Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 5727 |
|---|---|
| ensemblid | ENSG00000185920.19 |
| hgncid | 9585 |
| symbol | PTCH1 |
| name | patched 1 |
| refseq_nuc | NM_001083603.3 |
| refseq_prot | NP_001077072.1 |
| ensembl_nuc | ENST00000437951.6 |
| ensembl_prot | ENSP00000389744.2 |
| mane_status | MANE Plus Clinical |
| chr | chr9 |
| start | 95442980 |
| end | 95516971 |
| strand | - |
| ver | v1.2 |
| region | chr9:95442980-95516971 |
| region5000 | chr9:95437980-95521971 |
| regionname0 | PTCH1_chr9_95442980_95516971 |
| regionname5000 | PTCH1_chr9_95437980_95521971 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 1446 | 131 | 36 | 28 | 45 | 6 | 15 | 37 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0002 | 0/1 | 1446 | 86 | 15 | 13 | 48 | 4 | 5 | 35 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0003 | 0/0 | 1446 | 25 | 8 | 0 | 15 | 0 | 2 | 10 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0004 | 0/0 | 1446 | 15 | 14 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0005 | 0/0 | 1446 | 6 | 0 | 0 | 5 | 0 | 1 | 3 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0006 | 0/0 | 1446 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0007 | 0/0 | 1446 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0008 | 0/0 | 1446 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0009 | 0/0 | 1446 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0010 | 0/0 | 1446 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0011 | 0/0 | 1446 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0012 | 0/0 | 1446 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0013 | 0/0 | 1446 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0014 | 0/0 | 1446 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0015 | 0/0 | 1446 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0016 | 0/0 | 1446 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 4341 | 76 | 12 | 13 | 43 | 3 | 4 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| c0002 | 1/0 | 4341 | 49 | 12 | 18 | 9 | 2 | 7 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| c0003 | 0/0 | 4341 | 44 | 18 | 5 | 17 | 2 | 2 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| c0004 | 0/0 | 4341 | 22 | 1 | 2 | 15 | 1 | 3 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| c0005 | 0/0 | 4341 | 19 | 8 | 0 | 9 | 0 | 2 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| c0006 | 0/0 | 4341 | 14 | 13 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| c0007 | 0/0 | 4341 | 5 | 0 | 0 | 4 | 0 | 1 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| c0008 | 0/0 | 4341 | 4 | 0 | 0 | 3 | 0 | 1 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| c0009 | 0/0 | 4341 | 4 | 1 | 2 | 0 | 0 | 1 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| c0010 | 0/0 | 4341 | 4 | 4 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| c0011 | 0/0 | 4341 | 3 | 0 | 0 | 3 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| c0012 | 0/0 | 4341 | 3 | 0 | 0 | 3 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| c0013 | 0/0 | 4341 | 3 | 0 | 0 | 2 | 0 | 1 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| c0014 | 0/0 | 4341 | 2 | 2 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| c0015 | 0/0 | 4341 | 2 | 1 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| c0016 | 0/0 | 4341 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| c0017 | 0/0 | 4341 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| c0018 | 0/0 | 4341 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| c0019 | 0/0 | 4341 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| c0020 | 0/0 | 4341 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| c0021 | 0/0 | 4341 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| c0022 | 0/0 | 4341 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| c0023 | 0/0 | 4341 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| c0024 | 0/0 | 4341 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| c0025 | 0/0 | 4341 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| c0026 | 0/0 | 4341 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| c0027 | 0/0 | 4341 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| c0028 | 0/0 | 4341 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| c0029 | 0/0 | 4341 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| c0030 | 0/0 | 4341 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| c0031 | 0/0 | 4341 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| c0032 | 0/0 | 4341 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| c0033 | 0/0 | 4341 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| c0034 | 0/0 | 4341 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| c0035 | 0/0 | 4341 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| c0036 | 0/0 | 4341 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| c0037 | 0/0 | 4341 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| c0038 | 0/0 | 4341 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| c0039 | 0/0 | 4341 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 3564 | 117 | 10 | 19 | 67 | 4 | 15 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| t0002 | 0/0 | 3564 | 36 | 13 | 9 | 9 | 1 | 4 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| t0003 | 0/0 | 3570 | 24 | 1 | 5 | 14 | 2 | 2 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| t0004 | 0/0 | 3567 | 17 | 10 | 0 | 6 | 0 | 1 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| t0005 | 0/0 | 3566 | 8 | 7 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| t0006 | 0/0 | 3571 | 7 | 6 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| t0007 | 0/0 | 3565 | 6 | 5 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| t0008 | 0/0 | 3565 | 5 | 5 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| t0009 | 0/0 | 3571 | 5 | 5 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| t0010 | 0/0 | 3565 | 4 | 0 | 0 | 4 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| t0011 | 0/0 | 3565 | 4 | 2 | 2 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| t0012 | 0/0 | 3564 | 3 | 0 | 0 | 3 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| t0013 | 0/0 | 3561 | 3 | 1 | 2 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| t0014 | 0/0 | 3564 | 3 | 0 | 1 | 0 | 2 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| t0015 | 0/0 | 3549 | 2 | 0 | 0 | 1 | 0 | 1 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| t0016 | 0/0 | 3570 | 2 | 2 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| t0017 | 0/0 | 3563 | 2 | 0 | 0 | 2 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| t0018 | 0/0 | 3564 | 2 | 0 | 0 | 2 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| t0019 | 0/0 | 3564 | 2 | 0 | 0 | 2 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| t0020 | 0/0 | 3565 | 2 | 2 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| t0021 | 0/0 | 3565 | 2 | 2 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| t0022 | 0/0 | 3571 | 2 | 2 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| t0023 | 0/0 | 3565 | 2 | 2 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| t0024 | 0/0 | 3550 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| t0025 | 0/0 | 3564 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| t0026 | 0/0 | 3564 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| t0027 | 0/0 | 3564 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| t0028 | 0/0 | 3575 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| t0029 | 0/0 | 3570 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| t0030 | 0/0 | 3569 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| t0031 | 0/0 | 3570 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| t0032 | 0/0 | 3570 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| t0033 | 0/0 | 3564 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| t0034 | 0/0 | 3564 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| t0035 | 0/0 | 3564 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| t0036 | 0/0 | 3563 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| t0037 | 0/0 | 3564 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| t0038 | 0/0 | 3567 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| t0039 | 0/0 | 3565 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| t0040 | 0/0 | 3564 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| t0041 | 0/0 | 3564 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0002 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0120 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0132 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002 | 1/0 | 4341 | 49 | 12 | 18 | 9 | 2 | 7 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0001c0003 | 0/0 | 4341 | 44 | 18 | 5 | 17 | 2 | 2 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0001c0004 | 0/0 | 4341 | 22 | 1 | 2 | 15 | 1 | 3 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0001c0008 | 0/0 | 4341 | 4 | 0 | 0 | 3 | 0 | 1 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0001c0009 | 0/0 | 4341 | 4 | 1 | 2 | 0 | 0 | 1 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0001c0014 | 0/0 | 4341 | 2 | 2 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0001c0015 | 0/0 | 4341 | 2 | 1 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0001c0024 | 0/0 | 4341 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0001c0030 | 0/0 | 4341 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0001c0036 | 0/0 | 4341 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0001c0037 | 0/0 | 4341 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0002c0001 | 0/1 | 4341 | 76 | 12 | 13 | 43 | 3 | 4 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0002c0013 | 0/0 | 4341 | 3 | 0 | 0 | 2 | 0 | 1 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0002c0020 | 0/0 | 4341 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0002c0021 | 0/0 | 4341 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0002c0022 | 0/0 | 4341 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0002c0029 | 0/0 | 4341 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0002c0031 | 0/0 | 4341 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0002c0034 | 0/0 | 4341 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0002c0035 | 0/0 | 4341 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0003c0005 | 0/0 | 4341 | 19 | 8 | 0 | 9 | 0 | 2 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0003c0011 | 0/0 | 4341 | 3 | 0 | 0 | 3 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0003c0012 | 0/0 | 4341 | 3 | 0 | 0 | 3 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0004c0006 | 0/0 | 4341 | 14 | 13 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0004c0016 | 0/0 | 4341 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0005c0007 | 0/0 | 4341 | 5 | 0 | 0 | 4 | 0 | 1 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0005c0023 | 0/0 | 4341 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0006c0010 | 0/0 | 4341 | 4 | 4 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0007c0019 | 0/0 | 4341 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0007c0025 | 0/0 | 4341 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0008c0018 | 0/0 | 4341 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0009c0026 | 0/0 | 4341 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0010c0028 | 0/0 | 4341 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0011c0027 | 0/0 | 4341 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0012c0032 | 0/0 | 4341 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0013c0033 | 0/0 | 4341 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0014c0017 | 0/0 | 4341 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0015c0038 | 0/0 | 4341 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0016c0039 | 0/0 | 4341 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001 | 1/0 | 7904 | 16 | 0 | 5 | 5 | 1 | 4 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0001c0002t0002 | 0/0 | 7904 | 15 | 2 | 5 | 4 | 1 | 3 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0001c0002t0003 | 0/0 | 7910 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0001c0002t0004 | 0/0 | 7907 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0001c0002t0005 | 0/0 | 7906 | 5 | 4 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0001c0002t0007 | 0/0 | 7905 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0001c0002t0011 | 0/0 | 7905 | 4 | 2 | 2 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0001c0002t0013 | 0/0 | 7901 | 2 | 0 | 2 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0001c0002t0020 | 0/0 | 7905 | 2 | 2 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0001c0002t0033 | 0/0 | 7904 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0001c0002t0040 | 0/0 | 7904 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0001c0003t0001 | 0/0 | 7904 | 6 | 2 | 1 | 3 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0001c0003t0003 | 0/0 | 7910 | 19 | 1 | 4 | 11 | 1 | 2 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0001c0003t0004 | 0/0 | 7907 | 5 | 4 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0001c0003t0005 | 0/0 | 7906 | 3 | 3 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0001c0003t0008 | 0/0 | 7905 | 4 | 4 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0001c0003t0013 | 0/0 | 7901 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0001c0003t0023 | 0/0 | 7905 | 2 | 2 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0001c0003t0030 | 0/0 | 7909 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0001c0003t0031 | 0/0 | 7910 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0001c0003t0034 | 0/0 | 7904 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0001c0003t0037 | 0/0 | 7904 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0001c0004t0001 | 0/0 | 7904 | 15 | 1 | 1 | 9 | 1 | 3 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0001c0004t0002 | 0/0 | 7904 | 3 | 0 | 1 | 2 