Search by Gene
| Item | Value |
|---|---|
| geneid | 57037 |
| ensemblid | ENSG00000106524.9 |
| hgncid | 25370 |
| symbol | ANKMY2 |
| name | ankyrin repeat and MYND domain containing 2 |
| refseq_nuc | NM_020319.3 |
| refseq_prot | NP_064715.1 |
| ensembl_nuc | ENST00000306999.7 |
| ensembl_prot | ENSP00000303570.2 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 16599779 |
| end | 16645754 |
| strand | - |
| ver | v1.2 |
| region | chr7:16599779-16645754 |
| region5000 | chr7:16594779-16650754 |
| regionname0 | ANKMY2_chr7_16599779_16645754 |
| regionname5000 | ANKMY2_chr7_16594779_16650754 |
Multiple Alignments (by translate haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
Multiple Alignments (by aa haplotype frequency)
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 441 | 366 | 87 | 70 | 153 | 14 | 42 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | MVHIK others(436): Show |
chr7 | 16594779 | 16650754 |
| a0002 | 0/0 | 441 | 27 | 2 | 1 | 24 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | MVHIK others(436): Show |
chr7 | 16594779 | 16650754 |
| a0003 | 0/0 | 441 | 2 | 2 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | MVHIK others(436): Show |
chr7 | 16594779 | 16650754 |
| a0004 | 0/0 | 441 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | MVHIK others(436): Show |
chr7 | 16594779 | 16650754 |
| a0005 | 0/0 | 441 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | MVHIK others(436): Show |
chr7 | 16594779 | 16650754 |
| a0006 | 0/0 | 441 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | MVHIK others(436): Show |
chr7 | 16594779 | 16650754 |
| a0007 | 0/0 | 441 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | MVHIK others(436): Show |
chr7 | 16594779 | 16650754 |
| a0008 | 0/0 | 441 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | MVHIK others(436): Show |
chr7 | 16594779 | 16650754 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1323 | 187 | 46 | 33 | 80 | 3 | 25 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | ATGGT others(1318): Show |
chr7 | 16594779 | 16650754 | ||
| a0001c0002 | 0/0 | 1323 | 62 | 5 | 11 | 30 | 4 | 12 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | ATGGT others(1318): Show |
chr7 | 16594779 | 16650754 | ||
| a0001c0003 | 0/0 | 1323 | 47 | 25 | 11 | 8 | 0 | 3 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | ATGGT others(1318): Show |
chr7 | 16594779 | 16650754 | ||
| a0001c0004 | 0/0 | 1323 | 39 | 6 | 9 | 17 | 6 | 1 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | ATGGT others(1318): Show |
chr7 | 16594779 | 16650754 | ||
| a0001c0006 | 0/0 | 1323 | 10 | 0 | 1 | 9 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | ATGGT others(1318): Show |
chr7 | 16594779 | 16650754 | ||
| a0001c0007 | 0/0 | 1323 | 8 | 2 | 1 | 4 | 1 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | ATGGT others(1318): Show |
chr7 | 16594779 | 16650754 | ||
| a0001c0008 | 0/0 | 1323 | 7 | 0 | 4 | 3 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | ATGGT others(1318): Show |
chr7 | 16594779 | 16650754 | ||
| a0001c0011 | 0/0 | 1323 | 2 | 2 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | ATGGT others(1318): Show |
chr7 | 16594779 | 16650754 | ||
| a0001c0017 | 0/0 | 1323 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | ATGGT others(1318): Show |
chr7 | 16594779 | 16650754 | ||
| a0001c0020 | 0/0 | 1323 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | ATGGT others(1318): Show |
chr7 | 16594779 | 16650754 | ||
| a0001c0021 | 0/0 | 1323 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | ATGGT others(1318): Show |
chr7 | 16594779 | 16650754 | ||
| a0001c0022 | 0/0 | 1323 | 1 | 0 | 0 | 0 | 0 | 1 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | ATGGT others(1318): Show |
chr7 | 16594779 | 16650754 | ||
| a0002c0005 | 0/0 | 1323 | 23 | 1 | 1 | 21 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | ATGGT others(1318): Show |
chr7 | 16594779 | 16650754 | ||
| a0002c0009 | 0/0 | 1323 | 2 | 0 | 0 | 2 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | ATGGT others(1318): Show |
chr7 | 16594779 | 16650754 | ||
| a0002c0010 | 0/0 | 1323 | 2 | 1 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | ATGGT others(1318): Show |
chr7 | 16594779 | 16650754 | ||
| a0003c0013 | 0/0 | 1323 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | ATGGT others(1318): Show |
chr7 | 16594779 | 16650754 | ||
| a0003c0018 | 0/0 | 1323 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | ATGGT others(1318): Show |
chr7 | 16594779 | 16650754 | ||
| a0004c0016 | 0/0 | 1323 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | ATGGT others(1318): Show |
chr7 | 16594779 | 16650754 | ||
| a0005c0014 | 0/0 | 1323 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | ATGGT others(1318): Show |
chr7 | 16594779 | 16650754 | ||
| a0006c0019 | 0/0 | 1323 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | ATGGT others(1318): Show |
chr7 | 16594779 | 16650754 | ||
| a0007c0012 | 0/0 | 1323 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | ATGGT others(1318): Show |
chr7 | 16594779 | 16650754 | ||
| a0008c0015 | 0/0 | 1323 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | ATGGT others(1318): Show |
chr7 | 16594779 | 16650754 |
| acthapid | grch38/chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2489 | 79 | 14 | 15 | 41 | 0 | 9 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | GAGCT others(2484): Show |
chr7 | 16594779 | 16650754 |
| a0001c0001t0002 | 0/0 | 2489 | 51 | 11 | 9 | 18 | 1 | 12 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | GAGCT others(2484): Show |
chr7 | 16594779 | 16650754 |
| a0001c0001t0003 | 0/0 | 2489 | 38 | 6 | 7 | 20 | 2 | 3 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | GAGCT others(2484): Show |
chr7 | 16594779 | 16650754 |
| a0001c0001t0005 | 0/0 | 2489 | 7 | 7 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | GAGCT others(2484): Show |
chr7 | 16594779 | 16650754 |
| a0001c0001t0006 | 0/0 | 2489 | 5 | 5 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | GAGCT others(2484): Show |
chr7 | 16594779 | 16650754 |
| a0001c0001t0009 | 0/0 | 2489 | 2 | 2 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | GAGCT others(2484): Show |
chr7 | 16594779 | 16650754 |
| a0001c0001t0011 | 0/0 | 2489 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | GAGCT others(2484): Show |
chr7 | 16594779 | 16650754 |
| a0001c0001t0013 | 0/0 | 2489 | 1 | 0 | 0 | 0 | 0 | 1 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | GAGCT others(2484): Show |
chr7 | 16594779 | 16650754 |
| a0001c0001t0015 | 0/0 | 2489 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | GAGCT others(2484): Show |
chr7 | 16594779 | 16650754 |
| a0001c0001t0016 | 0/0 | 2489 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | GAGCT others(2484): Show |
chr7 | 16594779 | 16650754 |
| a0001c0001t0017 | 0/0 | 2489 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | GAGCT others(2484): Show |
chr7 | 16594779 | 16650754 |
| a0001c0002t0001 | 0/0 | 2489 | 13 | 1 | 5 | 6 | 0 | 1 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | GAGCT others(2484): Show |
chr7 | 16594779 | 16650754 |
| a0001c0002t0002 | 0/0 | 2489 | 32 | 1 | 4 | 13 | 4 | 10 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | GAGCT others(2484): Show |
chr7 | 16594779 | 16650754 |
| a0001c0002t0003 | 0/0 | 2489 | 16 | 3 | 1 | 11 | 0 | 1 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | GAGCT others(2484): Show |
chr7 | 16594779 | 16650754 |
| a0001c0002t0008 | 0/0 | 2489 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | GAGCT others(2484): Show |
chr7 | 16594779 | 16650754 |
| a0001c0003t0004 | 0/0 | 2489 | 45 | 24 | 10 | 8 | 0 | 3 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | GAGCT others(2484): Show |
chr7 | 16594779 | 16650754 |
| a0001c0003t0005 | 0/0 | 2489 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | GAGCT others(2484): Show |
chr7 | 16594779 | 16650754 |
| a0001c0003t0007 | 0/0 | 2489 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | GAGCT others(2484): Show |
chr7 | 16594779 | 16650754 |
| a0001c0004t0001 | 0/0 | 2489 | 12 | 1 | 1 | 9 | 0 | 1 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | GAGCT others(2484): Show |
chr7 | 16594779 | 16650754 |
| a0001c0004t0002 | 0/0 | 2489 | 15 | 3 | 5 | 4 | 3 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | GAGCT others(2484): Show |
chr7 | 16594779 | 16650754 |
| a0001c0004t0003 | 0/0 | 2489 | 10 | 2 | 1 | 4 | 3 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | GAGCT others(2484): Show |
chr7 | 16594779 | 16650754 |
| a0001c0004t0008 | 0/0 | 2489 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | GAGCT others(2484): Show |
chr7 | 16594779 | 16650754 |
| a0001c0004t0010 | 0/0 | 2489 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | GAGCT others(2484): Show |
chr7 | 16594779 | 16650754 |
| a0001c0006t0004 | 0/0 | 2489 | 10 | 0 | 1 | 9 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | GAGCT others(2484): Show |
chr7 | 16594779 | 16650754 |
| a0001c0007t0004 | 0/0 | 2489 | 7 | 1 | 1 | 4 | 1 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | GAGCT others(2484): Show |
chr7 | 16594779 | 16650754 |
| a0001c0007t0007 | 0/0 | 2489 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | GAGCT others(2484): Show |
chr7 | 16594779 | 16650754 |
| a0001c0008t0001 | 0/0 | 2489 | 3 | 0 | 0 | 3 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | GAGCT others(2484): Show |
chr7 | 16594779 | 16650754 |
| a0001c0008t0002 | 0/0 | 2489 | 3 | 0 | 3 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | GAGCT others(2484): Show |
chr7 | 16594779 | 16650754 |
| a0001c0008t0003 | 0/0 | 2489 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | GAGCT others(2484): Show |
chr7 | 16594779 | 16650754 |
| a0001c0011t0001 | 0/0 | 2489 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | GAGCT others(2484): Show |
chr7 | 16594779 | 16650754 |
| a0001c0011t0002 | 0/0 | 2489 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | GAGCT others(2484): Show |
chr7 | 16594779 | 16650754 |
| a0001c0017t0001 | 0/0 | 2489 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | GAGCT others(2484): Show |
chr7 | 16594779 | 16650754 |
| a0001c0020t0004 | 0/0 | 2489 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | GAGCT others(2484): Show |
chr7 | 16594779 | 16650754 |
| a0001c0021t0002 | 0/0 | 2489 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | GAGCT others(2484): Show |
chr7 | 16594779 | 16650754 |
| a0001c0022t0001 | 0/0 | 2489 | 1 | 0 | 0 | 0 | 0 | 1 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | GAGCT others(2484): Show |
chr7 | 16594779 | 16650754 |
| a0002c0005t0001 | 0/0 | 2489 | 7 | 0 | 0 | 7 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | GAGCT others(2484): Show |
chr7 | 16594779 | 16650754 |
| a0002c0005t0002 | 0/0 | 2489 | 9 | 0 | 0 | 9 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | GAGCT others(2484): Show |
chr7 | 16594779 | 16650754 |
| a0002c0005t0003 | 0/0 | 2489 | 6 | 1 | 1 | 4 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | GAGCT others(2484): Show |
chr7 | 16594779 | 16650754 |
| a0002c0005t0014 | 0/0 | 2489 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | GAGCT others(2484): Show |
chr7 | 16594779 | 16650754 |
| a0002c0009t0001 | 0/0 | 2489 | 2 | 0 | 0 | 2 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | GAGCT others(2484): Show |
chr7 | 16594779 | 16650754 |
| a0002c0010t0004 | 0/0 | 2489 | 2 | 1 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | GAGCT others(2484): Show |
chr7 | 16594779 | 16650754 |
| a0003c0013t0003 | 0/0 | 2489 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | GAGCT others(2484): Show |
chr7 | 16594779 | 16650754 |
| a0003c0018t0003 | 0/0 | 2489 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | GAGCT others(2484): Show |
chr7 | 16594779 | 16650754 |
| a0004c0016t0002 | 0/0 | 2489 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | GAGCT others(2484): Show |
chr7 | 16594779 | 16650754 |
| a0005c0014t0001 | 0/0 | 2489 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | GAGCT others(2484): Show |
chr7 | 16594779 | 16650754 |
| a0006c0019t0004 | 0/0 | 2489 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | GAGCT others(2484): Show |
chr7 | 16594779 | 16650754 |
| a0007c0012t0002 | 0/0 | 2489 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | GAGCT others(2484): Show |
chr7 | 16594779 | 16650754 |
| a0008c0015t0012 | 0/0 | 2489 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | GAGCT others(2484): Show |
chr7 | 16594779 | 16650754 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0001g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0001g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0001g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0001g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0001g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0002g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0002g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0002g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0002g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0003g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0003g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0003g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0003g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0003g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0003g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0003g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0005g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0005g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0005g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0005g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0005g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0005g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0006g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0006g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0006g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0006g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0006g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0009g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0011g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0013g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0015g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0016g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0001t0017g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0002t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0002t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0002t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0002t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0002t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0002t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0002t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0002t0002g0006 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0002t0002g0007 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0002t0002g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0002t0002g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0002t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0002t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0002t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0002t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0002t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0002t0002g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0002t0003g0004 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0002t0003g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0002t0003g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0002t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0002t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0002t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0002t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0002t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0002t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0002t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0002t0003g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0002t0003g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0002t0003g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0002t0008g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0003t0004g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0003t0004g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0003t0004g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0003t0004g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0003t0004g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0003t0004g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0003t0004g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0003t0004g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0003t0004g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0003t0004g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0003t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0003t0004g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0003t0004g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0003t0004g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0003t0004g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0003t0004g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0003t0004g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0003t0004g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0003t0004g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0003t0004g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0003t0004g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0003t0004g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0003t0004g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0003t0004g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0003t0004g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0003t0004g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0003t0004g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0003t0004g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0003t0004g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0003t0004g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0003t0004g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0003t0004g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0003t0004g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0003t0004g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0003t0004g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0003t0004g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0003t0004g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0003t0004g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0003t0004g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0003t0004g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0003t0004g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0003t0004g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0003t0004g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0003t0004g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0003t0004g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0003t0005g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0003t0007g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0004t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0004t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0004t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0004t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0004t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0004t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0004t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0004t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0004t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0004t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0004t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0004t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0004t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0004t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0004t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0004t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0004t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0004t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0004t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0004t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0004t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0004t0002g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0004t0002g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0004t0002g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0004t0002g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0004t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0004t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0004t0003g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0004t0003g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0004t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0004t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0004t0003g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0004t0003g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0004t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0004t0003g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0004t0003g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0004t0003g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0004t0008g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0004t0010g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0006t0004g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0006t0004g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0006t0004g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0006t0004g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0006t0004g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0006t0004g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0006t0004g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0006t0004g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0006t0004g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0007t0004g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0007t0004g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0007t0004g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0007t0004g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0007t0004g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0007t0004g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0007t0004g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0007t0007g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0008t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0008t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0008t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0008t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0008t0002g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0008t0003g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0011t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0011t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0017t0001g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0020t0004g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0021t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0001c0022t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0002c0005t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0002c0005t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0002c0005t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0002c0005t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0002c0005t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0002c0005t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0002c0005t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0002c0005t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0002c0005t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0002c0005t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0002c0005t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0002c0005t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0002c0005t0002g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0002c0005t0002g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0002c0005t0002g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0002c0005t0002g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0002c0005t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0002c0005t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0002c0005t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0002c0005t0003g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0002c0005t0003g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0002c0005t0003g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0002c0005t0014g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0002c0009t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0002c0009t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0002c0010t0004g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0002c0010t0004g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0003c0013t0003g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0003c0018t0003g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0004c0016t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0005c0014t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0006c0019t0004g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0007c0012t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| a0008c0015t0012g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0082 | EUR | GBR | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG00140 | hp2 | a0001 | c0004 | t0003 | g0177 | EUR | GBR | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG00280 | hp1 | a0001 | c0007 | t0004 | g0187 | EUR | FIN | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG00280 | hp2 | a0001 | c0004 | t0003 | g0303 | EUR | FIN | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG00323 | hp1 | a0001 | c0004 | t0002 | g0304 | EUR | FIN | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG00323 | hp2 | a0001 | c0004 | t0003 | g0178 | EUR | FIN | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG00408 | hp1 | a0001 | c0002 | t0002 | g0136 | EAS | CHS | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG00408 | hp2 | a0002 | c0005 | t0014 | g0209 | EAS | CHS | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | CHS | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG00423 | hp2 | a0002 | c0009 | t0001 | g0141 | EAS | CHS | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | CHS | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | CHS | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG00597 | hp1 | a0002 | c0005 | t0001 | g0293 | EAS | CHS | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG00597 | hp2 | a0001 | c0006 | t0004 | g0207 | EAS | CHS | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0340 | EAS | CHS | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | CHS | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG00621 | hp1 | a0001 | c0002 | t0002 | g0088 | EAS | CHS | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | CHS | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0323 | AMR | PUR | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG00642 | hp2 | a0002 | c0005 | t0003 | g0355 | AMR | PUR | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0315 | EAS | CHS | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG00673 | hp2 | a0001 | c0001 | t0003 | g0100 | EAS | CHS | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG00733 | hp1 | a0001 | c0006 | t0004 | g0075 | AMR | PUR | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0373 | AMR | PUR | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG00735 | hp2 | a0001 | c0001 | t0015 | g0174 | AMR | PUR | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG00738 | hp1 | a0001 | c0008 | t0002 | g0322 | AMR | PUR | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG00741 | hp1 | a0001 | c0008 | t0002 | g0190 | AMR | PUR | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG00741 | hp2 | a0001 | c0004 | t0002 | g0305 | AMR | PUR | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0183 | AMR | PUR | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0156 | AMR | PUR | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0155 | AMR | PUR | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0132 | AMR | PUR | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG01081 | hp2 | a0001 | c0003 | t0004 | g0368 | AMR | PUR | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG01099 | hp1 | a0001 | c0001 | t0016 | g0237 | AMR | PUR | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG01099 | hp2 | a0001 | c0004 | t0003 | g0219 | AMR | PUR | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG01106 | hp1 | a0001 | c0004 | t0010 | g0022 | AMR | PUR | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0251 | AMR | PUR | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0149 | AMR | PUR | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG01167 | hp2 | a0001 | c0004 | t0002 | g0063 | AMR | PUR | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0051 | AMR | PUR | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG01168 | hp2 | a0001 | c0002 | t0002 | g0325 | AMR | PUR | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0053 | AMR | PUR | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG01169 | hp2 | a0001 | c0004 | t0002 | g0064 | AMR | PUR | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0221 | AMR | PUR | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG01192 | hp2 | a0001 | c0004 | t0002 | g0307 | AMR | PUR | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG01243 | hp1 | a0001 | c0002 | t0008 | g0101 | AMR | PUR | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG01243 | hp2 | a0001 | c0003 | t0004 | g0215 | AMR | PUR | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0164 | AMR | CLM | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG01255 | hp2 | a0001 | c0007 | t0004 | g0320 | AMR | CLM | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG01256 | hp1 | a0001 | c0003 | t0004 | g0086 | AMR | CLM | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0360 | AMR | CLM | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG01257 | hp1 | a0004 | c0016 | t0002 | g0126 | AMR | CLM | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0069 | AMR | CLM | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG01261 | hp1 | a0001 | c0002 | t0003 | g0265 | AMR | CLM | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | CLM | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG01346 | hp1 | a0001 | c0004 | t0002 | g0192 | AMR | CLM | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG01346 | hp2 | a0001 | c0003 | t0005 | g0113 | AMR | CLM | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG01361 | hp1 | a0001 | c0003 | t0004 | g0118 | AMR | CLM | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG01361 | hp2 | a0001 | c0004 | t0001 | g0329 | AMR | CLM | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0071 | AMR | CLM | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | CLM | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG01496 | hp1 | a0001 | c0003 | t0004 | g0337 | AMR | CLM | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0054 | AMR | CLM | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0233 | EUR | IBS | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG01515 | hp2 | a0001 | c0004 | t0002 | g0214 | EUR | IBS | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG01516 | hp1 | a0001 | c0002 | t0002 | g0007 | EUR | IBS | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG01516 | hp2 | a0001 | c0002 | t0002 | g0121 | EUR | IBS | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0223 | EUR | IBS | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG01517 | hp2 | a0001 | c0002 | t0002 | g0120 | EUR | IBS | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG01884 | hp1 | a0001 | c0002 | t0002 | g0084 | AFR | ACB | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG01884 | hp2 | a0001 | c0003 | t0004 | g0250 | AFR | ACB | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG01891 | hp1 | a0001 | c0017 | t0001 | g0370 | AFR | ACB | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0236 | AFR | ACB | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PEL | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0094 | AMR | PEL | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG01934 | hp2 | a0001 | c0002 | t0002 | g0116 | AMR | PEL | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG01952 | hp1 | a0001 | c0002 | t0002 | g0006 | AMR | PEL | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG01952 | hp2 | a0001 | c0008 | t0003 | g0191 | AMR | PEL | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG01975 | hp1 | a0001 | c0003 | t0004 | g0231 | AMR | PEL | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG01975 | hp2 | a0001 | c0008 | t0002 | g0189 | AMR | PEL | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG01978 | hp1 | a0001 | c0002 | t0002 | g0091 | AMR | PEL | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG01978 | hp2 | a0001 | c0003 | t0004 | g0247 | AMR | PEL | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PEL | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG01981 | hp2 | a0001 | c0004 | t0008 | g0171 | AMR | PEL | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | KHV | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02015 | hp2 | a0002 | c0005 | t0001 | g0357 | EAS | KHV | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02027 | hp1 | a0001 | c0002 | t0002 | g0107 | EAS | KHV | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02040 | hp1 | a0001 | c0004 | t0001 | g0308 | EAS | KHV | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02055 | hp1 | a0001 | c0003 | t0004 | g0333 | AFR | ACB | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02055 | hp2 | a0001 | c0003 | t0004 | g0217 | AFR | ACB | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02056 | hp2 | a0001 | c0002 | t0002 | g0199 | EAS | KHV | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02074 | hp1 | a0001 | c0020 | t0004 | g0296 | EAS | KHV | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | KHV | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0319 | EAS | KHV | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02083 | hp1 | a0001 | c0002 | t0003 | g0004 | EAS | KHV | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02129 | hp1 | a0001 | c0006 | t0004 | g0104 | EAS | KHV | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0122 | EAS | KHV | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0159 | EAS | KHV | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02132 | hp2 | a0001 | c0003 | t0004 | g0316 | EAS | KHV | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02135 | hp1 | a0001 | c0003 | t0004 | g0347 | EAS | KHV | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02135 | hp2 | a0002 | c0005 | t0001 | g0288 | EAS | KHV | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0087 | AFR | ACB | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02145 | hp2 | a0001 | c0003 | t0004 | g0294 | AFR | ACB | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02148 | hp1 | a0001 | c0001 | t0003 | g0226 | AMR | PEL | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02148 | hp2 | a0001 | c0003 | t0004 | g0114 | AMR | PEL | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02155 | hp1 | a0002 | c0005 | t0001 | g0356 | EAS | CDX | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | CDX | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02165 | hp1 | a0001 | c0004 | t0001 | g0067 | EAS | CDX | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0263 | EAS | CDX | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02257 | hp1 | a0001 | c0001 | t0006 | g0366 | AFR | ACB | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02257 | hp2 | a0001 | c0004 | t0002 | g0302 | AFR | ACB | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02258 | hp1 | a0001 | c0003 | t0004 | g0153 | AFR | ACB | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02258 | hp2 | a0001 | c0001 | t0005 | g0257 | AFR | ACB | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02280 | hp1 | a0001 | c0002 | t0003 | g0078 | AFR | ACB | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02280 | hp2 | a0001 | c0001 | t0005 | g0134 | AFR | ACB | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02300 | hp1 | a0001 | c0003 | t0004 | g0146 | AMR | PEL | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02300 | hp2 | a0001 | c0003 | t0004 | g0238 | AMR | PEL | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0259 | AFR | ACB | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02451 | hp2 | a0001 | c0003 | t0004 | g0040 | AFR | ACB | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02523 | hp1 | a0001 | c0002 | t0002 | g0056 | EAS | KHV | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02523 | hp2 | a0001 | c0003 | t0004 | g0036 | EAS | KHV | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02572 | hp1 | a0001 | c0003 | t0004 | g0042 | AFR | GWD | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0212 | AFR | GWD | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02602 | hp1 | a0001 | c0002 | t0002 | g0083 | SAS | PJL | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0131 | AFR | GWD | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02615 | hp2 | a0001 | c0003 | t0004 | g0281 | AFR | GWD | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02622 | hp1 | a0001 | c0007 | t0004 | g0218 | AFR | GWD | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02622 | hp2 | a0001 | c0004 | t0002 | g0026 | AFR | GWD | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02630 | hp1 | a0005 | c0014 | t0001 | g0324 | AFR | GWD | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02630 | hp2 | a0001 | c0001 | t0006 | g0044 | AFR | GWD | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02683 | hp1 | a0001 | c0002 | t0002 | g0030 | SAS | PJL | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0182 | SAS | PJL | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0096 | SAS | PJL | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02698 | hp2 | a0001 | c0003 | t0004 | g0235 | SAS | PJL | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02717 | hp1 | a0001 | c0003 | t0007 | g0352 | AFR | GWD | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0049 | AFR | GWD | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0262 | AFR | GWD | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02723 | hp2 | a0001 | c0004 | t0001 | g0301 | AFR | GWD | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0224 | SAS | PJL | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02735 | hp2 | a0001 | c0002 | t0002 | g0006 | SAS | PJL | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02738 | hp1 | a0001 | c0002 | t0002 | g0200 | SAS | PJL | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02738 | hp2 | a0001 | c0001 | t0013 | g0043 | SAS | PJL | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0252 | AFR | GWD | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02809 | hp2 | a0001 | c0003 | t0004 | g0047 | AFR | GWD | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02818 | hp1 | a0001 | c0003 | t0004 | g0039 | AFR | GWD | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02818 | hp2 | a0001 | c0003 | t0004 | g0033 | AFR | GWD | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02886 | hp1 | a0001 | c0004 | t0003 | g0268 | AFR | GWD | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02886 | hp2 | a0001 | c0011 | t0001 | g0220 | AFR | GWD | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02895 | hp1 | a0006 | c0019 | t0004 | g0050 | AFR | GWD | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02895 | hp2 | a0001 | c0001 | t0009 | g0002 | AFR | GWD | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0128 | AFR | GWD | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0130 | AFR | GWD | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02897 | hp2 | a0001 | c0001 | t0009 | g0002 | AFR | GWD | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02922 | hp1 | a0001 | c0003 | t0004 | g0269 | AFR | ESN | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02922 | hp2 | a0001 | c0001 | t0011 | g0260 | AFR | ESN | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0195 | AFR | ESN | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02965 | hp2 | a0001 | c0003 | t0004 | g0046 | AFR | ESN | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02970 | hp1 | a0001 | c0001 | t0005 | g0021 | AFR | ESN | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02970 | hp2 | a0001 | c0003 | t0004 | g0185 | AFR | ESN | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02976 | hp1 | a0001 | c0003 | t0004 | g0332 | AFR | ESN | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0369 | AFR | ESN | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG03017 | hp1 | a0001 | c0002 | t0002 | g0029 | SAS | PJL | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0206 | SAS | PJL | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG03041 | hp1 | a0001 | c0001 | t0006 | g0045 | AFR | GWD | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG03041 | hp2 | a0001 | c0003 | t0004 | g0295 | AFR | GWD | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG03098 | hp1 | a0001 | c0001 | t0006 | g0255 | AFR | MSL | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0133 | AFR | MSL | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG03130 | hp1 | a0001 | c0003 | t0004 | g0027 | AFR | ESN | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0349 | AFR | ESN | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | ESN | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | ESN | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG03195 | hp1 | a0001 | c0002 | t0003 | g0326 | AFR | ESN | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG03195 | hp2 | a0001 | c0003 | t0004 | g0377 | AFR | ESN | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG03209 | hp1 | a0001 | c0011 | t0002 | g0025 | AFR | MSL | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG03209 | hp2 | a0001 | c0001 | t0006 | g0208 | AFR | MSL | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG03225 | hp1 | a0001 | c0007 | t0007 | g0274 | AFR | MSL | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG03225 | hp2 | a0001 | c0004 | t0003 | g0375 | AFR | MSL | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0169 | SAS | PJL | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0037 | SAS | PJL | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG03453 | hp1 | a0002 | c0010 | t0004 | g0350 | AFR | MSL | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG03453 | hp2 | a0001 | c0003 | t0004 | g0023 | AFR | MSL | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0280 | SAS | PJL | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0079 | SAS | PJL | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0145 | SAS | PJL | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG03492 | hp2 | a0001 | c0002 | t0003 | g0004 | SAS | PJL | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0362 | AFR | GWD | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG03540 | hp2 | a0001 | c0001 | t0005 | g0376 | AFR | GWD | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG03579 | hp1 | a0001 | c0004 | t0002 | g0065 | AFR | MSL | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0135 | AFR | MSL | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG03654 | hp1 | a0001 | c0004 | t0001 | g0052 | SAS | PJL | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0284 | SAS | PJL | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0261 | SAS | PJL | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG03669 | hp2 | a0001 | c0002 | t0002 | g0062 | SAS | PJL | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0035 | SAS | STU | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG03688 | hp2 | a0001 | c0002 | t0002 | g0092 | SAS | STU | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | BEB | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0229 | SAS | BEB | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG03834 | hp1 | a0001 | c0003 | t0004 | g0147 | SAS | BEB | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG03834 | hp2 | a0001 | c0002 | t0002 | g0081 | SAS | BEB | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG03927 | hp1 | a0001 | c0003 | t0004 | g0234 | SAS | BEB | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0241 | SAS | BEB | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0127 | SAS | BEB | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0246 | SAS | BEB | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0279 | SAS | STU | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG04115 | hp2 | a0001 | c0002 | t0002 | g0102 | SAS | STU | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | STU | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | STU | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG04204 | hp1 | a0001 | c0022 | t0001 | g0186 | SAS | STU | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG04204 | hp2 | a0001 | c0002 | t0002 | g0028 | SAS | STU | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0283 | SAS | STU | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | STU | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18522 | hp1 | a0001 | c0003 | t0004 | g0367 | AFR | YRI | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | YRI | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | CHB | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18612 | hp2 | a0001 | c0002 | t0003 | g0012 | EAS | CHB | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | YRI | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0129 | AFR | YRI | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18939 | hp1 | a0002 | c0005 | t0001 | g0144 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18939 | hp2 | a0001 | c0004 | t0003 | g0297 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18943 | hp2 | a0002 | c0005 | t0002 | g0327 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18944 | hp1 | a0001 | c0004 | t0002 | g0299 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18944 | hp2 | a0001 | c0002 | t0003 | g0167 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18945 | hp1 | a0001 | c0007 | t0004 | g0311 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18945 | hp2 | a0001 | c0008 | t0001 | g0020 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18947 | hp2 | a0001 | c0004 | t0001 | g0330 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18948 | hp2 | a0001 | c0001 | t0003 | g0060 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18949 | hp1 | a0001 | c0001 | t0003 | g0111 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18949 | hp2 | a0001 | c0004 | t0001 | g0313 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18950 | hp1 | a0001 | c0002 | t0002 | g0074 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0343 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18951 | hp2 | a0002 | c0005 | t0003 | g0139 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18952 | hp1 | a0001 | c0004 | t0002 | g0335 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0339 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18953 | hp2 | a0001 | c0002 | t0003 | g0148 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18956 | hp2 | a0001 | c0001 | t0003 | g0117 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18957 | hp1 | a0001 | c0003 | t0004 | g0232 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18957 | hp2 | a0001 | c0004 | t0001 | g0193 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18960 | hp1 | a0002 | c0005 | t0002 | g0138 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18961 | hp1 | a0001 | c0004 | t0003 | g0285 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18961 | hp2 | a0001 | c0002 | t0003 | g0012 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18962 | hp1 | a0002 | c0005 | t0002 | g0125 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18962 | hp2 | a0002 | c0005 | t0002 | g0353 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18964 | hp1 | a0001 | c0002 | t0002 | g0070 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18964 | hp2 | a0002 | c0005 | t0003 | g0290 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18965 | hp2 | a0002 | c0005 | t0003 | g0201 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18966 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18967 | hp2 | a0001 | c0021 | t0002 | g0205 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0068 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18969 | hp2 | a0001 | c0002 | t0002 | g0048 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18970 | hp1 | a0001 | c0008 | t0001 | g0020 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18974 | hp1 | a0001 | c0001 | t0003 | g0123 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18974 | hp2 | a0002 | c0005 | t0001 | g0140 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18977 | hp1 | a0001 | c0004 | t0002 | g0336 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0345 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18980 | hp1 | a0002 | c0005 | t0002 | g0359 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18980 | hp2 | a0002 | c0005 | t0003 | g0142 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18982 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18982 | hp2 | a0001 | c0003 | t0004 | g0243 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18983 | hp2 | a0007 | c0012 | t0002 | g0291 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18984 | hp1 | a0002 | c0005 | t0001 | g0289 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0342 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18986 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18987 | hp1 | a0001 | c0001 | t0017 | g0378 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18989 | hp1 | a0001 | c0004 | t0001 | g0314 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18989 | hp2 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18990 | hp1 | a0001 | c0003 | t0004 | g0344 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0361 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18991 | hp1 | a0002 | c0005 | t0002 | g0371 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18991 | hp2 | a0002 | c0010 | t0004 | g0354 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18992 | hp1 | a0002 | c0009 | t0001 | g0143 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18992 | hp2 | a0001 | c0006 | t0004 | g0105 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0119 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA19000 | hp1 | a0001 | c0002 | t0002 | g0080 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA19000 | hp2 | a0001 | c0007 | t0004 | g0310 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA19004 | hp1 | a0001 | c0004 | t0003 | g0211 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA19005 | hp1 | a0001 | c0002 | t0003 | g0203 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0099 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0348 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA19006 | hp2 | a0001 | c0002 | t0002 | g0103 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA19007 | hp1 | a0001 | c0002 | t0003 | g0011 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA19007 | hp2 | a0001 | c0006 | t0004 | g0008 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA19010 | hp2 | a0002 | c0005 | t0002 | g0124 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA19011 | hp2 | a0001 | c0006 | t0004 | g0008 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA19012 | hp2 | a0002 | c0005 | t0002 | g0292 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA19030 | hp1 | a0003 | c0013 | t0003 | g0372 | AFR | LWK | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA19030 | hp2 | a0002 | c0005 | t0003 | g0351 | AFR | LWK | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA19043 | hp1 | a0001 | c0002 | t0003 | g0264 | AFR | LWK | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA19043 | hp2 | a0001 | c0003 | t0004 | g0318 | AFR | LWK | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0057 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA19056 | hp2 | a0001 | c0006 | t0004 | g0090 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA19057 | hp1 | a0001 | c0006 | t0004 | g0093 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA19058 | hp2 | a0001 | c0001 | t0003 | g0180 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA19060 | hp2 | a0001 | c0002 | t0003 | g0168 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA19062 | hp1 | a0001 | c0007 | t0004 | g0328 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0112 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA19063 | hp2 | a0001 | c0002 | t0002 | g0317 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA19065 | hp1 | a0001 | c0004 | t0002 | g0300 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA19065 | hp2 | a0001 | c0008 | t0001 | g0306 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA19066 | hp1 | a0001 | c0006 | t0004 | g0106 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA19067 | hp1 | a0002 | c0005 | t0002 | g0358 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA19067 | hp2 | a0001 | c0007 | t0004 | g0312 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA19070 | hp1 | a0001 | c0004 | t0001 | g0309 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0346 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0341 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA19076 | hp1 | a0001 | c0002 | t0003 | g0031 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0110 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA19077 | hp2 | a0001 | c0004 | t0001 | g0066 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA19079 | hp1 | a0001 | c0002 | t0003 | g0072 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA19080 | hp1 | a0001 | c0002 | t0003 | g0011 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA19080 | hp2 | a0001 | c0006 | t0004 | g0089 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA19081 | hp2 | a0001 | c0001 | t0003 | g0032 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA19084 | hp2 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA19087 | hp1 | a0001 | c0003 | t0004 | g0287 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0363 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA19088 | hp2 | a0001 | c0004 | t0003 | g0210 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA19090 | hp2 | a0001 | c0003 | t0004 | g0152 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA19240 | hp1 | a0001 | c0001 | t0005 | g0365 | AFR | YRI | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | YRI | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | ASW | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA20129 | hp2 | a0001 | c0001 | t0005 | g0021 | AFR | ASW | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA20805 | hp1 | a0001 | c0002 | t0002 | g0007 | EUR | TSI | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA20805 | hp2 | a0001 | c0004 | t0002 | g0188 | EUR | TSI | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0228 | SAS | GIH | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | GIH | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0076 | AMR | CLM | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0150 | AMR | CLM | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02109 | hp1 | a0001 | c0003 | t0004 | g0034 | AFR | ACB | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0334 | AFR | ACB | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | ACB | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02486 | hp2 | a0001 | c0003 | t0004 | g0041 | AFR | ACB | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02559 | hp1 | a0003 | c0018 | t0003 | g0374 | AFR | ACB | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0321 | AFR | MSL | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG03471 | hp2 | a0001 | c0001 | t0005 | g0364 | AFR | MSL | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0273 | AFR | USA | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0085 | AFR | USA | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA18955 | hp2 | a0001 | c0004 | t0001 | g0298 | EAS | JPT | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA20300 | hp1 | a0001 | c0003 | t0004 | g0222 | AFR | USA | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | USA | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | LWK | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| NA21309 | hp2 | a0008 | c0015 | t0012 | g0194 | AFR | LWK | ANKMY2_chr7_16594779_16650754 | ANKMY2 | chr7 | 16594779 | 16650754 |
