR | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG00738 | hp1 | a0001 | c0001 | t0011 | g0104 | AMR | PUR | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG00738 | hp2 | a0001 | c0001 | t0026 | g0216 | AMR | PUR | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0193 | AMR | PUR | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0243 | AMR | PUR | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01069 | hp1 | a0001 | c0001 | t0011 | g0103 | AMR | PUR | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01069 | hp2 | a0001 | c0006 | t0013 | g0233 | AMR | PUR | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0285 | AMR | PUR | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0223 | AMR | PUR | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0090 | AMR | PUR | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0302 | AMR | PUR | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01081 | hp2 | a0001 | c0001 | t0008 | g0001 | AMR | PUR | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01099 | hp1 | a0001 | c0001 | t0005 | g0352 | AMR | PUR | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01099 | hp2 | a0001 | c0001 | t0011 | g0091 | AMR | PUR | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0088 | AMR | PUR | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01109 | hp1 | a0001 | c0001 | t0008 | g0270 | AMR | PUR | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01109 | hp2 | a0001 | c0001 | t0031 | g0326 | AMR | PUR | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0281 | AMR | PUR | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0102 | AMR | PUR | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0077 | AMR | PUR | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01175 | hp2 | a0001 | c0001 | t0016 | g0333 | AMR | PUR | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0140 | AMR | PUR | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01192 | hp2 | a0001 | c0001 | t0007 | g0273 | AMR | PUR | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01243 | hp1 | a0001 | c0003 | t0005 | g0314 | AMR | PUR | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01243 | hp2 | a0001 | c0002 | t0004 | g0158 | AMR | PUR | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01255 | hp1 | a0002 | c0004 | t0038 | g0358 | AMR | CLM | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01255 | hp2 | a0001 | c0002 | t0004 | g0214 | AMR | CLM | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | CLM | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | CLM | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0286 | AMR | CLM | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01257 | hp2 | a0001 | c0001 | t0024 | g0101 | AMR | CLM | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0324 | AMR | CLM | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | CLM | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01261 | hp2 | a0001 | c0001 | t0020 | g0157 | AMR | CLM | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | CLM | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0304 | AMR | CLM | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01361 | hp1 | a0001 | c0001 | t0042 | g0139 | AMR | CLM | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01361 | hp2 | a0001 | c0001 | t0049 | g0325 | AMR | CLM | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0089 | AMR | CLM | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01433 | hp2 | a0001 | c0001 | t0020 | g0156 | AMR | CLM | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | CLM | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01496 | hp2 | a0002 | c0004 | t0005 | g0366 | AMR | CLM | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0068 | EUR | IBS | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01515 | hp2 | a0001 | c0002 | t0004 | g0284 | EUR | IBS | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0246 | EUR | IBS | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01516 | hp2 | a0001 | c0001 | t0016 | g0236 | EUR | IBS | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0072 | EUR | IBS | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0247 | EUR | IBS | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01884 | hp1 | a0002 | c0004 | t0018 | g0360 | AFR | ACB | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0066 | AFR | ACB | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01891 | hp1 | a0001 | c0001 | t0040 | g0007 | AFR | ACB | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0118 | AFR | ACB | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01934 | hp1 | a0001 | c0001 | t0019 | g0225 | AMR | PEL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01934 | hp2 | a0001 | c0001 | t0016 | g0235 | AMR | PEL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01943 | hp1 | a0001 | c0001 | t0020 | g0207 | AMR | PEL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01975 | hp1 | a0001 | c0001 | t0011 | g0112 | AMR | PEL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01975 | hp2 | a0001 | c0002 | t0027 | g0189 | AMR | PEL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01978 | hp1 | a0001 | c0001 | t0016 | g0237 | AMR | PEL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PEL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0192 | AMR | PEL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0350 | AMR | PEL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | KHV | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02015 | hp2 | a0001 | c0010 | t0001 | g0003 | EAS | KHV | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02040 | hp1 | a0001 | c0002 | t0010 | g0336 | EAS | KHV | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | KHV | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02055 | hp1 | a0001 | c0003 | t0005 | g0292 | AFR | ACB | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02055 | hp2 | a0001 | c0003 | t0006 | g0322 | AFR | ACB | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02056 | hp1 | a0001 | c0001 | t0036 | g0023 | EAS | KHV | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02056 | hp2 | a0001 | c0001 | t0003 | g0086 | EAS | KHV | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02074 | hp2 | a0001 | c0002 | t0004 | g0190 | EAS | KHV | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02080 | hp1 | a0001 | c0002 | t0010 | g0338 | EAS | KHV | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | KHV | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02083 | hp1 | a0001 | c0005 | t0001 | g0219 | EAS | KHV | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0345 | EAS | KHV | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02132 | hp1 | a0001 | c0002 | t0010 | g0339 | EAS | KHV | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0268 | EAS | KHV | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02145 | hp1 | a0001 | c0002 | t0004 | g0147 | AFR | ACB | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02145 | hp2 | a0001 | c0003 | t0005 | g0008 | AFR | ACB | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02155 | hp1 | a0001 | c0001 | t0009 | g0111 | EAS | CDX | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0340 | EAS | CDX | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0341 | EAS | CDX | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0116 | EAS | CDX | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02257 | hp1 | a0007 | c0011 | t0001 | g0004 | AFR | ACB | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02257 | hp2 | a0001 | c0001 | t0041 | g0150 | AFR | ACB | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02258 | hp1 | a0004 | c0013 | t0003 | g0005 | AFR | ACB | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02258 | hp2 | a0001 | c0001 | t0023 | g0122 | AFR | ACB | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PEL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PEL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02280 | hp1 | a0002 | c0019 | t0006 | g0356 | AFR | ACB | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02280 | hp2 | a0001 | c0001 | t0005 | g0012 | AFR | ACB | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | PEL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02293 | hp2 | a0001 | c0001 | t0011 | g0155 | AMR | PEL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02300 | hp1 | a0001 | c0001 | t0011 | g0105 | AMR | PEL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02451 | hp1 | a0001 | c0003 | t0006 | g0042 | AFR | ACB | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02451 | hp2 | a0001 | c0001 | t0014 | g0300 | AFR | ACB | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02523 | hp1 | a0001 | c0001 | t0043 | g0251 | EAS | KHV | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02523 | hp2 | a0001 | c0002 | t0010 | g0335 | EAS | KHV | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0037 | AFR | GWD | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02572 | hp2 | a0001 | c0001 | t0014 | g0295 | AFR | GWD | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0264 | SAS | PJL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02602 | hp2 | a0001 | c0001 | t0017 | g0209 | SAS | PJL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0129 | AFR | GWD | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02615 | hp2 | a0001 | c0001 | t0008 | g0125 | AFR | GWD | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02622 | hp1 | a0001 | c0001 | t0005 | g0011 | AFR | GWD | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02622 | hp2 | a0002 | c0004 | t0005 | g0002 | AFR | GWD | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0017 | AFR | GWD | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02630 | hp2 | a0001 | c0003 | t0005 | g0332 | AFR | GWD | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02647 | hp1 | a0001 | c0003 | t0005 | g0151 | AFR | GWD | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02647 | hp2 | a0001 | c0002 | t0004 | g0015 | AFR | GWD | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02698 | hp1 | a0001 | c0002 | t0004 | g0307 | SAS | PJL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0320 | SAS | PJL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0113 | AFR | GWD | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02717 | hp2 | a0001 | c0003 | t0006 | g0014 | AFR | GWD | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02723 | hp1 | a0002 | c0004 | t0008 | g0361 | AFR | GWD | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0311 | AFR | GWD | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0283 | SAS | PJL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02735 | hp2 | a0001 | c0001 | t0017 | g0205 | SAS | PJL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0183 | SAS | PJL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02738 | hp2 | a0001 | c0001 | t0007 | g0181 | SAS | PJL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02809 | hp1 | a0001 | c0001 | t0014 | g0298 | AFR | GWD | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02809 | hp2 | a0001 | c0001 | t0021 | g0354 | AFR | GWD | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02818 | hp1 | a0006 | c0009 | t0012 | g0368 | AFR | GWD | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02818 | hp2 | a0002 | c0004 | t0005 | g0367 | AFR | GWD | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02886 | hp1 | a0003 | c0007 | t0012 | g0133 | AFR | GWD | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02886 | hp2 | a0002 | c0004 | t0023 | g0359 | AFR | GWD | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02895 | hp1 | a0002 | c0004 | t0018 | g0362 | AFR | GWD | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02895 | hp2 | a0001 | c0001 | t0005 | g0313 | AFR | GWD | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02897 | hp1 | a0002 | c0004 | t0018 | g0363 | AFR | GWD | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02897 | hp2 | a0001 | c0001 | t0005 | g0280 | AFR | GWD | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0100 | AFR | ESN | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02922 | hp2 | a0003 | c0007 | t0012 | g0131 | AFR | ESN | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02965 | hp1 | a0001 | c0001 | t0022 | g0166 | AFR | ESN | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02965 | hp2 | a0001 | c0001 | t0008 | g0096 | AFR | ESN | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02970 | hp1 | a0001 | c0001 | t0021 | g0303 | AFR | ESN | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02970 | hp2 | a0003 | c0007 | t0012 | g0092 | AFR | ESN | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02976 | hp1 | a0001 | c0003 | t0006 | g0010 | AFR | ESN | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02976 | hp2 | a0001 | c0003 | t0006 | g0044 | AFR | ESN | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03017 | hp1 | a0001 | c0001 | t0007 | g0329 | SAS | PJL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03017 | hp2 | a0001 | c0002 | t0004 | g0245 | SAS | PJL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03041 | hp1 | a0001 | c0001 | t0008 | g0170 | AFR | GWD | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03041 | hp2 | a0001 | c0003 | t0005 | g0347 | AFR | GWD | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0083 | AFR | MSL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03098 | hp2 | a0001 | c0001 | t0005 | g0080 | AFR | MSL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03139 | hp1 | a0001 | c0001 | t0037 | g0121 | AFR | ESN | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03139 | hp2 | a0003 | c0007 | t0012 | g0009 | AFR | ESN | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03195 | hp1 | a0001 | c0001 | t0008 | g0098 | AFR | ESN | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03195 | hp2 | a0001 | c0003 | t0006 | g0043 | AFR | ESN | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03209 | hp1 | a0001 | c0001 | t0035 | g0152 | AFR | MSL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03209 | hp2 | a0002 | c0004 | t0005 | g0002 | AFR | MSL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03225 | hp1 | a0001 | c0001 | t0008 | g0162 | AFR | MSL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03225 | hp2 | a0006 | c0009 | t0012 | g0357 | AFR | MSL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0160 | SAS | PJL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0258 | SAS | PJL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03453 | hp1 | a0001 | c0003 | t0005 | g0315 | AFR | MSL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03453 | hp2 | a0001 | c0003 | t0005 | g0316 | AFR | MSL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03486 | hp1 | a0001 | c0001 | t0014 | g0047 | AFR | MSL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03486 | hp2 | a0001 | c0001 | t0008 | g0097 | AFR | MSL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0145 | SAS | PJL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03491 | hp1 | a0001 | c0001 | t0019 | g0226 | SAS | PJL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0132 | AFR | ESN | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03516 | hp2 | a0001 | c0003 | t0006 | g0013 | AFR | ESN | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | GWD | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03540 | hp2 | a0002 | c0004 | t0008 | g0365 | AFR | GWD | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03579 | hp1 | a0001 | c0001 | t0034 | g0299 | AFR | MSL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03579 | hp2 | a0001 | c0001 | t0005 | g0169 | AFR | MSL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0232 | SAS | PJL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03654 | hp2 | a0010 | c0018 | t0001 | g0355 | SAS | PJL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03669 | hp1 | a0001 | c0002 | t0029 | g0075 | SAS | PJL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0067 | SAS | PJL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0136 | SAS | STU | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0076 | SAS | STU | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0306 | SAS | PJL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03710 | hp2 | a0001 | c0001 | t0030 | g0159 | SAS | PJL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03831 | hp1 | a0001 | c0006 | t0013 | g0276 | SAS | BEB | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03831 | hp2 | a0001 | c0001 | t0011 | g0137 | SAS | BEB | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | BEB | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03834 | hp2 | a0001 | c0001 | t0019 | g0069 | SAS | BEB | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03927 | hp1 | a0001 | c0006 | t0013 | g0176 | SAS | BEB | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03927 | hp2 | a0001 | c0002 | t0004 | g0294 | SAS | BEB | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0296 | SAS | BEB | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03942 | hp2 | a0001 | c0001 | t0026 | g0201 | SAS | BEB | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG04115 | hp1 | a0001 | c0001 | t0011 | g0128 | SAS | STU | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG04115 | hp2 | a0001 | c0006 | t0013 | g0194 | SAS | STU | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG04184 | hp1 | a0001 | c0002 | t0046 | g0171 | SAS | BEB | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0256 | SAS | BEB | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG04199 | hp1 | a0001 | c0006 | t0039 | g0144 | SAS | STU | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0227 | SAS | STU | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG04204 | hp1 | a0001 | c0001 | t0017 | g0211 | SAS | STU | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG04204 | hp2 | a0001 | c0005 | t0001 | g0254 | SAS | STU | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0109 | SAS | STU | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0242 | SAS | STU | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18522 | hp1 | a0003 | c0007 | t0012 | g0039 | AFR | YRI | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18522 | hp2 | a0002 | c0004 | t0018 | g0364 | AFR | YRI | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | CHB | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0186 | EAS | CHB | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | CHB | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | CHB | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18906 | hp1 | a0001 | c0001 | t0014 | g0278 | AFR | YRI | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18906 | hp2 | a0001 | c0001 | t0005 | g0164 | AFR | YRI | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18939 | hp2 | a0001 | c0002 | t0004 | g0230 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18940 | hp1 | a0001 | c0001 | t0007 | g0036 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18940 | hp2 | a0001 | c0002 | t0004 | g0079 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18941 | hp1 | a0001 | c0002 | t0010 | g0244 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18941 | hp2 | a0001 | c0001 | t0007 | g0019 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18942 | hp2 | a0001 | c0001 | t0045 | g0252 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18943 | hp1 | a0001 | c0005 | t0015 | g0032 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18943 | hp2 | a0001 | c0001 | t0025 | g0107 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18944 | hp1 | a0001 | c0005 | t0015 | g0029 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18944 | hp2 | a0001 | c0002 | t0004 | g0034 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18946 | hp1 | a0001 | c0001 | t0007 | g0025 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18947 | hp1 | a0001 | c0001 | t0009 | g0148 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18947 | hp2 | a0001 | c0001 | t0007 | g0033 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18952 | hp2 | a0001 | c0005 | t0015 | g0030 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18954 | hp1 | a0001 | c0002 | t0004 | g0287 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18959 | hp1 | a0001 | c0005 | t0015 | g0020 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18960 | hp2 | a0001 | c0002 | t0004 | g0228 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18963 | hp1 | a0001 | c0015 | t0007 | g0022 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18963 | hp2 | a0001 | c0002 | t0004 | g0261 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0114 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18970 | hp1 | a0001 | c0001 | t0032 | g0305 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18971 | hp1 | a0001 | c0002 | t0048 | g0222 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18973 | hp2 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0346 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18977 | hp1 | a0001 | c0001 | t0009 | g0021 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18977 | hp2 | a0001 | c0002 | t0004 | g0328 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18979 | hp2 | a0001 | c0001 | t0007 | g0179 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18981 | hp2 | a0001 | c0002 | t0010 | g0344 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18983 | hp1 | a0001 | c0001 | t0009 | g0202 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18983 | hp2 | a0001 | c0001 | t0044 | g0094 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18985 | hp1 | a0001 | c0002 | t0004 | g0289 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18990 | hp1 | a0001 | c0002 | t0004 | g0323 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18991 | hp1 | a0001 | c0003 | t0002 | g0064 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18991 | hp2 | a0001 | c0002 | t0004 | g0331 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18997 | hp1 | a0001 | c0002 | t0004 | g0185 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19002 | hp1 | a0001 | c0001 | t0007 | g0106 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19003 | hp2 | a0001 | c0002 | t0004 | g0290 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0343 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19005 | hp2 | a0001 | c0002 | t0004 | g0291 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19009 | hp1 | a0005 | c0008 | t0001 | g0249 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19010 | hp1 | a0001 | c0002 | t0004 | g0309 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0342 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19012 | hp2 | a0001 | c0002 | t0004 | g0288 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19030 | hp1 | a0001 | c0002 | t0047 | g0161 | AFR | LWK | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19030 | hp2 | a0001 | c0003 | t0006 | g0045 | AFR | LWK | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19043 | hp1 | a0001 | c0001 | t0021 | g0351 | AFR | LWK | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19043 | hp2 | a0001 | c0003 | t0006 | g0310 | AFR | LWK | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19054 | hp1 | a0001 | c0002 | t0004 | g0182 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19054 | hp2 | a0001 | c0001 | t0009 | g0312 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19055 | hp1 | a0001 | c0001 | t0025 | g0093 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19057 | hp1 | a0001 | c0001 | t0033 | g0126 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19057 | hp2 | a0001 | c0002 | t0010 | g0349 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0117 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19066 | hp1 | a0001 | c0002 | t0004 | g0127 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19077 | hp1 | a0001 | c0001 | t0007 | g0024 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19077 | hp2 | a0001 | c0002 | t0004 | g0260 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19079 | hp1 | a0001 | c0002 | t0004 | g0265 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0330 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19081 | hp1 | a0001 | c0002 | t0010 | g0337 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19081 | hp2 | a0005 | c0008 | t0001 | g0215 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19082 | hp1 | a0001 | c0002 | t0010 | g0321 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19087 | hp2 | a0001 | c0001 | t0009 | g0130 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19088 | hp2 | a0008 | c0014 | t0001 | g0213 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19090 | hp2 | a0001 | c0001 | t0007 | g0187 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19240 | hp1 | a0001 | c0003 | t0006 | g0082 | AFR | YRI | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19240 | hp2 | a0001 | c0001 | t0008 | g0001 | AFR | YRI | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA20129 | hp1 | a0001 | c0001 | t0005 | g0163 | AFR | ASW | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA20129 | hp2 | a0001 | c0003 | t0005 | g0334 | AFR | ASW | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0073 | EUR | TSI | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0191 | EUR | TSI | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA20805 | hp1 | a0001 | c0001 | t0022 | g0165 | EUR | TSI | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA20805 | hp2 | a0001 | c0001 | t0024 | g0099 | EUR | TSI | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0319 | SAS | GIH | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | GIH | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02109 | hp1 | a0001 | c0003 | t0006 | g0046 | AFR | ACB | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02109 | hp2 | a0001 | c0001 | t0005 | g0353 | AFR | ACB | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02486 | hp1 | a0001 | c0003 | t0005 | g0016 | AFR | ACB | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0259 | AFR | ACB | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0318 | AFR | ACB | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0040 | AFR | ACB | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03471 | hp1 | a0004 | c0012 | t0006 | g0006 | AFR | MSL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03471 | hp2 | a0001 | c0002 | t0004 | g0168 | AFR | MSL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0110 | AFR | USA | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG06807 | hp2 | a0001 | c0001 | t0008 | g0048 | AFR | USA | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18955 | hp1 | a0001 | c0001 | t0009 | g0081 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18955 | hp2 | a0001 | c0005 | t0001 | g0154 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA20300 | hp1 | a0001 | c0003 | t0028 | g0293 | AFR | USA | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0301 | AFR | USA | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA21309 | hp1 | a0001 | c0001 | t0017 | g0196 | AFR | LWK | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA21309 | hp2 | a0001 | c0016 | t0003 | g0065 | AFR | LWK | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0070 | REF | REF | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0004 | g0317 | REF | REF | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:2263342
|
G | A | 2 | a0003a0006 | 7 | HG02818.hp1 HG02886.hp1 HG02922.hp2 others(4): Show |
missense_variant | MODERATE | c.803C>T | p.Thr268Ile | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/11 | 823/4704 | 803/1398 | 268/465 | chr7 | 2263342 | ||
| chr7:2278158
|
A | C | 1 | a0008 | 1 | NA19088.hp2 | missense_variant | MODERATE | c.242T>G | p.Leu81Arg | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/11 | 262/4704 | 242/1398 | 81/465 | chr7 | 2278158 | ||
| chr7:2278266
|
ACGATGGC others(8): Show |
A | 1 | a0005 | 2 | NA19009.hp1 NA19081.hp2 |
disruptive_inframe_deletion | MODERATE | c.119_133delAGCCCCAG others(7): Show |
p.Glu40_Ile44del | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/11 | 153/4704 | 119/1398 | 40/465 | chr7 | 2278266 | ||
| chr7:2278294
|
G | GTGTCGGC others(22): Show |
1 | a0009 | 1 | HG00733.hp1 | frameshift_variant | HIGH | c.95-18_105dupTCACCA others(23): Show |
p.Pro36fs | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/11 | 125/4704 | 105/1398 | 35/465 | chr7 | 2278294 | ||
| chr7:2314345
|
G | A | 1 | a0010 | 1 | HG03654.hp2 | missense_variant | MODERATE | c.77C>T | p.Ala26Val | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/11 | 97/4704 | 77/1398 | 26/465 | chr7 | 2314345 | ||
| chr7:2314365
|
C | G | 1 | a0004 | 2 | HG02258.hp1 HG03471.hp1 |
missense_variant | MODERATE | c.57G>C | p.Glu19Asp | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/11 | 77/4704 | 57/1398 | 19/465 | chr7 | 2314365 | ||
| chr7:2314381
|
A | C | 1 | a0007 | 1 | HG02257.hp1 | missense_variant | MODERATE | c.41T>G | p.Val14Gly | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/11 | 61/4704 | 41/1398 | 14/465 | chr7 | 2314381 | ||
| chr7:2314399
|
G | C | 2 | a0002a0006 | 15 | HG01255.hp1 HG01496.hp2 HG01884.hp1 others(12): Show |
missense_variant | MODERATE | c.23C>G | p.Pro8Arg | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/11 | 43/4704 | 23/1398 | 8/465 | chr7 | 2314399 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:2257371
|
A | G | 18 | a0001c0001a0001c0003a0001c0005others(15): Show | 323 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(320): Show |
synonymous_variant | LOW | c.1128T>C | p.Ile376Ile | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 9/11 | 1148/4704 | 1128/1398 | 376/465 | chr7 | 2257371 | ||
| chr7:2257407
|
G | C | 1 | a0001c0015 | 1 | NA18963.hp1 | synonymous_variant | LOW | c.1092C>G | p.Arg364Arg | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 9/11 | 1112/4704 | 1092/1398 | 364/465 | chr7 | 2257407 | ||
| chr7:2264351
|
T | C | 15 | a0001c0001a0001c0005a0001c0006others(12): Show | 298 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(295): Show |
synonymous_variant | LOW | c.729A>G | p.Ala243Ala | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 6/11 | 749/4704 | 729/1398 | 243/465 | chr7 | 2264351 | ||
| chr7:2269574
|
C | T | 1 | a0001c0006 | 6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
synonymous_variant | LOW | c.606G>A | p.Leu202Leu | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/11 | 626/4704 | 606/1398 | 202/465 | chr7 | 2269574 | ||
| chr7:2275167
|
C | A | 1 | a0001c0016 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.363G>T | p.Leu121Leu | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/11 | 383/4704 | 363/1398 | 121/465 | chr7 | 2275167 | ||
| chr7:2275209
|
G | A | 2 | a0001c0005a0001c0010 | 10 | HG00423.hp1 HG00673.hp1 HG02015.hp2 others(7): Show |
synonymous_variant | LOW | c.321C>T | p.Tyr107Tyr | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/11 | 341/4704 | 321/1398 | 107/465 | chr7 | 2275209 | ||
| chr7:2314389
|
C | T | 1 | a0001c0010 | 1 | HG02015.hp2 | synonymous_variant | LOW | c.33G>A | p.Ala11Ala | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/11 | 53/4704 | 33/1398 | 11/465 | chr7 | 2314389 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:2251923
|
A | C | 1 | a0001c0001t0040 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3133T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 3133 | chr7 | 2251923 | |||||
| chr7:2252043
|
G | A | 1 | a0001c0001t0022 | 2 | HG02965.hp1 NA20805.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3013C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 3013 | chr7 | 2252043 | |||||
| chr7:2252143
|
ACCCCCCT others(7): Show |
A | 17 | a0001c0001t0002a0001c0001t0005a0001c0001t0009others(14): Show | 99 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*2899_*2912delCCGT others(10): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 2899 | chr7 | 2252143 | |||||
| chr7:2252162
|
G | A | 1 | a0001c0001t0043 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2894C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 2894 | chr7 | 2252162 | |||||
| chr7:2252169
|
G | A | 1 | a0001c0001t0044 | 1 | NA18983.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2887C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 2887 | chr7 | 2252169 | |||||
| chr7:2252259
|
A | AGCTTGG | 2 | a0001c0002t0010a0001c0002t0027 | 11 | HG00639.hp1 HG01975.hp2 HG02040.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2791_*2796dupCCAA others(2): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 2796 | chr7 | 2252259 | |||||
| chr7:2252275
|
G | A | 10 | a0001c0001t0003a0001c0001t0011a0001c0001t0023others(7): Show | 52 | HG00544.hp1 HG00639.hp2 HG00738.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*2781C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 2781 | chr7 | 2252275 | |||||
| chr7:2252308
|
G | A | 19 | a0001c0001t0001a0001c0001t0007a0001c0001t0016others(16): Show | 121 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*2748C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 2748 | chr7 | 2252308 | |||||
| chr7:2252389
|
G | A | 1 | a0001c0002t0046 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2667C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 2667 | chr7 | 2252389 | |||||
| chr7:2252533
|
GC | G | 1 | a0001c0005t0015 | 4 | NA18943.hp1 NA18944.hp1 NA18952.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2522delG | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 2522 | chr7 | 2252533 | |||||
| chr7:2252585
|
C | T | 1 | a0001c0001t0016 | 4 | HG01175.hp2 HG01516.hp2 HG01934.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2471G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 2471 | chr7 | 2252585 | |||||
| chr7:2252624
|
C | T | 3 | a0001c0001t0013a0001c0006t0013a0001c0006t0039 | 7 | HG00642.hp1 HG00735.hp2 HG01069.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2432G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 2432 | chr7 | 2252624 | |||||
| chr7:2252670
|
G | GC | 11 | a0001c0001t0005a0001c0001t0021a0001c0001t0036others(8): Show | 40 | HG01099.hp1 HG01243.hp1 HG01255.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*2385dupG | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 2385 | chr7 | 2252670 | |||||
| chr7:2252681
|
T | G | 61 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(58): Show | 323 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(320): Show |
3_prime_UTR_variant | MODIFIER | c.*2375A>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 2375 | chr7 | 2252681 | |||||
| chr7:2252695
|
C | CCACCCCT others(16): Show |
2 | a0001c0001t0008a0002c0004t0008 | 12 | HG01081.hp2 HG01109.hp1 HG02615.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2338_*2360dupAGGA others(19): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 2360 | chr7 | 2252695 | |||||
| chr7:2252711
|
GCTCTCCT others(18): Show |
G | 3 | a0001c0001t0017a0001c0001t0031a0002c0004t0018 | 9 | HG01109.hp2 HG01884.hp1 HG02602.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2320_*2344delAGCA others(21): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 2320 | chr7 | 2252711 | |||||
| chr7:2252848
|
TCTC | T | 1 | a0001c0001t0009 | 9 | HG00558.hp2 HG00673.hp2 HG02155.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2205_*2207delGAG | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 2205 | chr7 | 2252848 | |||||
| chr7:2252867
|
CTGCTCTC others(15): Show |
C | 2 | a0001c0001t0017a0002c0004t0018 | 8 | HG01884.hp1 HG02602.hp2 HG02735.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2167_*2188delAGGG others(18): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 2167 | chr7 | 2252867 | |||||
| chr7:2252891
|
GCT | G | 33 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(30): Show | 204 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(201): Show |
3_prime_UTR_variant | MODIFIER | c.*2163_*2164delAG | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 2163 | chr7 | 2252891 | |||||
| chr7:2252982
|
CCCTGTTC others(1): Show |
C | 13 | a0001c0001t0007a0001c0001t0017a0001c0001t0022others(10): Show | 31 | HG01192.hp2 HG01884.hp1 HG01891.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*2066_*2073delAGAA others(4): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 2066 | chr7 | 2252982 | |||||
| chr7:2253092
|
G | A | 1 | a0001c0001t0032 | 1 | NA18970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1964C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 1964 | chr7 | 2253092 | |||||
| chr7:2253126
|
T | C | 1 | a0001c0001t0041 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1930A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 1930 | chr7 | 2253126 | |||||
| chr7:2253246
|
C | CTG | 58 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(55): Show | 310 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(307): Show |
3_prime_UTR_variant | MODIFIER | c.*1808_*1809dupCA | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 1809 | chr7 | 2253246 | |||||
| chr7:2253292
|
A | G | 1 | a0001c0001t0017 | 4 | HG02602.hp2 HG02735.hp2 HG04204.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1764T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 1764 | chr7 | 2253292 | |||||
| chr7:2253423
|
G | C | 1 | a0001c0001t0042 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1633C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 1633 | chr7 | 2253423 | |||||
| chr7:2253486
|
G | A | 1 | a0002c0004t0038 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1570C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 1570 | chr7 | 2253486 | |||||
| chr7:2253570
|
G | GGCCAGAA others(7): Show |
1 | a0001c0001t0033 | 1 | NA19057.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1472_*1485dupTGCT others(10): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 1485 | chr7 | 2253570 | |||||
| chr7:2253590
|
C | T | 1 | a0001c0002t0027 | 2 | HG00639.hp1 HG01975.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1466G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 1466 | chr7 | 2253590 | |||||
| chr7:2253721
|
C | T | 1 | a0001c0001t0034 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1335G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 1335 | chr7 | 2253721 | |||||
| chr7:2253858
|
G | A | 1 | a0001c0001t0020 | 3 | HG01261.hp2 HG01433.hp2 HG01943.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1198C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 1198 | chr7 | 2253858 | |||||
| chr7:2253874
|
G | A | 20 | a0001c0001t0002a0001c0001t0005a0001c0001t0009others(17): Show | 104 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*1182C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 1182 | chr7 | 2253874 | |||||
| chr7:2253916
|
C | T | 7 | a0001c0001t0005a0001c0001t0021a0001c0001t0037others(4): Show | 31 | HG01099.hp1 HG01243.hp1 HG01255.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*1140G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 1140 | chr7 | 2253916 | |||||
| chr7:2253919
|
CCAGGGA | C | 4 | a0001c0001t0007a0001c0001t0025a0001c0001t0036others(1): Show | 15 | HG01192.hp2 HG02056.hp1 HG02738.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1131_*1136delTCCC others(2): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 1131 | chr7 | 2253919 | |||||
| chr7:2253926
|
G | A | 1 | a0001c0001t0025 | 2 | NA18943.hp2 NA19055.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1130C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 1130 | chr7 | 2253926 | |||||
| chr7:2253971
|
T | C | 1 | a0001c0001t0026 | 2 | HG00738.hp2 HG03942.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1085A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 1085 | chr7 | 2253971 | |||||
| chr7:2253974
|
A | G | 58 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(55): Show | 310 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(307): Show |
3_prime_UTR_variant | MODIFIER | c.*1082T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 1082 | chr7 | 2253974 | |||||
| chr7:2254249
|
C | T | 1 | a0001c0001t0035 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*807G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 807 | chr7 | 2254249 | |||||
| chr7:2254288
|
C | T | 2 | a0001c0001t0014a0001c0001t0034 | 6 | HG02451.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*768G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 768 | chr7 | 2254288 | |||||
| chr7:2254488
|
C | T | 15 | a0001c0001t0001a0001c0001t0016a0001c0001t0020others(12): Show | 106 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*568G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 568 | chr7 | 2254488 | |||||
| chr7:2254618
|
C | T | 1 | a0001c0002t0029 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*438G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 438 | chr7 | 2254618 | |||||
| chr7:2254749
|
T | C | 1 | a0001c0001t0049 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*307A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 307 | chr7 | 2254749 | |||||
| chr7:2254766
|
A | G | 1 | a0001c0001t0019 | 3 | HG01934.hp1 HG03491.hp1 HG03834.hp2 |
3_prime_UTR_variant | MODIFIER | c.*290T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 290 | chr7 | 2254766 | |||||
| chr7:2254864
|
A | T | 1 | a0001c0001t0022 | 2 | HG02965.hp1 NA20805.hp1 |
3_prime_UTR_variant | MODIFIER | c.*192T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 192 | chr7 | 2254864 | |||||
| chr7:2254947
|
G | A | 1 | a0001c0001t0021 | 3 | HG02809.hp2 HG02970.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*109C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 109 | chr7 | 2254947 | |||||