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0001c0004t0003 | 0/0 | 7910 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0001c0004t0019 | 0/0 | 7904 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0001c0004t0025 | 0/0 | 7904 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0001c0004t0041 | 0/0 | 7904 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0001c0008t0012 | 0/0 | 7904 | 3 | 0 | 0 | 3 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0001c0008t0015 | 0/0 | 7889 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0001c0009t0001 | 0/0 | 7904 | 4 | 1 | 2 | 0 | 0 | 1 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0001c0014t0021 | 0/0 | 7905 | 2 | 2 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0001c0015t0002 | 0/0 | 7904 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0001c0015t0039 | 0/0 | 7905 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0001c0024t0001 | 0/0 | 7904 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0001c0030t0032 | 0/0 | 7910 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0001c0036t0001 | 0/0 | 7904 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0001c0037t0024 | 0/0 | 7890 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0002c0001t0001 | 0/1 | 7904 | 50 | 3 | 9 | 34 | 1 | 2 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0002c0001t0002 | 0/0 | 7904 | 3 | 0 | 2 | 0 | 0 | 1 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0002c0001t0003 | 0/0 | 7910 | 2 | 0 | 0 | 2 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0002c0001t0004 | 0/0 | 7907 | 2 | 2 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0002c0001t0007 | 0/0 | 7905 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0002c0001t0009 | 0/0 | 7911 | 4 | 4 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0002c0001t0014 | 0/0 | 7904 | 3 | 0 | 1 | 0 | 2 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0002c0001t0016 | 0/0 | 7910 | 2 | 2 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0002c0001t0017 | 0/0 | 7903 | 2 | 0 | 0 | 2 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0002c0001t0018 | 0/0 | 7904 | 2 | 0 | 0 | 2 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0002c0001t0026 | 0/0 | 7904 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0002c0001t0028 | 0/0 | 7915 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0002c0001t0029 | 0/0 | 7910 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0002c0001t0035 | 0/0 | 7904 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0002c0001t0036 | 0/0 | 7903 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0002c0013t0001 | 0/0 | 7904 | 3 | 0 | 0 | 2 | 0 | 1 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0002c0020t0003 | 0/0 | 7910 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0002c0021t0009 | 0/0 | 7911 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0002c0022t0001 | 0/0 | 7904 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0002c0029t0001 | 0/0 | 7904 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0002c0031t0001 | 0/0 | 7904 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0002c0034t0001 | 0/0 | 7904 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0002c0035t0038 | 0/0 | 7907 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0003c0005t0001 | 0/0 | 7904 | 7 | 0 | 0 | 5 | 0 | 2 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0003c0005t0002 | 0/0 | 7904 | 5 | 5 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0003c0005t0004 | 0/0 | 7907 | 5 | 2 | 0 | 3 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0003c0005t0008 | 0/0 | 7905 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0003c0005t0019 | 0/0 | 7904 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0003c0011t0010 | 0/0 | 7905 | 3 | 0 | 0 | 3 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0003c0012t0002 | 0/0 | 7904 | 3 | 0 | 0 | 3 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0004c0006t0001 | 0/0 | 7904 | 2 | 2 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0004c0006t0002 | 0/0 | 7904 | 3 | 3 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0004c0006t0004 | 0/0 | 7907 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0004c0006t0006 | 0/0 | 7911 | 7 | 6 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0004c0006t0027 | 0/0 | 7904 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0004c0016t0002 | 0/0 | 7904 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0005c0007t0001 | 0/0 | 7904 | 4 | 0 | 0 | 4 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0005c0007t0004 | 0/0 | 7907 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0005c0023t0010 | 0/0 | 7905 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0006c0010t0007 | 0/0 | 7905 | 4 | 4 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0007c0019t0001 | 0/0 | 7904 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0007c0025t0004 | 0/0 | 7907 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0008c0018t0001 | 0/0 | 7904 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0009c0026t0002 | 0/0 | 7904 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0010c0028t0001 | 0/0 | 7904 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0011c0027t0001 | 0/0 | 7904 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0012c0032t0004 | 0/0 | 7907 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0013c0033t0002 | 0/0 | 7904 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0014c0017t0022 | 0/0 | 7911 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0015c0038t0015 | 0/0 | 7889 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| a0016c0039t0022 | 0/0 | 7911 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | copy fasta | chr9 | 95437980 | 95521971 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0002t0001g0132 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0002t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0002t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0002t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0002t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0002t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0002t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0002t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0002t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0002t0003g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0002t0004g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0002t0005g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0002t0005g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0002t0005g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0002t0005g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0002t0005g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0002t0007g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0002t0011g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0002t0011g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0002t0011g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0002t0013g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0002t0020g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0002t0020g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0002t0033g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0002t0040g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0003t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0003t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0003t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0003t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0003t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0003t0003g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0003t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0003t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0003t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0003t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0003t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0003t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0003t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0003t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0003t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0003t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0003t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0003t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0003t0003g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0003t0003g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0003t0003g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0003t0003g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0003t0003g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0003t0003g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0003t0004g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0003t0004g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0003t0004g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0003t0004g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0003t0004g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0003t0005g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0003t0005g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0003t0005g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0003t0008g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0003t0008g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0003t0008g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0003t0008g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0003t0013g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0003t0023g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0003t0023g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0003t0030g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0003t0031g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0003t0034g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0003t0037g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0004t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0004t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0004t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0004t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0004t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0004t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0004t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0004t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0004t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0004t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0004t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0004t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0004t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0004t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0004t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0004t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0004t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0004t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0004t0019g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0004t0025g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0004t0041g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0008t0012g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0008t0012g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0008t0012g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0008t0015g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0009t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0009t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0009t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0009t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0014t0021g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0014t0021g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0015t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0015t0039g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0024t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0030t0032g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0036t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0001c0037t0024g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0001t0001g0120 