Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55750 |
| ensemblid | ENSG00000006530.18 |
| hgncid | 21869 |
| symbol | AGK |
| name | acylglycerol kinase |
| refseq_nuc | NM_018238.4 |
| refseq_prot | NP_060708.1 |
| ensembl_nuc | ENST00000649286.2 |
| ensembl_prot | ENSP00000497280.1 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 141551410 |
| end | 141655244 |
| strand | + |
| ver | v1.2 |
| region | chr7:141551410-141655244 |
| region5000 | chr7:141546410-141660244 |
| regionname0 | AGK_chr7_141551410_141655244 |
| regionname5000 | AGK_chr7_141546410_141660244 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 422 | 268 | 68 | 43 | 115 | 8 | 32 | 83 | AGK_chr7_141546410_141660244 | AGK | MTVFF others(417): Show |
chr7 | 141546410 | 141660244 |
| a0002 | 0/0 | 422 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | MTVFF others(417): Show |
chr7 | 141546410 | 141660244 |
| a0003 | 0/0 | 422 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | MTVFF others(417): Show |
chr7 | 141546410 | 141660244 |
| a0004 | 0/0 | 422 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | MTVFF others(417): Show |
chr7 | 141546410 | 141660244 |
| a0005 | 0/0 | 422 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | MTVFF others(417): Show |
chr7 | 141546410 | 141660244 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1266 | 268 | 68 | 43 | 115 | 8 | 32 | AGK_chr7_141546410_141660244 | AGK | ATGAC others(1261): Show |
chr7 | 141546410 | 141660244 | ||
| a0002c0002 | 0/0 | 1266 | 3 | 2 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | ATGAC others(1261): Show |
chr7 | 141546410 | 141660244 | ||
| a0003c0005 | 0/0 | 1266 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | ATGAC others(1261): Show |
chr7 | 141546410 | 141660244 | ||
| a0004c0003 | 0/0 | 1266 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | ATGAC others(1261): Show |
chr7 | 141546410 | 141660244 | ||
| a0005c0004 | 0/0 | 1266 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | ATGAC others(1261): Show |
chr7 | 141546410 | 141660244 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3628 | 215 | 42 | 39 | 102 | 7 | 23 | AGK_chr7_141546410_141660244 | AGK | AGAGC others(3623): Show |
chr7 | 141546410 | 141660244 |
| a0001c0001t0002 | 0/0 | 3628 | 23 | 6 | 2 | 9 | 0 | 6 | AGK_chr7_141546410_141660244 | AGK | AGAGC others(3623): Show |
chr7 | 141546410 | 141660244 |
| a0001c0001t0003 | 0/0 | 3632 | 5 | 5 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | AGAGC others(3627): Show |
chr7 | 141546410 | 141660244 |
| a0001c0001t0004 | 0/0 | 3628 | 6 | 6 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | AGAGC others(3623): Show |
chr7 | 141546410 | 141660244 |
| a0001c0001t0005 | 0/0 | 3628 | 3 | 1 | 0 | 2 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | AGAGC others(3623): Show |
chr7 | 141546410 | 141660244 |
| a0001c0001t0006 | 0/0 | 3632 | 3 | 3 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | AGAGC others(3627): Show |
chr7 | 141546410 | 141660244 |
| a0001c0001t0007 | 0/0 | 3628 | 2 | 0 | 1 | 0 | 1 | 0 | AGK_chr7_141546410_141660244 | AGK | AGAGC others(3623): Show |
chr7 | 141546410 | 141660244 |
| a0001c0001t0008 | 0/0 | 3628 | 2 | 2 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | AGAGC others(3623): Show |
chr7 | 141546410 | 141660244 |
| a0001c0001t0009 | 0/0 | 3628 | 2 | 2 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | AGAGC others(3623): Show |
chr7 | 141546410 | 141660244 |
| a0001c0001t0011 | 0/0 | 3628 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | AGAGC others(3623): Show |
chr7 | 141546410 | 141660244 |
| a0001c0001t0012 | 0/0 | 3628 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | AGAGC others(3623): Show |
chr7 | 141546410 | 141660244 |
| a0001c0001t0013 | 0/0 | 3628 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | AGAGC others(3623): Show |
chr7 | 141546410 | 141660244 |
| a0001c0001t0014 | 0/0 | 3628 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | AGAGC others(3623): Show |
chr7 | 141546410 | 141660244 |
| a0001c0001t0015 | 0/0 | 3628 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | AGAGC others(3623): Show |
chr7 | 141546410 | 141660244 |
| a0001c0001t0016 | 0/0 | 3628 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | AGAGC others(3623): Show |
chr7 | 141546410 | 141660244 |
| a0001c0001t0017 | 0/0 | 3628 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | AGAGC others(3623): Show |
chr7 | 141546410 | 141660244 |
| a0002c0002t0003 | 0/0 | 3632 | 3 | 2 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | AGAGC others(3627): Show |
chr7 | 141546410 | 141660244 |
| a0003c0005t0001 | 0/0 | 3628 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | AGAGC others(3623): Show |
chr7 | 141546410 | 141660244 |
| a0004c0003t0010 | 0/0 | 3632 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | AGAGC others(3627): Show |
chr7 | 141546410 | 141660244 |
| a0005c0004t0002 | 0/0 | 3628 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | AGAGC others(3623): Show |
chr7 | 141546410 | 141660244 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0002 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0116 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0135 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0002g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0003g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0003g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0003g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0003g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0003g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0004g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0004g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0004g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0004g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0004g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0005g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0005g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0005g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0006g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0006g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0006g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0007g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0007g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0008g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0008g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0009g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0009g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0011g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0012g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0013g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0014g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0015g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0016g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0001c0001t0017g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0002c0002t0003g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0002c0002t0003g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0003c0005t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0004c0003t0010g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| a0005c0004t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG00140 | hp2 | a0001 | c0001 | t0007 | g0019 | EUR | GBR | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | CHS | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | CHS | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | CHS | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | CHS | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | CHS | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | CHS | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG00597 | hp2 | a0001 | c0001 | t0015 | g0057 | EAS | CHS | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | CHS | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | CHS | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | CHS | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0259 | AMR | PUR | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | CLM | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | CLM | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | CLM | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG01261 | hp1 | a0002 | c0002 | t0003 | g0008 | AMR | CLM | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG01361 | hp1 | a0001 | c0001 | t0012 | g0044 | AMR | CLM | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0038 | EUR | IBS | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0162 | EUR | IBS | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0260 | AFR | ACB | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | ACB | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | ACB | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PEL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0229 | AMR | PEL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PEL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0244 | EAS | KHV | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG02055 | hp1 | a0001 | c0001 | t0006 | g0224 | AFR | ACB | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | KHV | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | KHV | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | CDX | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | CDX | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG02258 | hp1 | a0001 | c0001 | t0005 | g0256 | AFR | ACB | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | ACB | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PEL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0239 | SAS | PJL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG02615 | hp1 | a0001 | c0001 | t0013 | g0139 | AFR | GWD | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG02622 | hp1 | a0001 | c0001 | t0009 | g0121 | AFR | GWD | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0251 | AFR | GWD | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0219 | AFR | GWD | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG02683 | hp1 | a0001 | c0001 | t0016 | g0172 | SAS | PJL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG02717 | hp2 | a0001 | c0001 | t0009 | g0122 | AFR | GWD | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0262 | AFR | GWD | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0246 | SAS | PJL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0232 | AFR | GWD | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG02895 | hp1 | a0001 | c0001 | t0008 | g0041 | AFR | GWD | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG02896 | hp1 | a0002 | c0002 | t0003 | g0266 | AFR | GWD | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | GWD | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | GWD | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG02897 | hp2 | a0001 | c0001 | t0008 | g0042 | AFR | GWD | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | ESN | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | ESN | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG02965 | hp1 | a0001 | c0001 | t0006 | g0226 | AFR | ESN | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0252 | AFR | ESN | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0264 | AFR | ESN | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | ESN | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | ESN | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG03041 | hp1 | a0003 | c0005 | t0001 | g0025 | AFR | GWD | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0231 | AFR | ESN | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ESN | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | ESN | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0250 | AFR | MSL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0261 | AFR | MSL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | MSL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG03225 | hp2 | a0002 | c0002 | t0003 | g0008 | AFR | MSL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | MSL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0265 | AFR | MSL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ESN | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | ESN | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0007 | AFR | GWD | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | MSL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0233 | AFR | MSL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | STU | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0242 | SAS | STU | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0236 | SAS | PJL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | BEB | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0237 | SAS | BEB | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0245 | SAS | BEB | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | BEB | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG03942 | hp1 | a0001 | c0001 | t0017 | g0240 | SAS | BEB | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | BEB | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | STU | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | STU | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | STU | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | STU | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | CHB | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | CHB | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | YRI | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA18906 | hp2 | a0004 | c0003 | t0010 | g0227 | AFR | YRI | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA18949 | hp2 | a0001 | c0001 | t0005 | g0258 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA18951 | hp2 | a0001 | c0001 | t0011 | g0186 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA19078 | hp1 | a0005 | c0004 | t0002 | g0241 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA19079 | hp1 | a0001 | c0001 | t0005 | g0257 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | YRI | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | YRI | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA20129 | hp1 | a0001 | c0001 | t0004 | g0007 | AFR | ASW | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | ASW | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0053 | EUR | TSI | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0117 | EUR | TSI | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0144 | EUR | TSI | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0040 | EUR | TSI | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | GIH | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA20905 | hp2 | a0001 | c0001 | t0014 | g0010 | SAS | GIH | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG01123 | hp2 | a0001 | c0001 | t0007 | g0056 | AMR | CLM | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG02109 | hp2 | a0001 | c0001 | t0006 | g0225 | AFR | ACB | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | ACB | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0263 | AFR | MSL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | USA | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | USA | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0116 | REF | REF | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0135 | REF | REF | AGK_chr7_141546410_141660244 | AGK | chr7 | 141546410 | 141660244 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:141555483 | A | G | 1 | a0002 | 3 | HG01261.hp1 HG02896.hp1 HG03225.hp2 |
missense_variant | MODERATE | c.17A>G | p.Lys6Arg | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/16 | 56/3628 | 17/1269 | 6/422 | chr7 | 141555483 | |||
| chr7:141596602 | A | G | 1 | a0003 | 1 | HG03041.hp1 | missense_variant | MODERATE | c.182A>G | p.Lys61Arg | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/16 | 221/3628 | 182/1269 | 61/422 | chr7 | 141596602 | |||
| chr7:141611252 | A | G | 1 | a0005 | 1 | NA19078.hp1 | missense_variant | MODERATE | c.355A>G | p.Ile119Val | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 6/16 | 394/3628 | 355/1269 | 119/422 | chr7 | 141611252 | |||
| chr7:141614171 | C | G | 1 | a0004 | 1 | NA18906.hp2 | missense_variant | MODERATE | c.416C>G | p.Thr139Arg | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 7/16 | 455/3628 | 416/1269 | 139/422 | chr7 | 141614171 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:141653065 | C | T | 1 | a0001c0001t0004 | 6 | HG01884.hp1 HG02630.hp1 HG02965.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*141C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 16/16 | 141 | chr7 | 141653065 | ||||||
| chr7:141653068 | C | A | 1 | a0004c0003t0010 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*144C>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 16/16 | 144 | chr7 | 141653068 | ||||||
| chr7:141653108 | C | T | 1 | a0001c0001t0009 | 2 | HG02622.hp1 HG02717.hp2 |
3_prime_UTR_variant | MODIFIER | c.*184C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 16/16 | 184 | chr7 | 141653108 | ||||||
| chr7:141653239 | C | T | 1 | a0001c0001t0017 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*315C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 16/16 | 315 | chr7 | 141653239 | ||||||
| chr7:141653244 | G | A | 3 | a0001c0001t0003 a0001c0001t0005 a0002c0002t0003 |
11 | HG01261.hp1 HG02258.hp1 HG02723.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*320G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 16/16 | 320 | chr7 | 141653244 | ||||||
| chr7:141653383 | T | A | 1 | a0001c0001t0011 | 1 | NA18951.hp2 | 3_prime_UTR_variant | MODIFIER | c.*459T>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 16/16 | 459 | chr7 | 141653383 | ||||||
| chr7:141653385 | C | CTGTT | 4 | a0001c0001t0003 a0001c0001t0006 a0002c0002t0003 others(1): Show |
12 | HG01261.hp1 HG02055.hp1 HG02109.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*463_*466dupGTTT | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 16/16 | 467 | INFO_REALIGN_3_PRIME | chr7 | 141653385 | |||||
| chr7:141653628 | A | G | 1 | a0001c0001t0016 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*704A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 16/16 | 704 | chr7 | 141653628 | ||||||
| chr7:141654099 | C | T | 4 | a0001c0001t0002 a0001c0001t0015 a0001c0001t0017 others(1): Show |
26 | HG00408.hp1 HG00597.hp2 HG01168.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*1175C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 16/16 | 1175 | chr7 | 141654099 | ||||||
| chr7:141654134 | A | T | 2 | a0001c0001t0006 a0004c0003t0010 |
4 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1210A>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 16/16 | 1210 | chr7 | 141654134 | ||||||
| chr7:141654391 | T | C | 1 | a0001c0001t0015 | 1 | HG00597.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1467T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 16/16 | 1467 | chr7 | 141654391 | ||||||
| chr7:141654673 | G | A | 1 | a0001c0001t0007 | 2 | HG00140.hp2 HG01123.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1749G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 16/16 | 1749 | chr7 | 141654673 | ||||||
| chr7:141654695 | G | A | 1 | a0001c0001t0012 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1771G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 16/16 | 1771 | chr7 | 141654695 | ||||||
| chr7:141654934 | A | G | 1 | a0001c0001t0008 | 2 | HG02895.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2010A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 16/16 | 2010 | chr7 | 141654934 | ||||||
| chr7:141654942 | C | T | 1 | a0001c0001t0014 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2018C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 16/16 | 2018 | chr7 | 141654942 | ||||||
| chr7:141655072 | C | A | 1 | a0001c0001t0006 | 3 | HG02055.hp1 HG02109.hp2 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2148C>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 16/16 | 2148 | chr7 | 141655072 | ||||||
| chr7:141655089 | G | A | 1 | a0001c0001t0013 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2165G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 16/16 | 2165 | chr7 | 141655089 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:141551465 | C | G | 47 | a0001c0001t0001g0228 a0001c0001t0001g0248 a0001c0001t0001g0249 others(44): Show |
51 | HG00408.hp1 HG01168.hp2 HG01261.hp1 others(48): Show |
intron_variant | MODIFIER | c.-15+31C>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 1/15 | chr7 | 141551465 | |||||||
| chr7:141551493 | G | T | 1 | a0001c0001t0001g0223 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-15+59G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 1/15 | chr7 | 141551493 | |||||||
| chr7:141551642 | C | A | 2 | a0001c0001t0001g0009 a0001c0001t0001g0223 |
2 | HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-15+208C>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 1/15 | chr7 | 141551642 | |||||||
| chr7:141551768 | C | T | 47 | a0001c0001t0001g0228 a0001c0001t0001g0248 a0001c0001t0001g0249 others(44): Show |
51 | HG00408.hp1 HG01168.hp2 HG01261.hp1 others(48): Show |
intron_variant | MODIFIER | c.-15+334C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 1/15 | chr7 | 141551768 | |||||||
| chr7:141551808 | GGGTT | G | 5 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(2): Show |
5 | HG00642.hp2 HG01168.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.-15+383_-15+386del others(4): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 141551808 | ||||||
| chr7:141551910 | T | G | 3 | a0001c0001t0006g0224 a0001c0001t0006g0225 a0001c0001t0006g0226 |
3 | HG02055.hp1 HG02109.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-15+476T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 1/15 | chr7 | 141551910 | |||||||
| chr7:141551973 | C | T | 1 | a0001c0001t0001g0014 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-15+539C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 1/15 | chr7 | 141551973 | |||||||
| chr7:141552086 | C | G | 7 | a0001c0001t0003g0261 a0001c0001t0003g0262 a0001c0001t0003g0263 others(4): Show |
8 | HG01261.hp1 HG02723.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-15+652C>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 1/15 | chr7 | 141552086 | |||||||
| chr7:141552380 | A | G | 1 | a0001c0001t0001g0222 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-15+946A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 1/15 | chr7 | 141552380 | |||||||
| chr7:141552479 | T | G | 4 | a0001c0001t0003g0261 a0001c0001t0003g0262 a0001c0001t0003g0263 others(1): Show |
4 | HG02723.hp1 HG02970.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+1045T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 1/15 | chr7 | 141552479 | |||||||
| chr7:141552605 | A | G | 2 | a0002c0002t0003g0008 a0002c0002t0003g0266 |
3 | HG01261.hp1 HG02896.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-15+1171A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 1/15 | chr7 | 141552605 | |||||||
| chr7:141552607 | G | A | 1 | a0004c0003t0010g0227 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-15+1173G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 1/15 | chr7 | 141552607 | |||||||
| chr7:141552623 | T | G | 1 | a0001c0001t0001g0015 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-15+1189T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 1/15 | chr7 | 141552623 | |||||||
| chr7:141552626 | C | T | 4 | a0001c0001t0003g0261 a0001c0001t0003g0262 a0001c0001t0003g0263 others(1): Show |
4 | HG02723.hp1 HG02970.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+1192C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 1/15 | chr7 | 141552626 | |||||||
| chr7:141552627 | G | A | 2 | a0001c0001t0001g0228 a0001c0001t0002g0229 |
2 | HG01952.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-15+1193G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 1/15 | chr7 | 141552627 | |||||||
| chr7:141552682 | G | T | 1 | a0001c0001t0001g0221 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-15+1248G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 1/15 | chr7 | 141552682 | |||||||
| chr7:141552753 | T | C | 148 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(145): Show |
152 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.-15+1319T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 1/15 | chr7 | 141552753 | |||||||
| chr7:141552762 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-15+1328G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 1/15 | chr7 | 141552762 | |||||||
| chr7:141553616 | G | T | 1 | a0001c0001t0003g0265 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-14-1837G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 1/15 | chr7 | 141553616 | |||||||
| chr7:141553729 | C | T | 1 | a0001c0001t0004g0260 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-14-1724C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 1/15 | chr7 | 141553729 | |||||||
| chr7:141553827 | G | A | 21 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0229 others(18): Show |
23 | HG00408.hp1 HG01952.hp2 HG02015.hp1 others(20): Show |
intron_variant | MODIFIER | c.-14-1626G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 1/15 | chr7 | 141553827 | |||||||
| chr7:141553915 | C | T | 3 | a0001c0001t0003g0262 a0001c0001t0003g0263 a0001c0001t0003g0264 |
3 | HG02723.hp1 HG02970.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-14-1538C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 1/15 | chr7 | 141553915 | |||||||
| chr7:141554051 | G | A | 1 | a0001c0001t0001g0016 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-14-1402G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 1/15 | chr7 | 141554051 | |||||||
| chr7:141554077 | C | T | 1 | a0001c0001t0001g0109 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-14-1376C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 1/15 | chr7 | 141554077 | |||||||
| chr7:141554338 | T | TA | 17 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(14): Show |
18 | HG01255.hp2 HG01884.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.-14-1096dupA | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 141554338 | ||||||
| chr7:141554481 | G | T | 1 | a0001c0001t0001g0220 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-14-972G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 1/15 | chr7 | 141554481 | |||||||
| chr7:141554495 | C | A | 1 | a0001c0001t0001g0113 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-14-958C>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 1/15 | chr7 | 141554495 | |||||||
| chr7:141554600 | G | A | 2 | a0001c0001t0001g0248 a0001c0001t0001g0249 |
2 | HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-14-853G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 1/15 | chr7 | 141554600 | |||||||
| chr7:141554691 | T | C | 1 | a0001c0001t0001g0114 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-14-762T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 1/15 | chr7 | 141554691 | |||||||
| chr7:141554694 | C | T | 45 | a0001c0001t0001g0228 a0001c0001t0001g0248 a0001c0001t0001g0249 others(42): Show |
49 | HG00408.hp1 HG01168.hp2 HG01261.hp1 others(46): Show |
intron_variant | MODIFIER | c.-14-759C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 1/15 | chr7 | 141554694 | |||||||
| chr7:141554923 | A | C | 1 | a0001c0001t0001g0108 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-14-530A>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 1/15 | chr7 | 141554923 | |||||||
| chr7:141555050 | T | C | 7 | a0001c0001t0003g0261 a0001c0001t0003g0262 a0001c0001t0003g0263 others(4): Show |
8 | HG01261.hp1 HG02723.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-14-403T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 1/15 | chr7 | 141555050 | |||||||
| chr7:141555096 | A | T | 1 | a0001c0001t0001g0107 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-14-357A>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 1/15 | chr7 | 141555096 | |||||||
| chr7:141555178 | G | C | 1 | a0001c0001t0002g0230 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-14-275G>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 1/15 | chr7 | 141555178 | |||||||
