Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 51768 |
| ensemblid | ENSG00000064115.11 |
| hgncid | 23049 |
| symbol | TM7SF3 |
| name | transmembrane 7 superfamily member 3 |
| refseq_nuc | NM_016551.3 |
| refseq_prot | NP_057635.1 |
| ensembl_nuc | ENST00000343028.9 |
| ensembl_prot | ENSP00000342322.4 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 26971579 |
| end | 27014384 |
| strand | - |
| ver | v1.2 |
| region | chr12:26971579-27014384 |
| region5000 | chr12:26966579-27019384 |
| regionname0 | TM7SF3_chr12_26971579_27014384 |
| regionname5000 | TM7SF3_chr12_26966579_27019384 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 570 | 381 | 73 | 64 | 181 | 16 | 45 | 142 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | MGFLQ others(565): Show |
chr12 | 26966579 | 27019384 |
| a0002 | 0/0 | 570 | 31 | 2 | 7 | 22 | 0 | 0 | 19 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | MGFLQ others(565): Show |
chr12 | 26966579 | 27019384 |
| a0003 | 0/0 | 570 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | MGFLQ others(565): Show |
chr12 | 26966579 | 27019384 |
| a0004 | 0/0 | 570 | 3 | 0 | 1 | 0 | 0 | 2 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | MGFLQ others(565): Show |
chr12 | 26966579 | 27019384 |
| a0005 | 0/0 | 570 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | MGFLQ others(565): Show |
chr12 | 26966579 | 27019384 |
| a0006 | 0/0 | 570 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | MGFLQ others(565): Show |
chr12 | 26966579 | 27019384 |
| a0007 | 0/0 | 570 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | MGFLQ others(565): Show |
chr12 | 26966579 | 27019384 |
| a0008 | 0/0 | 570 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | MGFLQ others(565): Show |
chr12 | 26966579 | 27019384 |
| a0009 | 0/0 | 570 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | MGFLQ others(565): Show |
chr12 | 26966579 | 27019384 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1710 | 379 | 73 | 64 | 179 | 16 | 45 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | ATGGG others(1705): Show |
chr12 | 26966579 | 27019384 | ||
| a0001c0005 | 0/0 | 1710 | 2 | 0 | 0 | 2 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | ATGGG others(1705): Show |
chr12 | 26966579 | 27019384 | ||
| a0002c0002 | 0/0 | 1710 | 31 | 2 | 7 | 22 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | ATGGG others(1705): Show |
chr12 | 26966579 | 27019384 | ||
| a0003c0003 | 0/0 | 1710 | 9 | 9 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | ATGGG others(1705): Show |
chr12 | 26966579 | 27019384 | ||
| a0004c0004 | 0/0 | 1710 | 3 | 0 | 1 | 0 | 0 | 2 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | ATGGG others(1705): Show |
chr12 | 26966579 | 27019384 | ||
| a0005c0006 | 0/0 | 1710 | 2 | 2 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | ATGGG others(1705): Show |
chr12 | 26966579 | 27019384 | ||
| a0006c0007 | 0/0 | 1710 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | ATGGG others(1705): Show |
chr12 | 26966579 | 27019384 | ||
| a0007c0010 | 0/0 | 1710 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | ATGGG others(1705): Show |
chr12 | 26966579 | 27019384 | ||
| a0008c0008 | 0/0 | 1710 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | ATGGG others(1705): Show |
chr12 | 26966579 | 27019384 | ||
| a0009c0009 | 0/0 | 1710 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | ATGGG others(1705): Show |
chr12 | 26966579 | 27019384 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4315 | 113 | 24 | 10 | 61 | 3 | 15 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | AGGTG others(4310): Show |
chr12 | 26966579 | 27019384 |
| a0001c0001t0002 | 0/0 | 4316 | 57 | 4 | 20 | 23 | 2 | 8 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | AGGTG others(4311): Show |
chr12 | 26966579 | 27019384 |
| a0001c0001t0003 | 0/0 | 4316 | 50 | 6 | 2 | 36 | 1 | 5 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | AGGTG others(4311): Show |
chr12 | 26966579 | 27019384 |
| a0001c0001t0004 | 0/0 | 4312 | 46 | 4 | 7 | 30 | 3 | 2 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | AGGTG others(4307): Show |
chr12 | 26966579 | 27019384 |
| a0001c0001t0005 | 0/0 | 4316 | 12 | 0 | 1 | 11 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | AGGTG others(4311): Show |
chr12 | 26966579 | 27019384 |
| a0001c0001t0006 | 0/0 | 4316 | 31 | 6 | 12 | 2 | 3 | 8 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | AGGTG others(4311): Show |
chr12 | 26966579 | 27019384 |
| a0001c0001t0007 | 0/1 | 4316 | 14 | 5 | 4 | 0 | 2 | 2 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | AGGTG others(4311): Show |
chr12 | 26966579 | 27019384 |
| a0001c0001t0008 | 1/0 | 4315 | 11 | 3 | 5 | 0 | 0 | 2 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | AGGTG others(4310): Show |
chr12 | 26966579 | 27019384 |
| a0001c0001t0010 | 0/0 | 4315 | 4 | 1 | 2 | 0 | 1 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | AGGTG others(4310): Show |
chr12 | 26966579 | 27019384 |
| a0001c0001t0011 | 0/0 | 4314 | 5 | 0 | 0 | 5 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | AGGTG others(4309): Show |
chr12 | 26966579 | 27019384 |
| a0001c0001t0013 | 0/0 | 4315 | 4 | 4 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | AGGTG others(4310): Show |
chr12 | 26966579 | 27019384 |
| a0001c0001t0014 | 0/0 | 4316 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | AGGTG others(4311): Show |
chr12 | 26966579 | 27019384 |
| a0001c0001t0015 | 0/0 | 4315 | 3 | 3 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | AGGTG others(4310): Show |
chr12 | 26966579 | 27019384 |
| a0001c0001t0016 | 0/0 | 4315 | 2 | 1 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | AGGTG others(4310): Show |
chr12 | 26966579 | 27019384 |
| a0001c0001t0017 | 0/0 | 4314 | 3 | 1 | 0 | 2 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | AGGTG others(4309): Show |
chr12 | 26966579 | 27019384 |
| a0001c0001t0018 | 0/0 | 4316 | 3 | 3 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | AGGTG others(4311): Show |
chr12 | 26966579 | 27019384 |
| a0001c0001t0019 | 0/0 | 4315 | 2 | 0 | 0 | 2 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | AGGTG others(4310): Show |
chr12 | 26966579 | 27019384 |
| a0001c0001t0020 | 0/0 | 4315 | 2 | 2 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | AGGTG others(4310): Show |
chr12 | 26966579 | 27019384 |
| a0001c0001t0024 | 0/0 | 4316 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | AGGTG others(4311): Show |
chr12 | 26966579 | 27019384 |
| a0001c0001t0025 | 0/0 | 4317 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | AGGTG others(4312): Show |
chr12 | 26966579 | 27019384 |
| a0001c0001t0026 | 0/0 | 4316 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | AGGTG others(4311): Show |
chr12 | 26966579 | 27019384 |
| a0001c0001t0027 | 0/0 | 4316 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | AGGTG others(4311): Show |
chr12 | 26966579 | 27019384 |
| a0001c0001t0028 | 0/0 | 4315 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | AGGTG others(4310): Show |
chr12 | 26966579 | 27019384 |
| a0001c0001t0029 | 0/0 | 4315 | 1 | 0 | 0 | 0 | 1 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | AGGTG others(4310): Show |
chr12 | 26966579 | 27019384 |
| a0001c0001t0030 | 0/0 | 4316 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | AGGTG others(4311): Show |
chr12 | 26966579 | 27019384 |
| a0001c0001t0031 | 0/0 | 4317 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | AGGTG others(4312): Show |
chr12 | 26966579 | 27019384 |
| a0001c0001t0032 | 0/0 | 4313 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | AGGTG others(4308): Show |
chr12 | 26966579 | 27019384 |
| a0001c0001t0033 | 0/0 | 4317 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | AGGTG others(4312): Show |
chr12 | 26966579 | 27019384 |
| a0001c0001t0034 | 0/0 | 4312 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | AGGTG others(4307): Show |
chr12 | 26966579 | 27019384 |
| a0001c0001t0035 | 0/0 | 4312 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | AGGTG others(4307): Show |
chr12 | 26966579 | 27019384 |
| a0001c0001t0037 | 0/0 | 4311 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | AGGTG others(4306): Show |
chr12 | 26966579 | 27019384 |
| a0001c0001t0038 | 0/0 | 4312 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | AGGTG others(4307): Show |
chr12 | 26966579 | 27019384 |
| a0001c0001t0039 | 0/0 | 4316 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | AGGTG others(4311): Show |
chr12 | 26966579 | 27019384 |
| a0001c0001t0040 | 0/0 | 4315 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | AGGTG others(4310): Show |
chr12 | 26966579 | 27019384 |
| a0001c0005t0005 | 0/0 | 4316 | 2 | 0 | 0 | 2 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | AGGTG others(4311): Show |
chr12 | 26966579 | 27019384 |
| a0002c0002t0001 | 0/0 | 4315 | 3 | 0 | 0 | 3 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | AGGTG others(4310): Show |
chr12 | 26966579 | 27019384 |
| a0002c0002t0004 | 0/0 | 4312 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | AGGTG others(4307): Show |
chr12 | 26966579 | 27019384 |
| a0002c0002t0005 | 0/0 | 4316 | 18 | 0 | 7 | 11 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | AGGTG others(4311): Show |
chr12 | 26966579 | 27019384 |
| a0002c0002t0012 | 0/0 | 4317 | 4 | 0 | 0 | 4 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | AGGTG others(4312): Show |
chr12 | 26966579 | 27019384 |
| a0002c0002t0014 | 0/0 | 4316 | 2 | 2 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | AGGTG others(4311): Show |
chr12 | 26966579 | 27019384 |
| a0002c0002t0021 | 0/0 | 4316 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | AGGTG others(4311): Show |
chr12 | 26966579 | 27019384 |
| a0002c0002t0022 | 0/0 | 4315 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | AGGTG others(4310): Show |
chr12 | 26966579 | 27019384 |
| a0002c0002t0023 | 0/0 | 4316 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | AGGTG others(4311): Show |
chr12 | 26966579 | 27019384 |
| a0003c0003t0009 | 0/0 | 4316 | 9 | 9 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | AGGTG others(4311): Show |
chr12 | 26966579 | 27019384 |
| a0004c0004t0010 | 0/0 | 4315 | 2 | 0 | 0 | 0 | 0 | 2 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | AGGTG others(4310): Show |
chr12 | 26966579 | 27019384 |
| a0004c0004t0016 | 0/0 | 4315 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | AGGTG others(4310): Show |
chr12 | 26966579 | 27019384 |
| a0005c0006t0004 | 0/0 | 4312 | 2 | 2 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | AGGTG others(4307): Show |
chr12 | 26966579 | 27019384 |
| a0006c0007t0004 | 0/0 | 4312 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | AGGTG others(4307): Show |
chr12 | 26966579 | 27019384 |
| a0007c0010t0003 | 0/0 | 4316 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | AGGTG others(4311): Show |
chr12 | 26966579 | 27019384 |
| a0008c0008t0036 | 0/0 | 4315 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | AGGTG others(4310): Show |
chr12 | 26966579 | 27019384 |
| a0009c0009t0001 | 0/0 | 4315 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | AGGTG others(4310): Show |
chr12 | 26966579 | 27019384 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 7 | 1 | 0 | 3 | 1 | 2 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0002 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0002g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0002g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0002g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0002g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0002g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0002g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0002g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0002g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0002g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0002g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0002g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0002g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0002g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0003g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0003g0016 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0003g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0003g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0003g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0003g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0004g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0004g0019 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0004g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0004g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0004g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0004g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0004g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0004g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0004g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0004g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0004g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0004g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0004g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0004g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0004g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0004g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0004g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0004g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0004g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0004g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0004g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0004g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0004g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0004g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0004g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0004g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0004g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0004g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0004g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0004g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0004g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0004g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0004g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0004g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0004g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0004g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0004g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0004g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0004g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0004g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0004g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0004g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0004g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0005g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0005g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0005g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0005g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0005g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0005g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0005g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0005g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0005g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0005g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0005g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0005g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0006g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0006g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0006g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0006g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0006g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0006g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0006g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0006g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0006g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0006g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0006g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0006g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0006g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0006g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0006g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0006g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0006g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0006g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0006g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0006g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0006g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0006g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0006g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0006g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0006g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0006g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0006g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0006g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0006g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0006g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0006g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0007g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0007g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0007g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0007g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0007g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0007g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0007g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0007g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0007g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0007g0241 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0007g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0007g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0007g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0008g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0008g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0008g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0008g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0008g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0008g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0008g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0008g0338 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0008g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0008g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0010g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0010g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0010g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0010g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0011g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0011g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0011g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0011g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0011g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0013g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0013g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0014g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0015g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0015g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0015g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0016g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0016g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0017g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0017g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0017g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0018g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0018g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0018g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0019g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0019g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0020g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0020g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0024g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0025g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0026g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0027g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0028g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0029g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0030g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0031g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0032g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0033g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0034g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0035g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0037g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0038g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0039g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0001t0040g0372 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0005t0005g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0001c0005t0005g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0002c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0002c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0002c0002t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0002c0002t0004g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0002c0002t0005g0013 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0002c0002t0005g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0002c0002t0005g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0002c0002t0005g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0002c0002t0005g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0002c0002t0005g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0002c0002t0005g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0002c0002t0005g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0002c0002t0005g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0002c0002t0005g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0002c0002t0005g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0002c0002t0005g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0002c0002t0005g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0002c0002t0005g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0002c0002t0005g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0002c0002t0012g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0002c0002t0012g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0002c0002t0012g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0002c0002t0014g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0002c0002t0014g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0002c0002t0021g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0002c0002t0022g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0002c0002t0023g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0003c0003t0009g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0003c0003t0009g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0003c0003t0009g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0003c0003t0009g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0003c0003t0009g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0003c0003t0009g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0004c0004t0010g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0004c0004t0010g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0004c0004t0016g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0005c0006t0004g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0005c0006t0004g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0006c0007t0004g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0007c0010t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0008c0008t0036g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| a0009c0009t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0016 | EUR | GBR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG00140 | hp1 | a0001 | c0001 | t0007 | g0058 | EUR | GBR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG00140 | hp2 | a0001 | c0001 | t0006 | g0074 | EUR | GBR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0062 | EUR | FIN | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG00280 | hp2 | a0001 | c0001 | t0010 | g0301 | EUR | FIN | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0063 | EUR | FIN | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG00323 | hp2 | a0001 | c0001 | t0006 | g0072 | EUR | FIN | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0256 | EAS | CHS | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | CHS | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG00544 | hp1 | a0001 | c0001 | t0004 | g0100 | EAS | CHS | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG00558 | hp1 | a0001 | c0001 | t0004 | g0130 | EAS | CHS | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG00558 | hp2 | a0001 | c0001 | t0019 | g0258 | EAS | CHS | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG00597 | hp1 | a0001 | c0001 | t0005 | g0164 | EAS | CHS | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0350 | EAS | CHS | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | CHS | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0203 | EAS | CHS | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | CHS | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0046 | AMR | PUR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0096 | AMR | PUR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG00673 | hp2 | a0001 | c0001 | t0004 | g0132 | EAS | CHS | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG00733 | hp1 | a0001 | c0001 | t0006 | g0161 | AMR | PUR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0032 | AMR | PUR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG00735 | hp1 | a0001 | c0001 | t0006 | g0075 | AMR | PUR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0043 | AMR | PUR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG00738 | hp1 | a0004 | c0004 | t0016 | g0227 | AMR | PUR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0044 | AMR | PUR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG00741 | hp1 | a0001 | c0001 | t0006 | g0237 | AMR | PUR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0326 | AMR | PUR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG01069 | hp1 | a0002 | c0002 | t0005 | g0356 | AMR | PUR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG01069 | hp2 | a0001 | c0001 | t0006 | g0169 | AMR | PUR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG01070 | hp1 | a0001 | c0001 | t0007 | g0014 | AMR | PUR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG01070 | hp2 | a0001 | c0001 | t0006 | g0076 | AMR | PUR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG01071 | hp1 | a0002 | c0002 | t0005 | g0035 | AMR | PUR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG01071 | hp2 | a0001 | c0001 | t0007 | g0014 | AMR | PUR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG01074 | hp1 | a0001 | c0001 | t0004 | g0283 | AMR | PUR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0031 | AMR | PUR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG01081 | hp2 | a0001 | c0001 | t0006 | g0037 | AMR | PUR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG01106 | hp1 | a0001 | c0001 | t0007 | g0059 | AMR | PUR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG01106 | hp2 | a0001 | c0001 | t0006 | g0204 | AMR | PUR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG01109 | hp1 | a0002 | c0002 | t0005 | g0013 | AMR | PUR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG01109 | hp2 | a0001 | c0001 | t0025 | g0060 | AMR | PUR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG01168 | hp2 | a0001 | c0001 | t0007 | g0166 | AMR | PUR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG01169 | hp2 | a0001 | c0001 | t0004 | g0177 | AMR | PUR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG01175 | hp1 | a0001 | c0001 | t0010 | g0217 | AMR | PUR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG01175 | hp2 | a0001 | c0001 | t0008 | g0091 | AMR | PUR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0287 | AMR | PUR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG01192 | hp2 | a0001 | c0001 | t0004 | g0176 | AMR | PUR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0039 | AMR | PUR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0316 | AMR | PUR | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0045 | AMR | CLM | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG01255 | hp2 | a0001 | c0001 | t0008 | g0344 | AMR | CLM | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG01256 | hp1 | a0001 | c0001 | t0006 | g0056 | AMR | CLM | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0331 | AMR | CLM | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0047 | AMR | CLM | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0349 | AMR | CLM | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG01261 | hp2 | a0001 | c0001 | t0010 | g0302 | AMR | CLM | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG01346 | hp2 | a0001 | c0001 | t0006 | g0057 | AMR | CLM | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0124 | AMR | CLM | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG01358 | hp2 | a0001 | c0001 | t0008 | g0337 | AMR | CLM | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG01433 | hp1 | a0001 | c0001 | t0008 | g0042 | AMR | CLM | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG01433 | hp2 | a0001 | c0001 | t0006 | g0068 | AMR | CLM | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0031 | AMR | CLM | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG01515 | hp1 | a0001 | c0001 | t0004 | g0019 | EUR | IBS | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0099 | EUR | IBS | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG01517 | hp1 | a0001 | c0001 | t0006 | g0073 | EUR | IBS | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG01517 | hp2 | a0001 | c0001 | t0004 | g0019 | EUR | IBS | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG01928 | hp1 | a0002 | c0002 | t0005 | g0321 | AMR | PEL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG01928 | hp2 | a0001 | c0001 | t0004 | g0040 | AMR | PEL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG01934 | hp1 | a0001 | c0001 | t0006 | g0335 | AMR | PEL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG01934 | hp2 | a0001 | c0001 | t0006 | g0051 | AMR | PEL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG01943 | hp1 | a0001 | c0001 | t0004 | g0049 | AMR | PEL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0325 | AMR | PEL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG01978 | hp1 | a0001 | c0001 | t0005 | g0342 | AMR | PEL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0323 | AMR | PEL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0327 | AMR | PEL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0206 | AMR | PEL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG01993 | hp1 | a0002 | c0002 | t0005 | g0355 | AMR | PEL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG01993 | hp2 | a0001 | c0001 | t0004 | g0041 | AMR | PEL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0328 | AMR | PEL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02004 | hp2 | a0002 | c0002 | t0005 | g0013 | AMR | PEL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02015 | hp2 | a0001 | c0001 | t0039 | g0070 | EAS | KHV | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | KHV | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02027 | hp2 | a0002 | c0002 | t0005 | g0255 | EAS | KHV | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | KHV | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02055 | hp1 | a0001 | c0001 | t0026 | g0159 | AFR | ACB | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0192 | AFR | ACB | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | KHV | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02056 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | KHV | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0162 | EAS | KHV | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02080 | hp1 | a0001 | c0001 | t0006 | g0315 | EAS | KHV | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02080 | hp2 | a0001 | c0001 | t0004 | g0346 | EAS | KHV | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02083 | hp2 | a0001 | c0001 | t0004 | g0230 | EAS | KHV | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0163 | EAS | KHV | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02132 | hp2 | a0001 | c0001 | t0006 | g0081 | EAS | KHV | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02135 | hp1 | a0001 | c0001 | t0005 | g0264 | EAS | KHV | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02135 | hp2 | a0002 | c0002 | t0005 | g0361 | EAS | KHV | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02145 | hp2 | a0001 | c0001 | t0028 | g0160 | AFR | ACB | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0330 | AMR | PEL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02148 | hp2 | a0001 | c0001 | t0004 | g0329 | AMR | PEL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | CDX | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | CDX | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | CDX | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0085 | AFR | ACB | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02257 | hp2 | a0001 | c0001 | t0015 | g0087 | AFR | ACB | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02280 | hp1 | a0001 | c0001 | t0006 | g0080 | AFR | ACB | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02280 | hp2 | a0001 | c0001 | t0006 | g0071 | AFR | ACB | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0324 | AMR | PEL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02300 | hp2 | a0002 | c0002 | t0005 | g0035 | AMR | PEL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02451 | hp1 | a0003 | c0003 | t0009 | g0010 | AFR | ACB | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02451 | hp2 | a0001 | c0001 | t0007 | g0240 | AFR | ACB | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02523 | hp1 | a0001 | c0001 | t0016 | g0101 | EAS | KHV | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02523 | hp2 | a0001 | c0001 | t0038 | g0281 | EAS | KHV | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02572 | hp1 | a0001 | c0001 | t0007 | g0239 | AFR | GWD | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02572 | hp2 | a0001 | c0001 | t0013 | g0012 | AFR | GWD | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0103 | SAS | PJL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0016 | AFR | GWD | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | GWD | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02630 | hp1 | a0001 | c0001 | t0013 | g0012 | AFR | GWD | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0358 | AFR | GWD | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0294 | AFR | GWD | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02647 | hp2 | a0001 | c0001 | t0006 | g0158 | AFR | GWD | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0317 | SAS | PJL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02683 | hp2 | a0001 | c0001 | t0006 | g0170 | SAS | PJL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0104 | SAS | PJL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0050 | SAS | PJL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02717 | hp1 | a0001 | c0001 | t0018 | g0137 | AFR | GWD | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02723 | hp1 | a0001 | c0001 | t0013 | g0306 | AFR | GWD | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02723 | hp2 | a0002 | c0002 | t0014 | g0354 | AFR | GWD | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0243 | SAS | PJL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02809 | hp2 | a0001 | c0001 | t0020 | g0357 | AFR | GWD | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02818 | hp1 | a0001 | c0001 | t0007 | g0299 | AFR | GWD | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02886 | hp1 | a0003 | c0003 | t0009 | g0234 | AFR | GWD | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0065 | AFR | GWD | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02895 | hp1 | a0001 | c0001 | t0007 | g0066 | AFR | GWD | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0178 | AFR | GWD | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0140 | AFR | GWD | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02897 | hp2 | a0001 | c0001 | t0037 | g0139 | AFR | GWD | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02922 | hp2 | a0001 | c0001 | t0027 | g0232 | AFR | ESN | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02965 | hp1 | a0003 | c0003 | t0009 | g0022 | AFR | ESN | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | ESN | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | ESN | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02970 | hp2 | a0001 | c0001 | t0006 | g0064 | AFR | ESN | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02976 | hp2 | a0003 | c0003 | t0009 | g0236 | AFR | ESN | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG03017 | hp2 | a0001 | c0001 | t0035 | g0038 | SAS | PJL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0116 | AFR | GWD | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG03041 | hp2 | a0002 | c0002 | t0014 | g0345 | AFR | GWD | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG03130 | hp1 | a0001 | c0001 | t0008 | g0033 | AFR | ESN | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0167 | AFR | ESN | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG03139 | hp2 | a0001 | c0001 | t0015 | g0088 | AFR | ESN | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | ESN | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG03209 | hp1 | a0003 | c0003 | t0009 | g0233 | AFR | MSL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG03209 | hp2 | a0001 | c0001 | t0016 | g0157 | AFR | MSL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG03225 | hp1 | a0001 | c0001 | t0008 | g0226 | AFR | MSL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0304 | AFR | MSL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG03239 | hp1 | a0001 | c0001 | t0007 | g0246 | SAS | PJL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0181 | SAS | PJL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG03453 | hp1 | a0001 | c0001 | t0018 | g0136 | AFR | MSL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG03453 | hp2 | a0001 | c0001 | t0014 | g0090 | AFR | MSL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG03486 | hp1 | a0001 | c0001 | t0004 | g0300 | AFR | MSL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG03486 | hp2 | a0001 | c0001 | t0013 | g0012 | AFR | MSL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG03491 | hp1 | a0004 | c0004 | t0010 | g0254 | SAS | PJL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0244 | SAS | PJL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG03492 | hp2 | a0004 | c0004 | t0010 | g0253 | SAS | PJL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG03516 | hp1 | a0001 | c0001 | t0015 | g0089 | AFR | ESN | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG03516 | hp2 | a0003 | c0003 | t0009 | g0010 | AFR | ESN | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG03540 | hp1 | a0001 | c0001 | t0030 | g0172 | AFR | GWD | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG03540 | hp2 | a0001 | c0001 | t0017 | g0228 | AFR | GWD | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0303 | AFR | MSL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0102 | SAS | PJL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG03669 | hp1 | a0001 | c0001 | t0040 | g0372 | SAS | PJL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG03669 | hp2 | a0001 | c0001 | t0006 | g0077 | SAS | PJL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG03688 | hp1 | a0001 | c0001 | t0004 | g0171 | SAS | STU | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG03704 | hp1 | a0001 | c0001 | t0008 | g0334 | SAS | PJL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG03710 | hp1 | a0001 | c0001 | t0006 | g0084 | SAS | PJL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG03710 | hp2 | a0001 | c0001 | t0006 | g0314 | SAS | PJL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG03831 | hp1 | a0001 | c0001 | t0006 | g0083 | SAS | BEB | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG03831 | hp2 | a0006 | c0007 | t0004 | g0347 | SAS | BEB | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | BEB | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG03834 | hp2 | a0001 | c0001 | t0007 | g0245 | SAS | BEB | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | BEB | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | BEB | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | BEB | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG03942 | hp2 | a0001 | c0001 | t0004 | g0197 | SAS | BEB | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0093 | SAS | STU | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0348 | SAS | STU | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0118 | SAS | BEB | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0208 | SAS | BEB | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG04199 | hp1 | a0001 | c0001 | t0008 | g0339 | SAS | STU | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG04199 | hp2 | a0001 | c0001 | t0006 | g0247 | SAS | STU | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG04204 | hp1 | a0001 | c0001 | t0006 | g0078 | SAS | STU | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0108 | SAS | STU | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0048 | SAS | STU | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG04228 | hp2 | a0001 | c0001 | t0033 | g0069 | SAS | STU | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | CHB | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | CHB | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18906 | hp1 | a0003 | c0003 | t0009 | g0235 | AFR | YRI | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18906 | hp2 | a0005 | c0006 | t0004 | g0189 | AFR | YRI | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18939 | hp1 | a0001 | c0001 | t0005 | g0107 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18944 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18946 | hp1 | a0001 | c0001 | t0024 | g0199 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18946 | hp2 | a0001 | c0001 | t0004 | g0216 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18947 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0152 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18948 | hp2 | a0001 | c0001 | t0004 | g0285 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18949 | hp1 | a0002 | c0002 | t0005 | g0353 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0129 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0106 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18951 | hp2 | a0001 | c0001 | t0004 | g0293 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18952 | hp2 | a0001 | c0005 | t0005 | g0175 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18953 | hp1 | a0001 | c0001 | t0004 | g0274 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18956 | hp1 | a0001 | c0001 | t0003 | g0123 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18956 | hp2 | a0002 | c0002 | t0005 | g0365 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18957 | hp1 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18957 | hp2 | a0001 | c0001 | t0004 | g0126 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18959 | hp2 | a0001 | c0001 | t0005 | g0249 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18961 | hp1 | a0001 | c0001 | t0004 | g0211 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0341 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18962 | hp1 | a0001 | c0001 | t0004 | g0296 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18965 | hp1 | a0001 | c0001 | t0003 | g0198 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18966 | hp2 | a0002 | c0002 | t0005 | g0362 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18967 | hp2 | a0001 | c0001 | t0003 | g0219 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18968 | hp1 | a0002 | c0002 | t0005 | g0366 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18969 | hp1 | a0002 | c0002 | t0001 | g0202 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18970 | hp1 | a0001 | c0001 | t0004 | g0298 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18972 | hp1 | a0001 | c0001 | t0003 | g0138 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18972 | hp2 | a0001 | c0001 | t0003 | g0220 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18973 | hp1 | a0007 | c0010 | t0003 | g0119 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18975 | hp1 | a0001 | c0001 | t0019 | g0259 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18975 | hp2 | a0001 | c0001 | t0003 | g0133 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18977 | hp1 | a0002 | c0002 | t0001 | g0320 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18977 | hp2 | a0002 | c0002 | t0005 | g0201 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0351 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18981 | hp1 | a0001 | c0001 | t0032 | g0282 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18982 | hp1 | a0001 | c0001 | t0003 | g0151 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0213 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18984 | hp1 | a0001 | c0001 | t0017 | g0309 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18984 | hp2 | a0001 | c0001 | t0005 | g0270 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18985 | hp1 | a0001 | c0001 | t0004 | g0278 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18989 | hp1 | a0002 | c0002 | t0012 | g0370 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18989 | hp2 | a0001 | c0001 | t0004 | g0295 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18991 | hp1 | a0001 | c0001 | t0004 | g0131 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18991 | hp2 | a0001 | c0001 | t0011 | g0263 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18992 | hp1 | a0002 | c0002 | t0022 | g0367 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0165 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18994 | hp2 | a0001 | c0001 | t0004 | g0272 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18995 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18997 | hp2 | a0001 | c0001 | t0004 | g0094 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18999 | hp1 | a0002 | c0002 | t0023 | g0363 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18999 | hp2 | a0001 | c0001 | t0004 | g0280 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19000 | hp1 | a0001 | c0001 | t0031 | g0194 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19002 | hp1 | a0001 | c0001 | t0004 | g0092 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19002 | hp2 | a0001 | c0001 | t0017 | g0312 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19003 | hp2 | a0008 | c0008 | t0036 | g0142 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19004 | hp1 | a0001 | c0001 | t0003 | g0289 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0224 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19006 | hp2 | a0001 | c0001 | t0011 | g0273 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19007 | hp2 | a0001 | c0001 | t0005 | g0251 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19009 | hp1 | a0001 | c0001 | t0005 | g0109 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19010 | hp1 | a0001 | c0001 | t0005 | g0114 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0095 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19012 | hp1 | a0001 | c0001 | t0011 | g0332 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19012 | hp2 | a0001 | c0001 | t0004 | g0205 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | LWK | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0359 | AFR | LWK | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0054 | AFR | LWK | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | LWK | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19055 | hp1 | a0009 | c0009 | t0001 | g0307 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19055 | hp2 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19057 | hp2 | a0001 | c0001 | t0005 | g0284 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19058 | hp2 | a0001 | c0001 | t0005 | g0122 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19060 | hp2 | a0002 | c0002 | t0005 | g0360 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0352 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19062 | hp2 | a0002 | c0002 | t0005 | g0013 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19063 | hp2 | a0001 | c0001 | t0004 | g0279 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19064 | hp1 | a0001 | c0005 | t0005 | g0173 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19065 | hp2 | a0001 | c0001 | t0004 | g0128 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19067 | hp1 | a0001 | c0001 | t0003 | g0242 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19067 | hp2 | a0002 | c0002 | t0005 | g0364 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19068 | hp2 | a0002 | c0002 | t0012 | g0020 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19076 | hp1 | a0001 | c0001 | t0004 | g0271 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19076 | hp2 | a0001 | c0001 | t0005 | g0225 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19077 | hp1 | a0001 | c0001 | t0011 | g0333 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0223 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19078 | hp1 | a0002 | c0002 | t0005 | g0371 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19078 | hp2 | a0001 | c0001 | t0003 | g0117 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0113 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19080 | hp1 | a0001 | c0001 | t0034 | g0262 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19080 | hp2 | a0001 | c0001 | t0003 | g0221 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19081 | hp1 | a0001 | c0001 | t0011 | g0266 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19081 | hp2 | a0001 | c0001 | t0003 | g0112 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19082 | hp2 | a0002 | c0002 | t0012 | g0369 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19084 | hp2 | a0002 | c0002 | t0012 | g0020 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19086 | hp1 | a0001 | c0001 | t0003 | g0115 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0222 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19088 | hp2 | a0001 | c0001 | t0004 | g0277 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19089 | hp1 | a0001 | c0001 | t0004 | g0200 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19089 | hp2 | a0002 | c0002 | t0021 | g0322 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19091 | hp1 | a0002 | c0002 | t0004 | g0368 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19091 | hp2 | a0001 | c0001 | t0003 | g0134 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19240 | hp1 | a0003 | c0003 | t0009 | g0010 | AFR | YRI | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0269 | AFR | YRI | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0218 | EUR | TSI | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA20752 | hp2 | a0001 | c0001 | t0029 | g0297 | EUR | TSI | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA20805 | hp1 | a0001 | c0001 | t0004 | g0168 | EUR | TSI | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA20805 | hp2 | a0001 | c0001 | t0007 | g0061 | EUR | TSI | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA20905 | hp1 | a0001 | c0001 | t0006 | g0079 | SAS | GIH | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0120 | SAS | GIH | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0032 | AMR | CLM | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG01123 | hp2 | a0001 | c0001 | t0008 | g0336 | AMR | CLM | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02109 | hp1 | a0001 | c0001 | t0020 | g0343 | AFR | ACB | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02109 | hp2 | a0001 | c0001 | t0008 | g0033 | AFR | ACB | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | ACB | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02486 | hp2 | a0001 | c0001 | t0010 | g0252 | AFR | ACB | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | ACB | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG02559 | hp2 | a0001 | c0001 | t0006 | g0156 | AFR | ACB | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG03471 | hp1 | a0001 | c0001 | t0018 | g0135 | AFR | MSL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0086 | AFR | MSL | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG06807 | hp1 | a0005 | c0006 | t0004 | g0190 | AFR | USA | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| HG06807 | hp2 | a0001 | c0001 | t0007 | g0210 | AFR | USA | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA18955 | hp2 | a0001 | c0001 | t0004 | g0127 | EAS | JPT | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA20300 | hp1 | a0003 | c0003 | t0009 | g0022 | AFR | USA | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA20300 | hp2 | a0001 | c0001 | t0006 | g0052 | AFR | USA | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0111 | AFR | LWK | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0318 | AFR | LWK | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0007 | g0241 | REF | REF | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0008 | g0338 | REF | REF | TM7SF3_chr12_26966579_27019384 | TM7SF3 | chr12 | 26966579 | 27019384 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:26990518 | G | A | 1 | a0004 | 3 | HG00738.hp1 HG03491.hp1 HG03492.hp2 |
missense_variant | MODERATE | c.800C>T | p.Ala267Val | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/12 | 1016/4315 | 800/1713 | 267/570 | chr12 | 26990518 | |||
| chr12:26990539 | T | G | 1 | a0008 | 1 | NA19003.hp2 | missense_variant | MODERATE | c.779A>C | p.Asp260Ala | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/12 | 995/4315 | 779/1713 | 260/570 | chr12 | 26990539 | |||
| chr12:26990540 | C | T | 1 | a0008 | 1 | NA19003.hp2 | missense_variant | MODERATE | c.778G>A | p.Asp260Asn | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/12 | 994/4315 | 778/1713 | 260/570 | chr12 | 26990540 | |||
| chr12:26990543 | A | C | 1 | a0008 | 1 | NA19003.hp2 | missense_variant | MODERATE | c.775T>G | p.Trp259Gly | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/12 | 991/4315 | 775/1713 | 259/570 | chr12 | 26990543 | |||
| chr12:26990575 | G | A | 1 | a0002 | 31 | HG00609.hp2 HG01069.hp1 HG01071.hp1 others(28): Show |
missense_variant | MODERATE | c.743C>T | p.Pro248Leu | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/12 | 959/4315 | 743/1713 | 248/570 | chr12 | 26990575 | |||
| chr12:26995244 | G | A | 1 | a0005 | 2 | HG06807.hp1 NA18906.hp2 |
missense_variant | MODERATE | c.683C>T | p.Ala228Val | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/12 | 899/4315 | 683/1713 | 228/570 | chr12 | 26995244 | |||
| chr12:26995391 | G | C | 1 | a0003 | 9 | HG02451.hp1 HG02886.hp1 HG02965.hp1 others(6): Show |
missense_variant | MODERATE | c.536C>G | p.Pro179Arg | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/12 | 752/4315 | 536/1713 | 179/570 | chr12 | 26995391 | |||
| chr12:26996745 | G | A | 1 | a0009 | 1 | NA19055.hp1 | missense_variant | MODERATE | c.515C>T | p.Ala172Val | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 4/12 | 731/4315 | 515/1713 | 172/570 | chr12 | 26996745 | |||
| chr12:26996781 | G | A | 1 | a0007 | 1 | NA18973.hp1 | missense_variant | MODERATE | c.479C>T | p.Thr160Met | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 4/12 | 695/4315 | 479/1713 | 160/570 | chr12 | 26996781 | |||
| chr12:27003328 | C | G | 1 | a0006 | 1 | HG03831.hp2 | missense_variant | MODERATE | c.154G>C | p.Glu52Gln | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/12 | 370/4315 | 154/1713 | 52/570 | chr12 | 27003328 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:26990466 | A | T | 1 | a0001c0005 | 2 | NA18952.hp2 NA19064.hp1 |
synonymous_variant | LOW | c.852T>A | p.Gly284Gly | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/12 | 1068/4315 | 852/1713 | 284/570 | chr12 | 26990466 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:26971595 | GATTT | G | 9 | a0001c0001t0004 a0001c0001t0032 a0001c0001t0034 others(6): Show |
55 | HG00544.hp1 HG00558.hp1 HG00673.hp2 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*2366_*2369delAAAT | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 12/12 | 2366 | chr12 | 26971595 | ||||||
| chr12:26971660 | G | A | 1 | a0001c0001t0027 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2305C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 12/12 | 2305 | chr12 | 26971660 | ||||||
| chr12:26971721 | T | C | 4 | a0001c0001t0014 a0001c0001t0026 a0001c0001t0028 others(1): Show |
5 | HG02055.hp1 HG02145.hp2 HG02723.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2244A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 12/12 | 2244 | chr12 | 26971721 | ||||||
| chr12:26971722 | A | G | 5 | a0001c0001t0006 a0001c0001t0015 a0001c0001t0018 others(2): Show |
39 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*2243T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 12/12 | 2243 | chr12 | 26971722 | ||||||
| chr12:26971806 | C | A | 1 | a0001c0001t0007 | 13 | HG00140.hp1 HG01070.hp1 HG01071.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2159G>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 12/12 | 2159 | chr12 | 26971806 | ||||||
| chr12:26971851 | T | C | 4 | a0001c0001t0006 a0001c0001t0018 a0001c0001t0033 others(1): Show |
36 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*2114A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 12/12 | 2114 | chr12 | 26971851 | ||||||
| chr12:26971943 | T | G | 49 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(46): Show |
416 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(413): Show |
3_prime_UTR_variant | MODIFIER | c.*2022A>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 12/12 | 2022 | chr12 | 26971943 | ||||||
| chr12:26972058 | A | G | 1 | a0001c0001t0035 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1907T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 12/12 | 1907 | chr12 | 26972058 | ||||||
| chr12:26972420 | CT | C | 16 | a0001c0001t0001 a0001c0001t0010 a0001c0001t0011 others(13): Show |
144 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(141): Show |
3_prime_UTR_variant | MODIFIER | c.*1544delA | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 12/12 | 1544 | chr12 | 26972420 | ||||||
| chr12:26972438 | C | T | 2 | a0001c0001t0010 a0004c0004t0010 |
6 | HG00280.hp2 HG01175.hp1 HG01261.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1527G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 12/12 | 1527 | chr12 | 26972438 | ||||||
| chr12:26972452 | G | A | 1 | a0001c0001t0019 | 2 | HG00558.hp2 NA18975.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1513C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 12/12 | 1513 | chr12 | 26972452 | ||||||
| chr12:26972477 | G | A | 1 | a0003c0003t0009 | 9 | HG02451.hp1 HG02886.hp1 HG02965.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1488C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 12/12 | 1488 | chr12 | 26972477 | ||||||
| chr12:26972527 | T | C | 1 | a0001c0001t0029 | 1 | NA20752.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1438A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 12/12 | 1438 | chr12 | 26972527 | ||||||
| chr12:26972800 | T | C | 1 | a0001c0001t0030 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1165A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 12/12 | 1165 | chr12 | 26972800 | ||||||
| chr12:26972870 | G | A | 1 | a0001c0001t0038 | 1 | HG02523.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1095C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 12/12 | 1095 | chr12 | 26972870 | ||||||
| chr12:26972959 | CA | C | 1 | a0001c0001t0011 | 5 | NA18991.hp2 NA19006.hp2 NA19012.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1005delT | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 12/12 | 1005 | chr12 | 26972959 | ||||||
| chr12:26973006 | G | A | 1 | a0001c0001t0020 | 2 | HG02109.hp1 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*959C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 12/12 | 959 | chr12 | 26973006 | ||||||
| chr12:26973023 | A | G | 1 | a0001c0001t0034 | 1 | NA19080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*942T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 12/12 | 942 | chr12 | 26973023 | ||||||
| chr12:26973109 | G | A | 1 | a0001c0001t0039 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*856C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 12/12 | 856 | chr12 | 26973109 | ||||||
| chr12:26973169 | A | C | 2 | a0001c0001t0014 a0002c0002t0014 |
3 | HG02723.hp2 HG03041.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*796T>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 12/12 | 796 | chr12 | 26973169 | ||||||
| chr12:26973175 | G | GT | 37 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(34): Show |
394 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(391): Show |
3_prime_UTR_variant | MODIFIER | c.*789dupA | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 12/12 | 789 | chr12 | 26973175 | ||||||
| chr12:26973175 | G | GTT | 6 | a0001c0001t0025 a0001c0001t0026 a0001c0001t0031 others(3): Show |
9 | HG01109.hp2 HG02055.hp1 HG04228.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*788_*789dupAA | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 12/12 | 789 | chr12 | 26973175 | ||||||
| chr12:26973179 | T | G | 1 | a0001c0001t0020 | 2 | HG02109.hp1 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*786A>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 12/12 | 786 | chr12 | 26973179 | ||||||
| chr12:26973179 | T | TG | 2 | a0001c0001t0018 a0002c0002t0023 |
4 | HG02717.hp1 HG03453.hp1 HG03471.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*785_*786insC | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 12/12 | 785 | chr12 | 26973179 | ||||||
| chr12:26973237 | A | G | 1 | a0002c0002t0021 | 1 | NA19089.hp2 | 3_prime_UTR_variant | MODIFIER | c.*728T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 12/12 | 728 | chr12 | 26973237 | ||||||
| chr12:26973263 | T | G | 18 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 others(15): Show |
172 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(169): Show |
3_prime_UTR_variant | MODIFIER | c.*702A>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 12/12 | 702 | chr12 | 26973263 | ||||||
| chr12:26973335 | G | A | 1 | a0001c0001t0013 | 4 | HG02572.hp2 HG02630.hp1 HG02723.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*630C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 12/12 | 630 | chr12 | 26973335 | ||||||
| chr12:26973367 | G | T | 1 | a0001c0001t0024 | 1 | NA18946.hp1 | 3_prime_UTR_variant | MODIFIER | c.*598C>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 12/12 | 598 | chr12 | 26973367 | ||||||
| chr12:26973743 | A | G | 7 | a0001c0001t0005 a0001c0005t0005 a0002c0002t0005 others(4): Show |
39 | HG00597.hp1 HG01069.hp1 HG01071.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*222T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 12/12 | 222 | chr12 | 26973743 | ||||||
| chr12:27014233 | C | A | 1 | a0001c0001t0040 | 1 | HG03669.hp1 | 5_prime_UTR_variant | MODIFIER | c.-65G>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/12 | 65 | chr12 | 27014233 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:26974392 | T | C | 1 | a0001c0001t0016g0157 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1451-165A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 11/11 | chr12 | 26974392 | |||||||
| chr12:26974704 | C | T | 45 | a0001c0001t0002g0099 a0001c0001t0002g0116 a0001c0001t0003g0005 others(42): Show |
51 | HG00099.hp2 HG00642.hp2 HG01109.hp2 others(48): Show |
intron_variant | MODIFIER | c.1451-477G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 11/11 | chr12 | 26974704 | |||||||
| chr12:26974711 | A | G | 1 | a0001c0001t0003g0129 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1451-484T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 11/11 | chr12 | 26974711 | |||||||
| chr12:26975078 | ACT | A | 35 | a0001c0001t0005g0107 a0001c0001t0005g0109 a0001c0001t0005g0114 others(32): Show |
39 | HG00597.hp1 HG01069.hp1 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.1450+416_1450+417d others(4): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 11/11 | chr12 | 26975078 | |||||||
| chr12:26975341 | C | T | 1 | a0001c0001t0004g0168 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1450+155G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 11/11 | chr12 | 26975341 | |||||||
| chr12:26975395 | T | C | 1 | a0001c0001t0004g0092 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1450+101A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 11/11 | chr12 | 26975395 | |||||||
| chr12:26975661 | G | GT | 109 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(106): Show |
144 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(141): Show |
splice_region_variant&intron_variant | LOW | c.1288-4dupA | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 10/11 | chr12 | 26975661 | |||||||
| chr12:26975791 | C | A | 1 | a0001c0001t0004g0167 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1288-133G>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 10/11 | chr12 | 26975791 | |||||||
| chr12:26975814 | A | G | 1 | a0001c0001t0003g0065 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1288-156T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 10/11 | chr12 | 26975814 | |||||||
| chr12:26976018 | T | C | 1 | a0001c0001t0002g0145 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1287+242A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 10/11 | chr12 | 26976018 | |||||||
| chr12:26976105 | G | A | 3 | a0001c0001t0001g0028 a0001c0001t0001g0267 a0001c0001t0001g0268 |
4 | HG00438.hp2 HG00544.hp2 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.1287+155C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 10/11 | chr12 | 26976105 | |||||||
| chr12:26976204 | A | G | 1 | a0001c0001t0001g0310 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1287+56T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 10/11 | chr12 | 26976204 | |||||||
| chr12:26976440 | T | C | 1 | a0002c0002t0005g0321 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1190-83A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 9/11 | chr12 | 26976440 | |||||||
| chr12:26976453 | T | C | 2 | a0001c0001t0015g0087 a0001c0001t0015g0088 |
2 | HG02257.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1190-96A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 9/11 | chr12 | 26976453 | |||||||
| chr12:26976582 | C | G | 1 | a0001c0001t0002g0324 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1190-225G>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 9/11 | chr12 | 26976582 | |||||||
| chr12:26977016 | A | G | 109 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(106): Show |
144 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.1190-659T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 9/11 | chr12 | 26977016 | |||||||
| chr12:26977153 | T | C | 2 | a0001c0001t0004g0140 a0001c0001t0037g0139 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1190-796A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 9/11 | chr12 | 26977153 | |||||||
| chr12:26977232 | C | A | 305 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(302): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.1190-875G>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 9/11 | chr12 | 26977232 | |||||||
| chr12:26977293 | G | C | 1 | a0001c0001t0006g0056 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1190-936C>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 9/11 | chr12 | 26977293 | |||||||
| chr12:26977396 | A | G | 100 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(97): Show |
133 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.1190-1039T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 9/11 | chr12 | 26977396 | |||||||