| chr7:2254972
|
C | T | 1 | a0001c0001t0011 | 8 | HG00738.hp1 HG01069.hp1 HG01099.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*84G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 84 | chr7 | 2254972 | |||||
| chr7:2255024
|
G | T | 1 | a0001c0003t0028 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*32C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 32 | chr7 | 2255024 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:2255209
|
C | T | 1 | a0001c0003t0005g0315 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1285-40G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 10/10 | chr7 | 2255209 | ||||||
| chr7:2255210
|
C | T | 1 | a0001c0001t0009g0108 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1285-41G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 10/10 | chr7 | 2255210 | ||||||
| chr7:2255348
|
G | A | 1 | a0002c0004t0023g0359 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1285-179C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 10/10 | chr7 | 2255348 | ||||||
| chr7:2255359
|
C | A | 1 | a0001c0001t0002g0109 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1285-190G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 10/10 | chr7 | 2255359 | ||||||
| chr7:2255582
|
C | G | 1 | a0001c0001t0008g0162 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1285-413G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 10/10 | chr7 | 2255582 | ||||||
| chr7:2255595
|
C | T | 2 | a0001c0001t0001g0199a0001c0001t0001g0258 | 2 | HG00735.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1285-426G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 10/10 | chr7 | 2255595 | ||||||
| chr7:2255886
|
G | T | 1 | a0001c0001t0001g0200 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1285-717C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 10/10 | chr7 | 2255886 | ||||||
| chr7:2256167
|
TA | T | 183 | a0001c0001t0001g0200a0001c0001t0002g0017a0001c0001t0002g0018others(180): Show | 185 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(182): Show |
intron_variant | MODIFIER | c.1284+706delT | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 10/10 | chr7 | 2256167 | ||||||
| chr7:2256278
|
C | G | 1 | a0001c0001t0007g0329 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1284+596G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 10/10 | chr7 | 2256278 | ||||||
| chr7:2256283
|
G | A | 1 | a0001c0001t0007g0329 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1284+591C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 10/10 | chr7 | 2256283 | ||||||
| chr7:2256418
|
G | C | 1 | a0001c0001t0007g0329 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1284+456C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 10/10 | chr7 | 2256418 | ||||||
| chr7:2256449
|
G | A | 2 | a0001c0001t0022g0165a0001c0001t0022g0166 | 2 | HG02965.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1284+425C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 10/10 | chr7 | 2256449 | ||||||
| chr7:2256495
|
G | A | 1 | a0001c0001t0030g0159 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1284+379C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 10/10 | chr7 | 2256495 | ||||||
| chr7:2256732
|
T | C | 1 | a0001c0001t0009g0312 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1284+142A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 10/10 | chr7 | 2256732 | ||||||
| chr7:2256787
|
G | A | 2 | a0001c0001t0003g0068a0001c0001t0003g0072 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1284+87C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 10/10 | chr7 | 2256787 | ||||||
| chr7:2256858
|
A | G | 294 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(291): Show | 295 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.1284+16T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 10/10 | chr7 | 2256858 | ||||||
| chr7:2256865
|
C | A | 5 | a0001c0001t0014g0047a0001c0001t0014g0278a0001c0001t0014g0295others(2): Show | 5 | HG02451.hp2 HG02572.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1284+9G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 10/10 | chr7 | 2256865 | ||||||
| chr7:2257061
|
C | A | 99 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0026others(96): Show | 100 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.1135-38G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 9/10 | chr7 | 2257061 | ||||||
| chr7:2257087
|
A | T | 70 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0026others(67): Show | 70 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.1135-64T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 9/10 | chr7 | 2257087 | ||||||
| chr7:2257088
|
C | T | 7 | a0001c0005t0001g0057a0001c0005t0001g0154a0001c0005t0001g0254others(4): Show | 7 | HG00423.hp1 HG04204.hp2 NA18943.hp1 others(4): Show |
intron_variant | MODIFIER | c.1135-65G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 9/10 | chr7 | 2257088 | ||||||
| chr7:2257095
|
G | A | 5 | a0001c0001t0003g0038a0001c0001t0003g0223a0001c0001t0023g0122others(2): Show | 5 | HG00639.hp2 HG01070.hp2 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.1135-72C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 9/10 | chr7 | 2257095 | ||||||
| chr7:2257104
|
G | A | 5 | a0001c0001t0001g0184a0001c0001t0001g0229a0001c0001t0001g0341others(2): Show | 5 | HG00423.hp2 HG00438.hp2 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.1135-81C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 9/10 | chr7 | 2257104 | ||||||
| chr7:2257189
|
G | A | 1 | a0001c0001t0003g0140 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1135-166C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 9/10 | chr7 | 2257189 | ||||||
| chr7:2257577
|
C | T | 42 | a0001c0001t0003g0066a0001c0001t0003g0067a0001c0001t0003g0068others(39): Show | 42 | HG00544.hp1 HG00738.hp1 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.985-63G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 8/10 | chr7 | 2257577 | ||||||
| chr7:2257596
|
C | T | 4 | a0001c0006t0013g0176a0001c0006t0013g0194a0001c0006t0013g0276others(1): Show | 4 | HG03831.hp1 HG03927.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.985-82G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 8/10 | chr7 | 2257596 | ||||||
| chr7:2257651
|
C | T | 1 | a0001c0001t0007g0329 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.984+84G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 8/10 | chr7 | 2257651 | ||||||
| chr7:2257663
|
G | T | 1 | a0001c0001t0003g0264 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.984+72C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 8/10 | chr7 | 2257663 | ||||||
| chr7:2257685
|
A | C | 1 | a0001c0002t0004g0307 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.984+50T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 8/10 | chr7 | 2257685 | ||||||
| chr7:2258008
|
C | CT | 39 | a0001c0001t0001g0197a0001c0001t0001g0275a0001c0001t0002g0071others(36): Show | 39 | HG00280.hp2 HG00642.hp1 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.916-206dupA | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2258008 | ||||||
| chr7:2258008
|
C | CTT | 31 | a0001c0001t0001g0119a0001c0001t0005g0011a0001c0001t0005g0012others(28): Show | 32 | HG01081.hp2 HG01109.hp1 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.916-207_916-206dup others(2): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2258008 | ||||||
| chr7:2258008
|
CT | C | 12 | a0001c0001t0003g0038a0001c0001t0003g0281a0001c0001t0023g0122others(9): Show | 12 | HG00639.hp2 HG01167.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.916-206delA | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2258008 | ||||||
| chr7:2258031
|
T | A | 5 | a0001c0003t0005g0316a0001c0003t0006g0010a0001c0003t0006g0013others(2): Show | 5 | HG02717.hp2 HG02976.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.916-228A>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2258031 | ||||||
| chr7:2258032
|
C | T | 38 | a0001c0001t0003g0066a0001c0001t0003g0067a0001c0001t0003g0068others(35): Show | 38 | HG00544.hp1 HG00738.hp1 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.916-229G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2258032 | ||||||
| chr7:2258038
|
CT | C | 5 | a0001c0003t0005g0316a0001c0003t0006g0010a0001c0003t0006g0013others(2): Show | 5 | HG02717.hp2 HG02976.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.916-236delA | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2258038 | ||||||
| chr7:2258062
|
A | G | 41 | a0001c0001t0003g0038a0001c0001t0003g0223a0001c0001t0005g0011others(38): Show | 42 | HG00639.hp2 HG01070.hp2 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.916-259T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2258062 | ||||||
| chr7:2258072
|
A | G | 38 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0003g0223others(35): Show | 39 | HG00639.hp2 HG01070.hp2 HG01081.hp2 others(36): Show |
intron_variant | MODIFIER | c.916-269T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2258072 | ||||||
| chr7:2258160
|
T | G | 5 | a0001c0001t0003g0038a0001c0001t0003g0223a0001c0001t0023g0122others(2): Show | 5 | HG00639.hp2 HG01070.hp2 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.916-357A>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2258160 | ||||||
| chr7:2258167
|
T | C | 1 | a0001c0001t0002g0026 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.916-364A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2258167 | ||||||
| chr7:2258184
|
GTATTTC | G | 4 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0008g0270others(1): Show | 4 | HG01109.hp1 HG02280.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.916-387_916-382del others(6): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2258184 | ||||||
| chr7:2258192
|
T | G | 4 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0008g0270others(1): Show | 4 | HG01109.hp1 HG02280.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.916-389A>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2258192 | ||||||
| chr7:2258206
|
C | T | 4 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0008g0270others(1): Show | 4 | HG01109.hp1 HG02280.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.916-403G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2258206 | ||||||
| chr7:2258284
|
G | A | 1 | a0001c0001t0001g0208 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.916-481C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2258284 | ||||||
| chr7:2258295
|
G | T | 1 | a0001c0001t0003g0223 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.916-492C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2258295 | ||||||
| chr7:2258436
|
A | G | 307 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(304): Show | 309 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.916-633T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2258436 | ||||||
| chr7:2258468
|
A | G | 10 | a0001c0001t0001g0119a0001c0001t0007g0019a0001c0001t0007g0024others(7): Show | 10 | HG02056.hp1 NA18940.hp1 NA18941.hp2 others(7): Show |
intron_variant | MODIFIER | c.916-665T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2258468 | ||||||
| chr7:2258568
|
G | A | 2 | a0001c0002t0004g0265a0001c0002t0004g0328 | 2 | NA18977.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.916-765C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2258568 | ||||||
| chr7:2258591
|
C | G | 7 | a0001c0001t0013g0074a0001c0006t0013g0176a0001c0006t0013g0194others(4): Show | 7 | HG00642.hp1 HG00735.hp2 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.916-788G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2258591 | ||||||
| chr7:2258592
|
C | T | 106 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(103): Show | 106 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.916-789G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2258592 | ||||||
| chr7:2258763
|
G | A | 1 | a0001c0002t0010g0338 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.916-960C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2258763 | ||||||
| chr7:2258892
|
T | C | 10 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0008g0270others(7): Show | 10 | HG01109.hp1 HG02280.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.916-1089A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2258892 | ||||||
| chr7:2259047
|
C | T | 3 | a0001c0001t0002g0141a0001c0001t0002g0142a0001c0001t0002g0143 | 3 | NA18995.hp1 NA19009.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.916-1244G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259047 | ||||||
| chr7:2259211
|
C | T | 12 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0008g0270others(9): Show | 12 | HG01109.hp1 HG01884.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.916-1408G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259211 | ||||||
| chr7:2259222
|
C | G | 1 | a0001c0001t0014g0047 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.916-1419G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259222 | ||||||
| chr7:2259250
|
G | A | 1 | a0001c0001t0001g0212 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.916-1447C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259250 | ||||||
| chr7:2259363
|
C | A | 7 | a0001c0001t0013g0074a0001c0006t0013g0176a0001c0006t0013g0194others(4): Show | 7 | HG00642.hp1 HG00735.hp2 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.916-1560G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259363 | ||||||
| chr7:2259375
|
C | G | 3 | a0001c0001t0013g0074a0001c0006t0013g0233a0001c0006t0013g0234 | 3 | HG00642.hp1 HG00735.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.916-1572G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259375 | ||||||
| chr7:2259427
|
T | C | 7 | a0001c0001t0013g0074a0001c0006t0013g0176a0001c0006t0013g0194others(4): Show | 7 | HG00642.hp1 HG00735.hp2 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.916-1624A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259427 | ||||||
| chr7:2259482
|
T | C | 1 | a0001c0001t0003g0037 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.916-1679A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259482 | ||||||
| chr7:2259497
|
G | A | 3 | a0001c0001t0001g0175a0001c0001t0001g0188a0001c0001t0001g0257 | 3 | HG00621.hp2 NA18978.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.916-1694C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259497 | ||||||
| chr7:2259497
|
G | C | 7 | a0001c0001t0013g0074a0001c0006t0013g0176a0001c0006t0013g0194others(4): Show | 7 | HG00642.hp1 HG00735.hp2 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.916-1694C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259497 | ||||||
| chr7:2259666
|
G | A | 8 | a0001c0001t0017g0196a0001c0001t0017g0205a0001c0001t0017g0209others(5): Show | 8 | HG01884.hp1 HG02602.hp2 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.916-1863C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259666 | ||||||
| chr7:2259676
|
G | A | 1 | a0001c0015t0007g0022 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.916-1873C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259676 | ||||||
| chr7:2259707
|
G | A | 1 | a0001c0003t0005g0151 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.916-1904C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259707 | ||||||
| chr7:2259793
|
C | G | 5 | a0001c0003t0005g0316a0001c0003t0006g0010a0001c0003t0006g0013others(2): Show | 5 | HG02717.hp2 HG02976.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.916-1990G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259793 | ||||||
| chr7:2259925
|
A | T | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2122T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259925 | ||||||
| chr7:2259926
|
G | T | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2123C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259926 | ||||||
| chr7:2259927
|
A | T | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2124T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259927 | ||||||
| chr7:2259929
|
G | T | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2126C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259929 | ||||||
| chr7:2259930
|
A | T | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2127T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259930 | ||||||
| chr7:2259932
|
T | G | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2129A>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259932 | ||||||
| chr7:2259935
|
T | A | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2132A>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259935 | ||||||
| chr7:2259948
|
A | T | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2145T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259948 | ||||||
| chr7:2259953
|
A | G | 3 | a0001c0001t0005g0163a0001c0001t0005g0164a0001c0001t0005g0169 | 3 | HG03579.hp2 NA18906.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.916-2150T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259953 | ||||||
| chr7:2259955
|
A | T | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2152T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259955 | ||||||
| chr7:2259957
|
G | A | 1 | a0001c0010t0001g0003 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.916-2154C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259957 | ||||||
| chr7:2259957
|
G | T | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2154C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259957 | ||||||
| chr7:2259958
|
C | G | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2155G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259958 | ||||||
| chr7:2259962
|
C | T | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2159G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259962 | ||||||
| chr7:2259964
|
C | T | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2161G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259964 | ||||||
| chr7:2259966
|
A | T | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2163T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259966 | ||||||
| chr7:2259968
|
G | T | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2165C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259968 | ||||||
| chr7:2259969
|
A | T | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2166T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259969 | ||||||
| chr7:2259970
|
T | C | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2167A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259970 | ||||||
| chr7:2259983
|
A | T | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2180T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259983 | ||||||
| chr7:2259984
|
A | C | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2181T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259984 | ||||||
| chr7:2259986
|
A | T | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2183T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259986 | ||||||
| chr7:2259987
|
A | T | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2184T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259987 | ||||||
| chr7:2259989
|
A | T | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2186T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259989 | ||||||
| chr7:2259990
|
A | T | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2187T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259990 | ||||||
| chr7:2259999
|
G | A | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2196C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259999 | ||||||
| chr7:2260007
|
AAAGAGAG others(38): Show |
A | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2249_916-2205d others(47): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260007 | ||||||
| chr7:2260053
|
G | T | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2250C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260053 | ||||||
| chr7:2260055
|
A | C | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2252T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260055 | ||||||
| chr7:2260056
|
G | T | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2253C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260056 | ||||||
| chr7:2260057
|
G | C | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2254C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260057 | ||||||
| chr7:2260059
|
C | A | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2256G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260059 | ||||||
| chr7:2260063
|
G | T | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2260C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260063 | ||||||
| chr7:2260065
|
G | C | 114 | a0001c0001t0001g0279a0001c0001t0002g0017a0001c0001t0002g0018others(111): Show | 116 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.916-2262C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260065 | ||||||
| chr7:2260067
|
A | C | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2264T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260067 | ||||||
| chr7:2260068
|
A | G | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2265T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260068 | ||||||
| chr7:2260073
|
C | A | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2270G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260073 | ||||||
| chr7:2260077
|
A | T | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2274T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260077 | ||||||
| chr7:2260080
|
T | G | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2277A>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260080 | ||||||
| chr7:2260083
|
T | G | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2280A>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260083 | ||||||
| chr7:2260084
|
C | G | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2281G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260084 | ||||||
| chr7:2260085
|
A | T | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2282T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260085 | ||||||
| chr7:2260086
|
G | A | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2283C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260086 | ||||||
| chr7:2260088
|
A | T | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2285T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260088 | ||||||
| chr7:2260090
|
G | C | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2287C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260090 | ||||||
| chr7:2260091
|
T | C | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2288A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260091 | ||||||
| chr7:2260095
|
C | A | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2292G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260095 | ||||||
| chr7:2260097
|
G | A | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2294C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260097 | ||||||
| chr7:2260098
|
A | ATAAGACC others(32): Show |
1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2296_916-2295i others(41): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260098 | ||||||
| chr7:2260102
|
G | T | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2299C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260102 | ||||||
| chr7:2260103
|
G | T | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2300C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260103 | ||||||
| chr7:2260104
|
C | T | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2301G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260104 | ||||||
| chr7:2260118
|
C | T | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2315G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260118 | ||||||
| chr7:2260135
|
A | G | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2332T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260135 | ||||||
| chr7:2260152
|
G | A | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2349C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260152 | ||||||
| chr7:2260156
|
C | T | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2353G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260156 | ||||||
| chr7:2260165
|
A | G | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2362T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260165 | ||||||
| chr7:2260169
|
C | CTCAGCTC others(6): Show |
1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2367_916-2366i others(15): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260169 | ||||||
| chr7:2260181
|
C | T | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2378G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260181 | ||||||
| chr7:2260182
|
G | A | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2379C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260182 | ||||||
| chr7:2260189
|
A | T | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2386T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260189 | ||||||
| chr7:2260191
|
G | T | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2388C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260191 | ||||||
| chr7:2260199
|
G | A | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2396C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260199 | ||||||
| chr7:2260214
|
C | T | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2411G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260214 | ||||||
| chr7:2260223
|
G | A | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2420C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260223 | ||||||
| chr7:2260232
|
A | G | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2429T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260232 | ||||||
| chr7:2260242
|
T | C | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2439A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260242 | ||||||
| chr7:2260243
|
G | A | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2440C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260243 | ||||||
| chr7:2260244
|
C | T | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2441G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260244 | ||||||
| chr7:2260247
|
G | A | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2444C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260247 | ||||||
| chr7:2260255
|
G | A | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2452C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260255 | ||||||
| chr7:2260258
|
T | C | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2455A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260258 | ||||||
| chr7:2260259
|
G | A | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2456C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260259 | ||||||
| chr7:2260265
|
T | A | 123 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(120): Show | 123 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.916-2462A>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260265 | ||||||
| chr7:2260266
|
G | T | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2463C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260266 | ||||||
| chr7:2260286
|
T | C | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2483A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260286 | ||||||
| chr7:2260287
|
G | A | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2484C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260287 | ||||||
| chr7:2260289
|
G | T | 1 | a0001c0001t0003g0264 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.916-2486C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260289 | ||||||
| chr7:2260395
|
A | G | 306 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(303): Show | 308 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.916-2592T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260395 | ||||||
| chr7:2260500
|
C | T | 3 | a0001c0001t0013g0074a0001c0006t0013g0233a0001c0006t0013g0234 | 3 | HG00642.hp1 HG00735.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.916-2697G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260500 | ||||||
| chr7:2260562
|
C | T | 2 | a0001c0006t0013g0233a0001c0006t0013g0234 | 2 | HG00735.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.915+2668G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260562 | ||||||
| chr7:2260724
|
T | A | 1 | a0001c0003t0005g0334 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.915+2506A>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260724 | ||||||
| chr7:2260923
|
G | T | 1 | a0001c0016t0003g0065 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.915+2307C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260923 | ||||||
| chr7:2261169
|
G | A | 1 | a0001c0003t0006g0082 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.915+2061C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2261169 | ||||||
| chr7:2261219
|
G | C | 1 | a0001c0001t0002g0060 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.915+2011C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2261219 | ||||||
| chr7:2261242
|
G | A | 5 | a0001c0001t0014g0278a0001c0001t0014g0295a0001c0001t0014g0298others(2): Show | 5 | HG02451.hp2 HG02572.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.915+1988C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2261242 | ||||||
| chr7:2261288
|
C | G | 4 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0008g0270others(1): Show | 4 | HG01109.hp1 HG02280.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.915+1942G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2261288 | ||||||
| chr7:2261290
|
G | A | 3 | a0001c0002t0004g0015a0001c0002t0004g0168a0001c0002t0047g0161 | 3 | HG02647.hp2 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.915+1940C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2261290 | ||||||
| chr7:2261319
|
G | A | 1 | a0001c0001t0002g0058 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.915+1911C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2261319 | ||||||
| chr7:2261340
|
G | A | 8 | a0001c0001t0017g0196a0001c0001t0017g0205a0001c0001t0017g0209others(5): Show | 8 | HG01884.hp1 HG02602.hp2 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.915+1890C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2261340 | ||||||
| chr7:2261352
|
G | T | 1 | a0001c0001t0001g0206 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.915+1878C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2261352 | ||||||
| chr7:2261428
|
G | A | 6 | a0001c0001t0014g0047a0001c0001t0014g0278a0001c0001t0014g0295others(3): Show | 6 | HG02451.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.915+1802C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2261428 | ||||||
| chr7:2261476
|
C | A | 2 | a0001c0002t0027g0189a0001c0002t0027g0348 | 2 | HG00639.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.915+1754G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2261476 | ||||||
| chr7:2261607
|
C | A | 4 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0008g0270others(1): Show | 4 | HG01109.hp1 HG02280.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.915+1623G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2261607 | ||||||
| chr7:2261745
|
C | T | 1 | a0001c0001t0001g0056 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.915+1485G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2261745 | ||||||
| chr7:2261745
|
CG | C | 4 | a0001c0001t0017g0196a0001c0001t0017g0205a0001c0001t0017g0209others(1): Show | 4 | HG02602.hp2 HG02735.hp2 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.915+1484delC | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2261745 | ||||||
| chr7:2261849
|
A | G | 123 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(120): Show | 123 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.915+1381T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2261849 | ||||||
| chr7:2261918
|
G | T | 4 | a0001c0001t0017g0196a0001c0001t0017g0205a0001c0001t0017g0209others(1): Show | 4 | HG02602.hp2 HG02735.hp2 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.915+1312C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2261918 | ||||||
| chr7:2261943
|
T | G | 123 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(120): Show | 123 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.915+1287A>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2261943 | ||||||
| chr7:2262008
|
G | A | 1 | a0001c0001t0001g0341 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.915+1222C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2262008 | ||||||
| chr7:2262195
|
C | A | 4 | a0001c0002t0004g0127a0001c0002t0004g0185a0001c0002t0004g0228others(1): Show | 4 | NA18960.hp2 NA18963.hp2 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.915+1035G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2262195 | ||||||
| chr7:2262204
|
A | T | 6 | a0001c0001t0014g0047a0001c0001t0014g0278a0001c0001t0014g0295others(3): Show | 6 | HG02451.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.915+1026T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2262204 | ||||||
| chr7:2262345
|
A | T | 17 | a0001c0001t0002g0076a0001c0001t0002g0077a0001c0001t0002g0180others(14): Show | 17 | HG00099.hp1 HG00642.hp2 HG00733.hp1 others(14): Show |
intron_variant | MODIFIER | c.915+885T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2262345 | ||||||
| chr7:2262354
|
C | T | 306 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(303): Show | 308 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.915+876G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2262354 | ||||||
| chr7:2262443
|
G | A | 4 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0008g0270others(1): Show | 4 | HG01109.hp1 HG02280.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.915+787C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2262443 | ||||||
| chr7:2262479
|
G | A | 1 | a0001c0001t0003g0037 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.915+751C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2262479 | ||||||
| chr7:2262496
|
G | C | 47 | a0001c0001t0003g0066a0001c0001t0003g0067a0001c0001t0003g0068others(44): Show | 47 | HG00544.hp1 HG00642.hp1 HG00738.hp1 others(44): Show |
intron_variant | MODIFIER | c.915+734C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2262496 | ||||||
| chr7:2262503
|
G | A | 5 | a0001c0001t0001g0184a0001c0001t0001g0229a0001c0001t0001g0341others(2): Show | 5 | HG00423.hp2 HG00438.hp2 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.915+727C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2262503 | ||||||
| chr7:2262726
|
C | A | 1 | a0001c0016t0003g0065 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.915+504G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2262726 | ||||||
| chr7:2262730
|
C | G | 2 | a0001c0001t0035g0152a0001c0001t0041g0150 | 2 | HG02257.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.915+500G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2262730 | ||||||
| chr7:2262746
|
C | T | 6 | a0001c0006t0013g0176a0001c0006t0013g0194a0001c0006t0013g0233others(3): Show | 6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.915+484G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2262746 | ||||||
| chr7:2262779
|
T | C | 306 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(303): Show | 308 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.915+451A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2262779 | ||||||
| chr7:2262836
|
G | A | 31 | a0001c0001t0002g0076a0001c0001t0002g0077a0001c0001t0002g0180others(28): Show | 31 | HG00099.hp1 HG00642.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.915+394C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2262836 | ||||||
| chr7:2262889
|
G | A | 6 | a0001c0001t0014g0047a0001c0001t0014g0278a0001c0001t0014g0295others(3): Show | 6 | HG02451.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.915+341C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2262889 | ||||||
| chr7:2262892
|
C | T | 17 | a0001c0001t0002g0076a0001c0001t0002g0077a0001c0001t0002g0180others(14): Show | 17 | HG00099.hp1 HG00642.hp2 HG00733.hp1 others(14): Show |
intron_variant | MODIFIER | c.915+338G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2262892 | ||||||
| chr7:2262930
|
G | A | 1 | a0001c0001t0003g0193 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.915+300C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2262930 | ||||||
| chr7:2263057
|
T | C | 14 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0008g0270others(11): Show | 14 | HG01109.hp1 HG01884.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.915+173A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2263057 | ||||||
| chr7:2263072
|
T | C | 2 | a0001c0001t0003g0140a0001c0001t0003g0243 | 2 | HG00741.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.915+158A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2263072 | ||||||
| chr7:2263101
|
G | A | 5 | a0001c0001t0003g0038a0001c0001t0003g0223a0001c0001t0023g0122others(2): Show | 5 | HG00639.hp2 HG01070.hp2 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.915+129C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2263101 | ||||||
| chr7:2263137
|
G | A | 6 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0008g0270others(3): Show | 6 | HG01109.hp1 HG02257.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.915+93C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2263137 | ||||||
| chr7:2263192
|
T | C | 3 | a0001c0001t0003g0223a0001c0001t0040g0007a0002c0004t0023g0359 | 3 | HG01070.hp2 HG01891.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.915+38A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2263192 | ||||||
| chr7:2263422
|
G | A | 1 | a0001c0002t0004g0245 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.783-60C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 6/10 | chr7 | 2263422 | ||||||
| chr7:2263436
|
C | T | 9 | a0001c0001t0008g0001a0001c0001t0008g0048a0001c0001t0008g0096others(6): Show | 10 | HG01081.hp2 HG02615.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.783-74G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 6/10 | chr7 | 2263436 | ||||||
| chr7:2263439
|
C | A | 4 | a0002c0004t0018g0360a0002c0004t0018g0362a0002c0004t0018g0363others(1): Show | 4 | HG01884.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.783-77G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 6/10 | chr7 | 2263439 | ||||||
| chr7:2263439
|
C | T | 15 | a0001c0001t0001g0119a0001c0001t0007g0019a0001c0001t0007g0024others(12): Show | 15 | HG01192.hp2 HG02056.hp1 HG03017.hp1 others(12): Show |
intron_variant | MODIFIER | c.783-77G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 6/10 | chr7 | 2263439 | ||||||
| chr7:2263465
|
C | T | 14 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0008g0270others(11): Show | 14 | HG01109.hp1 HG01884.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.783-103G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 6/10 | chr7 | 2263465 | ||||||
| chr7:2263474
|
G | A | 138 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(135): Show | 139 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.783-112C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 6/10 | chr7 | 2263474 | ||||||
| chr7:2263483
|
C | T | 3 | a0001c0001t0005g0163a0001c0001t0005g0164a0001c0001t0005g0169 | 3 | HG03579.hp2 NA18906.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.783-121G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 6/10 | chr7 | 2263483 | ||||||
| chr7:2263524
|
C | A | 1 | a0001c0001t0019g0225 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.783-162G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 6/10 | chr7 | 2263524 | ||||||
| chr7:2263524
|
C | T | 1 | a0001c0001t0003g0037 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.783-162G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 6/10 | chr7 | 2263524 | ||||||
| chr7:2263616
|
G | T | 1 | a0001c0002t0004g0127 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.783-254C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 6/10 | chr7 | 2263616 | ||||||
| chr7:2263643
|
G | A | 1 | a0001c0016t0003g0065 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.783-281C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 6/10 | chr7 | 2263643 | ||||||
| chr7:2263676
|
G | A | 4 | a0002c0004t0018g0360a0002c0004t0018g0362a0002c0004t0018g0363others(1): Show | 4 | HG01884.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.783-314C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 6/10 | chr7 | 2263676 | ||||||
| chr7:2263715
|
G | A | 4 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0008g0270others(1): Show | 4 | HG01109.hp1 HG02280.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.783-353C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 6/10 | chr7 | 2263715 | ||||||
| chr7:2263719
|
C | CT | 7 | a0001c0001t0003g0037a0001c0001t0005g0011a0001c0001t0005g0012others(4): Show | 7 | HG01109.hp1 HG02280.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.783-358dupA | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 6/10 | chr7 | 2263719 | ||||||
| chr7:2263725
|
T | G | 4 | a0002c0004t0018g0360a0002c0004t0018g0362a0002c0004t0018g0363others(1): Show | 4 | HG01884.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.783-363A>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 6/10 | chr7 | 2263725 | ||||||
