Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 2936 |
| ensemblid | ENSG00000104687.14 |
| hgncid | 4623 |
| symbol | GSR |
| name | glutathione-disulfide reductase |
| refseq_nuc | NM_000637.5 |
| refseq_prot | NP_000628.2 |
| ensembl_nuc | ENST00000221130.11 |
| ensembl_prot | ENSP00000221130.5 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 30678066 |
| end | 30727846 |
| strand | - |
| ver | v1.2 |
| region | chr8:30678066-30727846 |
| region5000 | chr8:30673066-30732846 |
| regionname0 | GSR_chr8_30678066_30727846 |
| regionname5000 | GSR_chr8_30673066_30732846 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 522 | 320 | 77 | 64 | 127 | 13 | 37 | 100 | GSR_chr8_30673066_30732846 | GSR | MALLP others(517): Show |
chr8 | 30673066 | 30732846 |
| a0002 | 0/0 | 522 | 18 | 10 | 0 | 5 | 0 | 3 | 4 | GSR_chr8_30673066_30732846 | GSR | MALLP others(517): Show |
chr8 | 30673066 | 30732846 |
| a0003 | 0/0 | 522 | 4 | 2 | 2 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | MALLP others(517): Show |
chr8 | 30673066 | 30732846 |
| a0004 | 0/0 | 522 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | MALLP others(517): Show |
chr8 | 30673066 | 30732846 |
| a0005 | 0/0 | 522 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | MALLP others(517): Show |
chr8 | 30673066 | 30732846 |
| a0006 | 0/0 | 522 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | MALLP others(517): Show |
chr8 | 30673066 | 30732846 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1566 | 306 | 65 | 64 | 126 | 12 | 37 | GSR_chr8_30673066_30732846 | GSR | ATGGC others(1561): Show |
chr8 | 30673066 | 30732846 | ||
| a0001c0003 | 0/0 | 1566 | 7 | 7 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | ATGGC others(1561): Show |
chr8 | 30673066 | 30732846 | ||
| a0001c0004 | 0/0 | 1566 | 6 | 5 | 0 | 0 | 1 | 0 | GSR_chr8_30673066_30732846 | GSR | ATGGC others(1561): Show |
chr8 | 30673066 | 30732846 | ||
| a0001c0009 | 0/0 | 1566 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | ATGGC others(1561): Show |
chr8 | 30673066 | 30732846 | ||
| a0002c0002 | 0/0 | 1566 | 17 | 9 | 0 | 5 | 0 | 3 | GSR_chr8_30673066_30732846 | GSR | ATGGC others(1561): Show |
chr8 | 30673066 | 30732846 | ||
| a0002c0010 | 0/0 | 1566 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | ATGGC others(1561): Show |
chr8 | 30673066 | 30732846 | ||
| a0003c0005 | 0/0 | 1566 | 4 | 2 | 2 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | ATGGC others(1561): Show |
chr8 | 30673066 | 30732846 | ||
| a0004c0006 | 0/0 | 1566 | 4 | 4 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | ATGGC others(1561): Show |
chr8 | 30673066 | 30732846 | ||
| a0005c0007 | 0/0 | 1566 | 1 | 0 | 0 | 0 | 1 | 0 | GSR_chr8_30673066_30732846 | GSR | ATGGC others(1561): Show |
chr8 | 30673066 | 30732846 | ||
| a0006c0008 | 0/0 | 1566 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | ATGGC others(1561): Show |
chr8 | 30673066 | 30732846 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3034 | 70 | 10 | 17 | 26 | 2 | 14 | GSR_chr8_30673066_30732846 | GSR | CTTCC others(3029): Show |
chr8 | 30673066 | 30732846 |
| a0001c0001t0002 | 0/0 | 3034 | 56 | 3 | 15 | 25 | 4 | 9 | GSR_chr8_30673066_30732846 | GSR | CTTCC others(3029): Show |
chr8 | 30673066 | 30732846 |
| a0001c0001t0003 | 0/0 | 3034 | 49 | 9 | 9 | 25 | 2 | 4 | GSR_chr8_30673066_30732846 | GSR | CTTCC others(3029): Show |
chr8 | 30673066 | 30732846 |
| a0001c0001t0004 | 0/0 | 3035 | 52 | 3 | 18 | 26 | 1 | 4 | GSR_chr8_30673066_30732846 | GSR | CTTCC others(3030): Show |
chr8 | 30673066 | 30732846 |
| a0001c0001t0005 | 0/0 | 3034 | 12 | 12 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | CTTCC others(3029): Show |
chr8 | 30673066 | 30732846 |
| a0001c0001t0006 | 0/0 | 3035 | 10 | 2 | 3 | 5 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | CTTCC others(3030): Show |
chr8 | 30673066 | 30732846 |
| a0001c0001t0007 | 0/0 | 3035 | 12 | 7 | 0 | 5 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | CTTCC others(3030): Show |
chr8 | 30673066 | 30732846 |
| a0001c0001t0008 | 0/0 | 3034 | 9 | 3 | 0 | 4 | 0 | 2 | GSR_chr8_30673066_30732846 | GSR | CTTCC others(3029): Show |
chr8 | 30673066 | 30732846 |
| a0001c0001t0009 | 0/0 | 3034 | 6 | 6 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | CTTCC others(3029): Show |
chr8 | 30673066 | 30732846 |
| a0001c0001t0010 | 0/0 | 3034 | 5 | 1 | 0 | 4 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | CTTCC others(3029): Show |
chr8 | 30673066 | 30732846 |
| a0001c0001t0011 | 0/0 | 3034 | 2 | 0 | 0 | 1 | 1 | 0 | GSR_chr8_30673066_30732846 | GSR | CTTCC others(3029): Show |
chr8 | 30673066 | 30732846 |
| a0001c0001t0012 | 0/0 | 3034 | 2 | 2 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | CTTCC others(3029): Show |
chr8 | 30673066 | 30732846 |
| a0001c0001t0013 | 0/0 | 3034 | 3 | 0 | 0 | 0 | 2 | 1 | GSR_chr8_30673066_30732846 | GSR | CTTCC others(3029): Show |
chr8 | 30673066 | 30732846 |
| a0001c0001t0014 | 0/0 | 3034 | 2 | 2 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | CTTCC others(3029): Show |
chr8 | 30673066 | 30732846 |
| a0001c0001t0015 | 0/0 | 3034 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | CTTCC others(3029): Show |
chr8 | 30673066 | 30732846 |
| a0001c0001t0016 | 0/0 | 3034 | 2 | 2 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | CTTCC others(3029): Show |
chr8 | 30673066 | 30732846 |
| a0001c0001t0018 | 0/0 | 3034 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | CTTCC others(3029): Show |
chr8 | 30673066 | 30732846 |
| a0001c0001t0019 | 0/0 | 3034 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | CTTCC others(3029): Show |
chr8 | 30673066 | 30732846 |
| a0001c0001t0020 | 0/0 | 3034 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | CTTCC others(3029): Show |
chr8 | 30673066 | 30732846 |
| a0001c0001t0021 | 0/0 | 3034 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | CTTCC others(3029): Show |
chr8 | 30673066 | 30732846 |
| a0001c0001t0022 | 0/0 | 3034 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | CTTCC others(3029): Show |
chr8 | 30673066 | 30732846 |
| a0001c0001t0023 | 0/0 | 3034 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | CTTCC others(3029): Show |
chr8 | 30673066 | 30732846 |
| a0001c0001t0025 | 0/0 | 3034 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | CTTCC others(3029): Show |
chr8 | 30673066 | 30732846 |
| a0001c0001t0026 | 0/1 | 3033 | 1 | 0 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | CTTCC others(3028): Show |
chr8 | 30673066 | 30732846 |
| a0001c0001t0027 | 0/0 | 3034 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | CTTCC others(3029): Show |
chr8 | 30673066 | 30732846 |
| a0001c0001t0028 | 0/0 | 3034 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | CTTCC others(3029): Show |
chr8 | 30673066 | 30732846 |
| a0001c0001t0030 | 0/0 | 3035 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | CTTCC others(3030): Show |
chr8 | 30673066 | 30732846 |
| a0001c0001t0032 | 0/0 | 3035 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | CTTCC others(3030): Show |
chr8 | 30673066 | 30732846 |
| a0001c0001t0033 | 0/0 | 3034 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | CTTCC others(3029): Show |
chr8 | 30673066 | 30732846 |
| a0001c0003t0002 | 0/0 | 3034 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | CTTCC others(3029): Show |
chr8 | 30673066 | 30732846 |
| a0001c0003t0003 | 0/0 | 3034 | 2 | 2 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | CTTCC others(3029): Show |
chr8 | 30673066 | 30732846 |
| a0001c0003t0005 | 0/0 | 3034 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | CTTCC others(3029): Show |
chr8 | 30673066 | 30732846 |
| a0001c0003t0017 | 0/0 | 3037 | 2 | 2 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | CTTCC others(3032): Show |
chr8 | 30673066 | 30732846 |
| a0001c0003t0029 | 0/0 | 3037 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | CTTCC others(3032): Show |
chr8 | 30673066 | 30732846 |
| a0001c0004t0001 | 0/0 | 3034 | 2 | 1 | 0 | 0 | 1 | 0 | GSR_chr8_30673066_30732846 | GSR | CTTCC others(3029): Show |
chr8 | 30673066 | 30732846 |
| a0001c0004t0003 | 0/0 | 3034 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | CTTCC others(3029): Show |
chr8 | 30673066 | 30732846 |
| a0001c0004t0005 | 0/0 | 3034 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | CTTCC others(3029): Show |
chr8 | 30673066 | 30732846 |
| a0001c0004t0009 | 0/0 | 3034 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | CTTCC others(3029): Show |
chr8 | 30673066 | 30732846 |
| a0001c0004t0031 | 0/0 | 3037 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | CTTCC others(3032): Show |
chr8 | 30673066 | 30732846 |
| a0001c0009t0002 | 0/0 | 3034 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | CTTCC others(3029): Show |
chr8 | 30673066 | 30732846 |
| a0002c0002t0001 | 0/0 | 3034 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | CTTCC others(3029): Show |
chr8 | 30673066 | 30732846 |
| a0002c0002t0002 | 0/0 | 3034 | 10 | 5 | 0 | 2 | 0 | 3 | GSR_chr8_30673066_30732846 | GSR | CTTCC others(3029): Show |
chr8 | 30673066 | 30732846 |
| a0002c0002t0003 | 0/0 | 3034 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | CTTCC others(3029): Show |
chr8 | 30673066 | 30732846 |
| a0002c0002t0006 | 0/0 | 3035 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | CTTCC others(3030): Show |
chr8 | 30673066 | 30732846 |
| a0002c0002t0010 | 0/0 | 3034 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | CTTCC others(3029): Show |
chr8 | 30673066 | 30732846 |
| a0002c0002t0011 | 0/0 | 3034 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | CTTCC others(3029): Show |
chr8 | 30673066 | 30732846 |
| a0002c0002t0012 | 0/0 | 3034 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | CTTCC others(3029): Show |
chr8 | 30673066 | 30732846 |
| a0002c0002t0015 | 0/0 | 3034 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | CTTCC others(3029): Show |
chr8 | 30673066 | 30732846 |
| a0002c0010t0002 | 0/0 | 3034 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | CTTCC others(3029): Show |
chr8 | 30673066 | 30732846 |
| a0003c0005t0003 | 0/0 | 3034 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | CTTCC others(3029): Show |
chr8 | 30673066 | 30732846 |
| a0003c0005t0004 | 0/0 | 3035 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | CTTCC others(3030): Show |
chr8 | 30673066 | 30732846 |
| a0003c0005t0006 | 0/0 | 3035 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | CTTCC others(3030): Show |
chr8 | 30673066 | 30732846 |
| a0003c0005t0034 | 0/0 | 3034 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | CTTCC others(3029): Show |
chr8 | 30673066 | 30732846 |
| a0004c0006t0003 | 0/0 | 3034 | 2 | 2 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | CTTCC others(3029): Show |
chr8 | 30673066 | 30732846 |
| a0004c0006t0006 | 0/0 | 3035 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | CTTCC others(3030): Show |
chr8 | 30673066 | 30732846 |
| a0004c0006t0008 | 0/0 | 3034 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | CTTCC others(3029): Show |
chr8 | 30673066 | 30732846 |
| a0005c0007t0002 | 0/0 | 3034 | 1 | 0 | 0 | 0 | 1 | 0 | GSR_chr8_30673066_30732846 | GSR | CTTCC others(3029): Show |
chr8 | 30673066 | 30732846 |
| a0006c0008t0024 | 0/0 | 3034 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | CTTCC others(3029): Show |
chr8 | 30673066 | 30732846 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0044 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0001 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0003g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0004g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0005g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0005g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0005g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0005g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0005g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0005g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0005g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0005g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0005g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0005g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0005g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0005g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0006g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0006g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0006g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0006g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0006g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0006g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0006g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0006g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0006g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0006g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0007g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0007g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0007g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0007g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0007g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0007g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0007g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0007g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0007g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0007g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0007g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0007g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0008g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0008g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0008g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0008g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0008g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0008g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0008g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0008g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0008g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0009g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0009g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0009g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0009g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0009g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0009g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0010g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0010g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0010g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0010g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0010g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0011g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0011g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0012g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0012g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0013g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0013g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0013g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0014g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0014g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0015g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0016g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0016g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0018g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0019g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0020g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0021g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0022g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0023g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0025g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0026g0163 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0027g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0028g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0030g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0032g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0001t0033g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0003t0002g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0003t0003g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0003t0003g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0003t0005g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0003t0017g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0003t0017g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0003t0029g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0004t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0004t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0004t0003g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0004t0005g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0004t0009g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0004t0031g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0001c0009t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0002c0002t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0002c0002t0002g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0002c0002t0002g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0002c0002t0002g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0002c0002t0002g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0002c0002t0002g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0002c0002t0002g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0002c0002t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0002c0002t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0002c0002t0002g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0002c0002t0002g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0002c0002t0003g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0002c0002t0006g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0002c0002t0010g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0002c0002t0011g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0002c0002t0012g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0002c0002t0015g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0002c0010t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0003c0005t0003g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0003c0005t0004g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0003c0005t0006g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0003c0005t0034g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0004c0006t0003g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0004c0006t0003g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0004c0006t0006g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0004c0006t0008g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0005c0007t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| a0006c0008t0024g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0255 | EUR | GBR | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0170 | EUR | GBR | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG00140 | hp1 | a0001 | c0001 | t0004 | g0107 | EUR | GBR | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG00140 | hp2 | a0001 | c0001 | t0013 | g0305 | EUR | GBR | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0143 | EUR | FIN | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0106 | EUR | FIN | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG00323 | hp1 | a0001 | c0001 | t0013 | g0307 | EUR | FIN | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG00323 | hp2 | a0005 | c0007 | t0002 | g0173 | EUR | FIN | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0244 | EAS | CHS | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | CHS | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG00438 | hp1 | a0001 | c0001 | t0022 | g0100 | EAS | CHS | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | CHS | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0078 | EAS | CHS | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | CHS | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG00558 | hp1 | a0001 | c0001 | t0010 | g0180 | EAS | CHS | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG00558 | hp2 | a0001 | c0001 | t0004 | g0188 | EAS | CHS | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | CHS | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | CHS | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | CHS | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG00621 | hp2 | a0002 | c0002 | t0010 | g0341 | EAS | CHS | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0133 | AMR | PUR | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG00642 | hp1 | a0001 | c0001 | t0004 | g0094 | AMR | PUR | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0091 | AMR | PUR | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | CHS | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG00673 | hp2 | a0001 | c0001 | t0003 | g0174 | EAS | CHS | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG00733 | hp1 | a0001 | c0001 | t0003 | g0092 | AMR | PUR | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0070 | AMR | PUR | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG00738 | hp1 | a0001 | c0001 | t0004 | g0286 | AMR | PUR | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG00738 | hp2 | a0003 | c0005 | t0003 | g0005 | AMR | PUR | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01069 | hp1 | a0001 | c0001 | t0018 | g0128 | AMR | PUR | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0124 | AMR | PUR | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0025 | AMR | PUR | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0165 | AMR | PUR | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01074 | hp1 | a0001 | c0001 | t0004 | g0121 | AMR | PUR | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0119 | AMR | PUR | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0026 | AMR | PUR | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01099 | hp1 | a0001 | c0001 | t0004 | g0093 | AMR | PUR | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0084 | AMR | PUR | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0164 | AMR | PUR | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0104 | AMR | PUR | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01175 | hp2 | a0001 | c0001 | t0004 | g0058 | AMR | PUR | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01243 | hp1 | a0003 | c0005 | t0006 | g0003 | AMR | PUR | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0172 | AMR | CLM | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01255 | hp2 | a0001 | c0001 | t0006 | g0243 | AMR | CLM | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | CLM | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0136 | AMR | CLM | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01257 | hp1 | a0001 | c0001 | t0006 | g0186 | AMR | CLM | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01257 | hp2 | a0001 | c0001 | t0004 | g0156 | AMR | CLM | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01258 | hp2 | a0001 | c0001 | t0004 | g0149 | AMR | CLM | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0083 | AMR | CLM | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0088 | AMR | CLM | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01358 | hp1 | a0001 | c0001 | t0006 | g0187 | AMR | CLM | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0109 | AMR | CLM | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0153 | AMR | CLM | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01361 | hp2 | a0001 | c0001 | t0004 | g0261 | AMR | CLM | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0024 | AMR | CLM | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01433 | hp2 | a0001 | c0001 | t0004 | g0053 | AMR | CLM | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0023 | EUR | IBS | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0131 | EUR | IBS | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01516 | hp1 | a0001 | c0001 | t0011 | g0073 | EUR | IBS | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0142 | EUR | IBS | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0101 | AFR | ACB | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | ACB | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01891 | hp1 | a0001 | c0003 | t0003 | g0012 | AFR | ACB | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01891 | hp2 | a0002 | c0002 | t0012 | g0322 | AFR | ACB | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01928 | hp1 | a0001 | c0001 | t0004 | g0185 | AMR | PEL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01928 | hp2 | a0001 | c0001 | t0004 | g0076 | AMR | PEL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0295 | AMR | PEL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01952 | hp1 | a0001 | c0001 | t0004 | g0061 | AMR | PEL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0081 | AMR | PEL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0294 | AMR | PEL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0105 | AMR | PEL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | PEL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0200 | AMR | PEL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | PEL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01981 | hp2 | a0001 | c0001 | t0004 | g0192 | AMR | PEL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PEL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01993 | hp2 | a0001 | c0001 | t0004 | g0148 | AMR | PEL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02004 | hp1 | a0001 | c0001 | t0015 | g0118 | AMR | PEL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0147 | AMR | PEL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | KHV | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | KHV | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02040 | hp1 | a0001 | c0001 | t0004 | g0182 | EAS | KHV | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0299 | EAS | KHV | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02055 | hp1 | a0001 | c0001 | t0012 | g0168 | AFR | ACB | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02055 | hp2 | a0001 | c0004 | t0005 | g0328 | AFR | ACB | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02056 | hp1 | a0001 | c0001 | t0004 | g0166 | EAS | KHV | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | KHV | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0229 | EAS | KHV | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02074 | hp2 | a0001 | c0001 | t0006 | g0085 | EAS | KHV | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02083 | hp1 | a0001 | c0001 | t0004 | g0120 | EAS | KHV | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02083 | hp2 | a0001 | c0001 | t0028 | g0159 | EAS | KHV | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0049 | AFR | ACB | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02145 | hp2 | a0003 | c0005 | t0004 | g0004 | AFR | ACB | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02155 | hp1 | a0001 | c0001 | t0004 | g0102 | EAS | CDX | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0226 | EAS | CDX | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02257 | hp1 | a0002 | c0002 | t0003 | g0320 | AFR | ACB | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0215 | AFR | ACB | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02258 | hp1 | a0001 | c0001 | t0008 | g0237 | AFR | ACB | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02258 | hp2 | a0001 | c0001 | t0007 | g0209 | AFR | ACB | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02273 | hp1 | a0001 | c0001 | t0004 | g0103 | AMR | PEL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0086 | AMR | PEL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02280 | hp1 | a0001 | c0001 | t0005 | g0281 | AFR | ACB | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02280 | hp2 | a0001 | c0001 | t0007 | g0217 | AFR | ACB | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02300 | hp1 | a0001 | c0001 | t0004 | g0150 | AMR | PEL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02451 | hp1 | a0004 | c0006 | t0003 | g0342 | AFR | ACB | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | ACB | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02572 | hp1 | a0001 | c0001 | t0010 | g0206 | AFR | GWD | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02572 | hp2 | a0001 | c0001 | t0005 | g0284 | AFR | GWD | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0052 | SAS | PJL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0298 | SAS | PJL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0030 | AFR | GWD | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0211 | AFR | GWD | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | GWD | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02630 | hp2 | a0001 | c0001 | t0005 | g0203 | AFR | GWD | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | GWD | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02647 | hp2 | a0001 | c0001 | t0008 | g0235 | AFR | GWD | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02683 | hp1 | a0001 | c0001 | t0008 | g0041 | SAS | PJL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0293 | SAS | PJL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02717 | hp1 | a0001 | c0001 | t0025 | g0214 | AFR | GWD | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02717 | hp2 | a0001 | c0001 | t0008 | g0236 | AFR | GWD | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02723 | hp1 | a0001 | c0001 | t0005 | g0249 | AFR | GWD | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02723 | hp2 | a0001 | c0001 | t0009 | g0020 | AFR | GWD | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02738 | hp1 | a0001 | c0001 | t0004 | g0199 | SAS | PJL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02738 | hp2 | a0002 | c0002 | t0002 | g0333 | SAS | PJL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02809 | hp1 | a0001 | c0004 | t0031 | g0330 | AFR | GWD | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02809 | hp2 | a0001 | c0001 | t0005 | g0282 | AFR | GWD | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02818 | hp1 | a0001 | c0001 | t0009 | g0022 | AFR | GWD | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | GWD | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02886 | hp1 | a0001 | c0003 | t0017 | g0010 | AFR | GWD | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02886 | hp2 | a0001 | c0003 | t0029 | g0007 | AFR | GWD | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02895 | hp1 | a0002 | c0002 | t0002 | g0337 | AFR | GWD | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02895 | hp2 | a0001 | c0001 | t0009 | g0019 | AFR | GWD | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | GWD | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02896 | hp2 | a0001 | c0001 | t0016 | g0213 | AFR | GWD | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02897 | hp1 | a0001 | c0001 | t0016 | g0212 | AFR | GWD | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02897 | hp2 | a0001 | c0001 | t0009 | g0021 | AFR | GWD | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0208 | AFR | ESN | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02922 | hp2 | a0002 | c0002 | t0002 | g0327 | AFR | ESN | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02965 | hp1 | a0001 | c0001 | t0032 | g0280 | AFR | ESN | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02965 | hp2 | a0001 | c0004 | t0009 | g0319 | AFR | ESN | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02970 | hp1 | a0001 | c0004 | t0001 | g0339 | AFR | ESN | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02970 | hp2 | a0003 | c0005 | t0034 | g0346 | AFR | ESN | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02976 | hp1 | a0001 | c0001 | t0005 | g0278 | AFR | ESN | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02976 | hp2 | a0002 | c0002 | t0002 | g0326 | AFR | ESN | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0139 | SAS | PJL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0232 | AFR | GWD | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03041 | hp2 | a0004 | c0006 | t0006 | g0343 | AFR | GWD | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03098 | hp1 | a0001 | c0001 | t0009 | g0017 | AFR | MSL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03098 | hp2 | a0001 | c0001 | t0005 | g0300 | AFR | MSL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03139 | hp1 | a0002 | c0002 | t0002 | g0324 | AFR | ESN | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0205 | AFR | ESN | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03195 | hp1 | a0006 | c0008 | t0024 | g0204 | AFR | ESN | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0216 | AFR | ESN | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03225 | hp1 | a0002 | c0002 | t0011 | g0321 | AFR | MSL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03225 | hp2 | a0001 | c0003 | t0017 | g0009 | AFR | MSL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03239 | hp2 | a0001 | c0001 | t0021 | g0158 | SAS | PJL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03453 | hp1 | a0001 | c0001 | t0009 | g0018 | AFR | MSL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0248 | AFR | MSL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03486 | hp1 | a0001 | c0001 | t0014 | g0031 | AFR | MSL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03486 | hp2 | a0001 | c0001 | t0007 | g0225 | AFR | MSL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03490 | hp1 | a0001 | c0001 | t0004 | g0296 | SAS | PJL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0247 | SAS | PJL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0241 | SAS | PJL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0035 | AFR | ESN | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03516 | hp2 | a0001 | c0004 | t0003 | g0323 | AFR | ESN | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03540 | hp1 | a0001 | c0001 | t0006 | g0055 | AFR | GWD | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | GWD | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03579 | hp1 | a0001 | c0001 | t0007 | g0219 | AFR | MSL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03579 | hp2 | a0001 | c0001 | t0005 | g0315 | AFR | MSL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03654 | hp1 | a0002 | c0002 | t0002 | g0340 | SAS | PJL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0127 | SAS | PJL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0252 | SAS | PJL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0063 | SAS | PJL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0240 | SAS | STU | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | STU | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0267 | SAS | PJL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03704 | hp2 | a0001 | c0001 | t0008 | g0042 | SAS | PJL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0157 | SAS | PJL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0268 | SAS | PJL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0067 | SAS | BEB | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03831 | hp2 | a0001 | c0001 | t0004 | g0068 | SAS | BEB | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0239 | SAS | BEB | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03834 | hp2 | a0001 | c0001 | t0027 | g0309 | SAS | BEB | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03942 | hp1 | a0001 | c0001 | t0004 | g0125 | SAS | BEB | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03942 | hp2 | a0002 | c0002 | t0002 | g0331 | SAS | BEB | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0310 | SAS | STU | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG04115 | hp2 | a0001 | c0001 | t0023 | g0197 | SAS | STU | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0098 | SAS | STU | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG04199 | hp2 | a0001 | c0001 | t0013 | g0303 | SAS | STU | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0129 | SAS | STU | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0114 | SAS | STU | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18522 | hp1 | a0001 | c0001 | t0007 | g0222 | AFR | YRI | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18522 | hp2 | a0001 | c0003 | t0005 | g0008 | AFR | YRI | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | CHB | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18612 | hp2 | a0001 | c0001 | t0004 | g0122 | EAS | CHB | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18906 | hp1 | a0002 | c0002 | t0015 | g0338 | AFR | YRI | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | YRI | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18941 | hp2 | a0001 | c0001 | t0006 | g0183 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18942 | hp2 | a0001 | c0001 | t0008 | g0037 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18943 | hp2 | a0001 | c0001 | t0003 | g0151 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18944 | hp1 | a0001 | c0001 | t0007 | g0048 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18945 | hp1 | a0001 | c0001 | t0004 | g0130 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18948 | hp1 | a0001 | c0001 | t0019 | g0137 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18952 | hp1 | a0001 | c0001 | t0004 | g0190 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18954 | hp1 | a0001 | c0001 | t0004 | g0108 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18960 | hp2 | a0002 | c0002 | t0002 | g0336 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18961 | hp1 | a0001 | c0001 | t0004 | g0054 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0144 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0189 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18964 | hp2 | a0001 | c0001 | t0004 | g0160 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18966 | hp1 | a0001 | c0001 | t0003 | g0154 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18966 | hp2 | a0001 | c0001 | t0004 | g0318 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18968 | hp2 | a0001 | c0001 | t0004 | g0317 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18970 | hp1 | a0001 | c0001 | t0007 | g0134 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18971 | hp1 | a0001 | c0001 | t0004 | g0112 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18975 | hp1 | a0001 | c0001 | t0007 | g0059 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0162 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18977 | hp2 | a0001 | c0001 | t0010 | g0195 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18979 | hp2 | a0001 | c0001 | t0004 | g0056 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18983 | hp1 | a0001 | c0001 | t0006 | g0146 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18983 | hp2 | a0001 | c0001 | t0004 | g0193 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18986 | hp2 | a0001 | c0001 | t0004 | g0116 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18988 | hp1 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18991 | hp1 | a0001 | c0001 | t0003 | g0077 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18991 | hp2 | a0002 | c0002 | t0002 | g0334 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18992 | hp1 | a0001 | c0001 | t0010 | g0181 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18992 | hp2 | a0001 | c0001 | t0006 | g0110 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18999 | hp1 | a0001 | c0001 | t0003 | g0202 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18999 | hp2 | a0001 | c0001 | t0004 | g0201 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19005 | hp1 | a0001 | c0001 | t0004 | g0072 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19005 | hp2 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19009 | hp2 | a0001 | c0001 | t0004 | g0079 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0132 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0302 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19012 | hp1 | a0001 | c0001 | t0004 | g0051 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0316 | AFR | LWK | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19030 | hp2 | a0001 | c0001 | t0006 | g0167 | AFR | LWK | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19043 | hp1 | a0001 | c0001 | t0033 | g0034 | AFR | LWK | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19043 | hp2 | a0001 | c0001 | t0012 | g0169 | AFR | LWK | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19058 | hp1 | a0001 | c0001 | t0004 | g0126 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0233 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19060 | hp2 | a0001 | c0001 | t0006 | g0191 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19062 | hp1 | a0001 | c0009 | t0002 | g0027 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0179 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19063 | hp1 | a0001 | c0001 | t0007 | g0075 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19064 | hp1 | a0001 | c0001 | t0004 | g0060 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19064 | hp2 | a0001 | c0001 | t0008 | g0043 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19065 | hp2 | a0001 | c0001 | t0004 | g0062 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19068 | hp1 | a0001 | c0001 | t0007 | g0074 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19068 | hp2 | a0001 | c0001 | t0020 | g0141 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19072 | hp1 | a0001 | c0001 | t0003 | g0177 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19072 | hp2 | a0001 | c0001 | t0030 | g0028 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0069 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19077 | hp2 | a0001 | c0001 | t0004 | g0194 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19079 | hp1 | a0002 | c0002 | t0006 | g0329 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0099 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19080 | hp2 | a0001 | c0001 | t0003 | g0178 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19081 | hp1 | a0001 | c0001 | t0008 | g0040 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19085 | hp1 | a0001 | c0001 | t0004 | g0047 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19088 | hp1 | a0001 | c0001 | t0011 | g0111 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19088 | hp2 | a0001 | c0001 | t0010 | g0276 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19090 | hp1 | a0001 | c0001 | t0008 | g0196 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19090 | hp2 | a0002 | c0002 | t0001 | g0335 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19240 | hp1 | a0004 | c0006 | t0003 | g0344 | AFR | YRI | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA19240 | hp2 | a0001 | c0001 | t0007 | g0220 | AFR | YRI | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA20129 | hp1 | a0001 | c0003 | t0003 | g0011 | AFR | ASW | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0117 | AFR | ASW | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0089 | EUR | TSI | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA20805 | hp2 | a0001 | c0004 | t0001 | g0332 | EUR | TSI | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0308 | SAS | GIH | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0175 | SAS | GIH | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | CLM | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG01123 | hp2 | a0001 | c0001 | t0004 | g0050 | AMR | CLM | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02109 | hp1 | a0004 | c0006 | t0008 | g0345 | AFR | ACB | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | ACB | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02486 | hp1 | a0001 | c0003 | t0002 | g0006 | AFR | ACB | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02486 | hp2 | a0001 | c0001 | t0014 | g0032 | AFR | ACB | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02559 | hp1 | a0001 | c0001 | t0007 | g0221 | AFR | ACB | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0314 | AFR | ACB | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0115 | AFR | MSL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG03471 | hp2 | a0002 | c0002 | t0002 | g0325 | AFR | MSL | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG06807 | hp1 | a0001 | c0001 | t0005 | g0279 | AFR | USA | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| HG06807 | hp2 | a0001 | c0001 | t0005 | g0207 | AFR | USA | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA18955 | hp2 | a0001 | c0001 | t0003 | g0184 | EAS | JPT | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA20300 | hp1 | a0001 | c0001 | t0005 | g0283 | AFR | USA | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0224 | AFR | USA | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA21309 | hp1 | a0002 | c0010 | t0002 | g0016 | AFR | LWK | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | LWK | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0026 | g0163 | REF | REF | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0044 | REF | REF | GSR_chr8_30673066_30732846 | GSR | chr8 | 30673066 | 30732846 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:30692985 | A | G | 1 | a0006 | 1 | HG03195.hp1 | missense_variant | MODERATE | c.866T>C | p.Val289Ala | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/13 | 877/3034 | 866/1569 | 289/522 | chr8 | 30692985 | |||
| chr8:30703138 | C | T | 1 | a0005 | 1 | HG00323.hp2 | missense_variant | MODERATE | c.595G>A | p.Ala199Thr | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/13 | 606/3034 | 595/1569 | 199/522 | chr8 | 30703138 | |||
| chr8:30708107 | G | A | 1 | a0002 | 18 | HG00621.hp2 HG01891.hp2 HG02257.hp1 others(15): Show |
missense_variant | MODERATE | c.457C>T | p.Arg153Cys | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/13 | 468/3034 | 457/1569 | 153/522 | chr8 | 30708107 | |||
| chr8:30727793 | T | C | 1 | a0004 | 4 | HG02109.hp1 HG02451.hp1 HG03041.hp2 others(1): Show |
missense_variant | MODERATE | c.43A>G | p.Ser15Gly | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/13 | 54/3034 | 43/1569 | 15/522 | chr8 | 30727793 | |||
| chr8:30727795 | G | T | 1 | a0003 | 4 | HG00738.hp2 HG01243.hp1 HG02145.hp2 others(1): Show |
missense_variant | MODERATE | c.41C>A | p.Pro14Gln | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/13 | 52/3034 | 41/1569 | 14/522 | chr8 | 30727795 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:30696473 | G | A | 1 | a0001c0009 | 1 | NA19062.hp1 | synonymous_variant | LOW | c.702C>T | p.Ser234Ser | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/13 | 713/3034 | 702/1569 | 234/522 | chr8 | 30696473 | |||
| chr8:30727575 | A | G | 4 | a0001c0003 a0001c0004 a0002c0002 others(1): Show |
34 | HG00621.hp2 HG01891.hp1 HG01891.hp2 others(31): Show |
synonymous_variant | LOW | c.261T>C | p.Gly87Gly | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/13 | 272/3034 | 261/1569 | 87/522 | chr8 | 30727575 | |||
| chr8:30727647 | G | A | 2 | a0001c0004 a0002c0002 |
23 | HG00621.hp2 HG01891.hp2 HG02055.hp2 others(20): Show |
synonymous_variant | LOW | c.189C>T | p.Ala63Ala | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/13 | 200/3034 | 189/1569 | 63/522 | chr8 | 30727647 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:30678101 | T | C | 1 | a0001c0001t0014 | 2 | HG02486.hp2 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1419A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 13/13 | 1419 | chr8 | 30678101 | ||||||
| chr8:30678116 | A | G | 1 | a0001c0001t0014 | 2 | HG02486.hp2 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1404T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 13/13 | 1404 | chr8 | 30678116 | ||||||
| chr8:30678143 | C | A | 13 | a0001c0001t0002 a0001c0001t0011 a0001c0001t0015 others(10): Show |
79 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*1377G>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 13/13 | 1377 | chr8 | 30678143 | ||||||
| chr8:30678210 | T | C | 1 | a0001c0001t0013 | 3 | HG00140.hp2 HG00323.hp1 HG04199.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1310A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 13/13 | 1310 | chr8 | 30678210 | ||||||
| chr8:30678340 | A | AAT | 3 | a0001c0003t0017 a0001c0003t0029 a0001c0004t0031 |
4 | HG02809.hp1 HG02886.hp1 HG02886.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1178_*1179dupAT | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 13/13 | 1179 | chr8 | 30678340 | ||||||
| chr8:30678357 | ATATT | A | 5 | a0001c0001t0003 a0001c0001t0009 a0001c0004t0009 others(2): Show |
14 | HG00738.hp2 HG01516.hp2 HG02723.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1159_*1162delAATA | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 13/13 | 1159 | chr8 | 30678357 | ||||||
| chr8:30678359 | AT | A | 7 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0013 others(4): Show |
59 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*1160delA | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 13/13 | 1160 | chr8 | 30678359 | ||||||
| chr8:30678359 | ATT | A | 4 | a0001c0001t0001 a0001c0001t0019 a0001c0001t0020 others(1): Show |
7 | HG00733.hp2 HG03239.hp1 HG03834.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1159_*1160delAA | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 13/13 | 1159 | chr8 | 30678359 | ||||||
| chr8:30678359 | ATTT | A | 10 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0006 others(7): Show |
83 | HG00140.hp1 HG00558.hp1 HG00558.hp2 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*1158_*1160delAAA | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 13/13 | 1158 | chr8 | 30678359 | ||||||
| chr8:30678359 | ATTTT | A | 18 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(15): Show |
76 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*1157_*1160delAAAA | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 13/13 | 1157 | chr8 | 30678359 | ||||||
| chr8:30678359 | ATTTTT | A | 13 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0011 others(10): Show |
77 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*1156_*1160delAAAA others(1): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 13/13 | 1156 | chr8 | 30678359 | ||||||
| chr8:30678361 | T | A | 6 | a0001c0001t0001 a0001c0001t0012 a0001c0003t0017 others(3): Show |
8 | HG01891.hp2 HG02055.hp1 HG02109.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1159A>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 13/13 | 1159 | chr8 | 30678361 | ||||||
| chr8:30678362 | T | A | 3 | a0001c0001t0001 a0001c0001t0003 a0003c0005t0004 |
9 | HG02145.hp2 HG02615.hp2 HG02683.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1158A>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 13/13 | 1158 | chr8 | 30678362 | ||||||
| chr8:30678363 | T | A | 5 | a0001c0001t0019 a0001c0001t0020 a0001c0001t0027 others(2): Show |
5 | HG02809.hp1 HG02886.hp2 HG03834.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1157A>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 13/13 | 1157 | chr8 | 30678363 | ||||||
| chr8:30678364 | T | A | 7 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0010 others(4): Show |
73 | HG00140.hp1 HG00558.hp1 HG00558.hp2 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*1156A>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 13/13 | 1156 | chr8 | 30678364 | ||||||
| chr8:30678365 | T | A | 13 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0015 others(10): Show |
32 | HG00438.hp1 HG02004.hp1 HG02055.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*1155A>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 13/13 | 1155 | chr8 | 30678365 | ||||||
| chr8:30678366 | T | A | 4 | a0001c0001t0007 a0001c0001t0011 a0001c0001t0023 others(1): Show |
16 | HG01516.hp1 HG02258.hp2 HG02280.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1154A>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 13/13 | 1154 | chr8 | 30678366 | ||||||
| chr8:30678367 | T | A | 5 | a0001c0001t0005 a0001c0001t0032 a0001c0003t0005 others(2): Show |
16 | HG02055.hp2 HG02280.hp1 HG02572.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1153A>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 13/13 | 1153 | chr8 | 30678367 | ||||||
| chr8:30678369 | T | A | 1 | a0006c0008t0024 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1151A>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 13/13 | 1151 | chr8 | 30678369 | ||||||
| chr8:30678518 | A | T | 1 | a0001c0001t0019 | 1 | NA18948.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1002T>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 13/13 | 1002 | chr8 | 30678518 | ||||||
| chr8:30678555 | T | G | 2 | a0001c0001t0009 a0001c0004t0009 |
7 | HG02723.hp2 HG02818.hp1 HG02895.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*965A>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 13/13 | 965 | chr8 | 30678555 | ||||||
| chr8:30678613 | C | T | 2 | a0001c0001t0012 a0002c0002t0012 |
3 | HG01891.hp2 HG02055.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*907G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 13/13 | 907 | chr8 | 30678613 | ||||||
| chr8:30678711 | G | A | 1 | a0001c0001t0028 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*809C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 13/13 | 809 | chr8 | 30678711 | ||||||
| chr8:30678952 | C | G | 1 | a0001c0001t0018 | 1 | HG01069.hp1 | 3_prime_UTR_variant | MODIFIER | c.*568G>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 13/13 | 568 | chr8 | 30678952 | ||||||
