Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10043 |
| ensemblid | ENSG00000100284.22 |
| hgncid | 11982 |
| symbol | TOM1 |
| name | target of myb1 membrane trafficking protein |
| refseq_nuc | NM_005488.3 |
| refseq_prot | NP_005479.1 |
| ensembl_nuc | ENST00000449058.7 |
| ensembl_prot | ENSP00000394466.2 |
| mane_status | MANE Select |
| chr | chr22 |
| start | 35299894 |
| end | 35347973 |
| strand | + |
| ver | v1.2 |
| region | chr22:35299894-35347973 |
| region5000 | chr22:35294894-35352973 |
| regionname0 | TOM1_chr22_35299894_35347973 |
| regionname5000 | TOM1_chr22_35294894_35352973 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 492 | 353 | 84 | 68 | 156 | 10 | 33 | 116 | TOM1_chr22_35294894_35352973 | TOM1 | MDFLL others(487): Show |
chr22 | 35294894 | 35352973 |
| a0002 | 0/0 | 492 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | MDFLL others(487): Show |
chr22 | 35294894 | 35352973 |
| a0003 | 0/0 | 492 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | MDFLL others(487): Show |
chr22 | 35294894 | 35352973 |
| a0004 | 0/0 | 492 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | MDFLL others(487): Show |
chr22 | 35294894 | 35352973 |
| a0005 | 0/0 | 492 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | MDFLL others(487): Show |
chr22 | 35294894 | 35352973 |
| a0006 | 0/0 | 492 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | MDFLL others(487): Show |
chr22 | 35294894 | 35352973 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1476 | 229 | 24 | 46 | 128 | 6 | 24 | TOM1_chr22_35294894_35352973 | TOM1 | ATGGA others(1471): Show |
chr22 | 35294894 | 35352973 | ||
| a0001c0002 | 0/1 | 1476 | 111 | 52 | 20 | 25 | 4 | 9 | TOM1_chr22_35294894_35352973 | TOM1 | ATGGA others(1471): Show |
chr22 | 35294894 | 35352973 | ||
| a0001c0003 | 0/0 | 1476 | 6 | 4 | 0 | 2 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | ATGGA others(1471): Show |
chr22 | 35294894 | 35352973 | ||
| a0001c0004 | 0/0 | 1476 | 2 | 1 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | ATGGA others(1471): Show |
chr22 | 35294894 | 35352973 | ||
| a0001c0006 | 0/0 | 1476 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | ATGGA others(1471): Show |
chr22 | 35294894 | 35352973 | ||
| a0001c0007 | 0/0 | 1476 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | ATGGA others(1471): Show |
chr22 | 35294894 | 35352973 | ||
| a0001c0010 | 0/0 | 1476 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | ATGGA others(1471): Show |
chr22 | 35294894 | 35352973 | ||
| a0001c0013 | 0/0 | 1476 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | ATGGA others(1471): Show |
chr22 | 35294894 | 35352973 | ||
| a0001c0014 | 0/0 | 1476 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | ATGGA others(1471): Show |
chr22 | 35294894 | 35352973 | ||
| a0002c0009 | 0/0 | 1476 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | ATGGA others(1471): Show |
chr22 | 35294894 | 35352973 | ||
| a0003c0005 | 0/0 | 1476 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | ATGGA others(1471): Show |
chr22 | 35294894 | 35352973 | ||
| a0004c0012 | 0/0 | 1476 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | ATGGA others(1471): Show |
chr22 | 35294894 | 35352973 | ||
| a0005c0008 | 0/0 | 1476 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | ATGGA others(1471): Show |
chr22 | 35294894 | 35352973 | ||
| a0006c0011 | 0/0 | 1476 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | ATGGA others(1471): Show |
chr22 | 35294894 | 35352973 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2278 | 225 | 22 | 46 | 126 | 6 | 24 | TOM1_chr22_35294894_35352973 | TOM1 | GATTC others(2273): Show |
chr22 | 35294894 | 35352973 |
| a0001c0001t0002 | 0/0 | 2278 | 2 | 2 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | GATTC others(2273): Show |
chr22 | 35294894 | 35352973 |
| a0001c0001t0004 | 0/0 | 2278 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | GATTC others(2273): Show |
chr22 | 35294894 | 35352973 |
| a0001c0001t0005 | 0/0 | 2278 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | GATTC others(2273): Show |
chr22 | 35294894 | 35352973 |
| a0001c0002t0001 | 0/1 | 2278 | 108 | 51 | 18 | 25 | 4 | 9 | TOM1_chr22_35294894_35352973 | TOM1 | GATTC others(2273): Show |
chr22 | 35294894 | 35352973 |
| a0001c0002t0002 | 0/0 | 2278 | 3 | 1 | 2 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | GATTC others(2273): Show |
chr22 | 35294894 | 35352973 |
| a0001c0003t0001 | 0/0 | 2278 | 3 | 2 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | GATTC others(2273): Show |
chr22 | 35294894 | 35352973 |
| a0001c0003t0002 | 0/0 | 2278 | 2 | 2 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | GATTC others(2273): Show |
chr22 | 35294894 | 35352973 |
| a0001c0003t0003 | 0/0 | 2278 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | GATTC others(2273): Show |
chr22 | 35294894 | 35352973 |
| a0001c0004t0001 | 0/0 | 2278 | 2 | 1 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | GATTC others(2273): Show |
chr22 | 35294894 | 35352973 |
| a0001c0006t0001 | 0/0 | 2278 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | GATTC others(2273): Show |
chr22 | 35294894 | 35352973 |
| a0001c0007t0001 | 0/0 | 2278 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | GATTC others(2273): Show |
chr22 | 35294894 | 35352973 |
| a0001c0010t0001 | 0/0 | 2278 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | GATTC others(2273): Show |
chr22 | 35294894 | 35352973 |
| a0001c0013t0001 | 0/0 | 2278 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | GATTC others(2273): Show |
chr22 | 35294894 | 35352973 |
| a0001c0014t0001 | 0/0 | 2278 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | GATTC others(2273): Show |
chr22 | 35294894 | 35352973 |
| a0002c0009t0001 | 0/0 | 2278 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | GATTC others(2273): Show |
chr22 | 35294894 | 35352973 |
| a0003c0005t0001 | 0/0 | 2278 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | GATTC others(2273): Show |
chr22 | 35294894 | 35352973 |
| a0004c0012t0001 | 0/0 | 2278 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | GATTC others(2273): Show |
chr22 | 35294894 | 35352973 |
| a0005c0008t0001 | 0/0 | 2278 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | GATTC others(2273): Show |
chr22 | 35294894 | 35352973 |
| a0006c0011t0001 | 0/0 | 2278 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | GATTC others(2273): Show |
chr22 | 35294894 | 35352973 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 4 | 0 | 0 | 1 | 1 | 2 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0006 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0291 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0002g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0002g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0004g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0001t0005g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0001 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0002 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0058 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0002g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0002g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0002t0002g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0003t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0003t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0003t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0003t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0003t0002g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0003t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0004t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0004t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0006t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0007t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0010t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0013t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0001c0014t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0002c0009t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0003c0005t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0004c0012t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0005c0008t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| a0006c0011t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0295 | EUR | GBR | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0062 | EUR | GBR | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0107 | EUR | FIN | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG00323 | hp2 | a0001 | c0002 | t0001 | g0088 | EUR | FIN | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | CHS | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | CHS | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0027 | EAS | CHS | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | CHS | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | CHS | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | CHS | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | CHS | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | CHS | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | CHS | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0243 | AMR | PUR | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | CHS | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | CHS | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0223 | AMR | PUR | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG01069 | hp2 | a0001 | c0002 | t0002 | g0298 | AMR | PUR | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG01070 | hp1 | a0001 | c0002 | t0001 | g0013 | AMR | PUR | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG01071 | hp1 | a0001 | c0002 | t0002 | g0296 | AMR | PUR | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0013 | AMR | PUR | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0225 | AMR | PUR | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG01081 | hp2 | a0002 | c0009 | t0001 | g0105 | AMR | PUR | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG01099 | hp2 | a0001 | c0004 | t0001 | g0245 | AMR | PUR | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0190 | AMR | PUR | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | PUR | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0285 | AMR | PUR | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0294 | AMR | PUR | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0234 | AMR | PUR | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | CLM | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG01255 | hp2 | a0001 | c0010 | t0001 | g0219 | AMR | CLM | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0023 | AMR | CLM | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | CLM | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | CLM | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0287 | AMR | CLM | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0023 | AMR | CLM | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG01261 | hp1 | a0003 | c0005 | t0001 | g0081 | AMR | CLM | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | CLM | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | CLM | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG01358 | hp2 | a0001 | c0002 | t0001 | g0221 | AMR | CLM | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | CLM | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0218 | AMR | CLM | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | CLM | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG01496 | hp2 | a0004 | c0012 | t0001 | g0229 | AMR | CLM | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0063 | EUR | IBS | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0289 | EUR | IBS | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0087 | EUR | IBS | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0290 | EUR | IBS | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | ACB | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0302 | AFR | ACB | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | ACB | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG01891 | hp2 | a0001 | c0002 | t0001 | g0255 | AFR | ACB | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0186 | AMR | PEL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG01943 | hp1 | a0001 | c0002 | t0001 | g0134 | AMR | PEL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | PEL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG01975 | hp2 | a0001 | c0002 | t0001 | g0131 | AMR | PEL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG01978 | hp1 | a0005 | c0008 | t0001 | g0163 | AMR | PEL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0129 | AMR | PEL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PEL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | KHV | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02040 | hp2 | a0001 | c0001 | t0004 | g0203 | EAS | KHV | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0233 | AFR | ACB | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02055 | hp2 | a0001 | c0014 | t0001 | g0309 | AFR | ACB | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0146 | EAS | KHV | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | KHV | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | KHV | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | KHV | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | KHV | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02148 | hp1 | a0001 | c0002 | t0001 | g0130 | AMR | PEL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | CDX | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | CDX | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0180 | AFR | ACB | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0002 | AFR | ACB | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | ACB | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0232 | AFR | ACB | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02280 | hp2 | a0001 | c0002 | t0001 | g0030 | AFR | ACB | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02293 | hp1 | a0001 | c0002 | t0001 | g0113 | AMR | PEL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | PEL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0222 | AMR | PEL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0154 | AFR | ACB | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0051 | AFR | ACB | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0002 | AFR | GWD | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02630 | hp1 | a0001 | c0004 | t0001 | g0250 | AFR | GWD | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | GWD | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0001 | AFR | GWD | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0284 | SAS | PJL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0104 | SAS | PJL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0009 | AFR | GWD | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0071 | AFR | GWD | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0282 | AFR | GWD | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0244 | SAS | PJL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | GWD | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02809 | hp2 | a0001 | c0002 | t0001 | g0002 | AFR | GWD | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | GWD | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0253 | AFR | GWD | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0297 | AFR | GWD | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0236 | AFR | GWD | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | GWD | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02896 | hp2 | a0001 | c0003 | t0002 | g0300 | AFR | GWD | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02897 | hp1 | a0001 | c0003 | t0002 | g0301 | AFR | GWD | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02897 | hp2 | a0001 | c0002 | t0001 | g0230 | AFR | GWD | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02922 | hp2 | a0001 | c0003 | t0001 | g0307 | AFR | ESN | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0002 | AFR | ESN | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02965 | hp2 | a0001 | c0002 | t0001 | g0246 | AFR | ESN | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | ESN | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | ESN | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02976 | hp2 | a0001 | c0002 | t0001 | g0009 | AFR | ESN | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0064 | SAS | PJL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG03041 | hp1 | a0001 | c0002 | t0001 | g0172 | AFR | GWD | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0305 | AFR | GWD | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG03098 | hp1 | a0001 | c0002 | t0001 | g0049 | AFR | MSL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | MSL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0258 | AFR | ESN | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0155 | AFR | ESN | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG03139 | hp1 | a0001 | c0002 | t0001 | g0257 | AFR | ESN | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0005 | AFR | ESN | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG03195 | hp1 | a0001 | c0002 | t0002 | g0304 | AFR | ESN | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0231 | AFR | ESN | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | MSL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG03209 | hp2 | a0001 | c0002 | t0001 | g0173 | AFR | MSL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | MSL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG03225 | hp2 | a0001 | c0006 | t0001 | g0189 | AFR | MSL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0299 | AFR | MSL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0025 | AFR | MSL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG03490 | hp2 | a0001 | c0002 | t0001 | g0128 | SAS | PJL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0273 | SAS | PJL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0286 | SAS | PJL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0050 | AFR | ESN | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0208 | AFR | ESN | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0009 | AFR | GWD | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0005 | AFR | GWD | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0132 | SAS | PJL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0235 | SAS | PJL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0241 | SAS | PJL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | BEB | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | BEB | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | BEB | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0292 | SAS | BEB | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | STU | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | STU | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0242 | SAS | STU | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | STU | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG04228 | hp1 | a0006 | c0011 | t0001 | g0188 | SAS | STU | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | STU | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0254 | AFR | YRI | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0002 | AFR | YRI | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | CHB | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | CHB | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | CHB | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18940 | hp1 | a0001 | c0002 | t0001 | g0276 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18943 | hp1 | a0001 | c0002 | t0001 | g0024 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18943 | hp2 | a0001 | c0003 | t0003 | g0056 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18944 | hp1 | a0001 | c0002 | t0001 | g0239 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0214 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0275 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18962 | hp1 | a0001 | c0001 | t0005 | g0091 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0237 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18963 | hp1 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18965 | hp2 | a0001 | c0002 | t0001 | g0240 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18969 | hp2 | a0001 | c0007 | t0001 | g0165 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0024 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18977 | hp2 | a0001 | c0002 | t0001 | g0213 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18981 | hp2 | a0001 | c0002 | t0001 | g0224 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0112 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA19009 | hp1 | a0001 | c0002 | t0001 | g0306 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0279 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0192 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA19030 | hp1 | a0001 | c0003 | t0001 | g0303 | AFR | LWK | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA19030 | hp2 | a0001 | c0002 | t0001 | g0212 | AFR | LWK | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | LWK | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA19043 | hp2 | a0001 | c0002 | t0001 | g0005 | AFR | LWK | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA19063 | hp1 | a0001 | c0003 | t0001 | g0096 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA19077 | hp1 | a0001 | c0002 | t0001 | g0281 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA19079 | hp1 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA19084 | hp2 | a0001 | c0002 | t0001 | g0170 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA19087 | hp1 | a0001 | c0002 | t0001 | g0099 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA19240 | hp1 | a0001 | c0013 | t0001 | g0308 | AFR | YRI | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0001 | AFR | YRI | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0033 | AFR | ASW | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0210 | AFR | ASW | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0215 | EUR | TSI | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0278 | AMR | CLM | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | ACB | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0025 | AFR | MSL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | MSL | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18955 | hp1 | a0001 | c0002 | t0001 | g0260 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0169 | AFR | USA | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0280 | AFR | USA | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA21309 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | LWK | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | LWK | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0058 | REF | REF | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0291 | REF | REF | TOM1_chr22_35294894_35352973 | TOM1 | chr22 | 35294894 | 35352973 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:35330471 | G | A | 1 | a0003 | 1 | HG01261.hp1 | missense_variant | MODERATE | c.890G>A | p.Arg297His | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 8/15 | 925/2278 | 890/1479 | 297/492 | chr22 | 35330471 | |||