| chr7:141555184 | A | G | 24 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0219 others(21): Show |
26 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(23): Show |
intron_variant | MODIFIER | c.-14-269A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 1/15 | chr7 | 141555184 | |||||||
| chr7:141555572 | C | T | 1 | a0001c0001t0003g0265 | 1 | HG03453.hp2 | splice_region_variant&intron_variant | LOW | c.101+5C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141555572 | |||||||
| chr7:141555638 | A | C | 1 | a0001c0001t0001g0218 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.101+71A>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141555638 | |||||||
| chr7:141556095 | T | C | 7 | a0001c0001t0003g0261 a0001c0001t0003g0262 a0001c0001t0003g0263 others(4): Show |
8 | HG01261.hp1 HG02723.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.101+528T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141556095 | |||||||
| chr7:141556289 | G | T | 1 | a0001c0001t0001g0217 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.101+722G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141556289 | |||||||
| chr7:141556489 | C | T | 23 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0219 others(20): Show |
25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.101+922C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141556489 | |||||||
| chr7:141556497 | G | A | 1 | a0001c0001t0001g0017 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.101+930G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141556497 | |||||||
| chr7:141556540 | C | CA | 13 | a0001c0001t0001g0018 a0001c0001t0001g0108 a0001c0001t0001g0115 others(10): Show |
13 | HG00140.hp2 HG01168.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.101+990dupA | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 141556540 | ||||||
| chr7:141556583 | C | T | 1 | a0004c0003t0010g0227 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.101+1016C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141556583 | |||||||
| chr7:141556748 | T | G | 1 | a0001c0001t0001g0118 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.101+1181T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141556748 | |||||||
| chr7:141557066 | C | G | 1 | a0001c0001t0001g0216 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.101+1499C>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141557066 | |||||||
| chr7:141557130 | T | C | 1 | a0001c0001t0001g0115 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.101+1563T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141557130 | |||||||
| chr7:141557196 | A | T | 1 | a0001c0001t0003g0261 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.101+1629A>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141557196 | |||||||
| chr7:141557247 | T | C | 1 | a0001c0001t0001g0119 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.101+1680T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141557247 | |||||||
| chr7:141557480 | G | A | 24 | a0001c0001t0001g0020 a0001c0001t0002g0005 a0001c0001t0002g0006 others(21): Show |
26 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(23): Show |
intron_variant | MODIFIER | c.101+1913G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141557480 | |||||||
| chr7:141557964 | A | G | 1 | a0001c0001t0005g0256 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.101+2397A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141557964 | |||||||
| chr7:141558007 | C | T | 3 | a0001c0001t0006g0224 a0001c0001t0006g0225 a0001c0001t0006g0226 |
3 | HG02055.hp1 HG02109.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.101+2440C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141558007 | |||||||
| chr7:141558180 | C | T | 2 | a0001c0001t0001g0105 a0001c0001t0001g0106 |
2 | HG02083.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.101+2613C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141558180 | |||||||
| chr7:141558250 | G | A | 9 | a0001c0001t0001g0120 a0001c0001t0001g0228 a0001c0001t0003g0261 others(6): Show |
10 | HG01261.hp1 HG02559.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.101+2683G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141558250 | |||||||
| chr7:141558347 | GT | G | 39 | a0001c0001t0001g0108 a0001c0001t0001g0228 a0001c0001t0002g0005 others(36): Show |
43 | HG00408.hp1 HG01168.hp2 HG01261.hp1 others(40): Show |
intron_variant | MODIFIER | c.101+2794delT | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 141558347 | ||||||
| chr7:141558348 | T | G | 3 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0002g0230 |
3 | HG01081.hp2 NA19064.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.101+2781T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141558348 | |||||||
| chr7:141558349 | T | G | 39 | a0001c0001t0001g0108 a0001c0001t0001g0228 a0001c0001t0002g0005 others(36): Show |
43 | HG00408.hp1 HG01168.hp2 HG01261.hp1 others(40): Show |
intron_variant | MODIFIER | c.101+2782T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141558349 | |||||||
| chr7:141558411 | C | A | 2 | a0001c0001t0009g0121 a0001c0001t0009g0122 |
2 | HG02622.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.101+2844C>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141558411 | |||||||
| chr7:141558457 | G | A | 3 | a0001c0001t0006g0224 a0001c0001t0006g0225 a0001c0001t0006g0226 |
3 | HG02055.hp1 HG02109.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.101+2890G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141558457 | |||||||
| chr7:141558500 | G | A | 4 | a0001c0001t0006g0224 a0001c0001t0006g0225 a0001c0001t0006g0226 others(1): Show |
4 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.101+2933G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141558500 | |||||||
| chr7:141558579 | T | C | 40 | a0001c0001t0001g0108 a0001c0001t0001g0228 a0001c0001t0002g0005 others(37): Show |
44 | HG00408.hp1 HG01168.hp2 HG01261.hp1 others(41): Show |
intron_variant | MODIFIER | c.101+3012T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141558579 | |||||||
| chr7:141558590 | A | G | 1 | a0001c0001t0001g0104 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.101+3023A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141558590 | |||||||
| chr7:141558652 | G | A | 4 | a0001c0001t0002g0229 a0001c0001t0002g0231 a0001c0001t0002g0232 others(1): Show |
4 | HG01952.hp2 HG02818.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.101+3085G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141558652 | |||||||
| chr7:141558720 | G | T | 1 | a0001c0001t0001g0215 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.101+3153G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141558720 | |||||||
| chr7:141558760 | T | A | 23 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0219 others(20): Show |
25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.101+3193T>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141558760 | |||||||
| chr7:141558805 | T | C | 2 | a0001c0001t0002g0230 a0001c0001t0002g0234 |
2 | NA18997.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.101+3238T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141558805 | |||||||
| chr7:141559004 | A | G | 2 | a0001c0001t0005g0257 a0001c0001t0005g0258 |
2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.101+3437A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141559004 | |||||||
| chr7:141559093 | C | T | 3 | a0001c0001t0002g0247 a0001c0001t0005g0257 a0001c0001t0005g0258 |
3 | NA18949.hp2 NA18959.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.101+3526C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141559093 | |||||||
| chr7:141559168 | T | A | 23 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0219 others(20): Show |
25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.101+3601T>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141559168 | |||||||
| chr7:141559238 | T | A | 2 | a0001c0001t0005g0257 a0001c0001t0005g0258 |
2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.101+3671T>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141559238 | |||||||
| chr7:141559387 | C | T | 7 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(4): Show |
7 | HG00544.hp2 HG03209.hp2 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.101+3820C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141559387 | |||||||
| chr7:141559665 | T | C | 5 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0001t0001g0253 others(2): Show |
5 | HG01891.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.101+4098T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141559665 | |||||||
| chr7:141559694 | C | G | 1 | a0001c0001t0001g0220 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.101+4127C>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141559694 | |||||||
| chr7:141559752 | CT | C | 21 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0229 others(18): Show |
23 | HG00408.hp1 HG01952.hp2 HG02015.hp1 others(20): Show |
intron_variant | MODIFIER | c.101+4188delT | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 141559752 | ||||||
| chr7:141559810 | T | C | 1 | a0001c0001t0001g0123 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.101+4243T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141559810 | |||||||
| chr7:141559959 | G | A | 1 | a0001c0001t0001g0124 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.101+4392G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141559959 | |||||||
| chr7:141559969 | C | CT | 65 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0101 others(62): Show |
68 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.101+4412dupT | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 141559969 | ||||||
| chr7:141560271 | C | G | 1 | a0001c0001t0001g0123 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.101+4704C>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141560271 | |||||||
| chr7:141560272 | G | T | 1 | a0001c0001t0003g0265 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.101+4705G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141560272 | |||||||
| chr7:141560284 | G | C | 1 | a0001c0001t0003g0265 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.101+4717G>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141560284 | |||||||
| chr7:141560403 | TTTC | T | 5 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0001t0001g0253 others(2): Show |
5 | HG01891.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.101+4848_101+4850d others(5): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 141560403 | ||||||
| chr7:141560560 | G | A | 1 | a0001c0001t0001g0021 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.101+4993G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141560560 | |||||||
| chr7:141560762 | A | G | 5 | a0001c0001t0004g0007 a0001c0001t0004g0250 a0001c0001t0004g0251 others(2): Show |
6 | HG01884.hp1 HG02630.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.101+5195A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141560762 | |||||||
| chr7:141560795 | C | CT | 108 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(105): Show |
108 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.101+5247dupT | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 141560795 | ||||||
| chr7:141560799 | T | C | 9 | a0001c0001t0001g0228 a0001c0001t0003g0261 a0001c0001t0003g0262 others(6): Show |
10 | HG01261.hp1 HG02258.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.101+5232T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141560799 | |||||||
| chr7:141560800 | T | C | 1 | a0001c0001t0001g0169 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.101+5233T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141560800 | |||||||
| chr7:141560852 | A | G | 34 | a0001c0001t0001g0228 a0001c0001t0002g0005 a0001c0001t0002g0006 others(31): Show |
37 | HG00408.hp1 HG01168.hp2 HG01261.hp1 others(34): Show |
intron_variant | MODIFIER | c.101+5285A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141560852 | |||||||
| chr7:141560859 | C | T | 1 | a0001c0001t0001g0009 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.101+5292C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141560859 | |||||||
| chr7:141560880 | T | TCCGC | 9 | a0001c0001t0001g0228 a0001c0001t0003g0261 a0001c0001t0003g0262 others(6): Show |
10 | HG01261.hp1 HG02258.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.101+5315_101+5318d others(6): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 141560880 | ||||||
| chr7:141560994 | C | T | 1 | a0001c0001t0001g0100 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.101+5427C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141560994 | |||||||
| chr7:141560995 | G | A | 1 | a0001c0001t0001g0125 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.101+5428G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141560995 | |||||||
| chr7:141561029 | G | A | 3 | a0001c0001t0003g0262 a0001c0001t0003g0263 a0001c0001t0003g0264 |
3 | HG02723.hp1 HG02970.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.101+5462G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141561029 | |||||||
| chr7:141561088 | C | T | 6 | a0001c0001t0001g0113 a0001c0001t0001g0162 a0001c0001t0001g0163 others(3): Show |
6 | HG01070.hp1 HG01099.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.101+5521C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141561088 | |||||||
| chr7:141561142 | T | C | 1 | a0001c0001t0003g0261 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.101+5575T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141561142 | |||||||
| chr7:141561354 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.101+5787C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141561354 | |||||||
| chr7:141561487 | TA | T | 5 | a0001c0001t0004g0007 a0001c0001t0004g0250 a0001c0001t0004g0251 others(2): Show |
6 | HG01884.hp1 HG02630.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.101+5921delA | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141561487 | |||||||
| chr7:141561496 | T | A | 2 | a0001c0001t0001g0167 a0001c0001t0001g0168 |
2 | HG01070.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.101+5929T>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141561496 | |||||||
| chr7:141561614 | A | AT | 6 | a0001c0001t0003g0261 a0001c0001t0003g0262 a0001c0001t0003g0263 others(3): Show |
7 | HG01261.hp1 HG02723.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.101+6057dupT | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 141561614 | ||||||
| chr7:141561623 | T | G | 1 | a0001c0001t0001g0228 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.101+6056T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141561623 | |||||||
| chr7:141561669 | G | T | 5 | a0001c0001t0004g0007 a0001c0001t0004g0250 a0001c0001t0004g0251 others(2): Show |
6 | HG01884.hp1 HG02630.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.101+6102G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141561669 | |||||||
| chr7:141561687 | C | T | 2 | a0001c0001t0005g0257 a0001c0001t0005g0258 |
2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.101+6120C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141561687 | |||||||
| chr7:141562150 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.101+6583C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141562150 | |||||||
| chr7:141562357 | C | G | 2 | a0001c0001t0005g0257 a0001c0001t0005g0258 |
2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.101+6790C>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141562357 | |||||||
| chr7:141562542 | A | G | 1 | a0001c0001t0001g0204 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.101+6975A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141562542 | |||||||
| chr7:141562585 | G | T | 1 | a0001c0001t0004g0252 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.101+7018G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141562585 | |||||||
| chr7:141562765 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.101+7198G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141562765 | |||||||
| chr7:141563026 | G | A | 7 | a0001c0001t0003g0261 a0001c0001t0003g0262 a0001c0001t0003g0263 others(4): Show |
8 | HG01261.hp1 HG02723.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.101+7459G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141563026 | |||||||
| chr7:141563106 | G | A | 5 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0001t0001g0253 others(2): Show |
5 | HG01891.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.101+7539G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141563106 | |||||||
| chr7:141563107 | T | G | 5 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0001t0001g0253 others(2): Show |
5 | HG01891.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.101+7540T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141563107 | |||||||
| chr7:141563226 | G | A | 1 | a0001c0001t0001g0170 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.101+7659G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141563226 | |||||||
| chr7:141563366 | T | G | 23 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0219 others(20): Show |
25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.101+7799T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141563366 | |||||||
| chr7:141563666 | G | T | 23 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0219 others(20): Show |
25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.101+8099G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141563666 | |||||||
| chr7:141563837 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.101+8270C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141563837 | |||||||
| chr7:141563963 | G | C | 1 | a0001c0001t0002g0259 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.101+8396G>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141563963 | |||||||
| chr7:141563989 | C | T | 2 | a0001c0001t0005g0257 a0001c0001t0005g0258 |
2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.101+8422C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141563989 | |||||||
| chr7:141563992 | G | A | 2 | a0001c0001t0001g0029 a0001c0001t0001g0126 |
2 | HG01496.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.101+8425G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141563992 | |||||||
| chr7:141564016 | A | G | 23 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0219 others(20): Show |
25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.101+8449A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141564016 | |||||||
| chr7:141564200 | T | C | 1 | a0001c0001t0001g0228 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.101+8633T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141564200 | |||||||
| chr7:141564251 | T | C | 2 | a0001c0001t0005g0257 a0001c0001t0005g0258 |
2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.101+8684T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141564251 | |||||||
| chr7:141564469 | AACTC | A | 21 | a0001c0001t0001g0015 a0001c0001t0001g0110 a0001c0001t0001g0112 others(18): Show |
21 | HG00642.hp1 HG01255.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.101+8910_101+8913d others(6): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 141564469 | ||||||
| chr7:141564531 | A | G | 4 | a0001c0001t0002g0229 a0001c0001t0002g0231 a0001c0001t0002g0232 others(1): Show |
4 | HG01952.hp2 HG02818.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.101+8964A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141564531 | |||||||
| chr7:141564551 | C | T | 1 | a0001c0001t0002g0219 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.101+8984C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141564551 | |||||||
| chr7:141564579 | G | T | 5 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0001t0001g0253 others(2): Show |
5 | HG01891.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.101+9012G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141564579 | |||||||
| chr7:141564647 | C | T | 1 | a0001c0001t0002g0233 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.101+9080C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141564647 | |||||||
| chr7:141564800 | A | G | 147 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(144): Show |
151 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.101+9233A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141564800 | |||||||
| chr7:141564844 | C | A | 1 | a0001c0001t0001g0108 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.101+9277C>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141564844 | |||||||
| chr7:141564898 | T | C | 23 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0219 others(20): Show |
25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.101+9331T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141564898 | |||||||
| chr7:141564956 | A | G | 1 | a0001c0001t0001g0223 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.101+9389A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141564956 | |||||||
| chr7:141565131 | C | T | 5 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0001t0001g0253 others(2): Show |
5 | HG01891.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.101+9564C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141565131 | |||||||
| chr7:141565244 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.101+9677C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141565244 | |||||||
| chr7:141565421 | C | T | 2 | a0001c0001t0005g0257 a0001c0001t0005g0258 |
2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.101+9854C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141565421 | |||||||
| chr7:141565448 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.101+9881C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141565448 | |||||||
| chr7:141565498 | A | C | 1 | a0001c0001t0001g0015 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.101+9931A>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141565498 | |||||||
| chr7:141565585 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.101+10018G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141565585 | |||||||
| chr7:141565637 | C | CA | 7 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0101 others(4): Show |
7 | HG01243.hp1 HG02683.hp2 HG04228.hp2 others(4): Show |
intron_variant | MODIFIER | c.101+10085dupA | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 141565637 | ||||||
| chr7:141565706 | C | G | 4 | a0001c0001t0001g0017 a0001c0001t0001g0096 a0001c0001t0001g0097 others(1): Show |
4 | HG00544.hp1 HG02040.hp2 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.101+10139C>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141565706 | |||||||
| chr7:141565800 | A | G | 3 | a0001c0001t0001g0110 a0001c0001t0001g0159 a0001c0001t0001g0160 |
3 | HG02602.hp1 HG03688.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.101+10233A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141565800 | |||||||
| chr7:141565891 | G | T | 1 | a0004c0003t0010g0227 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.101+10324G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141565891 | |||||||
| chr7:141566025 | G | C | 2 | a0001c0001t0001g0248 a0001c0001t0001g0249 |
2 | HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.101+10458G>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141566025 | |||||||
| chr7:141566086 | T | C | 10 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0001t0001g0253 others(7): Show |
11 | HG01884.hp1 HG01891.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.101+10519T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141566086 | |||||||
| chr7:141566104 | C | T | 2 | a0001c0001t0005g0257 a0001c0001t0005g0258 |
2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.101+10537C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141566104 | |||||||
| chr7:141566141 | A | G | 1 | a0001c0001t0001g0028 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.101+10574A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141566141 | |||||||
| chr7:141566208 | A | G | 2 | a0001c0001t0005g0257 a0001c0001t0005g0258 |
2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.101+10641A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141566208 | |||||||
| chr7:141566470 | G | A | 1 | a0001c0001t0001g0171 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.101+10903G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141566470 | |||||||
| chr7:141566587 | G | A | 2 | a0001c0001t0005g0257 a0001c0001t0005g0258 |
2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.101+11020G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141566587 | |||||||
| chr7:141566713 | G | A | 3 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0128 |
3 | HG01496.hp2 HG03704.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.101+11146G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141566713 | |||||||
| chr7:141566714 | C | G | 23 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0219 others(20): Show |
25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.101+11147C>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141566714 | |||||||
| chr7:141567021 | A | G | 5 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0001t0001g0253 others(2): Show |
5 | HG01891.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.101+11454A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141567021 | |||||||
| chr7:141567167 | C | A | 2 | a0001c0001t0001g0009 a0001c0001t0001g0223 |
2 | HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.101+11600C>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141567167 | |||||||
| chr7:141567194 | C | T | 2 | a0001c0001t0001g0113 a0001c0001t0001g0164 |
2 | HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.101+11627C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141567194 | |||||||
| chr7:141567433 | A | T | 1 | a0001c0001t0003g0265 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.101+11866A>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141567433 | |||||||
| chr7:141567469 | T | C | 1 | a0001c0001t0001g0120 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.101+11902T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141567469 | |||||||
| chr7:141567543 | A | G | 8 | a0001c0001t0003g0261 a0001c0001t0003g0262 a0001c0001t0003g0263 others(5): Show |
9 | HG01261.hp1 HG02258.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.101+11976A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141567543 | |||||||
| chr7:141567619 | T | C | 2 | a0001c0001t0005g0257 a0001c0001t0005g0258 |
2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.101+12052T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141567619 | |||||||
| chr7:141567852 | T | C | 2 | a0001c0001t0005g0257 a0001c0001t0005g0258 |
2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.101+12285T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141567852 | |||||||
| chr7:141568057 | C | T | 1 | a0001c0001t0001g0202 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.101+12490C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141568057 | |||||||
| chr7:141568218 | A | G | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | NA18977.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.101+12651A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141568218 | |||||||
| chr7:141568291 | G | A | 1 | a0001c0001t0001g0033 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.101+12724G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141568291 | |||||||
| chr7:141568574 | C | CT | 15 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0001t0001g0253 others(12): Show |
16 | HG01884.hp1 HG01891.hp2 HG02015.hp1 others(13): Show |
intron_variant | MODIFIER | c.101+13022dupT | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 141568574 | ||||||
| chr7:141568625 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.101+13058G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141568625 | |||||||
| chr7:141568657 | C | T | 1 | a0001c0001t0001g0221 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.101+13090C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141568657 | |||||||
| chr7:141568774 | C | A | 1 | a0001c0001t0002g0219 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.101+13207C>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141568774 | |||||||