| chr12:26977408 | A | G | 1 | a0002c0002t0023g0363 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1190-1051T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 9/11 | chr12 | 26977408 | |||||||
| chr12:26977520 | G | A | 1 | a0001c0001t0002g0181 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1190-1163C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 9/11 | chr12 | 26977520 | |||||||
| chr12:26977702 | T | C | 356 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(353): Show |
412 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(409): Show |
intron_variant | MODIFIER | c.1190-1345A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 9/11 | chr12 | 26977702 | |||||||
| chr12:26977766 | ATG | A | 238 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(235): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(280): Show |
intron_variant | MODIFIER | c.1190-1411_1190-141 others(6): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 9/11 | chr12 | 26977766 | |||||||
| chr12:26977766 | ATGTG | A | 111 | a0001c0001t0002g0007 a0001c0001t0002g0031 a0001c0001t0002g0032 others(108): Show |
122 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.1190-1413_1190-141 others(8): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 9/11 | chr12 | 26977766 | |||||||
| chr12:26977946 | G | A | 356 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(353): Show |
412 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(409): Show |
intron_variant | MODIFIER | c.1190-1589C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 9/11 | chr12 | 26977946 | |||||||
| chr12:26978506 | C | T | 1 | a0001c0001t0001g0030 | 2 | HG02155.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1189+1278G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 9/11 | chr12 | 26978506 | |||||||
| chr12:26978627 | A | G | 37 | a0001c0001t0006g0037 a0001c0001t0006g0051 a0001c0001t0006g0052 others(34): Show |
37 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.1189+1157T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 9/11 | chr12 | 26978627 | |||||||
| chr12:26978634 | T | C | 7 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0260 others(4): Show |
11 | HG00597.hp2 HG01257.hp2 NA18969.hp2 others(8): Show |
intron_variant | MODIFIER | c.1189+1150A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 9/11 | chr12 | 26978634 | |||||||
| chr12:26978744 | AT | A | 92 | a0001c0001t0001g0305 a0001c0001t0002g0007 a0001c0001t0002g0031 others(89): Show |
97 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.1189+1039delA | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 9/11 | chr12 | 26978744 | |||||||
| chr12:26978744 | ATT | A | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(209): Show |
260 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.1189+1038_1189+103 others(6): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 9/11 | chr12 | 26978744 | |||||||
| chr12:26978976 | A | C | 3 | a0001c0001t0014g0090 a0002c0002t0014g0345 a0002c0002t0014g0354 |
3 | HG02723.hp2 HG03041.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1189+808T>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 9/11 | chr12 | 26978976 | |||||||
| chr12:26979013 | G | GA | 11 | a0001c0001t0001g0015 a0001c0001t0001g0025 a0001c0001t0001g0028 others(8): Show |
14 | HG00438.hp2 HG00544.hp2 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.1189+770dupT | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 9/11 | chr12 | 26979013 | |||||||
| chr12:26979021 | A | C | 3 | a0001c0001t0002g0044 a0001c0001t0002g0062 a0001c0001t0002g0206 |
3 | HG00280.hp1 HG00738.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.1189+763T>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 9/11 | chr12 | 26979021 | |||||||
| chr12:26979025 | C | T | 1 | a0001c0001t0004g0346 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1189+759G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 9/11 | chr12 | 26979025 | |||||||
| chr12:26979096 | A | G | 35 | a0001c0001t0005g0107 a0001c0001t0005g0109 a0001c0001t0005g0114 others(32): Show |
39 | HG00597.hp1 HG01069.hp1 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.1189+688T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 9/11 | chr12 | 26979096 | |||||||
| chr12:26979174 | C | T | 1 | a0001c0001t0014g0090 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1189+610G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 9/11 | chr12 | 26979174 | |||||||
| chr12:26979281 | T | C | 1 | a0001c0001t0016g0157 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1189+503A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 9/11 | chr12 | 26979281 | |||||||
| chr12:26979309 | T | A | 2 | a0001c0001t0002g0181 a0001c0001t0002g0208 |
2 | HG03239.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.1189+475A>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 9/11 | chr12 | 26979309 | |||||||
| chr12:26979510 | C | T | 1 | a0004c0004t0016g0227 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1189+274G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 9/11 | chr12 | 26979510 | |||||||
| chr12:26979758 | C | CA | 94 | a0001c0001t0002g0099 a0001c0001t0002g0116 a0001c0001t0002g0141 others(91): Show |
104 | HG00099.hp2 HG00597.hp1 HG00642.hp2 others(101): Show |
intron_variant | MODIFIER | c.1189+25dupT | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 9/11 | chr12 | 26979758 | |||||||
| chr12:26979989 | C | T | 1 | a0001c0001t0030g0172 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1037-53G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 8/11 | chr12 | 26979989 | |||||||
| chr12:26980018 | G | C | 1 | a0001c0001t0017g0228 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1037-82C>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 8/11 | chr12 | 26980018 | |||||||
| chr12:26980060 | T | C | 35 | a0001c0001t0005g0107 a0001c0001t0005g0109 a0001c0001t0005g0114 others(32): Show |
39 | HG00597.hp1 HG01069.hp1 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.1037-124A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 8/11 | chr12 | 26980060 | |||||||
| chr12:26980134 | A | G | 1 | a0001c0001t0015g0089 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1037-198T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 8/11 | chr12 | 26980134 | |||||||
| chr12:26980150 | C | T | 1 | a0001c0001t0015g0089 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1037-214G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 8/11 | chr12 | 26980150 | |||||||
| chr12:26980292 | A | G | 1 | a0002c0002t0023g0363 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1036+274T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 8/11 | chr12 | 26980292 | |||||||
| chr12:26980516 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1036+50G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 8/11 | chr12 | 26980516 | |||||||
| chr12:26980835 | A | G | 1 | a0001c0001t0006g0080 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.956-189T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 7/11 | chr12 | 26980835 | |||||||
| chr12:26980894 | A | G | 1 | a0001c0001t0002g0327 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.956-248T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 7/11 | chr12 | 26980894 | |||||||
| chr12:26981142 | A | G | 2 | a0001c0001t0018g0135 a0001c0001t0018g0137 |
2 | HG02717.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.956-496T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 7/11 | chr12 | 26981142 | |||||||
| chr12:26981548 | C | T | 1 | a0002c0002t0005g0371 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.956-902G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 7/11 | chr12 | 26981548 | |||||||
| chr12:26981856 | A | G | 150 | a0001c0001t0002g0007 a0001c0001t0002g0031 a0001c0001t0002g0032 others(147): Show |
158 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.955+917T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 7/11 | chr12 | 26981856 | |||||||
| chr12:26981868 | T | C | 1 | a0001c0001t0001g0082 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.955+905A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 7/11 | chr12 | 26981868 | |||||||
| chr12:26981931 | A | G | 2 | a0001c0001t0002g0102 a0001c0001t0002g0103 |
2 | HG02602.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.955+842T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 7/11 | chr12 | 26981931 | |||||||
| chr12:26981981 | C | T | 2 | a0001c0001t0007g0014 a0001c0001t0007g0059 |
3 | HG01070.hp1 HG01071.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.955+792G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 7/11 | chr12 | 26981981 | |||||||
| chr12:26982426 | C | T | 1 | a0004c0004t0016g0227 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.955+347G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 7/11 | chr12 | 26982426 | |||||||
| chr12:26982472 | C | T | 1 | a0001c0001t0003g0117 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.955+301G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 7/11 | chr12 | 26982472 | |||||||
| chr12:26982498 | C | T | 2 | a0001c0001t0003g0115 a0001c0001t0003g0213 |
2 | NA18982.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.955+275G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 7/11 | chr12 | 26982498 | |||||||
| chr12:26982587 | C | T | 15 | a0001c0001t0002g0141 a0001c0001t0002g0143 a0001c0001t0002g0144 others(12): Show |
15 | NA18943.hp2 NA18946.hp1 NA18950.hp2 others(12): Show |
intron_variant | MODIFIER | c.955+186G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 7/11 | chr12 | 26982587 | |||||||
| chr12:26982736 | T | G | 57 | a0001c0001t0001g0105 a0001c0001t0002g0099 a0001c0001t0002g0116 others(54): Show |
63 | HG00099.hp2 HG00642.hp2 HG00738.hp1 others(60): Show |
intron_variant | MODIFIER | c.955+37A>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 7/11 | chr12 | 26982736 | |||||||
| chr12:26982861 | T | TA | 9 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0053 others(6): Show |
13 | HG00642.hp1 HG02109.hp1 HG02809.hp2 others(10): Show |
splice_region_variant&intron_variant | LOW | c.869-3dupT | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26982861 | |||||||
| chr12:26982969 | C | T | 9 | a0001c0001t0003g0129 a0001c0001t0004g0092 a0001c0001t0004g0094 others(6): Show |
9 | HG00558.hp1 HG00673.hp2 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.869-110G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26982969 | |||||||
| chr12:26982979 | T | C | 1 | a0001c0001t0001g0257 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.869-120A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26982979 | |||||||
| chr12:26982985 | A | G | 57 | a0001c0001t0001g0105 a0001c0001t0002g0099 a0001c0001t0002g0116 others(54): Show |
63 | HG00099.hp2 HG00642.hp2 HG00738.hp1 others(60): Show |
intron_variant | MODIFIER | c.869-126T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26982985 | |||||||
| chr12:26983247 | G | A | 1 | a0001c0001t0001g0036 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.869-388C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26983247 | |||||||
| chr12:26983320 | A | T | 1 | a0001c0001t0017g0228 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.869-461T>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26983320 | |||||||
| chr12:26983332 | ATTCAAAC others(6): Show |
A | 1 | a0001c0001t0003g0117 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.869-486_869-474del others(13): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26983332 | |||||||
| chr12:26983339 | C | T | 1 | a0001c0001t0017g0228 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.869-480G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26983339 | |||||||
| chr12:26983492 | C | G | 1 | a0001c0001t0002g0206 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.869-633G>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26983492 | |||||||
| chr12:26983635 | G | T | 1 | a0001c0001t0015g0089 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.869-776C>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26983635 | |||||||
| chr12:26983693 | G | T | 30 | a0001c0001t0006g0051 a0001c0001t0006g0052 a0001c0001t0006g0064 others(27): Show |
30 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.869-834C>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26983693 | |||||||
| chr12:26983721 | C | T | 3 | a0001c0001t0002g0146 a0001c0001t0002g0147 a0008c0008t0036g0142 |
3 | NA18979.hp2 NA19000.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.869-862G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26983721 | |||||||
| chr12:26983726 | A | G | 1 | a0001c0001t0015g0089 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.869-867T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26983726 | |||||||
| chr12:26984060 | C | T | 8 | a0001c0001t0001g0063 a0001c0001t0002g0062 a0001c0001t0007g0014 others(5): Show |
9 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(6): Show |
intron_variant | MODIFIER | c.869-1201G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26984060 | |||||||
| chr12:26984151 | C | T | 25 | a0002c0002t0001g0202 a0002c0002t0001g0203 a0002c0002t0001g0320 others(22): Show |
29 | HG00609.hp2 HG01069.hp1 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.869-1292G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26984151 | |||||||
| chr12:26984168 | G | A | 1 | a0001c0001t0030g0172 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.869-1309C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26984168 | |||||||
| chr12:26984205 | G | A | 1 | a0001c0001t0025g0060 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.869-1346C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26984205 | |||||||
| chr12:26984255 | A | C | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(130): Show |
171 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(168): Show |
intron_variant | MODIFIER | c.869-1396T>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26984255 | |||||||
| chr12:26984257 | C | T | 1 | a0004c0004t0016g0227 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.869-1398G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26984257 | |||||||
| chr12:26984300 | A | G | 1 | a0001c0001t0003g0054 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.869-1441T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26984300 | |||||||
| chr12:26984355 | G | A | 1 | a0001c0001t0001g0292 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.869-1496C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26984355 | |||||||
| chr12:26984406 | G | C | 2 | a0001c0001t0020g0343 a0001c0001t0020g0357 |
2 | HG02109.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.869-1547C>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26984406 | |||||||
| chr12:26984442 | C | T | 1 | a0002c0002t0023g0363 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.869-1583G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26984442 | |||||||
| chr12:26984449 | C | CA | 29 | a0001c0001t0006g0083 a0001c0001t0006g0170 a0001c0001t0015g0089 others(26): Show |
33 | HG00609.hp2 HG01069.hp1 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.869-1591dupT | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26984449 | |||||||
| chr12:26984449 | C | CAA | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(93): Show |
130 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.869-1592_869-1591d others(4): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26984449 | |||||||
| chr12:26984477 | C | T | 1 | a0001c0001t0004g0278 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.869-1618G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26984477 | |||||||
| chr12:26984550 | C | G | 1 | a0001c0001t0004g0171 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.869-1691G>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26984550 | |||||||
| chr12:26984639 | C | T | 1 | a0001c0001t0006g0072 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.869-1780G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26984639 | |||||||
| chr12:26984828 | G | A | 5 | a0001c0001t0002g0039 a0001c0001t0002g0045 a0001c0001t0002g0046 others(2): Show |
5 | HG00639.hp1 HG01243.hp1 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.869-1969C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26984828 | |||||||
| chr12:26984861 | C | T | 4 | a0001c0001t0003g0054 a0001c0001t0003g0085 a0001c0001t0003g0086 others(1): Show |
4 | HG02257.hp1 HG03471.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.869-2002G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26984861 | |||||||
| chr12:26985122 | C | T | 56 | a0001c0001t0001g0110 a0001c0001t0001g0121 a0001c0001t0001g0244 others(53): Show |
62 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.869-2263G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985122 | |||||||
| chr12:26985129 | A | G | 25 | a0002c0002t0001g0202 a0002c0002t0001g0203 a0002c0002t0001g0320 others(22): Show |
29 | HG00609.hp2 HG01069.hp1 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.869-2270T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985129 | |||||||
| chr12:26985201 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.869-2342C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985201 | |||||||
| chr12:26985367 | C | T | 4 | a0001c0001t0003g0054 a0001c0001t0003g0085 a0001c0001t0003g0086 others(1): Show |
4 | HG02257.hp1 HG03471.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.869-2508G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985367 | |||||||
| chr12:26985485 | T | C | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(243): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.869-2626A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985485 | |||||||
| chr12:26985621 | CA | C | 22 | a0001c0001t0002g0143 a0001c0001t0002g0146 a0001c0001t0002g0148 others(19): Show |
24 | HG01433.hp1 HG01943.hp1 HG02056.hp2 others(21): Show |
intron_variant | MODIFIER | c.869-2763delT | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985621 | |||||||
| chr12:26985621 | CAA | C | 26 | a0001c0001t0002g0144 a0001c0001t0002g0145 a0001c0001t0002g0147 others(23): Show |
27 | HG00558.hp1 HG00673.hp2 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.869-2764_869-2763d others(4): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985621 | |||||||
| chr12:26985621 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0010g0302 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.869-2773_869-2763d others(13): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985621 | |||||||
| chr12:26985621 | CAAAAAAA others(5): Show |
C | 5 | a0001c0001t0003g0086 a0001c0001t0005g0114 a0001c0001t0006g0078 others(2): Show |
5 | HG03471.hp2 HG04204.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.869-2774_869-2763d others(14): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985621 | |||||||
| chr12:26985621 | CAAAAAAA others(6): Show |
C | 6 | a0001c0001t0003g0054 a0001c0001t0003g0085 a0001c0001t0003g0117 others(3): Show |
6 | HG02257.hp1 HG02723.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.869-2775_869-2763d others(15): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985621 | |||||||
| chr12:26985621 | CAAAAAAA others(7): Show |
C | 7 | a0001c0001t0003g0016 a0001c0001t0003g0118 a0001c0001t0003g0124 others(4): Show |
8 | HG00099.hp2 HG01358.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.869-2776_869-2763d others(16): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985621 | |||||||
| chr12:26985621 | CAAAAAAA others(8): Show |
C | 1 | a0001c0001t0003g0220 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.869-2777_869-2763d others(17): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985621 | |||||||
| chr12:26985621 | CAAAAAAA others(9): Show |
C | 38 | a0001c0001t0001g0121 a0001c0001t0002g0099 a0001c0001t0002g0116 others(35): Show |
41 | HG00597.hp1 HG00642.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.869-2778_869-2763d others(18): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985621 | |||||||
| chr12:26985621 | CAAAAAAA others(10): Show |
C | 2 | a0001c0001t0003g0108 a0001c0001t0003g0111 |
2 | HG04204.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.869-2779_869-2763d others(19): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985621 | |||||||
| chr12:26985621 | CAAAAAAA others(11): Show |
C | 4 | a0001c0001t0006g0084 a0001c0001t0006g0315 a0001c0001t0006g0335 others(1): Show |
4 | HG01934.hp1 HG02015.hp2 HG02080.hp1 others(1): Show |
intron_variant | MODIFIER | c.869-2780_869-2763d others(20): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985621 | |||||||
| chr12:26985635 | AAAAAAAA others(12): Show |
A | 1 | a0001c0001t0016g0157 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.869-2795_869-2777d others(21): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985635 | |||||||
| chr12:26985636 | AAAAAAAA others(11): Show |
A | 14 | a0001c0001t0006g0051 a0001c0001t0006g0052 a0001c0001t0006g0057 others(11): Show |
14 | HG00140.hp2 HG00323.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.869-2795_869-2778d others(20): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985636 | |||||||
| chr12:26985637 | AAAAAAAA others(10): Show |
A | 1 | a0001c0001t0001g0110 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.869-2795_869-2779d others(19): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985637 | |||||||
| chr12:26985637 | AAAAAAAA others(12): Show |
A | 1 | a0001c0001t0030g0172 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.869-2797_869-2779d others(21): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985637 | |||||||
| chr12:26985638 | AAAAAAAA others(9): Show |
A | 8 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0138 others(5): Show |
10 | HG02074.hp1 HG02523.hp1 HG03669.hp1 others(7): Show |
intron_variant | MODIFIER | c.869-2795_869-2780d others(18): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985638 | |||||||
| chr12:26985638 | AAAAAAAA others(11): Show |
A | 6 | a0001c0001t0006g0056 a0001c0001t0006g0068 a0001c0001t0006g0080 others(3): Show |
6 | HG00733.hp1 HG01256.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.869-2797_869-2780d others(20): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985638 | |||||||
| chr12:26985638 | AAAAAAAA others(21): Show |
A | 1 | a0004c0004t0016g0227 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.869-2807_869-2780d others(30): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985638 | |||||||
| chr12:26985639 | AAAAAAAA others(10): Show |
A | 11 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(8): Show |
11 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.869-2797_869-2781d others(19): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985639 | |||||||
| chr12:26985639 | AAAAAAAA others(12): Show |
A | 1 | a0001c0001t0003g0065 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.869-2799_869-2781d others(21): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985639 | |||||||
| chr12:26985640 | AAAAAAAA others(9): Show |
A | 2 | a0001c0001t0001g0244 a0001c0001t0004g0100 |