| chr8:30678978 | C | G | 1 | a0001c0003t0029 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*542G>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 13/13 | 542 | chr8 | 30678978 | ||||||
| chr8:30679011 | T | C | 2 | a0001c0001t0016 a0001c0001t0025 |
3 | HG02717.hp1 HG02896.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*509A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 13/13 | 509 | chr8 | 30679011 | ||||||
| chr8:30679064 | A | G | 47 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(44): Show |
256 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(253): Show |
3_prime_UTR_variant | MODIFIER | c.*456T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 13/13 | 456 | chr8 | 30679064 | ||||||
| chr8:30679149 | C | CA | 12 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(9): Show |
84 | HG00140.hp1 HG00558.hp2 HG00642.hp1 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*370dupT | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 13/13 | 370 | chr8 | 30679149 | ||||||
| chr8:30679276 | T | G | 2 | a0001c0001t0009 a0001c0004t0009 |
7 | HG02723.hp2 HG02818.hp1 HG02895.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*244A>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 13/13 | 244 | chr8 | 30679276 | ||||||
| chr8:30679370 | G | C | 1 | a0001c0001t0033 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*150C>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 13/13 | 150 | chr8 | 30679370 | ||||||
| chr8:30727837 | C | A | 1 | a0003c0005t0034 | 1 | HG02970.hp2 | 5_prime_UTR_variant | MODIFIER | c.-2G>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/13 | 2 | chr8 | 30727837 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:30679706 | CT | C | 241 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0038 others(238): Show |
242 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.1420-38delA | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 12/12 | chr8 | 30679706 | |||||||
| chr8:30679710 | T | C | 1 | a0004c0006t0003g0344 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1420-41A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 12/12 | chr8 | 30679710 | |||||||
| chr8:30679727 | C | T | 1 | a0001c0001t0003g0205 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1420-58G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 12/12 | chr8 | 30679727 | |||||||
| chr8:30679780 | G | A | 1 | a0001c0001t0004g0261 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1420-111C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 12/12 | chr8 | 30679780 | |||||||
| chr8:30679798 | C | T | 2 | a0004c0006t0003g0344 a0004c0006t0006g0343 |
2 | HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1420-129G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 12/12 | chr8 | 30679798 | |||||||
| chr8:30679815 | C | A | 71 | a0001c0001t0003g0179 a0001c0001t0003g0215 a0001c0001t0004g0047 others(68): Show |
71 | HG00140.hp1 HG00558.hp2 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.1420-146G>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 12/12 | chr8 | 30679815 | |||||||
| chr8:30679831 | G | A | 1 | a0001c0001t0001g0292 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1420-162C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 12/12 | chr8 | 30679831 | |||||||
| chr8:30679852 | C | T | 1 | a0001c0001t0022g0100 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1420-183G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 12/12 | chr8 | 30679852 | |||||||
| chr8:30680033 | A | T | 1 | a0001c0001t0004g0296 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1420-364T>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 12/12 | chr8 | 30680033 | |||||||
| chr8:30680381 | G | GT | 20 | a0001c0001t0001g0250 a0001c0001t0001g0254 a0001c0001t0001g0259 others(17): Show |
20 | HG00558.hp2 HG00735.hp1 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.1419+522dupA | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 12/12 | chr8 | 30680381 | |||||||
| chr8:30680381 | G | GTT | 6 | a0001c0001t0001g0306 a0001c0001t0001g0313 a0001c0001t0007g0220 others(3): Show |
6 | HG02486.hp2 HG03041.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1419+521_1419+522d others(4): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 12/12 | chr8 | 30680381 | |||||||
| chr8:30680384 | T | TTG | 33 | a0001c0001t0002g0049 a0001c0001t0002g0064 a0001c0001t0002g0098 others(30): Show |
33 | HG00438.hp1 HG00673.hp2 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.1419+519_1419+520i others(4): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 12/12 | chr8 | 30680384 | |||||||
| chr8:30680385 | T | TG | 207 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0038 others(204): Show |
208 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.1419+518_1419+519i others(3): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 12/12 | chr8 | 30680385 | |||||||
| chr8:30680386 | T | G | 7 | a0001c0001t0009g0017 a0001c0001t0009g0018 a0001c0001t0009g0019 others(4): Show |
7 | HG02723.hp2 HG02818.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1419+518A>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 12/12 | chr8 | 30680386 | |||||||
| chr8:30680392 | T | G | 2 | a0001c0001t0003g0077 a0001c0001t0003g0078 |
2 | HG00544.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.1419+512A>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 12/12 | chr8 | 30680392 | |||||||
| chr8:30680397 | T | G | 1 | a0001c0001t0003g0030 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1419+507A>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 12/12 | chr8 | 30680397 | |||||||
| chr8:30680447 | G | T | 339 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0036 others(336): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.1419+457C>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 12/12 | chr8 | 30680447 | |||||||
| chr8:30680481 | G | A | 80 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(77): Show |
81 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.1419+423C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 12/12 | chr8 | 30680481 | |||||||
| chr8:30680537 | A | G | 269 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0038 others(266): Show |
270 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.1419+367T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 12/12 | chr8 | 30680537 | |||||||
| chr8:30680548 | T | C | 252 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0038 others(249): Show |
253 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.1419+356A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 12/12 | chr8 | 30680548 | |||||||
| chr8:30680560 | A | C | 248 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0038 others(245): Show |
249 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.1419+344T>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 12/12 | chr8 | 30680560 | |||||||
| chr8:30680582 | A | T | 2 | a0002c0002t0002g0334 a0002c0002t0002g0336 |
2 | NA18960.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.1419+322T>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 12/12 | chr8 | 30680582 | |||||||
| chr8:30681199 | T | C | 2 | a0001c0001t0014g0031 a0001c0001t0014g0032 |
2 | HG02486.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1286-162A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 11/12 | chr8 | 30681199 | |||||||
| chr8:30681388 | G | A | 1 | a0002c0010t0002g0016 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1286-351C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 11/12 | chr8 | 30681388 | |||||||
| chr8:30681448 | C | T | 2 | a0001c0001t0003g0232 a0001c0001t0003g0314 |
2 | HG02559.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1286-411G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 11/12 | chr8 | 30681448 | |||||||
| chr8:30681480 | G | A | 1 | a0002c0002t0003g0320 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1286-443C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 11/12 | chr8 | 30681480 | |||||||
| chr8:30681541 | A | G | 1 | a0002c0002t0003g0320 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1285+389T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 11/12 | chr8 | 30681541 | |||||||
| chr8:30681597 | G | A | 1 | a0001c0001t0004g0316 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1285+333C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 11/12 | chr8 | 30681597 | |||||||
| chr8:30681621 | A | G | 1 | a0001c0001t0033g0034 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1285+309T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 11/12 | chr8 | 30681621 | |||||||
| chr8:30681626 | A | C | 3 | a0001c0001t0001g0250 a0001c0001t0001g0294 a0001c0001t0001g0295 |
3 | HG01934.hp1 HG01975.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.1285+304T>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 11/12 | chr8 | 30681626 | |||||||
| chr8:30681648 | T | A | 1 | a0001c0001t0003g0087 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1285+282A>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 11/12 | chr8 | 30681648 | |||||||
| chr8:30681752 | C | T | 1 | a0001c0001t0005g0315 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1285+178G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 11/12 | chr8 | 30681752 | |||||||
| chr8:30681764 | A | G | 2 | a0003c0005t0003g0005 a0003c0005t0034g0346 |
2 | HG00738.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1285+166T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 11/12 | chr8 | 30681764 | |||||||
| chr8:30682106 | T | G | 249 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0038 others(246): Show |
250 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.1154-45A>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 10/12 | chr8 | 30682106 | |||||||
| chr8:30682402 | C | G | 2 | a0001c0001t0003g0215 a0001c0001t0033g0034 |
2 | HG02257.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1154-341G>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 10/12 | chr8 | 30682402 | |||||||
| chr8:30682454 | A | T | 269 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0038 others(266): Show |
270 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.1154-393T>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 10/12 | chr8 | 30682454 | |||||||
| chr8:30682561 | A | C | 1 | a0001c0001t0007g0225 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1154-500T>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 10/12 | chr8 | 30682561 | |||||||
| chr8:30682658 | C | T | 7 | a0001c0001t0009g0017 a0001c0001t0009g0018 a0001c0001t0009g0019 others(4): Show |
7 | HG02723.hp2 HG02818.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1154-597G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 10/12 | chr8 | 30682658 | |||||||
| chr8:30682770 | A | G | 254 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0038 others(251): Show |
255 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.1154-709T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 10/12 | chr8 | 30682770 | |||||||
| chr8:30682791 | C | T | 178 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0038 others(175): Show |
179 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.1154-730G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 10/12 | chr8 | 30682791 | |||||||
| chr8:30682792 | G | A | 70 | a0001c0001t0003g0179 a0001c0001t0003g0215 a0001c0001t0004g0047 others(67): Show |
70 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.1154-731C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 10/12 | chr8 | 30682792 | |||||||
| chr8:30682837 | T | A | 4 | a0001c0001t0003g0080 a0001c0001t0003g0081 a0001c0001t0003g0178 others(1): Show |
4 | HG01952.hp2 HG02486.hp1 NA19080.hp2 others(1): Show |
intron_variant | MODIFIER | c.1154-776A>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 10/12 | chr8 | 30682837 | |||||||
| chr8:30682958 | G | C | 1 | a0001c0001t0002g0052 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1154-897C>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 10/12 | chr8 | 30682958 | |||||||
| chr8:30682959 | C | G | 1 | a0001c0001t0002g0052 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1154-898G>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 10/12 | chr8 | 30682959 | |||||||
| chr8:30682972 | C | T | 1 | a0001c0001t0003g0035 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1154-911G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 10/12 | chr8 | 30682972 | |||||||
| chr8:30683181 | C | A | 7 | a0001c0001t0009g0017 a0001c0001t0009g0018 a0001c0001t0009g0019 others(4): Show |
7 | HG02723.hp2 HG02818.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1153+907G>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 10/12 | chr8 | 30683181 | |||||||
| chr8:30683440 | T | C | 1 | a0001c0001t0012g0168 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1153+648A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 10/12 | chr8 | 30683440 | |||||||
| chr8:30683589 | G | A | 2 | a0001c0001t0003g0215 a0001c0001t0033g0034 |
2 | HG02257.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1153+499C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 10/12 | chr8 | 30683589 | |||||||
| chr8:30683691 | G | A | 1 | a0001c0001t0025g0214 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1153+397C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 10/12 | chr8 | 30683691 | |||||||
| chr8:30683692 | T | G | 3 | a0001c0001t0005g0207 a0001c0001t0010g0206 a0006c0008t0024g0204 |
3 | HG02572.hp1 HG03195.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1153+396A>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 10/12 | chr8 | 30683692 | |||||||
| chr8:30683754 | C | CA | 79 | a0001c0001t0001g0263 a0001c0001t0002g0152 a0001c0001t0003g0087 others(76): Show |
79 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.1153+333dupT | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 10/12 | chr8 | 30683754 | |||||||
| chr8:30683754 | C | CAA | 189 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0038 others(186): Show |
190 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.1153+332_1153+333d others(4): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 10/12 | chr8 | 30683754 | |||||||
| chr8:30684398 | C | T | 254 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0038 others(251): Show |
255 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.1042-199G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30684398 | |||||||
| chr8:30684414 | A | G | 4 | a0001c0003t0017g0009 a0001c0003t0017g0010 a0001c0003t0029g0007 others(1): Show |
4 | HG02809.hp1 HG02886.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1042-215T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30684414 | |||||||
| chr8:30684418 | G | A | 81 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(78): Show |
82 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.1042-219C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30684418 | |||||||
| chr8:30684607 | G | T | 1 | a0001c0001t0008g0041 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1042-408C>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30684607 | |||||||
| chr8:30684747 | T | A | 2 | a0001c0001t0004g0149 a0001c0001t0004g0156 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1042-548A>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30684747 | |||||||
| chr8:30684809 | G | A | 4 | a0001c0001t0003g0216 a0001c0003t0003g0011 a0001c0004t0003g0323 others(1): Show |
4 | HG02451.hp1 HG03195.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1042-610C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30684809 | |||||||
| chr8:30684926 | T | C | 1 | a0001c0001t0002g0131 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1042-727A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30684926 | |||||||
| chr8:30684928 | CATTT | C | 61 | a0001c0001t0001g0036 a0001c0001t0001g0135 a0001c0001t0001g0230 others(58): Show |
61 | HG00323.hp2 HG00558.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.1042-733_1042-730d others(6): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30684928 | |||||||
| chr8:30684928 | CATTTATT others(1): Show |
C | 84 | a0001c0001t0001g0033 a0001c0001t0001g0038 a0001c0001t0001g0090 others(81): Show |
84 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(81): Show |
intron_variant | MODIFIER | c.1042-737_1042-730d others(10): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30684928 | |||||||
| chr8:30684928 | CATTTATT others(5): Show |
C | 76 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0210 others(73): Show |
77 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.1042-741_1042-730d others(14): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30684928 | |||||||
| chr8:30684928 | CATTTATT others(9): Show |
C | 74 | a0001c0001t0001g0285 a0001c0001t0001g0304 a0001c0001t0002g0001 others(71): Show |
75 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.1042-745_1042-730d others(18): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30684928 | |||||||
| chr8:30684928 | CATTTATT others(13): Show |
C | 9 | a0001c0001t0001g0245 a0001c0001t0001g0272 a0001c0001t0001g0274 others(6): Show |
9 | HG00099.hp2 HG00738.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1042-749_1042-730d others(22): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30684928 | |||||||
| chr8:30684928 | CATTTATT others(17): Show |
C | 10 | a0001c0001t0001g0311 a0001c0001t0002g0096 a0001c0001t0002g0152 others(7): Show |
10 | HG02004.hp2 HG02257.hp1 HG02273.hp2 others(7): Show |
intron_variant | MODIFIER | c.1042-753_1042-730d others(26): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30684928 | |||||||
| chr8:30684928 | CATTTATT others(21): Show |
C | 11 | a0001c0001t0004g0224 a0001c0001t0006g0167 a0001c0001t0007g0209 others(8): Show |
11 | HG01243.hp1 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1042-757_1042-730d others(30): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30684928 | |||||||
| chr8:30684954 | T | A | 1 | a0001c0001t0002g0052 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1042-755A>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30684954 | |||||||
| chr8:30684975 | T | G | 2 | a0001c0001t0003g0215 a0001c0001t0033g0034 |
2 | HG02257.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1042-776A>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30684975 | |||||||
| chr8:30685111 | C | T | 86 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0038 others(83): Show |
86 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1042-912G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30685111 | |||||||
| chr8:30685146 | G | A | 32 | a0001c0001t0001g0090 a0001c0001t0001g0210 a0001c0001t0001g0227 others(29): Show |
32 | HG00140.hp2 HG00323.hp1 HG01934.hp1 others(29): Show |
intron_variant | MODIFIER | c.1042-947C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30685146 | |||||||
| chr8:30685211 | C | T | 1 | a0002c0002t0002g0340 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1042-1012G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30685211 | |||||||
| chr8:30685246 | C | T | 1 | a0001c0001t0001g0289 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1042-1047G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30685246 | |||||||
| chr8:30685252 | G | A | 2 | a0001c0001t0002g0124 a0001c0001t0002g0165 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1042-1053C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30685252 | |||||||
| chr8:30685379 | C | A | 8 | a0001c0001t0003g0030 a0001c0001t0003g0035 a0001c0001t0003g0205 others(5): Show |
8 | HG01891.hp1 HG02257.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1042-1180G>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30685379 | |||||||
| chr8:30685558 | T | C | 1 | a0001c0003t0002g0006 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1042-1359A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30685558 | |||||||
| chr8:30685734 | G | A | 2 | a0003c0005t0003g0005 a0003c0005t0034g0346 |
2 | HG00738.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1042-1535C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30685734 | |||||||
| chr8:30685751 | G | A | 1 | a0002c0002t0003g0320 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1042-1552C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30685751 | |||||||
| chr8:30685901 | C | T | 2 | a0001c0001t0003g0179 a0001c0001t0006g0110 |
2 | NA18992.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.1042-1702G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30685901 | |||||||
| chr8:30685913 | G | A | 1 | a0001c0001t0003g0215 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1042-1714C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30685913 | |||||||
| chr8:30685985 | C | CA | 13 | a0001c0001t0001g0218 a0001c0001t0001g0313 a0001c0001t0003g0081 others(10): Show |
13 | HG01952.hp2 HG02155.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.1042-1787dupT | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30685985 | |||||||
| chr8:30685985 | C | CAA | 10 | a0001c0001t0004g0224 a0001c0001t0007g0209 a0001c0001t0007g0217 others(7): Show |
10 | HG00738.hp2 HG01243.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1042-1788_1042-178 others(6): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30685985 | |||||||
| chr8:30685985 | C | CAAA | 6 | a0001c0001t0004g0116 a0001c0001t0006g0110 a0001c0001t0006g0167 others(3): Show |
6 | HG01257.hp1 HG02559.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1042-1789_1042-178 others(7): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30685985 | |||||||
| chr8:30685985 | C | CAAAA | 50 | a0001c0001t0003g0177 a0001c0001t0003g0179 a0001c0001t0004g0047 others(47): Show |
50 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.1042-1790_1042-178 others(8): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30685985 | |||||||
| chr8:30685985 | C | CAAAAA | 13 | a0001c0001t0004g0058 a0001c0001t0004g0068 a0001c0001t0004g0070 others(10): Show |
13 | HG00642.hp1 HG00735.hp2 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.1042-1791_1042-178 others(9): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30685985 | |||||||
| chr8:30685985 | CA | C | 94 | a0001c0001t0001g0251 a0001c0001t0001g0304 a0001c0001t0001g0308 others(91): Show |
95 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.1042-1787delT | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30685985 | |||||||
| chr8:30685985 | CAA | C | 9 | a0001c0001t0003g0030 a0001c0001t0003g0035 a0001c0001t0003g0205 others(6): Show |
9 | HG01891.hp1 HG02257.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1042-1788_1042-178 others(6): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30685985 | |||||||
| chr8:30685985 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0113 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1042-1797_1042-178 others(15): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30685985 | |||||||
| chr8:30685985 | CAAAAAAA others(5): Show |
C | 5 | a0001c0001t0001g0250 a0001c0001t0001g0294 a0001c0001t0001g0295 others(2): Show |
5 | HG01934.hp1 HG01975.hp1 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.1042-1798_1042-178 others(16): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30685985 | |||||||
| chr8:30686118 | C | T | 3 | a0001c0001t0007g0209 a0001c0001t0007g0220 a0001c0001t0007g0222 |
3 | HG02258.hp2 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1042-1919G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30686118 | |||||||
| chr8:30686221 | T | A | 1 | a0001c0001t0003g0179 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1042-2022A>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30686221 | |||||||
| chr8:30686221 | T | C | 1 | a0001c0001t0003g0030 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1042-2022A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30686221 | |||||||
| chr8:30686690 | A | G | 180 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0038 others(177): Show |
181 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.1041+2471T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30686690 | |||||||
| chr8:30686702 | C | A | 1 | a0001c0001t0002g0052 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1041+2459G>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30686702 | |||||||
| chr8:30686703 | A | C | 68 | a0001c0001t0003g0177 a0001c0001t0003g0179 a0001c0001t0004g0047 others(65): Show |
68 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.1041+2458T>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30686703 | |||||||
| chr8:30686704 | A | C | 2 | a0001c0001t0004g0286 a0005c0007t0002g0173 |
2 | HG00323.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.1041+2457T>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30686704 | |||||||
| chr8:30686841 | G | GT | 8 | a0001c0001t0001g0260 a0001c0001t0002g0228 a0001c0001t0003g0216 others(5): Show |
8 | HG01175.hp2 HG01978.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1041+2319dupA | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30686841 | |||||||
| chr8:30686841 | G | T | 1 | a0001c0001t0001g0251 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1041+2320C>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30686841 | |||||||
| chr8:30686885 | G | A | 3 | a0001c0001t0001g0250 a0001c0001t0001g0294 a0001c0001t0001g0295 |
3 | HG01934.hp1 HG01975.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.1041+2276C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30686885 | |||||||
| chr8:30686897 | C | T | 3 | a0001c0001t0004g0116 a0001c0001t0004g0199 a0001c0001t0023g0197 |
3 | HG02738.hp1 HG04115.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.1041+2264G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30686897 | |||||||
| chr8:30686997 | T | C | 180 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0038 others(177): Show |
181 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.1041+2164A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30686997 | |||||||
| chr8:30687046 | A | G | 1 | a0001c0001t0002g0052 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1041+2115T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30687046 | |||||||
| chr8:30687129 | G | A | 1 | a0001c0001t0033g0034 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1041+2032C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30687129 | |||||||
| chr8:30687206 | T | C | 1 | a0001c0001t0002g0049 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1041+1955A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30687206 | |||||||
| chr8:30687374 | A | AG | 7 | a0001c0001t0009g0017 a0001c0001t0009g0018 a0001c0001t0009g0019 others(4): Show |
