| 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 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and 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 | copy fasta | chr11 | 34911618 | 35001128 |
| a0002 | 0/0 | 501 | 76 | 42 | 7 | 19 | 1 | 7 | 15 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| a0003 | 0/0 | 501 | 12 | 1 | 4 | 0 | 2 | 5 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| a0004 | 0/0 | 501 | 4 | 0 | 1 | 0 | 3 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| a0005 | 0/0 | 501 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| a0006 | 0/0 | 501 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| a0007 | 0/0 | 501 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| a0008 | 0/1 | 501 | 2 | 0 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| a0009 | 0/0 | 501 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| a0010 | 0/0 | 501 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| a0011 | 0/0 | 501 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 1506 | 120 | 18 | 27 | 58 | 4 | 13 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| c0002 | 1/0 | 1506 | 78 | 20 | 17 | 32 | 0 | 8 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| c0003 | 0/0 | 1506 | 29 | 4 | 6 | 17 | 1 | 1 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| c0004 | 0/0 | 1506 | 14 | 13 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| c0005 | 0/0 | 1506 | 13 | 13 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| c0006 | 0/0 | 1506 | 12 | 1 | 4 | 0 | 2 | 5 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| c0007 | 0/0 | 1506 | 8 | 0 | 0 | 2 | 0 | 6 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| c0008 | 0/0 | 1506 | 8 | 8 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| c0009 | 0/0 | 1506 | 3 | 3 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| c0010 | 0/0 | 1506 | 3 | 0 | 0 | 0 | 3 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| c0011 | 0/0 | 1506 | 3 | 3 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| c0012 | 0/0 | 1506 | 3 | 3 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| c0013 | 0/0 | 1506 | 2 | 0 | 0 | 1 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| c0014 | 0/0 | 1506 | 2 | 0 | 2 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| c0015 | 0/1 | 1506 | 2 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| c0016 | 0/0 | 1506 | 2 | 0 | 0 | 2 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| c0017 | 0/0 | 1506 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| c0018 | 0/0 | 1506 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| c0019 | 0/0 | 1506 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| c0020 | 0/0 | 1506 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| c0021 | 0/0 | 1521 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| c0022 | 0/0 | 1506 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| c0023 | 0/0 | 1506 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| c0024 | 0/0 | 1506 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| c0025 | 0/0 | 1506 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| c0026 | 0/0 | 1506 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| c0027 | 0/0 | 1506 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| c0028 | 0/0 | 1506 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 995 | 134 | 23 | 31 | 56 | 6 | 18 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| t0002 | 1/0 | 995 | 81 | 17 | 17 | 33 | 3 | 10 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| t0003 | 0/0 | 995 | 30 | 8 | 6 | 14 | 1 | 1 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| t0004 | 0/1 | 995 | 23 | 12 | 2 | 2 | 0 | 6 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| t0005 | 0/0 | 995 | 14 | 14 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| t0006 | 0/0 | 995 | 8 | 8 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| t0007 | 0/0 | 995 | 6 | 6 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| t0008 | 0/0 | 995 | 4 | 0 | 0 | 4 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| t0009 | 0/0 | 995 | 3 | 1 | 2 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| t0010 | 0/0 | 995 | 3 | 0 | 0 | 3 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| t0011 | 0/0 | 991 | 2 | 0 | 1 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| t0012 | 0/0 | 995 | 2 | 0 | 0 | 2 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| t0013 | 0/0 | 995 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| t0014 | 0/0 | 945 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| t0015 | 0/0 | 991 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| t0016 | 0/0 | 995 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0009 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0025 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0165 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0227 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1506 | 120 | 18 | 27 | 58 | 4 | 13 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| a0001c0002 | 1/0 | 1506 | 78 | 20 | 17 | 32 | 0 | 8 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| a0001c0013 | 0/0 | 1506 | 2 | 0 | 0 | 1 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| a0001c0014 | 0/0 | 1506 | 2 | 0 | 2 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| a0001c0017 | 0/0 | 1506 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| a0001c0018 | 0/0 | 1506 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| a0001c0020 | 0/0 | 1506 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| a0001c0021 | 0/0 | 1521 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| a0001c0023 | 0/0 | 1506 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| a0001c0024 | 0/0 | 1506 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| a0001c0026 | 0/0 | 1506 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| a0002c0003 | 0/0 | 1506 | 29 | 4 | 6 | 17 | 1 | 1 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| a0002c0004 | 0/0 | 1506 | 14 | 13 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| a0002c0005 | 0/0 | 1506 | 13 | 13 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| a0002c0007 | 0/0 | 1506 | 8 | 0 | 0 | 2 | 0 | 6 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| a0002c0008 | 0/0 | 1506 | 8 | 8 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| a0002c0012 | 0/0 | 1506 | 3 | 3 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| a0002c0027 | 0/0 | 1506 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| a0003c0006 | 0/0 | 1506 | 12 | 1 | 4 | 0 | 2 | 5 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| a0004c0010 | 0/0 | 1506 | 3 | 0 | 0 | 0 | 3 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| a0004c0022 | 0/0 | 1506 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| a0005c0009 | 0/0 | 1506 | 3 | 3 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| a0006c0011 | 0/0 | 1506 | 3 | 3 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| a0007c0016 | 0/0 | 1506 | 2 | 0 | 0 | 2 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| a0008c0015 | 0/1 | 1506 | 2 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| a0009c0028 | 0/0 | 1506 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| a0010c0019 | 0/0 | 1506 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| a0011c0025 | 0/0 | 1506 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | 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 | copy fasta | chr11 | 34911618 | 35001128 |
| a0001c0001t0008 | 0/0 | 2500 | 4 | 0 | 0 | 4 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| a0001c0001t0011 | 0/0 | 2496 | 2 | 0 | 1 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| a0001c0002t0002 | 1/0 | 2500 | 70 | 14 | 17 | 30 | 0 | 8 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| a0001c0002t0007 | 0/0 | 2500 | 5 | 5 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| a0001c0002t0012 | 0/0 | 2500 | 2 | 0 | 0 | 2 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| a0001c0002t0014 | 0/0 | 2450 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| a0001c0013t0002 | 0/0 | 2500 | 2 | 0 | 0 | 1 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| a0001c0014t0009 | 0/0 | 2500 | 2 | 0 | 2 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| a0001c0017t0007 | 0/0 | 2500 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| a0001c0018t0001 | 0/0 | 2500 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| a0001c0020t0002 | 0/0 | 2500 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| a0001c0021t0002 | 0/0 | 2515 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| a0001c0023t0009 | 0/0 | 2500 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| a0001c0024t0001 | 0/0 | 2500 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| a0001c0026t0013 | 0/0 | 2500 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| a0002c0003t0003 | 0/0 | 2500 | 26 | 4 | 6 | 14 | 1 | 1 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| a0002c0003t0010 | 0/0 | 2500 | 3 | 0 | 0 | 3 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| a0002c0004t0004 | 0/0 | 2500 | 13 | 12 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| a0002c0004t0005 | 0/0 | 2500 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| a0002c0005t0005 | 0/0 | 2500 | 13 | 13 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| a0002c0007t0004 | 0/0 | 2500 | 8 | 0 | 0 | 2 | 0 | 6 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| a0002c0008t0006 | 0/0 | 2500 | 8 | 8 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| a0002c0012t0003 | 0/0 | 2500 | 3 | 3 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| a0002c0027t0003 | 0/0 | 2500 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| a0003c0006t0001 | 0/0 | 2500 | 12 | 1 | 4 | 0 | 2 | 5 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| a0004c0010t0002 | 0/0 | 2500 | 3 | 0 | 0 | 0 | 3 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| a0004c0022t0015 | 0/0 | 2496 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| a0005c0009t0002 | 0/0 | 2500 | 3 | 3 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| a0006c0011t0001 | 0/0 | 2500 | 3 | 3 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| a0007c0016t0001 | 0/0 | 2500 | 2 | 0 | 0 | 2 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| a0008c0015t0004 | 0/1 | 2500 | 2 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| a0009c0028t0016 | 0/0 | 2500 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| a0010c0019t0002 | 0/0 | 2500 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| a0011c0025t0001 | 0/0 | 2500 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | copy fasta | chr11 | 34911618 | 35001128 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and 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 | 0 | 1 | 0 | 1 | 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 | 2 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 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 | 0 | 1 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0060 | 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 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 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 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 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 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0001g0091 | 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 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0097 | 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 | 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 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 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 | 0 | 1 | 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 |
| a0001c0001t0008g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0008g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0008g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0008g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0011g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0001t0011g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 |
| a0001c0014t0009g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0001c0014t0009g0110 | 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 |
| a0001c0026t0013g0054 | 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 |
| a0007c0016t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0007c0016t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0008c0015t0004g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0008c0015t0004g0227 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0009c0028t0016g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0010c0019t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| a0011c0025t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | 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 | g0009 | 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 | g0033 | 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 | g0100 | EAS | CHS | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG00558 | hp1 | a0001 | c0001 | t0008 | g0062 | EAS | CHS | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0061 | 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 | g0114 | 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 | g0014 | 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 | g0057 | 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 | g0059 | AMR | PUR | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0121 | 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 | g0076 | 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 | g0082 | 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 | g0088 | 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 | g0014 | 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 | g0055 | AMR | PUR | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0089 | 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 | g0084 | 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 | g0109 | 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 | g0052 | AMR | PUR | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0070 | 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 | g0049 | AMR | CLM | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0117 | 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 | g0119 | 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 | g0120 | AMR | CLM | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0009 | 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 | a0008 | c0015 | t0004 | g0225 | AMR | CLM | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | CLM | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0038 | 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 | g0083 | 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 | g0085 | 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 | g0036 | 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 | g0110 | 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 | g0044 | 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 | g0060 | 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 | g0077 | 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 | g0102 | 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 | g0063 | 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 | g0066 | 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 | a0011 | c0025 | t0001 | g0215 | AFR | ACB | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | CDX | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG02165 | hp2 | a0001 | c0001 | t0008 | g0065 | 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 | g0050 | 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 | g0010 | 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 | g0010 | 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 | g0111 | 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 | g0104 | SAS | PJL | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG02738 | hp1 | a0001 | c0001 | t0011 | g0115 | 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 | g0035 | 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 | a0009 | 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 | g0086 | 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 | g0122 | 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 | g0012 | 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 | g0011 | 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 | g0012 | 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 | a0010 | c0019 | t0002 | g0159 | SAS | STU | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0118 | 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 | g0046 | 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 | g0107 | SAS | BEB | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0080 | 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 | g0112 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0090 | 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 | g0081 | 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 | g0092 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA18950 | hp1 | a0001 | c0001 | t0008 | g0064 | 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 | g0099 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0087 | 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 | g0041 | 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 | g0079 | 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 | a0007 | c0016 | t0001 | g0101 | 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 | g0042 | 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 | g0098 | 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 | g0123 | 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 | g0078 | 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 | g0103 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0034 | 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 | g0097 | 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 | g0093 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA18986 | hp1 | a0007 | c0016 | t0001 | g0095 | 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 | g0075 | 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 | g0069 | 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 | g0108 | 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 | g0096 | 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 | g0015 | 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 | g0013 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0073 | 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 | g0068 | 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 | g0091 | 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 | g0011 | 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 | g0043 | 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 | g0015 | 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 | g0105 | 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 | g0074 | 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 | g0013 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0072 | 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 | g0056 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0067 | 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 | g0094 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA19087 | hp2 | a0001 | c0001 | t0008 | g0113 | EAS | JPT | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0040 | 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 | g0054 | 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 | g0053 | 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 | g0071 | 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 | g0051 | 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 | hp1 | a0008 | c0015 | t0004 | g0227 | REF | REF | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0002 | g0165 | REF | REF | PDHX_chr11_34911618_35001128 | PDHX | chr11 | 34911618 | 35001128 |
| 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 | a0007 | 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 | a0002a0008a0009 | 79 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(76): 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 | a0009 | 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 | a0011 | 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 | a0010 | 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 | a0008 | 2 | HG01361.hp1 homoSapiens_chm13v2.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 |
| 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 | a0001c0001a0001c0013a0001c0014others(16): Show | 224 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(221): 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 | a0002c0003a0002c0004a0002c0005others(6): Show | 79 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(76): 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 | a0001c0026a0002c0005 | 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 | a0001c0014a0002c0007a0008c0015 | 12 | HG01192.hp2 HG01361.hp1 HG01943.hp2 others(9): 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 | a0009c0028 | 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 | a0001c0014a0001c0017a0001c0023others(5): Show | 42 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(39): 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 | a0001c0001a0001c0018a0001c0024others(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 |
| 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 | a0002c0003t0003a0002c0003t0010a0002c0004t0004others(8): Show | 79 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(76): 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 | a0001c0026t0013a0002c0004t0005a0002c0005t0005 | 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 | a0001c0026t0013a0002c0004t0005a0002c0005t0005 | 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 | a0001c0001t0001a0001c0001t0008a0001c0001t0011others(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 | a0001c0001t0011a0004c0022t0015 | 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 | a0009c0028t0016 | 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 | a0001c0001t0001a0001c0001t0008a0001c0001t0011others(23): Show | 228 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(225): 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 | a0001c0014t0009a0001c0023t0009a0002c0004t0004others(2): Show | 26 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(23): 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 | a0009c0028t0016 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*904G>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 11/11 | 904 | chr11 | 34996076 |
| 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 | a0002c0003t0003g0276a0002c0003t0003g0277a0002c0003t0003g0278others(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 | 68 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(65): Show | 79 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(76): 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 | 68 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(65): Show | 79 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(76): 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 | a0001c0002t0002g0216a0001c0002t0002g0217a0001c0002t0002g0218others(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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | 68 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(65): Show | 79 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(76): Show |
intron_variant | MODIFIER | c.160+478T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34917293 | ||||||
| chr11:34917388
|
A | G | 68 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(65): Show | 79 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(76): Show |
intron_variant | MODIFIER | c.160+573A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34917388 | ||||||
| chr11:34917402
|
T | G | 19 | a0002c0004t0004g0222a0002c0004t0004g0224a0002c0004t0004g0232others(16): Show | 20 | HG01361.hp1 HG01496.hp2 HG02280.hp1 others(17): 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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0001c0002t0012g0128a0001c0002t0012g0129 | 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 | 68 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(65): Show | 79 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(76): 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 | a0002c0004t0004g0236a0002c0004t0004g0237a0002c0004t0004g0238others(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 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(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 | a0001c0002t0002g0130a0001c0002t0002g0131 | 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 | a0001c0013t0002g0213a0003c0006t0001g0202a0003c0006t0001g0203others(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 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(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 | 68 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(65): Show | 79 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(76): 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 | a0002c0004t0004g0222a0002c0004t0004g0236a0002c0004t0004g0237others(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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0001c0002t0007g0187a0001c0002t0007g0188a0001c0002t0007g0189others(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 | 183 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(180): Show | 205 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(202): 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 | a0002c0004t0004g0222a0002c0004t0004g0236a0002c0004t0004g0237others(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 | a0001c0001t0001g0030a0001c0001t0001g0031 | 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 | a0002c0012t0003g0242a0002c0012t0003g0243 | 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 | 68 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(65): Show | 79 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(76): 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 | a0001c0002t0007g0187a0001c0002t0007g0188a0001c0002t0007g0189others(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 | 200 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(197): Show | 223 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(220): 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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | 68 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(65): Show | 79 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(76): 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 | a0001c0013t0002g0213a0002c0004t0004g0224a0003c0006t0001g0202others(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 | 68 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(65): Show | 79 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(76): 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 | a0001c0002t0002g0017a0001c0002t0002g0130a0001c0002t0002g0131others(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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | 68 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(65): Show | 79 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(76): 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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0001c0013t0002g0213a0003c0006t0001g0202a0003c0006t0001g0203others(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 | a0001c0002t0002g0140a0001c0002t0002g0141a0004c0010t0002g0138others(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 | 68 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(65): Show | 79 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(76): Show |
intron_variant | MODIFIER | c.160+2996A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34919811 | ||||||
| chr11:34919817
|
C | G | 68 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(65): Show | 79 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(76): 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 | 201 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(198): Show | 224 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(221): 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 | 9 | a0002c0007t0004g0022a0002c0007t0004g0223a0002c0007t0004g0226others(6): Show | 10 | HG01361.hp1 HG02602.hp2 HG02738.hp2 others(7): 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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | 200 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(197): Show | 223 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(220): 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 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(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 | 68 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(65): Show | 79 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(76): 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 | a0001c0013t0002g0213a0003c0006t0001g0202a0003c0006t0001g0203others(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 | a0002c0008t0006g0001a0002c0008t0006g0270a0002c0008t0006g0271others(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 | a0002c0008t0006g0001a0002c0008t0006g0270a0002c0008t0006g0271others(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 | a0001c0013t0002g0213a0003c0006t0001g0202a0003c0006t0001g0203others(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 | a0002c0004t0004g0265a0002c0004t0004g0266 | 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 | 200 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(197): Show | 223 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(220): 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 | a0001c0013t0002g0213a0003c0006t0001g0202a0003c0006t0001g0203others(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 | 68 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(65): Show | 79 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(76): 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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | 9 | a0002c0007t0004g0022a0002c0007t0004g0223a0002c0007t0004g0226others(6): Show | 10 | HG01361.hp1 HG02602.hp2 HG02738.hp2 others(7): 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 | a0002c0004t0004g0265a0002c0004t0004g0266a0002c0005t0005g0263others(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 | 201 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(198): Show | 224 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(221): 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 | 66 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(63): Show | 77 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(74): Show |
intron_variant | MODIFIER | c.160+5129G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34921944 | ||||||
| chr11:34922200
|
T | G | 200 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(197): Show | 223 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.160+5385T>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34922200 | ||||||
| chr11:34922407
|
A | G | 68 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(65): Show | 79 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(76): 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 | a0009c0028t0016g0275 | 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 | a0001c0013t0002g0213a0003c0006t0001g0202a0003c0006t0001g0203others(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 | 68 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(65): Show | 79 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(76): 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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0001c0002t0007g0187a0001c0002t0007g0188a0001c0002t0007g0189others(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 | a0001c0001t0001g0032a0001c0002t0002g0132 | 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 | a0001c0002t0002g0182a0001c0002t0002g0183a0001c0002t0007g0188others(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 | a0002c0003t0003g0245a0002c0003t0003g0246a0002c0004t0005g0007others(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 | a0001c0001t0001g0194a0001c0001t0001g0195a0002c0003t0003g0023others(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 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0002t0002g0133others(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 |