| chr7:2263783
|
G | A | 1 | a0001c0001t0003g0037 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.783-421C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 6/10 | chr7 | 2263783 | ||||||
| chr7:2263838
|
G | A | 1 | a0001c0001t0041g0150 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.782+460C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 6/10 | chr7 | 2263838 | ||||||
| chr7:2263928
|
C | A | 1 | a0001c0001t0002g0129 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.782+370G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 6/10 | chr7 | 2263928 | ||||||
| chr7:2263946
|
C | CCTCGTGA others(17): Show |
1 | a0001c0001t0009g0312 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.782+328_782+351dup others(24): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 6/10 | chr7 | 2263946 | ||||||
| chr7:2264263
|
G | A | 1 | a0001c0002t0010g0338 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.782+35C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 6/10 | chr7 | 2264263 | ||||||
| chr7:2264495
|
C | T | 6 | a0001c0001t0014g0047a0001c0001t0014g0278a0001c0001t0014g0295others(3): Show | 6 | HG02451.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.622-37G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2264495 | ||||||
| chr7:2264556
|
A | C | 306 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(303): Show | 308 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.622-98T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2264556 | ||||||
| chr7:2264640
|
C | T | 132 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(129): Show | 132 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.622-182G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2264640 | ||||||
| chr7:2264670
|
G | A | 1 | a0001c0001t0011g0155 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.622-212C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2264670 | ||||||
| chr7:2264805
|
C | T | 9 | a0001c0001t0008g0001a0001c0001t0008g0048a0001c0001t0008g0096others(6): Show | 10 | HG01081.hp2 HG02615.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.622-347G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2264805 | ||||||
| chr7:2265008
|
T | C | 306 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(303): Show | 308 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.622-550A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2265008 | ||||||
| chr7:2265014
|
G | A | 4 | a0001c0001t0016g0235a0001c0001t0016g0236a0001c0001t0016g0237others(1): Show | 4 | HG01175.hp2 HG01516.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.622-556C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2265014 | ||||||
| chr7:2265035
|
AAAAC | A | 6 | a0001c0006t0013g0176a0001c0006t0013g0194a0001c0006t0013g0233others(3): Show | 6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.622-581_622-578del others(4): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2265035 | ||||||
| chr7:2265194
|
T | G | 1 | a0001c0001t0037g0121 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.622-736A>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2265194 | ||||||
| chr7:2265199
|
G | A | 1 | a0001c0001t0003g0037 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.622-741C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2265199 | ||||||
| chr7:2265396
|
C | T | 5 | a0001c0001t0003g0038a0001c0001t0003g0223a0001c0001t0023g0122others(2): Show | 5 | HG00639.hp2 HG01070.hp2 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.622-938G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2265396 | ||||||
| chr7:2265736
|
C | T | 1 | a0001c0001t0019g0225 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.622-1278G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2265736 | ||||||
| chr7:2265737
|
G | A | 6 | a0001c0006t0013g0176a0001c0006t0013g0194a0001c0006t0013g0233others(3): Show | 6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.622-1279C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2265737 | ||||||
| chr7:2265756
|
T | G | 1 | a0001c0001t0035g0152 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.622-1298A>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2265756 | ||||||
| chr7:2266172
|
T | C | 1 | a0001c0003t0005g0315 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.622-1714A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2266172 | ||||||
| chr7:2266179
|
T | TTTG | 4 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0008g0270others(1): Show | 4 | HG01109.hp1 HG02280.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.622-1724_622-1722d others(5): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2266179 | ||||||
| chr7:2266247
|
C | T | 6 | a0001c0001t0014g0047a0001c0001t0014g0278a0001c0001t0014g0295others(3): Show | 6 | HG02451.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.622-1789G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2266247 | ||||||
| chr7:2266289
|
G | A | 6 | a0001c0006t0013g0176a0001c0006t0013g0194a0001c0006t0013g0233others(3): Show | 6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.622-1831C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2266289 | ||||||
| chr7:2266308
|
C | A | 4 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0008g0270others(1): Show | 4 | HG01109.hp1 HG02280.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.622-1850G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2266308 | ||||||
| chr7:2266351
|
A | AT | 243 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(240): Show | 245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.622-1894dupA | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2266351 | ||||||
| chr7:2266386
|
G | A | 6 | a0001c0006t0013g0176a0001c0006t0013g0194a0001c0006t0013g0233others(3): Show | 6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.622-1928C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2266386 | ||||||
| chr7:2266395
|
G | A | 1 | a0001c0001t0001g0221 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.622-1937C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2266395 | ||||||
| chr7:2266575
|
G | C | 6 | a0001c0006t0013g0176a0001c0006t0013g0194a0001c0006t0013g0233others(3): Show | 6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.622-2117C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2266575 | ||||||
| chr7:2266577
|
C | T | 2 | a0001c0001t0020g0156a0001c0001t0020g0157 | 2 | HG01261.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.622-2119G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2266577 | ||||||
| chr7:2266608
|
G | C | 8 | a0001c0001t0002g0118a0003c0007t0012g0009a0003c0007t0012g0039others(5): Show | 8 | HG01891.hp2 HG02818.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.622-2150C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2266608 | ||||||
| chr7:2266641
|
G | A | 9 | a0001c0001t0008g0001a0001c0001t0008g0048a0001c0001t0008g0096others(6): Show | 10 | HG01081.hp2 HG02615.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.622-2183C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2266641 | ||||||
| chr7:2266643
|
C | A | 6 | a0001c0006t0013g0176a0001c0006t0013g0194a0001c0006t0013g0233others(3): Show | 6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.622-2185G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2266643 | ||||||
| chr7:2266675
|
G | C | 15 | a0001c0001t0001g0119a0001c0001t0007g0019a0001c0001t0007g0024others(12): Show | 15 | HG01192.hp2 HG02056.hp1 HG03017.hp1 others(12): Show |
intron_variant | MODIFIER | c.622-2217C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2266675 | ||||||
| chr7:2266690
|
T | A | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.622-2232A>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2266690 | ||||||
| chr7:2266763
|
C | T | 6 | a0001c0001t0014g0047a0001c0001t0014g0278a0001c0001t0014g0295others(3): Show | 6 | HG02451.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.622-2305G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2266763 | ||||||
| chr7:2266813
|
G | A | 1 | a0001c0002t0004g0190 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.622-2355C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2266813 | ||||||
| chr7:2266962
|
C | G | 307 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(304): Show | 309 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.622-2504G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2266962 | ||||||
| chr7:2266977
|
G | A | 1 | a0001c0001t0003g0086 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.622-2519C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2266977 | ||||||
| chr7:2267020
|
G | A | 132 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(129): Show | 132 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.621+2539C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267020 | ||||||
| chr7:2267046
|
G | A | 2 | a0001c0001t0003g0114a0001c0001t0003g0117 | 2 | NA18966.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.621+2513C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267046 | ||||||
| chr7:2267073
|
C | T | 56 | a0001c0001t0002g0026a0001c0001t0002g0041a0001c0001t0002g0054others(53): Show | 56 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.621+2486G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267073 | ||||||
| chr7:2267106
|
T | C | 4 | a0002c0004t0018g0360a0002c0004t0018g0362a0002c0004t0018g0363others(1): Show | 4 | HG01884.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.621+2453A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267106 | ||||||
| chr7:2267142
|
T | C | 2 | a0001c0001t0022g0165a0001c0001t0022g0166 | 2 | HG02965.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.621+2417A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267142 | ||||||
| chr7:2267159
|
C | T | 41 | a0001c0001t0003g0066a0001c0001t0003g0067a0001c0001t0003g0068others(38): Show | 41 | HG00544.hp1 HG00642.hp1 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.621+2400G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267159 | ||||||
| chr7:2267178
|
C | T | 1 | a0001c0001t0021g0303 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.621+2381G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267178 | ||||||
| chr7:2267211
|
G | A | 283 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(280): Show | 285 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.621+2348C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267211 | ||||||
| chr7:2267256
|
G | T | 6 | a0001c0006t0013g0176a0001c0006t0013g0194a0001c0006t0013g0233others(3): Show | 6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.621+2303C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267256 | ||||||
| chr7:2267299
|
GCCCTCTC others(5): Show |
G | 1 | a0002c0004t0005g0366 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.621+2248_621+2259d others(14): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267299 | ||||||
| chr7:2267305
|
TCCCTCC | T | 34 | a0001c0001t0001g0119a0001c0001t0002g0153a0001c0001t0003g0038others(31): Show | 34 | HG00639.hp2 HG00735.hp2 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.621+2248_621+2253d others(8): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267305 | ||||||
| chr7:2267335
|
T | C | 2 | a0001c0001t0021g0303a0001c0001t0021g0354 | 2 | HG02809.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.621+2224A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267335 | ||||||
| chr7:2267339
|
T | G | 10 | a0001c0001t0014g0047a0001c0001t0014g0278a0001c0001t0014g0295others(7): Show | 10 | HG01884.hp1 HG02451.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.621+2220A>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267339 | ||||||
| chr7:2267349
|
C | T | 150 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0026others(147): Show | 152 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(149): Show |
intron_variant | MODIFIER | c.621+2210G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267349 | ||||||
| chr7:2267375
|
C | T | 16 | a0001c0001t0001g0119a0001c0001t0007g0019a0001c0001t0007g0024others(13): Show | 16 | HG01192.hp2 HG02056.hp1 HG02738.hp2 others(13): Show |
intron_variant | MODIFIER | c.621+2184G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267375 | ||||||
| chr7:2267402
|
C | G | 4 | a0002c0004t0018g0360a0002c0004t0018g0362a0002c0004t0018g0363others(1): Show | 4 | HG01884.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.621+2157G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267402 | ||||||
| chr7:2267411
|
G | A | 133 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(130): Show | 133 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.621+2148C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267411 | ||||||
| chr7:2267442
|
T | C | 56 | a0001c0001t0002g0026a0001c0001t0002g0041a0001c0001t0002g0054others(53): Show | 56 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.621+2117A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267442 | ||||||
| chr7:2267450
|
A | G | 56 | a0001c0001t0002g0026a0001c0001t0002g0041a0001c0001t0002g0054others(53): Show | 56 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.621+2109T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267450 | ||||||
| chr7:2267457
|
C | T | 73 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0026others(70): Show | 73 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.621+2102G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267457 | ||||||
| chr7:2267503
|
G | C | 6 | a0001c0006t0013g0176a0001c0006t0013g0194a0001c0006t0013g0233others(3): Show | 6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.621+2056C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267503 | ||||||
| chr7:2267511
|
G | A | 6 | a0001c0006t0013g0176a0001c0006t0013g0194a0001c0006t0013g0233others(3): Show | 6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.621+2048C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267511 | ||||||
| chr7:2267536
|
G | A | 6 | a0001c0001t0014g0047a0001c0001t0014g0278a0001c0001t0014g0295others(3): Show | 6 | HG02451.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.621+2023C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267536 | ||||||
| chr7:2267565
|
C | T | 5 | a0001c0001t0001g0184a0001c0001t0001g0229a0001c0001t0001g0341others(2): Show | 5 | HG00423.hp2 HG00438.hp2 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.621+1994G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267565 | ||||||
| chr7:2267570
|
T | A | 1 | a0001c0016t0003g0065 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.621+1989A>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267570 | ||||||
| chr7:2267601
|
C | A | 10 | a0001c0006t0013g0176a0001c0006t0013g0194a0001c0006t0013g0233others(7): Show | 10 | HG00735.hp2 HG01069.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.621+1958G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267601 | ||||||
| chr7:2267618
|
A | G | 6 | a0001c0006t0013g0176a0001c0006t0013g0194a0001c0006t0013g0233others(3): Show | 6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.621+1941T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267618 | ||||||
| chr7:2267635
|
G | A | 5 | a0001c0001t0001g0184a0001c0001t0001g0229a0001c0001t0001g0341others(2): Show | 5 | HG00423.hp2 HG00438.hp2 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.621+1924C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267635 | ||||||
| chr7:2267643
|
A | G | 8 | a0001c0001t0003g0038a0001c0001t0023g0122a0001c0006t0013g0176others(5): Show | 8 | HG00639.hp2 HG00735.hp2 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.621+1916T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267643 | ||||||
| chr7:2267644
|
C | A | 1 | a0001c0002t0004g0294 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.621+1915G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267644 | ||||||
| chr7:2267644
|
C | T | 2 | a0001c0001t0003g0038a0001c0001t0023g0122 | 2 | HG00639.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.621+1915G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267644 | ||||||
| chr7:2267729
|
G | A | 1 | a0001c0001t0003g0037 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.621+1830C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267729 | ||||||
| chr7:2267732
|
A | AC | 12 | a0001c0001t0001g0027a0001c0001t0001g0175a0001c0001t0001g0224others(9): Show | 12 | HG00438.hp1 HG00741.hp2 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.621+1826dupG | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267732 | ||||||
| chr7:2267735
|
CCGTCTGG others(32): Show |
C | 2 | a0001c0001t0022g0165a0001c0001t0022g0166 | 2 | HG02965.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.621+1785_621+1823d others(41): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267735 | ||||||
| chr7:2267754
|
T | C | 1 | a0001c0001t0003g0037 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.621+1805A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267754 | ||||||
| chr7:2267775
|
C | A | 16 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(13): Show | 16 | HG00544.hp2 HG00597.hp1 NA18747.hp1 others(13): Show |
intron_variant | MODIFIER | c.621+1784G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267775 | ||||||
| chr7:2267784
|
TGTGAGGA others(492): Show |
T | 9 | a0001c0001t0008g0001a0001c0001t0008g0048a0001c0001t0008g0096others(6): Show | 10 | HG01081.hp2 HG02615.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.621+1276_621+1774d others(2): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267784 | ||||||
| chr7:2267785
|
G | A | 1 | a0001c0001t0002g0256 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.621+1774C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267785 | ||||||
| chr7:2267795
|
C | T | 1 | a0001c0001t0002g0256 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.621+1764G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267795 | ||||||
| chr7:2267912
|
T | G | 6 | a0001c0006t0013g0176a0001c0006t0013g0194a0001c0006t0013g0233others(3): Show | 6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.621+1647A>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267912 | ||||||
| chr7:2267931
|
A | C | 298 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(295): Show | 299 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.621+1628T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267931 | ||||||
| chr7:2267944
|
GGGAGCGC others(30): Show |
G | 1 | a0001c0001t0001g0200 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.621+1578_621+1614d others(39): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267944 | ||||||
| chr7:2267986
|
C | T | 1 | a0002c0004t0038g0358 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.621+1573G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267986 | ||||||
| chr7:2267996
|
C | G | 1 | a0001c0002t0046g0171 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.621+1563G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267996 | ||||||
| chr7:2268008
|
C | T | 142 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0026others(139): Show | 143 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.621+1551G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268008 | ||||||
| chr7:2268047
|
C | T | 2 | a0001c0006t0013g0233a0001c0006t0013g0234 | 2 | HG00735.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.621+1512G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268047 | ||||||
| chr7:2268054
|
G | A | 7 | a0001c0001t0002g0040a0001c0006t0013g0176a0001c0006t0013g0194others(4): Show | 7 | HG00735.hp2 HG01069.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.621+1505C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268054 | ||||||
| chr7:2268071
|
G | A | 1 | a0001c0001t0002g0040 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.621+1488C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268071 | ||||||
| chr7:2268080
|
A | C | 6 | a0001c0006t0013g0176a0001c0006t0013g0194a0001c0006t0013g0233others(3): Show | 6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.621+1479T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268080 | ||||||
| chr7:2268081
|
C | A | 10 | a0001c0001t0014g0047a0001c0001t0014g0278a0001c0001t0014g0295others(7): Show | 10 | HG01884.hp1 HG02451.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.621+1478G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268081 | ||||||
| chr7:2268086
|
T | C | 6 | a0001c0006t0013g0176a0001c0006t0013g0194a0001c0006t0013g0233others(3): Show | 6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.621+1473A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268086 | ||||||
| chr7:2268105
|
G | C | 1 | a0001c0002t0004g0015 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.621+1454C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268105 | ||||||
| chr7:2268121
|
GTCAGCCC others(42): Show |
G | 1 | a0001c0006t0013g0176 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.621+1389_621+1437d others(51): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268121 | ||||||
| chr7:2268135
|
TGGCCAGC others(43): Show |
T | 5 | a0001c0006t0013g0194a0001c0006t0013g0233a0001c0006t0013g0234others(2): Show | 5 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.621+1374_621+1423d others(52): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268135 | ||||||
| chr7:2268179
|
T | C | 1 | a0001c0006t0013g0176 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.621+1380A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268179 | ||||||
| chr7:2268185
|
C | T | 1 | a0001c0006t0013g0176 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.621+1374G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268185 | ||||||
| chr7:2268226
|
C | T | 4 | a0002c0004t0018g0360a0002c0004t0018g0362a0002c0004t0018g0363others(1): Show | 4 | HG01884.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.621+1333G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268226 | ||||||
| chr7:2268229
|
C | T | 2 | a0001c0001t0001g0246a0001c0001t0001g0247 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.621+1330G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268229 | ||||||
| chr7:2268230
|
G | A | 6 | a0001c0006t0013g0176a0001c0006t0013g0194a0001c0006t0013g0233others(3): Show | 6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.621+1329C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268230 | ||||||
| chr7:2268244
|
G | C | 2 | a0001c0001t0022g0165a0001c0001t0022g0166 | 2 | HG02965.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.621+1315C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268244 | ||||||
| chr7:2268256
|
G | A | 1 | a0001c0001t0003g0037 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.621+1303C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268256 | ||||||
| chr7:2268317
|
C | A | 4 | a0001c0002t0004g0127a0001c0002t0004g0185a0001c0002t0004g0228others(1): Show | 4 | NA18960.hp2 NA18963.hp2 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.621+1242G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268317 | ||||||
| chr7:2268336
|
T | C | 4 | a0001c0003t0006g0010a0001c0003t0006g0013a0001c0003t0006g0014others(1): Show | 4 | HG02717.hp2 HG02976.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.621+1223A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268336 | ||||||
| chr7:2268339
|
G | A | 1 | a0001c0003t0005g0008 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.621+1220C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268339 | ||||||
| chr7:2268354
|
T | C | 6 | a0001c0006t0013g0176a0001c0006t0013g0194a0001c0006t0013g0233others(3): Show | 6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.621+1205A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268354 | ||||||
| chr7:2268385
|
C | A | 6 | a0001c0006t0013g0176a0001c0006t0013g0194a0001c0006t0013g0233others(3): Show | 6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.621+1174G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268385 | ||||||
| chr7:2268394
|
C | G | 5 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0053others(2): Show | 5 | HG01256.hp2 HG01258.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.621+1165G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268394 | ||||||
| chr7:2268435
|
A | G | 6 | a0001c0006t0013g0176a0001c0006t0013g0194a0001c0006t0013g0233others(3): Show | 6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.621+1124T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268435 | ||||||
| chr7:2268443
|
G | A | 106 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0026others(103): Show | 108 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.621+1116C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268443 | ||||||
| chr7:2268449
|
T | C | 6 | a0001c0006t0013g0176a0001c0006t0013g0194a0001c0006t0013g0233others(3): Show | 6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.621+1110A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268449 | ||||||
| chr7:2268514
|
C | A | 4 | a0002c0004t0018g0360a0002c0004t0018g0362a0002c0004t0018g0363others(1): Show | 4 | HG01884.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.621+1045G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268514 | ||||||
| chr7:2268520
|
C | T | 110 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(107): Show | 110 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.621+1039G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268520 | ||||||
| chr7:2268537
|
C | T | 4 | a0002c0004t0018g0360a0002c0004t0018g0362a0002c0004t0018g0363others(1): Show | 4 | HG01884.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.621+1022G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268537 | ||||||
| chr7:2268586
|
C | T | 3 | a0001c0001t0003g0223a0001c0001t0040g0007a0002c0004t0023g0359 | 3 | HG01070.hp2 HG01891.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.621+973G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268586 | ||||||
| chr7:2268598
|
G | T | 1 | a0001c0016t0003g0065 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.621+961C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268598 | ||||||
| chr7:2268635
|
T | TGGGAGGT others(122): Show |
3 | a0001c0002t0004g0015a0001c0002t0004g0168a0001c0002t0047g0161 | 3 | HG02647.hp2 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.621+795_621+923dup others(129): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268635 | ||||||
| chr7:2268635
|
T | TGGGAGGT others(121): Show |
20 | a0001c0001t0001g0119a0001c0001t0005g0011a0001c0001t0005g0012others(17): Show | 20 | HG01109.hp1 HG01192.hp2 HG02056.hp1 others(17): Show |
intron_variant | MODIFIER | c.621+923_621+924ins others(128): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268635 | ||||||
| chr7:2268660
|
G | A | 1 | a0001c0001t0003g0037 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.621+899C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268660 | ||||||
| chr7:2268686
|
CCCCTCTG others(122): Show |
C | 1 | a0001c0001t0005g0353 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.621+744_621+872del | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268686 | ||||||
| chr7:2268694
|
C | CCCGGCCA others(43): Show |
1 | a0001c0001t0002g0141 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.621+864_621+865ins others(50): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268694 | ||||||
| chr7:2268694
|
C | CCCGGCCA others(42): Show |
107 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0026others(104): Show | 109 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.621+864_621+865ins others(49): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268694 | ||||||
| chr7:2268694
|
C | CCCGGCCA others(41): Show |
1 | a0001c0001t0009g0312 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.621+864_621+865ins others(48): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268694 | ||||||
| chr7:2268697
|
A | AGCCAGCC others(43): Show |
4 | a0001c0001t0003g0086a0001c0001t0003g0136a0001c0001t0003g0183others(1): Show | 4 | HG02056.hp2 HG02738.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.621+861_621+862ins others(50): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268697 | ||||||
| chr7:2268697
|
A | AGCCAGCC others(42): Show |
47 | a0001c0001t0003g0038a0001c0001t0003g0066a0001c0001t0003g0067others(44): Show | 47 | HG00544.hp1 HG00639.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.621+861_621+862ins others(49): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268697 | ||||||
| chr7:2268697
|
A | G | 255 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(252): Show | 257 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.621+862T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268697 | ||||||
| chr7:2268714
|
G | A | 6 | a0001c0006t0013g0176a0001c0006t0013g0194a0001c0006t0013g0233others(3): Show | 6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.621+845C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268714 | ||||||
| chr7:2268714
|
G | GGGAGGGA others(122): Show |
2 | a0001c0001t0001g0258a0001c0001t0007g0187 | 2 | HG03239.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.621+844_621+845ins others(129): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268714 | ||||||
| chr7:2268714
|
G | GGGAGGGA others(121): Show |
102 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0035others(99): Show | 102 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.621+844_621+845ins others(128): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268714 | ||||||
| chr7:2268724
|
T | TGGGGGTG others(122): Show |
5 | a0001c0001t0001g0031a0001c0001t0001g0049a0001c0001t0001g0175others(2): Show | 5 | HG00544.hp2 HG00597.hp1 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.621+834_621+835ins others(129): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268724 | ||||||
| chr7:2268724
|
T | TGGGGGTG others(122): Show |
1 | a0001c0001t0007g0181 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.621+834_621+835ins others(129): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268724 | ||||||
| chr7:2268724
|
T | TGGGGGTG others(43): Show |
3 | a0001c0001t0002g0227a0001c0001t0002g0304a0001c0003t0005g0292 | 3 | HG01346.hp2 HG02055.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.621+834_621+835ins others(50): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268724 | ||||||
| chr7:2268727
|
G | GGGTGTCA others(42): Show |
5 | a0001c0001t0009g0021a0001c0001t0009g0081a0001c0001t0009g0108others(2): Show | 5 | HG00673.hp2 HG02155.hp1 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.621+831_621+832ins others(49): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268727 | ||||||
| chr7:2268731
|
G | T | 8 | a0001c0001t0001g0279a0001c0006t0013g0176a0001c0006t0013g0194others(5): Show | 8 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(5): Show |
intron_variant | MODIFIER | c.621+828C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268731 | ||||||
| chr7:2268743
|
A | C | 306 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(303): Show | 308 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.621+816T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268743 | ||||||
| chr7:2268747
|
C | T | 1 | a0001c0001t0002g0118 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.621+812G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268747 | ||||||
| chr7:2268762
|
T | TCCGGGAG others(122): Show |
1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.621+796_621+797ins others(129): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268762 | ||||||
| chr7:2268793
|
G | A | 4 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0008g0270others(1): Show | 4 | HG01109.hp1 HG02280.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.621+766C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268793 | ||||||
| chr7:2268815
|
G | C | 306 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(303): Show | 308 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.621+744C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268815 | ||||||
| chr7:2268826
|
G | A | 1 | a0001c0001t0003g0136 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.621+733C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268826 | ||||||
| chr7:2268834
|
G | A | 6 | a0001c0006t0013g0176a0001c0006t0013g0194a0001c0006t0013g0233others(3): Show | 6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.621+725C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268834 | ||||||
| chr7:2268838
|
C | CGCCCGGG others(39): Show |
1 | a0001c0001t0035g0152 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.621+720_621+721ins others(46): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268838 | ||||||
| chr7:2268853
|
TG | T | 125 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(122): Show | 125 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.621+705delC | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268853 | ||||||
| chr7:2268853
|
TGGGGGGG others(43): Show |
T | 3 | a0001c0001t0002g0083a0001c0001t0002g0132a0001c0001t0008g0162 | 3 | HG03098.hp1 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.621+656_621+705del others(50): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268853 | ||||||
| chr7:2268854
|
G | GGGGGGGG others(122): Show |
1 | a0001c0015t0007g0022 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.621+704_621+705ins others(129): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268854 | ||||||
| chr7:2268859
|
G | T | 1 | a0001c0001t0003g0136 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.621+700C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268859 | ||||||
| chr7:2268870
|
C | CTGCCCGG others(150): Show |
6 | a0001c0006t0013g0176a0001c0006t0013g0194a0001c0006t0013g0233others(3): Show | 6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.621+688_621+689ins others(157): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268870 | ||||||
| chr7:2268871
|
G | A | 5 | a0001c0001t0001g0203a0001c0001t0016g0235a0001c0001t0016g0236others(2): Show | 5 | HG01175.hp2 HG01256.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.621+688C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268871 | ||||||
| chr7:2268871
|
G | C | 1 | a0001c0001t0003g0136 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.621+688C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268871 | ||||||
| chr7:2268872
|
C | G | 1 | a0001c0001t0003g0136 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.621+687G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268872 | ||||||
| chr7:2268874
|
CGGCCAGC others(45): Show |
C | 2 | a0001c0001t0011g0128a0001c0001t0011g0137 | 2 | HG03831.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.621+633_621+684del others(52): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268874 | ||||||
| chr7:2268902
|
TG | T | 346 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(343): Show | 348 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(345): Show |
intron_variant | MODIFIER | c.621+656delC | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268902 | ||||||
| chr7:2268904
|
G | GGGGGGGT others(120): Show |
1 | a0001c0001t0003g0136 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.621+654_621+655ins others(127): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268904 | ||||||
| chr7:2268906
|
G | A | 4 | a0002c0004t0018g0360a0002c0004t0018g0362a0002c0004t0018g0363others(1): Show | 4 | HG01884.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.621+653C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268906 | ||||||
| chr7:2268906
|
G | C | 107 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0026others(104): Show | 109 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.621+653C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268906 | ||||||
| chr7:2268907
|
G | A | 1 | a0001c0001t0002g0018 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.621+652C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268907 | ||||||
| chr7:2268922
|
T | C | 1 | a0001c0001t0003g0070 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.621+637A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268922 | ||||||
| chr7:2268926
|
T | C | 8 | a0001c0001t0003g0070a0001c0001t0003g0136a0001c0006t0013g0176others(5): Show | 8 | HG00735.hp2 HG01069.hp2 HG03688.hp1 others(5): Show |
intron_variant | MODIFIER | c.621+633A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268926 | ||||||
| chr7:2268944
|
G | A | 2 | a0001c0001t0001g0173a0001c0001t0041g0150 | 2 | HG02257.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.621+615C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268944 | ||||||
| chr7:2268972
|
A | G | 6 | a0001c0006t0013g0176a0001c0006t0013g0194a0001c0006t0013g0233others(3): Show | 6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.621+587T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268972 | ||||||
| chr7:2269005
|
G | A | 3 | a0001c0001t0003g0223a0001c0001t0040g0007a0002c0004t0023g0359 | 3 | HG01070.hp2 HG01891.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.621+554C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2269005 | ||||||
| chr7:2269012
|
A | AC | 4 | a0001c0001t0001g0138a0001c0001t0002g0141a0001c0002t0004g0328others(1): Show | 4 | NA18977.hp2 NA18991.hp1 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.621+546dupG | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2269012 | ||||||
| chr7:2269015
|
C | T | 1 | a0002c0004t0038g0358 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.621+544G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2269015 | ||||||
| chr7:2269070
|
G | A | 1 | a0001c0002t0004g0245 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.621+489C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2269070 | ||||||
| chr7:2269108
|
G | A | 2 | a0001c0001t0035g0152a0001c0001t0041g0150 | 2 | HG02257.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.621+451C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2269108 | ||||||
| chr7:2269156
|
TG | T | 6 | a0001c0006t0013g0176a0001c0006t0013g0194a0001c0006t0013g0233others(3): Show | 6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.621+402delC | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2269156 | ||||||
| chr7:2269161
|
G | A | 4 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0008g0270others(1): Show | 4 | HG01109.hp1 HG02280.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.621+398C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2269161 | ||||||
| chr7:2269161
|
G | C | 9 | a0001c0001t0008g0001a0001c0001t0008g0048a0001c0001t0008g0096others(6): Show | 10 | HG01081.hp2 HG02615.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.621+398C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2269161 | ||||||
| chr7:2269222
|
G | C | 2 | a0001c0001t0021g0303a0001c0001t0021g0354 | 2 | HG02809.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.621+337C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2269222 | ||||||
| chr7:2269238
|
C | CTGTGCTC others(9): Show |
9 | a0001c0001t0002g0076a0001c0001t0002g0180a0001c0001t0002g0231others(6): Show | 9 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.621+320_621+321ins others(16): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2269238 | ||||||
| chr7:2269279
|
G | A | 1 | a0001c0002t0004g0079 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.621+280C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2269279 | ||||||
| chr7:2269282
|
G | A | 10 | a0001c0001t0014g0047a0001c0001t0014g0278a0001c0001t0014g0295others(7): Show | 10 | HG01884.hp1 HG02451.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.621+277C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2269282 | ||||||
| chr7:2269299
|
C | T | 6 | a0001c0006t0013g0176a0001c0006t0013g0194a0001c0006t0013g0233others(3): Show | 6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.621+260G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2269299 | ||||||
| chr7:2269323
|
G | A | 9 | a0001c0001t0008g0001a0001c0001t0008g0048a0001c0001t0008g0096others(6): Show | 10 | HG01081.hp2 HG02615.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.621+236C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2269323 | ||||||
| chr7:2269384
|
C | T | 52 | a0001c0001t0003g0038a0001c0001t0003g0066a0001c0001t0003g0067others(49): Show | 52 | HG00544.hp1 HG00639.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.621+175G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2269384 | ||||||
| chr7:2269391
|
T | A | 307 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(304): Show | 309 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.621+168A>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2269391 | ||||||
| chr7:2269479
|
C | T | 2 | a0001c0001t0022g0165a0001c0001t0022g0166 | 2 | HG02965.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.621+80G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2269479 | ||||||
| chr7:2269523
|
T | TA | 7 | a0001c0001t0002g0077a0001c0006t0013g0176a0001c0006t0013g0194others(4): Show | 7 | HG00735.hp2 HG01069.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.621+35dupT | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2269523 | ||||||
| chr7:2269523
|
TA | T | 19 | a0001c0001t0003g0243a0001c0001t0003g0319a0001c0001t0005g0011others(16): Show | 19 | HG00741.hp2 HG01109.hp1 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.621+35delT | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2269523 | ||||||
| chr7:2269524
|