| chr22:35338744 | G | A | 1 | a0005 | 1 | HG01978.hp1 | missense_variant | MODERATE | c.1180G>A | p.Gly394Ser | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/15 | 1215/2278 | 1180/1479 | 394/492 | chr22 | 35338744 | |||
| chr22:35346940 | C | T | 1 | a0004 | 1 | HG01496.hp2 | missense_variant | MODERATE | c.1295C>T | p.Ala432Val | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 14/15 | 1330/2278 | 1295/1479 | 432/492 | chr22 | 35346940 | |||
| chr22:35347097 | G | A | 1 | a0002 | 1 | HG01081.hp2 | missense_variant | MODERATE | c.1367G>A | p.Arg456Gln | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 15/15 | 1402/2278 | 1367/1479 | 456/492 | chr22 | 35347097 | |||
| chr22:35347136 | C | T | 1 | a0006 | 1 | HG04228.hp1 | missense_variant | MODERATE | c.1406C>T | p.Pro469Leu | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 15/15 | 1441/2278 | 1406/1479 | 469/492 | chr22 | 35347136 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:35317938 | C | T | 2 | a0001c0013 a0001c0014 |
2 | HG02055.hp2 NA19240.hp1 |
synonymous_variant | LOW | c.114C>T | p.Asp38Asp | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/15 | 149/2278 | 114/1479 | 38/492 | chr22 | 35317938 | |||
| chr22:35327327 | G | A | 1 | a0001c0004 | 2 | HG01099.hp2 HG02630.hp1 |
synonymous_variant | LOW | c.705G>A | p.Ser235Ser | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/15 | 740/2278 | 705/1479 | 235/492 | chr22 | 35327327 | |||
| chr22:35333424 | G | A | 1 | a0001c0006 | 1 | HG03225.hp2 | synonymous_variant | LOW | c.954G>A | p.Pro318Pro | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 10/15 | 989/2278 | 954/1479 | 318/492 | chr22 | 35333424 | |||
| chr22:35334410 | G | A | 1 | a0001c0007 | 1 | NA18969.hp2 | synonymous_variant | LOW | c.1110G>A | p.Ala370Ala | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/15 | 1145/2278 | 1110/1479 | 370/492 | chr22 | 35334410 | |||
| chr22:35346932 | T | G | 5 | a0001c0002 a0001c0003 a0001c0013 others(2): Show |
119 | HG00099.hp2 HG00323.hp2 HG00544.hp1 others(116): Show |
splice_region_variant&synonymous_variant | LOW | c.1287T>G | p.Gly429Gly | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 14/15 | 1322/2278 | 1287/1479 | 429/492 | chr22 | 35346932 | |||
| chr22:35347131 | G | C | 3 | a0001c0002 a0001c0013 a0005c0008 |
112 | HG00099.hp2 HG00323.hp2 HG00544.hp1 others(109): Show |
synonymous_variant | LOW | c.1401G>C | p.Gly467Gly | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 15/15 | 1436/2278 | 1401/1479 | 467/492 | chr22 | 35347131 | |||
| chr22:35347185 | T | C | 1 | a0001c0010 | 1 | HG01255.hp2 | synonymous_variant | LOW | c.1455T>C | p.Asp485Asp | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 15/15 | 1490/2278 | 1455/1479 | 485/492 | chr22 | 35347185 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:35299901 | G | A | 3 | a0001c0001t0002 a0001c0002t0002 a0001c0003t0002 |
7 | HG01069.hp2 HG01071.hp1 HG02886.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-28G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/15 | 28 | chr22 | 35299901 | ||||||
| chr22:35347210 | G | C | 1 | a0001c0003t0003 | 1 | NA18943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1G>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 15/15 | 1 | chr22 | 35347210 | ||||||
| chr22:35347342 | C | T | 1 | a0001c0001t0005 | 1 | NA18962.hp1 | 3_prime_UTR_variant | MODIFIER | c.*133C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 15/15 | 133 | chr22 | 35347342 | ||||||
| chr22:35347886 | G | T | 1 | a0001c0001t0004 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*677G>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 15/15 | 677 | chr22 | 35347886 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:35300021 | C | G | 2 | a0001c0013t0001g0308 a0001c0014t0001g0309 |
2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.52+41C>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35300021 | |||||||
| chr22:35300084 | G | A | 25 | a0001c0001t0001g0004 a0001c0001t0001g0031 a0001c0001t0001g0032 others(22): Show |
29 | HG01168.hp1 HG01169.hp2 HG02027.hp2 others(26): Show |
intron_variant | MODIFIER | c.52+104G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35300084 | |||||||
| chr22:35300084 | G | C | 132 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(129): Show |
151 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.52+104G>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35300084 | |||||||
| chr22:35300099 | G | T | 1 | a0001c0003t0001g0307 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.52+119G>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35300099 | |||||||
| chr22:35300148 | G | A | 1 | a0001c0002t0001g0170 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.52+168G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35300148 | |||||||
| chr22:35300287 | G | T | 1 | a0001c0002t0001g0306 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.52+307G>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35300287 | |||||||
| chr22:35300322 | G | A | 4 | a0001c0001t0001g0171 a0001c0002t0001g0009 a0001c0002t0001g0172 others(1): Show |
6 | HG02717.hp1 HG02976.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.52+342G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35300322 | |||||||
| chr22:35300511 | G | A | 2 | a0001c0013t0001g0308 a0001c0014t0001g0309 |
2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.52+531G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35300511 | |||||||
| chr22:35300515 | C | T | 2 | a0001c0002t0001g0002 a0001c0002t0001g0305 |
6 | HG02258.hp1 HG02572.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.52+535C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35300515 | |||||||
| chr22:35300737 | A | G | 1 | a0001c0001t0001g0052 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.52+757A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35300737 | |||||||
| chr22:35300905 | AC | A | 132 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(129): Show |
151 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.52+926delC | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35300905 | |||||||
| chr22:35300938 | A | G | 167 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(164): Show |
190 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.52+958A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35300938 | |||||||
| chr22:35301048 | C | CA | 55 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0031 others(52): Show |
59 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.52+1089dupA | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 35301048 | ||||||
| chr22:35301048 | CA | C | 5 | a0001c0001t0001g0052 a0001c0001t0001g0295 a0001c0002t0001g0005 others(2): Show |
7 | HG00099.hp1 HG02451.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.52+1089delA | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 35301048 | ||||||
| chr22:35301048 | CAAAAA | C | 125 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(122): Show |
144 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.52+1085_52+1089del others(5): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 35301048 | ||||||
| chr22:35301267 | T | A | 2 | a0001c0001t0001g0174 a0001c0001t0001g0175 |
2 | HG01192.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.52+1287T>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35301267 | |||||||
| chr22:35301273 | A | T | 1 | a0001c0001t0001g0294 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.52+1293A>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35301273 | |||||||
| chr22:35301312 | ATATATAT | A | 4 | a0001c0001t0001g0052 a0001c0002t0001g0005 a0001c0002t0001g0050 others(1): Show |
6 | HG02451.hp2 HG02818.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.52+1338_52+1344del others(7): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 35301312 | ||||||
| chr22:35301314 | ATATAT | A | 132 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(129): Show |
151 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.52+1340_52+1344del others(5): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 35301314 | ||||||
| chr22:35301370 | A | G | 9 | a0001c0001t0002g0297 a0001c0001t0002g0299 a0001c0002t0001g0302 others(6): Show |
9 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.52+1390A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35301370 | |||||||
| chr22:35301399 | A | G | 132 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(129): Show |
151 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.52+1419A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35301399 | |||||||
| chr22:35301523 | T | A | 1 | a0001c0001t0001g0176 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.52+1543T>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35301523 | |||||||
| chr22:35301527 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.52+1547C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35301527 | |||||||
| chr22:35301619 | G | C | 152 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(149): Show |
175 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.52+1639G>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35301619 | |||||||
| chr22:35301697 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.52+1717C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35301697 | |||||||
| chr22:35301702 | T | C | 1 | a0001c0001t0001g0037 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.52+1722T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35301702 | |||||||
| chr22:35301811 | C | CT | 132 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(129): Show |
151 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.52+1831_52+1832ins others(1): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35301811 | |||||||
| chr22:35301978 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.52+1998C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35301978 | |||||||
| chr22:35302037 | A | G | 1 | a0001c0002t0001g0173 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.52+2057A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35302037 | |||||||
| chr22:35302056 | C | T | 2 | a0001c0013t0001g0308 a0001c0014t0001g0309 |
2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.52+2076C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35302056 | |||||||
| chr22:35302069 | G | C | 4 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0002t0001g0030 others(1): Show |
4 | HG02280.hp2 HG02572.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.52+2089G>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35302069 | |||||||
| chr22:35302074 | G | A | 1 | a0001c0002t0001g0210 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.52+2094G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35302074 | |||||||
| chr22:35302255 | A | C | 4 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(1): Show |
4 | HG01168.hp1 HG01169.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.52+2275A>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35302255 | |||||||
| chr22:35302306 | T | C | 1 | a0001c0001t0001g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.52+2326T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35302306 | |||||||
| chr22:35302330 | CT | C | 220 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(217): Show |
259 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.52+2372delT | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 35302330 | ||||||
| chr22:35302330 | CTT | C | 26 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0034 others(23): Show |
30 | HG01257.hp2 HG02027.hp2 HG02132.hp2 others(27): Show |
intron_variant | MODIFIER | c.52+2371_52+2372del others(2): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 35302330 | ||||||
| chr22:35302330 | CTTT | C | 16 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0002g0297 others(13): Show |
18 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.52+2370_52+2372del others(3): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 35302330 | ||||||
| chr22:35302330 | CTTTT | C | 10 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0037 others(7): Show |
10 | HG01168.hp1 HG01169.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.52+2369_52+2372del others(4): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 35302330 | ||||||
| chr22:35302336 | T | C | 1 | a0001c0001t0001g0211 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.52+2356T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35302336 | |||||||
| chr22:35302337 | T | C | 3 | a0001c0002t0001g0002 a0001c0002t0001g0212 a0001c0002t0001g0305 |
7 | HG02258.hp1 HG02572.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.52+2357T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35302337 | |||||||
| chr22:35302358 | T | G | 132 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(129): Show |
151 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.52+2378T>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35302358 | |||||||
| chr22:35302422 | G | A | 130 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(127): Show |
149 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.52+2442G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35302422 | |||||||
| chr22:35302462 | AG | A | 152 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(149): Show |
175 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.52+2484delG | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 35302462 | ||||||
| chr22:35302484 | G | A | 1 | a0001c0001t0001g0037 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.52+2504G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35302484 | |||||||
| chr22:35302489 | G | A | 2 | a0001c0001t0001g0157 a0001c0001t0001g0158 |
2 | NA18939.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.52+2509G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35302489 | |||||||
| chr22:35302498 | G | A | 132 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(129): Show |
151 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.52+2518G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35302498 | |||||||
| chr22:35302600 | G | T | 1 | a0001c0001t0001g0156 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.52+2620G>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35302600 | |||||||
| chr22:35302620 | C | T | 2 | a0001c0002t0001g0154 a0001c0002t0001g0155 |
2 | HG02451.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.52+2640C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35302620 | |||||||
| chr22:35302697 | T | C | 1 | a0001c0001t0001g0061 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.52+2717T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35302697 | |||||||
| chr22:35302896 | C | A | 1 | a0001c0001t0001g0278 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.52+2916C>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35302896 | |||||||
| chr22:35302993 | C | T | 1 | a0001c0001t0001g0277 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.52+3013C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35302993 | |||||||
| chr22:35303052 | A | C | 132 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(129): Show |
151 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.52+3072A>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35303052 | |||||||
| chr22:35303110 | T | G | 2 | a0001c0002t0001g0062 a0001c0002t0001g0063 |
2 | HG00099.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.52+3130T>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35303110 | |||||||
| chr22:35303111 | T | G | 15 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0035 others(12): Show |
19 | HG02027.hp2 HG02132.hp2 HG02155.hp1 others(16): Show |
intron_variant | MODIFIER | c.52+3131T>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35303111 | |||||||
| chr22:35303131 | A | AACACACA others(3): Show |
140 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(137): Show |
163 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.52+3160_52+3169dup others(10): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 35303131 | ||||||
| chr22:35303131 | A | AACACACA others(5): Show |
6 | a0001c0001t0001g0038 a0001c0001t0001g0053 a0001c0001t0001g0065 others(3): Show |
6 | HG02735.hp1 HG03017.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.52+3158_52+3169dup others(12): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 35303131 | ||||||
| chr22:35303131 | A | AACACACA others(11): Show |
4 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0002t0001g0030 others(1): Show |
4 | HG02280.hp2 HG02572.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.52+3152_52+3169dup others(18): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 35303131 | ||||||
| chr22:35303202 | C | T | 1 | a0001c0001t0001g0044 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.52+3222C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35303202 | |||||||
| chr22:35303272 | C | T | 15 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0035 others(12): Show |
19 | HG02027.hp2 HG02132.hp2 HG02155.hp1 others(16): Show |
intron_variant | MODIFIER | c.52+3292C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35303272 | |||||||
| chr22:35303379 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.52+3399C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35303379 | |||||||
| chr22:35303460 | A | G | 132 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(129): Show |
151 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.52+3480A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35303460 | |||||||
| chr22:35303504 | C | CT | 14 | a0001c0001t0001g0036 a0001c0001t0001g0149 a0001c0001t0001g0150 others(11): Show |
14 | HG01175.hp1 HG02135.hp2 HG03098.hp1 others(11): Show |
intron_variant | MODIFIER | c.52+3542dupT | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 35303504 | ||||||
| chr22:35303504 | CT | C | 8 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0177 others(5): Show |
8 | HG01069.hp1 HG01123.hp1 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.52+3542delT | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 35303504 | ||||||
| chr22:35303589 | C | T | 132 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(129): Show |
151 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.52+3609C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35303589 | |||||||
| chr22:35303620 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.52+3640C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35303620 | |||||||
| chr22:35303670 | G | A | 132 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(129): Show |
151 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.52+3690G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35303670 | |||||||
| chr22:35303766 | G | A | 132 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(129): Show |
151 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.52+3786G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35303766 | |||||||
| chr22:35303772 | G | A | 132 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(129): Show |
151 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.52+3792G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35303772 | |||||||
| chr22:35303823 | A | G | 1 | a0001c0001t0001g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.52+3843A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35303823 | |||||||
| chr22:35303826 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.52+3846C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35303826 | |||||||
| chr22:35303831 | A | G | 28 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0176 others(25): Show |
32 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.52+3851A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35303831 | |||||||