12 | a0001c0002t0002g0017a0001c0002t0002g0136a0001c0002t0002g0137others(9): Show | 14 | HG02602.hp2 HG02615.hp2 HG02647.hp1 others(11): 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 | a0001c0002t0002g0130a0001c0002t0002g0131a0001c0017t0007g0144others(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 | a0002c0003t0003g0278a0002c0003t0003g0279 | 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 | a0002c0005t0005g0263a0002c0012t0003g0242a0002c0012t0003g0264 | 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 | a0002c0004t0004g0239a0002c0008t0006g0001a0002c0008t0006g0270others(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 | a0002c0004t0004g0236a0002c0004t0004g0237a0002c0004t0004g0238others(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 | a0001c0013t0002g0213a0003c0006t0001g0202a0003c0006t0001g0203others(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 | a0001c0001t0001g0009a0001c0001t0001g0033a0001c0001t0001g0034others(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 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(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 | a0001c0001t0001g0032a0001c0001t0001g0121a0001c0001t0001g0122others(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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(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 | a0001c0001t0001g0009a0001c0001t0001g0032a0001c0001t0001g0033others(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 | a0001c0002t0002g0180a0001c0002t0002g0181 | 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 | 207 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(204): Show | 230 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.160+6162C>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34922977 | ||||||
| chr11:34923019
|
A | C | 200 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(197): Show | 223 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(220): 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 | a0002c0012t0003g0242a0002c0012t0003g0243 | 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 | 200 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(197): Show | 223 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(220): 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 | a0002c0004t0004g0232a0002c0004t0004g0235 | 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 | 68 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(65): Show | 79 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(76): 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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | 26 | a0002c0004t0004g0222a0002c0004t0004g0224a0002c0004t0004g0232others(23): Show | 29 | HG01361.hp1 HG01496.hp2 HG02145.hp1 others(26): 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 | 69 | a0001c0001t0001g0114a0002c0003t0003g0023a0002c0003t0003g0024others(66): Show | 80 | HG00423.hp1 HG00621.hp2 HG00673.hp1 others(77): 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 | a0002c0008t0006g0001a0002c0008t0006g0270a0002c0008t0006g0271others(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 | a0005c0009t0002g0177a0005c0009t0002g0178a0005c0009t0002g0179 | 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 | 68 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(65): Show | 79 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(76): 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 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(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 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(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 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(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 | 201 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(198): Show | 224 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(221): Show |
intron_variant | MODIFIER | c.161-6783A>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34924621 | ||||||
| chr11:34924756
|
A | G | 68 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(65): Show | 79 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(76): Show |
intron_variant | MODIFIER | c.161-6648A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34924756 | ||||||
| chr11:34924760
|
G | A | 68 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(65): Show | 79 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(76): 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 | a0001c0001t0001g0037 | 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 | a0001c0013t0002g0213a0003c0006t0001g0202a0003c0006t0001g0203others(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 | 68 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(65): Show | 79 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(76): Show |
intron_variant | MODIFIER | c.161-5911C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34925493 | ||||||
| chr11:34925509
|
G | A | 200 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(197): Show | 223 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(220): 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 | a0002c0004t0004g0265a0002c0004t0004g0266a0002c0005t0005g0263others(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 | 68 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(65): Show | 79 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(76): 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 | a0001c0001t0001g0037 | 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 | a0002c0008t0006g0001a0002c0008t0006g0270a0002c0008t0006g0271others(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 | a0001c0013t0002g0213a0003c0006t0001g0202a0003c0006t0001g0203others(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 | a0009c0028t0016g0275 | 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 | a0001c0001t0001g0010 | 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 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(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 | a0002c0008t0006g0001a0002c0008t0006g0270a0002c0008t0006g0271others(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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0001c0002t0007g0187a0001c0002t0007g0188a0001c0002t0007g0189others(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 | 201 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(198): Show | 224 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(221): 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 | a0001c0002t0002g0017a0001c0002t0002g0130a0001c0002t0002g0131others(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 | a0001c0023t0009g0199a0006c0011t0001g0198a0006c0011t0001g0200others(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 | a0002c0004t0005g0007a0002c0005t0005g0007a0002c0005t0005g0008others(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 | a0001c0001t0001g0038a0001c0001t0001g0039 | 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 | 67 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(64): Show | 78 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(75): 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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | 201 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(198): Show | 224 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(221): 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 | 68 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(65): Show | 79 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(76): Show |
intron_variant | MODIFIER | c.161-4124G>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34927280 | ||||||
| chr11:34927329
|
C | G | 68 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(65): Show | 79 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(76): 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 | a0002c0008t0006g0001a0002c0008t0006g0270a0002c0008t0006g0271others(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 | 200 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(197): Show | 223 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(220): 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 | a0001c0001t0001g0040 | 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 | a0001c0013t0002g0213a0003c0006t0001g0202a0003c0006t0001g0203others(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 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(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 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119 | 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 | a0002c0004t0004g0222a0002c0004t0004g0236a0002c0004t0004g0237others(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 | a0001c0002t0007g0187a0001c0002t0007g0188a0001c0002t0007g0189others(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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | 69 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0002t0012g0129others(66): Show | 80 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(77): 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 | a0002c0004t0004g0265a0002c0004t0004g0266a0002c0005t0005g0263others(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 | 66 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(63): Show | 77 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(74): 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 | a0002c0004t0004g0265a0002c0004t0004g0266 | 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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | 207 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(204): Show | 230 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(227): 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 | 68 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(65): Show | 79 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(76): 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 | a0001c0002t0007g0187a0001c0002t0007g0188a0001c0002t0007g0189others(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 | 68 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(65): Show | 79 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(76): 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 | a0001c0002t0002g0175a0001c0002t0002g0176 | 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 | 68 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(65): Show | 79 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(76): 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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0001c0001t0008g0113a0001c0017t0007g0144 | 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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0001c0001t0001g0112 | 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 | a0002c0003t0003g0278a0002c0003t0003g0279 | 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 | 9 | a0002c0007t0004g0022a0002c0007t0004g0223a0002c0007t0004g0226others(6): Show | 10 | HG01361.hp1 HG02602.hp2 HG02738.hp2 others(7): Show |
intron_variant | MODIFIER | c.161-1418T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34929986 | ||||||
| chr11:34930059
|
T | C | 68 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(65): Show | 79 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(76): Show |
intron_variant | MODIFIER | c.161-1345T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34930059 | ||||||
| chr11:34930398
|
A | G | 68 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(65): Show | 79 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(76): 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 | a0001c0001t0001g0111 | 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 | 201 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(198): Show | 224 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(221): Show |
intron_variant | MODIFIER | c.161-958G>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34930446 | ||||||
| chr11:34930568
|
T | C | 201 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(198): Show | 224 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(221): 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 | a0001c0013t0002g0213a0003c0006t0001g0202a0003c0006t0001g0203others(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 | a0001c0002t0002g0149a0001c0002t0002g0150a0001c0002t0002g0151others(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 | 68 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(65): Show | 79 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(76): 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 | a0001c0013t0002g0213a0003c0006t0001g0202a0003c0006t0001g0203others(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 | a0001c0013t0002g0213a0003c0006t0001g0202a0003c0006t0001g0203others(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 | 200 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(197): Show | 223 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(220): 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 | a0001c0013t0002g0213a0003c0006t0001g0202a0003c0006t0001g0203others(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 | a0003c0006t0001g0202a0003c0006t0001g0203a0003c0006t0001g0204others(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 | 68 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(65): Show | 79 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(76): Show |
intron_variant | MODIFIER | c.161-542T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 1/10 | chr11 | 34930862 | ||||||
| chr11:34931018
|
G | C | 200 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(197): Show | 223 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(220): 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 | a0002c0004t0005g0007a0002c0005t0005g0007a0002c0005t0005g0008others(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 | 68 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(65): Show | 79 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(76): Show |
intron_variant | MODIFIER | c.241+24C>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34931508 | ||||||
| chr11:34931536
|
G | GT | 62 | a0001c0001t0001g0123a0001c0014t0009g0109a0001c0014t0009g0110others(59): Show | 73 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(70): 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 | a0002c0003t0003g0255a0002c0003t0003g0259a0002c0004t0004g0238others(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 | a0001c0001t0001g0041 | 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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | 71 | a0001c0001t0001g0123a0001c0014t0009g0109a0001c0014t0009g0110others(68): Show | 82 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(79): 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 | a0002c0004t0004g0265a0002c0004t0004g0266 | 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 | a0001c0001t0001g0044a0001c0001t0001g0194a0001c0002t0002g0004others(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 | a0001c0002t0002g0018a0001c0002t0002g0019a0001c0002t0002g0152others(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 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(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 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(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 | a0001c0002t0007g0192a0001c0017t0007g0144a0002c0008t0006g0270others(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 | a0002c0003t0003g0247a0002c0003t0003g0276a0002c0003t0003g0277others(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 | 57 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(54): Show | 66 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(63): 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 | 68 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(65): Show | 79 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(76): Show |
intron_variant | MODIFIER | c.241+493A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34931977 | ||||||
| chr11:34931982
|
G | A | 68 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(65): Show | 79 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(76): 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 | a0001c0001t0001g0002a0001c0001t0001g0044a0001c0001t0001g0048others(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 | a0002c0004t0004g0265a0002c0004t0004g0266 | 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 | 207 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(204): Show | 230 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(227): 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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | 201 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(198): Show | 224 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(221): Show |
intron_variant | MODIFIER | c.241+1448G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34932932 | ||||||
| chr11:34932992