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0001t0004g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0001t0004g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0001t0007g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0001t0009g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0001t0009g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0001t0009g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0001t0009g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0001t0014g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0001t0014g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0001t0014g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0001t0016g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0001t0016g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0001t0017g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0001t0017g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0001t0018g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0001t0018g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0001t0026g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0001t0028g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0001t0029g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0001t0035g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0001t0036g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0013t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0013t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0013t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0020t0003g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0021t0009g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0022t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0029t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0031t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0034t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0002c0035t0038g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0003c0005t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0003c0005t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0003c0005t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0003c0005t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0003c0005t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0003c0005t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0003c0005t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0003c0005t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0003c0005t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0003c0005t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0003c0005t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0003c0005t0004g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0003c0005t0004g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0003c0005t0004g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0003c0005t0004g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0003c0005t0004g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0003c0005t0008g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0003c0005t0019g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0003c0011t0010g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0003c0011t0010g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0003c0012t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0003c0012t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0003c0012t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0004c0006t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0004c0006t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0004c0006t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0004c0006t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0004c0006t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0004c0006t0004g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0004c0006t0006g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0004c0006t0006g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0004c0006t0006g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0004c0006t0006g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0004c0006t0006g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0004c0006t0006g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0004c0006t0027g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0004c0016t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0005c0007t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0005c0007t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0005c0007t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0005c0007t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0005c0007t0004g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0005c0023t0010g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0006c0010t0007g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0006c0010t0007g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0006c0010t0007g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0007c0019t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0007c0025t0004g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0008c0018t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0009c0026t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0010c0028t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0011c0027t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0012c0032t0004g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0013c0033t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0014c0017t0022g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0015c0038t0015g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| a0016c0039t0022g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0002 | c0001 | t0001 | g0136 | EUR | GBR | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG00140 | hp2 | a0001 | c0004 | t0001 | g0256 | EUR | GBR | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG00408 | hp1 | a0002 | c0001 | t0001 | g0043 | EAS | CHS | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG00408 | hp2 | a0001 | c0002 | t0001 | g0254 | EAS | CHS | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG00423 | hp1 | a0002 | c0001 | t0001 | g0124 | EAS | CHS | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG00423 | hp2 | a0001 | c0008 | t0012 | g0017 | EAS | CHS | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG00558 | hp1 | a0002 | c0029 | t0001 | g0116 | EAS | CHS | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG00558 | hp2 | a0007 | c0019 | t0001 | g0109 | EAS | CHS | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG00597 | hp1 | a0001 | c0003 | t0003 | g0171 | EAS | CHS | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG00597 | hp2 | a0002 | c0001 | t0001 | g0122 | EAS | CHS | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG00609 | hp1 | a0003 | c0011 | t0010 | g0123 | EAS | CHS | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG00609 | hp2 | a0002 | c0013 | t0001 | g0233 | EAS | CHS | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0073 | AMR | PUR | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG00639 | hp2 | a0002 | c0001 | t0036 | g0127 | AMR | PUR | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG00673 | hp1 | a0002 | c0001 | t0001 | g0004 | EAS | CHS | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG00673 | hp2 | a0005 | c0023 | t0010 | g0218 | EAS | CHS | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG00738 | hp1 | a0002 | c0001 | t0001 | g0152 | AMR | PUR | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG00738 | hp2 | a0001 | c0003 | t0001 | g0160 | AMR | PUR | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG01069 | hp1 | a0001 | c0002 | t0013 | g0009 | AMR | PUR | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG01069 | hp2 | a0008 | c0018 | t0001 | g0154 | AMR | PUR | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG01071 | hp1 | a0001 | c0002 | t0002 | g0139 | AMR | PUR | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG01071 | hp2 | a0001 | c0002 | t0013 | g0009 | AMR | PUR | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG01074 | hp1 | a0001 | c0002 | t0002 | g0107 | AMR | PUR | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG01074 | hp2 | a0001 | c0002 | t0003 | g0235 | AMR | PUR | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG01081 | hp1 | a0001 | c0002 | t0005 | g0207 | AMR | PUR | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG01081 | hp2 | a0001 | c0015 | t0039 | g0130 | AMR | PUR | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG01099 | hp1 | a0001 | c0003 | t0003 | g0180 | AMR | PUR | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG01099 | hp2 | a0002 | c0001 | t0001 | g0006 | AMR | PUR | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0156 | AMR | PUR | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG01106 | hp2 | a0002 | c0001 | t0002 | g0060 | AMR | PUR | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0074 | AMR | PUR | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG01109 | hp2 | a0001 | c0002 | t0011 | g0188 | AMR | PUR | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG01167 | hp1 | a0001 | c0003 | t0003 | g0183 | AMR | PUR | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0093 | AMR | PUR | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG01175 | hp1 | a0001 | c0004 | t0002 | g0240 | AMR | PUR | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG01175 | hp2 | a0002 | c0001 | t0001 | g0082 | AMR | PUR | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG01192 | hp1 | a0002 | c0001 | t0001 | g0006 | AMR | PUR | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG01192 | hp2 | a0001 | c0003 | t0003 | g0181 | AMR | PUR | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG01243 | hp1 | a0001 | c0002 | t0011 | g0008 | AMR | PUR | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG01243 | hp2 | a0004 | c0006 | t0006 | g0028 | AMR | PUR | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG01255 | hp1 | a0001 | c0002 | t0002 | g0195 | AMR | CLM | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG01255 | hp2 | a0001 | c0003 | t0003 | g0179 | AMR | CLM | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG01358 | hp1 | a0001 | c0002 | t0002 | g0067 | AMR | CLM | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG01358 | hp2 | a0001 | c0002 | t0040 | g0230 | AMR | CLM | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG01361 | hp1 | a0001 | c0009 | t0001 | g0248 | AMR | CLM | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG01361 | hp2 | a0002 | c0001 | t0001 | g0133 | AMR | CLM | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG01516 | hp1 | a0002 | c0001 | t0014 | g0058 | EUR | IBS | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG01516 | hp2 | a0001 | c0002 | t0002 | g0104 | EUR | IBS | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG01517 | hp1 | a0002 | c0020 | t0003 | g0178 | EUR | IBS | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG01517 | hp2 | a0002 | c0001 | t0014 | g0057 | EUR | IBS | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG01884 | hp1 | a0004 | c0006 | t0001 | g0033 | AFR | ACB | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG01884 | hp2 | a0003 | c0005 | t0002 | g0206 | AFR | ACB | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG01934 | hp1 | a0002 | c0001 | t0001 | g0137 | AMR | PEL | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG01934 | hp2 | a0001 | c0002 | t0002 | g0126 | AMR | PEL | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG01952 | hp1 | a0009 | c0026 | t0002 | g0190 | AMR | PEL | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG01952 | hp2 | a0002 | c0001 | t0002 | g0054 | AMR | PEL | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG01975 | hp1 | a0002 | c0001 | t0001 | g0062 | AMR | PEL | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG01975 | hp2 | a0001 | c0004 | t0001 | g0238 | AMR | PEL | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0155 | AMR | PEL | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG02004 | hp2 | a0002 | c0001 | t0001 | g0056 | AMR | PEL | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG02015 | hp1 | a0003 | c0005 | t0001 | g0011 | EAS | KHV | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG02015 | hp2 | a0001 | c0037 | t0024 | g0016 | EAS | KHV | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG02027 | hp1 | a0001 | c0003 | t0003 | g0174 | EAS | KHV | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG02027 | hp2 | a0002 | c0001 | t0001 | g0121 | EAS | KHV | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG02040 | hp1 | a0002 | c0001 | t0035 | g0113 | EAS | KHV | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG02040 | hp2 | a0002 | c0001 | t0001 | g0125 | EAS | KHV | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG02055 | hp1 | a0001 | c0009 | t0001 | g0249 | AFR | ACB | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG02055 | hp2 | a0002 | c0001 | t0001 | g0117 | AFR | ACB | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG02056 | hp1 | a0001 | c0003 | t0003 | g0164 | EAS | KHV | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG02056 | hp2 | a0003 | c0011 | t0010 | g0010 | EAS | KHV | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG02071 | hp1 | a0002 | c0001 | t0018 | g0077 | EAS | KHV | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG02071 | hp2 | a0015 | c0038 | t0015 | g0019 | EAS | KHV | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG02129 | hp1 | a0007 | c0025 | t0004 | g0224 | EAS | KHV | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG02129 | hp2 | a0002 | c0001 | t0001 | g0092 | EAS | KHV | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG02135 | hp1 | a0003 | c0005 | t0001 | g0011 | EAS | KHV | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG02135 | hp2 | a0001 | c0002 | t0002 | g0041 | EAS | KHV | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG02145 | hp1 | a0006 | c0010 | t0007 | g0264 | AFR | ACB | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG02145 | hp2 | a0001 | c0003 | t0004 | g0196 | AFR | ACB | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG02155 | hp1 | a0001 | c0004 | t0001 | g0239 | EAS | CDX | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG02155 | hp2 | a0002 | c0001 | t0001 | g0088 | EAS | CDX | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG02257 | hp1 | a0001 | c0002 | t0005 | g0201 | AFR | ACB | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG02257 | hp2 | a0002 | c0021 | t0009 | g0047 | AFR | ACB | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG02300 | hp1 | a0001 | c0009 | t0001 | g0247 | AMR | PEL | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG02300 | hp2 | a0002 | c0001 | t0001 | g0143 | AMR | PEL | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG02451 | hp1 | a0004 | c0006 | t0027 | g0025 | AFR | ACB | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG02451 | hp2 | a0001 | c0003 | t0023 | g0039 | AFR | ACB | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG02523 | hp1 | a0005 | c0007 | t0001 | g0189 | EAS | KHV | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG02523 | hp2 | a0012 | c0032 | t0004 | g0089 | EAS | KHV | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG02572 | hp1 | a0001 | c0030 | t0032 | g0211 | AFR | GWD | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG02572 | hp2 | a0006 | c0010 | t0007 | g0263 | AFR | GWD | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG02615 | hp1 | a0001 | c0003 | t0005 | g0197 | AFR | GWD | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG02615 | hp2 | a0001 | c0002 | t0005 | g0259 | AFR | GWD | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG02622 | hp1 | a0004 | c0006 | t0002 | g0022 | AFR | GWD | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG02622 | hp2 | a0001 | c0003 | t0001 | g0191 | AFR | GWD | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG02630 | hp1 | a0002 | c0001 | t0009 | g0095 | AFR | GWD | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG02630 | hp2 | a0001 | c0003 | t0008 | g0202 | AFR | GWD | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG02647 | hp1 | a0003 | c0005 | t0004 | g0076 | AFR | GWD | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG02647 | hp2 | a0001 | c0003 | t0023 | g0038 | AFR | GWD | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG02683 | hp1 | a0001 | c0002 | t0002 | g0141 | SAS | PJL | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG02683 | hp2 | a0001 | c0024 | t0001 | g0227 | SAS | PJL | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG02717 | hp1 | a0004 | c0006 | t0002 | g0026 | AFR | GWD | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG02717 | hp2 | a0002 | c0035 | t0038 | g0099 | AFR | GWD | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG02723 | hp1 | a0004 | c0016 | t0002 | g0024 | AFR | GWD | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG02723 | hp2 | a0016 | c0039 | t0022 | g0262 | AFR | GWD | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG02735 | hp1 | a0001 | c0002 | t0002 | g0119 | SAS | PJL | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG02735 | hp2 | a0001 | c0009 | t0001 | g0246 | SAS | PJL | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG02738 | hp1 | a0001 | c0004 | t0001 | g0229 | SAS | PJL | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0144 | SAS | PJL | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG02809 | hp1 | a0001 | c0002 | t0007 | g0036 | AFR | GWD | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG02809 | hp2 | a0002 | c0001 | t0028 | g0105 | AFR | GWD | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG02818 | hp1 | a0001 | c0014 | t0021 | g0212 | AFR | GWD | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG02818 | hp2 | a0014 | c0017 | t0022 | g0020 | AFR | GWD | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG02895 | hp1 | a0001 | c0003 | t0008 | g0203 | AFR | GWD | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG02895 | hp2 | a0006 | c0010 | t0007 | g0013 | AFR | GWD | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG02897 | hp1 | a0002 | c0001 | t0009 | g0080 | AFR | GWD | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG02897 | hp2 | a0006 | c0010 | t0007 | g0013 | AFR | GWD | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG02922 | hp1 | a0004 | c0006 | t0006 | g0001 | AFR | ESN | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG02922 | hp2 | a0003 | c0005 | t0008 | g0226 | AFR | ESN | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG02965 | hp1 | a0002 | c0001 | t0004 | g0070 | AFR | ESN | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG02965 | hp2 | a0001 | c0003 | t0037 | g0037 | AFR | ESN | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG02976 | hp1 | a0001 | c0003 | t0005 | g0208 | AFR | ESN | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG02976 | hp2 | a0003 | c0005 | t0002 | g0225 | AFR | ESN | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG03041 | hp1 | a0002 | c0001 | t0016 | g0081 | AFR | GWD | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG03041 | hp2 | a0001 | c0014 | t0021 | g0213 | AFR | GWD | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG03098 | hp1 | a0004 | c0006 | t0004 | g0027 | AFR | MSL | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG03098 | hp2 | a0004 | c0006 | t0006 | g0030 | AFR | MSL | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG03130 | hp1 | a0001 | c0002 | t0011 | g0008 | AFR | ESN | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG03130 | hp2 | a0003 | c0005 | t0004 | g0108 | AFR | ESN | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG03139 | hp1 | a0001 | c0003 | t0008 | g0193 | AFR | ESN | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG03139 | hp2 | a0002 | c0001 | t0009 | g0260 | AFR | ESN | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG03195 | hp1 | a0003 | c0005 | t0002 | g0079 | AFR | ESN | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG03195 | hp2 | a0001 | c0003 | t0004 | g0199 | AFR | ESN | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG03239 | hp1 | a0002 | c0001 | t0001 | g0138 | SAS | PJL | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG03239 | hp2 | a0001 | c0004 | t0001 | g0242 | SAS | PJL | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG03453 | hp1 | a0001 | c0003 | t0005 | g0210 | AFR | MSL | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG03453 | hp2 | a0001 | c0003 | t0001 | g0192 | AFR | MSL | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG03486 | hp1 | a0001 | c0002 | t0020 | g0035 | AFR | MSL | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG03486 | hp2 | a0001 | c0002 | t0002 | g0214 | AFR | MSL | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0061 | SAS | PJL | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG03490 | hp2 | a0001 | c0004 | t0001 | g0078 | SAS | PJL | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG03491 | hp1 | a0001 | c0002 | t0002 | g0147 | SAS | PJL | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0083 | SAS | PJL | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG03516 | hp1 | a0004 | c0006 | t0006 | g0001 | AFR | ESN | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG03516 | hp2 | a0003 | c0005 | t0002 | g0129 | AFR | ESN | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG03540 | hp1 | a0002 | c0001 | t0004 | g0094 | AFR | GWD | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG03540 | hp2 | a0001 | c0002 | t0011 | g0185 | AFR | GWD | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG03579 | hp1 | a0002 | c0001 | t0001 | g0072 | AFR | MSL | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG03579 | hp2 | a0004 | c0006 | t0006 | g0031 | AFR | MSL | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0085 | SAS | PJL | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG03669 | hp2 | a0002 | c0001 | t0007 | g0066 | SAS | PJL | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG03704 | hp1 | a0002 | c0013 | t0001 | g0258 | SAS | PJL | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG03704 | hp2 | a0001 | c0003 | t0003 | g0182 | SAS | PJL | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG03710 | hp1 | a0003 | c0005 | t0001 | g0140 | SAS | PJL | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG03710 | hp2 | a0002 | c0001 | t0002 | g0131 | SAS | PJL | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG04184 | hp1 | a0001 | c0003 | t0003 | g0110 | SAS | BEB | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG04184 | hp2 | a0005 | c0007 | t0004 | g0158 | SAS | BEB | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG04199 | hp1 | a0001 | c0008 | t0015 | g0015 | SAS | STU | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG04199 | hp2 | a0011 | c0027 | t0001 | g0142 | SAS | STU | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA18747 | hp1 | a0002 | c0001 | t0001 | g0097 | EAS | CHB | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA18747 | hp2 | a0003 | c0012 | t0002 | g0184 | EAS | CHB | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA18906 | hp1 | a0002 | c0034 | t0001 | g0145 | AFR | YRI | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA18906 | hp2 | a0001 | c0003 | t0004 | g0200 | AFR | YRI | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA18939 | hp1 | a0002 | c0001 | t0017 | g0100 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA18939 | hp2 | a0001 | c0003 | t0003 | g0165 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA18940 | hp1 | a0002 | c0001 | t0001 | g0115 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA18940 | hp2 | a0001 | c0004 | t0002 | g0250 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA18943 | hp1 | a0002 | c0013 | t0001 | g0241 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA18943 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA18944 | hp1 | a0001 | c0003 | t0003 | g0169 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA18944 | hp2 | a0002 | c0001 | t0001 | g0103 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA18946 | hp1 | a0001 | c0004 | t0025 | g0236 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA18946 | hp2 | a0002 | c0001 | t0001 | g0134 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA18952 | hp1 | a0003 | c0005 | t0001 | g0175 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA18952 | hp2 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA18954 | hp1 | a0001 | c0003 | t0001 | g0007 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA18954 | hp2 | a0002 | c0001 | t0003 | g0101 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA18956 | hp1 | a0001 | c0003 | t0003 | g0162 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA18956 | hp2 | a0002 | c0001 | t0001 | g0149 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA18957 | hp1 | a0002 | c0001 | t0001 | g0098 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA18957 | hp2 | a0003 | c0005 | t0004 | g0216 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA18960 | hp1 | a0002 | c0001 | t0001 | g0053 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA18960 | hp2 | a0002 | c0001 | t0001 | g0052 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA18962 | hp1 | a0001 | c0004 | t0019 | g0251 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA18962 | hp2 | a0001 | c0003 | t0003 | g0163 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA18965 | hp1 | a0001 | c0008 | t0012 | g0014 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA18965 | hp2 | a0010 | c0028 | t0001 | g0150 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA18967 | hp1 | a0001 | c0003 | t0031 | g0253 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA18967 | hp2 | a0002 | c0001 | t0001 | g0049 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA18968 | hp1 | a0001 | c0003 | t0001 | g0166 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA18968 | hp2 | a0003 | c0005 | t0001 | g0223 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA18969 | hp1 | a0002 | c0001 | t0001 | g0051 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA18969 | hp2 | a0001 | c0004 | t0002 | g0252 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA18970 | hp1 | a0002 | c0001 | t0001 | g0065 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA18970 | hp2 | a0003 | c0012 | t0002 | g0186 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA18971 | hp1 | a0002 | c0001 | t0001 | g0135 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA18971 | hp2 | a0001 | c0004 | t0003 | g0255 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA18973 | hp1 | a0001 | c0004 | t0001 | g0243 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA18973 | hp2 | a0002 | c0031 | t0001 | g0091 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA18975 | hp1 | a0002 | c0001 | t0001 | g0048 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA18975 | hp2 | a0003 | c0011 | t0010 | g0010 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA18977 | hp1 | a0003 | c0005 | t0004 | g0219 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA18977 | hp2 | a0002 | c0001 | t0018 | g0102 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA18979 | hp1 | a0003 | c0005 | t0004 | g0215 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA18979 | hp2 | a0002 | c0001 | t0001 | g0084 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA18982 | hp1 | a0002 | c0001 | t0001 | g0090 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA18982 | hp2 | a0002 | c0001 | t0017 | g0046 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA18983 | hp1 | a0002 | c0001 | t0001 | g0003 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA18983 | hp2 | a0001 | c0004 | t0001 | g0012 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA18986 | hp1 | a0005 | c0007 | t0001 | g0222 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA18986 | hp2 | a0001 | c0003 | t0004 | g0159 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA18988 | hp1 | a0003 | c0012 | t0002 | g0187 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA18988 | hp2 | a0002 | c0001 | t0029 | g0040 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA18991 | hp1 | a0002 | c0001 | t0001 | g0050 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA18991 | hp2 | a0001 | c0004 | t0001 | g0245 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA18994 | hp1 | a0005 | c0007 | t0001 | g0217 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA18994 | hp2 | a0001 | c0004 | t0001 | g0231 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA18999 | hp1 | a0002 | c0001 | t0001 | g0086 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA18999 | hp2 | a0001 | c0004 | t0001 | g0257 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA19000 | hp1 | a0002 | c0001 | t0001 | g0087 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA19000 | hp2 | a0001 | c0003 | t0003 | g0167 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA19003 | hp1 | a0002 | c0001 | t0001 | g0045 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA19003 | hp2 | a0001 | c0002 | t0001 | g0106 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA19004 | hp1 | a0001 | c0003 | t0001 | g0007 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA19004 | hp2 | a0001 | c0002 | t0001 | g0112 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA19005 | hp1 | a0002 | c0001 | t0001 | g0063 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA19005 | hp2 | a0003 | c0005 | t0001 | g0176 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA19007 | hp1 | a0002 | c0001 | t0001 | g0064 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA19007 | hp2 | a0001 | c0004 | t0001 | g0244 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA19030 | hp1 | a0001 | c0002 | t0002 | g0261 | AFR | LWK | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA19030 | hp2 | a0003 | c0005 | t0002 | g0128 | AFR | LWK | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA19043 | hp1 | a0002 | c0001 | t0016 | g0096 | AFR | LWK | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA19043 | hp2 | a0001 | c0003 | t0004 | g0198 | AFR | LWK | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA19056 | hp1 | a0002 | c0001 | t0003 | g0151 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA19056 | hp2 | a0001 | c0003 | t0030 | g0173 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA19062 | hp1 | a0002 | c0001 | t0026 | g0044 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA19062 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA19064 | hp1 | a0005 | c0007 | t0001 | g0221 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA19064 | hp2 | a0001 | c0003 | t0003 | g0161 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA19066 | hp1 | a0001 | c0008 | t0012 | g0018 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA19066 | hp2 | a0002 | c0022 | t0001 | g0075 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA19068 | hp1 | a0001 | c0004 | t0041 | g0265 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA19068 | hp2 | a0001 | c0002 | t0001 | g0034 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA19079 | hp1 | a0001 | c0004 | t0001 | g0237 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA19079 | hp2 | a0002 | c0001 | t0001 | g0003 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA19083 | hp1 | a0003 | c0005 | t0019 | g0220 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA19083 | hp2 | a0002 | c0001 | t0001 | g0146 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA19086 | hp1 | a0001 | c0002 | t0001 | g0153 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA19086 | hp2 | a0001 | c0004 | t0001 | g0012 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA19090 | hp1 | a0001 | c0003 | t0003 | g0170 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA19090 | hp2 | a0002 | c0001 | t0001 | g0004 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA19240 | hp1 | a0004 | c0006 | t0006 | g0021 | AFR | YRI | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA19240 | hp2 | a0001 | c0002 | t0005 | g0204 | AFR | YRI | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA20129 | hp1 | a0004 | c0006 | t0006 | g0029 | AFR | ASW | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA20129 | hp2 | a0004 | c0006 | t0002 | g0023 | AFR | ASW | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0148 | EUR | TSI | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA20752 | hp2 | a0001 | c0003 | t0003 | g0177 | EUR | TSI | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA20805 | hp1 | a0001 | c0036 | t0001 | g0234 | EUR | TSI | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA20805 | hp2 | a0001 | c0003 | t0034 | g0068 | EUR | TSI | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA20905 | hp1 | a0002 | c0001 | t0001 | g0002 | SAS | GIH | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA20905 | hp2 | a0003 | c0005 | t0001 | g0228 | SAS | GIH | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG01123 | hp1 | a0001 | c0002 | t0033 | g0157 | AMR | CLM | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG01123 | hp2 | a0002 | c0001 | t0014 | g0059 | AMR | CLM | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG02109 | hp1 | a0001 | c0002 | t0005 | g0205 | AFR | ACB | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG02109 | hp2 | a0001 | c0003 | t0013 | g0209 | AFR | ACB | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG02486 | hp1 | a0004 | c0006 | t0001 | g0032 | AFR | ACB | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG02486 | hp2 | a0001 | c0004 | t0001 | g0232 | AFR | ACB | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG02559 | hp1 | a0001 | c0003 | t0003 | g0168 | AFR | ACB | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG02559 | hp2 | a0001 | c0002 | t0004 | g0071 | AFR | ACB | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG03471 | hp1 | a0002 | c0001 | t0009 | g0114 | AFR | MSL | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG03471 | hp2 | a0001 | c0002 | t0020 | g0042 | AFR | MSL | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG06807 | hp1 | a0002 | c0001 | t0001 | g0069 | AFR | USA | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| HG06807 | hp2 | a0001 | c0015 | t0002 | g0055 | AFR | USA | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA18955 | hp1 | a0001 | c0003 | t0003 | g0172 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA18955 | hp2 | a0001 | c0002 | t0002 | g0111 | EAS | JPT | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA21309 | hp1 | a0001 | c0003 | t0008 | g0194 | AFR | LWK | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| NA21309 | hp2 | a0013 | c0033 | t0002 | g0118 | AFR | LWK | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0001 | t0001 | g0120 | REF | REF | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0132 | REF | REF | PTCH1_chr9_95437980_95521971 | PTCH1 | chr9 | 95437980 | 95521971 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:95446931
|
C | T | 1 | a0010 | 1 | NA18965.hp2 | missense_variant | MODERATE | c.4322G>A | p.Arg1441Gln | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 23/24 | 4473/7905 | 4322/4341 | 1441/1446 | chr9 | 95446931 | ||
| chr9:95446967
|
A | G | 1 | a0014 | 1 | HG02818.hp2 | missense_variant | MODERATE | c.4286T>C | p.Ile1429Thr | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 23/24 | 4437/7905 | 4286/4341 | 1429/1446 | chr9 | 95446967 | ||
| chr9:95447108
|
G | A | 1 | a0011 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.4145C>T | p.Pro1382Leu | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 23/24 | 4296/7905 | 4145/4341 | 1382/1446 | chr9 | 95447108 | ||
| chr9:95447312
|
G | A | 6 | a0002a0005a0010others(3): Show | 96 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(93): Show |
missense_variant | MODERATE | c.3941C>T | p.Pro1314Leu | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 23/24 | 4092/7905 | 3941/4341 | 1314/1446 | chr9 | 95447312 | ||
| chr9:95447349
|
G | A | 1 | a0007 | 2 | HG00558.hp2 HG02129.hp1 |
missense_variant | MODERATE | c.3904C>T | p.Arg1302Cys | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 23/24 | 4055/7905 | 3904/4341 | 1302/1446 | chr9 | 95447349 | ||
| chr9:95447411
|
G | A | 1 | a0006 | 4 | HG02145.hp1 HG02572.hp2 HG02895.hp2 others(1): Show |
missense_variant | MODERATE | c.3842C>T | p.Pro1281Leu | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 23/24 | 3993/7905 | 3842/4341 | 1281/1446 | chr9 | 95447411 | ||
| chr9:95449107
|
C | T | 1 | a0009 | 1 | HG01952.hp1 | missense_variant | MODERATE | c.3763G>A | p.Val1255Met | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 22/24 | 3914/7905 | 3763/4341 | 1255/1446 | chr9 | 95449107 | ||
| chr9:95449290
|
T | A | 3 | a0003a0005a0007 | 33 | HG00558.hp2 HG00609.hp1 HG00673.hp2 others(30): Show |
missense_variant | MODERATE | c.3580A>T | p.Thr1194Ser | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 22/24 | 3731/7905 | 3580/4341 | 1194/1446 | chr9 | 95449290 | ||
| chr9:95467197
|
T | C | 1 | a0015 | 1 | HG02071.hp2 | missense_variant | MODERATE | c.2476A>G | p.Ser826Gly | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 15/24 | 2627/7905 | 2476/4341 | 826/1446 | chr9 | 95467197 | ||
| chr9:95468779
|
G | A | 1 | a0012 | 1 | HG02523.hp2 | missense_variant | MODERATE | c.2219C>T | p.Ala740Val | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 14/24 | 2370/7905 | 2219/4341 | 740/1446 | chr9 | 95468779 | ||
| chr9:95468828
|
G | A | 1 | a0013 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.2170C>T | p.Pro724Ser | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 14/24 | 2321/7905 | 2170/4341 | 724/1446 | chr9 | 95468828 | ||
| chr9:95476101
|
C | T | 1 | a0008 | 1 | HG01069.hp2 | missense_variant | MODERATE | c.1658G>A | p.Ser553Asn | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 12/24 | 1809/7905 | 1658/4341 | 553/1446 | chr9 | 95476101 | ||
| chr9:95516658
|
C | G | 2 | a0004a0014 | 16 | HG01243.hp2 HG01884.hp1 HG02451.hp1 others(13): Show |
missense_variant | MODERATE | c.163G>C | p.Asp55His | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/24 | 314/7905 | 163/4341 | 55/1446 | chr9 | 95516658 | ||
| chr9:95516690
|
T | C | 3 | a0006a0015a0016 | 6 | HG02071.hp2 HG02145.hp1 HG02572.hp2 others(3): Show |
missense_variant | MODERATE | c.131A>G | p.Glu44Gly | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/24 | 282/7905 | 131/4341 | 44/1446 | chr9 | 95516690 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:95447176
|
G | A | 2 | a0001c0036a0002c0029 | 2 | HG00558.hp1 NA20805.hp1 |
synonymous_variant | LOW | c.4077C>T | p.Ser1359Ser | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 23/24 | 4228/7905 | 4077/4341 | 1359/1446 | chr9 | 95447176 | ||
| chr9:95449186
|
C | T | 1 | a0004c0016 | 1 | HG02723.hp1 | synonymous_variant | LOW | c.3684G>A | p.Thr1228Thr | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 22/24 | 3835/7905 | 3684/4341 | 1228/1446 | chr9 | 95449186 | ||
| chr9:95449249
|
G | A | 1 | a0001c0030 | 1 | HG02572.hp1 | synonymous_variant | LOW | c.3621C>T | p.Ala1207Ala | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 22/24 | 3772/7905 | 3621/4341 | 1207/1446 | chr9 | 95449249 | ||
| chr9:95449306
|
G | A | 1 | a0001c0015 | 2 | HG01081.hp2 HG06807.hp2 |
synonymous_variant | LOW | c.3564C>T | p.Gly1188Gly | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 22/24 | 3715/7905 | 3564/4341 | 1188/1446 | chr9 | 95449306 | ||
| chr9:95453540
|
G | A | 1 | a0002c0031 | 1 | NA18973.hp2 | synonymous_variant | LOW | c.3384C>T | p.Gly1128Gly | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 20/24 | 3535/7905 | 3384/4341 | 1128/1446 | chr9 | 95453540 | ||
| chr9:95456387
|
G | A | 1 | a0002c0035 | 1 | HG02717.hp2 | synonymous_variant | LOW | c.3192C>T | p.Val1064Val | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 19/24 | 3343/7905 | 3192/4341 | 1064/1446 | chr9 | 95456387 | ||
| chr9:95458040
|
A | C | 7 | a0001c0024a0003c0005a0003c0011others(4): Show | 31 | HG00558.hp2 HG00609.hp1 HG00673.hp2 others(28): Show |
synonymous_variant | LOW | c.3138T>G | p.Leu1046Leu | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 18/24 | 3289/7905 | 3138/4341 | 1046/1446 | chr9 | 95458040 | ||
| chr9:95458268
|
A | G | 2 | a0003c0011a0005c0023 | 4 | HG00609.hp1 HG00673.hp2 HG02056.hp2 others(1): Show |
synonymous_variant | LOW | c.2910T>C | p.Tyr970Tyr | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 18/24 | 3061/7905 | 2910/4341 | 970/1446 | chr9 | 95458268 | ||
| chr9:95458271
|
C | T | 1 | a0002c0022 | 1 | NA19066.hp2 | synonymous_variant | LOW | c.2907G>A | p.Glu969Glu | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 18/24 | 3058/7905 | 2907/4341 | 969/1446 | chr9 | 95458271 | ||
| chr9:95459688
|
C | T | 1 | a0001c0014 | 2 | HG02818.hp1 HG03041.hp2 |
synonymous_variant | LOW | c.2796G>A | p.Ala932Ala | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 17/24 | 2947/7905 | 2796/4341 | 932/1446 | chr9 | 95459688 | ||
| chr9:95468802
|
T | C | 3 | a0001c0008a0001c0037a0015c0038 | 6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
synonymous_variant | LOW | c.2196A>G | p.Ser732Ser | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 14/24 | 2347/7905 | 2196/4341 | 732/1446 | chr9 | 95468802 | ||
| chr9:95469039
|
C | T | 1 | a0002c0021 | 1 | HG02257.hp2 | synonymous_variant | LOW | c.1959G>A | p.Thr653Thr | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 14/24 | 2110/7905 | 1959/4341 | 653/1446 | chr9 | 95469039 | ||
| chr9:95469147
|
G | A | 2 | a0002c0034a0002c0035 | 2 | HG02717.hp2 NA18906.hp1 |
synonymous_variant | LOW | c.1851C>T | p.Cys617Cys | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 14/24 | 2002/7905 | 1851/4341 | 617/1446 | chr9 | 95469147 | ||
| chr9:95476076
|
G | A | 4 | a0001c0004a0001c0009a0001c0036others(1): Show | 30 | HG00140.hp2 HG00609.hp2 HG01175.hp1 others(27): Show |
synonymous_variant | LOW | c.1683C>T | p.Ala561Ala | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 12/24 | 1834/7905 | 1683/4341 | 561/1446 | chr9 | 95476076 | ||
| chr9:95476097
|
A | G | 6 | a0001c0003a0001c0008a0001c0037others(3): Show | 52 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(49): Show |
synonymous_variant | LOW | c.1662T>C | p.Asn554Asn | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 12/24 | 1813/7905 | 1662/4341 | 554/1446 | chr9 | 95476097 | ||
| chr9:95481960
|
T | C | 1 | a0001c0009 | 4 | HG01361.hp1 HG02055.hp1 HG02300.hp1 others(1): Show |
synonymous_variant | LOW | c.732A>G | p.Thr244Thr | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 5/24 | 883/7905 | 732/4341 | 244/1446 | chr9 | 95481960 | ||
| chr9:95506597
|
C | A | 1 | a0001c0037 | 1 | HG02015.hp2 | splice_region_variant&synonymous_variant | LOW | c.201G>T | p.Gly67Gly | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/24 | 352/7905 | 201/4341 | 67/1446 | chr9 | 95506597 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:95443161
|
C | A | 15 | a0001c0002t0002a0001c0003t0034a0001c0004t0002others(12): Show | 41 | HG00639.hp2 HG01071.hp1 HG01074.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*3232G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 24/24 | 3751 | chr9 | 95443161 | |||||
| chr9:95443236
|
C | T | 3 | a0001c0008t0015a0001c0037t0024a0015c0038t0015 | 3 | HG02015.hp2 HG02071.hp2 HG04199.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3157G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 24/24 | 3676 | chr9 | 95443236 | |||||
| chr9:95443363
|
T | C | 31 | a0001c0002t0003a0001c0002t0004a0001c0002t0005others(28): Show | 78 | HG00597.hp1 HG01074.hp2 HG01081.hp1 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*3030A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 24/24 | 3549 | chr9 | 95443363 | |||||