7 | HG02723.hp2 HG02818.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1041+1786dupC | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30687374 | |||||||
| chr8:30687413 | C | T | 2 | a0001c0001t0003g0035 a0002c0002t0003g0320 |
2 | HG02257.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1041+1748G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30687413 | |||||||
| chr8:30687429 | T | G | 3 | a0001c0001t0001g0250 a0001c0001t0001g0294 a0001c0001t0001g0295 |
3 | HG01934.hp1 HG01975.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.1041+1732A>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30687429 | |||||||
| chr8:30687444 | G | A | 1 | a0004c0006t0003g0344 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1041+1717C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30687444 | |||||||
| chr8:30687520 | C | T | 45 | a0001c0001t0003g0013 a0001c0001t0003g0024 a0001c0001t0003g0025 others(42): Show |
45 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.1041+1641G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30687520 | |||||||
| chr8:30687621 | T | C | 2 | a0002c0002t0002g0331 a0002c0002t0002g0333 |
2 | HG02738.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1041+1540A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30687621 | |||||||
| chr8:30687647 | A | AAAAC | 6 | a0001c0001t0001g0263 a0001c0001t0001g0265 a0001c0001t0001g0266 others(3): Show |
6 | HG02258.hp2 HG02451.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1041+1510_1041+151 others(8): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30687647 | |||||||
| chr8:30687755 | T | C | 1 | a0001c0001t0004g0121 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1041+1406A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30687755 | |||||||
| chr8:30687800 | T | C | 1 | a0003c0005t0004g0004 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1041+1361A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30687800 | |||||||
| chr8:30688134 | C | T | 4 | a0001c0001t0003g0216 a0001c0003t0003g0011 a0001c0004t0003g0323 others(1): Show |
4 | HG02451.hp1 HG03195.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1041+1027G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30688134 | |||||||
| chr8:30688221 | A | C | 1 | a0002c0010t0002g0016 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1041+940T>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30688221 | |||||||
| chr8:30688245 | C | T | 4 | a0001c0003t0017g0009 a0001c0003t0017g0010 a0001c0003t0029g0007 others(1): Show |
4 | HG02809.hp1 HG02886.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1041+916G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30688245 | |||||||
| chr8:30688310 | G | A | 72 | a0001c0001t0003g0179 a0001c0001t0003g0215 a0001c0001t0004g0047 others(69): Show |
72 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.1041+851C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30688310 | |||||||
| chr8:30688513 | A | C | 1 | a0001c0001t0006g0146 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1041+648T>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30688513 | |||||||
| chr8:30688578 | C | CA | 85 | a0001c0001t0001g0262 a0001c0001t0003g0013 a0001c0001t0003g0024 others(82): Show |
85 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.1041+582dupT | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30688578 | |||||||
| chr8:30688578 | C | CAA | 99 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0038 others(96): Show |
100 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.1041+581_1041+582d others(4): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30688578 | |||||||
| chr8:30688578 | C | CAAA | 10 | a0001c0001t0002g0127 a0001c0001t0002g0155 a0001c0001t0002g0244 others(7): Show |
10 | HG00408.hp1 HG00621.hp2 HG02040.hp2 others(7): Show |
intron_variant | MODIFIER | c.1041+580_1041+582d others(5): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30688578 | |||||||
| chr8:30688578 | CA | C | 71 | a0001c0001t0001g0266 a0001c0001t0003g0179 a0001c0001t0003g0215 others(68): Show |
71 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.1041+582delT | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30688578 | |||||||
| chr8:30688600 | G | A | 1 | a0004c0006t0003g0344 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1041+561C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30688600 | |||||||
| chr8:30688714 | G | A | 1 | a0001c0001t0022g0100 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1041+447C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30688714 | |||||||
| chr8:30688963 | A | C | 1 | a0001c0001t0002g0101 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1041+198T>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30688963 | |||||||
| chr8:30689119 | T | C | 199 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0038 others(196): Show |
200 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.1041+42A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 9/12 | chr8 | 30689119 | |||||||
| chr8:30689324 | T | G | 1 | a0001c0001t0004g0112 | 1 | NA18971.hp1 | splice_region_variant&intron_variant | LOW | c.883-5A>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30689324 | |||||||
| chr8:30689449 | G | C | 246 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0038 others(243): Show |
247 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.883-130C>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30689449 | |||||||
| chr8:30689746 | G | GTA | 12 | a0001c0001t0001g0135 a0001c0001t0001g0223 a0001c0001t0001g0269 others(9): Show |
12 | HG02145.hp2 HG02280.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.883-429_883-428dup others(2): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30689746 | |||||||
| chr8:30689746 | GTA | G | 264 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0038 others(261): Show |
265 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.883-429_883-428del others(2): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30689746 | |||||||
| chr8:30689750 | A | G | 4 | a0001c0001t0003g0216 a0001c0003t0003g0011 a0001c0004t0003g0323 others(1): Show |
4 | HG02451.hp1 HG03195.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.883-431T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30689750 | |||||||
| chr8:30689773 | T | C | 4 | a0001c0001t0003g0216 a0001c0003t0003g0011 a0001c0004t0003g0323 others(1): Show |
4 | HG02451.hp1 HG03195.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.883-454A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30689773 | |||||||
| chr8:30689897 | AT | A | 3 | a0001c0001t0003g0030 a0001c0001t0003g0232 a0001c0001t0003g0314 |
3 | HG02559.hp2 HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.883-579delA | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30689897 | |||||||
| chr8:30689923 | GT | G | 6 | a0001c0001t0009g0017 a0001c0001t0009g0018 a0001c0001t0009g0019 others(3): Show |
6 | HG02723.hp2 HG02818.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.883-605delA | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30689923 | |||||||
| chr8:30689968 | TTA | T | 5 | a0001c0001t0003g0030 a0001c0001t0003g0065 a0001c0001t0003g0232 others(2): Show |
5 | HG02559.hp2 HG02615.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.883-651_883-650del others(2): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30689968 | |||||||
| chr8:30689984 | A | ATATATAT others(37): Show |
2 | a0001c0001t0001g0033 a0001c0001t0001g0038 |
2 | HG01934.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.883-666_883-665ins others(44): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30689984 | |||||||
| chr8:30690006 | ATATAT | A | 138 | a0001c0001t0001g0239 a0001c0001t0001g0304 a0001c0001t0001g0306 others(135): Show |
139 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.883-692_883-688del others(5): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30690006 | |||||||
| chr8:30690022 | G | A | 25 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0038 others(22): Show |
25 | HG01243.hp2 HG01891.hp1 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.883-703C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30690022 | |||||||
| chr8:30690029 | T | C | 3 | a0001c0001t0003g0030 a0001c0001t0003g0232 a0001c0001t0003g0314 |
3 | HG02559.hp2 HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.883-710A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30690029 | |||||||
| chr8:30690046 | TATAA | T | 6 | a0001c0001t0009g0017 a0001c0001t0009g0018 a0001c0001t0009g0019 others(3): Show |
6 | HG02723.hp2 HG02818.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.883-731_883-728del others(4): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30690046 | |||||||
| chr8:30690073 | C | T | 1 | a0001c0001t0004g0103 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.883-754G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30690073 | |||||||
| chr8:30690098 | TAAA | T | 4 | a0001c0001t0003g0215 a0001c0001t0004g0316 a0001c0001t0033g0034 others(1): Show |
4 | HG02257.hp2 HG02486.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.883-782_883-780del others(3): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30690098 | |||||||
| chr8:30690141 | C | T | 1 | a0001c0001t0003g0162 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.883-822G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30690141 | |||||||
| chr8:30690155 | A | AATTT | 5 | a0001c0001t0004g0286 a0001c0001t0006g0146 a0002c0002t0001g0335 others(2): Show |
5 | HG00323.hp2 HG00738.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.883-837_883-836ins others(4): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30690155 | |||||||
| chr8:30690158 | A | ATATT | 223 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0239 others(220): Show |
224 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.883-843_883-840dup others(4): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30690158 | |||||||
| chr8:30690158 | A | T | 5 | a0001c0001t0004g0286 a0001c0001t0006g0146 a0002c0002t0001g0335 others(2): Show |
5 | HG00323.hp2 HG00738.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.883-839T>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30690158 | |||||||
| chr8:30690541 | G | A | 10 | a0001c0001t0005g0203 a0001c0001t0005g0278 a0001c0001t0005g0279 others(7): Show |
10 | HG02280.hp1 HG02572.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.883-1222C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30690541 | |||||||
| chr8:30690637 | G | A | 59 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0095 others(56): Show |
60 | HG00099.hp1 HG00280.hp2 HG00733.hp2 others(57): Show |
intron_variant | MODIFIER | c.883-1318C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30690637 | |||||||
| chr8:30690906 | A | T | 1 | a0001c0001t0004g0201 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.883-1587T>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30690906 | |||||||
| chr8:30690907 | T | A | 4 | a0001c0001t0002g0029 a0001c0001t0002g0198 a0001c0001t0004g0149 others(1): Show |
4 | HG00408.hp2 HG00621.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.883-1588A>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30690907 | |||||||
| chr8:30690947 | A | G | 1 | a0001c0001t0001g0285 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.883-1628T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30690947 | |||||||
| chr8:30691180 | A | G | 5 | a0001c0001t0001g0002 a0001c0001t0001g0242 a0001c0001t0001g0253 others(2): Show |
6 | HG00099.hp1 HG00735.hp1 HG01109.hp1 others(3): Show |
intron_variant | MODIFIER | c.882+1789T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30691180 | |||||||
| chr8:30691227 | C | T | 3 | a0001c0001t0003g0205 a0001c0001t0003g0211 a0001c0003t0003g0012 |
3 | HG01891.hp1 HG02615.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.882+1742G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30691227 | |||||||
| chr8:30691281 | G | T | 1 | a0001c0001t0023g0197 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.882+1688C>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30691281 | |||||||
| chr8:30691282 | G | C | 1 | a0001c0001t0023g0197 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.882+1687C>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30691282 | |||||||
| chr8:30691321 | C | T | 1 | a0001c0001t0002g0175 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.882+1648G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30691321 | |||||||
| chr8:30692079 | G | A | 2 | a0001c0001t0002g0244 a0001c0001t0002g0299 |
2 | HG00408.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.882+890C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30692079 | |||||||
| chr8:30692108 | G | GA | 11 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0038 others(8): Show |
11 | HG01243.hp2 HG01934.hp2 HG02300.hp2 others(8): Show |
intron_variant | MODIFIER | c.882+860dupT | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30692108 | |||||||
| chr8:30692108 | GA | G | 66 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0095 others(63): Show |
67 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.882+860delT | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30692108 | |||||||
| chr8:30692196 | C | CT | 108 | a0001c0001t0001g0090 a0001c0001t0001g0239 a0001c0001t0001g0240 others(105): Show |
109 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.882+772dupA | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30692196 | |||||||
| chr8:30692196 | C | CTT | 44 | a0001c0001t0001g0223 a0001c0001t0002g0014 a0001c0001t0002g0015 others(41): Show |
44 | HG00597.hp1 HG00735.hp2 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.882+771_882+772dup others(2): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30692196 | |||||||
| chr8:30692196 | C | CTTT | 7 | a0001c0001t0004g0199 a0001c0001t0006g0167 a0001c0001t0007g0217 others(4): Show |
7 | HG02145.hp2 HG02280.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.882+770_882+772dup others(3): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30692196 | |||||||
| chr8:30692196 | CT | C | 14 | a0001c0001t0001g0039 a0001c0001t0001g0253 a0001c0001t0003g0144 others(11): Show |
14 | HG01243.hp2 HG01256.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.882+772delA | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30692196 | |||||||
| chr8:30692196 | CTT | C | 18 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0038 others(15): Show |
18 | HG01934.hp2 HG02257.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.882+771_882+772del others(2): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30692196 | |||||||
| chr8:30692253 | G | A | 1 | a0001c0001t0003g0248 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.882+716C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30692253 | |||||||
| chr8:30692268 | A | C | 1 | a0001c0001t0008g0037 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.882+701T>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30692268 | |||||||
| chr8:30692368 | GT | G | 7 | a0001c0001t0004g0224 a0001c0001t0007g0217 a0001c0001t0007g0219 others(4): Show |
7 | HG02280.hp2 HG02559.hp1 HG03486.hp2 others(4): Show |
intron_variant | MODIFIER | c.882+600delA | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30692368 | |||||||
| chr8:30692495 | C | CT | 197 | a0001c0001t0001g0033 a0001c0001t0001g0135 a0001c0001t0001g0223 others(194): Show |
198 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.882+473dupA | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30692495 | |||||||
| chr8:30692495 | C | CTT | 101 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0095 others(98): Show |
102 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.882+472_882+473dup others(2): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30692495 | |||||||
| chr8:30692495 | C | CTTT | 14 | a0001c0001t0001g0138 a0001c0001t0001g0241 a0001c0001t0001g0251 others(11): Show |
14 | HG00735.hp1 HG01081.hp1 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.882+471_882+473dup others(3): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30692495 | |||||||
| chr8:30692857 | A | C | 1 | a0001c0001t0001g0269 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.882+112T>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 8/12 | chr8 | 30692857 | |||||||
| chr8:30693144 | A | T | 1 | a0001c0001t0005g0203 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.796-89T>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/12 | chr8 | 30693144 | |||||||
| chr8:30693245 | T | C | 1 | a0001c0001t0006g0167 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.796-190A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/12 | chr8 | 30693245 | |||||||
| chr8:30693399 | T | C | 2 | a0001c0001t0001g0033 a0001c0001t0001g0038 |
2 | HG01934.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.796-344A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/12 | chr8 | 30693399 | |||||||
| chr8:30693416 | T | C | 4 | a0001c0001t0003g0216 a0001c0003t0003g0011 a0001c0004t0003g0323 others(1): Show |
4 | HG02451.hp1 HG03195.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.796-361A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/12 | chr8 | 30693416 | |||||||
| chr8:30693533 | A | AT | 5 | a0001c0001t0001g0135 a0001c0001t0001g0269 a0001c0001t0006g0167 others(2): Show |
5 | HG02630.hp1 HG03492.hp2 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.796-479dupA | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/12 | chr8 | 30693533 | |||||||
| chr8:30693533 | A | ATG | 4 | a0001c0003t0017g0009 a0001c0003t0029g0007 a0001c0004t0009g0319 others(1): Show |
4 | HG02809.hp1 HG02886.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.796-479_796-478ins others(2): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/12 | chr8 | 30693533 | |||||||
| chr8:30693534 | T | C | 1 | a0002c0002t0010g0341 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.796-479A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/12 | chr8 | 30693534 | |||||||
| chr8:30693538 | T | C | 1 | a0001c0001t0003g0139 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.796-483A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/12 | chr8 | 30693538 | |||||||
| chr8:30693538 | TA | T | 6 | a0001c0001t0001g0295 a0001c0001t0002g0105 a0001c0001t0002g0117 others(3): Show |
6 | HG00323.hp1 HG00558.hp2 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.796-484delT | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/12 | chr8 | 30693538 | |||||||
| chr8:30693539 | A | T | 338 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0036 others(335): Show |
340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.796-484T>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/12 | chr8 | 30693539 | |||||||
| chr8:30693696 | C | T | 256 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0036 others(253): Show |
258 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.796-641G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/12 | chr8 | 30693696 | |||||||
| chr8:30694182 | C | T | 1 | a0001c0001t0009g0020 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.796-1127G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/12 | chr8 | 30694182 | |||||||
| chr8:30694291 | G | A | 1 | a0001c0001t0010g0180 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.796-1236C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/12 | chr8 | 30694291 | |||||||
| chr8:30694443 | G | A | 1 | a0001c0001t0002g0252 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.796-1388C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/12 | chr8 | 30694443 | |||||||
| chr8:30694544 | T | G | 2 | a0001c0001t0003g0132 a0001c0001t0004g0116 |
2 | NA18986.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.796-1489A>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/12 | chr8 | 30694544 | |||||||
| chr8:30694882 | A | G | 2 | a0001c0001t0014g0031 a0001c0001t0014g0032 |
2 | HG02486.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.795+1498T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/12 | chr8 | 30694882 | |||||||
| chr8:30694897 | C | CA | 90 | a0001c0001t0001g0002 a0001c0001t0001g0036 a0001c0001t0001g0038 others(87): Show |
91 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.795+1482dupT | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/12 | chr8 | 30694897 | |||||||
| chr8:30694897 | C | CAA | 109 | a0001c0001t0001g0033 a0001c0001t0001g0218 a0001c0001t0001g0239 others(106): Show |
110 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.795+1481_795+1482d others(4): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/12 | chr8 | 30694897 | |||||||
| chr8:30694897 | C | CAAA | 10 | a0001c0001t0002g0052 a0001c0001t0003g0132 a0001c0001t0003g0177 others(7): Show |
10 | HG01069.hp1 HG01123.hp2 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.795+1480_795+1482d others(5): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/12 | chr8 | 30694897 | |||||||
| chr8:30694986 | A | G | 1 | a0001c0001t0004g0125 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.795+1394T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/12 | chr8 | 30694986 | |||||||
| chr8:30695112 | T | C | 1 | a0002c0002t0012g0322 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.795+1268A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/12 | chr8 | 30695112 | |||||||
| chr8:30695176 | C | T | 22 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0005g0203 others(19): Show |
22 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.795+1204G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/12 | chr8 | 30695176 | |||||||
| chr8:30695183 | A | T | 22 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0005g0203 others(19): Show |
22 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.795+1197T>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/12 | chr8 | 30695183 | |||||||
| chr8:30695276 | C | T | 3 | a0001c0001t0001g0135 a0001c0001t0001g0269 a0001c0004t0001g0332 |
3 | HG02630.hp1 HG03492.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.795+1104G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/12 | chr8 | 30695276 | |||||||
| chr8:30695290 | C | A | 3 | a0001c0001t0003g0205 a0001c0001t0003g0211 a0001c0003t0003g0012 |
3 | HG01891.hp1 HG02615.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.795+1090G>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/12 | chr8 | 30695290 | |||||||
| chr8:30695482 | C | T | 2 | a0004c0006t0003g0344 a0004c0006t0006g0343 |
2 | HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.795+898G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/12 | chr8 | 30695482 | |||||||
| chr8:30695485 | C | T | 3 | a0001c0001t0001g0135 a0001c0001t0001g0269 a0001c0004t0001g0332 |
3 | HG02630.hp1 HG03492.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.795+895G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/12 | chr8 | 30695485 | |||||||
| chr8:30695522 | A | C | 1 | a0001c0001t0007g0075 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.795+858T>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/12 | chr8 | 30695522 | |||||||
| chr8:30695697 | G | A | 2 | a0001c0003t0017g0009 a0001c0003t0017g0010 |
2 | HG02886.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.795+683C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/12 | chr8 | 30695697 | |||||||
| chr8:30695780 | C | G | 3 | a0001c0001t0003g0071 a0001c0001t0003g0189 a0001c0009t0002g0027 |
3 | NA18964.hp1 NA18988.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.795+600G>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/12 | chr8 | 30695780 | |||||||
| chr8:30695813 | G | A | 1 | a0001c0001t0003g0248 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.795+567C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/12 | chr8 | 30695813 | |||||||
| chr8:30695913 | A | G | 212 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0036 others(209): Show |
214 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.795+467T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/12 | chr8 | 30695913 | |||||||
| chr8:30695951 | A | T | 1 | a0001c0001t0003g0154 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.795+429T>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/12 | chr8 | 30695951 | |||||||
| chr8:30695954 | C | T | 4 | a0001c0001t0004g0316 a0001c0001t0006g0167 a0001c0001t0012g0168 others(1): Show |
4 | HG02055.hp1 NA19030.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.795+426G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/12 | chr8 | 30695954 | |||||||
| chr8:30696114 | G | A | 2 | a0001c0001t0002g0124 a0001c0001t0002g0165 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.795+266C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/12 | chr8 | 30696114 | |||||||
| chr8:30696283 | C | T | 1 | a0001c0001t0002g0015 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.795+97G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 7/12 | chr8 | 30696283 | |||||||
| chr8:30696489 | G | A | 138 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0038 others(135): Show |
139 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(136): Show |
intron_variant | MODIFIER | c.696-10C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30696489 | |||||||
| chr8:30696656 | C | T | 1 | a0001c0001t0004g0316 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.696-177G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30696656 | |||||||
| chr8:30696749 | G | A | 12 | a0001c0001t0001g0135 a0001c0001t0001g0223 a0001c0001t0001g0269 others(9): Show |
12 | HG02145.hp2 HG02280.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.696-270C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30696749 | |||||||
| chr8:30696827 | C | A | 2 | a0002c0002t0002g0331 a0002c0002t0002g0333 |
2 | HG02738.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.696-348G>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30696827 | |||||||
| chr8:30697211 | C | T | 2 | a0001c0001t0004g0093 a0001c0001t0004g0094 |
2 | HG00642.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.696-732G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30697211 | |||||||
| chr8:30697241 | C | T | 3 | a0001c0001t0001g0135 a0001c0001t0001g0269 a0001c0004t0001g0332 |
3 | HG02630.hp1 HG03492.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.696-762G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30697241 | |||||||
| chr8:30697367 | T | C | 9 | a0001c0001t0001g0223 a0001c0001t0004g0224 a0001c0001t0007g0217 others(6): Show |
9 | HG02145.hp2 HG02280.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.696-888A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30697367 | |||||||
| chr8:30697408 | T | C | 2 | a0001c0001t0014g0031 a0001c0001t0014g0032 |
2 | HG02486.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.696-929A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30697408 | |||||||