|
C | A | 1 | a0008c0015t0004g0227 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.241+1508C>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34932992 | ||||||
| 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 | 68 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(65): Show | 79 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(76): 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 | a0002c0004t0005g0007a0002c0005t0005g0007a0002c0005t0005g0026others(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 | 68 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(65): Show | 79 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(76): 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 | a0002c0004t0004g0222a0002c0004t0004g0236a0002c0004t0004g0237others(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 | a0009c0028t0016g0275 | 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 | a0001c0023t0009g0199a0006c0011t0001g0198a0006c0011t0001g0200others(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 | 68 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(65): Show | 79 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(76): 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 | a0001c0001t0001g0196a0001c0001t0001g0197 | 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 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0051others(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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | 68 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(65): Show | 79 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(76): 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 | a0002c0003t0003g0258a0002c0003t0003g0259 | 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 | a0010c0019t0002g0159 | 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 | 37 | a0001c0001t0001g0197a0001c0002t0002g0021a0001c0002t0002g0137others(34): Show | 39 | HG00280.hp1 HG00621.hp1 HG00735.hp1 others(36): 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 | a0002c0003t0010g0254a0002c0004t0004g0224a0002c0004t0005g0007others(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 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(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 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0001c0001t0001g0055a0001c0001t0001g0082a0001c0001t0001g0083others(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 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | 68 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(65): Show | 79 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(76): 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 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0248others(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 | 84 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0107others(81): Show | 95 | HG00280.hp1 HG00423.hp1 HG00673.hp1 others(92): 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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | 84 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0107others(81): Show | 95 | HG00280.hp1 HG00423.hp1 HG00673.hp1 others(92): 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 | 68 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(65): Show | 79 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(76): 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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | 68 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(65): Show | 79 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(76): 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 | a0001c0013t0002g0213a0003c0006t0001g0202a0003c0006t0001g0203others(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 | a0001c0002t0002g0006a0001c0002t0002g0021a0001c0002t0002g0146others(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 | 26 | a0002c0004t0004g0222a0002c0004t0004g0224a0002c0004t0004g0232others(23): Show | 29 | HG01361.hp1 HG01496.hp2 HG02145.hp1 others(26): 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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0001c0002t0007g0187a0001c0002t0007g0188a0001c0002t0007g0189others(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 | a0002c0004t0005g0007a0002c0005t0005g0007a0002c0005t0005g0008others(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 | 68 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(65): Show | 79 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(76): Show |
intron_variant | MODIFIER | c.241+4180A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34935664 | ||||||
| chr11:34935726
|
C | T | 68 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(65): Show | 79 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(76): Show |
intron_variant | MODIFIER | c.241+4242C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34935726 | ||||||
| chr11:34935737
|
G | T | 200 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(197): Show | 223 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.241+4253G>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34935737 | ||||||
| chr11:34935804
|
T | C | 68 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(65): Show | 79 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(76): 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 | a0002c0004t0004g0265a0002c0004t0004g0266a0002c0012t0003g0264 | 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 | a0001c0013t0002g0213a0003c0006t0001g0202a0003c0006t0001g0203others(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 | a0001c0013t0002g0213a0003c0006t0001g0202a0003c0006t0001g0203others(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 | a0002c0003t0003g0276a0002c0003t0003g0277 | 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 | a0001c0001t0001g0086a0001c0001t0001g0111 | 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 | a0001c0001t0001g0057 | 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 | 68 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(65): Show | 79 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(76): Show |
intron_variant | MODIFIER | c.241+4785A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34936269 | ||||||
| chr11:34936275
|
A | C | 68 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(65): Show | 79 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(76): Show |
intron_variant | MODIFIER | c.241+4791A>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34936275 | ||||||
| chr11:34936286
|
T | A | 68 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(65): Show | 79 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(76): Show |
intron_variant | MODIFIER | c.241+4802T>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34936286 | ||||||
| chr11:34936291
|
G | A | 68 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(65): Show | 79 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(76): Show |
intron_variant | MODIFIER | c.241+4807G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34936291 | ||||||
| chr11:34936363
|
C | G | 68 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(65): Show | 79 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(76): 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 | 68 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(65): Show | 79 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(76): 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 | a0002c0004t0005g0007a0002c0005t0005g0007a0002c0005t0005g0008others(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 | 201 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(198): Show | 224 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(221): 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 | a0001c0013t0002g0213a0003c0006t0001g0202a0003c0006t0001g0203others(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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(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 | a0001c0013t0002g0213a0001c0023t0009g0199a0002c0012t0003g0242others(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 | a0001c0002t0002g0134a0001c0002t0002g0151a0001c0002t0002g0181others(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 | 17 | a0002c0003t0003g0261a0002c0004t0004g0222a0002c0004t0004g0232others(14): Show | 18 | HG01361.hp1 HG01496.hp2 HG02015.hp2 others(15): 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 | a0001c0001t0001g0047a0001c0001t0001g0057a0001c0001t0001g0080others(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 | a0002c0004t0004g0224a0002c0004t0004g0236a0002c0004t0004g0237others(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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(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 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(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 | a0001c0013t0002g0213a0003c0006t0001g0202a0003c0006t0001g0203others(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 | a0001c0013t0002g0213a0003c0006t0001g0202a0003c0006t0001g0203others(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 | 196 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(193): Show | 219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): 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 | a0001c0013t0002g0213a0003c0006t0001g0202a0003c0006t0001g0203others(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 | 201 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(198): Show | 224 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(221): 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 | a0002c0004t0005g0007a0002c0005t0005g0007a0002c0005t0005g0008others(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 | a0001c0001t0001g0014a0001c0001t0001g0057a0001c0001t0001g0075others(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 | a0003c0006t0001g0202a0003c0006t0001g0203a0003c0006t0001g0204others(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 | 185 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(182): Show | 206 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(203): 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 | a0001c0001t0001g0034a0001c0001t0001g0074a0002c0008t0006g0001others(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 | 67 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(64): Show | 78 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.241+6027A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34937511 | ||||||
| chr11:34937687
|
T | C | 9 | a0002c0007t0004g0022a0002c0007t0004g0223a0002c0007t0004g0226others(6): Show | 10 | HG01361.hp1 HG02602.hp2 HG02738.hp2 others(7): 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 | a0001c0002t0007g0187a0001c0002t0007g0188a0001c0002t0007g0189others(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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0002c0004t0005g0007a0002c0005t0005g0007a0002c0005t0005g0026others(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 | a0001c0001t0001g0104 | 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 | a0001c0001t0001g0055a0001c0001t0001g0082a0001c0001t0001g0083others(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 | 65 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(62): Show | 76 | HG00673.hp2 HG01106.hp1 HG01168.hp2 others(73): Show |
intron_variant | MODIFIER | c.241+7144T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34938628 | ||||||
| chr11:34938798
|
T | C | 13 | a0002c0004t0004g0232a0002c0004t0004g0233a0002c0004t0004g0234others(10): Show | 14 | HG01361.hp1 HG01496.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.241+7314T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34938798 | ||||||
| chr11:34938872
|
T | C | 65 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(62): Show | 76 | HG00673.hp2 HG01106.hp1 HG01168.hp2 others(73): 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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | 65 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(62): Show | 76 | HG00673.hp2 HG01106.hp1 HG01168.hp2 others(73): Show |
intron_variant | MODIFIER | c.241+7694G>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34939178 | ||||||
| chr11:34939361
|
G | A | 197 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(194): Show | 220 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(217): 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 | a0001c0001t0001g0046a0001c0001t0001g0100a0001c0001t0001g0111others(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 | 160 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(157): Show | 181 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(178): 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 | a0001c0001t0001g0047a0001c0002t0002g0161a0001c0021t0002g0166others(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 | a0001c0002t0007g0192a0002c0003t0003g0276a0002c0003t0003g0277others(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 | a0001c0002t0007g0187a0001c0002t0007g0188a0001c0002t0007g0189others(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 | a0001c0001t0001g0125a0002c0004t0004g0222 | 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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0001c0023t0009g0199a0006c0011t0001g0198a0006c0011t0001g0200 | 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 | 65 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(62): Show | 76 | HG00673.hp2 HG01106.hp1 HG01168.hp2 others(73): 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 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(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 | a0001c0002t0007g0187a0001c0002t0007g0188a0001c0002t0007g0189others(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 | 65 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(62): Show | 76 | HG00673.hp2 HG01106.hp1 HG01168.hp2 others(73): Show |
intron_variant | MODIFIER | c.242-7895A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34939611 | ||||||
| chr11:34939614
|
A | G | 65 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(62): Show | 76 | HG00673.hp2 HG01106.hp1 HG01168.hp2 others(73): Show |
intron_variant | MODIFIER | c.242-7892A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34939614 | ||||||
| chr11:34939863
|
T | C | 65 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(62): Show | 76 | HG00673.hp2 HG01106.hp1 HG01168.hp2 others(73): Show |
intron_variant | MODIFIER | c.242-7643T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34939863 | ||||||
| chr11:34940064
|
C | A | 65 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(62): Show | 76 | HG00673.hp2 HG01106.hp1 HG01168.hp2 others(73): 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 | a0001c0002t0002g0180a0001c0002t0002g0181 | 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 | 198 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(195): Show | 221 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(218): 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 | a0001c0001t0001g0013a0001c0001t0001g0081 | 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 | a0001c0001t0001g0099 | 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 | a0001c0001t0001g0050 | 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 | 26 | a0002c0004t0004g0222a0002c0004t0004g0224a0002c0004t0004g0232others(23): Show | 29 | HG01361.hp1 HG01496.hp2 HG02145.hp1 others(26): Show |
intron_variant | MODIFIER | c.242-6933A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34940573 | ||||||
| chr11:34940607
|
A | G | 65 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(62): Show | 76 | HG00673.hp2 HG01106.hp1 HG01168.hp2 others(73): 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 | a0001c0013t0002g0213a0003c0006t0001g0202a0003c0006t0001g0203others(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 | 65 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(62): Show | 76 | HG00673.hp2 HG01106.hp1 HG01168.hp2 others(73): 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 | a0001c0013t0002g0213a0003c0006t0001g0202a0003c0006t0001g0203others(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 | a0001c0023t0009g0199a0006c0011t0001g0198a0006c0011t0001g0200others(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 | 204 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(201): Show | 227 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(224): 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 | a0001c0001t0001g0016a0001c0001t0001g0029 | 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 | a0002c0008t0006g0273a0002c0008t0006g0274 | 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 | a0001c0013t0002g0213a0003c0006t0001g0202a0003c0006t0001g0203others(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 | a0001c0001t0001g0086 | 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 | 204 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(201): Show | 227 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.242-6125T>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34941381 | ||||||