A | T | 12 | a0001c0001t0001g0177a0001c0001t0005g0313a0001c0003t0005g0008others(9): Show | 12 | HG01243.hp1 HG02055.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.621+35T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2269524 | ||||||
| chr7:2269535
|
A | G | 2 | a0001c0001t0002g0055a0001c0003t0002g0064 | 2 | NA18971.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.621+24T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2269535 | ||||||
| chr7:2269536
|
A | G | 1 | a0001c0001t0003g0090 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.621+23T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2269536 | ||||||
| chr7:2269540
|
A | G | 1 | a0001c0005t0015g0020 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.621+19T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2269540 | ||||||
| chr7:2269720
|
G | A | 104 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0026others(101): Show | 106 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.541-81C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2269720 | ||||||
| chr7:2269903
|
G | A | 6 | a0001c0006t0013g0176a0001c0006t0013g0194a0001c0006t0013g0233others(3): Show | 6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.541-264C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2269903 | ||||||
| chr7:2269903
|
G | T | 2 | a0001c0001t0003g0264a0001c0001t0013g0074 | 2 | HG00642.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.541-264C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2269903 | ||||||
| chr7:2270014
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.541-375C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2270014 | ||||||
| chr7:2270134
|
C | T | 1 | a0001c0001t0008g0162 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.541-495G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2270134 | ||||||
| chr7:2270167
|
A | C | 6 | a0001c0006t0013g0176a0001c0006t0013g0194a0001c0006t0013g0233others(3): Show | 6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.541-528T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2270167 | ||||||
| chr7:2270255
|
C | G | 6 | a0001c0006t0013g0176a0001c0006t0013g0194a0001c0006t0013g0233others(3): Show | 6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.541-616G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2270255 | ||||||
| chr7:2270314
|
C | CA | 13 | a0001c0002t0004g0127a0001c0002t0004g0147a0001c0002t0004g0185others(10): Show | 13 | HG01884.hp1 HG02080.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.541-676dupT | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2270314 | ||||||
| chr7:2270314
|
C | CAA | 16 | a0001c0001t0001g0056a0001c0001t0001g0120a0001c0001t0001g0208others(13): Show | 16 | HG00639.hp2 HG01070.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.541-677_541-676dup others(2): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2270314 | ||||||
| chr7:2270314
|
C | CAAA | 90 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0035others(87): Show | 90 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.541-678_541-676dup others(3): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2270314 | ||||||
| chr7:2270314
|
C | CAAAA | 113 | a0001c0001t0001g0031a0001c0001t0001g0062a0001c0001t0001g0084others(110): Show | 114 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.541-679_541-676dup others(4): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2270314 | ||||||
| chr7:2270314
|
C | CAAAAA | 28 | a0001c0001t0002g0040a0001c0001t0002g0063a0001c0001t0002g0083others(25): Show | 28 | HG00741.hp2 HG01346.hp2 HG01361.hp1 others(25): Show |
intron_variant | MODIFIER | c.541-680_541-676dup others(5): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2270314 | ||||||
| chr7:2270314
|
C | CAAAAAA | 21 | a0001c0001t0002g0134a0001c0001t0002g0142a0001c0001t0005g0080others(18): Show | 22 | HG01099.hp1 HG01243.hp1 HG01255.hp1 others(19): Show |
intron_variant | MODIFIER | c.541-681_541-676dup others(6): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2270314 | ||||||
| chr7:2270314
|
C | CAAAAAAA | 10 | a0001c0001t0002g0078a0001c0001t0005g0313a0001c0001t0005g0353others(7): Show | 10 | HG01496.hp2 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.541-682_541-676dup others(7): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2270314 | ||||||
| chr7:2270314
|
CA | C | 14 | a0001c0002t0004g0015a0001c0002t0004g0158a0001c0002t0004g0168others(11): Show | 14 | HG01243.hp2 HG02055.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.541-676delT | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2270314 | ||||||
| chr7:2270314
|
CAAA | C | 15 | a0001c0001t0001g0119a0001c0001t0007g0019a0001c0001t0007g0024others(12): Show | 15 | HG01192.hp2 HG02056.hp1 HG02738.hp2 others(12): Show |
intron_variant | MODIFIER | c.541-678_541-676del others(3): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2270314 | ||||||
| chr7:2270314
|
CAAAAAAA others(4): Show |
C | 3 | a0001c0001t0022g0165a0001c0001t0022g0166a0001c0002t0004g0230 | 3 | HG02965.hp1 NA18939.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.541-686_541-676del others(11): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2270314 | ||||||
| chr7:2270397
|
C | T | 1 | a0001c0002t0004g0147 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.541-758G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2270397 | ||||||
| chr7:2270398
|
G | A | 9 | a0001c0003t0006g0042a0001c0003t0006g0043a0001c0003t0006g0044others(6): Show | 9 | HG02055.hp2 HG02109.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.541-759C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2270398 | ||||||
| chr7:2270408
|
C | T | 6 | a0001c0006t0013g0176a0001c0006t0013g0194a0001c0006t0013g0233others(3): Show | 6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.541-769G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2270408 | ||||||
| chr7:2270466
|
A | G | 6 | a0001c0006t0013g0176a0001c0006t0013g0194a0001c0006t0013g0233others(3): Show | 6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.541-827T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2270466 | ||||||
| chr7:2270520
|
G | A | 1 | a0001c0001t0002g0304 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.541-881C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2270520 | ||||||
| chr7:2270558
|
A | G | 255 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(252): Show | 257 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.541-919T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2270558 | ||||||
| chr7:2270707
|
G | A | 16 | a0001c0001t0001g0119a0001c0001t0007g0019a0001c0001t0007g0024others(13): Show | 16 | HG01192.hp2 HG02056.hp1 HG02738.hp2 others(13): Show |
intron_variant | MODIFIER | c.541-1068C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2270707 | ||||||
| chr7:2270756
|
C | T | 1 | a0001c0001t0003g0037 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.540+1094G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2270756 | ||||||
| chr7:2270932
|
C | T | 6 | a0001c0003t0006g0042a0001c0003t0006g0043a0001c0003t0006g0044others(3): Show | 6 | HG02109.hp1 HG02451.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.540+918G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2270932 | ||||||
| chr7:2270988
|
C | T | 6 | a0001c0006t0013g0176a0001c0006t0013g0194a0001c0006t0013g0233others(3): Show | 6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.540+862G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2270988 | ||||||
| chr7:2271042
|
G | A | 1 | a0001c0016t0003g0065 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.540+808C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2271042 | ||||||
| chr7:2271082
|
C | T | 2 | a0001c0002t0029g0075a0001c0002t0046g0171 | 2 | HG03669.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.540+768G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2271082 | ||||||
| chr7:2271339
|
C | T | 130 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(127): Show | 130 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.540+511G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2271339 | ||||||
| chr7:2271370
|
T | G | 1 | a0001c0001t0001g0217 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.540+480A>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2271370 | ||||||
| chr7:2271438
|
A | C | 1 | a0001c0003t0002g0064 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.540+412T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2271438 | ||||||
| chr7:2271611
|
G | A | 2 | a0001c0001t0002g0232a0001c0001t0002g0304 | 2 | HG01346.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.540+239C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2271611 | ||||||
| chr7:2271617
|
C | T | 1 | a0001c0003t0006g0043 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.540+233G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2271617 | ||||||
| chr7:2271628
|
C | T | 1 | a0001c0001t0002g0113 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.540+222G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2271628 | ||||||
| chr7:2271629
|
G | A | 2 | a0001c0001t0003g0037a0001c0002t0010g0349 | 2 | HG02572.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.540+221C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2271629 | ||||||
| chr7:2271631
|
G | A | 109 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(106): Show | 109 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.540+219C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2271631 | ||||||
| chr7:2271754
|
A | G | 1 | a0001c0001t0014g0298 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.540+96T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2271754 | ||||||
| chr7:2271806
|
G | A | 2 | a0001c0002t0004g0147a0001c0002t0004g0158 | 2 | HG01243.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.540+44C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2271806 | ||||||
| chr7:2272013
|
C | T | 1 | a0001c0001t0001g0282 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.419-42G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2272013 | ||||||
| chr7:2272075
|
A | G | 11 | a0001c0001t0014g0047a0001c0001t0014g0278a0001c0001t0014g0295others(8): Show | 11 | HG01255.hp1 HG01884.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.419-104T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2272075 | ||||||
| chr7:2272138
|
C | T | 2 | a0001c0002t0027g0189a0001c0002t0027g0348 | 2 | HG00639.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.419-167G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2272138 | ||||||
| chr7:2272139
|
G | A | 1 | a0001c0001t0041g0150 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.419-168C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2272139 | ||||||
| chr7:2272201
|
C | A | 11 | a0001c0001t0014g0047a0001c0001t0014g0278a0001c0001t0014g0295others(8): Show | 11 | HG01255.hp1 HG01884.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.419-230G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2272201 | ||||||
| chr7:2272207
|
A | G | 6 | a0001c0006t0013g0176a0001c0006t0013g0194a0001c0006t0013g0233others(3): Show | 6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.419-236T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2272207 | ||||||
| chr7:2272255
|
G | A | 1 | a0001c0002t0010g0338 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.419-284C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2272255 | ||||||
| chr7:2272324
|
A | G | 6 | a0001c0006t0013g0176a0001c0006t0013g0194a0001c0006t0013g0233others(3): Show | 6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.419-353T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2272324 | ||||||
| chr7:2272377
|
C | CT | 16 | a0001c0001t0001g0119a0001c0001t0007g0019a0001c0001t0007g0024others(13): Show | 16 | HG01192.hp2 HG02056.hp1 HG02738.hp2 others(13): Show |
intron_variant | MODIFIER | c.419-407dupA | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2272377 | ||||||
| chr7:2272377
|
CT | C | 7 | a0001c0001t0003g0038a0001c0001t0003g0223a0001c0001t0023g0122others(4): Show | 7 | HG00639.hp2 HG01070.hp2 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.419-407delA | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2272377 | ||||||
| chr7:2272529
|
A | C | 6 | a0001c0006t0013g0176a0001c0006t0013g0194a0001c0006t0013g0233others(3): Show | 6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.419-558T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2272529 | ||||||
| chr7:2272628
|
G | A | 4 | a0002c0004t0018g0360a0002c0004t0018g0362a0002c0004t0018g0363others(1): Show | 4 | HG01884.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.419-657C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2272628 | ||||||
| chr7:2272730
|
A | T | 1 | a0001c0001t0030g0159 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.419-759T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2272730 | ||||||
| chr7:2272872
|
C | T | 249 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(246): Show | 251 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.419-901G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2272872 | ||||||
| chr7:2272929
|
G | T | 6 | a0001c0001t0014g0047a0001c0001t0014g0278a0001c0001t0014g0295others(3): Show | 6 | HG02451.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.419-958C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2272929 | ||||||
| chr7:2272933
|
A | G | 109 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(106): Show | 109 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.419-962T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2272933 | ||||||
| chr7:2272936
|
C | T | 3 | a0001c0001t0008g0001a0001c0001t0008g0048a0001c0001t0008g0162 | 4 | HG01081.hp2 HG03225.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.419-965G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2272936 | ||||||
| chr7:2273091
|
C | A | 2 | a0001c0001t0001g0208a0001c0001t0001g0297 | 2 | HG02015.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.419-1120G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2273091 | ||||||
| chr7:2273370
|
G | A | 6 | a0001c0001t0014g0047a0001c0001t0014g0278a0001c0001t0014g0295others(3): Show | 6 | HG02451.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.419-1399C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2273370 | ||||||
| chr7:2273442
|
C | A | 1 | a0001c0001t0003g0286 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.419-1471G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2273442 | ||||||
| chr7:2273447
|
G | A | 6 | a0001c0001t0014g0047a0001c0001t0014g0278a0001c0001t0014g0295others(3): Show | 6 | HG02451.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.419-1476C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2273447 | ||||||
| chr7:2273543
|
A | T | 1 | a0001c0001t0043g0251 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.418+1569T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2273543 | ||||||
| chr7:2273552
|
C | G | 1 | a0001c0006t0013g0176 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.418+1560G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2273552 | ||||||
| chr7:2273630
|
G | A | 16 | a0001c0001t0001g0119a0001c0001t0007g0019a0001c0001t0007g0024others(13): Show | 16 | HG01192.hp2 HG02056.hp1 HG02738.hp2 others(13): Show |
intron_variant | MODIFIER | c.418+1482C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2273630 | ||||||
| chr7:2273662
|
G | C | 6 | a0001c0001t0014g0047a0001c0001t0014g0278a0001c0001t0014g0295others(3): Show | 6 | HG02451.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.418+1450C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2273662 | ||||||
| chr7:2273699
|
T | C | 1 | a0001c0001t0014g0047 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.418+1413A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2273699 | ||||||
| chr7:2273794
|
C | T | 1 | a0001c0001t0007g0329 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.418+1318G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2273794 | ||||||
| chr7:2273902
|
T | TA | 34 | a0001c0001t0001g0062a0001c0001t0001g0172a0001c0001t0001g0218others(31): Show | 34 | HG00438.hp1 HG01070.hp2 HG01192.hp1 others(31): Show |
intron_variant | MODIFIER | c.418+1209dupT | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2273902 | ||||||
| chr7:2273903
|
A | T | 1 | a0001c0002t0004g0323 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.418+1209T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2273903 | ||||||
| chr7:2273972
|
T | C | 45 | a0001c0001t0003g0066a0001c0001t0003g0067a0001c0001t0003g0068others(42): Show | 45 | HG00544.hp1 HG00642.hp1 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.418+1140A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2273972 | ||||||
| chr7:2274014
|
C | T | 45 | a0001c0001t0003g0066a0001c0001t0003g0067a0001c0001t0003g0068others(42): Show | 45 | HG00544.hp1 HG00642.hp1 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.418+1098G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2274014 | ||||||
| chr7:2274029
|
G | T | 1 | a0001c0001t0017g0196 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.418+1083C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2274029 | ||||||
| chr7:2274128
|
T | A | 1 | a0001c0006t0039g0144 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.418+984A>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2274128 | ||||||
| chr7:2274129
|
C | A | 1 | a0001c0006t0039g0144 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.418+983G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2274129 | ||||||
| chr7:2274171
|
G | A | 1 | a0001c0001t0021g0351 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.418+941C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2274171 | ||||||
| chr7:2274178
|
G | A | 4 | a0002c0004t0018g0360a0002c0004t0018g0362a0002c0004t0018g0363others(1): Show | 4 | HG01884.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.418+934C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2274178 | ||||||
| chr7:2274209
|
C | G | 7 | a0001c0001t0003g0066a0001c0001t0003g0067a0001c0001t0003g0183others(4): Show | 7 | HG00741.hp1 HG01884.hp2 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.418+903G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2274209 | ||||||
| chr7:2274290
|
C | T | 1 | a0001c0002t0010g0336 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.418+822G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2274290 | ||||||
| chr7:2274291
|
G | T | 6 | a0001c0006t0013g0176a0001c0006t0013g0194a0001c0006t0013g0233others(3): Show | 6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.418+821C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2274291 | ||||||
| chr7:2274351
|
C | T | 1 | a0001c0001t0005g0012 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.418+761G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2274351 | ||||||
| chr7:2274356
|
T | C | 1 | a0002c0019t0006g0356 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.418+756A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2274356 | ||||||
| chr7:2274412
|
T | G | 2 | a0001c0001t0001g0263a0001c0001t0001g0267 | 2 | NA18954.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.418+700A>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2274412 | ||||||
| chr7:2274502
|
G | A | 1 | a0001c0003t0006g0014 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.418+610C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2274502 | ||||||
| chr7:2274513
|
G | A | 1 | a0001c0001t0003g0037 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.418+599C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2274513 | ||||||
| chr7:2274519
|
A | G | 6 | a0001c0006t0013g0176a0001c0006t0013g0194a0001c0006t0013g0233others(3): Show | 6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.418+593T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2274519 | ||||||
| chr7:2274620
|
C | T | 1 | a0001c0001t0019g0069 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.418+492G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2274620 | ||||||
| chr7:2274992
|
TC | T | 321 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(318): Show | 323 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.418+119delG | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2274992 | ||||||
| chr7:2275017
|
G | A | 125 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(122): Show | 125 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.418+95C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2275017 | ||||||
| chr7:2275087
|
C | T | 1 | a0001c0001t0009g0130 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.418+25G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2275087 | ||||||
| chr7:2275259
|
G | A | 1 | a0001c0001t0002g0191 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.301-30C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2275259 | ||||||
| chr7:2275372
|
G | A | 1 | a0001c0003t0005g0315 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.301-143C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2275372 | ||||||
| chr7:2275373
|
G | C | 305 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(302): Show | 307 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.301-144C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2275373 | ||||||
| chr7:2275421
|
C | T | 116 | a0001c0001t0001g0146a0001c0001t0002g0017a0001c0001t0002g0018others(113): Show | 118 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(115): Show |
intron_variant | MODIFIER | c.301-192G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2275421 | ||||||
| chr7:2275470
|
C | T | 126 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(123): Show | 126 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.301-241G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2275470 | ||||||
| chr7:2275571
|
G | A | 2 | a0001c0001t0001g0175a0001c0001t0001g0257 | 2 | NA18978.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.301-342C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2275571 | ||||||
| chr7:2275575
|
G | A | 1 | a0001c0001t0001g0272 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.301-346C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2275575 | ||||||
| chr7:2275584
|
C | G | 1 | a0001c0001t0009g0312 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.301-355G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2275584 | ||||||
| chr7:2275589
|
C | G | 1 | a0001c0001t0009g0312 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.301-360G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2275589 | ||||||
| chr7:2275590
|
T | G | 1 | a0001c0001t0009g0312 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.301-361A>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2275590 | ||||||
| chr7:2275594
|
T | G | 1 | a0001c0001t0009g0312 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.301-365A>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2275594 | ||||||
| chr7:2275596
|
G | A | 1 | a0001c0001t0009g0312 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.301-367C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2275596 | ||||||
| chr7:2275689
|
G | A | 45 | a0001c0001t0003g0066a0001c0001t0003g0067a0001c0001t0003g0068others(42): Show | 45 | HG00544.hp1 HG00642.hp1 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.301-460C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2275689 | ||||||
| chr7:2275765
|
G | A | 9 | a0001c0001t0003g0037a0001c0001t0021g0303a0001c0001t0021g0354others(6): Show | 9 | HG00735.hp2 HG01069.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.301-536C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2275765 | ||||||
| chr7:2275942
|
G | A | 1 | a0001c0002t0004g0287 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.301-713C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2275942 | ||||||
| chr7:2275954
|
C | T | 6 | a0001c0006t0013g0176a0001c0006t0013g0194a0001c0006t0013g0233others(3): Show | 6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.301-725G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2275954 | ||||||
| chr7:2275985
|
G | A | 1 | a0001c0001t0005g0164 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.301-756C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2275985 | ||||||
| chr7:2275997
|
C | CA | 12 | a0001c0001t0001g0028a0001c0001t0001g0138a0001c0001t0002g0304others(9): Show | 12 | HG01069.hp2 HG01192.hp1 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.301-769dupT | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2275997 | ||||||
| chr7:2276146
|
G | A | 1 | a0001c0001t0001g0210 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.301-917C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2276146 | ||||||
| chr7:2276163
|
G | C | 22 | a0001c0001t0001g0119a0001c0001t0005g0011a0001c0001t0005g0012others(19): Show | 22 | HG01109.hp1 HG01192.hp2 HG02056.hp1 others(19): Show |
intron_variant | MODIFIER | c.301-934C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2276163 | ||||||
| chr7:2276204
|
G | A | 8 | a0001c0001t0014g0047a0001c0001t0014g0278a0001c0001t0014g0295others(5): Show | 8 | HG02451.hp2 HG02572.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.301-975C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2276204 | ||||||
| chr7:2276267
|
G | A | 12 | a0001c0001t0014g0047a0001c0001t0014g0278a0001c0001t0014g0295others(9): Show | 12 | HG01884.hp1 HG02451.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.301-1038C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2276267 | ||||||
| chr7:2276315
|
C | T | 131 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(128): Show | 131 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.301-1086G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2276315 | ||||||
| chr7:2276329
|
G | A | 1 | a0001c0002t0004g0265 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.301-1100C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2276329 | ||||||
| chr7:2276417
|
G | A | 1 | a0001c0001t0002g0041 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.301-1188C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2276417 | ||||||
| chr7:2276480
|
A | G | 8 | a0001c0001t0001g0175a0001c0001t0001g0177a0001c0001t0001g0188others(5): Show | 8 | HG00621.hp2 NA18612.hp1 NA18612.hp2 others(5): Show |
intron_variant | MODIFIER | c.301-1251T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2276480 | ||||||
| chr7:2276642
|
T | TA | 16 | a0001c0001t0002g0330a0001c0001t0009g0312a0001c0001t0021g0351others(13): Show | 16 | HG01243.hp2 HG02055.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.301-1414dupT | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2276642 | ||||||
| chr7:2276642
|
TA | T | 142 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(139): Show | 142 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.301-1414delT | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2276642 | ||||||
| chr7:2276886
|
AGT | A | 131 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(128): Show | 131 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.300+1212_300+1213d others(4): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2276886 | ||||||
| chr7:2276942
|
C | G | 2 | a0001c0001t0035g0152a0001c0001t0041g0150 | 2 | HG02257.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.300+1158G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2276942 | ||||||
| chr7:2277003
|
C | G | 6 | a0001c0006t0013g0176a0001c0006t0013g0194a0001c0006t0013g0233others(3): Show | 6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.300+1097G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2277003 | ||||||
| chr7:2277199
|
G | A | 1 | a0001c0001t0003g0115 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.300+901C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2277199 | ||||||
| chr7:2277217
|
C | T | 131 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(128): Show | 131 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.300+883G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2277217 | ||||||
| chr7:2277229
|
C | G | 1 | a0001c0002t0004g0245 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.300+871G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2277229 | ||||||
| chr7:2277263
|
C | G | 1 | a0001c0001t0009g0021 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.300+837G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2277263 | ||||||
| chr7:2277425
|
G | A | 1 | a0001c0001t0002g0256 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.300+675C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2277425 | ||||||
| chr7:2277449
|
G | A | 2 | a0001c0001t0022g0165a0001c0001t0022g0166 | 2 | HG02965.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.300+651C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2277449 | ||||||
| chr7:2277523
|
G | C | 2 | a0001c0001t0035g0152a0001c0001t0041g0150 | 2 | HG02257.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.300+577C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2277523 | ||||||
| chr7:2277564
|
G | T | 1 | a0001c0001t0023g0122 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.300+536C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2277564 | ||||||
| chr7:2277611
|
T | C | 6 | a0001c0001t0014g0047a0001c0001t0014g0278a0001c0001t0014g0295others(3): Show | 6 | HG02451.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.300+489A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2277611 | ||||||
| chr7:2277636
|
TA | T | 303 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(300): Show | 305 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.300+463delT | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2277636 | ||||||
| chr7:2277794
|
A | G | 257 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(254): Show | 259 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.300+306T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2277794 | ||||||
| chr7:2277804
|
A | G | 3 | a0001c0001t0011g0103a0001c0001t0011g0128a0001c0001t0011g0137 | 3 | HG01069.hp1 HG03831.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.300+296T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2277804 | ||||||
| chr7:2277806
|
C | T | 2 | a0001c0001t0003g0286a0001c0001t0003g0324 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.300+294G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2277806 | ||||||
| chr7:2277810
|
GA | G | 133 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(130): Show | 133 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.300+289delT | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2277810 | ||||||
| chr7:2277836
|
A | G | 1 | a0005c0008t0001g0249 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.300+264T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2277836 | ||||||
| chr7:2278055
|
T | C | 4 | a0002c0004t0018g0360a0002c0004t0018g0362a0002c0004t0018g0363others(1): Show | 4 | HG01884.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.300+45A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2278055 | ||||||
| chr7:2278589
|
CACTCACT others(76): Show |
C | 6 | a0001c0001t0014g0047a0001c0001t0014g0278a0001c0001t0014g0295others(3): Show | 6 | HG02451.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-367_95-285delCC others(81): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278589 | ||||||
| chr7:2278599
|
C | T | 4 | a0002c0004t0018g0360a0002c0004t0018g0362a0002c0004t0018g0363others(1): Show | 4 | HG01884.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-294G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278599 | ||||||
| chr7:2278618
|
GACTC | G | 131 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(128): Show | 131 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.95-317_95-314delGA others(2): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278618 | ||||||
| chr7:2278633
|
C | T | 131 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(128): Show | 131 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.95-328G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278633 | ||||||
| chr7:2278642
|
AGCCGGAC others(47): Show |
A | 4 | a0001c0006t0013g0176a0001c0006t0013g0194a0001c0006t0013g0276others(1): Show | 4 | HG03831.hp1 HG03927.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-391_95-338delGT others(52): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278642 | ||||||
| chr7:2278645
|
C | T | 107 | a0001c0001t0001g0146a0001c0001t0002g0017a0001c0001t0002g0018others(104): Show | 109 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.95-340G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278645 | ||||||
| chr7:2278646
|
G | A | 44 | a0001c0001t0003g0066a0001c0001t0003g0067a0001c0001t0003g0068others(41): Show | 44 | HG00544.hp1 HG00642.hp1 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.95-341C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278646 | ||||||
| chr7:2278661
|
A | C | 1 | a0001c0001t0011g0103 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.95-356T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278661 | ||||||
| chr7:2278667
|
C | A | 2 | a0001c0006t0013g0233a0001c0006t0013g0234 | 2 | HG00735.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.95-362G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278667 | ||||||
| chr7:2278667
|
C | T | 1 | a0001c0001t0003g0037 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.95-362G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278667 | ||||||
| chr7:2278667
|
CGCCGGAC others(362): Show |
C | 2 | a0001c0001t0022g0165a0001c0001t0022g0166 | 2 | HG02965.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.95-731_95-363del | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278667 | ||||||
| chr7:2278700
|
G | A | 1 | a0001c0001t0005g0080 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.95-395C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278700 | ||||||
| chr7:2278709
|
C | G | 5 | a0001c0003t0005g0008a0001c0006t0013g0176a0001c0006t0013g0194others(2): Show | 5 | HG02145.hp2 HG03831.hp1 HG03927.hp1 others(2): Show |
intron_variant | MODIFIER | c.95-404G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278709 | ||||||
| chr7:2278722
|
C | T | 70 | a0001c0001t0001g0146a0001c0001t0002g0017a0001c0001t0002g0018others(67): Show | 71 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.95-417G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278722 | ||||||
| chr7:2278723
|
G | A | 1 | a0001c0001t0001g0217 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.95-418C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278723 | ||||||
| chr7:2278725
|
A | C | 6 | a0001c0001t0016g0235a0001c0001t0016g0236a0001c0001t0016g0237others(3): Show | 6 | HG00735.hp2 HG01069.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.95-420T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278725 | ||||||
| chr7:2278738
|
C | CACACTAC others(109): Show |
1 | a0001c0001t0002g0311 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.95-434_95-433insCA others(114): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278738 | ||||||
| chr7:2278738
|
C | G | 107 | a0001c0001t0001g0146a0001c0001t0002g0017a0001c0001t0002g0018others(104): Show | 109 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.95-433G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278738 | ||||||
| chr7:2278754
|
A | C | 6 | a0001c0006t0013g0176a0001c0006t0013g0194a0001c0006t0013g0233others(3): Show | 6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-449T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278754 | ||||||
| chr7:2278754
|
AGCCGGAC others(22): Show |
A | 1 | a0001c0001t0003g0037 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.95-478_95-450delGT others(27): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278754 | ||||||
| chr7:2278758
|
G | A | 1 | a0001c0002t0004g0331 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.95-453C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278758 | ||||||
| chr7:2278788
|
GACTC | G | 4 | a0001c0006t0013g0176a0001c0006t0013g0194a0001c0006t0013g0276others(1): Show | 4 | HG03831.hp1 HG03927.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-487_95-484delGA others(2): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278788 | ||||||
| chr7:2278792
|
CACTCACA others(18): Show |
C | 134 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(131): Show | 134 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.95-512_95-488delCC others(23): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278792 | ||||||
| chr7:2278792
|
CACTCACA others(246): Show |
C | 4 | a0001c0001t0016g0235a0001c0001t0016g0236a0001c0001t0016g0237others(1): Show | 4 | HG01175.hp2 HG01516.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-740_95-488del | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278792 | ||||||
| chr7:2278812
|
CGCCGGAC others(217): Show |
C | 3 | a0001c0001t0001g0175a0001c0001t0035g0152a0001c0001t0041g0150 | 3 | HG02257.hp2 HG03209.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.95-731_95-508del | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278812 | ||||||
| chr7:2278812
|
CGCCGGAC others(275): Show |
C | 2 | a0001c0001t0001g0242a0001c0001t0001g0258 | 2 | HG03239.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.95-789_95-508del | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278812 | ||||||
| chr7:2278816
|
G | A | 2 | a0001c0001t0003g0038a0001c0001t0023g0122 | 2 | HG00639.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.95-511C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278816 | ||||||
| chr7:2278817
|
G | GACTC | 13 | a0001c0001t0002g0078a0001c0001t0002g0095a0001c0001t0002g0134others(10): Show | 13 | HG02280.hp1 HG03831.hp1 HG03927.hp1 others(10): Show |
intron_variant | MODIFIER | c.95-516_95-513dupGA others(2): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278817 | ||||||
| chr7:2278817
|
G | GACTCACA others(22): Show |
1 | a0001c0001t0002g0102 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.95-541_95-513dupGA others(27): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278817 | ||||||
| chr7:2278834
|
C | T | 49 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0003g0066others(46): Show | 49 | HG00544.hp1 HG00639.hp2 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.95-529G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278834 | ||||||
| chr7:2278837
|
C | A | 2 | a0001c0006t0013g0233a0001c0006t0013g0234 | 2 | HG00735.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.95-532G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278837 | ||||||
| chr7:2278864
|
G | A | 1 | a0001c0003t0005g0316 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.95-559C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278864 | ||||||
| chr7:2278866
|
C | A | 7 | a0001c0001t0002g0095a0001c0001t0002g0134a0001c0001t0002g0330others(4): Show | 7 | HG03831.hp1 HG03927.hp1 HG04115.hp2 others(4): Show |
intron_variant | MODIFIER | c.95-561G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278866 | ||||||
| chr7:2278866
|
CGCCGGAC others(221): Show |
C | 100 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(97): Show | 100 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.95-789_95-562del | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278866 | ||||||
| chr7:2278895
|
A | C | 19 | a0001c0001t0001g0073a0001c0001t0001g0195a0001c0001t0002g0095others(16): Show | 19 | HG00735.hp2 HG01069.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.95-590T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278895 | ||||||
| chr7:2278953
|
C | A | 4 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0008g0270others(1): Show | 4 | HG01109.hp1 HG02280.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-648G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278953 | ||||||
| chr7:2278953
|
CGCCGGAC others(192): Show |
C | 2 | a0001c0001t0001g0073a0001c0001t0001g0195 | 2 | HG01496.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.95-847_95-649del | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278953 | ||||||
| chr7:2278962
|
CACTCACA others(18): Show |
C | 1 | a0001c0001t0003g0037 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.95-682_95-658delCC others(23): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278962 | ||||||
| chr7:2278982
|
C | A | 2 | a0001c0006t0013g0233a0001c0006t0013g0234 | 2 | HG00735.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.95-677G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278982 | ||||||
| chr7:2278982
|
CGCCGGAC others(47): Show |
C | 1 | a0001c0001t0007g0106 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.95-731_95-678delTT others(52): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278982 | ||||||
| chr7:2278982
|
CGCCGGAC others(105): Show |
C | 25 | a0001c0001t0001g0119a0001c0001t0007g0019a0001c0001t0007g0024others(22): Show | 25 | HG01192.hp2 HG01884.hp1 HG02056.hp1 others(22): Show |
intron_variant | MODIFIER | c.95-789_95-678del | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278982 | ||||||
| chr7:2278982
|
CGCCGGAC others(163): Show |
C | 4 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0008g0270others(1): Show | 4 | HG01109.hp1 HG02280.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-847_95-678del | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278982 | ||||||
| chr7:2278987
|
G | GACTC | 13 | a0001c0001t0002g0095a0001c0001t0002g0102a0001c0001t0002g0109others(10): Show | 13 | HG00735.hp2 HG01069.hp2 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.95-686_95-683dupGA others(2): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278987 | ||||||
