Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 8050 |
| ensemblid | ENSG00000110435.13 |
| hgncid | 21350 |
| symbol | PDHX |
| name | pyruvate dehydrogenase complex component X |
| refseq_nuc | NM_003477.3 |
| refseq_prot | NP_003468.2 |
| ensembl_nuc | ENST00000227868.9 |
| ensembl_prot | ENSP00000227868.4 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 34916618 |
| end | 34996128 |
| strand | + |
| ver | v1.2 |
| region | chr11:34916618-34996128 |
| region5000 | chr11:34911618-35001128 |
| regionname0 | PDHX_chr11_34916618_34996128 |
| regionname5000 | PDHX_chr11_34911618_35001128 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 501 | 209 | 41 | 47 | 93 | 4 | 23 | 75 | PDHX_chr11_34911618_35001128 | PDHX | MAASW others(496): Show |
chr11 | 34911618 | 35001128 |
| a0002 | 0/0 | 501 | 76 | 42 | 7 | 19 | 1 | 7 | 15 | PDHX_chr11_34911618_35001128 | PDHX | MAASW others(496): Show |
chr11 | 34911618 | 35001128 |
| a0003 | 0/0 | 501 | 12 | 1 | 4 | 0 | 2 | 5 | 0 | PDHX_chr11_34911618_35001128 | PDHX | MAASW others(496): Show |
chr11 | 34911618 | 35001128 |
| a0004 | 0/0 | 501 | 4 | 0 | 1 | 0 | 3 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | MAASW others(496): Show |
chr11 | 34911618 | 35001128 |
| a0005 | 0/0 | 501 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | MAASW others(496): Show |
chr11 | 34911618 | 35001128 |
| a0006 | 0/0 | 501 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | MAASW others(496): Show |
chr11 | 34911618 | 35001128 |
| a0007 | 0/1 | 501 | 2 | 0 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | MAASW others(496): Show |
chr11 | 34911618 | 35001128 |
| a0008 | 0/0 | 501 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | PDHX_chr11_34911618_35001128 | PDHX | MAASW others(496): Show |
chr11 | 34911618 | 35001128 |
| a0009 | 0/0 | 501 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | MAASW others(496): Show |
chr11 | 34911618 | 35001128 |
| a0010 | 0/0 | 501 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | MAASW others(496): Show |
chr11 | 34911618 | 35001128 |
| a0011 | 0/0 | 501 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PDHX_chr11_34911618_35001128 | PDHX | MAASW others(496): Show |
chr11 | 34911618 | 35001128 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1503 | 120 | 18 | 27 | 58 | 4 | 13 | PDHX_chr11_34911618_35001128 | PDHX | ATGGC others(1498): Show |
chr11 | 34911618 | 35001128 | ||
| a0001c0002 | 1/0 | 1503 | 78 | 20 | 17 | 32 | 0 | 8 | PDHX_chr11_34911618_35001128 | PDHX | ATGGC others(1498): Show |
chr11 | 34911618 | 35001128 | ||
| a0001c0013 | 0/0 | 1503 | 2 | 0 | 0 | 1 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | ATGGC others(1498): Show |
chr11 | 34911618 | 35001128 | ||
| a0001c0014 | 0/0 | 1503 | 2 | 0 | 2 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | ATGGC others(1498): Show |
chr11 | 34911618 | 35001128 | ||
| a0001c0017 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | ATGGC others(1498): Show |
chr11 | 34911618 | 35001128 | ||
| a0001c0018 | 0/0 | 1503 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | ATGGC others(1498): Show |
chr11 | 34911618 | 35001128 | ||
| a0001c0020 | 0/0 | 1503 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | ATGGC others(1498): Show |
chr11 | 34911618 | 35001128 | ||
| a0001c0021 | 0/0 | 1518 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | ATGGC others(1513): Show |
chr11 | 34911618 | 35001128 | ||
| a0001c0023 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | ATGGC others(1498): Show |
chr11 | 34911618 | 35001128 | ||
| a0001c0024 | 0/0 | 1503 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | ATGGC others(1498): Show |
chr11 | 34911618 | 35001128 | ||
| a0001c0026 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | ATGGC others(1498): Show |
chr11 | 34911618 | 35001128 | ||
| a0002c0003 | 0/0 | 1503 | 29 | 4 | 6 | 17 | 1 | 1 | PDHX_chr11_34911618_35001128 | PDHX | ATGGC others(1498): Show |
chr11 | 34911618 | 35001128 | ||
| a0002c0004 | 0/0 | 1503 | 14 | 13 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | ATGGC others(1498): Show |
chr11 | 34911618 | 35001128 | ||
| a0002c0005 | 0/0 | 1503 | 13 | 13 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | ATGGC others(1498): Show |
chr11 | 34911618 | 35001128 | ||
| a0002c0007 | 0/0 | 1503 | 8 | 0 | 0 | 2 | 0 | 6 | PDHX_chr11_34911618_35001128 | PDHX | ATGGC others(1498): Show |
chr11 | 34911618 | 35001128 | ||
| a0002c0008 | 0/0 | 1503 | 8 | 8 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | ATGGC others(1498): Show |
chr11 | 34911618 | 35001128 | ||
| a0002c0012 | 0/0 | 1503 | 3 | 3 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | ATGGC others(1498): Show |
chr11 | 34911618 | 35001128 | ||
| a0002c0027 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | ATGGC others(1498): Show |
chr11 | 34911618 | 35001128 | ||
| a0003c0006 | 0/0 | 1503 | 12 | 1 | 4 | 0 | 2 | 5 | PDHX_chr11_34911618_35001128 | PDHX | ATGGC others(1498): Show |
chr11 | 34911618 | 35001128 | ||
| a0004c0010 | 0/0 | 1503 | 3 | 0 | 0 | 0 | 3 | 0 | PDHX_chr11_34911618_35001128 | PDHX | ATGGC others(1498): Show |
chr11 | 34911618 | 35001128 | ||
| a0004c0022 | 0/0 | 1503 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | ATGGC others(1498): Show |
chr11 | 34911618 | 35001128 | ||
| a0005c0009 | 0/0 | 1503 | 3 | 3 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | ATGGC others(1498): Show |
chr11 | 34911618 | 35001128 | ||
| a0006c0011 | 0/0 | 1503 | 3 | 3 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | ATGGC others(1498): Show |
chr11 | 34911618 | 35001128 | ||
| a0007c0015 | 0/1 | 1503 | 2 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | ATGGC others(1498): Show |
chr11 | 34911618 | 35001128 | ||
| a0008c0016 | 0/0 | 1503 | 2 | 0 | 0 | 2 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | ATGGC others(1498): Show |
chr11 | 34911618 | 35001128 | ||
| a0009c0025 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | ATGGC others(1498): Show |
chr11 | 34911618 | 35001128 | ||
| a0010c0028 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | ATGGC others(1498): Show |
chr11 | 34911618 | 35001128 | ||
| a0011c0019 | 0/0 | 1503 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | ATGGC others(1498): Show |
chr11 | 34911618 | 35001128 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2500 | 114 | 18 | 26 | 54 | 4 | 12 | PDHX_chr11_34911618_35001128 | PDHX | AGGCT others(2495): Show |
chr11 | 34911618 | 35001128 |
| a0001c0001t0008 | 0/0 | 2500 | 4 | 0 | 0 | 4 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | AGGCT others(2495): Show |
chr11 | 34911618 | 35001128 |
| a0001c0001t0011 | 0/0 | 2496 | 2 | 0 | 1 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | AGGCT others(2491): Show |
chr11 | 34911618 | 35001128 |
| a0001c0002t0002 | 1/0 | 2500 | 70 | 14 | 17 | 30 | 0 | 8 | PDHX_chr11_34911618_35001128 | PDHX | AGGCT others(2495): Show |
chr11 | 34911618 | 35001128 |
| a0001c0002t0007 | 0/0 | 2500 | 5 | 5 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | AGGCT others(2495): Show |
chr11 | 34911618 | 35001128 |
| a0001c0002t0012 | 0/0 | 2500 | 2 | 0 | 0 | 2 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | AGGCT others(2495): Show |
chr11 | 34911618 | 35001128 |
| a0001c0002t0014 | 0/0 | 2450 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | AGGCT others(2445): Show |
chr11 | 34911618 | 35001128 |
| a0001c0013t0002 | 0/0 | 2500 | 2 | 0 | 0 | 1 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | AGGCT others(2495): Show |
chr11 | 34911618 | 35001128 |
| a0001c0014t0009 | 0/0 | 2500 | 2 | 0 | 2 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | AGGCT others(2495): Show |
chr11 | 34911618 | 35001128 |
| a0001c0017t0007 | 0/0 | 2500 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | AGGCT others(2495): Show |
chr11 | 34911618 | 35001128 |
| a0001c0018t0001 | 0/0 | 2500 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | AGGCT others(2495): Show |
chr11 | 34911618 | 35001128 |
| a0001c0020t0002 | 0/0 | 2500 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | AGGCT others(2495): Show |
chr11 | 34911618 | 35001128 |
| a0001c0021t0002 | 0/0 | 2515 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | AGGCT others(2510): Show |
chr11 | 34911618 | 35001128 |
| a0001c0023t0009 | 0/0 | 2500 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | AGGCT others(2495): Show |
chr11 | 34911618 | 35001128 |
| a0001c0024t0001 | 0/0 | 2500 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | AGGCT others(2495): Show |
chr11 | 34911618 | 35001128 |
| a0001c0026t0013 | 0/0 | 2500 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | AGGCT others(2495): Show |
chr11 | 34911618 | 35001128 |
| a0002c0003t0003 | 0/0 | 2500 | 26 | 4 | 6 | 14 | 1 | 1 | PDHX_chr11_34911618_35001128 | PDHX | AGGCT others(2495): Show |
chr11 | 34911618 | 35001128 |
| a0002c0003t0010 | 0/0 | 2500 | 3 | 0 | 0 | 3 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | AGGCT others(2495): Show |
chr11 | 34911618 | 35001128 |
| a0002c0004t0004 | 0/0 | 2500 | 13 | 12 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | AGGCT others(2495): Show |
chr11 | 34911618 | 35001128 |
| a0002c0004t0005 | 0/0 | 2500 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | AGGCT others(2495): Show |
chr11 | 34911618 | 35001128 |
| a0002c0005t0005 | 0/0 | 2500 | 13 | 13 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | AGGCT others(2495): Show |
chr11 | 34911618 | 35001128 |
| a0002c0007t0004 | 0/0 | 2500 | 8 | 0 | 0 | 2 | 0 | 6 | PDHX_chr11_34911618_35001128 | PDHX | AGGCT others(2495): Show |
chr11 | 34911618 | 35001128 |
| a0002c0008t0006 | 0/0 | 2500 | 8 | 8 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | AGGCT others(2495): Show |
chr11 | 34911618 | 35001128 |
| a0002c0012t0003 | 0/0 | 2500 | 3 | 3 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | AGGCT others(2495): Show |
chr11 | 34911618 | 35001128 |
| a0002c0027t0003 | 0/0 | 2500 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | AGGCT others(2495): Show |
chr11 | 34911618 | 35001128 |
| a0003c0006t0001 | 0/0 | 2500 | 12 | 1 | 4 | 0 | 2 | 5 | PDHX_chr11_34911618_35001128 | PDHX | AGGCT others(2495): Show |
chr11 | 34911618 | 35001128 |
| a0004c0010t0002 | 0/0 | 2500 | 3 | 0 | 0 | 0 | 3 | 0 | PDHX_chr11_34911618_35001128 | PDHX | AGGCT others(2495): Show |
chr11 | 34911618 | 35001128 |
| a0004c0022t0015 | 0/0 | 2496 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | AGGCT others(2491): Show |
chr11 | 34911618 | 35001128 |
| a0005c0009t0002 | 0/0 | 2500 | 3 | 3 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | AGGCT others(2495): Show |
chr11 | 34911618 | 35001128 |
| a0006c0011t0001 | 0/0 | 2500 | 3 | 3 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | AGGCT others(2495): Show |
chr11 | 34911618 | 35001128 |
| a0007c0015t0004 | 0/1 | 2500 | 2 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | AGGCT others(2495): Show |
chr11 | 34911618 | 35001128 |
| a0008c0016t0001 | 0/0 | 2500 | 2 | 0 | 0 | 2 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | AGGCT others(2495): Show |
chr11 | 34911618 | 35001128 |
| a0009c0025t0001 | 0/0 | 2500 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | AGGCT others(2495): Show |
chr11 | 34911618 | 35001128 |
| a0010c0028t0016 | 0/0 | 2500 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | AGGCT others(2495): Show |
chr11 | 34911618 | 35001128 |
| a0011c0019t0002 | 0/0 | 2500 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | AGGCT others(2495): Show |
chr11 | 34911618 | 35001128 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0008g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0008g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0008g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0008g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0011g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0011g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0002t0002g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0002t0002g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0002t0002g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0002t0002g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0002t0002g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0002t0002g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0002t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0002t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0002t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0002t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0002t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0002t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0002t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0002t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0002t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0002t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0002t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0002t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0002t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0002t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0002t0002g0165 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0002t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0002t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0002t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0002t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0002t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0002t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0002t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0002t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0002t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0002t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0002t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0002t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0002t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0002t0007g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0002t0007g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0002t0007g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0002t0007g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0002t0007g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0002t0012g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0002t0012g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0002t0014g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0013t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0013t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0014t0009g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0014t0009g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0017t0007g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0018t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0020t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0021t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0023t0009g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0024t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0026t0013g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0002c0003t0003g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0002c0003t0003g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0002c0003t0003g0025 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0002c0003t0003g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0002c0003t0003g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0002c0003t0003g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0002c0003t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0002c0003t0003g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0002c0003t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0002c0003t0003g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0002c0003t0003g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0002c0003t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0002c0003t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0002c0003t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0002c0003t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0002c0003t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0002c0003t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0002c0003t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0002c0003t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0002c0003t0003g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0002c0003t0003g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0002c0003t0003g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0002c0003t0003g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0002c0003t0010g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0002c0003t0010g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0002c0003t0010g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0002c0004t0004g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0002c0004t0004g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0002c0004t0004g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0002c0004t0004g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0002c0004t0004g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0002c0004t0004g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0002c0004t0004g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0002c0004t0004g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0002c0004t0004g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0002c0004t0004g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0002c0004t0004g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0002c0004t0004g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0002c0004t0004g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0002c0004t0005g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0002c0005t0005g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0002c0005t0005g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0002c0005t0005g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0002c0005t0005g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0002c0005t0005g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0002c0005t0005g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0002c0005t0005g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0002c0005t0005g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0002c0007t0004g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0002c0007t0004g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0002c0007t0004g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0002c0007t0004g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0002c0007t0004g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0002c0007t0004g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0002c0007t0004g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0002c0008t0006g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0002c0008t0006g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0002c0008t0006g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0002c0008t0006g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0002c0008t0006g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0002c0008t0006g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0002c0012t0003g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0002c0012t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0002c0012t0003g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0002c0027t0003g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0003c0006t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0003c0006t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0003c0006t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0003c0006t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0003c0006t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0003c0006t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0003c0006t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0003c0006t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0003c0006t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0003c0006t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0003c0006t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0003c0006t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0004c0010t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0004c0010t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0004c0010t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0004c0022t0015g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0005c0009t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0005c0009t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0005c0009t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0006c0011t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0006c0011t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0006c0011t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0007c0015t0004g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0007c0015t0004g0227 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0008c0016t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0008c0016t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0009c0025t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0010c0028t0016g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0011c0019t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0004 | c0010 | t0002 | g0142 | EUR | GBR | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | GBR | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG00280 | hp1 | a0003 | c0006 | t0001 | g0204 | EUR | FIN | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0112 | EUR | FIN | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG00423 | hp1 | a0002 | c0003 | t0010 | g0241 | EAS | CHS | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | CHS | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG00558 | hp1 | a0001 | c0001 | t0008 | g0057 | EAS | CHS | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | CHS | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG00609 | hp2 | a0001 | c0002 | t0002 | g0157 | EAS | CHS | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG00621 | hp1 | a0001 | c0002 | t0002 | g0145 | EAS | CHS | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | CHS | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG00642 | hp1 | a0001 | c0002 | t0002 | g0162 | AMR | PUR | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG00673 | hp1 | a0002 | c0003 | t0010 | g0251 | EAS | CHS | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG00673 | hp2 | a0002 | c0003 | t0003 | g0256 | EAS | CHS | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG00735 | hp1 | a0001 | c0002 | t0002 | g0182 | AMR | PUR | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG00738 | hp1 | a0001 | c0002 | t0002 | g0184 | AMR | PUR | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG01071 | hp2 | a0001 | c0002 | t0002 | g0185 | AMR | PUR | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG01074 | hp2 | a0001 | c0002 | t0002 | g0219 | AMR | PUR | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG01081 | hp2 | a0004 | c0022 | t0015 | g0143 | AMR | PUR | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG01106 | hp1 | a0002 | c0003 | t0003 | g0249 | AMR | PUR | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG01109 | hp1 | a0003 | c0006 | t0001 | g0211 | AMR | PUR | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG01109 | hp2 | a0001 | c0002 | t0002 | g0158 | AMR | PUR | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG01168 | hp2 | a0002 | c0003 | t0003 | g0025 | AMR | PUR | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG01169 | hp2 | a0002 | c0003 | t0003 | g0252 | AMR | PUR | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG01175 | hp1 | a0001 | c0002 | t0002 | g0172 | AMR | PUR | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG01175 | hp2 | a0002 | c0003 | t0003 | g0245 | AMR | PUR | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG01192 | hp1 | a0002 | c0003 | t0003 | g0253 | AMR | PUR | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG01192 | hp2 | a0001 | c0014 | t0009 | g0105 | AMR | PUR | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG01243 | hp1 | a0003 | c0006 | t0001 | g0207 | AMR | PUR | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG01255 | hp2 | a0001 | c0002 | t0002 | g0181 | AMR | CLM | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG01256 | hp1 | a0001 | c0002 | t0002 | g0149 | AMR | CLM | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | CLM | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | CLM | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG01257 | hp2 | a0002 | c0003 | t0003 | g0246 | AMR | CLM | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG01258 | hp1 | a0001 | c0002 | t0002 | g0150 | AMR | CLM | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG01261 | hp1 | a0001 | c0002 | t0002 | g0163 | AMR | CLM | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG01261 | hp2 | a0001 | c0001 | t0011 | g0111 | AMR | CLM | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG01358 | hp2 | a0001 | c0002 | t0002 | g0151 | AMR | CLM | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG01361 | hp1 | a0007 | c0015 | t0004 | g0225 | AMR | CLM | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | CLM | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG01433 | hp2 | a0001 | c0002 | t0002 | g0180 | AMR | CLM | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG01496 | hp1 | a0001 | c0018 | t0001 | g0164 | AMR | CLM | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG01496 | hp2 | a0002 | c0004 | t0004 | g0233 | AMR | CLM | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG01515 | hp1 | a0003 | c0006 | t0001 | g0208 | EUR | IBS | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG01515 | hp2 | a0004 | c0010 | t0002 | g0139 | EUR | IBS | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG01516 | hp1 | a0002 | c0003 | t0003 | g0025 | EUR | IBS | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0079 | EUR | IBS | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG01517 | hp1 | a0004 | c0010 | t0002 | g0138 | EUR | IBS | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0081 | EUR | IBS | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG01884 | hp1 | a0002 | c0027 | t0003 | g0244 | AFR | ACB | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG01884 | hp2 | a0001 | c0002 | t0014 | g0191 | AFR | ACB | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG01891 | hp2 | a0001 | c0002 | t0002 | g0131 | AFR | ACB | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG01943 | hp1 | a0003 | c0006 | t0001 | g0206 | AMR | PEL | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG01943 | hp2 | a0001 | c0014 | t0009 | g0106 | AMR | PEL | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG01952 | hp1 | a0001 | c0002 | t0002 | g0218 | AMR | PEL | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PEL | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG01975 | hp2 | a0001 | c0002 | t0002 | g0217 | AMR | PEL | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG01993 | hp1 | a0001 | c0002 | t0002 | g0173 | AMR | PEL | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | KHV | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG02015 | hp2 | a0002 | c0003 | t0003 | g0261 | EAS | KHV | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG02040 | hp2 | a0001 | c0002 | t0002 | g0156 | EAS | KHV | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG02055 | hp1 | a0002 | c0005 | t0005 | g0027 | AFR | ACB | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG02055 | hp2 | a0001 | c0002 | t0002 | g0140 | AFR | ACB | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG02056 | hp2 | a0001 | c0002 | t0002 | g0155 | EAS | KHV | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG02083 | hp1 | a0001 | c0002 | t0002 | g0135 | EAS | KHV | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | KHV | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG02129 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | KHV | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | KHV | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG02145 | hp1 | a0002 | c0008 | t0006 | g0274 | AFR | ACB | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG02145 | hp2 | a0009 | c0025 | t0001 | g0215 | AFR | ACB | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | CDX | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG02165 | hp2 | a0001 | c0001 | t0008 | g0060 | EAS | CDX | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG02257 | hp1 | a0001 | c0002 | t0002 | g0018 | AFR | ACB | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG02257 | hp2 | a0005 | c0009 | t0002 | g0177 | AFR | ACB | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG02280 | hp1 | a0002 | c0004 | t0004 | g0236 | AFR | ACB | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG02280 | hp2 | a0002 | c0005 | t0005 | g0268 | AFR | ACB | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG02293 | hp2 | a0001 | c0002 | t0002 | g0174 | AMR | PEL | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG02300 | hp2 | a0003 | c0006 | t0001 | g0203 | AMR | PEL | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG02451 | hp1 | a0002 | c0008 | t0006 | g0272 | AFR | ACB | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG02572 | hp1 | a0002 | c0004 | t0004 | g0235 | AFR | GWD | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG02572 | hp2 | a0001 | c0002 | t0007 | g0189 | AFR | GWD | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG02602 | hp1 | a0001 | c0002 | t0002 | g0141 | SAS | PJL | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG02602 | hp2 | a0002 | c0007 | t0004 | g0228 | SAS | PJL | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG02615 | hp1 | a0002 | c0008 | t0006 | g0271 | AFR | GWD | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG02615 | hp2 | a0002 | c0003 | t0003 | g0276 | AFR | GWD | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG02622 | hp1 | a0002 | c0004 | t0004 | g0224 | AFR | GWD | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG02630 | hp1 | a0002 | c0003 | t0003 | g0279 | AFR | GWD | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG02647 | hp1 | a0002 | c0003 | t0003 | g0277 | AFR | GWD | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG02647 | hp2 | a0002 | c0005 | t0005 | g0263 | AFR | GWD | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG02717 | hp1 | a0002 | c0004 | t0004 | g0232 | AFR | GWD | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG02723 | hp1 | a0001 | c0002 | t0007 | g0192 | AFR | GWD | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG02723 | hp2 | a0001 | c0002 | t0002 | g0017 | AFR | GWD | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG02735 | hp1 | a0003 | c0006 | t0001 | g0210 | SAS | PJL | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG02738 | hp1 | a0001 | c0001 | t0011 | g0114 | SAS | PJL | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG02738 | hp2 | a0002 | c0007 | t0004 | g0230 | SAS | PJL | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG02809 | hp2 | a0002 | c0005 | t0005 | g0026 | AFR | GWD | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG02886 | hp1 | a0002 | c0008 | t0006 | g0001 | AFR | GWD | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG02886 | hp2 | a0001 | c0002 | t0002 | g0169 | AFR | GWD | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG02895 | hp2 | a0001 | c0002 | t0007 | g0187 | AFR | GWD | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG02896 | hp2 | a0002 | c0005 | t0005 | g0267 | AFR | GWD | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG02897 | hp2 | a0002 | c0005 | t0005 | g0007 | AFR | GWD | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG02922 | hp1 | a0010 | c0028 | t0016 | g0275 | AFR | ESN | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG02922 | hp2 | a0002 | c0008 | t0006 | g0273 | AFR | ESN | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG02965 | hp1 | a0002 | c0005 | t0005 | g0027 | AFR | ESN | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG02965 | hp2 | a0005 | c0009 | t0002 | g0178 | AFR | ESN | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG02970 | hp1 | a0001 | c0002 | t0002 | g0019 | AFR | ESN | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG02970 | hp2 | a0001 | c0002 | t0007 | g0190 | AFR | ESN | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG02976 | hp1 | a0002 | c0004 | t0004 | g0240 | AFR | ESN | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ESN | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG03017 | hp1 | a0001 | c0002 | t0002 | g0193 | SAS | PJL | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG03041 | hp1 | a0002 | c0004 | t0004 | g0237 | AFR | GWD | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG03041 | hp2 | a0002 | c0005 | t0005 | g0269 | AFR | GWD | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG03098 | hp1 | a0002 | c0004 | t0004 | g0238 | AFR | MSL | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG03098 | hp2 | a0002 | c0008 | t0006 | g0001 | AFR | MSL | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG03130 | hp1 | a0001 | c0002 | t0002 | g0019 | AFR | ESN | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | ESN | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG03139 | hp1 | a0006 | c0011 | t0001 | g0200 | AFR | ESN | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG03139 | hp2 | a0002 | c0005 | t0005 | g0007 | AFR | ESN | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG03195 | hp1 | a0002 | c0004 | t0004 | g0266 | AFR | ESN | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG03195 | hp2 | a0002 | c0005 | t0005 | g0008 | AFR | ESN | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG03209 | hp1 | a0002 | c0004 | t0004 | g0234 | AFR | MSL | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG03225 | hp1 | a0002 | c0004 | t0004 | g0239 | AFR | MSL | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG03225 | hp2 | a0002 | c0003 | t0003 | g0278 | AFR | MSL | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG03239 | hp1 | a0003 | c0006 | t0001 | g0214 | SAS | PJL | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG03239 | hp2 | a0001 | c0002 | t0002 | g0148 | SAS | PJL | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG03453 | hp1 | a0002 | c0008 | t0006 | g0001 | AFR | MSL | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG03490 | hp2 | a0001 | c0002 | t0002 | g0132 | SAS | PJL | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG03491 | hp1 | a0003 | c0006 | t0001 | g0202 | SAS | PJL | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG03491 | hp2 | a0001 | c0024 | t0001 | g0116 | SAS | PJL | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG03492 | hp1 | a0003 | c0006 | t0001 | g0205 | SAS | PJL | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG03516 | hp1 | a0006 | c0011 | t0001 | g0201 | AFR | ESN | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG03516 | hp2 | a0001 | c0002 | t0002 | g0017 | AFR | ESN | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG03540 | hp1 | a0002 | c0008 | t0006 | g0270 | AFR | GWD | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG03540 | hp2 | a0001 | c0002 | t0002 | g0160 | AFR | GWD | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG03579 | hp2 | a0001 | c0002 | t0002 | g0018 | AFR | MSL | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG03654 | hp1 | a0002 | c0007 | t0004 | g0022 | SAS | PJL | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG03688 | hp1 | a0001 | c0002 | t0002 | g0136 | SAS | STU | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG03688 | hp2 | a0011 | c0019 | t0002 | g0159 | SAS | STU | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG03710 | hp1 | a0002 | c0007 | t0004 | g0226 | SAS | PJL | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG03927 | hp1 | a0001 | c0013 | t0002 | g0213 | SAS | BEB | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG03927 | hp2 | a0001 | c0002 | t0002 | g0133 | SAS | BEB | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | BEB | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG03942 | hp2 | a0001 | c0002 | t0002 | g0137 | SAS | BEB | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG04184 | hp1 | a0002 | c0007 | t0004 | g0229 | SAS | BEB | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | BEB | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | STU | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG04199 | hp2 | a0001 | c0002 | t0002 | g0134 | SAS | STU | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | STU | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG04204 | hp2 | a0002 | c0007 | t0004 | g0022 | SAS | STU | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG04228 | hp1 | a0003 | c0006 | t0001 | g0212 | SAS | STU | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG04228 | hp2 | a0002 | c0003 | t0003 | g0247 | SAS | STU | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA18522 | hp1 | a0006 | c0011 | t0001 | g0198 | AFR | YRI | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA18522 | hp2 | a0001 | c0002 | t0002 | g0152 | AFR | YRI | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA18906 | hp1 | a0002 | c0004 | t0005 | g0007 | AFR | YRI | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA18906 | hp2 | a0001 | c0002 | t0002 | g0153 | AFR | YRI | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA18940 | hp1 | a0002 | c0003 | t0003 | g0259 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA18945 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA18948 | hp1 | a0001 | c0002 | t0002 | g0146 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA18949 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA18950 | hp1 | a0001 | c0001 | t0008 | g0059 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA18950 | hp2 | a0001 | c0002 | t0002 | g0147 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA18952 | hp1 | a0001 | c0021 | t0002 | g0166 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA18953 | hp2 | a0001 | c0002 | t0002 | g0170 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA18957 | hp2 | a0001 | c0002 | t0002 | g0175 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA18962 | hp1 | a0001 | c0002 | t0012 | g0129 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA18962 | hp2 | a0002 | c0003 | t0003 | g0258 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA18964 | hp1 | a0002 | c0003 | t0003 | g0257 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA18964 | hp2 | a0008 | c0016 | t0001 | g0097 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA18965 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA18967 | hp1 | a0001 | c0002 | t0002 | g0020 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA18972 | hp1 | a0001 | c0002 | t0002 | g0176 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA18972 | hp2 | a0002 | c0003 | t0003 | g0255 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA18973 | hp2 | a0002 | c0003 | t0003 | g0023 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA18975 | hp1 | a0001 | c0002 | t0002 | g0161 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA18977 | hp1 | a0002 | c0003 | t0003 | g0248 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA18978 | hp2 | a0001 | c0002 | t0002 | g0020 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA18980 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA18986 | hp1 | a0008 | c0016 | t0001 | g0091 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA18986 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA18988 | hp2 | a0001 | c0002 | t0012 | g0128 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA18994 | hp1 | a0001 | c0002 | t0002 | g0021 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA18995 | hp1 | a0001 | c0020 | t0002 | g0220 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA18997 | hp1 | a0002 | c0003 | t0003 | g0024 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA18998 | hp1 | a0002 | c0003 | t0003 | g0260 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA18999 | hp1 | a0002 | c0003 | t0003 | g0023 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA19001 | hp2 | a0001 | c0013 | t0002 | g0028 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA19002 | hp1 | a0001 | c0002 | t0002 | g0167 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA19003 | hp2 | a0002 | c0003 | t0003 | g0250 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA19012 | hp1 | a0001 | c0002 | t0002 | g0216 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA19030 | hp1 | a0001 | c0002 | t0007 | g0188 | AFR | LWK | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA19030 | hp2 | a0002 | c0012 | t0003 | g0242 | AFR | LWK | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | LWK | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA19043 | hp2 | a0002 | c0004 | t0004 | g0222 | AFR | LWK | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA19054 | hp2 | a0002 | c0007 | t0004 | g0231 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA19056 | hp2 | a0002 | c0003 | t0003 | g0024 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA19063 | hp1 | a0001 | c0002 | t0002 | g0021 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA19064 | hp2 | a0002 | c0003 | t0003 | g0262 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA19068 | hp2 | a0001 | c0002 | t0002 | g0183 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA19072 | hp1 | a0002 | c0003 | t0010 | g0254 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA19077 | hp1 | a0001 | c0002 | t0002 | g0154 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA19078 | hp2 | a0002 | c0007 | t0004 | g0223 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA19082 | hp1 | a0001 | c0002 | t0002 | g0171 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA19085 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA19086 | hp1 | a0001 | c0002 | t0002 | g0168 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA19087 | hp2 | a0001 | c0001 | t0008 | g0109 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA19091 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA20129 | hp1 | a0002 | c0004 | t0004 | g0265 | AFR | ASW | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA20129 | hp2 | a0002 | c0012 | t0003 | g0243 | AFR | ASW | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG02109 | hp1 | a0001 | c0017 | t0007 | g0144 | AFR | ACB | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG02109 | hp2 | a0001 | c0026 | t0013 | g0050 | AFR | ACB | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG02486 | hp1 | a0002 | c0005 | t0005 | g0008 | AFR | ACB | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG02486 | hp2 | a0001 | c0002 | t0002 | g0186 | AFR | ACB | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG02559 | hp1 | a0005 | c0009 | t0002 | g0179 | AFR | ACB | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG02559 | hp2 | a0001 | c0023 | t0009 | g0199 | AFR | ACB | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | MSL | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | MSL | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG06807 | hp1 | a0002 | c0012 | t0003 | g0264 | AFR | USA | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG06807 | hp2 | a0002 | c0005 | t0005 | g0026 | AFR | USA | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA18955 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | USA | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA20300 | hp2 | a0001 | c0002 | t0002 | g0130 | AFR | USA | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA21309 | hp1 | a0002 | c0005 | t0005 | g0008 | AFR | LWK | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA21309 | hp2 | a0003 | c0006 | t0001 | g0209 | AFR | LWK | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| homoSapiens | chm13v2 | a0007 | c0015 | t0004 | g0227 | REF | REF | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0002 | g0165 | REF | REF | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:34916702 | A | C | 1 | a0008 | 2 | NA18964.hp2 NA18986.hp1 |