| chr9:95443397
|
TACAA | T | 2 | a0001c0002t0013a0001c0003t0013 | 3 | HG01069.hp1 HG01071.hp2 HG02109.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2992_*2995delTTGT | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 24/24 | 3511 | chr9 | 95443397 | |||||
| chr9:95443613
|
T | A | 1 | a0002c0001t0035 | 1 | HG02040.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2780A>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 24/24 | 3299 | chr9 | 95443613 | |||||
| chr9:95443735
|
A | C | 1 | a0002c0035t0038 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2658T>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 24/24 | 3177 | chr9 | 95443735 | |||||
| chr9:95444104
|
G | GT | 10 | a0001c0002t0004a0001c0003t0004a0002c0001t0004others(7): Show | 21 | HG00609.hp1 HG00673.hp2 HG02056.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2288dupA | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 24/24 | 2807 | chr9 | 95444104 | |||||
| chr9:95444104
|
GT | G | 4 | a0001c0003t0030a0001c0003t0037a0002c0001t0017others(1): Show | 5 | HG00639.hp2 HG02965.hp2 NA18939.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2288delA | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 24/24 | 2807 | chr9 | 95444104 | |||||
| chr9:95444117
|
T | A | 1 | a0001c0014t0021 | 2 | HG02818.hp1 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2276A>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 24/24 | 2795 | chr9 | 95444117 | |||||
| chr9:95444117
|
TA | T | 3 | a0001c0008t0015a0002c0001t0016a0015c0038t0015 | 4 | HG02071.hp2 HG03041.hp1 HG04199.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2275delT | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 24/24 | 2794 | chr9 | 95444117 | |||||
| chr9:95444118
|
A | T | 14 | a0001c0002t0011a0001c0002t0013a0001c0003t0008others(11): Show | 30 | HG01069.hp1 HG01071.hp2 HG01109.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*2275T>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 24/24 | 2794 | chr9 | 95444118 | |||||
| chr9:95444488
|
G | C | 7 | a0002c0001t0009a0002c0001t0016a0002c0001t0028others(4): Show | 17 | HG01243.hp2 HG02257.hp2 HG02630.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1905C>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 24/24 | 2424 | chr9 | 95444488 | |||||
| chr9:95444491
|
ACACACAC others(11): Show |
A | 3 | a0001c0008t0015a0001c0037t0024a0015c0038t0015 | 3 | HG02015.hp2 HG02071.hp2 HG04199.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1884_*1901delCGTG others(14): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 24/24 | 2403 | chr9 | 95444491 | |||||
| chr9:95444501
|
G | A | 1 | a0001c0002t0033 | 1 | HG01123.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1892C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 24/24 | 2411 | chr9 | 95444501 | |||||
| chr9:95444509
|
G | GCA | 20 | a0001c0002t0003a0001c0002t0004a0001c0002t0005others(17): Show | 54 | HG00597.hp1 HG01074.hp2 HG01081.hp1 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*1882_*1883dupTG | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 24/24 | 2402 | chr9 | 95444509 | |||||
| chr9:95444509
|
G | GCACACA | 6 | a0002c0001t0009a0002c0001t0016a0002c0021t0009others(3): Show | 16 | HG01243.hp2 HG02257.hp2 HG02630.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1878_*1883dupTGTG others(2): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 24/24 | 2402 | chr9 | 95444509 | |||||
| chr9:95444509
|
G | GCACACAC others(3): Show |
1 | a0002c0001t0028 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1874_*1883dupTGTG others(6): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 24/24 | 2402 | chr9 | 95444509 | |||||
| chr9:95444513
|
A | G | 1 | a0001c0002t0033 | 1 | HG01123.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1880T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 24/24 | 2399 | chr9 | 95444513 | |||||
| chr9:95444571
|
T | G | 1 | a0001c0003t0031 | 1 | NA18967.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1822A>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 24/24 | 2341 | chr9 | 95444571 | |||||
| chr9:95444684
|
C | T | 7 | a0002c0001t0009a0002c0001t0016a0002c0001t0028others(4): Show | 17 | HG01243.hp2 HG02257.hp2 HG02630.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1709G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 24/24 | 2228 | chr9 | 95444684 | |||||
| chr9:95444685
|
G | A | 3 | a0002c0001t0018a0003c0011t0010a0005c0023t0010 | 6 | HG00609.hp1 HG00673.hp2 HG02056.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1708C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 24/24 | 2227 | chr9 | 95444685 | |||||
| chr9:95444691
|
G | A | 4 | a0002c0001t0009a0002c0001t0016a0002c0001t0028others(1): Show | 8 | HG02257.hp2 HG02630.hp1 HG02809.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1702C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 24/24 | 2221 | chr9 | 95444691 | |||||
| chr9:95444777
|
T | G | 7 | a0002c0001t0009a0002c0001t0016a0002c0001t0028others(4): Show | 17 | HG01243.hp2 HG02257.hp2 HG02630.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1616A>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 24/24 | 2135 | chr9 | 95444777 | |||||
| chr9:95444848
|
A | G | 3 | a0001c0002t0020a0001c0003t0023a0001c0015t0039 | 5 | HG01081.hp2 HG02451.hp2 HG02647.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1545T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 24/24 | 2064 | chr9 | 95444848 | |||||
| chr9:95444858
|
A | G | 3 | a0001c0002t0020a0001c0003t0023a0001c0015t0039 | 5 | HG01081.hp2 HG02451.hp2 HG02647.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1535T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 24/24 | 2054 | chr9 | 95444858 | |||||
| chr9:95445020
|
C | G | 8 | a0001c0002t0003a0001c0003t0003a0001c0003t0030others(5): Show | 27 | HG00597.hp1 HG01074.hp2 HG01099.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*1373G>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 24/24 | 1892 | chr9 | 95445020 | |||||
| chr9:95445327
|
T | G | 2 | a0001c0003t0023a0001c0015t0039 | 3 | HG01081.hp2 HG02451.hp2 HG02647.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1066A>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 24/24 | 1585 | chr9 | 95445327 | |||||
| chr9:95445542
|
C | G | 1 | a0004c0006t0006 | 7 | HG01243.hp2 HG02922.hp1 HG03098.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*851G>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 24/24 | 1370 | chr9 | 95445542 | |||||
| chr9:95445592
|
G | A | 1 | a0001c0015t0039 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*801C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 24/24 | 1320 | chr9 | 95445592 | |||||
| chr9:95445606
|
G | A | 2 | a0001c0004t0019a0003c0005t0019 | 2 | NA18962.hp1 NA19083.hp1 |
3_prime_UTR_variant | MODIFIER | c.*787C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 24/24 | 1306 | chr9 | 95445606 | |||||
| chr9:95445613
|
G | A | 3 | a0001c0008t0015a0001c0037t0024a0015c0038t0015 | 3 | HG02015.hp2 HG02071.hp2 HG04199.hp1 |
3_prime_UTR_variant | MODIFIER | c.*780C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 24/24 | 1299 | chr9 | 95445613 | |||||
| chr9:95445644
|
G | GAAAT | 3 | a0001c0008t0015a0001c0037t0024a0015c0038t0015 | 3 | HG02015.hp2 HG02071.hp2 HG04199.hp1 |
3_prime_UTR_variant | MODIFIER | c.*748_*749insATTT | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 24/24 | 1267 | chr9 | 95445644 | |||||
| chr9:95445644
|
G | GAAGT | 9 | a0001c0002t0003a0001c0003t0003a0001c0003t0030others(6): Show | 28 | HG00597.hp1 HG01074.hp2 HG01099.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*748_*749insACTT | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 24/24 | 1267 | chr9 | 95445644 | |||||
| chr9:95445728
|
C | CA | 21 | a0001c0002t0007a0001c0002t0011a0001c0002t0013others(18): Show | 44 | HG01069.hp1 HG01071.hp2 HG01081.hp2 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*664dupT | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 24/24 | 1183 | chr9 | 95445728 | |||||
| chr9:95445943
|
T | G | 1 | a0001c0002t0040 | 1 | HG01358.hp2 | 3_prime_UTR_variant | MODIFIER | c.*450A>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 24/24 | 969 | chr9 | 95445943 | |||||
| chr9:95446156
|
C | G | 10 | a0001c0002t0013a0001c0003t0008a0001c0003t0013others(7): Show | 24 | HG01069.hp1 HG01071.hp2 HG01243.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*237G>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 24/24 | 756 | chr9 | 95446156 | |||||
| chr9:95446162
|
A | G | 1 | a0002c0001t0014 | 3 | HG01123.hp2 HG01516.hp1 HG01517.hp2 |
3_prime_UTR_variant | MODIFIER | c.*231T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 24/24 | 750 | chr9 | 95446162 | |||||
| chr9:95446248
|
A | G | 1 | a0002c0001t0026 | 1 | NA19062.hp1 | 3_prime_UTR_variant | MODIFIER | c.*145T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 24/24 | 664 | chr9 | 95446248 | |||||
| chr9:95446288
|
C | T | 1 | a0001c0004t0025 | 1 | NA18946.hp1 | 3_prime_UTR_variant | MODIFIER | c.*105G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 24/24 | 624 | chr9 | 95446288 | |||||
| chr9:95446308
|
C | T | 2 | a0001c0002t0013a0001c0003t0013 | 3 | HG01069.hp1 HG01071.hp2 HG02109.hp2 |
3_prime_UTR_variant | MODIFIER | c.*85G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 24/24 | 604 | chr9 | 95446308 | |||||
| chr9:95516875
|
T | A | 1 | a0001c0004t0041 | 1 | NA19068.hp1 | 5_prime_UTR_variant | MODIFIER | c.-55A>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/24 | 55 | chr9 | 95516875 | |||||
| chr9:95516878
|
C | A | 1 | a0001c0004t0041 | 1 | NA19068.hp1 | 5_prime_UTR_variant | MODIFIER | c.-58G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/24 | 58 | chr9 | 95516878 | |||||
| chr9:95516952
|
C | T | 4 | a0001c0008t0012a0001c0008t0015a0001c0037t0024others(1): Show | 6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-132G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/24 | chr9 | 95516952 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:95446437
|
G | A | 1 | a0001c0002t0011g0188 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.*2-46C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 23/23 | chr9 | 95446437 | ||||||
| chr9:95446505
|
G | A | 5 | a0001c0002t0001g0106a0001c0002t0001g0112a0001c0002t0001g0153others(2): Show | 5 | NA18962.hp1 NA19003.hp2 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.*2-114C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 23/23 | chr9 | 95446505 | ||||||
| chr9:95446508
|
G | A | 1 | a0002c0001t0003g0101 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.*2-117C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 23/23 | chr9 | 95446508 | ||||||
| chr9:95446571
|
C | T | 1 | a0001c0009t0001g0247 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.*2-180G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 23/23 | chr9 | 95446571 | ||||||
| chr9:95446682
|
C | T | 2 | a0001c0002t0003g0235a0001c0003t0003g0168 | 2 | HG01074.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.*1+229G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 23/23 | chr9 | 95446682 | ||||||
| chr9:95446773
|
A | G | 2 | a0002c0035t0038g0099a0004c0006t0006g0021 | 2 | HG02717.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.*1+138T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 23/23 | chr9 | 95446773 | ||||||
| chr9:95446812
|
C | T | 2 | a0002c0001t0001g0052a0002c0001t0001g0064 | 2 | NA18960.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.*1+99G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 23/23 | chr9 | 95446812 | ||||||
| chr9:95446874
|
T | C | 20 | a0001c0004t0001g0245a0002c0001t0001g0003a0002c0001t0001g0045others(17): Show | 21 | HG00597.hp2 HG02040.hp1 NA18939.hp1 others(18): Show |
intron_variant | MODIFIER | c.*1+37A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 23/23 | chr9 | 95446874 | ||||||
| chr9:95446904
|
C | T | 1 | a0002c0001t0001g0048 | 1 | NA18975.hp1 | splice_region_variant&intron_variant | LOW | c.*1+7G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 23/23 | chr9 | 95446904 | ||||||
| chr9:95447460
|
G | A | 2 | a0002c0001t0001g0090a0010c0028t0001g0150 | 2 | NA18965.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.3802-9C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 22/23 | chr9 | 95447460 | ||||||
| chr9:95447617
|
C | T | 8 | a0001c0008t0012g0014a0001c0008t0012g0017a0001c0008t0012g0018others(5): Show | 9 | HG00423.hp2 HG00609.hp1 HG02015.hp2 others(6): Show |
intron_variant | MODIFIER | c.3802-166G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 22/23 | chr9 | 95447617 | ||||||
| chr9:95447648
|
A | T | 8 | a0001c0002t0002g0214a0001c0002t0013g0009a0001c0003t0013g0209others(5): Show | 9 | HG01069.hp1 HG01071.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.3802-197T>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 22/23 | chr9 | 95447648 | ||||||
| chr9:95447676
|
G | A | 27 | a0001c0002t0002g0214a0001c0002t0007g0036a0001c0002t0011g0008others(24): Show | 31 | HG00423.hp2 HG00609.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.3802-225C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 22/23 | chr9 | 95447676 | ||||||
| chr9:95447802
|
G | A | 1 | a0001c0030t0032g0211 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3802-351C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 22/23 | chr9 | 95447802 | ||||||
| chr9:95447888
|
G | A | 8 | a0001c0002t0004g0071a0003c0005t0002g0206a0003c0005t0002g0225others(5): Show | 8 | HG01884.hp2 HG02559.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.3802-437C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 22/23 | chr9 | 95447888 | ||||||
| chr9:95448223
|
C | T | 2 | a0001c0002t0005g0204a0001c0002t0005g0205 | 2 | HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3802-772G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 22/23 | chr9 | 95448223 | ||||||