| chr22:35303864 | T | C | 2 | a0001c0001t0001g0070 a0001c0002t0001g0071 |
2 | HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.52+3884T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35303864 | |||||||
| chr22:35303890 | C | T | 132 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(129): Show |
151 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.52+3910C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35303890 | |||||||
| chr22:35303937 | T | C | 9 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0074 others(6): Show |
9 | HG00597.hp1 HG00609.hp1 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.52+3957T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35303937 | |||||||
| chr22:35303990 | C | T | 11 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0035 others(8): Show |
13 | HG02027.hp2 HG02132.hp2 HG02155.hp1 others(10): Show |
intron_variant | MODIFIER | c.52+4010C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35303990 | |||||||
| chr22:35304183 | C | T | 7 | a0001c0001t0001g0022 a0001c0001t0001g0144 a0001c0001t0001g0145 others(4): Show |
8 | HG00438.hp2 HG02056.hp1 NA18949.hp1 others(5): Show |
intron_variant | MODIFIER | c.52+4203C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35304183 | |||||||
| chr22:35304262 | A | G | 132 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(129): Show |
151 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.52+4282A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35304262 | |||||||
| chr22:35304419 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.52+4439G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35304419 | |||||||
| chr22:35304474 | G | A | 132 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(129): Show |
151 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.52+4494G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35304474 | |||||||
| chr22:35304495 | A | C | 1 | a0001c0002t0001g0013 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.52+4515A>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35304495 | |||||||
| chr22:35304495 | A | T | 131 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(128): Show |
149 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.52+4515A>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35304495 | |||||||
| chr22:35304526 | G | T | 132 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(129): Show |
151 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.52+4546G>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35304526 | |||||||
| chr22:35304624 | A | G | 197 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(194): Show |
224 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(221): Show |
intron_variant | MODIFIER | c.52+4644A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35304624 | |||||||
| chr22:35304730 | G | A | 1 | a0001c0001t0001g0082 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.52+4750G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35304730 | |||||||
| chr22:35304770 | A | G | 132 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(129): Show |
151 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.52+4790A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35304770 | |||||||
| chr22:35304774 | G | A | 132 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(129): Show |
151 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.52+4794G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35304774 | |||||||
| chr22:35304811 | A | T | 132 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(129): Show |
151 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.52+4831A>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35304811 | |||||||
| chr22:35305170 | C | T | 1 | a0001c0002t0001g0292 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.52+5190C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35305170 | |||||||
| chr22:35305230 | G | A | 132 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(129): Show |
151 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.52+5250G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35305230 | |||||||
| chr22:35305261 | G | A | 4 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(1): Show |
4 | HG01168.hp1 HG01169.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.52+5281G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35305261 | |||||||
| chr22:35305433 | G | A | 132 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(129): Show |
151 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.52+5453G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35305433 | |||||||
| chr22:35305457 | T | C | 294 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(291): Show |
341 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(338): Show |
intron_variant | MODIFIER | c.52+5477T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35305457 | |||||||
| chr22:35305464 | A | G | 32 | a0001c0001t0001g0012 a0001c0001t0001g0171 a0001c0001t0001g0191 others(29): Show |
36 | HG00423.hp1 HG00609.hp2 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.52+5484A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35305464 | |||||||
| chr22:35305580 | A | G | 132 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(129): Show |
151 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.52+5600A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35305580 | |||||||
| chr22:35305616 | C | T | 132 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(129): Show |
151 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.52+5636C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35305616 | |||||||
| chr22:35305658 | CAA | C | 132 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(129): Show |
151 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.52+5693_52+5694del others(2): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 35305658 | ||||||
| chr22:35305729 | T | G | 132 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(129): Show |
151 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.52+5749T>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35305729 | |||||||
| chr22:35305730 | G | A | 132 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(129): Show |
151 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.52+5750G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35305730 | |||||||
| chr22:35305859 | C | T | 4 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0142 others(1): Show |
6 | HG02293.hp2 NA18974.hp1 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.52+5879C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35305859 | |||||||
| chr22:35305860 | G | A | 1 | a0001c0001t0001g0045 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.52+5880G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35305860 | |||||||
| chr22:35305905 | A | AGAGTG | 132 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(129): Show |
151 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.52+5927_52+5928ins others(5): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 35305905 | ||||||
| chr22:35305967 | C | T | 1 | a0001c0001t0001g0251 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.52+5987C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35305967 | |||||||
| chr22:35306057 | G | T | 3 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0002t0001g0030 |
3 | HG02280.hp2 HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.52+6077G>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35306057 | |||||||
| chr22:35306075 | A | C | 198 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(195): Show |
225 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(222): Show |
intron_variant | MODIFIER | c.52+6095A>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35306075 | |||||||
| chr22:35306088 | A | G | 1 | a0001c0002t0001g0306 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.52+6108A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35306088 | |||||||
| chr22:35306144 | CT | C | 133 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(130): Show |
152 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.52+6174delT | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 35306144 | ||||||
| chr22:35306154 | T | C | 1 | a0001c0001t0001g0193 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.52+6174T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35306154 | |||||||
| chr22:35306181 | A | T | 132 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(129): Show |
151 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.52+6201A>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35306181 | |||||||
| chr22:35306303 | G | A | 4 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(1): Show |
4 | HG01168.hp1 HG01169.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.52+6323G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35306303 | |||||||
| chr22:35306379 | T | G | 2 | a0001c0013t0001g0308 a0001c0014t0001g0309 |
2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.52+6399T>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35306379 | |||||||
| chr22:35306446 | G | A | 15 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0035 others(12): Show |
19 | HG02027.hp2 HG02132.hp2 HG02155.hp1 others(16): Show |
intron_variant | MODIFIER | c.52+6466G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35306446 | |||||||
| chr22:35306711 | G | C | 1 | a0001c0002t0001g0218 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.52+6731G>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35306711 | |||||||
| chr22:35306748 | A | AC | 132 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(129): Show |
151 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.52+6771dupC | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 35306748 | ||||||
| chr22:35306958 | T | A | 1 | a0001c0001t0001g0159 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.52+6978T>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35306958 | |||||||
| chr22:35307041 | A | C | 1 | a0001c0001t0001g0207 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.52+7061A>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35307041 | |||||||
| chr22:35307135 | T | C | 130 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(127): Show |
149 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.52+7155T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35307135 | |||||||
| chr22:35307235 | T | C | 1 | a0001c0001t0001g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.52+7255T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35307235 | |||||||
| chr22:35307288 | A | G | 129 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(126): Show |
148 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.52+7308A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35307288 | |||||||
| chr22:35307323 | G | A | 2 | a0001c0013t0001g0308 a0001c0014t0001g0309 |
2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.52+7343G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35307323 | |||||||
| chr22:35307329 | T | G | 129 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(126): Show |
148 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.52+7349T>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35307329 | |||||||
| chr22:35307373 | T | C | 129 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(126): Show |
148 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.52+7393T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35307373 | |||||||
| chr22:35307462 | G | A | 4 | a0001c0001t0001g0028 a0001c0001t0001g0141 a0001c0001t0001g0284 others(1): Show |
5 | HG00099.hp1 HG02698.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.52+7482G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35307462 | |||||||
| chr22:35307464 | A | T | 1 | a0001c0002t0001g0281 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.52+7484A>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35307464 | |||||||
| chr22:35307558 | T | A | 284 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(281): Show |
331 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(328): Show |
intron_variant | MODIFIER | c.52+7578T>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35307558 | |||||||
| chr22:35307661 | T | C | 8 | a0001c0001t0002g0297 a0001c0001t0002g0299 a0001c0002t0002g0296 others(5): Show |
8 | HG01069.hp2 HG01071.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.52+7681T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35307661 | |||||||
| chr22:35308087 | C | A | 5 | a0001c0001t0001g0068 a0001c0001t0001g0083 a0001c0001t0001g0084 others(2): Show |
5 | HG00733.hp1 HG00741.hp1 HG01069.hp1 others(2): Show |
intron_variant | MODIFIER | c.52+8107C>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35308087 | |||||||
| chr22:35308155 | T | C | 1 | a0001c0010t0001g0219 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.52+8175T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35308155 | |||||||
| chr22:35308189 | A | G | 1 | a0001c0002t0001g0033 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.52+8209A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35308189 | |||||||
| chr22:35308199 | C | T | 3 | a0001c0002t0001g0005 a0001c0002t0001g0050 a0001c0002t0001g0051 |
5 | HG02451.hp2 HG03139.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.52+8219C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35308199 | |||||||
| chr22:35308217 | T | C | 3 | a0001c0002t0001g0002 a0001c0002t0001g0212 a0001c0002t0001g0305 |
7 | HG02258.hp1 HG02572.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.52+8237T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35308217 | |||||||
| chr22:35308228 | G | C | 130 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(127): Show |
149 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.52+8248G>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35308228 | |||||||
| chr22:35308275 | CT | C | 132 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(129): Show |
152 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.52+8310delT | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 35308275 | ||||||
| chr22:35308290 | T | C | 1 | a0001c0001t0001g0252 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.52+8310T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35308290 | |||||||
| chr22:35308291 | C | CT | 23 | a0001c0001t0001g0012 a0001c0001t0001g0036 a0001c0001t0001g0039 others(20): Show |
25 | HG00423.hp1 HG00609.hp2 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.52+8321dupT | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 35308291 | ||||||
| chr22:35308291 | C | T | 1 | a0001c0001t0001g0252 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.52+8311C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35308291 | |||||||
| chr22:35308355 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.52+8375C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35308355 | |||||||
| chr22:35308421 | C | G | 1 | a0001c0001t0001g0272 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.52+8441C>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35308421 | |||||||
| chr22:35308441 | A | G | 27 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0176 others(24): Show |
31 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.52+8461A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35308441 | |||||||
| chr22:35308602 | TCCCTGAC others(5): Show |
T | 1 | a0001c0001t0001g0216 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.52+8624_52+8635del others(12): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 35308602 | ||||||
| chr22:35308619 | G | C | 179 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(176): Show |
209 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(206): Show |
intron_variant | MODIFIER | c.52+8639G>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35308619 | |||||||
| chr22:35308654 | A | G | 1 | a0001c0001t0001g0143 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.52+8674A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35308654 | |||||||
| chr22:35309239 | G | T | 1 | a0001c0001t0001g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.53-8638G>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35309239 | |||||||
| chr22:35309366 | A | G | 160 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(157): Show |
184 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.53-8511A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35309366 | |||||||
| chr22:35309476 | T | C | 1 | a0001c0001t0001g0195 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.53-8401T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35309476 | |||||||
| chr22:35309523 | A | G | 1 | a0001c0002t0001g0064 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.53-8354A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35309523 | |||||||
| chr22:35309568 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.53-8309G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35309568 | |||||||
| chr22:35309636 | T | C | 1 | a0001c0001t0001g0087 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.53-8241T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35309636 | |||||||
| chr22:35309643 | C | CA | 127 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(124): Show |
146 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.53-8217dupA | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 35309643 | ||||||
| chr22:35309643 | CA | C | 6 | a0001c0001t0001g0216 a0001c0001t0001g0271 a0001c0002t0001g0236 others(3): Show |
6 | HG02723.hp2 HG02735.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.53-8217delA | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 35309643 | ||||||
| chr22:35309659 | A | G | 8 | a0001c0001t0001g0216 a0001c0001t0001g0238 a0001c0002t0001g0026 others(5): Show |
10 | HG00544.hp1 NA18939.hp2 NA18944.hp1 others(7): Show |
intron_variant | MODIFIER | c.53-8218A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35309659 | |||||||
| chr22:35309738 | A | T | 3 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0002t0001g0180 |
3 | HG02257.hp2 HG02818.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.53-8139A>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35309738 | |||||||
| chr22:35309875 | C | A | 1 | a0001c0002t0001g0253 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.53-8002C>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35309875 | |||||||
| chr22:35309878 | G | C | 1 | a0001c0002t0001g0088 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.53-7999G>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35309878 | |||||||
| chr22:35309949 | G | C | 128 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(125): Show |
147 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.53-7928G>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35309949 | |||||||
| chr22:35310040 | C | T | 2 | a0001c0001t0001g0019 a0001c0001t0001g0137 |
3 | HG03704.hp2 HG03834.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.53-7837C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35310040 | |||||||
| chr22:35310261 | T | TTAAAAGT others(311): Show |
4 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0002t0001g0030 others(1): Show |
4 | HG02280.hp2 HG02572.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.53-7604_53-7603ins others(318): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 35310261 | ||||||
| chr22:35310537 | G | C | 1 | a0001c0002t0001g0302 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.53-7340G>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35310537 | |||||||
| chr22:35310577 | G | A | 15 | a0001c0001t0001g0012 a0001c0001t0001g0252 a0001c0001t0001g0259 others(12): Show |
17 | HG00423.hp1 HG00609.hp2 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.53-7300G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35310577 | |||||||
| chr22:35310586 | A | G | 2 | a0001c0013t0001g0308 a0001c0014t0001g0309 |
2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.53-7291A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35310586 | |||||||
| chr22:35310670 | A | T | 2 | a0001c0013t0001g0308 a0001c0014t0001g0309 |
2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.53-7207A>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35310670 | |||||||
| chr22:35310727 | G | GGTACTGC others(5): Show |
1 | a0001c0001t0001g0216 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.53-7149_53-7138dup others(12): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 35310727 | ||||||
| chr22:35310743 | C | G | 1 | a0001c0001t0001g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.53-7134C>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35310743 | |||||||
| chr22:35310959 | G | A | 4 | a0001c0001t0001g0052 a0001c0002t0001g0005 a0001c0002t0001g0050 others(1): Show |
6 | HG02451.hp2 HG02818.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.53-6918G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35310959 | |||||||
| chr22:35311243 | G | A | 177 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(174): Show |
207 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(204): Show |
intron_variant | MODIFIER | c.53-6634G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35311243 | |||||||
| chr22:35311258 | C | A | 2 | a0001c0013t0001g0308 a0001c0014t0001g0309 |
2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.53-6619C>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35311258 | |||||||
| chr22:35311280 | G | T | 4 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0002t0001g0030 others(1): Show |