| chr7:141568842 | C | T | 1 | a0004c0003t0010g0227 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.101+13275C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141568842 | |||||||
| chr7:141568971 | T | C | 4 | a0001c0001t0001g0110 a0001c0001t0001g0148 a0001c0001t0001g0159 others(1): Show |
4 | HG02602.hp1 HG03688.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.101+13404T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141568971 | |||||||
| chr7:141569047 | C | T | 2 | a0001c0001t0005g0257 a0001c0001t0005g0258 |
2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.101+13480C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141569047 | |||||||
| chr7:141569217 | C | T | 1 | a0001c0001t0001g0098 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.101+13650C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141569217 | |||||||
| chr7:141569232 | C | T | 1 | a0001c0001t0001g0093 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.101+13665C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141569232 | |||||||
| chr7:141569306 | C | T | 9 | a0001c0001t0001g0114 a0001c0001t0001g0194 a0001c0001t0001g0195 others(6): Show |
9 | HG00558.hp1 HG00621.hp1 HG00673.hp2 others(6): Show |
intron_variant | MODIFIER | c.101+13739C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141569306 | |||||||
| chr7:141569464 | G | A | 2 | a0001c0001t0005g0257 a0001c0001t0005g0258 |
2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.101+13897G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141569464 | |||||||
| chr7:141569592 | C | T | 46 | a0001c0001t0001g0017 a0001c0001t0001g0021 a0001c0001t0001g0026 others(43): Show |
46 | HG00423.hp2 HG00544.hp1 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.101+14025C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141569592 | |||||||
| chr7:141569634 | A | G | 9 | a0001c0001t0001g0228 a0001c0001t0003g0261 a0001c0001t0003g0262 others(6): Show |
10 | HG01261.hp1 HG02258.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.101+14067A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141569634 | |||||||
| chr7:141569693 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.101+14126C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141569693 | |||||||
| chr7:141569704 | G | A | 1 | a0001c0001t0002g0219 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.101+14137G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141569704 | |||||||
| chr7:141569782 | G | A | 1 | a0001c0001t0016g0172 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.101+14215G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141569782 | |||||||
| chr7:141569827 | A | T | 3 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0092 |
3 | HG01081.hp1 HG01255.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.101+14260A>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141569827 | |||||||
| chr7:141569829 | C | T | 10 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0001t0001g0253 others(7): Show |
11 | HG01884.hp1 HG01891.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.101+14262C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141569829 | |||||||
| chr7:141569923 | G | A | 23 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0219 others(20): Show |
25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.101+14356G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141569923 | |||||||
| chr7:141570061 | G | A | 4 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0202 others(1): Show |
4 | NA18948.hp1 NA19000.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.101+14494G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141570061 | |||||||
| chr7:141570100 | A | G | 2 | a0001c0001t0005g0257 a0001c0001t0005g0258 |
2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.101+14533A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141570100 | |||||||
| chr7:141570123 | C | T | 23 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0219 others(20): Show |
25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.101+14556C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141570123 | |||||||
| chr7:141570295 | CAGA | C | 3 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 |
3 | HG01081.hp2 HG03927.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.101+14730_101+1473 others(7): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 141570295 | ||||||
| chr7:141570436 | A | T | 1 | a0001c0001t0001g0143 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.101+14869A>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141570436 | |||||||
| chr7:141570462 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.101+14895C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141570462 | |||||||
| chr7:141570646 | A | T | 1 | a0001c0001t0001g0119 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.101+15079A>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141570646 | |||||||
| chr7:141571266 | T | C | 9 | a0001c0001t0001g0228 a0001c0001t0003g0261 a0001c0001t0003g0262 others(6): Show |
10 | HG01261.hp1 HG02258.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.101+15699T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141571266 | |||||||
| chr7:141571823 | G | C | 1 | a0001c0001t0002g0246 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.101+16256G>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141571823 | |||||||
| chr7:141571841 | A | G | 1 | a0001c0001t0001g0063 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.101+16274A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141571841 | |||||||
| chr7:141572242 | A | C | 1 | a0001c0001t0007g0019 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.101+16675A>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141572242 | |||||||
| chr7:141572499 | T | G | 1 | a0001c0001t0001g0169 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.101+16932T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141572499 | |||||||
| chr7:141572731 | G | A | 2 | a0001c0001t0001g0009 a0001c0001t0001g0223 |
2 | HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.101+17164G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141572731 | |||||||
| chr7:141572803 | TG | T | 24 | a0001c0001t0001g0228 a0001c0001t0002g0005 a0001c0001t0002g0006 others(21): Show |
26 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(23): Show |
intron_variant | MODIFIER | c.101+17245delG | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 141572803 | ||||||
| chr7:141572806 | G | C | 5 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0001t0001g0253 others(2): Show |
5 | HG01891.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.101+17239G>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141572806 | |||||||
| chr7:141572807 | G | C | 2 | a0001c0001t0005g0257 a0001c0001t0005g0258 |
2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.101+17240G>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141572807 | |||||||
| chr7:141572809 | G | C | 1 | a0001c0001t0001g0220 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.101+17242G>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141572809 | |||||||
| chr7:141572828 | C | T | 1 | a0001c0001t0002g0242 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.101+17261C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141572828 | |||||||
| chr7:141572916 | G | A | 41 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0015 others(38): Show |
42 | HG00140.hp1 HG00642.hp1 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.101+17349G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141572916 | |||||||
| chr7:141573016 | G | T | 34 | a0001c0001t0001g0228 a0001c0001t0002g0005 a0001c0001t0002g0006 others(31): Show |
37 | HG00408.hp1 HG01168.hp2 HG01261.hp1 others(34): Show |
intron_variant | MODIFIER | c.101+17449G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141573016 | |||||||
| chr7:141573226 | T | A | 1 | a0001c0001t0001g0065 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.101+17659T>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141573226 | |||||||
| chr7:141573360 | A | T | 3 | a0001c0001t0001g0110 a0001c0001t0001g0159 a0001c0001t0001g0160 |
3 | HG02602.hp1 HG03688.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.101+17793A>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141573360 | |||||||
| chr7:141573703 | C | T | 5 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0001t0001g0253 others(2): Show |
5 | HG01891.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.101+18136C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141573703 | |||||||
| chr7:141573796 | G | A | 33 | a0001c0001t0001g0228 a0001c0001t0002g0005 a0001c0001t0002g0006 others(30): Show |
36 | HG00408.hp1 HG01168.hp2 HG01261.hp1 others(33): Show |
intron_variant | MODIFIER | c.101+18229G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141573796 | |||||||
| chr7:141573827 | T | C | 2 | a0001c0001t0005g0257 a0001c0001t0005g0258 |
2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.101+18260T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141573827 | |||||||
| chr7:141573829 | C | T | 10 | a0001c0001t0001g0228 a0001c0001t0003g0261 a0001c0001t0003g0262 others(7): Show |
11 | HG01261.hp1 HG02723.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.101+18262C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141573829 | |||||||
| chr7:141574443 | G | A | 1 | a0002c0002t0003g0008 | 2 | HG01261.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.102-18703G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141574443 | |||||||
| chr7:141574578 | G | A | 1 | a0001c0001t0001g0124 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.102-18568G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141574578 | |||||||
| chr7:141574591 | G | C | 1 | a0001c0001t0001g0223 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.102-18555G>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141574591 | |||||||
| chr7:141574637 | A | T | 3 | a0001c0001t0006g0224 a0001c0001t0006g0225 a0001c0001t0006g0226 |
3 | HG02055.hp1 HG02109.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.102-18509A>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141574637 | |||||||
| chr7:141574754 | A | G | 1 | a0001c0001t0001g0114 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.102-18392A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141574754 | |||||||
| chr7:141574758 | G | A | 23 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0219 others(20): Show |
25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.102-18388G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141574758 | |||||||
| chr7:141574860 | GGGAGCGA others(9): Show |
G | 1 | a0001c0001t0001g0223 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.102-18283_102-1826 others(20): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 141574860 | ||||||
| chr7:141574944 | G | T | 1 | a0005c0004t0002g0241 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.102-18202G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141574944 | |||||||
| chr7:141575009 | A | G | 1 | a0001c0001t0017g0240 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.102-18137A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141575009 | |||||||
| chr7:141575119 | G | A | 23 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0219 others(20): Show |
25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.102-18027G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141575119 | |||||||
| chr7:141575457 | T | A | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | NA18991.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.102-17689T>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141575457 | |||||||
| chr7:141575654 | C | CT | 62 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0030 others(59): Show |
62 | HG00423.hp2 HG00558.hp1 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.102-17463dupT | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 141575654 | ||||||
| chr7:141575654 | C | CTT | 9 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0032 others(6): Show |
9 | HG00558.hp2 HG00642.hp2 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.102-17464_102-1746 others(6): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 141575654 | ||||||
| chr7:141575654 | CT | C | 5 | a0001c0001t0001g0124 a0001c0001t0001g0149 a0001c0001t0001g0220 others(2): Show |
5 | HG02055.hp1 HG02109.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.102-17463delT | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 141575654 | ||||||
| chr7:141575654 | CTTT | C | 5 | a0001c0001t0002g0006 a0001c0001t0002g0239 a0001c0001t0002g0244 others(2): Show |
6 | HG02015.hp1 HG02258.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.102-17465_102-1746 others(7): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 141575654 | ||||||
| chr7:141575654 | CTTTT | C | 17 | a0001c0001t0001g0228 a0001c0001t0002g0005 a0001c0001t0002g0230 others(14): Show |
18 | HG00408.hp1 HG02155.hp1 HG02630.hp1 others(15): Show |
intron_variant | MODIFIER | c.102-17466_102-1746 others(8): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 141575654 | ||||||
| chr7:141575654 | CTTTTT | C | 12 | a0001c0001t0002g0219 a0001c0001t0002g0229 a0001c0001t0002g0231 others(9): Show |
13 | HG01168.hp2 HG01884.hp1 HG01952.hp2 others(10): Show |
intron_variant | MODIFIER | c.102-17467_102-1746 others(9): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 141575654 | ||||||
| chr7:141575654 | CTTTTTT | C | 5 | a0001c0001t0003g0262 a0001c0001t0003g0263 a0001c0001t0003g0265 others(2): Show |
6 | HG01261.hp1 HG02723.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.102-17468_102-1746 others(10): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 141575654 | ||||||
| chr7:141575654 | CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0001g0175 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.102-17475_102-1746 others(17): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 141575654 | ||||||
| chr7:141575683 | T | G | 2 | a0002c0002t0003g0008 a0002c0002t0003g0266 |
3 | HG01261.hp1 HG02896.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.102-17463T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141575683 | |||||||
| chr7:141575687 | C | G | 23 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0219 others(20): Show |
25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.102-17459C>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141575687 | |||||||
| chr7:141575837 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.102-17309C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141575837 | |||||||
| chr7:141576246 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.102-16900A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141576246 | |||||||
| chr7:141576263 | A | G | 34 | a0001c0001t0001g0228 a0001c0001t0002g0005 a0001c0001t0002g0006 others(31): Show |
37 | HG00408.hp1 HG01168.hp2 HG01261.hp1 others(34): Show |
intron_variant | MODIFIER | c.102-16883A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141576263 | |||||||
| chr7:141576334 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.102-16812C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141576334 | |||||||
| chr7:141576355 | CTTG | C | 3 | a0001c0001t0006g0224 a0001c0001t0006g0225 a0001c0001t0006g0226 |
3 | HG02055.hp1 HG02109.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.102-16786_102-1678 others(7): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 141576355 | ||||||
| chr7:141576404 | A | G | 23 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0219 others(20): Show |
25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.102-16742A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141576404 | |||||||
| chr7:141576427 | A | G | 1 | a0001c0001t0001g0128 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.102-16719A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141576427 | |||||||
| chr7:141576485 | A | G | 1 | a0001c0001t0001g0009 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.102-16661A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141576485 | |||||||
| chr7:141576632 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.102-16514C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141576632 | |||||||
| chr7:141576633 | G | A | 7 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0001t0001g0253 others(4): Show |
7 | HG01891.hp2 HG02622.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.102-16513G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141576633 | |||||||
| chr7:141576651 | A | G | 1 | a0001c0001t0001g0062 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.102-16495A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141576651 | |||||||
| chr7:141576765 | C | T | 2 | a0001c0001t0005g0257 a0001c0001t0005g0258 |
2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.102-16381C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141576765 | |||||||
| chr7:141576847 | C | T | 2 | a0001c0001t0005g0257 a0001c0001t0005g0258 |
2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.102-16299C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141576847 | |||||||
| chr7:141577035 | G | A | 95 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(92): Show |
95 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.102-16111G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141577035 | |||||||
| chr7:141577239 | A | G | 2 | a0002c0002t0003g0008 a0002c0002t0003g0266 |
3 | HG01261.hp1 HG02896.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.102-15907A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141577239 | |||||||
| chr7:141577418 | C | T | 23 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0219 others(20): Show |
25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.102-15728C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141577418 | |||||||
| chr7:141577614 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.102-15532G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141577614 | |||||||
| chr7:141577633 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.102-15513G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141577633 | |||||||
| chr7:141577742 | C | T | 1 | a0001c0001t0005g0256 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.102-15404C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141577742 | |||||||
| chr7:141577796 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.102-15350C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141577796 | |||||||
| chr7:141577818 | C | CT | 16 | a0001c0001t0001g0015 a0001c0001t0001g0108 a0001c0001t0001g0125 others(13): Show |
16 | HG01168.hp2 HG02055.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.102-15310dupT | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 141577818 | ||||||
| chr7:141577818 | C | CTT | 19 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0219 others(16): Show |
21 | HG00408.hp1 HG01952.hp2 HG02015.hp1 others(18): Show |
intron_variant | MODIFIER | c.102-15311_102-1531 others(6): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 141577818 | ||||||
| chr7:141577818 | CT | C | 12 | a0001c0001t0001g0017 a0001c0001t0001g0066 a0001c0001t0001g0092 others(9): Show |
13 | HG01256.hp1 HG01884.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.102-15310delT | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 141577818 | ||||||
| chr7:141577935 | C | G | 1 | a0001c0001t0003g0261 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.102-15211C>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141577935 | |||||||
| chr7:141578085 | CGTCCATG others(5958): Show |
C | 3 | a0001c0001t0003g0262 a0001c0001t0003g0263 a0001c0001t0003g0264 |
3 | HG02723.hp1 HG02970.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.102-14991_102-9027 others(3): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 141578085 | ||||||
| chr7:141578143 | C | A | 2 | a0001c0001t0005g0257 a0001c0001t0005g0258 |
2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.102-15003C>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141578143 | |||||||
| chr7:141578156 | G | T | 1 | a0001c0001t0001g0133 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.102-14990G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141578156 | |||||||
| chr7:141578313 | G | T | 2 | a0001c0001t0005g0257 a0001c0001t0005g0258 |
2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.102-14833G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141578313 | |||||||
| chr7:141578323 | G | A | 1 | a0001c0001t0001g0037 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.102-14823G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141578323 | |||||||
| chr7:141578396 | C | G | 2 | a0001c0001t0005g0257 a0001c0001t0005g0258 |
2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.102-14750C>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141578396 | |||||||
| chr7:141578401 | G | T | 2 | a0001c0001t0001g0047 a0001c0001t0001g0222 |
2 | HG00408.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.102-14745G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141578401 | |||||||
| chr7:141578402 | C | T | 2 | a0001c0001t0001g0047 a0001c0001t0001g0222 |
2 | HG00408.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.102-14744C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141578402 | |||||||
| chr7:141578469 | C | G | 2 | a0001c0001t0005g0257 a0001c0001t0005g0258 |
2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.102-14677C>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141578469 | |||||||
| chr7:141578776 | CGAATAAG others(4): Show |
C | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | NA18991.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.102-14366_102-1435 others(15): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 141578776 | ||||||
| chr7:141578847 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.102-14299G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141578847 | |||||||
| chr7:141579017 | A | G | 1 | a0001c0001t0001g0228 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.102-14129A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141579017 | |||||||
| chr7:141579027 | A | T | 2 | a0001c0001t0001g0065 a0001c0001t0001g0100 |
2 | NA18975.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.102-14119A>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141579027 | |||||||
| chr7:141579152 | G | C | 1 | a0001c0001t0005g0256 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.102-13994G>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141579152 | |||||||
| chr7:141579249 | G | C | 1 | a0001c0001t0002g0246 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.102-13897G>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141579249 | |||||||
| chr7:141579270 | C | T | 2 | a0001c0001t0005g0257 a0001c0001t0005g0258 |
2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.102-13876C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141579270 | |||||||
| chr7:141579308 | G | A | 2 | a0001c0001t0005g0257 a0001c0001t0005g0258 |
2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.102-13838G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141579308 | |||||||
| chr7:141579336 | A | C | 2 | a0001c0001t0005g0257 a0001c0001t0005g0258 |
2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.102-13810A>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141579336 | |||||||
| chr7:141579370 | T | C | 5 | a0001c0001t0003g0261 a0001c0001t0003g0265 a0001c0001t0005g0256 others(2): Show |
6 | HG01261.hp1 HG02258.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.102-13776T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141579370 | |||||||
| chr7:141579380 | C | T | 1 | a0001c0001t0001g0104 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.102-13766C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141579380 | |||||||
| chr7:141579456 | G | A | 23 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0219 others(20): Show |
25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.102-13690G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141579456 | |||||||
| chr7:141579527 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.102-13619G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141579527 | |||||||
| chr7:141579597 | C | T | 7 | a0001c0001t0004g0007 a0001c0001t0004g0250 a0001c0001t0004g0251 others(4): Show |
8 | HG01884.hp1 HG02630.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.102-13549C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141579597 | |||||||
| chr7:141579689 | G | T | 1 | a0001c0001t0001g0108 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.102-13457G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141579689 | |||||||
| chr7:141579779 | C | T | 1 | a0001c0001t0002g0259 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.102-13367C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141579779 | |||||||
| chr7:141579847 | T | C | 10 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0001t0001g0253 others(7): Show |
11 | HG01884.hp1 HG01891.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.102-13299T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141579847 | |||||||
| chr7:141579983 | G | T | 2 | a0002c0002t0003g0008 a0002c0002t0003g0266 |
3 | HG01261.hp1 HG02896.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.102-13163G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141579983 | |||||||
| chr7:141580005 | G | A | 1 | a0001c0001t0003g0261 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.102-13141G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141580005 | |||||||
| chr7:141580220 | G | A | 1 | a0001c0001t0001g0031 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.102-12926G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141580220 | |||||||
| chr7:141580273 | A | G | 23 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0219 others(20): Show |
25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.102-12873A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141580273 | |||||||
| chr7:141580278 | G | C | 95 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(92): Show |
95 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.102-12868G>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141580278 | |||||||
| chr7:141580279 | G | A | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | NA18977.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.102-12867G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141580279 | |||||||
| chr7:141580385 | G | A | 4 | a0001c0001t0003g0261 a0001c0001t0003g0265 a0002c0002t0003g0008 others(1): Show |
5 | HG01261.hp1 HG02896.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.102-12761G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141580385 | |||||||
| chr7:141580409 | T | C | 4 | a0001c0001t0001g0048 a0001c0001t0001g0058 a0001c0001t0008g0041 others(1): Show |
4 | HG02572.hp2 HG02818.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.102-12737T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141580409 | |||||||
| chr7:141580506 | C | T | 5 | a0001c0001t0004g0007 a0001c0001t0004g0250 a0001c0001t0004g0251 others(2): Show |
6 | HG01884.hp1 HG02630.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.102-12640C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141580506 | |||||||
| chr7:141580625 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.102-12521G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141580625 | |||||||
| chr7:141580705 | C | T | 2 | a0001c0001t0001g0018 a0001c0001t0001g0046 |
2 | HG02027.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.102-12441C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141580705 | |||||||
| chr7:141580706 | G | A | 6 | a0001c0001t0003g0261 a0001c0001t0003g0265 a0001c0001t0005g0257 others(3): Show |
7 | HG01261.hp1 HG02896.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.102-12440G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141580706 | |||||||
| chr7:141580798 | G | A | 95 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(92): Show |
95 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.102-12348G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141580798 | |||||||
| chr7:141580891 | C | T | 1 | a0001c0001t0005g0256 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.102-12255C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141580891 | |||||||