| chr8:30697421 | C | A | 135 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0038 others(132): Show |
136 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(133): Show |
intron_variant | MODIFIER | c.696-942G>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30697421 | |||||||
| chr8:30697422 | A | AAAAC | 80 | a0001c0001t0001g0227 a0001c0001t0001g0230 a0001c0001t0001g0231 others(77): Show |
80 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.696-947_696-944dup others(4): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30697422 | |||||||
| chr8:30697422 | AAAAC | A | 11 | a0001c0001t0001g0285 a0001c0001t0003g0216 a0001c0001t0003g0298 others(8): Show |
11 | HG02451.hp1 HG02602.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.696-947_696-944del others(4): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30697422 | |||||||
| chr8:30697425 | A | AAC | 9 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0038 others(6): Show |
9 | HG01243.hp2 HG01934.hp2 HG02300.hp2 others(6): Show |
intron_variant | MODIFIER | c.696-947_696-946ins others(2): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30697425 | |||||||
| chr8:30697426 | C | A | 10 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0038 others(7): Show |
10 | HG01243.hp2 HG01934.hp2 HG02300.hp2 others(7): Show |
intron_variant | MODIFIER | c.696-947G>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30697426 | |||||||
| chr8:30697426 | C | CA | 127 | a0001c0001t0001g0239 a0001c0001t0002g0001 a0001c0001t0002g0014 others(124): Show |
128 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(125): Show |
intron_variant | MODIFIER | c.696-948dupT | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30697426 | |||||||
| chr8:30697429 | A | C | 1 | a0001c0001t0008g0040 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.696-950T>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30697429 | |||||||
| chr8:30697430 | C | A | 1 | a0001c0001t0008g0040 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.696-951G>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30697430 | |||||||
| chr8:30697567 | G | GCAGTGAG others(1): Show |
3 | a0001c0001t0003g0205 a0001c0001t0003g0211 a0001c0003t0003g0012 |
3 | HG01891.hp1 HG02615.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.696-1096_696-1089d others(10): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30697567 | |||||||
| chr8:30697826 | C | A | 1 | a0001c0001t0002g0119 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.696-1347G>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30697826 | |||||||
| chr8:30697933 | C | T | 4 | a0001c0001t0002g0066 a0001c0001t0003g0205 a0001c0001t0003g0211 others(1): Show |
4 | HG00597.hp2 HG01891.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.696-1454G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30697933 | |||||||
| chr8:30697973 | T | A | 1 | a0004c0006t0006g0343 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.696-1494A>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30697973 | |||||||
| chr8:30698080 | A | G | 1 | a0001c0001t0003g0205 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.696-1601T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30698080 | |||||||
| chr8:30698081 | C | T | 6 | a0001c0001t0009g0017 a0001c0001t0009g0018 a0001c0001t0009g0019 others(3): Show |
6 | HG02723.hp2 HG02818.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.696-1602G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30698081 | |||||||
| chr8:30698098 | C | T | 2 | a0001c0001t0005g0208 a0001c0001t0007g0209 |
2 | HG02258.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.696-1619G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30698098 | |||||||
| chr8:30698224 | G | A | 1 | a0001c0003t0017g0009 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.696-1745C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30698224 | |||||||
| chr8:30698413 | G | A | 1 | a0001c0001t0006g0110 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.695+1668C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30698413 | |||||||
| chr8:30698416 | A | G | 1 | a0004c0006t0003g0344 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.695+1665T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30698416 | |||||||
| chr8:30698492 | G | A | 1 | a0001c0001t0004g0166 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.695+1589C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30698492 | |||||||
| chr8:30698576 | A | G | 8 | a0001c0001t0009g0017 a0001c0001t0009g0018 a0001c0001t0009g0019 others(5): Show |
8 | HG02486.hp2 HG02723.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.695+1505T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30698576 | |||||||
| chr8:30698638 | C | T | 1 | a0004c0006t0006g0343 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.695+1443G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30698638 | |||||||
| chr8:30698864 | T | TCC | 116 | a0001c0001t0001g0227 a0001c0001t0001g0230 a0001c0001t0001g0231 others(113): Show |
116 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.695+1215_695+1216d others(4): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30698864 | |||||||
| chr8:30698876 | C | T | 1 | a0001c0001t0021g0158 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.695+1205G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30698876 | |||||||
| chr8:30698884 | A | C | 8 | a0001c0001t0001g0223 a0001c0001t0004g0224 a0001c0001t0007g0217 others(5): Show |
8 | HG02280.hp2 HG02559.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.695+1197T>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30698884 | |||||||
| chr8:30699094 | T | C | 116 | a0001c0001t0001g0227 a0001c0001t0001g0230 a0001c0001t0001g0231 others(113): Show |
116 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.695+987A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30699094 | |||||||
| chr8:30699265 | T | C | 1 | a0001c0001t0003g0081 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.695+816A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30699265 | |||||||
| chr8:30699292 | A | T | 88 | a0001c0001t0001g0227 a0001c0001t0001g0230 a0001c0001t0001g0231 others(85): Show |
88 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.695+789T>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30699292 | |||||||
| chr8:30699312 | A | T | 14 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0038 others(11): Show |
14 | HG01243.hp2 HG01934.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.695+769T>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30699312 | |||||||
| chr8:30699361 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.695+720G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30699361 | |||||||
| chr8:30699448 | A | G | 2 | a0002c0002t0011g0321 a0002c0002t0012g0322 |
2 | HG01891.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.695+633T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 6/12 | chr8 | 30699448 | |||||||
| chr8:30700190 | T | C | 2 | a0001c0001t0003g0232 a0001c0001t0003g0314 |
2 | HG02559.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.641-55A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30700190 | |||||||
| chr8:30700454 | G | A | 1 | a0001c0001t0006g0186 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.641-319C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30700454 | |||||||
| chr8:30700481 | C | T | 1 | a0001c0001t0005g0282 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.641-346G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30700481 | |||||||
| chr8:30700530 | C | G | 2 | a0001c0001t0002g0124 a0001c0001t0002g0165 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.641-395G>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30700530 | |||||||
| chr8:30700648 | T | C | 1 | a0004c0006t0003g0342 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.641-513A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30700648 | |||||||
| chr8:30700722 | C | CAAAAAAA others(3): Show |
1 | a0001c0001t0004g0160 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.641-588_641-587ins others(10): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30700722 | |||||||
| chr8:30700722 | C | CAAAAAAA others(4): Show |
2 | a0001c0001t0001g0223 a0001c0001t0007g0221 |
2 | HG02559.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.641-588_641-587ins others(11): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30700722 | |||||||
| chr8:30700722 | C | CAAAAAAA others(5): Show |
6 | a0001c0001t0007g0059 a0001c0001t0007g0217 a0001c0001t0007g0219 others(3): Show |
6 | HG02280.hp2 HG03486.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.641-588_641-587ins others(12): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30700722 | |||||||
| chr8:30700723 | C | A | 11 | a0001c0001t0001g0223 a0001c0001t0004g0160 a0001c0001t0004g0224 others(8): Show |
11 | HG01891.hp1 HG02280.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.641-588G>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30700723 | |||||||
| chr8:30700723 | C | CAAAAAAA others(1): Show |
15 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0038 others(12): Show |
15 | HG01515.hp1 HG01934.hp2 HG02300.hp2 others(12): Show |
intron_variant | MODIFIER | c.641-596_641-589dup others(8): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30700723 | |||||||
| chr8:30700723 | C | CAAAAAAA others(2): Show |
14 | a0001c0001t0001g0039 a0001c0001t0002g0109 a0001c0001t0002g0117 others(11): Show |
14 | HG01074.hp2 HG01243.hp2 HG01358.hp2 others(11): Show |
intron_variant | MODIFIER | c.641-597_641-589dup others(9): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30700723 | |||||||
| chr8:30700723 | C | CAAAAAAA others(3): Show |
32 | a0001c0001t0001g0239 a0001c0001t0002g0123 a0001c0001t0004g0056 others(29): Show |
32 | HG00558.hp2 HG01074.hp1 HG01257.hp1 others(29): Show |
intron_variant | MODIFIER | c.641-598_641-589dup others(10): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30700723 | |||||||
| chr8:30700723 | C | CAAAAAAA others(4): Show |
38 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(35): Show |
39 | HG00597.hp1 HG00639.hp2 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.641-599_641-589dup others(11): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30700723 | |||||||
| chr8:30700723 | C | CAAAAAAA others(5): Show |
21 | a0001c0001t0002g0052 a0001c0001t0002g0091 a0001c0001t0002g0129 others(18): Show |
21 | HG00639.hp1 HG00642.hp1 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.641-600_641-589dup others(12): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30700723 | |||||||
| chr8:30700723 | C | CAAAAAAA others(6): Show |
8 | a0001c0001t0002g0049 a0001c0001t0002g0088 a0001c0001t0002g0096 others(5): Show |
8 | HG01261.hp2 HG01361.hp1 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.641-601_641-589dup others(13): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30700723 | |||||||
| chr8:30700723 | C | CAAAAAAA others(7): Show |
2 | a0001c0001t0003g0132 a0001c0001t0003g0179 |
2 | NA19011.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.641-602_641-589dup others(14): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30700723 | |||||||
| chr8:30700723 | C | CAAAAAAA others(12): Show |
1 | a0001c0001t0002g0084 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.641-607_641-589dup others(19): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30700723 | |||||||
| chr8:30700723 | C | CAAAAAAA others(17): Show |
1 | a0001c0001t0003g0248 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.641-612_641-589dup others(24): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30700723 | |||||||
| chr8:30700723 | CAAAA | C | 7 | a0001c0001t0002g0145 a0001c0001t0003g0035 a0001c0001t0003g0077 others(4): Show |
7 | HG00621.hp2 HG00673.hp1 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.641-592_641-589del others(4): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30700723 | |||||||
| chr8:30700723 | CAAAAA | C | 61 | a0001c0001t0001g0227 a0001c0001t0001g0269 a0001c0001t0002g0029 others(58): Show |
61 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.641-593_641-589del others(5): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30700723 | |||||||
| chr8:30700723 | CAAAAAA | C | 36 | a0001c0001t0001g0135 a0001c0001t0001g0230 a0001c0001t0001g0231 others(33): Show |
36 | HG00738.hp2 HG01243.hp1 HG01884.hp2 others(33): Show |
intron_variant | MODIFIER | c.641-594_641-589del others(6): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30700723 | |||||||
| chr8:30700723 | CAAAAAAA | C | 14 | a0001c0001t0001g0210 a0001c0001t0001g0292 a0001c0001t0001g0304 others(11): Show |
14 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(11): Show |
intron_variant | MODIFIER | c.641-595_641-589del others(7): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30700723 | |||||||
| chr8:30700723 | CAAAAAAA others(1): Show |
C | 61 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0095 others(58): Show |
62 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.641-596_641-589del others(8): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30700723 | |||||||
| chr8:30700723 | CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0004g0166 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.641-601_641-589del others(13): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30700723 | |||||||
| chr8:30701022 | C | G | 1 | a0001c0001t0001g0106 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.641-887G>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30701022 | |||||||
| chr8:30701114 | T | C | 1 | a0001c0001t0001g0285 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.641-979A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30701114 | |||||||
| chr8:30701334 | C | T | 1 | a0001c0001t0001g0264 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.641-1199G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30701334 | |||||||
| chr8:30701337 | A | G | 1 | a0001c0001t0001g0264 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.641-1202T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30701337 | |||||||
| chr8:30701370 | G | A | 21 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0005g0208 others(18): Show |
21 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.641-1235C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30701370 | |||||||
| chr8:30701488 | A | T | 1 | a0001c0001t0005g0203 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.641-1353T>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30701488 | |||||||
| chr8:30701571 | A | G | 1 | a0001c0001t0004g0112 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.641-1436T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30701571 | |||||||
| chr8:30701605 | C | T | 4 | a0001c0003t0005g0008 a0001c0003t0017g0009 a0001c0003t0017g0010 others(1): Show |
4 | HG02886.hp1 HG02886.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.641-1470G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30701605 | |||||||
| chr8:30701606 | G | A | 2 | a0001c0001t0003g0179 a0001c0001t0006g0110 |
2 | NA18992.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.641-1471C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30701606 | |||||||
| chr8:30701635 | C | CA | 119 | a0001c0001t0001g0113 a0001c0001t0001g0239 a0001c0001t0002g0001 others(116): Show |
120 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.640+1457dupT | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30701635 | |||||||
| chr8:30701717 | C | T | 36 | a0001c0001t0001g0218 a0001c0001t0001g0238 a0001c0001t0001g0250 others(33): Show |
36 | HG00140.hp2 HG00323.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.640+1376G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30701717 | |||||||
| chr8:30701718 | G | A | 4 | a0001c0001t0002g0133 a0001c0001t0002g0153 a0001c0001t0002g0200 others(1): Show |
4 | HG00639.hp1 HG01361.hp1 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.640+1375C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30701718 | |||||||
| chr8:30701749 | C | T | 2 | a0001c0001t0003g0065 a0001c0001t0003g0086 |
2 | HG02273.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.640+1344G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30701749 | |||||||
| chr8:30701794 | C | CA | 12 | a0001c0001t0003g0030 a0001c0001t0003g0035 a0001c0001t0003g0205 others(9): Show |
12 | HG01891.hp1 HG02145.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.640+1298dupT | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30701794 | |||||||
| chr8:30701794 | CA | C | 152 | a0001c0001t0001g0002 a0001c0001t0001g0036 a0001c0001t0001g0090 others(149): Show |
153 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.640+1298delT | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30701794 | |||||||
| chr8:30701794 | CAA | C | 155 | a0001c0001t0001g0033 a0001c0001t0001g0038 a0001c0001t0001g0039 others(152): Show |
156 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.640+1297_640+1298d others(4): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30701794 | |||||||
| chr8:30702010 | T | C | 1 | a0001c0001t0007g0134 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.640+1083A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30702010 | |||||||
| chr8:30702098 | C | T | 13 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0038 others(10): Show |
13 | HG01243.hp2 HG01934.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.640+995G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30702098 | |||||||
| chr8:30702522 | T | C | 1 | a0001c0001t0004g0192 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.640+571A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30702522 | |||||||
| chr8:30702632 | T | C | 1 | a0004c0006t0003g0344 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.640+461A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30702632 | |||||||
| chr8:30702671 | G | A | 48 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0038 others(45): Show |
48 | HG00140.hp2 HG00323.hp1 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.640+422C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 5/12 | chr8 | 30702671 | |||||||
| chr8:30703244 | A | C | 1 | a0004c0006t0003g0344 | 1 | NA19240.hp1 | splice_region_variant&intron_variant | LOW | c.493-4T>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30703244 | |||||||
| chr8:30703294 | T | C | 1 | a0001c0001t0004g0286 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.493-54A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30703294 | |||||||
| chr8:30703370 | C | T | 121 | a0001c0001t0001g0113 a0001c0001t0001g0239 a0001c0001t0002g0001 others(118): Show |
122 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.493-130G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30703370 | |||||||
| chr8:30703389 | G | C | 1 | a0001c0001t0004g0061 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.493-149C>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30703389 | |||||||
| chr8:30703502 | T | A | 1 | a0001c0001t0003g0030 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.493-262A>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30703502 | |||||||
| chr8:30703782 | C | G | 48 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0038 others(45): Show |
48 | HG00140.hp2 HG00323.hp1 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.493-542G>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30703782 | |||||||
| chr8:30703914 | G | C | 1 | a0004c0006t0006g0343 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.493-674C>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30703914 | |||||||
| chr8:30704008 | G | A | 2 | a0001c0001t0003g0248 a0001c0001t0005g0249 |
2 | HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.493-768C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30704008 | |||||||
| chr8:30704090 | C | T | 8 | a0001c0001t0001g0223 a0001c0001t0004g0224 a0001c0001t0007g0217 others(5): Show |
8 | HG02280.hp2 HG02559.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.493-850G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30704090 | |||||||
| chr8:30704228 | G | A | 1 | a0001c0001t0003g0215 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.493-988C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30704228 | |||||||
| chr8:30704444 | T | C | 3 | a0001c0001t0009g0019 a0001c0001t0009g0021 a0001c0001t0009g0022 |
3 | HG02818.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.493-1204A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30704444 | |||||||
| chr8:30704503 | C | T | 35 | a0001c0001t0001g0218 a0001c0001t0001g0238 a0001c0001t0001g0250 others(32): Show |
35 | HG00140.hp2 HG00323.hp1 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.493-1263G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30704503 | |||||||
| chr8:30704549 | T | C | 7 | a0001c0001t0009g0017 a0001c0001t0009g0018 a0001c0001t0009g0019 others(4): Show |
7 | HG02109.hp1 HG02723.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.493-1309A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30704549 | |||||||
| chr8:30704604 | C | T | 110 | a0001c0001t0001g0113 a0001c0001t0001g0239 a0001c0001t0002g0001 others(107): Show |
111 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.493-1364G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30704604 | |||||||
| chr8:30704721 | T | C | 1 | a0001c0001t0001g0293 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.493-1481A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30704721 | |||||||
| chr8:30704952 | A | G | 1 | a0001c0001t0011g0111 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.493-1712T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30704952 | |||||||
| chr8:30704959 | T | C | 1 | a0001c0001t0001g0293 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.493-1719A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30704959 | |||||||
| chr8:30705131 | TA | T | 35 | a0001c0001t0001g0218 a0001c0001t0001g0238 a0001c0001t0001g0250 others(32): Show |
35 | HG00140.hp2 HG00323.hp1 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.493-1892delT | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30705131 | |||||||
| chr8:30705262 | C | CA | 338 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0036 others(335): Show |
340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.493-2023dupT | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30705262 | |||||||
| chr8:30705270 | T | A | 38 | a0001c0001t0001g0033 a0001c0001t0001g0218 a0001c0001t0001g0238 others(35): Show |
38 | HG00140.hp2 HG00323.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.493-2030A>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30705270 | |||||||
| chr8:30705313 | A | G | 113 | a0001c0001t0001g0113 a0001c0001t0001g0135 a0001c0001t0001g0239 others(110): Show |
114 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.493-2073T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30705313 | |||||||
| chr8:30705319 | G | C | 1 | a0001c0001t0003g0026 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.493-2079C>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30705319 | |||||||
| chr8:30705372 | C | T | 2 | a0001c0001t0003g0248 a0001c0001t0005g0249 |
2 | HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.493-2132G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30705372 | |||||||
| chr8:30705437 | A | AT | 4 | a0001c0001t0005g0315 a0001c0001t0016g0212 a0001c0001t0016g0213 others(1): Show |
4 | HG02717.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.493-2198dupA | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30705437 | |||||||
| chr8:30705508 | C | T | 3 | a0001c0001t0008g0235 a0001c0001t0008g0236 a0001c0001t0008g0237 |
3 | HG02258.hp1 HG02647.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.493-2268G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30705508 | |||||||
| chr8:30705554 | G | T | 1 | a0001c0001t0002g0109 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.493-2314C>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30705554 | |||||||
| chr8:30705694 | T | G | 5 | a0001c0001t0004g0316 a0003c0005t0003g0005 a0003c0005t0004g0004 others(2): Show |
5 | HG00738.hp2 HG01243.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.492+2378A>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30705694 | |||||||
| chr8:30705750 | A | G | 3 | a0001c0001t0003g0216 a0001c0003t0003g0011 a0004c0006t0003g0342 |
3 | HG02451.hp1 HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.492+2322T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30705750 | |||||||
| chr8:30705925 | C | T | 171 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0038 others(168): Show |
172 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.492+2147G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30705925 | |||||||
| chr8:30706023 | G | A | 1 | a0001c0001t0001g0262 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.492+2049C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30706023 | |||||||
| chr8:30706174 | CA | C | 38 | a0001c0001t0001g0218 a0001c0001t0001g0238 a0001c0001t0001g0250 others(35): Show |
38 | HG00140.hp2 HG00323.hp1 HG01256.hp1 others(35): Show |
intron_variant | MODIFIER | c.492+1897delT | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30706174 | |||||||
| chr8:30706174 | CAA | C | 6 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0001g0312 others(3): Show |
6 | HG00738.hp1 HG02965.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.492+1896_492+1897d others(4): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30706174 | |||||||
| chr8:30706366 | G | C | 7 | a0001c0001t0009g0017 a0001c0001t0009g0018 a0001c0001t0009g0019 others(4): Show |
7 | HG02109.hp1 HG02723.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.492+1706C>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30706366 | |||||||
| chr8:30706383 | G | C | 5 | a0001c0001t0004g0316 a0003c0005t0003g0005 a0003c0005t0004g0004 others(2): Show |
5 | HG00738.hp2 HG01243.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.492+1689C>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30706383 | |||||||
| chr8:30706393 | C | T | 1 | a0001c0001t0003g0215 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.492+1679G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30706393 | |||||||
| chr8:30706395 | C | T | 3 | a0001c0001t0001g0308 a0001c0001t0001g0310 a0001c0001t0027g0309 |
3 | HG03834.hp2 HG04115.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.492+1677G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30706395 | |||||||
| chr8:30706508 | T | TAAAC | 14 | a0002c0002t0001g0335 a0002c0002t0002g0324 a0002c0002t0002g0325 others(11): Show |