4 | HG02280.hp2 HG02572.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.53-6597G>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35311280 | |||||||
| chr22:35311335 | A | G | 1 | a0001c0001t0001g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.53-6542A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35311335 | |||||||
| chr22:35311358 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.53-6519C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35311358 | |||||||
| chr22:35311424 | G | A | 6 | a0001c0001t0001g0187 a0001c0001t0001g0277 a0001c0002t0001g0186 others(3): Show |
6 | HG01123.hp2 HG01358.hp2 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.53-6453G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35311424 | |||||||
| chr22:35311430 | T | C | 1 | a0001c0001t0001g0149 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.53-6447T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35311430 | |||||||
| chr22:35311431 | C | T | 1 | a0001c0001t0001g0149 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.53-6446C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35311431 | |||||||
| chr22:35311510 | G | A | 1 | a0001c0001t0001g0039 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.53-6367G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35311510 | |||||||
| chr22:35311595 | C | T | 10 | a0001c0001t0001g0187 a0001c0001t0001g0277 a0001c0002t0001g0186 others(7): Show |
10 | HG01106.hp1 HG01123.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.53-6282C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35311595 | |||||||
| chr22:35311604 | G | A | 2 | a0001c0013t0001g0308 a0001c0014t0001g0309 |
2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.53-6273G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35311604 | |||||||
| chr22:35311841 | A | C | 1 | a0001c0001t0001g0136 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.53-6036A>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35311841 | |||||||
| chr22:35311869 | G | A | 1 | a0001c0002t0001g0254 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.53-6008G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35311869 | |||||||
| chr22:35312176 | G | A | 1 | a0001c0002t0001g0255 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.53-5701G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35312176 | |||||||
| chr22:35312243 | CA | C | 26 | a0001c0001t0001g0038 a0001c0001t0001g0046 a0001c0001t0001g0047 others(23): Show |
28 | HG01069.hp2 HG01071.hp1 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.53-5618delA | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 35312243 | ||||||
| chr22:35312243 | CAA | C | 116 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(113): Show |
139 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(136): Show |
intron_variant | MODIFIER | c.53-5619_53-5618del others(2): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 35312243 | ||||||
| chr22:35312369 | G | A | 1 | a0001c0002t0001g0223 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.53-5508G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35312369 | |||||||
| chr22:35312438 | C | T | 2 | a0001c0013t0001g0308 a0001c0014t0001g0309 |
2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.53-5439C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35312438 | |||||||
| chr22:35312529 | G | A | 4 | a0001c0001t0001g0052 a0001c0002t0001g0005 a0001c0002t0001g0050 others(1): Show |
6 | HG02451.hp2 HG02818.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.53-5348G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35312529 | |||||||
| chr22:35312576 | A | G | 10 | a0001c0001t0001g0133 a0001c0002t0001g0062 a0001c0002t0001g0063 others(7): Show |
10 | HG00099.hp2 HG00323.hp2 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.53-5301A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35312576 | |||||||
| chr22:35312797 | C | T | 130 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(127): Show |
149 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.53-5080C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35312797 | |||||||
| chr22:35312806 | G | A | 128 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(125): Show |
147 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.53-5071G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35312806 | |||||||
| chr22:35312815 | A | G | 1 | a0001c0013t0001g0308 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.53-5062A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35312815 | |||||||
| chr22:35312828 | T | G | 1 | a0001c0001t0001g0070 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.53-5049T>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35312828 | |||||||
| chr22:35312843 | C | T | 1 | a0001c0001t0001g0127 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.53-5034C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35312843 | |||||||
| chr22:35313072 | G | A | 128 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(125): Show |
147 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.53-4805G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35313072 | |||||||
| chr22:35313117 | C | T | 1 | a0001c0001t0001g0041 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.53-4760C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35313117 | |||||||
| chr22:35313144 | C | T | 2 | a0001c0001t0001g0205 a0001c0001t0001g0206 |
2 | HG00438.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.53-4733C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35313144 | |||||||
| chr22:35313228 | T | C | 1 | a0001c0001t0001g0135 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.53-4649T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35313228 | |||||||
| chr22:35313240 | G | A | 1 | a0001c0001t0001g0041 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.53-4637G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35313240 | |||||||
| chr22:35313261 | C | T | 1 | a0001c0001t0001g0268 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.53-4616C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35313261 | |||||||
| chr22:35313313 | C | T | 2 | a0001c0001t0001g0157 a0001c0001t0001g0158 |
2 | NA18939.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.53-4564C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35313313 | |||||||
| chr22:35313344 | C | CA | 5 | a0001c0001t0001g0052 a0001c0001t0001g0089 a0001c0002t0001g0005 others(2): Show |
7 | HG02451.hp2 HG02818.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.53-4521dupA | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 35313344 | ||||||
| chr22:35313416 | G | A | 1 | a0001c0002t0001g0255 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.53-4461G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35313416 | |||||||
| chr22:35313551 | A | G | 2 | a0001c0001t0001g0174 a0001c0001t0001g0175 |
2 | HG01192.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.53-4326A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35313551 | |||||||
| chr22:35313772 | C | T | 10 | a0001c0001t0002g0297 a0001c0001t0002g0299 a0001c0002t0001g0302 others(7): Show |
10 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.53-4105C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35313772 | |||||||
| chr22:35313867 | C | T | 4 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(1): Show |
4 | HG01168.hp1 HG01169.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.53-4010C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35313867 | |||||||
| chr22:35313908 | G | A | 4 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0002t0001g0030 others(1): Show |
4 | HG02280.hp2 HG02572.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.53-3969G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35313908 | |||||||
| chr22:35314141 | A | G | 1 | a0001c0001t0001g0267 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.53-3736A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35314141 | |||||||
| chr22:35314180 | G | A | 3 | a0001c0002t0001g0213 a0001c0002t0001g0224 a0001c0002t0001g0279 |
3 | NA18977.hp2 NA18981.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.53-3697G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35314180 | |||||||
| chr22:35314217 | A | ATG | 131 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(128): Show |
150 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.53-3658_53-3657dup others(2): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 35314217 | ||||||
| chr22:35314224 | A | G | 3 | a0001c0002t0001g0013 a0001c0002t0001g0154 a0001c0002t0001g0155 |
4 | HG01070.hp1 HG01071.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.53-3653A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35314224 | |||||||
| chr22:35314238 | G | A | 24 | a0001c0001t0001g0004 a0001c0001t0001g0031 a0001c0001t0001g0032 others(21): Show |
29 | HG00642.hp1 HG01175.hp1 HG01255.hp2 others(26): Show |
intron_variant | MODIFIER | c.53-3639G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35314238 | |||||||
| chr22:35314324 | C | T | 10 | a0001c0001t0002g0297 a0001c0001t0002g0299 a0001c0002t0001g0302 others(7): Show |
10 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.53-3553C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35314324 | |||||||
| chr22:35314363 | A | G | 3 | a0001c0001t0001g0004 a0001c0001t0001g0035 a0001c0001t0001g0044 |
5 | HG02027.hp2 NA18612.hp1 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.53-3514A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35314363 | |||||||
| chr22:35314456 | C | T | 1 | a0001c0002t0001g0063 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.53-3421C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35314456 | |||||||
| chr22:35314456 | CG | C | 15 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0041 others(12): Show |
16 | HG00642.hp1 HG01175.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.53-3415delG | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 35314456 | ||||||
| chr22:35314712 | C | T | 2 | a0001c0003t0002g0300 a0001c0003t0002g0301 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.53-3165C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35314712 | |||||||
| chr22:35314879 | C | CTCATGAG others(1): Show |
10 | a0001c0001t0001g0038 a0001c0001t0001g0220 a0001c0001t0001g0294 others(7): Show |
11 | HG00642.hp1 HG01175.hp1 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.53-2996_53-2989dup others(8): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 35314879 | ||||||
| chr22:35315097 | C | T | 2 | a0001c0013t0001g0308 a0001c0014t0001g0309 |
2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.53-2780C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35315097 | |||||||
| chr22:35315105 | A | G | 130 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(127): Show |
149 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.53-2772A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35315105 | |||||||
| chr22:35315196 | A | G | 7 | a0001c0001t0001g0038 a0001c0001t0001g0052 a0001c0001t0002g0299 others(4): Show |
9 | HG02451.hp2 HG02818.hp2 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.53-2681A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35315196 | |||||||
| chr22:35315260 | G | C | 7 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0035 others(4): Show |
9 | HG02027.hp2 HG02132.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.53-2617G>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35315260 | |||||||
| chr22:35315328 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.53-2549G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35315328 | |||||||
| chr22:35315393 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.53-2484G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35315393 | |||||||
| chr22:35315451 | C | G | 1 | a0001c0001t0001g0271 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.53-2426C>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35315451 | |||||||
| chr22:35315452 | C | T | 1 | a0001c0001t0001g0271 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.53-2425C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35315452 | |||||||
| chr22:35315550 | A | C | 26 | a0001c0001t0001g0004 a0001c0001t0001g0031 a0001c0001t0001g0032 others(23): Show |
29 | HG00642.hp1 HG01175.hp1 HG01255.hp2 others(26): Show |
intron_variant | MODIFIER | c.53-2327A>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35315550 | |||||||
| chr22:35315718 | C | A | 1 | a0001c0002t0001g0210 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.53-2159C>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35315718 | |||||||
| chr22:35315820 | G | A | 2 | a0001c0013t0001g0308 a0001c0014t0001g0309 |
2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.53-2057G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35315820 | |||||||
| chr22:35315895 | A | G | 1 | a0001c0002t0001g0180 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.53-1982A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35315895 | |||||||
| chr22:35315938 | G | A | 1 | a0001c0002t0001g0224 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.53-1939G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35315938 | |||||||
| chr22:35315948 | C | T | 2 | a0001c0002t0001g0190 a0001c0002t0001g0215 |
2 | HG01106.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.53-1929C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35315948 | |||||||
| chr22:35315975 | G | A | 2 | a0001c0001t0001g0038 a0001c0001t0001g0065 |
2 | HG03471.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.53-1902G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35315975 | |||||||
| chr22:35316139 | C | T | 128 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(125): Show |
147 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.53-1738C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35316139 | |||||||
| chr22:35316184 | C | T | 128 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(125): Show |
147 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.53-1693C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35316184 | |||||||
| chr22:35316498 | T | C | 10 | a0001c0001t0002g0297 a0001c0001t0002g0299 a0001c0002t0001g0302 others(7): Show |
10 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.53-1379T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35316498 | |||||||
| chr22:35316560 | A | G | 160 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(157): Show |
184 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.53-1317A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35316560 | |||||||
| chr22:35316585 | G | A | 1 | a0001c0002t0001g0128 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.53-1292G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35316585 | |||||||
| chr22:35316621 | C | T | 128 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(125): Show |
147 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.53-1256C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35316621 | |||||||
| chr22:35316622 | G | A | 1 | a0001c0002t0001g0033 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.53-1255G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35316622 | |||||||
| chr22:35316629 | G | A | 2 | a0001c0013t0001g0308 a0001c0014t0001g0309 |
2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.53-1248G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35316629 | |||||||
| chr22:35317000 | C | T | 5 | a0001c0001t0001g0126 a0001c0001t0001g0187 a0001c0002t0001g0186 others(2): Show |
5 | HG01123.hp2 HG01358.hp2 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.53-877C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35317000 | |||||||
| chr22:35317091 | G | A | 1 | a0001c0001t0005g0091 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.53-786G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35317091 | |||||||
| chr22:35317206 | G | T | 5 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0125 others(2): Show |
7 | HG00597.hp2 NA18970.hp1 NA18971.hp2 others(4): Show |
intron_variant | MODIFIER | c.53-671G>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35317206 | |||||||
| chr22:35317353 | C | G | 2 | a0001c0001t0001g0174 a0001c0001t0001g0175 |
2 | HG01192.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.53-524C>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35317353 | |||||||
| chr22:35317468 | G | A | 2 | a0001c0013t0001g0308 a0001c0014t0001g0309 |
2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.53-409G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35317468 | |||||||
| chr22:35317523 | A | G | 3 | a0001c0002t0001g0213 a0001c0002t0001g0224 a0001c0002t0001g0279 |
3 | NA18977.hp2 NA18981.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.53-354A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35317523 | |||||||
| chr22:35317581 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.53-296G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35317581 | |||||||
| chr22:35317839 | A | G | 1 | a0001c0001t0001g0177 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.53-38A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 1/14 | chr22 | 35317839 | |||||||
| chr22:35318011 | C | T | 1 | a0001c0013t0001g0308 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.137+50C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | chr22 | 35318011 | |||||||
| chr22:35318052 | G | C | 1 | a0001c0001t0001g0191 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.137+91G>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | chr22 | 35318052 | |||||||
| chr22:35318214 | C | T | 2 | a0001c0013t0001g0308 a0001c0014t0001g0309 |
2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.137+253C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | chr22 | 35318214 | |||||||
| chr22:35318318 | G | A | 3 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0002t0001g0030 |
3 | HG02280.hp2 HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.137+357G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | chr22 | 35318318 | |||||||
| chr22:35318466 | G | A | 1 | a0001c0001t0001g0144 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.137+505G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | chr22 | 35318466 | |||||||
| chr22:35318645 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.137+684C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | chr22 | 35318645 | |||||||
| chr22:35318657 | G | T | 3 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0002t0001g0030 |
3 | HG02280.hp2 HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.137+696G>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | chr22 | 35318657 | |||||||
| chr22:35318747 | G | T | 24 | a0001c0001t0001g0004 a0001c0001t0001g0031 a0001c0001t0001g0032 others(21): Show |
27 | HG00642.hp1 HG01175.hp1 HG01255.hp2 others(24): Show |
intron_variant | MODIFIER | c.137+786G>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | chr22 | 35318747 | |||||||
| chr22:35318760 | G | A | 24 | a0001c0001t0001g0004 a0001c0001t0001g0031 a0001c0001t0001g0032 others(21): Show |
27 | HG00642.hp1 HG01175.hp1 HG01255.hp2 others(24): Show |
intron_variant | MODIFIER | c.137+799G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | chr22 | 35318760 | |||||||
| chr22:35318986 | T | C | 12 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0035 others(9): Show |
14 | HG02027.hp2 HG02132.hp2 HG02155.hp1 others(11): Show |
intron_variant | MODIFIER | c.137+1025T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | chr22 | 35318986 | |||||||
| chr22:35319271 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.137+1310C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | chr22 | 35319271 | |||||||
| chr22:35319275 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.137+1314G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | chr22 | 35319275 | |||||||
| chr22:35319392 | G | A | 5 | a0001c0001t0001g0068 a0001c0001t0001g0083 a0001c0001t0001g0084 others(2): Show |
5 | HG00733.hp1 HG00741.hp1 HG01069.hp1 others(2): Show |
intron_variant | MODIFIER | c.137+1431G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | chr22 | 35319392 | |||||||
| chr22:35319816 | G | C | 27 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0176 others(24): Show |
31 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.137+1855G>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | chr22 | 35319816 | |||||||
| chr22:35319848 | T | C | 1 | a0001c0001t0001g0159 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.137+1887T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | chr22 | 35319848 | |||||||
| chr22:35319857 | G | A | 21 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0035 others(18): Show |
24 | HG00642.hp1 HG01175.hp1 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.137+1896G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | chr22 | 35319857 | |||||||
| chr22:35319949 | G | A | 3 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0002t0001g0030 |
3 | HG02280.hp2 HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.137+1988G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | chr22 | 35319949 | |||||||
| chr22:35319964 | C | T | 11 | a0001c0001t0001g0171 a0001c0002t0001g0009 a0001c0002t0001g0172 others(8): Show |
13 | HG01891.hp2 HG02717.hp1 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.138-1995C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | chr22 | 35319964 | |||||||
| chr22:35320122 | A | C | 1 | a0001c0001t0001g0124 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.138-1837A>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | chr22 | 35320122 | |||||||