| chr11:34941499
|
A | G | 198 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(195): Show | 221 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.242-6007A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34941499 | ||||||
| chr11:34941555
|
A | G | 65 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(62): Show | 76 | HG00673.hp2 HG01106.hp1 HG01168.hp2 others(73): 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 | a0001c0001t0001g0194a0001c0001t0001g0195 | 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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(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 | 198 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(195): Show | 221 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.242-5637T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34941869 | ||||||
| chr11:34941912
|
T | C | 65 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(62): Show | 76 | HG00673.hp2 HG01106.hp1 HG01168.hp2 others(73): 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 | a0001c0001t0001g0011a0001c0001t0001g0030a0001c0001t0001g0031others(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 | a0001c0001t0001g0078a0001c0001t0001g0079 | 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 | a0002c0004t0005g0007a0002c0005t0005g0007a0002c0005t0005g0008others(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 | 197 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(194): Show | 220 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(217): 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 | a0001c0013t0002g0213a0003c0006t0001g0202a0003c0006t0001g0203others(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 | a0001c0001t0001g0075a0001c0002t0002g0154a0002c0003t0003g0257others(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 | 197 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(194): Show | 220 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(217): 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 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(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 | a0001c0013t0002g0213a0003c0006t0001g0202a0003c0006t0001g0203others(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 | 65 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(62): Show | 76 | HG00673.hp2 HG01106.hp1 HG01168.hp2 others(73): Show |
intron_variant | MODIFIER | c.242-4728G>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34942778 | ||||||
| chr11:34942797
|
T | C | 204 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(201): Show | 227 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(224): 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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0001c0013t0002g0213a0003c0006t0001g0202a0003c0006t0001g0203others(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 | 204 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(201): Show | 227 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(224): 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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(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 | a0002c0003t0003g0024a0002c0003t0003g0250 | 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 | a0001c0001t0001g0046a0001c0001t0001g0047 | 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 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(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 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0001c0001t0001g0058 | 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 | 18 | a0002c0004t0004g0222a0002c0004t0004g0224a0002c0004t0004g0232others(15): Show | 19 | HG01361.hp1 HG01496.hp2 HG02280.hp1 others(16): 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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0001c0023t0009g0199a0006c0011t0001g0198a0006c0011t0001g0200others(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 | a0003c0006t0001g0202a0003c0006t0001g0203a0003c0006t0001g0204others(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 | 65 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(62): Show | 76 | HG00673.hp2 HG01106.hp1 HG01168.hp2 others(73): 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 | 197 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(194): Show | 220 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(217): 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 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(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 | a0003c0006t0001g0202a0003c0006t0001g0203a0003c0006t0001g0204others(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 | a0001c0001t0001g0046a0001c0001t0001g0047 | 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 | a0011c0025t0001g0215 | 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 | a0001c0001t0001g0040 | 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 | a0003c0006t0001g0202a0003c0006t0001g0203a0003c0006t0001g0204others(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 | 183 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(180): Show | 206 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(203): Show |
intron_variant | MODIFIER | c.242-1764G>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34945742 | ||||||
| chr11:34945781
|
A | G | 82 | a0001c0023t0009g0199a0002c0003t0003g0023a0002c0003t0003g0024others(79): Show | 93 | HG00280.hp1 HG00673.hp2 HG01106.hp1 others(90): 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 | a0001c0001t0001g0013a0001c0001t0001g0081 | 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 | a0001c0001t0001g0073 | 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 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(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 | a0001c0001t0001g0035a0001c0001t0001g0036a0002c0003t0003g0277others(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 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0002t0002g0160others(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 | 169 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(166): Show | 187 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.242-726C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 2/10 | chr11 | 34946780 | ||||||
| chr11:34946976
|
A | G | 172 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(169): Show | 192 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(189): 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 | a0002c0008t0006g0001a0002c0008t0006g0272 | 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 | a0002c0003t0003g0278a0002c0003t0003g0279 | 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 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0106 | 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 | a0001c0002t0002g0006a0001c0002t0002g0021a0001c0002t0002g0146others(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 | a0001c0001t0001g0104 | 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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0009c0028t0016g0275 | 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 | 205 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(202): Show | 228 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.342+473A>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34948079 | ||||||
| chr11:34948093
|
T | A | 205 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(202): Show | 228 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.342+487T>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34948093 | ||||||
| chr11:34948175
|
A | G | 11 | a0001c0014t0009g0109a0001c0014t0009g0110a0002c0007t0004g0022others(8): Show | 12 | HG01192.hp2 HG01361.hp1 HG01943.hp2 others(9): 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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | 43 | a0001c0001t0001g0089a0001c0001t0001g0106a0001c0001t0001g0194others(40): Show | 49 | HG00558.hp2 HG01168.hp1 HG01192.hp2 others(46): 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 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(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 | a0001c0001t0001g0033 | 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 | a0009c0028t0016g0275 | 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 | a0002c0008t0006g0001a0002c0008t0006g0270a0002c0008t0006g0271others(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 | a0002c0004t0004g0232a0002c0004t0004g0233a0002c0004t0004g0234others(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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | 26 | a0001c0014t0009g0109a0001c0014t0009g0110a0001c0017t0007g0144others(23): Show | 27 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(24): Show |
intron_variant | MODIFIER | c.342+1650G>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34949256 | ||||||
| chr11:34949270
|
T | C | 172 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(169): Show | 192 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(189): 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 |
36 | a0001c0014t0009g0109a0001c0014t0009g0110a0001c0017t0007g0144others(33): Show | 42 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(39): 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 | 172 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(169): Show | 192 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(189): 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 | a0002c0008t0006g0001a0002c0008t0006g0270a0002c0008t0006g0271others(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 | 36 | a0001c0014t0009g0109a0001c0014t0009g0110a0001c0017t0007g0144others(33): Show | 42 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(39): 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 | a0001c0023t0009g0199a0002c0004t0004g0236a0002c0004t0004g0237others(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 | a0001c0026t0013g0054a0002c0004t0005g0007a0002c0005t0005g0007others(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 | a0001c0001t0001g0122 | 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 | a0001c0001t0001g0058a0001c0001t0001g0099 | 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 | a0001c0002t0002g0145a0001c0002t0002g0148 | 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 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0221others(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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0001c0001t0001g0053 | 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 | a0001c0001t0001g0072 | 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 | a0002c0008t0006g0001a0002c0008t0006g0270a0002c0008t0006g0271others(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 | a0001c0001t0001g0071a0001c0001t0001g0098a0001c0001t0001g0126others(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 | 172 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(169): Show | 192 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(189): 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 | a0001c0001t0001g0090 | 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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | 26 | a0001c0014t0009g0109a0001c0014t0009g0110a0001c0017t0007g0144others(23): Show | 27 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(24): 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 | 166 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(163): Show | 184 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(181): 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 | a0001c0002t0002g0017a0001c0002t0002g0130a0001c0002t0002g0131others(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 | a0001c0001t0001g0045a0001c0001t0001g0056a0001c0001t0001g0069others(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 | a0001c0001t0001g0014a0001c0001t0001g0032a0001c0001t0001g0040others(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 | 33 | a0001c0014t0009g0109a0001c0014t0009g0110a0001c0017t0007g0144others(30): Show | 39 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(36): 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 | a0002c0003t0003g0258a0002c0003t0003g0259 | 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 | 205 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(202): Show | 228 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(225): 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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | 36 | a0001c0014t0009g0109a0001c0014t0009g0110a0001c0017t0007g0144others(33): Show | 42 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(39): 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 | a0002c0012t0003g0242a0002c0012t0003g0243 | 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 | a0002c0008t0006g0001a0002c0008t0006g0270a0002c0008t0006g0271others(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 | 36 | a0001c0014t0009g0109a0001c0014t0009g0110a0001c0017t0007g0144others(33): Show | 42 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(39): Show |
intron_variant | MODIFIER | c.342+3644G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34951250 | ||||||
| chr11:34951295
|
A | G | 172 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(169): Show | 192 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(189): 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 | a0001c0002t0007g0187a0001c0002t0007g0188a0001c0002t0007g0189others(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 | a0001c0026t0013g0054a0002c0004t0005g0007a0002c0005t0005g0007others(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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0001c0002t0002g0130a0001c0002t0002g0131 | 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 | a0002c0004t0004g0232a0002c0004t0004g0235 | 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 | a0001c0001t0001g0059 | 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 | a0001c0002t0002g0018a0001c0002t0002g0019a0001c0002t0002g0152others(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 | 166 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(163): Show | 184 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.342+4326T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34951932 | ||||||
| chr11:34951999
|
A | G | 205 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(202): Show | 228 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(225): 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 | a0009c0028t0016g0275 | 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 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(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 | a0009c0028t0016g0275 | 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 | 36 | a0001c0014t0009g0109a0001c0014t0009g0110a0001c0017t0007g0144others(33): Show | 42 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(39): 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 | a0001c0026t0013g0054 | 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 | 36 | a0001c0014t0009g0109a0001c0014t0009g0110a0001c0017t0007g0144others(33): Show | 42 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(39): 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 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(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 | a0001c0002t0002g0130a0001c0002t0002g0131 | 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 | a0001c0002t0007g0187a0001c0002t0007g0188a0001c0002t0007g0189others(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 | a0006c0011t0001g0198a0006c0011t0001g0200a0006c0011t0001g0201 | 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 | 172 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(169): Show | 192 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(189): 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 | a0001c0001t0001g0045a0001c0001t0008g0113a0001c0002t0002g0174 | 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 | a0001c0026t0013g0054a0002c0004t0005g0007a0002c0005t0005g0007others(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 | 205 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(202): Show | 228 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(225): 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 | a0001c0001t0001g0035a0001c0001t0001g0036 | 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 | a0001c0026t0013g0054a0002c0004t0005g0007a0002c0005t0005g0007others(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 | a0002c0008t0006g0001a0002c0008t0006g0270a0002c0008t0006g0271others(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 | a0001c0001t0001g0075 | 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 | a0001c0001t0001g0097 | 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 | 36 | a0001c0014t0009g0109a0001c0014t0009g0110a0001c0017t0007g0144others(33): Show | 42 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(39): Show |