| view | chr:pos | ref | alt | # # of ahapid:amio-acid(protein) level
|
ahapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:16600820 | C | T | 1 | a0008 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.1267G>A | p.Glu423Lys | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 10/10 | 1448/2489 | 1267/1326 | 423/441 | chr7 | 16600820 | |||
| chr7:16600829 | G | A | 1 | a0004 | 1 | HG01257.hp1 | missense_variant | MODERATE | c.1258C>T | p.Leu420Phe | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 10/10 | 1439/2489 | 1258/1326 | 420/441 | chr7 | 16600829 | |||
| chr7:16602428 | C | T | 1 | a0005 | 1 | HG02630.hp1 | missense_variant | MODERATE | c.1093G>A | p.Glu365Lys | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 9/10 | 1274/2489 | 1093/1326 | 365/441 | chr7 | 16602428 | |||
| chr7:16604753 | C | T | 1 | a0007 | 1 | NA18983.hp2 | missense_variant | MODERATE | c.979G>A | p.Gly327Arg | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 8/10 | 1160/2489 | 979/1326 | 327/441 | chr7 | 16604753 | |||
| chr7:16610723 | T | G | 1 | a0003 | 2 | HG02559.hp1 NA19030.hp1 |
missense_variant | MODERATE | c.572A>C | p.Glu191Ala | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 6/10 | 753/2489 | 572/1326 | 191/441 | chr7 | 16610723 | |||
| chr7:16615764 | T | C | 1 | a0006 | 1 | HG02895.hp1 | missense_variant | MODERATE | c.511A>G | p.Thr171Ala | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 5/10 | 692/2489 | 511/1326 | 171/441 | chr7 | 16615764 | |||
| chr7:16627100 | C | T | 2 | a0002a0007 | 28 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(25): Show |
missense_variant | MODERATE | c.211G>A | p.Asp71Asn | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 3/10 | 392/2489 | 211/1326 | 71/441 | chr7 | 16627100 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:16600866 | G | A | 6 | a0001c0003a0001c0006a0001c0007others(3): Show | 69 | HG00280.hp1 HG00597.hp2 HG00733.hp1 others(66): Show |
synonymous_variant | LOW | c.1221C>T | p.Ser407Ser | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 10/10 | 1402/2489 | 1221/1326 | 407/441 | chr7 | 16600866 | |||
| chr7:16609666 | G | C | 1 | a0001c0017 | 1 | HG01891.hp1 | synonymous_variant | LOW | c.846C>G | p.Leu282Leu | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/10 | 1027/2489 | 846/1326 | 282/441 | chr7 | 16609666 | |||
| chr7:16610722 | T | C | 1 | a0001c0021 | 1 | NA18967.hp2 | synonymous_variant | LOW | c.573A>G | p.Glu191Glu | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 6/10 | 754/2489 | 573/1326 | 191/441 | chr7 | 16610722 | |||
| chr7:16615762 | C | T | 6 | a0001c0002a0001c0006a0001c0008others(3): Show | 83 | HG00408.hp1 HG00423.hp2 HG00597.hp2 others(80): Show |
synonymous_variant | LOW | c.513G>A | p.Thr171Thr | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 5/10 | 694/2489 | 513/1326 | 171/441 | chr7 | 16615762 | |||
| chr7:16627068 | G | A | 1 | a0001c0022 | 1 | HG04204.hp1 | synonymous_variant | LOW | c.243C>T | p.Tyr81Tyr | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 3/10 | 424/2489 | 243/1326 | 81/441 | chr7 | 16627068 | |||
| chr7:16627116 | T | G | 6 | a0001c0004a0001c0007a0001c0008others(3): Show | 57 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(54): Show |
synonymous_variant | LOW | c.195A>C | p.Leu65Leu | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 3/10 | 376/2489 | 195/1326 | 65/441 | chr7 | 16627116 | |||
| chr7:16627134 | G | C | 6 | a0001c0004a0001c0007a0001c0008others(3): Show | 57 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(54): Show |
synonymous_variant | LOW | c.177C>G | p.Leu59Leu | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 3/10 | 358/2489 | 177/1326 | 59/441 | chr7 | 16627134 | |||
| chr7:16636394 | G | A | 1 | a0001c0011 | 2 | HG02886.hp2 HG03209.hp1 |
synonymous_variant | LOW | c.129C>T | p.Asp43Asp | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/10 | 310/2489 | 129/1326 | 43/441 | chr7 | 16636394 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:16599951 | T | G | 2 | a0001c0001t0011a0008c0015t0012 | 2 | HG02922.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*810A>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 10/10 | 810 | chr7 | 16599951 | ||||||
| chr7:16599990 | A | C | 14 | a0001c0001t0002a0001c0001t0009a0001c0001t0013others(11): Show | 121 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*771T>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 10/10 | 771 | chr7 | 16599990 | ||||||
| chr7:16599999 | C | T | 2 | a0001c0002t0008a0001c0004t0008 | 2 | HG01243.hp1 HG01981.hp2 |
3_prime_UTR_variant | MODIFIER | c.*762G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 10/10 | 762 | chr7 | 16599999 | ||||||
| chr7:16600020 | T | C | 1 | a0001c0001t0006 | 5 | HG02257.hp1 HG02630.hp2 HG03041.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*741A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 10/10 | 741 | chr7 | 16600020 | ||||||
| chr7:16600099 | C | G | 1 | a0001c0001t0006 | 5 | HG02257.hp1 HG02630.hp2 HG03041.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*662G>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 10/10 | 662 | chr7 | 16600099 | ||||||
| chr7:16600360 | T | C | 1 | a0001c0001t0015 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*401A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 10/10 | 401 | chr7 | 16600360 | ||||||
| chr7:16600433 | C | G | 1 | a0002c0005t0014 | 1 | HG00408.hp2 | 3_prime_UTR_variant | MODIFIER | c.*328G>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 10/10 | 328 | chr7 | 16600433 | ||||||
| chr7:16600498 | G | C | 1 | a0001c0001t0016 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*263C>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 10/10 | 263 | chr7 | 16600498 | ||||||
| chr7:16600572 | T | C | 13 | a0001c0001t0001a0001c0001t0006a0001c0001t0009others(10): Show | 128 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(125): Show |
3_prime_UTR_variant | MODIFIER | c.*189A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 10/10 | 189 | chr7 | 16600572 | ||||||
| chr7:16600576 | G | C | 12 | a0001c0001t0002a0001c0001t0015a0001c0001t0016others(9): Show | 118 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(115): Show |
3_prime_UTR_variant | MODIFIER | c.*185C>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 10/10 | 185 | chr7 | 16600576 | ||||||
| chr7:16600675 | A | G | 13 | a0001c0001t0001a0001c0001t0005a0001c0001t0009others(10): Show | 130 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(127): Show |
3_prime_UTR_variant | MODIFIER | c.*86T>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 10/10 | 86 | chr7 | 16600675 | ||||||
| chr7:16600733 | T | C | 36 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(33): Show | 323 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(320): Show |
3_prime_UTR_variant | MODIFIER | c.*28A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 10/10 | 28 | chr7 | 16600733 | ||||||
| chr7:16600746 | C | T | 2 | a0001c0003t0007a0001c0007t0007 | 2 | HG02717.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*15G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 10/10 | 15 | chr7 | 16600746 | ||||||
| chr7:16645600 | C | T | 1 | a0001c0004t0010 | 1 | HG01106.hp1 | 5_prime_UTR_variant | MODIFIER | c.-27G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/10 | 27 | chr7 | 16645600 | ||||||
| chr7:16645704 | C | A | 1 | a0001c0001t0017 | 1 | NA18987.hp1 | 5_prime_UTR_variant | MODIFIER | c.-131G>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/10 | 131 | chr7 | 16645704 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:16601289 | C | T | 2 | a0001c0004t0003g0297a0002c0005t0003g0201 | 2 | NA18939.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.1142-344G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 9/9 | chr7 | 16601289 | |||||||
| chr7:16601551 | C | T | 1 | a0008c0015t0012g0194 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1142-606G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 9/9 | chr7 | 16601551 | |||||||
| chr7:16601617 | T | C | 3 | a0001c0001t0003g0273a0001c0004t0003g0268a0001c0004t0003g0375 | 3 | HG02886.hp1 HG03225.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1142-672A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 9/9 | chr7 | 16601617 | |||||||
| chr7:16601636 | C | T | 94 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0015others(91): Show | 105 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.1142-691G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 9/9 | chr7 | 16601636 | |||||||
| chr7:16601637 | G | A | 43 | a0001c0003t0004g0023a0001c0003t0004g0036a0001c0003t0004g0086others(40): Show | 44 | HG00280.hp1 HG00597.hp2 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.1142-692C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 9/9 | chr7 | 16601637 | |||||||
| chr7:16601696 | C | G | 64 | a0001c0001t0002g0014a0001c0001t0002g0035a0001c0001t0002g0054others(61): Show | 66 | HG00408.hp1 HG00408.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.1141+684G>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 9/9 | chr7 | 16601696 | |||||||
| chr7:16601765 | G | T | 119 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0015others(116): Show | 132 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(129): Show |
intron_variant | MODIFIER | c.1141+615C>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 9/9 | chr7 | 16601765 | |||||||
| chr7:16601819 | T | A | 3 | a0001c0001t0002g0014a0001c0002t0002g0048a0001c0004t0002g0299 | 4 | NA18944.hp1 NA18969.hp2 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.1141+561A>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 9/9 | chr7 | 16601819 | |||||||
| chr7:16601859 | A | C | 5 | a0001c0001t0006g0044a0001c0001t0006g0045a0001c0001t0006g0208others(2): Show | 5 | HG02257.hp1 HG02630.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1141+521T>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 9/9 | chr7 | 16601859 | |||||||
| chr7:16601867 | A | G | 11 | a0001c0001t0005g0021a0001c0001t0005g0134a0001c0001t0005g0257others(8): Show | 12 | HG02257.hp1 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.1141+513T>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 9/9 | chr7 | 16601867 | |||||||
| chr7:16602124 | A | C | 178 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0015others(175): Show | 191 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(188): Show |
intron_variant | MODIFIER | c.1141+256T>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 9/9 | chr7 | 16602124 | |||||||
| chr7:16602144 | A | G | 7 | a0001c0001t0001g0001a0001c0001t0001g0115a0001c0001t0001g0151others(4): Show | 11 | HG00642.hp1 HG00738.hp2 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.1141+236T>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 9/9 | chr7 | 16602144 | |||||||
| chr7:16602308 | C | T | 1 | a0001c0001t0003g0228 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1141+72G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 9/9 | chr7 | 16602308 | |||||||
| chr7:16602357 | G | A | 1 | a0001c0001t0002g0340 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1141+23C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 9/9 | chr7 | 16602357 | |||||||
| chr7:16602376 | A | G | 1 | a0008c0015t0012g0194 | 1 | NA21309.hp2 | splice_region_variant&intron_variant | LOW | c.1141+4T>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 9/9 | chr7 | 16602376 | |||||||
| chr7:16602820 | T | C | 60 | a0001c0003t0004g0023a0001c0003t0004g0027a0001c0003t0004g0033others(57): Show | 62 | HG00280.hp1 HG00597.hp2 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.1012-311A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 8/9 | chr7 | 16602820 | |||||||
| chr7:16603006 | T | C | 1 | a0001c0003t0004g0153 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1012-497A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 8/9 | chr7 | 16603006 | |||||||
| chr7:16603051 | C | T | 116 | a0001c0001t0001g0338a0001c0001t0001g0342a0001c0001t0002g0014others(113): Show | 120 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.1012-542G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 8/9 | chr7 | 16603051 | |||||||
| chr7:16603213 | T | C | 12 | a0001c0001t0005g0021a0001c0001t0005g0134a0001c0001t0005g0257others(9): Show | 13 | HG01069.hp1 HG02257.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1012-704A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 8/9 | chr7 | 16603213 | |||||||
| chr7:16603290 | A | T | 1 | a0001c0001t0001g0165 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1012-781T>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 8/9 | chr7 | 16603290 | |||||||
| chr7:16603370 | G | A | 58 | a0001c0003t0004g0023a0001c0003t0004g0027a0001c0003t0004g0033others(55): Show | 59 | HG00280.hp1 HG00597.hp2 HG00733.hp1 others(56): Show |
intron_variant | MODIFIER | c.1012-861C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 8/9 | chr7 | 16603370 | |||||||
| chr7:16603548 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1012-1039G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 8/9 | chr7 | 16603548 | |||||||
| chr7:16603715 | C | G | 1 | a0001c0004t0001g0052 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1011+1006G>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 8/9 | chr7 | 16603715 | |||||||
| chr7:16603730 | T | C | 1 | a0001c0001t0001g0256 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1011+991A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 8/9 | chr7 | 16603730 | |||||||
| chr7:16603774 | C | T | 1 | a0008c0015t0012g0194 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1011+947G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 8/9 | chr7 | 16603774 | |||||||
| chr7:16603793 | G | A | 5 | a0001c0001t0002g0229a0001c0002t0002g0028a0001c0002t0002g0083others(2): Show | 5 | HG01934.hp2 HG02602.hp1 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.1011+928C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 8/9 | chr7 | 16603793 | |||||||
| chr7:16603842 | T | A | 43 | a0001c0003t0004g0023a0001c0003t0004g0036a0001c0003t0004g0086others(40): Show | 44 | HG00280.hp1 HG00597.hp2 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.1011+879A>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 8/9 | chr7 | 16603842 | |||||||
| chr7:16603941 | G | A | 3 | a0001c0001t0003g0321a0003c0013t0003g0372a0003c0018t0003g0374 | 3 | HG02559.hp1 HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1011+780C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 8/9 | chr7 | 16603941 | |||||||
| chr7:16603992 | C | A | 1 | a0001c0001t0005g0021 | 2 | HG02970.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1011+729G>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 8/9 | chr7 | 16603992 | |||||||
| chr7:16604218 | C | T | 1 | a0001c0001t0003g0252 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1011+503G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 8/9 | chr7 | 16604218 | |||||||
| chr7:16604236 | C | G | 1 | a0001c0001t0001g0170 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1011+485G>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 8/9 | chr7 | 16604236 | |||||||
| chr7:16604394 | A | G | 2 | a0001c0001t0005g0134a0001c0001t0005g0364 | 2 | HG02280.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1011+327T>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 8/9 | chr7 | 16604394 | |||||||
| chr7:16604432 | TTTCTC | T | 43 | a0001c0003t0004g0023a0001c0003t0004g0036a0001c0003t0004g0086others(40): Show | 44 | HG00280.hp1 HG00597.hp2 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.1011+284_1011+288d others(7): Show |
ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 8/9 | chr7 | 16604432 | |||||||
| chr7:16604438 | T | C | 2 | a0001c0003t0004g0281a0001c0003t0004g0332 | 2 | HG02615.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1011+283A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 8/9 | chr7 | 16604438 | |||||||
| chr7:16604516 | T | G | 96 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0015others(93): Show | 107 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.1011+205A>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 8/9 | chr7 | 16604516 | |||||||
| chr7:16604583 | A | G | 1 | a0001c0004t0003g0285 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1011+138T>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 8/9 | chr7 | 16604583 | |||||||
| chr7:16604605 | G | A | 2 | a0001c0002t0002g0092a0001c0002t0002g0116 | 2 | HG01934.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1011+116C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 8/9 | chr7 | 16604605 | |||||||
| chr7:16604937 | C | T | 3 | a0001c0001t0003g0273a0001c0004t0003g0268a0001c0004t0003g0375 | 3 | HG02886.hp1 HG03225.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.883-88G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/9 | chr7 | 16604937 | |||||||
| chr7:16605034 | G | A | 1 | a0001c0004t0003g0285 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.883-185C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/9 | chr7 | 16605034 | |||||||
| chr7:16605090 | C | A | 1 | a0001c0002t0002g0083 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.883-241G>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/9 | chr7 | 16605090 | |||||||
| chr7:16605143 | T | C | 3 | a0001c0001t0003g0273a0001c0004t0003g0268a0001c0004t0003g0375 | 3 | HG02886.hp1 HG03225.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.883-294A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/9 | chr7 | 16605143 | |||||||
| chr7:16605190 | G | A | 6 | a0001c0001t0005g0021a0001c0001t0005g0134a0001c0001t0005g0257others(3): Show | 7 | HG02258.hp2 HG02280.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.883-341C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/9 | chr7 | 16605190 | |||||||
| chr7:16605417 | A | G | 4 | a0001c0001t0006g0044a0001c0001t0006g0208a0001c0001t0006g0255others(1): Show | 4 | HG02257.hp1 HG02630.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.883-568T>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/9 | chr7 | 16605417 | |||||||
| chr7:16605583 | C | T | 1 | a0001c0001t0001g0227 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.883-734G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/9 | chr7 | 16605583 | |||||||
| chr7:16605600 | C | A | 1 | a0001c0001t0002g0096 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.883-751G>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/9 | chr7 | 16605600 | |||||||
| chr7:16605646 | C | T | 1 | a0001c0004t0001g0330 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.883-797G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/9 | chr7 | 16605646 | |||||||
| chr7:16605658 | C | T | 1 | a0008c0015t0012g0194 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.883-809G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/9 | chr7 | 16605658 | |||||||
| chr7:16605672 | TA | T | 86 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0015others(83): Show | 97 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.883-824delT | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/9 | chr7 | 16605672 | |||||||
| chr7:16605673 | A | C | 8 | a0001c0001t0001g0202a0001c0001t0001g0239a0001c0001t0001g0276others(5): Show | 8 | HG00621.hp2 HG01928.hp1 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.883-824T>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/9 | chr7 | 16605673 | |||||||
| chr7:16605674 | C | CT | 51 | a0001c0001t0002g0076a0001c0001t0002g0094a0001c0001t0002g0109others(48): Show | 51 | HG00408.hp1 HG00408.hp2 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.883-826dupA | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/9 | chr7 | 16605674 | |||||||
| chr7:16605674 | CT | C | 29 | a0001c0001t0001g0038a0001c0001t0001g0216a0001c0001t0001g0253others(26): Show | 31 | HG00639.hp1 HG00639.hp2 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.883-826delA | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/9 | chr7 | 16605674 | |||||||
| chr7:16605674 | CTT | C | 40 | a0001c0001t0001g0254a0001c0003t0004g0023a0001c0003t0004g0036others(37): Show | 41 | HG00280.hp1 HG00597.hp2 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.883-827_883-826del others(2): Show |
ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/9 | chr7 | 16605674 | |||||||
| chr7:16605674 | CTTTTTTT others(4): Show |
C | 1 | a0001c0003t0004g0332 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.883-836_883-826del others(11): Show |
ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/9 | chr7 | 16605674 | |||||||
| chr7:16605674 | CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0003g0085 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.883-839_883-826del others(14): Show |
ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/9 | chr7 | 16605674 | |||||||
| chr7:16605675 | T | C | 86 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0015others(83): Show | 97 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.883-826A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/9 | chr7 | 16605675 | |||||||
| chr7:16605680 | T | G | 7 | a0001c0001t0001g0202a0001c0001t0001g0239a0001c0001t0001g0276others(4): Show | 7 | HG00621.hp2 HG01928.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.883-831A>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/9 | chr7 | 16605680 | |||||||
| chr7:16605681 | T | G | 83 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0015others(80): Show | 93 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.883-832A>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/9 | chr7 | 16605681 | |||||||
| chr7:16605705 | C | T | 1 | a0001c0001t0001g0024 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.883-856G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/9 | chr7 | 16605705 | |||||||
| chr7:16605722 | G | A | 2 | a0001c0001t0003g0251a0001c0001t0003g0262 | 2 | HG01109.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.883-873C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/9 | chr7 | 16605722 | |||||||
| chr7:16605831 | C | T | 94 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0015others(91): Show | 105 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.883-982G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/9 | chr7 | 16605831 | |||||||
| chr7:16605843 | C | T | 6 | a0001c0001t0006g0044a0001c0001t0006g0045a0001c0001t0006g0208others(3): Show | 6 | HG02257.hp1 HG02630.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.883-994G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/9 | chr7 | 16605843 | |||||||
| chr7:16605847 | T | A | 4 | a0001c0001t0001g0369a0001c0001t0009g0002a0001c0004t0001g0301others(1): Show | 5 | HG02723.hp2 HG02886.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-998A>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/9 | chr7 | 16605847 | |||||||
| chr7:16606113 | G | A | 1 | a0001c0002t0002g0091 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.883-1264C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/9 | chr7 | 16606113 | |||||||
| chr7:16606130 | T | C | 112 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0015others(109): Show | 124 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(121): Show |
intron_variant | MODIFIER | c.883-1281A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/9 | chr7 | 16606130 | |||||||
| chr7:16606165 | T | C | 1 | a0002c0005t0014g0209 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.883-1316A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/9 | chr7 | 16606165 | |||||||
| chr7:16606166 | A | G | 6 | a0001c0001t0005g0021a0001c0001t0005g0134a0001c0001t0005g0257others(3): Show | 7 | HG02258.hp2 HG02280.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.883-1317T>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/9 | chr7 | 16606166 | |||||||
| chr7:16606190 | C | T | 1 | a0002c0005t0001g0293 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.883-1341G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/9 | chr7 | 16606190 | |||||||
| chr7:16606191 | G | A | 6 | a0001c0001t0002g0079a0001c0001t0002g0087a0001c0001t0002g0145others(3): Show | 6 | HG01516.hp2 HG01517.hp2 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.883-1342C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/9 | chr7 | 16606191 | |||||||
| chr7:16606246 | C | T | 3 | a0001c0001t0003g0273a0001c0004t0003g0268a0001c0004t0003g0375 | 3 | HG02886.hp1 HG03225.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.883-1397G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/9 | chr7 | 16606246 | |||||||
| chr7:16606260 | G | A | 7 | a0001c0003t0004g0039a0001c0003t0004g0040a0001c0003t0004g0047others(4): Show | 7 | HG01884.hp2 HG02451.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.883-1411C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/9 | chr7 | 16606260 | |||||||
| chr7:16606297 | G | A | 3 | a0001c0001t0003g0273a0001c0004t0003g0268a0001c0004t0003g0375 | 3 | HG02886.hp1 HG03225.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.883-1448C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/9 | chr7 | 16606297 | |||||||
| chr7:16606364 | G | A | 1 | a0001c0021t0002g0205 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.883-1515C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/9 | chr7 | 16606364 | |||||||
| chr7:16606382 | T | C | 1 | a0001c0008t0003g0191 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.883-1533A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/9 | chr7 | 16606382 | |||||||
| chr7:16606403 | T | C | 1 | a0008c0015t0012g0194 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.883-1554A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/9 | chr7 | 16606403 | |||||||
| chr7:16606420 | C | A | 1 | a0001c0001t0001g0363 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.883-1571G>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/9 | chr7 | 16606420 | |||||||
| chr7:16606429 | T | TA | 289 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0015others(286): Show | 306 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(303): Show |
intron_variant | MODIFIER | c.883-1581dupT | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/9 | chr7 | 16606429 | |||||||
| chr7:16606429 | T | TAA | 7 | a0001c0001t0001g0362a0001c0001t0001g0369a0001c0001t0005g0257others(4): Show | 8 | HG02258.hp2 HG02723.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.883-1582_883-1581d others(4): Show |
ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/9 | chr7 | 16606429 | |||||||
| chr7:16606604 | T | C | 3 | a0001c0001t0001g0338a0001c0001t0001g0342a0001c0004t0001g0308 | 3 | HG02040.hp1 NA18984.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.883-1755A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/9 | chr7 | 16606604 | |||||||
| chr7:16606704 | A | T | 1 | a0002c0005t0003g0351 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.883-1855T>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/9 | chr7 | 16606704 | |||||||
| chr7:16606799 | T | A | 1 | a0003c0018t0003g0374 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.883-1950A>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/9 | chr7 | 16606799 | |||||||
| chr7:16606966 | T | C | 7 | a0001c0003t0004g0039a0001c0003t0004g0040a0001c0003t0004g0047others(4): Show | 7 | HG01884.hp2 HG02451.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.883-2117A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/9 | chr7 | 16606966 | |||||||
| chr7:16607107 | G | A | 109 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0015others(106): Show | 120 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(117): Show |
intron_variant | MODIFIER | c.883-2258C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/9 | chr7 | 16607107 | |||||||
| chr7:16607277 | T | C | 96 | a0001c0001t0002g0014a0001c0001t0002g0035a0001c0001t0002g0054others(93): Show | 98 | HG00408.hp1 HG00408.hp2 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.882+2353A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/9 | chr7 | 16607277 | |||||||
| chr7:16607281 | C | G | 3 | a0001c0002t0002g0091a0001c0002t0002g0120a0001c0002t0002g0121 | 3 | HG01516.hp2 HG01517.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.882+2349G>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/9 | chr7 | 16607281 | |||||||
| chr7:16607410 | G | A | 13 | a0001c0003t0004g0027a0001c0003t0004g0033a0001c0003t0004g0034others(10): Show | 13 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.882+2220C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/9 | chr7 | 16607410 | |||||||
| chr7:16607516 | T | C | 375 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0015others(372): Show | 399 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(396): Show |
intron_variant | MODIFIER | c.882+2114A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/9 | chr7 | 16607516 | |||||||
| chr7:16607553 | A | G | 334 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0015others(331): Show | 356 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(353): Show |
intron_variant | MODIFIER | c.882+2077T>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/9 | chr7 | 16607553 | |||||||
| chr7:16607580 | A | T | 6 | a0001c0003t0004g0033a0001c0003t0004g0034a0001c0003t0004g0041others(3): Show | 6 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.882+2050T>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/9 | chr7 | 16607580 | |||||||
| chr7:16607653 | C | T | 1 | a0001c0003t0004g0217 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.882+1977G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/9 | chr7 | 16607653 | |||||||
| chr7:16607665 | CTGCT | C | 6 | a0001c0001t0002g0275a0001c0001t0002g0282a0001c0002t0002g0199others(3): Show | 6 | HG02056.hp2 NA18960.hp2 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.882+1961_882+1964d others(6): Show |
ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/9 | chr7 | 16607665 | |||||||
| chr7:16607668 | CT | C | 87 | a0001c0001t0002g0014a0001c0001t0002g0071a0001c0001t0002g0094others(84): Show | 89 | HG00408.hp1 HG00408.hp2 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.882+1961delA | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/9 | chr7 | 16607668 | |||||||
| chr7:16607668 | CTT | C | 76 | a0001c0001t0001g0077a0001c0001t0001g0283a0001c0001t0002g0054others(73): Show | 83 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.882+1960_882+1961d others(4): Show |
ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/9 | chr7 | 16607668 | |||||||
| chr7:16607668 | CTTTTTTT others(7): Show |
C | 157 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0015others(154): Show | 170 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(167): Show |
intron_variant | MODIFIER | c.882+1948_882+1961d others(16): Show |
ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/9 | chr7 | 16607668 | |||||||
| chr7:16607724 | G | GT | 88 | a0001c0001t0002g0014a0001c0001t0002g0035a0001c0001t0002g0054others(85): Show | 90 | HG00408.hp1 HG00408.hp2 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.882+1905dupA | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/9 | chr7 | 16607724 | |||||||
| chr7:16607737 | A | C | 2 | a0001c0001t0003g0212a0002c0005t0003g0351 | 2 | HG02572.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.882+1893T>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/9 | chr7 | 16607737 | |||||||
| chr7:16607801 | C | T | 3 | a0001c0003t0004g0146a0001c0006t0004g0075a0001c0007t0004g0187 | 3 | HG00280.hp1 HG00733.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.882+1829G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/9 | chr7 | 16607801 | |||||||
| chr7:16608115 | T | C | 2 | a0001c0003t0004g0281a0001c0003t0004g0332 | 2 | HG02615.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.882+1515A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/9 | chr7 | 16608115 | |||||||
| chr7:16608207 | A | G | 88 | a0001c0001t0002g0014a0001c0001t0002g0035a0001c0001t0002g0054others(85): Show | 90 | HG00408.hp1 HG00408.hp2 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.882+1423T>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/9 | chr7 | 16608207 | |||||||
| chr7:16608573 | G | C | 5 | a0001c0001t0002g0129a0001c0001t0002g0131a0001c0001t0002g0132others(2): Show | 5 | HG01074.hp1 HG02615.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.882+1057C>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/9 | chr7 | 16608573 | |||||||
| chr7:16608641 | C | G | 37 | a0001c0003t0004g0036a0001c0003t0004g0086a0001c0003t0004g0114others(34): Show | 38 | HG00280.hp1 HG00597.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.882+989G>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/9 | chr7 | 16608641 | |||||||
| chr7:16608688 | G | A | 1 | a0008c0015t0012g0194 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.882+942C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/9 | chr7 | 16608688 | |||||||
| chr7:16608799 | G | A | 3 | a0001c0001t0003g0273a0001c0004t0003g0268a0001c0004t0003g0375 | 3 | HG02886.hp1 HG03225.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.882+831C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/9 | chr7 | 16608799 | |||||||
| chr7:16608818 | T | A | 1 | a0001c0001t0001g0163 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.882+812A>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/9 | chr7 | 16608818 | |||||||
| chr7:16608915 | C | T | 1 | a0008c0015t0012g0194 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.882+715G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/9 | chr7 | 16608915 | |||||||
| chr7:16609260 | T | C | 97 | a0001c0001t0002g0014a0001c0001t0002g0035a0001c0001t0002g0054others(94): Show | 100 | HG00408.hp1 HG00408.hp2 HG00609.hp1 others(97): Show |
intron_variant | MODIFIER | c.882+370A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/9 | chr7 | 16609260 | |||||||
| chr7:16609401 | G | A | 1 | a0001c0001t0002g0279 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.882+229C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/9 | chr7 | 16609401 | |||||||
| chr7:16609410 | T | C | 1 | a0001c0001t0002g0035 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.882+220A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/9 | chr7 | 16609410 | |||||||
| chr7:16609451 | C | T | 1 | a0001c0002t0001g0068 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.882+179G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/9 | chr7 | 16609451 | |||||||
| chr7:16609461 | G | T | 3 | a0001c0001t0005g0021a0001c0001t0005g0257a0001c0001t0005g0376 | 4 | HG02258.hp2 HG02970.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.882+169C>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/9 | chr7 | 16609461 | |||||||
| chr7:16609576 | T | C | 2 | a0001c0001t0005g0365a0001c0001t0011g0260 | 2 | HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.882+54A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 7/9 | chr7 | 16609576 | |||||||
| chr7:16609866 | T | A | 64 | a0001c0001t0001g0077a0001c0001t0002g0261a0001c0001t0003g0009others(61): Show | 70 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.747-101A>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 6/9 | chr7 | 16609866 | |||||||
| chr7:16609911 | C | G | 1 | a0001c0001t0002g0229 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.747-146G>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 6/9 | chr7 | 16609911 | |||||||
| chr7:16610210 | C | T | 50 | a0001c0001t0002g0014a0001c0001t0002g0035a0001c0001t0002g0054others(47): Show | 53 | HG00609.hp1 HG00609.hp2 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.746+339G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 6/9 | chr7 | 16610210 | |||||||
| chr7:16610310 | C | T | 1 | a0001c0001t0001g0227 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.746+239G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 6/9 | chr7 | 16610310 | |||||||
| chr7:16610402 | T | G | 14 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0270others(11): Show | 15 | HG00639.hp1 HG01891.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.746+147A>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 6/9 | chr7 | 16610402 | |||||||
| chr7:16610513 | G | A | 1 | a0006c0019t0004g0050 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.746+36C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 6/9 | chr7 | 16610513 | |||||||
| chr7:16610802 | C | G | 296 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0015others(293): Show | 318 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(315): Show |
intron_variant | MODIFIER | c.532-39G>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 5/9 | chr7 | 16610802 | |||||||
| chr7:16610824 | G | A | 1 | a0008c0015t0012g0194 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.532-61C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 5/9 | chr7 | 16610824 | |||||||
| chr7:16610883 | G | A | 1 | a0001c0003t0004g0316 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.532-120C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 5/9 | chr7 | 16610883 | |||||||
| chr7:16611022 | A | G | 2 | a0001c0004t0003g0297a0002c0005t0003g0201 | 2 | NA18939.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.532-259T>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 5/9 | chr7 | 16611022 | |||||||
| chr7:16611162 | C | T | 5 | a0001c0001t0003g0150a0001c0001t0003g0223a0001c0001t0003g0228others(2): Show | 5 | HG01123.hp2 HG01261.hp1 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.532-399G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 5/9 | chr7 | 16611162 | |||||||
| chr7:16611182 | G | A | 3 | a0001c0001t0003g0273a0001c0004t0003g0268a0001c0004t0003g0375 | 3 | HG02886.hp1 HG03225.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.532-419C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 5/9 | chr7 | 16611182 | |||||||
| chr7:16611331 | G | A | 7 | a0001c0003t0004g0039a0001c0003t0004g0040a0001c0003t0004g0047others(4): Show | 7 | HG01884.hp2 HG02451.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.532-568C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 5/9 | chr7 | 16611331 | |||||||
| chr7:16611521 | C | T | 3 | a0001c0001t0005g0021a0001c0001t0005g0257a0001c0001t0005g0376 | 4 | HG02258.hp2 HG02970.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.532-758G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 5/9 | chr7 | 16611521 | |||||||
| chr7:16611536 | G | C | 1 | a0001c0008t0003g0191 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.532-773C>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 5/9 | chr7 | 16611536 | |||||||
| chr7:16611602 | T | C | 165 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0015others(162): Show | 178 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(175): Show |
intron_variant | MODIFIER | c.532-839A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 5/9 | chr7 | 16611602 | |||||||
| chr7:16611689 | G | A | 1 | a0001c0001t0001g0162 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.532-926C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 5/9 | chr7 | 16611689 | |||||||
| chr7:16611692 | T | C | 80 | a0001c0001t0002g0014a0001c0001t0002g0035a0001c0001t0002g0054others(77): Show | 83 | HG00408.hp1 HG00408.hp2 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.532-929A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 5/9 | chr7 | 16611692 | |||||||
| chr7:16611790 | A | C | 44 | a0001c0003t0004g0023a0001c0003t0004g0036a0001c0003t0004g0086others(41): Show | 45 | HG00280.hp1 HG00597.hp2 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.532-1027T>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 5/9 | chr7 | 16611790 | |||||||
| chr7:16611918 | C | T | 1 | a0008c0015t0012g0194 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.532-1155G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 5/9 | chr7 | 16611918 | |||||||
| chr7:16611919 | G | A | 4 | a0001c0001t0002g0261a0001c0001t0003g0037a0001c0001t0003g0085others(1): Show | 4 | HG01243.hp1 HG03239.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.532-1156C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 5/9 | chr7 | 16611919 | |||||||
| chr7:16611976 | T | C | 1 | a0006c0019t0004g0050 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.532-1213A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 5/9 | chr7 | 16611976 | |||||||
| chr7:16612161 | C | A | 3 | a0001c0004t0001g0066a0001c0004t0001g0309a0001c0004t0001g0314 | 3 | NA18989.hp1 NA19070.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.532-1398G>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 5/9 | chr7 | 16612161 | |||||||
| chr7:16612264 | G | C | 1 | a0001c0001t0017g0378 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.532-1501C>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 5/9 | chr7 | 16612264 | |||||||
| chr7:16612325 | C | T | 2 | a0001c0003t0004g0281a0001c0003t0004g0332 | 2 | HG02615.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.532-1562G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 5/9 | chr7 | 16612325 | |||||||
| chr7:16612404 | T | G | 1 | a0001c0001t0003g0321 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.532-1641A>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 5/9 | chr7 | 16612404 | |||||||
| chr7:16612586 | T | C | 2 | a0001c0001t0001g0095a0001c0001t0001g0097 | 2 | HG00735.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.532-1823A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 5/9 | chr7 | 16612586 | |||||||
| chr7:16612591 | T | C | 82 | a0001c0001t0002g0014a0001c0001t0002g0035a0001c0001t0002g0054others(79): Show | 84 | HG00408.hp1 HG00408.hp2 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.532-1828A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 5/9 | chr7 | 16612591 | |||||||
| chr7:16612609 | G | A | 1 | a0001c0001t0003g0252 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.532-1846C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 5/9 | chr7 | 16612609 | |||||||
| chr7:16612745 | G | A | 1 | a0001c0001t0003g0273 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.532-1982C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 5/9 | chr7 | 16612745 | |||||||
| chr7:16612853 | T | G | 44 | a0001c0003t0004g0023a0001c0003t0004g0036a0001c0003t0004g0086others(41): Show | 45 | HG00280.hp1 HG00597.hp2 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.532-2090A>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 5/9 | chr7 | 16612853 | |||||||
| chr7:16612898 | A | G | 65 | a0001c0001t0001g0077a0001c0001t0001g0198a0001c0001t0002g0096others(62): Show | 71 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.532-2135T>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 5/9 | chr7 | 16612898 | |||||||
| chr7:16612989 | A | G | 1 | a0008c0015t0012g0194 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.532-2226T>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 5/9 | chr7 | 16612989 | |||||||
| chr7:16613014 | C | G | 15 | a0001c0002t0002g0084a0001c0003t0004g0027a0001c0003t0004g0033others(12): Show | 15 | HG01346.hp1 HG01884.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.532-2251G>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 5/9 | chr7 | 16613014 | |||||||
| chr7:16613055 | A | T | 4 | a0001c0001t0001g0038a0001c0003t0004g0046a0001c0003t0004g0281others(1): Show | 4 | HG02615.hp2 HG02896.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.532-2292T>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 5/9 | chr7 | 16613055 | |||||||
| chr7:16613298 | G | C | 98 | a0001c0001t0002g0014a0001c0001t0002g0035a0001c0001t0002g0054others(95): Show | 100 | HG00408.hp1 HG00408.hp2 HG00609.hp1 others(97): Show |
intron_variant | MODIFIER | c.531+2446C>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 5/9 | chr7 | 16613298 | |||||||
| chr7:16613424 | C | G | 2 | a0001c0003t0004g0281a0001c0003t0004g0332 | 2 | HG02615.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.531+2320G>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 5/9 | chr7 | 16613424 | |||||||
| chr7:16613469 | G | A | 39 | a0001c0001t0002g0014a0001c0001t0002g0035a0001c0001t0002g0054others(36): Show | 41 | HG00609.hp1 HG00609.hp2 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.531+2275C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 5/9 | chr7 | 16613469 | |||||||
| chr7:16613539 | C | A | 1 | a0001c0003t0004g0040 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.531+2205G>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 5/9 | chr7 | 16613539 | |||||||
| chr7:16613570 | T | A | 1 | a0001c0008t0003g0191 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.531+2174A>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 5/9 | chr7 | 16613570 | |||||||
| chr7:16613680 | T | C | 1 | a0001c0001t0001g0115 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.531+2064A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 5/9 | chr7 | 16613680 | |||||||
| chr7:16613825 | A | G | 3 | a0001c0001t0003g0273a0001c0004t0003g0268a0001c0004t0003g0375 | 3 | HG02886.hp1 HG03225.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.531+1919T>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 5/9 | chr7 | 16613825 | |||||||
| chr7:16613854 | T | C | 2 | a0001c0001t0005g0365a0001c0001t0011g0260 | 2 | HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.531+1890A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 5/9 | chr7 | 16613854 | |||||||
| chr7:16613896 | G | A | 10 | a0001c0003t0004g0036a0001c0003t0004g0152a0001c0003t0004g0232others(7): Show | 11 | HG02074.hp1 HG02135.hp1 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.531+1848C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 5/9 | chr7 | 16613896 | |||||||
| chr7:16613912 | C | A | 1 | a0001c0017t0001g0370 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.531+1832G>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 5/9 | chr7 | 16613912 | |||||||
| chr7:16613920 | C | CA | 159 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0015others(156): Show | 171 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.531+1823dupT | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 5/9 | chr7 | 16613920 | |||||||
| chr7:16613920 | C | CAA | 9 | a0001c0001t0001g0024a0001c0001t0001g0158a0001c0001t0001g0197others(6): Show | 9 | HG02109.hp2 HG02145.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.531+1822_531+1823d others(4): Show |
ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 5/9 | chr7 | 16613920 | |||||||
| chr7:16613920 | CA | C | 9 | a0001c0001t0002g0054a0001c0001t0002g0169a0001c0001t0002g0195others(6): Show | 9 | HG01496.hp2 HG02886.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.531+1823delT | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 5/9 | chr7 | 16613920 | |||||||
| chr7:16613983 | A | G | 67 | a0001c0001t0002g0014a0001c0001t0002g0035a0001c0001t0002g0054others(64): Show | 69 | HG00408.hp1 HG00408.hp2 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.531+1761T>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 5/9 | chr7 | 16613983 | |||||||
| chr7:16614012 | A | G | 1 | a0001c0001t0002g0164 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.531+1732T>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 5/9 | chr7 | 16614012 | |||||||
| chr7:16614041 | G | C | 1 | a0001c0002t0002g0028 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.531+1703C>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 5/9 | chr7 | 16614041 | |||||||
| chr7:16614133 | A | G | 3 | a0001c0003t0004g0114a0001c0003t0004g0231a0001c0003t0004g0238 | 3 | HG01975.hp1 HG02148.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.531+1611T>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 5/9 | chr7 | 16614133 | |||||||
| chr7:16614396 | A | C | 4 | a0001c0001t0003g0273a0001c0001t0005g0021a0001c0001t0005g0257others(1): Show | 5 | HG02258.hp2 HG02970.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.531+1348T>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 5/9 | chr7 | 16614396 | |||||||
| chr7:16614437 | C | A | 1 | a0008c0015t0012g0194 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.531+1307G>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 5/9 | chr7 | 16614437 | |||||||
| chr7:16614485 | C | G | 1 | a0001c0004t0003g0303 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.531+1259G>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 5/9 | chr7 | 16614485 | |||||||
| chr7:16614666 | C | A | 55 | a0001c0001t0003g0273a0001c0001t0005g0021a0001c0001t0005g0376others(52): Show | 57 | HG00280.hp1 HG00597.hp2 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.531+1078G>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 5/9 | chr7 | 16614666 | |||||||
| chr7:16614709 | T | C | 36 | a0001c0001t0002g0014a0001c0001t0002g0054a0001c0001t0002g0071others(33): Show | 38 | HG00609.hp1 HG00609.hp2 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.531+1035A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 5/9 | chr7 | 16614709 | |||||||
| chr7:16614712 | G | A | 8 | a0001c0003t0004g0039a0001c0003t0004g0040a0001c0003t0004g0047others(5): Show | 8 | HG01884.hp2 HG02451.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.531+1032C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 5/9 | chr7 | 16614712 | |||||||
| chr7:16615084 | A | C | 2 | a0001c0002t0003g0264a0001c0002t0003g0326 | 2 | HG03195.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.531+660T>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 5/9 | chr7 | 16615084 | |||||||
| chr7:16615096 | A | G | 5 | a0001c0001t0005g0021a0001c0001t0006g0045a0001c0003t0004g0047others(2): Show | 6 | HG01884.hp2 HG02809.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.531+648T>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 5/9 | chr7 | 16615096 | |||||||
| chr7:16615112 | T | C | 1 | a0001c0008t0003g0191 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.531+632A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 5/9 | chr7 | 16615112 | |||||||
| chr7:16615329 | A | T | 1 | a0003c0018t0003g0374 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.531+415T>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 5/9 | chr7 | 16615329 | |||||||
| chr7:16615334 | C | T | 2 | a0001c0001t0002g0069a0001c0001t0002g0076 | 2 | HG01123.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.531+410G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 5/9 | chr7 | 16615334 | |||||||
| chr7:16615416 | G | C | 1 | a0001c0001t0003g0273 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.531+328C>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 5/9 | chr7 | 16615416 | |||||||
| chr7:16615446 | T | C | 1 | a0005c0014t0001g0324 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.531+298A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 5/9 | chr7 | 16615446 | |||||||
| chr7:16615523 | G | A | 2 | a0001c0004t0002g0214a0001c0004t0003g0178 | 2 | HG00323.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.531+221C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 5/9 | chr7 | 16615523 | |||||||
| chr7:16615533 | C | T | 2 | a0001c0004t0003g0210a0001c0004t0003g0211 | 2 | NA19004.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.531+211G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 5/9 | chr7 | 16615533 | |||||||
| chr7:16615598 | A | C | 3 | a0001c0001t0006g0366a0001c0003t0004g0367a0001c0003t0004g0368 | 3 | HG01081.hp2 HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.531+146T>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 5/9 | chr7 | 16615598 | |||||||
| chr7:16615994 | T | C | 6 | a0001c0004t0002g0302a0001c0004t0002g0304a0001c0004t0002g0305others(3): Show | 6 | HG00280.hp2 HG00323.hp1 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.371-90A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16615994 | |||||||
| chr7:16616007 | C | T | 47 | a0001c0001t0001g0198a0001c0001t0002g0071a0001c0001t0002g0079others(44): Show | 47 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.371-103G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16616007 | |||||||
| chr7:16616139 | C | T | 269 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0024others(266): Show | 288 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.371-235G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16616139 | |||||||
| chr7:16616313 | T | C | 4 | a0001c0001t0002g0154a0001c0001t0003g0155a0001c0001t0003g0156others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.371-409A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16616313 | |||||||
| chr7:16616538 | C | T | 30 | a0001c0001t0002g0094a0001c0003t0004g0036a0001c0004t0001g0301others(27): Show | 30 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.371-634G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16616538 | |||||||
| chr7:16616553 | G | C | 1 | a0001c0001t0002g0263 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.371-649C>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16616553 | |||||||
| chr7:16616569 | G | A | 3 | a0001c0001t0003g0122a0001c0001t0003g0123a0001c0001t0017g0378 | 3 | HG02129.hp2 NA18974.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.371-665C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16616569 | |||||||
| chr7:16616571 | CG | C | 196 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0024others(193): Show | 212 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(209): Show |
intron_variant | MODIFIER | c.371-668delC | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16616571 | |||||||
| chr7:16616572 | G | A | 1 | a0001c0004t0001g0314 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.371-668C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16616572 | |||||||
| chr7:16616572 | G | C | 31 | a0001c0001t0001g0225a0001c0001t0002g0082a0001c0001t0005g0365others(28): Show | 31 | HG00140.hp1 HG00280.hp1 HG01255.hp2 others(28): Show |
intron_variant | MODIFIER | c.371-668C>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16616572 | |||||||
| chr7:16616572 | G | T | 4 | a0001c0002t0002g0056a0001c0002t0002g0136a0001c0002t0002g0199others(1): Show | 4 | HG00408.hp1 HG00597.hp2 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.371-668C>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16616572 | |||||||