2 | HG00544.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.869-2797_869-2782d others(18): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985640 | |||||||
| chr12:26985640 | AAAAAAAA others(11): Show |
A | 6 | a0001c0001t0001g0009 a0001c0001t0001g0067 a0001c0001t0001g0248 others(3): Show |
6 | HG02486.hp1 HG02922.hp1 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.869-2799_869-2782d others(20): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985640 | |||||||
| chr12:26985641 | AAAAAAAA others(8): Show |
A | 4 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0305 others(1): Show |
4 | HG00438.hp2 NA18939.hp2 NA19086.hp2 others(1): Show |
intron_variant | MODIFIER | c.869-2797_869-2783d others(17): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985641 | |||||||
| chr12:26985641 | AAAAAAAA others(10): Show |
A | 72 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(69): Show |
93 | HG00099.hp1 HG00280.hp2 HG00609.hp1 others(90): Show |
intron_variant | MODIFIER | c.869-2799_869-2783d others(19): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985641 | |||||||
| chr12:26985641 | AAAAAAAA others(12): Show |
A | 3 | a0002c0002t0005g0362 a0002c0002t0005g0364 a0002c0002t0022g0367 |
3 | NA18966.hp2 NA18992.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.869-2801_869-2783d others(21): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985641 | |||||||
| chr12:26985642 | AAAAAAAA others(9): Show |
A | 3 | a0001c0001t0001g0028 a0001c0001t0001g0275 a0001c0001t0001g0311 |
3 | HG00544.hp2 NA18943.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.869-2799_869-2784d others(18): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985642 | |||||||
| chr12:26985642 | AAAAAAAA others(11): Show |
A | 1 | a0001c0001t0001g0294 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.869-2801_869-2784d others(20): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985642 | |||||||
| chr12:26985642 | AAAAAAAA others(13): Show |
A | 1 | a0002c0002t0004g0368 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.869-2803_869-2784d others(22): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985642 | |||||||
| chr12:26985643 | AAAAAAAA others(8): Show |
A | 2 | a0001c0001t0001g0003 a0001c0001t0001g0196 |
3 | HG02602.hp1 NA18985.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.869-2799_869-2785d others(17): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985643 | |||||||
| chr12:26985643 | AAAAAAAA others(10): Show |
A | 10 | a0001c0001t0001g0001 a0001c0001t0001g0024 a0001c0001t0001g0027 others(7): Show |
10 | HG00597.hp2 HG01257.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.869-2801_869-2785d others(19): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985643 | |||||||
| chr12:26985643 | AAAAAAAA others(12): Show |
A | 19 | a0002c0002t0001g0202 a0002c0002t0001g0203 a0002c0002t0001g0320 others(16): Show |
22 | HG00609.hp2 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.869-2803_869-2785d others(21): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985643 | |||||||
| chr12:26985644 | AAAAAAAA others(3): Show |
A | 3 | a0001c0001t0001g0036 a0001c0001t0020g0343 a0001c0001t0020g0357 |
3 | HG01496.hp2 HG02109.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.869-2795_869-2786d others(12): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985644 | |||||||
| chr12:26985644 | AAAAAAAA others(9): Show |
A | 4 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0154 others(1): Show |
4 | HG02145.hp1 HG04199.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.869-2801_869-2786d others(18): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985644 | |||||||
| chr12:26985644 | AAAAAAAA others(11): Show |
A | 2 | a0002c0002t0005g0255 a0002c0002t0005g0361 |
2 | HG02027.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.869-2803_869-2786d others(20): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985644 | |||||||
| chr12:26985645 | AAAAAAAA others(10): Show |
A | 1 | a0001c0001t0001g0003 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.869-2803_869-2787d others(19): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985645 | |||||||
| chr12:26985645 | AAAAAAAA others(12): Show |
A | 1 | a0002c0002t0005g0013 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.869-2805_869-2787d others(21): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985645 | |||||||
| chr12:26985646 | A | T | 2 | a0001c0001t0002g0181 a0001c0001t0027g0232 |
2 | HG02922.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.869-2787T>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985646 | |||||||
| chr12:26985648 | A | ATAT | 9 | a0001c0001t0001g0023 a0001c0001t0002g0031 a0001c0001t0002g0032 others(6): Show |
11 | HG00733.hp2 HG00741.hp2 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.869-2790_869-2789i others(5): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985648 | |||||||
| chr12:26985648 | A | T | 5 | a0001c0001t0002g0048 a0001c0001t0002g0181 a0001c0001t0003g0124 others(2): Show |
5 | HG01358.hp1 HG02523.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.869-2789T>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985648 | |||||||
| chr12:26985650 | A | ATAT | 4 | a0001c0001t0002g0178 a0001c0001t0002g0324 a0001c0001t0002g0328 others(1): Show |
4 | HG02004.hp1 HG02300.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.869-2792_869-2791i others(5): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985650 | |||||||
| chr12:26985650 | A | T | 36 | a0001c0001t0001g0023 a0001c0001t0002g0007 a0001c0001t0002g0031 others(33): Show |
38 | HG00558.hp2 HG00733.hp2 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.869-2791T>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985650 | |||||||
| chr12:26985652 | A | AAAATATA others(5): Show |
2 | a0003c0003t0009g0010 a0003c0003t0009g0022 |
4 | HG02451.hp1 HG03516.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.869-2794_869-2793i others(14): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985652 | |||||||
| chr12:26985652 | A | AAATATAT others(4): Show |
1 | a0003c0003t0009g0022 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.869-2794_869-2793i others(13): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985652 | |||||||
| chr12:26985652 | A | ATATATAT others(4): Show |
1 | a0003c0003t0009g0236 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.869-2794_869-2793i others(13): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985652 | |||||||
| chr12:26985652 | A | ATATATAT others(6): Show |
1 | a0003c0003t0009g0235 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.869-2794_869-2793i others(15): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985652 | |||||||
| chr12:26985652 | A | T | 80 | a0001c0001t0001g0023 a0001c0001t0001g0207 a0001c0001t0001g0257 others(77): Show |
86 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.869-2793T>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985652 | |||||||
| chr12:26985652 | AAT | A | 7 | a0001c0001t0001g0034 a0001c0001t0002g0141 a0001c0001t0004g0040 others(4): Show |
8 | HG01168.hp1 HG01169.hp1 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.869-2795_869-2794d others(4): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985652 | |||||||
| chr12:26985653 | AT | A | 4 | a0001c0001t0002g0149 a0001c0001t0004g0131 a0001c0001t0004g0205 others(1): Show |
4 | NA18973.hp2 NA18991.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.869-2795delA | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985653 | |||||||
| chr12:26985654 | T | A | 4 | a0001c0001t0002g0102 a0001c0001t0008g0033 a0001c0001t0008g0226 others(1): Show |
4 | HG03130.hp1 HG03225.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.869-2795A>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985654 | |||||||
| chr12:26985656 | T | A | 1 | a0001c0001t0004g0280 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.869-2797A>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985656 | |||||||
| chr12:26985658 | T | A | 1 | a0001c0001t0008g0336 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.869-2799A>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985658 | |||||||
| chr12:26985678 | T | C | 6 | a0001c0001t0007g0299 a0001c0001t0027g0232 a0003c0003t0009g0010 others(3): Show |
9 | HG02451.hp1 HG02818.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.869-2819A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985678 | |||||||
| chr12:26985678 | T | TATATATA others(5): Show |
1 | a0003c0003t0009g0234 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.869-2820_869-2819i others(14): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985678 | |||||||
| chr12:26985678 | T | TATATATA others(7): Show |
1 | a0003c0003t0009g0233 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.869-2820_869-2819i others(16): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985678 | |||||||
| chr12:26985680 | C | T | 90 | a0001c0001t0001g0110 a0001c0001t0001g0121 a0001c0001t0001g0244 others(87): Show |
96 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.869-2821G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985680 | |||||||
| chr12:26985806 | G | GT | 84 | a0001c0001t0001g0036 a0001c0001t0001g0063 a0001c0001t0001g0110 others(81): Show |
93 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.869-2948dupA | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985806 | |||||||
| chr12:26985806 | G | GTT | 107 | a0001c0001t0001g0023 a0001c0001t0001g0207 a0001c0001t0001g0257 others(104): Show |
116 | HG00140.hp1 HG00438.hp1 HG00621.hp1 others(113): Show |
intron_variant | MODIFIER | c.869-2949_869-2948d others(4): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985806 | |||||||
| chr12:26985806 | G | GTTT | 7 | a0001c0001t0002g0043 a0001c0001t0002g0146 a0001c0001t0002g0182 others(4): Show |
7 | HG00735.hp2 HG00738.hp1 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.869-2950_869-2948d others(5): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985806 | |||||||
| chr12:26985806 | G | GTTTTT | 7 | a0002c0002t0001g0202 a0002c0002t0004g0368 a0002c0002t0005g0356 others(4): Show |
7 | HG01069.hp1 NA18969.hp1 NA18989.hp1 others(4): Show |
intron_variant | MODIFIER | c.869-2952_869-2948d others(7): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985806 | |||||||
| chr12:26985806 | G | GTTTTTT | 17 | a0002c0002t0001g0203 a0002c0002t0001g0320 a0002c0002t0005g0013 others(14): Show |
21 | HG00609.hp2 HG01071.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.869-2953_869-2948d others(8): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985806 | |||||||
| chr12:26985806 | GT | G | 60 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(57): Show |
76 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.869-2948delA | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985806 | |||||||
| chr12:26985806 | GTT | G | 50 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(47): Show |
68 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.869-2949_869-2948d others(4): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985806 | |||||||
| chr12:26985845 | G | C | 15 | a0001c0001t0001g0015 a0001c0001t0001g0025 a0001c0001t0001g0028 others(12): Show |
18 | HG00438.hp2 HG00544.hp2 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.869-2986C>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985845 | |||||||
| chr12:26985888 | A | ACTGCCAG | 128 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(125): Show |
166 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(163): Show |
intron_variant | MODIFIER | c.869-3036_869-3030d others(9): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985888 | |||||||
| chr12:26985929 | T | C | 1 | a0001c0001t0003g0117 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.869-3070A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985929 | |||||||
| chr12:26985946 | A | G | 26 | a0001c0001t0004g0127 a0002c0002t0001g0202 a0002c0002t0001g0203 others(23): Show |
30 | HG00609.hp2 HG01069.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.869-3087T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985946 | |||||||
| chr12:26985968 | C | T | 1 | a0001c0001t0001g0186 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.869-3109G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985968 | |||||||
| chr12:26985981 | G | A | 2 | a0002c0002t0014g0345 a0002c0002t0014g0354 |
2 | HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.869-3122C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985981 | |||||||
| chr12:26985998 | G | GT | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(93): Show |
128 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.869-3140dupA | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985998 | |||||||
| chr12:26985998 | G | GTT | 4 | a0001c0001t0013g0012 a0001c0001t0013g0306 a0001c0001t0015g0089 others(1): Show |
6 | HG02572.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.869-3141_869-3140d others(4): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26985998 | |||||||
| chr12:26986018 | C | T | 241 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(238): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.869-3159G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26986018 | |||||||
| chr12:26986029 | T | C | 1 | a0001c0001t0002g0181 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.869-3170A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26986029 | |||||||
| chr12:26986123 | C | T | 9 | a0001c0001t0015g0087 a0001c0001t0015g0088 a0001c0001t0027g0232 others(6): Show |
12 | HG02257.hp2 HG02451.hp1 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.869-3264G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26986123 | |||||||
| chr12:26986124 | G | A | 1 | a0001c0001t0019g0259 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.869-3265C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26986124 | |||||||
| chr12:26986175 | C | T | 6 | a0003c0003t0009g0010 a0003c0003t0009g0022 a0003c0003t0009g0233 others(3): Show |
9 | HG02451.hp1 HG02886.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.869-3316G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26986175 | |||||||
| chr12:26986383 | C | A | 2 | a0001c0001t0015g0087 a0001c0001t0015g0088 |
2 | HG02257.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.869-3524G>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26986383 | |||||||
| chr12:26986405 | C | T | 1 | a0001c0001t0007g0058 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.869-3546G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26986405 | |||||||
| chr12:26986541 | C | T | 3 | a0001c0001t0008g0091 a0001c0001t0008g0336 a0001c0001t0008g0337 |
3 | HG01123.hp2 HG01175.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.869-3682G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26986541 | |||||||
| chr12:26986618 | G | A | 4 | a0001c0001t0003g0054 a0001c0001t0003g0085 a0001c0001t0003g0086 others(1): Show |
4 | HG02257.hp1 HG03471.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.869-3759C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26986618 | |||||||
| chr12:26986790 | C | T | 1 | a0001c0001t0004g0205 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.868+3660G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26986790 | |||||||
| chr12:26986791 | T | A | 2 | a0001c0001t0026g0159 a0001c0001t0028g0160 |
2 | HG02055.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.868+3659A>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26986791 | |||||||
| chr12:26986928 | T | G | 2 | a0001c0001t0020g0343 a0001c0001t0020g0357 |
2 | HG02109.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.868+3522A>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26986928 | |||||||
| chr12:26986994 | C | T | 6 | a0003c0003t0009g0010 a0003c0003t0009g0022 a0003c0003t0009g0233 others(3): Show |
9 | HG02451.hp1 HG02886.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.868+3456G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26986994 | |||||||
| chr12:26987019 | T | C | 1 | a0002c0002t0005g0362 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.868+3431A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26987019 | |||||||
| chr12:26987044 | G | T | 2 | a0001c0001t0020g0343 a0001c0001t0020g0357 |
2 | HG02109.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.868+3406C>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26987044 | |||||||
| chr12:26987054 | T | A | 25 | a0002c0002t0001g0202 a0002c0002t0001g0203 a0002c0002t0001g0320 others(22): Show |
29 | HG00609.hp2 HG01069.hp1 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.868+3396A>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26987054 | |||||||
| chr12:26987104 | C | A | 4 | a0001c0001t0003g0054 a0001c0001t0003g0085 a0001c0001t0003g0086 others(1): Show |
4 | HG02257.hp1 HG03471.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.868+3346G>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26987104 | |||||||
| chr12:26987335 | C | A | 1 | a0002c0002t0005g0321 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.868+3115G>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26987335 | |||||||
| chr12:26987426 | C | A | 7 | a0001c0001t0004g0359 a0001c0001t0020g0343 a0001c0001t0020g0357 others(4): Show |
7 | HG00738.hp1 HG02109.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.868+3024G>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26987426 | |||||||
| chr12:26987593 | T | C | 2 | a0001c0001t0006g0158 a0001c0001t0016g0157 |
2 | HG02647.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.868+2857A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26987593 | |||||||
| chr12:26987616 | C | T | 6 | a0001c0001t0010g0217 a0001c0001t0010g0252 a0001c0001t0010g0301 others(3): Show |
6 | HG00280.hp2 HG01175.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.868+2834G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26987616 | |||||||
| chr12:26988062 | TA | T | 12 | a0001c0001t0001g0214 a0001c0001t0003g0104 a0001c0001t0004g0216 others(9): Show |
12 | HG01256.hp1 HG01993.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.868+2387delT | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26988062 | |||||||
| chr12:26988177 | C | T | 4 | a0001c0001t0003g0054 a0001c0001t0003g0085 a0001c0001t0003g0086 others(1): Show |
4 | HG02257.hp1 HG03471.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.868+2273G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26988177 | |||||||
| chr12:26988212 | G | C | 33 | a0001c0001t0001g0036 a0001c0001t0006g0051 a0001c0001t0006g0052 others(30): Show |
33 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.868+2238C>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26988212 | |||||||
| chr12:26988231 | C | T | 2 | a0001c0001t0015g0087 a0001c0001t0015g0088 |
2 | HG02257.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.868+2219G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26988231 | |||||||
| chr12:26988281 | A | G | 1 | a0001c0001t0006g0158 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.868+2169T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26988281 | |||||||
| chr12:26988462 | C | T | 4 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0138 others(1): Show |
6 | NA18947.hp2 NA18951.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.868+1988G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26988462 | |||||||
| chr12:26988471 | A | T | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(121): Show |
162 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(159): Show |
intron_variant | MODIFIER | c.868+1979T>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26988471 | |||||||
| chr12:26988484 | T | C | 1 | a0001c0001t0001g0244 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.868+1966A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26988484 | |||||||
| chr12:26988628 | T | C | 2 | a0001c0001t0002g0178 a0001c0001t0002g0192 |
2 | HG02055.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.868+1822A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26988628 | |||||||
| chr12:26988672 | T | TTG | 10 | a0001c0001t0001g0318 a0001c0001t0002g0328 a0001c0001t0004g0300 others(7): Show |
10 | HG01256.hp1 HG02004.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.868+1776_868+1777d others(4): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26988672 | |||||||
| chr12:26988672 | T | TTGTG | 17 | a0001c0001t0003g0005 a0001c0001t0003g0095 a0001c0001t0003g0096 others(14): Show |
19 | HG00642.hp2 HG01255.hp2 HG02015.hp2 others(16): Show |
intron_variant | MODIFIER | c.868+1774_868+1777d others(6): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26988672 | |||||||
| chr12:26988672 | T | TTGTGTG | 24 | a0001c0001t0003g0021 a0001c0001t0003g0151 a0001c0001t0003g0219 others(21): Show |
25 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.868+1772_868+1777d others(8): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26988672 | |||||||
| chr12:26988672 | T | TTGTGTGT others(1): Show |
50 | a0001c0001t0001g0036 a0001c0001t0001g0097 a0001c0001t0001g0098 others(47): Show |
52 | HG00544.hp1 HG00597.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.868+1770_868+1777d others(10): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26988672 | |||||||
| chr12:26988672 | T | TTGTGTGT others(3): Show |
12 | a0001c0001t0002g0116 a0001c0001t0002g0150 a0001c0001t0003g0054 others(9): Show |
12 | HG02129.hp1 HG02257.hp1 HG02523.hp1 others(9): Show |
intron_variant | MODIFIER | c.868+1768_868+1777d others(12): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26988672 | |||||||
| chr12:26988672 | T | TTGTGTGT others(5): Show |
7 | a0001c0001t0003g0016 a0001c0001t0003g0065 a0001c0001t0003g0086 others(4): Show |
8 | HG00099.hp2 HG02615.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.868+1766_868+1777d others(14): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26988672 | |||||||
| chr12:26988672 | T | TTGTGTGT others(7): Show |
1 | a0001c0001t0003g0165 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.868+1764_868+1777d others(16): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26988672 | |||||||
| chr12:26988672 | TTG | T | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(146): Show |
188 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.868+1776_868+1777d others(4): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26988672 | |||||||
| chr12:26988672 | TTGTG | T | 25 | a0001c0001t0001g0319 a0002c0002t0001g0202 a0002c0002t0001g0203 others(22): Show |
29 | HG00609.hp2 HG01069.hp1 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.868+1774_868+1777d others(6): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26988672 | |||||||
| chr12:26989008 | T | C | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(118): Show |
159 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(156): Show |
intron_variant | MODIFIER | c.868+1442A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26989008 | |||||||