| chr22:35320269 | A | G | 1 | a0001c0001t0001g0149 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.138-1690A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | chr22 | 35320269 | |||||||
| chr22:35320364 | G | A | 2 | a0001c0001t0001g0157 a0001c0001t0001g0158 |
2 | NA18939.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.138-1595G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | chr22 | 35320364 | |||||||
| chr22:35320497 | G | A | 1 | a0001c0002t0001g0241 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.138-1462G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | chr22 | 35320497 | |||||||
| chr22:35320601 | G | C | 155 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(152): Show |
179 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.138-1358G>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | chr22 | 35320601 | |||||||
| chr22:35320987 | G | GA | 25 | a0001c0001t0001g0004 a0001c0001t0001g0031 a0001c0001t0001g0032 others(22): Show |
28 | HG00642.hp1 HG01175.hp1 HG01255.hp2 others(25): Show |
intron_variant | MODIFIER | c.138-958dupA | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr22 | 35320987 | ||||||
| chr22:35320987 | G | GAAAAAAA others(5): Show |
1 | a0001c0002t0001g0033 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.138-969_138-958dup others(12): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr22 | 35320987 | ||||||
| chr22:35320987 | G | GAAAAAAA others(6): Show |
2 | a0001c0001t0001g0038 a0001c0001t0001g0123 |
2 | HG01099.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.138-970_138-958dup others(13): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr22 | 35320987 | ||||||
| chr22:35320987 | G | GAAAAAAA others(7): Show |
87 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(84): Show |
102 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.138-971_138-958dup others(14): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr22 | 35320987 | ||||||
| chr22:35320987 | G | GAAAAAAA others(8): Show |
40 | a0001c0001t0001g0014 a0001c0001t0001g0019 a0001c0001t0001g0053 others(37): Show |
44 | HG00438.hp2 HG01346.hp2 HG01433.hp1 others(41): Show |
intron_variant | MODIFIER | c.138-958_138-957ins others(15): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr22 | 35320987 | ||||||
| chr22:35320987 | G | GAAAAAAA others(9): Show |
1 | a0001c0001t0001g0092 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.138-958_138-957ins others(16): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr22 | 35320987 | ||||||
| chr22:35320987 | G | GAAAAAAA others(10): Show |
1 | a0001c0002t0001g0129 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.138-958_138-957ins others(17): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr22 | 35320987 | ||||||
| chr22:35321000 | A | AAAAAAAA others(7): Show |
4 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0125 others(1): Show |
6 | HG00597.hp2 NA18971.hp2 NA18973.hp2 others(3): Show |
intron_variant | MODIFIER | c.138-958_138-957ins others(14): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr22 | 35321000 | ||||||
| chr22:35321222 | G | T | 2 | a0001c0013t0001g0308 a0001c0014t0001g0309 |
2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.138-737G>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | chr22 | 35321222 | |||||||
| chr22:35321253 | T | C | 160 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(157): Show |
184 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.138-706T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | chr22 | 35321253 | |||||||
| chr22:35321382 | C | A | 1 | a0001c0001t0001g0083 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.138-577C>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | chr22 | 35321382 | |||||||
| chr22:35321406 | T | C | 3 | a0001c0001t0001g0022 a0001c0001t0001g0089 a0001c0001t0001g0148 |
4 | NA18981.hp1 NA18990.hp2 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.138-553T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | chr22 | 35321406 | |||||||
| chr22:35321547 | T | C | 24 | a0001c0001t0001g0004 a0001c0001t0001g0031 a0001c0001t0001g0032 others(21): Show |
27 | HG00642.hp1 HG01175.hp1 HG01255.hp2 others(24): Show |
intron_variant | MODIFIER | c.138-412T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | chr22 | 35321547 | |||||||
| chr22:35321601 | G | A | 1 | a0001c0002t0001g0064 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.138-358G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | chr22 | 35321601 | |||||||
| chr22:35321750 | C | T | 1 | a0001c0002t0001g0275 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.138-209C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | chr22 | 35321750 | |||||||
| chr22:35321842 | A | C | 8 | a0001c0002t0001g0001 a0001c0002t0001g0025 a0001c0002t0001g0208 others(5): Show |
16 | HG01884.hp1 HG02055.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.138-117A>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | chr22 | 35321842 | |||||||
| chr22:35321878 | A | G | 1 | a0001c0001t0001g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.138-81A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 2/14 | chr22 | 35321878 | |||||||
| chr22:35322108 | C | T | 1 | a0001c0001t0001g0034 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.216+71C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 3/14 | chr22 | 35322108 | |||||||
| chr22:35322247 | G | A | 2 | a0001c0001t0001g0038 a0001c0002t0001g0033 |
2 | HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.216+210G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 3/14 | chr22 | 35322247 | |||||||
| chr22:35322255 | C | A | 1 | a0001c0001t0001g0093 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.216+218C>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 3/14 | chr22 | 35322255 | |||||||
| chr22:35322297 | C | T | 19 | a0001c0001t0001g0004 a0001c0001t0001g0031 a0001c0001t0001g0032 others(16): Show |
22 | HG00642.hp1 HG01175.hp1 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.216+260C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 3/14 | chr22 | 35322297 | |||||||
| chr22:35322325 | C | T | 1 | a0001c0001t0001g0166 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.216+288C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 3/14 | chr22 | 35322325 | |||||||
| chr22:35322360 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.216+323G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 3/14 | chr22 | 35322360 | |||||||
| chr22:35322384 | G | A | 2 | a0001c0001t0001g0052 a0001c0002t0001g0033 |
2 | HG02818.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.216+347G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 3/14 | chr22 | 35322384 | |||||||
| chr22:35322437 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.216+400C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 3/14 | chr22 | 35322437 | |||||||
| chr22:35322798 | T | G | 1 | a0001c0001t0001g0082 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.217-230T>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 3/14 | chr22 | 35322798 | |||||||
| chr22:35322823 | C | T | 2 | a0001c0013t0001g0308 a0001c0014t0001g0309 |
2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.217-205C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 3/14 | chr22 | 35322823 | |||||||
| chr22:35322941 | G | A | 1 | a0001c0002t0001g0242 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.217-87G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 3/14 | chr22 | 35322941 | |||||||
| chr22:35323290 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.366+113C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 4/14 | chr22 | 35323290 | |||||||
| chr22:35323308 | G | A | 17 | a0001c0001t0001g0216 a0001c0001t0001g0238 a0001c0002t0001g0024 others(14): Show |
19 | HG00733.hp2 HG01074.hp1 HG02698.hp2 others(16): Show |
intron_variant | MODIFIER | c.366+131G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 4/14 | chr22 | 35323308 | |||||||
| chr22:35323313 | G | C | 1 | a0001c0002t0001g0218 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.366+136G>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 4/14 | chr22 | 35323313 | |||||||
| chr22:35323385 | T | TA | 36 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0031 others(33): Show |
41 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.367-96dupA | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr22 | 35323385 | ||||||
| chr22:35323641 | T | G | 1 | a0001c0001t0001g0187 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.501+11T>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 5/14 | chr22 | 35323641 | |||||||
| chr22:35323732 | C | T | 2 | a0001c0001t0001g0174 a0001c0001t0001g0175 |
2 | HG01192.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.502-36C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 5/14 | chr22 | 35323732 | |||||||
| chr22:35323961 | A | G | 1 | a0001c0002t0001g0258 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.648+47A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 6/14 | chr22 | 35323961 | |||||||
| chr22:35324142 | T | A | 1 | a0001c0001t0001g0145 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.648+228T>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 6/14 | chr22 | 35324142 | |||||||
| chr22:35324412 | C | CA | 30 | a0001c0001t0001g0019 a0001c0001t0001g0052 a0001c0001t0001g0053 others(27): Show |
43 | HG00423.hp2 HG01884.hp1 HG01943.hp2 others(40): Show |
intron_variant | MODIFIER | c.648+522dupA | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr22 | 35324412 | ||||||
| chr22:35324412 | C | CAA | 38 | a0001c0001t0001g0012 a0001c0001t0001g0032 a0001c0001t0001g0036 others(35): Show |
42 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.648+521_648+522dup others(2): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr22 | 35324412 | ||||||
| chr22:35324412 | C | CAAA | 6 | a0001c0001t0001g0031 a0001c0001t0001g0259 a0001c0002t0001g0192 others(3): Show |
6 | HG02572.hp2 NA18522.hp1 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.648+520_648+522dup others(3): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr22 | 35324412 | ||||||
| chr22:35324412 | CA | C | 16 | a0001c0001t0001g0038 a0001c0001t0001g0067 a0001c0001t0001g0082 others(13): Show |
16 | HG00323.hp2 HG01069.hp2 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.648+522delA | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr22 | 35324412 | ||||||
| chr22:35324412 | CAA | C | 8 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(5): Show |
8 | HG01099.hp2 HG01168.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.648+521_648+522del others(2): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr22 | 35324412 | ||||||
| chr22:35324950 | G | A | 1 | a0001c0001t0001g0267 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.648+1036G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 6/14 | chr22 | 35324950 | |||||||
| chr22:35324955 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.648+1041G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 6/14 | chr22 | 35324955 | |||||||
| chr22:35324996 | C | T | 1 | a0001c0001t0001g0061 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.648+1082C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 6/14 | chr22 | 35324996 | |||||||
| chr22:35325098 | T | C | 9 | a0001c0001t0001g0038 a0001c0001t0001g0046 a0001c0001t0001g0047 others(6): Show |
9 | HG01099.hp2 HG01168.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.648+1184T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 6/14 | chr22 | 35325098 | |||||||
| chr22:35325172 | G | A | 1 | a0001c0001t0001g0039 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.648+1258G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 6/14 | chr22 | 35325172 | |||||||
| chr22:35325218 | C | T | 2 | a0001c0003t0001g0303 a0001c0003t0001g0307 |
2 | HG02922.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.648+1304C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 6/14 | chr22 | 35325218 | |||||||
| chr22:35325285 | G | A | 2 | a0001c0003t0001g0303 a0001c0003t0001g0307 |
2 | HG02922.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.648+1371G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 6/14 | chr22 | 35325285 | |||||||
| chr22:35325495 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.648+1581G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 6/14 | chr22 | 35325495 | |||||||
| chr22:35325742 | T | C | 3 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0272 |
3 | HG01261.hp2 HG01943.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.649-1529T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 6/14 | chr22 | 35325742 | |||||||
| chr22:35325761 | T | G | 2 | a0001c0003t0001g0303 a0001c0003t0001g0307 |
2 | HG02922.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.649-1510T>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 6/14 | chr22 | 35325761 | |||||||
| chr22:35325796 | A | G | 1 | a0001c0001t0001g0171 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.649-1475A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 6/14 | chr22 | 35325796 | |||||||
| chr22:35325857 | A | T | 39 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0018 others(36): Show |
42 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.649-1414A>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 6/14 | chr22 | 35325857 | |||||||
| chr22:35326018 | G | A | 59 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0031 others(56): Show |
65 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.649-1253G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 6/14 | chr22 | 35326018 | |||||||
| chr22:35326133 | T | C | 28 | a0001c0001t0001g0012 a0001c0001t0001g0036 a0001c0001t0001g0039 others(25): Show |
30 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.649-1138T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 6/14 | chr22 | 35326133 | |||||||
| chr22:35326358 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.649-913C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 6/14 | chr22 | 35326358 | |||||||
| chr22:35326444 | C | T | 3 | a0001c0002t0001g0005 a0001c0002t0001g0050 a0001c0002t0001g0051 |
5 | HG02451.hp2 HG03139.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.649-827C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 6/14 | chr22 | 35326444 | |||||||
| chr22:35326452 | C | G | 2 | a0001c0001t0001g0289 a0001c0001t0001g0290 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.649-819C>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 6/14 | chr22 | 35326452 | |||||||
| chr22:35326470 | T | C | 1 | a0001c0001t0001g0045 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.649-801T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 6/14 | chr22 | 35326470 | |||||||
| chr22:35326590 | G | A | 2 | a0001c0002t0001g0154 a0001c0002t0001g0155 |
2 | HG02451.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.649-681G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 6/14 | chr22 | 35326590 | |||||||
| chr22:35326668 | G | A | 2 | a0001c0001t0001g0020 a0001c0001t0001g0143 |
3 | NA18975.hp1 NA19012.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.649-603G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 6/14 | chr22 | 35326668 | |||||||
| chr22:35326688 | G | A | 2 | a0001c0001t0001g0034 a0001c0001t0001g0151 |
2 | HG02132.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.649-583G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 6/14 | chr22 | 35326688 | |||||||
| chr22:35326757 | C | T | 1 | a0001c0001t0001g0122 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.649-514C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 6/14 | chr22 | 35326757 | |||||||
| chr22:35326822 | G | T | 1 | a0001c0001t0001g0052 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.649-449G>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 6/14 | chr22 | 35326822 | |||||||
| chr22:35327238 | G | T | 1 | a0001c0001t0001g0074 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.649-33G>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 6/14 | chr22 | 35327238 | |||||||
| chr22:35327252 | G | A | 3 | a0001c0001t0001g0045 a0001c0001t0001g0256 a0001c0002t0001g0130 |
3 | HG02148.hp1 HG02809.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.649-19G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 6/14 | chr22 | 35327252 | |||||||
| chr22:35327456 | C | G | 1 | a0001c0002t0001g0033 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.765+69C>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35327456 | |||||||
| chr22:35327457 | A | G | 1 | a0001c0001t0002g0299 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.765+70A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35327457 | |||||||
| chr22:35327559 | G | A | 1 | a0001c0002t0001g0050 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.765+172G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35327559 | |||||||
| chr22:35327635 | A | G | 1 | a0004c0012t0001g0229 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.765+248A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35327635 | |||||||
| chr22:35327660 | T | C | 1 | a0001c0002t0001g0129 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.765+273T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35327660 | |||||||
| chr22:35327725 | C | T | 5 | a0001c0001t0001g0004 a0001c0001t0001g0035 a0001c0001t0001g0044 others(2): Show |
7 | HG02027.hp2 HG02809.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.765+338C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35327725 | |||||||
| chr22:35327746 | A | G | 3 | a0001c0001t0001g0220 a0001c0001t0001g0289 a0001c0001t0001g0290 |
3 | HG01256.hp2 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.765+359A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35327746 | |||||||
| chr22:35327757 | G | A | 1 | a0001c0001t0001g0106 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.765+370G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35327757 | |||||||
| chr22:35327827 | G | A | 1 | a0001c0003t0001g0307 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.765+440G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35327827 | |||||||
| chr22:35327838 | A | G | 243 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(240): Show |
287 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(284): Show |
intron_variant | MODIFIER | c.765+451A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35327838 | |||||||
| chr22:35327862 | A | G | 1 | a0001c0001t0001g0065 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.765+475A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35327862 | |||||||
| chr22:35327877 | C | T | 6 | a0001c0001t0001g0036 a0001c0001t0001g0039 a0001c0001t0001g0040 others(3): Show |
6 | HG00621.hp2 HG02155.hp1 NA18957.hp2 others(3): Show |
intron_variant | MODIFIER | c.765+490C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35327877 | |||||||
| chr22:35328131 | C | T | 2 | a0001c0013t0001g0308 a0001c0014t0001g0309 |
2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.765+744C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35328131 | |||||||
| chr22:35328238 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.765+851C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35328238 | |||||||
| chr22:35328260 | G | A | 1 | a0001c0001t0001g0274 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.765+873G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35328260 | |||||||
| chr22:35328271 | G | C | 23 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0054 others(20): Show |
27 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(24): Show |
intron_variant | MODIFIER | c.765+884G>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35328271 | |||||||
| chr22:35328293 | G | A | 35 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0031 others(32): Show |
39 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.765+906G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35328293 | |||||||
| chr22:35328430 | C | T | 1 | a0001c0002t0001g0050 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.765+1043C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35328430 | |||||||
| chr22:35328491 | C | T | 2 | a0001c0003t0002g0300 a0001c0003t0002g0301 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.765+1104C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35328491 | |||||||
| chr22:35328504 | A | T | 1 | a0001c0004t0001g0245 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.765+1117A>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35328504 | |||||||
| chr22:35328511 | G | A | 1 | a0001c0004t0001g0245 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.765+1124G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35328511 | |||||||
| chr22:35328539 | G | A | 2 | a0001c0001t0001g0015 a0001c0001t0001g0059 |
3 | HG01175.hp2 HG01257.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.765+1152G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35328539 | |||||||
| chr22:35328666 | C | A | 109 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(106): Show |
137 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.765+1279C>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35328666 | |||||||
| chr22:35328808 | G | A | 2 | a0001c0002t0001g0154 a0001c0002t0001g0155 |
2 | HG02451.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.765+1421G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35328808 | |||||||
| chr22:35328822 | G | A | 12 | a0001c0001t0001g0004 a0001c0001t0001g0035 a0001c0001t0001g0036 others(9): Show |
14 | HG00621.hp2 HG01175.hp1 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.765+1435G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35328822 | |||||||