| chr7:16616573 | C | A | 31 | a0001c0001t0001g0225a0001c0001t0002g0082a0001c0001t0005g0365others(28): Show | 31 | HG00140.hp1 HG00280.hp1 HG01255.hp2 others(28): Show |
intron_variant | MODIFIER | c.371-669G>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16616573 | |||||||
| chr7:16616573 | C | T | 196 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0024others(193): Show | 212 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(209): Show |
intron_variant | MODIFIER | c.371-669G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16616573 | |||||||
| chr7:16616578 | C | T | 3 | a0001c0002t0001g0049a0001c0003t0004g0269a0003c0013t0003g0372 | 3 | HG02717.hp2 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.371-674G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16616578 | |||||||
| chr7:16616579 | C | G | 15 | a0001c0001t0002g0109a0001c0001t0002g0261a0001c0001t0002g0279others(12): Show | 18 | HG00423.hp1 HG00438.hp1 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.371-675G>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16616579 | |||||||
| chr7:16616580 | C | A | 1 | a0001c0003t0004g0034 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.371-676G>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16616580 | |||||||
| chr7:16616580 | C | G | 4 | a0001c0001t0005g0364a0001c0001t0006g0208a0001c0002t0003g0264others(1): Show | 4 | HG03195.hp1 HG03209.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.371-676G>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16616580 | |||||||
| chr7:16616667 | G | A | 206 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0024others(203): Show | 224 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(221): Show |
intron_variant | MODIFIER | c.371-763C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16616667 | |||||||
| chr7:16616756 | G | A | 5 | a0001c0003t0004g0027a0001c0003t0004g0047a0001c0003t0004g0185others(2): Show | 5 | HG02145.hp2 HG02809.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.371-852C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16616756 | |||||||
| chr7:16616828 | C | A | 1 | a0002c0005t0001g0289 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.371-924G>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16616828 | |||||||
| chr7:16616921 | C | T | 272 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0024others(269): Show | 291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.371-1017G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16616921 | |||||||
| chr7:16617045 | T | C | 1 | a0001c0001t0003g0212 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.371-1141A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16617045 | |||||||
| chr7:16617061 | A | G | 1 | a0008c0015t0012g0194 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.371-1157T>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16617061 | |||||||
| chr7:16617077 | C | CT | 99 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0001g0098others(96): Show | 110 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.371-1174dupA | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16617077 | |||||||
| chr7:16617077 | C | CTT | 5 | a0001c0001t0002g0069a0001c0001t0002g0076a0001c0002t0001g0003others(2): Show | 6 | HG00733.hp1 HG01074.hp2 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.371-1175_371-1174d others(4): Show |
ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16617077 | |||||||
| chr7:16617382 | A | G | 7 | a0001c0001t0001g0055a0001c0001t0001g0077a0001c0001t0002g0179others(4): Show | 7 | NA18948.hp1 NA18950.hp2 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.371-1478T>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16617382 | |||||||
| chr7:16617424 | G | C | 57 | a0001c0001t0001g0373a0001c0001t0002g0082a0001c0004t0001g0052others(54): Show | 58 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.371-1520C>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16617424 | |||||||
| chr7:16617525 | C | T | 1 | a0001c0003t0004g0344 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.371-1621G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16617525 | |||||||
| chr7:16617549 | A | G | 26 | a0001c0001t0002g0094a0002c0005t0001g0140a0002c0005t0001g0144others(23): Show | 26 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(23): Show |
intron_variant | MODIFIER | c.371-1645T>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16617549 | |||||||
| chr7:16617664 | C | T | 108 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0038others(105): Show | 115 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.371-1760G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16617664 | |||||||
| chr7:16617681 | G | A | 3 | a0001c0004t0003g0268a0001c0004t0003g0375a0001c0007t0007g0274 | 3 | HG02886.hp1 HG03225.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.371-1777C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16617681 | |||||||
| chr7:16617692 | A | G | 2 | a0001c0001t0005g0365a0001c0001t0011g0260 | 2 | HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.371-1788T>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16617692 | |||||||
| chr7:16617917 | G | GT | 41 | a0001c0001t0001g0158a0001c0001t0001g0160a0001c0001t0001g0166others(38): Show | 42 | HG00140.hp2 HG00323.hp2 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.371-2014dupA | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16617917 | |||||||
| chr7:16617917 | G | GTT | 24 | a0001c0001t0001g0024a0001c0001t0001g0270a0001c0001t0002g0094others(21): Show | 24 | HG00408.hp2 HG00597.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.371-2015_371-2014d others(4): Show |
ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16617917 | |||||||
| chr7:16617917 | G | GTTT | 14 | a0001c0001t0001g0271a0001c0001t0003g0273a0001c0011t0001g0220others(11): Show | 14 | HG00423.hp2 HG01891.hp1 HG02886.hp2 others(11): Show |
intron_variant | MODIFIER | c.371-2016_371-2014d others(5): Show |
ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16617917 | |||||||
| chr7:16617917 | G | GTTTTTTT others(3): Show |
1 | a0001c0001t0011g0260 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.371-2023_371-2014d others(12): Show |
ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16617917 | |||||||
| chr7:16617917 | G | GTTTTTTT others(4): Show |
1 | a0001c0001t0005g0365 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.371-2024_371-2014d others(13): Show |
ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16617917 | |||||||
| chr7:16617917 | GT | G | 128 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0038others(125): Show | 142 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.371-2014delA | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16617917 | |||||||
| chr7:16617917 | GTTTTTTT others(6): Show |
G | 16 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0256others(13): Show | 16 | HG00639.hp1 HG01109.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.371-2026_371-2014d others(15): Show |
ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16617917 | |||||||
| chr7:16617930 | T | G | 85 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0001g0098others(82): Show | 94 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.371-2026A>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16617930 | |||||||
| chr7:16617930 | T | TG | 5 | a0001c0001t0001g0334a0001c0003t0004g0041a0001c0003t0004g0042others(2): Show | 5 | HG02055.hp1 HG02109.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.371-2027_371-2026i others(3): Show |
ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16617930 | |||||||
| chr7:16617941 | T | G | 1 | a0001c0001t0003g0262 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.371-2037A>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16617941 | |||||||
| chr7:16617980 | T | C | 1 | a0001c0001t0015g0174 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.371-2076A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16617980 | |||||||
| chr7:16617987 | A | G | 58 | a0001c0001t0001g0373a0001c0001t0002g0082a0001c0004t0001g0052others(55): Show | 59 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.371-2083T>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16617987 | |||||||
| chr7:16618041 | A | C | 167 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0001g0098others(164): Show | 177 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.371-2137T>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16618041 | |||||||
| chr7:16618052 | C | T | 88 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0001g0098others(85): Show | 97 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.371-2148G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16618052 | |||||||
| chr7:16618174 | C | A | 8 | a0001c0002t0001g0099a0001c0002t0002g0088a0001c0006t0004g0008others(5): Show | 9 | HG00621.hp1 HG02129.hp1 NA18992.hp2 others(6): Show |
intron_variant | MODIFIER | c.371-2270G>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16618174 | |||||||
| chr7:16618300 | CA | C | 5 | a0002c0005t0002g0124a0002c0005t0002g0125a0002c0005t0002g0358others(2): Show | 5 | HG00408.hp2 NA18962.hp1 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.371-2397delT | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16618300 | |||||||
| chr7:16618403 | A | G | 58 | a0001c0001t0001g0373a0001c0001t0002g0082a0001c0004t0001g0052others(55): Show | 59 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.371-2499T>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16618403 | |||||||
| chr7:16618421 | C | A | 58 | a0001c0001t0001g0373a0001c0001t0002g0082a0001c0004t0001g0052others(55): Show | 59 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.371-2517G>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16618421 | |||||||
| chr7:16618445 | G | C | 1 | a0001c0007t0004g0320 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.371-2541C>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16618445 | |||||||
| chr7:16618503 | T | C | 1 | a0001c0001t0001g0163 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.371-2599A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16618503 | |||||||
| chr7:16618541 | A | T | 58 | a0001c0001t0001g0373a0001c0001t0002g0082a0001c0004t0001g0052others(55): Show | 59 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.371-2637T>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16618541 | |||||||
| chr7:16618594 | G | A | 1 | a0001c0001t0002g0137 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.371-2690C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16618594 | |||||||
| chr7:16618622 | C | T | 58 | a0001c0001t0001g0373a0001c0001t0002g0082a0001c0004t0001g0052others(55): Show | 59 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.371-2718G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16618622 | |||||||
| chr7:16618624 | T | C | 58 | a0001c0001t0001g0373a0001c0001t0002g0082a0001c0004t0001g0052others(55): Show | 59 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.371-2720A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16618624 | |||||||
| chr7:16618858 | C | CT | 58 | a0001c0001t0001g0373a0001c0001t0002g0082a0001c0004t0001g0052others(55): Show | 59 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.371-2955_371-2954i others(3): Show |
ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16618858 | |||||||
| chr7:16618859 | G | A | 8 | a0001c0002t0001g0049a0001c0003t0004g0027a0001c0003t0004g0047others(5): Show | 8 | HG02145.hp2 HG02717.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.371-2955C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16618859 | |||||||
| chr7:16618865 | G | A | 58 | a0001c0001t0001g0373a0001c0001t0002g0082a0001c0004t0001g0052others(55): Show | 59 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.371-2961C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16618865 | |||||||
| chr7:16618889 | C | CTAGCTT | 58 | a0001c0001t0001g0373a0001c0001t0002g0082a0001c0004t0001g0052others(55): Show | 59 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.371-2986_371-2985i others(8): Show |
ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16618889 | |||||||
| chr7:16618987 | T | C | 3 | a0001c0003t0004g0039a0001c0003t0004g0040a0001c0003t0004g0318 | 3 | HG02451.hp2 HG02818.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.371-3083A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16618987 | |||||||
| chr7:16619081 | G | C | 6 | a0001c0001t0001g0334a0001c0001t0003g0321a0001c0003t0004g0041others(3): Show | 6 | HG02055.hp1 HG02109.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.371-3177C>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16619081 | |||||||
| chr7:16619093 | C | T | 56 | a0001c0004t0001g0052a0001c0004t0001g0066a0001c0004t0001g0067others(53): Show | 57 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.371-3189G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16619093 | |||||||
| chr7:16619133 | A | G | 1 | a0001c0004t0002g0065 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.371-3229T>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16619133 | |||||||
| chr7:16619155 | C | CT | 22 | a0001c0001t0001g0202a0001c0001t0001g0334a0001c0001t0002g0277others(19): Show | 24 | HG00621.hp2 HG00639.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.371-3252dupA | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16619155 | |||||||
| chr7:16619155 | CT | C | 5 | a0001c0001t0005g0021a0001c0001t0005g0365a0001c0001t0011g0260others(2): Show | 6 | HG02922.hp2 HG02970.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.371-3252delA | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16619155 | |||||||
| chr7:16619157 | T | C | 1 | a0002c0005t0003g0351 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.371-3253A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16619157 | |||||||
| chr7:16619193 | G | T | 1 | a0001c0001t0006g0208 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.371-3289C>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16619193 | |||||||
| chr7:16619216 | C | T | 4 | a0001c0004t0002g0335a0001c0004t0002g0336a0001c0007t0004g0310others(1): Show | 4 | NA18945.hp1 NA18952.hp1 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.371-3312G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16619216 | |||||||
| chr7:16619261 | C | T | 6 | a0001c0001t0001g0334a0001c0001t0003g0321a0001c0003t0004g0041others(3): Show | 6 | HG02055.hp1 HG02109.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.371-3357G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16619261 | |||||||
| chr7:16619279 | G | A | 1 | a0001c0001t0002g0164 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.371-3375C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16619279 | |||||||
| chr7:16619310 | C | T | 4 | a0001c0001t0005g0021a0001c0001t0005g0365a0001c0001t0011g0260others(1): Show | 5 | HG02922.hp2 HG02970.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.371-3406G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16619310 | |||||||
| chr7:16619326 | T | A | 58 | a0001c0001t0001g0373a0001c0001t0002g0082a0001c0004t0001g0052others(55): Show | 59 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.371-3422A>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16619326 | |||||||
| chr7:16619329 | T | C | 2 | a0001c0001t0002g0079a0001c0001t0002g0145 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.371-3425A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16619329 | |||||||
| chr7:16619374 | G | A | 50 | a0001c0004t0001g0052a0001c0004t0001g0066a0001c0004t0001g0067others(47): Show | 51 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.371-3470C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16619374 | |||||||
| chr7:16619393 | A | T | 2 | a0001c0001t0003g0051a0001c0001t0003g0053 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.371-3489T>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16619393 | |||||||
| chr7:16619450 | G | A | 1 | a0001c0002t0002g0028 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.371-3546C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16619450 | |||||||
| chr7:16619533 | C | T | 31 | a0001c0001t0001g0018a0001c0001t0001g0170a0001c0001t0001g0202others(28): Show | 34 | HG00438.hp2 HG00609.hp1 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.371-3629G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16619533 | |||||||
| chr7:16619568 | T | G | 4 | a0001c0001t0001g0115a0001c0003t0004g0118a0001c0003t0004g0222others(1): Show | 4 | HG01346.hp2 HG01361.hp1 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.371-3664A>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16619568 | |||||||
| chr7:16619583 | A | C | 61 | a0001c0001t0001g0373a0001c0001t0002g0082a0001c0003t0004g0039others(58): Show | 62 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.371-3679T>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16619583 | |||||||
| chr7:16619617 | C | A | 1 | a0001c0004t0002g0300 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.371-3713G>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16619617 | |||||||
| chr7:16619632 | G | T | 59 | a0001c0003t0004g0039a0001c0003t0004g0040a0001c0003t0004g0318others(56): Show | 60 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.371-3728C>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16619632 | |||||||
| chr7:16619698 | A | G | 4 | a0001c0001t0005g0021a0001c0001t0005g0365a0001c0001t0011g0260others(1): Show | 5 | HG02922.hp2 HG02970.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.371-3794T>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16619698 | |||||||
| chr7:16619801 | C | G | 50 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0038others(47): Show | 56 | HG00609.hp2 HG00642.hp1 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.371-3897G>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16619801 | |||||||
| chr7:16619841 | A | G | 2 | a0001c0001t0006g0045a0001c0003t0004g0046 | 2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.371-3937T>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16619841 | |||||||
| chr7:16619848 | C | A | 3 | a0001c0003t0004g0039a0001c0003t0004g0040a0001c0003t0004g0318 | 3 | HG02451.hp2 HG02818.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.371-3944G>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16619848 | |||||||
| chr7:16620014 | C | G | 59 | a0001c0003t0004g0039a0001c0003t0004g0040a0001c0003t0004g0318others(56): Show | 60 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.371-4110G>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16620014 | |||||||
| chr7:16620102 | T | C | 12 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0256others(9): Show | 12 | HG00639.hp1 HG01109.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.371-4198A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16620102 | |||||||
| chr7:16620178 | T | C | 50 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0038others(47): Show | 56 | HG00609.hp2 HG00642.hp1 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.371-4274A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16620178 | |||||||
| chr7:16620348 | G | C | 59 | a0001c0003t0004g0039a0001c0003t0004g0040a0001c0003t0004g0318others(56): Show | 60 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.371-4444C>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16620348 | |||||||
| chr7:16620379 | AT | A | 7 | a0001c0002t0001g0183a0001c0002t0002g0083a0001c0002t0002g0084others(4): Show | 7 | HG01069.hp1 HG01516.hp2 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.371-4476delA | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16620379 | |||||||
| chr7:16620459 | T | C | 50 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0038others(47): Show | 56 | HG00609.hp2 HG00642.hp1 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.370+4524A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16620459 | |||||||
| chr7:16620474 | G | A | 59 | a0001c0003t0004g0039a0001c0003t0004g0040a0001c0003t0004g0318others(56): Show | 60 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.370+4509C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16620474 | |||||||
| chr7:16620591 | T | TAC | 31 | a0001c0001t0001g0024a0001c0001t0001g0077a0001c0001t0001g0270others(28): Show | 32 | HG00673.hp2 HG00735.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.370+4390_370+4391d others(4): Show |
ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16620591 | |||||||
| chr7:16620591 | T | TACAC | 49 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0058others(46): Show | 55 | HG00639.hp1 HG00642.hp1 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.370+4388_370+4391d others(6): Show |
ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16620591 | |||||||
| chr7:16620591 | T | TACACAC | 35 | a0001c0001t0001g0038a0001c0001t0001g0241a0001c0001t0002g0094others(32): Show | 35 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.370+4386_370+4391d others(8): Show |
ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16620591 | |||||||
| chr7:16620591 | T | TACACACA others(1): Show |
10 | a0001c0001t0005g0021a0001c0001t0013g0043a0001c0003t0004g0039others(7): Show | 11 | HG00423.hp2 HG02451.hp2 HG02698.hp2 others(8): Show |
intron_variant | MODIFIER | c.370+4384_370+4391d others(10): Show |
ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16620591 | |||||||
| chr7:16620591 | T | TACACACA others(3): Show |
4 | a0001c0001t0001g0258a0002c0005t0001g0357a0006c0019t0004g0050others(1): Show | 4 | HG02015.hp2 HG02895.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.370+4382_370+4391d others(12): Show |
ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16620591 | |||||||
| chr7:16620591 | T | TACACACA others(5): Show |
1 | a0003c0018t0003g0374 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.370+4380_370+4391d others(14): Show |
ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16620591 | |||||||
| chr7:16620591 | T | TACACACA others(7): Show |
9 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0256others(6): Show | 9 | HG01109.hp1 HG01884.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.370+4378_370+4391d others(16): Show |
ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16620591 | |||||||
| chr7:16620591 | T | TACACACA others(9): Show |
2 | a0001c0001t0005g0257a0005c0014t0001g0324 | 2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.370+4376_370+4391d others(18): Show |
ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16620591 | |||||||
| chr7:16620591 | TAC | T | 56 | a0001c0002t0001g0183a0001c0002t0002g0083a0001c0002t0002g0084others(53): Show | 57 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.370+4390_370+4391d others(4): Show |
ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16620591 | |||||||
| chr7:16620591 | TACAC | T | 8 | a0001c0001t0001g0170a0001c0001t0003g0182a0001c0004t0001g0301others(5): Show | 8 | HG01167.hp2 HG01169.hp2 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.370+4388_370+4391d others(6): Show |
ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16620591 | |||||||
| chr7:16620591 | TACACACA others(1): Show |
T | 6 | a0001c0001t0003g0212a0001c0001t0005g0365a0001c0001t0005g0376others(3): Show | 6 | HG01081.hp2 HG02257.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.370+4384_370+4391d others(10): Show |
ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16620591 | |||||||
| chr7:16620863 | A | T | 12 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0256others(9): Show | 12 | HG00639.hp1 HG01109.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.370+4120T>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16620863 | |||||||
| chr7:16620889 | A | G | 7 | a0001c0001t0001g0024a0001c0001t0001g0270a0001c0001t0001g0271others(4): Show | 7 | HG01891.hp1 HG02486.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.370+4094T>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16620889 | |||||||
| chr7:16621098 | C | T | 4 | a0001c0001t0001g0266a0003c0018t0003g0374a0005c0014t0001g0324others(1): Show | 4 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.370+3885G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16621098 | |||||||
| chr7:16621099 | G | C | 59 | a0001c0003t0004g0039a0001c0003t0004g0040a0001c0003t0004g0318others(56): Show | 60 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.370+3884C>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16621099 | |||||||
| chr7:16621132 | C | T | 1 | a0001c0002t0001g0068 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.370+3851G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16621132 | |||||||
| chr7:16621208 | C | T | 1 | a0001c0002t0003g0031 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.370+3775G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16621208 | |||||||
| chr7:16621212 | C | T | 1 | a0001c0002t0003g0031 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.370+3771G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16621212 | |||||||
| chr7:16621213 | C | T | 1 | a0001c0002t0003g0031 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.370+3770G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16621213 | |||||||
| chr7:16621216 | G | A | 1 | a0001c0002t0003g0031 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.370+3767C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16621216 | |||||||
| chr7:16621218 | G | A | 1 | a0001c0002t0003g0031 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.370+3765C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16621218 | |||||||
| chr7:16621219 | G | T | 1 | a0001c0002t0003g0031 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.370+3764C>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16621219 | |||||||
| chr7:16621223 | G | T | 1 | a0001c0002t0003g0031 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.370+3760C>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16621223 | |||||||
| chr7:16621226 | A | T | 1 | a0001c0002t0003g0031 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.370+3757T>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16621226 | |||||||
| chr7:16621227 | C | T | 1 | a0001c0002t0003g0031 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.370+3756G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16621227 | |||||||
| chr7:16621228 | C | A | 1 | a0001c0002t0003g0031 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.370+3755G>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16621228 | |||||||
| chr7:16621230 | C | T | 1 | a0001c0002t0003g0031 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.370+3753G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16621230 | |||||||
| chr7:16621232 | A | T | 1 | a0001c0002t0003g0031 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.370+3751T>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16621232 | |||||||
| chr7:16621241 | G | T | 1 | a0001c0002t0003g0031 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.370+3742C>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16621241 | |||||||
| chr7:16621243 | A | T | 1 | a0001c0002t0003g0031 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.370+3740T>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16621243 | |||||||
| chr7:16621247 | A | T | 1 | a0001c0002t0003g0031 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.370+3736T>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16621247 | |||||||
| chr7:16621250 | T | A | 1 | a0001c0002t0003g0031 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.370+3733A>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16621250 | |||||||
| chr7:16621257 | G | T | 1 | a0001c0002t0003g0031 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.370+3726C>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16621257 | |||||||
| chr7:16621261 | G | T | 1 | a0001c0002t0003g0031 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.370+3722C>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16621261 | |||||||