| chr12:26989054 | C | T | 2 | a0001c0001t0008g0091 a0001c0001t0008g0336 |
2 | HG01123.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.868+1396G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26989054 | |||||||
| chr12:26989092 | G | A | 2 | a0001c0001t0003g0162 a0001c0001t0016g0101 |
2 | HG02074.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.868+1358C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26989092 | |||||||
| chr12:26989144 | G | A | 9 | a0001c0001t0002g0007 a0001c0001t0002g0174 a0001c0001t0002g0182 others(6): Show |
11 | NA18941.hp2 NA18942.hp2 NA18953.hp2 others(8): Show |
intron_variant | MODIFIER | c.868+1306C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26989144 | |||||||
| chr12:26989253 | T | C | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(93): Show |
130 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.868+1197A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26989253 | |||||||
| chr12:26989465 | G | A | 320 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(317): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.868+985C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26989465 | |||||||
| chr12:26989668 | T | C | 90 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(87): Show |
122 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.868+782A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26989668 | |||||||
| chr12:26989668 | T | TAC | 59 | a0001c0001t0001g0023 a0001c0001t0001g0207 a0001c0001t0001g0257 others(56): Show |
64 | HG00438.hp1 HG00558.hp2 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.868+780_868+781dup others(2): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26989668 | |||||||
| chr12:26989668 | T | TACAC | 58 | a0001c0001t0002g0141 a0001c0001t0002g0143 a0001c0001t0002g0144 others(55): Show |
61 | HG00558.hp1 HG00673.hp2 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.868+778_868+781dup others(4): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26989668 | |||||||
| chr12:26989898 | A | G | 1 | a0001c0001t0006g0064 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.868+552T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26989898 | |||||||
| chr12:26990083 | T | C | 238 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(235): Show |
284 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(281): Show |
intron_variant | MODIFIER | c.868+367A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26990083 | |||||||
| chr12:26990160 | G | A | 1 | a0001c0001t0002g0358 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.868+290C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26990160 | |||||||
| chr12:26990370 | T | C | 1 | a0001c0001t0006g0080 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.868+80A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 6/11 | chr12 | 26990370 | |||||||
| chr12:26990646 | C | T | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(93): Show |
130 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.691-19G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26990646 | |||||||
| chr12:26990646 | CAT | C | 3 | a0001c0001t0027g0232 a0002c0002t0014g0345 a0002c0002t0014g0354 |
3 | HG02723.hp2 HG02922.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.691-21_691-20delAT | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26990646 | |||||||
| chr12:26990699 | C | T | 92 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(89): Show |
126 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.691-72G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26990699 | |||||||
| chr12:26991059 | G | A | 5 | a0001c0001t0003g0065 a0001c0001t0014g0090 a0001c0001t0015g0087 others(2): Show |
5 | HG02257.hp2 HG02886.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.691-432C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26991059 | |||||||
| chr12:26991089 | A | G | 25 | a0002c0002t0001g0202 a0002c0002t0001g0203 a0002c0002t0001g0320 others(22): Show |
29 | HG00609.hp2 HG01069.hp1 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.691-462T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26991089 | |||||||
| chr12:26991139 | T | C | 1 | a0001c0001t0002g0212 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.691-512A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26991139 | |||||||
| chr12:26991141 | C | CT | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(114): Show |
155 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(152): Show |
intron_variant | MODIFIER | c.691-515dupA | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26991141 | |||||||
| chr12:26991141 | C | CTT | 12 | a0001c0001t0001g0185 a0001c0001t0001g0244 a0001c0001t0001g0261 others(9): Show |
12 | HG00642.hp1 HG02723.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.691-516_691-515dup others(2): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26991141 | |||||||
| chr12:26991141 | CT | C | 6 | a0001c0001t0001g0063 a0001c0001t0001g0318 a0001c0001t0002g0047 others(3): Show |
6 | HG00280.hp1 HG00323.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.691-515delA | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26991141 | |||||||
| chr12:26991141 | CTTTTTTT others(2): Show |
C | 6 | a0001c0001t0020g0343 a0001c0001t0020g0357 a0001c0001t0027g0232 others(3): Show |
6 | HG00738.hp1 HG02109.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.691-523_691-515del others(9): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26991141 | |||||||
| chr12:26991176 | C | T | 8 | a0001c0001t0001g0063 a0001c0001t0002g0062 a0001c0001t0007g0014 others(5): Show |
9 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(6): Show |
intron_variant | MODIFIER | c.691-549G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26991176 | |||||||
| chr12:26991242 | T | C | 69 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0105 others(66): Show |
75 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.691-615A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26991242 | |||||||
| chr12:26991253 | C | T | 3 | a0001c0001t0027g0232 a0002c0002t0014g0345 a0002c0002t0014g0354 |
3 | HG02723.hp2 HG02922.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.691-626G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26991253 | |||||||
| chr12:26991301 | C | T | 1 | a0001c0001t0001g0287 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.691-674G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26991301 | |||||||
| chr12:26991302 | G | A | 70 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0105 others(67): Show |
76 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.691-675C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26991302 | |||||||
| chr12:26991320 | T | C | 25 | a0002c0002t0001g0202 a0002c0002t0001g0203 a0002c0002t0001g0320 others(22): Show |
29 | HG00609.hp2 HG01069.hp1 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.691-693A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26991320 | |||||||
| chr12:26991373 | C | T | 1 | a0001c0001t0027g0232 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.691-746G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26991373 | |||||||
| chr12:26991379 | C | T | 1 | a0001c0001t0017g0312 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.691-752G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26991379 | |||||||
| chr12:26991418 | C | CTGGGATT others(4): Show |
1 | a0002c0002t0012g0370 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.691-802_691-792dup others(11): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26991418 | |||||||
| chr12:26991527 | C | T | 25 | a0002c0002t0001g0202 a0002c0002t0001g0203 a0002c0002t0001g0320 others(22): Show |
29 | HG00609.hp2 HG01069.hp1 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.691-900G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26991527 | |||||||
| chr12:26991629 | G | A | 2 | a0001c0001t0004g0197 a0001c0001t0035g0038 |
2 | HG03017.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.691-1002C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26991629 | |||||||
| chr12:26991793 | C | T | 1 | a0001c0001t0001g0286 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.691-1166G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26991793 | |||||||
| chr12:26991865 | G | C | 3 | a0001c0001t0018g0135 a0001c0001t0018g0136 a0001c0001t0018g0137 |
3 | HG02717.hp1 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.691-1238C>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26991865 | |||||||
| chr12:26991904 | C | A | 1 | a0008c0008t0036g0142 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.691-1277G>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26991904 | |||||||
| chr12:26991905 | A | C | 1 | a0008c0008t0036g0142 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.691-1278T>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26991905 | |||||||
| chr12:26991906 | C | A | 1 | a0008c0008t0036g0142 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.691-1279G>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26991906 | |||||||
| chr12:26991947 | C | T | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(93): Show |
130 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.691-1320G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26991947 | |||||||
| chr12:26992001 | T | A | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(93): Show |
130 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.691-1374A>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26992001 | |||||||
| chr12:26992156 | G | A | 1 | a0001c0001t0004g0167 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.691-1529C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26992156 | |||||||
| chr12:26992225 | G | T | 1 | a0001c0001t0001g0082 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.691-1598C>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26992225 | |||||||
| chr12:26992270 | T | A | 10 | a0001c0001t0001g0063 a0001c0001t0002g0062 a0001c0001t0006g0056 others(7): Show |
11 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(8): Show |
intron_variant | MODIFIER | c.691-1643A>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26992270 | |||||||
| chr12:26992273 | A | T | 4 | a0001c0001t0003g0065 a0001c0001t0004g0171 a0001c0001t0014g0090 others(1): Show |
4 | HG02886.hp2 HG03453.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.691-1646T>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26992273 | |||||||
| chr12:26992364 | T | C | 4 | a0001c0001t0001g0028 a0001c0001t0001g0267 a0001c0001t0001g0268 others(1): Show |
5 | HG00438.hp2 HG00544.hp2 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.691-1737A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26992364 | |||||||
| chr12:26992428 | G | A | 1 | a0001c0001t0001g0294 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.691-1801C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26992428 | |||||||
| chr12:26992506 | G | A | 1 | a0001c0001t0004g0130 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.691-1879C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26992506 | |||||||
| chr12:26992576 | G | A | 1 | a0001c0001t0005g0249 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.691-1949C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26992576 | |||||||
| chr12:26992580 | G | A | 2 | a0001c0001t0015g0087 a0001c0001t0015g0088 |
2 | HG02257.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.691-1953C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26992580 | |||||||
| chr12:26992654 | G | A | 2 | a0001c0001t0001g0063 a0001c0001t0002g0062 |
2 | HG00280.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.691-2027C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26992654 | |||||||
| chr12:26992659 | C | T | 1 | a0001c0001t0020g0343 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.691-2032G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26992659 | |||||||
| chr12:26992666 | C | T | 1 | a0001c0001t0006g0080 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.691-2039G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26992666 | |||||||
| chr12:26992668 | G | A | 1 | a0001c0001t0006g0247 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.691-2041C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26992668 | |||||||
| chr12:26992864 | T | C | 92 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(89): Show |
126 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.691-2237A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26992864 | |||||||
| chr12:26992905 | C | CT | 51 | a0001c0001t0001g0207 a0001c0001t0001g0229 a0001c0001t0001g0238 others(48): Show |
51 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.691-2279dupA | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26992905 | |||||||
| chr12:26992905 | C | CTT | 70 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0105 others(67): Show |
76 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.691-2280_691-2279d others(4): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26992905 | |||||||
| chr12:26992905 | CT | C | 36 | a0001c0001t0004g0205 a0001c0001t0013g0012 a0001c0001t0013g0306 others(33): Show |
45 | HG00609.hp2 HG01069.hp1 HG01071.hp1 others(42): Show |
intron_variant | MODIFIER | c.691-2279delA | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26992905 | |||||||
| chr12:26992905 | CTT | C | 12 | a0001c0001t0004g0359 a0001c0001t0015g0089 a0001c0001t0017g0228 others(9): Show |
12 | HG00738.hp1 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.691-2280_691-2279d others(4): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26992905 | |||||||
| chr12:26992980 | G | A | 1 | a0001c0001t0006g0170 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.690+2257C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26992980 | |||||||
| chr12:26993108 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.690+2129C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26993108 | |||||||
| chr12:26993509 | A | G | 326 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(323): Show |
382 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(379): Show |
intron_variant | MODIFIER | c.690+1728T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26993509 | |||||||
| chr12:26993586 | C | A | 1 | a0001c0001t0002g0062 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.690+1651G>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26993586 | |||||||
| chr12:26993645 | C | T | 1 | a0001c0001t0029g0297 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.690+1592G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26993645 | |||||||
| chr12:26994084 | T | A | 306 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(303): Show |
361 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(358): Show |
intron_variant | MODIFIER | c.690+1153A>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26994084 | |||||||
| chr12:26994146 | G | A | 1 | a0001c0001t0004g0295 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.690+1091C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26994146 | |||||||
| chr12:26994307 | G | T | 2 | a0002c0002t0014g0345 a0002c0002t0014g0354 |
2 | HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.690+930C>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26994307 | |||||||
| chr12:26994422 | T | C | 26 | a0001c0001t0035g0038 a0002c0002t0001g0202 a0002c0002t0001g0203 others(23): Show |
30 | HG00609.hp2 HG01069.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.690+815A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26994422 | |||||||
| chr12:26994578 | C | T | 1 | a0001c0001t0027g0232 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.690+659G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26994578 | |||||||
| chr12:26994672 | C | G | 5 | a0001c0001t0003g0054 a0001c0001t0003g0085 a0001c0001t0003g0086 others(2): Show |
5 | HG00738.hp1 HG02257.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.690+565G>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26994672 | |||||||
| chr12:26994951 | G | A | 1 | a0001c0001t0010g0302 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.690+286C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26994951 | |||||||
| chr12:26994967 | C | T | 2 | a0001c0001t0001g0303 a0001c0001t0001g0304 |
2 | HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.690+270G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26994967 | |||||||
| chr12:26995181 | C | T | 1 | a0001c0001t0002g0050 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.690+56G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 5/11 | chr12 | 26995181 | |||||||
| chr12:26995464 | TA | T | 5 | a0001c0001t0003g0054 a0001c0001t0003g0085 a0001c0001t0003g0086 others(2): Show |
5 | HG00738.hp1 HG02257.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.519-57delT | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 4/11 | chr12 | 26995464 | |||||||
| chr12:26995578 | T | C | 3 | a0001c0001t0018g0135 a0001c0001t0018g0136 a0001c0001t0018g0137 |
3 | HG02717.hp1 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.519-170A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 4/11 | chr12 | 26995578 | |||||||
| chr12:26995797 | C | T | 2 | a0001c0001t0003g0065 a0001c0001t0014g0090 |
2 | HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.519-389G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 4/11 | chr12 | 26995797 | |||||||
| chr12:26995930 | A | T | 26 | a0001c0001t0035g0038 a0002c0002t0001g0202 a0002c0002t0001g0203 others(23): Show |
30 | HG00609.hp2 HG01069.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.519-522T>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 4/11 | chr12 | 26995930 | |||||||
| chr12:26996008 | G | A | 357 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(354): Show |
413 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(410): Show |
intron_variant | MODIFIER | c.519-600C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 4/11 | chr12 | 26996008 | |||||||
| chr12:26996016 | A | T | 1 | a0006c0007t0004g0347 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.519-608T>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 4/11 | chr12 | 26996016 | |||||||
| chr12:26996024 | T | A | 2 | a0001c0001t0004g0140 a0001c0001t0037g0139 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.519-616A>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 4/11 | chr12 | 26996024 | |||||||
| chr12:26996025 | A | T | 1 | a0001c0001t0002g0206 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.519-617T>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 4/11 | chr12 | 26996025 | |||||||
| chr12:26996153 | TA | T | 7 | a0001c0001t0003g0198 a0001c0001t0005g0225 a0001c0001t0017g0312 others(4): Show |
7 | HG02723.hp2 HG02897.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.518+588delT | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 4/11 | chr12 | 26996153 | |||||||
| chr12:26996317 | C | T | 6 | a0001c0001t0010g0217 a0001c0001t0010g0252 a0001c0001t0010g0301 others(3): Show |
6 | HG00280.hp2 HG01175.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.518+425G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 4/11 | chr12 | 26996317 | |||||||
| chr12:26996376 | G | T | 6 | a0001c0001t0002g0039 a0001c0001t0002g0044 a0001c0001t0002g0045 others(3): Show |
6 | HG00639.hp1 HG00738.hp2 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.518+366C>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 4/11 | chr12 | 26996376 | |||||||
| chr12:26996535 | A | G | 1 | a0001c0001t0002g0206 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.518+207T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 4/11 | chr12 | 26996535 | |||||||
| chr12:26996624 | C | A | 2 | a0002c0002t0014g0345 a0002c0002t0014g0354 |
2 | HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.518+118G>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 4/11 | chr12 | 26996624 | |||||||
| chr12:26996973 | A | G | 4 | a0001c0001t0015g0089 a0001c0001t0017g0228 a0001c0001t0026g0159 others(1): Show |
4 | HG02055.hp1 HG02145.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.398-111T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 3/11 | chr12 | 26996973 | |||||||
| chr12:26996981 | C | T | 1 | a0001c0001t0002g0326 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.398-119G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 3/11 | chr12 | 26996981 | |||||||
| chr12:26997095 | T | C | 1 | a0001c0001t0001g0310 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.398-233A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 3/11 | chr12 | 26997095 | |||||||
| chr12:26997177 | A | G | 114 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(111): Show |
143 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(140): Show |
intron_variant | MODIFIER | c.398-315T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 3/11 | chr12 | 26997177 | |||||||
| chr12:26997330 | G | A | 1 | a0001c0001t0003g0120 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.398-468C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 3/11 | chr12 | 26997330 | |||||||
| chr12:26997479 | T | C | 1 | a0001c0001t0004g0131 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.398-617A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 3/11 | chr12 | 26997479 | |||||||
| chr12:26997481 | T | C | 3 | a0001c0001t0006g0077 a0001c0001t0006g0078 a0001c0001t0006g0079 |
3 | HG03669.hp2 HG04204.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.398-619A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 3/11 | chr12 | 26997481 | |||||||
| chr12:26997546 | G | C | 100 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(97): Show |
129 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.398-684C>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 3/11 | chr12 | 26997546 | |||||||
| chr12:26997823 | C | CT | 18 | a0001c0001t0001g0015 a0001c0001t0003g0017 a0001c0001t0003g0018 others(15): Show |
21 | HG00544.hp1 HG00673.hp1 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.398-962dupA | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 3/11 | chr12 | 26997823 | |||||||
| chr12:26997823 | C | CTTT | 81 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0053 others(78): Show |
92 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.398-964_398-962dup others(3): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 3/11 | chr12 | 26997823 | |||||||
| chr12:26997823 | CT | C | 160 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(157): Show |
193 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.398-962delA | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 3/11 | chr12 | 26997823 | |||||||
| chr12:26997853 | TCTTGCTC others(11): Show |
T | 1 | a0001c0001t0004g0359 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.398-1009_398-992de others(19): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 3/11 | chr12 | 26997853 | |||||||
| chr12:26997940 | C | T | 1 | a0001c0001t0002g0325 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.398-1078G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 3/11 | chr12 | 26997940 | |||||||