| chr7:2278987
|
G | GACTCACT others(26): Show |
74 | a0001c0001t0001g0146a0001c0001t0002g0017a0001c0001t0002g0018others(71): Show | 75 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.95-683_95-682insGA others(31): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278987 | ||||||
| chr7:2278987
|
G | GACTCACT others(55): Show |
23 | a0001c0001t0005g0080a0001c0001t0005g0100a0001c0001t0005g0163others(20): Show | 24 | HG01099.hp1 HG01243.hp1 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.95-683_95-682insGA others(60): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278987 | ||||||
| chr7:2278987
|
G | GACTCACT others(84): Show |
1 | a0001c0001t0005g0280 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.95-683_95-682insGA others(89): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278987 | ||||||
| chr7:2278987
|
G | GACTCACT others(482): Show |
2 | a0001c0001t0021g0303a0001c0001t0021g0354 | 2 | HG02809.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.95-683_95-682insGA others(487): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278987 | ||||||
| chr7:2278998
|
C | T | 2 | a0001c0002t0027g0189a0001c0002t0027g0348 | 2 | HG00639.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.95-693G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278998 | ||||||
| chr7:2279007
|
C | A | 4 | a0001c0006t0013g0176a0001c0006t0013g0194a0001c0006t0013g0276others(1): Show | 4 | HG03831.hp1 HG03927.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-702G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2279007 | ||||||
| chr7:2279036
|
A | C | 115 | a0001c0001t0001g0146a0001c0001t0002g0017a0001c0001t0002g0018others(112): Show | 117 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(114): Show |
intron_variant | MODIFIER | c.95-731T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2279036 | ||||||
| chr7:2279040
|
G | A | 1 | a0001c0001t0003g0136 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.95-735C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2279040 | ||||||
| chr7:2279065
|
C | A | 8 | a0001c0001t0022g0165a0001c0001t0022g0166a0001c0001t0035g0152others(5): Show | 8 | HG02257.hp2 HG02965.hp1 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.95-760G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2279065 | ||||||
| chr7:2279094
|
A | AGCCGGAC others(22): Show |
1 | a0001c0001t0003g0306 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.95-790_95-789insGT others(27): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2279094 | ||||||
| chr7:2279094
|
A | AGCCGGAC others(22): Show |
42 | a0001c0001t0003g0066a0001c0001t0003g0068a0001c0001t0003g0070others(39): Show | 42 | HG00544.hp1 HG00642.hp1 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.95-818_95-790dupGT others(27): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2279094 | ||||||
| chr7:2279094
|
A | AGCCGGAC others(80): Show |
1 | a0001c0003t0006g0310 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.95-876_95-790dupGT others(85): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2279094 | ||||||
| chr7:2279094
|
A | C | 121 | a0001c0001t0001g0146a0001c0001t0001g0175a0001c0001t0002g0017others(118): Show | 123 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.95-789T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2279094 | ||||||
| chr7:2279098
|
GGACTCAC others(21): Show |
G | 1 | a0001c0001t0001g0175 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.95-821_95-794delGG others(26): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2279098 | ||||||
| chr7:2279115
|
G | GGAGTCGA others(22): Show |
1 | a0001c0001t0002g0153 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.95-811_95-810insGG others(27): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2279115 | ||||||
| chr7:2279120
|
C | T | 6 | a0001c0003t0005g0316a0001c0003t0006g0010a0001c0003t0006g0013others(3): Show | 6 | HG02717.hp2 HG02886.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-815G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2279120 | ||||||
| chr7:2279123
|
CGCCGGAC others(22): Show |
C | 1 | a0001c0001t0007g0106 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.95-847_95-819delTT others(27): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2279123 | ||||||
| chr7:2279152
|
A | C | 281 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(278): Show | 283 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.95-847T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2279152 | ||||||
| chr7:2279184
|
C | T | 2 | a0001c0001t0022g0165a0001c0001t0022g0166 | 2 | HG02965.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.95-879G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2279184 | ||||||
| chr7:2279239
|
CGCCGGAC others(22): Show |
C | 4 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0008g0270others(1): Show | 4 | HG01109.hp1 HG02280.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-963_95-935delTT others(27): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2279239 | ||||||
| chr7:2279268
|
A | C | 1 | a0001c0001t0003g0067 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.95-963T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2279268 | ||||||
| chr7:2279288
|
C | T | 1 | a0009c0017t0002g0327 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.95-983G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2279288 | ||||||
| chr7:2279297
|
A | C | 1 | a0001c0001t0007g0329 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.95-992T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2279297 | ||||||
| chr7:2279300
|
CGGACTCA others(22): Show |
C | 1 | a0001c0001t0003g0067 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.95-1024_95-996delA others(28): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2279300 | ||||||
| chr7:2279355
|
C | A | 1 | a0001c0001t0003g0067 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.95-1050G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2279355 | ||||||
| chr7:2279358
|
T | C | 1 | a0001c0001t0003g0067 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.95-1053A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2279358 | ||||||
| chr7:2279444
|
G | A | 2 | a0001c0001t0001g0138a0001c0001t0001g0250 | 2 | NA19003.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.95-1139C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2279444 | ||||||
| chr7:2279494
|
G | A | 48 | a0001c0001t0003g0038a0001c0001t0003g0066a0001c0001t0003g0067others(45): Show | 48 | HG00544.hp1 HG00639.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.95-1189C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2279494 | ||||||
| chr7:2279544
|
G | A | 1 | a0001c0001t0003g0223 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.95-1239C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2279544 | ||||||
| chr7:2279571
|
G | A | 4 | a0002c0004t0018g0360a0002c0004t0018g0362a0002c0004t0018g0363others(1): Show | 4 | HG01884.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-1266C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2279571 | ||||||
| chr7:2279612
|
G | A | 5 | a0001c0001t0005g0080a0001c0001t0005g0352a0001c0001t0005g0353others(2): Show | 6 | HG01099.hp1 HG02109.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.95-1307C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2279612 | ||||||
| chr7:2279697
|
G | A | 12 | a0001c0001t0014g0047a0001c0001t0014g0278a0001c0001t0014g0295others(9): Show | 12 | HG01884.hp1 HG02451.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.95-1392C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2279697 | ||||||
| chr7:2279762
|
G | A | 1 | a0001c0001t0001g0175 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.95-1457C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2279762 | ||||||
| chr7:2279762
|
G | GA | 19 | a0001c0001t0001g0056a0001c0001t0001g0084a0001c0001t0001g0250others(16): Show | 19 | HG01934.hp2 HG02056.hp1 HG02083.hp2 others(16): Show |
intron_variant | MODIFIER | c.95-1458dupT | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2279762 | ||||||
| chr7:2279762
|
GA | G | 51 | a0001c0001t0001g0206a0001c0001t0001g0271a0001c0001t0002g0145others(48): Show | 51 | HG00544.hp1 HG00639.hp2 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.95-1458delT | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2279762 | ||||||
| chr7:2279762
|
GAAAAAAA | G | 8 | a0001c0001t0014g0047a0001c0001t0014g0278a0001c0001t0014g0295others(5): Show | 8 | HG02451.hp2 HG02572.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.95-1464_95-1458del others(7): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2279762 | ||||||
| chr7:2279951
|
C | T | 4 | a0002c0004t0018g0360a0002c0004t0018g0362a0002c0004t0018g0363others(1): Show | 4 | HG01884.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-1646G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2279951 | ||||||
| chr7:2279981
|
T | C | 1 | a0001c0001t0001g0120 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.95-1676A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2279981 | ||||||
| chr7:2280116
|
A | G | 2 | a0001c0001t0035g0152a0001c0001t0041g0150 | 2 | HG02257.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.95-1811T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2280116 | ||||||
| chr7:2280220
|
G | A | 3 | a0001c0001t0003g0038a0001c0001t0003g0223a0001c0001t0023g0122 | 3 | HG00639.hp2 HG01070.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.95-1915C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2280220 | ||||||
| chr7:2280234
|
G | C | 2 | a0001c0001t0001g0035a0001c0001t0001g0217 | 2 | NA18960.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.95-1929C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2280234 | ||||||
| chr7:2280304
|
GA | G | 4 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0008g0270others(1): Show | 4 | HG01109.hp1 HG02280.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-2000delT | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2280304 | ||||||
| chr7:2280413
|
C | T | 1 | a0001c0005t0001g0057 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.95-2108G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2280413 | ||||||
| chr7:2280477
|
CA | C | 9 | a0001c0001t0002g0078a0001c0001t0014g0047a0001c0001t0014g0278others(6): Show | 9 | HG02451.hp2 HG02572.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.95-2173delT | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2280477 | ||||||
| chr7:2280493
|
T | C | 1 | a0001c0001t0002g0118 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.95-2188A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2280493 | ||||||
| chr7:2280723
|
C | T | 12 | a0001c0001t0014g0047a0001c0001t0014g0278a0001c0001t0014g0295others(9): Show | 12 | HG01884.hp1 HG02451.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.95-2418G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2280723 | ||||||
| chr7:2280747
|
T | C | 6 | a0001c0001t0014g0047a0001c0001t0014g0278a0001c0001t0014g0295others(3): Show | 6 | HG02451.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-2442A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2280747 | ||||||
| chr7:2280765
|
A | C | 1 | a0002c0004t0018g0360 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.95-2460T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2280765 | ||||||
| chr7:2280792
|
C | CT | 237 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(234): Show | 239 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.95-2488dupA | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2280792 | ||||||
| chr7:2280825
|
C | T | 1 | a0001c0001t0002g0311 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.95-2520G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2280825 | ||||||
| chr7:2281225
|
G | A | 3 | a0001c0001t0017g0205a0001c0001t0017g0209a0001c0001t0017g0211 | 3 | HG02602.hp2 HG02735.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.95-2920C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2281225 | ||||||
| chr7:2281469
|
C | T | 5 | a0001c0001t0001g0184a0001c0001t0001g0229a0001c0001t0001g0341others(2): Show | 5 | HG00423.hp2 HG00438.hp2 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.95-3164G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2281469 | ||||||
| chr7:2281497
|
G | A | 3 | a0001c0001t0008g0001a0001c0001t0008g0048a0001c0001t0008g0162 | 4 | HG01081.hp2 HG03225.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-3192C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2281497 | ||||||
| chr7:2281544
|
G | A | 1 | a0001c0001t0002g0311 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.95-3239C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2281544 | ||||||
| chr7:2281547
|
A | G | 16 | a0001c0001t0001g0119a0001c0001t0007g0019a0001c0001t0007g0024others(13): Show | 16 | HG01192.hp2 HG02056.hp1 HG02738.hp2 others(13): Show |
intron_variant | MODIFIER | c.95-3242T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2281547 | ||||||
| chr7:2281612
|
A | G | 7 | a0001c0001t0003g0037a0001c0006t0013g0176a0001c0006t0013g0194others(4): Show | 7 | HG00735.hp2 HG01069.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.95-3307T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2281612 | ||||||
| chr7:2281647
|
A | T | 1 | a0001c0002t0010g0335 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.95-3342T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2281647 | ||||||
| chr7:2281797
|
G | A | 1 | a0001c0002t0004g0158 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.95-3492C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2281797 | ||||||
| chr7:2281838
|
T | C | 4 | a0002c0004t0018g0360a0002c0004t0018g0362a0002c0004t0018g0363others(1): Show | 4 | HG01884.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-3533A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2281838 | ||||||
| chr7:2281925
|
C | A | 1 | a0001c0001t0003g0037 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.95-3620G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2281925 | ||||||
| chr7:2282031
|
T | C | 1 | a0010c0018t0001g0355 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.95-3726A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2282031 | ||||||
| chr7:2282413
|
C | T | 1 | a0001c0001t0003g0037 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.95-4108G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2282413 | ||||||
| chr7:2282469
|
A | G | 2 | a0001c0006t0013g0233a0001c0006t0013g0234 | 2 | HG00735.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.95-4164T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2282469 | ||||||
| chr7:2282495
|
T | G | 13 | a0001c0001t0003g0037a0001c0001t0014g0047a0001c0001t0014g0278others(10): Show | 13 | HG01884.hp1 HG02451.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.95-4190A>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2282495 | ||||||
| chr7:2282521
|
A | G | 15 | a0001c0001t0001g0119a0001c0001t0007g0019a0001c0001t0007g0024others(12): Show | 15 | HG01192.hp2 HG02056.hp1 HG02738.hp2 others(12): Show |
intron_variant | MODIFIER | c.95-4216T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2282521 | ||||||
| chr7:2282703
|
G | A | 42 | a0001c0001t0003g0066a0001c0001t0003g0067a0001c0001t0003g0068others(39): Show | 42 | HG00544.hp1 HG00642.hp1 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.95-4398C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2282703 | ||||||
| chr7:2282768
|
G | A | 46 | a0001c0001t0003g0038a0001c0001t0003g0066a0001c0001t0003g0067others(43): Show | 46 | HG00544.hp1 HG00639.hp2 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.95-4463C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2282768 | ||||||
| chr7:2282859
|
C | G | 3 | a0001c0001t0005g0080a0001c0001t0005g0352a0001c0001t0005g0353 | 3 | HG01099.hp1 HG02109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.95-4554G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2282859 | ||||||
| chr7:2282860
|
G | A | 2 | a0001c0001t0009g0312a0001c0002t0029g0075 | 2 | HG03669.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.95-4555C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2282860 | ||||||
| chr7:2282949
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.95-4644C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2282949 | ||||||
| chr7:2282978
|
G | A | 1 | a0001c0001t0003g0037 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.95-4673C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2282978 | ||||||
| chr7:2282982
|
G | A | 283 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(280): Show | 285 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.95-4677C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2282982 | ||||||
| chr7:2282989
|
C | A | 46 | a0001c0001t0003g0038a0001c0001t0003g0066a0001c0001t0003g0067others(43): Show | 46 | HG00544.hp1 HG00639.hp2 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.95-4684G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2282989 | ||||||
| chr7:2282992
|
A | G | 46 | a0001c0001t0003g0038a0001c0001t0003g0066a0001c0001t0003g0067others(43): Show | 46 | HG00544.hp1 HG00639.hp2 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.95-4687T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2282992 | ||||||
| chr7:2282993
|
A | C | 46 | a0001c0001t0003g0038a0001c0001t0003g0066a0001c0001t0003g0067others(43): Show | 46 | HG00544.hp1 HG00639.hp2 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.95-4688T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2282993 | ||||||
| chr7:2282998
|
G | A | 1 | a0002c0004t0005g0366 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.95-4693C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2282998 | ||||||
| chr7:2283014
|
G | A | 1 | a0001c0001t0003g0037 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.95-4709C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2283014 | ||||||
| chr7:2283028
|
G | A | 61 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0003g0066others(58): Show | 61 | HG00544.hp1 HG00639.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.95-4723C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2283028 | ||||||
| chr7:2283037
|
T | C | 46 | a0001c0001t0003g0038a0001c0001t0003g0066a0001c0001t0003g0067others(43): Show | 46 | HG00544.hp1 HG00639.hp2 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.95-4732A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2283037 | ||||||
| chr7:2283075
|
C | T | 2 | a0001c0001t0001g0263a0001c0001t0001g0267 | 2 | NA18954.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.95-4770G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2283075 | ||||||
| chr7:2283076
|
G | A | 2 | a0001c0001t0001g0056a0001c0001t0009g0021 | 2 | NA18977.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.95-4771C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2283076 | ||||||
| chr7:2283088
|
T | G | 6 | a0001c0006t0013g0176a0001c0006t0013g0194a0001c0006t0013g0233others(3): Show | 6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-4783A>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2283088 | ||||||
| chr7:2283104
|
A | G | 6 | a0001c0006t0013g0176a0001c0006t0013g0194a0001c0006t0013g0233others(3): Show | 6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-4799T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2283104 | ||||||
| chr7:2283106
|
A | G | 6 | a0001c0006t0013g0176a0001c0006t0013g0194a0001c0006t0013g0233others(3): Show | 6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-4801T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2283106 | ||||||
| chr7:2283129
|
A | T | 2 | a0001c0001t0035g0152a0001c0001t0041g0150 | 2 | HG02257.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.95-4824T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2283129 | ||||||
| chr7:2283130
|
A | C | 6 | a0001c0006t0013g0176a0001c0006t0013g0194a0001c0006t0013g0233others(3): Show | 6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-4825T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2283130 | ||||||
| chr7:2283157
|
G | A | 4 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0008g0270others(1): Show | 4 | HG01109.hp1 HG02280.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-4852C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2283157 | ||||||
| chr7:2283176
|
C | G | 8 | a0001c0001t0014g0047a0001c0001t0014g0278a0001c0001t0014g0295others(5): Show | 8 | HG02451.hp2 HG02572.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.95-4871G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2283176 | ||||||
| chr7:2283177
|
G | A | 6 | a0001c0006t0013g0176a0001c0006t0013g0194a0001c0006t0013g0233others(3): Show | 6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-4872C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2283177 | ||||||
| chr7:2283254
|
G | A | 6 | a0001c0006t0013g0176a0001c0006t0013g0194a0001c0006t0013g0233others(3): Show | 6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-4949C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2283254 | ||||||
| chr7:2283267
|
G | C | 1 | a0001c0001t0014g0047 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.95-4962C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2283267 | ||||||
| chr7:2283308
|
T | C | 239 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(236): Show | 241 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(238): Show |
intron_variant | MODIFIER | c.95-5003A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2283308 | ||||||
| chr7:2283339
|
A | C | 1 | a0001c0001t0003g0037 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.95-5034T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2283339 | ||||||
| chr7:2283363
|
T | A | 2 | a0001c0001t0035g0152a0001c0001t0041g0150 | 2 | HG02257.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.95-5058A>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2283363 | ||||||
| chr7:2283384
|
C | G | 122 | a0001c0001t0001g0119a0001c0001t0001g0146a0001c0001t0002g0017others(119): Show | 124 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(121): Show |
intron_variant | MODIFIER | c.95-5079G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2283384 | ||||||
| chr7:2283408
|
C | T | 1 | a0005c0008t0001g0249 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.95-5103G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2283408 | ||||||
| chr7:2283411
|
C | T | 1 | a0001c0001t0001g0274 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.95-5106G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2283411 | ||||||
| chr7:2283526
|
T | C | 6 | a0001c0006t0013g0176a0001c0006t0013g0194a0001c0006t0013g0233others(3): Show | 6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-5221A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2283526 | ||||||
| chr7:2283532
|
G | C | 246 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(243): Show | 248 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.95-5227C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2283532 | ||||||
| chr7:2283602
|
G | A | 9 | a0001c0003t0006g0042a0001c0003t0006g0043a0001c0003t0006g0044others(6): Show | 9 | HG02055.hp2 HG02109.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.95-5297C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2283602 | ||||||
| chr7:2283638
|
G | A | 4 | a0001c0001t0011g0091a0001c0001t0011g0105a0001c0001t0011g0112others(1): Show | 4 | HG01099.hp2 HG01975.hp1 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-5333C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2283638 | ||||||
| chr7:2283670
|
G | A | 10 | a0001c0005t0001g0057a0001c0005t0001g0154a0001c0005t0001g0219others(7): Show | 10 | HG00423.hp1 HG00673.hp1 HG02015.hp2 others(7): Show |
intron_variant | MODIFIER | c.95-5365C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2283670 | ||||||
| chr7:2283758
|
G | A | 2 | a0001c0001t0003g0066a0001c0001t0003g0067 | 2 | HG01884.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.95-5453C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2283758 | ||||||
| chr7:2283814
|
G | T | 4 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0008g0270others(1): Show | 4 | HG01109.hp1 HG02280.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-5509C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2283814 | ||||||
| chr7:2283853
|
T | C | 106 | a0001c0001t0001g0146a0001c0001t0002g0017a0001c0001t0002g0018others(103): Show | 106 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.95-5548A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2283853 | ||||||
| chr7:2283951
|
A | G | 4 | a0002c0004t0018g0360a0002c0004t0018g0362a0002c0004t0018g0363others(1): Show | 4 | HG01884.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-5646T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2283951 | ||||||
| chr7:2284044
|
C | T | 4 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0008g0270others(1): Show | 4 | HG01109.hp1 HG02280.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-5739G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2284044 | ||||||
| chr7:2284077
|
C | T | 1 | a0001c0002t0004g0284 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.95-5772G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2284077 | ||||||
| chr7:2284121
|
G | T | 54 | a0001c0001t0001g0119a0001c0001t0002g0083a0001c0001t0002g0132others(51): Show | 56 | HG01081.hp2 HG01099.hp1 HG01192.hp2 others(53): Show |
intron_variant | MODIFIER | c.95-5816C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2284121 | ||||||
| chr7:2284209
|
C | T | 2 | a0001c0002t0029g0075a0001c0002t0046g0171 | 2 | HG03669.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.95-5904G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2284209 | ||||||
| chr7:2284258
|
G | A | 1 | a0001c0001t0019g0069 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.95-5953C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2284258 | ||||||
| chr7:2284276
|
G | A | 1 | a0001c0001t0002g0153 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.95-5971C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2284276 | ||||||
| chr7:2284326
|
G | A | 5 | a0001c0001t0014g0047a0001c0001t0014g0278a0001c0001t0014g0295others(2): Show | 5 | HG02572.hp2 HG02809.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.95-6021C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2284326 | ||||||
| chr7:2284344
|
C | T | 3 | a0001c0001t0014g0300a0001c0001t0022g0165a0001c0001t0022g0166 | 3 | HG02451.hp2 HG02965.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.95-6039G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2284344 | ||||||
| chr7:2284345
|
G | A | 5 | a0001c0001t0014g0047a0001c0001t0014g0278a0001c0001t0014g0295others(2): Show | 5 | HG02572.hp2 HG02809.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.95-6040C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2284345 | ||||||
| chr7:2284350
|
C | T | 1 | a0001c0001t0001g0283 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.95-6045G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2284350 | ||||||
| chr7:2284396
|
C | CT | 137 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(134): Show | 137 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.95-6092dupA | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2284396 | ||||||
| chr7:2284396
|
C | CTT | 89 | a0001c0001t0001g0073a0001c0001t0001g0084a0001c0001t0001g0177others(86): Show | 90 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.95-6093_95-6092dup others(2): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2284396 | ||||||
| chr7:2284396
|
C | CTTT | 19 | a0001c0001t0002g0132a0001c0001t0003g0070a0001c0001t0003g0085others(16): Show | 20 | HG00738.hp1 HG01070.hp2 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.95-6094_95-6092dup others(3): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2284396 | ||||||
| chr7:2284422
|
G | A | 1 | a0001c0001t0009g0108 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.95-6117C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2284422 | ||||||
| chr7:2284432
|
C | T | 52 | a0001c0001t0001g0119a0001c0001t0002g0083a0001c0001t0002g0132others(49): Show | 54 | HG01081.hp2 HG01099.hp1 HG01192.hp2 others(51): Show |
intron_variant | MODIFIER | c.95-6127G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2284432 | ||||||
| chr7:2284458
|
A | G | 2 | a0001c0001t0002g0078a0001c0001t0044g0094 | 2 | NA18983.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.95-6153T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2284458 | ||||||
| chr7:2284587
|
G | A | 1 | a0001c0001t0002g0102 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.95-6282C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2284587 | ||||||
| chr7:2284625
|
C | T | 1 | a0001c0001t0002g0232 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.95-6320G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2284625 | ||||||
| chr7:2284647
|
G | A | 5 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0008g0270others(2): Show | 5 | HG01109.hp1 HG02258.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-6342C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2284647 | ||||||
| chr7:2284690
|
C | T | 5 | a0001c0001t0009g0148a0001c0001t0009g0149a0001c0001t0009g0202others(2): Show | 5 | HG00558.hp2 NA18947.hp1 NA18981.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-6385G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2284690 | ||||||
| chr7:2284693
|
T | C | 5 | a0001c0001t0009g0148a0001c0001t0009g0149a0001c0001t0009g0202others(2): Show | 5 | HG00558.hp2 NA18947.hp1 NA18981.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-6388A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2284693 | ||||||
| chr7:2284709
|
C | T | 14 | a0001c0001t0002g0083a0001c0001t0002g0132a0001c0001t0008g0001others(11): Show | 15 | HG01081.hp2 HG02451.hp2 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.95-6404G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2284709 | ||||||
| chr7:2284746
|
G | A | 44 | a0001c0001t0001g0119a0001c0001t0003g0038a0001c0001t0005g0080others(41): Show | 45 | HG00639.hp2 HG01099.hp1 HG01192.hp2 others(42): Show |
intron_variant | MODIFIER | c.95-6441C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2284746 | ||||||
| chr7:2284953
|
T | C | 5 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0008g0270others(2): Show | 5 | HG01109.hp1 HG02258.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-6648A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2284953 | ||||||
| chr7:2284954
|
G | A | 2 | a0001c0001t0020g0156a0001c0001t0020g0157 | 2 | HG01261.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.95-6649C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2284954 | ||||||
| chr7:2284983
|
T | C | 4 | a0001c0006t0013g0176a0001c0006t0013g0194a0001c0006t0013g0276others(1): Show | 4 | HG03831.hp1 HG03927.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-6678A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2284983 | ||||||
| chr7:2284995
|
A | G | 2 | a0001c0001t0032g0305a0001c0002t0004g0328 | 2 | NA18970.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.95-6690T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2284995 | ||||||
| chr7:2285008
|
C | G | 1 | a0001c0001t0002g0304 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.95-6703G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2285008 | ||||||
| chr7:2285009
|
G | A | 134 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(131): Show | 134 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.95-6704C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2285009 | ||||||
| chr7:2285023
|
T | C | 6 | a0001c0001t0005g0163a0001c0001t0005g0164a0001c0001t0005g0169others(3): Show | 6 | HG02647.hp1 HG03139.hp1 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.95-6718A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2285023 | ||||||
| chr7:2285030
|
A | G | 51 | a0001c0001t0002g0311a0001c0001t0003g0038a0001c0001t0003g0160others(48): Show | 51 | HG00639.hp2 HG01070.hp2 HG01109.hp1 others(48): Show |
intron_variant | MODIFIER | c.95-6725T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2285030 | ||||||
| chr7:2285078
|
G | A | 6 | a0001c0001t0003g0160a0001c0001t0003g0281a0001c0001t0003g0296others(3): Show | 6 | HG01167.hp1 HG02559.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.95-6773C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2285078 | ||||||
| chr7:2285113
|
G | A | 105 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(102): Show | 105 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.95-6808C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2285113 | ||||||
| chr7:2285144
|
A | G | 5 | a0001c0001t0005g0080a0001c0001t0005g0352a0001c0001t0005g0353others(2): Show | 6 | HG01099.hp1 HG02109.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.95-6839T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2285144 | ||||||
| chr7:2285147
|
A | G | 5 | a0001c0001t0005g0080a0001c0001t0005g0352a0001c0001t0005g0353others(2): Show | 6 | HG01099.hp1 HG02109.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.95-6842T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2285147 | ||||||
| chr7:2285148
|
G | C | 180 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(177): Show | 181 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.95-6843C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2285148 | ||||||
| chr7:2285177
|
A | C | 1 | a0001c0001t0003g0160 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.95-6872T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2285177 | ||||||
| chr7:2285207
|
G | A | 3 | a0001c0001t0003g0160a0001c0001t0003g0296a0001c0001t0030g0159 | 3 | HG03239.hp1 HG03710.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.95-6902C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2285207 | ||||||
| chr7:2285211
|
C | CA | 132 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(129): Show | 132 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.95-6907dupT | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2285211 | ||||||
| chr7:2285211
|
C | CAA | 36 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(33): Show | 36 | HG00738.hp2 HG01192.hp2 HG01256.hp2 others(33): Show |
intron_variant | MODIFIER | c.95-6908_95-6907dup others(2): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2285211 | ||||||
| chr7:2285211
|
CA | C | 9 | a0001c0002t0004g0185a0001c0002t0010g0244a0001c0002t0010g0335others(6): Show | 9 | HG00639.hp1 HG01975.hp2 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.95-6907delT | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2285211 | ||||||
| chr7:2285341
|
T | A | 174 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(171): Show | 174 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(171): Show |
intron_variant | MODIFIER | c.95-7036A>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2285341 | ||||||
| chr7:2285415
|
C | A | 6 | a0001c0003t0006g0042a0001c0003t0006g0043a0001c0003t0006g0044others(3): Show | 6 | HG02109.hp1 HG02451.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.95-7110G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2285415 | ||||||
| chr7:2285514
|
C | T | 30 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(27): Show | 30 | HG01192.hp2 HG01256.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.95-7209G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2285514 | ||||||
| chr7:2285597
|
T | C | 12 | a0001c0001t0002g0083a0001c0001t0002g0132a0001c0001t0008g0001others(9): Show | 13 | HG01081.hp2 HG02615.hp2 HG02965.hp1 others(10): Show |
intron_variant | MODIFIER | c.95-7292A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2285597 | ||||||
| chr7:2285659
|
ACTTT | A | 5 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0008g0270others(2): Show | 5 | HG01109.hp1 HG02258.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-7358_95-7355del others(4): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2285659 | ||||||
| chr7:2285672
|
A | AT | 27 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(24): Show | 27 | HG01192.hp2 HG01256.hp2 HG01258.hp2 others(24): Show |
intron_variant | MODIFIER | c.95-7368dupA | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2285672 | ||||||
| chr7:2285748
|
C | G | 3 | a0001c0001t0001g0173a0001c0001t0001g0262a0001c0001t0001g0271 | 3 | NA18747.hp1 NA18946.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.95-7443G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2285748 | ||||||
| chr7:2285786
|
C | G | 1 | a0001c0001t0001g0120 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.95-7481G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2285786 | ||||||
| chr7:2285833
|
A | T | 1 | a0001c0001t0001g0297 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.95-7528T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2285833 | ||||||
| chr7:2285868
|
C | CG | 11 | a0001c0001t0005g0163a0001c0001t0005g0164a0001c0001t0005g0169others(8): Show | 11 | HG01255.hp1 HG03041.hp1 HG03139.hp1 others(8): Show |
intron_variant | MODIFIER | c.95-7564dupC | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2285868 | ||||||
| chr7:2285902
|
C | T | 1 | a0002c0004t0008g0365 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.95-7597G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2285902 | ||||||
| chr7:2286007
|
CT | C | 10 | a0001c0001t0001g0053a0001c0001t0001g0269a0001c0001t0003g0070others(7): Show | 10 | HG01109.hp1 HG01167.hp1 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.95-7703delA | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2286007 | ||||||
| chr7:2286201
|
G | A | 1 | a0001c0006t0039g0144 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.95-7896C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2286201 | ||||||
| chr7:2286201
|
G | C | 1 | a0001c0001t0002g0231 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.95-7896C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2286201 | ||||||
| chr7:2286236
|
T | C | 1 | a0001c0001t0002g0259 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.95-7931A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2286236 | ||||||
| chr7:2286318
|
G | A | 1 | a0001c0001t0032g0305 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.95-8013C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2286318 | ||||||
| chr7:2286358
|
T | C | 3 | a0001c0001t0002g0311a0001c0001t0007g0273a0001c0002t0047g0161 | 3 | HG01192.hp2 HG02723.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.95-8053A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2286358 | ||||||
| chr7:2286444
|
T | TGTACA | 6 | a0001c0001t0003g0160a0001c0001t0003g0281a0001c0001t0003g0296others(3): Show | 6 | HG01167.hp1 HG02559.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.95-8144_95-8140dup others(5): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2286444 | ||||||
| chr7:2286478
|
T | C | 5 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0008g0270others(2): Show | 5 | HG01109.hp1 HG02258.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-8173A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2286478 | ||||||
| chr7:2286521
|
A | AT | 123 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(120): Show | 123 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.95-8217_95-8216ins others(1): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2286521 | ||||||
| chr7:2286522
|
A | T | 5 | a0001c0001t0003g0038a0001c0001t0021g0351a0001c0001t0023g0122others(2): Show | 5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-8217T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2286522 | ||||||
| chr7:2286523
|
T | A | 5 | a0001c0001t0003g0038a0001c0001t0021g0351a0001c0001t0023g0122others(2): Show | 5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-8218A>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2286523 | ||||||
| chr7:2286523
|
T | TA | 3 | a0001c0001t0002g0256a0001c0006t0013g0194a0001c0006t0013g0276 | 3 | HG03831.hp1 HG04115.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.95-8219_95-8218ins others(1): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2286523 | ||||||
| chr7:2286524
|
T | A | 124 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(121): Show | 124 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.95-8219A>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2286524 | ||||||
| chr7:2286525
|
T | A | 8 | a0001c0001t0002g0256a0001c0001t0003g0038a0001c0001t0021g0351others(5): Show | 8 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.95-8220A>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2286525 | ||||||
| chr7:2286526
|
T | A | 124 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(121): Show | 124 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.95-8221A>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2286526 | ||||||
| chr7:2286527
|
T | A | 8 | a0001c0001t0002g0256a0001c0001t0003g0038a0001c0001t0021g0351others(5): Show | 8 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.95-8222A>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2286527 | ||||||
| chr7:2286528
|
T | A | 122 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(119): Show | 122 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.95-8223A>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2286528 | ||||||
| chr7:2286529
|
T | A | 2 | a0001c0001t0002g0256a0001c0001t0003g0038 | 2 | HG00639.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.95-8224A>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2286529 | ||||||
| chr7:2286567
|