| chr7:141580915 | G | A | 2 | a0001c0001t0001g0065 a0001c0001t0001g0100 |
2 | NA18975.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.102-12231G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141580915 | |||||||
| chr7:141581010 | G | A | 3 | a0001c0001t0001g0043 a0001c0001t0001g0055 a0001c0001t0001g0104 |
3 | HG02080.hp2 NA18948.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.102-12136G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141581010 | |||||||
| chr7:141581081 | C | T | 1 | a0001c0001t0001g0009 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.102-12065C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141581081 | |||||||
| chr7:141581246 | G | T | 1 | a0001c0001t0001g0108 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.102-11900G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141581246 | |||||||
| chr7:141581458 | G | C | 1 | a0001c0001t0005g0256 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.102-11688G>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141581458 | |||||||
| chr7:141581632 | A | G | 1 | a0001c0001t0001g0212 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.102-11514A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141581632 | |||||||
| chr7:141581883 | T | C | 5 | a0001c0001t0004g0007 a0001c0001t0004g0250 a0001c0001t0004g0251 others(2): Show |
6 | HG01884.hp1 HG02630.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.102-11263T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141581883 | |||||||
| chr7:141581930 | G | A | 2 | a0001c0001t0005g0257 a0001c0001t0005g0258 |
2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.102-11216G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141581930 | |||||||
| chr7:141582002 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.102-11144C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141582002 | |||||||
| chr7:141582012 | G | A | 1 | a0001c0001t0009g0122 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.102-11134G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141582012 | |||||||
| chr7:141582069 | C | T | 39 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0219 others(36): Show |
43 | HG00408.hp1 HG01168.hp2 HG01261.hp1 others(40): Show |
intron_variant | MODIFIER | c.102-11077C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141582069 | |||||||
| chr7:141582208 | G | A | 2 | a0001c0001t0001g0136 a0001c0001t0013g0139 |
2 | HG02615.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.102-10938G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141582208 | |||||||
| chr7:141582295 | G | A | 2 | a0001c0001t0001g0137 a0001c0001t0001g0138 |
2 | HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.102-10851G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141582295 | |||||||
| chr7:141582340 | G | A | 2 | a0002c0002t0003g0008 a0002c0002t0003g0266 |
3 | HG01261.hp1 HG02896.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.102-10806G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141582340 | |||||||
| chr7:141582529 | G | A | 2 | a0001c0001t0001g0113 a0001c0001t0001g0164 |
2 | HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.102-10617G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141582529 | |||||||
| chr7:141582624 | T | A | 1 | a0001c0001t0001g0120 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.102-10522T>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141582624 | |||||||
| chr7:141582768 | C | G | 1 | a0001c0001t0005g0256 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.102-10378C>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141582768 | |||||||
| chr7:141582898 | G | A | 23 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0219 others(20): Show |
25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.102-10248G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141582898 | |||||||
| chr7:141582957 | A | T | 1 | a0001c0001t0003g0261 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.102-10189A>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141582957 | |||||||
| chr7:141582968 | A | G | 1 | a0001c0001t0001g0191 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.102-10178A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141582968 | |||||||
| chr7:141583060 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.102-10086G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141583060 | |||||||
| chr7:141583236 | A | T | 1 | a0001c0001t0001g0091 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.102-9910A>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141583236 | |||||||
| chr7:141583256 | C | A | 1 | a0001c0001t0003g0261 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.102-9890C>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141583256 | |||||||
| chr7:141583353 | A | G | 1 | a0001c0001t0001g0217 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.102-9793A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141583353 | |||||||
| chr7:141583476 | C | T | 1 | a0001c0001t0003g0265 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.102-9670C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141583476 | |||||||
| chr7:141583541 | T | C | 201 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(198): Show |
206 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.102-9605T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141583541 | |||||||
| chr7:141583573 | A | C | 23 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0219 others(20): Show |
25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.102-9573A>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141583573 | |||||||
| chr7:141583618 | C | A | 1 | a0001c0001t0001g0108 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.102-9528C>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141583618 | |||||||
| chr7:141583711 | G | A | 1 | a0001c0001t0001g0223 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.102-9435G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141583711 | |||||||
| chr7:141583737 | G | A | 4 | a0001c0001t0003g0261 a0001c0001t0003g0265 a0002c0002t0003g0008 others(1): Show |
5 | HG01261.hp1 HG02896.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.102-9409G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141583737 | |||||||
| chr7:141583810 | C | T | 3 | a0001c0001t0006g0224 a0001c0001t0006g0225 a0001c0001t0006g0226 |
3 | HG02055.hp1 HG02109.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.102-9336C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141583810 | |||||||
| chr7:141583951 | T | C | 1 | a0001c0001t0001g0024 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.102-9195T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141583951 | |||||||
| chr7:141584049 | G | A | 2 | a0001c0001t0005g0257 a0001c0001t0005g0258 |
2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.102-9097G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141584049 | |||||||
| chr7:141584059 | G | T | 1 | a0001c0001t0001g0165 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.102-9087G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141584059 | |||||||
| chr7:141584125 | C | T | 1 | a0001c0001t0001g0216 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.102-9021C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141584125 | |||||||
| chr7:141584131 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.102-9015C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141584131 | |||||||
| chr7:141584140 | A | G | 1 | a0001c0001t0004g0260 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.102-9006A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141584140 | |||||||
| chr7:141584166 | G | A | 2 | a0001c0001t0005g0257 a0001c0001t0005g0258 |
2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.102-8980G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141584166 | |||||||
| chr7:141584256 | A | G | 3 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0128 |
3 | HG01496.hp2 HG03704.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.102-8890A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141584256 | |||||||
| chr7:141584445 | C | A | 1 | a0001c0001t0001g0176 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.102-8701C>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141584445 | |||||||
| chr7:141584587 | A | C | 1 | a0001c0001t0001g0155 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.102-8559A>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141584587 | |||||||
| chr7:141584593 | T | G | 2 | a0001c0001t0005g0257 a0001c0001t0005g0258 |
2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.102-8553T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141584593 | |||||||
| chr7:141584865 | C | G | 1 | a0001c0001t0001g0117 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.102-8281C>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141584865 | |||||||
| chr7:141584911 | G | A | 1 | a0001c0001t0004g0260 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.102-8235G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141584911 | |||||||
| chr7:141584930 | T | C | 1 | a0001c0001t0001g0124 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.102-8216T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141584930 | |||||||
| chr7:141585002 | A | G | 2 | a0001c0001t0001g0176 a0001c0001t0001g0207 |
2 | NA18957.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.102-8144A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141585002 | |||||||
| chr7:141585110 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.102-8036G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141585110 | |||||||
| chr7:141585111 | T | G | 1 | a0001c0001t0001g0050 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.102-8035T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141585111 | |||||||
| chr7:141585174 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.102-7972G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141585174 | |||||||
| chr7:141585379 | C | T | 38 | a0001c0001t0001g0228 a0001c0001t0002g0005 a0001c0001t0002g0006 others(35): Show |
41 | HG00408.hp1 HG01168.hp2 HG01261.hp1 others(38): Show |
intron_variant | MODIFIER | c.102-7767C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141585379 | |||||||
| chr7:141585409 | G | C | 1 | a0001c0001t0001g0194 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.102-7737G>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141585409 | |||||||
| chr7:141585555 | G | A | 7 | a0001c0001t0003g0261 a0001c0001t0003g0262 a0001c0001t0003g0263 others(4): Show |
8 | HG01261.hp1 HG02723.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.102-7591G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141585555 | |||||||
| chr7:141585706 | A | G | 1 | a0001c0001t0003g0265 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.102-7440A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141585706 | |||||||
| chr7:141585910 | T | C | 1 | a0001c0001t0001g0132 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.102-7236T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141585910 | |||||||
| chr7:141586034 | G | A | 2 | a0001c0001t0003g0262 a0001c0001t0003g0264 |
2 | HG02723.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.102-7112G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141586034 | |||||||
| chr7:141586098 | C | T | 3 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 |
3 | HG02055.hp2 HG02486.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.102-7048C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141586098 | |||||||
| chr7:141586156 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.102-6990C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141586156 | |||||||
| chr7:141586337 | C | T | 2 | a0001c0001t0001g0013 a0001c0001t0001g0049 |
2 | HG00735.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.102-6809C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141586337 | |||||||
| chr7:141586475 | A | T | 1 | a0001c0001t0001g0145 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.102-6671A>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141586475 | |||||||
| chr7:141586663 | A | C | 2 | a0001c0001t0001g0136 a0001c0001t0013g0139 |
2 | HG02615.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.102-6483A>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141586663 | |||||||
| chr7:141586672 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.102-6474A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141586672 | |||||||
| chr7:141586831 | G | T | 1 | a0001c0001t0001g0185 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.102-6315G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141586831 | |||||||
| chr7:141586956 | G | A | 9 | a0001c0001t0003g0261 a0001c0001t0003g0262 a0001c0001t0003g0263 others(6): Show |
10 | HG01261.hp1 HG02723.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.102-6190G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141586956 | |||||||
| chr7:141587021 | C | T | 38 | a0001c0001t0001g0228 a0001c0001t0002g0005 a0001c0001t0002g0006 others(35): Show |
41 | HG00408.hp1 HG01168.hp2 HG01261.hp1 others(38): Show |
intron_variant | MODIFIER | c.102-6125C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141587021 | |||||||
| chr7:141587040 | G | A | 1 | a0001c0001t0001g0036 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.102-6106G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141587040 | |||||||
| chr7:141587067 | G | A | 6 | a0001c0001t0001g0022 a0001c0001t0001g0028 a0001c0001t0001g0037 others(3): Show |
6 | HG02735.hp2 HG02738.hp2 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.102-6079G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141587067 | |||||||
| chr7:141587085 | T | C | 150 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(147): Show |
154 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.102-6061T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141587085 | |||||||
| chr7:141587484 | T | C | 1 | a0001c0001t0001g0062 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.102-5662T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141587484 | |||||||
| chr7:141587584 | C | T | 4 | a0001c0001t0006g0224 a0001c0001t0006g0225 a0001c0001t0006g0226 others(1): Show |
4 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.102-5562C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141587584 | |||||||
| chr7:141587671 | A | G | 1 | a0001c0001t0001g0098 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.102-5475A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141587671 | |||||||
| chr7:141587729 | A | G | 1 | a0001c0001t0001g0228 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.102-5417A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141587729 | |||||||
| chr7:141587792 | T | C | 10 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0001t0001g0253 others(7): Show |
11 | HG01884.hp1 HG01891.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.102-5354T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141587792 | |||||||
| chr7:141587852 | G | A | 95 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(92): Show |
95 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.102-5294G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141587852 | |||||||
| chr7:141587949 | A | G | 1 | a0001c0001t0001g0214 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.102-5197A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141587949 | |||||||
| chr7:141588114 | T | G | 1 | a0001c0001t0001g0063 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.102-5032T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141588114 | |||||||
| chr7:141588135 | A | T | 2 | a0001c0001t0005g0257 a0001c0001t0005g0258 |
2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.102-5011A>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141588135 | |||||||
| chr7:141588270 | G | T | 1 | a0001c0001t0001g0059 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.102-4876G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141588270 | |||||||
| chr7:141588617 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.102-4529G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141588617 | |||||||
| chr7:141588617 | G | GA | 8 | a0001c0001t0001g0067 a0001c0001t0001g0228 a0001c0001t0002g0219 others(5): Show |
8 | HG02055.hp1 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.102-4516dupA | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 141588617 | ||||||
| chr7:141588966 | G | A | 7 | a0001c0001t0003g0261 a0001c0001t0003g0262 a0001c0001t0003g0263 others(4): Show |
8 | HG01261.hp1 HG02723.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.102-4180G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141588966 | |||||||
| chr7:141589347 | T | C | 1 | a0001c0001t0001g0228 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.102-3799T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141589347 | |||||||
| chr7:141589563 | A | AT | 7 | a0001c0001t0001g0118 a0001c0001t0001g0248 a0001c0001t0001g0249 others(4): Show |
7 | HG01891.hp2 HG02109.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.102-3569dupT | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 141589563 | ||||||
| chr7:141589749 | G | A | 1 | a0004c0003t0010g0227 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.102-3397G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141589749 | |||||||
| chr7:141589751 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.102-3395G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141589751 | |||||||
| chr7:141589787 | C | T | 2 | a0001c0001t0001g0048 a0001c0001t0001g0058 |
2 | HG02572.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.102-3359C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141589787 | |||||||
| chr7:141590271 | T | C | 48 | a0001c0001t0001g0228 a0001c0001t0001g0248 a0001c0001t0001g0249 others(45): Show |
52 | HG00408.hp1 HG01168.hp2 HG01261.hp1 others(49): Show |
intron_variant | MODIFIER | c.102-2875T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141590271 | |||||||
| chr7:141590384 | G | A | 5 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0001g0039 others(2): Show |
5 | HG00735.hp1 HG01192.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.102-2762G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141590384 | |||||||
| chr7:141590457 | G | A | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | NA18977.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.102-2689G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141590457 | |||||||
| chr7:141590507 | T | C | 2 | a0002c0002t0003g0008 a0002c0002t0003g0266 |
3 | HG01261.hp1 HG02896.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.102-2639T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141590507 | |||||||
| chr7:141590518 | G | A | 7 | a0001c0001t0003g0261 a0001c0001t0003g0262 a0001c0001t0003g0263 others(4): Show |
8 | HG01261.hp1 HG02723.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.102-2628G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141590518 | |||||||
| chr7:141590623 | CTT | C | 9 | a0001c0001t0003g0261 a0001c0001t0003g0262 a0001c0001t0003g0263 others(6): Show |
10 | HG01261.hp1 HG02723.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.102-2521_102-2520d others(4): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 141590623 | ||||||
| chr7:141590930 | G | T | 2 | a0001c0001t0005g0257 a0001c0001t0005g0258 |
2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.102-2216G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141590930 | |||||||
| chr7:141590953 | A | G | 2 | a0001c0001t0001g0137 a0001c0001t0001g0138 |
2 | HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.102-2193A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141590953 | |||||||
| chr7:141591058 | T | A | 1 | a0001c0001t0001g0209 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.102-2088T>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141591058 | |||||||
| chr7:141591082 | G | GT | 14 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0061 others(11): Show |
14 | HG00735.hp2 HG01952.hp2 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.102-2037dupT | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 141591082 | ||||||
| chr7:141591082 | GT | G | 150 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(147): Show |
152 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.102-2037delT | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 141591082 | ||||||
| chr7:141591082 | GTT | G | 10 | a0001c0001t0001g0053 a0001c0001t0001g0073 a0001c0001t0001g0074 others(7): Show |
11 | HG01346.hp1 HG01884.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.102-2038_102-2037d others(4): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 141591082 | ||||||
| chr7:141591082 | GTTTTTTT others(6): Show |
G | 8 | a0001c0001t0003g0261 a0001c0001t0003g0262 a0001c0001t0003g0263 others(5): Show |
9 | HG01261.hp1 HG02258.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.102-2049_102-2037d others(15): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 141591082 | ||||||
| chr7:141591083 | T | A | 1 | a0001c0001t0002g0219 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.102-2063T>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141591083 | |||||||
| chr7:141591086 | T | G | 5 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0001t0001g0253 others(2): Show |
5 | HG01891.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.102-2060T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141591086 | |||||||
| chr7:141591087 | T | G | 1 | a0001c0001t0006g0226 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.102-2059T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141591087 | |||||||
| chr7:141591088 | T | G | 6 | a0001c0001t0004g0007 a0001c0001t0004g0250 a0001c0001t0004g0251 others(3): Show |
7 | HG01884.hp1 HG02630.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.102-2058T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141591088 | |||||||
| chr7:141591096 | T | G | 1 | a0001c0001t0001g0068 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.102-2050T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141591096 | |||||||
| chr7:141591114 | CAG | C | 3 | a0001c0001t0003g0262 a0001c0001t0003g0263 a0001c0001t0003g0264 |
3 | HG02723.hp1 HG02970.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.102-2029_102-2028d others(4): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 141591114 | ||||||
| chr7:141591323 | C | G | 1 | a0001c0001t0001g0185 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.102-1823C>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141591323 | |||||||
| chr7:141591340 | A | G | 4 | a0001c0001t0006g0224 a0001c0001t0006g0225 a0001c0001t0006g0226 others(1): Show |
4 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.102-1806A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141591340 | |||||||
| chr7:141591466 | C | A | 1 | a0001c0001t0001g0037 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.102-1680C>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141591466 | |||||||
| chr7:141591610 | T | G | 1 | a0001c0001t0004g0260 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.102-1536T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141591610 | |||||||
| chr7:141591712 | C | T | 1 | a0001c0001t0003g0262 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.102-1434C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141591712 | |||||||
| chr7:141591751 | T | C | 1 | a0001c0001t0001g0037 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.102-1395T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141591751 | |||||||
| chr7:141592043 | C | A | 1 | a0001c0001t0001g0151 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.102-1103C>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141592043 | |||||||
| chr7:141592273 | G | A | 1 | a0001c0001t0001g0053 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.102-873G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141592273 | |||||||
| chr7:141592345 | T | A | 2 | a0001c0001t0005g0257 a0001c0001t0005g0258 |
2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.102-801T>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141592345 | |||||||
| chr7:141592613 | A | G | 1 | a0001c0001t0005g0256 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.102-533A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141592613 | |||||||
| chr7:141592641 | C | A | 1 | a0001c0001t0001g0108 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.102-505C>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141592641 | |||||||
| chr7:141592743 | G | A | 1 | a0001c0001t0003g0265 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.102-403G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141592743 | |||||||
| chr7:141592746 | C | T | 1 | a0001c0001t0004g0260 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.102-400C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141592746 | |||||||
| chr7:141592964 | AAAGTGCT others(10): Show |
A | 6 | a0001c0001t0003g0261 a0001c0001t0003g0262 a0001c0001t0003g0263 others(3): Show |
7 | HG01261.hp1 HG02723.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.102-181_102-165del others(17): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 2/15 | chr7 | 141592964 | |||||||
| chr7:141593452 | C | T | 7 | a0001c0001t0003g0261 a0001c0001t0003g0262 a0001c0001t0003g0263 others(4): Show |
8 | HG01261.hp1 HG02723.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.141+267C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 3/15 | chr7 | 141593452 | |||||||
| chr7:141593617 | A | G | 1 | a0001c0001t0001g0016 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.141+432A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 3/15 | chr7 | 141593617 | |||||||
| chr7:141593995 | C | T | 1 | a0001c0001t0014g0010 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.141+810C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 3/15 | chr7 | 141593995 | |||||||
| chr7:141594535 | G | C | 4 | a0001c0001t0002g0229 a0001c0001t0002g0231 a0001c0001t0002g0232 others(1): Show |
4 | HG01952.hp2 HG02818.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.141+1350G>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 3/15 | chr7 | 141594535 | |||||||
| chr7:141594684 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.141+1499G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 3/15 | chr7 | 141594684 | |||||||
| chr7:141594798 | A | T | 1 | a0001c0001t0005g0256 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.141+1613A>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 3/15 | chr7 | 141594798 | |||||||
| chr7:141594949 | C | G | 2 | a0001c0001t0001g0137 a0001c0001t0001g0138 |
2 | HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.142-1613C>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 3/15 | chr7 | 141594949 | |||||||
| chr7:141595059 | C | A | 1 | a0001c0001t0001g0228 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.142-1503C>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 3/15 | chr7 | 141595059 | |||||||
| chr7:141595128 | A | T | 1 | a0001c0001t0001g0133 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.142-1434A>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 3/15 | chr7 | 141595128 | |||||||
| chr7:141595258 | T | C | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0015 others(74): Show |
79 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.142-1304T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 3/15 | chr7 | 141595258 | |||||||
| chr7:141595371 | A | G | 1 | a0001c0001t0001g0228 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.142-1191A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 3/15 | chr7 | 141595371 | |||||||
| chr7:141595669 | A | T | 2 | a0001c0001t0001g0047 a0001c0001t0001g0222 |
2 | HG00408.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.142-893A>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 3/15 | chr7 | 141595669 | |||||||
| chr7:141595811 | C | A | 1 | a0001c0001t0001g0228 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.142-751C>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 3/15 | chr7 | 141595811 | |||||||
| chr7:141596081 | C | T | 1 | a0001c0001t0001g0171 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.142-481C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 3/15 | chr7 | 141596081 | |||||||