14 | HG00621.hp2 HG01891.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.492+1560_492+1563d others(6): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30706508 | |||||||
| chr8:30706508 | TAAAC | T | 3 | a0001c0001t0003g0092 a0001c0001t0022g0100 a0001c0003t0002g0006 |
3 | HG00438.hp1 HG00733.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.492+1560_492+1563d others(6): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30706508 | |||||||
| chr8:30706537 | G | A | 1 | a0001c0001t0003g0147 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.492+1535C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30706537 | |||||||
| chr8:30706591 | G | A | 1 | a0001c0001t0009g0017 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.492+1481C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30706591 | |||||||
| chr8:30706874 | C | T | 1 | a0001c0001t0003g0226 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.492+1198G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30706874 | |||||||
| chr8:30706890 | A | G | 1 | a0001c0001t0003g0071 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.492+1182T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30706890 | |||||||
| chr8:30706954 | G | A | 2 | a0001c0001t0002g0244 a0001c0001t0002g0299 |
2 | HG00408.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.492+1118C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30706954 | |||||||
| chr8:30707219 | C | A | 1 | a0001c0001t0033g0034 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.492+853G>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30707219 | |||||||
| chr8:30707226 | A | G | 1 | a0001c0001t0033g0034 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.492+846T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30707226 | |||||||
| chr8:30707270 | G | A | 1 | a0001c0001t0004g0296 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.492+802C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30707270 | |||||||
| chr8:30707680 | T | C | 333 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0036 others(330): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.492+392A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30707680 | |||||||
| chr8:30707730 | A | G | 139 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0095 others(136): Show |
140 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.492+342T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30707730 | |||||||
| chr8:30707734 | C | A | 11 | a0001c0001t0001g0223 a0001c0001t0004g0224 a0001c0001t0005g0203 others(8): Show |
11 | HG02280.hp2 HG02559.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.492+338G>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30707734 | |||||||
| chr8:30707765 | G | A | 1 | a0001c0001t0004g0051 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.492+307C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30707765 | |||||||
| chr8:30708035 | C | T | 1 | a0001c0001t0002g0198 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.492+37G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 4/12 | chr8 | 30708035 | |||||||
| chr8:30708245 | T | C | 1 | a0001c0003t0017g0010 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.423-104A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 3/12 | chr8 | 30708245 | |||||||
| chr8:30708258 | C | T | 1 | a0001c0001t0001g0210 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.423-117G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 3/12 | chr8 | 30708258 | |||||||
| chr8:30708367 | A | G | 333 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0036 others(330): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.423-226T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 3/12 | chr8 | 30708367 | |||||||
| chr8:30708376 | C | T | 4 | a0003c0005t0003g0005 a0003c0005t0004g0004 a0003c0005t0006g0003 others(1): Show |
4 | HG00738.hp2 HG01243.hp1 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.423-235G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 3/12 | chr8 | 30708376 | |||||||
| chr8:30708377 | G | A | 35 | a0001c0001t0001g0218 a0001c0001t0001g0238 a0001c0001t0001g0250 others(32): Show |
35 | HG00140.hp2 HG00323.hp1 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.423-236C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 3/12 | chr8 | 30708377 | |||||||
| chr8:30708428 | C | T | 170 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0038 others(167): Show |
171 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.423-287G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 3/12 | chr8 | 30708428 | |||||||
| chr8:30708488 | A | G | 1 | a0001c0001t0004g0107 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.423-347T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 3/12 | chr8 | 30708488 | |||||||
| chr8:30708493 | T | C | 34 | a0001c0001t0001g0218 a0001c0001t0001g0238 a0001c0001t0001g0250 others(31): Show |
34 | HG00140.hp2 HG00323.hp1 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.423-352A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 3/12 | chr8 | 30708493 | |||||||
| chr8:30708646 | T | C | 1 | a0001c0001t0003g0030 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.423-505A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 3/12 | chr8 | 30708646 | |||||||
| chr8:30708691 | T | C | 6 | a0001c0001t0004g0070 a0001c0001t0004g0185 a0001c0001t0004g0188 others(3): Show |
6 | HG00558.hp2 HG00735.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.423-550A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 3/12 | chr8 | 30708691 | |||||||
| chr8:30708750 | A | C | 1 | a0001c0001t0001g0223 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.423-609T>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 3/12 | chr8 | 30708750 | |||||||
| chr8:30708760 | T | C | 4 | a0001c0003t0005g0008 a0001c0003t0017g0009 a0001c0003t0017g0010 others(1): Show |
4 | HG02886.hp1 HG02886.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.423-619A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 3/12 | chr8 | 30708760 | |||||||
| chr8:30708831 | T | C | 300 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0036 others(297): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.423-690A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 3/12 | chr8 | 30708831 | |||||||
| chr8:30708833 | C | A | 1 | a0001c0001t0023g0197 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.423-692G>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 3/12 | chr8 | 30708833 | |||||||
| chr8:30708958 | C | CA | 31 | a0001c0001t0001g0033 a0001c0001t0001g0038 a0001c0001t0001g0039 others(28): Show |
31 | HG00621.hp2 HG00735.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.423-818dupT | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 3/12 | chr8 | 30708958 | |||||||
| chr8:30709192 | T | C | 38 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0106 others(35): Show |
39 | HG00099.hp1 HG00280.hp2 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.422+622A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 3/12 | chr8 | 30709192 | |||||||
| chr8:30709222 | A | G | 1 | a0001c0001t0003g0184 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.422+592T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 3/12 | chr8 | 30709222 | |||||||
| chr8:30709225 | C | T | 42 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0106 others(39): Show |
43 | HG00099.hp1 HG00280.hp2 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.422+589G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 3/12 | chr8 | 30709225 | |||||||
| chr8:30709269 | G | A | 41 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0218 others(38): Show |
42 | HG00099.hp1 HG00733.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.422+545C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 3/12 | chr8 | 30709269 | |||||||
| chr8:30709269 | G | T | 30 | a0001c0001t0001g0210 a0001c0001t0001g0230 a0001c0001t0001g0231 others(27): Show |
30 | HG00621.hp2 HG01884.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.422+545C>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 3/12 | chr8 | 30709269 | |||||||
| chr8:30709271 | G | A | 1 | a0001c0001t0003g0099 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.422+543C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 3/12 | chr8 | 30709271 | |||||||
| chr8:30709331 | C | T | 1 | a0001c0001t0001g0218 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.422+483G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 3/12 | chr8 | 30709331 | |||||||
| chr8:30709612 | T | A | 5 | a0001c0001t0004g0076 a0001c0001t0004g0148 a0001c0001t0004g0149 others(2): Show |
5 | HG01257.hp2 HG01258.hp2 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.422+202A>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 3/12 | chr8 | 30709612 | |||||||
| chr8:30709632 | G | A | 4 | a0001c0001t0001g0218 a0001c0001t0003g0215 a0001c0004t0001g0339 others(1): Show |
4 | HG02257.hp2 HG02818.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.422+182C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 3/12 | chr8 | 30709632 | |||||||
| chr8:30709700 | G | A | 2 | a0001c0001t0002g0001 a0001c0001t0002g0104 |
3 | HG00639.hp2 HG01169.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.422+114C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 3/12 | chr8 | 30709700 | |||||||
| chr8:30709762 | A | C | 1 | a0001c0001t0004g0076 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.422+52T>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 3/12 | chr8 | 30709762 | |||||||
| chr8:30709905 | G | GT | 6 | a0001c0001t0004g0316 a0003c0005t0003g0005 a0003c0005t0004g0004 others(3): Show |
6 | HG00738.hp2 HG01243.hp1 HG02145.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.334-4dupA | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30709905 | |||||||
| chr8:30709906 | T | TA | 13 | a0001c0001t0001g0255 a0001c0001t0003g0035 a0001c0001t0003g0078 others(10): Show |
13 | HG00099.hp1 HG00544.hp1 HG00621.hp2 others(10): Show |
splice_region_variant&intron_variant | LOW | c.334-5dupT | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30709906 | |||||||
| chr8:30709906 | TA | T | 13 | a0001c0001t0001g0218 a0001c0001t0001g0245 a0001c0001t0001g0272 others(10): Show |
13 | HG00323.hp1 HG01975.hp2 HG02257.hp2 others(10): Show |
splice_region_variant&intron_variant | LOW | c.334-5delT | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30709906 | |||||||
| chr8:30709907 | A | T | 3 | a0001c0003t0017g0009 a0001c0003t0017g0010 a0001c0003t0029g0007 |
3 | HG02886.hp1 HG02886.hp2 HG03225.hp2 |
splice_region_variant&intron_variant | LOW | c.334-5T>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30709907 | |||||||
| chr8:30709908 | A | T | 1 | a0001c0003t0005g0008 | 1 | NA18522.hp2 | splice_region_variant&intron_variant | LOW | c.334-6T>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30709908 | |||||||
| chr8:30710011 | C | T | 8 | a0001c0001t0005g0278 a0001c0001t0005g0279 a0001c0001t0005g0281 others(5): Show |
8 | HG02280.hp1 HG02572.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.334-109G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30710011 | |||||||
| chr8:30710013 | C | T | 1 | a0001c0001t0002g0088 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.334-111G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30710013 | |||||||
| chr8:30710044 | G | A | 1 | a0001c0001t0005g0203 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.334-142C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30710044 | |||||||
| chr8:30710535 | G | A | 3 | a0001c0001t0006g0167 a0001c0001t0012g0168 a0001c0001t0012g0169 |
3 | HG02055.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.334-633C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30710535 | |||||||
| chr8:30710541 | A | C | 11 | a0001c0001t0003g0248 a0001c0001t0005g0249 a0001c0001t0005g0278 others(8): Show |
11 | HG02280.hp1 HG02572.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.334-639T>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30710541 | |||||||
| chr8:30710687 | G | A | 1 | a0001c0001t0014g0032 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.334-785C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30710687 | |||||||
| chr8:30710714 | C | CA | 6 | a0001c0001t0001g0218 a0001c0001t0005g0249 a0001c0001t0005g0278 others(3): Show |
6 | HG02280.hp1 HG02723.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.334-813dupT | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30710714 | |||||||
| chr8:30710714 | C | CAA | 6 | a0001c0001t0005g0282 a0001c0001t0005g0283 a0001c0001t0005g0284 others(3): Show |
6 | HG02572.hp2 HG02809.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.334-814_334-813dup others(2): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30710714 | |||||||
| chr8:30710714 | CA | C | 12 | a0001c0001t0003g0035 a0001c0001t0003g0205 a0001c0001t0003g0211 others(9): Show |
12 | HG02145.hp2 HG02257.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.334-813delT | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30710714 | |||||||
| chr8:30710714 | CAA | C | 9 | a0001c0001t0003g0030 a0001c0001t0004g0316 a0001c0001t0005g0203 others(6): Show |
9 | HG00738.hp2 HG01243.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.334-814_334-813del others(2): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30710714 | |||||||
| chr8:30710714 | CAAA | C | 32 | a0001c0001t0001g0095 a0001c0001t0002g0029 a0001c0001t0002g0049 others(29): Show |
32 | HG00408.hp2 HG00544.hp1 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.334-815_334-813del others(3): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30710714 | |||||||
| chr8:30710714 | CAAAA | C | 158 | a0001c0001t0001g0106 a0001c0001t0001g0113 a0001c0001t0001g0135 others(155): Show |
159 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.334-816_334-813del others(4): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30710714 | |||||||
| chr8:30710714 | CAAAAA | C | 39 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0038 others(36): Show |
39 | HG00140.hp2 HG00323.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.334-817_334-813del others(5): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30710714 | |||||||
| chr8:30710714 | CAAAAAAA others(4): Show |
C | 7 | a0001c0001t0004g0224 a0001c0001t0007g0217 a0001c0001t0007g0219 others(4): Show |
7 | HG02280.hp2 HG02559.hp1 HG03486.hp2 others(4): Show |
intron_variant | MODIFIER | c.334-823_334-813del others(11): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30710714 | |||||||
| chr8:30710714 | CAAAAAAA others(10): Show |
C | 1 | a0001c0001t0006g0167 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.334-829_334-813del others(17): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30710714 | |||||||
| chr8:30710714 | CAAAAAAA others(13): Show |
C | 67 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0210 others(64): Show |
68 | HG00099.hp1 HG00621.hp2 HG00733.hp2 others(65): Show |
intron_variant | MODIFIER | c.334-832_334-813del others(20): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30710714 | |||||||
| chr8:30710741 | A | G | 1 | a0001c0001t0013g0303 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.334-839T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30710741 | |||||||
| chr8:30710757 | AAAG | A | 32 | a0001c0001t0001g0002 a0001c0001t0001g0234 a0001c0001t0001g0239 others(29): Show |
33 | HG00099.hp1 HG00733.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.334-858_334-856del others(3): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30710757 | |||||||
| chr8:30710758 | AAG | A | 32 | a0001c0001t0001g0090 a0001c0001t0001g0210 a0001c0001t0001g0230 others(29): Show |
32 | HG00621.hp2 HG01884.hp2 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.334-858_334-857del others(2): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30710758 | |||||||
| chr8:30710764 | A | T | 23 | a0001c0001t0001g0090 a0001c0001t0001g0210 a0001c0001t0001g0230 others(20): Show |
23 | HG00733.hp2 HG01099.hp2 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.334-862T>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30710764 | |||||||
| chr8:30710766 | A | T | 54 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0210 others(51): Show |
55 | HG00099.hp1 HG00621.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.334-864T>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30710766 | |||||||
| chr8:30710768 | A | AT | 5 | a0001c0001t0001g0218 a0001c0001t0003g0215 a0001c0001t0003g0216 others(2): Show |
5 | HG02257.hp2 HG02818.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.334-867_334-866ins others(1): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30710768 | |||||||
| chr8:30710768 | A | T | 263 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0095 others(260): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.334-866T>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30710768 | |||||||
| chr8:30710844 | C | T | 2 | a0001c0003t0003g0011 a0004c0006t0003g0342 |
2 | HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.334-942G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30710844 | |||||||
| chr8:30711117 | A | G | 1 | a0001c0001t0004g0079 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.333+945T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30711117 | |||||||
| chr8:30711118 | C | G | 200 | a0001c0001t0001g0095 a0001c0001t0001g0106 a0001c0001t0001g0113 others(197): Show |
201 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.333+944G>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30711118 | |||||||
| chr8:30711120 | G | A | 2 | a0001c0003t0003g0011 a0004c0006t0003g0342 |
2 | HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.333+942C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30711120 | |||||||
| chr8:30711125 | G | A | 2 | a0001c0001t0003g0077 a0001c0001t0003g0078 |
2 | HG00544.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.333+937C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30711125 | |||||||
| chr8:30711173 | G | A | 1 | a0001c0001t0010g0181 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.333+889C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30711173 | |||||||
| chr8:30711252 | G | A | 40 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0038 others(37): Show |
40 | HG00140.hp2 HG00323.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.333+810C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30711252 | |||||||
| chr8:30711498 | T | A | 2 | a0001c0003t0003g0011 a0004c0006t0003g0342 |
2 | HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.333+564A>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30711498 | |||||||
| chr8:30711525 | C | T | 1 | a0001c0001t0001g0223 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.333+537G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30711525 | |||||||
| chr8:30711594 | G | A | 2 | a0001c0003t0003g0011 a0004c0006t0003g0342 |
2 | HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.333+468C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30711594 | |||||||
| chr8:30711621 | C | T | 2 | a0001c0001t0003g0232 a0001c0001t0003g0314 |
2 | HG02559.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.333+441G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30711621 | |||||||
| chr8:30711649 | C | T | 1 | a0001c0004t0031g0330 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.333+413G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30711649 | |||||||
| chr8:30711650 | G | A | 2 | a0001c0003t0003g0011 a0004c0006t0003g0342 |
2 | HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.333+412C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30711650 | |||||||
| chr8:30711653 | G | A | 40 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0038 others(37): Show |
40 | HG00140.hp2 HG00323.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.333+409C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30711653 | |||||||
| chr8:30711733 | T | C | 1 | a0001c0001t0007g0225 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.333+329A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 2/12 | chr8 | 30711733 | |||||||
| chr8:30712135 | C | T | 5 | a0001c0001t0001g0218 a0001c0001t0003g0215 a0001c0001t0003g0216 others(2): Show |
5 | HG02257.hp2 HG02818.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.307-47G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30712135 | |||||||
| chr8:30712309 | C | T | 5 | a0001c0001t0001g0218 a0001c0001t0003g0215 a0001c0001t0003g0216 others(2): Show |
5 | HG02257.hp2 HG02818.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.307-221G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30712309 | |||||||
| chr8:30712310 | G | A | 195 | a0001c0001t0001g0095 a0001c0001t0001g0106 a0001c0001t0001g0113 others(192): Show |
196 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.307-222C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30712310 | |||||||
| chr8:30712350 | G | A | 1 | a0001c0001t0022g0100 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.307-262C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30712350 | |||||||
| chr8:30712501 | G | A | 2 | a0001c0001t0002g0101 a0001c0001t0021g0158 |
2 | HG01884.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.307-413C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30712501 | |||||||
| chr8:30712509 | G | A | 1 | a0001c0001t0004g0094 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.307-421C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30712509 | |||||||
| chr8:30712553 | G | A | 42 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0038 others(39): Show |
42 | HG00140.hp2 HG00323.hp1 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.307-465C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30712553 | |||||||
| chr8:30712607 | AAGGCTGC others(11): Show |
A | 1 | a0001c0004t0005g0328 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.307-537_307-520del others(18): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30712607 | |||||||
| chr8:30712640 | A | G | 2 | a0001c0001t0012g0168 a0001c0001t0012g0169 |
2 | HG02055.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.307-552T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30712640 | |||||||
| chr8:30712706 | G | A | 1 | a0001c0001t0003g0030 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.307-618C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30712706 | |||||||
| chr8:30712766 | C | T | 1 | a0001c0001t0002g0049 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.307-678G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30712766 | |||||||
| chr8:30712768 | T | C | 1 | a0001c0001t0004g0188 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.307-680A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30712768 | |||||||
| chr8:30712832 | T | G | 200 | a0001c0001t0001g0095 a0001c0001t0001g0106 a0001c0001t0001g0113 others(197): Show |
201 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.307-744A>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30712832 | |||||||
| chr8:30713065 | C | T | 1 | a0001c0001t0004g0160 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.307-977G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30713065 | |||||||
| chr8:30713225 | T | TG | 10 | a0001c0001t0004g0316 a0001c0003t0005g0008 a0001c0003t0017g0009 others(7): Show |
10 | HG00738.hp2 HG01243.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.307-1138dupC | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30713225 | |||||||
| chr8:30713256 | C | T | 2 | a0001c0001t0002g0001 a0001c0001t0002g0104 |
3 | HG00639.hp2 HG01169.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.307-1168G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30713256 | |||||||
| chr8:30713286 | C | T | 5 | a0001c0001t0001g0218 a0001c0001t0003g0215 a0001c0001t0003g0216 others(2): Show |
5 | HG02257.hp2 HG02818.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.307-1198G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30713286 | |||||||
| chr8:30713389 | C | T | 194 | a0001c0001t0001g0095 a0001c0001t0001g0106 a0001c0001t0001g0113 others(191): Show |
195 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.307-1301G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30713389 | |||||||
| chr8:30713435 | T | C | 2 | a0001c0001t0004g0160 a0001c0001t0007g0059 |
2 | NA18964.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.307-1347A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30713435 | |||||||
| chr8:30713585 | A | T | 6 | a0001c0001t0004g0054 a0001c0001t0004g0060 a0001c0001t0004g0061 others(3): Show |
6 | HG01952.hp1 HG02155.hp1 HG02273.hp1 others(3): Show |
intron_variant | MODIFIER | c.307-1497T>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30713585 | |||||||
| chr8:30713658 | C | T | 1 | a0001c0001t0001g0266 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.307-1570G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30713658 | |||||||
| chr8:30713985 | A | C | 13 | a0001c0001t0001g0210 a0001c0001t0001g0230 a0001c0001t0001g0231 others(10): Show |
13 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.307-1897T>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30713985 | |||||||
| chr8:30714180 | C | T | 2 | a0002c0002t0002g0331 a0002c0002t0002g0333 |
2 | HG02738.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.307-2092G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30714180 | |||||||
| chr8:30714202 | C | CT | 21 | a0001c0001t0001g0036 a0001c0001t0001g0251 a0001c0001t0003g0035 others(18): Show |
21 | HG01891.hp1 HG01891.hp2 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.307-2115dupA | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30714202 | |||||||
| chr8:30714202 | CT | C | 98 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0095 others(95): Show |
99 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.307-2115delA | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30714202 | |||||||
| chr8:30714202 | CTT | C | 164 | a0001c0001t0001g0106 a0001c0001t0001g0113 a0001c0001t0001g0135 others(161): Show |
165 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.307-2116_307-2115d others(4): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30714202 | |||||||
| chr8:30714294 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.307-2206G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30714294 | |||||||
| chr8:30714395 | C | T | 3 | a0001c0001t0004g0053 a0001c0001t0004g0093 a0001c0001t0004g0094 |
3 | HG00642.hp1 HG01099.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.307-2307G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30714395 | |||||||
| chr8:30714446 | C | T | 176 | a0001c0001t0001g0095 a0001c0001t0001g0106 a0001c0001t0001g0113 others(173): Show |
177 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.307-2358G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30714446 | |||||||