missense_variant | MODERATE | c.47A>C | p.Tyr16Ser | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/11 | 85/2500 | 47/1506 | 16/501 | chr11 | 34916702 | |||
| chr11:34916722 | C | T | 3 | a0002 a0007 a0010 |
78 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(75): Show |
missense_variant | MODERATE | c.67C>T | p.Arg23Cys | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/11 | 105/2500 | 67/1506 | 23/501 | chr11 | 34916722 | |||
| chr11:34916725 | C | G | 1 | a0004 | 4 | HG00140.hp1 HG01081.hp2 HG01515.hp2 others(1): Show |
missense_variant | MODERATE | c.70C>G | p.Arg24Gly | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/11 | 108/2500 | 70/1506 | 24/501 | chr11 | 34916725 | |||
| chr11:34947565 | A | G | 1 | a0003 | 12 | HG00280.hp1 HG01109.hp1 HG01243.hp1 others(9): Show |
missense_variant | MODERATE | c.301A>G | p.Thr101Ala | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/11 | 339/2500 | 301/1506 | 101/501 | chr11 | 34947565 | |||
| chr11:34960443 | G | A | 1 | a0005 | 3 | HG02257.hp2 HG02559.hp1 HG02965.hp2 |
missense_variant | MODERATE | c.566G>A | p.Arg189His | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/11 | 604/2500 | 566/1506 | 189/501 | chr11 | 34960443 | |||
| chr11:34960466 | C | A | 1 | a0010 | 1 | HG02922.hp1 | missense_variant | MODERATE | c.589C>A | p.Leu197Met | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/11 | 627/2500 | 589/1506 | 197/501 | chr11 | 34960466 | |||
| chr11:34966750 | C | T | 1 | a0009 | 1 | HG02145.hp2 | missense_variant | MODERATE | c.752C>T | p.Ala251Val | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 6/11 | 790/2500 | 752/1506 | 251/501 | chr11 | 34966750 | |||
| chr11:34994932 | G | A | 1 | a0011 | 1 | HG03688.hp2 | missense_variant | MODERATE | c.1266G>A | p.Met422Ile | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 11/11 | 1304/2500 | 1266/1506 | 422/501 | chr11 | 34994932 | |||
| chr11:34994997 | G | A | 1 | a0006 | 3 | HG03139.hp1 HG03516.hp1 NA18522.hp1 |
missense_variant | MODERATE | c.1331G>A | p.Arg444Lys | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 11/11 | 1369/2500 | 1331/1506 | 444/501 | chr11 | 34994997 | |||
| chr11:34994999 | T | G | 1 | a0007 | 1 | HG01361.hp1 | missense_variant | MODERATE | c.1333T>G | p.Phe445Val | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 11/11 | 1371/2500 | 1333/1506 | 445/501 | chr11 | 34994999 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:34916718 | C | T | 19 | a0001c0001 a0001c0013 a0001c0014 others(16): Show |
223 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(220): Show |
synonymous_variant | LOW | c.63C>T | p.Pro21Pro | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/11 | 101/2500 | 63/1506 | 21/501 | chr11 | 34916718 | |||
| chr11:34916763 | T | C | 9 | a0002c0003 a0002c0004 a0002c0005 others(6): Show |
78 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(75): Show |
synonymous_variant | LOW | c.108T>C | p.Ser36Ser | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/11 | 146/2500 | 108/1506 | 36/501 | chr11 | 34916763 | |||
| chr11:34947603 | C | T | 2 | a0001c0026 a0002c0005 |
14 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(11): Show |
synonymous_variant | LOW | c.339C>T | p.Ile113Ile | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/11 | 377/2500 | 339/1506 | 113/501 | chr11 | 34947603 | |||
| chr11:34957479 | C | T | 1 | a0002c0008 | 8 | HG02145.hp1 HG02451.hp1 HG02615.hp1 others(5): Show |
synonymous_variant | LOW | c.438C>T | p.Asp146Asp | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 4/11 | 476/2500 | 438/1506 | 146/501 | chr11 | 34957479 | |||
| chr11:34957515 | G | A | 1 | a0002c0027 | 1 | HG01884.hp1 | synonymous_variant | LOW | c.474G>A | p.Glu158Glu | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 4/11 | 512/2500 | 474/1506 | 158/501 | chr11 | 34957515 | |||
| chr11:34957548 | C | T | 3 | a0001c0014 a0002c0007 a0007c0015 |
11 | HG01192.hp2 HG01361.hp1 HG01943.hp2 others(8): Show |
synonymous_variant | LOW | c.507C>T | p.Ile169Ile | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 4/11 | 545/2500 | 507/1506 | 169/501 | chr11 | 34957548 | |||
| chr11:34957572 | C | T | 1 | a0002c0008 | 8 | HG02145.hp1 HG02451.hp1 HG02615.hp1 others(5): Show |
synonymous_variant | LOW | c.531C>T | p.Pro177Pro | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 4/11 | 569/2500 | 531/1506 | 177/501 | chr11 | 34957572 | |||
| chr11:34960495 | C | G | 1 | a0010c0028 | 1 | HG02922.hp1 | synonymous_variant | LOW | c.618C>G | p.Gly206Gly | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/11 | 656/2500 | 618/1506 | 206/501 | chr11 | 34960495 | |||
| chr11:34966796 | T | C | 8 | a0001c0014 a0001c0017 a0001c0023 others(5): Show |
41 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(38): Show |
synonymous_variant | LOW | c.798T>C | p.Pro266Pro | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 6/11 | 836/2500 | 798/1506 | 266/501 | chr11 | 34966796 | |||
| chr11:34970180 | T | C | 9 | a0001c0001 a0001c0018 a0001c0024 others(6): Show |
142 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(139): Show |
synonymous_variant | LOW | c.858T>C | p.Val286Val | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/11 | 896/2500 | 858/1506 | 286/501 | chr11 | 34970180 | |||
| chr11:34970279 | G | A | 1 | a0002c0012 | 3 | HG06807.hp1 NA19030.hp2 NA20129.hp2 |
synonymous_variant | LOW | c.957G>A | p.Leu319Leu | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/11 | 995/2500 | 957/1506 | 319/501 | chr11 | 34970279 | |||
| chr11:34992320 | A | G | 1 | a0001c0024 | 1 | HG03491.hp2 | synonymous_variant | LOW | c.1188A>G | p.Leu396Leu | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 10/11 | 1226/2500 | 1188/1506 | 396/501 | chr11 | 34992320 | |||
| chr11:34994989 | G | A | 1 | a0001c0020 | 1 | NA18995.hp1 | synonymous_variant | LOW | c.1323G>A | p.Ala441Ala | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 11/11 | 1361/2500 | 1323/1506 | 441/501 | chr11 | 34994989 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:34916633 | C | A | 1 | a0001c0001t0008 | 4 | HG00558.hp1 HG02165.hp2 NA18950.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-23C>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/11 | 23 | chr11 | 34916633 | ||||||
| chr11:34916652 | C | G | 11 | a0002c0003t0003 a0002c0003t0010 a0002c0004t0004 others(8): Show |
78 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(75): Show |
5_prime_UTR_variant | MODIFIER | c.-4C>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/11 | 4 | chr11 | 34916652 | ||||||
| chr11:34995166 | T | TGCCTAGT others(8): Show |
1 | a0001c0021t0002 | 1 | NA18952.hp1 | 3_prime_UTR_variant | MODIFIER | c.1501_*9dupGCCTAGTC others(7): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 11/11 | 10 | INFO_REALIGN_3_PRIME | chr11 | 34995166 | |||||
| chr11:34995199 | A | C | 1 | a0001c0002t0012 | 2 | NA18962.hp1 NA18988.hp2 |
3_prime_UTR_variant | MODIFIER | c.*27A>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 11/11 | 27 | chr11 | 34995199 | ||||||
| chr11:34995286 | A | G | 1 | a0004c0022t0015 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*114A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 11/11 | 114 | chr11 | 34995286 | ||||||
| chr11:34995295 | A | G | 1 | a0002c0008t0006 | 8 | HG02145.hp1 HG02451.hp1 HG02615.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*123A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 11/11 | 123 | chr11 | 34995295 | ||||||
| chr11:34995345 | G | A | 3 | a0001c0026t0013 a0002c0004t0005 a0002c0005t0005 |
15 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*173G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 11/11 | 173 | chr11 | 34995345 | ||||||
| chr11:34995372 | T | C | 3 | a0001c0026t0013 a0002c0004t0005 a0002c0005t0005 |
15 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*200T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 11/11 | 200 | chr11 | 34995372 | ||||||
| chr11:34995435 | AAAGGGAA others(43): Show |
A | 1 | a0001c0002t0014 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*265_*314delAGGGAA others(44): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 11/11 | 265 | INFO_REALIGN_3_PRIME | chr11 | 34995435 | |||||
| chr11:34995658 | G | T | 14 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0011 others(11): Show |
157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
3_prime_UTR_variant | MODIFIER | c.*486G>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 11/11 | 486 | chr11 | 34995658 | ||||||
| chr11:34995679 | TAATA | T | 2 | a0001c0001t0011 a0004c0022t0015 |
3 | HG01081.hp2 HG01261.hp2 HG02738.hp1 |
3_prime_UTR_variant | MODIFIER | c.*517_*520delATAA | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 11/11 | 517 | INFO_REALIGN_3_PRIME | chr11 | 34995679 | |||||
| chr11:34995744 | A | G | 1 | a0010c0028t0016 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*572A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 11/11 | 572 | chr11 | 34995744 | ||||||
| chr11:34995816 | C | A | 26 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0011 others(23): Show |
227 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(224): Show |
3_prime_UTR_variant | MODIFIER | c.*644C>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 11/11 | 644 | chr11 | 34995816 | ||||||
| chr11:34996062 | T | C | 5 | a0001c0014t0009 a0001c0023t0009 a0002c0004t0004 others(2): Show |
25 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*890T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 11/11 | 890 | chr11 | 34996062 | ||||||
| chr11:34996076 | G | T | 1 | a0010c0028t0016 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*904G>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 11/11 | 904 | chr11 | 34996076 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:34916827 | G | C | 1 | a0002c0008t0006g0001 | 3 | HG02886.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.160+12G>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34916827 | |||||||
| chr11:34916830 | C | G | 4 | a0002c0003t0003g0276 a0002c0003t0003g0277 a0002c0003t0003g0278 others(1): Show |
4 | HG02615.hp2 HG02630.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.160+15C>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34916830 | |||||||
| chr11:34916909 | A | G | 67 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(64): Show |
78 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.160+94A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34916909 | |||||||
| chr11:34916936 | C | T | 1 | a0001c0001t0001g0221 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.160+121C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34916936 | |||||||
| chr11:34917004 | A | G | 67 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(64): Show |
78 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.160+189A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34917004 | |||||||
| chr11:34917104 | C | T | 5 | a0001c0002t0002g0216 a0001c0002t0002g0217 a0001c0002t0002g0218 others(2): Show |
5 | HG01074.hp2 HG01952.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.160+289C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34917104 | |||||||
| chr11:34917236 | G | A | 111 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(108): Show |
123 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.160+421G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34917236 | |||||||
| chr11:34917244 | C | T | 1 | a0001c0001t0001g0016 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.160+429C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34917244 | |||||||
| chr11:34917293 | T | C | 67 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(64): Show |
78 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.160+478T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34917293 | |||||||
| chr11:34917388 | A | G | 67 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(64): Show |
78 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.160+573A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34917388 | |||||||
| chr11:34917402 | T | G | 18 | a0002c0004t0004g0222 a0002c0004t0004g0224 a0002c0004t0004g0232 others(15): Show |
19 | HG01361.hp1 HG01496.hp2 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.160+587T>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34917402 | |||||||
| chr11:34917415 | A | G | 132 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(129): Show |
144 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.160+600A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34917415 | |||||||
| chr11:34917509 | T | A | 1 | a0002c0004t0004g0240 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.160+694T>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34917509 | |||||||
| chr11:34917677 | C | A | 2 | a0001c0002t0012g0128 a0001c0002t0012g0129 |
2 | NA18962.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.160+862C>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34917677 | |||||||
| chr11:34917745 | G | A | 67 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(64): Show |
78 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.160+930G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34917745 | |||||||
| chr11:34917894 | A | G | 4 | a0002c0004t0004g0236 a0002c0004t0004g0237 a0002c0004t0004g0238 others(1): Show |
4 | HG02280.hp1 HG03041.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.160+1079A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34917894 | |||||||
| chr11:34917896 | T | G | 41 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(38): Show |
49 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.160+1081T>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34917896 | |||||||
| chr11:34917920 | A | G | 1 | a0001c0001t0001g0127 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.160+1105A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34917920 | |||||||
| chr11:34917950 | G | A | 2 | a0001c0002t0002g0130 a0001c0002t0002g0131 |
2 | HG01891.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.160+1135G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34917950 | |||||||
| chr11:34917969 | A | G | 14 | a0001c0013t0002g0213 a0003c0006t0001g0202 a0003c0006t0001g0203 others(11): Show |
14 | HG00280.hp1 HG01109.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.160+1154A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34917969 | |||||||
| chr11:34917990 | G | A | 4 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(1): Show |
4 | HG02451.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.160+1175G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34917990 | |||||||
| chr11:34918084 | C | T | 67 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(64): Show |
78 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.160+1269C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34918084 | |||||||
| chr11:34918203 | G | A | 5 | a0002c0004t0004g0222 a0002c0004t0004g0236 a0002c0004t0004g0237 others(2): Show |
5 | HG02280.hp1 HG03041.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.160+1388G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34918203 | |||||||
| chr11:34918265 | C | T | 1 | a0001c0002t0002g0193 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.160+1450C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34918265 | |||||||
| chr11:34918276 | T | TA | 109 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(106): Show |
121 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.160+1474dupA | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 34918276 | ||||||
| chr11:34918383 | G | A | 1 | a0002c0007t0004g0223 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.160+1568G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34918383 | |||||||
| chr11:34918441 | GA | G | 20 | a0001c0002t0007g0187 a0001c0002t0007g0188 a0001c0002t0007g0189 others(17): Show |
20 | HG00280.hp1 HG01109.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.160+1640delA | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 34918441 | ||||||
| chr11:34918441 | GAA | G | 182 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(179): Show |
204 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(201): Show |
intron_variant | MODIFIER | c.160+1639_160+1640d others(4): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 34918441 | ||||||
| chr11:34918444 | A | G | 5 | a0002c0004t0004g0222 a0002c0004t0004g0236 a0002c0004t0004g0237 others(2): Show |
5 | HG02280.hp1 HG03041.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.160+1629A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34918444 | |||||||
| chr11:34918498 | G | A | 2 | a0001c0001t0001g0030 a0001c0001t0001g0031 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.160+1683G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34918498 | |||||||
| chr11:34918772 | G | A | 1 | a0002c0003t0003g0276 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.160+1957G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34918772 | |||||||
| chr11:34918795 | G | A | 2 | a0002c0012t0003g0242 a0002c0012t0003g0243 |
2 | NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.160+1980G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34918795 | |||||||
| chr11:34918806 | C | G | 67 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(64): Show |
78 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.160+1991C>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34918806 | |||||||
| chr11:34918859 | T | C | 6 | a0001c0002t0007g0187 a0001c0002t0007g0188 a0001c0002t0007g0189 others(3): Show |
6 | HG01884.hp2 HG02572.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.160+2044T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34918859 | |||||||
| chr11:34918899 | G | A | 199 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(196): Show |
222 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.160+2084G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34918899 | |||||||
| chr11:34919021 | A | G | 118 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(115): Show |
130 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.160+2206A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34919021 | |||||||
| chr11:34919190 | A | G | 67 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(64): Show |
78 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.160+2375A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34919190 | |||||||
| chr11:34919279 | CTG | C | 15 | a0001c0013t0002g0213 a0002c0004t0004g0224 a0003c0006t0001g0202 others(12): Show |
15 | HG00280.hp1 HG01109.hp1 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.160+2467_160+2468d others(4): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 34919279 | ||||||
| chr11:34919297 | G | A | 67 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(64): Show |
78 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.160+2482G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34919297 | |||||||
| chr11:34919360 | G | A | 10 | a0001c0002t0002g0017 a0001c0002t0002g0130 a0001c0002t0002g0131 others(7): Show |
11 | HG01891.hp2 HG02083.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.160+2545G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34919360 | |||||||
| chr11:34919435 | G | A | 132 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(129): Show |
144 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.160+2620G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34919435 | |||||||
| chr11:34919478 | G | T | 132 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(129): Show |
144 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.160+2663G>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34919478 | |||||||
| chr11:34919501 | T | G | 67 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(64): Show |
78 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.160+2686T>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34919501 | |||||||
| chr11:34919541 | C | T | 118 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(115): Show |
130 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.160+2726C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34919541 | |||||||
| chr11:34919551 | C | G | 14 | a0001c0013t0002g0213 a0003c0006t0001g0202 a0003c0006t0001g0203 others(11): Show |
14 | HG00280.hp1 HG01109.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.160+2736C>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34919551 | |||||||
| chr11:34919580 | T | C | 6 | a0001c0002t0002g0140 a0001c0002t0002g0141 a0004c0010t0002g0138 others(3): Show |
6 | HG00140.hp1 HG01081.hp2 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.160+2765T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34919580 | |||||||
| chr11:34919744 | A | G | 1 | a0001c0002t0002g0186 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.160+2929A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34919744 | |||||||
| chr11:34919811 | A | G | 67 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(64): Show |
78 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.160+2996A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34919811 | |||||||
| chr11:34919817 | C | G | 67 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(64): Show |
78 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.160+3002C>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34919817 | |||||||
| chr11:34919887 | A | G | 1 | a0001c0002t0002g0185 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.160+3072A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34919887 | |||||||
| chr11:34919909 | A | G | 1 | a0001c0002t0002g0184 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.160+3094A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34919909 | |||||||
| chr11:34919947 | G | A | 200 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(197): Show |
223 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.160+3132G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34919947 | |||||||
| chr11:34919988 | A | G | 1 | a0001c0001t0001g0221 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.160+3173A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34919988 | |||||||
| chr11:34920050 | C | A | 8 | a0002c0007t0004g0022 a0002c0007t0004g0223 a0002c0007t0004g0226 others(5): Show |
9 | HG01361.hp1 HG02602.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.160+3235C>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34920050 | |||||||
| chr11:34920298 | G | A | 118 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(115): Show |
130 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.160+3483G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34920298 | |||||||
| chr11:34920329 | G | A | 199 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(196): Show |
222 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.160+3514G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34920329 | |||||||
| chr11:34920366 | A | G | 16 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(13): Show |
21 | HG02055.hp1 HG02280.hp2 HG02451.hp2 others(18): Show |
intron_variant | MODIFIER | c.160+3551A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34920366 | |||||||
| chr11:34920422 | A | G | 67 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(64): Show |
78 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.160+3607A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34920422 | |||||||
| chr11:34920443 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.160+3628A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34920443 | |||||||
| chr11:34920463 | A | G | 14 | a0001c0013t0002g0213 a0003c0006t0001g0202 a0003c0006t0001g0203 others(11): Show |
14 | HG00280.hp1 HG01109.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.160+3648A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34920463 | |||||||
| chr11:34920601 | G | A | 6 | a0002c0008t0006g0001 a0002c0008t0006g0270 a0002c0008t0006g0271 others(3): Show |
8 | HG02145.hp1 HG02451.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.160+3786G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34920601 | |||||||
| chr11:34920704 | G | A | 1 | a0001c0002t0002g0145 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.160+3889G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34920704 | |||||||
| chr11:34920723 | T | A | 4 | a0002c0008t0006g0001 a0002c0008t0006g0270 a0002c0008t0006g0271 others(1): Show |
6 | HG02451.hp1 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.160+3908T>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34920723 | |||||||
| chr11:34920766 | T | C | 14 | a0001c0013t0002g0213 a0003c0006t0001g0202 a0003c0006t0001g0203 others(11): Show |
14 | HG00280.hp1 HG01109.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.160+3951T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34920766 | |||||||
| chr11:34920854 | A | G | 2 | a0002c0004t0004g0265 a0002c0004t0004g0266 |
2 | HG03195.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.160+4039A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34920854 | |||||||
| chr11:34920972 | C | A | 199 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(196): Show |
222 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.160+4157C>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34920972 | |||||||
| chr11:34921029 | G | A | 14 | a0001c0013t0002g0213 a0003c0006t0001g0202 a0003c0006t0001g0203 others(11): Show |
14 | HG00280.hp1 HG01109.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.160+4214G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34921029 | |||||||
| chr11:34921044 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.160+4229C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34921044 | |||||||
| chr11:34921289 | C | G | 67 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(64): Show |
78 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.160+4474C>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34921289 | |||||||
| chr11:34921378 | C | G | 1 | a0003c0006t0001g0214 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.160+4563C>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34921378 | |||||||
| chr11:34921444 | A | AACTG | 192 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(189): Show |
214 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.160+4632_160+4635d others(6): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 34921444 | ||||||
| chr11:34921447 | T | TGACG | 8 | a0002c0007t0004g0022 a0002c0007t0004g0223 a0002c0007t0004g0226 others(5): Show |
9 | HG01361.hp1 HG02602.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.160+4635_160+4636i others(6): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 34921447 | ||||||
| chr11:34921636 | C | T | 6 | a0002c0004t0004g0265 a0002c0004t0004g0266 a0002c0005t0005g0263 others(3): Show |
6 | HG02647.hp2 HG03195.hp1 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.160+4821C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34921636 | |||||||
| chr11:34921682 | G | C | 200 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(197): Show |
223 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.160+4867G>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34921682 | |||||||
| chr11:34921803 | A | G | 1 | a0001c0013t0002g0213 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.160+4988A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34921803 | |||||||
| chr11:34921944 | G | A | 65 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(62): Show |
76 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(73): Show |
intron_variant | MODIFIER | c.160+5129G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34921944 | |||||||
| chr11:34922200 | T | G | 199 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(196): Show |
222 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.160+5385T>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34922200 | |||||||
| chr11:34922407 | A | G | 67 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(64): Show |
78 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.160+5592A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34922407 | |||||||
| chr11:34922553 | G | A | 1 | a0010c0028t0016g0275 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.160+5738G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34922553 | |||||||
| chr11:34922617 | C | T | 14 | a0001c0013t0002g0213 a0003c0006t0001g0202 a0003c0006t0001g0203 others(11): Show |
14 | HG00280.hp1 HG01109.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.160+5802C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34922617 | |||||||
| chr11:34922650 | T | G | 1 | a0002c0004t0004g0240 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.160+5835T>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34922650 | |||||||
| chr11:34922665 | A | G | 67 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(64): Show |
78 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.160+5850A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34922665 | |||||||
| chr11:34922801 | CTTG | C | 132 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(129): Show |
144 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.160+5994_160+5996d others(5): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 34922801 | ||||||
| chr11:34922824 | T | C | 132 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(129): Show |
144 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.160+6009T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34922824 | |||||||
| chr11:34922826 | G | C | 1 | a0002c0004t0004g0240 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.160+6011G>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34922826 | |||||||
| chr11:34922835 | G | A | 6 | a0001c0002t0007g0187 a0001c0002t0007g0188 a0001c0002t0007g0189 others(3): Show |
6 | HG01884.hp2 HG02572.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.160+6020G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34922835 | |||||||
| chr11:34922864 | T | G | 2 | a0001c0001t0001g0032 a0001c0002t0002g0132 |
2 | HG00741.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.160+6049T>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34922864 | |||||||
| chr11:34922864 | T | TTG | 15 | a0001c0002t0002g0182 a0001c0002t0002g0183 a0001c0002t0007g0188 others(12): Show |
15 | HG00735.hp1 HG01884.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.160+6083_160+6084d others(4): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 34922864 | ||||||
| chr11:34922864 | T | TTGTG | 10 | a0002c0003t0003g0245 a0002c0003t0003g0246 a0002c0004t0005g0007 others(7): Show |
15 | HG01175.hp2 HG01257.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.160+6081_160+6084d others(6): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 34922864 | ||||||
| chr11:34922864 | T | TTGTGTG | 20 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0002c0003t0003g0023 others(17): Show |
23 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.160+6079_160+6084d others(8): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 34922864 | ||||||
| chr11:34922864 | T | TTGTGTGT others(1): Show |
12 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0002t0002g0133 others(9): Show |
12 | HG01361.hp1 HG01496.hp2 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.160+6077_160+6084d others(10): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 34922864 | ||||||
| chr11:34922864 | T | TTGTGTGT others(3): Show |
11 | a0001c0002t0002g0017 a0001c0002t0002g0136 a0001c0002t0002g0137 others(8): Show |
13 | HG02602.hp2 HG02615.hp2 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.160+6075_160+6084d others(12): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 34922864 | ||||||
| chr11:34922864 | T | TTGTGTGT others(5): Show |
6 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0017t0007g0144 others(3): Show |
6 | HG01891.hp2 HG02109.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.160+6073_160+6084d others(14): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 34922864 | ||||||
| chr11:34922864 | T | TTGTGTGT others(7): Show |
2 | a0002c0003t0003g0278 a0002c0003t0003g0279 |
2 | HG02630.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.160+6071_160+6084d others(16): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 34922864 | ||||||
| chr11:34922864 | TTGTG | T | 3 | a0002c0005t0005g0263 a0002c0012t0003g0242 a0002c0012t0003g0264 |
3 | HG02647.hp2 HG06807.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.160+6081_160+6084d others(6): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 34922864 | ||||||
| chr11:34922864 | TTGTGTGT others(1): Show |
T | 8 | a0002c0004t0004g0239 a0002c0008t0006g0001 a0002c0008t0006g0270 others(5): Show |
10 | HG02145.hp1 HG02451.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.160+6077_160+6084d others(10): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 34922864 | ||||||
| chr11:34922864 | TTGTGTGT others(3): Show |
T | 4 | a0002c0004t0004g0236 a0002c0004t0004g0237 a0002c0004t0004g0238 others(1): Show |
4 | HG02280.hp1 HG02976.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.160+6075_160+6084d others(12): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 34922864 | ||||||
| chr11:34922892 | GTGTGTGT others(1): Show |
G | 14 | a0001c0013t0002g0213 a0003c0006t0001g0202 a0003c0006t0001g0203 others(11): Show |
14 | HG00280.hp1 HG01109.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.160+6081_160+6088d others(10): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 34922892 | ||||||