intron_variant | MODIFIER | c.343-4609G>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34952775 | ||||||
| chr11:34952860
|
T | A | 205 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(202): Show | 228 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(225): 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 | a0001c0001t0001g0047 | 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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | 172 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(169): Show | 192 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(189): 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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0002c0008t0006g0001a0002c0008t0006g0270a0002c0008t0006g0271others(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 | a0001c0001t0001g0011a0001c0001t0001g0030a0001c0001t0001g0031 | 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 | 162 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(159): Show | 177 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(174): 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 | a0001c0001t0001g0040a0001c0001t0001g0041 | 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 | a0001c0002t0002g0158a0005c0009t0002g0177a0005c0009t0002g0178others(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 | a0001c0002t0007g0187a0001c0002t0007g0188a0001c0002t0007g0189others(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 | 36 | a0001c0014t0009g0109a0001c0014t0009g0110a0001c0017t0007g0144others(33): Show | 42 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(39): Show |
intron_variant | MODIFIER | c.343-2614delC | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34954769 | ||||||
| chr11:34954823
|
A | T | 12 | a0003c0006t0001g0202a0003c0006t0001g0203a0003c0006t0001g0204others(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 | a0009c0028t0016g0275 | 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 | 11 | a0001c0014t0009g0109a0001c0014t0009g0110a0002c0007t0004g0022others(8): Show | 12 | HG01192.hp2 HG01361.hp1 HG01943.hp2 others(9): 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 | a0001c0001t0001g0059a0001c0001t0001g0122a0001c0001t0001g0125 | 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 | a0009c0028t0016g0275 | 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 | a0009c0028t0016g0275 | 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 | 36 | a0001c0014t0009g0109a0001c0014t0009g0110a0001c0017t0007g0144others(33): Show | 42 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(39): 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 | a0010c0019t0002g0159 | 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 | a0002c0008t0006g0001a0002c0008t0006g0270a0002c0008t0006g0271others(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 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0001c0002t0002g0162a0001c0002t0002g0163a0001c0002t0002g0169 | 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 | a0003c0006t0001g0202a0003c0006t0001g0205 | 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 | a0001c0002t0002g0017a0001c0002t0002g0130a0001c0002t0002g0131 | 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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0001c0002t0007g0187a0001c0002t0007g0188a0001c0002t0007g0189others(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 | 36 | a0001c0014t0009g0109a0001c0014t0009g0110a0001c0017t0007g0144others(33): Show | 42 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(39): Show |
intron_variant | MODIFIER | c.343-938A>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34956446 | ||||||
| chr11:34956458
|
G | T | 36 | a0001c0014t0009g0109a0001c0014t0009g0110a0001c0017t0007g0144others(33): Show | 42 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(39): Show |
intron_variant | MODIFIER | c.343-926G>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34956458 | ||||||
| chr11:34956549
|
T | C | 172 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(169): Show | 192 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.343-835T>C | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 3/10 | chr11 | 34956549 | ||||||
| chr11:34956654
|
C | G | 17 | a0001c0014t0009g0109a0001c0014t0009g0110a0002c0004t0004g0232others(14): Show | 18 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(15): 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 | a0001c0026t0013g0054a0002c0004t0005g0007a0002c0005t0005g0007others(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 | 156 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(153): Show | 169 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(166): 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 | a0009c0028t0016g0275 | 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 | 36 | a0001c0014t0009g0109a0001c0014t0009g0110a0001c0017t0007g0144others(33): Show | 42 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(39): 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 | a0001c0026t0013g0054a0002c0004t0005g0007a0002c0005t0005g0007others(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 | a0006c0011t0001g0198a0006c0011t0001g0200a0006c0011t0001g0201 | 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 | a0001c0002t0007g0187a0001c0002t0007g0188a0001c0002t0007g0189others(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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0001c0001t0001g0088 | 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 | 25 | a0001c0014t0009g0109a0001c0014t0009g0110a0001c0023t0009g0199others(22): Show | 26 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(23): 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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | 170 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(167): Show | 190 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(187): 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 | 166 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(163): Show | 184 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(181): 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 | a0001c0001t0001g0097a0007c0016t0001g0095a0009c0028t0016g0275 | 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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | 36 | a0001c0014t0009g0109a0001c0014t0009g0110a0001c0017t0007g0144others(33): Show | 42 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(39): 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 | a0009c0028t0016g0275 | 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 | a0001c0014t0009g0110 | 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 | 36 | a0001c0014t0009g0109a0001c0014t0009g0110a0001c0017t0007g0144others(33): Show | 42 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(39): Show |
intron_variant | MODIFIER | c.542+720G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 4/10 | chr11 | 34958303 | ||||||
| chr11:34958305
|
C | T | 26 | a0001c0014t0009g0109a0001c0014t0009g0110a0001c0017t0007g0144others(23): Show | 27 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(24): Show |
intron_variant | MODIFIER | c.542+722C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 4/10 | chr11 | 34958305 | ||||||
| chr11:34958341
|
T | C | 172 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(169): Show | 192 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(189): 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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0001c0026t0013g0054a0002c0004t0005g0007a0002c0005t0005g0007others(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 | 205 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(202): Show | 228 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(225): 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 | 36 | a0001c0014t0009g0109a0001c0014t0009g0110a0001c0017t0007g0144others(33): Show | 42 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(39): 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 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(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 | a0002c0003t0003g0276a0002c0003t0003g0277 | 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 | a0009c0028t0016g0275 | 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 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0002c0012t0003g0242a0002c0012t0003g0243 | 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 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0068 | 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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0001c0002t0007g0187a0001c0002t0007g0188a0001c0002t0007g0189others(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 | a0001c0001t0001g0089 | 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 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0034others(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 | 36 | a0001c0014t0009g0109a0001c0014t0009g0110a0001c0017t0007g0144others(33): Show | 42 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(39): 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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0002c0008t0006g0001a0002c0008t0006g0270a0002c0008t0006g0271others(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 | a0006c0011t0001g0198a0006c0011t0001g0200a0006c0011t0001g0201 | 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 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(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 | a0001c0001t0001g0117a0001c0001t0001g0119 | 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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0001c0026t0013g0054a0002c0004t0005g0007a0002c0005t0005g0007others(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 | a0001c0002t0007g0187a0001c0002t0007g0188a0001c0002t0007g0189others(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 | 36 | a0001c0014t0009g0109a0001c0014t0009g0110a0001c0017t0007g0144others(33): Show | 42 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(39): 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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0009c0028t0016g0275 | 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 | a0002c0008t0006g0001a0002c0008t0006g0270a0002c0008t0006g0271others(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 | a0002c0008t0006g0001a0002c0008t0006g0270a0002c0008t0006g0271others(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 | a0002c0008t0006g0001a0002c0008t0006g0270a0002c0008t0006g0271others(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 | a0001c0026t0013g0054a0002c0004t0005g0007a0002c0005t0005g0007others(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 | a0006c0011t0001g0198a0006c0011t0001g0200a0006c0011t0001g0201 | 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 | a0009c0028t0016g0275 | 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 | a0001c0002t0007g0187a0001c0002t0007g0188a0001c0002t0007g0189others(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 | 205 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(202): Show | 228 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.641+2507G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | chr11 | 34963025 | ||||||
| chr11:34963028
|
T | C | 36 | a0001c0014t0009g0109a0001c0014t0009g0110a0001c0017t0007g0144others(33): Show | 42 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(39): 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 | a0009c0028t0016g0275 | 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 | a0001c0002t0002g0149a0001c0002t0002g0150a0001c0002t0002g0151 | 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 | 36 | a0001c0014t0009g0109a0001c0014t0009g0110a0001c0017t0007g0144others(33): Show | 42 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(39): Show |
intron_variant | MODIFIER | c.641+3042G>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | chr11 | 34963560 | ||||||
| chr11:34963780
|
G | C | 36 | a0001c0014t0009g0109a0001c0014t0009g0110a0001c0017t0007g0144others(33): Show | 42 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(39): 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 | 166 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(163): Show | 184 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.642-2741C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 5/10 | chr11 | 34963899 | ||||||
| chr11:34963901
|
A | G | 17 | a0001c0014t0009g0109a0001c0014t0009g0110a0002c0004t0004g0232others(14): Show | 18 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(15): 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 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0068others(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 | a0001c0023t0009g0199a0002c0004t0004g0222a0002c0004t0004g0236others(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 | a0001c0023t0009g0199a0002c0004t0004g0222a0002c0004t0004g0224others(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 | a0001c0001t0001g0039 | 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 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0040others(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 | a0002c0008t0006g0001a0002c0008t0006g0270a0002c0008t0006g0271others(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 |