G | A | 7 | a0001c0001t0040g0007a0001c0003t0005g0316a0001c0003t0006g0010others(4): Show | 7 | HG01891.hp1 HG02717.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.95-8262C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2286567 | ||||||
| chr7:2286580
|
C | T | 1 | a0001c0001t0003g0223 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.95-8275G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2286580 | ||||||
| chr7:2286614
|
G | A | 1 | a0001c0001t0001g0283 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.95-8309C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2286614 | ||||||
| chr7:2286624
|
T | C | 1 | a0001c0001t0001g0197 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.95-8319A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2286624 | ||||||
| chr7:2286626
|
C | A | 7 | a0003c0007t0012g0009a0003c0007t0012g0039a0003c0007t0012g0092others(4): Show | 7 | HG02818.hp1 HG02886.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.95-8321G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2286626 | ||||||
| chr7:2286651
|
C | T | 225 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(222): Show | 227 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(224): Show |
intron_variant | MODIFIER | c.95-8346G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2286651 | ||||||
| chr7:2286680
|
G | A | 1 | a0001c0001t0014g0300 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.95-8375C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2286680 | ||||||
| chr7:2286706
|
G | C | 7 | a0001c0001t0040g0007a0001c0003t0005g0316a0001c0003t0006g0010others(4): Show | 7 | HG01891.hp1 HG02717.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.95-8401C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2286706 | ||||||
| chr7:2286818
|
A | C | 13 | a0001c0002t0004g0034a0001c0002t0004g0079a0001c0002t0004g0230others(10): Show | 13 | HG00558.hp1 HG02698.hp1 NA18939.hp2 others(10): Show |
intron_variant | MODIFIER | c.95-8513T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2286818 | ||||||
| chr7:2286927
|
T | G | 1 | a0001c0001t0016g0237 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.95-8622A>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2286927 | ||||||
| chr7:2287011
|
C | A | 3 | a0001c0001t0003g0114a0001c0001t0003g0116a0001c0001t0003g0117 | 3 | HG02165.hp2 NA18966.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.95-8706G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2287011 | ||||||
| chr7:2287181
|
C | T | 122 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(119): Show | 122 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.95-8876G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2287181 | ||||||
| chr7:2287246
|
ACT | A | 122 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(119): Show | 122 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.95-8943_95-8942del others(2): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2287246 | ||||||
| chr7:2287297
|
T | C | 1 | a0001c0002t0004g0167 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.95-8992A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2287297 | ||||||
| chr7:2287483
|
G | A | 1 | a0001c0016t0003g0065 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.95-9178C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2287483 | ||||||
| chr7:2287500
|
A | G | 1 | a0001c0001t0037g0121 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.95-9195T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2287500 | ||||||
| chr7:2287686
|
G | A | 1 | a0005c0008t0001g0215 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.95-9381C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2287686 | ||||||
| chr7:2287769
|
A | AAAC | 4 | a0002c0004t0018g0360a0002c0004t0018g0362a0002c0004t0018g0363others(1): Show | 4 | HG01884.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-9467_95-9465dup others(3): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2287769 | ||||||
| chr7:2287784
|
C | A | 8 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0008g0270others(5): Show | 8 | HG01109.hp1 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.95-9479G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2287784 | ||||||
| chr7:2287784
|
CAAA | C | 5 | a0001c0001t0003g0038a0001c0001t0021g0351a0001c0001t0023g0122others(2): Show | 5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-9482_95-9480del others(3): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2287784 | ||||||
| chr7:2287787
|
A | C | 10 | a0001c0003t0006g0042a0001c0003t0006g0043a0001c0003t0006g0044others(7): Show | 10 | HG02109.hp1 HG02451.hp1 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.95-9482T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2287787 | ||||||
| chr7:2287811
|
G | A | 1 | a0001c0001t0014g0300 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.95-9506C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2287811 | ||||||
| chr7:2287869
|
C | T | 1 | a0001c0001t0002g0231 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.95-9564G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2287869 | ||||||
| chr7:2287894
|
GA | G | 9 | a0001c0001t0002g0077a0001c0001t0002g0191a0001c0001t0003g0066others(6): Show | 9 | HG00741.hp1 HG01175.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.95-9590delT | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2287894 | ||||||
| chr7:2287923
|
G | A | 1 | a0001c0001t0002g0304 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.95-9618C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2287923 | ||||||
| chr7:2287942
|
T | C | 1 | a0001c0001t0001g0224 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.95-9637A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2287942 | ||||||
| chr7:2287991
|
T | C | 1 | a0001c0001t0021g0351 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.95-9686A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2287991 | ||||||
| chr7:2288084
|
C | T | 6 | a0001c0001t0005g0163a0001c0001t0005g0164a0001c0001t0005g0169others(3): Show | 6 | HG01255.hp1 HG03041.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-9779G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2288084 | ||||||
| chr7:2288287
|
T | C | 2 | a0001c0001t0003g0038a0001c0001t0023g0122 | 2 | HG00639.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.95-9982A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2288287 | ||||||
| chr7:2288347
|
T | TA | 30 | a0001c0001t0001g0056a0001c0001t0001g0084a0001c0001t0001g0238others(27): Show | 31 | HG00738.hp2 HG01099.hp1 HG01175.hp1 others(28): Show |
intron_variant | MODIFIER | c.95-10043dupT | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2288347 | ||||||
| chr7:2288347
|
T | TAA | 6 | a0001c0001t0005g0163a0001c0001t0005g0164a0001c0001t0005g0169others(3): Show | 6 | HG01255.hp1 HG03041.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-10044_95-10043d others(4): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2288347 | ||||||
| chr7:2288347
|
TA | T | 45 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(42): Show | 45 | HG00639.hp1 HG01069.hp1 HG01081.hp1 others(42): Show |
intron_variant | MODIFIER | c.95-10043delT | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2288347 | ||||||
| chr7:2288580
|
G | A | 1 | a0001c0001t0003g0193 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.95-10275C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2288580 | ||||||
| chr7:2288660
|
A | G | 2 | a0001c0001t0001g0246a0001c0001t0001g0247 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.95-10355T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2288660 | ||||||
| chr7:2288951
|
G | A | 1 | a0001c0001t0021g0351 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.95-10646C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2288951 | ||||||
| chr7:2288989
|
A | G | 4 | a0002c0004t0018g0360a0002c0004t0018g0362a0002c0004t0018g0363others(1): Show | 4 | HG01884.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-10684T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2288989 | ||||||
| chr7:2289059
|
G | T | 1 | a0001c0001t0001g0146 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.95-10754C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2289059 | ||||||
| chr7:2289079
|
G | A | 4 | a0002c0004t0018g0360a0002c0004t0018g0362a0002c0004t0018g0363others(1): Show | 4 | HG01884.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-10774C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2289079 | ||||||
| chr7:2289170
|
C | A | 2 | a0001c0003t0005g0292a0001c0003t0028g0293 | 2 | HG02055.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.95-10865G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2289170 | ||||||
| chr7:2289186
|
C | T | 5 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0008g0270others(2): Show | 5 | HG01109.hp1 HG02258.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-10881G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2289186 | ||||||
| chr7:2289237
|
T | C | 2 | a0001c0001t0022g0165a0001c0001t0022g0166 | 2 | HG02965.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.95-10932A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2289237 | ||||||
| chr7:2289251
|
G | A | 1 | a0001c0001t0003g0223 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.95-10946C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2289251 | ||||||
| chr7:2289254
|
G | A | 2 | a0001c0001t0041g0150a0001c0003t0005g0151 | 2 | HG02257.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.95-10949C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2289254 | ||||||
| chr7:2289276
|
G | A | 5 | a0001c0001t0003g0038a0001c0001t0021g0351a0001c0001t0023g0122others(2): Show | 5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-10971C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2289276 | ||||||
| chr7:2289308
|
G | A | 2 | a0003c0007t0012g0092a0003c0007t0012g0131 | 2 | HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.95-11003C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2289308 | ||||||
| chr7:2289319
|
A | G | 6 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(3): Show | 6 | HG01256.hp2 HG01258.hp2 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.95-11014T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2289319 | ||||||
| chr7:2289452
|
C | G | 1 | a0001c0001t0002g0145 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.95-11147G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2289452 | ||||||
| chr7:2289495
|
G | C | 4 | a0002c0004t0018g0360a0002c0004t0018g0362a0002c0004t0018g0363others(1): Show | 4 | HG01884.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-11190C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2289495 | ||||||
| chr7:2289560
|
T | C | 1 | a0001c0001t0005g0080 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.95-11255A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2289560 | ||||||
| chr7:2289647
|
A | G | 4 | a0001c0006t0013g0176a0001c0006t0013g0194a0001c0006t0013g0276others(1): Show | 4 | HG03831.hp1 HG03927.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-11342T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2289647 | ||||||
| chr7:2289671
|
T | C | 1 | a0001c0001t0013g0074 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.95-11366A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2289671 | ||||||
| chr7:2289699
|
C | T | 1 | a0001c0001t0003g0223 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.95-11394G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2289699 | ||||||
| chr7:2289753
|
C | T | 1 | a0001c0001t0026g0216 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.95-11448G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2289753 | ||||||
| chr7:2289754
|
G | A | 2 | a0001c0001t0002g0017a0001c0001t0002g0018 | 2 | HG02630.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.95-11449C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2289754 | ||||||
| chr7:2289809
|
G | A | 1 | a0002c0019t0006g0356 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.95-11504C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2289809 | ||||||
| chr7:2289829
|
G | A | 2 | a0001c0001t0001g0073a0001c0001t0001g0195 | 2 | HG01496.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.95-11524C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2289829 | ||||||
| chr7:2289856
|
C | G | 1 | a0001c0001t0003g0037 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.95-11551G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2289856 | ||||||
| chr7:2289862
|
G | A | 190 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(187): Show | 190 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(187): Show |
intron_variant | MODIFIER | c.95-11557C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2289862 | ||||||
| chr7:2289873
|
G | A | 1 | a0001c0001t0001g0210 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.95-11568C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2289873 | ||||||
| chr7:2289964
|
G | A | 26 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(23): Show | 26 | HG01192.hp2 HG01256.hp2 HG01258.hp2 others(23): Show |
intron_variant | MODIFIER | c.95-11659C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2289964 | ||||||
| chr7:2289967
|
T | C | 26 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(23): Show | 26 | HG01192.hp2 HG01256.hp2 HG01258.hp2 others(23): Show |
intron_variant | MODIFIER | c.95-11662A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2289967 | ||||||
| chr7:2289979
|
G | T | 1 | a0001c0001t0025g0107 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.95-11674C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2289979 | ||||||
| chr7:2290428
|
CAGGAGGT | C | 28 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(25): Show | 28 | HG01192.hp2 HG01256.hp2 HG01258.hp2 others(25): Show |
intron_variant | MODIFIER | c.95-12130_95-12124d others(9): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2290428 | ||||||
| chr7:2290510
|
TAAAGA | T | 7 | a0001c0001t0001g0177a0001c0001t0005g0163a0001c0001t0005g0164others(4): Show | 7 | HG01255.hp1 HG03041.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.95-12210_95-12206d others(7): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2290510 | ||||||
| chr7:2290714
|
A | C | 1 | a0001c0001t0002g0191 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.95-12409T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2290714 | ||||||
| chr7:2290752
|
G | A | 1 | a0001c0001t0001g0241 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.95-12447C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2290752 | ||||||
| chr7:2290834
|
C | T | 8 | a0001c0001t0003g0160a0001c0001t0003g0281a0001c0001t0003g0296others(5): Show | 8 | HG01167.hp1 HG02559.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.95-12529G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2290834 | ||||||
| chr7:2290861
|
A | G | 138 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(135): Show | 138 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.95-12556T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2290861 | ||||||
| chr7:2290942
|
G | C | 1 | a0001c0001t0014g0300 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.95-12637C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2290942 | ||||||
| chr7:2290969
|
T | C | 1 | a0001c0001t0002g0145 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.95-12664A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2290969 | ||||||
| chr7:2291151
|
C | A | 2 | a0001c0001t0001g0283a0001c0001t0026g0216 | 2 | HG00738.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.95-12846G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2291151 | ||||||
| chr7:2291239
|
G | A | 1 | a0001c0001t0003g0136 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.95-12934C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2291239 | ||||||
| chr7:2291330
|
G | A | 1 | a0001c0002t0004g0261 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.95-13025C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2291330 | ||||||
| chr7:2291787
|
A | G | 1 | a0001c0001t0001g0248 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.95-13482T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2291787 | ||||||
| chr7:2291934
|
C | T | 5 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0008g0270others(2): Show | 5 | HG01109.hp1 HG02258.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-13629G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2291934 | ||||||
| chr7:2292092
|
T | C | 1 | a0001c0001t0014g0300 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.95-13787A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2292092 | ||||||
| chr7:2292106
|
A | C | 4 | a0001c0006t0013g0176a0001c0006t0013g0194a0001c0006t0013g0276others(1): Show | 4 | HG03831.hp1 HG03927.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-13801T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2292106 | ||||||
| chr7:2292109
|
C | T | 8 | a0001c0001t0003g0160a0001c0001t0003g0281a0001c0001t0003g0296others(5): Show | 8 | HG01167.hp1 HG02559.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.95-13804G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2292109 | ||||||
| chr7:2292409
|
G | A | 1 | a0001c0001t0035g0152 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.95-14104C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2292409 | ||||||
| chr7:2292443
|
G | C | 2 | a0001c0001t0040g0007a0002c0004t0023g0359 | 2 | HG01891.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.95-14138C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2292443 | ||||||
| chr7:2292474
|
C | T | 1 | a0001c0001t0017g0211 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.95-14169G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2292474 | ||||||
| chr7:2292475
|
G | A | 6 | a0001c0001t0005g0163a0001c0001t0005g0164a0001c0001t0005g0169others(3): Show | 6 | HG01255.hp1 HG03041.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-14170C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2292475 | ||||||
| chr7:2292480
|
C | T | 6 | a0001c0001t0005g0080a0001c0001t0005g0352a0001c0001t0005g0353others(3): Show | 7 | HG01099.hp1 HG01496.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.95-14175G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2292480 | ||||||
| chr7:2292539
|
G | C | 2 | a0001c0001t0003g0286a0001c0001t0003g0324 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.95-14234C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2292539 | ||||||
| chr7:2292590
|
T | C | 2 | a0001c0001t0003g0286a0001c0001t0003g0324 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.95-14285A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2292590 | ||||||
| chr7:2292704
|
C | A | 28 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(25): Show | 28 | HG01256.hp2 HG01258.hp2 HG01943.hp2 others(25): Show |
intron_variant | MODIFIER | c.95-14399G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2292704 | ||||||
| chr7:2292706
|
C | A | 1 | a0001c0001t0001g0297 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.95-14401G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2292706 | ||||||
| chr7:2292839
|
G | T | 1 | a0002c0004t0008g0365 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.95-14534C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2292839 | ||||||
| chr7:2292878
|
C | T | 1 | a0001c0001t0003g0186 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.95-14573G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2292878 | ||||||
| chr7:2293139
|
C | T | 2 | a0001c0001t0005g0163a0001c0001t0005g0169 | 2 | HG03579.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.95-14834G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2293139 | ||||||
| chr7:2293245
|
G | T | 131 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(128): Show | 131 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.95-14940C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2293245 | ||||||
| chr7:2293333
|
G | T | 131 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(128): Show | 131 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.95-15028C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2293333 | ||||||
| chr7:2293371
|
C | T | 2 | a0001c0001t0003g0068a0001c0001t0003g0072 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.95-15066G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2293371 | ||||||
| chr7:2293384
|
G | A | 29 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(26): Show | 29 | HG01256.hp2 HG01258.hp2 HG01943.hp2 others(26): Show |
intron_variant | MODIFIER | c.95-15079C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2293384 | ||||||
| chr7:2293393
|
C | T | 4 | a0001c0006t0013g0176a0001c0006t0013g0194a0001c0006t0013g0276others(1): Show | 4 | HG03831.hp1 HG03927.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-15088G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2293393 | ||||||
| chr7:2293422
|
A | G | 191 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(188): Show | 191 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(188): Show |
intron_variant | MODIFIER | c.95-15117T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2293422 | ||||||
| chr7:2293439
|
A | T | 1 | a0001c0001t0007g0329 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.95-15134T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2293439 | ||||||
| chr7:2293441
|
G | C | 1 | a0001c0016t0003g0065 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.95-15136C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2293441 | ||||||
| chr7:2293469
|
C | A | 6 | a0001c0001t0005g0163a0001c0001t0005g0164a0001c0001t0005g0169others(3): Show | 6 | HG01255.hp1 HG03041.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-15164G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2293469 | ||||||
| chr7:2293578
|
C | A | 2 | a0001c0001t0003g0038a0001c0001t0023g0122 | 2 | HG00639.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.95-15273G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2293578 | ||||||
| chr7:2293604
|
G | A | 5 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0008g0270others(2): Show | 5 | HG01109.hp1 HG02258.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-15299C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2293604 | ||||||
| chr7:2293618
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.95-15313G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2293618 | ||||||
| chr7:2293735
|
C | T | 2 | a0001c0001t0001g0119a0001c0001t0033g0126 | 2 | NA18964.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.95-15430G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2293735 | ||||||
| chr7:2293907
|
A | G | 153 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(150): Show | 153 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.95-15602T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2293907 | ||||||
| chr7:2293911
|
A | C | 1 | a0001c0001t0008g0097 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.95-15606T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2293911 | ||||||
| chr7:2293966
|
C | CA | 30 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(27): Show | 30 | HG01256.hp2 HG01258.hp2 HG01943.hp2 others(27): Show |
intron_variant | MODIFIER | c.95-15662dupT | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2293966 | ||||||
| chr7:2293998
|
T | C | 2 | a0001c0002t0004g0015a0001c0002t0004g0168 | 2 | HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.95-15693A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2293998 | ||||||
| chr7:2294026
|
G | A | 1 | a0001c0002t0029g0075 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.95-15721C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2294026 | ||||||
| chr7:2294268
|
T | C | 1 | a0001c0001t0041g0150 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.95-15963A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2294268 | ||||||
| chr7:2294309
|
C | T | 4 | a0002c0004t0018g0360a0002c0004t0018g0362a0002c0004t0018g0363others(1): Show | 4 | HG01884.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-16004G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2294309 | ||||||
| chr7:2294349
|
T | C | 1 | a0001c0002t0010g0344 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.95-16044A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2294349 | ||||||
| chr7:2294390
|
G | C | 176 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(173): Show | 176 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.95-16085C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2294390 | ||||||
| chr7:2294515
|
T | C | 4 | a0002c0004t0018g0360a0002c0004t0018g0362a0002c0004t0018g0363others(1): Show | 4 | HG01884.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-16210A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2294515 | ||||||
| chr7:2294518
|
G | A | 1 | a0001c0001t0035g0152 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.95-16213C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2294518 | ||||||
| chr7:2294600
|
G | A | 5 | a0001c0001t0003g0038a0001c0001t0021g0351a0001c0001t0023g0122others(2): Show | 5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-16295C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2294600 | ||||||
| chr7:2294693
|
G | A | 5 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0008g0270others(2): Show | 5 | HG01109.hp1 HG02258.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-16388C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2294693 | ||||||
| chr7:2294729
|
G | A | 29 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(26): Show | 29 | HG01256.hp2 HG01258.hp2 HG01943.hp2 others(26): Show |
intron_variant | MODIFIER | c.95-16424C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2294729 | ||||||
| chr7:2294751
|
G | A | 2 | a0001c0001t0001g0246a0001c0001t0001g0247 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.95-16446C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2294751 | ||||||
| chr7:2294766
|
G | A | 29 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(26): Show | 29 | HG01256.hp2 HG01258.hp2 HG01943.hp2 others(26): Show |
intron_variant | MODIFIER | c.95-16461C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2294766 | ||||||
| chr7:2294851
|
T | C | 1 | a0001c0001t0014g0300 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.95-16546A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2294851 | ||||||
| chr7:2295045
|
T | C | 5 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0008g0270others(2): Show | 5 | HG01109.hp1 HG02258.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-16740A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2295045 | ||||||
| chr7:2295131
|
G | A | 4 | a0002c0004t0018g0360a0002c0004t0018g0362a0002c0004t0018g0363others(1): Show | 4 | HG01884.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-16826C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2295131 | ||||||
| chr7:2295353
|
G | A | 29 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(26): Show | 29 | HG01256.hp2 HG01258.hp2 HG01943.hp2 others(26): Show |
intron_variant | MODIFIER | c.95-17048C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2295353 | ||||||
| chr7:2295359
|
G | C | 1 | a0001c0001t0001g0178 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.95-17054C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2295359 | ||||||
| chr7:2295378
|
G | A | 1 | a0001c0016t0003g0065 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.95-17073C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2295378 | ||||||
| chr7:2295402
|
C | CA | 146 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(143): Show | 146 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.95-17098dupT | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2295402 | ||||||
| chr7:2295465
|
G | A | 1 | a0001c0002t0010g0337 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.95-17160C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2295465 | ||||||
| chr7:2295563
|
G | A | 2 | a0001c0001t0008g0001a0001c0001t0008g0048 | 3 | HG01081.hp2 HG06807.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.95-17258C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2295563 | ||||||
| chr7:2295592
|
C | CA | 23 | a0001c0001t0001g0073a0001c0001t0003g0088a0001c0001t0003g0115others(20): Show | 23 | HG00544.hp1 HG00597.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.95-17288dupT | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2295592 | ||||||
| chr7:2295592
|
CA | C | 6 | a0001c0001t0002g0302a0001c0001t0003g0324a0001c0001t0019g0069others(3): Show | 6 | HG01081.hp1 HG01257.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-17288delT | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2295592 | ||||||
| chr7:2295592
|
CAAA | C | 7 | a0001c0001t0003g0038a0001c0001t0021g0351a0001c0001t0023g0122others(4): Show | 7 | HG00639.hp2 HG02258.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.95-17290_95-17288d others(5): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2295592 | ||||||
| chr7:2295592
|
CAAAA | C | 13 | a0001c0001t0001g0052a0001c0001t0005g0163a0001c0001t0005g0164others(10): Show | 13 | HG01255.hp1 HG02257.hp2 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.95-17291_95-17288d others(6): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2295592 | ||||||
| chr7:2295592
|
CAAAAA | C | 28 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0053others(25): Show | 28 | HG01256.hp2 HG01258.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.95-17292_95-17288d others(7): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2295592 | ||||||
| chr7:2295592
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0003g0223 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.95-17298_95-17288d others(13): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2295592 | ||||||
| chr7:2295592
|
CAAAAAAA others(5): Show |
C | 5 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0008g0270others(2): Show | 5 | HG01109.hp1 HG02258.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-17299_95-17288d others(14): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2295592 | ||||||
| chr7:2295592
|
CAAAAAAA others(6): Show |
C | 2 | a0001c0001t0007g0036a0001c0005t0015g0032 | 2 | NA18940.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.95-17300_95-17288d others(15): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2295592 | ||||||
| chr7:2295592
|
CAAAAAAA others(7): Show |
C | 124 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(121): Show | 124 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.95-17301_95-17288d others(16): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2295592 | ||||||
| chr7:2295763
|
G | A | 1 | a0001c0003t0005g0151 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.95-17458C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2295763 | ||||||
| chr7:2295766
|
G | A | 1 | a0001c0005t0001g0057 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.95-17461C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2295766 | ||||||
| chr7:2296038
|
G | A | 2 | a0001c0001t0003g0038a0001c0001t0023g0122 | 2 | HG00639.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.95-17733C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2296038 | ||||||
| chr7:2296180
|
CACAATAT others(2498): Show |
C | 5 | a0001c0001t0003g0038a0001c0001t0021g0351a0001c0001t0023g0122others(2): Show | 5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+15643_95-17876d others(2): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2296180 | ||||||
| chr7:2296241
|
A | G | 29 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(26): Show | 29 | HG01256.hp2 HG01258.hp2 HG01943.hp2 others(26): Show |
intron_variant | MODIFIER | c.95-17936T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2296241 | ||||||
| chr7:2296453
|
T | C | 1 | a0001c0001t0025g0093 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.94+17875A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2296453 | ||||||
| chr7:2296517
|
T | C | 1 | a0001c0001t0009g0202 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.94+17811A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2296517 | ||||||
| chr7:2296559
|
A | G | 1 | a0001c0001t0002g0118 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.94+17769T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2296559 | ||||||
| chr7:2296671
|
C | T | 6 | a0001c0001t0005g0163a0001c0001t0005g0164a0001c0001t0005g0169others(3): Show | 6 | HG01255.hp1 HG03041.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+17657G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2296671 | ||||||
| chr7:2296697
|
G | A | 1 | a0001c0002t0029g0075 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.94+17631C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2296697 | ||||||
| chr7:2296717
|
G | C | 2 | a0001c0001t0001g0124a0001c0005t0001g0154 | 2 | HG00621.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.94+17611C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2296717 | ||||||
| chr7:2296759
|
C | G | 1 | a0001c0001t0002g0102 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.94+17569G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2296759 | ||||||
| chr7:2296788
|
G | A | 5 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0008g0270others(2): Show | 5 | HG01109.hp1 HG02258.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+17540C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2296788 | ||||||
| chr7:2296903
|
C | A | 11 | a0001c0001t0007g0273a0001c0001t0008g0001a0001c0001t0008g0048others(8): Show | 12 | HG01081.hp2 HG01192.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.94+17425G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2296903 | ||||||
| chr7:2297027
|
G | A | 1 | a0001c0001t0013g0074 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.94+17301C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2297027 | ||||||
| chr7:2297196
|
A | G | 1 | a0001c0001t0019g0225 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.94+17132T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2297196 | ||||||
| chr7:2297364
|
A | T | 1 | a0001c0001t0003g0037 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.94+16964T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2297364 | ||||||
| chr7:2297406
|
C | T | 2 | a0001c0001t0003g0037a0001c0001t0007g0329 | 2 | HG02572.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.94+16922G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2297406 | ||||||
| chr7:2297437
|
C | G | 5 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0008g0270others(2): Show | 5 | HG01109.hp1 HG02258.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+16891G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2297437 | ||||||
| chr7:2297525
|
G | A | 3 | a0001c0001t0003g0088a0001c0001t0003g0089a0001c0001t0003g0090 | 3 | HG01074.hp2 HG01106.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.94+16803C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2297525 | ||||||
| chr7:2297550
|
C | CA | 69 | a0001c0001t0001g0146a0001c0001t0001g0195a0001c0001t0002g0040others(66): Show | 69 | HG00544.hp1 HG00597.hp2 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.94+16777dupT | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2297550 | ||||||
| chr7:2297550
|
C | CAA | 22 | a0001c0001t0001g0073a0001c0001t0002g0077a0001c0001t0002g0095others(19): Show | 22 | HG00642.hp1 HG00741.hp1 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.94+16776_94+16777d others(4): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2297550 | ||||||
| chr7:2297550
|
C | CAAA | 6 | a0001c0001t0001g0084a0001c0001t0003g0223a0002c0004t0018g0360others(3): Show | 6 | HG01070.hp2 HG01884.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+16775_94+16777d others(5): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2297550 | ||||||
| chr7:2297550
|
C | CAAAAA | 62 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0035others(59): Show | 62 | HG00099.hp2 HG00280.hp1 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.94+16773_94+16777d others(7): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2297550 | ||||||
| chr7:2297550
|
C | CAAAAAA | 58 | a0001c0001t0001g0031a0001c0001t0001g0049a0001c0001t0001g0124others(55): Show | 58 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.94+16772_94+16777d others(8): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2297550 | ||||||
| chr7:2297550
|
C | CAAAAAAA | 6 | a0001c0001t0001g0197a0001c0001t0001g0200a0001c0001t0001g0279others(3): Show | 6 | HG00738.hp2 HG01074.hp1 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.94+16771_94+16777d others(9): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2297550 | ||||||
| chr7:2297550
|
CA | C | 16 | a0001c0001t0001g0119a0001c0001t0002g0026a0001c0001t0002g0041others(13): Show | 16 | HG02040.hp1 HG02080.hp1 HG02080.hp2 others(13): Show |
intron_variant | MODIFIER | c.94+16777delT | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2297550 | ||||||
| chr7:2297550
|
CAA | C | 9 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(6): Show | 9 | HG01256.hp2 HG01258.hp2 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.94+16776_94+16777d others(4): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2297550 | ||||||
| chr7:2297550
|
CAAAAAAA others(5): Show |
C | 3 | a0001c0001t0003g0286a0001c0001t0024g0099a0001c0001t0024g0101 | 3 | HG01257.hp1 HG01257.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.94+16766_94+16777d others(14): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2297550 | ||||||
| chr7:2297647
|
G | A | 3 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0001g0274 | 3 | HG00733.hp2 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.94+16681C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2297647 | ||||||
| chr7:2297796
|
C | G | 4 | a0001c0001t0014g0278a0001c0001t0014g0295a0001c0001t0014g0298others(1): Show | 4 | HG02572.hp2 HG02809.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.94+16532G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2297796 | ||||||
| chr7:2297838
|
C | G | 1 | a0001c0001t0002g0145 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.94+16490G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2297838 | ||||||
| chr7:2297959
|
A | G | 1 | a0001c0002t0029g0075 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.94+16369T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2297959 | ||||||
| chr7:2297968
|
C | T | 3 | a0001c0001t0003g0037a0001c0001t0007g0329a0001c0001t0035g0152 | 3 | HG02572.hp1 HG03017.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.94+16360G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2297968 | ||||||
| chr7:2297981
|
C | T | 2 | a0001c0005t0001g0057a0001c0005t0001g0254 | 2 | HG00423.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.94+16347G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2297981 | ||||||
| chr7:2298023
|
T | C | 4 | a0002c0004t0018g0360a0002c0004t0018g0362a0002c0004t0018g0363others(1): Show | 4 | HG01884.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.94+16305A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298023 | ||||||
| chr7:2298072
|
T | C | 1 | a0001c0001t0021g0303 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.94+16256A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298072 | ||||||
| chr7:2298087
|
C | G | 6 | a0001c0001t0005g0163a0001c0001t0005g0164a0001c0001t0005g0169others(3): Show | 6 | HG01255.hp1 HG03041.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+16241G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298087 | ||||||
| chr7:2298091
|
G | A | 1 | a0001c0001t0007g0329 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.94+16237C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298091 | ||||||
| chr7:2298130
|
A | G | 6 | a0001c0001t0005g0163a0001c0001t0005g0164a0001c0001t0005g0169others(3): Show | 6 | HG01255.hp1 HG03041.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+16198T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298130 | ||||||
| chr7:2298172
|
G | A | 29 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(26): Show | 29 | HG01256.hp2 HG01258.hp2 HG01943.hp2 others(26): Show |
intron_variant | MODIFIER | c.94+16156C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298172 | ||||||
| chr7:2298290
|
T | A | 1 | a0001c0001t0008g0170 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.94+16038A>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298290 | ||||||
| chr7:2298319
|
A | G | 27 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(24): Show | 27 | HG01256.hp2 HG01258.hp2 HG01943.hp2 others(24): Show |
intron_variant | MODIFIER | c.94+16009T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298319 | ||||||
| chr7:2298452
|
C | A | 126 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(123): Show | 126 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.94+15876G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298452 | ||||||
| chr7:2298662
|
A | G | 1 | a0001c0001t0001g0056 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.94+15666T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298662 | ||||||
| chr7:2298690
|
G | T | 5 | a0001c0001t0003g0038a0001c0001t0021g0351a0001c0001t0023g0122others(2): Show | 5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+15638C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298690 | ||||||
| chr7:2298697
|
G | T | 5 | a0001c0001t0003g0038a0001c0001t0021g0351a0001c0001t0023g0122others(2): Show | 5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+15631C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298697 | ||||||