| chr11:34922894 | GTGTGTA | G | 5 | a0001c0001t0001g0015 a0001c0001t0001g0112 a0001c0001t0001g0113 others(2): Show |
6 | HG00140.hp2 HG00280.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.160+6083_160+6088d others(8): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 34922894 | ||||||
| chr11:34922898 | GTA | G | 5 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(2): Show |
5 | HG01257.hp1 HG01258.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.160+6085_160+6086d others(4): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 34922898 | ||||||
| chr11:34922900 | A | G | 14 | a0001c0001t0001g0032 a0001c0001t0001g0115 a0001c0001t0001g0117 others(11): Show |
14 | HG00741.hp1 HG00741.hp2 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.160+6085A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34922900 | |||||||
| chr11:34922902 | GTATT | G | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(91): Show |
105 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.160+6088_160+6091d others(6): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34922902 | |||||||
| chr11:34922906 | T | G | 38 | a0001c0001t0001g0015 a0001c0001t0001g0032 a0001c0001t0001g0112 others(35): Show |
39 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(36): Show |
intron_variant | MODIFIER | c.160+6091T>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34922906 | |||||||
| chr11:34922920 | G | T | 2 | a0001c0002t0002g0180 a0001c0002t0002g0181 |
2 | HG01255.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.160+6105G>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34922920 | |||||||
| chr11:34922977 | C | A | 206 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(203): Show |
229 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.160+6162C>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34922977 | |||||||
| chr11:34923019 | A | C | 199 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(196): Show |
222 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.160+6204A>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34923019 | |||||||
| chr11:34923088 | C | T | 2 | a0002c0012t0003g0242 a0002c0012t0003g0243 |
2 | NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.160+6273C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34923088 | |||||||
| chr11:34923199 | TG | T | 199 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(196): Show |
222 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.160+6387delG | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 34923199 | ||||||
| chr11:34923299 | A | G | 1 | a0001c0017t0007g0144 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.160+6484A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34923299 | |||||||
| chr11:34923363 | T | C | 2 | a0002c0004t0004g0232 a0002c0004t0004g0235 |
2 | HG02572.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.160+6548T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34923363 | |||||||
| chr11:34923635 | TC | T | 67 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(64): Show |
78 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.160+6822delC | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 34923635 | ||||||
| chr11:34923681 | G | A | 110 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(107): Show |
122 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.160+6866G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34923681 | |||||||
| chr11:34923858 | G | A | 1 | a0002c0004t0004g0240 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.160+7043G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34923858 | |||||||
| chr11:34923902 | G | A | 25 | a0002c0004t0004g0222 a0002c0004t0004g0224 a0002c0004t0004g0232 others(22): Show |
28 | HG01361.hp1 HG01496.hp2 HG02145.hp1 others(25): Show |
intron_variant | MODIFIER | c.160+7087G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34923902 | |||||||
| chr11:34924177 | A | G | 1 | a0001c0013t0002g0213 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.161-7227A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34924177 | |||||||
| chr11:34924280 | C | T | 68 | a0001c0001t0001g0110 a0002c0003t0003g0023 a0002c0003t0003g0024 others(65): Show |
79 | HG00423.hp1 HG00621.hp2 HG00673.hp1 others(76): Show |
intron_variant | MODIFIER | c.161-7124C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34924280 | |||||||
| chr11:34924284 | C | T | 4 | a0002c0008t0006g0001 a0002c0008t0006g0270 a0002c0008t0006g0271 others(1): Show |
6 | HG02451.hp1 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.161-7120C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34924284 | |||||||
| chr11:34924409 | C | T | 3 | a0005c0009t0002g0177 a0005c0009t0002g0178 a0005c0009t0002g0179 |
3 | HG02257.hp2 HG02559.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.161-6995C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34924409 | |||||||
| chr11:34924430 | A | T | 67 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(64): Show |
78 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.161-6974A>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34924430 | |||||||
| chr11:34924467 | C | A | 4 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(1): Show |
4 | HG02451.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.161-6937C>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34924467 | |||||||
| chr11:34924568 | G | A | 41 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(38): Show |
49 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.161-6836G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34924568 | |||||||
| chr11:34924620 | T | A | 41 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(38): Show |
49 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.161-6784T>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34924620 | |||||||
| chr11:34924621 | A | T | 200 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(197): Show |
223 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.161-6783A>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34924621 | |||||||
| chr11:34924756 | A | G | 67 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(64): Show |
78 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.161-6648A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34924756 | |||||||
| chr11:34924760 | G | A | 67 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(64): Show |
78 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.161-6644G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34924760 | |||||||
| chr11:34924970 | G | C | 1 | a0001c0001t0001g0033 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.161-6434G>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34924970 | |||||||
| chr11:34925119 | C | T | 1 | a0002c0004t0004g0240 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.161-6285C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34925119 | |||||||
| chr11:34925165 | A | G | 14 | a0001c0013t0002g0213 a0003c0006t0001g0202 a0003c0006t0001g0203 others(11): Show |
14 | HG00280.hp1 HG01109.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.161-6239A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34925165 | |||||||
| chr11:34925412 | G | A | 1 | a0002c0007t0004g0226 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.161-5992G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34925412 | |||||||
| chr11:34925493 | C | T | 67 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(64): Show |
78 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.161-5911C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34925493 | |||||||
| chr11:34925509 | G | A | 199 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(196): Show |
222 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.161-5895G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34925509 | |||||||
| chr11:34925642 | T | C | 7 | a0002c0004t0004g0265 a0002c0004t0004g0266 a0002c0005t0005g0263 others(4): Show |
7 | HG01884.hp1 HG02647.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.161-5762T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34925642 | |||||||
| chr11:34925949 | A | G | 67 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(64): Show |
78 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.161-5455A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34925949 | |||||||
| chr11:34925965 | A | T | 1 | a0001c0001t0001g0033 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.161-5439A>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34925965 | |||||||
| chr11:34925987 | A | G | 6 | a0002c0008t0006g0001 a0002c0008t0006g0270 a0002c0008t0006g0271 others(3): Show |
8 | HG02145.hp1 HG02451.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.161-5417A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34925987 | |||||||
| chr11:34926082 | G | A | 1 | a0001c0002t0002g0146 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.161-5322G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34926082 | |||||||
| chr11:34926146 | A | G | 14 | a0001c0013t0002g0213 a0003c0006t0001g0202 a0003c0006t0001g0203 others(11): Show |
14 | HG00280.hp1 HG01109.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.161-5258A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34926146 | |||||||
| chr11:34926219 | C | T | 1 | a0010c0028t0016g0275 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.161-5185C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34926219 | |||||||
| chr11:34926248 | T | G | 1 | a0001c0001t0001g0009 | 2 | HG02622.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.161-5156T>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34926248 | |||||||
| chr11:34926317 | T | C | 41 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(38): Show |
49 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.161-5087T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34926317 | |||||||
| chr11:34926340 | A | G | 1 | a0002c0027t0003g0244 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.161-5064A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34926340 | |||||||
| chr11:34926379 | C | T | 4 | a0002c0008t0006g0001 a0002c0008t0006g0270 a0002c0008t0006g0271 others(1): Show |
6 | HG02451.hp1 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.161-5025C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34926379 | |||||||
| chr11:34926397 | A | C | 132 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(129): Show |
144 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.161-5007A>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34926397 | |||||||
| chr11:34926581 | T | C | 1 | a0001c0002t0002g0147 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.161-4823T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34926581 | |||||||
| chr11:34926621 | A | G | 1 | a0002c0003t0003g0257 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.161-4783A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34926621 | |||||||
| chr11:34926669 | A | C | 6 | a0001c0002t0007g0187 a0001c0002t0007g0188 a0001c0002t0007g0189 others(3): Show |
6 | HG01884.hp2 HG02572.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.161-4735A>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34926669 | |||||||
| chr11:34926670 | AT | A | 200 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(197): Show |
223 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.161-4724delT | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 34926670 | ||||||
| chr11:34926749 | G | GAAGTATG others(12): Show |
10 | a0001c0002t0002g0017 a0001c0002t0002g0130 a0001c0002t0002g0131 others(7): Show |
11 | HG01891.hp2 HG02083.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.161-4654_161-4636d others(21): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 34926749 | ||||||
| chr11:34926767 | T | C | 4 | a0001c0023t0009g0199 a0006c0011t0001g0198 a0006c0011t0001g0200 others(1): Show |
4 | HG02559.hp2 HG03139.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.161-4637T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34926767 | |||||||
| chr11:34926805 | A | C | 8 | a0002c0004t0005g0007 a0002c0005t0005g0007 a0002c0005t0005g0008 others(5): Show |
13 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.161-4599A>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34926805 | |||||||
| chr11:34926895 | G | T | 1 | a0002c0004t0004g0224 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.161-4509G>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34926895 | |||||||
| chr11:34926999 | G | A | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | HG01167.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.161-4405G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34926999 | |||||||
| chr11:34927014 | T | TA | 66 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(63): Show |
77 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(74): Show |
intron_variant | MODIFIER | c.161-4383dupA | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 34927014 | ||||||
| chr11:34927039 | G | A | 118 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(115): Show |
130 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.161-4365G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34927039 | |||||||
| chr11:34927226 | A | AG | 200 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(197): Show |
223 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.161-4178_161-4177i others(3): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34927226 | |||||||
| chr11:34927280 | G | C | 67 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(64): Show |
78 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.161-4124G>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34927280 | |||||||
| chr11:34927329 | C | G | 67 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(64): Show |
78 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.161-4075C>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34927329 | |||||||
| chr11:34927489 | A | C | 6 | a0002c0008t0006g0001 a0002c0008t0006g0270 a0002c0008t0006g0271 others(3): Show |
8 | HG02145.hp1 HG02451.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.161-3915A>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34927489 | |||||||
| chr11:34927569 | T | C | 199 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(196): Show |
222 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.161-3835T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34927569 | |||||||
| chr11:34927612 | G | A | 1 | a0001c0001t0001g0036 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.161-3792G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34927612 | |||||||
| chr11:34927651 | G | T | 14 | a0001c0013t0002g0213 a0003c0006t0001g0202 a0003c0006t0001g0203 others(11): Show |
14 | HG00280.hp1 HG01109.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.161-3753G>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34927651 | |||||||
| chr11:34927872 | A | G | 1 | a0002c0004t0004g0240 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.161-3532A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34927872 | |||||||
| chr11:34927955 | G | A | 33 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(30): Show |
36 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.161-3449G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34927955 | |||||||
| chr11:34928024 | A | T | 3 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 |
3 | HG01257.hp1 HG01258.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.161-3380A>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34928024 | |||||||
| chr11:34928066 | C | T | 5 | a0002c0004t0004g0222 a0002c0004t0004g0236 a0002c0004t0004g0237 others(2): Show |
5 | HG02280.hp1 HG03041.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.161-3338C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34928066 | |||||||
| chr11:34928179 | G | A | 6 | a0001c0002t0007g0187 a0001c0002t0007g0188 a0001c0002t0007g0189 others(3): Show |
6 | HG01884.hp2 HG02572.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.161-3225G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34928179 | |||||||
| chr11:34928319 | T | C | 110 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(107): Show |
122 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.161-3085T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34928319 | |||||||
| chr11:34928371 | C | CT | 68 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0002t0012g0129 others(65): Show |
79 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(76): Show |
intron_variant | MODIFIER | c.161-3021dupT | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 34928371 | ||||||
| chr11:34928413 | T | G | 6 | a0002c0004t0004g0265 a0002c0004t0004g0266 a0002c0005t0005g0263 others(3): Show |
6 | HG02647.hp2 HG03195.hp1 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.161-2991T>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34928413 | |||||||
| chr11:34928444 | T | G | 65 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(62): Show |
76 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(73): Show |
intron_variant | MODIFIER | c.161-2960T>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34928444 | |||||||
| chr11:34928445 | T | G | 2 | a0002c0004t0004g0265 a0002c0004t0004g0266 |
2 | HG03195.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.161-2959T>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34928445 | |||||||
| chr11:34928649 | G | C | 132 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(129): Show |
144 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.161-2755G>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34928649 | |||||||
| chr11:34929162 | C | CA | 206 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(203): Show |
229 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.161-2241dupA | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 34929162 | ||||||
| chr11:34929198 | T | C | 67 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(64): Show |
78 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.161-2206T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34929198 | |||||||
| chr11:34929258 | C | T | 6 | a0001c0002t0007g0187 a0001c0002t0007g0188 a0001c0002t0007g0189 others(3): Show |
6 | HG01884.hp2 HG02572.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.161-2146C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34929258 | |||||||
| chr11:34929278 | C | T | 1 | a0002c0004t0004g0240 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.161-2126C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34929278 | |||||||
| chr11:34929314 | A | G | 67 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(64): Show |
78 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.161-2090A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34929314 | |||||||
| chr11:34929316 | C | G | 2 | a0001c0002t0002g0175 a0001c0002t0002g0176 |
2 | NA18957.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.161-2088C>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34929316 | |||||||
| chr11:34929357 | A | G | 67 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(64): Show |
78 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.161-2047A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34929357 | |||||||
| chr11:34929373 | G | C | 132 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(129): Show |
144 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.161-2031G>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34929373 | |||||||
| chr11:34929375 | C | T | 2 | a0001c0001t0008g0109 a0001c0017t0007g0144 |
2 | HG02109.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.161-2029C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34929375 | |||||||
| chr11:34929403 | A | G | 132 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(129): Show |
144 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.161-2001A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34929403 | |||||||
| chr11:34929412 | T | C | 1 | a0001c0002t0002g0148 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.161-1992T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34929412 | |||||||
| chr11:34929650 | G | A | 1 | a0002c0004t0004g0240 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.161-1754G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34929650 | |||||||
| chr11:34929657 | A | G | 1 | a0001c0001t0001g0108 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.161-1747A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34929657 | |||||||
| chr11:34929793 | C | T | 1 | a0001c0002t0002g0135 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.161-1611C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34929793 | |||||||
| chr11:34929942 | G | A | 2 | a0002c0003t0003g0278 a0002c0003t0003g0279 |
2 | HG02630.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.161-1462G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34929942 | |||||||
| chr11:34929986 | T | C | 8 | a0002c0007t0004g0022 a0002c0007t0004g0223 a0002c0007t0004g0226 others(5): Show |
9 | HG01361.hp1 HG02602.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.161-1418T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34929986 | |||||||
| chr11:34930059 | T | C | 67 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(64): Show |
78 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.161-1345T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34930059 | |||||||
| chr11:34930398 | A | G | 67 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(64): Show |
78 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.161-1006A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34930398 | |||||||
| chr11:34930408 | A | G | 1 | a0002c0003t0003g0256 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.161-996A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34930408 | |||||||
| chr11:34930416 | A | G | 1 | a0001c0001t0001g0107 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.161-988A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34930416 | |||||||
| chr11:34930446 | G | T | 200 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(197): Show |
223 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.161-958G>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34930446 | |||||||
| chr11:34930568 | T | C | 200 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(197): Show |
223 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.161-836T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34930568 | |||||||
| chr11:34930611 | T | C | 14 | a0001c0013t0002g0213 a0003c0006t0001g0202 a0003c0006t0001g0203 others(11): Show |
14 | HG00280.hp1 HG01109.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.161-793T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34930611 | |||||||
| chr11:34930611 | T | G | 7 | a0001c0002t0002g0149 a0001c0002t0002g0150 a0001c0002t0002g0151 others(4): Show |
7 | HG00735.hp1 HG01071.hp2 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.161-793T>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34930611 | |||||||
| chr11:34930630 | G | T | 67 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(64): Show |
78 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.161-774G>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34930630 | |||||||
| chr11:34930640 | A | G | 14 | a0001c0013t0002g0213 a0003c0006t0001g0202 a0003c0006t0001g0203 others(11): Show |
14 | HG00280.hp1 HG01109.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.161-764A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34930640 | |||||||
| chr11:34930642 | G | A | 14 | a0001c0013t0002g0213 a0003c0006t0001g0202 a0003c0006t0001g0203 others(11): Show |
14 | HG00280.hp1 HG01109.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.161-762G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34930642 | |||||||
| chr11:34930694 | G | C | 199 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(196): Show |
222 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.161-710G>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34930694 | |||||||
| chr11:34930784 | G | T | 1 | a0001c0001t0001g0016 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.161-620G>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34930784 | |||||||
| chr11:34930786 | G | A | 14 | a0001c0013t0002g0213 a0003c0006t0001g0202 a0003c0006t0001g0203 others(11): Show |
14 | HG00280.hp1 HG01109.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.161-618G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34930786 | |||||||
| chr11:34930805 | G | A | 5 | a0003c0006t0001g0202 a0003c0006t0001g0203 a0003c0006t0001g0204 others(2): Show |
5 | HG00280.hp1 HG01943.hp1 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.161-599G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34930805 | |||||||
| chr11:34930862 | T | C | 67 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(64): Show |
78 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.161-542T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34930862 | |||||||
| chr11:34931018 | G | C | 199 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(196): Show |
222 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.161-386G>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34931018 | |||||||
| chr11:34931322 | C | T | 1 | a0002c0007t0004g0230 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.161-82C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34931322 | |||||||
| chr11:34931487 | G | A | 8 | a0002c0004t0005g0007 a0002c0005t0005g0007 a0002c0005t0005g0008 others(5): Show |
13 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(10): Show |
splice_region_variant&intron_variant | LOW | c.241+3G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34931487 | |||||||
| chr11:34931508 | C | A | 67 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(64): Show |
78 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.241+24C>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34931508 | |||||||
| chr11:34931536 | G | GT | 61 | a0001c0001t0001g0118 a0001c0014t0009g0105 a0001c0014t0009g0106 others(58): Show |
72 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(69): Show |
intron_variant | MODIFIER | c.241+56dupT | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 34931536 | ||||||
| chr11:34931536 | G | GTT | 4 | a0002c0003t0003g0255 a0002c0003t0003g0259 a0002c0004t0004g0238 others(1): Show |
4 | HG03098.hp1 NA18940.hp1 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.241+55_241+56dupTT | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 34931536 | ||||||
| chr11:34931537 | T | G | 1 | a0001c0001t0001g0037 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.241+53T>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34931537 | |||||||
| chr11:34931541 | G | GT | 127 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(124): Show |
139 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.241+68dupT | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 34931541 | ||||||
| chr11:34931541 | G | T | 70 | a0001c0001t0001g0118 a0001c0014t0009g0105 a0001c0014t0009g0106 others(67): Show |
81 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(78): Show |
intron_variant | MODIFIER | c.241+57G>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34931541 | |||||||
| chr11:34931657 | G | A | 2 | a0002c0004t0004g0265 a0002c0004t0004g0266 |
2 | HG03195.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.241+173G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34931657 | |||||||
| chr11:34931812 | T | TTG | 35 | a0001c0001t0001g0040 a0001c0001t0001g0194 a0001c0002t0002g0004 others(32): Show |
40 | HG00140.hp1 HG00609.hp2 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.241+366_241+367dup others(2): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 34931812 | ||||||
| chr11:34931812 | T | TTGTG | 7 | a0001c0002t0002g0018 a0001c0002t0002g0019 a0001c0002t0002g0152 others(4): Show |
9 | HG01515.hp2 HG01517.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.241+364_241+367dup others(4): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 34931812 | ||||||
| chr11:34931812 | TTG | T | 24 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(21): Show |
28 | HG01175.hp1 HG01192.hp2 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.241+366_241+367del others(2): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 34931812 | ||||||
| chr11:34931812 | TTGTG | T | 102 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(99): Show |
110 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.241+364_241+367del others(4): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 34931812 | ||||||
| chr11:34931812 | TTGTGTGT others(1): Show |
T | 4 | a0001c0002t0007g0192 a0001c0017t0007g0144 a0002c0008t0006g0270 others(1): Show |
4 | HG02109.hp1 HG02723.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.241+360_241+367del others(8): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 34931812 | ||||||
| chr11:34931812 | TTGTGTGT others(3): Show |
T | 9 | a0002c0003t0003g0247 a0002c0003t0003g0276 a0002c0003t0003g0277 others(6): Show |
11 | HG01884.hp1 HG02451.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.241+358_241+367del others(10): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 34931812 | ||||||
| chr11:34931812 | TTGTGTGT others(5): Show |
T | 56 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(53): Show |
65 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(62): Show |
intron_variant | MODIFIER | c.241+356_241+367del others(12): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 34931812 | ||||||
| chr11:34931968 | A | C | 1 | a0002c0003t0010g0254 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.241+484A>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34931968 | |||||||
| chr11:34931973 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.241+489T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34931973 | |||||||
| chr11:34931977 | A | G | 67 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(64): Show |
78 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.241+493A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34931977 | |||||||
| chr11:34931982 | G | A | 67 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(64): Show |
78 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.241+498G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34931982 | |||||||
| chr11:34932032 | A | G | 1 | a0002c0004t0004g0237 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.241+548A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34932032 | |||||||
| chr11:34932358 | A | G | 5 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0044 others(2): Show |
7 | HG01256.hp2 HG01952.hp2 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.241+874A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34932358 | |||||||
| chr11:34932388 | G | A | 2 | a0002c0004t0004g0265 a0002c0004t0004g0266 |
2 | HG03195.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.241+904G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34932388 | |||||||
| chr11:34932435 | A | G | 206 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(203): Show |
229 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.241+951A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34932435 | |||||||
| chr11:34932482 | C | T | 1 | a0002c0005t0005g0027 | 2 | HG02055.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.241+998C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34932482 | |||||||
| chr11:34932685 | T | A | 110 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(107): Show |
122 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.241+1201T>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34932685 | |||||||
| chr11:34932783 | C | T | 1 | a0003c0006t0001g0212 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.241+1299C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34932783 | |||||||
| chr11:34932885 | C | T | 1 | a0001c0017t0007g0144 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.241+1401C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34932885 | |||||||
| chr11:34932932 | G | A | 200 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(197): Show |
223 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.241+1448G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34932932 | |||||||
| chr11:34933057 | A | G | 1 | a0002c0007t0004g0230 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.241+1573A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34933057 | |||||||
| chr11:34933061 | A | C | 1 | a0001c0002t0002g0171 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.241+1577A>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34933061 | |||||||
| chr11:34933168 | A | G | 67 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(64): Show |
78 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.241+1684A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34933168 | |||||||
| chr11:34933345 | G | A | 5 | a0002c0004t0005g0007 a0002c0005t0005g0007 a0002c0005t0005g0026 others(2): Show |
7 | HG02280.hp2 HG02809.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.241+1861G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34933345 | |||||||
| chr11:34933346 | A | G | 67 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(64): Show |
78 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.241+1862A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34933346 | |||||||
| chr11:34933426 | A | G | 5 | a0002c0004t0004g0222 a0002c0004t0004g0236 a0002c0004t0004g0237 others(2): Show |
5 | HG02280.hp1 HG03041.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.241+1942A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34933426 | |||||||
| chr11:34933438 | A | C | 1 | a0002c0005t0005g0026 | 2 | HG02809.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.241+1954A>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34933438 | |||||||
| chr11:34933737 | A | G | 1 | a0010c0028t0016g0275 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.241+2253A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34933737 | |||||||
| chr11:34933843 | CTAAGGAT others(2): Show |
C | 4 | a0001c0023t0009g0199 a0006c0011t0001g0198 a0006c0011t0001g0200 others(1): Show |
4 | HG02559.hp2 HG03139.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.241+2371_241+2379d others(11): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 34933843 | ||||||
| chr11:34933860 | A | G | 67 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(64): Show |
78 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.241+2376A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34933860 | |||||||
| chr11:34933872 | A | G | 2 | a0001c0001t0001g0196 a0001c0001t0001g0197 |
2 | HG02451.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.241+2388A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34933872 | |||||||
| chr11:34933979 | T | C | 6 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0047 others(3): Show |
8 | HG01243.hp2 HG02109.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.241+2495T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34933979 | |||||||
| chr11:34934037 | T | G | 118 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(115): Show |
130 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.241+2553T>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34934037 | |||||||
| chr11:34934127 | C | T | 67 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(64): Show |
78 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.241+2643C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34934127 | |||||||
| chr11:34934301 | A | G | 2 | a0002c0003t0003g0258 a0002c0003t0003g0259 |
2 | NA18940.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.241+2817A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34934301 | |||||||
| chr11:34934308 | A | G | 1 | a0011c0019t0002g0159 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.241+2824A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34934308 | |||||||
| chr11:34934460 | C | T | 1 | a0002c0004t0004g0224 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.241+2976C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34934460 | |||||||
| chr11:34934571 | A | AT | 36 | a0001c0001t0001g0197 a0001c0002t0002g0021 a0001c0002t0002g0137 others(33): Show |
38 | HG00280.hp1 HG00621.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.241+3111dupT | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 34934571 | ||||||
| chr11:34934571 | A | ATT | 13 | a0002c0003t0010g0254 a0002c0004t0004g0224 a0002c0004t0005g0007 others(10): Show |
18 | HG01884.hp1 HG02055.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.241+3110_241+3111d others(4): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 34934571 | ||||||
| chr11:34934571 | A | ATTT | 26 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(23): Show |
29 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.241+3109_241+3111d others(5): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 34934571 | ||||||
| chr11:34934571 | AT | A | 58 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0016 others(55): Show |
63 | HG00423.hp2 HG00558.hp2 HG00741.hp1 others(60): Show |
intron_variant | MODIFIER | c.241+3111delT | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 34934571 | ||||||
| chr11:34934571 | ATT | A | 63 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(60): Show |
72 | HG00140.hp2 HG00280.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.241+3110_241+3111d others(4): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 34934571 | ||||||
| chr11:34934663 | A | G | 1 | a0001c0017t0007g0144 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.241+3179A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34934663 | |||||||
| chr11:34934670 | T | C | 5 | a0001c0001t0001g0051 a0001c0001t0001g0078 a0001c0001t0001g0079 others(2): Show |
5 | HG01074.hp1 HG01167.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.241+3186T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34934670 | |||||||
| chr11:34934744 | A | G | 41 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(38): Show |
49 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.241+3260A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34934744 | |||||||
| chr11:34934772 | T | C | 1 | a0002c0027t0003g0244 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.241+3288T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34934772 | |||||||
| chr11:34934789 | C | T | 1 | a0002c0004t0004g0222 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.241+3305C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34934789 | |||||||