26 | a0001c0002t0002g0005a0001c0014t0009g0109a0001c0014t0009g0110others(23): Show | 29 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(26): 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 | a0001c0017t0007g0144a0001c0026t0013g0054a0002c0004t0005g0007others(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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0001c0002t0007g0187a0001c0002t0007g0188a0001c0002t0007g0189others(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 | a0001c0001t0001g0121 | 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 | a0001c0001t0001g0010 | 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 | a0002c0008t0006g0001a0002c0008t0006g0270a0002c0008t0006g0271others(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 | 178 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(175): Show | 198 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(195): 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 | a0001c0001t0001g0094 | 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 | a0002c0007t0004g0223a0002c0007t0004g0231 | 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 | a0001c0001t0001g0100 | 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 | a0002c0004t0004g0232a0002c0004t0004g0233a0002c0004t0004g0234others(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 | a0002c0008t0006g0001a0002c0008t0006g0270a0002c0008t0006g0271others(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 | a0002c0008t0006g0001a0002c0008t0006g0270a0002c0008t0006g0271others(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 | a0001c0001t0001g0003a0001c0001t0001g0060a0001c0001t0001g0074 | 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 | 206 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(203): Show | 229 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(226): 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 | a0001c0001t0001g0038a0001c0001t0001g0039 | 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 | a0002c0004t0004g0232a0002c0004t0004g0233a0002c0004t0004g0234others(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 | a0001c0001t0001g0107 | 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 | a0001c0002t0002g0132a0001c0002t0002g0133a0001c0002t0002g0134others(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 | 26 | a0001c0014t0009g0109a0001c0014t0009g0110a0001c0017t0007g0144others(23): Show | 27 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(24): 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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0002c0012t0003g0242a0002c0012t0003g0243a0002c0012t0003g0264 | 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 | a0001c0001t0001g0061 | 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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | 36 | a0001c0014t0009g0109a0001c0014t0009g0110a0001c0017t0007g0144others(33): Show | 42 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(39): 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 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(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 | 172 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(169): Show | 192 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(189): 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 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(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 | a0001c0001t0001g0086 | 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 | a0001c0001t0001g0046 | 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 | a0001c0002t0007g0187a0001c0002t0007g0188a0001c0002t0007g0189others(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 | 166 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(163): Show | 184 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(181): 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 | a0001c0002t0007g0187a0001c0002t0007g0188a0001c0002t0007g0189others(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 | a0001c0001t0001g0127a0001c0001t0001g0221 | 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 | a0001c0023t0009g0199a0002c0004t0004g0222a0002c0004t0004g0224others(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 | a0001c0026t0013g0054a0002c0004t0005g0007a0002c0005t0005g0007others(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 | 36 | a0001c0014t0009g0109a0001c0014t0009g0110a0001c0017t0007g0144others(33): Show | 42 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(39): 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 | a0001c0001t0001g0055a0001c0001t0001g0083a0001c0001t0001g0084others(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 | a0001c0001t0001g0055a0001c0001t0001g0083a0001c0001t0001g0084others(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 | a0001c0001t0001g0055a0001c0001t0001g0083a0001c0001t0001g0084others(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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0001c0001t0001g0055a0001c0001t0001g0082a0001c0001t0001g0083others(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 | 36 | a0001c0014t0009g0109a0001c0014t0009g0110a0001c0017t0007g0144others(33): Show | 42 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(39): 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 | a0001c0002t0002g0180a0001c0002t0002g0181 | 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 | a0009c0028t0016g0275 | 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 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(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 | a0001c0002t0007g0187a0001c0002t0007g0188a0001c0002t0007g0189others(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 | a0001c0002t0002g0006a0001c0002t0002g0021a0001c0002t0002g0146others(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 | a0001c0001t0008g0065 | 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 | a0001c0001t0001g0123a0001c0002t0002g0148 | 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 | a0009c0028t0016g0275 | 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 | a0001c0002t0002g0149a0001c0002t0002g0150a0001c0002t0002g0151others(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 | 166 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(163): Show | 184 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(181): 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 | a0006c0011t0001g0198a0006c0011t0001g0200a0006c0011t0001g0201 | 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 | a0002c0012t0003g0242a0002c0012t0003g0243a0002c0012t0003g0264 | 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 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0068 | 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 | 172 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(169): Show | 192 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(189): 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 | a0001c0001t0001g0032a0001c0001t0001g0124a0004c0022t0015g0143 | 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 | 205 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(202): Show | 228 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(225): 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 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(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 | a0002c0003t0003g0278a0002c0003t0003g0279 | 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 | a0002c0012t0003g0242a0002c0012t0003g0243 | 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 | a0003c0006t0001g0202a0003c0006t0001g0203a0003c0006t0001g0204others(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 | 35 | a0001c0014t0009g0109a0001c0014t0009g0110a0001c0017t0007g0144others(32): Show | 41 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(38): 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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0001c0002t0007g0187a0001c0002t0007g0189a0001c0002t0007g0190others(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 | 166 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(163): Show | 184 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(181): 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 | a0001c0002t0007g0187a0001c0002t0007g0188a0001c0002t0007g0189others(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 | a0002c0008t0006g0001a0002c0008t0006g0270a0002c0008t0006g0271others(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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(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 | a0001c0026t0013g0054a0002c0004t0005g0007a0002c0005t0005g0007others(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 | a0001c0002t0007g0187a0001c0002t0007g0188a0001c0002t0007g0189others(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 | a0001c0001t0001g0055a0001c0001t0001g0082a0001c0001t0001g0083others(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 | a0001c0001t0008g0062 | 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 | 205 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(202): Show | 228 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(225): 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 | a0001c0002t0007g0187a0001c0002t0007g0188a0001c0002t0007g0189others(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 | 172 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(169): Show | 192 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(189): 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 | a0001c0001t0001g0077 | 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 | 36 | a0001c0014t0009g0109a0001c0014t0009g0110a0001c0017t0007g0144others(33): Show | 42 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(39): 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 | a0002c0003t0003g0276a0002c0003t0003g0277a0002c0003t0003g0278others(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 | 36 | a0001c0014t0009g0109a0001c0014t0009g0110a0001c0017t0007g0144others(33): Show | 42 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(39): 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 | a0011c0025t0001g0215 | 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 | a0009c0028t0016g0275 | 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 | a0001c0026t0013g0054a0002c0004t0005g0007a0002c0005t0005g0007others(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 | 166 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(163): Show | 184 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(181): 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 | a0001c0002t0007g0187a0001c0002t0007g0188a0001c0002t0007g0189others(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 | 166 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(163): Show | 184 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(181): 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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0002c0008t0006g0001a0002c0008t0006g0270a0002c0008t0006g0271others(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 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0051others(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 | 36 | a0001c0014t0009g0109a0001c0014t0009g0110a0001c0017t0007g0144others(33): Show | 42 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(39): 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 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(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 | a0009c0028t0016g0275 | 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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | 17 | a0001c0014t0009g0109a0001c0014t0009g0110a0002c0004t0004g0232others(14): Show | 18 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(15): 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 | a0001c0001t0001g0055a0001c0001t0001g0082a0001c0001t0001g0083others(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 | 36 | a0001c0014t0009g0109a0001c0014t0009g0110a0001c0017t0007g0144others(33): Show | 42 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(39): Show |
intron_variant | MODIFIER | c.965-1657C>T | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | chr11 | 34976467 | ||||||
| chr11:34976604
|
T | C | 205 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(202): Show | 228 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(225): 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 | a0001c0026t0013g0054a0002c0004t0005g0007a0002c0005t0005g0007others(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 | a0006c0011t0001g0198a0006c0011t0001g0200a0006c0011t0001g0201 | 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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | 36 | a0001c0014t0009g0109a0001c0014t0009g0110a0001c0017t0007g0144others(33): Show | 42 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(39): Show |
intron_variant | MODIFIER | c.965-1178A>G | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 7/10 | chr11 | 34976946 | ||||||
| chr11:34977199
|
G | A | 166 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(163): Show | 184 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(181): 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 | a0001c0001t0001g0093a0001c0001t0001g0098 | 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 | a0002c0003t0003g0278a0002c0003t0003g0279 | 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 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(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 | a0001c0001t0001g0015 | 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 | 205 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(202): Show | 228 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(225): 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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0001c0023t0009g0199a0002c0004t0004g0222a0002c0004t0004g0236others(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 | 26 | a0001c0014t0009g0109a0001c0014t0009g0110a0001c0017t0007g0144others(23): Show | 27 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(24): 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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0001c0002t0002g0018a0001c0002t0002g0019a0001c0002t0002g0152others(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 | a0001c0026t0013g0054a0002c0004t0005g0007a0002c0005t0005g0007others(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 | a0002c0003t0003g0276a0002c0003t0003g0277 | 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 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0001c0001t0001g0076 | 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 | a0002c0008t0006g0001a0002c0008t0006g0270a0002c0008t0006g0271others(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 | a0001c0001t0001g0080 | 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 | 6 | a0002c0007t0004g0022a0002c0007t0004g0228a0002c0007t0004g0229others(3): Show | 7 | HG01361.hp1 HG02602.hp2 HG02738.hp2 others(4): 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 | a0001c0002t0002g0132a0001c0002t0002g0134 | 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 | a0001c0026t0013g0054a0002c0004t0005g0007a0002c0005t0005g0007others(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 | a0001c0001t0001g0032a0001c0001t0001g0124a0004c0022t0015g0143 | 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 | a0001c0001t0001g0123 | 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 | a0001c0026t0013g0054a0002c0004t0005g0007a0002c0005t0005g0007others(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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0001c0001t0001g0055a0001c0001t0001g0083a0001c0001t0001g0084others(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 | a0001c0026t0013g0054a0002c0004t0005g0007a0002c0005t0005g0007others(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 | a0002c0004t0004g0224a0002c0004t0004g0232a0002c0004t0004g0234others(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 |
22 | a0001c0014t0009g0109a0001c0014t0009g0110a0001c0017t0007g0144others(19): Show | 23 | HG01169.hp2 HG01192.hp2 HG01361.hp1 others(20): 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 | a0001c0001t0001g0082a0002c0003t0003g0023a0002c0003t0003g0024others(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 | a0001c0001t0001g0036 | 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 | a0001c0001t0001g0083a0001c0001t0001g0085a0001c0002t0007g0187others(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 | a0001c0001t0001g0030a0001c0001t0001g0035a0001c0001t0001g0055others(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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(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 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0033others(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 | a0006c0011t0001g0198a0006c0011t0001g0200a0006c0011t0001g0201 | 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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0001c0026t0013g0054a0002c0004t0005g0007a0002c0005t0005g0007others(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 | a0002c0008t0006g0273a0002c0008t0006g0274 | 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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0001c0001t0001g0090 | 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 | a0001c0001t0001g0123 | 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 | a0001c0002t0007g0187a0001c0002t0007g0188a0001c0002t0007g0189others(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 | a0001c0026t0013g0054a0002c0004t0005g0007a0002c0005t0005g0007others(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 | a0001c0002t0007g0187a0001c0002t0007g0188a0001c0002t0007g0189others(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 | a0001c0026t0013g0054a0002c0004t0005g0007a0002c0005t0005g0007others(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 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(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 | 26 | a0001c0014t0009g0109a0001c0014t0009g0110a0001c0017t0007g0144others(23): Show | 27 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(24): 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 | a0001c0001t0001g0042 | 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 | a0002c0008t0006g0001a0002c0008t0006g0270a0002c0008t0006g0271others(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 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0051others(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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0001c0001t0001g0091 | 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 | a0001c0026t0013g0054a0002c0004t0005g0007a0002c0005t0005g0007others(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 | a0002c0012t0003g0242a0002c0012t0003g0243 | 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 | a0001c0001t0001g0014a0001c0001t0001g0076 | 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 | a0001c0002t0002g0017a0001c0002t0002g0130a0001c0002t0002g0131others(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 | a0009c0028t0016g0275 | 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 | 25 | a0001c0014t0009g0109a0001c0014t0009g0110a0001c0023t0009g0199others(22): Show | 26 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(23): Show |