| chr22:35328856 | C | A | 1 | a0001c0001t0001g0082 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.765+1469C>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35328856 | |||||||
| chr22:35328857 | A | G | 1 | a0001c0001t0001g0082 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.765+1470A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35328857 | |||||||
| chr22:35328901 | C | G | 1 | a0001c0001t0001g0093 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.766-1446C>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35328901 | |||||||
| chr22:35328978 | C | T | 4 | a0001c0001t0001g0074 a0001c0001t0001g0094 a0001c0001t0001g0120 others(1): Show |
4 | HG01074.hp2 HG01928.hp1 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.766-1369C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35328978 | |||||||
| chr22:35329207 | C | T | 4 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0143 others(1): Show |
6 | HG02293.hp2 NA18974.hp1 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.766-1140C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35329207 | |||||||
| chr22:35329545 | A | G | 59 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0031 others(56): Show |
65 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.766-802A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35329545 | |||||||
| chr22:35329656 | A | G | 1 | a0001c0002t0001g0030 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.766-691A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35329656 | |||||||
| chr22:35329734 | T | C | 4 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0209 others(1): Show |
4 | HG00544.hp2 HG00673.hp1 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.766-613T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35329734 | |||||||
| chr22:35329801 | G | A | 14 | a0001c0001t0001g0171 a0001c0001t0001g0191 a0001c0002t0001g0009 others(11): Show |
16 | HG01099.hp2 HG01884.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.766-546G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35329801 | |||||||
| chr22:35329813 | G | A | 7 | a0001c0001t0001g0004 a0001c0001t0001g0035 a0001c0001t0001g0044 others(4): Show |
9 | HG01175.hp1 HG02027.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.766-534G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35329813 | |||||||
| chr22:35330030 | A | T | 2 | a0001c0002t0001g0024 a0001c0002t0001g0170 |
3 | NA18943.hp1 NA18970.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.766-317A>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35330030 | |||||||
| chr22:35330144 | C | T | 1 | a0001c0002t0001g0134 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.766-203C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35330144 | |||||||
| chr22:35330287 | A | G | 2 | a0001c0001t0001g0289 a0001c0001t0001g0290 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.766-60A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35330287 | |||||||
| chr22:35330294 | C | T | 1 | a0001c0001t0001g0201 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.766-53C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 7/14 | chr22 | 35330294 | |||||||
| chr22:35330792 | G | A | 1 | a0001c0003t0001g0303 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.899+312G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 8/14 | chr22 | 35330792 | |||||||
| chr22:35330821 | C | A | 1 | a0001c0001t0001g0220 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.899+341C>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 8/14 | chr22 | 35330821 | |||||||
| chr22:35330842 | G | A | 2 | a0001c0002t0001g0230 a0001c0002t0001g0236 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.899+362G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 8/14 | chr22 | 35330842 | |||||||
| chr22:35331093 | C | CT | 57 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(54): Show |
63 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.899+633dupT | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr22 | 35331093 | ||||||
| chr22:35331093 | C | CTT | 5 | a0001c0001t0001g0004 a0001c0001t0001g0035 a0001c0001t0001g0044 others(2): Show |
7 | HG02027.hp2 NA18612.hp1 NA18977.hp1 others(4): Show |
intron_variant | MODIFIER | c.899+632_899+633dup others(2): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr22 | 35331093 | ||||||
| chr22:35331093 | CT | C | 15 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0059 others(12): Show |
15 | HG01099.hp2 HG01167.hp1 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.899+633delT | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr22 | 35331093 | ||||||
| chr22:35331093 | CTT | C | 13 | a0001c0001t0001g0046 a0001c0001t0001g0171 a0001c0001t0001g0191 others(10): Show |
15 | HG01169.hp2 HG01884.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.899+632_899+633del others(2): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr22 | 35331093 | ||||||
| chr22:35331161 | T | C | 2 | a0001c0001t0001g0108 a0001c0001t0001g0159 |
2 | HG02135.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.899+681T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 8/14 | chr22 | 35331161 | |||||||
| chr22:35331272 | CT | C | 11 | a0001c0001t0001g0004 a0001c0001t0001g0031 a0001c0001t0001g0032 others(8): Show |
13 | HG01175.hp1 HG02027.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.899+805delT | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr22 | 35331272 | ||||||
| chr22:35331510 | C | G | 1 | a0001c0002t0001g0210 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.899+1030C>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 8/14 | chr22 | 35331510 | |||||||
| chr22:35331983 | G | A | 3 | a0001c0001t0001g0098 a0001c0001t0001g0109 a0001c0001t0001g0110 |
3 | HG00642.hp2 HG02148.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.900-998G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 8/14 | chr22 | 35331983 | |||||||
| chr22:35331985 | A | G | 1 | a0001c0002t0001g0279 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.900-996A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 8/14 | chr22 | 35331985 | |||||||
| chr22:35332106 | C | T | 2 | a0001c0013t0001g0308 a0001c0014t0001g0309 |
2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.900-875C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 8/14 | chr22 | 35332106 | |||||||
| chr22:35332150 | G | T | 2 | a0001c0003t0001g0303 a0001c0003t0001g0307 |
2 | HG02922.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.900-831G>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 8/14 | chr22 | 35332150 | |||||||
| chr22:35332293 | A | G | 1 | a0001c0010t0001g0219 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.900-688A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 8/14 | chr22 | 35332293 | |||||||
| chr22:35332362 | G | T | 1 | a0001c0001t0001g0090 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.900-619G>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 8/14 | chr22 | 35332362 | |||||||
| chr22:35332473 | T | C | 152 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(149): Show |
181 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(178): Show |
intron_variant | MODIFIER | c.900-508T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 8/14 | chr22 | 35332473 | |||||||
| chr22:35332554 | G | A | 2 | a0001c0001t0001g0037 a0001c0001t0002g0299 |
2 | HG02976.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.900-427G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 8/14 | chr22 | 35332554 | |||||||
| chr22:35332597 | CACACACA others(3): Show |
C | 122 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(119): Show |
149 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.900-374_900-365del others(10): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr22 | 35332597 | ||||||
| chr22:35332599 | CACACACA others(1): Show |
C | 5 | a0001c0001t0001g0038 a0001c0001t0001g0144 a0001c0001t0001g0171 others(2): Show |
5 | HG03098.hp2 HG03225.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.900-374_900-367del others(8): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr22 | 35332599 | ||||||
| chr22:35332605 | CAT | C | 56 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(53): Show |
62 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.900-374_900-373del others(2): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr22 | 35332605 | ||||||
| chr22:35332607 | T | C | 6 | a0001c0001t0001g0004 a0001c0001t0001g0035 a0001c0001t0001g0044 others(3): Show |
8 | HG01993.hp1 HG02027.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.900-374T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 8/14 | chr22 | 35332607 | |||||||
| chr22:35332676 | A | T | 2 | a0001c0003t0001g0303 a0001c0003t0001g0307 |
2 | HG02922.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.900-305A>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 8/14 | chr22 | 35332676 | |||||||
| chr22:35332714 | A | G | 1 | a0001c0003t0001g0303 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.900-267A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 8/14 | chr22 | 35332714 | |||||||
| chr22:35332810 | A | G | 1 | a0001c0001t0001g0151 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.900-171A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 8/14 | chr22 | 35332810 | |||||||
| chr22:35332883 | G | A | 1 | a0001c0002t0001g0243 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.900-98G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 8/14 | chr22 | 35332883 | |||||||
| chr22:35333282 | T | A | 12 | a0001c0001t0001g0171 a0001c0001t0001g0191 a0001c0002t0001g0009 others(9): Show |
14 | HG01884.hp2 HG01891.hp2 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.934-122T>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 9/14 | chr22 | 35333282 | |||||||
| chr22:35333316 | G | C | 5 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0125 others(2): Show |
7 | HG00597.hp2 NA18971.hp2 NA18973.hp2 others(4): Show |
intron_variant | MODIFIER | c.934-88G>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 9/14 | chr22 | 35333316 | |||||||
| chr22:35333588 | A | G | 2 | a0001c0004t0001g0245 a0001c0004t0001g0250 |
2 | HG01099.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1027+91A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 10/14 | chr22 | 35333588 | |||||||
| chr22:35333614 | C | T | 7 | a0001c0001t0001g0011 a0001c0001t0001g0116 a0001c0001t0001g0147 others(4): Show |
9 | HG00558.hp2 HG02040.hp2 NA18942.hp2 others(6): Show |
intron_variant | MODIFIER | c.1027+117C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 10/14 | chr22 | 35333614 | |||||||
| chr22:35333660 | G | A | 2 | a0001c0004t0001g0245 a0001c0004t0001g0250 |
2 | HG01099.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1027+163G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 10/14 | chr22 | 35333660 | |||||||
| chr22:35333673 | C | T | 1 | a0001c0002t0001g0033 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1027+176C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 10/14 | chr22 | 35333673 | |||||||
| chr22:35333677 | C | A | 1 | a0001c0002t0001g0013 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1027+180C>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 10/14 | chr22 | 35333677 | |||||||
| chr22:35333728 | G | A | 106 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(103): Show |
131 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.1027+231G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 10/14 | chr22 | 35333728 | |||||||
| chr22:35333743 | A | G | 1 | a0001c0001t0001g0256 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1027+246A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 10/14 | chr22 | 35333743 | |||||||
| chr22:35333849 | G | A | 2 | a0001c0013t0001g0308 a0001c0014t0001g0309 |
2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1027+352G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 10/14 | chr22 | 35333849 | |||||||
| chr22:35333853 | A | C | 1 | a0001c0003t0001g0307 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1027+356A>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 10/14 | chr22 | 35333853 | |||||||
| chr22:35333949 | C | G | 1 | a0001c0002t0001g0155 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1028-379C>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 10/14 | chr22 | 35333949 | |||||||
| chr22:35334092 | A | C | 182 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(179): Show |
217 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(214): Show |
intron_variant | MODIFIER | c.1028-236A>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 10/14 | chr22 | 35334092 | |||||||
| chr22:35334104 | C | T | 3 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0202 |
3 | HG02015.hp1 HG02818.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1028-224C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 10/14 | chr22 | 35334104 | |||||||
| chr22:35334197 | C | T | 1 | a0001c0001t0001g0127 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1028-131C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 10/14 | chr22 | 35334197 | |||||||
| chr22:35334200 | G | A | 1 | a0001c0002t0001g0186 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1028-128G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 10/14 | chr22 | 35334200 | |||||||
| chr22:35334204 | A | T | 3 | a0001c0002t0001g0005 a0001c0002t0001g0050 a0001c0002t0001g0051 |
5 | HG02451.hp2 HG03139.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1028-124A>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 10/14 | chr22 | 35334204 | |||||||
| chr22:35334261 | T | C | 1 | a0001c0003t0001g0307 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1028-67T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 10/14 | chr22 | 35334261 | |||||||
| chr22:35334616 | T | A | 1 | a0001c0001t0001g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1148+168T>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35334616 | |||||||
| chr22:35334771 | A | G | 1 | a0001c0001t0001g0075 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1148+323A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35334771 | |||||||
| chr22:35334786 | G | A | 1 | a0001c0002t0001g0129 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1148+338G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35334786 | |||||||
| chr22:35334841 | C | A | 1 | a0001c0001t0001g0259 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1148+393C>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35334841 | |||||||
| chr22:35334841 | C | G | 1 | a0001c0003t0001g0307 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1148+393C>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35334841 | |||||||
| chr22:35334850 | A | C | 13 | a0001c0001t0001g0019 a0001c0001t0001g0114 a0001c0001t0001g0115 others(10): Show |
14 | HG01106.hp1 HG01358.hp2 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.1148+402A>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35334850 | |||||||
| chr22:35334862 | A | C | 6 | a0001c0001t0002g0297 a0001c0002t0001g0172 a0001c0002t0002g0296 others(3): Show |
6 | HG01069.hp2 HG01071.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1148+414A>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35334862 | |||||||
| chr22:35334993 | C | T | 2 | a0001c0001t0001g0205 a0001c0001t0001g0206 |
2 | HG00438.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.1148+545C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35334993 | |||||||
| chr22:35335101 | G | A | 117 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0012 others(114): Show |
143 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.1148+653G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35335101 | |||||||
| chr22:35335109 | C | T | 27 | a0001c0001t0001g0008 a0001c0001t0001g0034 a0001c0001t0001g0039 others(24): Show |
30 | HG00544.hp2 HG00558.hp1 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.1148+661C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35335109 | |||||||
| chr22:35335182 | G | A | 7 | a0001c0001t0001g0006 a0001c0001t0001g0111 a0001c0001t0001g0138 others(4): Show |
10 | HG01070.hp1 HG01071.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.1148+734G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35335182 | |||||||
| chr22:35335252 | T | C | 254 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(251): Show |
300 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(297): Show |
intron_variant | MODIFIER | c.1148+804T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35335252 | |||||||
| chr22:35335411 | G | T | 4 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0002g0297 others(1): Show |
4 | HG02257.hp2 HG02818.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1148+963G>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35335411 | |||||||
| chr22:35335652 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1148+1204C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35335652 | |||||||
| chr22:35335653 | G | A | 1 | a0001c0003t0001g0303 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1148+1205G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35335653 | |||||||
| chr22:35335668 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1148+1220G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35335668 | |||||||
| chr22:35335680 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1148+1232C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35335680 | |||||||
| chr22:35335704 | G | A | 1 | a0001c0001t0001g0015 | 2 | HG01175.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1148+1256G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35335704 | |||||||
| chr22:35335762 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1148+1314G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35335762 | |||||||
| chr22:35335774 | T | C | 4 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(1): Show |
4 | HG01168.hp1 HG01169.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1148+1326T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35335774 | |||||||
| chr22:35335929 | G | A | 1 | a0004c0012t0001g0229 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1148+1481G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35335929 | |||||||
| chr22:35335964 | G | T | 4 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0002g0297 others(1): Show |
4 | HG02257.hp2 HG02818.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1148+1516G>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35335964 | |||||||
| chr22:35336193 | G | A | 1 | a0001c0001t0001g0042 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1148+1745G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35336193 | |||||||
| chr22:35336257 | G | A | 1 | a0001c0002t0001g0154 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1148+1809G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35336257 | |||||||
| chr22:35336307 | G | C | 1 | a0001c0001t0001g0117 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1148+1859G>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35336307 | |||||||
| chr22:35336574 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1148+2126G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35336574 | |||||||
| chr22:35336610 | C | T | 85 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(82): Show |
98 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.1149-2103C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35336610 | |||||||
| chr22:35336704 | C | T | 1 | a0001c0002t0001g0104 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1149-2009C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35336704 | |||||||
| chr22:35336847 | C | T | 1 | a0001c0001t0001g0294 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1149-1866C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35336847 | |||||||
| chr22:35336864 | C | T | 4 | a0001c0002t0001g0190 a0001c0002t0001g0215 a0001c0002t0001g0234 others(1): Show |
4 | HG01106.hp1 HG01192.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.1149-1849C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35336864 | |||||||
| chr22:35336911 | G | A | 114 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(111): Show |
131 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.1149-1802G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35336911 | |||||||
| chr22:35336942 | CT | C | 191 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(188): Show |
232 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(229): Show |
intron_variant | MODIFIER | c.1149-1755delT | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr22 | 35336942 | ||||||
| chr22:35337000 | G | A | 117 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(114): Show |
134 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.1149-1713G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35337000 | |||||||
| chr22:35337082 | G | A | 2 | a0001c0001t0001g0174 a0001c0001t0001g0175 |
2 | HG01192.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1149-1631G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35337082 | |||||||
| chr22:35337093 | C | T | 1 | a0001c0013t0001g0308 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1149-1620C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35337093 | |||||||
| chr22:35337180 | C | T | 2 | a0001c0002t0001g0186 a0001c0002t0001g0222 |
2 | HG01928.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.1149-1533C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35337180 | |||||||
| chr22:35337259 | T | C | 1 | a0001c0001t0001g0247 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1149-1454T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35337259 | |||||||