| chr7:2298704
|
G | T | 5 | a0001c0001t0003g0038a0001c0001t0021g0351a0001c0001t0023g0122others(2): Show | 5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+15624C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298704 | ||||||
| chr7:2298714
|
T | C | 5 | a0001c0001t0003g0038a0001c0001t0021g0351a0001c0001t0023g0122others(2): Show | 5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+15614A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298714 | ||||||
| chr7:2298722
|
T | C | 5 | a0001c0001t0003g0038a0001c0001t0021g0351a0001c0001t0023g0122others(2): Show | 5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+15606A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298722 | ||||||
| chr7:2298731
|
C | G | 5 | a0001c0001t0003g0038a0001c0001t0021g0351a0001c0001t0023g0122others(2): Show | 5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+15597G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298731 | ||||||
| chr7:2298737
|
C | G | 5 | a0001c0001t0003g0038a0001c0001t0021g0351a0001c0001t0023g0122others(2): Show | 5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+15591G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298737 | ||||||
| chr7:2298738
|
C | CCGGACTG | 5 | a0001c0001t0003g0038a0001c0001t0021g0351a0001c0001t0023g0122others(2): Show | 5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+15589_94+15590i others(9): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298738 | ||||||
| chr7:2298739
|
T | C | 5 | a0001c0001t0003g0038a0001c0001t0021g0351a0001c0001t0023g0122others(2): Show | 5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+15589A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298739 | ||||||
| chr7:2298743
|
G | A | 1 | a0001c0001t0009g0111 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.94+15585C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298743 | ||||||
| chr7:2298743
|
G | C | 5 | a0001c0001t0003g0038a0001c0001t0021g0351a0001c0001t0023g0122others(2): Show | 5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+15585C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298743 | ||||||
| chr7:2298753
|
A | G | 5 | a0001c0001t0003g0038a0001c0001t0021g0351a0001c0001t0023g0122others(2): Show | 5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+15575T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298753 | ||||||
| chr7:2298755
|
G | A | 6 | a0001c0001t0003g0038a0001c0001t0003g0223a0001c0001t0021g0351others(3): Show | 6 | HG00639.hp2 HG01070.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.94+15573C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298755 | ||||||
| chr7:2298761
|
A | G | 5 | a0001c0001t0003g0038a0001c0001t0021g0351a0001c0001t0023g0122others(2): Show | 5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+15567T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298761 | ||||||
| chr7:2298773
|
C | A | 1 | a0001c0001t0003g0038 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.94+15555G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298773 | ||||||
| chr7:2298773
|
C | G | 4 | a0001c0001t0021g0351a0001c0001t0023g0122a0001c0001t0041g0150others(1): Show | 4 | HG02257.hp2 HG02258.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.94+15555G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298773 | ||||||
| chr7:2298778
|
A | G | 5 | a0001c0001t0003g0038a0001c0001t0021g0351a0001c0001t0023g0122others(2): Show | 5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+15550T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298778 | ||||||
| chr7:2298780
|
C | T | 5 | a0001c0001t0003g0038a0001c0001t0021g0351a0001c0001t0023g0122others(2): Show | 5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+15548G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298780 | ||||||
| chr7:2298785
|
A | G | 5 | a0001c0001t0003g0038a0001c0001t0021g0351a0001c0001t0023g0122others(2): Show | 5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+15543T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298785 | ||||||
| chr7:2298792
|
A | C | 5 | a0001c0001t0003g0038a0001c0001t0021g0351a0001c0001t0023g0122others(2): Show | 5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+15536T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298792 | ||||||
| chr7:2298794
|
A | C | 5 | a0001c0001t0003g0038a0001c0001t0021g0351a0001c0001t0023g0122others(2): Show | 5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+15534T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298794 | ||||||
| chr7:2298795
|
G | C | 5 | a0001c0001t0003g0038a0001c0001t0021g0351a0001c0001t0023g0122others(2): Show | 5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+15533C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298795 | ||||||
| chr7:2298802
|
A | C | 5 | a0001c0001t0003g0038a0001c0001t0021g0351a0001c0001t0023g0122others(2): Show | 5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+15526T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298802 | ||||||
| chr7:2298804
|
A | G | 5 | a0001c0001t0003g0038a0001c0001t0021g0351a0001c0001t0023g0122others(2): Show | 5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+15524T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298804 | ||||||
| chr7:2298817
|
G | A | 2 | a0001c0001t0003g0264a0001c0001t0013g0074 | 2 | HG00642.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.94+15511C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298817 | ||||||
| chr7:2298817
|
G | C | 5 | a0001c0001t0003g0038a0001c0001t0021g0351a0001c0001t0023g0122others(2): Show | 5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+15511C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298817 | ||||||
| chr7:2298820
|
C | T | 5 | a0001c0001t0003g0038a0001c0001t0021g0351a0001c0001t0023g0122others(2): Show | 5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+15508G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298820 | ||||||
| chr7:2298829
|
T | C | 5 | a0001c0001t0003g0038a0001c0001t0021g0351a0001c0001t0023g0122others(2): Show | 5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+15499A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298829 | ||||||
| chr7:2298837
|
A | G | 5 | a0001c0001t0003g0038a0001c0001t0021g0351a0001c0001t0023g0122others(2): Show | 5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+15491T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298837 | ||||||
| chr7:2298839
|
A | C | 5 | a0001c0001t0003g0038a0001c0001t0021g0351a0001c0001t0023g0122others(2): Show | 5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+15489T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298839 | ||||||
| chr7:2298840
|
T | C | 5 | a0001c0001t0003g0038a0001c0001t0021g0351a0001c0001t0023g0122others(2): Show | 5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+15488A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298840 | ||||||
| chr7:2298843
|
T | C | 5 | a0001c0001t0003g0038a0001c0001t0021g0351a0001c0001t0023g0122others(2): Show | 5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+15485A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298843 | ||||||
| chr7:2298847
|
A | G | 5 | a0001c0001t0003g0038a0001c0001t0021g0351a0001c0001t0023g0122others(2): Show | 5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+15481T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298847 | ||||||
| chr7:2298852
|
T | C | 5 | a0001c0001t0003g0038a0001c0001t0021g0351a0001c0001t0023g0122others(2): Show | 5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+15476A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298852 | ||||||
| chr7:2298853
|
A | G | 5 | a0001c0001t0003g0038a0001c0001t0021g0351a0001c0001t0023g0122others(2): Show | 5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+15475T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298853 | ||||||
| chr7:2298866
|
G | T | 5 | a0001c0001t0003g0038a0001c0001t0021g0351a0001c0001t0023g0122others(2): Show | 5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+15462C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298866 | ||||||
| chr7:2298873
|
G | A | 5 | a0001c0001t0003g0038a0001c0001t0021g0351a0001c0001t0023g0122others(2): Show | 5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+15455C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298873 | ||||||
| chr7:2298882
|
A | G | 5 | a0001c0001t0003g0038a0001c0001t0021g0351a0001c0001t0023g0122others(2): Show | 5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+15446T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298882 | ||||||
| chr7:2299079
|
A | T | 1 | a0001c0001t0009g0081 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.94+15249T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2299079 | ||||||
| chr7:2299300
|
T | G | 1 | a0001c0001t0008g0270 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.94+15028A>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2299300 | ||||||
| chr7:2299309
|
G | A | 4 | a0002c0004t0018g0360a0002c0004t0018g0362a0002c0004t0018g0363others(1): Show | 4 | HG01884.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.94+15019C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2299309 | ||||||
| chr7:2299373
|
CAG | C | 9 | a0001c0001t0003g0160a0001c0001t0003g0223a0001c0001t0003g0281others(6): Show | 9 | HG01070.hp2 HG01167.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.94+14953_94+14954d others(4): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2299373 | ||||||
| chr7:2299391
|
G | A | 10 | a0001c0001t0005g0163a0001c0001t0005g0164a0001c0001t0005g0169others(7): Show | 10 | HG01255.hp1 HG01884.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.94+14937C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2299391 | ||||||
| chr7:2299468
|
C | T | 1 | a0001c0001t0001g0258 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.94+14860G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2299468 | ||||||
| chr7:2299634
|
C | G | 1 | a0001c0001t0026g0201 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.94+14694G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2299634 | ||||||
| chr7:2299651
|
A | G | 4 | a0001c0006t0013g0176a0001c0006t0013g0194a0001c0006t0013g0276others(1): Show | 4 | HG03831.hp1 HG03927.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.94+14677T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2299651 | ||||||
| chr7:2299770
|
G | T | 178 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(175): Show | 178 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.94+14558C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2299770 | ||||||
| chr7:2299872
|
T | C | 22 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(19): Show | 22 | HG01256.hp2 HG01258.hp2 HG01943.hp2 others(19): Show |
intron_variant | MODIFIER | c.94+14456A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2299872 | ||||||
| chr7:2299973
|
A | C | 6 | a0003c0007t0012g0009a0003c0007t0012g0039a0003c0007t0012g0092others(3): Show | 6 | HG02818.hp1 HG02922.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.94+14355T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2299973 | ||||||
| chr7:2300247
|
C | T | 1 | a0001c0016t0003g0065 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.94+14081G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2300247 | ||||||
| chr7:2300313
|
A | C | 1 | a0001c0002t0004g0158 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.94+14015T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2300313 | ||||||
| chr7:2300424
|
T | C | 7 | a0001c0001t0003g0160a0001c0001t0003g0296a0001c0001t0003g0318others(4): Show | 7 | HG02559.hp1 HG02809.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.94+13904A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2300424 | ||||||
| chr7:2300482
|
A | G | 147 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(144): Show | 147 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.94+13846T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2300482 | ||||||
| chr7:2300652
|
A | T | 48 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(45): Show | 49 | HG01099.hp1 HG01243.hp1 HG01243.hp2 others(46): Show |
intron_variant | MODIFIER | c.94+13676T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2300652 | ||||||
| chr7:2300663
|
A | C | 13 | a0001c0001t0001g0073a0001c0001t0001g0084a0001c0001t0001g0195others(10): Show | 13 | HG00544.hp1 HG00642.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.94+13665T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2300663 | ||||||
| chr7:2300813
|
T | C | 4 | a0002c0004t0018g0360a0002c0004t0018g0362a0002c0004t0018g0363others(1): Show | 4 | HG01884.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.94+13515A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2300813 | ||||||
| chr7:2300974
|
G | A | 4 | a0002c0004t0018g0360a0002c0004t0018g0362a0002c0004t0018g0363others(1): Show | 4 | HG01884.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.94+13354C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2300974 | ||||||
| chr7:2301007
|
C | T | 6 | a0001c0001t0003g0160a0001c0001t0003g0296a0001c0001t0003g0318others(3): Show | 6 | HG02559.hp1 HG02809.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.94+13321G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2301007 | ||||||
| chr7:2301306
|
GCAC | G | 32 | a0001c0001t0001g0073a0001c0001t0001g0084a0001c0001t0001g0195others(29): Show | 32 | HG00544.hp1 HG00642.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.94+13019_94+13021d others(5): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2301306 | ||||||
| chr7:2301325
|
G | A | 22 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(19): Show | 22 | HG01256.hp2 HG01258.hp2 HG01943.hp2 others(19): Show |
intron_variant | MODIFIER | c.94+13003C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2301325 | ||||||
| chr7:2301420
|
C | T | 126 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(123): Show | 126 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.94+12908G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2301420 | ||||||
| chr7:2301427
|
G | C | 1 | a0001c0001t0001g0197 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.94+12901C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2301427 | ||||||
| chr7:2301462
|
G | A | 1 | a0001c0005t0001g0254 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.94+12866C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2301462 | ||||||
| chr7:2301516
|
G | A | 5 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0008g0270others(2): Show | 5 | HG01109.hp1 HG02258.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+12812C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2301516 | ||||||
| chr7:2301644
|
A | C | 3 | a0001c0001t0014g0300a0001c0001t0022g0165a0001c0001t0022g0166 | 3 | HG02451.hp2 HG02965.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.94+12684T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2301644 | ||||||
| chr7:2301903
|
C | T | 1 | a0002c0004t0005g0366 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.94+12425G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2301903 | ||||||
| chr7:2301904
|
A | C | 6 | a0001c0001t0005g0163a0001c0001t0005g0164a0001c0001t0005g0169others(3): Show | 6 | HG01255.hp1 HG03041.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+12424T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2301904 | ||||||
| chr7:2301970
|
C | T | 5 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0008g0270others(2): Show | 5 | HG01109.hp1 HG02258.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+12358G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2301970 | ||||||
| chr7:2302028
|
G | A | 2 | a0001c0001t0002g0083a0001c0001t0002g0132 | 2 | HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.94+12300C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2302028 | ||||||
| chr7:2302089
|
A | ACCCTCTC others(17): Show |
1 | a0001c0001t0003g0306 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.94+12215_94+12238d others(26): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2302089 | ||||||
| chr7:2302106
|
G | A | 3 | a0001c0001t0001g0035a0001c0001t0001g0217a0001c0006t0039g0144 | 3 | HG04199.hp1 NA18960.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.94+12222C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2302106 | ||||||
| chr7:2302106
|
GACGGTCT others(18): Show |
G | 5 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0008g0270others(2): Show | 5 | HG01109.hp1 HG02258.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+12197_94+12221d others(27): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2302106 | ||||||
| chr7:2302147
|
T | G | 32 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(29): Show | 32 | HG01256.hp2 HG01258.hp2 HG01943.hp2 others(29): Show |
intron_variant | MODIFIER | c.94+12181A>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2302147 | ||||||
| chr7:2302156
|
G | A | 2 | a0001c0002t0010g0321a0001c0002t0010g0349 | 2 | NA19057.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.94+12172C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2302156 | ||||||
| chr7:2302240
|
T | C | 22 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(19): Show | 22 | HG01256.hp2 HG01258.hp2 HG01943.hp2 others(19): Show |
intron_variant | MODIFIER | c.94+12088A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2302240 | ||||||
| chr7:2302347
|
A | G | 357 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(354): Show | 359 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(356): Show |
intron_variant | MODIFIER | c.94+11981T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2302347 | ||||||
| chr7:2302356
|
G | A | 26 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(23): Show | 26 | HG00544.hp2 HG02056.hp1 NA18747.hp1 others(23): Show |
intron_variant | MODIFIER | c.94+11972C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2302356 | ||||||
| chr7:2302391
|
A | C | 1 | a0001c0001t0035g0152 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.94+11937T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2302391 | ||||||
| chr7:2302391
|
A | G | 1 | a0001c0001t0001g0297 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.94+11937T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2302391 | ||||||
| chr7:2302431
|
T | C | 120 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(117): Show | 120 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.94+11897A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2302431 | ||||||
| chr7:2302434
|
T | C | 121 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(118): Show | 121 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.94+11894A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2302434 | ||||||
| chr7:2302461
|
C | G | 32 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(29): Show | 32 | HG01256.hp2 HG01258.hp2 HG01943.hp2 others(29): Show |
intron_variant | MODIFIER | c.94+11867G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2302461 | ||||||
| chr7:2302462
|
C | T | 32 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(29): Show | 32 | HG01256.hp2 HG01258.hp2 HG01943.hp2 others(29): Show |
intron_variant | MODIFIER | c.94+11866G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2302462 | ||||||
| chr7:2302470
|
C | T | 1 | a0001c0002t0004g0290 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.94+11858G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2302470 | ||||||
| chr7:2302500
|
T | C | 4 | a0002c0004t0018g0360a0002c0004t0018g0362a0002c0004t0018g0363others(1): Show | 4 | HG01884.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.94+11828A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2302500 | ||||||
| chr7:2302515
|
G | A | 1 | a0001c0001t0001g0123 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.94+11813C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2302515 | ||||||
| chr7:2302541
|
G | A | 1 | a0001c0001t0035g0152 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.94+11787C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2302541 | ||||||
| chr7:2302547
|
CTCTGCCT others(32): Show |
C | 5 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0008g0270others(2): Show | 5 | HG01109.hp1 HG02258.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+11742_94+11780d others(41): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2302547 | ||||||
| chr7:2302559
|
G | A | 1 | a0001c0001t0003g0070 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.94+11769C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2302559 | ||||||
| chr7:2302579
|
G | A | 1 | a0001c0001t0001g0200 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.94+11749C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2302579 | ||||||
| chr7:2302586
|
T | C | 6 | a0001c0001t0005g0163a0001c0001t0005g0164a0001c0001t0005g0169others(3): Show | 6 | HG01255.hp1 HG03041.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+11742A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2302586 | ||||||
| chr7:2302675
|
G | A | 6 | a0001c0001t0005g0163a0001c0001t0005g0164a0001c0001t0005g0169others(3): Show | 6 | HG01255.hp1 HG03041.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+11653C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2302675 | ||||||
| chr7:2302689
|
G | A | 1 | a0001c0001t0001g0283 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.94+11639C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2302689 | ||||||
| chr7:2302739
|
C | T | 4 | a0001c0006t0013g0176a0001c0006t0013g0194a0001c0006t0013g0276others(1): Show | 4 | HG03831.hp1 HG03927.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.94+11589G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2302739 | ||||||
| chr7:2302751
|
A | G | 193 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(190): Show | 193 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(190): Show |
intron_variant | MODIFIER | c.94+11577T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2302751 | ||||||
| chr7:2302758
|
C | T | 4 | a0001c0006t0013g0176a0001c0006t0013g0194a0001c0006t0013g0276others(1): Show | 4 | HG03831.hp1 HG03927.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.94+11570G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2302758 | ||||||
| chr7:2302772
|
G | A | 4 | a0001c0006t0013g0176a0001c0006t0013g0194a0001c0006t0013g0276others(1): Show | 4 | HG03831.hp1 HG03927.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.94+11556C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2302772 | ||||||
| chr7:2302817
|
G | A | 9 | a0001c0001t0007g0273a0001c0001t0008g0001a0001c0001t0008g0048others(6): Show | 10 | HG01081.hp2 HG01192.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.94+11511C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2302817 | ||||||
| chr7:2302870
|
C | T | 1 | a0001c0001t0007g0181 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.94+11458G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2302870 | ||||||
| chr7:2302876
|
G | A | 1 | a0001c0001t0008g0270 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.94+11452C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2302876 | ||||||
| chr7:2302895
|
C | CCTCCGCC others(33): Show |
1 | a0001c0001t0002g0077 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.94+11393_94+11432d others(42): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2302895 | ||||||
| chr7:2302910
|
C | T | 9 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0008g0270others(6): Show | 9 | HG01109.hp1 HG01884.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.94+11418G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2302910 | ||||||
| chr7:2302927
|
G | A | 6 | a0001c0001t0005g0163a0001c0001t0005g0164a0001c0001t0005g0169others(3): Show | 6 | HG01255.hp1 HG03041.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+11401C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2302927 | ||||||
| chr7:2303000
|
G | A | 1 | a0001c0001t0003g0038 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.94+11328C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303000 | ||||||
| chr7:2303010
|
TGGGGGTC others(41): Show |
T | 1 | a0001c0002t0010g0349 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.94+11270_94+11317d others(50): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303010 | ||||||
| chr7:2303011
|
G | A | 1 | a0001c0001t0001g0282 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.94+11317C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303011 | ||||||
| chr7:2303023
|
C | G | 6 | a0001c0003t0006g0042a0001c0003t0006g0043a0001c0003t0006g0044others(3): Show | 6 | HG02109.hp1 HG02451.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.94+11305G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303023 | ||||||
| chr7:2303061
|
A | AGGTCAGC others(218): Show |
1 | a0001c0001t0001g0200 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.94+11266_94+11267i others(227): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303061 | ||||||
| chr7:2303074
|
A | G | 182 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(179): Show | 182 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(179): Show |
intron_variant | MODIFIER | c.94+11254T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303074 | ||||||
| chr7:2303087
|
C | T | 1 | a0001c0016t0003g0065 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.94+11241G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303087 | ||||||
| chr7:2303090
|
C | T | 1 | a0001c0002t0004g0182 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.94+11238G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303090 | ||||||
| chr7:2303117
|
C | A | 1 | a0001c0001t0011g0112 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.94+11211G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303117 | ||||||
| chr7:2303144
|
G | A | 2 | a0001c0002t0046g0171a0001c0005t0001g0220 | 2 | HG00673.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.94+11184C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303144 | ||||||
| chr7:2303168
|
A | G | 3 | a0001c0001t0021g0351a0001c0001t0041g0150a0001c0003t0005g0151 | 3 | HG02257.hp2 HG02647.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.94+11160T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303168 | ||||||
| chr7:2303218
|
G | A | 167 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(164): Show | 167 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.94+11110C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303218 | ||||||
| chr7:2303234
|
AGGGGGTC others(42): Show |
A | 6 | a0001c0001t0005g0163a0001c0001t0005g0164a0001c0001t0005g0169others(3): Show | 6 | HG01255.hp1 HG03041.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+11045_94+11093d others(51): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303234 | ||||||
| chr7:2303287
|
G | T | 27 | a0001c0001t0001g0229a0001c0001t0002g0330a0001c0001t0003g0306others(24): Show | 27 | HG00423.hp2 HG00558.hp1 HG00597.hp2 others(24): Show |
intron_variant | MODIFIER | c.94+11041C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303287 | ||||||
| chr7:2303299
|
G | C | 1 | a0001c0001t0001g0218 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.94+11029C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303299 | ||||||
| chr7:2303307
|
A | T | 4 | a0002c0004t0018g0360a0002c0004t0018g0362a0002c0004t0018g0363others(1): Show | 4 | HG01884.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.94+11021T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303307 | ||||||
| chr7:2303309
|
C | T | 4 | a0002c0004t0018g0360a0002c0004t0018g0362a0002c0004t0018g0363others(1): Show | 4 | HG01884.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.94+11019G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303309 | ||||||
| chr7:2303315
|
C | T | 2 | a0001c0006t0013g0233a0001c0006t0013g0234 | 2 | HG00735.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.94+11013G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303315 | ||||||
| chr7:2303347
|
C | T | 3 | a0001c0001t0005g0163a0001c0001t0005g0164a0001c0001t0005g0169 | 3 | HG03579.hp2 NA18906.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.94+10981G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303347 | ||||||
| chr7:2303360
|
G | A | 1 | a0001c0001t0003g0090 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.94+10968C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303360 | ||||||
| chr7:2303382
|
C | T | 18 | a0001c0001t0002g0330a0001c0002t0004g0034a0001c0002t0004g0079others(15): Show | 18 | HG00558.hp1 HG00597.hp2 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.94+10946G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303382 | ||||||
| chr7:2303396
|
C | A | 2 | a0001c0001t0020g0156a0001c0001t0020g0157 | 2 | HG01261.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.94+10932G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303396 | ||||||
| chr7:2303397
|
G | A | 7 | a0001c0001t0003g0223a0001c0001t0005g0163a0001c0001t0005g0164others(4): Show | 7 | HG01070.hp2 HG01255.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.94+10931C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303397 | ||||||
| chr7:2303423
|
T | C | 1 | a0001c0001t0002g0058 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.94+10905A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303423 | ||||||
| chr7:2303426
|
G | A | 1 | a0001c0001t0002g0058 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.94+10902C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303426 | ||||||
| chr7:2303441
|
C | T | 1 | a0001c0001t0003g0306 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.94+10887G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303441 | ||||||
| chr7:2303453
|
G | A | 1 | a0001c0001t0002g0058 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.94+10875C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303453 | ||||||
| chr7:2303512
|
G | A | 13 | a0001c0002t0004g0034a0001c0002t0004g0079a0001c0002t0004g0230others(10): Show | 13 | HG00558.hp1 HG02698.hp1 NA18939.hp2 others(10): Show |
intron_variant | MODIFIER | c.94+10816C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303512 | ||||||
| chr7:2303521
|
A | G | 5 | a0001c0005t0001g0057a0001c0005t0001g0219a0001c0005t0001g0220others(2): Show | 5 | HG00423.hp1 HG00673.hp1 HG02015.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+10807T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303521 | ||||||
| chr7:2303544
|
C | T | 5 | a0001c0001t0003g0038a0001c0001t0021g0351a0001c0001t0023g0122others(2): Show | 5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+10784G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303544 | ||||||
| chr7:2303557
|
T | G | 5 | a0001c0005t0001g0057a0001c0005t0001g0219a0001c0005t0001g0220others(2): Show | 5 | HG00423.hp1 HG00673.hp1 HG02015.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+10771A>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303557 | ||||||
| chr7:2303577
|
G | A | 4 | a0001c0001t0002g0191a0001c0001t0003g0183a0001c0001t0003g0192others(1): Show | 4 | HG00741.hp1 HG01981.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.94+10751C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303577 | ||||||
| chr7:2303656
|
A | C | 2 | a0001c0001t0001g0199a0001c0001t0001g0258 | 2 | HG00735.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.94+10672T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303656 | ||||||
| chr7:2303657
|
C | T | 1 | a0001c0001t0001g0173 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.94+10671G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303657 | ||||||
| chr7:2303664
|
T | C | 2 | a0001c0001t0001g0199a0001c0001t0001g0258 | 2 | HG00735.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.94+10664A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303664 | ||||||
| chr7:2303702
|
A | G | 1 | a0001c0001t0002g0026 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.94+10626T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303702 | ||||||
| chr7:2303727
|
A | G | 7 | a0001c0001t0001g0199a0001c0001t0001g0258a0001c0001t0002g0026others(4): Show | 7 | HG00735.hp1 HG01884.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.94+10601T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303727 | ||||||
| chr7:2303762
|
C | G | 5 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0008g0270others(2): Show | 5 | HG01109.hp1 HG02258.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+10566G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303762 | ||||||
| chr7:2303763
|
G | A | 1 | a0001c0001t0003g0193 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.94+10565C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303763 | ||||||
| chr7:2303816
|
T | C | 1 | a0001c0001t0003g0037 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.94+10512A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303816 | ||||||
| chr7:2303822
|
G | T | 7 | a0001c0001t0003g0160a0001c0001t0003g0281a0001c0001t0003g0318others(4): Show | 7 | HG01167.hp1 HG02559.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.94+10506C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303822 | ||||||
| chr7:2303878
|
C | T | 1 | a0001c0001t0002g0256 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.94+10450G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303878 | ||||||
| chr7:2303978
|
A | T | 125 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(122): Show | 125 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.94+10350T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303978 | ||||||
| chr7:2303979
|
A | T | 1 | a0001c0001t0001g0297 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.94+10349T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303979 | ||||||
| chr7:2303986
|
A | T | 187 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(184): Show | 187 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.94+10342T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303986 | ||||||
| chr7:2303995
|
TA | T | 33 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(30): Show | 33 | HG01256.hp2 HG01258.hp2 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.94+10332delT | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303995 | ||||||
| chr7:2304060
|
G | A | 2 | a0001c0005t0001g0057a0001c0005t0001g0254 | 2 | HG00423.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.94+10268C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304060 | ||||||
| chr7:2304110
|
T | A | 1 | a0001c0003t0005g0347 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.94+10218A>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304110 | ||||||
| chr7:2304129
|
T | C | 32 | a0001c0001t0001g0073a0001c0001t0001g0084a0001c0001t0001g0195others(29): Show | 32 | HG00544.hp1 HG00642.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.94+10199A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304129 | ||||||
| chr7:2304166
|
CA | C | 11 | a0001c0001t0001g0198a0001c0001t0001g0269a0001c0001t0003g0160others(8): Show | 11 | HG01167.hp1 HG02559.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.94+10161delT | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304166 | ||||||
| chr7:2304181
|
A | G | 1 | a0001c0001t0002g0071 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.94+10147T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304181 | ||||||
| chr7:2304271
|
A | G | 1 | a0001c0001t0003g0186 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.94+10057T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304271 | ||||||
| chr7:2304272
|
C | T | 28 | a0001c0001t0001g0229a0001c0001t0002g0330a0001c0001t0003g0296others(25): Show | 28 | HG00423.hp2 HG00558.hp1 HG00597.hp2 others(25): Show |
intron_variant | MODIFIER | c.94+10056G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304272 | ||||||
| chr7:2304275
|
C | T | 28 | a0001c0001t0001g0229a0001c0001t0002g0330a0001c0001t0003g0296others(25): Show | 28 | HG00423.hp2 HG00558.hp1 HG00597.hp2 others(25): Show |
intron_variant | MODIFIER | c.94+10053G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304275 | ||||||
| chr7:2304276
|
A | G | 28 | a0001c0001t0001g0229a0001c0001t0002g0330a0001c0001t0003g0296others(25): Show | 28 | HG00423.hp2 HG00558.hp1 HG00597.hp2 others(25): Show |
intron_variant | MODIFIER | c.94+10052T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304276 | ||||||
| chr7:2304282
|
C | T | 28 | a0001c0001t0001g0229a0001c0001t0002g0330a0001c0001t0003g0296others(25): Show | 28 | HG00423.hp2 HG00558.hp1 HG00597.hp2 others(25): Show |
intron_variant | MODIFIER | c.94+10046G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304282 | ||||||
| chr7:2304288
|
G | A | 1 | a0001c0001t0002g0304 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.94+10040C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304288 | ||||||
| chr7:2304288
|
G | T | 28 | a0001c0001t0001g0229a0001c0001t0002g0330a0001c0001t0003g0296others(25): Show | 28 | HG00423.hp2 HG00558.hp1 HG00597.hp2 others(25): Show |
intron_variant | MODIFIER | c.94+10040C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304288 | ||||||
| chr7:2304310
|
C | G | 5 | a0001c0001t0003g0038a0001c0001t0021g0351a0001c0001t0023g0122others(2): Show | 5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+10018G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304310 | ||||||
| chr7:2304311
|
A | G | 52 | a0001c0001t0001g0073a0001c0001t0001g0084a0001c0001t0001g0184others(49): Show | 52 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.94+10017T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304311 | ||||||
| chr7:2304315
|
T | C | 31 | a0001c0001t0001g0184a0001c0001t0001g0229a0001c0001t0002g0330others(28): Show | 31 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.94+10013A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304315 | ||||||
| chr7:2304319
|
C | A | 20 | a0001c0001t0001g0073a0001c0001t0001g0084a0001c0001t0001g0195others(17): Show | 20 | HG00544.hp1 HG00642.hp1 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.94+10009G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304319 | ||||||
| chr7:2304320
|
A | G | 52 | a0001c0001t0001g0073a0001c0001t0001g0084a0001c0001t0001g0184others(49): Show | 52 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.94+10008T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304320 | ||||||
| chr7:2304327
|
G | A | 1 | a0001c0001t0007g0329 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.94+10001C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304327 | ||||||
| chr7:2304333
|
A | G | 4 | a0001c0001t0002g0227a0001c0001t0019g0069a0001c0001t0019g0225others(1): Show | 4 | HG01934.hp1 HG03491.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.94+9995T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304333 | ||||||
| chr7:2304338
|
A | T | 1 | a0001c0001t0002g0041 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.94+9990T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304338 | ||||||
| chr7:2304339
|
T | C | 13 | a0001c0001t0001g0073a0001c0001t0001g0084a0001c0001t0001g0195others(10): Show | 13 | HG00544.hp1 HG00642.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.94+9989A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304339 | ||||||
| chr7:2304340
|
A | C | 175 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(172): Show | 175 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.94+9988T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304340 | ||||||
| chr7:2304340
|
A | G | 1 | a0001c0001t0007g0329 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.94+9988T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304340 | ||||||
| chr7:2304341
|
G | A | 3 | a0001c0001t0001g0221a0001c0001t0001g0255a0001c0003t0005g0008 | 3 | HG02145.hp2 NA18939.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.94+9987C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304341 | ||||||
| chr7:2304344
|
A | G | 4 | a0001c0001t0014g0300a0001c0001t0022g0165a0001c0001t0022g0166others(1): Show | 4 | HG02451.hp2 HG02965.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.94+9984T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304344 | ||||||
| chr7:2304345
|
C | T | 1 | a0001c0001t0003g0088 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.94+9983G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304345 | ||||||
| chr7:2304360
|
G | C | 6 | a0001c0001t0007g0329a0001c0001t0014g0295a0001c0001t0014g0298others(3): Show | 6 | HG00423.hp1 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+9968C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304360 | ||||||
| chr7:2304360
|
G | T | 2 | a0001c0001t0007g0024a0001c0001t0007g0025 | 2 | NA18946.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.94+9968C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304360 | ||||||
| chr7:2304361
|
G | A | 3 | a0001c0001t0014g0295a0001c0001t0014g0298a0001c0001t0034g0299 | 3 | HG02572.hp2 HG02809.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.94+9967C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304361 | ||||||
| chr7:2304372
|
A | G | 2 | a0001c0001t0001g0238a0001c0001t0001g0271 | 2 | HG01978.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.94+9956T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304372 | ||||||
| chr7:2304401
|
A | G | 1 | a0001c0002t0027g0189 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.94+9927T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304401 | ||||||
| chr7:2304405
|
G | A | 5 | a0001c0001t0003g0160a0001c0001t0007g0273a0001c0002t0004g0015others(2): Show | 5 | HG01192.hp2 HG01243.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+9923C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304405 | ||||||