| chr7:141596670 | T | G | 1 | a0001c0001t0001g0069 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.221+29T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | chr7 | 141596670 | |||||||
| chr7:141596749 | A | G | 1 | a0001c0001t0017g0240 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.221+108A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | chr7 | 141596749 | |||||||
| chr7:141596848 | G | A | 3 | a0001c0001t0003g0262 a0001c0001t0003g0263 a0001c0001t0003g0264 |
3 | HG02723.hp1 HG02970.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.221+207G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | chr7 | 141596848 | |||||||
| chr7:141596921 | C | T | 1 | a0001c0001t0004g0260 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.221+280C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | chr7 | 141596921 | |||||||
| chr7:141596929 | G | A | 1 | a0001c0001t0001g0032 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.221+288G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | chr7 | 141596929 | |||||||
| chr7:141597735 | G | A | 1 | a0004c0003t0010g0227 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.221+1094G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | chr7 | 141597735 | |||||||
| chr7:141597876 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.221+1235G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | chr7 | 141597876 | |||||||
| chr7:141597890 | C | CA | 16 | a0001c0001t0001g0001 a0001c0001t0001g0052 a0001c0001t0001g0054 others(13): Show |
17 | HG00140.hp1 HG01192.hp1 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.221+1278dupA | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr7 | 141597890 | ||||||
| chr7:141597890 | CA | C | 20 | a0001c0001t0001g0099 a0001c0001t0001g0108 a0001c0001t0001g0112 others(17): Show |
21 | HG00673.hp2 HG01255.hp2 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.221+1278delA | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr7 | 141597890 | ||||||
| chr7:141597890 | CAA | C | 12 | a0001c0001t0001g0167 a0001c0001t0001g0228 a0001c0001t0001g0248 others(9): Show |
12 | HG01099.hp2 HG01891.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.221+1277_221+1278d others(4): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr7 | 141597890 | ||||||
| chr7:141597890 | CAAA | C | 23 | a0001c0001t0001g0253 a0001c0001t0001g0254 a0001c0001t0002g0005 others(20): Show |
25 | HG00408.hp1 HG01261.hp1 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.221+1276_221+1278d others(5): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr7 | 141597890 | ||||||
| chr7:141597890 | CAAAA | C | 5 | a0001c0001t0002g0006 a0001c0001t0002g0259 a0001c0001t0005g0257 others(2): Show |
6 | HG01168.hp2 HG02486.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.221+1275_221+1278d others(6): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr7 | 141597890 | ||||||
| chr7:141597890 | CAAAAAAA others(4): Show |
C | 5 | a0001c0001t0001g0034 a0001c0001t0001g0063 a0001c0001t0001g0070 others(2): Show |
5 | HG00673.hp1 HG01070.hp1 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.221+1268_221+1278d others(13): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr7 | 141597890 | ||||||
| chr7:141597890 | CAAAAAAA others(5): Show |
C | 73 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(70): Show |
73 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.221+1267_221+1278d others(14): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr7 | 141597890 | ||||||
| chr7:141597890 | CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0001g0087 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.221+1266_221+1278d others(15): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr7 | 141597890 | ||||||
| chr7:141597890 | CAAAAAAA others(9): Show |
C | 4 | a0001c0001t0006g0224 a0001c0001t0006g0225 a0001c0001t0006g0226 others(1): Show |
4 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.221+1263_221+1278d others(18): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr7 | 141597890 | ||||||
| chr7:141598116 | G | A | 3 | a0001c0001t0006g0224 a0001c0001t0006g0225 a0001c0001t0006g0226 |
3 | HG02055.hp1 HG02109.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.221+1475G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | chr7 | 141598116 | |||||||
| chr7:141598179 | C | G | 11 | a0001c0001t0001g0001 a0001c0001t0001g0126 a0001c0001t0001g0127 others(8): Show |
12 | HG00140.hp1 HG01081.hp2 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.221+1538C>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | chr7 | 141598179 | |||||||
| chr7:141598259 | C | T | 2 | a0001c0001t0001g0009 a0001c0001t0001g0223 |
2 | HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.221+1618C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | chr7 | 141598259 | |||||||
| chr7:141598967 | A | G | 10 | a0001c0001t0003g0261 a0001c0001t0003g0262 a0001c0001t0003g0263 others(7): Show |
11 | HG01261.hp1 HG02258.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.222-2238A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | chr7 | 141598967 | |||||||
| chr7:141599061 | A | G | 2 | a0001c0001t0005g0257 a0001c0001t0005g0258 |
2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.222-2144A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | chr7 | 141599061 | |||||||
| chr7:141599169 | T | C | 1 | a0001c0001t0003g0265 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.222-2036T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | chr7 | 141599169 | |||||||
| chr7:141599172 | C | G | 3 | a0001c0001t0001g0110 a0001c0001t0001g0159 a0001c0001t0001g0160 |
3 | HG02602.hp1 HG03688.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.222-2033C>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | chr7 | 141599172 | |||||||
| chr7:141599233 | T | A | 8 | a0001c0001t0001g0119 a0001c0001t0001g0123 a0001c0001t0001g0129 others(5): Show |
8 | HG01261.hp2 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.222-1972T>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | chr7 | 141599233 | |||||||
| chr7:141599249 | C | T | 1 | a0004c0003t0010g0227 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.222-1956C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | chr7 | 141599249 | |||||||
| chr7:141599271 | G | T | 1 | a0001c0001t0001g0086 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.222-1934G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | chr7 | 141599271 | |||||||
| chr7:141599339 | GCTAAAAG others(3): Show |
G | 1 | a0001c0001t0001g0119 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.222-1861_222-1852d others(12): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr7 | 141599339 | ||||||
| chr7:141599371 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.222-1834G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | chr7 | 141599371 | |||||||
| chr7:141599435 | A | G | 2 | a0001c0001t0005g0257 a0001c0001t0005g0258 |
2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.222-1770A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | chr7 | 141599435 | |||||||
| chr7:141599527 | A | G | 3 | a0001c0001t0001g0123 a0001c0001t0001g0147 a0001c0001t0001g0218 |
3 | HG02572.hp1 HG02895.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.222-1678A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | chr7 | 141599527 | |||||||
| chr7:141599696 | G | A | 7 | a0001c0001t0001g0119 a0001c0001t0001g0123 a0001c0001t0001g0129 others(4): Show |
7 | HG01261.hp2 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.222-1509G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | chr7 | 141599696 | |||||||
| chr7:141599865 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.222-1340C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | chr7 | 141599865 | |||||||
| chr7:141600013 | G | T | 1 | a0001c0001t0001g0037 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.222-1192G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | chr7 | 141600013 | |||||||
| chr7:141600099 | T | C | 11 | a0001c0001t0001g0131 a0001c0001t0001g0248 a0001c0001t0001g0249 others(8): Show |
12 | HG01884.hp1 HG01891.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.222-1106T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | chr7 | 141600099 | |||||||
| chr7:141600228 | G | A | 1 | a0001c0001t0014g0010 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.222-977G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | chr7 | 141600228 | |||||||
| chr7:141600239 | A | C | 23 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0219 others(20): Show |
25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.222-966A>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | chr7 | 141600239 | |||||||
| chr7:141600270 | T | C | 2 | a0001c0001t0001g0176 a0001c0001t0001g0207 |
2 | NA18957.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.222-935T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | chr7 | 141600270 | |||||||
| chr7:141600696 | A | G | 48 | a0001c0001t0001g0228 a0001c0001t0001g0248 a0001c0001t0001g0249 others(45): Show |
52 | HG00408.hp1 HG01168.hp2 HG01261.hp1 others(49): Show |
intron_variant | MODIFIER | c.222-509A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | chr7 | 141600696 | |||||||
| chr7:141600811 | T | C | 34 | a0001c0001t0001g0228 a0001c0001t0002g0005 a0001c0001t0002g0006 others(31): Show |
37 | HG00408.hp1 HG01168.hp2 HG01261.hp1 others(34): Show |
intron_variant | MODIFIER | c.222-394T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | chr7 | 141600811 | |||||||
| chr7:141600957 | C | T | 2 | a0001c0001t0001g0182 a0001c0001t0001g0184 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.222-248C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | chr7 | 141600957 | |||||||
| chr7:141601077 | T | C | 8 | a0001c0001t0003g0261 a0001c0001t0003g0262 a0001c0001t0003g0263 others(5): Show |
9 | HG01261.hp1 HG02258.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.222-128T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 4/15 | chr7 | 141601077 | |||||||
| chr7:141601298 | A | G | 2 | a0002c0002t0003g0008 a0002c0002t0003g0266 |
3 | HG01261.hp1 HG02896.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.297+18A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141601298 | |||||||
| chr7:141601404 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.297+124C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141601404 | |||||||
| chr7:141601891 | T | C | 1 | a0001c0001t0001g0228 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.297+611T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141601891 | |||||||
| chr7:141602033 | C | CAT | 38 | a0001c0001t0001g0228 a0001c0001t0002g0005 a0001c0001t0002g0006 others(35): Show |
41 | HG00408.hp1 HG01168.hp2 HG01261.hp1 others(38): Show |
intron_variant | MODIFIER | c.297+756_297+757dup others(2): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141602033 | ||||||
| chr7:141602045 | C | T | 4 | a0001c0001t0003g0261 a0001c0001t0003g0262 a0001c0001t0003g0263 others(1): Show |
4 | HG02723.hp1 HG02970.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.297+765C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141602045 | |||||||
| chr7:141602073 | A | G | 48 | a0001c0001t0001g0228 a0001c0001t0001g0248 a0001c0001t0001g0249 others(45): Show |
52 | HG00408.hp1 HG01168.hp2 HG01261.hp1 others(49): Show |
intron_variant | MODIFIER | c.297+793A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141602073 | |||||||
| chr7:141602172 | C | CGTGTGT | 10 | a0001c0001t0002g0005 a0001c0001t0002g0230 a0001c0001t0002g0234 others(7): Show |
11 | HG00408.hp1 HG02015.hp1 HG02155.hp1 others(8): Show |
intron_variant | MODIFIER | c.297+892_297+893ins others(6): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141602172 | |||||||
| chr7:141602172 | C | CGTGTGTG others(3): Show |
3 | a0001c0001t0002g0245 a0001c0001t0003g0265 a0001c0001t0004g0007 |
4 | HG03453.hp2 HG03540.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.297+892_297+893ins others(10): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141602172 | |||||||
| chr7:141602172 | C | CGTGTGTG others(5): Show |
9 | a0001c0001t0001g0228 a0001c0001t0002g0229 a0001c0001t0002g0232 others(6): Show |
9 | HG01952.hp2 HG02258.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.297+892_297+893ins others(12): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141602172 | |||||||
| chr7:141602172 | C | CGTGTGTG others(7): Show |
6 | a0001c0001t0001g0043 a0001c0001t0002g0231 a0001c0001t0003g0261 others(3): Show |
6 | HG01884.hp1 HG02970.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.297+892_297+893ins others(14): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141602172 | |||||||
| chr7:141602172 | C | CGTGTGTG others(9): Show |
2 | a0001c0001t0002g0006 a0001c0001t0004g0252 |
3 | HG02486.hp1 HG02965.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.297+892_297+893ins others(16): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141602172 | |||||||
| chr7:141602172 | C | CGTGTGTG others(11): Show |
3 | a0001c0001t0004g0250 a0002c0002t0003g0008 a0002c0002t0003g0266 |
4 | HG01261.hp1 HG02896.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.297+892_297+893ins others(18): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141602172 | |||||||
| chr7:141602172 | C | CGTGTGTG others(13): Show |
2 | a0001c0001t0002g0219 a0001c0001t0003g0263 |
2 | HG02647.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.297+892_297+893ins others(20): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141602172 | |||||||
| chr7:141602172 | C | CGTGTGTG others(15): Show |
2 | a0001c0001t0001g0055 a0001c0001t0001g0071 |
2 | HG01070.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.297+892_297+893ins others(22): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141602172 | |||||||
| chr7:141602172 | C | CGTGTGTG others(21): Show |
1 | a0001c0001t0001g0072 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.297+892_297+893ins others(28): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141602172 | |||||||
| chr7:141602172 | C | CGTGTGTG others(23): Show |
1 | a0001c0001t0001g0095 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.297+892_297+893ins others(30): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141602172 | |||||||
| chr7:141602172 | C | CGTGTGTG others(25): Show |
1 | a0001c0001t0001g0094 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.297+892_297+893ins others(32): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141602172 | |||||||
| chr7:141602173 | T | G | 44 | a0001c0001t0001g0043 a0001c0001t0001g0055 a0001c0001t0001g0071 others(41): Show |
48 | HG00408.hp1 HG01070.hp2 HG01168.hp2 others(45): Show |
intron_variant | MODIFIER | c.297+893T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141602173 | |||||||
| chr7:141602173 | T | TGTGTGTG others(22): Show |
1 | a0001c0001t0001g0100 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.297+893_297+894ins others(29): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141602173 | |||||||
| chr7:141602173 | T | TTG | 23 | a0001c0001t0001g0009 a0001c0001t0001g0028 a0001c0001t0001g0030 others(20): Show |
23 | HG01070.hp1 HG01081.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.297+931_297+932dup others(2): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141602173 | ||||||
| chr7:141602173 | T | TTGTG | 6 | a0001c0001t0001g0148 a0001c0001t0001g0163 a0001c0001t0001g0165 others(3): Show |
6 | HG01243.hp2 HG02723.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.297+929_297+932dup others(4): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141602173 | ||||||
| chr7:141602173 | T | TTGTGTGT others(1): Show |
4 | a0001c0001t0001g0108 a0001c0001t0001g0253 a0001c0001t0001g0254 others(1): Show |
4 | HG01891.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.297+925_297+932dup others(8): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141602173 | ||||||
| chr7:141602173 | T | TTGTGTGT others(3): Show |
2 | a0001c0001t0006g0224 a0001c0001t0006g0226 |
2 | HG02055.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.297+923_297+932dup others(10): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141602173 | ||||||
| chr7:141602173 | T | TTGTGTGT others(5): Show |
4 | a0001c0001t0001g0026 a0001c0001t0001g0054 a0001c0001t0001g0062 others(1): Show |
4 | HG02109.hp2 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.297+921_297+932dup others(12): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141602173 | ||||||
| chr7:141602173 | T | TTGTGTGT others(7): Show |
6 | a0001c0001t0001g0016 a0001c0001t0001g0034 a0001c0001t0001g0035 others(3): Show |
6 | HG02615.hp2 HG02717.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.297+919_297+932dup others(14): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141602173 | ||||||
| chr7:141602173 | T | TTGTGTGT others(9): Show |
4 | a0001c0001t0001g0066 a0001c0001t0001g0090 a0001c0001t0001g0221 others(1): Show |
4 | HG01081.hp1 HG01123.hp2 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.297+917_297+932dup others(16): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141602173 | ||||||
| chr7:141602173 | T | TTGTGTGT others(11): Show |
7 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0069 others(4): Show |
7 | HG00140.hp2 HG00423.hp2 HG00642.hp2 others(4): Show |
intron_variant | MODIFIER | c.297+915_297+932dup others(18): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141602173 | ||||||
| chr7:141602173 | T | TTGTGTGT others(13): Show |
8 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0038 others(5): Show |
8 | HG01256.hp1 HG01361.hp1 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.297+913_297+932dup others(20): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141602173 | ||||||
| chr7:141602173 | T | TTGTGTGT others(15): Show |
15 | a0001c0001t0001g0021 a0001c0001t0001g0033 a0001c0001t0001g0039 others(12): Show |
15 | HG00408.hp2 HG00544.hp1 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.297+911_297+932dup others(22): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141602173 | ||||||
| chr7:141602173 | T | TTGTGTGT others(17): Show |
18 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0027 others(15): Show |
18 | HG00558.hp2 HG01168.hp1 HG01943.hp1 others(15): Show |
intron_variant | MODIFIER | c.297+909_297+932dup others(24): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141602173 | ||||||
| chr7:141602173 | T | TTGTGTGT others(19): Show |
10 | a0001c0001t0001g0032 a0001c0001t0001g0036 a0001c0001t0001g0053 others(7): Show |
10 | HG00597.hp2 HG00673.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.297+907_297+932dup others(26): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141602173 | ||||||
| chr7:141602173 | T | TTGTGTGT others(21): Show |
4 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0046 others(1): Show |
4 | HG02027.hp1 NA18954.hp1 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.297+905_297+932dup others(28): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141602173 | ||||||
| chr7:141602173 | T | TTGTGTGT others(23): Show |
2 | a0001c0001t0001g0040 a0001c0001t0001g0098 |
2 | NA19056.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.297+903_297+932dup others(30): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141602173 | ||||||
| chr7:141602173 | T | TTGTGTGT others(27): Show |
1 | a0001c0001t0001g0083 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.297+899_297+932dup others(34): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141602173 | ||||||
| chr7:141602173 | T | TTGTGTGT others(29): Show |
1 | a0001c0001t0001g0084 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.297+897_297+932dup others(36): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141602173 | ||||||
| chr7:141602173 | T | TTGTGTGT others(31): Show |
1 | a0001c0001t0001g0085 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.297+895_297+932dup others(38): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141602173 | ||||||
| chr7:141602173 | TTG | T | 6 | a0001c0001t0001g0037 a0001c0001t0001g0050 a0001c0001t0001g0125 others(3): Show |
6 | HG02080.hp1 HG02155.hp2 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.297+931_297+932del others(2): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141602173 | ||||||
| chr7:141602175 | G | T | 2 | a0001c0001t0005g0257 a0001c0001t0005g0258 |
2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.297+895G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141602175 | |||||||
| chr7:141602177 | G | T | 1 | a0001c0001t0005g0258 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.297+897G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141602177 | |||||||
| chr7:141602213 | A | G | 3 | a0001c0001t0003g0262 a0001c0001t0003g0263 a0001c0001t0003g0264 |
3 | HG02723.hp1 HG02970.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.297+933A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141602213 | |||||||
| chr7:141602301 | C | T | 1 | a0001c0001t0005g0256 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.297+1021C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141602301 | |||||||
| chr7:141602342 | C | T | 34 | a0001c0001t0001g0228 a0001c0001t0002g0005 a0001c0001t0002g0006 others(31): Show |
37 | HG00408.hp1 HG01168.hp2 HG01261.hp1 others(34): Show |
intron_variant | MODIFIER | c.297+1062C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141602342 | |||||||
| chr7:141602369 | A | C | 1 | a0001c0001t0001g0174 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.297+1089A>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141602369 | |||||||
| chr7:141602786 | T | C | 8 | a0001c0001t0003g0261 a0001c0001t0003g0262 a0001c0001t0003g0263 others(5): Show |
9 | HG01261.hp1 HG02258.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.297+1506T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141602786 | |||||||
| chr7:141602921 | G | C | 8 | a0001c0001t0001g0021 a0001c0001t0001g0033 a0001c0001t0001g0066 others(5): Show |
8 | HG02040.hp1 NA18956.hp1 NA18960.hp1 others(5): Show |
intron_variant | MODIFIER | c.297+1641G>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141602921 | |||||||
| chr7:141603121 | A | G | 48 | a0001c0001t0001g0228 a0001c0001t0001g0248 a0001c0001t0001g0249 others(45): Show |
52 | HG00408.hp1 HG01168.hp2 HG01261.hp1 others(49): Show |
intron_variant | MODIFIER | c.297+1841A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141603121 | |||||||
| chr7:141603266 | A | G | 4 | a0001c0001t0004g0007 a0001c0001t0004g0250 a0001c0001t0004g0251 others(1): Show |
5 | HG02630.hp1 HG02965.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.297+1986A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141603266 | |||||||
| chr7:141603346 | T | C | 2 | a0001c0001t0005g0257 a0001c0001t0005g0258 |
2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.297+2066T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141603346 | |||||||
| chr7:141603421 | A | G | 10 | a0001c0001t0003g0261 a0001c0001t0003g0262 a0001c0001t0003g0263 others(7): Show |
11 | HG01261.hp1 HG02258.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.297+2141A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141603421 | |||||||
| chr7:141603731 | G | A | 2 | a0002c0002t0003g0008 a0002c0002t0003g0266 |
3 | HG01261.hp1 HG02896.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.297+2451G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141603731 | |||||||
| chr7:141603890 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.297+2610C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141603890 | |||||||
| chr7:141604051 | T | C | 3 | a0001c0001t0006g0224 a0001c0001t0006g0225 a0001c0001t0006g0226 |
3 | HG02055.hp1 HG02109.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.297+2771T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141604051 | |||||||
| chr7:141604310 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.297+3030C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141604310 | |||||||
| chr7:141604346 | G | A | 1 | a0001c0001t0001g0009 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.297+3066G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141604346 | |||||||
| chr7:141604372 | G | GTATATAT others(3): Show |
2 | a0001c0001t0001g0016 a0001c0001t0001g0062 |
2 | HG02717.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.297+3093_297+3094i others(12): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141604372 | ||||||
| chr7:141604374 | G | A | 3 | a0001c0001t0001g0016 a0001c0001t0001g0054 a0001c0001t0001g0062 |
3 | HG02717.hp1 HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.297+3094G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141604374 | |||||||
| chr7:141604374 | G | GTA | 29 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(26): Show |
31 | HG00140.hp1 HG00642.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.297+3123_297+3124d others(4): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141604374 | ||||||
| chr7:141604374 | G | GTATA | 10 | a0001c0001t0001g0094 a0001c0001t0001g0129 a0001c0001t0001g0130 others(7): Show |
10 | HG01081.hp2 HG01261.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.297+3121_297+3124d others(6): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141604374 | ||||||
| chr7:141604374 | G | GTATATA | 24 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0026 others(21): Show |
24 | HG00140.hp2 HG00642.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.297+3119_297+3124d others(8): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141604374 | ||||||
| chr7:141604374 | G | GTATATAT others(1): Show |
24 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0017 others(21): Show |
24 | HG00408.hp2 HG00544.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.297+3117_297+3124d others(10): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141604374 | ||||||
| chr7:141604374 | G | GTATATAT others(3): Show |
30 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0023 others(27): Show |
30 | HG00558.hp2 HG00597.hp2 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.297+3115_297+3124d others(12): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141604374 | ||||||
| chr7:141604374 | G | GTATATAT others(5): Show |
8 | a0001c0001t0001g0022 a0001c0001t0001g0049 a0001c0001t0001g0067 others(5): Show |
8 | HG00735.hp1 HG02148.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.297+3113_297+3124d others(14): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141604374 | ||||||
| chr7:141604374 | G | GTATATAT others(7): Show |
7 | a0001c0001t0001g0027 a0001c0001t0001g0073 a0001c0001t0001g0088 others(4): Show |
7 | HG00423.hp2 HG01346.hp1 HG02040.hp2 others(4): Show |
intron_variant | MODIFIER | c.297+3111_297+3124d others(16): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141604374 | ||||||
| chr7:141604374 | G | GTATATAT others(9): Show |
5 | a0001c0001t0001g0029 a0001c0001t0001g0040 a0001c0001t0001g0063 others(2): Show |
5 | HG01099.hp1 HG02273.hp2 HG02293.hp2 others(2): Show |
intron_variant | MODIFIER | c.297+3109_297+3124d others(18): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141604374 | ||||||
| chr7:141604374 | G | GTGTA | 4 | a0001c0001t0004g0250 a0001c0001t0004g0252 a0002c0002t0003g0266 others(1): Show |
4 | HG02896.hp1 HG02965.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.297+3095_297+3096i others(6): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141604374 | ||||||
| chr7:141604374 | G | GTGTATA | 2 | a0001c0001t0001g0059 a0002c0002t0003g0008 |
3 | HG01261.hp1 HG02615.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.297+3095_297+3096i others(8): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141604374 | ||||||
| chr7:141604374 | G | GTGTATAT others(1): Show |
4 | a0001c0001t0001g0045 a0001c0001t0001g0095 a0001c0001t0001g0100 others(1): Show |
4 | HG01884.hp1 HG04204.hp1 NA19085.hp1 others(1): Show |
intron_variant | MODIFIER | c.297+3095_297+3096i others(10): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141604374 | ||||||
| chr7:141604374 | G | GTGTATAT others(3): Show |
2 | a0001c0001t0004g0007 a0001c0001t0004g0251 |
3 | HG02630.hp1 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.297+3095_297+3096i others(12): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141604374 | ||||||
| chr7:141604374 | G | GTGTATAT others(5): Show |
2 | a0001c0001t0001g0101 a0001c0001t0001g0248 |