| chr12:26997984 | CCTGA | C | 21 | a0001c0001t0003g0129 a0001c0001t0004g0006 a0001c0001t0004g0019 others(18): Show |
24 | HG00558.hp1 HG00673.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.398-1126_398-1123d others(6): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 3/11 | chr12 | 26997984 | |||||||
| chr12:26998123 | G | A | 2 | a0001c0001t0015g0087 a0001c0001t0015g0088 |
2 | HG02257.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.398-1261C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 3/11 | chr12 | 26998123 | |||||||
| chr12:26998385 | C | T | 1 | a0001c0001t0004g0171 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.397+1141G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 3/11 | chr12 | 26998385 | |||||||
| chr12:26998457 | G | A | 3 | a0001c0001t0027g0232 a0002c0002t0014g0345 a0002c0002t0014g0354 |
3 | HG02723.hp2 HG02922.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.397+1069C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 3/11 | chr12 | 26998457 | |||||||
| chr12:26998747 | A | G | 127 | a0001c0001t0001g0015 a0001c0001t0001g0063 a0001c0001t0001g0097 others(124): Show |
142 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.397+779T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 3/11 | chr12 | 26998747 | |||||||
| chr12:26998856 | G | T | 1 | a0001c0001t0002g0324 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.397+670C>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 3/11 | chr12 | 26998856 | |||||||
| chr12:26998888 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.397+638G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 3/11 | chr12 | 26998888 | |||||||
| chr12:26998958 | C | T | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(228): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.397+568G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 3/11 | chr12 | 26998958 | |||||||
| chr12:26999338 | G | C | 1 | a0001c0001t0004g0296 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.397+188C>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 3/11 | chr12 | 26999338 | |||||||
| chr12:26999395 | C | CA | 115 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0015 others(112): Show |
139 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(136): Show |
intron_variant | MODIFIER | c.397+130dupT | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 3/11 | chr12 | 26999395 | |||||||
| chr12:26999395 | CA | C | 21 | a0001c0001t0001g0036 a0001c0001t0006g0051 a0001c0001t0006g0052 others(18): Show |
21 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.397+130delT | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 3/11 | chr12 | 26999395 | |||||||
| chr12:26999411 | G | A | 1 | a0001c0001t0004g0359 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.397+115C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 3/11 | chr12 | 26999411 | |||||||
| chr12:26999446 | A | G | 3 | a0001c0001t0027g0232 a0002c0002t0014g0345 a0002c0002t0014g0354 |
3 | HG02723.hp2 HG02922.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.397+80T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 3/11 | chr12 | 26999446 | |||||||
| chr12:26999733 | T | C | 353 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(350): Show |
409 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(406): Show |
intron_variant | MODIFIER | c.247-57A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 26999733 | |||||||
| chr12:26999742 | C | T | 1 | a0001c0001t0007g0245 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.247-66G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 26999742 | |||||||
| chr12:26999751 | A | G | 4 | a0001c0001t0003g0065 a0001c0001t0014g0090 a0001c0001t0015g0087 others(1): Show |
4 | HG02257.hp2 HG02886.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.247-75T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 26999751 | |||||||
| chr12:26999794 | C | A | 1 | a0001c0001t0001g0311 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.247-118G>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 26999794 | |||||||
| chr12:26999894 | T | G | 4 | a0001c0001t0001g0121 a0001c0001t0005g0122 a0001c0001t0005g0164 others(1): Show |
4 | HG00597.hp1 NA19058.hp2 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.247-218A>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 26999894 | |||||||
| chr12:27000056 | C | T | 3 | a0001c0001t0027g0232 a0002c0002t0014g0345 a0002c0002t0014g0354 |
3 | HG02723.hp2 HG02922.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.247-380G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27000056 | |||||||
| chr12:27000101 | T | C | 1 | a0001c0001t0001g0063 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.247-425A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27000101 | |||||||
| chr12:27000142 | G | A | 1 | a0001c0001t0008g0339 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.247-466C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27000142 | |||||||
| chr12:27000255 | C | G | 26 | a0001c0001t0035g0038 a0002c0002t0001g0202 a0002c0002t0001g0203 others(23): Show |
30 | HG00609.hp2 HG01069.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.247-579G>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27000255 | |||||||
| chr12:27000307 | T | C | 1 | a0001c0001t0003g0054 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.247-631A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27000307 | |||||||
| chr12:27000522 | C | T | 4 | a0001c0001t0015g0089 a0001c0001t0017g0228 a0001c0001t0026g0159 others(1): Show |
4 | HG02055.hp1 HG02145.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.247-846G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27000522 | |||||||
| chr12:27000567 | C | T | 1 | a0001c0001t0003g0065 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.247-891G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27000567 | |||||||
| chr12:27000584 | C | G | 1 | a0001c0001t0001g0267 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.247-908G>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27000584 | |||||||
| chr12:27000585 | A | G | 1 | a0001c0001t0001g0267 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.247-909T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27000585 | |||||||
| chr12:27000597 | C | T | 2 | a0001c0001t0001g0097 a0001c0001t0001g0098 |
2 | HG01261.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.247-921G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27000597 | |||||||
| chr12:27000600 | C | T | 21 | a0001c0001t0003g0129 a0001c0001t0004g0006 a0001c0001t0004g0019 others(18): Show |
24 | HG00558.hp1 HG00673.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.247-924G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27000600 | |||||||
| chr12:27000650 | G | A | 1 | a0001c0001t0003g0123 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.247-974C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27000650 | |||||||
| chr12:27000701 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.247-1025G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27000701 | |||||||
| chr12:27000739 | G | A | 1 | a0001c0001t0001g0125 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.247-1063C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27000739 | |||||||
| chr12:27000785 | A | G | 8 | a0001c0001t0001g0025 a0001c0001t0001g0265 a0001c0001t0005g0264 others(5): Show |
9 | HG02135.hp1 HG02165.hp1 NA18942.hp1 others(6): Show |
intron_variant | MODIFIER | c.247-1109T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27000785 | |||||||
| chr12:27000821 | T | C | 1 | a0001c0001t0002g0212 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.247-1145A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27000821 | |||||||
| chr12:27000835 | A | C | 1 | a0001c0001t0004g0359 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.247-1159T>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27000835 | |||||||
| chr12:27000857 | C | T | 2 | a0001c0001t0015g0087 a0001c0001t0015g0088 |
2 | HG02257.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.247-1181G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27000857 | |||||||
| chr12:27001197 | G | A | 21 | a0001c0001t0001g0036 a0001c0001t0006g0051 a0001c0001t0006g0052 others(18): Show |
21 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.247-1521C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27001197 | |||||||
| chr12:27001238 | G | T | 63 | a0001c0001t0001g0015 a0001c0001t0001g0097 a0001c0001t0001g0098 others(60): Show |
70 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.247-1562C>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27001238 | |||||||
| chr12:27001437 | C | T | 1 | a0001c0001t0003g0093 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.247-1761G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27001437 | |||||||
| chr12:27001609 | C | T | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.246+1627G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27001609 | |||||||
| chr12:27001679 | C | T | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.246+1557G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27001679 | |||||||
| chr12:27001726 | A | T | 1 | a0001c0001t0002g0044 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.246+1510T>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27001726 | |||||||
| chr12:27001812 | C | A | 2 | a0001c0001t0003g0065 a0001c0001t0014g0090 |
2 | HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.246+1424G>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27001812 | |||||||
| chr12:27001891 | C | T | 1 | a0001c0001t0004g0167 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.246+1345G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27001891 | |||||||
| chr12:27001938 | G | A | 1 | a0001c0001t0002g0243 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.246+1298C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27001938 | |||||||
| chr12:27002037 | T | C | 233 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(230): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.246+1199A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27002037 | |||||||
| chr12:27002117 | G | A | 8 | a0001c0001t0001g0063 a0001c0001t0002g0062 a0001c0001t0007g0014 others(5): Show |
9 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(6): Show |
intron_variant | MODIFIER | c.246+1119C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27002117 | |||||||
| chr12:27002187 | G | T | 1 | a0001c0001t0027g0232 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.246+1049C>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27002187 | |||||||
| chr12:27002235 | G | A | 2 | a0001c0001t0020g0343 a0001c0001t0020g0357 |
2 | HG02109.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.246+1001C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27002235 | |||||||
| chr12:27002237 | C | A | 304 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(301): Show |
359 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(356): Show |
intron_variant | MODIFIER | c.246+999G>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27002237 | |||||||
| chr12:27002297 | T | C | 1 | a0001c0001t0003g0086 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.246+939A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27002297 | |||||||
| chr12:27002299 | C | CA | 176 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(173): Show |
198 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(195): Show |
intron_variant | MODIFIER | c.246+936dupT | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27002299 | |||||||
| chr12:27002352 | C | T | 100 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(97): Show |
129 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.246+884G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27002352 | |||||||
| chr12:27002454 | T | A | 1 | a0002c0002t0005g0364 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.246+782A>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27002454 | |||||||
| chr12:27002630 | G | C | 1 | a0001c0001t0006g0037 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.246+606C>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27002630 | |||||||
| chr12:27002709 | T | C | 5 | a0001c0001t0003g0054 a0001c0001t0003g0085 a0001c0001t0003g0086 others(2): Show |
5 | HG00738.hp1 HG02257.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.246+527A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27002709 | |||||||
| chr12:27003095 | T | C | 1 | a0001c0001t0006g0052 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.246+141A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27003095 | |||||||
| chr12:27003111 | T | A | 110 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(107): Show |
139 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.246+125A>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27003111 | |||||||
| chr12:27003143 | A | G | 1 | a0002c0002t0005g0364 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.246+93T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27003143 | |||||||
| chr12:27003180 | T | TACCAGAC others(4): Show |
1 | a0002c0002t0005g0364 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.246+45_246+55dupGG others(9): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 2/11 | chr12 | 27003180 | |||||||
| chr12:27003609 | T | C | 1 | a0001c0001t0004g0041 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.92-219A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27003609 | |||||||
| chr12:27003713 | G | C | 26 | a0001c0001t0035g0038 a0002c0002t0001g0202 a0002c0002t0001g0203 others(23): Show |
30 | HG00609.hp2 HG01069.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.92-323C>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27003713 | |||||||
| chr12:27003783 | G | A | 1 | a0001c0001t0006g0084 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.92-393C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27003783 | |||||||
| chr12:27003803 | A | G | 26 | a0001c0001t0035g0038 a0002c0002t0001g0202 a0002c0002t0001g0203 others(23): Show |
30 | HG00609.hp2 HG01069.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.92-413T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27003803 | |||||||
| chr12:27003859 | T | C | 1 | a0001c0001t0006g0080 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.92-469A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27003859 | |||||||
| chr12:27004153 | T | A | 1 | a0001c0001t0008g0334 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.92-763A>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27004153 | |||||||
| chr12:27004260 | C | A | 1 | a0002c0002t0001g0203 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.92-870G>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27004260 | |||||||
| chr12:27004285 | C | G | 1 | a0001c0001t0002g0323 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.92-895G>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27004285 | |||||||
| chr12:27004589 | G | A | 1 | a0001c0001t0004g0132 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.92-1199C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27004589 | |||||||
| chr12:27004671 | A | G | 104 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(101): Show |
133 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(130): Show |
intron_variant | MODIFIER | c.92-1281T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27004671 | |||||||
| chr12:27004964 | G | A | 4 | a0001c0001t0006g0156 a0001c0001t0027g0232 a0002c0002t0014g0345 others(1): Show |
4 | HG02559.hp2 HG02723.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.92-1574C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27004964 | |||||||
| chr12:27004964 | G | T | 26 | a0001c0001t0035g0038 a0002c0002t0001g0202 a0002c0002t0001g0203 others(23): Show |
30 | HG00609.hp2 HG01069.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.92-1574C>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27004964 | |||||||
| chr12:27005173 | C | A | 1 | a0001c0001t0029g0297 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.92-1783G>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27005173 | |||||||
| chr12:27005223 | A | T | 12 | a0001c0001t0001g0063 a0001c0001t0002g0062 a0001c0001t0004g0140 others(9): Show |
13 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(10): Show |
intron_variant | MODIFIER | c.92-1833T>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27005223 | |||||||
| chr12:27005347 | T | C | 7 | a0001c0001t0003g0054 a0001c0001t0003g0065 a0001c0001t0003g0085 others(4): Show |
7 | HG00738.hp1 HG02257.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.92-1957A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27005347 | |||||||
| chr12:27005355 | A | G | 1 | a0004c0004t0016g0227 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.92-1965T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27005355 | |||||||
| chr12:27005356 | C | G | 2 | a0001c0001t0003g0095 a0001c0001t0003g0096 |
2 | HG00642.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.92-1966G>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27005356 | |||||||
| chr12:27005405 | C | A | 1 | a0001c0001t0004g0298 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.92-2015G>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27005405 | |||||||
| chr12:27005506 | T | A | 74 | a0001c0001t0001g0015 a0001c0001t0001g0097 a0001c0001t0001g0098 others(71): Show |
81 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.92-2116A>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27005506 | |||||||
| chr12:27005555 | C | T | 67 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0011 others(64): Show |
83 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.92-2165G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27005555 | |||||||
| chr12:27005561 | A | G | 2 | a0002c0002t0014g0345 a0002c0002t0014g0354 |
2 | HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.92-2171T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27005561 | |||||||
| chr12:27005764 | G | A | 1 | a0001c0001t0001g0244 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.92-2374C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27005764 | |||||||
| chr12:27005788 | G | C | 12 | a0001c0001t0001g0063 a0001c0001t0002g0062 a0001c0001t0004g0140 others(9): Show |
13 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(10): Show |
intron_variant | MODIFIER | c.92-2398C>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27005788 | |||||||
| chr12:27005804 | A | AT | 6 | a0001c0001t0001g0125 a0001c0001t0003g0065 a0001c0001t0004g0271 others(3): Show |
6 | HG02886.hp2 HG03453.hp2 NA18994.hp2 others(3): Show |
intron_variant | MODIFIER | c.92-2415dupA | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27005804 | |||||||
| chr12:27005877 | T | C | 1 | a0001c0001t0001g0034 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.92-2487A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27005877 | |||||||
| chr12:27005958 | C | T | 1 | a0001c0001t0008g0334 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.92-2568G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27005958 | |||||||
| chr12:27005989 | G | A | 3 | a0002c0002t0001g0202 a0002c0002t0001g0203 a0002c0002t0005g0201 |
3 | HG00609.hp2 NA18969.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.92-2599C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27005989 | |||||||
| chr12:27006015 | G | T | 70 | a0001c0001t0001g0015 a0001c0001t0001g0097 a0001c0001t0001g0098 others(67): Show |
77 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.92-2625C>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27006015 | |||||||
| chr12:27006019 | C | T | 1 | a0001c0001t0003g0095 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.92-2629G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27006019 | |||||||
| chr12:27006029 | A | G | 114 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(111): Show |
143 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(140): Show |
intron_variant | MODIFIER | c.92-2639T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27006029 | |||||||
| chr12:27006096 | G | A | 1 | a0001c0001t0004g0359 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.92-2706C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27006096 | |||||||
| chr12:27006140 | C | CT | 22 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(19): Show |
26 | HG00438.hp2 HG00544.hp2 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.92-2751dupA | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27006140 | |||||||
| chr12:27006144 | T | C | 5 | a0001c0001t0006g0156 a0001c0001t0006g0158 a0001c0001t0027g0232 others(2): Show |
5 | HG02559.hp2 HG02647.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.92-2754A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27006144 | |||||||
| chr12:27006146 | T | C | 6 | a0001c0001t0003g0054 a0001c0001t0003g0085 a0001c0001t0003g0086 others(3): Show |
6 | HG00738.hp1 HG02132.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.92-2756A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27006146 | |||||||
| chr12:27006178 | C | T | 2 | a0001c0001t0015g0087 a0001c0001t0015g0088 |
2 | HG02257.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.92-2788G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27006178 | |||||||
| chr12:27006200 | G | A | 26 | a0001c0001t0035g0038 a0002c0002t0001g0202 a0002c0002t0001g0203 others(23): Show |
30 | HG00609.hp2 HG01069.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.92-2810C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27006200 | |||||||
| chr12:27006284 | T | G | 1 | a0001c0001t0003g0124 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.92-2894A>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27006284 | |||||||
| chr12:27006372 | C | T | 7 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0260 others(4): Show |
11 | HG00597.hp2 HG01257.hp2 NA18969.hp2 others(8): Show |
intron_variant | MODIFIER | c.92-2982G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27006372 | |||||||
| chr12:27006415 | G | A | 1 | a0001c0001t0017g0312 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.92-3025C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27006415 | |||||||
| chr12:27006490 | G | C | 1 | a0001c0001t0001g0313 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.92-3100C>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27006490 | |||||||
| chr12:27006493 | C | T | 2 | a0001c0001t0003g0065 a0001c0001t0014g0090 |
2 | HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.92-3103G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27006493 | |||||||
| chr12:27006545 | T | C | 2 | a0001c0001t0020g0343 a0001c0001t0020g0357 |
2 | HG02109.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.92-3155A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27006545 | |||||||