| chr7:2304406
|
T | C | 1 | a0001c0001t0003g0140 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.94+9922A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304406 | ||||||
| chr7:2304416
|
C | T | 5 | a0001c0001t0014g0047a0001c0001t0014g0278a0001c0001t0014g0295others(2): Show | 5 | HG02572.hp2 HG02809.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.94+9912G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304416 | ||||||
| chr7:2304421
|
G | A | 1 | a0001c0001t0001g0283 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.94+9907C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304421 | ||||||
| chr7:2304424
|
G | T | 1 | a0001c0001t0001g0271 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.94+9904C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304424 | ||||||
| chr7:2304488
|
G | A | 1 | a0001c0001t0035g0152 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.94+9840C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304488 | ||||||
| chr7:2304539
|
A | G | 1 | a0001c0001t0001g0123 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.94+9789T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304539 | ||||||
| chr7:2304568
|
C | T | 151 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(148): Show | 151 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.94+9760G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304568 | ||||||
| chr7:2304668
|
C | T | 5 | a0001c0001t0003g0038a0001c0001t0021g0351a0001c0001t0023g0122others(2): Show | 5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+9660G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304668 | ||||||
| chr7:2304738
|
G | A | 1 | a0001c0001t0009g0021 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.94+9590C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304738 | ||||||
| chr7:2304830
|
G | A | 1 | a0001c0001t0035g0152 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.94+9498C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304830 | ||||||
| chr7:2304860
|
G | A | 1 | a0001c0001t0002g0256 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.94+9468C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304860 | ||||||
| chr7:2304966
|
G | C | 4 | a0002c0004t0018g0360a0002c0004t0018g0362a0002c0004t0018g0363others(1): Show | 4 | HG01884.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.94+9362C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304966 | ||||||
| chr7:2305048
|
G | A | 18 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(15): Show | 18 | HG00639.hp2 HG01256.hp2 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.94+9280C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2305048 | ||||||
| chr7:2305086
|
G | A | 9 | a0001c0001t0001g0175a0001c0001t0001g0188a0001c0001t0001g0257others(6): Show | 9 | HG00621.hp2 NA18612.hp2 NA18978.hp2 others(6): Show |
intron_variant | MODIFIER | c.94+9242C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2305086 | ||||||
| chr7:2305093
|
G | A | 1 | a0001c0001t0002g0118 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.94+9235C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2305093 | ||||||
| chr7:2305110
|
C | CA | 5 | a0001c0001t0003g0281a0001c0001t0003g0318a0001c0001t0005g0280others(2): Show | 5 | HG01167.hp1 HG01192.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.94+9217dupT | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2305110 | ||||||
| chr7:2305213
|
C | T | 5 | a0001c0001t0003g0281a0001c0001t0003g0318a0001c0001t0005g0280others(2): Show | 5 | HG01167.hp1 HG01192.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.94+9115G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2305213 | ||||||
| chr7:2305360
|
TTTTG | T | 5 | a0001c0001t0003g0281a0001c0001t0003g0318a0001c0001t0005g0280others(2): Show | 5 | HG01167.hp1 HG01192.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.94+8964_94+8967del others(4): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2305360 | ||||||
| chr7:2305456
|
T | C | 185 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(182): Show | 186 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.94+8872A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2305456 | ||||||
| chr7:2305520
|
C | G | 1 | a0001c0001t0001g0177 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.94+8808G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2305520 | ||||||
| chr7:2305565
|
T | C | 3 | a0001c0001t0014g0300a0001c0001t0022g0165a0001c0001t0022g0166 | 3 | HG02451.hp2 HG02965.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.94+8763A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2305565 | ||||||
| chr7:2305953
|
G | A | 1 | a0001c0001t0001g0119 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.94+8375C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2305953 | ||||||
| chr7:2306077
|
G | C | 1 | a0003c0007t0012g0133 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.94+8251C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2306077 | ||||||
| chr7:2306139
|
T | G | 3 | a0001c0001t0014g0300a0001c0001t0022g0165a0001c0001t0022g0166 | 3 | HG02451.hp2 HG02965.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.94+8189A>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2306139 | ||||||
| chr7:2306161
|
T | A | 1 | a0001c0001t0001g0172 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.94+8167A>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2306161 | ||||||
| chr7:2306205
|
G | A | 1 | a0001c0001t0035g0152 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.94+8123C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2306205 | ||||||
| chr7:2306273
|
G | A | 2 | a0001c0001t0002g0040a0002c0019t0006g0356 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.94+8055C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2306273 | ||||||
| chr7:2306300
|
G | C | 6 | a0001c0001t0002g0040a0001c0001t0008g0270a0001c0001t0035g0152others(3): Show | 6 | HG01109.hp1 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+8028C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2306300 | ||||||
| chr7:2306400
|
G | A | 1 | a0001c0001t0001g0224 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.94+7928C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2306400 | ||||||
| chr7:2306480
|
C | T | 167 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(164): Show | 168 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.94+7848G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2306480 | ||||||
| chr7:2306493
|
T | C | 3 | a0001c0001t0014g0300a0001c0001t0022g0165a0001c0001t0022g0166 | 3 | HG02451.hp2 HG02965.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.94+7835A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2306493 | ||||||
| chr7:2306584
|
C | T | 1 | a0001c0001t0002g0304 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.94+7744G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2306584 | ||||||
| chr7:2306638
|
C | T | 2 | a0001c0001t0003g0038a0001c0001t0023g0122 | 2 | HG00639.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.94+7690G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2306638 | ||||||
| chr7:2306639
|
A | T | 8 | a0001c0001t0002g0078a0001c0001t0002g0095a0001c0001t0002g0134others(5): Show | 8 | NA18978.hp1 NA18983.hp2 NA18988.hp2 others(5): Show |
intron_variant | MODIFIER | c.94+7689T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2306639 | ||||||
| chr7:2306646
|
C | G | 1 | a0001c0001t0036g0023 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.94+7682G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2306646 | ||||||
| chr7:2306708
|
G | A | 4 | a0002c0004t0018g0360a0002c0004t0018g0362a0002c0004t0018g0363others(1): Show | 4 | HG01884.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.94+7620C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2306708 | ||||||
| chr7:2306739
|
T | G | 2 | a0001c0001t0014g0300a0001c0001t0035g0152 | 2 | HG02451.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.94+7589A>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2306739 | ||||||
| chr7:2306745
|
A | G | 4 | a0001c0001t0003g0038a0001c0001t0003g0140a0001c0001t0021g0351others(1): Show | 4 | HG00639.hp2 HG01192.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.94+7583T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2306745 | ||||||
| chr7:2306765
|
G | A | 1 | a0001c0016t0003g0065 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.94+7563C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2306765 | ||||||
| chr7:2306929
|
A | G | 2 | a0001c0001t0021g0303a0001c0003t0006g0322 | 2 | HG02055.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.94+7399T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2306929 | ||||||
| chr7:2306977
|
T | A | 135 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(132): Show | 135 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.94+7351A>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2306977 | ||||||
| chr7:2306983
|
A | AATT | 135 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(132): Show | 135 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.94+7344_94+7345ins others(3): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2306983 | ||||||
| chr7:2307173
|
T | C | 1 | a0001c0001t0001g0120 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.94+7155A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2307173 | ||||||
| chr7:2307273
|
AT | A | 187 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(184): Show | 188 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.94+7054delA | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2307273 | ||||||
| chr7:2307359
|
G | A | 1 | a0001c0002t0004g0147 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.94+6969C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2307359 | ||||||
| chr7:2307384
|
G | A | 3 | a0001c0001t0035g0152a0001c0001t0041g0150a0001c0003t0005g0151 | 3 | HG02257.hp2 HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.94+6944C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2307384 | ||||||
| chr7:2307403
|
C | CG | 13 | a0001c0001t0008g0048a0001c0001t0014g0047a0001c0001t0014g0278others(10): Show | 13 | HG02109.hp1 HG02451.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.94+6924dupC | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2307403 | ||||||
| chr7:2307544
|
C | T | 2 | a0001c0001t0002g0017a0001c0001t0002g0018 | 2 | HG02630.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.94+6784G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2307544 | ||||||
| chr7:2307581
|
G | A | 3 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0001g0258 | 3 | HG01516.hp1 HG01517.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.94+6747C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2307581 | ||||||
| chr7:2307606
|
TG | T | 3 | a0001c0001t0003g0160a0001c0001t0030g0159a0001c0002t0004g0158 | 3 | HG01243.hp2 HG03239.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.94+6721delC | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2307606 | ||||||
| chr7:2307634
|
C | CA | 73 | a0001c0001t0001g0073a0001c0001t0001g0084a0001c0001t0001g0119others(70): Show | 73 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.94+6693dupT | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2307634 | ||||||
| chr7:2307634
|
C | CAA | 21 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0138others(18): Show | 21 | HG00621.hp1 HG01106.hp2 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.94+6692_94+6693dup others(2): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2307634 | ||||||
| chr7:2307634
|
CA | C | 130 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.94+6693delT | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2307634 | ||||||
| chr7:2307634
|
CAA | C | 7 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0008g0001others(4): Show | 8 | HG01081.hp2 HG02145.hp2 HG02293.hp2 others(5): Show |
intron_variant | MODIFIER | c.94+6692_94+6693del others(2): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2307634 | ||||||
| chr7:2307634
|
CAAA | C | 7 | a0001c0001t0002g0040a0001c0001t0005g0012a0001c0002t0004g0015others(4): Show | 7 | HG02280.hp2 HG02486.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.94+6691_94+6693del others(3): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2307634 | ||||||
| chr7:2307634
|
CAAAA | C | 18 | a0001c0001t0003g0088a0001c0001t0003g0089a0001c0001t0003g0090others(15): Show | 19 | HG01074.hp2 HG01106.hp1 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.94+6690_94+6693del others(4): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2307634 | ||||||
| chr7:2307644
|
A | T | 3 | a0001c0001t0035g0152a0001c0001t0041g0150a0001c0003t0005g0151 | 3 | HG02257.hp2 HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.94+6684T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2307644 | ||||||
| chr7:2307657
|
AAG | A | 24 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(21): Show | 24 | HG00423.hp1 HG00597.hp1 HG01256.hp2 others(21): Show |
intron_variant | MODIFIER | c.94+6669_94+6670del others(2): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2307657 | ||||||
| chr7:2307798
|
G | A | 45 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(42): Show | 46 | HG00423.hp1 HG00597.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.94+6530C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2307798 | ||||||
| chr7:2307870
|
T | C | 2 | a0001c0001t0002g0017a0001c0001t0002g0018 | 2 | HG02630.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.94+6458A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2307870 | ||||||
| chr7:2307978
|
A | AT | 26 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(23): Show | 26 | HG00423.hp1 HG00597.hp1 HG01256.hp2 others(23): Show |
intron_variant | MODIFIER | c.94+6349dupA | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2307978 | ||||||
| chr7:2308118
|
C | T | 85 | a0001c0001t0001g0073a0001c0001t0001g0084a0001c0001t0001g0119others(82): Show | 85 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.94+6210G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2308118 | ||||||
| chr7:2308219
|
G | C | 92 | a0001c0001t0001g0073a0001c0001t0001g0084a0001c0001t0001g0119others(89): Show | 92 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.94+6109C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2308219 | ||||||
| chr7:2308229
|
T | C | 16 | a0001c0001t0002g0040a0002c0004t0005g0002a0002c0004t0005g0366others(13): Show | 17 | HG01255.hp1 HG01496.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.94+6099A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2308229 | ||||||
| chr7:2308230
|
A | G | 3 | a0001c0001t0003g0038a0001c0016t0003g0065a0004c0013t0003g0005 | 3 | HG00639.hp2 HG02258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.94+6098T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2308230 | ||||||
| chr7:2308352
|
C | G | 2 | a0001c0001t0003g0038a0001c0016t0003g0065 | 2 | HG00639.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.94+5976G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2308352 | ||||||
| chr7:2308447
|
C | T | 5 | a0001c0001t0003g0140a0001c0001t0005g0352a0001c0001t0005g0353others(2): Show | 5 | HG01099.hp1 HG01192.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+5881G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2308447 | ||||||
| chr7:2308496
|
C | T | 4 | a0001c0001t0002g0134a0001c0001t0003g0085a0001c0001t0003g0086others(1): Show | 4 | HG02056.hp2 NA18973.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.94+5832G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2308496 | ||||||
| chr7:2308604
|
T | G | 1 | a0001c0001t0001g0267 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.94+5724A>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2308604 | ||||||
| chr7:2308665
|
C | CA | 51 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(48): Show | 51 | HG00544.hp2 HG00733.hp1 HG01109.hp1 others(48): Show |
intron_variant | MODIFIER | c.94+5662dupT | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2308665 | ||||||
| chr7:2308665
|
CA | C | 85 | a0001c0001t0001g0073a0001c0001t0001g0119a0001c0001t0001g0120others(82): Show | 85 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.94+5662delT | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2308665 | ||||||
| chr7:2308681
|
A | AG | 7 | a0001c0001t0035g0152a0001c0001t0040g0007a0001c0001t0041g0150others(4): Show | 7 | HG01891.hp1 HG02145.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.94+5646_94+5647ins others(1): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2308681 | ||||||
| chr7:2308687
|
A | G | 89 | a0001c0001t0001g0073a0001c0001t0001g0084a0001c0001t0001g0119others(86): Show | 89 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.94+5641T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2308687 | ||||||
| chr7:2308704
|
C | T | 1 | a0001c0001t0001g0184 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.94+5624G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2308704 | ||||||
| chr7:2308774
|
G | C | 1 | a0001c0001t0002g0268 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.94+5554C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2308774 | ||||||
| chr7:2308780
|
A | AT | 53 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(50): Show | 54 | HG00597.hp1 HG00639.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.94+5547dupA | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2308780 | ||||||
| chr7:2308912
|
C | T | 133 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.94+5416G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2308912 | ||||||
| chr7:2308915
|
G | A | 6 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0002t0004g0015others(3): Show | 6 | HG02280.hp2 HG02486.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+5413C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2308915 | ||||||
| chr7:2308978
|
G | A | 7 | a0001c0001t0035g0152a0001c0001t0040g0007a0001c0001t0041g0150others(4): Show | 7 | HG01891.hp1 HG02145.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.94+5350C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2308978 | ||||||
| chr7:2308981
|
G | T | 2 | a0001c0001t0001g0173a0001c0001t0001g0174 | 2 | NA18952.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.94+5347C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2308981 | ||||||
| chr7:2309017
|
G | T | 1 | a0001c0002t0004g0294 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.94+5311C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2309017 | ||||||
| chr7:2309052
|
G | A | 6 | a0001c0003t0006g0042a0001c0003t0006g0043a0001c0003t0006g0044others(3): Show | 6 | HG02109.hp1 HG02451.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.94+5276C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2309052 | ||||||
| chr7:2309131
|
C | T | 6 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0002t0004g0015others(3): Show | 6 | HG02280.hp2 HG02486.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+5197G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2309131 | ||||||
| chr7:2309255
|
A | C | 153 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(150): Show | 155 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(152): Show |
intron_variant | MODIFIER | c.94+5073T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2309255 | ||||||
| chr7:2309280
|
G | C | 26 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(23): Show | 26 | HG00423.hp1 HG00597.hp1 HG01256.hp2 others(23): Show |
intron_variant | MODIFIER | c.94+5048C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2309280 | ||||||
| chr7:2309305
|
T | C | 26 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(23): Show | 26 | HG00423.hp1 HG00597.hp1 HG01256.hp2 others(23): Show |
intron_variant | MODIFIER | c.94+5023A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2309305 | ||||||
| chr7:2309454
|
G | A | 1 | a0006c0009t0012g0368 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.94+4874C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2309454 | ||||||
| chr7:2309496
|
C | T | 1 | a0001c0001t0003g0037 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.94+4832G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2309496 | ||||||
| chr7:2309510
|
T | C | 48 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(45): Show | 50 | HG00423.hp1 HG00597.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.94+4818A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2309510 | ||||||
| chr7:2309624
|
A | G | 1 | a0001c0001t0001g0172 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.94+4704T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2309624 | ||||||
| chr7:2309697
|
C | G | 1 | a0001c0001t0008g0001 | 2 | HG01081.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.94+4631G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2309697 | ||||||
| chr7:2309717
|
G | C | 1 | a0001c0003t0005g0334 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.94+4611C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2309717 | ||||||
| chr7:2309765
|
G | A | 1 | a0001c0002t0046g0171 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.94+4563C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2309765 | ||||||
| chr7:2309788
|
T | C | 1 | a0001c0002t0004g0147 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.94+4540A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2309788 | ||||||
| chr7:2309835
|
T | C | 152 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(149): Show | 154 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(151): Show |
intron_variant | MODIFIER | c.94+4493A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2309835 | ||||||
| chr7:2309864
|
G | A | 1 | a0001c0001t0002g0077 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.94+4464C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2309864 | ||||||
| chr7:2309865
|
C | T | 2 | a0001c0001t0003g0160a0001c0001t0030g0159 | 2 | HG03239.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.94+4463G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2309865 | ||||||
| chr7:2309973
|
G | A | 150 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(147): Show | 151 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(148): Show |
intron_variant | MODIFIER | c.94+4355C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2309973 | ||||||
| chr7:2310111
|
G | A | 12 | a0001c0001t0001g0340a0001c0001t0001g0341a0001c0001t0001g0342others(9): Show | 12 | HG02040.hp1 HG02080.hp1 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.94+4217C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2310111 | ||||||
| chr7:2310151
|
G | A | 3 | a0001c0001t0005g0352a0001c0001t0005g0353a0001c0001t0021g0351 | 3 | HG01099.hp1 HG02109.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.94+4177C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2310151 | ||||||
| chr7:2310230
|
G | A | 1 | a0001c0005t0001g0154 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.94+4098C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2310230 | ||||||
| chr7:2310484
|
G | A | 1 | a0001c0003t0005g0347 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.94+3844C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2310484 | ||||||
| chr7:2310513
|
A | G | 12 | a0001c0001t0001g0073a0001c0001t0002g0071a0001c0001t0002g0076others(9): Show | 12 | HG00280.hp2 HG00642.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.94+3815T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2310513 | ||||||
| chr7:2310549
|
T | C | 151 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(148): Show | 153 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(150): Show |
intron_variant | MODIFIER | c.94+3779A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2310549 | ||||||
| chr7:2310593
|
C | T | 2 | a0001c0001t0003g0066a0001c0001t0003g0067 | 2 | HG01884.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.94+3735G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2310593 | ||||||
| chr7:2310681
|
G | A | 1 | a0001c0001t0001g0271 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.94+3647C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2310681 | ||||||
| chr7:2310688
|
G | A | 26 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(23): Show | 26 | HG00423.hp1 HG00597.hp1 HG01256.hp2 others(23): Show |
intron_variant | MODIFIER | c.94+3640C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2310688 | ||||||
| chr7:2310733
|
T | C | 97 | a0001c0001t0001g0073a0001c0001t0001g0084a0001c0001t0001g0119others(94): Show | 97 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.94+3595A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2310733 | ||||||
| chr7:2310757
|
T | TG | 97 | a0001c0001t0001g0073a0001c0001t0001g0084a0001c0001t0001g0119others(94): Show | 97 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.94+3570dupC | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2310757 | ||||||
| chr7:2310777
|
A | G | 1 | a0001c0001t0007g0273 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.94+3551T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2310777 | ||||||
| chr7:2310798
|
G | A | 150 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(147): Show | 152 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(149): Show |
intron_variant | MODIFIER | c.94+3530C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2310798 | ||||||
| chr7:2310816
|
G | A | 103 | a0001c0001t0001g0073a0001c0001t0001g0084a0001c0001t0001g0119others(100): Show | 103 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.94+3512C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2310816 | ||||||
| chr7:2310845
|
C | T | 4 | a0001c0002t0004g0288a0001c0002t0004g0289a0001c0002t0004g0290others(1): Show | 4 | NA18985.hp1 NA19003.hp2 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.94+3483G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2310845 | ||||||
| chr7:2310860
|
G | C | 3 | a0001c0001t0001g0146a0001c0001t0002g0145a0001c0006t0039g0144 | 3 | HG03490.hp2 HG03834.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.94+3468C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2310860 | ||||||
| chr7:2310880
|
T | C | 136 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.94+3448A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2310880 | ||||||
| chr7:2311068
|
T | A | 6 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0002t0004g0015others(3): Show | 6 | HG02280.hp2 HG02486.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+3260A>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2311068 | ||||||
| chr7:2311115
|
T | G | 14 | a0002c0004t0005g0002a0002c0004t0005g0366a0002c0004t0005g0367others(11): Show | 15 | HG01255.hp1 HG01496.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.94+3213A>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2311115 | ||||||
| chr7:2311306
|
C | G | 1 | a0001c0001t0014g0278 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.94+3022G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2311306 | ||||||
| chr7:2311312
|
G | A | 1 | a0001c0003t0005g0008 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.94+3016C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2311312 | ||||||
| chr7:2311324
|
C | T | 47 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(44): Show | 49 | HG00423.hp1 HG00597.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.94+3004G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2311324 | ||||||
| chr7:2311373
|
C | T | 4 | a0001c0001t0040g0007a0001c0003t0005g0008a0001c0003t0006g0010others(1): Show | 4 | HG01891.hp1 HG02145.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.94+2955G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2311373 | ||||||
| chr7:2311447
|
G | C | 23 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(20): Show | 23 | HG00423.hp1 HG00597.hp1 HG01256.hp2 others(20): Show |
intron_variant | MODIFIER | c.94+2881C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2311447 | ||||||
| chr7:2311554
|
C | T | 1 | a0001c0002t0004g0158 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.94+2774G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2311554 | ||||||
| chr7:2311613
|
T | G | 2 | a0001c0001t0002g0017a0001c0001t0002g0018 | 2 | HG02630.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.94+2715A>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2311613 | ||||||
| chr7:2311794
|
G | A | 1 | a0001c0001t0007g0273 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.94+2534C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2311794 | ||||||
| chr7:2311810
|
G | C | 2 | a0001c0003t0006g0010a0003c0007t0012g0009 | 2 | HG02976.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.94+2518C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2311810 | ||||||
| chr7:2311854
|
A | G | 151 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(148): Show | 153 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(150): Show |
intron_variant | MODIFIER | c.94+2474T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2311854 | ||||||
| chr7:2311860
|
C | T | 1 | a0003c0007t0012g0039 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.94+2468G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2311860 | ||||||
| chr7:2311884
|
C | A | 2 | a0001c0001t0002g0017a0001c0001t0002g0018 | 2 | HG02630.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.94+2444G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2311884 | ||||||
| chr7:2312020
|
G | A | 1 | a0001c0002t0004g0147 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.94+2308C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2312020 | ||||||
| chr7:2312039
|
C | T | 1 | a0001c0002t0004g0287 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.94+2289G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2312039 | ||||||
| chr7:2312125
|
C | T | 2 | a0001c0001t0020g0156a0001c0001t0020g0157 | 2 | HG01261.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.94+2203G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2312125 | ||||||
| chr7:2312174
|
G | GATCCAGC others(10): Show |
1 | a0001c0001t0001g0272 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.94+2153_94+2154ins others(17): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2312174 | ||||||
| chr7:2312176
|
A | T | 1 | a0001c0001t0001g0272 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.94+2152T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2312176 | ||||||
| chr7:2312177
|
A | C | 1 | a0001c0001t0001g0272 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.94+2151T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2312177 | ||||||
| chr7:2312179
|
T | C | 1 | a0001c0001t0001g0272 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.94+2149A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2312179 | ||||||
| chr7:2312198
|
A | G | 1 | a0001c0001t0001g0272 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.94+2130T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2312198 | ||||||
| chr7:2312200
|
G | C | 1 | a0001c0001t0001g0272 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.94+2128C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2312200 | ||||||
| chr7:2312201
|
G | C | 1 | a0001c0001t0001g0272 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.94+2127C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2312201 | ||||||
| chr7:2312203
|
G | A | 1 | a0001c0001t0001g0272 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.94+2125C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2312203 | ||||||
| chr7:2312209
|
C | T | 1 | a0001c0001t0001g0272 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.94+2119G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2312209 | ||||||
| chr7:2312217
|
A | C | 1 | a0001c0001t0001g0272 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.94+2111T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2312217 | ||||||
| chr7:2312220
|
G | T | 1 | a0001c0001t0001g0272 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.94+2108C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2312220 | ||||||
| chr7:2312224
|
CCTCAGGT others(8): Show |
C | 1 | a0001c0001t0001g0272 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.94+2089_94+2103del others(15): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2312224 | ||||||
| chr7:2312268
|
T | G | 1 | a0001c0001t0001g0272 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.94+2060A>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2312268 | ||||||
| chr7:2312346
|
T | C | 150 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(147): Show | 152 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(149): Show |
intron_variant | MODIFIER | c.94+1982A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2312346 | ||||||
| chr7:2312418
|
C | A | 6 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0002t0004g0015others(3): Show | 6 | HG02280.hp2 HG02486.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+1910G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2312418 | ||||||
| chr7:2312581
|
GAC | G | 5 | a0001c0003t0006g0042a0001c0003t0006g0043a0001c0003t0006g0044others(2): Show | 5 | HG02109.hp1 HG02451.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+1745_94+1746del others(2): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2312581 | ||||||
| chr7:2312590
|
T | G | 1 | a0001c0001t0014g0278 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.94+1738A>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2312590 | ||||||
| chr7:2312609
|
C | T | 3 | a0001c0001t0005g0352a0001c0001t0005g0353a0001c0001t0021g0351 | 3 | HG01099.hp1 HG02109.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.94+1719G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2312609 | ||||||
| chr7:2312727
|
C | G | 4 | a0001c0001t0005g0352a0001c0001t0005g0353a0001c0001t0021g0351others(1): Show | 4 | HG01099.hp1 HG02109.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.94+1601G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2312727 | ||||||
| chr7:2312741
|
A | T | 4 | a0001c0001t0005g0352a0001c0001t0005g0353a0001c0001t0021g0351others(1): Show | 4 | HG01099.hp1 HG02109.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.94+1587T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2312741 | ||||||
| chr7:2312747
|
CA | C | 6 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0002t0004g0015others(3): Show | 6 | HG02280.hp2 HG02486.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+1580delT | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2312747 | ||||||
| chr7:2312755
|
T | TCC | 24 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(21): Show | 24 | HG00423.hp1 HG00597.hp1 HG01192.hp2 others(21): Show |
intron_variant | MODIFIER | c.94+1571_94+1572dup others(2): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2312755 | ||||||
| chr7:2312763
|
C | G | 2 | a0001c0001t0003g0038a0001c0016t0003g0065 | 2 | HG00639.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.94+1565G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2312763 | ||||||
| chr7:2312912
|
T | G | 6 | a0001c0001t0005g0352a0001c0001t0005g0353a0001c0001t0009g0148others(3): Show | 6 | HG00558.hp2 HG01099.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.94+1416A>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2312912 | ||||||
| chr7:2312959
|
G | C | 93 | a0001c0001t0001g0073a0001c0001t0001g0084a0001c0001t0001g0119others(90): Show | 93 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.94+1369C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2312959 | ||||||
| chr7:2312960
|
C | G | 4 | a0001c0001t0040g0007a0001c0003t0005g0008a0001c0003t0006g0010others(1): Show | 4 | HG01891.hp1 HG02145.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.94+1368G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2312960 | ||||||
| chr7:2312992
|
G | C | 1 | a0001c0001t0001g0279 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.94+1336C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2312992 | ||||||
| chr7:2313023
|
G | C | 1 | a0001c0001t0001g0283 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.94+1305C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2313023 | ||||||
| chr7:2313055
|
G | A | 2 | a0001c0002t0010g0349a0001c0002t0027g0348 | 2 | HG00639.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.94+1273C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2313055 | ||||||
| chr7:2313058
|
T | C | 93 | a0001c0001t0001g0073a0001c0001t0001g0084a0001c0001t0001g0119others(90): Show | 93 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.94+1270A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2313058 | ||||||
| chr7:2313090
|
A | C | 1 | a0001c0001t0001g0350 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.94+1238T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2313090 | ||||||
| chr7:2313090
|
A | G | 3 | a0001c0001t0005g0352a0001c0001t0005g0353a0001c0001t0021g0351 | 3 | HG01099.hp1 HG02109.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.94+1238T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2313090 | ||||||
| chr7:2313176
|
A | C | 105 | a0001c0001t0001g0073a0001c0001t0001g0084a0001c0001t0001g0119others(102): Show | 106 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.94+1152T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2313176 | ||||||
| chr7:2313189
|
G | A | 1 | a0001c0016t0003g0065 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.94+1139C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2313189 | ||||||
| chr7:2313195
|
A | G | 1 | a0001c0001t0011g0155 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.94+1133T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2313195 | ||||||
| chr7:2313317
|
G | A | 1 | a0004c0012t0006g0006 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.94+1011C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2313317 | ||||||
| chr7:2313391
|
T | C | 1 | a0001c0001t0001g0274 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.94+937A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2313391 | ||||||
| chr7:2313523
|
C | CA | 7 | a0001c0001t0001g0275a0001c0001t0001g0277a0001c0001t0001g0279others(4): Show | 7 | HG01981.hp2 HG03831.hp1 NA18906.hp1 others(4): Show |
intron_variant | MODIFIER | c.94+804dupT | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2313523 | ||||||
| chr7:2313523
|
CA | C | 109 | a0001c0001t0001g0073a0001c0001t0001g0084a0001c0001t0001g0119others(106): Show | 109 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.94+804delT | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2313523 | ||||||
| chr7:2313530
|
A | G | 86 | a0001c0001t0001g0073a0001c0001t0001g0084a0001c0001t0001g0119others(83): Show | 86 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.94+798T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2313530 | ||||||
| chr7:2313535
|
A | G | 44 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(41): Show | 45 | HG00423.hp1 HG00597.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.94+793T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2313535 | ||||||
| chr7:2313545
|
G | C | 2 | a0001c0001t0003g0281a0001c0001t0005g0280 | 2 | HG01167.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.94+783C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2313545 | ||||||
| chr7:2313602
|
C | T | 1 | a0001c0001t0003g0037 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.94+726G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2313602 | ||||||
| chr7:2313706
|
A | T | 18 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(15): Show | 18 | HG00544.hp2 HG02056.hp1 NA18940.hp1 others(15): Show |
intron_variant | MODIFIER | c.94+622T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2313706 | ||||||
| chr7:2313714
|
T | C | 1 | a0001c0001t0001g0282 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.94+614A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2313714 | ||||||
| chr7:2313732
|
C | T | 2 | a0001c0001t0002g0017a0001c0001t0002g0018 | 2 | HG02630.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.94+596G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2313732 | ||||||
| chr7:2313772
|
G | C | 1 | a0001c0001t0001g0283 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.94+556C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2313772 | ||||||
| chr7:2313857
|
TACTGGCC others(7): Show |
T | 1 | a0001c0002t0004g0284 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.94+457_94+470delGG others(12): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2313857 | ||||||
| chr7:2313965
|
A | G | 301 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(298): Show | 303 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.94+363T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2313965 | ||||||
| chr7:2313975
|
G | T | 6 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0002t0004g0015others(3): Show | 6 | HG02280.hp2 HG02486.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+353C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2313975 | ||||||
| chr7:2314008
|
A | C | 4 | a0001c0001t0040g0007a0001c0003t0005g0008a0001c0003t0006g0010others(1): Show | 4 | HG01891.hp1 HG02145.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.94+320T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2314008 | ||||||
| chr7:2314220
|
G | A | 4 | a0001c0001t0005g0352a0001c0001t0005g0353a0001c0001t0021g0351others(1): Show | 4 | HG01099.hp1 HG02109.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.94+108C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2314220 |