2 | HG02970.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.297+3095_297+3096i others(14): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141604374 | ||||||
| chr7:141604374 | G | GTGTATAT others(7): Show |
3 | a0001c0001t0001g0249 a0001c0001t0001g0253 a0001c0001t0001g0254 |
3 | HG02896.hp2 HG02897.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.297+3095_297+3096i others(16): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141604374 | ||||||
| chr7:141604374 | G | GTGTGTAT others(17): Show |
1 | a0001c0001t0001g0255 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.297+3095_297+3096i others(26): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141604374 | ||||||
| chr7:141604374 | GTA | G | 12 | a0001c0001t0001g0003 a0001c0001t0001g0110 a0001c0001t0001g0120 others(9): Show |
13 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(10): Show |
intron_variant | MODIFIER | c.297+3123_297+3124d others(4): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141604374 | ||||||
| chr7:141604374 | GTATA | G | 21 | a0001c0001t0001g0197 a0001c0001t0002g0005 a0001c0001t0002g0006 others(18): Show |
23 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(20): Show |
intron_variant | MODIFIER | c.297+3121_297+3124d others(6): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141604374 | ||||||
| chr7:141604374 | GTATATAT others(3): Show |
G | 2 | a0001c0001t0001g0218 a0001c0001t0006g0225 |
2 | HG02109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.297+3115_297+3124d others(12): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141604374 | ||||||
| chr7:141604374 | GTATATAT others(5): Show |
G | 1 | a0001c0001t0001g0123 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.297+3113_297+3124d others(14): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141604374 | ||||||
| chr7:141604376 | A | G | 9 | a0001c0001t0001g0192 a0001c0001t0001g0212 a0001c0001t0002g0219 others(6): Show |
9 | HG02056.hp2 HG02258.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.297+3096A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141604376 | |||||||
| chr7:141604378 | A | G | 2 | a0001c0001t0001g0120 a0001c0001t0002g0243 |
2 | HG02559.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.297+3098A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141604378 | |||||||
| chr7:141604380 | A | G | 20 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0229 others(17): Show |
22 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(19): Show |
intron_variant | MODIFIER | c.297+3100A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141604380 | |||||||
| chr7:141604382 | A | G | 2 | a0001c0001t0002g0234 a0005c0004t0002g0241 |
2 | NA18997.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.297+3102A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141604382 | |||||||
| chr7:141604384 | A | G | 2 | a0001c0001t0006g0224 a0001c0001t0006g0226 |
2 | HG02055.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.297+3104A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141604384 | |||||||
| chr7:141604386 | A | G | 1 | a0001c0001t0006g0225 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.297+3106A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141604386 | |||||||
| chr7:141604394 | A | G | 2 | a0001c0001t0005g0257 a0001c0001t0005g0258 |
2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.297+3114A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141604394 | |||||||
| chr7:141604403 | T | C | 13 | a0001c0001t0001g0171 a0001c0001t0003g0261 a0001c0001t0003g0262 others(10): Show |
15 | HG01261.hp1 HG01884.hp1 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.297+3123T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141604403 | |||||||
| chr7:141604403 | T | TATATATA others(9): Show |
1 | a0001c0001t0005g0256 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.297+3124_297+3125i others(18): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141604403 | ||||||
| chr7:141604443 | G | C | 7 | a0001c0001t0001g0016 a0001c0001t0001g0030 a0001c0001t0001g0054 others(4): Show |
7 | HG01243.hp1 HG02615.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.297+3163G>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141604443 | |||||||
| chr7:141604566 | A | G | 1 | a0001c0001t0001g0050 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.297+3286A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141604566 | |||||||
| chr7:141604582 | A | AT | 5 | a0001c0001t0001g0199 a0001c0001t0001g0228 a0001c0001t0002g0235 others(2): Show |
5 | HG02738.hp1 HG02922.hp2 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.297+3322dupT | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141604582 | ||||||
| chr7:141604582 | A | ATT | 7 | a0001c0001t0003g0261 a0001c0001t0003g0262 a0001c0001t0003g0264 others(4): Show |
8 | HG01261.hp1 HG02258.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.297+3321_297+3322d others(4): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141604582 | ||||||
| chr7:141604582 | AT | A | 12 | a0001c0001t0001g0043 a0001c0001t0001g0087 a0001c0001t0001g0106 others(9): Show |
12 | HG01168.hp2 HG01256.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.297+3322delT | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141604582 | ||||||
| chr7:141604622 | T | C | 23 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0219 others(20): Show |
25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.297+3342T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141604622 | |||||||
| chr7:141604669 | C | T | 5 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0001t0001g0253 others(2): Show |
5 | HG01891.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.297+3389C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141604669 | |||||||
| chr7:141604984 | C | T | 1 | a0001c0001t0001g0036 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.297+3704C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141604984 | |||||||
| chr7:141605152 | A | G | 34 | a0001c0001t0001g0228 a0001c0001t0002g0005 a0001c0001t0002g0006 others(31): Show |
37 | HG00408.hp1 HG01168.hp2 HG01261.hp1 others(34): Show |
intron_variant | MODIFIER | c.297+3872A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141605152 | |||||||
| chr7:141605168 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.297+3888G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141605168 | |||||||
| chr7:141605292 | A | G | 1 | a0001c0001t0002g0219 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.297+4012A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141605292 | |||||||
| chr7:141605848 | T | C | 1 | a0001c0001t0015g0057 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.297+4568T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141605848 | |||||||
| chr7:141605861 | C | G | 23 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0219 others(20): Show |
25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.297+4581C>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141605861 | |||||||
| chr7:141606011 | G | A | 143 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(140): Show |
147 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.297+4731G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141606011 | |||||||
| chr7:141606017 | C | T | 5 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0001t0001g0253 others(2): Show |
5 | HG01891.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.297+4737C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141606017 | |||||||
| chr7:141606495 | T | A | 1 | a0001c0001t0002g0259 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.298-4700T>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141606495 | |||||||
| chr7:141606502 | A | G | 95 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(92): Show |
95 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.298-4693A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141606502 | |||||||
| chr7:141606641 | A | C | 1 | a0001c0001t0001g0195 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.298-4554A>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141606641 | |||||||
| chr7:141606723 | G | T | 2 | a0001c0001t0009g0121 a0001c0001t0009g0122 |
2 | HG02622.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.298-4472G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141606723 | |||||||
| chr7:141607303 | C | T | 3 | a0001c0001t0003g0261 a0002c0002t0003g0008 a0002c0002t0003g0266 |
4 | HG01261.hp1 HG02896.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.298-3892C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141607303 | |||||||
| chr7:141607501 | G | A | 2 | a0001c0001t0001g0048 a0001c0001t0001g0140 |
2 | HG02486.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.298-3694G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141607501 | |||||||
| chr7:141607658 | T | A | 3 | a0001c0001t0001g0022 a0001c0001t0001g0052 a0001c0001t0001g0099 |
3 | HG02735.hp2 HG03942.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.298-3537T>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141607658 | |||||||
| chr7:141607719 | A | G | 3 | a0001c0001t0001g0173 a0001c0001t0001g0202 a0001c0001t0001g0205 |
3 | NA19000.hp2 NA19007.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.298-3476A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141607719 | |||||||
| chr7:141607817 | T | C | 23 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0219 others(20): Show |
25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.298-3378T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141607817 | |||||||
| chr7:141607832 | G | A | 23 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0219 others(20): Show |
25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.298-3363G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141607832 | |||||||
| chr7:141608108 | C | T | 1 | a0001c0001t0001g0053 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.298-3087C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141608108 | |||||||
| chr7:141608660 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.298-2535C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141608660 | |||||||
| chr7:141608728 | C | T | 22 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0229 others(19): Show |
24 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(21): Show |
intron_variant | MODIFIER | c.298-2467C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141608728 | |||||||
| chr7:141608767 | C | T | 3 | a0001c0001t0003g0262 a0001c0001t0003g0263 a0001c0001t0003g0264 |
3 | HG02723.hp1 HG02970.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.298-2428C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141608767 | |||||||
| chr7:141608805 | A | G | 48 | a0001c0001t0001g0228 a0001c0001t0001g0248 a0001c0001t0001g0249 others(45): Show |
52 | HG00408.hp1 HG01168.hp2 HG01261.hp1 others(49): Show |
intron_variant | MODIFIER | c.298-2390A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141608805 | |||||||
| chr7:141609245 | C | T | 5 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0001t0001g0253 others(2): Show |
5 | HG01891.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.298-1950C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141609245 | |||||||
| chr7:141609464 | G | A | 43 | a0001c0001t0001g0228 a0001c0001t0002g0005 a0001c0001t0002g0006 others(40): Show |
47 | HG00408.hp1 HG01168.hp2 HG01261.hp1 others(44): Show |
intron_variant | MODIFIER | c.298-1731G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141609464 | |||||||
| chr7:141609487 | A | C | 23 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0219 others(20): Show |
25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.298-1708A>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141609487 | |||||||
| chr7:141609604 | A | T | 1 | a0001c0001t0005g0256 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.298-1591A>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141609604 | |||||||
| chr7:141609691 | G | A | 5 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0001t0001g0253 others(2): Show |
5 | HG01891.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.298-1504G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141609691 | |||||||
| chr7:141609759 | G | A | 1 | a0001c0001t0001g0038 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.298-1436G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141609759 | |||||||
| chr7:141609799 | A | G | 2 | a0001c0001t0001g0113 a0001c0001t0001g0164 |
2 | HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.298-1396A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141609799 | |||||||
| chr7:141609868 | G | A | 1 | a0004c0003t0010g0227 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.298-1327G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141609868 | |||||||
| chr7:141609971 | G | GT | 6 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0037 others(3): Show |
6 | HG02027.hp1 HG02922.hp2 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.298-1212dupT | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr7 | 141609971 | ||||||
| chr7:141610102 | A | G | 1 | a0001c0001t0001g0190 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.298-1093A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141610102 | |||||||
| chr7:141610241 | A | G | 4 | a0001c0001t0006g0224 a0001c0001t0006g0225 a0001c0001t0006g0226 others(1): Show |
4 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.298-954A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141610241 | |||||||
| chr7:141610396 | T | C | 2 | a0001c0001t0005g0257 a0001c0001t0005g0258 |
2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.298-799T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141610396 | |||||||
| chr7:141610402 | T | G | 1 | a0001c0001t0003g0265 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.298-793T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141610402 | |||||||
| chr7:141610540 | C | A | 4 | a0001c0001t0006g0224 a0001c0001t0006g0225 a0001c0001t0006g0226 others(1): Show |
4 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.298-655C>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141610540 | |||||||
| chr7:141610840 | T | C | 149 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(146): Show |
153 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.298-355T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141610840 | |||||||
| chr7:141611055 | T | A | 1 | a0001c0001t0001g0060 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.298-140T>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141611055 | |||||||
| chr7:141611089 | G | A | 5 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0001t0001g0253 others(2): Show |
5 | HG01891.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.298-106G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 5/15 | chr7 | 141611089 | |||||||
| chr7:141612197 | T | C | 1 | a0004c0003t0010g0227 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.390+910T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 6/15 | chr7 | 141612197 | |||||||
| chr7:141612229 | A | G | 23 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0219 others(20): Show |
25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.390+942A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 6/15 | chr7 | 141612229 | |||||||
| chr7:141612249 | G | A | 4 | a0001c0001t0001g0048 a0001c0001t0001g0058 a0001c0001t0008g0041 others(1): Show |
4 | HG02572.hp2 HG02818.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.390+962G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 6/15 | chr7 | 141612249 | |||||||
| chr7:141612297 | C | A | 1 | a0001c0001t0001g0108 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.390+1010C>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 6/15 | chr7 | 141612297 | |||||||
| chr7:141612525 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.390+1238G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 6/15 | chr7 | 141612525 | |||||||
| chr7:141612557 | A | G | 1 | a0001c0001t0001g0053 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.390+1270A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 6/15 | chr7 | 141612557 | |||||||
| chr7:141612616 | G | A | 4 | a0001c0001t0006g0224 a0001c0001t0006g0225 a0001c0001t0006g0226 others(1): Show |
4 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.390+1329G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 6/15 | chr7 | 141612616 | |||||||
| chr7:141612861 | G | A | 1 | a0001c0001t0001g0216 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.391-1285G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 6/15 | chr7 | 141612861 | |||||||
| chr7:141612906 | A | G | 1 | a0001c0001t0001g0030 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.391-1240A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 6/15 | chr7 | 141612906 | |||||||
| chr7:141612930 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.391-1216C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 6/15 | chr7 | 141612930 | |||||||
| chr7:141613123 | T | G | 23 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0219 others(20): Show |
25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.391-1023T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 6/15 | chr7 | 141613123 | |||||||
| chr7:141613159 | A | C | 5 | a0001c0001t0004g0007 a0001c0001t0004g0250 a0001c0001t0004g0251 others(2): Show |
6 | HG01884.hp1 HG02630.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.391-987A>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 6/15 | chr7 | 141613159 | |||||||
| chr7:141613426 | G | A | 7 | a0001c0001t0003g0261 a0001c0001t0003g0262 a0001c0001t0003g0263 others(4): Show |
8 | HG01261.hp1 HG02723.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.391-720G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 6/15 | chr7 | 141613426 | |||||||
| chr7:141613534 | G | A | 4 | a0001c0001t0003g0261 a0001c0001t0003g0262 a0001c0001t0003g0263 others(1): Show |
4 | HG02723.hp1 HG02970.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.391-612G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 6/15 | chr7 | 141613534 | |||||||
| chr7:141613619 | A | G | 1 | a0001c0001t0005g0256 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.391-527A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 6/15 | chr7 | 141613619 | |||||||
| chr7:141613797 | A | G | 147 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(144): Show |
151 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.391-349A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 6/15 | chr7 | 141613797 | |||||||
| chr7:141614087 | C | A | 5 | a0001c0001t0004g0007 a0001c0001t0004g0250 a0001c0001t0004g0251 others(2): Show |
6 | HG01884.hp1 HG02630.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.391-59C>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 6/15 | chr7 | 141614087 | |||||||
| chr7:141614360 | G | A | 9 | a0001c0001t0003g0261 a0001c0001t0003g0262 a0001c0001t0003g0263 others(6): Show |
10 | HG01261.hp1 HG02723.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.423+182G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 7/15 | chr7 | 141614360 | |||||||
| chr7:141614595 | T | TTTCTACA others(320): Show |
1 | a0001c0001t0002g0259 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.423+429_423+430ins others(327): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr7 | 141614595 | ||||||
| chr7:141614595 | T | TTTCTACA others(314): Show |
1 | a0001c0001t0002g0243 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.423+431_423+432ins others(321): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr7 | 141614595 | ||||||
| chr7:141614595 | T | TTTCTACA others(315): Show |
5 | a0001c0001t0002g0005 a0001c0001t0002g0236 a0001c0001t0002g0239 others(2): Show |
6 | HG02015.hp1 HG02155.hp1 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.423+431_423+432ins others(322): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr7 | 141614595 | ||||||
| chr7:141614595 | T | TTTCTACA others(316): Show |
13 | a0001c0001t0002g0219 a0001c0001t0002g0229 a0001c0001t0002g0230 others(10): Show |
13 | HG00408.hp1 HG01952.hp2 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.423+431_423+432ins others(323): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr7 | 141614595 | ||||||
| chr7:141614595 | T | TTTCTACA others(317): Show |
3 | a0001c0001t0002g0006 a0001c0001t0002g0232 a0005c0004t0002g0241 |
4 | HG02486.hp1 HG02818.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.423+431_423+432ins others(324): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr7 | 141614595 | ||||||
| chr7:141614596 | T | A | 2 | a0002c0002t0003g0008 a0002c0002t0003g0266 |
3 | HG01261.hp1 HG02896.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.423+418T>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 7/15 | chr7 | 141614596 | |||||||
| chr7:141614791 | CAT | C | 95 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(92): Show |
95 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.423+616_423+617del others(2): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr7 | 141614791 | ||||||
| chr7:141614928 | G | A | 5 | a0001c0001t0004g0007 a0001c0001t0004g0250 a0001c0001t0004g0251 others(2): Show |
6 | HG01884.hp1 HG02630.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.424-543G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 7/15 | chr7 | 141614928 | |||||||
| chr7:141615467 | C | G | 1 | a0001c0001t0001g0123 | 1 | HG02572.hp1 | splice_region_variant&intron_variant | LOW | c.424-4C>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 7/15 | chr7 | 141615467 | |||||||
| chr7:141615600 | G | T | 4 | a0001c0001t0006g0224 a0001c0001t0006g0225 a0001c0001t0006g0226 others(1): Show |
4 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.518+35G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141615600 | |||||||
| chr7:141615645 | TC | T | 5 | a0001c0001t0004g0007 a0001c0001t0004g0250 a0001c0001t0004g0251 others(2): Show |
6 | HG01884.hp1 HG02630.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.518+81delC | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141615645 | |||||||
| chr7:141615874 | A | G | 1 | a0001c0001t0001g0228 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.518+309A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141615874 | |||||||
| chr7:141615919 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.518+354C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141615919 | |||||||
| chr7:141616084 | A | G | 23 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0219 others(20): Show |
25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.518+519A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141616084 | |||||||
| chr7:141616198 | A | G | 1 | a0001c0001t0002g0006 | 2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.518+633A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141616198 | |||||||
| chr7:141616204 | A | G | 100 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(97): Show |
100 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.518+639A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141616204 | |||||||
| chr7:141616207 | T | C | 100 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(97): Show |
100 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.518+642T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141616207 | |||||||
| chr7:141616233 | A | G | 3 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0092 |
3 | HG01081.hp1 HG01255.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.518+668A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141616233 | |||||||
| chr7:141616262 | A | G | 3 | a0001c0001t0001g0173 a0001c0001t0001g0202 a0001c0001t0001g0205 |
3 | NA19000.hp2 NA19007.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.518+697A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141616262 | |||||||
| chr7:141616341 | A | G | 1 | a0003c0005t0001g0025 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.518+776A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141616341 | |||||||
| chr7:141616762 | C | CT | 13 | a0001c0001t0001g0021 a0001c0001t0001g0032 a0001c0001t0001g0033 others(10): Show |
13 | HG01070.hp2 HG01258.hp2 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.518+1211dupT | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr7 | 141616762 | ||||||
| chr7:141616805 | C | G | 2 | a0001c0001t0001g0113 a0001c0001t0001g0164 |
2 | HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.518+1240C>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141616805 | |||||||
| chr7:141616843 | C | A | 1 | a0001c0001t0013g0139 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.518+1278C>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141616843 | |||||||
| chr7:141616853 | G | A | 3 | a0001c0001t0003g0262 a0001c0001t0003g0263 a0001c0001t0003g0264 |
3 | HG02723.hp1 HG02970.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.518+1288G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141616853 | |||||||
| chr7:141616943 | C | G | 3 | a0001c0001t0006g0224 a0001c0001t0006g0225 a0001c0001t0006g0226 |
3 | HG02055.hp1 HG02109.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.518+1378C>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141616943 | |||||||
| chr7:141616999 | C | T | 10 | a0001c0001t0003g0261 a0001c0001t0003g0262 a0001c0001t0003g0263 others(7): Show |
11 | HG01261.hp1 HG02258.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.518+1434C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141616999 | |||||||
| chr7:141617034 | C | T | 100 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(97): Show |
100 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.518+1469C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141617034 | |||||||
| chr7:141617585 | T | G | 1 | a0001c0001t0002g0234 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.518+2020T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141617585 | |||||||
| chr7:141618243 | T | A | 4 | a0001c0001t0006g0224 a0001c0001t0006g0225 a0001c0001t0006g0226 others(1): Show |
4 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.518+2678T>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141618243 | |||||||
| chr7:141618441 | G | A | 34 | a0001c0001t0001g0228 a0001c0001t0002g0005 a0001c0001t0002g0006 others(31): Show |
37 | HG00408.hp1 HG01168.hp2 HG01261.hp1 others(34): Show |
intron_variant | MODIFIER | c.518+2876G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141618441 | |||||||
| chr7:141618455 | G | A | 1 | a0001c0001t0001g0017 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.518+2890G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141618455 | |||||||
| chr7:141618705 | A | G | 6 | a0001c0001t0001g0114 a0001c0001t0001g0194 a0001c0001t0001g0198 others(3): Show |
6 | HG00558.hp1 HG00621.hp1 HG00673.hp2 others(3): Show |
intron_variant | MODIFIER | c.519-3027A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141618705 | |||||||
| chr7:141618827 | C | T | 17 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0230 others(14): Show |
19 | HG00408.hp1 HG02015.hp1 HG02155.hp1 others(16): Show |
intron_variant | MODIFIER | c.519-2905C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141618827 | |||||||
| chr7:141618890 | G | A | 1 | a0001c0001t0005g0258 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.519-2842G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141618890 | |||||||
| chr7:141619115 | T | G | 1 | a0001c0001t0005g0256 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.519-2617T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141619115 | |||||||
| chr7:141619116 | T | A | 1 | a0001c0001t0005g0256 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.519-2616T>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141619116 | |||||||
| chr7:141619149 | T | A | 1 | a0001c0001t0003g0261 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.519-2583T>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141619149 | |||||||
| chr7:141619207 | A | G | 23 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0219 others(20): Show |
25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.519-2525A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141619207 | |||||||
| chr7:141619222 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.519-2510G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141619222 | |||||||