| chr7:16621262 | G | A | 1 | a0001c0002t0003g0031 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.370+3721C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16621262 | |||||||
| chr7:16621274 | G | A | 1 | a0001c0002t0003g0031 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.370+3709C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16621274 | |||||||
| chr7:16621275 | G | T | 1 | a0001c0002t0003g0031 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.370+3708C>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16621275 | |||||||
| chr7:16621283 | T | A | 1 | a0001c0002t0003g0031 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.370+3700A>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16621283 | |||||||
| chr7:16621512 | C | T | 59 | a0001c0003t0004g0039a0001c0003t0004g0040a0001c0003t0004g0318others(56): Show | 60 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.370+3471G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16621512 | |||||||
| chr7:16621516 | G | A | 2 | a0001c0004t0003g0210a0001c0004t0003g0211 | 2 | NA19004.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.370+3467C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16621516 | |||||||
| chr7:16621519 | G | C | 1 | a0001c0001t0001g0348 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.370+3464C>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16621519 | |||||||
| chr7:16621550 | G | A | 1 | a0001c0003t0004g0235 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.370+3433C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16621550 | |||||||
| chr7:16621563 | C | T | 1 | a0001c0002t0001g0016 | 2 | NA18989.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.370+3420G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16621563 | |||||||
| chr7:16621667 | T | C | 1 | a0001c0008t0003g0191 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.370+3316A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16621667 | |||||||
| chr7:16621855 | G | A | 1 | a0001c0003t0007g0352 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.370+3128C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16621855 | |||||||
| chr7:16621917 | C | T | 1 | a0001c0004t0010g0022 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.370+3066G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16621917 | |||||||
| chr7:16621939 | A | T | 16 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0256others(13): Show | 16 | HG00639.hp1 HG01109.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.370+3044T>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16621939 | |||||||
| chr7:16621964 | A | G | 61 | a0001c0001t0001g0373a0001c0001t0002g0082a0001c0003t0004g0039others(58): Show | 62 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.370+3019T>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16621964 | |||||||
| chr7:16621975 | A | G | 2 | a0001c0001t0002g0079a0001c0001t0002g0145 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.370+3008T>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16621975 | |||||||
| chr7:16621976 | T | A | 22 | a0001c0001t0001g0213a0001c0001t0001g0266a0001c0001t0001g0331others(19): Show | 22 | HG00438.hp2 HG00673.hp1 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.370+3007A>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16621976 | |||||||
| chr7:16621978 | A | T | 59 | a0001c0003t0004g0039a0001c0003t0004g0040a0001c0003t0004g0318others(56): Show | 60 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.370+3005T>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16621978 | |||||||
| chr7:16621995 | A | G | 61 | a0001c0001t0001g0373a0001c0001t0002g0082a0001c0003t0004g0039others(58): Show | 62 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.370+2988T>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16621995 | |||||||
| chr7:16622069 | A | G | 59 | a0001c0003t0004g0039a0001c0003t0004g0040a0001c0003t0004g0318others(56): Show | 60 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.370+2914T>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16622069 | |||||||
| chr7:16622094 | AAAG | A | 3 | a0001c0001t0001g0165a0001c0001t0001g0176a0008c0015t0012g0194 | 3 | HG02080.hp2 HG02083.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.370+2886_370+2888d others(5): Show |
ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16622094 | |||||||
| chr7:16622107 | AAGG | A | 43 | a0001c0001t0001g0024a0001c0001t0001g0270a0001c0001t0001g0271others(40): Show | 43 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.370+2873_370+2875d others(5): Show |
ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16622107 | |||||||
| chr7:16622179 | T | C | 59 | a0001c0003t0004g0039a0001c0003t0004g0040a0001c0003t0004g0318others(56): Show | 60 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.370+2804A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16622179 | |||||||
| chr7:16622201 | T | C | 7 | a0001c0001t0001g0024a0001c0001t0001g0270a0001c0001t0001g0271others(4): Show | 7 | HG01891.hp1 HG02486.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.370+2782A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16622201 | |||||||
| chr7:16622277 | A | G | 1 | a0006c0019t0004g0050 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.370+2706T>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16622277 | |||||||
| chr7:16622290 | G | T | 1 | a0001c0001t0003g0037 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.370+2693C>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16622290 | |||||||
| chr7:16622383 | T | C | 273 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0024others(270): Show | 290 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.370+2600A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16622383 | |||||||
| chr7:16622384 | C | G | 3 | a0001c0002t0002g0006a0001c0002t0002g0007a0001c0002t0002g0102 | 5 | HG01516.hp1 HG01952.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.370+2599G>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16622384 | |||||||
| chr7:16622470 | T | G | 59 | a0001c0003t0004g0039a0001c0003t0004g0040a0001c0003t0004g0318others(56): Show | 60 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.370+2513A>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16622470 | |||||||
| chr7:16622504 | C | T | 5 | a0001c0001t0003g0212a0001c0001t0005g0376a0001c0001t0006g0366others(2): Show | 5 | HG01081.hp2 HG02257.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.370+2479G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16622504 | |||||||
| chr7:16622509 | C | T | 1 | a0001c0001t0003g0073 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.370+2474G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16622509 | |||||||
| chr7:16622567 | T | C | 16 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0256others(13): Show | 16 | HG00639.hp1 HG01109.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.370+2416A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16622567 | |||||||
| chr7:16622672 | G | A | 10 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0256others(7): Show | 10 | HG01109.hp1 HG01884.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.370+2311C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16622672 | |||||||
| chr7:16622704 | C | T | 59 | a0001c0003t0004g0039a0001c0003t0004g0040a0001c0003t0004g0318others(56): Show | 60 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.370+2279G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16622704 | |||||||
| chr7:16622721 | C | A | 6 | a0001c0001t0001g0334a0001c0001t0003g0321a0001c0003t0004g0041others(3): Show | 6 | HG02055.hp1 HG02109.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.370+2262G>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16622721 | |||||||
| chr7:16622729 | G | C | 1 | a0008c0015t0012g0194 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.370+2254C>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16622729 | |||||||
| chr7:16622735 | A | G | 59 | a0001c0003t0004g0039a0001c0003t0004g0040a0001c0003t0004g0318others(56): Show | 60 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.370+2248T>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16622735 | |||||||
| chr7:16622750 | G | A | 59 | a0001c0003t0004g0039a0001c0003t0004g0040a0001c0003t0004g0318others(56): Show | 60 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.370+2233C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16622750 | |||||||
| chr7:16622750 | G | GAATA | 13 | a0001c0001t0001g0019a0001c0001t0001g0038a0001c0001t0001g0166others(10): Show | 15 | HG01070.hp1 HG01071.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.370+2229_370+2232d others(6): Show |
ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16622750 | |||||||
| chr7:16622750 | GAATA | G | 131 | a0001c0001t0001g0024a0001c0001t0001g0095a0001c0001t0001g0097others(128): Show | 140 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.370+2229_370+2232d others(6): Show |
ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16622750 | |||||||
| chr7:16622750 | GAATAAAT others(1): Show |
G | 68 | a0001c0001t0001g0001a0001c0001t0001g0058a0001c0001t0001g0059others(65): Show | 73 | HG00609.hp2 HG00639.hp1 HG00642.hp1 others(70): Show |
intron_variant | MODIFIER | c.370+2225_370+2232d others(10): Show |
ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16622750 | |||||||
| chr7:16622750 | GAATAAAT others(5): Show |
G | 2 | a0001c0001t0005g0021a0001c0003t0004g0377 | 3 | HG02970.hp1 HG03195.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.370+2221_370+2232d others(14): Show |
ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16622750 | |||||||
| chr7:16622770 | AAATAAAT others(8): Show |
A | 59 | a0001c0003t0004g0039a0001c0003t0004g0040a0001c0003t0004g0318others(56): Show | 60 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.370+2198_370+2212d others(17): Show |
ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16622770 | |||||||
| chr7:16622782 | A | G | 94 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0001g0098others(91): Show | 103 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.370+2201T>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16622782 | |||||||
| chr7:16622810 | G | C | 59 | a0001c0003t0004g0039a0001c0003t0004g0040a0001c0003t0004g0318others(56): Show | 60 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.370+2173C>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16622810 | |||||||
| chr7:16622882 | C | T | 1 | a0001c0001t0001g0172 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.370+2101G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16622882 | |||||||
| chr7:16622939 | G | C | 1 | a0002c0005t0003g0351 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.370+2044C>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16622939 | |||||||
| chr7:16622959 | G | A | 1 | a0001c0004t0001g0067 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.370+2024C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16622959 | |||||||
| chr7:16622974 | C | G | 8 | a0001c0002t0001g0049a0001c0003t0004g0027a0001c0003t0004g0047others(5): Show | 8 | HG02145.hp2 HG02717.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.370+2009G>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16622974 | |||||||
| chr7:16622977 | A | T | 1 | a0001c0001t0001g0175 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.370+2006T>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16622977 | |||||||
| chr7:16622995 | T | G | 49 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0038others(46): Show | 55 | HG00609.hp2 HG00642.hp1 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.370+1988A>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16622995 | |||||||
| chr7:16623030 | T | C | 59 | a0001c0003t0004g0039a0001c0003t0004g0040a0001c0003t0004g0318others(56): Show | 60 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.370+1953A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16623030 | |||||||
| chr7:16623039 | C | G | 1 | a0001c0001t0003g0262 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.370+1944G>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16623039 | |||||||
| chr7:16623116 | T | C | 1 | a0001c0003t0004g0146 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.370+1867A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16623116 | |||||||
| chr7:16623153 | A | G | 59 | a0001c0003t0004g0039a0001c0003t0004g0040a0001c0003t0004g0318others(56): Show | 60 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.370+1830T>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16623153 | |||||||
| chr7:16623195 | C | G | 1 | a0001c0001t0002g0259 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.370+1788G>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16623195 | |||||||
| chr7:16623257 | AGGGT | A | 3 | a0001c0002t0003g0167a0001c0002t0003g0168a0001c0002t0003g0203 | 3 | NA18944.hp2 NA19005.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.370+1722_370+1725d others(6): Show |
ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16623257 | |||||||
| chr7:16623280 | T | C | 12 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0256others(9): Show | 12 | HG00639.hp1 HG01109.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.370+1703A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16623280 | |||||||
| chr7:16623353 | T | C | 2 | a0001c0001t0001g0266a0005c0014t0001g0324 | 2 | HG02630.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.370+1630A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16623353 | |||||||
| chr7:16623605 | A | T | 2 | a0002c0009t0001g0141a0002c0009t0001g0143 | 2 | HG00423.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.370+1378T>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16623605 | |||||||
| chr7:16623734 | G | C | 1 | a0001c0001t0002g0071 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.370+1249C>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16623734 | |||||||
| chr7:16623821 | G | T | 59 | a0001c0003t0004g0039a0001c0003t0004g0040a0001c0003t0004g0318others(56): Show | 60 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.370+1162C>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16623821 | |||||||
| chr7:16623851 | A | T | 1 | a0001c0004t0001g0314 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.370+1132T>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16623851 | |||||||
| chr7:16623889 | G | A | 86 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0001g0098others(83): Show | 95 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.370+1094C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16623889 | |||||||
| chr7:16623924 | A | G | 3 | a0001c0001t0002g0261a0001c0001t0002g0279a0001c0001t0002g0280 | 3 | HG03491.hp1 HG03669.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.370+1059T>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16623924 | |||||||
| chr7:16624017 | C | T | 59 | a0001c0003t0004g0039a0001c0003t0004g0040a0001c0003t0004g0318others(56): Show | 60 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.370+966G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16624017 | |||||||
| chr7:16624081 | G | A | 86 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0001g0098others(83): Show | 95 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.370+902C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16624081 | |||||||
| chr7:16624106 | T | C | 1 | a0001c0003t0004g0215 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.370+877A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16624106 | |||||||
| chr7:16624107 | T | G | 1 | a0001c0002t0002g0199 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.370+876A>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16624107 | |||||||
| chr7:16624117 | A | T | 59 | a0001c0003t0004g0039a0001c0003t0004g0040a0001c0003t0004g0318others(56): Show | 60 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.370+866T>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16624117 | |||||||
| chr7:16624223 | C | G | 6 | a0001c0001t0001g0024a0001c0001t0001g0270a0001c0001t0001g0271others(3): Show | 6 | HG01891.hp1 HG02486.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.370+760G>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16624223 | |||||||
| chr7:16624235 | G | A | 1 | a0001c0001t0002g0169 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.370+748C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16624235 | |||||||
| chr7:16624363 | C | T | 59 | a0001c0003t0004g0039a0001c0003t0004g0040a0001c0003t0004g0318others(56): Show | 60 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.370+620G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16624363 | |||||||
| chr7:16624368 | G | C | 56 | a0001c0004t0001g0052a0001c0004t0001g0066a0001c0004t0001g0067others(53): Show | 57 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.370+615C>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16624368 | |||||||
| chr7:16624650 | A | T | 1 | a0001c0002t0002g0081 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.370+333T>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16624650 | |||||||
| chr7:16624700 | G | C | 1 | a0001c0004t0003g0285 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.370+283C>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16624700 | |||||||
| chr7:16624760 | C | A | 59 | a0001c0003t0004g0039a0001c0003t0004g0040a0001c0003t0004g0318others(56): Show | 60 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.370+223G>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16624760 | |||||||
| chr7:16624780 | GTA | G | 8 | a0001c0002t0001g0049a0001c0003t0004g0027a0001c0003t0004g0047others(5): Show | 8 | HG02145.hp2 HG02717.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.370+201_370+202del others(2): Show |
ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16624780 | |||||||
| chr7:16624801 | C | T | 1 | a0001c0001t0001g0245 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.370+182G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16624801 | |||||||
| chr7:16624805 | A | C | 2 | a0001c0001t0006g0045a0001c0003t0004g0046 | 2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.370+178T>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16624805 | |||||||
| chr7:16624851 | C | A | 8 | a0001c0002t0001g0049a0001c0003t0004g0027a0001c0003t0004g0047others(5): Show | 8 | HG02145.hp2 HG02717.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.370+132G>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16624851 | |||||||
| chr7:16624886 | A | AC | 59 | a0001c0003t0004g0039a0001c0003t0004g0040a0001c0003t0004g0318others(56): Show | 60 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.370+96dupG | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 4/9 | chr7 | 16624886 | |||||||
| chr7:16625107 | G | A | 4 | a0001c0001t0005g0021a0001c0001t0005g0365a0001c0001t0011g0260others(1): Show | 5 | HG02922.hp2 HG02970.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.272-26C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 3/9 | chr7 | 16625107 | |||||||
| chr7:16625194 | T | G | 6 | a0001c0001t0001g0334a0001c0001t0003g0321a0001c0003t0004g0041others(3): Show | 6 | HG02055.hp1 HG02109.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.272-113A>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 3/9 | chr7 | 16625194 | |||||||
| chr7:16625339 | C | T | 1 | a0002c0005t0002g0353 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.272-258G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 3/9 | chr7 | 16625339 | |||||||
| chr7:16625437 | C | T | 1 | a0001c0003t0004g0344 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.272-356G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 3/9 | chr7 | 16625437 | |||||||
| chr7:16625520 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.272-439G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 3/9 | chr7 | 16625520 | |||||||
| chr7:16625613 | A | G | 56 | a0001c0004t0001g0052a0001c0004t0001g0066a0001c0004t0001g0067others(53): Show | 57 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.272-532T>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 3/9 | chr7 | 16625613 | |||||||
| chr7:16625643 | A | C | 57 | a0001c0001t0002g0149a0001c0004t0001g0052a0001c0004t0001g0066others(54): Show | 58 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.272-562T>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 3/9 | chr7 | 16625643 | |||||||
| chr7:16625691 | G | C | 1 | a0001c0002t0001g0016 | 2 | NA18989.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.272-610C>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 3/9 | chr7 | 16625691 | |||||||
| chr7:16625754 | A | C | 3 | a0001c0001t0002g0154a0001c0001t0003g0155a0001c0001t0003g0156 | 3 | HG01070.hp1 HG01071.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.272-673T>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 3/9 | chr7 | 16625754 | |||||||
| chr7:16625814 | T | G | 56 | a0001c0004t0001g0052a0001c0004t0001g0066a0001c0004t0001g0067others(53): Show | 57 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.272-733A>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 3/9 | chr7 | 16625814 | |||||||
| chr7:16625909 | G | A | 1 | a0001c0001t0002g0054 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.272-828C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 3/9 | chr7 | 16625909 | |||||||
| chr7:16625962 | C | A | 56 | a0001c0004t0001g0052a0001c0004t0001g0066a0001c0004t0001g0067others(53): Show | 57 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.272-881G>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 3/9 | chr7 | 16625962 | |||||||
| chr7:16625979 | C | CT | 38 | a0001c0001t0001g0055a0001c0001t0001g0158a0001c0001t0001g0216others(35): Show | 39 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.272-899dupA | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 3/9 | chr7 | 16625979 | |||||||
| chr7:16625979 | CT | C | 157 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0038others(154): Show | 172 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(169): Show |
intron_variant | MODIFIER | c.272-899delA | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 3/9 | chr7 | 16625979 | |||||||
| chr7:16625979 | CTTTT | C | 53 | a0001c0004t0001g0052a0001c0004t0001g0066a0001c0004t0001g0067others(50): Show | 54 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(51): Show |
intron_variant | MODIFIER | c.272-902_272-899del others(4): Show |
ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 3/9 | chr7 | 16625979 | |||||||
| chr7:16626116 | C | G | 56 | a0001c0004t0001g0052a0001c0004t0001g0066a0001c0004t0001g0067others(53): Show | 57 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.271+924G>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 3/9 | chr7 | 16626116 | |||||||
| chr7:16626167 | G | C | 1 | a0001c0003t0004g0034 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.271+873C>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 3/9 | chr7 | 16626167 | |||||||
| chr7:16626169 | C | T | 2 | a0001c0001t0005g0021a0001c0003t0004g0377 | 3 | HG02970.hp1 HG03195.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.271+871G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 3/9 | chr7 | 16626169 | |||||||
| chr7:16626179 | T | C | 273 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0024others(270): Show | 290 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.271+861A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 3/9 | chr7 | 16626179 | |||||||
| chr7:16626232 | G | A | 6 | a0001c0004t0001g0301a0001c0004t0002g0026a0001c0004t0002g0063others(3): Show | 6 | HG01167.hp2 HG01169.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.271+808C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 3/9 | chr7 | 16626232 | |||||||
| chr7:16626292 | A | T | 56 | a0001c0004t0001g0052a0001c0004t0001g0066a0001c0004t0001g0067others(53): Show | 57 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.271+748T>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 3/9 | chr7 | 16626292 | |||||||
| chr7:16626327 | A | G | 56 | a0001c0004t0001g0052a0001c0004t0001g0066a0001c0004t0001g0067others(53): Show | 57 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.271+713T>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 3/9 | chr7 | 16626327 | |||||||
| chr7:16626339 | T | A | 3 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0003t0004g0238 | 3 | HG01928.hp1 HG01981.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.271+701A>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 3/9 | chr7 | 16626339 | |||||||
| chr7:16626350 | T | C | 56 | a0001c0004t0001g0052a0001c0004t0001g0066a0001c0004t0001g0067others(53): Show | 57 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.271+690A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 3/9 | chr7 | 16626350 | |||||||
| chr7:16626426 | G | A | 2 | a0001c0001t0002g0131a0001c0001t0002g0132 | 2 | HG01074.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.271+614C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 3/9 | chr7 | 16626426 | |||||||
| chr7:16626439 | T | C | 1 | a0001c0001t0002g0054 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.271+601A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 3/9 | chr7 | 16626439 | |||||||
| chr7:16626615 | C | T | 2 | a0001c0001t0001g0157a0001c0001t0002g0035 | 2 | HG03688.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.271+425G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 3/9 | chr7 | 16626615 | |||||||
| chr7:16626629 | A | C | 1 | a0001c0003t0004g0033 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.271+411T>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 3/9 | chr7 | 16626629 | |||||||
| chr7:16626676 | G | A | 91 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0001g0098others(88): Show | 100 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.271+364C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 3/9 | chr7 | 16626676 | |||||||
| chr7:16626829 | T | C | 50 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0038others(47): Show | 57 | HG00609.hp2 HG00642.hp1 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.271+211A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 3/9 | chr7 | 16626829 | |||||||
| chr7:16626982 | T | C | 1 | a0001c0001t0001g0343 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.271+58A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 3/9 | chr7 | 16626982 | |||||||
| chr7:16627232 | C | T | 1 | a0001c0001t0002g0181 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.133-54G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16627232 | |||||||
| chr7:16627327 | T | G | 56 | a0001c0004t0001g0052a0001c0004t0001g0066a0001c0004t0001g0067others(53): Show | 57 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.133-149A>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16627327 | |||||||
| chr7:16627382 | C | T | 4 | a0001c0002t0001g0323a0001c0003t0004g0039a0001c0003t0004g0040others(1): Show | 4 | HG00639.hp1 HG02451.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.133-204G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16627382 | |||||||
| chr7:16627383 | G | A | 8 | a0001c0002t0001g0049a0001c0003t0004g0027a0001c0003t0004g0047others(5): Show | 8 | HG02145.hp2 HG02717.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.133-205C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16627383 | |||||||
| chr7:16627390 | C | G | 3 | a0001c0003t0004g0039a0001c0003t0004g0040a0001c0003t0004g0318 | 3 | HG02451.hp2 HG02818.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.133-212G>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16627390 | |||||||