| chr11:34934794 | G | A | 132 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(129): Show |
144 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.241+3310G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34934794 | |||||||
| chr11:34934828 | C | T | 67 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(64): Show |
78 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.241+3344C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34934828 | |||||||
| chr11:34934874 | C | A | 13 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0248 others(10): Show |
15 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(12): Show |
intron_variant | MODIFIER | c.241+3390C>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34934874 | |||||||
| chr11:34934932 | TA | T | 83 | a0001c0001t0001g0103 a0001c0001t0001g0119 a0001c0001t0001g0120 others(80): Show |
94 | HG00280.hp1 HG00423.hp1 HG00673.hp1 others(91): Show |
intron_variant | MODIFIER | c.241+3460delA | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 34934932 | ||||||
| chr11:34934933 | A | T | 121 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(118): Show |
133 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.241+3449A>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34934933 | |||||||
| chr11:34934934 | A | T | 83 | a0001c0001t0001g0103 a0001c0001t0001g0119 a0001c0001t0001g0120 others(80): Show |
94 | HG00280.hp1 HG00423.hp1 HG00673.hp1 others(91): Show |
intron_variant | MODIFIER | c.241+3450A>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34934934 | |||||||
| chr11:34934935 | A | T | 1 | a0002c0004t0004g0240 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.241+3451A>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34934935 | |||||||
| chr11:34934940 | A | G | 1 | a0001c0002t0002g0135 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.241+3456A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34934940 | |||||||
| chr11:34934953 | A | G | 67 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(64): Show |
78 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.241+3469A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34934953 | |||||||
| chr11:34935020 | C | A | 118 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(115): Show |
130 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.241+3536C>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34935020 | |||||||
| chr11:34935069 | G | A | 67 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(64): Show |
78 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.241+3585G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34935069 | |||||||
| chr11:34935087 | A | G | 14 | a0001c0013t0002g0213 a0003c0006t0001g0202 a0003c0006t0001g0203 others(11): Show |
14 | HG00280.hp1 HG01109.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.241+3603A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34935087 | |||||||
| chr11:34935093 | A | G | 1 | a0002c0004t0004g0240 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.241+3609A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34935093 | |||||||
| chr11:34935111 | A | T | 11 | a0001c0002t0002g0006 a0001c0002t0002g0021 a0001c0002t0002g0146 others(8): Show |
14 | NA18948.hp1 NA18949.hp1 NA18950.hp2 others(11): Show |
intron_variant | MODIFIER | c.241+3627A>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34935111 | |||||||
| chr11:34935418 | A | G | 25 | a0002c0004t0004g0222 a0002c0004t0004g0224 a0002c0004t0004g0232 others(22): Show |
28 | HG01361.hp1 HG01496.hp2 HG02145.hp1 others(25): Show |
intron_variant | MODIFIER | c.241+3934A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34935418 | |||||||
| chr11:34935510 | T | G | 1 | a0001c0001t0001g0194 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.241+4026T>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34935510 | |||||||
| chr11:34935527 | T | C | 132 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(129): Show |
144 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.241+4043T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34935527 | |||||||
| chr11:34935542 | T | A | 6 | a0001c0002t0007g0187 a0001c0002t0007g0188 a0001c0002t0007g0189 others(3): Show |
6 | HG01884.hp2 HG02572.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.241+4058T>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34935542 | |||||||
| chr11:34935582 | T | G | 1 | a0005c0009t0002g0177 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.241+4098T>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34935582 | |||||||
| chr11:34935602 | C | T | 8 | a0002c0004t0005g0007 a0002c0005t0005g0007 a0002c0005t0005g0008 others(5): Show |
13 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.241+4118C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34935602 | |||||||
| chr11:34935664 | A | G | 67 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(64): Show |
78 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.241+4180A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34935664 | |||||||
| chr11:34935726 | C | T | 67 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(64): Show |
78 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.241+4242C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34935726 | |||||||
| chr11:34935737 | G | T | 199 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(196): Show |
222 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.241+4253G>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34935737 | |||||||
| chr11:34935804 | T | C | 67 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(64): Show |
78 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.241+4320T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34935804 | |||||||
| chr11:34935847 | A | T | 3 | a0002c0004t0004g0265 a0002c0004t0004g0266 a0002c0012t0003g0264 |
3 | HG03195.hp1 HG06807.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.241+4363A>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34935847 | |||||||
| chr11:34935908 | A | G | 14 | a0001c0013t0002g0213 a0003c0006t0001g0202 a0003c0006t0001g0203 others(11): Show |
14 | HG00280.hp1 HG01109.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.241+4424A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34935908 | |||||||
| chr11:34935970 | C | G | 14 | a0001c0013t0002g0213 a0003c0006t0001g0202 a0003c0006t0001g0203 others(11): Show |
14 | HG00280.hp1 HG01109.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.241+4486C>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34935970 | |||||||
| chr11:34936036 | C | A | 1 | a0002c0027t0003g0244 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.241+4552C>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34936036 | |||||||
| chr11:34936048 | C | T | 2 | a0002c0003t0003g0276 a0002c0003t0003g0277 |
2 | HG02615.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.241+4564C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34936048 | |||||||
| chr11:34936067 | G | C | 1 | a0001c0017t0007g0144 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.241+4583G>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34936067 | |||||||
| chr11:34936141 | G | A | 2 | a0001c0001t0001g0082 a0001c0001t0001g0107 |
2 | HG02717.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.241+4657G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34936141 | |||||||
| chr11:34936170 | T | C | 1 | a0001c0001t0001g0052 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.241+4686T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34936170 | |||||||
| chr11:34936269 | A | G | 67 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(64): Show |
78 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.241+4785A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34936269 | |||||||
| chr11:34936275 | A | C | 67 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(64): Show |
78 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.241+4791A>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34936275 | |||||||
| chr11:34936286 | T | A | 67 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(64): Show |
78 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.241+4802T>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34936286 | |||||||
| chr11:34936291 | G | A | 67 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(64): Show |
78 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.241+4807G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34936291 | |||||||
| chr11:34936363 | C | G | 67 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(64): Show |
78 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.241+4879C>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34936363 | |||||||
| chr11:34936377 | G | A | 1 | a0002c0004t0004g0240 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.241+4893G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34936377 | |||||||
| chr11:34936390 | A | G | 67 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(64): Show |
78 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.241+4906A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34936390 | |||||||
| chr11:34936423 | G | A | 8 | a0002c0004t0005g0007 a0002c0005t0005g0007 a0002c0005t0005g0008 others(5): Show |
13 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.241+4939G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34936423 | |||||||
| chr11:34936461 | G | A | 200 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(197): Show |
223 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.241+4977G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34936461 | |||||||
| chr11:34936732 | A | G | 14 | a0001c0013t0002g0213 a0003c0006t0001g0202 a0003c0006t0001g0203 others(11): Show |
14 | HG00280.hp1 HG01109.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.241+5248A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34936732 | |||||||
| chr11:34936739 | T | A | 57 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(54): Show |
64 | HG00140.hp2 HG00280.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.241+5255T>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34936739 | |||||||
| chr11:34936769 | G | GTTTCT | 34 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(31): Show |
42 | HG00673.hp1 HG00673.hp2 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.241+5299_241+5303d others(7): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 34936769 | ||||||
| chr11:34936769 | G | GTTTCTTT others(3): Show |
20 | a0001c0013t0002g0213 a0001c0023t0009g0199 a0002c0012t0003g0242 others(17): Show |
20 | HG00280.hp1 HG01109.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.241+5294_241+5303d others(12): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 34936769 | ||||||
| chr11:34936783 | C | CT | 9 | a0001c0002t0002g0134 a0001c0002t0002g0151 a0001c0002t0002g0181 others(6): Show |
9 | HG01255.hp2 HG01358.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.241+5321dupT | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 34936783 | ||||||
| chr11:34936784 | T | TTTTC | 16 | a0002c0003t0003g0261 a0002c0004t0004g0222 a0002c0004t0004g0232 others(13): Show |
17 | HG01361.hp1 HG01496.hp2 HG02015.hp2 others(14): Show |
intron_variant | MODIFIER | c.241+5303_241+5304i others(6): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 34936784 | ||||||
| chr11:34936784 | T | TTTTCTTT others(2): Show |
6 | a0001c0001t0001g0043 a0001c0001t0001g0052 a0001c0001t0001g0076 others(3): Show |
6 | HG00735.hp2 HG03704.hp1 HG04199.hp1 others(3): Show |
intron_variant | MODIFIER | c.241+5303_241+5304i others(11): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 34936784 | ||||||
| chr11:34936785 | T | TTTC | 9 | a0002c0004t0004g0224 a0002c0004t0004g0236 a0002c0004t0004g0237 others(6): Show |
11 | HG02280.hp1 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.241+5303_241+5304i others(5): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 34936785 | ||||||
| chr11:34936785 | T | TTTCTTTT others(1): Show |
102 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(99): Show |
114 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.241+5303_241+5304i others(10): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 34936785 | ||||||
| chr11:34936788 | T | C | 4 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(1): Show |
4 | HG02451.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.241+5304T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34936788 | |||||||
| chr11:34936793 | T | C | 4 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(1): Show |
4 | HG02451.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.241+5309T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34936793 | |||||||
| chr11:34936797 | T | G | 14 | a0001c0013t0002g0213 a0003c0006t0001g0202 a0003c0006t0001g0203 others(11): Show |
14 | HG00280.hp1 HG01109.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.241+5313T>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34936797 | |||||||
| chr11:34936802 | T | G | 14 | a0001c0013t0002g0213 a0003c0006t0001g0202 a0003c0006t0001g0203 others(11): Show |
14 | HG00280.hp1 HG01109.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.241+5318T>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34936802 | |||||||
| chr11:34936806 | C | T | 195 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(192): Show |
218 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.241+5322C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34936806 | |||||||
| chr11:34936893 | A | G | 1 | a0001c0001t0001g0016 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.241+5409A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34936893 | |||||||
| chr11:34936920 | C | G | 13 | a0001c0013t0002g0213 a0003c0006t0001g0202 a0003c0006t0001g0203 others(10): Show |
13 | HG00280.hp1 HG01109.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.241+5436C>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34936920 | |||||||
| chr11:34936950 | A | G | 200 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(197): Show |
223 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.241+5466A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34936950 | |||||||
| chr11:34937219 | A | T | 8 | a0002c0004t0005g0007 a0002c0005t0005g0007 a0002c0005t0005g0008 others(5): Show |
13 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.241+5735A>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34937219 | |||||||
| chr11:34937264 | G | A | 1 | a0001c0017t0007g0144 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.241+5780G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34937264 | |||||||
| chr11:34937286 | C | G | 7 | a0001c0001t0001g0013 a0001c0001t0001g0052 a0001c0001t0001g0071 others(4): Show |
8 | HG00642.hp2 HG00735.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.241+5802C>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34937286 | |||||||
| chr11:34937301 | TTA | T | 7 | a0003c0006t0001g0202 a0003c0006t0001g0203 a0003c0006t0001g0204 others(4): Show |
7 | HG00280.hp1 HG01243.hp1 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.241+5820_241+5821d others(4): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 34937301 | ||||||
| chr11:34937355 | C | T | 1 | a0002c0004t0004g0240 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.241+5871C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34937355 | |||||||
| chr11:34937381 | G | A | 1 | a0002c0004t0004g0240 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.241+5897G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34937381 | |||||||
| chr11:34937442 | C | CTT | 184 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(181): Show |
205 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.241+5973_241+5974d others(4): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 34937442 | ||||||
| chr11:34937442 | C | CTTT | 11 | a0001c0001t0001g0070 a0001c0001t0001g0113 a0002c0008t0006g0001 others(8): Show |
13 | HG01109.hp1 HG02145.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.241+5972_241+5974d others(5): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 34937442 | ||||||
| chr11:34937511 | A | G | 66 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(63): Show |
77 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(74): Show |
intron_variant | MODIFIER | c.241+6027A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34937511 | |||||||
| chr11:34937687 | T | C | 8 | a0002c0007t0004g0022 a0002c0007t0004g0223 a0002c0007t0004g0226 others(5): Show |
9 | HG01361.hp1 HG02602.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.241+6203T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34937687 | |||||||
| chr11:34937804 | C | T | 1 | a0002c0004t0004g0222 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.241+6320C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34937804 | |||||||
| chr11:34937851 | G | T | 6 | a0001c0002t0007g0187 a0001c0002t0007g0188 a0001c0002t0007g0189 others(3): Show |
6 | HG01884.hp2 HG02572.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.241+6367G>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34937851 | |||||||
| chr11:34937909 | C | A | 118 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(115): Show |
130 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.241+6425C>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34937909 | |||||||
| chr11:34937922 | G | A | 5 | a0002c0004t0005g0007 a0002c0005t0005g0007 a0002c0005t0005g0026 others(2): Show |
7 | HG02280.hp2 HG02809.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.241+6438G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34937922 | |||||||
| chr11:34937931 | A | G | 1 | a0001c0001t0001g0100 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.241+6447A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34937931 | |||||||
| chr11:34938090 | A | G | 1 | a0003c0006t0001g0212 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.241+6606A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34938090 | |||||||
| chr11:34938294 | G | A | 1 | a0002c0005t0005g0269 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.241+6810G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34938294 | |||||||
| chr11:34938421 | C | T | 6 | a0001c0001t0001g0051 a0001c0001t0001g0078 a0001c0001t0001g0079 others(3): Show |
6 | HG01074.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.241+6937C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34938421 | |||||||
| chr11:34938425 | T | A | 1 | a0001c0002t0002g0136 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.241+6941T>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34938425 | |||||||
| chr11:34938628 | T | C | 64 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(61): Show |
75 | HG00673.hp2 HG01106.hp1 HG01168.hp2 others(72): Show |
intron_variant | MODIFIER | c.241+7144T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34938628 | |||||||
| chr11:34938798 | T | C | 12 | a0002c0004t0004g0232 a0002c0004t0004g0233 a0002c0004t0004g0234 others(9): Show |
13 | HG01361.hp1 HG01496.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.241+7314T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34938798 | |||||||
| chr11:34938872 | T | C | 64 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(61): Show |
75 | HG00673.hp2 HG01106.hp1 HG01168.hp2 others(72): Show |
intron_variant | MODIFIER | c.241+7388T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34938872 | |||||||
| chr11:34938947 | A | G | 1 | a0001c0017t0007g0144 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.241+7463A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34938947 | |||||||
| chr11:34939039 | T | G | 1 | a0001c0017t0007g0144 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.241+7555T>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34939039 | |||||||
| chr11:34939139 | CCATT | C | 118 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(115): Show |
130 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.241+7660_241+7663d others(6): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 34939139 | ||||||
| chr11:34939178 | G | C | 64 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(61): Show |
75 | HG00673.hp2 HG01106.hp1 HG01168.hp2 others(72): Show |
intron_variant | MODIFIER | c.241+7694G>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34939178 | |||||||
| chr11:34939361 | G | A | 196 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(193): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.241+7877G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34939361 | |||||||
| chr11:34939468 | GGT | G | 41 | a0001c0001t0001g0042 a0001c0001t0001g0096 a0001c0001t0001g0107 others(38): Show |
44 | HG00280.hp1 HG00423.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.242-8002_242-8001d others(4): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 34939468 | ||||||
| chr11:34939468 | GGTGT | G | 159 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(156): Show |
180 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.242-8004_242-8001d others(6): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 34939468 | ||||||
| chr11:34939468 | GGTGTGT | G | 17 | a0001c0001t0001g0043 a0001c0002t0002g0161 a0001c0021t0002g0166 others(14): Show |
19 | HG00423.hp1 HG00673.hp1 HG01496.hp2 others(16): Show |
intron_variant | MODIFIER | c.242-8006_242-8001d others(8): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 34939468 | ||||||
| chr11:34939468 | GGTGTGTG others(1): Show |
G | 12 | a0001c0002t0007g0192 a0002c0003t0003g0276 a0002c0003t0003g0277 others(9): Show |
12 | HG01884.hp1 HG02615.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.242-8008_242-8001d others(10): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 34939468 | ||||||
| chr11:34939468 | GGTGTGTG others(3): Show |
G | 32 | a0001c0002t0007g0187 a0001c0002t0007g0188 a0001c0002t0007g0189 others(29): Show |
40 | HG00673.hp2 HG01106.hp1 HG01168.hp2 others(37): Show |
intron_variant | MODIFIER | c.242-8010_242-8001d others(12): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 34939468 | ||||||
| chr11:34939502 | T | C | 2 | a0001c0001t0001g0125 a0002c0004t0004g0222 |
2 | HG04204.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.242-8004T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34939502 | |||||||
| chr11:34939504 | T | C | 128 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(125): Show |
140 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.242-8002T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34939504 | |||||||
| chr11:34939504 | T | TGTGTGTG others(5): Show |
3 | a0001c0023t0009g0199 a0006c0011t0001g0198 a0006c0011t0001g0200 |
3 | HG02559.hp2 HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.242-8001_242-8000i others(14): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 34939504 | ||||||
| chr11:34939504 | T | TGTGTGTG others(7): Show |
1 | a0006c0011t0001g0201 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.242-8001_242-8000i others(16): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 34939504 | ||||||
| chr11:34939517 | G | A | 64 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(61): Show |
75 | HG00673.hp2 HG01106.hp1 HG01168.hp2 others(72): Show |
intron_variant | MODIFIER | c.242-7989G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34939517 | |||||||
| chr11:34939519 | G | A | 30 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(27): Show |
33 | HG00673.hp2 HG01106.hp1 HG01168.hp2 others(30): Show |
intron_variant | MODIFIER | c.242-7987G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34939519 | |||||||
| chr11:34939572 | A | C | 6 | a0001c0002t0007g0187 a0001c0002t0007g0188 a0001c0002t0007g0189 others(3): Show |
6 | HG01884.hp2 HG02572.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.242-7934A>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34939572 | |||||||
| chr11:34939611 | A | G | 64 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(61): Show |
75 | HG00673.hp2 HG01106.hp1 HG01168.hp2 others(72): Show |
intron_variant | MODIFIER | c.242-7895A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34939611 | |||||||
| chr11:34939614 | A | G | 64 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(61): Show |
75 | HG00673.hp2 HG01106.hp1 HG01168.hp2 others(72): Show |
intron_variant | MODIFIER | c.242-7892A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34939614 | |||||||
| chr11:34939863 | T | C | 64 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(61): Show |
75 | HG00673.hp2 HG01106.hp1 HG01168.hp2 others(72): Show |
intron_variant | MODIFIER | c.242-7643T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34939863 | |||||||
| chr11:34940064 | C | A | 64 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(61): Show |
75 | HG00673.hp2 HG01106.hp1 HG01168.hp2 others(72): Show |
intron_variant | MODIFIER | c.242-7442C>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34940064 | |||||||
| chr11:34940101 | A | G | 2 | a0001c0002t0002g0180 a0001c0002t0002g0181 |
2 | HG01255.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.242-7405A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34940101 | |||||||
| chr11:34940209 | C | A | 197 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(194): Show |
220 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.242-7297C>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34940209 | |||||||
| chr11:34940211 | A | G | 2 | a0001c0001t0001g0012 a0001c0001t0001g0077 |
3 | NA18948.hp2 NA18999.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.242-7295A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34940211 | |||||||
| chr11:34940328 | C | A | 1 | a0002c0004t0004g0240 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.242-7178C>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34940328 | |||||||
| chr11:34940340 | A | G | 1 | a0001c0001t0001g0095 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.242-7166A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34940340 | |||||||
| chr11:34940396 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.242-7110A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34940396 | |||||||
| chr11:34940421 | A | G | 1 | a0001c0001t0001g0046 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.242-7085A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34940421 | |||||||
| chr11:34940488 | T | C | 1 | a0001c0017t0007g0144 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.242-7018T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34940488 | |||||||
| chr11:34940573 | A | G | 25 | a0002c0004t0004g0222 a0002c0004t0004g0224 a0002c0004t0004g0232 others(22): Show |
28 | HG01361.hp1 HG01496.hp2 HG02145.hp1 others(25): Show |
intron_variant | MODIFIER | c.242-6933A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34940573 | |||||||
| chr11:34940607 | A | G | 64 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(61): Show |
75 | HG00673.hp2 HG01106.hp1 HG01168.hp2 others(72): Show |
intron_variant | MODIFIER | c.242-6899A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34940607 | |||||||
| chr11:34940725 | A | T | 14 | a0001c0013t0002g0213 a0003c0006t0001g0202 a0003c0006t0001g0203 others(11): Show |
14 | HG00280.hp1 HG01109.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.242-6781A>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34940725 | |||||||
| chr11:34940786 | G | A | 64 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(61): Show |
75 | HG00673.hp2 HG01106.hp1 HG01168.hp2 others(72): Show |
intron_variant | MODIFIER | c.242-6720G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34940786 | |||||||
| chr11:34940852 | A | G | 14 | a0001c0013t0002g0213 a0003c0006t0001g0202 a0003c0006t0001g0203 others(11): Show |
14 | HG00280.hp1 HG01109.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.242-6654A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34940852 | |||||||
| chr11:34940884 | G | A | 4 | a0001c0023t0009g0199 a0006c0011t0001g0198 a0006c0011t0001g0200 others(1): Show |
4 | HG02559.hp2 HG03139.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.242-6622G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34940884 | |||||||
| chr11:34941074 | C | CTTAA | 203 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(200): Show |
226 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.242-6430_242-6429i others(6): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 34941074 | ||||||
| chr11:34941199 | A | G | 1 | a0002c0003t0003g0248 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.242-6307A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34941199 | |||||||
| chr11:34941206 | T | C | 2 | a0001c0001t0001g0016 a0001c0001t0001g0029 |
3 | HG03490.hp1 HG03492.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.242-6300T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34941206 | |||||||
| chr11:34941208 | G | A | 2 | a0002c0008t0006g0273 a0002c0008t0006g0274 |
2 | HG02145.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.242-6298G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34941208 | |||||||
| chr11:34941352 | T | G | 14 | a0001c0013t0002g0213 a0003c0006t0001g0202 a0003c0006t0001g0203 others(11): Show |
14 | HG00280.hp1 HG01109.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.242-6154T>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34941352 | |||||||
| chr11:34941355 | A | G | 1 | a0001c0001t0001g0082 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.242-6151A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34941355 | |||||||
| chr11:34941381 | T | G | 203 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(200): Show |
226 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.242-6125T>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34941381 | |||||||
| chr11:34941499 | A | G | 197 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(194): Show |
220 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.242-6007A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34941499 | |||||||
| chr11:34941555 | A | G | 64 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(61): Show |
75 | HG00673.hp2 HG01106.hp1 HG01168.hp2 others(72): Show |
intron_variant | MODIFIER | c.242-5951A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34941555 | |||||||
| chr11:34941625 | G | A | 2 | a0001c0001t0001g0194 a0001c0001t0001g0195 |
2 | HG02809.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.242-5881G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34941625 | |||||||
| chr11:34941677 | C | T | 118 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(115): Show |
130 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.242-5829C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34941677 | |||||||
| chr11:34941773 | C | A | 8 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(5): Show |
8 | HG02451.hp2 HG02559.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.242-5733C>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34941773 | |||||||
| chr11:34941869 | T | C | 197 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(194): Show |
220 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.242-5637T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34941869 | |||||||
| chr11:34941912 | T | C | 64 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(61): Show |
75 | HG00673.hp2 HG01106.hp1 HG01168.hp2 others(72): Show |
intron_variant | MODIFIER | c.242-5594T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34941912 | |||||||
| chr11:34941939 | A | G | 4 | a0001c0001t0001g0010 a0001c0001t0001g0030 a0001c0001t0001g0031 others(1): Show |
5 | HG01515.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.242-5567A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34941939 | |||||||
| chr11:34941959 | G | T | 2 | a0001c0001t0001g0074 a0001c0001t0001g0075 |
2 | NA18961.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.242-5547G>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34941959 | |||||||
| chr11:34942081 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.242-5425C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34942081 | |||||||
| chr11:34942177 | G | GT | 8 | a0002c0004t0005g0007 a0002c0005t0005g0007 a0002c0005t0005g0008 others(5): Show |
13 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.242-5327dupT | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 34942177 | ||||||
| chr11:34942181 | G | A | 196 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(193): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.242-5325G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34942181 | |||||||
| chr11:34942216 | T | C | 14 | a0001c0013t0002g0213 a0003c0006t0001g0202 a0003c0006t0001g0203 others(11): Show |
14 | HG00280.hp1 HG01109.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.242-5290T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34942216 | |||||||
| chr11:34942250 | G | GA | 5 | a0001c0001t0001g0071 a0001c0002t0002g0154 a0002c0003t0003g0257 others(2): Show |
5 | HG02145.hp2 NA18964.hp1 NA18988.hp1 others(2): Show |
intron_variant | MODIFIER | c.242-5249dupA | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 34942250 | ||||||
| chr11:34942313 | A | T | 196 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(193): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.242-5193A>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34942313 | |||||||
| chr11:34942369 | A | G | 38 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(35): Show |
46 | HG00673.hp2 HG01106.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.242-5137A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34942369 | |||||||
| chr11:34942535 | C | T | 14 | a0001c0013t0002g0213 a0003c0006t0001g0202 a0003c0006t0001g0203 others(11): Show |
14 | HG00280.hp1 HG01109.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.242-4971C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34942535 | |||||||
| chr11:34942741 | A | T | 1 | a0002c0027t0003g0244 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.242-4765A>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34942741 | |||||||
| chr11:34942778 | G | T | 64 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(61): Show |
75 | HG00673.hp2 HG01106.hp1 HG01168.hp2 others(72): Show |
intron_variant | MODIFIER | c.242-4728G>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34942778 | |||||||
| chr11:34942797 | T | C | 203 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(200): Show |
226 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.242-4709T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34942797 | |||||||
| chr11:34942894 | T | C | 110 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(107): Show |
122 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.242-4612T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34942894 | |||||||
| chr11:34942944 | A | G | 14 | a0001c0013t0002g0213 a0003c0006t0001g0202 a0003c0006t0001g0203 others(11): Show |
14 | HG00280.hp1 HG01109.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.242-4562A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34942944 | |||||||
| chr11:34943004 | A | G | 203 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(200): Show |
226 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.242-4502A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34943004 | |||||||
| chr11:34943056 | G | GT | 132 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(129): Show |
144 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.242-4443dupT | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 34943056 | ||||||
| chr11:34943089 | T | C | 38 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(35): Show |
46 | HG00673.hp2 HG01106.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.242-4417T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34943089 | |||||||
| chr11:34943334 | T | C | 1 | a0002c0004t0004g0240 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.242-4172T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34943334 | |||||||
| chr11:34943408 | A | G | 2 | a0002c0003t0003g0024 a0002c0003t0003g0250 |
3 | NA18997.hp1 NA19003.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.242-4098A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34943408 | |||||||
| chr11:34943500 | G | A | 1 | a0003c0006t0001g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.242-4006G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34943500 | |||||||
| chr11:34943681 | G | C | 1 | a0002c0004t0004g0240 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.242-3825G>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34943681 | |||||||
| chr11:34943776 | T | G | 2 | a0001c0001t0001g0042 a0001c0001t0001g0043 |
2 | HG03704.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.242-3730T>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34943776 | |||||||
| chr11:34943860 | A | G | 30 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(27): Show |
33 | HG00673.hp2 HG01106.hp1 HG01168.hp2 others(30): Show |
intron_variant | MODIFIER | c.242-3646A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34943860 | |||||||
| chr11:34943861 | C | T | 38 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(35): Show |
46 | HG00673.hp2 HG01106.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.242-3645C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34943861 | |||||||
| chr11:34944010 | C | T | 118 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(115): Show |
130 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.242-3496C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34944010 | |||||||
| chr11:34944037 | T | C | 1 | a0001c0001t0001g0053 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.242-3469T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34944037 | |||||||
| chr11:34944079 | A | ACG | 17 | a0002c0004t0004g0222 a0002c0004t0004g0224 a0002c0004t0004g0232 others(14): Show |
18 | HG01361.hp1 HG01496.hp2 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.242-3427_242-3426i others(4): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34944079 | |||||||
| chr11:34944079 | ATGTG | A | 132 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(129): Show |
144 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.242-3415_242-3412d others(6): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 34944079 | ||||||
| chr11:34944080 | T | C | 46 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(43): Show |
56 | HG00673.hp2 HG01106.hp1 HG01168.hp2 others(53): Show |
intron_variant | MODIFIER | c.242-3426T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34944080 | |||||||
| chr11:34944084 | T | C | 132 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(129): Show |