| chr22:35337311 | A | G | 1 | a0001c0001t0001g0057 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1149-1402A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35337311 | |||||||
| chr22:35337314 | C | T | 6 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(3): Show |
6 | HG01168.hp1 HG01169.hp2 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.1149-1399C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35337314 | |||||||
| chr22:35337343 | G | C | 114 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(111): Show |
131 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.1149-1370G>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35337343 | |||||||
| chr22:35337399 | C | T | 11 | a0001c0001t0001g0004 a0001c0001t0001g0035 a0001c0001t0001g0044 others(8): Show |
13 | HG00323.hp1 HG00544.hp2 HG00673.hp1 others(10): Show |
intron_variant | MODIFIER | c.1149-1314C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35337399 | |||||||
| chr22:35337462 | G | A | 2 | a0001c0001t0001g0122 a0001c0001t0001g0162 |
2 | HG00423.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.1149-1251G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35337462 | |||||||
| chr22:35337661 | G | A | 110 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(107): Show |
127 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.1149-1052G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35337661 | |||||||
| chr22:35337715 | C | T | 117 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(114): Show |
134 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.1149-998C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35337715 | |||||||
| chr22:35337729 | G | A | 11 | a0001c0001t0001g0004 a0001c0001t0001g0035 a0001c0001t0001g0044 others(8): Show |
13 | HG00323.hp1 HG00544.hp2 HG00673.hp1 others(10): Show |
intron_variant | MODIFIER | c.1149-984G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35337729 | |||||||
| chr22:35337929 | G | A | 1 | a0001c0001t0001g0248 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1149-784G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35337929 | |||||||
| chr22:35338109 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1149-604G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35338109 | |||||||
| chr22:35338154 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1149-559A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35338154 | |||||||
| chr22:35338265 | C | T | 1 | a0001c0001t0001g0037 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1149-448C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35338265 | |||||||
| chr22:35338314 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1149-399C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35338314 | |||||||
| chr22:35338429 | A | T | 1 | a0001c0001t0001g0093 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1149-284A>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35338429 | |||||||
| chr22:35338638 | C | T | 1 | a0001c0006t0001g0189 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1149-75C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 11/14 | chr22 | 35338638 | |||||||
| chr22:35339062 | G | A | 1 | a0001c0001t0001g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1224+274G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35339062 | |||||||
| chr22:35339108 | A | G | 1 | a0001c0001t0001g0167 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1224+320A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35339108 | |||||||
| chr22:35339366 | G | A | 1 | a0001c0001t0001g0183 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1224+578G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35339366 | |||||||
| chr22:35339615 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1224+827C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35339615 | |||||||
| chr22:35339661 | T | C | 1 | a0001c0002t0001g0186 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1224+873T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35339661 | |||||||
| chr22:35339711 | C | T | 1 | a0001c0002t0001g0305 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1224+923C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35339711 | |||||||
| chr22:35339732 | G | A | 1 | a0001c0002t0001g0128 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1224+944G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35339732 | |||||||
| chr22:35339759 | C | T | 4 | a0001c0001t0001g0037 a0001c0001t0001g0171 a0001c0001t0001g0191 others(1): Show |
4 | HG02976.hp1 HG03098.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1224+971C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35339759 | |||||||
| chr22:35339767 | G | A | 215 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(212): Show |
256 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(253): Show |
intron_variant | MODIFIER | c.1224+979G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35339767 | |||||||
| chr22:35339844 | C | G | 7 | a0001c0001t0001g0040 a0001c0001t0001g0066 a0001c0001t0001g0108 others(4): Show |
7 | HG02135.hp1 HG02523.hp1 NA18957.hp2 others(4): Show |
intron_variant | MODIFIER | c.1224+1056C>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35339844 | |||||||
| chr22:35339898 | C | T | 1 | a0001c0001t0001g0294 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1224+1110C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35339898 | |||||||
| chr22:35339903 | CA | C | 94 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(91): Show |
107 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.1224+1129delA | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 35339903 | ||||||
| chr22:35339910 | A | G | 16 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0053 others(13): Show |
20 | HG00438.hp1 HG00558.hp2 HG02040.hp2 others(17): Show |
intron_variant | MODIFIER | c.1224+1122A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35339910 | |||||||
| chr22:35339928 | T | C | 1 | a0001c0001t0001g0037 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1224+1140T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35339928 | |||||||
| chr22:35340144 | G | A | 3 | a0001c0002t0001g0025 a0001c0002t0001g0208 a0001c0002t0002g0304 |
4 | HG03195.hp1 HG03453.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1224+1356G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35340144 | |||||||
| chr22:35340209 | G | C | 1 | a0001c0003t0001g0303 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1224+1421G>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35340209 | |||||||
| chr22:35340233 | C | CGAGGAGG others(3): Show |
1 | a0001c0001t0001g0187 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1224+1455_1224+146 others(14): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 35340233 | ||||||
| chr22:35340315 | G | A | 5 | a0001c0001t0001g0037 a0001c0001t0001g0171 a0001c0001t0001g0191 others(2): Show |
5 | HG02976.hp1 HG03098.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1224+1527G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35340315 | |||||||
| chr22:35340434 | A | C | 1 | a0001c0001t0001g0294 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1224+1646A>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35340434 | |||||||
| chr22:35340715 | C | G | 20 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0037 others(17): Show |
24 | HG00438.hp1 HG00558.hp2 HG02040.hp2 others(21): Show |
intron_variant | MODIFIER | c.1224+1927C>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35340715 | |||||||
| chr22:35340738 | C | T | 2 | a0001c0001t0001g0006 a0001c0001t0001g0138 |
4 | HG01167.hp2 HG01168.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.1224+1950C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35340738 | |||||||
| chr22:35340827 | C | G | 1 | a0001c0001t0001g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1224+2039C>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35340827 | |||||||
| chr22:35341221 | C | G | 93 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(90): Show |
106 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.1224+2433C>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35341221 | |||||||
| chr22:35341229 | A | C | 3 | a0001c0003t0002g0300 a0001c0003t0002g0301 a0001c0014t0001g0309 |
3 | HG02055.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1224+2441A>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35341229 | |||||||
| chr22:35341252 | A | G | 3 | a0001c0003t0002g0300 a0001c0003t0002g0301 a0001c0014t0001g0309 |
3 | HG02055.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1224+2464A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35341252 | |||||||
| chr22:35341253 | C | A | 3 | a0001c0003t0002g0300 a0001c0003t0002g0301 a0001c0014t0001g0309 |
3 | HG02055.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1224+2465C>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35341253 | |||||||
| chr22:35341302 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1224+2514G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35341302 | |||||||
| chr22:35341348 | C | T | 2 | a0001c0001t0001g0046 a0001c0001t0001g0048 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1224+2560C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35341348 | |||||||
| chr22:35341399 | C | A | 3 | a0001c0001t0001g0227 a0001c0001t0001g0228 a0001c0001t0001g0277 |
3 | HG02074.hp1 HG02080.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.1224+2611C>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35341399 | |||||||
| chr22:35341468 | G | A | 101 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(98): Show |
114 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.1224+2680G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35341468 | |||||||
| chr22:35341539 | C | T | 3 | a0001c0003t0002g0300 a0001c0003t0002g0301 a0001c0014t0001g0309 |
3 | HG02055.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1224+2751C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35341539 | |||||||
| chr22:35341582 | C | T | 1 | a0001c0002t0001g0279 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1224+2794C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35341582 | |||||||
| chr22:35341583 | G | A | 1 | a0001c0013t0001g0308 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1224+2795G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35341583 | |||||||
| chr22:35341732 | T | C | 1 | a0001c0001t0001g0093 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1224+2944T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35341732 | |||||||
| chr22:35341746 | C | A | 1 | a0001c0001t0001g0267 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1224+2958C>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35341746 | |||||||
| chr22:35341825 | C | T | 2 | a0001c0001t0001g0093 a0001c0002t0001g0104 |
2 | HG02698.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1224+3037C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35341825 | |||||||
| chr22:35342038 | G | GGCTGAAG others(34): Show |
1 | a0001c0002t0001g0280 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1224+3251_1224+329 others(45): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 35342038 | ||||||
| chr22:35342222 | G | A | 1 | a0001c0001t0001g0151 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1224+3434G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342222 | |||||||
| chr22:35342293 | G | A | 1 | a0001c0002t0001g0013 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1225-3432G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342293 | |||||||
| chr22:35342390 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1225-3335C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342390 | |||||||
| chr22:35342412 | A | C | 4 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0037 others(1): Show |
4 | HG02572.hp2 HG02630.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1225-3313A>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342412 | |||||||
| chr22:35342495 | C | T | 217 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(214): Show |
258 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(255): Show |
intron_variant | MODIFIER | c.1225-3230C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342495 | |||||||
| chr22:35342554 | G | GGGATCCT others(3): Show |
17 | a0001c0001t0001g0004 a0001c0001t0001g0031 a0001c0001t0001g0032 others(14): Show |
19 | HG00323.hp1 HG00544.hp2 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.1225-3167_1225-315 others(14): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 35342554 | ||||||
| chr22:35342593 | T | G | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-3132T>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342593 | |||||||
| chr22:35342609 | T | A | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-3116T>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342609 | |||||||
| chr22:35342627 | T | G | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-3098T>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342627 | |||||||
| chr22:35342638 | A | T | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-3087A>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342638 | |||||||
| chr22:35342643 | T | G | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-3082T>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342643 | |||||||
| chr22:35342646 | T | G | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-3079T>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342646 | |||||||
| chr22:35342661 | T | G | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-3064T>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342661 | |||||||
| chr22:35342669 | A | T | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-3056A>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342669 | |||||||
| chr22:35342681 | T | G | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-3044T>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342681 | |||||||
| chr22:35342687 | C | A | 1 | a0001c0013t0001g0308 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1225-3038C>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342687 | |||||||
| chr22:35342688 | T | C | 1 | a0001c0013t0001g0308 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1225-3037T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342688 | |||||||
| chr22:35342727 | C | G | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2998C>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342727 | |||||||
| chr22:35342728 | A | C | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2997A>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342728 | |||||||
| chr22:35342729 | C | A | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2996C>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342729 | |||||||
| chr22:35342733 | A | T | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2992A>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342733 | |||||||
| chr22:35342741 | C | G | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2984C>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342741 | |||||||
| chr22:35342743 | A | C | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2982A>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342743 | |||||||
| chr22:35342750 | T | G | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2975T>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342750 | |||||||
| chr22:35342751 | A | T | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2974A>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342751 | |||||||
| chr22:35342753 | A | T | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2972A>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342753 | |||||||
| chr22:35342755 | A | T | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2970A>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342755 | |||||||
| chr22:35342766 | A | T | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2959A>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342766 | |||||||
| chr22:35342768 | A | T | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2957A>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342768 | |||||||
| chr22:35342774 | A | G | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2951A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342774 | |||||||
| chr22:35342775 | C | A | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2950C>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342775 | |||||||
| chr22:35342776 | A | C | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2949A>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342776 | |||||||
| chr22:35342777 | C | T | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2948C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342777 | |||||||
| chr22:35342780 | ACCACACA others(5): Show |
A | 3 | a0001c0001t0001g0122 a0001c0001t0001g0149 a0001c0001t0001g0262 |
3 | HG02074.hp2 NA18979.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.1225-2932_1225-292 others(16): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 35342780 | ||||||
| chr22:35342795 | A | T | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2930A>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342795 | |||||||
| chr22:35342804 | T | G | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2921T>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342804 | |||||||
| chr22:35342807 | A | T | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2918A>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342807 | |||||||
| chr22:35342815 | A | T | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2910A>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342815 | |||||||
| chr22:35342825 | A | T | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2900A>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342825 | |||||||
| chr22:35342829 | C | A | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2896C>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342829 | |||||||
| chr22:35342832 | T | G | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2893T>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342832 | |||||||
| chr22:35342838 | C | T | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2887C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342838 | |||||||
| chr22:35342843 | C | T | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2882C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342843 | |||||||
| chr22:35342844 | A | C | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2881A>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342844 | |||||||
| chr22:35342854 | A | T | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2871A>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342854 | |||||||
| chr22:35342857 | C | G | 1 | a0001c0003t0001g0303 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1225-2868C>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342857 | |||||||
| chr22:35342868 | A | T | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2857A>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342868 | |||||||
| chr22:35342870 | A | T | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2855A>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342870 | |||||||
| chr22:35342882 | A | T | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2843A>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342882 | |||||||
| chr22:35342886 | C | A | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2839C>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342886 | |||||||
| chr22:35342887 | A | T | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2838A>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342887 | |||||||
| chr22:35342889 | ACACACAT others(34): Show |
A | 1 | a0001c0002t0001g0280 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1225-2834_1225-279 others(45): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 35342889 | ||||||
| chr22:35342912 | A | T | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2813A>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342912 | |||||||
| chr22:35342917 | T | G | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2808T>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342917 | |||||||
| chr22:35342922 | A | T | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2803A>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342922 | |||||||
| chr22:35342925 | T | G | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2800T>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342925 | |||||||
| chr22:35342929 | A | G | 32 | a0001c0002t0001g0016 a0001c0002t0001g0023 a0001c0002t0001g0024 others(29): Show |
37 | HG00544.hp1 HG00642.hp1 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.1225-2796A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342929 | |||||||
| chr22:35342932 | T | G | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2793T>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342932 | |||||||
| chr22:35342935 | A | T | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2790A>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342935 | |||||||
| chr22:35342943 | A | G | 1 | a0001c0001t0001g0193 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1225-2782A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342943 | |||||||
| chr22:35342949 | A | T | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2776A>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342949 | |||||||