| chr7:16627517 | T | C | 56 | a0001c0004t0001g0052a0001c0004t0001g0066a0001c0004t0001g0067others(53): Show | 57 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.133-339A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16627517 | |||||||
| chr7:16627622 | T | G | 6 | a0001c0001t0002g0094a0001c0002t0001g0221a0001c0002t0002g0006others(3): Show | 8 | HG01192.hp1 HG01516.hp1 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.133-444A>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16627622 | |||||||
| chr7:16627649 | A | T | 50 | a0001c0001t0001g0024a0001c0001t0001g0270a0001c0001t0001g0271others(47): Show | 51 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.133-471T>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16627649 | |||||||
| chr7:16627711 | AT | A | 4 | a0001c0001t0005g0376a0001c0001t0006g0366a0001c0003t0004g0367others(1): Show | 4 | HG01081.hp2 HG02257.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.133-534delA | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16627711 | |||||||
| chr7:16627732 | C | CCAAATCA others(92): Show |
53 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0038others(50): Show | 59 | HG00609.hp2 HG00642.hp1 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.133-653_133-555dup others(99): Show |
ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16627732 | |||||||
| chr7:16627732 | CCAAATCA others(92): Show |
C | 56 | a0001c0004t0001g0052a0001c0004t0001g0066a0001c0004t0001g0067others(53): Show | 57 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.133-653_133-555del others(99): Show |
ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16627732 | |||||||
| chr7:16627935 | T | C | 56 | a0001c0004t0001g0052a0001c0004t0001g0066a0001c0004t0001g0067others(53): Show | 57 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.133-757A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16627935 | |||||||
| chr7:16627953 | C | T | 56 | a0001c0004t0001g0052a0001c0004t0001g0066a0001c0004t0001g0067others(53): Show | 57 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.133-775G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16627953 | |||||||
| chr7:16627957 | C | CATATGAT others(92): Show |
87 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0001g0098others(84): Show | 96 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.133-780_133-779ins others(99): Show |
ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16627957 | |||||||
| chr7:16628061 | A | G | 220 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0024others(217): Show | 236 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(233): Show |
intron_variant | MODIFIER | c.133-883T>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16628061 | |||||||
| chr7:16628061 | A | T | 55 | a0001c0004t0001g0066a0001c0004t0001g0067a0001c0004t0001g0193others(52): Show | 56 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.133-883T>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16628061 | |||||||
| chr7:16628154 | G | A | 1 | a0008c0015t0012g0194 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.133-976C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16628154 | |||||||
| chr7:16628226 | C | A | 35 | a0001c0001t0001g0024a0001c0001t0001g0270a0001c0001t0001g0271others(32): Show | 35 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.133-1048G>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16628226 | |||||||
| chr7:16628295 | G | A | 88 | a0001c0001t0001g0077a0001c0001t0001g0095a0001c0001t0001g0097others(85): Show | 97 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.133-1117C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16628295 | |||||||
| chr7:16628385 | C | T | 96 | a0001c0001t0001g0077a0001c0001t0001g0095a0001c0001t0001g0097others(93): Show | 105 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.133-1207G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16628385 | |||||||
| chr7:16628409 | C | T | 55 | a0001c0004t0001g0066a0001c0004t0001g0067a0001c0004t0001g0193others(52): Show | 56 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.133-1231G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16628409 | |||||||
| chr7:16628500 | A | G | 1 | a0001c0002t0003g0078 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.133-1322T>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16628500 | |||||||
| chr7:16628605 | C | A | 1 | a0001c0001t0001g0278 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.133-1427G>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16628605 | |||||||
| chr7:16628744 | G | A | 3 | a0001c0001t0002g0154a0001c0001t0003g0155a0001c0001t0003g0156 | 3 | HG01070.hp1 HG01071.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.133-1566C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16628744 | |||||||
| chr7:16628777 | T | C | 55 | a0001c0004t0001g0066a0001c0004t0001g0067a0001c0004t0001g0193others(52): Show | 56 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.133-1599A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16628777 | |||||||
| chr7:16628787 | T | A | 269 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0024others(266): Show | 286 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.133-1609A>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16628787 | |||||||
| chr7:16628907 | TTAAACA | T | 53 | a0001c0004t0001g0066a0001c0004t0001g0067a0001c0004t0001g0193others(50): Show | 54 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(51): Show |
intron_variant | MODIFIER | c.133-1735_133-1730d others(8): Show |
ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16628907 | |||||||
| chr7:16628908 | T | TAAACA | 63 | a0001c0001t0001g0038a0001c0001t0001g0058a0001c0001t0001g0059others(60): Show | 67 | HG00140.hp1 HG00621.hp1 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.133-1735_133-1731d others(7): Show |
ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16628908 | |||||||
| chr7:16628908 | T | TAAACAAA others(3): Show |
26 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0001g0098others(23): Show | 29 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(26): Show |
intron_variant | MODIFIER | c.133-1740_133-1731d others(12): Show |
ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16628908 | |||||||
| chr7:16628908 | T | TAAACAAA others(8): Show |
5 | a0001c0001t0002g0319a0001c0001t0003g0100a0001c0003t0004g0118others(2): Show | 5 | HG00673.hp2 HG01346.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.133-1745_133-1731d others(17): Show |
ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16628908 | |||||||
| chr7:16628908 | TAAACA | T | 72 | a0001c0001t0001g0151a0001c0001t0001g0173a0001c0001t0001g0253others(69): Show | 73 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.133-1735_133-1731d others(7): Show |
ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16628908 | |||||||
| chr7:16628908 | TAAACAAA others(3): Show |
T | 10 | a0001c0001t0001g0024a0001c0001t0001g0270a0001c0001t0001g0271others(7): Show | 10 | HG01891.hp1 HG02486.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.133-1740_133-1731d others(12): Show |
ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16628908 | |||||||
| chr7:16628908 | TAAACAAA others(13): Show |
T | 6 | a0001c0001t0001g0334a0001c0001t0003g0321a0001c0003t0004g0041others(3): Show | 6 | HG02055.hp1 HG02109.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.133-1750_133-1731d others(22): Show |
ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16628908 | |||||||
| chr7:16628974 | A | G | 55 | a0001c0004t0001g0066a0001c0004t0001g0067a0001c0004t0001g0193others(52): Show | 56 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.133-1796T>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16628974 | |||||||
| chr7:16629144 | C | T | 1 | a0001c0002t0003g0148 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.133-1966G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16629144 | |||||||
| chr7:16629196 | A | T | 1 | a0001c0001t0001g0055 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.133-2018T>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16629196 | |||||||
| chr7:16629256 | C | T | 1 | a0001c0001t0003g0073 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.133-2078G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16629256 | |||||||
| chr7:16629282 | T | A | 15 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0256others(12): Show | 15 | HG00639.hp1 HG01109.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.133-2104A>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16629282 | |||||||
| chr7:16629305 | G | T | 6 | a0001c0004t0002g0302a0001c0004t0002g0304a0001c0004t0002g0305others(3): Show | 6 | HG00280.hp2 HG00323.hp1 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.133-2127C>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16629305 | |||||||
| chr7:16629356 | C | G | 1 | a0001c0004t0002g0307 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.133-2178G>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16629356 | |||||||
| chr7:16629542 | A | C | 7 | a0001c0001t0001g0024a0001c0001t0001g0270a0001c0001t0001g0271others(4): Show | 7 | HG01891.hp1 HG02486.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.133-2364T>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16629542 | |||||||
| chr7:16629619 | A | G | 55 | a0001c0004t0001g0066a0001c0004t0001g0067a0001c0004t0001g0193others(52): Show | 56 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.133-2441T>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16629619 | |||||||
| chr7:16629694 | T | C | 2 | a0001c0001t0003g0273a0001c0001t0006g0208 | 2 | HG03209.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.133-2516A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16629694 | |||||||
| chr7:16629708 | A | C | 50 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0038others(47): Show | 56 | HG00609.hp2 HG00642.hp1 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.133-2530T>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16629708 | |||||||
| chr7:16629970 | T | C | 2 | a0001c0001t0005g0365a0001c0001t0011g0260 | 2 | HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.133-2792A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16629970 | |||||||
| chr7:16630127 | C | G | 15 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0256others(12): Show | 15 | HG00639.hp1 HG01109.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.133-2949G>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16630127 | |||||||
| chr7:16630174 | G | A | 15 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0256others(12): Show | 15 | HG00639.hp1 HG01109.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.133-2996C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16630174 | |||||||
| chr7:16630231 | C | A | 1 | a0001c0002t0008g0101 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.133-3053G>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16630231 | |||||||
| chr7:16630267 | T | C | 1 | a0001c0004t0002g0188 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.133-3089A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16630267 | |||||||
| chr7:16630381 | C | T | 1 | a0001c0003t0004g0033 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.133-3203G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16630381 | |||||||
| chr7:16630432 | T | C | 1 | a0001c0001t0002g0259 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.133-3254A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16630432 | |||||||
| chr7:16630692 | A | G | 3 | a0001c0001t0001g0338a0001c0001t0001g0342a0001c0001t0001g0343 | 3 | NA18951.hp1 NA18984.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.133-3514T>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16630692 | |||||||
| chr7:16630703 | T | C | 2 | a0001c0001t0003g0273a0001c0001t0006g0208 | 2 | HG03209.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.133-3525A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16630703 | |||||||
| chr7:16630765 | A | C | 4 | a0001c0004t0001g0066a0001c0004t0001g0308a0001c0004t0001g0309others(1): Show | 4 | HG02040.hp1 NA18989.hp1 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.133-3587T>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16630765 | |||||||
| chr7:16630846 | A | G | 50 | a0001c0001t0001g0024a0001c0001t0001g0270a0001c0001t0001g0271others(47): Show | 51 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.133-3668T>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16630846 | |||||||
| chr7:16631167 | G | GTGA | 50 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0038others(47): Show | 56 | HG00609.hp2 HG00642.hp1 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.133-3992_133-3990d others(5): Show |
ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16631167 | |||||||
| chr7:16631365 | T | C | 13 | a0001c0004t0002g0192a0001c0004t0002g0214a0001c0004t0002g0302others(10): Show | 14 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.133-4187A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16631365 | |||||||
| chr7:16631511 | C | T | 37 | a0001c0001t0001g0024a0001c0001t0001g0270a0001c0001t0001g0271others(34): Show | 37 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.133-4333G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16631511 | |||||||
| chr7:16631691 | T | C | 15 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0256others(12): Show | 15 | HG00639.hp1 HG01109.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.133-4513A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16631691 | |||||||
| chr7:16631759 | C | T | 4 | a0001c0001t0001g0266a0003c0018t0003g0374a0005c0014t0001g0324others(1): Show | 4 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.133-4581G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16631759 | |||||||
| chr7:16632018 | C | A | 7 | a0001c0001t0001g0024a0001c0001t0001g0270a0001c0001t0001g0271others(4): Show | 7 | HG01891.hp1 HG02486.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.132+4373G>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16632018 | |||||||
| chr7:16632111 | C | A | 1 | a0001c0001t0002g0054 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.132+4280G>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16632111 | |||||||
| chr7:16632133 | C | T | 5 | a0001c0001t0003g0212a0001c0001t0005g0376a0001c0001t0006g0366others(2): Show | 5 | HG01081.hp2 HG02257.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.132+4258G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16632133 | |||||||
| chr7:16632211 | T | C | 4 | a0001c0001t0001g0266a0003c0018t0003g0374a0005c0014t0001g0324others(1): Show | 4 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.132+4180A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16632211 | |||||||
| chr7:16632238 | TTTA | T | 35 | a0001c0001t0001g0024a0001c0001t0001g0270a0001c0001t0001g0271others(32): Show | 35 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.132+4150_132+4152d others(5): Show |
ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16632238 | |||||||
| chr7:16632304 | T | A | 284 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0024others(281): Show | 301 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.132+4087A>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16632304 | |||||||
| chr7:16632395 | T | C | 7 | a0001c0001t0005g0021a0001c0001t0005g0365a0001c0001t0011g0260others(4): Show | 8 | HG02886.hp1 HG02922.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.132+3996A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16632395 | |||||||
| chr7:16632493 | G | A | 46 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0038others(43): Show | 52 | HG00609.hp2 HG00642.hp1 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.132+3898C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16632493 | |||||||
| chr7:16632518 | G | A | 3 | a0001c0001t0002g0133a0001c0001t0002g0349a0001c0001t0005g0134 | 3 | HG02280.hp2 HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.132+3873C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16632518 | |||||||
| chr7:16632569 | G | A | 1 | a0001c0011t0001g0220 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.132+3822C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16632569 | |||||||
| chr7:16632630 | C | T | 1 | a0001c0002t0002g0317 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.132+3761G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16632630 | |||||||
| chr7:16632645 | G | A | 2 | a0001c0002t0002g0007a0001c0002t0002g0102 | 3 | HG01516.hp1 HG04115.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.132+3746C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16632645 | |||||||
| chr7:16632648 | T | C | 28 | a0002c0005t0001g0140a0002c0005t0001g0144a0002c0005t0001g0288others(25): Show | 28 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(25): Show |
intron_variant | MODIFIER | c.132+3743A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16632648 | |||||||
| chr7:16632850 | C | A | 10 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0256others(7): Show | 10 | HG01109.hp1 HG01884.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.132+3541G>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16632850 | |||||||
| chr7:16632860 | T | A | 1 | a0001c0004t0002g0192 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.132+3531A>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16632860 | |||||||
| chr7:16632881 | G | A | 1 | a0001c0002t0002g0200 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.132+3510C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16632881 | |||||||
| chr7:16632905 | C | T | 8 | a0001c0001t0001g0055a0001c0001t0001g0276a0001c0001t0001g0278others(5): Show | 8 | NA18948.hp1 NA18950.hp2 NA18953.hp1 others(5): Show |
intron_variant | MODIFIER | c.132+3486G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16632905 | |||||||
| chr7:16632940 | A | G | 1 | a0001c0002t0003g0072 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.132+3451T>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16632940 | |||||||
| chr7:16632950 | A | G | 53 | a0001c0001t0001g0024a0001c0001t0001g0266a0001c0001t0001g0270others(50): Show | 53 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.132+3441T>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16632950 | |||||||
| chr7:16633025 | T | C | 1 | a0001c0004t0002g0307 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.132+3366A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16633025 | |||||||
| chr7:16633066 | C | A | 28 | a0002c0005t0001g0140a0002c0005t0001g0144a0002c0005t0001g0288others(25): Show | 28 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(25): Show |
intron_variant | MODIFIER | c.132+3325G>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16633066 | |||||||
| chr7:16633080 | C | T | 49 | a0001c0001t0001g0061a0001c0001t0002g0272a0001c0004t0001g0066others(46): Show | 50 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(47): Show |
intron_variant | MODIFIER | c.132+3311G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16633080 | |||||||
| chr7:16633096 | T | G | 2 | a0001c0001t0005g0365a0001c0001t0011g0260 | 2 | HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.132+3295A>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16633096 | |||||||
| chr7:16633133 | T | A | 278 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0024others(275): Show | 295 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.132+3258A>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16633133 | |||||||
| chr7:16633356 | C | T | 102 | a0001c0001t0001g0077a0001c0001t0001g0095a0001c0001t0001g0097others(99): Show | 111 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.132+3035G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16633356 | |||||||
| chr7:16633610 | C | T | 2 | a0001c0001t0001g0369a0001c0001t0006g0044 | 2 | HG02630.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.132+2781G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16633610 | |||||||
| chr7:16633766 | G | C | 46 | a0001c0001t0001g0024a0001c0001t0001g0270a0001c0001t0001g0271others(43): Show | 46 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.132+2625C>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16633766 | |||||||
| chr7:16633767 | G | A | 2 | a0002c0009t0001g0141a0002c0009t0001g0143 | 2 | HG00423.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.132+2624C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16633767 | |||||||
| chr7:16633772 | C | T | 1 | a0001c0001t0013g0043 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.132+2619G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16633772 | |||||||
| chr7:16633830 | G | C | 1 | a0001c0001t0003g0037 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.132+2561C>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16633830 | |||||||
| chr7:16633944 | T | A | 1 | a0001c0001t0001g0038 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.132+2447A>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16633944 | |||||||
| chr7:16634366 | T | C | 3 | a0001c0004t0003g0268a0001c0004t0003g0375a0001c0007t0007g0274 | 3 | HG02886.hp1 HG03225.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.132+2025A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16634366 | |||||||
| chr7:16634490 | C | A | 2 | a0001c0001t0005g0365a0001c0001t0011g0260 | 2 | HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.132+1901G>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16634490 | |||||||
| chr7:16634505 | G | C | 1 | a0001c0001t0001g0241 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.132+1886C>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16634505 | |||||||
| chr7:16634514 | G | A | 3 | a0001c0003t0004g0039a0001c0003t0004g0040a0001c0003t0004g0318 | 3 | HG02451.hp2 HG02818.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.132+1877C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16634514 | |||||||
| chr7:16634548 | G | A | 12 | a0001c0004t0001g0066a0001c0004t0001g0308a0001c0004t0001g0309others(9): Show | 12 | HG02040.hp1 NA18945.hp1 NA18947.hp2 others(9): Show |
intron_variant | MODIFIER | c.132+1843C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16634548 | |||||||
| chr7:16634567 | T | C | 1 | a0001c0004t0001g0193 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.132+1824A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16634567 | |||||||
| chr7:16634659 | G | C | 15 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0256others(12): Show | 15 | HG00639.hp1 HG01109.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.132+1732C>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16634659 | |||||||
| chr7:16634697 | A | T | 4 | a0001c0001t0001g0266a0003c0018t0003g0374a0005c0014t0001g0324others(1): Show | 4 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.132+1694T>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16634697 | |||||||
| chr7:16634698 | G | C | 3 | a0001c0001t0001g0242a0001c0001t0002g0244a0001c0003t0004g0243 | 3 | HG00609.hp2 NA18982.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.132+1693C>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16634698 | |||||||
| chr7:16634713 | C | T | 99 | a0001c0001t0001g0077a0001c0001t0001g0095a0001c0001t0001g0097others(96): Show | 108 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.132+1678G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16634713 | |||||||
| chr7:16634720 | A | G | 2 | a0001c0001t0006g0045a0001c0003t0004g0046 | 2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.132+1671T>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16634720 | |||||||
| chr7:16635009 | T | C | 46 | a0001c0001t0001g0024a0001c0001t0001g0270a0001c0001t0001g0271others(43): Show | 46 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.132+1382A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16635009 | |||||||
| chr7:16635114 | C | T | 102 | a0001c0001t0001g0077a0001c0001t0001g0095a0001c0001t0001g0097others(99): Show | 111 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.132+1277G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16635114 | |||||||
| chr7:16635128 | G | T | 10 | a0001c0001t0003g0212a0001c0001t0005g0376a0001c0001t0006g0366others(7): Show | 10 | HG01081.hp2 HG02145.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.132+1263C>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16635128 | |||||||
| chr7:16635151 | T | C | 35 | a0001c0001t0001g0024a0001c0001t0001g0270a0001c0001t0001g0271others(32): Show | 35 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.132+1240A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16635151 | |||||||
| chr7:16635311 | T | C | 1 | a0001c0002t0002g0107 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.132+1080A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16635311 | |||||||
| chr7:16635337 | T | C | 56 | a0001c0001t0001g0061a0001c0001t0001g0266a0001c0001t0002g0272others(53): Show | 57 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.132+1054A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16635337 | |||||||
| chr7:16635417 | G | A | 274 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0024others(271): Show | 290 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(287): Show |
intron_variant | MODIFIER | c.132+974C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16635417 | |||||||
| chr7:16635662 | C | G | 15 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0256others(12): Show | 15 | HG00639.hp1 HG01109.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.132+729G>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16635662 | |||||||
| chr7:16636041 | C | G | 46 | a0001c0001t0001g0024a0001c0001t0001g0270a0001c0001t0001g0271others(43): Show | 46 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.132+350G>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16636041 | |||||||
| chr7:16636068 | G | C | 7 | a0001c0001t0001g0266a0001c0001t0003g0262a0001c0001t0006g0045others(4): Show | 7 | HG02559.hp1 HG02630.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.132+323C>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16636068 | |||||||
| chr7:16636100 | C | T | 15 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0256others(12): Show | 15 | HG00639.hp1 HG01109.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.132+291G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16636100 | |||||||
| chr7:16636118 | T | C | 280 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0024others(277): Show | 297 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(294): Show |
intron_variant | MODIFIER | c.132+273A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16636118 | |||||||
| chr7:16636269 | T | C | 110 | a0001c0001t0001g0077a0001c0001t0001g0095a0001c0001t0001g0097others(107): Show | 119 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.132+122A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16636269 | |||||||
| chr7:16636280 | G | A | 3 | a0001c0002t0002g0056a0001c0002t0002g0136a0001c0006t0004g0207 | 3 | HG00408.hp1 HG00597.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.132+111C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16636280 | |||||||
| chr7:16636282 | G | A | 55 | a0001c0001t0001g0061a0001c0001t0001g0334a0001c0001t0002g0272others(52): Show | 56 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.132+109C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16636282 | |||||||
| chr7:16636302 | C | CA | 49 | a0001c0001t0001g0015a0001c0001t0001g0115a0001c0001t0001g0173others(46): Show | 51 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(48): Show |
intron_variant | MODIFIER | c.132+88dupT | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16636302 | |||||||
| chr7:16636302 | C | CAA | 8 | a0001c0001t0003g0119a0001c0001t0003g0321a0001c0003t0004g0247others(5): Show | 8 | HG01978.hp2 HG03471.hp1 NA18980.hp1 others(5): Show |
intron_variant | MODIFIER | c.132+87_132+88dupTT | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16636302 | |||||||