144 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.242-3422T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34944084 | |||||||
| chr11:34944120 | AATT | A | 4 | a0001c0023t0009g0199 a0006c0011t0001g0198 a0006c0011t0001g0200 others(1): Show |
4 | HG02559.hp2 HG03139.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.242-3376_242-3374d others(5): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 34944120 | ||||||
| chr11:34944287 | T | C | 1 | a0002c0004t0004g0239 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.242-3219T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34944287 | |||||||
| chr11:34944912 | G | A | 13 | a0003c0006t0001g0202 a0003c0006t0001g0203 a0003c0006t0001g0204 others(10): Show |
13 | HG00280.hp1 HG01109.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.242-2594G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34944912 | |||||||
| chr11:34944945 | T | C | 64 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(61): Show |
75 | HG00673.hp2 HG01106.hp1 HG01168.hp2 others(72): Show |
intron_variant | MODIFIER | c.242-2561T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34944945 | |||||||
| chr11:34944986 | A | C | 1 | a0001c0002t0002g0185 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.242-2520A>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34944986 | |||||||
| chr11:34944999 | A | C | 196 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(193): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.242-2507A>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34944999 | |||||||
| chr11:34945012 | CCT | C | 8 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(5): Show |
8 | HG02451.hp2 HG02559.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.242-2491_242-2490d others(4): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 34945012 | ||||||
| chr11:34945208 | C | T | 13 | a0003c0006t0001g0202 a0003c0006t0001g0203 a0003c0006t0001g0204 others(10): Show |
13 | HG00280.hp1 HG01109.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.242-2298C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34945208 | |||||||
| chr11:34945223 | T | C | 2 | a0001c0001t0001g0042 a0001c0001t0001g0043 |
2 | HG03704.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.242-2283T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34945223 | |||||||
| chr11:34945396 | G | A | 1 | a0009c0025t0001g0215 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.242-2110G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34945396 | |||||||
| chr11:34945648 | A | G | 1 | a0001c0001t0001g0036 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.242-1858A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34945648 | |||||||
| chr11:34945742 | G | C | 13 | a0003c0006t0001g0202 a0003c0006t0001g0203 a0003c0006t0001g0204 others(10): Show |
13 | HG00280.hp1 HG01109.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.242-1764G>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34945742 | |||||||
| chr11:34945742 | G | T | 182 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(179): Show |
205 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(202): Show |
intron_variant | MODIFIER | c.242-1764G>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34945742 | |||||||
| chr11:34945781 | A | G | 81 | a0001c0023t0009g0199 a0002c0003t0003g0023 a0002c0003t0003g0024 others(78): Show |
92 | HG00280.hp1 HG00673.hp2 HG01106.hp1 others(89): Show |
intron_variant | MODIFIER | c.242-1725A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34945781 | |||||||
| chr11:34945825 | TC | T | 2 | a0001c0001t0001g0012 a0001c0001t0001g0077 |
3 | NA18948.hp2 NA18999.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.242-1680delC | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34945825 | |||||||
| chr11:34945878 | G | A | 1 | a0002c0027t0003g0244 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.242-1628G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34945878 | |||||||
| chr11:34945909 | C | G | 1 | a0001c0002t0007g0192 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.242-1597C>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34945909 | |||||||
| chr11:34945983 | C | T | 1 | a0001c0001t0001g0069 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.242-1523C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34945983 | |||||||
| chr11:34946034 | C | A | 1 | a0002c0004t0004g0224 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.242-1472C>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34946034 | |||||||
| chr11:34946136 | G | A | 1 | a0001c0002t0007g0192 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.242-1370G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34946136 | |||||||
| chr11:34946196 | A | G | 4 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(1): Show |
4 | HG02451.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.242-1310A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34946196 | |||||||
| chr11:34946341 | G | T | 1 | a0003c0006t0001g0206 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.242-1165G>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34946341 | |||||||
| chr11:34946371 | T | C | 1 | a0001c0013t0002g0213 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.242-1135T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34946371 | |||||||
| chr11:34946461 | C | T | 4 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0002c0003t0003g0277 others(1): Show |
4 | HG01891.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.242-1045C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34946461 | |||||||
| chr11:34946478 | T | C | 1 | a0002c0003t0003g0250 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.242-1028T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34946478 | |||||||
| chr11:34946668 | C | T | 28 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0002t0002g0160 others(25): Show |
33 | HG01496.hp2 HG01891.hp1 HG02055.hp1 others(30): Show |
intron_variant | MODIFIER | c.242-838C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34946668 | |||||||
| chr11:34946680 | A | G | 1 | a0001c0001t0001g0194 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.242-826A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34946680 | |||||||
| chr11:34946780 | C | T | 168 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(165): Show |
186 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.242-726C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34946780 | |||||||
| chr11:34946976 | A | G | 171 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(168): Show |
191 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.242-530A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34946976 | |||||||
| chr11:34947019 | T | A | 2 | a0002c0008t0006g0001 a0002c0008t0006g0272 |
4 | HG02451.hp1 HG02886.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.242-487T>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34947019 | |||||||
| chr11:34947348 | C | G | 2 | a0002c0003t0003g0278 a0002c0003t0003g0279 |
2 | HG02630.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.242-158C>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34947348 | |||||||
| chr11:34947405 | C | T | 3 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0102 |
3 | HG00558.hp2 HG02056.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.242-101C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34947405 | |||||||
| chr11:34947442 | G | A | 1 | a0001c0024t0001g0116 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.242-64G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34947442 | |||||||
| chr11:34947708 | G | A | 1 | a0002c0003t0010g0251 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.342+102G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34947708 | |||||||
| chr11:34947724 | A | AT | 14 | a0001c0002t0002g0006 a0001c0002t0002g0021 a0001c0002t0002g0146 others(11): Show |
17 | HG00642.hp1 HG01261.hp1 HG02886.hp2 others(14): Show |
intron_variant | MODIFIER | c.342+119dupT | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 34947724 | ||||||
| chr11:34947916 | G | C | 1 | a0001c0001t0001g0100 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.342+310G>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34947916 | |||||||
| chr11:34947987 | G | A | 130 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(127): Show |
142 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.342+381G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34947987 | |||||||
| chr11:34948063 | T | C | 1 | a0010c0028t0016g0275 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.342+457T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34948063 | |||||||
| chr11:34948074 | A | G | 1 | a0001c0002t0002g0145 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.342+468A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34948074 | |||||||
| chr11:34948079 | A | T | 204 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(201): Show |
227 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.342+473A>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34948079 | |||||||
| chr11:34948093 | T | A | 204 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(201): Show |
227 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.342+487T>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34948093 | |||||||
| chr11:34948175 | A | G | 10 | a0001c0014t0009g0105 a0001c0014t0009g0106 a0002c0007t0004g0022 others(7): Show |
11 | HG01192.hp2 HG01361.hp1 HG01943.hp2 others(8): Show |
intron_variant | MODIFIER | c.342+569A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34948175 | |||||||
| chr11:34948573 | CT | C | 130 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(127): Show |
142 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.342+983delT | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 34948573 | ||||||
| chr11:34948573 | CTT | C | 42 | a0001c0001t0001g0085 a0001c0001t0001g0102 a0001c0001t0001g0194 others(39): Show |
48 | HG00558.hp2 HG01168.hp1 HG01192.hp2 others(45): Show |
intron_variant | MODIFIER | c.342+982_342+983del others(2): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 34948573 | ||||||
| chr11:34948617 | G | A | 19 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(16): Show |
22 | HG00673.hp2 HG01106.hp1 HG01168.hp2 others(19): Show |
intron_variant | MODIFIER | c.342+1011G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34948617 | |||||||
| chr11:34948759 | G | A | 1 | a0001c0017t0007g0144 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.342+1153G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34948759 | |||||||
| chr11:34948799 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.342+1193A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34948799 | |||||||
| chr11:34948965 | T | G | 1 | a0010c0028t0016g0275 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.342+1359T>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34948965 | |||||||
| chr11:34948970 | C | A | 1 | a0002c0027t0003g0244 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.342+1364C>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34948970 | |||||||
| chr11:34949057 | A | C | 6 | a0002c0008t0006g0001 a0002c0008t0006g0270 a0002c0008t0006g0271 others(3): Show |
8 | HG02145.hp1 HG02451.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.342+1451A>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34949057 | |||||||
| chr11:34949138 | T | C | 6 | a0002c0004t0004g0232 a0002c0004t0004g0233 a0002c0004t0004g0234 others(3): Show |
6 | HG01496.hp2 HG02572.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.342+1532T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34949138 | |||||||
| chr11:34949195 | G | A | 129 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(126): Show |
141 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.342+1589G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34949195 | |||||||
| chr11:34949256 | G | C | 25 | a0001c0014t0009g0105 a0001c0014t0009g0106 a0001c0017t0007g0144 others(22): Show |
26 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(23): Show |
intron_variant | MODIFIER | c.342+1650G>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34949256 | |||||||
| chr11:34949270 | T | C | 171 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(168): Show |
191 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.342+1664T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34949270 | |||||||
| chr11:34949285 | G | T | 1 | a0002c0004t0004g0240 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.342+1679G>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34949285 | |||||||
| chr11:34949320 | A | ACCTCCGC others(25): Show |
35 | a0001c0014t0009g0105 a0001c0014t0009g0106 a0001c0017t0007g0144 others(32): Show |
41 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(38): Show |
intron_variant | MODIFIER | c.342+1719_342+1750d others(34): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 34949320 | ||||||
| chr11:34949512 | T | C | 171 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(168): Show |
191 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.342+1906T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34949512 | |||||||
| chr11:34949781 | A | C | 4 | a0002c0008t0006g0001 a0002c0008t0006g0270 a0002c0008t0006g0271 others(1): Show |
6 | HG02451.hp1 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.342+2175A>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34949781 | |||||||
| chr11:34949821 | T | C | 35 | a0001c0014t0009g0105 a0001c0014t0009g0106 a0001c0017t0007g0144 others(32): Show |
41 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(38): Show |
intron_variant | MODIFIER | c.342+2215T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34949821 | |||||||
| chr11:34949918 | A | G | 5 | a0001c0023t0009g0199 a0002c0004t0004g0236 a0002c0004t0004g0237 others(2): Show |
5 | HG02280.hp1 HG02559.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.342+2312A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34949918 | |||||||
| chr11:34949956 | T | A | 10 | a0001c0026t0013g0050 a0002c0004t0005g0007 a0002c0005t0005g0007 others(7): Show |
15 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.342+2350T>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34949956 | |||||||
| chr11:34949957 | A | T | 1 | a0001c0001t0001g0117 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.342+2351A>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34949957 | |||||||
| chr11:34950022 | A | G | 1 | a0001c0017t0007g0144 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.342+2416A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34950022 | |||||||
| chr11:34950086 | A | G | 2 | a0001c0001t0001g0053 a0001c0001t0001g0095 |
2 | HG01361.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.342+2480A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34950086 | |||||||
| chr11:34950116 | C | T | 2 | a0001c0002t0002g0145 a0001c0002t0002g0148 |
2 | HG00621.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.342+2510C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34950116 | |||||||
| chr11:34950304 | T | C | 1 | a0001c0017t0007g0144 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.342+2698T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34950304 | |||||||
| chr11:34950370 | T | TTTA | 4 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0221 others(1): Show |
4 | HG01891.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.342+2784_342+2786d others(5): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 34950370 | ||||||
| chr11:34950421 | A | G | 136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(133): Show |
150 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.342+2815A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34950421 | |||||||
| chr11:34950438 | A | T | 1 | a0001c0001t0001g0049 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.342+2832A>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34950438 | |||||||
| chr11:34950492 | A | T | 1 | a0001c0001t0001g0068 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.342+2886A>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34950492 | |||||||
| chr11:34950499 | A | G | 6 | a0002c0008t0006g0001 a0002c0008t0006g0270 a0002c0008t0006g0271 others(3): Show |
8 | HG02145.hp1 HG02451.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.342+2893A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34950499 | |||||||
| chr11:34950524 | C | CT | 5 | a0001c0001t0001g0067 a0001c0001t0001g0094 a0001c0001t0001g0126 others(2): Show |
5 | HG01257.hp2 HG02809.hp1 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.342+2920dupT | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 34950524 | ||||||
| chr11:34950532 | C | G | 1 | a0002c0004t0004g0224 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.342+2926C>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34950532 | |||||||
| chr11:34950607 | C | T | 171 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(168): Show |
191 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.342+3001C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34950607 | |||||||
| chr11:34950644 | T | A | 1 | a0001c0002t0002g0184 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.342+3038T>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34950644 | |||||||
| chr11:34950646 | A | G | 1 | a0001c0002t0002g0184 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.342+3040A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34950646 | |||||||
| chr11:34950652 | T | C | 1 | a0001c0001t0001g0086 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.342+3046T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34950652 | |||||||
| chr11:34950653 | A | G | 1 | a0001c0002t0002g0184 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.342+3047A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34950653 | |||||||
| chr11:34950655 | T | C | 1 | a0001c0002t0002g0184 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.342+3049T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34950655 | |||||||
| chr11:34950666 | A | G | 1 | a0001c0002t0002g0184 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.342+3060A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34950666 | |||||||
| chr11:34950674 | T | C | 1 | a0001c0002t0002g0184 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.342+3068T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34950674 | |||||||
| chr11:34950899 | G | T | 130 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(127): Show |
142 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.342+3293G>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34950899 | |||||||
| chr11:34950929 | T | C | 25 | a0001c0014t0009g0105 a0001c0014t0009g0106 a0001c0017t0007g0144 others(22): Show |
26 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(23): Show |
intron_variant | MODIFIER | c.342+3323T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34950929 | |||||||
| chr11:34950956 | C | T | 1 | a0002c0027t0003g0244 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.342+3350C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34950956 | |||||||
| chr11:34950992 | G | A | 1 | a0001c0017t0007g0144 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.342+3386G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34950992 | |||||||
| chr11:34951005 | A | G | 165 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(162): Show |
183 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.342+3399A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34951005 | |||||||
| chr11:34951011 | A | G | 10 | a0001c0002t0002g0017 a0001c0002t0002g0130 a0001c0002t0002g0131 others(7): Show |
11 | HG01891.hp2 HG02083.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.342+3405A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34951011 | |||||||
| chr11:34951049 | C | CT | 31 | a0001c0001t0001g0041 a0001c0001t0001g0064 a0001c0001t0001g0065 others(28): Show |
32 | HG00140.hp1 HG00609.hp2 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.342+3468dupT | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 34951049 | ||||||
| chr11:34951049 | CT | C | 13 | a0001c0001t0001g0013 a0001c0001t0001g0032 a0001c0001t0001g0036 others(10): Show |
14 | HG00642.hp2 HG00735.hp2 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.342+3468delT | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 34951049 | ||||||
| chr11:34951049 | CTT | C | 32 | a0001c0014t0009g0105 a0001c0014t0009g0106 a0001c0017t0007g0144 others(29): Show |
38 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(35): Show |
intron_variant | MODIFIER | c.342+3467_342+3468d others(4): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 34951049 | ||||||
| chr11:34951079 | C | T | 1 | a0003c0006t0001g0211 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.342+3473C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34951079 | |||||||
| chr11:34951080 | G | A | 2 | a0002c0003t0003g0258 a0002c0003t0003g0259 |
2 | NA18940.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.342+3474G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34951080 | |||||||
| chr11:34951081 | C | G | 204 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(201): Show |
227 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.342+3475C>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34951081 | |||||||
| chr11:34951117 | C | T | 130 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(127): Show |
142 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.342+3511C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34951117 | |||||||
| chr11:34951182 | G | A | 35 | a0001c0014t0009g0105 a0001c0014t0009g0106 a0001c0017t0007g0144 others(32): Show |
41 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(38): Show |
intron_variant | MODIFIER | c.342+3576G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34951182 | |||||||
| chr11:34951205 | C | T | 2 | a0002c0012t0003g0242 a0002c0012t0003g0243 |
2 | NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.342+3599C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34951205 | |||||||
| chr11:34951217 | C | T | 6 | a0002c0008t0006g0001 a0002c0008t0006g0270 a0002c0008t0006g0271 others(3): Show |
8 | HG02145.hp1 HG02451.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.342+3611C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34951217 | |||||||
| chr11:34951250 | G | A | 35 | a0001c0014t0009g0105 a0001c0014t0009g0106 a0001c0017t0007g0144 others(32): Show |
41 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(38): Show |
intron_variant | MODIFIER | c.342+3644G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34951250 | |||||||
| chr11:34951295 | A | G | 171 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(168): Show |
191 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.342+3689A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34951295 | |||||||
| chr11:34951297 | G | T | 6 | a0001c0002t0007g0187 a0001c0002t0007g0188 a0001c0002t0007g0189 others(3): Show |
6 | HG01884.hp2 HG02572.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.342+3691G>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34951297 | |||||||
| chr11:34951326 | T | TG | 10 | a0001c0026t0013g0050 a0002c0004t0005g0007 a0002c0005t0005g0007 others(7): Show |
15 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.342+3723dupG | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 34951326 | ||||||
| chr11:34951350 | C | T | 61 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(58): Show |
68 | HG00140.hp2 HG00280.hp2 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.342+3744C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34951350 | |||||||
| chr11:34951356 | G | T | 2 | a0001c0002t0002g0130 a0001c0002t0002g0131 |
2 | HG01891.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.342+3750G>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34951356 | |||||||
| chr11:34951381 | C | T | 2 | a0002c0004t0004g0232 a0002c0004t0004g0235 |
2 | HG02572.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.342+3775C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34951381 | |||||||
| chr11:34951745 | T | C | 1 | a0001c0001t0001g0054 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.342+4139T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34951745 | |||||||
| chr11:34951885 | G | A | 4 | a0001c0002t0002g0018 a0001c0002t0002g0019 a0001c0002t0002g0152 others(1): Show |
6 | HG02257.hp1 HG02486.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.342+4279G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34951885 | |||||||
| chr11:34951932 | T | C | 165 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(162): Show |
183 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.342+4326T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34951932 | |||||||
| chr11:34951999 | A | G | 204 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(201): Show |
227 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.342+4393A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34951999 | |||||||
| chr11:34952013 | T | C | 1 | a0010c0028t0016g0275 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.342+4407T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34952013 | |||||||
| chr11:34952015 | C | T | 27 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(24): Show |
30 | HG00673.hp2 HG01106.hp1 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.342+4409C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34952015 | |||||||
| chr11:34952019 | G | A | 1 | a0010c0028t0016g0275 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.342+4413G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34952019 | |||||||
| chr11:34952148 | G | C | 35 | a0001c0014t0009g0105 a0001c0014t0009g0106 a0001c0017t0007g0144 others(32): Show |
41 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(38): Show |
intron_variant | MODIFIER | c.342+4542G>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34952148 | |||||||
| chr11:34952151 | G | C | 1 | a0001c0026t0013g0050 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.342+4545G>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34952151 | |||||||
| chr11:34952153 | A | ATC | 35 | a0001c0014t0009g0105 a0001c0014t0009g0106 a0001c0017t0007g0144 others(32): Show |
41 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(38): Show |
intron_variant | MODIFIER | c.342+4549_342+4550d others(4): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 34952153 | ||||||
| chr11:34952217 | G | C | 19 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(16): Show |
22 | HG00673.hp2 HG01106.hp1 HG01168.hp2 others(19): Show |
intron_variant | MODIFIER | c.342+4611G>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34952217 | |||||||
| chr11:34952241 | A | G | 1 | a0001c0001t0001g0194 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.342+4635A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34952241 | |||||||
| chr11:34952252 | A | G | 2 | a0001c0002t0002g0130 a0001c0002t0002g0131 |
2 | HG01891.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.342+4646A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34952252 | |||||||
| chr11:34952306 | T | C | 1 | a0002c0004t0004g0224 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.342+4700T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34952306 | |||||||
| chr11:34952370 | G | T | 1 | a0002c0004t0004g0222 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.342+4764G>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34952370 | |||||||
| chr11:34952422 | A | G | 6 | a0001c0002t0007g0187 a0001c0002t0007g0188 a0001c0002t0007g0189 others(3): Show |
6 | HG01884.hp2 HG02572.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.342+4816A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34952422 | |||||||
| chr11:34952509 | A | G | 3 | a0006c0011t0001g0198 a0006c0011t0001g0200 a0006c0011t0001g0201 |
3 | HG03139.hp1 HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.343-4875A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34952509 | |||||||
| chr11:34952535 | G | T | 171 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(168): Show |
191 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.343-4849G>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34952535 | |||||||
| chr11:34952539 | C | T | 3 | a0001c0001t0001g0041 a0001c0001t0008g0109 a0001c0002t0002g0174 |
3 | HG02293.hp2 NA19087.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.343-4845C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34952539 | |||||||
| chr11:34952540 | G | C | 10 | a0001c0026t0013g0050 a0002c0004t0005g0007 a0002c0005t0005g0007 others(7): Show |
15 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.343-4844G>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34952540 | |||||||
| chr11:34952562 | A | G | 204 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(201): Show |
227 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.343-4822A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34952562 | |||||||
| chr11:34952582 | A | G | 2 | a0001c0001t0001g0119 a0001c0001t0001g0120 |
2 | HG01891.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.343-4802A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34952582 | |||||||
| chr11:34952614 | G | A | 9 | a0001c0026t0013g0050 a0002c0004t0005g0007 a0002c0005t0005g0007 others(6): Show |
14 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.343-4770G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34952614 | |||||||
| chr11:34952634 | T | C | 6 | a0002c0008t0006g0001 a0002c0008t0006g0270 a0002c0008t0006g0271 others(3): Show |
8 | HG02145.hp1 HG02451.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.343-4750T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34952634 | |||||||
| chr11:34952684 | T | C | 1 | a0001c0001t0001g0071 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.343-4700T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34952684 | |||||||
| chr11:34952711 | A | G | 1 | a0001c0001t0001g0093 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.343-4673A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34952711 | |||||||
| chr11:34952775 | G | T | 35 | a0001c0014t0009g0105 a0001c0014t0009g0106 a0001c0017t0007g0144 others(32): Show |
41 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(38): Show |
intron_variant | MODIFIER | c.343-4609G>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34952775 | |||||||
| chr11:34952860 | T | A | 204 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(201): Show |
227 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.343-4524T>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34952860 | |||||||
| chr11:34952877 | A | G | 1 | a0001c0001t0001g0043 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.343-4507A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34952877 | |||||||
| chr11:34952904 | C | T | 1 | a0001c0002t0002g0160 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.343-4480C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34952904 | |||||||
| chr11:34952916 | C | T | 130 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(127): Show |
142 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.343-4468C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34952916 | |||||||
| chr11:34952946 | T | C | 171 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(168): Show |
191 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.343-4438T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34952946 | |||||||
| chr11:34952965 | C | T | 1 | a0001c0002t0002g0162 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.343-4419C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34952965 | |||||||
| chr11:34953011 | A | G | 122 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(119): Show |
134 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.343-4373A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34953011 | |||||||
| chr11:34953013 | G | A | 1 | a0001c0002t0002g0158 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.343-4371G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34953013 | |||||||
| chr11:34953035 | T | A | 130 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(127): Show |
142 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.343-4349T>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34953035 | |||||||
| chr11:34953130 | AC | A | 6 | a0002c0008t0006g0001 a0002c0008t0006g0270 a0002c0008t0006g0271 others(3): Show |
8 | HG02145.hp1 HG02451.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.343-4253delC | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34953130 | |||||||
| chr11:34953161 | A | G | 3 | a0001c0001t0001g0010 a0001c0001t0001g0030 a0001c0001t0001g0031 |
4 | HG02895.hp1 HG02897.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.343-4223A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34953161 | |||||||
| chr11:34953520 | G | C | 161 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(158): Show |
176 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.343-3864G>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34953520 | |||||||
| chr11:34953750 | A | T | 2 | a0001c0001t0001g0036 a0001c0001t0001g0037 |
2 | NA18957.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.343-3634A>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34953750 | |||||||
| chr11:34953893 | GC | G | 4 | a0001c0002t0002g0158 a0005c0009t0002g0177 a0005c0009t0002g0178 others(1): Show |
4 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.343-3490delC | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34953893 | |||||||
| chr11:34954141 | T | G | 1 | a0002c0003t0003g0262 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.343-3243T>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34954141 | |||||||
| chr11:34954330 | C | G | 1 | a0001c0017t0007g0144 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.343-3054C>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34954330 | |||||||
| chr11:34954629 | G | T | 6 | a0001c0002t0007g0187 a0001c0002t0007g0188 a0001c0002t0007g0189 others(3): Show |
6 | HG01884.hp2 HG02572.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.343-2755G>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34954629 | |||||||
| chr11:34954769 | TC | T | 35 | a0001c0014t0009g0105 a0001c0014t0009g0106 a0001c0017t0007g0144 others(32): Show |
41 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(38): Show |
intron_variant | MODIFIER | c.343-2614delC | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34954769 | |||||||
| chr11:34954823 | A | T | 12 | a0003c0006t0001g0202 a0003c0006t0001g0203 a0003c0006t0001g0204 others(9): Show |
12 | HG00280.hp1 HG01109.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.343-2561A>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34954823 | |||||||
| chr11:34954879 | A | T | 1 | a0010c0028t0016g0275 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.343-2505A>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34954879 | |||||||
| chr11:34954891 | T | C | 10 | a0001c0014t0009g0105 a0001c0014t0009g0106 a0002c0007t0004g0022 others(7): Show |
11 | HG01192.hp2 HG01361.hp1 HG01943.hp2 others(8): Show |
intron_variant | MODIFIER | c.343-2493T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34954891 | |||||||
| chr11:34954932 | A | C | 3 | a0001c0001t0001g0054 a0001c0001t0001g0117 a0001c0001t0001g0125 |
3 | HG00738.hp2 HG03017.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.343-2452A>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34954932 | |||||||
| chr11:34955028 | A | G | 1 | a0010c0028t0016g0275 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.343-2356A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34955028 | |||||||
| chr11:34955036 | A | G | 1 | a0002c0004t0004g0222 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.343-2348A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34955036 | |||||||
| chr11:34955193 | A | G | 1 | a0010c0028t0016g0275 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.343-2191A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34955193 | |||||||
| chr11:34955325 | A | G | 35 | a0001c0014t0009g0105 a0001c0014t0009g0106 a0001c0017t0007g0144 others(32): Show |
41 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(38): Show |
intron_variant | MODIFIER | c.343-2059A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34955325 | |||||||
| chr11:34955351 | G | A | 1 | a0011c0019t0002g0159 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.343-2033G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34955351 | |||||||
| chr11:34955708 | A | G | 4 | a0002c0008t0006g0001 a0002c0008t0006g0270 a0002c0008t0006g0271 others(1): Show |
6 | HG02451.hp1 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.343-1676A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34955708 | |||||||
| chr11:34955765 | G | A | 27 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(24): Show |
30 | HG00673.hp2 HG01106.hp1 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.343-1619G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34955765 | |||||||
| chr11:34955810 | CTTTT | C | 122 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(119): Show |
134 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.343-1570_343-1567d others(6): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 34955810 | ||||||
| chr11:34955817 | T | A | 122 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(119): Show |
134 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.343-1567T>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34955817 | |||||||
| chr11:34955830 | T | C | 3 | a0001c0002t0002g0162 a0001c0002t0002g0163 a0001c0002t0002g0169 |
3 | HG00642.hp1 HG01261.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.343-1554T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34955830 | |||||||
| chr11:34955860 | A | G | 2 | a0003c0006t0001g0202 a0003c0006t0001g0205 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.343-1524A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34955860 | |||||||
| chr11:34955900 | G | A | 1 | a0001c0002t0002g0157 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.343-1484G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34955900 | |||||||
| chr11:34956084 | G | T | 3 | a0001c0002t0002g0017 a0001c0002t0002g0130 a0001c0002t0002g0131 |
4 | HG01891.hp2 HG02723.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.343-1300G>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34956084 | |||||||
| chr11:34956205 | CAT | C | 129 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(126): Show |
141 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.343-1166_343-1165d others(4): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 34956205 | ||||||