| chr22:35342953 | A | G | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2772A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342953 | |||||||
| chr22:35342954 | C | T | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2771C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342954 | |||||||
| chr22:35342955 | C | T | 1 | a0001c0002t0001g0180 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1225-2770C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342955 | |||||||
| chr22:35342956 | C | A | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2769C>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342956 | |||||||
| chr22:35342959 | A | C | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2766A>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342959 | |||||||
| chr22:35342961 | A | C | 1 | a0001c0002t0001g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1225-2764A>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35342961 | |||||||
| chr22:35342963 | ACAC | A | 177 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0014 others(174): Show |
207 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(204): Show |
intron_variant | MODIFIER | c.1225-2758_1225-275 others(7): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 35342963 | ||||||
| chr22:35342978 | ACT | A | 90 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0014 others(87): Show |
98 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.1225-2745_1225-274 others(6): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 35342978 | ||||||
| chr22:35343022 | C | T | 92 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0005 others(89): Show |
114 | HG00099.hp2 HG00323.hp2 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.1225-2703C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35343022 | |||||||
| chr22:35343072 | G | C | 1 | a0001c0001t0001g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1225-2653G>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35343072 | |||||||
| chr22:35343104 | ACCACACA others(3): Show |
A | 1 | a0001c0001t0001g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1225-2609_1225-260 others(14): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 35343104 | ||||||
| chr22:35343105 | CCA | C | 5 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(2): Show |
5 | HG01168.hp1 HG01169.hp2 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.1225-2612_1225-261 others(6): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 35343105 | ||||||
| chr22:35343117 | A | C | 1 | a0001c0001t0001g0052 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1225-2608A>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35343117 | |||||||
| chr22:35343122 | C | CAACACAC others(99): Show |
1 | a0001c0001t0001g0196 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1225-2602_1225-260 others(110): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 35343122 | ||||||
| chr22:35343132 | ACAC | A | 3 | a0001c0003t0002g0300 a0001c0003t0002g0301 a0001c0014t0001g0309 |
3 | HG02055.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1225-2592_1225-259 others(7): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35343132 | |||||||
| chr22:35343134 | ACAT | A | 5 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0078 others(2): Show |
7 | HG00597.hp2 NA18971.hp2 NA19000.hp1 others(4): Show |
intron_variant | MODIFIER | c.1225-2589_1225-258 others(7): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 35343134 | ||||||
| chr22:35343136 | A | C | 1 | a0001c0001t0001g0196 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1225-2589A>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35343136 | |||||||
| chr22:35343137 | T | A | 1 | a0001c0001t0001g0196 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1225-2588T>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35343137 | |||||||
| chr22:35343158 | T | A | 1 | a0001c0001t0001g0196 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1225-2567T>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35343158 | |||||||
| chr22:35343165 | A | T | 1 | a0001c0001t0001g0196 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1225-2560A>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35343165 | |||||||
| chr22:35343167 | C | A | 1 | a0001c0001t0001g0196 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1225-2558C>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35343167 | |||||||
| chr22:35343174 | A | C | 2 | a0001c0002t0001g0023 a0001c0002t0001g0243 |
3 | HG00642.hp1 HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1225-2551A>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35343174 | |||||||
| chr22:35343187 | C | T | 1 | a0001c0001t0001g0196 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1225-2538C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35343187 | |||||||
| chr22:35343188 | T | A | 1 | a0001c0001t0001g0196 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1225-2537T>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35343188 | |||||||
| chr22:35343189 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1225-2536C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35343189 | |||||||
| chr22:35343193 | T | A | 1 | a0001c0001t0001g0196 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1225-2532T>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35343193 | |||||||
| chr22:35343195 | A | C | 1 | a0001c0001t0001g0196 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1225-2530A>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35343195 | |||||||
| chr22:35343196 | T | A | 1 | a0001c0001t0001g0196 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1225-2529T>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35343196 | |||||||
| chr22:35343199 | G | C | 1 | a0001c0001t0001g0196 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1225-2526G>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35343199 | |||||||
| chr22:35343202 | T | A | 1 | a0001c0001t0001g0196 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1225-2523T>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35343202 | |||||||
| chr22:35343203 | A | C | 1 | a0001c0001t0001g0196 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1225-2522A>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35343203 | |||||||
| chr22:35343204 | CACACACA others(5): Show |
C | 1 | a0001c0002t0001g0180 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1225-2511_1225-250 others(16): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 35343204 | ||||||
| chr22:35343216 | T | C | 1 | a0001c0001t0001g0196 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1225-2509T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35343216 | |||||||
| chr22:35343253 | A | C | 1 | a0001c0001t0001g0196 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1225-2472A>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35343253 | |||||||
| chr22:35343254 | C | T | 1 | a0001c0001t0001g0196 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1225-2471C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35343254 | |||||||
| chr22:35343270 | C | G | 1 | a0001c0001t0001g0196 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1225-2455C>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35343270 | |||||||
| chr22:35343294 | T | TACACACC others(116): Show |
1 | a0001c0002t0001g0246 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1225-2421_1225-242 others(127): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 35343294 | ||||||
| chr22:35343305 | C | CCTACACA others(116): Show |
194 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
235 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(232): Show |
intron_variant | MODIFIER | c.1225-2374_1225-237 others(127): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 35343305 | ||||||
| chr22:35343305 | C | CCTACACA others(116): Show |
1 | a0001c0002t0001g0302 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1225-2374_1225-237 others(127): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 35343305 | ||||||
| chr22:35343305 | C | CCTACACA others(114): Show |
17 | a0001c0001t0001g0004 a0001c0001t0001g0031 a0001c0001t0001g0032 others(14): Show |
19 | HG00323.hp1 HG00544.hp2 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.1225-2353_1225-235 others(125): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 35343305 | ||||||
| chr22:35343305 | C | CCTACACA others(112): Show |
87 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0017 others(84): Show |
93 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.1225-2384_1225-238 others(123): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 35343305 | ||||||
| chr22:35343305 | C | G | 2 | a0001c0001t0001g0196 a0001c0002t0001g0246 |
2 | HG02965.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.1225-2420C>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35343305 | |||||||
| chr22:35343334 | A | ACACACAC others(116): Show |
5 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(2): Show |
5 | HG01168.hp1 HG01169.hp2 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.1225-2374_1225-237 others(127): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 35343334 | ||||||
| chr22:35343336 | A | ACACACCA others(108): Show |
1 | a0001c0001t0001g0181 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1225-2384_1225-238 others(119): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 35343336 | ||||||
| chr22:35343437 | A | G | 2 | a0001c0001t0001g0171 a0001c0001t0001g0191 |
2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1225-2288A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35343437 | |||||||
| chr22:35343518 | T | C | 18 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0037 others(15): Show |
22 | HG00558.hp2 HG02040.hp2 HG02976.hp1 others(19): Show |
intron_variant | MODIFIER | c.1225-2207T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35343518 | |||||||
| chr22:35343584 | ACCTACAC others(5): Show |
A | 3 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0249 |
3 | HG01891.hp1 HG02258.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1225-2128_1225-211 others(16): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 35343584 | ||||||
| chr22:35343678 | ACAC | A | 7 | a0001c0001t0001g0004 a0001c0001t0001g0035 a0001c0001t0001g0044 others(4): Show |
9 | HG00544.hp2 HG00673.hp1 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.1225-2043_1225-204 others(7): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 35343678 | ||||||
| chr22:35343731 | CCCA | C | 9 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(6): Show |
9 | HG01168.hp1 HG01169.hp2 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.1225-1989_1225-198 others(7): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 35343731 | ||||||
| chr22:35343736 | C | CACACCTA others(20): Show |
89 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0014 others(86): Show |
97 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.1225-1972_1225-197 others(31): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 35343736 | ||||||
| chr22:35343736 | C | CGCACCTA others(20): Show |
1 | a0001c0001t0001g0127 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1225-1989_1225-198 others(31): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35343736 | |||||||
| chr22:35343761 | CTACACA | C | 3 | a0001c0001t0001g0004 a0001c0001t0001g0035 a0001c0001t0001g0044 |
5 | HG02027.hp2 NA18612.hp1 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.1225-1957_1225-195 others(10): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 35343761 | ||||||
| chr22:35343807 | C | A | 88 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0005 others(85): Show |
110 | HG00099.hp2 HG00323.hp2 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.1225-1918C>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35343807 | |||||||
| chr22:35343866 | C | A | 1 | a0001c0002t0001g0186 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1225-1859C>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35343866 | |||||||
| chr22:35343934 | A | C | 90 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0014 others(87): Show |
98 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.1225-1791A>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35343934 | |||||||
| chr22:35343941 | CTACACAC others(6): Show |
C | 2 | a0001c0002t0001g0230 a0001c0002t0001g0236 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1225-1779_1225-176 others(17): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 35343941 | ||||||
| chr22:35344004 | TACACCTA others(5): Show |
T | 3 | a0001c0003t0002g0300 a0001c0003t0002g0301 a0001c0014t0001g0309 |
3 | HG02055.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1225-1710_1225-169 others(16): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 35344004 | ||||||
| chr22:35344055 | A | C | 3 | a0001c0002t0001g0172 a0001c0002t0002g0296 a0001c0002t0002g0298 |
3 | HG01069.hp2 HG01071.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1225-1670A>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35344055 | |||||||
| chr22:35344081 | G | A | 1 | a0001c0001t0001g0251 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1225-1644G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35344081 | |||||||
| chr22:35344135 | G | A | 97 | a0001c0001t0001g0006 a0001c0001t0001g0138 a0001c0002t0001g0001 others(94): Show |
121 | HG00099.hp2 HG00323.hp2 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.1225-1590G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35344135 | |||||||
| chr22:35344171 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1225-1554C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35344171 | |||||||
| chr22:35344210 | G | A | 3 | a0001c0003t0002g0300 a0001c0003t0002g0301 a0001c0014t0001g0309 |
3 | HG02055.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1225-1515G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35344210 | |||||||
| chr22:35344278 | A | C | 3 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0249 |
3 | HG01891.hp1 HG02258.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1225-1447A>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35344278 | |||||||
| chr22:35344281 | C | T | 7 | a0001c0001t0001g0135 a0001c0001t0001g0217 a0001c0001t0001g0273 others(4): Show |
7 | HG01109.hp1 HG01123.hp1 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1225-1444C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35344281 | |||||||
| chr22:35344324 | G | A | 1 | a0001c0001t0001g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1225-1401G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35344324 | |||||||
| chr22:35344354 | G | A | 13 | a0001c0001t0001g0004 a0001c0001t0001g0035 a0001c0001t0001g0044 others(10): Show |
15 | HG00323.hp1 HG00544.hp2 HG00673.hp1 others(12): Show |
intron_variant | MODIFIER | c.1225-1371G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35344354 | |||||||
| chr22:35344449 | C | A | 87 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0017 others(84): Show |
93 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.1225-1276C>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35344449 | |||||||
| chr22:35344494 | C | T | 2 | a0001c0002t0001g0257 a0001c0002t0001g0280 |
2 | HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1225-1231C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35344494 | |||||||
| chr22:35344496 | G | C | 3 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0002g0297 |
3 | HG02818.hp1 HG02886.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1225-1229G>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35344496 | |||||||
| chr22:35344533 | G | T | 1 | a0001c0002t0001g0275 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1225-1192G>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35344533 | |||||||
| chr22:35344650 | G | T | 18 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0037 others(15): Show |
22 | HG00558.hp2 HG02040.hp2 HG02976.hp1 others(19): Show |
intron_variant | MODIFIER | c.1225-1075G>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35344650 | |||||||
| chr22:35344707 | CTCTG | C | 5 | a0001c0001t0001g0011 a0001c0001t0001g0116 a0001c0001t0001g0204 others(2): Show |
7 | HG00558.hp2 HG03654.hp2 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.1225-1010_1225-100 others(8): Show |
TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 35344707 | ||||||
| chr22:35344843 | A | C | 4 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0002g0297 others(1): Show |
4 | HG02818.hp1 HG02886.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1225-882A>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35344843 | |||||||
| chr22:35344873 | G | A | 13 | a0001c0001t0001g0004 a0001c0001t0001g0035 a0001c0001t0001g0044 others(10): Show |
15 | HG00323.hp1 HG00544.hp2 HG00673.hp1 others(12): Show |
intron_variant | MODIFIER | c.1225-852G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35344873 | |||||||
| chr22:35344899 | T | C | 1 | a0001c0001t0001g0093 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1225-826T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35344899 | |||||||
| chr22:35345041 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1225-684C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35345041 | |||||||
| chr22:35345042 | G | A | 3 | a0001c0001t0001g0075 a0001c0001t0001g0157 a0001c0001t0001g0158 |
3 | HG00597.hp1 NA18939.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.1225-683G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35345042 | |||||||
| chr22:35345088 | G | A | 1 | a0001c0002t0001g0180 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1225-637G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35345088 | |||||||
| chr22:35345145 | C | T | 1 | a0001c0002t0001g0231 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1225-580C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35345145 | |||||||
| chr22:35345172 | T | C | 2 | a0001c0001t0001g0171 a0001c0001t0001g0191 |
2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1225-553T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35345172 | |||||||
| chr22:35345178 | T | C | 223 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(220): Show |
259 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(256): Show |
intron_variant | MODIFIER | c.1225-547T>C | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35345178 | |||||||
| chr22:35345346 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1225-379C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 12/14 | chr22 | 35345346 | |||||||
| chr22:35345818 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1284+34G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 13/14 | chr22 | 35345818 | |||||||
| chr22:35345823 | A | G | 1 | a0001c0001t0001g0198 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1284+39A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 13/14 | chr22 | 35345823 | |||||||
| chr22:35345827 | G | A | 82 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0017 others(79): Show |
88 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.1284+43G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 13/14 | chr22 | 35345827 | |||||||
| chr22:35345870 | A | G | 228 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(225): Show |
264 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(261): Show |
intron_variant | MODIFIER | c.1284+86A>G | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 13/14 | chr22 | 35345870 | |||||||
| chr22:35346002 | C | T | 1 | a0004c0012t0001g0229 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1284+218C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 13/14 | chr22 | 35346002 | |||||||
| chr22:35346075 | C | T | 6 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(3): Show |
6 | HG01099.hp2 HG01168.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.1284+291C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 13/14 | chr22 | 35346075 | |||||||
| chr22:35346110 | G | A | 3 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0294 |
3 | HG01175.hp1 HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1284+326G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 13/14 | chr22 | 35346110 | |||||||
| chr22:35346360 | G | A | 5 | a0001c0001t0001g0014 a0001c0001t0001g0092 a0001c0001t0001g0181 others(2): Show |
6 | HG00621.hp1 NA18612.hp2 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.1285-570G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 13/14 | chr22 | 35346360 | |||||||
| chr22:35346492 | C | T | 1 | a0001c0002t0001g0221 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1285-438C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 13/14 | chr22 | 35346492 | |||||||
| chr22:35346531 | C | T | 186 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0014 others(183): Show |
216 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(213): Show |
intron_variant | MODIFIER | c.1285-399C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 13/14 | chr22 | 35346531 | |||||||
| chr22:35346625 | G | A | 3 | a0001c0003t0002g0300 a0001c0003t0002g0301 a0001c0014t0001g0309 |
3 | HG02055.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1285-305G>A | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 13/14 | chr22 | 35346625 | |||||||
| chr22:35346769 | C | T | 10 | a0001c0001t0001g0004 a0001c0001t0001g0035 a0001c0001t0001g0044 others(7): Show |
12 | HG00323.hp1 HG00544.hp2 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.1285-161C>T | TOM1 | ENSG00000100284.22 | transcript | ENST00000449058.7 | protein_coding | 13/14 | chr22 | 35346769 |