| chr8:30714488 | A | G | 1 | a0001c0001t0003g0232 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.307-2400T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30714488 | |||||||
| chr8:30714504 | C | T | 1 | a0001c0001t0003g0202 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.307-2416G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30714504 | |||||||
| chr8:30714509 | T | A | 3 | a0001c0001t0001g0250 a0001c0001t0001g0294 a0001c0001t0001g0295 |
3 | HG01934.hp1 HG01975.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.307-2421A>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30714509 | |||||||
| chr8:30714668 | C | A | 4 | a0001c0001t0005g0315 a0001c0001t0016g0212 a0001c0001t0016g0213 others(1): Show |
4 | HG02717.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.307-2580G>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30714668 | |||||||
| chr8:30714695 | T | A | 1 | a0001c0001t0004g0224 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.307-2607A>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30714695 | |||||||
| chr8:30714738 | G | A | 2 | a0001c0004t0031g0330 a0006c0008t0024g0204 |
2 | HG02809.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.307-2650C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30714738 | |||||||
| chr8:30714824 | C | T | 1 | a0001c0003t0029g0007 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.307-2736G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30714824 | |||||||
| chr8:30714973 | T | A | 3 | a0001c0001t0003g0205 a0001c0001t0003g0211 a0001c0003t0003g0012 |
3 | HG01891.hp1 HG02615.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.307-2885A>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30714973 | |||||||
| chr8:30715013 | C | T | 2 | a0001c0001t0003g0083 a0001c0001t0003g0092 |
2 | HG00733.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.307-2925G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30715013 | |||||||
| chr8:30715027 | A | G | 43 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0038 others(40): Show |
43 | HG00140.hp2 HG00323.hp1 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.307-2939T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30715027 | |||||||
| chr8:30715061 | T | C | 195 | a0001c0001t0001g0095 a0001c0001t0001g0106 a0001c0001t0001g0113 others(192): Show |
196 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.307-2973A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30715061 | |||||||
| chr8:30715198 | C | T | 41 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0038 others(38): Show |
41 | HG00140.hp2 HG00323.hp1 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.307-3110G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30715198 | |||||||
| chr8:30715392 | G | A | 2 | a0001c0001t0002g0161 a0001c0001t0003g0162 |
2 | HG02015.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.307-3304C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30715392 | |||||||
| chr8:30715572 | C | T | 1 | a0001c0001t0003g0314 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.307-3484G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30715572 | |||||||
| chr8:30715574 | T | G | 1 | a0001c0001t0002g0029 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.307-3486A>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30715574 | |||||||
| chr8:30715583 | G | A | 6 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0005g0315 others(3): Show |
6 | HG01884.hp2 HG02109.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.307-3495C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30715583 | |||||||
| chr8:30715632 | C | G | 1 | a0001c0001t0002g0091 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.307-3544G>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30715632 | |||||||
| chr8:30715825 | T | C | 5 | a0001c0003t0005g0008 a0001c0003t0017g0009 a0001c0003t0017g0010 others(2): Show |
5 | HG02886.hp1 HG02886.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.307-3737A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30715825 | |||||||
| chr8:30715890 | T | A | 282 | a0001c0001t0001g0002 a0001c0001t0001g0095 a0001c0001t0001g0106 others(279): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.307-3802A>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30715890 | |||||||
| chr8:30715960 | G | A | 29 | a0001c0001t0001g0238 a0001c0001t0001g0250 a0001c0001t0001g0251 others(26): Show |
29 | HG00140.hp2 HG00323.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.307-3872C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30715960 | |||||||
| chr8:30715961 | C | A | 1 | a0001c0001t0004g0201 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.307-3873G>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30715961 | |||||||
| chr8:30715967 | T | A | 1 | a0001c0001t0003g0081 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.307-3879A>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30715967 | |||||||
| chr8:30716230 | C | A | 48 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0038 others(45): Show |
48 | HG00140.hp2 HG00323.hp1 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.307-4142G>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30716230 | |||||||
| chr8:30716491 | C | A | 10 | a0001c0001t0003g0248 a0001c0001t0005g0249 a0001c0001t0005g0278 others(7): Show |
10 | HG02280.hp1 HG02572.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.307-4403G>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30716491 | |||||||
| chr8:30716668 | T | G | 319 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0036 others(316): Show |
321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.307-4580A>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30716668 | |||||||
| chr8:30716744 | C | G | 1 | a0001c0001t0005g0278 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.307-4656G>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30716744 | |||||||
| chr8:30716806 | C | A | 1 | a0004c0006t0008g0345 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.307-4718G>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30716806 | |||||||
| chr8:30716814 | A | C | 1 | a0001c0001t0003g0226 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.307-4726T>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30716814 | |||||||
| chr8:30716819 | T | C | 1 | a0001c0001t0005g0203 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.307-4731A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30716819 | |||||||
| chr8:30716914 | C | A | 2 | a0001c0001t0012g0168 a0001c0001t0012g0169 |
2 | HG02055.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.307-4826G>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30716914 | |||||||
| chr8:30716916 | A | C | 1 | a0001c0001t0005g0203 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.307-4828T>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30716916 | |||||||
| chr8:30716952 | C | T | 1 | a0001c0001t0001g0263 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.307-4864G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30716952 | |||||||
| chr8:30716973 | T | C | 3 | a0001c0001t0005g0203 a0001c0004t0031g0330 a0006c0008t0024g0204 |
3 | HG02630.hp2 HG02809.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.307-4885A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30716973 | |||||||
| chr8:30717042 | A | G | 1 | a0001c0001t0003g0030 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.307-4954T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30717042 | |||||||
| chr8:30717119 | C | A | 1 | a0001c0001t0004g0072 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.307-5031G>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30717119 | |||||||
| chr8:30717152 | G | A | 25 | a0001c0001t0001g0218 a0001c0001t0003g0215 a0001c0001t0003g0216 others(22): Show |
25 | HG00621.hp2 HG01891.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.307-5064C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30717152 | |||||||
| chr8:30717232 | T | C | 207 | a0001c0001t0001g0095 a0001c0001t0001g0106 a0001c0001t0001g0113 others(204): Show |
208 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.307-5144A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30717232 | |||||||
| chr8:30717249 | G | GAAACAAA others(5): Show |
3 | a0001c0001t0002g0164 a0001c0001t0002g0165 a0001c0001t0002g0172 |
3 | HG01071.hp2 HG01169.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.307-5173_307-5162d others(14): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30717249 | |||||||
| chr8:30717369 | G | A | 1 | a0001c0001t0004g0166 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.307-5281C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30717369 | |||||||
| chr8:30717423 | G | C | 244 | a0001c0001t0001g0095 a0001c0001t0001g0106 a0001c0001t0001g0113 others(241): Show |
245 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.307-5335C>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30717423 | |||||||
| chr8:30717468 | G | A | 36 | a0001c0001t0001g0002 a0001c0001t0001g0234 a0001c0001t0001g0239 others(33): Show |
37 | HG00099.hp1 HG00733.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.307-5380C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30717468 | |||||||
| chr8:30717499 | T | C | 3 | a0001c0001t0006g0167 a0001c0001t0012g0168 a0001c0001t0012g0169 |
3 | HG02055.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.307-5411A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30717499 | |||||||
| chr8:30717543 | T | C | 242 | a0001c0001t0001g0002 a0001c0001t0001g0095 a0001c0001t0001g0106 others(239): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.307-5455A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30717543 | |||||||
| chr8:30717762 | CA | C | 32 | a0001c0001t0001g0218 a0001c0001t0003g0215 a0001c0001t0003g0216 others(29): Show |
32 | HG00621.hp2 HG00738.hp2 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.307-5675delT | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30717762 | |||||||
| chr8:30717827 | G | A | 4 | a0001c0003t0005g0008 a0001c0003t0017g0009 a0001c0003t0017g0010 others(1): Show |
4 | HG02886.hp1 HG02886.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.307-5739C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30717827 | |||||||
| chr8:30717866 | C | T | 242 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0095 others(239): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.307-5778G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30717866 | |||||||
| chr8:30717872 | G | A | 3 | a0001c0004t0001g0332 a0002c0002t0002g0337 a0002c0002t0015g0338 |
3 | HG02895.hp1 NA18906.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.307-5784C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30717872 | |||||||
| chr8:30717892 | G | A | 3 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0170 |
3 | HG00099.hp2 HG01071.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.307-5804C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30717892 | |||||||
| chr8:30717909 | G | C | 6 | a0001c0001t0001g0218 a0001c0001t0003g0215 a0001c0001t0003g0216 others(3): Show |
6 | HG02055.hp2 HG02257.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.307-5821C>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30717909 | |||||||
| chr8:30717930 | G | T | 3 | a0001c0001t0002g0052 a0001c0001t0002g0088 a0001c0001t0002g0089 |
3 | HG01261.hp2 HG02602.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.307-5842C>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30717930 | |||||||
| chr8:30718089 | G | T | 7 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(4): Show |
7 | HG00733.hp2 HG01099.hp2 HG01123.hp1 others(4): Show |
intron_variant | MODIFIER | c.307-6001C>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30718089 | |||||||
| chr8:30718111 | A | AAAAT | 221 | a0001c0001t0001g0090 a0001c0001t0001g0095 a0001c0001t0001g0106 others(218): Show |
222 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.307-6027_307-6024d others(6): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30718111 | |||||||
| chr8:30718111 | A | AAAATAAA others(1): Show |
24 | a0001c0001t0001g0002 a0001c0001t0001g0223 a0001c0001t0001g0240 others(21): Show |
25 | HG00099.hp1 HG00735.hp1 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.307-6031_307-6024d others(10): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30718111 | |||||||
| chr8:30718111 | A | AAAATAAA others(5): Show |
1 | a0001c0001t0002g0252 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.307-6035_307-6024d others(14): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30718111 | |||||||
| chr8:30718282 | T | C | 278 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0095 others(275): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.307-6194A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30718282 | |||||||
| chr8:30718321 | T | C | 36 | a0001c0001t0001g0002 a0001c0001t0001g0234 a0001c0001t0001g0239 others(33): Show |
37 | HG00099.hp1 HG00733.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.307-6233A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30718321 | |||||||
| chr8:30718357 | G | C | 206 | a0001c0001t0001g0090 a0001c0001t0001g0095 a0001c0001t0001g0106 others(203): Show |
207 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.307-6269C>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30718357 | |||||||
| chr8:30718489 | C | T | 1 | a0001c0001t0002g0252 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.307-6401G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30718489 | |||||||
| chr8:30718696 | C | G | 234 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0095 others(231): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.307-6608G>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30718696 | |||||||
| chr8:30718775 | A | T | 4 | a0001c0003t0005g0008 a0001c0003t0017g0009 a0001c0003t0017g0010 others(1): Show |
4 | HG02886.hp1 HG02886.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.307-6687T>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30718775 | |||||||
| chr8:30718891 | C | T | 1 | a0001c0001t0010g0180 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.307-6803G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30718891 | |||||||
| chr8:30718920 | GT | G | 241 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0095 others(238): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.307-6833delA | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30718920 | |||||||
| chr8:30718926 | T | G | 234 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0095 others(231): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.307-6838A>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30718926 | |||||||
| chr8:30718999 | G | A | 2 | a0001c0001t0014g0031 a0001c0001t0014g0032 |
2 | HG02486.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.307-6911C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30718999 | |||||||
| chr8:30719104 | AT | A | 302 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0036 others(299): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.307-7017delA | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30719104 | |||||||
| chr8:30719104 | ATT | A | 10 | a0001c0001t0001g0247 a0001c0001t0001g0251 a0001c0001t0009g0017 others(7): Show |
10 | HG02109.hp1 HG02723.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.307-7018_307-7017d others(4): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30719104 | |||||||
| chr8:30719164 | T | A | 19 | a0001c0004t0001g0332 a0001c0004t0003g0323 a0002c0002t0001g0335 others(16): Show |
19 | HG00621.hp2 HG01891.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.307-7076A>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30719164 | |||||||
| chr8:30719249 | G | C | 2 | a0001c0004t0031g0330 a0006c0008t0024g0204 |
2 | HG02809.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.307-7161C>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30719249 | |||||||
| chr8:30719273 | AAT | A | 233 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0095 others(230): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.307-7187_307-7186d others(4): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30719273 | |||||||
| chr8:30719287 | T | A | 234 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0095 others(231): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.307-7199A>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30719287 | |||||||
| chr8:30719309 | A | T | 1 | a0001c0001t0002g0082 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.307-7221T>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30719309 | |||||||
| chr8:30719318 | G | A | 230 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0095 others(227): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.307-7230C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30719318 | |||||||
| chr8:30719512 | A | G | 2 | a0001c0001t0014g0031 a0001c0001t0014g0032 |
2 | HG02486.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.307-7424T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30719512 | |||||||
| chr8:30719572 | T | C | 235 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0095 others(232): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.307-7484A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30719572 | |||||||
| chr8:30719679 | C | T | 232 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0095 others(229): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.307-7591G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30719679 | |||||||
| chr8:30719683 | G | T | 2 | a0001c0001t0005g0208 a0001c0001t0007g0209 |
2 | HG02258.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.307-7595C>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30719683 | |||||||
| chr8:30719712 | T | C | 1 | a0001c0001t0033g0034 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.307-7624A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30719712 | |||||||
| chr8:30719884 | A | G | 1 | a0001c0001t0004g0190 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.306+7646T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30719884 | |||||||
| chr8:30719928 | G | C | 282 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0095 others(279): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.306+7602C>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30719928 | |||||||
| chr8:30719950 | G | A | 233 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0095 others(230): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.306+7580C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30719950 | |||||||
| chr8:30720087 | G | A | 1 | a0001c0001t0004g0296 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.306+7443C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30720087 | |||||||
| chr8:30720171 | C | T | 1 | a0001c0001t0005g0203 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.306+7359G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30720171 | |||||||
| chr8:30720357 | G | C | 3 | a0001c0001t0005g0203 a0001c0004t0031g0330 a0006c0008t0024g0204 |
3 | HG02630.hp2 HG02809.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.306+7173C>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30720357 | |||||||
| chr8:30720389 | T | C | 233 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0095 others(230): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.306+7141A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30720389 | |||||||
| chr8:30720477 | A | G | 1 | a0001c0001t0001g0218 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.306+7053T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30720477 | |||||||
| chr8:30720657 | A | G | 282 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0095 others(279): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.306+6873T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30720657 | |||||||
| chr8:30720671 | G | GAA | 229 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0095 others(226): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.306+6857_306+6858d others(4): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30720671 | |||||||
| chr8:30720765 | A | G | 41 | a0001c0001t0001g0218 a0001c0001t0001g0223 a0001c0001t0003g0215 others(38): Show |
41 | HG00621.hp2 HG00738.hp2 HG01243.hp1 others(38): Show |
intron_variant | MODIFIER | c.306+6765T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30720765 | |||||||
| chr8:30720856 | CACAGGT | C | 233 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0095 others(230): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.306+6668_306+6673d others(8): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30720856 | |||||||
| chr8:30720863 | G | C | 233 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0095 others(230): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.306+6667C>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30720863 | |||||||
| chr8:30720934 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.306+6596C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30720934 | |||||||
| chr8:30720939 | C | T | 1 | a0001c0001t0003g0202 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.306+6591G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30720939 | |||||||
| chr8:30720949 | C | A | 1 | a0004c0006t0006g0343 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.306+6581G>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30720949 | |||||||
| chr8:30720967 | C | T | 233 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0095 others(230): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.306+6563G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30720967 | |||||||
| chr8:30720969 | G | A | 46 | a0001c0001t0001g0218 a0001c0001t0001g0223 a0001c0001t0003g0215 others(43): Show |
46 | HG00621.hp2 HG00738.hp2 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.306+6561C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30720969 | |||||||
| chr8:30721012 | T | C | 233 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0095 others(230): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.306+6518A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30721012 | |||||||
| chr8:30721064 | C | A | 233 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0095 others(230): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.306+6466G>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30721064 | |||||||
| chr8:30721087 | C | A | 39 | a0001c0001t0001g0002 a0001c0001t0001g0234 a0001c0001t0001g0240 others(36): Show |
40 | HG00099.hp1 HG00408.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.306+6443G>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30721087 | |||||||
| chr8:30721128 | T | C | 1 | a0001c0001t0002g0172 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.306+6402A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30721128 | |||||||
| chr8:30721134 | C | CTCTG | 233 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0095 others(230): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.306+6395_306+6396i others(6): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30721134 | |||||||
| chr8:30721143 | G | A | 1 | a0005c0007t0002g0173 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.306+6387C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30721143 | |||||||
| chr8:30721151 | GAAGA | G | 233 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0095 others(230): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.306+6375_306+6378d others(6): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30721151 | |||||||
| chr8:30721213 | C | A | 1 | a0001c0001t0003g0202 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.306+6317G>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30721213 | |||||||
| chr8:30721421 | T | C | 233 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0095 others(230): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.306+6109A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30721421 | |||||||
| chr8:30721426 | G | A | 3 | a0001c0001t0003g0205 a0001c0001t0003g0211 a0001c0003t0003g0012 |
3 | HG01891.hp1 HG02615.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.306+6104C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30721426 | |||||||
| chr8:30721451 | G | C | 226 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0095 others(223): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.306+6079C>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30721451 | |||||||
| chr8:30721480 | G | T | 7 | a0001c0001t0009g0017 a0001c0001t0009g0018 a0001c0001t0009g0019 others(4): Show |
7 | HG02109.hp1 HG02723.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.306+6050C>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30721480 | |||||||
| chr8:30721522 | G | A | 1 | a0001c0001t0003g0174 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.306+6008C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30721522 | |||||||
| chr8:30721577 | T | C | 280 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0095 others(277): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.306+5953A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30721577 | |||||||
| chr8:30721658 | GA | G | 232 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0095 others(229): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.306+5871delT | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30721658 | |||||||
| chr8:30721693 | T | A | 1 | a0004c0006t0003g0344 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.306+5837A>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30721693 | |||||||
| chr8:30721717 | T | C | 2 | a0001c0003t0003g0011 a0004c0006t0003g0342 |
2 | HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.306+5813A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30721717 | |||||||
| chr8:30721768 | C | T | 173 | a0001c0001t0001g0090 a0001c0001t0001g0095 a0001c0001t0001g0106 others(170): Show |
174 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.306+5762G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30721768 | |||||||
| chr8:30721800 | C | T | 1 | a0002c0002t0011g0321 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.306+5730G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30721800 | |||||||
| chr8:30721850 | G | A | 233 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0095 others(230): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.306+5680C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30721850 | |||||||
| chr8:30721875 | G | A | 1 | a0001c0001t0001g0297 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.306+5655C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30721875 | |||||||
| chr8:30721887 | C | T | 7 | a0001c0001t0009g0017 a0001c0001t0009g0018 a0001c0001t0009g0019 others(4): Show |