intron_variant | MODIFIER | c.1024-1858G>A | PDHX | ENSG00000110435.13 | transcript | ENST00000227868.9 | protein_coding | 8/10 | chr11 | 34982712 | ||||||
| chr11:34982729
|
C | G | 25 | a0001c0014t0009g0109a0001c0014t0009g0110a0001c0023t0009g0199others(22): Show | 26 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(23): 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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0001c0026t0013g0054a0002c0004t0005g0007a0002c0005t0005g0007others(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 | a0001c0026t0013g0054a0002c0004t0005g0007a0002c0005t0005g0007others(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 | a0001c0026t0013g0054a0002c0004t0005g0007a0002c0005t0005g0007others(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 | 11 | a0001c0014t0009g0109a0001c0014t0009g0110a0002c0007t0004g0022others(8): Show | 12 | HG01192.hp2 HG01361.hp1 HG01943.hp2 others(9): 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 | a0002c0008t0006g0001a0002c0008t0006g0270a0002c0008t0006g0271others(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 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(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 | a0001c0026t0013g0054a0002c0004t0005g0007a0002c0005t0005g0007others(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 | 244 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(241): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): 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 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0051others(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 | a0001c0026t0013g0054a0002c0004t0005g0007a0002c0005t0005g0007others(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 | a0001c0026t0013g0054a0002c0004t0005g0007a0002c0005t0005g0007others(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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0001c0026t0013g0054a0002c0004t0005g0007a0002c0005t0005g0007others(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 | a0002c0012t0003g0242a0002c0012t0003g0243 | 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 | a0001c0002t0002g0018a0001c0002t0002g0019a0001c0002t0002g0152others(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 | a0001c0026t0013g0054a0002c0004t0005g0007a0002c0005t0005g0007others(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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0001c0026t0013g0054a0002c0004t0005g0007a0002c0005t0005g0007others(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 | a0001c0026t0013g0054a0002c0004t0005g0007a0002c0005t0005g0007others(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 | a0001c0026t0013g0054a0002c0004t0005g0007a0002c0005t0005g0007others(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 | a0001c0026t0013g0054a0002c0004t0005g0007a0002c0005t0005g0007others(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 | a0001c0001t0001g0077 | 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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0001c0026t0013g0054a0002c0004t0005g0007a0002c0005t0005g0007others(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 | a0001c0026t0013g0054a0002c0004t0005g0007a0002c0005t0005g0007others(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 | a0003c0006t0001g0202a0003c0006t0001g0203a0003c0006t0001g0204others(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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0001c0001t0001g0058 | 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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0001c0026t0013g0054a0002c0004t0005g0007a0002c0005t0005g0007others(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 | 25 | a0001c0014t0009g0109a0001c0014t0009g0110a0001c0023t0009g0199others(22): Show | 26 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(23): 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 | a0001c0026t0013g0054a0002c0004t0005g0007a0002c0005t0005g0007others(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 | a0001c0026t0013g0054a0002c0004t0005g0007a0002c0005t0005g0007others(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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0003c0006t0001g0202a0003c0006t0001g0203a0003c0006t0001g0204others(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 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(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 | a0001c0026t0013g0054a0002c0004t0005g0007a0002c0005t0005g0007others(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 | a0010c0019t0002g0159 | 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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0001c0026t0013g0054a0002c0004t0005g0007a0002c0005t0005g0007others(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 | a0001c0023t0009g0199a0002c0004t0004g0236a0002c0004t0004g0238 | 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 | a0002c0008t0006g0001a0002c0008t0006g0270a0002c0008t0006g0271others(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 | a0001c0002t0007g0187a0001c0002t0007g0188a0001c0002t0007g0189others(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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0002c0003t0003g0279a0009c0028t0016g0275 | 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 | a0001c0023t0009g0199a0002c0004t0004g0222a0002c0004t0004g0236others(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 | a0001c0026t0013g0054a0002c0004t0005g0007a0002c0005t0005g0007others(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 | a0009c0028t0016g0275 | 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 | a0001c0026t0013g0054a0002c0004t0005g0007a0002c0005t0005g0007others(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 | a0001c0026t0013g0054a0002c0004t0005g0007a0002c0005t0005g0007others(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 | a0001c0026t0013g0054a0002c0004t0005g0007a0002c0005t0005g0007others(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 | a0001c0001t0001g0122 | 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 | a0001c0002t0007g0190a0001c0002t0007g0192a0002c0003t0003g0023others(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 | 28 | a0001c0002t0007g0187a0001c0002t0007g0189a0001c0002t0014g0191others(25): Show | 29 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(26): 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 | a0001c0002t0002g0146a0001c0002t0002g0152a0001c0002t0002g0167others(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 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0089others(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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0001c0001t0008g0064 | 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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0002c0012t0003g0242a0002c0012t0003g0243a0002c0012t0003g0264 | 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 | a0002c0012t0003g0242a0002c0012t0003g0243 | 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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0009c0028t0016g0275 | 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 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0051others(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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(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 | a0001c0026t0013g0054a0002c0004t0005g0007a0002c0005t0005g0007others(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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0001c0002t0002g0141a0004c0010t0002g0138a0004c0010t0002g0139others(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 | 30 | a0001c0014t0009g0109a0001c0014t0009g0110a0001c0023t0009g0199others(27): Show | 33 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(30): 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 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0010others(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 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0041others(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 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0029others(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 | a0001c0026t0013g0054a0002c0004t0005g0007a0002c0005t0005g0007others(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 | a0001c0002t0002g0156a0001c0002t0002g0157 | 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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0001c0001t0001g0015a0002c0008t0006g0001a0002c0008t0006g0270others(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 | 96 | a0001c0002t0002g0006a0001c0002t0002g0018a0001c0002t0002g0019others(93): Show | 105 | HG00140.hp1 HG00642.hp1 HG00673.hp2 others(102): 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 | a0001c0026t0013g0054a0002c0004t0005g0007a0002c0005t0005g0007others(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 | a0001c0001t0001g0059 | 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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0001c0001t0008g0065 | 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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0002c0008t0006g0001a0002c0008t0006g0270a0002c0008t0006g0271others(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 | a0002c0012t0003g0242a0002c0012t0003g0243 | 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 | 25 | a0001c0014t0009g0109a0001c0014t0009g0110a0001c0023t0009g0199others(22): Show | 26 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(23): 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 | a0001c0026t0013g0054a0002c0004t0005g0007a0002c0005t0005g0007others(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 | a0001c0002t0002g0018a0001c0002t0002g0019a0001c0002t0002g0152others(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 | a0001c0026t0013g0054a0002c0004t0005g0007a0002c0005t0005g0007others(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 | a0011c0025t0001g0215 | 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 | a0006c0011t0001g0200a0006c0011t0001g0201 | 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 | 25 | a0001c0014t0009g0109a0001c0014t0009g0110a0001c0023t0009g0199others(22): Show | 26 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(23): 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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0001c0026t0013g0054a0002c0004t0005g0007a0002c0005t0005g0007others(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 | a0001c0026t0013g0054a0002c0004t0005g0007a0002c0005t0005g0007others(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 | a0002c0003t0003g0276a0002c0003t0003g0277 | 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 | a0001c0001t0001g0034a0001c0001t0001g0069a0001c0001t0001g0073 | 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 | a0001c0001t0008g0065 | 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 | a0002c0012t0003g0242a0002c0012t0003g0243 | 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 | 11 | a0001c0014t0009g0109a0001c0014t0009g0110a0002c0007t0004g0022others(8): Show | 12 | HG01192.hp2 HG01361.hp1 HG01943.hp2 others(9): 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 | a0001c0002t0007g0187a0001c0002t0007g0188a0001c0002t0007g0189others(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 | a0009c0028t0016g0275 | 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 | a0001c0026t0013g0054a0002c0004t0005g0007a0002c0005t0005g0007others(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 | a0001c0002t0007g0187a0001c0002t0007g0188a0001c0002t0007g0189others(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 | a0002c0003t0003g0276a0002c0003t0003g0277 | 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 | a0002c0008t0006g0273a0002c0008t0006g0274 | 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 | a0002c0007t0004g0223a0002c0007t0004g0231 | 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 | a0008c0015t0004g0225 | 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 | a0001c0001t0001g0117a0001c0001t0001g0119 | 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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0001c0001t0001g0046a0001c0001t0001g0052a0001c0001t0001g0063others(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 | a0002c0008t0006g0001a0002c0008t0006g0270a0002c0008t0006g0271others(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 | a0001c0026t0013g0054a0002c0004t0005g0007a0002c0005t0005g0007others(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 | a0001c0026t0013g0054a0002c0004t0005g0007a0002c0005t0005g0007others(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 | a0002c0004t0004g0232a0002c0004t0004g0233a0002c0004t0004g0234others(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 | a0009c0028t0016g0275 | 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 | a0001c0001t0001g0042 | 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 | a0001c0001t0001g0040a0001c0001t0001g0041 | 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 | a0001c0002t0007g0187a0001c0002t0007g0188a0001c0002t0007g0189others(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 | a0001c0002t0007g0187a0001c0002t0007g0188a0001c0002t0007g0189others(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 | a0001c0002t0007g0187a0001c0002t0007g0188a0001c0002t0007g0189others(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 | a0001c0026t0013g0054a0002c0004t0005g0007a0002c0005t0005g0007others(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 | a0009c0028t0016g0275 | 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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0001c0026t0013g0054a0002c0004t0005g0007a0002c0005t0005g0007others(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 | a0001c0001t0001g0061 | 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 | a0001c0001t0001g0100 | 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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0001c0026t0013g0054a0002c0004t0005g0007a0002c0005t0005g0007others(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 | a0002c0008t0006g0001a0002c0008t0006g0270a0002c0008t0006g0271others(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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0001c0001t0001g0072 | 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 | 17 | a0001c0014t0009g0109a0001c0014t0009g0110a0002c0004t0004g0232others(14): Show | 18 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(15): 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 | a0002c0003t0003g0023a0002c0003t0003g0024a0002c0003t0003g0025others(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 | 17 | a0001c0014t0009g0109a0001c0014t0009g0110a0002c0004t0004g0232others(14): Show | 18 | HG01192.hp2 HG01361.hp1 HG01496.hp2 others(15): 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 | a0001c0026t0013g0054a0002c0004t0005g0007a0002c0005t0005g0007others(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 | a0001c0001t0001g0060 | 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 | a0001c0002t0002g0004a0001c0002t0002g0020a0001c0002t0002g0154others(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 | a0001c0001t0001g0079a0001c0001t0001g0221 | 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 | a0001c0001t0001g0077 | 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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0001c0001t0001g0045 | 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 | a0007c0016t0001g0095 | 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 | a0001c0002t0002g0018a0001c0002t0002g0019a0001c0002t0002g0152others(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 |