| chr11:34956247 | C | T | 1 | a0003c0006t0001g0212 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.343-1137C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34956247 | |||||||
| chr11:34956346 | G | A | 6 | a0001c0002t0007g0187 a0001c0002t0007g0188 a0001c0002t0007g0189 others(3): Show |
6 | HG01884.hp2 HG02572.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.343-1038G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34956346 | |||||||
| chr11:34956446 | A | C | 35 | a0001c0014t0009g0105 a0001c0014t0009g0106 a0001c0017t0007g0144 others(32): Show |
41 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(38): Show |
intron_variant | MODIFIER | c.343-938A>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34956446 | |||||||
| chr11:34956458 | G | T | 35 | a0001c0014t0009g0105 a0001c0014t0009g0106 a0001c0017t0007g0144 others(32): Show |
41 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(38): Show |
intron_variant | MODIFIER | c.343-926G>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34956458 | |||||||
| chr11:34956549 | T | C | 171 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(168): Show |
191 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.343-835T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34956549 | |||||||
| chr11:34956654 | C | G | 16 | a0001c0014t0009g0105 a0001c0014t0009g0106 a0002c0004t0004g0232 others(13): Show |
17 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.343-730C>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34956654 | |||||||
| chr11:34956701 | AG | A | 10 | a0001c0026t0013g0050 a0002c0004t0005g0007 a0002c0005t0005g0007 others(7): Show |
15 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.343-682delG | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34956701 | |||||||
| chr11:34956702 | G | A | 155 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(152): Show |
168 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.343-682G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34956702 | |||||||
| chr11:34956724 | A | G | 1 | a0010c0028t0016g0275 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.343-660A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34956724 | |||||||
| chr11:34956808 | A | G | 35 | a0001c0014t0009g0105 a0001c0014t0009g0106 a0001c0017t0007g0144 others(32): Show |
41 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(38): Show |
intron_variant | MODIFIER | c.343-576A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34956808 | |||||||
| chr11:34956840 | A | G | 10 | a0001c0026t0013g0050 a0002c0004t0005g0007 a0002c0005t0005g0007 others(7): Show |
15 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.343-544A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34956840 | |||||||
| chr11:34956846 | AC | A | 3 | a0006c0011t0001g0198 a0006c0011t0001g0200 a0006c0011t0001g0201 |
3 | HG03139.hp1 HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.343-537delC | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34956846 | |||||||
| chr11:34956860 | C | A | 6 | a0001c0002t0007g0187 a0001c0002t0007g0188 a0001c0002t0007g0189 others(3): Show |
6 | HG01884.hp2 HG02572.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.343-524C>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34956860 | |||||||
| chr11:34956973 | C | T | 129 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(126): Show |
141 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.343-411C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34956973 | |||||||
| chr11:34957154 | T | A | 1 | a0002c0004t0004g0239 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.343-230T>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34957154 | |||||||
| chr11:34957317 | A | G | 1 | a0001c0001t0001g0084 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.343-67A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34957317 | |||||||
| chr11:34957326 | CTACT | C | 24 | a0001c0014t0009g0105 a0001c0014t0009g0106 a0001c0023t0009g0199 others(21): Show |
25 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.343-55_343-52delCT others(2): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 34957326 | ||||||
| chr11:34957345 | G | A | 122 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(119): Show |
134 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.343-39G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34957345 | |||||||
| chr11:34957666 | G | A | 1 | a0001c0002t0002g0018 | 2 | HG02257.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.542+83G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 4/10 | chr11 | 34957666 | |||||||
| chr11:34957680 | A | G | 1 | a0002c0004t0004g0240 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.542+97A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 4/10 | chr11 | 34957680 | |||||||
| chr11:34957729 | GT | G | 169 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(166): Show |
189 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.542+157delT | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 34957729 | ||||||
| chr11:34957775 | C | T | 165 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(162): Show |
183 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.542+192C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 4/10 | chr11 | 34957775 | |||||||
| chr11:34957891 | A | G | 3 | a0001c0001t0001g0093 a0008c0016t0001g0091 a0010c0028t0016g0275 |
3 | HG02922.hp1 NA18980.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.542+308A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 4/10 | chr11 | 34957891 | |||||||
| chr11:34957958 | C | G | 130 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(127): Show |
142 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.542+375C>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 4/10 | chr11 | 34957958 | |||||||
| chr11:34958001 | C | T | 35 | a0001c0014t0009g0105 a0001c0014t0009g0106 a0001c0017t0007g0144 others(32): Show |
41 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(38): Show |
intron_variant | MODIFIER | c.542+418C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 4/10 | chr11 | 34958001 | |||||||
| chr11:34958005 | C | A | 1 | a0001c0023t0009g0199 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.542+422C>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 4/10 | chr11 | 34958005 | |||||||
| chr11:34958007 | T | C | 1 | a0010c0028t0016g0275 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.542+424T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 4/10 | chr11 | 34958007 | |||||||
| chr11:34958163 | A | G | 1 | a0002c0027t0003g0244 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.542+580A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 4/10 | chr11 | 34958163 | |||||||
| chr11:34958234 | A | G | 1 | a0001c0014t0009g0106 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.542+651A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 4/10 | chr11 | 34958234 | |||||||
| chr11:34958303 | G | A | 35 | a0001c0014t0009g0105 a0001c0014t0009g0106 a0001c0017t0007g0144 others(32): Show |
41 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(38): Show |
intron_variant | MODIFIER | c.542+720G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 4/10 | chr11 | 34958303 | |||||||
| chr11:34958305 | C | T | 25 | a0001c0014t0009g0105 a0001c0014t0009g0106 a0001c0017t0007g0144 others(22): Show |
26 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(23): Show |
intron_variant | MODIFIER | c.542+722C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 4/10 | chr11 | 34958305 | |||||||
| chr11:34958341 | T | C | 171 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(168): Show |
191 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.542+758T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 4/10 | chr11 | 34958341 | |||||||
| chr11:34958463 | G | C | 1 | a0001c0002t0002g0169 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.542+880G>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 4/10 | chr11 | 34958463 | |||||||
| chr11:34958556 | C | T | 130 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(127): Show |
142 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.542+973C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 4/10 | chr11 | 34958556 | |||||||
| chr11:34958592 | C | T | 10 | a0001c0026t0013g0050 a0002c0004t0005g0007 a0002c0005t0005g0007 others(7): Show |
15 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.542+1009C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 4/10 | chr11 | 34958592 | |||||||
| chr11:34958635 | C | CAA | 204 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(201): Show |
227 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.542+1053_542+1054i others(4): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 34958635 | ||||||
| chr11:34958767 | G | A | 35 | a0001c0014t0009g0105 a0001c0014t0009g0106 a0001c0017t0007g0144 others(32): Show |
41 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(38): Show |
intron_variant | MODIFIER | c.542+1184G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 4/10 | chr11 | 34958767 | |||||||
| chr11:34958823 | G | T | 7 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(4): Show |
7 | HG02451.hp2 HG02809.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.542+1240G>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 4/10 | chr11 | 34958823 | |||||||
| chr11:34958889 | A | T | 2 | a0002c0003t0003g0276 a0002c0003t0003g0277 |
2 | HG02615.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.542+1306A>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 4/10 | chr11 | 34958889 | |||||||
| chr11:34958940 | A | G | 1 | a0010c0028t0016g0275 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.542+1357A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 4/10 | chr11 | 34958940 | |||||||
| chr11:34958995 | T | G | 27 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(24): Show |
30 | HG00673.hp2 HG01106.hp1 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.542+1412T>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 4/10 | chr11 | 34958995 | |||||||
| chr11:34959015 | A | G | 130 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(127): Show |
142 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.543-1405A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 4/10 | chr11 | 34959015 | |||||||
| chr11:34959312 | A | G | 2 | a0002c0012t0003g0242 a0002c0012t0003g0243 |
2 | NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.543-1108A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 4/10 | chr11 | 34959312 | |||||||
| chr11:34959329 | A | G | 3 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0066 |
3 | NA19003.hp1 NA19082.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.543-1091A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 4/10 | chr11 | 34959329 | |||||||
| chr11:34959402 | AAAAC | A | 129 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(126): Show |
141 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.543-1002_543-999de others(5): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 34959402 | ||||||
| chr11:34959563 | A | G | 1 | a0002c0003t0003g0253 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.543-857A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 4/10 | chr11 | 34959563 | |||||||
| chr11:34959652 | G | A | 1 | a0001c0017t0007g0144 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.543-768G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 4/10 | chr11 | 34959652 | |||||||
| chr11:34959825 | A | G | 130 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(127): Show |
142 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.543-595A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 4/10 | chr11 | 34959825 | |||||||
| chr11:34960161 | TAGC | T | 5 | a0001c0002t0007g0187 a0001c0002t0007g0188 a0001c0002t0007g0189 others(2): Show |
5 | HG01884.hp2 HG02572.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.543-255_543-253del others(3): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 34960161 | ||||||
| chr11:34960330 | T | A | 1 | a0001c0001t0001g0085 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.543-90T>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 4/10 | chr11 | 34960330 | |||||||
| chr11:34960522 | T | C | 33 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0033 others(30): Show |
36 | HG00558.hp1 HG00609.hp1 HG00621.hp2 others(33): Show |
splice_region_variant&intron_variant | LOW | c.641+4T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | chr11 | 34960522 | |||||||
| chr11:34960594 | G | A | 35 | a0001c0014t0009g0105 a0001c0014t0009g0106 a0001c0017t0007g0144 others(32): Show |
41 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(38): Show |
intron_variant | MODIFIER | c.641+76G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | chr11 | 34960594 | |||||||
| chr11:34960599 | T | G | 129 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(126): Show |
141 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.641+81T>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | chr11 | 34960599 | |||||||
| chr11:34960601 | C | A | 122 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(119): Show |
134 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.641+83C>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | chr11 | 34960601 | |||||||
| chr11:34960686 | A | G | 129 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(126): Show |
141 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.641+168A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | chr11 | 34960686 | |||||||
| chr11:34961019 | C | A | 6 | a0002c0008t0006g0001 a0002c0008t0006g0270 a0002c0008t0006g0271 others(3): Show |
8 | HG02145.hp1 HG02451.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.641+501C>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | chr11 | 34961019 | |||||||
| chr11:34961061 | A | G | 1 | a0002c0007t0004g0230 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.641+543A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | chr11 | 34961061 | |||||||
| chr11:34961296 | T | C | 1 | a0001c0018t0001g0164 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.641+778T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | chr11 | 34961296 | |||||||
| chr11:34961409 | T | C | 3 | a0006c0011t0001g0198 a0006c0011t0001g0200 a0006c0011t0001g0201 |
3 | HG03139.hp1 HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.641+891T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | chr11 | 34961409 | |||||||
| chr11:34961466 | AAGCAATG others(1): Show |
A | 7 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(4): Show |
7 | HG02451.hp2 HG02809.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.641+950_641+957del others(8): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr11 | 34961466 | ||||||
| chr11:34961721 | C | G | 2 | a0001c0001t0001g0121 a0001c0001t0001g0123 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.641+1203C>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | chr11 | 34961721 | |||||||
| chr11:34961774 | G | A | 129 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(126): Show |
141 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.641+1256G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | chr11 | 34961774 | |||||||
| chr11:34961786 | C | A | 1 | a0001c0001t0001g0194 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.641+1268C>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | chr11 | 34961786 | |||||||
| chr11:34961802 | TC | T | 10 | a0001c0026t0013g0050 a0002c0004t0005g0007 a0002c0005t0005g0007 others(7): Show |
15 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.641+1285delC | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | chr11 | 34961802 | |||||||
| chr11:34961961 | A | C | 6 | a0001c0002t0007g0187 a0001c0002t0007g0188 a0001c0002t0007g0189 others(3): Show |
6 | HG01884.hp2 HG02572.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.641+1443A>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | chr11 | 34961961 | |||||||
| chr11:34962114 | T | C | 1 | a0002c0004t0004g0224 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.641+1596T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | chr11 | 34962114 | |||||||
| chr11:34962115 | A | G | 35 | a0001c0014t0009g0105 a0001c0014t0009g0106 a0001c0017t0007g0144 others(32): Show |
41 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(38): Show |
intron_variant | MODIFIER | c.641+1597A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | chr11 | 34962115 | |||||||
| chr11:34962280 | T | C | 129 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(126): Show |
141 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.641+1762T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | chr11 | 34962280 | |||||||
| chr11:34962286 | G | A | 1 | a0010c0028t0016g0275 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.641+1768G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | chr11 | 34962286 | |||||||
| chr11:34962343 | G | A | 6 | a0002c0008t0006g0001 a0002c0008t0006g0270 a0002c0008t0006g0271 others(3): Show |
8 | HG02145.hp1 HG02451.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.641+1825G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | chr11 | 34962343 | |||||||
| chr11:34962359 | T | C | 1 | a0001c0002t0002g0153 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.641+1841T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | chr11 | 34962359 | |||||||
| chr11:34962645 | A | G | 6 | a0002c0008t0006g0001 a0002c0008t0006g0270 a0002c0008t0006g0271 others(3): Show |
8 | HG02145.hp1 HG02451.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.641+2127A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | chr11 | 34962645 | |||||||
| chr11:34962703 | C | A | 1 | a0005c0009t0002g0178 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.641+2185C>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | chr11 | 34962703 | |||||||
| chr11:34962822 | C | T | 1 | a0001c0002t0002g0193 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.641+2304C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | chr11 | 34962822 | |||||||
| chr11:34962868 | G | A | 6 | a0002c0008t0006g0001 a0002c0008t0006g0270 a0002c0008t0006g0271 others(3): Show |
8 | HG02145.hp1 HG02451.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.641+2350G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | chr11 | 34962868 | |||||||
| chr11:34962878 | T | G | 10 | a0001c0026t0013g0050 a0002c0004t0005g0007 a0002c0005t0005g0007 others(7): Show |
15 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.641+2360T>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | chr11 | 34962878 | |||||||
| chr11:34962978 | T | G | 3 | a0006c0011t0001g0198 a0006c0011t0001g0200 a0006c0011t0001g0201 |
3 | HG03139.hp1 HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.641+2460T>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | chr11 | 34962978 | |||||||
| chr11:34962998 | C | A | 1 | a0010c0028t0016g0275 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.641+2480C>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | chr11 | 34962998 | |||||||
| chr11:34963004 | C | T | 13 | a0001c0002t0007g0187 a0001c0002t0007g0188 a0001c0002t0007g0189 others(10): Show |
15 | HG01884.hp2 HG02145.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.641+2486C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | chr11 | 34963004 | |||||||
| chr11:34963019 | G | A | 1 | a0001c0017t0007g0144 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.641+2501G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | chr11 | 34963019 | |||||||
| chr11:34963025 | G | A | 204 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(201): Show |
227 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.641+2507G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | chr11 | 34963025 | |||||||
| chr11:34963028 | T | C | 35 | a0001c0014t0009g0105 a0001c0014t0009g0106 a0001c0017t0007g0144 others(32): Show |
41 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(38): Show |
intron_variant | MODIFIER | c.641+2510T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | chr11 | 34963028 | |||||||
| chr11:34963039 | A | G | 1 | a0010c0028t0016g0275 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.641+2521A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | chr11 | 34963039 | |||||||
| chr11:34963276 | A | C | 3 | a0001c0002t0002g0149 a0001c0002t0002g0150 a0001c0002t0002g0151 |
3 | HG01256.hp1 HG01258.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.641+2758A>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | chr11 | 34963276 | |||||||
| chr11:34963523 | T | C | 1 | a0002c0004t0004g0240 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.641+3005T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | chr11 | 34963523 | |||||||
| chr11:34963560 | G | T | 35 | a0001c0014t0009g0105 a0001c0014t0009g0106 a0001c0017t0007g0144 others(32): Show |
41 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(38): Show |
intron_variant | MODIFIER | c.641+3042G>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | chr11 | 34963560 | |||||||
| chr11:34963780 | G | C | 35 | a0001c0014t0009g0105 a0001c0014t0009g0106 a0001c0017t0007g0144 others(32): Show |
41 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(38): Show |
intron_variant | MODIFIER | c.642-2860G>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | chr11 | 34963780 | |||||||
| chr11:34963877 | A | G | 1 | a0002c0004t0004g0240 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.642-2763A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | chr11 | 34963877 | |||||||
| chr11:34963899 | C | T | 165 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(162): Show |
183 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.642-2741C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | chr11 | 34963899 | |||||||
| chr11:34963901 | A | G | 16 | a0001c0014t0009g0105 a0001c0014t0009g0106 a0002c0004t0004g0232 others(13): Show |
17 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.642-2739A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | chr11 | 34963901 | |||||||
| chr11:34963939 | C | T | 5 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0065 others(2): Show |
5 | HG01255.hp1 NA19003.hp1 NA19072.hp2 others(2): Show |
intron_variant | MODIFIER | c.642-2701C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | chr11 | 34963939 | |||||||
| chr11:34963998 | A | G | 6 | a0001c0023t0009g0199 a0002c0004t0004g0222 a0002c0004t0004g0236 others(3): Show |
6 | HG02280.hp1 HG02559.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.642-2642A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | chr11 | 34963998 | |||||||
| chr11:34964189 | G | C | 1 | a0002c0003t0003g0247 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.642-2451G>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | chr11 | 34964189 | |||||||
| chr11:34964269 | A | G | 8 | a0001c0023t0009g0199 a0002c0004t0004g0222 a0002c0004t0004g0224 others(5): Show |
8 | HG02280.hp1 HG02559.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.642-2371A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | chr11 | 34964269 | |||||||
| chr11:34964349 | A | G | 1 | a0001c0001t0001g0035 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.642-2291A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | chr11 | 34964349 | |||||||
| chr11:34964419 | C | T | 13 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0036 others(10): Show |
16 | HG01256.hp2 HG01952.hp2 HG01975.hp1 others(13): Show |
intron_variant | MODIFIER | c.642-2221C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | chr11 | 34964419 | |||||||
| chr11:34964731 | T | C | 6 | a0002c0008t0006g0001 a0002c0008t0006g0270 a0002c0008t0006g0271 others(3): Show |
8 | HG02145.hp1 HG02451.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.642-1909T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | chr11 | 34964731 | |||||||
| chr11:34964773 | A | ATATTAGC others(15): Show |
25 | a0001c0002t0002g0005 a0001c0014t0009g0105 a0001c0014t0009g0106 others(22): Show |
28 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(25): Show |
intron_variant | MODIFIER | c.642-1820_642-1799d others(24): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr11 | 34964773 | ||||||
| chr11:34964773 | A | ATATTAGC others(37): Show |
11 | a0001c0017t0007g0144 a0001c0026t0013g0050 a0002c0004t0005g0007 others(8): Show |
16 | HG02055.hp1 HG02109.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.642-1842_642-1799d others(46): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr11 | 34964773 | ||||||
| chr11:34964773 | ATATTAGC others(15): Show |
A | 129 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(126): Show |
141 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.642-1820_642-1799d others(24): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr11 | 34964773 | ||||||
| chr11:34964773 | ATATTAGC others(37): Show |
A | 6 | a0001c0002t0007g0187 a0001c0002t0007g0188 a0001c0002t0007g0189 others(3): Show |
6 | HG01884.hp2 HG02572.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.642-1842_642-1799d others(46): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr11 | 34964773 | ||||||
| chr11:34964813 | TTAGCTAT others(19): Show |
T | 1 | a0001c0001t0001g0115 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.642-1812_642-1787d others(28): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr11 | 34964813 | ||||||
| chr11:34964921 | G | A | 1 | a0001c0001t0001g0009 | 2 | HG02622.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.642-1719G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | chr11 | 34964921 | |||||||
| chr11:34964949 | T | A | 6 | a0002c0008t0006g0001 a0002c0008t0006g0270 a0002c0008t0006g0271 others(3): Show |
8 | HG02145.hp1 HG02451.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.642-1691T>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | chr11 | 34964949 | |||||||
| chr11:34964964 | G | A | 177 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(174): Show |
197 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.642-1676G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | chr11 | 34964964 | |||||||
| chr11:34964990 | C | G | 1 | a0001c0001t0001g0090 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.642-1650C>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | chr11 | 34964990 | |||||||
| chr11:34965047 | G | T | 1 | a0001c0017t0007g0144 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.642-1593G>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | chr11 | 34965047 | |||||||
| chr11:34965060 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.642-1580C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | chr11 | 34965060 | |||||||
| chr11:34965285 | C | T | 2 | a0002c0007t0004g0223 a0002c0007t0004g0231 |
2 | NA19054.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.642-1355C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | chr11 | 34965285 | |||||||
| chr11:34965321 | G | T | 1 | a0001c0001t0001g0096 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.642-1319G>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | chr11 | 34965321 | |||||||
| chr11:34965419 | T | C | 1 | a0003c0006t0001g0208 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.642-1221T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | chr11 | 34965419 | |||||||
| chr11:34965474 | G | A | 6 | a0002c0004t0004g0232 a0002c0004t0004g0233 a0002c0004t0004g0234 others(3): Show |
6 | HG01496.hp2 HG02572.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.642-1166G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | chr11 | 34965474 | |||||||
| chr11:34965500 | A | C | 6 | a0002c0008t0006g0001 a0002c0008t0006g0270 a0002c0008t0006g0271 others(3): Show |
8 | HG02145.hp1 HG02451.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.642-1140A>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | chr11 | 34965500 | |||||||
| chr11:34965557 | A | G | 6 | a0002c0008t0006g0001 a0002c0008t0006g0270 a0002c0008t0006g0271 others(3): Show |
8 | HG02145.hp1 HG02451.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.642-1083A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | chr11 | 34965557 | |||||||
| chr11:34965712 | ATGCTCAA others(4): Show |
A | 3 | a0001c0001t0001g0003 a0001c0001t0001g0055 a0001c0001t0001g0070 |
5 | HG02015.hp1 NA18971.hp1 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.642-923_642-913del others(11): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr11 | 34965712 | ||||||
| chr11:34965804 | G | A | 1 | a0002c0004t0004g0240 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.642-836G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | chr11 | 34965804 | |||||||
| chr11:34965810 | T | C | 205 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(202): Show |
228 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.642-830T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | chr11 | 34965810 | |||||||
| chr11:34965975 | T | C | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | HG01167.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.642-665T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | chr11 | 34965975 | |||||||
| chr11:34966220 | T | C | 6 | a0002c0004t0004g0232 a0002c0004t0004g0233 a0002c0004t0004g0234 others(3): Show |
6 | HG01496.hp2 HG02572.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.642-420T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | chr11 | 34966220 | |||||||
| chr11:34966525 | A | G | 1 | a0001c0001t0001g0103 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.642-115A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | chr11 | 34966525 | |||||||
| chr11:34966621 | A | G | 1 | a0006c0011t0001g0200 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.642-19A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | chr11 | 34966621 | |||||||
| chr11:34967067 | G | A | 1 | a0002c0004t0004g0222 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.816+253G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 6/10 | chr11 | 34967067 | |||||||
| chr11:34967234 | T | A | 6 | a0001c0002t0002g0132 a0001c0002t0002g0133 a0001c0002t0002g0134 others(3): Show |
6 | HG03017.hp1 HG03490.hp2 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.816+420T>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 6/10 | chr11 | 34967234 | |||||||
| chr11:34967292 | G | C | 1 | a0001c0002t0002g0186 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.816+478G>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 6/10 | chr11 | 34967292 | |||||||
| chr11:34967307 | T | A | 25 | a0001c0014t0009g0105 a0001c0014t0009g0106 a0001c0017t0007g0144 others(22): Show |
26 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(23): Show |
intron_variant | MODIFIER | c.816+493T>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 6/10 | chr11 | 34967307 | |||||||
| chr11:34967457 | A | G | 1 | a0001c0002t0002g0219 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.816+643A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 6/10 | chr11 | 34967457 | |||||||
| chr11:34967498 | C | T | 122 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(119): Show |
134 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.816+684C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 6/10 | chr11 | 34967498 | |||||||
| chr11:34967524 | T | C | 3 | a0002c0012t0003g0242 a0002c0012t0003g0243 a0002c0012t0003g0264 |
3 | HG06807.hp1 NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.816+710T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 6/10 | chr11 | 34967524 | |||||||
| chr11:34967993 | G | C | 1 | a0001c0001t0001g0056 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.816+1179G>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 6/10 | chr11 | 34967993 | |||||||
| chr11:34968029 | G | A | 1 | a0001c0020t0002g0220 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.816+1215G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 6/10 | chr11 | 34968029 | |||||||
| chr11:34968223 | T | C | 1 | a0002c0027t0003g0244 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.816+1409T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 6/10 | chr11 | 34968223 | |||||||
| chr11:34968260 | C | CA | 130 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(127): Show |
142 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.816+1463dupA | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 34968260 | ||||||
| chr11:34968279 | T | G | 35 | a0001c0014t0009g0105 a0001c0014t0009g0106 a0001c0017t0007g0144 others(32): Show |
41 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(38): Show |
intron_variant | MODIFIER | c.816+1465T>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 6/10 | chr11 | 34968279 | |||||||
| chr11:34968354 | G | T | 27 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(24): Show |
30 | HG00673.hp2 HG01106.hp1 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.816+1540G>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 6/10 | chr11 | 34968354 | |||||||
| chr11:34968372 | A | G | 171 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(168): Show |
191 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.816+1558A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 6/10 | chr11 | 34968372 | |||||||
| chr11:34968407 | A | G | 4 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(1): Show |
4 | HG02451.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+1593A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 6/10 | chr11 | 34968407 | |||||||
| chr11:34968413 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.816+1599C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 6/10 | chr11 | 34968413 | |||||||
| chr11:34968467 | T | C | 1 | a0001c0001t0001g0042 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.816+1653T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 6/10 | chr11 | 34968467 | |||||||
| chr11:34968471 | G | A | 6 | a0001c0002t0007g0187 a0001c0002t0007g0188 a0001c0002t0007g0189 others(3): Show |
6 | HG01884.hp2 HG02572.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.816+1657G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 6/10 | chr11 | 34968471 | |||||||
| chr11:34968510 | G | A | 165 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(162): Show |
183 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.817-1629G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 6/10 | chr11 | 34968510 | |||||||
| chr11:34968772 | C | G | 6 | a0001c0002t0007g0187 a0001c0002t0007g0188 a0001c0002t0007g0189 others(3): Show |
6 | HG01884.hp2 HG02572.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.817-1367C>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 6/10 | chr11 | 34968772 | |||||||
| chr11:34968853 | A | G | 2 | a0001c0001t0001g0127 a0001c0001t0001g0221 |
2 | NA18961.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.817-1286A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 6/10 | chr11 | 34968853 | |||||||
| chr11:34968855 | C | A | 8 | a0001c0023t0009g0199 a0002c0004t0004g0222 a0002c0004t0004g0224 others(5): Show |
8 | HG02280.hp1 HG02559.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.817-1284C>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 6/10 | chr11 | 34968855 | |||||||
| chr11:34969125 | A | G | 10 | a0001c0026t0013g0050 a0002c0004t0005g0007 a0002c0005t0005g0007 others(7): Show |
15 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.817-1014A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 6/10 | chr11 | 34969125 | |||||||
| chr11:34969158 | G | A | 35 | a0001c0014t0009g0105 a0001c0014t0009g0106 a0001c0017t0007g0144 others(32): Show |
41 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(38): Show |
intron_variant | MODIFIER | c.817-981G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 6/10 | chr11 | 34969158 | |||||||
| chr11:34969186 | TGTTC | T | 4 | a0001c0001t0001g0051 a0001c0001t0001g0079 a0001c0001t0001g0080 others(1): Show |
4 | HG01167.hp1 HG01169.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.817-952_817-949del others(4): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 6/10 | chr11 | 34969186 | |||||||
| chr11:34969191 | A | T | 4 | a0001c0001t0001g0051 a0001c0001t0001g0079 a0001c0001t0001g0080 others(1): Show |
4 | HG01167.hp1 HG01169.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.817-948A>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 6/10 | chr11 | 34969191 | |||||||
| chr11:34969192 | G | A | 4 | a0001c0001t0001g0051 a0001c0001t0001g0079 a0001c0001t0001g0080 others(1): Show |
4 | HG01167.hp1 HG01169.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.817-947G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 6/10 | chr11 | 34969192 | |||||||
| chr11:34969210 | A | T | 122 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(119): Show |
134 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.817-929A>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 6/10 | chr11 | 34969210 | |||||||
| chr11:34969242 | G | A | 6 | a0001c0001t0001g0051 a0001c0001t0001g0078 a0001c0001t0001g0079 others(3): Show |
6 | HG01074.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.817-897G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 6/10 | chr11 | 34969242 | |||||||
| chr11:34969302 | G | C | 1 | a0001c0001t0001g0124 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.817-837G>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 6/10 | chr11 | 34969302 | |||||||
| chr11:34969312 | T | C | 35 | a0001c0014t0009g0105 a0001c0014t0009g0106 a0001c0017t0007g0144 others(32): Show |
41 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(38): Show |
intron_variant | MODIFIER | c.817-827T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 6/10 | chr11 | 34969312 | |||||||
| chr11:34969337 | G | T | 2 | a0001c0002t0002g0180 a0001c0002t0002g0181 |
2 | HG01255.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.817-802G>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 6/10 | chr11 | 34969337 | |||||||
| chr11:34969360 | T | C | 1 | a0010c0028t0016g0275 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.817-779T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 6/10 | chr11 | 34969360 | |||||||
| chr11:34969435 | C | T | 27 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(24): Show |
30 | HG00673.hp2 HG01106.hp1 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.817-704C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 6/10 | chr11 | 34969435 | |||||||
| chr11:34969626 | T | C | 6 | a0001c0002t0007g0187 a0001c0002t0007g0188 a0001c0002t0007g0189 others(3): Show |
6 | HG01884.hp2 HG02572.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.817-513T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 6/10 | chr11 | 34969626 | |||||||