7 | HG02109.hp1 HG02723.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.306+5643G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30721887 | |||||||
| chr8:30721939 | C | A | 233 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0095 others(230): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.306+5591G>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30721939 | |||||||
| chr8:30721953 | T | C | 1 | a0001c0001t0003g0216 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.306+5577A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30721953 | |||||||
| chr8:30721982 | T | C | 233 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0095 others(230): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.306+5548A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30721982 | |||||||
| chr8:30722007 | C | A | 1 | a0001c0001t0008g0042 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.306+5523G>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30722007 | |||||||
| chr8:30722013 | C | CA | 12 | a0001c0001t0002g0175 a0001c0001t0002g0176 a0001c0001t0003g0215 others(9): Show |
12 | HG02074.hp1 HG02257.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.306+5516dupT | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30722013 | |||||||
| chr8:30722231 | G | T | 47 | a0001c0001t0001g0218 a0001c0001t0001g0223 a0001c0001t0003g0215 others(44): Show |
47 | HG00621.hp2 HG00738.hp2 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.306+5299C>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30722231 | |||||||
| chr8:30722236 | C | T | 233 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0095 others(230): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.306+5294G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30722236 | |||||||
| chr8:30722454 | G | A | 4 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0003g0013 others(1): Show |
4 | HG00438.hp2 HG00597.hp1 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.306+5076C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30722454 | |||||||
| chr8:30722518 | G | GAGTTCGA others(7): Show |
231 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0095 others(228): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.306+4998_306+5011d others(16): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30722518 | |||||||
| chr8:30722523 | C | CGAGACCA others(7): Show |
2 | a0001c0001t0003g0077 a0001c0001t0003g0078 |
2 | HG00544.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.306+5006_306+5007i others(16): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30722523 | |||||||
| chr8:30722589 | A | T | 233 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0095 others(230): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.306+4941T>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30722589 | |||||||
| chr8:30722596 | T | C | 1 | a0001c0001t0003g0229 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.306+4934A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30722596 | |||||||
| chr8:30722630 | G | A | 233 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0095 others(230): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.306+4900C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30722630 | |||||||
| chr8:30722691 | C | T | 1 | a0001c0001t0004g0076 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.306+4839G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30722691 | |||||||
| chr8:30722692 | C | T | 47 | a0001c0001t0001g0218 a0001c0001t0001g0223 a0001c0001t0003g0215 others(44): Show |
47 | HG00621.hp2 HG00738.hp2 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.306+4838G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30722692 | |||||||
| chr8:30722696 | C | A | 233 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0095 others(230): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.306+4834G>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30722696 | |||||||
| chr8:30722731 | C | CAA | 7 | a0001c0001t0009g0018 a0001c0001t0009g0019 a0001c0001t0009g0020 others(4): Show |
7 | HG02109.hp1 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.306+4797_306+4798d others(4): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30722731 | |||||||
| chr8:30722731 | CA | C | 94 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0038 others(91): Show |
94 | HG00140.hp2 HG00323.hp1 HG00738.hp1 others(91): Show |
intron_variant | MODIFIER | c.306+4798delT | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30722731 | |||||||
| chr8:30722731 | CAA | C | 8 | a0001c0004t0003g0323 a0002c0002t0002g0324 a0002c0002t0002g0325 others(5): Show |
8 | HG01891.hp2 HG02257.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.306+4797_306+4798d others(4): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30722731 | |||||||
| chr8:30722731 | CAAAAAAA others(1): Show |
C | 223 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0095 others(220): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.306+4791_306+4798d others(10): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30722731 | |||||||
| chr8:30722777 | C | T | 233 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0095 others(230): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.306+4753G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30722777 | |||||||
| chr8:30722814 | T | A | 7 | a0001c0001t0009g0017 a0001c0001t0009g0018 a0001c0001t0009g0019 others(4): Show |
7 | HG02109.hp1 HG02723.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.306+4716A>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30722814 | |||||||
| chr8:30722833 | T | C | 2 | a0001c0003t0003g0011 a0004c0006t0003g0342 |
2 | HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.306+4697A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30722833 | |||||||
| chr8:30722998 | T | A | 2 | a0001c0001t0005g0203 a0006c0008t0024g0204 |
2 | HG02630.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.306+4532A>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30722998 | |||||||
| chr8:30723060 | G | A | 226 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0095 others(223): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.306+4470C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30723060 | |||||||
| chr8:30723067 | G | A | 226 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0095 others(223): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.306+4463C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30723067 | |||||||
| chr8:30723092 | C | T | 2 | a0001c0001t0010g0180 a0001c0001t0010g0181 |
2 | HG00558.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.306+4438G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30723092 | |||||||
| chr8:30723190 | G | A | 233 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0095 others(230): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.306+4340C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30723190 | |||||||
| chr8:30723309 | T | C | 2 | a0001c0001t0010g0180 a0001c0001t0010g0181 |
2 | HG00558.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.306+4221A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30723309 | |||||||
| chr8:30723363 | C | G | 20 | a0001c0004t0001g0332 a0001c0004t0003g0323 a0001c0004t0031g0330 others(17): Show |
20 | HG00621.hp2 HG01891.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.306+4167G>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30723363 | |||||||
| chr8:30723384 | C | T | 1 | a0001c0001t0003g0013 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.306+4146G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30723384 | |||||||
| chr8:30723385 | G | A | 1 | a0001c0001t0004g0182 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.306+4145C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30723385 | |||||||
| chr8:30723518 | C | T | 1 | a0001c0001t0004g0193 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.306+4012G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30723518 | |||||||
| chr8:30723556 | T | C | 233 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0095 others(230): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.306+3974A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30723556 | |||||||
| chr8:30723575 | T | G | 1 | a0001c0001t0006g0183 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.306+3955A>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30723575 | |||||||
| chr8:30723578 | G | T | 7 | a0001c0001t0009g0017 a0001c0001t0009g0018 a0001c0001t0009g0019 others(4): Show |
7 | HG02109.hp1 HG02723.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.306+3952C>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30723578 | |||||||
| chr8:30723588 | C | T | 4 | a0001c0001t0004g0047 a0001c0001t0007g0048 a0001c0001t0007g0074 others(1): Show |
4 | NA18944.hp1 NA19063.hp1 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.306+3942G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30723588 | |||||||
| chr8:30723608 | T | C | 1 | a0001c0001t0003g0184 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.306+3922A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30723608 | |||||||
| chr8:30723643 | T | A | 233 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0095 others(230): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.306+3887A>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30723643 | |||||||
| chr8:30723783 | A | AAC | 5 | a0001c0001t0001g0285 a0001c0001t0005g0207 a0001c0001t0010g0206 others(2): Show |
5 | HG02486.hp2 HG02572.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.306+3745_306+3746d others(4): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30723783 | |||||||
| chr8:30723783 | AAC | A | 50 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0001g0039 others(47): Show |
50 | HG00140.hp2 HG00323.hp1 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.306+3745_306+3746d others(4): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30723783 | |||||||
| chr8:30723783 | AACAC | A | 41 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0003g0215 others(38): Show |
41 | HG00621.hp2 HG00738.hp2 HG01243.hp1 others(38): Show |
intron_variant | MODIFIER | c.306+3743_306+3746d others(6): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30723783 | |||||||
| chr8:30723783 | AACACACA others(1): Show |
A | 41 | a0001c0001t0001g0002 a0001c0001t0001g0234 a0001c0001t0001g0239 others(38): Show |
42 | HG00099.hp1 HG00408.hp1 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.306+3739_306+3746d others(10): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30723783 | |||||||
| chr8:30723783 | AACACACA others(3): Show |
A | 192 | a0001c0001t0001g0090 a0001c0001t0001g0095 a0001c0001t0001g0106 others(189): Show |
193 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.306+3737_306+3746d others(12): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30723783 | |||||||
| chr8:30723818 | A | C | 220 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0095 others(217): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.306+3712T>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30723818 | |||||||
| chr8:30723826 | C | T | 5 | a0001c0003t0002g0006 a0001c0003t0005g0008 a0001c0003t0017g0009 others(2): Show |
5 | HG02486.hp1 HG02886.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.306+3704G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30723826 | |||||||
| chr8:30723841 | A | G | 1 | a0001c0001t0004g0072 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.306+3689T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30723841 | |||||||
| chr8:30723883 | C | T | 3 | a0001c0001t0003g0071 a0001c0001t0003g0189 a0001c0009t0002g0027 |
3 | NA18964.hp1 NA18988.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.306+3647G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30723883 | |||||||
| chr8:30723984 | C | A | 47 | a0001c0001t0001g0218 a0001c0001t0001g0223 a0001c0001t0003g0215 others(44): Show |
47 | HG00621.hp2 HG00738.hp2 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.306+3546G>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30723984 | |||||||
| chr8:30724078 | A | G | 47 | a0001c0001t0001g0218 a0001c0001t0001g0223 a0001c0001t0003g0215 others(44): Show |
47 | HG00621.hp2 HG00738.hp2 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.306+3452T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30724078 | |||||||
| chr8:30724261 | C | T | 47 | a0001c0001t0001g0218 a0001c0001t0001g0223 a0001c0001t0003g0215 others(44): Show |
47 | HG00621.hp2 HG00738.hp2 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.306+3269G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30724261 | |||||||
| chr8:30724311 | C | G | 1 | a0001c0004t0031g0330 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.306+3219G>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30724311 | |||||||
| chr8:30724338 | A | G | 302 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0095 others(299): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.306+3192T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30724338 | |||||||
| chr8:30724544 | C | CT | 41 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0038 others(38): Show |
41 | HG01243.hp2 HG01884.hp2 HG01891.hp1 others(38): Show |
intron_variant | MODIFIER | c.306+2985dupA | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30724544 | |||||||
| chr8:30724544 | C | CTT | 80 | a0001c0001t0001g0002 a0001c0001t0001g0223 a0001c0001t0001g0234 others(77): Show |
81 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.306+2984_306+2985d others(4): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30724544 | |||||||
| chr8:30724544 | C | CTTT | 190 | a0001c0001t0001g0090 a0001c0001t0001g0095 a0001c0001t0001g0106 others(187): Show |
191 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.306+2983_306+2985d others(5): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30724544 | |||||||
| chr8:30724544 | C | CTTTT | 31 | a0001c0001t0002g0049 a0001c0001t0002g0052 a0001c0001t0002g0057 others(28): Show |
31 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(28): Show |
intron_variant | MODIFIER | c.306+2982_306+2985d others(6): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30724544 | |||||||
| chr8:30724694 | C | T | 2 | a0001c0001t0002g0045 a0001c0001t0002g0046 |
2 | NA18944.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.306+2836G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30724694 | |||||||
| chr8:30724724 | C | T | 255 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0095 others(252): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.306+2806G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30724724 | |||||||
| chr8:30724787 | T | C | 309 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0095 others(306): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.306+2743A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30724787 | |||||||
| chr8:30724788 | G | T | 7 | a0001c0001t0009g0017 a0001c0001t0009g0018 a0001c0001t0009g0019 others(4): Show |
7 | HG02109.hp1 HG02723.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.306+2742C>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30724788 | |||||||
| chr8:30724794 | C | T | 1 | a0004c0006t0006g0343 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.306+2736G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30724794 | |||||||
| chr8:30724834 | T | A | 255 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0095 others(252): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.306+2696A>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30724834 | |||||||
| chr8:30724885 | A | C | 7 | a0001c0001t0009g0017 a0001c0001t0009g0018 a0001c0001t0009g0019 others(4): Show |
7 | HG02109.hp1 HG02723.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.306+2645T>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30724885 | |||||||
| chr8:30725015 | T | G | 3 | a0001c0001t0004g0193 a0001c0001t0004g0194 a0001c0001t0010g0195 |
3 | NA18977.hp2 NA18983.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.306+2515A>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30725015 | |||||||
| chr8:30725106 | T | G | 54 | a0001c0001t0001g0218 a0001c0001t0001g0223 a0001c0001t0003g0215 others(51): Show |
54 | HG00621.hp2 HG00738.hp2 HG01243.hp1 others(51): Show |
intron_variant | MODIFIER | c.306+2424A>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30725106 | |||||||
| chr8:30725137 | C | T | 47 | a0001c0001t0001g0218 a0001c0001t0001g0223 a0001c0001t0003g0215 others(44): Show |
47 | HG00621.hp2 HG00738.hp2 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.306+2393G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30725137 | |||||||
| chr8:30725307 | C | T | 2 | a0001c0001t0003g0215 a0001c0001t0003g0216 |
2 | HG02257.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.306+2223G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30725307 | |||||||
| chr8:30725311 | C | T | 1 | a0001c0001t0003g0030 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.306+2219G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30725311 | |||||||
| chr8:30725351 | T | G | 174 | a0001c0001t0001g0090 a0001c0001t0001g0095 a0001c0001t0001g0106 others(171): Show |
175 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.306+2179A>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30725351 | |||||||
| chr8:30725375 | G | A | 20 | a0001c0004t0001g0332 a0001c0004t0003g0323 a0001c0004t0031g0330 others(17): Show |
20 | HG00621.hp2 HG01891.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.306+2155C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30725375 | |||||||
| chr8:30725410 | A | G | 1 | a0001c0001t0001g0239 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.306+2120T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30725410 | |||||||
| chr8:30725414 | G | A | 54 | a0001c0001t0001g0218 a0001c0001t0001g0223 a0001c0001t0003g0215 others(51): Show |
54 | HG00621.hp2 HG00738.hp2 HG01243.hp1 others(51): Show |
intron_variant | MODIFIER | c.306+2116C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30725414 | |||||||
| chr8:30725491 | C | T | 54 | a0001c0001t0001g0218 a0001c0001t0001g0223 a0001c0001t0003g0215 others(51): Show |
54 | HG00621.hp2 HG00738.hp2 HG01243.hp1 others(51): Show |
intron_variant | MODIFIER | c.306+2039G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30725491 | |||||||
| chr8:30725519 | C | T | 1 | a0001c0001t0001g0238 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.306+2011G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30725519 | |||||||
| chr8:30725559 | C | T | 8 | a0001c0004t0003g0323 a0002c0002t0002g0324 a0002c0002t0002g0325 others(5): Show |
8 | HG01891.hp2 HG02257.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.306+1971G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30725559 | |||||||
| chr8:30725580 | C | A | 54 | a0001c0001t0001g0218 a0001c0001t0001g0223 a0001c0001t0003g0215 others(51): Show |
54 | HG00621.hp2 HG00738.hp2 HG01243.hp1 others(51): Show |
intron_variant | MODIFIER | c.306+1950G>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30725580 | |||||||
| chr8:30725881 | C | CA | 30 | a0001c0001t0001g0304 a0001c0001t0001g0306 a0001c0001t0001g0308 others(27): Show |
30 | HG00140.hp2 HG00323.hp1 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.306+1648dupT | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30725881 | |||||||
| chr8:30725881 | C | CAA | 39 | a0001c0001t0001g0218 a0001c0001t0001g0223 a0001c0001t0001g0313 others(36): Show |
39 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(36): Show |
intron_variant | MODIFIER | c.306+1647_306+1648d others(4): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30725881 | |||||||
| chr8:30725881 | C | CAAA | 7 | a0001c0001t0007g0225 a0001c0003t0002g0006 a0001c0003t0003g0011 others(4): Show |
7 | HG00621.hp2 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.306+1646_306+1648d others(5): Show |
GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30725881 | |||||||
| chr8:30725881 | CA | C | 7 | a0001c0001t0001g0234 a0001c0001t0002g0023 a0001c0001t0002g0029 others(4): Show |
7 | HG00408.hp2 HG01515.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.306+1648delT | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30725881 | |||||||
| chr8:30725888 | A | C | 1 | a0001c0009t0002g0027 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.306+1642T>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30725888 | |||||||
| chr8:30725918 | G | C | 1 | a0001c0001t0005g0203 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.306+1612C>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30725918 | |||||||
| chr8:30726064 | C | T | 45 | a0001c0001t0001g0218 a0001c0001t0001g0223 a0001c0001t0004g0224 others(42): Show |
45 | HG00621.hp2 HG00738.hp2 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.306+1466G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30726064 | |||||||
| chr8:30726186 | C | A | 1 | a0001c0001t0005g0203 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.306+1344G>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30726186 | |||||||
| chr8:30726197 | A | G | 51 | a0001c0001t0001g0218 a0001c0001t0001g0223 a0001c0001t0004g0224 others(48): Show |
51 | HG00621.hp2 HG00738.hp2 HG01243.hp1 others(48): Show |
intron_variant | MODIFIER | c.306+1333T>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30726197 | |||||||
| chr8:30726249 | G | A | 45 | a0001c0001t0001g0218 a0001c0001t0001g0223 a0001c0001t0004g0224 others(42): Show |
45 | HG00621.hp2 HG00738.hp2 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.306+1281C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30726249 | |||||||
| chr8:30726292 | G | T | 6 | a0001c0001t0009g0017 a0001c0001t0009g0018 a0001c0001t0009g0019 others(3): Show |
6 | HG02723.hp2 HG02818.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.306+1238C>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30726292 | |||||||
| chr8:30726387 | C | T | 4 | a0001c0001t0002g0023 a0001c0001t0003g0024 a0001c0001t0003g0025 others(1): Show |
4 | HG01071.hp1 HG01081.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.306+1143G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30726387 | |||||||
| chr8:30726429 | T | C | 1 | a0006c0008t0024g0204 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.306+1101A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30726429 | |||||||
| chr8:30726471 | T | C | 15 | a0001c0001t0001g0210 a0001c0001t0001g0230 a0001c0001t0001g0231 others(12): Show |
15 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.306+1059A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30726471 | |||||||
| chr8:30726547 | C | T | 6 | a0001c0001t0009g0017 a0001c0001t0009g0018 a0001c0001t0009g0019 others(3): Show |
6 | HG02723.hp2 HG02818.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.306+983G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30726547 | |||||||
| chr8:30726554 | G | T | 45 | a0001c0001t0001g0218 a0001c0001t0001g0223 a0001c0001t0004g0224 others(42): Show |
45 | HG00621.hp2 HG01891.hp2 HG02055.hp2 others(42): Show |
intron_variant | MODIFIER | c.306+976C>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30726554 | |||||||
| chr8:30726601 | A | C | 1 | a0002c0010t0002g0016 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.306+929T>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30726601 | |||||||
| chr8:30726632 | G | A | 9 | a0001c0001t0001g0218 a0001c0001t0001g0223 a0001c0001t0004g0224 others(6): Show |
9 | HG02280.hp2 HG02559.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.306+898C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30726632 | |||||||
| chr8:30726661 | C | A | 1 | a0001c0003t0002g0006 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.306+869G>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30726661 | |||||||
| chr8:30726713 | G | C | 4 | a0001c0001t0001g0227 a0001c0001t0002g0228 a0001c0001t0003g0226 others(1): Show |
4 | HG02074.hp1 HG02155.hp2 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.306+817C>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30726713 | |||||||
| chr8:30726991 | A | C | 1 | a0001c0003t0002g0006 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.306+539T>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30726991 | |||||||
| chr8:30727137 | T | C | 36 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0003t0002g0006 others(33): Show |
36 | HG00621.hp2 HG01884.hp2 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.306+393A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30727137 | |||||||
| chr8:30727237 | C | T | 3 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0003g0013 |
3 | HG00438.hp2 HG00597.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.306+293G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30727237 | |||||||
| chr8:30727300 | C | T | 1 | a0001c0001t0003g0232 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.306+230G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30727300 | |||||||
| chr8:30727301 | C | A | 1 | a0001c0001t0003g0232 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.306+229G>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30727301 | |||||||
| chr8:30727332 | G | C | 2 | a0001c0001t0003g0233 a0003c0005t0003g0005 |
2 | HG00738.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.306+198C>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30727332 | |||||||
| chr8:30727362 | T | C | 7 | a0001c0001t0003g0314 a0001c0001t0004g0316 a0001c0001t0005g0315 others(4): Show |
7 | HG00738.hp2 HG01243.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.306+168A>G | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30727362 | |||||||
| chr8:30727365 | C | T | 34 | a0001c0003t0002g0006 a0001c0003t0003g0011 a0001c0003t0003g0012 others(31): Show |
34 | HG00621.hp2 HG01891.hp1 HG01891.hp2 others(31): Show |
intron_variant | MODIFIER | c.306+165G>A | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30727365 | |||||||
| chr8:30727406 | G | A | 90 | a0001c0001t0001g0002 a0001c0001t0001g0234 a0001c0001t0001g0238 others(87): Show |
91 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.306+124C>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30727406 | |||||||
| chr8:30727427 | C | G | 34 | a0001c0003t0002g0006 a0001c0003t0003g0011 a0001c0003t0003g0012 others(31): Show |
34 | HG00621.hp2 HG01891.hp1 HG01891.hp2 others(31): Show |
intron_variant | MODIFIER | c.306+103G>C | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30727427 | |||||||
| chr8:30727483 | C | A | 2 | a0001c0001t0004g0317 a0001c0001t0004g0318 |
2 | NA18966.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.306+47G>T | GSR | ENSG00000104687.14 | transcript | ENST00000221130.11 | protein_coding | 1/12 | chr8 | 30727483 |