| chr7:141619507 | C | T | 5 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0001t0001g0253 others(2): Show |
5 | HG01891.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.519-2225C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141619507 | |||||||
| chr7:141619643 | A | G | 1 | a0001c0001t0002g0233 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.519-2089A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141619643 | |||||||
| chr7:141619673 | GA | G | 5 | a0001c0001t0004g0007 a0001c0001t0004g0250 a0001c0001t0004g0251 others(2): Show |
6 | HG01884.hp1 HG02630.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.519-2048delA | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr7 | 141619673 | ||||||
| chr7:141619685 | GCAAA | G | 3 | a0001c0001t0006g0224 a0001c0001t0006g0225 a0001c0001t0006g0226 |
3 | HG02055.hp1 HG02109.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.519-2042_519-2039d others(6): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr7 | 141619685 | ||||||
| chr7:141619690 | CAAA | C | 5 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0001t0001g0253 others(2): Show |
5 | HG01891.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.519-2039_519-2037d others(5): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr7 | 141619690 | ||||||
| chr7:141619754 | G | T | 1 | a0001c0001t0001g0228 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.519-1978G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141619754 | |||||||
| chr7:141619767 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.519-1965G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141619767 | |||||||
| chr7:141619888 | G | T | 1 | a0001c0001t0001g0228 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.519-1844G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141619888 | |||||||
| chr7:141619986 | A | G | 1 | a0004c0003t0010g0227 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.519-1746A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141619986 | |||||||
| chr7:141620063 | G | C | 2 | a0001c0001t0001g0137 a0001c0001t0001g0223 |
2 | HG02109.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.519-1669G>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141620063 | |||||||
| chr7:141620526 | CAG | C | 97 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(94): Show |
97 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.519-1205_519-1204d others(4): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141620526 | |||||||
| chr7:141620566 | CTGGAAAC others(5): Show |
C | 84 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(81): Show |
84 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.519-1144_519-1133d others(14): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr7 | 141620566 | ||||||
| chr7:141620729 | TCCAGGAG others(5): Show |
T | 23 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0219 others(20): Show |
25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.519-991_519-980del others(12): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr7 | 141620729 | ||||||
| chr7:141620772 | A | G | 5 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0001t0001g0253 others(2): Show |
5 | HG01891.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.519-960A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141620772 | |||||||
| chr7:141620828 | A | G | 7 | a0001c0001t0003g0261 a0001c0001t0003g0262 a0001c0001t0003g0263 others(4): Show |
8 | HG01261.hp1 HG02723.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.519-904A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141620828 | |||||||
| chr7:141620937 | C | T | 1 | a0004c0003t0010g0227 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.519-795C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141620937 | |||||||
| chr7:141620976 | G | A | 1 | a0001c0001t0001g0065 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.519-756G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141620976 | |||||||
| chr7:141621002 | C | T | 10 | a0001c0001t0003g0261 a0001c0001t0003g0262 a0001c0001t0003g0263 others(7): Show |
11 | HG01261.hp1 HG02258.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.519-730C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141621002 | |||||||
| chr7:141621050 | C | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | NA18991.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.519-682C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141621050 | |||||||
| chr7:141621094 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.519-638A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141621094 | |||||||
| chr7:141621209 | C | T | 3 | a0001c0001t0006g0224 a0001c0001t0006g0225 a0001c0001t0006g0226 |
3 | HG02055.hp1 HG02109.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.519-523C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141621209 | |||||||
| chr7:141621437 | A | G | 3 | a0001c0001t0003g0262 a0001c0001t0003g0263 a0001c0001t0003g0264 |
3 | HG02723.hp1 HG02970.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.519-295A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | chr7 | 141621437 | |||||||
| chr7:141621634 | ATG | A | 3 | a0001c0001t0003g0262 a0001c0001t0003g0263 a0001c0001t0003g0264 |
3 | HG02723.hp1 HG02970.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.519-84_519-83delGT | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr7 | 141621634 | ||||||
| chr7:141622012 | A | T | 23 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0219 others(20): Show |
25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.588+211A>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141622012 | |||||||
| chr7:141622237 | C | T | 1 | a0001c0001t0004g0260 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.588+436C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141622237 | |||||||
| chr7:141622408 | G | C | 2 | a0001c0001t0002g0230 a0001c0001t0002g0234 |
2 | NA18997.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.588+607G>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141622408 | |||||||
| chr7:141622818 | G | T | 1 | a0001c0001t0015g0057 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.588+1017G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141622818 | |||||||
| chr7:141622918 | T | TA | 32 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0229 others(29): Show |
35 | HG00408.hp1 HG01168.hp2 HG01261.hp1 others(32): Show |
intron_variant | MODIFIER | c.588+1128dupA | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 141622918 | ||||||
| chr7:141623125 | A | G | 6 | a0001c0001t0002g0005 a0001c0001t0002g0235 a0001c0001t0002g0238 others(3): Show |
7 | HG00408.hp1 HG02155.hp1 HG03688.hp2 others(4): Show |
intron_variant | MODIFIER | c.588+1324A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141623125 | |||||||
| chr7:141623335 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.588+1534C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141623335 | |||||||
| chr7:141623336 | G | A | 4 | a0001c0001t0006g0224 a0001c0001t0006g0225 a0001c0001t0006g0226 others(1): Show |
4 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.588+1535G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141623336 | |||||||
| chr7:141623379 | CA | C | 26 | a0001c0001t0001g0017 a0001c0001t0001g0228 a0001c0001t0002g0229 others(23): Show |
28 | HG01168.hp2 HG01261.hp1 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.588+1591delA | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 141623379 | ||||||
| chr7:141623391 | AAGAAAAA others(10): Show |
A | 1 | a0001c0001t0002g0219 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.588+1592_588+1608d others(19): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 141623391 | ||||||
| chr7:141623409 | A | G | 1 | a0001c0001t0002g0219 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.588+1608A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141623409 | |||||||
| chr7:141623412 | A | G | 1 | a0001c0001t0005g0256 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.588+1611A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141623412 | |||||||
| chr7:141623413 | A | T | 2 | a0001c0001t0005g0257 a0001c0001t0005g0258 |
2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.588+1612A>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141623413 | |||||||
| chr7:141623818 | G | A | 1 | a0001c0001t0001g0033 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.588+2017G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141623818 | |||||||
| chr7:141623825 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.588+2024C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141623825 | |||||||
| chr7:141623852 | G | A | 10 | a0001c0001t0003g0261 a0001c0001t0003g0262 a0001c0001t0003g0263 others(7): Show |
11 | HG01261.hp1 HG02258.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.588+2051G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141623852 | |||||||
| chr7:141624195 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.588+2394C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141624195 | |||||||
| chr7:141624437 | T | A | 1 | a0001c0001t0001g0103 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.588+2636T>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141624437 | |||||||
| chr7:141624559 | A | G | 4 | a0001c0001t0006g0224 a0001c0001t0006g0225 a0001c0001t0006g0226 others(1): Show |
4 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.588+2758A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141624559 | |||||||
| chr7:141624632 | A | T | 1 | a0001c0001t0001g0099 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.588+2831A>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141624632 | |||||||
| chr7:141624694 | G | A | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | NA18991.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.588+2893G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141624694 | |||||||
| chr7:141624923 | C | T | 43 | a0001c0001t0001g0228 a0001c0001t0002g0005 a0001c0001t0002g0006 others(40): Show |
47 | HG00408.hp1 HG01168.hp2 HG01261.hp1 others(44): Show |
intron_variant | MODIFIER | c.588+3122C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141624923 | |||||||
| chr7:141625108 | T | A | 1 | a0001c0001t0001g0148 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.588+3307T>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141625108 | |||||||
| chr7:141625263 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.588+3462C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141625263 | |||||||
| chr7:141625542 | A | C | 1 | a0001c0001t0001g0118 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.588+3741A>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141625542 | |||||||
| chr7:141625822 | T | C | 34 | a0001c0001t0001g0228 a0001c0001t0002g0005 a0001c0001t0002g0006 others(31): Show |
37 | HG00408.hp1 HG01168.hp2 HG01261.hp1 others(34): Show |
intron_variant | MODIFIER | c.588+4021T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141625822 | |||||||
| chr7:141625847 | T | G | 1 | a0001c0001t0001g0022 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.588+4046T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141625847 | |||||||
| chr7:141625899 | G | A | 1 | a0001c0001t0003g0265 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.588+4098G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141625899 | |||||||
| chr7:141625918 | G | C | 1 | a0001c0001t0005g0256 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.588+4117G>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141625918 | |||||||
| chr7:141626116 | A | G | 1 | a0001c0001t0001g0024 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.588+4315A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141626116 | |||||||
| chr7:141626137 | A | G | 1 | a0001c0001t0001g0130 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.588+4336A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141626137 | |||||||
| chr7:141626206 | G | A | 1 | a0001c0001t0003g0265 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.588+4405G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141626206 | |||||||
| chr7:141626328 | A | T | 1 | a0001c0001t0005g0256 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.588+4527A>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141626328 | |||||||
| chr7:141626482 | A | G | 1 | a0001c0001t0001g0108 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.588+4681A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141626482 | |||||||
| chr7:141626950 | C | T | 1 | a0001c0001t0001g0001 | 2 | HG00140.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.588+5149C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141626950 | |||||||
| chr7:141627003 | A | G | 2 | a0001c0001t0005g0257 a0001c0001t0005g0258 |
2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.588+5202A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141627003 | |||||||
| chr7:141627210 | T | G | 10 | a0001c0001t0003g0261 a0001c0001t0003g0262 a0001c0001t0003g0263 others(7): Show |
11 | HG01261.hp1 HG02258.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.588+5409T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141627210 | |||||||
| chr7:141627286 | A | AT | 12 | a0001c0001t0002g0229 a0001c0001t0002g0231 a0001c0001t0002g0232 others(9): Show |
13 | HG01261.hp1 HG01952.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.588+5494dupT | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 141627286 | ||||||
| chr7:141627367 | T | C | 8 | a0001c0001t0001g0119 a0001c0001t0001g0123 a0001c0001t0001g0129 others(5): Show |
8 | HG01261.hp2 HG01891.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.588+5566T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141627367 | |||||||
| chr7:141627596 | C | T | 10 | a0001c0001t0003g0261 a0001c0001t0003g0262 a0001c0001t0003g0263 others(7): Show |
11 | HG01261.hp1 HG02258.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.588+5795C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141627596 | |||||||
| chr7:141627709 | C | T | 7 | a0001c0001t0001g0119 a0001c0001t0001g0123 a0001c0001t0001g0129 others(4): Show |
7 | HG01261.hp2 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.588+5908C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141627709 | |||||||
| chr7:141627769 | A | C | 1 | a0001c0001t0001g0021 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.588+5968A>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141627769 | |||||||
| chr7:141627856 | A | T | 1 | a0001c0001t0003g0261 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.589-6045A>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141627856 | |||||||
| chr7:141627967 | C | T | 1 | a0001c0001t0001g0026 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.589-5934C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141627967 | |||||||
| chr7:141628051 | T | G | 1 | a0001c0001t0002g0219 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.589-5850T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141628051 | |||||||
| chr7:141628183 | G | T | 2 | a0002c0002t0003g0008 a0002c0002t0003g0266 |
3 | HG01261.hp1 HG02896.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.589-5718G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141628183 | |||||||
| chr7:141628338 | G | A | 1 | a0004c0003t0010g0227 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.589-5563G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141628338 | |||||||
| chr7:141628673 | C | T | 2 | a0001c0001t0001g0029 a0001c0001t0001g0080 |
2 | HG02273.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.589-5228C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141628673 | |||||||
| chr7:141628722 | C | T | 5 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0001t0001g0253 others(2): Show |
5 | HG01891.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.589-5179C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141628722 | |||||||
| chr7:141628965 | C | T | 1 | a0001c0001t0003g0261 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.589-4936C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141628965 | |||||||
| chr7:141629845 | T | C | 1 | a0001c0001t0001g0189 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.589-4056T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141629845 | |||||||
| chr7:141629851 | T | C | 138 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(135): Show |
141 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.589-4050T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141629851 | |||||||
| chr7:141629916 | G | T | 1 | a0001c0001t0001g0108 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.589-3985G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141629916 | |||||||
| chr7:141630106 | T | G | 1 | a0001c0001t0001g0134 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.589-3795T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141630106 | |||||||
| chr7:141630167 | G | T | 1 | a0002c0002t0003g0008 | 2 | HG01261.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.589-3734G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141630167 | |||||||
| chr7:141630379 | C | T | 1 | a0001c0001t0001g0174 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.589-3522C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141630379 | |||||||
| chr7:141630433 | G | A | 2 | a0001c0001t0005g0257 a0001c0001t0005g0258 |
2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.589-3468G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141630433 | |||||||
| chr7:141630534 | A | G | 1 | a0001c0001t0001g0012 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.589-3367A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141630534 | |||||||
| chr7:141630539 | AAAT | A | 3 | a0001c0001t0006g0224 a0001c0001t0006g0225 a0001c0001t0006g0226 |
3 | HG02055.hp1 HG02109.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.589-3355_589-3353d others(5): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 141630539 | ||||||
| chr7:141630938 | G | T | 1 | a0002c0002t0003g0008 | 2 | HG01261.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.589-2963G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141630938 | |||||||
| chr7:141630999 | A | C | 1 | a0001c0001t0001g0120 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.589-2902A>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141630999 | |||||||
| chr7:141631093 | A | G | 5 | a0001c0001t0004g0007 a0001c0001t0004g0250 a0001c0001t0004g0251 others(2): Show |
6 | HG01884.hp1 HG02630.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.589-2808A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141631093 | |||||||
| chr7:141631409 | G | C | 10 | a0001c0001t0003g0261 a0001c0001t0003g0262 a0001c0001t0003g0263 others(7): Show |
11 | HG01261.hp1 HG02258.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.589-2492G>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141631409 | |||||||
| chr7:141631527 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.589-2374C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141631527 | |||||||
| chr7:141631575 | C | A | 1 | a0001c0001t0001g0207 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.589-2326C>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141631575 | |||||||
| chr7:141631891 | T | C | 1 | a0001c0001t0001g0148 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.589-2010T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141631891 | |||||||
| chr7:141631954 | T | C | 149 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(146): Show |
153 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.589-1947T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141631954 | |||||||
| chr7:141632076 | C | A | 2 | a0001c0001t0001g0017 a0001c0001t0001g0018 |
2 | HG02027.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.589-1825C>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141632076 | |||||||
| chr7:141632187 | T | C | 149 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(146): Show |
153 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.589-1714T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141632187 | |||||||
| chr7:141632230 | T | TA | 13 | a0001c0001t0001g0032 a0001c0001t0001g0104 a0001c0001t0001g0115 others(10): Show |
13 | HG01361.hp2 HG01891.hp2 HG02293.hp1 others(10): Show |
intron_variant | MODIFIER | c.589-1657dupA | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 141632230 | ||||||
| chr7:141632230 | TA | T | 9 | a0001c0001t0003g0261 a0001c0001t0003g0262 a0001c0001t0003g0263 others(6): Show |
10 | HG01261.hp1 HG02723.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.589-1657delA | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 141632230 | ||||||
| chr7:141632245 | CAAAA | C | 4 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0167 others(1): Show |
4 | HG01070.hp1 HG01099.hp2 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.589-1651_589-1648d others(6): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 141632245 | ||||||
| chr7:141632253 | A | C | 1 | a0001c0001t0001g0228 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.589-1648A>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141632253 | |||||||
| chr7:141632435 | T | C | 2 | a0001c0001t0001g0017 a0001c0001t0001g0018 |
2 | HG02027.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.589-1466T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141632435 | |||||||
| chr7:141632443 | T | C | 4 | a0001c0001t0001g0228 a0001c0001t0006g0224 a0001c0001t0006g0225 others(1): Show |
4 | HG02055.hp1 HG02109.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.589-1458T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141632443 | |||||||
| chr7:141632930 | G | A | 99 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(96): Show |
99 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.589-971G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141632930 | |||||||
| chr7:141633140 | C | A | 23 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0219 others(20): Show |
25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.589-761C>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141633140 | |||||||
| chr7:141633180 | C | T | 7 | a0001c0001t0003g0261 a0001c0001t0003g0262 a0001c0001t0003g0263 others(4): Show |
8 | HG01261.hp1 HG02723.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.589-721C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141633180 | |||||||
| chr7:141633409 | CACTTTTT others(6): Show |
C | 5 | a0001c0001t0001g0228 a0001c0001t0006g0224 a0001c0001t0006g0225 others(2): Show |
5 | HG02055.hp1 HG02109.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.589-484_589-472del others(13): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 141633409 | ||||||
| chr7:141633458 | T | A | 1 | a0001c0001t0001g0228 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.589-443T>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141633458 | |||||||
| chr7:141633553 | T | A | 1 | a0001c0001t0001g0063 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.589-348T>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141633553 | |||||||
| chr7:141633635 | A | C | 6 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0051 others(3): Show |
7 | HG00735.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.589-266A>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 9/15 | chr7 | 141633635 | |||||||
| chr7:141634141 | T | G | 1 | a0001c0001t0003g0261 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.668+161T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 10/15 | chr7 | 141634141 | |||||||
| chr7:141634257 | G | T | 1 | a0001c0001t0001g0108 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.668+277G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 10/15 | chr7 | 141634257 | |||||||
| chr7:141634345 | G | A | 1 | a0001c0001t0001g0026 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.668+365G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 10/15 | chr7 | 141634345 | |||||||
| chr7:141634460 | C | T | 2 | a0001c0001t0002g0230 a0001c0001t0002g0234 |
2 | NA18997.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.668+480C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 10/15 | chr7 | 141634460 | |||||||
| chr7:141634730 | C | T | 1 | a0001c0001t0001g0144 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.668+750C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 10/15 | chr7 | 141634730 | |||||||
| chr7:141634738 | T | G | 1 | a0001c0001t0001g0048 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.668+758T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 10/15 | chr7 | 141634738 | |||||||
| chr7:141634830 | C | CT | 12 | a0001c0001t0001g0082 a0001c0001t0001g0112 a0001c0001t0001g0179 others(9): Show |
13 | HG01255.hp2 HG01261.hp1 HG01993.hp1 others(10): Show |
intron_variant | MODIFIER | c.668+865dupT | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr7 | 141634830 | ||||||
| chr7:141634830 | CT | C | 25 | a0001c0001t0001g0074 a0001c0001t0001g0081 a0001c0001t0002g0005 others(22): Show |
27 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(24): Show |
intron_variant | MODIFIER | c.668+865delT | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr7 | 141634830 | ||||||
| chr7:141634990 | ATGATTAT others(8): Show |
A | 5 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0001t0001g0253 others(2): Show |
5 | HG01891.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.668+1011_668+1025d others(17): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 10/15 | chr7 | 141634990 | |||||||
| chr7:141635007 | C | T | 5 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0001t0001g0253 others(2): Show |
5 | HG01891.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.668+1027C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 10/15 | chr7 | 141635007 | |||||||
| chr7:141635096 | C | G | 2 | a0001c0001t0005g0257 a0001c0001t0005g0258 |
2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.668+1116C>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 10/15 | chr7 | 141635096 | |||||||
| chr7:141635161 | A | G | 2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | HG01261.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.668+1181A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 10/15 | chr7 | 141635161 | |||||||
| chr7:141635186 | G | A | 4 | a0001c0001t0006g0224 a0001c0001t0006g0225 a0001c0001t0006g0226 others(1): Show |
4 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.668+1206G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 10/15 | chr7 | 141635186 | |||||||
| chr7:141635301 | AATC | A | 7 | a0001c0001t0003g0261 a0001c0001t0003g0262 a0001c0001t0003g0263 others(4): Show |
8 | HG01261.hp1 HG02723.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.668+1324_668+1326d others(5): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr7 | 141635301 | ||||||
| chr7:141635320 | G | GTA | 9 | a0001c0001t0003g0261 a0001c0001t0003g0262 a0001c0001t0003g0263 others(6): Show |
10 | HG01261.hp1 HG02723.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.668+1341_668+1342d others(4): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr7 | 141635320 | ||||||
| chr7:141635526 | C | A | 1 | a0001c0001t0001g0011 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.669-1434C>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 10/15 | chr7 | 141635526 | |||||||
| chr7:141635550 | C | T | 5 | a0001c0001t0001g0228 a0001c0001t0006g0224 a0001c0001t0006g0225 others(2): Show |
5 | HG02055.hp1 HG02109.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.669-1410C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 10/15 | chr7 | 141635550 | |||||||
| chr7:141635603 | A | G | 1 | a0001c0001t0001g0037 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.669-1357A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 10/15 | chr7 | 141635603 | |||||||
| chr7:141635647 | C | A | 1 | a0001c0001t0015g0057 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.669-1313C>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 10/15 | chr7 | 141635647 | |||||||
| chr7:141635671 | T | C | 23 | a0001c0001t0001g0220 a0001c0001t0002g0005 a0001c0001t0002g0006 others(20): Show |
25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.669-1289T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 10/15 | chr7 | 141635671 | |||||||