| chr11:34969634 | C | T | 12 | a0001c0002t0002g0006 a0001c0002t0002g0021 a0001c0002t0002g0146 others(9): Show |
15 | HG02109.hp1 NA18948.hp1 NA18949.hp1 others(12): Show |
intron_variant | MODIFIER | c.817-505C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 6/10 | chr11 | 34969634 | |||||||
| chr11:34969663 | T | A | 1 | a0001c0002t0002g0184 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.817-476T>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 6/10 | chr11 | 34969663 | |||||||
| chr11:34969713 | T | A | 1 | a0001c0002t0002g0167 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.817-426T>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 6/10 | chr11 | 34969713 | |||||||
| chr11:34969791 | G | A | 1 | a0001c0001t0008g0060 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.817-348G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 6/10 | chr11 | 34969791 | |||||||
| chr11:34969953 | C | T | 2 | a0001c0001t0001g0118 a0001c0002t0002g0148 |
2 | HG03239.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.817-186C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 6/10 | chr11 | 34969953 | |||||||
| chr11:34969989 | A | C | 1 | a0002c0004t0004g0222 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.817-150A>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 6/10 | chr11 | 34969989 | |||||||
| chr11:34970096 | A | G | 1 | a0001c0017t0007g0144 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.817-43A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 6/10 | chr11 | 34970096 | |||||||
| chr11:34970135 | G | T | 1 | a0001c0023t0009g0199 | 1 | HG02559.hp2 | splice_region_variant&intron_variant | LOW | c.817-4G>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 6/10 | chr11 | 34970135 | |||||||
| chr11:34970345 | C | T | 1 | a0010c0028t0016g0275 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.964+59C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | chr11 | 34970345 | |||||||
| chr11:34970529 | C | A | 1 | a0002c0004t0004g0235 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.964+243C>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | chr11 | 34970529 | |||||||
| chr11:34970666 | C | T | 4 | a0001c0002t0002g0149 a0001c0002t0002g0150 a0001c0002t0002g0151 others(1): Show |
4 | HG00735.hp1 HG01256.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+380C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | chr11 | 34970666 | |||||||
| chr11:34970904 | T | A | 165 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(162): Show |
183 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.964+618T>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | chr11 | 34970904 | |||||||
| chr11:34970996 | G | C | 1 | a0001c0001t0001g0125 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.964+710G>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | chr11 | 34970996 | |||||||
| chr11:34971192 | A | T | 1 | a0002c0004t0004g0239 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.964+906A>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | chr11 | 34971192 | |||||||
| chr11:34971315 | T | C | 3 | a0006c0011t0001g0198 a0006c0011t0001g0200 a0006c0011t0001g0201 |
3 | HG03139.hp1 HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.964+1029T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | chr11 | 34971315 | |||||||
| chr11:34971759 | A | G | 3 | a0002c0012t0003g0242 a0002c0012t0003g0243 a0002c0012t0003g0264 |
3 | HG06807.hp1 NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.964+1473A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | chr11 | 34971759 | |||||||
| chr11:34971797 | A | G | 3 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0066 |
3 | NA19003.hp1 NA19082.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.964+1511A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | chr11 | 34971797 | |||||||
| chr11:34971930 | G | A | 171 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(168): Show |
191 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.964+1644G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | chr11 | 34971930 | |||||||
| chr11:34972041 | T | C | 3 | a0001c0001t0001g0032 a0001c0001t0001g0124 a0004c0022t0015g0143 |
3 | HG00741.hp2 HG01081.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.964+1755T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | chr11 | 34972041 | |||||||
| chr11:34972141 | G | A | 204 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(201): Show |
227 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.964+1855G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | chr11 | 34972141 | |||||||
| chr11:34972230 | T | G | 27 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(24): Show |
30 | HG00673.hp2 HG01106.hp1 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.964+1944T>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | chr11 | 34972230 | |||||||
| chr11:34972235 | T | A | 1 | a0001c0001t0001g0221 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.964+1949T>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | chr11 | 34972235 | |||||||
| chr11:34972323 | T | A | 2 | a0002c0003t0003g0278 a0002c0003t0003g0279 |
2 | HG02630.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.964+2037T>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | chr11 | 34972323 | |||||||
| chr11:34972385 | A | G | 2 | a0002c0012t0003g0242 a0002c0012t0003g0243 |
2 | NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.964+2099A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | chr11 | 34972385 | |||||||
| chr11:34972391 | G | A | 12 | a0003c0006t0001g0202 a0003c0006t0001g0203 a0003c0006t0001g0204 others(9): Show |
12 | HG00280.hp1 HG01109.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.964+2105G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | chr11 | 34972391 | |||||||
| chr11:34972395 | A | AT | 34 | a0001c0014t0009g0105 a0001c0014t0009g0106 a0001c0017t0007g0144 others(31): Show |
40 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(37): Show |
intron_variant | MODIFIER | c.964+2123dupT | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr11 | 34972395 | ||||||
| chr11:34972395 | AT | A | 126 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(123): Show |
138 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.964+2123delT | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr11 | 34972395 | ||||||
| chr11:34972407 | T | C | 4 | a0001c0002t0007g0187 a0001c0002t0007g0189 a0001c0002t0007g0190 others(1): Show |
4 | HG01884.hp2 HG02572.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.964+2121T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | chr11 | 34972407 | |||||||
| chr11:34972551 | C | T | 1 | a0003c0006t0001g0214 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.964+2265C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | chr11 | 34972551 | |||||||
| chr11:34972554 | T | C | 1 | a0001c0002t0002g0005 | 3 | NA18980.hp2 NA19085.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.964+2268T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | chr11 | 34972554 | |||||||
| chr11:34972590 | T | G | 165 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(162): Show |
183 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.964+2304T>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | chr11 | 34972590 | |||||||
| chr11:34972620 | A | C | 1 | a0006c0011t0001g0200 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.964+2334A>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | chr11 | 34972620 | |||||||
| chr11:34972628 | G | T | 33 | a0001c0002t0007g0187 a0001c0002t0007g0188 a0001c0002t0007g0189 others(30): Show |
36 | HG00673.hp2 HG01106.hp1 HG01168.hp2 others(33): Show |
intron_variant | MODIFIER | c.964+2342G>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | chr11 | 34972628 | |||||||
| chr11:34972690 | C | T | 6 | a0002c0008t0006g0001 a0002c0008t0006g0270 a0002c0008t0006g0271 others(3): Show |
8 | HG02145.hp1 HG02451.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.964+2404C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | chr11 | 34972690 | |||||||
| chr11:34972975 | T | C | 129 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(126): Show |
141 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.964+2689T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | chr11 | 34972975 | |||||||
| chr11:34972976 | G | A | 4 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(1): Show |
4 | HG02451.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.964+2690G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | chr11 | 34972976 | |||||||
| chr11:34973083 | T | C | 10 | a0001c0026t0013g0050 a0002c0004t0005g0007 a0002c0005t0005g0007 others(7): Show |
15 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.964+2797T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | chr11 | 34973083 | |||||||
| chr11:34973122 | T | G | 6 | a0001c0002t0007g0187 a0001c0002t0007g0188 a0001c0002t0007g0189 others(3): Show |
6 | HG01884.hp2 HG02572.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.964+2836T>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | chr11 | 34973122 | |||||||
| chr11:34973399 | C | T | 6 | a0001c0001t0001g0051 a0001c0001t0001g0078 a0001c0001t0001g0079 others(3): Show |
6 | HG01074.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.964+3113C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | chr11 | 34973399 | |||||||
| chr11:34973503 | T | C | 1 | a0001c0001t0008g0057 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.964+3217T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | chr11 | 34973503 | |||||||
| chr11:34973563 | C | T | 204 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(201): Show |
227 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.964+3277C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | chr11 | 34973563 | |||||||
| chr11:34973617 | G | A | 6 | a0001c0002t0007g0187 a0001c0002t0007g0188 a0001c0002t0007g0189 others(3): Show |
6 | HG01884.hp2 HG02572.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.964+3331G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | chr11 | 34973617 | |||||||
| chr11:34973889 | A | ACTT | 171 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(168): Show |
191 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.964+3606_964+3608d others(5): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr11 | 34973889 | ||||||
| chr11:34974056 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.964+3770C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | chr11 | 34974056 | |||||||
| chr11:34974227 | G | A | 35 | a0001c0014t0009g0105 a0001c0014t0009g0106 a0001c0017t0007g0144 others(32): Show |
41 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(38): Show |
intron_variant | MODIFIER | c.965-3897G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | chr11 | 34974227 | |||||||
| chr11:34974282 | C | T | 4 | a0002c0003t0003g0276 a0002c0003t0003g0277 a0002c0003t0003g0278 others(1): Show |
4 | HG02615.hp2 HG02630.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-3842C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | chr11 | 34974282 | |||||||
| chr11:34974370 | C | G | 35 | a0001c0014t0009g0105 a0001c0014t0009g0106 a0001c0017t0007g0144 others(32): Show |
41 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(38): Show |
intron_variant | MODIFIER | c.965-3754C>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | chr11 | 34974370 | |||||||
| chr11:34974676 | A | G | 1 | a0009c0025t0001g0215 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.965-3448A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | chr11 | 34974676 | |||||||
| chr11:34974765 | C | T | 1 | a0010c0028t0016g0275 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.965-3359C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | chr11 | 34974765 | |||||||
| chr11:34975098 | C | A | 10 | a0001c0026t0013g0050 a0002c0004t0005g0007 a0002c0005t0005g0007 others(7): Show |
15 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.965-3026C>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | chr11 | 34975098 | |||||||
| chr11:34975129 | G | A | 165 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(162): Show |
183 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.965-2995G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | chr11 | 34975129 | |||||||
| chr11:34975170 | G | A | 33 | a0001c0002t0007g0187 a0001c0002t0007g0188 a0001c0002t0007g0189 others(30): Show |
36 | HG00673.hp2 HG01106.hp1 HG01168.hp2 others(33): Show |
intron_variant | MODIFIER | c.965-2954G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | chr11 | 34975170 | |||||||
| chr11:34975191 | T | TC | 165 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(162): Show |
183 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.965-2933_965-2932i others(3): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | chr11 | 34975191 | |||||||
| chr11:34975406 | A | G | 130 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(127): Show |
142 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.965-2718A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | chr11 | 34975406 | |||||||
| chr11:34975521 | A | G | 1 | a0002c0004t0004g0224 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.965-2603A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | chr11 | 34975521 | |||||||
| chr11:34975563 | G | A | 6 | a0002c0008t0006g0001 a0002c0008t0006g0270 a0002c0008t0006g0271 others(3): Show |
8 | HG02145.hp1 HG02451.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.965-2561G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | chr11 | 34975563 | |||||||
| chr11:34975563 | G | T | 1 | a0001c0002t0002g0160 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.965-2561G>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | chr11 | 34975563 | |||||||
| chr11:34975633 | A | G | 1 | a0002c0005t0005g0027 | 2 | HG02055.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.965-2491A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | chr11 | 34975633 | |||||||
| chr11:34975737 | T | G | 5 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0047 others(2): Show |
7 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.965-2387T>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | chr11 | 34975737 | |||||||
| chr11:34975767 | A | G | 35 | a0001c0014t0009g0105 a0001c0014t0009g0106 a0001c0017t0007g0144 others(32): Show |
41 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(38): Show |
intron_variant | MODIFIER | c.965-2357A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | chr11 | 34975767 | |||||||
| chr11:34975783 | C | T | 4 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(1): Show |
4 | HG02451.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.965-2341C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | chr11 | 34975783 | |||||||
| chr11:34976006 | A | T | 1 | a0010c0028t0016g0275 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.965-2118A>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | chr11 | 34976006 | |||||||
| chr11:34976015 | T | C | 129 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(126): Show |
141 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.965-2109T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | chr11 | 34976015 | |||||||
| chr11:34976154 | A | G | 16 | a0001c0014t0009g0105 a0001c0014t0009g0106 a0002c0004t0004g0232 others(13): Show |
17 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.965-1970A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | chr11 | 34976154 | |||||||
| chr11:34976208 | A | C | 6 | a0001c0001t0001g0051 a0001c0001t0001g0078 a0001c0001t0001g0079 others(3): Show |
6 | HG01074.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.965-1916A>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | chr11 | 34976208 | |||||||
| chr11:34976467 | C | T | 35 | a0001c0014t0009g0105 a0001c0014t0009g0106 a0001c0017t0007g0144 others(32): Show |
41 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(38): Show |
intron_variant | MODIFIER | c.965-1657C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | chr11 | 34976467 | |||||||
| chr11:34976604 | T | C | 204 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(201): Show |
227 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.965-1520T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | chr11 | 34976604 | |||||||
| chr11:34976644 | A | G | 1 | a0001c0002t0002g0005 | 3 | NA18980.hp2 NA19085.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.965-1480A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | chr11 | 34976644 | |||||||
| chr11:34976665 | T | C | 9 | a0001c0026t0013g0050 a0002c0004t0005g0007 a0002c0005t0005g0007 others(6): Show |
14 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.965-1459T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | chr11 | 34976665 | |||||||
| chr11:34976684 | T | G | 1 | a0003c0006t0001g0208 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.965-1440T>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | chr11 | 34976684 | |||||||
| chr11:34976688 | G | C | 3 | a0006c0011t0001g0198 a0006c0011t0001g0200 a0006c0011t0001g0201 |
3 | HG03139.hp1 HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.965-1436G>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | chr11 | 34976688 | |||||||
| chr11:34976743 | A | T | 130 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(127): Show |
142 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.965-1381A>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | chr11 | 34976743 | |||||||
| chr11:34976764 | A | C | 1 | a0001c0017t0007g0144 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.965-1360A>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | chr11 | 34976764 | |||||||
| chr11:34976946 | A | G | 35 | a0001c0014t0009g0105 a0001c0014t0009g0106 a0001c0017t0007g0144 others(32): Show |
41 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(38): Show |
intron_variant | MODIFIER | c.965-1178A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | chr11 | 34976946 | |||||||
| chr11:34977199 | G | A | 165 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(162): Show |
183 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.965-925G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | chr11 | 34977199 | |||||||
| chr11:34977290 | G | T | 2 | a0001c0001t0001g0089 a0001c0001t0001g0094 |
2 | NA18967.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.965-834G>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | chr11 | 34977290 | |||||||
| chr11:34977479 | C | T | 2 | a0002c0003t0003g0278 a0002c0003t0003g0279 |
2 | HG02630.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.965-645C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | chr11 | 34977479 | |||||||
| chr11:34977533 | G | C | 19 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(16): Show |
22 | HG00673.hp2 HG01106.hp1 HG01168.hp2 others(19): Show |
intron_variant | MODIFIER | c.965-591G>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | chr11 | 34977533 | |||||||
| chr11:34977581 | C | T | 1 | a0001c0001t0001g0014 | 2 | NA18998.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.965-543C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | chr11 | 34977581 | |||||||
| chr11:34977937 | G | T | 204 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(201): Show |
227 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.965-187G>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | chr11 | 34977937 | |||||||
| chr11:34978198 | C | G | 112 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(109): Show |
123 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.1023+16C>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34978198 | |||||||
| chr11:34978200 | A | G | 7 | a0001c0023t0009g0199 a0002c0004t0004g0222 a0002c0004t0004g0236 others(4): Show |
7 | HG02280.hp1 HG02559.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1023+18A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34978200 | |||||||
| chr11:34978314 | G | A | 25 | a0001c0014t0009g0105 a0001c0014t0009g0106 a0001c0017t0007g0144 others(22): Show |
26 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(23): Show |
intron_variant | MODIFIER | c.1023+132G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34978314 | |||||||
| chr11:34978811 | G | A | 129 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(126): Show |
141 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.1023+629G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34978811 | |||||||
| chr11:34978941 | G | A | 8 | a0001c0002t0002g0018 a0001c0002t0002g0019 a0001c0002t0002g0152 others(5): Show |
10 | HG01109.hp2 HG02257.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1023+759G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34978941 | |||||||
| chr11:34979122 | G | A | 11 | a0001c0026t0013g0050 a0002c0004t0005g0007 a0002c0005t0005g0007 others(8): Show |
16 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.1023+940G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34979122 | |||||||
| chr11:34979196 | A | G | 2 | a0002c0003t0003g0276 a0002c0003t0003g0277 |
2 | HG02615.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1023+1014A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34979196 | |||||||
| chr11:34979302 | G | C | 27 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(24): Show |
30 | HG00673.hp2 HG01106.hp1 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.1023+1120G>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34979302 | |||||||
| chr11:34979409 | A | G | 1 | a0001c0017t0007g0144 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1023+1227A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34979409 | |||||||
| chr11:34979436 | C | T | 129 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(126): Show |
141 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.1023+1254C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34979436 | |||||||
| chr11:34979597 | T | C | 1 | a0001c0001t0001g0072 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1023+1415T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34979597 | |||||||
| chr11:34979616 | A | G | 6 | a0002c0008t0006g0001 a0002c0008t0006g0270 a0002c0008t0006g0271 others(3): Show |
8 | HG02145.hp1 HG02451.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1023+1434A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34979616 | |||||||
| chr11:34979633 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1023+1451T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34979633 | |||||||
| chr11:34979890 | C | T | 5 | a0002c0007t0004g0022 a0002c0007t0004g0228 a0002c0007t0004g0229 others(2): Show |
6 | HG01361.hp1 HG02602.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1023+1708C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34979890 | |||||||
| chr11:34979916 | A | G | 2 | a0001c0002t0002g0132 a0001c0002t0002g0134 |
2 | HG03490.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1023+1734A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34979916 | |||||||
| chr11:34979926 | T | A | 11 | a0001c0026t0013g0050 a0002c0004t0005g0007 a0002c0005t0005g0007 others(8): Show |
16 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.1023+1744T>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34979926 | |||||||
| chr11:34979949 | T | C | 3 | a0001c0001t0001g0032 a0001c0001t0001g0124 a0004c0022t0015g0143 |
3 | HG00741.hp2 HG01081.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.1023+1767T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34979949 | |||||||
| chr11:34980113 | C | T | 1 | a0001c0001t0001g0118 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1023+1931C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34980113 | |||||||
| chr11:34980141 | G | T | 1 | a0002c0004t0004g0222 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1023+1959G>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34980141 | |||||||
| chr11:34980152 | T | TTTAAA | 11 | a0001c0026t0013g0050 a0002c0004t0005g0007 a0002c0005t0005g0007 others(8): Show |
16 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.1023+1972_1023+197 others(9): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr11 | 34980152 | ||||||
| chr11:34980152 | T | TTTTAA | 129 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(126): Show |
141 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.1023+1973_1023+197 others(9): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr11 | 34980152 | ||||||
| chr11:34980278 | C | T | 4 | a0001c0001t0001g0051 a0001c0001t0001g0079 a0001c0001t0001g0080 others(1): Show |
4 | HG01167.hp1 HG01169.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1023+2096C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34980278 | |||||||
| chr11:34980294 | G | T | 1 | a0002c0004t0004g0224 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1023+2112G>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34980294 | |||||||
| chr11:34980352 | C | CTTTT | 11 | a0001c0026t0013g0050 a0002c0004t0005g0007 a0002c0005t0005g0007 others(8): Show |
16 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.1023+2181_1023+218 others(8): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr11 | 34980352 | ||||||
| chr11:34980352 | C | CTTTTTTT others(3): Show |
10 | a0002c0004t0004g0224 a0002c0004t0004g0232 a0002c0004t0004g0234 others(7): Show |
12 | HG02451.hp1 HG02572.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.1023+2175_1023+218 others(14): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr11 | 34980352 | ||||||
| chr11:34980352 | C | CTTTTTTT others(4): Show |
21 | a0001c0014t0009g0105 a0001c0014t0009g0106 a0001c0017t0007g0144 others(18): Show |
22 | HG01169.hp2 HG01192.hp2 HG01361.hp1 others(19): Show |
intron_variant | MODIFIER | c.1023+2174_1023+218 others(15): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr11 | 34980352 | ||||||
| chr11:34980352 | C | CTTTTTTT others(5): Show |
23 | a0001c0001t0001g0078 a0002c0003t0003g0023 a0002c0003t0003g0024 others(20): Show |
26 | HG00673.hp2 HG01074.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.1023+2173_1023+218 others(16): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr11 | 34980352 | ||||||
| chr11:34980352 | C | CTTTTTTT others(8): Show |
1 | a0001c0001t0001g0120 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1023+2182_1023+218 others(19): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr11 | 34980352 | ||||||
| chr11:34980352 | C | CTTTTTTT others(6): Show |
11 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0002t0007g0187 others(8): Show |
11 | HG01175.hp2 HG01516.hp2 HG01517.hp2 others(8): Show |
intron_variant | MODIFIER | c.1023+2172_1023+218 others(17): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr11 | 34980352 | ||||||
| chr11:34980352 | C | CTTTTTTT others(7): Show |
10 | a0001c0001t0001g0030 a0001c0001t0001g0051 a0001c0001t0001g0080 others(7): Show |
10 | HG01167.hp1 HG01169.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1023+2171_1023+218 others(18): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr11 | 34980352 | ||||||
| chr11:34980352 | C | CTTTTTTT others(8): Show |
96 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(93): Show |
106 | HG00280.hp1 HG00423.hp2 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.1023+2184_1023+218 others(19): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr11 | 34980352 | ||||||
| chr11:34980352 | C | CTTTTTTT others(9): Show |
15 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0037 others(12): Show |
17 | HG00140.hp2 HG00280.hp2 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.1023+2184_1023+218 others(20): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr11 | 34980352 | ||||||
| chr11:34980352 | C | CTTTTTTT others(10): Show |
3 | a0006c0011t0001g0198 a0006c0011t0001g0200 a0006c0011t0001g0201 |
3 | HG03139.hp1 HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1023+2184_1023+218 others(21): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr11 | 34980352 | ||||||
| chr11:34980392 | G | A | 1 | a0001c0024t0001g0116 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1023+2210G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34980392 | |||||||
| chr11:34980572 | T | G | 1 | a0001c0002t0002g0167 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1023+2390T>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34980572 | |||||||
| chr11:34980599 | C | G | 1 | a0002c0004t0004g0240 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1023+2417C>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34980599 | |||||||
| chr11:34980611 | G | A | 1 | a0002c0004t0004g0240 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1023+2429G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34980611 | |||||||
| chr11:34980982 | T | C | 129 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(126): Show |
141 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.1023+2800T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34980982 | |||||||
| chr11:34981003 | T | A | 1 | a0002c0027t0003g0244 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1023+2821T>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34981003 | |||||||
| chr11:34981469 | A | G | 10 | a0001c0026t0013g0050 a0002c0004t0005g0007 a0002c0005t0005g0007 others(7): Show |
15 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1024-3101A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34981469 | |||||||
| chr11:34981619 | A | G | 2 | a0002c0008t0006g0273 a0002c0008t0006g0274 |
2 | HG02145.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1024-2951A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34981619 | |||||||
| chr11:34981686 | T | C | 140 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(137): Show |
157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.1024-2884T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34981686 | |||||||
| chr11:34981687 | G | A | 1 | a0001c0001t0001g0086 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1024-2883G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34981687 | |||||||
| chr11:34981741 | T | C | 1 | a0001c0001t0001g0118 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1024-2829T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34981741 | |||||||
| chr11:34981749 | T | G | 5 | a0001c0002t0007g0187 a0001c0002t0007g0188 a0001c0002t0007g0189 others(2): Show |
5 | HG01884.hp2 HG02572.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1024-2821T>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34981749 | |||||||
| chr11:34981751 | GTGA | G | 10 | a0001c0026t0013g0050 a0002c0004t0005g0007 a0002c0005t0005g0007 others(7): Show |
15 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1024-2812_1024-281 others(7): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr11 | 34981751 | ||||||
| chr11:34981761 | G | T | 1 | a0002c0004t0004g0240 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1024-2809G>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34981761 | |||||||
| chr11:34981943 | C | T | 1 | a0001c0002t0002g0133 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1024-2627C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34981943 | |||||||
| chr11:34981945 | G | T | 1 | a0001c0002t0002g0133 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1024-2625G>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34981945 | |||||||
| chr11:34981952 | G | C | 6 | a0001c0002t0007g0187 a0001c0002t0007g0188 a0001c0002t0007g0189 others(3): Show |
6 | HG01884.hp2 HG02572.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1024-2618G>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34981952 | |||||||
| chr11:34982029 | G | T | 10 | a0001c0026t0013g0050 a0002c0004t0005g0007 a0002c0005t0005g0007 others(7): Show |
15 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1024-2541G>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34982029 | |||||||
| chr11:34982095 | G | A | 4 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(1): Show |
4 | HG02451.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1024-2475G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34982095 | |||||||
| chr11:34982128 | G | T | 25 | a0001c0014t0009g0105 a0001c0014t0009g0106 a0001c0017t0007g0144 others(22): Show |
26 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(23): Show |
intron_variant | MODIFIER | c.1024-2442G>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34982128 | |||||||
| chr11:34982135 | G | T | 1 | a0001c0001t0001g0038 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1024-2435G>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34982135 | |||||||
| chr11:34982141 | C | T | 6 | a0002c0008t0006g0001 a0002c0008t0006g0270 a0002c0008t0006g0271 others(3): Show |
8 | HG02145.hp1 HG02451.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1024-2429C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34982141 | |||||||
| chr11:34982144 | T | G | 5 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0047 others(2): Show |
7 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1024-2426T>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34982144 | |||||||
| chr11:34982180 | A | C | 129 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(126): Show |
141 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.1024-2390A>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34982180 | |||||||
| chr11:34982236 | C | T | 1 | a0001c0001t0001g0087 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1024-2334C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34982236 | |||||||
| chr11:34982431 | C | A | 11 | a0001c0026t0013g0050 a0002c0004t0005g0007 a0002c0005t0005g0007 others(8): Show |
16 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.1024-2139C>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34982431 | |||||||
| chr11:34982487 | G | A | 2 | a0002c0012t0003g0242 a0002c0012t0003g0243 |
2 | NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1024-2083G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34982487 | |||||||
| chr11:34982532 | T | A | 2 | a0001c0001t0001g0013 a0001c0001t0001g0072 |
3 | HG00642.hp2 HG01071.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.1024-2038T>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34982532 | |||||||
| chr11:34982626 | CAG | C | 10 | a0001c0002t0002g0017 a0001c0002t0002g0130 a0001c0002t0002g0131 others(7): Show |
11 | HG01891.hp2 HG02083.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.1024-1940_1024-193 others(6): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr11 | 34982626 | ||||||
| chr11:34982651 | G | A | 1 | a0010c0028t0016g0275 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1024-1919G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34982651 | |||||||
| chr11:34982712 | G | A | 24 | a0001c0014t0009g0105 a0001c0014t0009g0106 a0001c0023t0009g0199 others(21): Show |
25 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.1024-1858G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34982712 | |||||||
| chr11:34982729 | C | G | 24 | a0001c0014t0009g0105 a0001c0014t0009g0106 a0001c0023t0009g0199 others(21): Show |
25 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.1024-1841C>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34982729 | |||||||
| chr11:34982793 | C | G | 129 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(126): Show |
141 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.1024-1777C>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34982793 | |||||||
| chr11:34982794 | T | C | 10 | a0001c0026t0013g0050 a0002c0004t0005g0007 a0002c0005t0005g0007 others(7): Show |
15 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1024-1776T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34982794 | |||||||
| chr11:34982800 | A | G | 10 | a0001c0026t0013g0050 a0002c0004t0005g0007 a0002c0005t0005g0007 others(7): Show |
15 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1024-1770A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34982800 | |||||||
| chr11:34982818 | A | T | 1 | a0002c0004t0004g0224 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1024-1752A>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34982818 | |||||||
| chr11:34982828 | G | A | 11 | a0001c0026t0013g0050 a0002c0004t0005g0007 a0002c0005t0005g0007 others(8): Show |
16 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.1024-1742G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34982828 | |||||||
| chr11:34982854 | G | T | 10 | a0001c0014t0009g0105 a0001c0014t0009g0106 a0002c0007t0004g0022 others(7): Show |
11 | HG01192.hp2 HG01361.hp1 HG01943.hp2 others(8): Show |
intron_variant | MODIFIER | c.1024-1716G>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34982854 | |||||||
| chr11:34982967 | C | A | 1 | a0006c0011t0001g0198 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1024-1603C>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34982967 | |||||||
| chr11:34983007 | C | T | 6 | a0002c0008t0006g0001 a0002c0008t0006g0270 a0002c0008t0006g0271 others(3): Show |
8 | HG02145.hp1 HG02451.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1024-1563C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34983007 | |||||||
| chr11:34983076 | C | T | 23 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(20): Show |
26 | HG00673.hp2 HG01106.hp1 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.1024-1494C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34983076 | |||||||
| chr11:34983131 | A | G | 10 | a0001c0026t0013g0050 a0002c0004t0005g0007 a0002c0005t0005g0007 others(7): Show |
15 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1024-1439A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34983131 | |||||||
| chr11:34983149 | G | A | 243 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(240): Show |
272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.1024-1421G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34983149 | |||||||
| chr11:34983180 | T | G | 5 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0047 others(2): Show |
7 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1024-1390T>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34983180 | |||||||
| chr11:34983225 | A | C | 10 | a0001c0026t0013g0050 a0002c0004t0005g0007 a0002c0005t0005g0007 others(7): Show |
15 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1024-1345A>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34983225 | |||||||
| chr11:34983239 | A | T | 10 | a0001c0026t0013g0050 a0002c0004t0005g0007 a0002c0005t0005g0007 others(7): Show |
15 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1024-1331A>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34983239 | |||||||
| chr11:34983267 | C | T | 1 | a0002c0003t0003g0256 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1024-1303C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34983267 | |||||||