| chr12:27006701 | G | A | 236 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(233): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.92-3311C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27006701 | |||||||
| chr12:27006796 | A | G | 27 | a0001c0001t0001g0036 a0001c0001t0006g0051 a0001c0001t0006g0052 others(24): Show |
27 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.92-3406T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27006796 | |||||||
| chr12:27006851 | A | G | 52 | a0001c0001t0001g0063 a0001c0001t0002g0062 a0001c0001t0004g0140 others(49): Show |
60 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.92-3461T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27006851 | |||||||
| chr12:27007028 | T | C | 2 | a0001c0001t0020g0343 a0001c0001t0020g0357 |
2 | HG02109.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.92-3638A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27007028 | |||||||
| chr12:27007243 | C | T | 3 | a0001c0001t0010g0252 a0004c0004t0010g0253 a0004c0004t0010g0254 |
3 | HG02486.hp2 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.92-3853G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27007243 | |||||||
| chr12:27007278 | C | G | 1 | a0001c0001t0003g0085 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.92-3888G>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27007278 | |||||||
| chr12:27007350 | A | G | 3 | a0001c0001t0006g0156 a0001c0001t0006g0158 a0001c0001t0027g0232 |
3 | HG02559.hp2 HG02647.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.92-3960T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27007350 | |||||||
| chr12:27007422 | C | T | 63 | a0001c0001t0001g0015 a0001c0001t0001g0097 a0001c0001t0001g0098 others(60): Show |
70 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.92-4032G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27007422 | |||||||
| chr12:27007461 | T | C | 2 | a0001c0001t0015g0089 a0001c0001t0017g0228 |
2 | HG03516.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.92-4071A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27007461 | |||||||
| chr12:27007535 | A | T | 1 | a0001c0001t0001g0250 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.92-4145T>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27007535 | |||||||
| chr12:27007729 | G | A | 30 | a0001c0001t0001g0036 a0001c0001t0001g0055 a0001c0001t0001g0082 others(27): Show |
30 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.92-4339C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27007729 | |||||||
| chr12:27007800 | T | C | 1 | a0001c0001t0001g0318 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.92-4410A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27007800 | |||||||
| chr12:27007897 | T | A | 2 | a0001c0001t0015g0087 a0001c0001t0015g0088 |
2 | HG02257.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.92-4507A>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27007897 | |||||||
| chr12:27008073 | CTGTGAGT others(1351): Show |
C | 4 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0138 others(1): Show |
6 | NA18947.hp2 NA18951.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+4647_92-4684del | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27008073 | |||||||
| chr12:27008196 | G | A | 31 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0002g0323 others(28): Show |
36 | HG00733.hp2 HG00741.hp2 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.92-4806C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27008196 | |||||||
| chr12:27008262 | T | C | 2 | a0002c0002t0014g0345 a0002c0002t0014g0354 |
2 | HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.92-4872A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27008262 | |||||||
| chr12:27008269 | C | T | 45 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0002g0039 others(42): Show |
50 | HG00639.hp1 HG00733.hp2 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.92-4879G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27008269 | |||||||
| chr12:27008446 | C | T | 45 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0002g0039 others(42): Show |
50 | HG00639.hp1 HG00733.hp2 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.92-5056G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27008446 | |||||||
| chr12:27008592 | T | C | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(147): Show |
184 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(181): Show |
intron_variant | MODIFIER | c.92-5202A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27008592 | |||||||
| chr12:27008670 | C | T | 1 | a0001c0001t0005g0164 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.92-5280G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27008670 | |||||||
| chr12:27008695 | G | A | 1 | a0001c0001t0015g0089 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.92-5305C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27008695 | |||||||
| chr12:27008975 | C | T | 44 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0002g0039 others(41): Show |
49 | HG00639.hp1 HG00733.hp2 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.91+5103G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27008975 | |||||||
| chr12:27009055 | T | C | 1 | a0001c0001t0004g0359 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.91+5023A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27009055 | |||||||
| chr12:27009122 | CTTAT | C | 2 | a0001c0001t0003g0213 a0002c0002t0012g0020 |
3 | NA18982.hp2 NA19068.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.91+4952_91+4955del others(4): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27009122 | |||||||
| chr12:27009161 | A | G | 1 | a0001c0001t0002g0243 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.91+4917T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27009161 | |||||||
| chr12:27009270 | A | G | 2 | a0001c0001t0002g0043 a0001c0001t0008g0042 |
2 | HG00735.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.91+4808T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27009270 | |||||||
| chr12:27009285 | C | A | 81 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0011 others(78): Show |
99 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.91+4793G>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27009285 | |||||||
| chr12:27009287 | A | C | 14 | a0001c0001t0002g0039 a0001c0001t0002g0043 a0001c0001t0002g0044 others(11): Show |
14 | HG00639.hp1 HG00735.hp2 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.91+4791T>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27009287 | |||||||
| chr12:27009343 | A | G | 302 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(299): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.91+4735T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27009343 | |||||||
| chr12:27009401 | G | A | 2 | a0002c0002t0014g0345 a0002c0002t0014g0354 |
2 | HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.91+4677C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27009401 | |||||||
| chr12:27009432 | T | C | 4 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0138 others(1): Show |
6 | NA18947.hp2 NA18951.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+4646A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27009432 | |||||||
| chr12:27009434 | T | A | 4 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0138 others(1): Show |
6 | NA18947.hp2 NA18951.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+4644A>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27009434 | |||||||
| chr12:27009436 | T | A | 4 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0138 others(1): Show |
6 | NA18947.hp2 NA18951.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+4642A>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27009436 | |||||||
| chr12:27009442 | A | C | 4 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0138 others(1): Show |
6 | NA18947.hp2 NA18951.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+4636T>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27009442 | |||||||
| chr12:27009443 | T | A | 4 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0138 others(1): Show |
6 | NA18947.hp2 NA18951.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+4635A>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27009443 | |||||||
| chr12:27009444 | G | GCAC | 4 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0138 others(1): Show |
6 | NA18947.hp2 NA18951.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+4633_91+4634ins others(3): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27009444 | |||||||
| chr12:27009447 | GA | G | 4 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0138 others(1): Show |
6 | NA18947.hp2 NA18951.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+4630delT | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27009447 | |||||||
| chr12:27009449 | G | C | 4 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0138 others(1): Show |
6 | NA18947.hp2 NA18951.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+4629C>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27009449 | |||||||
| chr12:27009451 | T | A | 4 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0138 others(1): Show |
6 | NA18947.hp2 NA18951.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+4627A>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27009451 | |||||||
| chr12:27009452 | G | C | 4 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0138 others(1): Show |
6 | NA18947.hp2 NA18951.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+4626C>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27009452 | |||||||
| chr12:27009455 | T | A | 4 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0138 others(1): Show |
6 | NA18947.hp2 NA18951.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+4623A>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27009455 | |||||||
| chr12:27009456 | T | C | 4 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0138 others(1): Show |
6 | NA18947.hp2 NA18951.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+4622A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27009456 | |||||||
| chr12:27009457 | A | C | 4 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0138 others(1): Show |
6 | NA18947.hp2 NA18951.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+4621T>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27009457 | |||||||
| chr12:27009458 | T | A | 4 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0138 others(1): Show |
6 | NA18947.hp2 NA18951.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+4620A>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27009458 | |||||||
| chr12:27009460 | T | A | 4 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0138 others(1): Show |
6 | NA18947.hp2 NA18951.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+4618A>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27009460 | |||||||
| chr12:27009461 | T | G | 4 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0138 others(1): Show |
6 | NA18947.hp2 NA18951.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+4617A>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27009461 | |||||||
| chr12:27009464 | T | G | 4 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0138 others(1): Show |
6 | NA18947.hp2 NA18951.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+4614A>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27009464 | |||||||
| chr12:27009539 | T | C | 2 | a0001c0001t0004g0140 a0001c0001t0037g0139 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.91+4539A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27009539 | |||||||
| chr12:27009651 | A | G | 1 | a0001c0001t0005g0249 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.91+4427T>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27009651 | |||||||
| chr12:27009679 | G | A | 1 | a0001c0001t0006g0083 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.91+4399C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27009679 | |||||||
| chr12:27009839 | T | G | 2 | a0001c0001t0026g0159 a0001c0001t0028g0160 |
2 | HG02055.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.91+4239A>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27009839 | |||||||
| chr12:27009842 | A | AT | 44 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0002g0039 others(41): Show |
49 | HG00639.hp1 HG00733.hp2 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.91+4235dupA | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27009842 | |||||||
| chr12:27009901 | T | C | 1 | a0001c0001t0004g0359 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.91+4177A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27009901 | |||||||
| chr12:27010157 | A | T | 2 | a0001c0001t0007g0239 a0001c0001t0007g0240 |
2 | HG02451.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.91+3921T>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27010157 | |||||||
| chr12:27010303 | A | C | 1 | a0001c0001t0001g0248 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.91+3775T>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27010303 | |||||||
| chr12:27010332 | C | T | 1 | a0001c0001t0004g0359 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.91+3746G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27010332 | |||||||
| chr12:27010341 | T | C | 1 | a0001c0001t0001g0319 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.91+3737A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27010341 | |||||||
| chr12:27010410 | T | C | 125 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(122): Show |
156 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.91+3668A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27010410 | |||||||
| chr12:27010426 | C | T | 1 | a0001c0001t0015g0089 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.91+3652G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27010426 | |||||||
| chr12:27010533 | C | T | 4 | a0001c0001t0003g0198 a0001c0001t0004g0200 a0001c0001t0004g0211 others(1): Show |
4 | NA18946.hp1 NA18961.hp1 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.91+3545G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27010533 | |||||||
| chr12:27011159 | C | T | 1 | a0001c0001t0004g0094 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.91+2919G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27011159 | |||||||
| chr12:27011275 | C | T | 1 | a0001c0001t0001g0238 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.91+2803G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27011275 | |||||||
| chr12:27011316 | C | T | 1 | a0001c0001t0015g0089 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.91+2762G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27011316 | |||||||
| chr12:27011317 | G | A | 32 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0002g0323 others(29): Show |
37 | HG00733.hp2 HG00741.hp2 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.91+2761C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27011317 | |||||||
| chr12:27011786 | C | T | 1 | a0001c0001t0003g0093 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.91+2292G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27011786 | |||||||
| chr12:27012075 | T | G | 2 | a0001c0001t0006g0158 a0001c0001t0007g0210 |
2 | HG02647.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.91+2003A>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27012075 | |||||||
| chr12:27012088 | G | A | 8 | a0001c0001t0006g0237 a0001c0001t0027g0232 a0003c0003t0009g0010 others(5): Show |
11 | HG00741.hp1 HG02451.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.91+1990C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27012088 | |||||||
| chr12:27012162 | G | A | 2 | a0001c0001t0011g0332 a0001c0001t0011g0333 |
2 | NA19012.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.91+1916C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27012162 | |||||||
| chr12:27012170 | T | C | 4 | a0001c0001t0003g0005 a0001c0001t0003g0151 a0001c0001t0003g0152 others(1): Show |
6 | NA18945.hp2 NA18948.hp1 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+1908A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27012170 | |||||||
| chr12:27012205 | T | C | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(135): Show |
173 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(170): Show |
intron_variant | MODIFIER | c.91+1873A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27012205 | |||||||
| chr12:27012231 | C | T | 3 | a0002c0002t0005g0035 a0002c0002t0005g0355 a0002c0002t0005g0356 |
4 | HG01069.hp1 HG01071.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.91+1847G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27012231 | |||||||
| chr12:27012249 | G | A | 2 | a0001c0001t0015g0087 a0001c0001t0015g0088 |
2 | HG02257.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.91+1829C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27012249 | |||||||
| chr12:27012264 | A | C | 331 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(328): Show |
386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
intron_variant | MODIFIER | c.91+1814T>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27012264 | |||||||
| chr12:27012270 | T | C | 8 | a0001c0001t0003g0198 a0001c0001t0004g0200 a0001c0001t0004g0211 others(5): Show |
8 | HG00609.hp2 NA18946.hp1 NA18946.hp2 others(5): Show |
intron_variant | MODIFIER | c.91+1808A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27012270 | |||||||
| chr12:27012297 | C | T | 1 | a0001c0001t0004g0092 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.91+1781G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27012297 | |||||||
| chr12:27012299 | C | A | 2 | a0001c0001t0001g0340 a0001c0001t0001g0341 |
2 | NA18961.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.91+1779G>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27012299 | |||||||
| chr12:27012338 | T | A | 1 | a0001c0001t0005g0342 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.91+1740A>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27012338 | |||||||
| chr12:27012343 | C | T | 1 | a0001c0001t0001g0218 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.91+1735G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27012343 | |||||||
| chr12:27012358 | G | C | 30 | a0001c0001t0002g0039 a0001c0001t0002g0043 a0001c0001t0002g0044 others(27): Show |
31 | HG00639.hp1 HG00735.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.91+1720C>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27012358 | |||||||
| chr12:27012449 | T | C | 2 | a0001c0001t0020g0343 a0001c0001t0020g0357 |
2 | HG02109.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.91+1629A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27012449 | |||||||
| chr12:27012566 | A | C | 1 | a0001c0001t0010g0217 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.91+1512T>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27012566 | |||||||
| chr12:27012751 | G | A | 74 | a0001c0001t0001g0015 a0001c0001t0001g0097 a0001c0001t0001g0098 others(71): Show |
80 | HG00099.hp2 HG00544.hp1 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.91+1327C>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27012751 | |||||||
| chr12:27012810 | C | T | 6 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0002g0212 others(3): Show |
7 | HG02155.hp1 NA18946.hp2 NA18982.hp2 others(4): Show |
intron_variant | MODIFIER | c.91+1268G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27012810 | |||||||
| chr12:27012965 | T | C | 4 | a0001c0001t0006g0158 a0001c0001t0016g0157 a0001c0001t0026g0159 others(1): Show |
4 | HG02055.hp1 HG02145.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.91+1113A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27012965 | |||||||
| chr12:27012988 | A | T | 37 | a0001c0001t0002g0039 a0001c0001t0002g0043 a0001c0001t0002g0044 others(34): Show |
38 | HG00639.hp1 HG00735.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.91+1090T>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27012988 | |||||||
| chr12:27012994 | T | C | 1 | a0001c0001t0008g0344 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.91+1084A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27012994 | |||||||
| chr12:27012995 | C | CA | 124 | a0001c0001t0001g0015 a0001c0001t0001g0036 a0001c0001t0001g0053 others(121): Show |
131 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.91+1082dupT | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27012995 | |||||||
| chr12:27012995 | C | CAA | 35 | a0001c0001t0002g0039 a0001c0001t0002g0043 a0001c0001t0002g0044 others(32): Show |
36 | HG00597.hp1 HG00639.hp1 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.91+1081_91+1082dup others(2): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27012995 | |||||||
| chr12:27012995 | C | CAAA | 47 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0185 others(44): Show |
56 | HG00609.hp2 HG00621.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.91+1080_91+1082dup others(3): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27012995 | |||||||
| chr12:27012995 | C | CAAAA | 8 | a0001c0001t0001g0207 a0001c0001t0002g0206 a0001c0001t0002g0208 others(5): Show |
8 | HG01106.hp2 HG01981.hp2 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.91+1079_91+1082dup others(4): Show |
TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27012995 | |||||||
| chr12:27013087 | A | C | 2 | a0001c0001t0001g0053 a0001c0001t0003g0054 |
2 | HG02970.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.91+991T>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27013087 | |||||||
| chr12:27013225 | A | C | 2 | a0001c0001t0006g0051 a0001c0001t0006g0052 |
2 | HG01934.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.91+853T>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27013225 | |||||||
| chr12:27013289 | C | A | 1 | a0001c0001t0004g0359 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.91+789G>T | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27013289 | |||||||
| chr12:27013642 | C | T | 173 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(170): Show |
189 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.91+436G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27013642 | |||||||
| chr12:27013743 | T | C | 12 | a0002c0002t0004g0368 a0002c0002t0005g0360 a0002c0002t0005g0361 others(9): Show |
12 | HG02135.hp2 NA18956.hp2 NA18966.hp2 others(9): Show |
intron_variant | MODIFIER | c.91+335A>G | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27013743 | |||||||
| chr12:27013763 | C | T | 14 | a0001c0001t0002g0039 a0001c0001t0002g0043 a0001c0001t0002g0044 others(11): Show |
14 | HG00639.hp1 HG00735.hp2 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.91+315G>A | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27013763 | |||||||
| chr12:27014021 | C | G | 1 | a0001c0001t0001g0036 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.91+57G>C | TM7SF3 | ENSG00000064115.11 | transcript | ENST00000343028.9 | protein_coding | 1/11 | chr12 | 27014021 |