| chr7:141635885 | A | G | 1 | a0001c0001t0001g0045 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.669-1075A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 10/15 | chr7 | 141635885 | |||||||
| chr7:141635943 | A | G | 7 | a0001c0001t0003g0261 a0001c0001t0003g0262 a0001c0001t0003g0263 others(4): Show |
8 | HG01261.hp1 HG02723.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.669-1017A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 10/15 | chr7 | 141635943 | |||||||
| chr7:141636516 | G | A | 23 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0219 others(20): Show |
25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.669-444G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 10/15 | chr7 | 141636516 | |||||||
| chr7:141636748 | G | A | 32 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0219 others(29): Show |
35 | HG00408.hp1 HG01168.hp2 HG01261.hp1 others(32): Show |
intron_variant | MODIFIER | c.669-212G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 10/15 | chr7 | 141636748 | |||||||
| chr7:141636767 | T | C | 1 | a0001c0001t0016g0172 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.669-193T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 10/15 | chr7 | 141636767 | |||||||
| chr7:141637174 | G | A | 5 | a0001c0001t0001g0001 a0001c0001t0001g0126 a0001c0001t0001g0127 others(2): Show |
6 | HG00140.hp1 HG01192.hp1 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.726+157G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 11/15 | chr7 | 141637174 | |||||||
| chr7:141637204 | T | C | 49 | a0001c0001t0001g0220 a0001c0001t0001g0228 a0001c0001t0001g0248 others(46): Show |
53 | HG00408.hp1 HG01168.hp2 HG01261.hp1 others(50): Show |
intron_variant | MODIFIER | c.726+187T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 11/15 | chr7 | 141637204 | |||||||
| chr7:141637279 | A | G | 2 | a0001c0001t0001g0126 a0001c0001t0001g0128 |
2 | HG01496.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.726+262A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 11/15 | chr7 | 141637279 | |||||||
| chr7:141637430 | G | A | 4 | a0001c0001t0004g0007 a0001c0001t0004g0250 a0001c0001t0004g0251 others(1): Show |
5 | HG02630.hp1 HG02965.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.726+413G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 11/15 | chr7 | 141637430 | |||||||
| chr7:141637725 | G | A | 1 | a0001c0001t0001g0185 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.726+708G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 11/15 | chr7 | 141637725 | |||||||
| chr7:141637767 | T | C | 4 | a0001c0001t0006g0224 a0001c0001t0006g0225 a0001c0001t0006g0226 others(1): Show |
4 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.726+750T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 11/15 | chr7 | 141637767 | |||||||
| chr7:141637853 | A | G | 1 | a0001c0001t0006g0225 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.726+836A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 11/15 | chr7 | 141637853 | |||||||
| chr7:141637965 | GT | G | 10 | a0001c0001t0001g0015 a0001c0001t0001g0111 a0001c0001t0001g0118 others(7): Show |
10 | HG02083.hp1 NA18951.hp1 NA18951.hp2 others(7): Show |
intron_variant | MODIFIER | c.726+949delT | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 11/15 | chr7 | 141637965 | |||||||
| chr7:141638304 | T | C | 1 | a0001c0001t0001g0197 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.726+1287T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 11/15 | chr7 | 141638304 | |||||||
| chr7:141638547 | A | G | 38 | a0001c0001t0001g0228 a0001c0001t0002g0005 a0001c0001t0002g0006 others(35): Show |
41 | HG00408.hp1 HG01168.hp2 HG01261.hp1 others(38): Show |
intron_variant | MODIFIER | c.726+1530A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 11/15 | chr7 | 141638547 | |||||||
| chr7:141638973 | G | A | 3 | a0001c0001t0001g0124 a0001c0001t0001g0210 a0001c0001t0001g0211 |
3 | HG00544.hp2 NA18974.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.726+1956G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 11/15 | chr7 | 141638973 | |||||||
| chr7:141639275 | C | G | 261 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(258): Show |
269 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.727-1973C>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 11/15 | chr7 | 141639275 | |||||||
| chr7:141639404 | G | C | 1 | a0001c0001t0001g0002 | 2 | HG00735.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.727-1844G>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 11/15 | chr7 | 141639404 | |||||||
| chr7:141639508 | T | C | 1 | a0001c0001t0001g0203 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.727-1740T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 11/15 | chr7 | 141639508 | |||||||
| chr7:141639807 | C | T | 1 | a0001c0001t0005g0256 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.727-1441C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 11/15 | chr7 | 141639807 | |||||||
| chr7:141639929 | C | A | 1 | a0001c0001t0001g0037 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.727-1319C>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 11/15 | chr7 | 141639929 | |||||||
| chr7:141640003 | A | G | 1 | a0001c0001t0001g0001 | 2 | HG00140.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.727-1245A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 11/15 | chr7 | 141640003 | |||||||
| chr7:141640026 | C | A | 1 | a0001c0001t0003g0263 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.727-1222C>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 11/15 | chr7 | 141640026 | |||||||
| chr7:141640245 | A | G | 3 | a0001c0001t0006g0224 a0001c0001t0006g0225 a0001c0001t0006g0226 |
3 | HG02055.hp1 HG02109.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.727-1003A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 11/15 | chr7 | 141640245 | |||||||
| chr7:141640257 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.727-991C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 11/15 | chr7 | 141640257 | |||||||
| chr7:141640287 | A | C | 5 | a0001c0001t0001g0228 a0001c0001t0006g0224 a0001c0001t0006g0225 others(2): Show |
5 | HG02055.hp1 HG02109.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.727-961A>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 11/15 | chr7 | 141640287 | |||||||
| chr7:141640307 | T | TAGAAGCA others(11): Show |
2 | a0001c0001t0005g0257 a0001c0001t0005g0258 |
2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.727-937_727-920dup others(18): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr7 | 141640307 | ||||||
| chr7:141640476 | G | C | 23 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0219 others(20): Show |
25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.727-772G>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 11/15 | chr7 | 141640476 | |||||||
| chr7:141640518 | C | A | 1 | a0001c0001t0007g0056 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.727-730C>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 11/15 | chr7 | 141640518 | |||||||
| chr7:141640697 | G | A | 1 | a0001c0001t0001g0176 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.727-551G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 11/15 | chr7 | 141640697 | |||||||
| chr7:141640876 | G | A | 1 | a0004c0003t0010g0227 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.727-372G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 11/15 | chr7 | 141640876 | |||||||
| chr7:141640993 | G | A | 2 | a0001c0001t0005g0257 a0001c0001t0005g0258 |
2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.727-255G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 11/15 | chr7 | 141640993 | |||||||
| chr7:141641038 | G | A | 1 | a0001c0001t0002g0244 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.727-210G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 11/15 | chr7 | 141641038 | |||||||
| chr7:141641577 | A | C | 1 | a0001c0001t0001g0133 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.877+179A>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 12/15 | chr7 | 141641577 | |||||||
| chr7:141641595 | A | G | 3 | a0001c0001t0003g0262 a0001c0001t0003g0263 a0001c0001t0003g0264 |
3 | HG02723.hp1 HG02970.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.877+197A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 12/15 | chr7 | 141641595 | |||||||
| chr7:141641706 | C | T | 1 | a0001c0001t0001g0171 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.878-105C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 12/15 | chr7 | 141641706 | |||||||
| chr7:141641773 | A | G | 1 | a0001c0001t0001g0148 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.878-38A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 12/15 | chr7 | 141641773 | |||||||
| chr7:141642129 | A | G | 1 | a0001c0001t0001g0216 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.975+221A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141642129 | |||||||
| chr7:141642170 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.975+262G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141642170 | |||||||
| chr7:141642343 | T | G | 32 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0219 others(29): Show |
35 | HG00408.hp1 HG01168.hp2 HG01261.hp1 others(32): Show |
intron_variant | MODIFIER | c.975+435T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141642343 | |||||||
| chr7:141642545 | C | T | 3 | a0001c0001t0006g0224 a0001c0001t0006g0225 a0001c0001t0006g0226 |
3 | HG02055.hp1 HG02109.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.975+637C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141642545 | |||||||
| chr7:141642852 | T | C | 3 | a0001c0001t0001g0149 a0001c0001t0001g0154 a0001c0001t0001g0156 |
3 | HG00642.hp1 HG02258.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.975+944T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141642852 | |||||||
| chr7:141642959 | A | G | 2 | a0001c0001t0002g0230 a0001c0001t0002g0234 |
2 | NA18997.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.975+1051A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141642959 | |||||||
| chr7:141643222 | C | T | 9 | a0001c0001t0003g0261 a0001c0001t0003g0262 a0001c0001t0003g0263 others(6): Show |
10 | HG01261.hp1 HG02723.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.975+1314C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141643222 | |||||||
| chr7:141643287 | C | T | 100 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(97): Show |
100 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.975+1379C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141643287 | |||||||
| chr7:141643417 | G | A | 2 | a0001c0001t0001g0002 a0001c0001t0001g0134 |
3 | HG00735.hp2 HG02630.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.975+1509G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141643417 | |||||||
| chr7:141643594 | C | T | 4 | a0001c0001t0004g0007 a0001c0001t0004g0250 a0001c0001t0004g0251 others(1): Show |
5 | HG02630.hp1 HG02965.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.975+1686C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141643594 | |||||||
| chr7:141643746 | G | A | 22 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0229 others(19): Show |
24 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(21): Show |
intron_variant | MODIFIER | c.975+1838G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141643746 | |||||||
| chr7:141644052 | T | C | 1 | a0004c0003t0010g0227 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.975+2144T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141644052 | |||||||
| chr7:141644091 | T | C | 5 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0001t0001g0253 others(2): Show |
5 | HG01891.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.975+2183T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141644091 | |||||||
| chr7:141644094 | T | TA | 9 | a0001c0001t0001g0157 a0001c0001t0001g0171 a0001c0001t0001g0213 others(6): Show |
9 | HG02055.hp1 HG02109.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.975+2199dupA | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr7 | 141644094 | ||||||
| chr7:141644094 | TA | T | 99 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(96): Show |
99 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.975+2199delA | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr7 | 141644094 | ||||||
| chr7:141644322 | T | G | 3 | a0001c0001t0003g0262 a0001c0001t0003g0263 a0001c0001t0003g0264 |
3 | HG02723.hp1 HG02970.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.975+2414T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141644322 | |||||||
| chr7:141644418 | A | G | 32 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0219 others(29): Show |
35 | HG00408.hp1 HG01168.hp2 HG01261.hp1 others(32): Show |
intron_variant | MODIFIER | c.975+2510A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141644418 | |||||||
| chr7:141644730 | A | G | 5 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0001t0001g0253 others(2): Show |
5 | HG01891.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.975+2822A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141644730 | |||||||
| chr7:141644750 | ATAAG | A | 5 | a0001c0001t0001g0228 a0001c0001t0006g0224 a0001c0001t0006g0225 others(2): Show |
5 | HG02055.hp1 HG02109.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.975+2844_975+2847d others(6): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr7 | 141644750 | ||||||
| chr7:141644946 | A | T | 1 | a0001c0001t0001g0047 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.975+3038A>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141644946 | |||||||
| chr7:141644984 | TATA | T | 23 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0219 others(20): Show |
25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.975+3081_975+3083d others(5): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr7 | 141644984 | ||||||
| chr7:141644988 | A | G | 3 | a0001c0001t0003g0262 a0001c0001t0003g0263 a0001c0001t0003g0264 |
3 | HG02723.hp1 HG02970.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.975+3080A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141644988 | |||||||
| chr7:141645072 | T | C | 23 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0219 others(20): Show |
25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.975+3164T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141645072 | |||||||
| chr7:141645566 | G | C | 1 | a0001c0001t0001g0024 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.975+3658G>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141645566 | |||||||
| chr7:141645587 | C | T | 1 | a0001c0001t0001g0066 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.976-3676C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141645587 | |||||||
| chr7:141645863 | G | A | 1 | a0001c0001t0001g0046 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.976-3400G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141645863 | |||||||
| chr7:141646176 | A | C | 1 | a0001c0001t0001g0133 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.976-3087A>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141646176 | |||||||
| chr7:141646283 | T | C | 5 | a0001c0001t0001g0029 a0001c0001t0001g0073 a0001c0001t0001g0080 others(2): Show |
5 | HG01346.hp1 HG02273.hp2 HG02293.hp2 others(2): Show |
intron_variant | MODIFIER | c.976-2980T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141646283 | |||||||
| chr7:141646372 | CAATT | C | 4 | a0001c0001t0004g0007 a0001c0001t0004g0250 a0001c0001t0004g0251 others(1): Show |
5 | HG02630.hp1 HG02965.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.976-2889_976-2886d others(6): Show |
AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr7 | 141646372 | ||||||
| chr7:141646384 | A | G | 1 | a0001c0001t0001g0015 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.976-2879A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141646384 | |||||||
| chr7:141646427 | A | G | 2 | a0001c0001t0008g0041 a0001c0001t0008g0042 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.976-2836A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141646427 | |||||||
| chr7:141646440 | G | C | 48 | a0001c0001t0001g0228 a0001c0001t0001g0248 a0001c0001t0001g0249 others(45): Show |
52 | HG00408.hp1 HG01168.hp2 HG01261.hp1 others(49): Show |
intron_variant | MODIFIER | c.976-2823G>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141646440 | |||||||
| chr7:141646645 | T | C | 1 | a0001c0001t0002g0259 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.976-2618T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141646645 | |||||||
| chr7:141646816 | G | A | 3 | a0001c0001t0001g0003 a0001c0001t0001g0185 a0001c0001t0001g0188 |
4 | HG00423.hp1 HG00597.hp1 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.976-2447G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141646816 | |||||||
| chr7:141646866 | C | G | 1 | a0001c0001t0001g0136 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.976-2397C>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141646866 | |||||||
| chr7:141647158 | A | T | 1 | a0001c0001t0002g0006 | 2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.976-2105A>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141647158 | |||||||
| chr7:141647245 | T | G | 2 | a0001c0001t0005g0257 a0001c0001t0005g0258 |
2 | NA18949.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.976-2018T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141647245 | |||||||
| chr7:141647298 | T | C | 23 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0219 others(20): Show |
25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.976-1965T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141647298 | |||||||
| chr7:141647309 | T | C | 5 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0001t0001g0253 others(2): Show |
5 | HG01891.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.976-1954T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141647309 | |||||||
| chr7:141647367 | T | C | 3 | a0001c0001t0001g0119 a0001c0001t0001g0129 a0001c0001t0001g0130 |
3 | HG01261.hp2 HG02559.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.976-1896T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141647367 | |||||||
| chr7:141647423 | C | T | 1 | a0001c0001t0005g0256 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.976-1840C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141647423 | |||||||
| chr7:141647431 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.976-1832C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141647431 | |||||||
| chr7:141647733 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.976-1530C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141647733 | |||||||
| chr7:141647774 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.976-1489G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141647774 | |||||||
| chr7:141647829 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.976-1434C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141647829 | |||||||
| chr7:141647859 | C | T | 1 | a0001c0001t0002g0219 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.976-1404C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141647859 | |||||||
| chr7:141647873 | G | A | 1 | a0004c0003t0010g0227 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.976-1390G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141647873 | |||||||
| chr7:141647880 | G | A | 25 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0219 others(22): Show |
27 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(24): Show |
intron_variant | MODIFIER | c.976-1383G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141647880 | |||||||
| chr7:141648080 | G | A | 1 | a0001c0001t0001g0021 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.976-1183G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141648080 | |||||||
| chr7:141648127 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.976-1136G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141648127 | |||||||
| chr7:141648195 | G | A | 1 | a0001c0001t0001g0037 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.976-1068G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141648195 | |||||||
| chr7:141648517 | A | C | 1 | a0001c0001t0001g0163 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.976-746A>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141648517 | |||||||
| chr7:141648579 | A | G | 2 | a0001c0001t0001g0043 a0001c0001t0001g0055 |
2 | HG02080.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.976-684A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141648579 | |||||||
| chr7:141648595 | A | G | 5 | a0001c0001t0004g0007 a0001c0001t0004g0250 a0001c0001t0004g0251 others(2): Show |
6 | HG01884.hp1 HG02630.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.976-668A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141648595 | |||||||
| chr7:141648619 | G | A | 1 | a0001c0001t0005g0256 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.976-644G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141648619 | |||||||
| chr7:141648804 | G | T | 2 | a0002c0002t0003g0008 a0002c0002t0003g0266 |
3 | HG01261.hp1 HG02896.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.976-459G>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141648804 | |||||||
| chr7:141649013 | T | C | 23 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0219 others(20): Show |
25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.976-250T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141649013 | |||||||
| chr7:141649094 | G | GA | 12 | a0001c0001t0001g0024 a0001c0001t0001g0088 a0001c0001t0001g0113 others(9): Show |
12 | HG01261.hp2 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.976-152dupA | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr7 | 141649094 | ||||||
| chr7:141649094 | GA | G | 36 | a0001c0001t0001g0009 a0001c0001t0001g0026 a0001c0001t0001g0048 others(33): Show |
37 | HG01952.hp2 HG02015.hp1 HG02055.hp1 others(34): Show |
intron_variant | MODIFIER | c.976-152delA | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr7 | 141649094 | ||||||
| chr7:141649114 | T | C | 48 | a0001c0001t0001g0228 a0001c0001t0001g0248 a0001c0001t0001g0249 others(45): Show |
52 | HG00408.hp1 HG01168.hp2 HG01261.hp1 others(49): Show |
intron_variant | MODIFIER | c.976-149T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141649114 | |||||||
| chr7:141649216 | T | G | 1 | a0001c0001t0001g0163 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.976-47T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 13/15 | chr7 | 141649216 | |||||||
| chr7:141649483 | T | G | 3 | a0001c0001t0001g0075 a0001c0001t0001g0079 a0001c0001t0001g0087 |
3 | HG01943.hp1 HG01993.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.1046+150T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 14/15 | chr7 | 141649483 | |||||||
| chr7:141649599 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1046+266G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 14/15 | chr7 | 141649599 | |||||||
| chr7:141649611 | G | A | 1 | a0001c0001t0001g0212 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1046+278G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 14/15 | chr7 | 141649611 | |||||||
| chr7:141649674 | G | A | 2 | a0002c0002t0003g0008 a0002c0002t0003g0266 |
3 | HG01261.hp1 HG02896.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1046+341G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 14/15 | chr7 | 141649674 | |||||||
| chr7:141649703 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1046+370G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 14/15 | chr7 | 141649703 | |||||||
| chr7:141649734 | T | C | 4 | a0001c0001t0006g0224 a0001c0001t0006g0225 a0001c0001t0006g0226 others(1): Show |
4 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1046+401T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 14/15 | chr7 | 141649734 | |||||||
| chr7:141649743 | T | C | 1 | a0001c0001t0001g0214 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1046+410T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 14/15 | chr7 | 141649743 | |||||||
| chr7:141649967 | C | T | 1 | a0001c0001t0005g0256 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1046+634C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 14/15 | chr7 | 141649967 | |||||||
| chr7:141650054 | T | G | 1 | a0001c0001t0001g0138 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1046+721T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 14/15 | chr7 | 141650054 | |||||||
| chr7:141650065 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1046+732G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 14/15 | chr7 | 141650065 | |||||||
| chr7:141650132 | C | T | 1 | a0001c0001t0005g0256 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1046+799C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 14/15 | chr7 | 141650132 | |||||||
| chr7:141650718 | T | C | 1 | a0004c0003t0010g0227 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1047-807T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 14/15 | chr7 | 141650718 | |||||||
| chr7:141650734 | C | T | 1 | a0001c0001t0004g0252 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1047-791C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 14/15 | chr7 | 141650734 | |||||||
| chr7:141650780 | C | T | 1 | a0001c0001t0002g0236 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1047-745C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 14/15 | chr7 | 141650780 | |||||||
| chr7:141650919 | G | A | 1 | a0001c0001t0003g0265 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1047-606G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 14/15 | chr7 | 141650919 | |||||||
| chr7:141650960 | G | C | 9 | a0001c0001t0003g0261 a0001c0001t0003g0262 a0001c0001t0003g0263 others(6): Show |
10 | HG01261.hp1 HG02723.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.1047-565G>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 14/15 | chr7 | 141650960 | |||||||
| chr7:141651170 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1047-355C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 14/15 | chr7 | 141651170 | |||||||
| chr7:141651290 | A | G | 23 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0219 others(20): Show |
25 | HG00408.hp1 HG01168.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.1047-235A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 14/15 | chr7 | 141651290 | |||||||
| chr7:141651467 | T | C | 1 | a0001c0001t0001g0108 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1047-58T>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 14/15 | chr7 | 141651467 | |||||||
| chr7:141652122 | C | CG | 7 | a0001c0001t0001g0068 a0001c0001t0001g0075 a0001c0001t0001g0079 others(4): Show |
7 | HG00558.hp2 HG01943.hp1 HG01993.hp2 others(4): Show |
intron_variant | MODIFIER | c.1131+515dupG | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr7 | 141652122 | ||||||
| chr7:141652122 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1131+513C>T | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 15/15 | chr7 | 141652122 | |||||||
| chr7:141652189 | A | G | 1 | a0001c0001t0001g0009 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1131+580A>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 15/15 | chr7 | 141652189 | |||||||
| chr7:141652229 | G | A | 4 | a0001c0001t0001g0108 a0001c0001t0001g0209 a0001c0001t0001g0212 others(1): Show |
4 | HG03225.hp1 NA18956.hp2 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.1132-558G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 15/15 | chr7 | 141652229 | |||||||
| chr7:141652304 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1132-483G>A | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 15/15 | chr7 | 141652304 | |||||||
| chr7:141652308 | A | C | 1 | a0001c0001t0001g0152 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1132-479A>C | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 15/15 | chr7 | 141652308 | |||||||
| chr7:141652747 | T | G | 6 | a0001c0001t0001g0022 a0001c0001t0001g0028 a0001c0001t0001g0037 others(3): Show |
6 | HG02735.hp2 HG02738.hp2 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.1132-40T>G | AGK | ENSG00000006530.18 | transcript | ENST00000649286.2 | protein_coding | 15/15 | chr7 | 141652747 |