| chr11:34983287 | C | G | 140 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(137): Show |
157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.1024-1283C>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34983287 | |||||||
| chr11:34983315 | T | C | 129 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(126): Show |
141 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.1024-1255T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34983315 | |||||||
| chr11:34983326 | A | G | 10 | a0001c0026t0013g0050 a0002c0004t0005g0007 a0002c0005t0005g0007 others(7): Show |
15 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1024-1244A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34983326 | |||||||
| chr11:34983346 | G | C | 2 | a0002c0012t0003g0242 a0002c0012t0003g0243 |
2 | NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1024-1224G>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34983346 | |||||||
| chr11:34983410 | G | T | 4 | a0001c0002t0002g0018 a0001c0002t0002g0019 a0001c0002t0002g0152 others(1): Show |
6 | HG02257.hp1 HG02486.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1024-1160G>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34983410 | |||||||
| chr11:34983438 | A | G | 10 | a0001c0026t0013g0050 a0002c0004t0005g0007 a0002c0005t0005g0007 others(7): Show |
15 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1024-1132A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34983438 | |||||||
| chr11:34983466 | A | G | 122 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(119): Show |
134 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.1024-1104A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34983466 | |||||||
| chr11:34983569 | A | T | 1 | a0001c0002t0002g0158 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1024-1001A>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34983569 | |||||||
| chr11:34983583 | A | T | 1 | a0001c0002t0002g0219 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1024-987A>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34983583 | |||||||
| chr11:34983584 | T | C | 10 | a0001c0026t0013g0050 a0002c0004t0005g0007 a0002c0005t0005g0007 others(7): Show |
15 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1024-986T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34983584 | |||||||
| chr11:34983588 | C | A | 10 | a0001c0026t0013g0050 a0002c0004t0005g0007 a0002c0005t0005g0007 others(7): Show |
15 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1024-982C>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34983588 | |||||||
| chr11:34983597 | T | G | 10 | a0001c0026t0013g0050 a0002c0004t0005g0007 a0002c0005t0005g0007 others(7): Show |
15 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1024-973T>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34983597 | |||||||
| chr11:34983598 | G | A | 10 | a0001c0026t0013g0050 a0002c0004t0005g0007 a0002c0005t0005g0007 others(7): Show |
15 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1024-972G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34983598 | |||||||
| chr11:34983604 | A | G | 1 | a0001c0001t0001g0073 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1024-966A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34983604 | |||||||
| chr11:34983611 | T | G | 146 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(143): Show |
165 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.1024-959T>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34983611 | |||||||
| chr11:34983627 | A | G | 10 | a0001c0026t0013g0050 a0002c0004t0005g0007 a0002c0005t0005g0007 others(7): Show |
15 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1024-943A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34983627 | |||||||
| chr11:34983628 | T | C | 10 | a0001c0026t0013g0050 a0002c0004t0005g0007 a0002c0005t0005g0007 others(7): Show |
15 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1024-942T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34983628 | |||||||
| chr11:34983689 | A | G | 7 | a0003c0006t0001g0202 a0003c0006t0001g0203 a0003c0006t0001g0204 others(4): Show |
7 | HG00280.hp1 HG01243.hp1 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1024-881A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34983689 | |||||||
| chr11:34983761 | G | A | 146 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(143): Show |
165 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.1024-809G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34983761 | |||||||
| chr11:34983811 | G | C | 1 | a0001c0001t0001g0053 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1024-759G>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34983811 | |||||||
| chr11:34983823 | C | T | 130 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(127): Show |
142 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.1024-747C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34983823 | |||||||
| chr11:34983824 | G | A | 10 | a0001c0026t0013g0050 a0002c0004t0005g0007 a0002c0005t0005g0007 others(7): Show |
15 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1024-746G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34983824 | |||||||
| chr11:34983870 | A | G | 24 | a0001c0014t0009g0105 a0001c0014t0009g0106 a0001c0023t0009g0199 others(21): Show |
25 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.1024-700A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34983870 | |||||||
| chr11:34983903 | T | A | 1 | a0003c0006t0001g0207 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1024-667T>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34983903 | |||||||
| chr11:34983956 | C | T | 1 | a0001c0002t0002g0158 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1024-614C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34983956 | |||||||
| chr11:34984022 | C | T | 10 | a0001c0026t0013g0050 a0002c0004t0005g0007 a0002c0005t0005g0007 others(7): Show |
15 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1024-548C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34984022 | |||||||
| chr11:34984105 | T | C | 1 | a0003c0006t0001g0211 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1024-465T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34984105 | |||||||
| chr11:34984116 | T | A | 10 | a0001c0026t0013g0050 a0002c0004t0005g0007 a0002c0005t0005g0007 others(7): Show |
15 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1024-454T>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34984116 | |||||||
| chr11:34984139 | A | T | 129 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(126): Show |
141 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.1024-431A>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34984139 | |||||||
| chr11:34984221 | A | T | 12 | a0003c0006t0001g0202 a0003c0006t0001g0203 a0003c0006t0001g0204 others(9): Show |
12 | HG00280.hp1 HG01109.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.1024-349A>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34984221 | |||||||
| chr11:34984355 | A | T | 27 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(24): Show |
30 | HG00673.hp2 HG01106.hp1 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.1024-215A>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34984355 | |||||||
| chr11:34984517 | C | T | 10 | a0001c0026t0013g0050 a0002c0004t0005g0007 a0002c0005t0005g0007 others(7): Show |
15 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1024-53C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34984517 | |||||||
| chr11:34984826 | T | A | 1 | a0001c0002t0007g0192 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1182+98T>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34984826 | |||||||
| chr11:34984851 | T | C | 1 | a0011c0019t0002g0159 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1182+123T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34984851 | |||||||
| chr11:34984918 | A | T | 129 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(126): Show |
141 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.1182+190A>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34984918 | |||||||
| chr11:34984973 | A | G | 10 | a0001c0026t0013g0050 a0002c0004t0005g0007 a0002c0005t0005g0007 others(7): Show |
15 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1182+245A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34984973 | |||||||
| chr11:34985079 | A | G | 1 | a0001c0002t0002g0131 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1182+351A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34985079 | |||||||
| chr11:34985133 | A | G | 3 | a0001c0023t0009g0199 a0002c0004t0004g0236 a0002c0004t0004g0238 |
3 | HG02280.hp1 HG02559.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1182+405A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34985133 | |||||||
| chr11:34985137 | T | C | 4 | a0002c0008t0006g0001 a0002c0008t0006g0270 a0002c0008t0006g0271 others(1): Show |
6 | HG02451.hp1 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1182+409T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34985137 | |||||||
| chr11:34985160 | C | T | 6 | a0001c0002t0007g0187 a0001c0002t0007g0188 a0001c0002t0007g0189 others(3): Show |
6 | HG01884.hp2 HG02572.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1182+432C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34985160 | |||||||
| chr11:34985161 | G | A | 129 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(126): Show |
141 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.1182+433G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34985161 | |||||||
| chr11:34985168 | C | T | 2 | a0002c0003t0003g0279 a0010c0028t0016g0275 |
2 | HG02630.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1182+440C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34985168 | |||||||
| chr11:34985171 | G | A | 6 | a0001c0023t0009g0199 a0002c0004t0004g0222 a0002c0004t0004g0236 others(3): Show |
6 | HG02280.hp1 HG02559.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1182+443G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34985171 | |||||||
| chr11:34985172 | G | T | 1 | a0002c0012t0003g0264 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1182+444G>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34985172 | |||||||
| chr11:34985196 | G | A | 10 | a0001c0026t0013g0050 a0002c0004t0005g0007 a0002c0005t0005g0007 others(7): Show |
15 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1182+468G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34985196 | |||||||
| chr11:34985280 | A | C | 1 | a0002c0005t0005g0026 | 2 | HG02809.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1182+552A>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34985280 | |||||||
| chr11:34985309 | C | T | 1 | a0010c0028t0016g0275 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1182+581C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34985309 | |||||||
| chr11:34985561 | G | A | 10 | a0001c0026t0013g0050 a0002c0004t0005g0007 a0002c0005t0005g0007 others(7): Show |
15 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1182+833G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34985561 | |||||||
| chr11:34985816 | C | A | 10 | a0001c0026t0013g0050 a0002c0004t0005g0007 a0002c0005t0005g0007 others(7): Show |
15 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1182+1088C>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34985816 | |||||||
| chr11:34985955 | C | A | 10 | a0001c0026t0013g0050 a0002c0004t0005g0007 a0002c0005t0005g0007 others(7): Show |
15 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1182+1227C>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34985955 | |||||||
| chr11:34986092 | G | A | 1 | a0002c0003t0003g0253 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1182+1364G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34986092 | |||||||
| chr11:34986125 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1182+1397C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34986125 | |||||||
| chr11:34986212 | T | C | 1 | a0002c0004t0004g0240 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1182+1484T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34986212 | |||||||
| chr11:34986307 | C | CA | 35 | a0001c0002t0007g0190 a0001c0002t0007g0192 a0002c0003t0003g0023 others(32): Show |
40 | HG00673.hp2 HG01106.hp1 HG01168.hp2 others(37): Show |
intron_variant | MODIFIER | c.1182+1598dupA | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 34986307 | ||||||
| chr11:34986307 | C | CAA | 27 | a0001c0002t0007g0187 a0001c0002t0007g0189 a0001c0002t0014g0191 others(24): Show |
28 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(25): Show |
intron_variant | MODIFIER | c.1182+1597_1182+159 others(6): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 34986307 | ||||||
| chr11:34986307 | CA | C | 18 | a0001c0002t0002g0146 a0001c0002t0002g0152 a0001c0002t0002g0167 others(15): Show |
23 | HG01993.hp1 HG02055.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.1182+1598delA | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 34986307 | ||||||
| chr11:34986322 | A | AAG | 8 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0085 others(5): Show |
8 | HG01167.hp2 HG01168.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.1182+1595_1182+159 others(6): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 34986322 | ||||||
| chr11:34986322 | A | AG | 121 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(118): Show |
133 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.1182+1594_1182+159 others(5): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34986322 | |||||||
| chr11:34986322 | A | G | 1 | a0001c0001t0008g0059 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1182+1594A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34986322 | |||||||
| chr11:34986531 | T | C | 140 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(137): Show |
157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.1182+1803T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34986531 | |||||||
| chr11:34986532 | G | A | 1 | a0002c0005t0005g0008 | 3 | HG02486.hp1 HG03195.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1182+1804G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34986532 | |||||||
| chr11:34986541 | G | C | 3 | a0002c0012t0003g0242 a0002c0012t0003g0243 a0002c0012t0003g0264 |
3 | HG06807.hp1 NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1182+1813G>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34986541 | |||||||
| chr11:34986734 | G | A | 2 | a0002c0012t0003g0242 a0002c0012t0003g0243 |
2 | NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1182+2006G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34986734 | |||||||
| chr11:34986836 | G | A | 122 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(119): Show |
134 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.1182+2108G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34986836 | |||||||
| chr11:34987007 | T | A | 1 | a0010c0028t0016g0275 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1182+2279T>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34987007 | |||||||
| chr11:34987153 | G | A | 5 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0047 others(2): Show |
7 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1182+2425G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34987153 | |||||||
| chr11:34987229 | G | A | 140 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(137): Show |
157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.1182+2501G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34987229 | |||||||
| chr11:34987370 | C | T | 4 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(1): Show |
4 | HG02451.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1182+2642C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34987370 | |||||||
| chr11:34987428 | T | A | 1 | a0002c0005t0005g0268 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1182+2700T>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34987428 | |||||||
| chr11:34987438 | A | G | 10 | a0001c0026t0013g0050 a0002c0004t0005g0007 a0002c0005t0005g0007 others(7): Show |
15 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1182+2710A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34987438 | |||||||
| chr11:34987539 | C | T | 129 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(126): Show |
141 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.1182+2811C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34987539 | |||||||
| chr11:34987656 | A | G | 130 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(127): Show |
142 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.1182+2928A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34987656 | |||||||
| chr11:34987686 | T | C | 146 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(143): Show |
165 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.1182+2958T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34987686 | |||||||
| chr11:34987708 | A | G | 4 | a0001c0002t0002g0141 a0004c0010t0002g0138 a0004c0010t0002g0139 others(1): Show |
4 | HG00140.hp1 HG01515.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.1182+2980A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34987708 | |||||||
| chr11:34987729 | A | AGT | 29 | a0001c0014t0009g0105 a0001c0014t0009g0106 a0001c0023t0009g0199 others(26): Show |
32 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(29): Show |
intron_variant | MODIFIER | c.1182+3020_1182+302 others(6): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 34987729 | ||||||
| chr11:34987729 | A | AGTGT | 110 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(107): Show |
119 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.1182+3018_1182+302 others(8): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 34987729 | ||||||
| chr11:34987729 | A | AGTGTGT | 20 | a0001c0001t0001g0003 a0001c0001t0001g0036 a0001c0001t0001g0037 others(17): Show |
27 | HG00423.hp2 HG02055.hp1 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.1182+3016_1182+302 others(10): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 34987729 | ||||||
| chr11:34987750 | A | G | 35 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0029 others(32): Show |
37 | HG00423.hp2 HG00558.hp2 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.1182+3022A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34987750 | |||||||
| chr11:34987942 | C | T | 1 | a0002c0007t0004g0228 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1182+3214C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34987942 | |||||||
| chr11:34988108 | G | C | 10 | a0001c0026t0013g0050 a0002c0004t0005g0007 a0002c0005t0005g0007 others(7): Show |
15 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1182+3380G>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34988108 | |||||||
| chr11:34988437 | T | G | 2 | a0001c0002t0002g0156 a0001c0002t0002g0157 |
2 | HG00609.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.1182+3709T>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34988437 | |||||||
| chr11:34988558 | C | CA | 112 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(109): Show |
123 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.1183-3741dupA | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 34988558 | ||||||
| chr11:34988558 | C | CAA | 12 | a0001c0001t0001g0014 a0002c0008t0006g0001 a0002c0008t0006g0270 others(9): Show |
15 | HG02145.hp1 HG02300.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.1183-3742_1183-374 others(6): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 34988558 | ||||||
| chr11:34988558 | CA | C | 95 | a0001c0002t0002g0006 a0001c0002t0002g0018 a0001c0002t0002g0019 others(92): Show |
104 | HG00140.hp1 HG00642.hp1 HG00673.hp2 others(101): Show |
intron_variant | MODIFIER | c.1183-3741delA | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 34988558 | ||||||
| chr11:34988562 | A | AG | 9 | a0001c0026t0013g0050 a0002c0004t0005g0007 a0002c0005t0005g0007 others(6): Show |
14 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.1183-3753_1183-375 others(5): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34988562 | |||||||
| chr11:34988573 | A | G | 1 | a0001c0001t0001g0054 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1183-3742A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34988573 | |||||||
| chr11:34988782 | T | C | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(136): Show |
156 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.1183-3533T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34988782 | |||||||
| chr11:34988856 | A | G | 1 | a0001c0001t0008g0060 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1183-3459A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34988856 | |||||||
| chr11:34988922 | A | G | 140 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(137): Show |
157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.1183-3393A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34988922 | |||||||
| chr11:34988985 | A | C | 1 | a0001c0017t0007g0144 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1183-3330A>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34988985 | |||||||
| chr11:34989033 | T | C | 6 | a0002c0008t0006g0001 a0002c0008t0006g0270 a0002c0008t0006g0271 others(3): Show |
8 | HG02145.hp1 HG02451.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1183-3282T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34989033 | |||||||
| chr11:34989096 | G | A | 2 | a0002c0012t0003g0242 a0002c0012t0003g0243 |
2 | NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1183-3219G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34989096 | |||||||
| chr11:34989317 | C | G | 24 | a0001c0014t0009g0105 a0001c0014t0009g0106 a0001c0023t0009g0199 others(21): Show |
25 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.1183-2998C>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34989317 | |||||||
| chr11:34989379 | G | GA | 10 | a0001c0026t0013g0050 a0002c0004t0005g0007 a0002c0005t0005g0007 others(7): Show |
15 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1183-2929dupA | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 34989379 | ||||||
| chr11:34989437 | A | C | 4 | a0001c0002t0002g0018 a0001c0002t0002g0019 a0001c0002t0002g0152 others(1): Show |
6 | HG02257.hp1 HG02486.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1183-2878A>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34989437 | |||||||
| chr11:34989544 | G | GAGT | 10 | a0001c0026t0013g0050 a0002c0004t0005g0007 a0002c0005t0005g0007 others(7): Show |
15 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1183-2767_1183-276 others(7): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 34989544 | ||||||
| chr11:34989694 | T | G | 1 | a0001c0013t0002g0213 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1183-2621T>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34989694 | |||||||
| chr11:34989718 | C | T | 1 | a0009c0025t0001g0215 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1183-2597C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34989718 | |||||||
| chr11:34989804 | A | G | 2 | a0006c0011t0001g0200 a0006c0011t0001g0201 |
2 | HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1183-2511A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34989804 | |||||||
| chr11:34989943 | T | A | 24 | a0001c0014t0009g0105 a0001c0014t0009g0106 a0001c0023t0009g0199 others(21): Show |
25 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.1183-2372T>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34989943 | |||||||
| chr11:34990092 | G | C | 1 | a0002c0007t0004g0230 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1183-2223G>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34990092 | |||||||
| chr11:34990196 | T | A | 146 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(143): Show |
165 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.1183-2119T>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34990196 | |||||||
| chr11:34990211 | G | A | 9 | a0001c0026t0013g0050 a0002c0004t0005g0007 a0002c0005t0005g0007 others(6): Show |
14 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.1183-2104G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34990211 | |||||||
| chr11:34990340 | A | G | 10 | a0001c0026t0013g0050 a0002c0004t0005g0007 a0002c0005t0005g0007 others(7): Show |
15 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1183-1975A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34990340 | |||||||
| chr11:34990402 | A | G | 2 | a0002c0003t0003g0276 a0002c0003t0003g0277 |
2 | HG02615.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1183-1913A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34990402 | |||||||
| chr11:34990487 | G | T | 1 | a0002c0007t0004g0223 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1183-1828G>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34990487 | |||||||
| chr11:34990675 | G | A | 3 | a0001c0001t0001g0064 a0001c0001t0001g0069 a0001c0001t0001g0113 |
3 | NA18978.hp1 NA18994.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.1183-1640G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34990675 | |||||||
| chr11:34990698 | C | A | 1 | a0001c0001t0008g0060 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1183-1617C>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34990698 | |||||||
| chr11:34990707 | T | A | 2 | a0002c0012t0003g0242 a0002c0012t0003g0243 |
2 | NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1183-1608T>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34990707 | |||||||
| chr11:34990947 | A | C | 10 | a0001c0014t0009g0105 a0001c0014t0009g0106 a0002c0007t0004g0022 others(7): Show |
11 | HG01192.hp2 HG01361.hp1 HG01943.hp2 others(8): Show |
intron_variant | MODIFIER | c.1183-1368A>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34990947 | |||||||
| chr11:34990985 | T | C | 6 | a0001c0002t0007g0187 a0001c0002t0007g0188 a0001c0002t0007g0189 others(3): Show |
6 | HG01884.hp2 HG02572.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1183-1330T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34990985 | |||||||
| chr11:34991008 | G | A | 1 | a0010c0028t0016g0275 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1183-1307G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34991008 | |||||||
| chr11:34991118 | A | AT | 10 | a0001c0026t0013g0050 a0002c0004t0005g0007 a0002c0005t0005g0007 others(7): Show |
15 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1183-1194dupT | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 34991118 | ||||||
| chr11:34991167 | C | T | 6 | a0001c0002t0007g0187 a0001c0002t0007g0188 a0001c0002t0007g0189 others(3): Show |
6 | HG01884.hp2 HG02572.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1183-1148C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34991167 | |||||||
| chr11:34991195 | G | A | 2 | a0002c0003t0003g0276 a0002c0003t0003g0277 |
2 | HG02615.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1183-1120G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34991195 | |||||||
| chr11:34991218 | C | T | 1 | a0001c0017t0007g0144 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1183-1097C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34991218 | |||||||
| chr11:34991224 | A | G | 1 | a0002c0004t0004g0224 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1183-1091A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34991224 | |||||||
| chr11:34991479 | A | C | 2 | a0002c0008t0006g0273 a0002c0008t0006g0274 |
2 | HG02145.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1183-836A>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34991479 | |||||||
| chr11:34991675 | G | A | 2 | a0002c0007t0004g0223 a0002c0007t0004g0231 |
2 | NA19054.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.1183-640G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34991675 | |||||||
| chr11:34991771 | G | A | 1 | a0002c0004t0004g0232 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1183-544G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34991771 | |||||||
| chr11:34991783 | G | A | 1 | a0007c0015t0004g0225 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1183-532G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34991783 | |||||||
| chr11:34991807 | C | T | 2 | a0001c0001t0001g0121 a0001c0001t0001g0123 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1183-508C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34991807 | |||||||
| chr11:34991903 | T | C | 142 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(139): Show |
159 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.1183-412T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34991903 | |||||||
| chr11:34991906 | C | CA | 29 | a0001c0001t0001g0042 a0001c0001t0001g0048 a0001c0001t0001g0058 others(26): Show |
29 | HG00423.hp2 HG00735.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.1183-387dupA | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 34991906 | ||||||
| chr11:34991906 | C | CAA | 7 | a0002c0008t0006g0001 a0002c0008t0006g0270 a0002c0008t0006g0271 others(4): Show |
9 | HG02145.hp1 HG02451.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1183-388_1183-387d others(4): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 34991906 | ||||||
| chr11:34991906 | CAA | C | 9 | a0001c0026t0013g0050 a0002c0004t0005g0007 a0002c0005t0005g0007 others(6): Show |
14 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.1183-388_1183-387d others(4): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 34991906 | ||||||
| chr11:34991973 | T | TC | 10 | a0001c0026t0013g0050 a0002c0004t0005g0007 a0002c0005t0005g0007 others(7): Show |
15 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1183-341dupC | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 34991973 | ||||||
| chr11:34992018 | A | G | 6 | a0002c0004t0004g0232 a0002c0004t0004g0233 a0002c0004t0004g0234 others(3): Show |
6 | HG01496.hp2 HG02572.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1183-297A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 9/10 | chr11 | 34992018 | |||||||
| chr11:34992391 | A | G | 1 | a0002c0003t0003g0276 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1247+12A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 10/10 | chr11 | 34992391 | |||||||
| chr11:34992475 | T | A | 1 | a0010c0028t0016g0275 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1247+96T>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 10/10 | chr11 | 34992475 | |||||||
| chr11:34992492 | A | T | 1 | a0001c0002t0002g0146 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1247+113A>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 10/10 | chr11 | 34992492 | |||||||
| chr11:34992494 | A | G | 1 | a0001c0002t0002g0218 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1247+115A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 10/10 | chr11 | 34992494 | |||||||
| chr11:34992589 | G | A | 1 | a0002c0007t0004g0226 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1247+210G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 10/10 | chr11 | 34992589 | |||||||
| chr11:34992774 | G | A | 1 | a0001c0001t0001g0038 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1247+395G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 10/10 | chr11 | 34992774 | |||||||
| chr11:34992894 | A | G | 2 | a0001c0001t0001g0036 a0001c0001t0001g0037 |
2 | NA18957.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1247+515A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 10/10 | chr11 | 34992894 | |||||||
| chr11:34992904 | G | GGAAACTT others(1): Show |
5 | a0001c0002t0007g0187 a0001c0002t0007g0188 a0001c0002t0007g0189 others(2): Show |
5 | HG01884.hp2 HG02572.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1247+525_1247+526i others(10): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 10/10 | chr11 | 34992904 | |||||||
| chr11:34992905 | C | T | 5 | a0001c0002t0007g0187 a0001c0002t0007g0188 a0001c0002t0007g0189 others(2): Show |
5 | HG01884.hp2 HG02572.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1247+526C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 10/10 | chr11 | 34992905 | |||||||
| chr11:34992907 | G | A | 5 | a0001c0002t0007g0187 a0001c0002t0007g0188 a0001c0002t0007g0189 others(2): Show |
5 | HG01884.hp2 HG02572.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1247+528G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 10/10 | chr11 | 34992907 | |||||||
| chr11:34993105 | G | A | 10 | a0001c0026t0013g0050 a0002c0004t0005g0007 a0002c0005t0005g0007 others(7): Show |
15 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1247+726G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 10/10 | chr11 | 34993105 | |||||||
| chr11:34993172 | T | C | 1 | a0010c0028t0016g0275 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1247+793T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 10/10 | chr11 | 34993172 | |||||||
| chr11:34993195 | T | C | 140 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(137): Show |
157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.1247+816T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 10/10 | chr11 | 34993195 | |||||||
| chr11:34993242 | T | C | 10 | a0001c0026t0013g0050 a0002c0004t0005g0007 a0002c0005t0005g0007 others(7): Show |
15 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1247+863T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 10/10 | chr11 | 34993242 | |||||||
| chr11:34993287 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1247+908G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 10/10 | chr11 | 34993287 | |||||||
| chr11:34993289 | A | G | 1 | a0001c0001t0001g0096 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1247+910A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 10/10 | chr11 | 34993289 | |||||||
| chr11:34993350 | A | G | 140 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(137): Show |
157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.1247+971A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 10/10 | chr11 | 34993350 | |||||||
| chr11:34993413 | A | G | 1 | a0001c0002t0002g0158 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1247+1034A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 10/10 | chr11 | 34993413 | |||||||
| chr11:34993425 | G | A | 129 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(126): Show |
141 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.1247+1046G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 10/10 | chr11 | 34993425 | |||||||
| chr11:34993580 | A | G | 10 | a0001c0026t0013g0050 a0002c0004t0005g0007 a0002c0005t0005g0007 others(7): Show |
15 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1247+1201A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 10/10 | chr11 | 34993580 | |||||||
| chr11:34993636 | T | G | 6 | a0002c0008t0006g0001 a0002c0008t0006g0270 a0002c0008t0006g0271 others(3): Show |
8 | HG02145.hp1 HG02451.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1247+1257T>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 10/10 | chr11 | 34993636 | |||||||
| chr11:34993731 | G | A | 130 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(127): Show |
142 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.1248-1183G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 10/10 | chr11 | 34993731 | |||||||
| chr11:34993837 | A | T | 1 | a0001c0001t0001g0068 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1248-1077A>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 10/10 | chr11 | 34993837 | |||||||
| chr11:34993875 | G | A | 16 | a0001c0014t0009g0105 a0001c0014t0009g0106 a0002c0004t0004g0232 others(13): Show |
17 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.1248-1039G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 10/10 | chr11 | 34993875 | |||||||
| chr11:34993890 | G | A | 27 | a0002c0003t0003g0023 a0002c0003t0003g0024 a0002c0003t0003g0025 others(24): Show |
30 | HG00673.hp2 HG01106.hp1 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.1248-1024G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 10/10 | chr11 | 34993890 | |||||||
| chr11:34993930 | T | A | 16 | a0001c0014t0009g0105 a0001c0014t0009g0106 a0002c0004t0004g0232 others(13): Show |
17 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.1248-984T>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 10/10 | chr11 | 34993930 | |||||||
| chr11:34993935 | G | A | 10 | a0001c0026t0013g0050 a0002c0004t0005g0007 a0002c0005t0005g0007 others(7): Show |
15 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1248-979G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 10/10 | chr11 | 34993935 | |||||||
| chr11:34993950 | A | G | 1 | a0001c0001t0001g0055 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1248-964A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 10/10 | chr11 | 34993950 | |||||||
| chr11:34994256 | T | C | 18 | a0001c0002t0002g0004 a0001c0002t0002g0020 a0001c0002t0002g0154 others(15): Show |
21 | HG00423.hp1 HG00673.hp1 HG01074.hp2 others(18): Show |
intron_variant | MODIFIER | c.1248-658T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 10/10 | chr11 | 34994256 | |||||||
| chr11:34994459 | A | G | 2 | a0001c0001t0001g0075 a0001c0001t0001g0221 |
2 | NA18961.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.1248-455A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 10/10 | chr11 | 34994459 | |||||||
| chr11:34994462 | CACTACTG others(3): Show |
C | 1 | a0001c0001t0001g0073 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1248-448_1248-439d others(12): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr11 | 34994462 | ||||||
| chr11:34994485 | C | T | 1 | a0002c0027t0003g0244 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1248-429C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 10/10 | chr11 | 34994485 | |||||||
| chr11:34994555 | G | C | 130 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(127): Show |
142 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.1248-359G>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 10/10 | chr11 | 34994555 | |||||||
| chr11:34994610 | G | A | 1 | a0001c0001t0001g0041 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1248-304G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 10/10 | chr11 | 34994610 | |||||||
| chr11:34994628 | C | T | 1 | a0008c0016t0001g0091 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1248-286C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 10/10 | chr11 | 34994628 | |||||||
| chr11:34994719 | TTATC | T | 4 | a0001c0002t0002g0018 a0001c0002t0002g0019 a0001c0002t0002g0152 others(1): Show |
6 | HG02257.hp1 HG02486.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1248-191_1248-188d others(6): Show |
PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr11 | 34994719 |