| chr7:16636302 | CA | C | 70 | a0001c0001t0001g0019a0001c0001t0001g0038a0001c0001t0001g0055others(67): Show | 73 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.132+88delT | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16636302 | |||||||
| chr7:16636302 | CAA | C | 17 | a0001c0001t0001g0266a0001c0001t0003g0212a0001c0001t0003g0273others(14): Show | 17 | HG01081.hp2 HG02145.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.132+87_132+88delTT | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16636302 | |||||||
| chr7:16636353 | A | AG | 7 | a0001c0001t0001g0266a0001c0001t0003g0262a0001c0001t0006g0045others(4): Show | 7 | HG02559.hp1 HG02630.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.132+37dupC | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16636353 | |||||||
| chr7:16636365 | C | A | 1 | a0001c0001t0009g0002 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.132+26G>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 2/9 | chr7 | 16636365 | |||||||
| chr7:16636457 | T | TA | 69 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0038others(66): Show | 78 | HG00423.hp1 HG00438.hp1 HG00609.hp2 others(75): Show |
splice_region_variant&intron_variant | LOW | c.68-3dupT | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16636457 | |||||||
| chr7:16636492 | G | A | 3 | a0001c0001t0002g0179a0001c0001t0002g0181a0001c0001t0003g0180 | 3 | NA18950.hp2 NA18956.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.68-37C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16636492 | |||||||
| chr7:16636539 | G | C | 50 | a0001c0001t0001g0024a0001c0001t0001g0266a0001c0001t0001g0270others(47): Show | 50 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.68-84C>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16636539 | |||||||
| chr7:16636725 | G | A | 1 | a0001c0001t0002g0341 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.68-270C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16636725 | |||||||
| chr7:16636749 | A | C | 6 | a0001c0001t0001g0334a0001c0001t0003g0321a0001c0003t0004g0041others(3): Show | 6 | HG02055.hp1 HG02109.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.68-294T>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16636749 | |||||||
| chr7:16636764 | GA | G | 7 | a0001c0001t0001g0266a0001c0001t0003g0262a0001c0001t0006g0045others(4): Show | 7 | HG02559.hp1 HG02630.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.68-310delT | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16636764 | |||||||
| chr7:16636781 | G | T | 3 | a0001c0001t0001g0362a0001c0003t0004g0033a0001c0003t0004g0034 | 3 | HG02109.hp1 HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.68-326C>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16636781 | |||||||
| chr7:16637175 | G | A | 28 | a0002c0005t0001g0140a0002c0005t0001g0144a0002c0005t0001g0288others(25): Show | 28 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(25): Show |
intron_variant | MODIFIER | c.68-720C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16637175 | |||||||
| chr7:16637178 | A | T | 2 | a0002c0005t0003g0351a0002c0010t0004g0350 | 2 | HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.68-723T>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16637178 | |||||||
| chr7:16637245 | C | G | 49 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0038others(46): Show | 55 | HG00609.hp2 HG00642.hp1 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.68-790G>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16637245 | |||||||
| chr7:16637330 | C | A | 173 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0024others(170): Show | 180 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.68-875G>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16637330 | |||||||
| chr7:16637559 | A | G | 276 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0024others(273): Show | 292 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(289): Show |
intron_variant | MODIFIER | c.68-1104T>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16637559 | |||||||
| chr7:16637711 | C | T | 1 | a0001c0001t0001g0270 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.68-1256G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16637711 | |||||||
| chr7:16637752 | G | A | 5 | a0001c0001t0005g0365a0001c0001t0005g0376a0001c0001t0006g0366others(2): Show | 5 | HG01081.hp2 HG02257.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-1297C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16637752 | |||||||
| chr7:16637757 | C | T | 1 | a0008c0015t0012g0194 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.68-1302G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16637757 | |||||||
| chr7:16637893 | A | G | 276 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0024others(273): Show | 292 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(289): Show |
intron_variant | MODIFIER | c.68-1438T>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16637893 | |||||||
| chr7:16638498 | T | C | 280 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0024others(277): Show | 297 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(294): Show |
intron_variant | MODIFIER | c.68-2043A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16638498 | |||||||
| chr7:16638574 | C | T | 1 | a0001c0002t0001g0323 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.68-2119G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16638574 | |||||||
| chr7:16638637 | C | G | 1 | a0001c0001t0011g0260 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.68-2182G>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16638637 | |||||||
| chr7:16638716 | C | T | 1 | a0001c0001t0001g0019 | 2 | NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.68-2261G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16638716 | |||||||
| chr7:16638787 | T | C | 6 | a0001c0001t0001g0334a0001c0001t0003g0321a0001c0003t0004g0041others(3): Show | 6 | HG02055.hp1 HG02109.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.68-2332A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16638787 | |||||||
| chr7:16638864 | C | CT | 277 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0024others(274): Show | 294 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(291): Show |
intron_variant | MODIFIER | c.68-2410_68-2409ins others(1): Show |
ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16638864 | |||||||
| chr7:16639116 | G | A | 26 | a0002c0005t0001g0140a0002c0005t0001g0144a0002c0005t0001g0288others(23): Show | 26 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(23): Show |
intron_variant | MODIFIER | c.68-2661C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16639116 | |||||||
| chr7:16639311 | G | A | 47 | a0001c0001t0001g0024a0001c0001t0001g0270a0001c0001t0001g0271others(44): Show | 47 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.68-2856C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16639311 | |||||||
| chr7:16639552 | G | A | 3 | a0001c0004t0003g0268a0001c0004t0003g0375a0001c0007t0007g0274 | 3 | HG02886.hp1 HG03225.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.68-3097C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16639552 | |||||||
| chr7:16639931 | G | A | 10 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0256others(7): Show | 10 | HG01109.hp1 HG01884.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.68-3476C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16639931 | |||||||
| chr7:16639997 | T | TA | 13 | a0001c0001t0001g0266a0001c0001t0001g0334a0001c0001t0003g0262others(10): Show | 13 | HG02055.hp1 HG02109.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.68-3543dupT | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16639997 | |||||||
| chr7:16640031 | T | G | 11 | a0001c0001t0003g0212a0001c0001t0005g0365a0001c0001t0005g0376others(8): Show | 11 | HG01081.hp2 HG02145.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.68-3576A>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16640031 | |||||||
| chr7:16640067 | G | A | 2 | a0001c0002t0002g0120a0001c0002t0002g0121 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.68-3612C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16640067 | |||||||
| chr7:16640076 | G | C | 1 | a0001c0003t0004g0023 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.68-3621C>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16640076 | |||||||
| chr7:16640105 | G | A | 1 | a0001c0001t0003g0262 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.68-3650C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16640105 | |||||||
| chr7:16640310 | T | A | 47 | a0001c0001t0001g0024a0001c0001t0001g0270a0001c0001t0001g0271others(44): Show | 47 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.68-3855A>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16640310 | |||||||
| chr7:16640389 | C | T | 1 | a0001c0002t0001g0068 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.68-3934G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16640389 | |||||||
| chr7:16640449 | T | C | 3 | a0001c0001t0003g0122a0001c0001t0003g0123a0001c0001t0017g0378 | 3 | HG02129.hp2 NA18974.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.68-3994A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16640449 | |||||||
| chr7:16640469 | C | T | 1 | a0001c0022t0001g0186 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.68-4014G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16640469 | |||||||
| chr7:16640482 | G | C | 6 | a0001c0001t0001g0334a0001c0001t0003g0321a0001c0003t0004g0041others(3): Show | 6 | HG02055.hp1 HG02109.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.68-4027C>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16640482 | |||||||
| chr7:16640625 | A | G | 2 | a0003c0018t0003g0374a0006c0019t0004g0050 | 2 | HG02559.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.68-4170T>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16640625 | |||||||
| chr7:16640647 | G | A | 3 | a0001c0002t0001g0049a0001c0003t0004g0269a0003c0013t0003g0372 | 3 | HG02717.hp2 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.68-4192C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16640647 | |||||||
| chr7:16640686 | T | C | 1 | a0002c0005t0001g0144 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.68-4231A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16640686 | |||||||
| chr7:16640709 | A | G | 103 | a0001c0001t0001g0077a0001c0001t0001g0095a0001c0001t0001g0097others(100): Show | 112 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.68-4254T>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16640709 | |||||||
| chr7:16640710 | C | T | 276 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0024others(273): Show | 293 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(290): Show |
intron_variant | MODIFIER | c.68-4255G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16640710 | |||||||
| chr7:16640749 | T | C | 5 | a0001c0002t0001g0323a0001c0003t0004g0039a0001c0003t0004g0040others(2): Show | 5 | HG00639.hp1 HG02451.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.68-4294A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16640749 | |||||||
| chr7:16641034 | C | T | 4 | a0001c0001t0001g0266a0003c0018t0003g0374a0005c0014t0001g0324others(1): Show | 4 | HG02559.hp1 HG02630.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+4473G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16641034 | |||||||
| chr7:16641106 | C | T | 6 | a0001c0001t0001g0334a0001c0001t0003g0321a0001c0003t0004g0041others(3): Show | 6 | HG02055.hp1 HG02109.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.67+4401G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16641106 | |||||||
| chr7:16641124 | C | T | 41 | a0001c0001t0001g0024a0001c0001t0001g0270a0001c0001t0001g0271others(38): Show | 41 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.67+4383G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16641124 | |||||||
| chr7:16641151 | T | C | 14 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0256others(11): Show | 14 | HG01109.hp1 HG01884.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.67+4356A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16641151 | |||||||
| chr7:16641181 | C | T | 2 | a0001c0001t0006g0045a0001c0003t0004g0046 | 2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.67+4326G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16641181 | |||||||
| chr7:16641199 | A | G | 15 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0256others(12): Show | 15 | HG00639.hp1 HG01109.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.67+4308T>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16641199 | |||||||
| chr7:16641241 | G | GAC | 118 | a0001c0001t0001g0077a0001c0001t0001g0095a0001c0001t0001g0097others(115): Show | 127 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.67+4264_67+4265dup others(2): Show |
ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16641241 | |||||||
| chr7:16641247 | C | A | 7 | a0001c0001t0001g0266a0001c0001t0003g0262a0001c0001t0006g0045others(4): Show | 7 | HG02559.hp1 HG02630.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.67+4260G>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16641247 | |||||||
| chr7:16641288 | A | G | 1 | a0002c0005t0002g0138 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.67+4219T>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16641288 | |||||||
| chr7:16641353 | T | A | 1 | a0001c0001t0002g0135 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.67+4154A>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16641353 | |||||||
| chr7:16641381 | T | A | 5 | a0001c0001t0001g0334a0001c0003t0004g0041a0001c0003t0004g0042others(2): Show | 5 | HG02055.hp1 HG02109.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+4126A>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16641381 | |||||||
| chr7:16641403 | G | A | 281 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0024others(278): Show | 298 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(295): Show |
intron_variant | MODIFIER | c.67+4104C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16641403 | |||||||
| chr7:16641435 | G | A | 27 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0003g0212others(24): Show | 27 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.67+4072C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16641435 | |||||||
| chr7:16641454 | T | G | 2 | a0001c0001t0001g0248a0001c0001t0001g0249 | 2 | NA19060.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.67+4053A>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16641454 | |||||||
| chr7:16641466 | C | T | 68 | a0001c0001t0001g0286a0001c0001t0001g0331a0001c0001t0001g0369others(65): Show | 70 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.67+4041G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16641466 | |||||||
| chr7:16641509 | T | G | 47 | a0001c0001t0001g0001a0001c0001t0001g0058a0001c0001t0001g0059others(44): Show | 53 | HG00609.hp2 HG00642.hp1 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.67+3998A>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16641509 | |||||||
| chr7:16641608 | C | T | 1 | a0001c0001t0003g0212 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.67+3899G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16641608 | |||||||
| chr7:16641694 | C | G | 297 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0024others(294): Show | 315 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(312): Show |
intron_variant | MODIFIER | c.67+3813G>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16641694 | |||||||
| chr7:16641719 | T | C | 8 | a0001c0001t0001g0369a0001c0001t0005g0364a0001c0001t0005g0365others(5): Show | 8 | HG01081.hp2 HG01891.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+3788A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16641719 | |||||||
| chr7:16641748 | G | A | 1 | a0001c0002t0001g0127 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.67+3759C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16641748 | |||||||
| chr7:16641810 | T | C | 1 | a0001c0001t0003g0182 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.67+3697A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16641810 | |||||||
| chr7:16641894 | G | A | 9 | a0001c0001t0002g0128a0001c0001t0002g0129a0001c0001t0002g0130others(6): Show | 9 | HG01074.hp1 HG02280.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.67+3613C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16641894 | |||||||
| chr7:16641964 | T | C | 2 | a0001c0004t0002g0063a0001c0004t0002g0064 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.67+3543A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16641964 | |||||||
| chr7:16642061 | T | TAA | 300 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0024others(297): Show | 317 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(314): Show |
intron_variant | MODIFIER | c.67+3445_67+3446ins others(2): Show |
ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16642061 | |||||||
| chr7:16642107 | C | T | 6 | a0001c0001t0001g0334a0001c0003t0004g0041a0001c0003t0004g0042others(3): Show | 6 | HG01243.hp2 HG02055.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.67+3400G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16642107 | |||||||
| chr7:16642110 | T | C | 16 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0256others(13): Show | 16 | HG01109.hp1 HG01884.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.67+3397A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16642110 | |||||||
| chr7:16642353 | A | G | 12 | a0001c0001t0001g0216a0001c0001t0001g0334a0001c0001t0009g0002others(9): Show | 13 | HG00639.hp2 HG01243.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.67+3154T>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16642353 | |||||||
| chr7:16642383 | T | C | 1 | a0001c0001t0001g0184 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.67+3124A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16642383 | |||||||
| chr7:16642546 | A | G | 1 | a0001c0002t0001g0323 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.67+2961T>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16642546 | |||||||
| chr7:16642652 | GA | G | 11 | a0001c0001t0001g0334a0001c0001t0003g0212a0001c0001t0009g0002others(8): Show | 12 | HG01243.hp2 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.67+2854delT | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16642652 | |||||||
| chr7:16642696 | C | A | 1 | a0001c0008t0002g0322 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.67+2811G>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16642696 | |||||||
| chr7:16642820 | G | A | 1 | a0001c0001t0001g0362 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.67+2687C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16642820 | |||||||
| chr7:16642862 | T | C | 46 | a0001c0001t0001g0213a0001c0001t0001g0270a0001c0001t0001g0271others(43): Show | 46 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.67+2645A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16642862 | |||||||
| chr7:16642912 | G | A | 294 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0024others(291): Show | 311 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(308): Show |
intron_variant | MODIFIER | c.67+2595C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16642912 | |||||||
| chr7:16643076 | T | C | 1 | a0005c0014t0001g0324 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.67+2431A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16643076 | |||||||
| chr7:16643114 | C | A | 2 | a0001c0003t0004g0039a0001c0003t0004g0040 | 2 | HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.67+2393G>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16643114 | |||||||
| chr7:16643122 | G | T | 3 | a0001c0001t0001g0373a0001c0002t0001g0003a0001c0002t0002g0325 | 4 | HG00733.hp2 HG01074.hp2 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+2385C>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16643122 | |||||||
| chr7:16643171 | A | T | 1 | a0001c0001t0003g0273 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.67+2336T>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16643171 | |||||||
| chr7:16643266 | C | G | 1 | a0001c0002t0002g0062 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.67+2241G>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16643266 | |||||||
| chr7:16643366 | A | G | 1 | a0001c0003t0004g0146 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.67+2141T>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16643366 | |||||||
| chr7:16643393 | C | T | 2 | a0001c0001t0006g0045a0001c0003t0004g0046 | 2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.67+2114G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16643393 | |||||||
| chr7:16643503 | GTCCAATG others(451): Show |
G | 6 | a0001c0001t0001g0334a0001c0003t0004g0041a0001c0003t0004g0042others(3): Show | 6 | HG01243.hp2 HG02055.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.67+1546_67+2003del | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16643503 | |||||||
| chr7:16643592 | A | C | 172 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0024others(169): Show | 187 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.67+1915T>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16643592 | |||||||
| chr7:16643776 | A | C | 209 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(206): Show | 225 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(222): Show |
intron_variant | MODIFIER | c.67+1731T>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16643776 | |||||||
| chr7:16643787 | G | A | 1 | a0001c0001t0002g0195 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.67+1720C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16643787 | |||||||
| chr7:16643843 | A | AC | 75 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0024others(72): Show | 82 | HG00609.hp2 HG00639.hp2 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.67+1663dupG | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16643843 | |||||||
| chr7:16643864 | C | CA | 33 | a0001c0001t0001g0038a0001c0001t0001g0196a0001c0001t0001g0197others(30): Show | 33 | HG00621.hp2 HG01081.hp2 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.67+1642dupT | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16643864 | |||||||
| chr7:16643896 | C | T | 58 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0024others(55): Show | 64 | HG00609.hp2 HG00642.hp1 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.67+1611G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16643896 | |||||||
| chr7:16644122 | G | A | 1 | a0001c0001t0001g0213 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.67+1385C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16644122 | |||||||
| chr7:16644366 | C | A | 1 | a0001c0001t0002g0206 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.67+1141G>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16644366 | |||||||
| chr7:16644391 | T | A | 1 | a0001c0006t0004g0207 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.67+1116A>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16644391 | |||||||
| chr7:16644422 | C | T | 7 | a0001c0001t0001g0216a0001c0001t0009g0002a0001c0003t0004g0023others(4): Show | 8 | HG00639.hp2 HG01243.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.67+1085G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16644422 | |||||||
| chr7:16644446 | A | G | 1 | a0001c0001t0006g0208 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.67+1061T>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16644446 | |||||||
| chr7:16644463 | C | T | 1 | a0001c0004t0002g0214 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.67+1044G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16644463 | |||||||
| chr7:16644474 | G | A | 43 | a0001c0001t0001g0018a0001c0001t0001g0213a0001c0001t0001g0334others(40): Show | 44 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.67+1033C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16644474 | |||||||
| chr7:16644494 | G | GCTA | 8 | a0001c0001t0001g0369a0001c0001t0005g0364a0001c0001t0005g0365others(5): Show | 8 | HG01081.hp2 HG01891.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+1010_67+1012dup others(3): Show |
ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16644494 | |||||||
| chr7:16644549 | T | C | 1 | a0002c0005t0002g0371 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.67+958A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16644549 | |||||||
| chr7:16644572 | T | C | 1 | a0001c0001t0001g0019 | 2 | NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.67+935A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16644572 | |||||||
| chr7:16644573 | G | A | 1 | a0001c0001t0006g0045 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.67+934C>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16644573 | |||||||
| chr7:16644586 | T | C | 2 | a0001c0002t0001g0049a0003c0013t0003g0372 | 2 | HG02717.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.67+921A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16644586 | |||||||
| chr7:16644622 | G | C | 191 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(188): Show | 200 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(197): Show |
intron_variant | MODIFIER | c.67+885C>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16644622 | |||||||
| chr7:16644660 | A | C | 2 | a0001c0001t0006g0045a0001c0002t0001g0049 | 2 | HG02717.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.67+847T>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16644660 | |||||||
| chr7:16644673 | C | T | 1 | a0001c0002t0002g0048 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.67+834G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16644673 | |||||||
| chr7:16644751 | T | C | 1 | a0001c0001t0001g0373 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.67+756A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16644751 | |||||||
| chr7:16644773 | G | C | 1 | a0001c0008t0001g0020 | 2 | NA18945.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.67+734C>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16644773 | |||||||
| chr7:16644867 | T | C | 1 | a0003c0018t0003g0374 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.67+640A>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16644867 | |||||||
| chr7:16645147 | C | G | 3 | a0001c0001t0006g0045a0001c0003t0004g0046a0001c0003t0004g0047 | 3 | HG02809.hp2 HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.67+360G>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16645147 | |||||||
| chr7:16645193 | A | G | 1 | a0001c0001t0006g0044 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.67+314T>C | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16645193 | |||||||
| chr7:16645240 | G | C | 2 | a0001c0001t0005g0376a0001c0004t0003g0375 | 2 | HG03225.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.67+267C>G | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16645240 | |||||||
| chr7:16645431 | C | T | 16 | a0001c0001t0001g0038a0001c0001t0002g0035a0001c0001t0003g0032others(13): Show | 16 | HG02109.hp1 HG02451.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.67+76G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16645431 | |||||||
| chr7:16645438 | C | T | 5 | a0001c0001t0001g0024a0001c0003t0004g0023a0001c0003t0004g0027others(2): Show | 5 | HG02559.hp2 HG02622.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.67+69G>A | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16645438 | |||||||
| chr7:16645460 | C | A | 2 | a0001c0001t0005g0021a0001c0003t0004g0377 | 3 | HG02970.hp1 HG03195.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.67+47G>T | ANKMY2 | ENSG00000106524.9 | transcript | ENST00000306999.7 | protein_coding | 1/9 | chr7 | 16645460 |