| chr9:95448224
|
G | A | 1 | a0004c0006t0006g0021 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3802-773C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 22/23 | chr9 | 95448224 | ||||||
| chr9:95448227
|
C | T | 1 | a0001c0002t0002g0261 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3802-776G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 22/23 | chr9 | 95448227 | ||||||
| chr9:95448659
|
G | T | 59 | a0001c0002t0002g0261a0001c0002t0003g0235a0001c0002t0005g0201others(56): Show | 60 | HG00423.hp2 HG00597.hp1 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.3801+410C>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 22/23 | chr9 | 95448659 | ||||||
| chr9:95448730
|
G | GA | 33 | a0001c0002t0001g0106a0001c0003t0003g0174a0003c0005t0001g0011others(30): Show | 35 | HG00558.hp2 HG00609.hp1 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.3801+338dupT | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 22/23 | chr9 | 95448730 | ||||||
| chr9:95449438
|
C | A | 2 | a0001c0003t0001g0191a0001c0003t0001g0192 | 2 | HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.3547-115G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 21/23 | chr9 | 95449438 | ||||||
| chr9:95449661
|
G | A | 1 | a0001c0003t0001g0007 | 2 | NA18954.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.3546+180C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 21/23 | chr9 | 95449661 | ||||||
| chr9:95449678
|
C | G | 1 | a0001c0009t0001g0246 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.3546+163G>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 21/23 | chr9 | 95449678 | ||||||
| chr9:95449706
|
C | T | 6 | a0001c0008t0012g0014a0001c0008t0012g0017a0001c0008t0012g0018others(3): Show | 6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.3546+135G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 21/23 | chr9 | 95449706 | ||||||
| chr9:95449803
|
C | A | 2 | a0001c0014t0021g0212a0001c0014t0021g0213 | 2 | HG02818.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.3546+38G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 21/23 | chr9 | 95449803 | ||||||
| chr9:95450027
|
C | T | 1 | a0001c0003t0003g0174 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.3447-87G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 20/23 | chr9 | 95450027 | ||||||
| chr9:95450072
|
A | C | 2 | a0001c0003t0001g0191a0001c0003t0001g0192 | 2 | HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.3447-132T>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 20/23 | chr9 | 95450072 | ||||||
| chr9:95450238
|
A | G | 1 | a0002c0034t0001g0145 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3447-298T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 20/23 | chr9 | 95450238 | ||||||
| chr9:95450270
|
C | T | 8 | a0001c0002t0002g0261a0001c0002t0005g0201a0001c0002t0005g0204others(5): Show | 8 | HG01952.hp1 HG02109.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.3447-330G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 20/23 | chr9 | 95450270 | ||||||
| chr9:95450326
|
C | T | 29 | a0001c0002t0003g0235a0001c0003t0001g0007a0001c0003t0001g0160others(26): Show | 30 | HG00597.hp1 HG00738.hp2 HG01074.hp2 others(27): Show |
intron_variant | MODIFIER | c.3447-386G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 20/23 | chr9 | 95450326 | ||||||
| chr9:95450788
|
G | C | 3 | a0001c0003t0004g0196a0001c0003t0005g0197a0009c0026t0002g0190 | 3 | HG01952.hp1 HG02145.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.3447-848C>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 20/23 | chr9 | 95450788 | ||||||
| chr9:95451004
|
A | AG | 29 | a0001c0002t0011g0188a0001c0002t0040g0230a0001c0004t0001g0012others(26): Show | 30 | HG00140.hp2 HG01109.hp2 HG01175.hp1 others(27): Show |
intron_variant | MODIFIER | c.3447-1065dupC | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 20/23 | chr9 | 95451004 | ||||||
| chr9:95451071
|
T | G | 2 | a0001c0015t0002g0055a0001c0015t0039g0130 | 2 | HG01081.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.3447-1131A>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 20/23 | chr9 | 95451071 | ||||||
| chr9:95451404
|
G | C | 1 | a0001c0003t0008g0194 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3447-1464C>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 20/23 | chr9 | 95451404 | ||||||
| chr9:95451446
|
C | G | 28 | a0001c0002t0040g0230a0001c0004t0001g0012a0001c0004t0001g0078others(25): Show | 29 | HG00140.hp2 HG01175.hp1 HG01358.hp2 others(26): Show |
intron_variant | MODIFIER | c.3447-1506G>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 20/23 | chr9 | 95451446 | ||||||
| chr9:95451478
|
G | A | 1 | a0001c0004t0001g0232 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3447-1538C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 20/23 | chr9 | 95451478 | ||||||
| chr9:95451627
|
T | C | 2 | a0001c0002t0005g0204a0001c0002t0005g0205 | 2 | HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3447-1687A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 20/23 | chr9 | 95451627 | ||||||
| chr9:95452085
|
A | G | 28 | a0001c0002t0040g0230a0001c0004t0001g0012a0001c0004t0001g0078others(25): Show | 29 | HG00140.hp2 HG01175.hp1 HG01358.hp2 others(26): Show |
intron_variant | MODIFIER | c.3446+1393T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 20/23 | chr9 | 95452085 | ||||||
| chr9:95452328
|
G | GAC | 5 | a0001c0002t0001g0083a0001c0002t0002g0195a0002c0001t0003g0151others(2): Show | 5 | HG01255.hp1 HG02451.hp1 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.3446+1148_3446+114 others(6): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 20/23 | chr9 | 95452328 | ||||||
| chr9:95452328
|
G | GACACAC | 12 | a0001c0002t0002g0261a0001c0002t0005g0207a0001c0002t0013g0009others(9): Show | 14 | HG01069.hp1 HG01071.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.3446+1144_3446+114 others(10): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 20/23 | chr9 | 95452328 | ||||||
| chr9:95452328
|
G | GACACACA others(1): Show |
7 | a0001c0002t0002g0214a0001c0002t0040g0230a0001c0036t0001g0234others(4): Show | 7 | HG01358.hp2 HG01884.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.3446+1142_3446+114 others(12): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 20/23 | chr9 | 95452328 | ||||||
| chr9:95452328
|
G | GACACACA others(3): Show |
32 | a0001c0002t0005g0201a0001c0002t0005g0259a0001c0002t0020g0035others(29): Show | 33 | HG00140.hp2 HG01175.hp1 HG01361.hp1 others(30): Show |
intron_variant | MODIFIER | c.3446+1140_3446+114 others(14): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 20/23 | chr9 | 95452328 | ||||||
| chr9:95452328
|
G | GACACACA others(5): Show |
11 | a0001c0003t0003g0169a0001c0003t0003g0181a0001c0003t0004g0196others(8): Show | 11 | HG00423.hp2 HG01192.hp2 HG01952.hp1 others(8): Show |
intron_variant | MODIFIER | c.3446+1138_3446+114 others(16): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 20/23 | chr9 | 95452328 | ||||||
| chr9:95452328
|
G | GACACACA others(7): Show |
10 | a0001c0002t0005g0204a0001c0002t0005g0205a0001c0003t0003g0174others(7): Show | 10 | HG02027.hp1 HG02109.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.3446+1136_3446+114 others(18): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 20/23 | chr9 | 95452328 | ||||||
| chr9:95452328
|
G | GACACACA others(9): Show |
25 | a0001c0003t0001g0007a0001c0003t0001g0160a0001c0003t0001g0166others(22): Show | 26 | HG00738.hp2 HG01099.hp1 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.3446+1134_3446+114 others(20): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 20/23 | chr9 | 95452328 | ||||||
| chr9:95452328
|
G | GACACACA others(11): Show |
5 | a0001c0003t0003g0170a0001c0004t0003g0255a0001c0008t0015g0015others(2): Show | 5 | HG01517.hp1 HG02015.hp2 HG04199.hp1 others(2): Show |
intron_variant | MODIFIER | c.3446+1132_3446+114 others(22): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 20/23 | chr9 | 95452328 | ||||||
| chr9:95452328
|
G | GACACACA others(13): Show |
1 | a0001c0003t0004g0159 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.3446+1130_3446+114 others(24): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 20/23 | chr9 | 95452328 | ||||||
| chr9:95452328
|
G | GACACACA others(15): Show |
1 | a0001c0003t0003g0171 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.3446+1128_3446+114 others(26): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 20/23 | chr9 | 95452328 | ||||||
| chr9:95452328
|
GAC | G | 92 | a0001c0002t0001g0061a0001c0002t0001g0085a0001c0002t0001g0254others(89): Show | 99 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.3446+1148_3446+114 others(6): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 20/23 | chr9 | 95452328 | ||||||
| chr9:95452356
|
C | CACACACA others(6): Show |
1 | a0001c0002t0003g0235 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.3446+1121_3446+112 others(17): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 20/23 | chr9 | 95452356 | ||||||
| chr9:95452357
|
A | ACACACAC others(12): Show |
1 | a0001c0003t0031g0253 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.3446+1120_3446+112 others(23): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 20/23 | chr9 | 95452357 | ||||||
| chr9:95452476
|
C | T | 38 | a0001c0002t0002g0214a0001c0002t0013g0009a0001c0002t0040g0230others(35): Show | 40 | HG00140.hp2 HG01069.hp1 HG01071.hp2 others(37): Show |
intron_variant | MODIFIER | c.3446+1002G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 20/23 | chr9 | 95452476 | ||||||
| chr9:95452903
|
T | C | 29 | a0001c0002t0003g0235a0001c0003t0001g0007a0001c0003t0001g0160others(26): Show | 30 | HG00597.hp1 HG00738.hp2 HG01074.hp2 others(27): Show |
intron_variant | MODIFIER | c.3446+575A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 20/23 | chr9 | 95452903 | ||||||
| chr9:95453024
|
C | T | 50 | a0001c0002t0002g0214a0001c0002t0007g0036a0001c0002t0013g0009others(47): Show | 54 | HG00140.hp2 HG01069.hp1 HG01071.hp2 others(51): Show |
intron_variant | MODIFIER | c.3446+454G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 20/23 | chr9 | 95453024 | ||||||
| chr9:95453046
|
T | C | 6 | a0004c0006t0006g0001a0004c0006t0006g0021a0004c0006t0006g0028others(3): Show | 7 | HG01243.hp2 HG02922.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.3446+432A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 20/23 | chr9 | 95453046 | ||||||
| chr9:95453113
|
C | A | 1 | a0003c0005t0002g0128 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3446+365G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 20/23 | chr9 | 95453113 | ||||||
| chr9:95453114
|
G | A | 1 | a0001c0003t0003g0165 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.3446+364C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 20/23 | chr9 | 95453114 | ||||||
| chr9:95453141
|
T | A | 2 | a0001c0002t0011g0008a0001c0002t0011g0185 | 3 | HG01243.hp1 HG03130.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.3446+337A>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 20/23 | chr9 | 95453141 | ||||||
| chr9:95453244
|
G | A | 1 | a0001c0009t0001g0248 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.3446+234C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 20/23 | chr9 | 95453244 | ||||||
| chr9:95453349
|
T | C | 40 | a0001c0002t0003g0235a0001c0003t0001g0007a0001c0003t0001g0160others(37): Show | 41 | HG00597.hp1 HG00738.hp2 HG01074.hp2 others(38): Show |
intron_variant | MODIFIER | c.3446+129A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 20/23 | chr9 | 95453349 | ||||||
| chr9:95453686
|
C | G | 31 | a0003c0005t0001g0011a0003c0005t0001g0140a0003c0005t0001g0175others(28): Show | 33 | HG00558.hp2 HG00609.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.3304-66G>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 19/23 | chr9 | 95453686 | ||||||
| chr9:95453772
|
C | A | 1 | a0002c0001t0001g0050 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3304-152G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 19/23 | chr9 | 95453772 | ||||||
| chr9:95453772
|
C | T | 6 | a0001c0002t0005g0201a0001c0002t0005g0204a0001c0002t0005g0205others(3): Show | 6 | HG01952.hp1 HG02109.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.3304-152G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 19/23 | chr9 | 95453772 | ||||||
| chr9:95453991
|
T | C | 6 | a0004c0006t0006g0001a0004c0006t0006g0021a0004c0006t0006g0028others(3): Show | 7 | HG01243.hp2 HG02922.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.3304-371A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 19/23 | chr9 | 95453991 | ||||||
| chr9:95454363
|
A | G | 6 | a0001c0008t0012g0014a0001c0008t0012g0017a0001c0008t0012g0018others(3): Show | 6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.3304-743T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 19/23 | chr9 | 95454363 | ||||||
| chr9:95454594
|
A | G | 151 | a0001c0002t0002g0214a0001c0002t0002g0261a0001c0002t0003g0235others(148): Show | 159 | HG00140.hp2 HG00423.hp2 HG00558.hp2 others(156): Show |
intron_variant | MODIFIER | c.3304-974T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 19/23 | chr9 | 95454594 | ||||||
| chr9:95454804
|
C | G | 1 | a0001c0002t0002g0214 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3304-1184G>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 19/23 | chr9 | 95454804 | ||||||
| chr9:95455066
|
A | G | 96 | a0001c0002t0002g0261a0001c0002t0003g0235a0001c0002t0005g0201others(93): Show | 100 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(97): Show |
intron_variant | MODIFIER | c.3303+1210T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 19/23 | chr9 | 95455066 | ||||||
| chr9:95455226
|
C | T | 1 | a0001c0002t0001g0083 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.3303+1050G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 19/23 | chr9 | 95455226 | ||||||
| chr9:95455299
|
T | C | 151 | a0001c0002t0002g0214a0001c0002t0002g0261a0001c0002t0003g0235others(148): Show | 159 | HG00140.hp2 HG00423.hp2 HG00558.hp2 others(156): Show |
intron_variant | MODIFIER | c.3303+977A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 19/23 | chr9 | 95455299 | ||||||
| chr9:95455328
|
G | A | 2 | a0001c0002t0002g0107a0001c0002t0002g0139 | 2 | HG01071.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.3303+948C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 19/23 | chr9 | 95455328 | ||||||
| chr9:95455442
|
C | G | 9 | a0001c0003t0004g0198a0001c0003t0004g0199a0001c0003t0004g0200others(6): Show | 9 | HG02630.hp2 HG02895.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.3303+834G>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 19/23 | chr9 | 95455442 | ||||||
| chr9:95455462
|
C | T | 2 | a0004c0006t0001g0032a0004c0006t0001g0033 | 2 | HG01884.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.3303+814G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 19/23 | chr9 | 95455462 | ||||||
| chr9:95455495
|
T | C | 2 | a0001c0014t0021g0212a0001c0014t0021g0213 | 2 | HG02818.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.3303+781A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 19/23 | chr9 | 95455495 | ||||||
| chr9:95455507
|
A | G | 3 | a0001c0003t0023g0038a0001c0015t0002g0055a0001c0015t0039g0130 | 3 | HG01081.hp2 HG02647.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.3303+769T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 19/23 | chr9 | 95455507 | ||||||
| chr9:95455728
|
T | G | 2 | a0001c0002t0013g0009a0001c0003t0013g0209 | 3 | HG01069.hp1 HG01071.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.3303+548A>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 19/23 | chr9 | 95455728 | ||||||
| chr9:95455759
|
C | T | 8 | a0001c0002t0005g0201a0001c0002t0005g0204a0001c0002t0005g0205others(5): Show | 8 | HG01952.hp1 HG02109.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.3303+517G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 19/23 | chr9 | 95455759 | ||||||
| chr9:95455760
|
G | A | 2 | a0001c0014t0021g0212a0001c0014t0021g0213 | 2 | HG02818.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.3303+516C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 19/23 | chr9 | 95455760 | ||||||
| chr9:95455960
|
G | A | 2 | a0002c0034t0001g0145a0002c0035t0038g0099 | 2 | HG02717.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3303+316C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 19/23 | chr9 | 95455960 | ||||||
| chr9:95456030
|
C | T | 1 | a0003c0005t0001g0223 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.3303+246G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 19/23 | chr9 | 95456030 | ||||||
| chr9:95456160
|
G | A | 2 | a0001c0014t0021g0212a0001c0014t0021g0213 | 2 | HG02818.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.3303+116C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 19/23 | chr9 | 95456160 | ||||||
| chr9:95456192
|
G | GC | 152 | a0001c0002t0002g0214a0001c0002t0002g0261a0001c0002t0003g0235others(149): Show | 160 | HG00140.hp2 HG00423.hp2 HG00558.hp2 others(157): Show |
intron_variant | MODIFIER | c.3303+83dupG | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 19/23 | chr9 | 95456192 | ||||||
| chr9:95456418
|
A | G | 1 | a0001c0002t0001g0083 | 1 | HG03491.hp2 | splice_region_variant&intron_variant | LOW | c.3166-5T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 18/23 | chr9 | 95456418 | ||||||
| chr9:95456710
|
G | A | 1 | a0003c0005t0002g0225 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3166-297C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 18/23 | chr9 | 95456710 | ||||||
| chr9:95456755
|
C | T | 2 | a0001c0014t0021g0212a0001c0014t0021g0213 | 2 | HG02818.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.3166-342G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 18/23 | chr9 | 95456755 | ||||||
| chr9:95456761
|
T | TCA | 8 | a0001c0008t0012g0014a0001c0008t0012g0017a0001c0008t0012g0018others(5): Show | 8 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.3166-350_3166-349d others(4): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 18/23 | chr9 | 95456761 | ||||||
| chr9:95456984
|
G | A | 1 | a0002c0022t0001g0075 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.3166-571C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 18/23 | chr9 | 95456984 | ||||||
| chr9:95457009
|
C | T | 4 | a0001c0002t0002g0005a0001c0002t0002g0041a0001c0002t0002g0067others(1): Show | 5 | HG01358.hp1 HG01934.hp2 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.3166-596G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 18/23 | chr9 | 95457009 | ||||||
| chr9:95457022
|
C | G | 1 | a0001c0002t0005g0207 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3166-609G>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 18/23 | chr9 | 95457022 | ||||||
| chr9:95457565
|
T | C | 4 | a0002c0001t0001g0049a0002c0001t0001g0050a0002c0001t0001g0051others(1): Show | 4 | NA18939.hp1 NA18967.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.3165+448A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 18/23 | chr9 | 95457565 | ||||||
| chr9:95457667
|
T | C | 1 | a0002c0001t0001g0138 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3165+346A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 18/23 | chr9 | 95457667 | ||||||
| chr9:95457755
|
G | A | 5 | a0002c0001t0001g0056a0002c0001t0001g0062a0002c0001t0014g0057others(2): Show | 5 | HG01123.hp2 HG01516.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.3165+258C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 18/23 | chr9 | 95457755 | ||||||
| chr9:95457777
|
G | C | 1 | a0001c0002t0002g0261 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3165+236C>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 18/23 | chr9 | 95457777 | ||||||
| chr9:95457780
|
C | T | 1 | a0003c0005t0002g0206 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3165+233G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 18/23 | chr9 | 95457780 | ||||||
| chr9:95457793
|
C | T | 1 | a0002c0001t0002g0131 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.3165+220G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 18/23 | chr9 | 95457793 | ||||||
| chr9:95458432
|
T | C | 2 | a0001c0014t0021g0212a0001c0014t0021g0213 | 2 | HG02818.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2885-139A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 17/23 | chr9 | 95458432 | ||||||
| chr9:95458564
|
C | T | 2 | a0004c0006t0001g0032a0004c0006t0001g0033 | 2 | HG01884.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.2885-271G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 17/23 | chr9 | 95458564 | ||||||
| chr9:95458576
|
AT | A | 6 | a0001c0008t0012g0014a0001c0008t0012g0017a0001c0008t0012g0018others(3): Show | 6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.2885-284delA | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 17/23 | chr9 | 95458576 | ||||||
| chr9:95458939
|
C | T | 2 | a0001c0002t0020g0035a0001c0002t0020g0042 | 2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2885-646G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 17/23 | chr9 | 95458939 | ||||||
| chr9:95459017
|
G | A | 1 | a0001c0002t0001g0112 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.2884+583C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 17/23 | chr9 | 95459017 | ||||||
| chr9:95459272
|
C | T | 3 | a0003c0011t0010g0010a0003c0011t0010g0123a0005c0023t0010g0218 | 4 | HG00609.hp1 HG00673.hp2 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.2884+328G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 17/23 | chr9 | 95459272 | ||||||
| chr9:95459306
|
C | T | 1 | a0001c0003t0008g0194 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2884+294G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 17/23 | chr9 | 95459306 | ||||||
| chr9:95459340
|
G | A | 1 | a0001c0015t0039g0130 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2884+260C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 17/23 | chr9 | 95459340 | ||||||
| chr9:95459418
|
G | A | 6 | a0001c0008t0012g0014a0001c0008t0012g0017a0001c0008t0012g0018others(3): Show | 6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.2884+182C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 17/23 | chr9 | 95459418 | ||||||
| chr9:95459512
|
G | A | 1 | a0002c0001t0001g0088 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2884+88C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 17/23 | chr9 | 95459512 | ||||||
| chr9:95459563
|
T | C | 3 | a0001c0002t0011g0008a0001c0002t0011g0185a0001c0002t0011g0188 | 4 | HG01109.hp2 HG01243.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.2884+37A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 17/23 | chr9 | 95459563 | ||||||
| chr9:95459579
|
T | C | 151 | a0001c0002t0002g0214a0001c0002t0002g0261a0001c0002t0003g0235others(148): Show | 159 | HG00140.hp2 HG00423.hp2 HG00558.hp2 others(156): Show |
intron_variant | MODIFIER | c.2884+21A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 17/23 | chr9 | 95459579 | ||||||
| chr9:95459891
|
T | C | 2 | a0001c0002t0002g0119a0001c0002t0002g0147 | 2 | HG02735.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.2701-108A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 16/23 | chr9 | 95459891 | ||||||
| chr9:95460072
|
A | G | 1 | a0001c0002t0005g0207 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2701-289T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 16/23 | chr9 | 95460072 | ||||||
| chr9:95460145
|
C | T | 4 | a0002c0001t0001g0049a0002c0001t0001g0050a0002c0001t0001g0051others(1): Show | 4 | NA18939.hp1 NA18967.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.2701-362G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 16/23 | chr9 | 95460145 | ||||||
| chr9:95460298
|
G | A | 4 | a0001c0002t0007g0036a0006c0010t0007g0013a0006c0010t0007g0263others(1): Show | 5 | HG02145.hp1 HG02572.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2701-515C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 16/23 | chr9 | 95460298 | ||||||
| chr9:95460299
|
T | G | 1 | a0002c0001t0002g0131 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2701-516A>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 16/23 | chr9 | 95460299 | ||||||
| chr9:95460349
|
G | A | 1 | a0009c0026t0002g0190 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2701-566C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 16/23 | chr9 | 95460349 | ||||||
| chr9:95460365
|
C | T | 1 | a0001c0002t0001g0254 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2701-582G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 16/23 | chr9 | 95460365 | ||||||
| chr9:95460369
|
C | T | 33 | a0001c0024t0001g0227a0003c0005t0001g0011a0003c0005t0001g0140others(30): Show | 35 | HG00558.hp2 HG00609.hp1 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.2701-586G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 16/23 | chr9 | 95460369 | ||||||
| chr9:95460371
|
C | T | 1 | a0001c0030t0032g0211 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2701-588G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 16/23 | chr9 | 95460371 | ||||||
| chr9:95460383
|
C | T | 38 | a0001c0002t0002g0214a0001c0002t0007g0036a0001c0002t0013g0009others(35): Show | 41 | HG00140.hp2 HG00609.hp2 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.2701-600G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 16/23 | chr9 | 95460383 | ||||||
| chr9:95460404
|
G | A | 3 | a0001c0002t0005g0204a0001c0002t0005g0205a0009c0026t0002g0190 | 3 | HG01952.hp1 HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2701-621C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 16/23 | chr9 | 95460404 | ||||||
| chr9:95460416
|
T | C | 1 | a0001c0003t0003g0179 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2701-633A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 16/23 | chr9 | 95460416 | ||||||
| chr9:95460467
|
C | T | 6 | a0001c0008t0012g0014a0001c0008t0012g0017a0001c0008t0012g0018others(3): Show | 6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.2701-684G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 16/23 | chr9 | 95460467 | ||||||
| chr9:95460505
|
T | G | 1 | a0002c0001t0009g0114 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2701-722A>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 16/23 | chr9 | 95460505 | ||||||
| chr9:95460510
|
A | G | 2 | a0001c0002t0005g0204a0001c0002t0005g0205 | 2 | HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2701-727T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 16/23 | chr9 | 95460510 | ||||||
| chr9:95460527
|
C | T | 1 | a0001c0003t0037g0037 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2701-744G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 16/23 | chr9 | 95460527 | ||||||
| chr9:95460588
|
G | C | 1 | a0001c0002t0003g0235 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2701-805C>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 16/23 | chr9 | 95460588 | ||||||
| chr9:95460646
|
A | C | 1 | a0001c0004t0001g0238 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2701-863T>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 16/23 | chr9 | 95460646 | ||||||
| chr9:95460751
|
G | C | 1 | a0002c0035t0038g0099 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2701-968C>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 16/23 | chr9 | 95460751 | ||||||
| chr9:95461155
|
A | G | 6 | a0004c0006t0006g0001a0004c0006t0006g0021a0004c0006t0006g0028others(3): Show | 7 | HG01243.hp2 HG02922.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.2700+701T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 16/23 | chr9 | 95461155 | ||||||
| chr9:95461179
|
T | C | 2 | a0014c0017t0022g0020a0016c0039t0022g0262 | 2 | HG02723.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.2700+677A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 16/23 | chr9 | 95461179 | ||||||
| chr9:95461230
|
A | T | 1 | a0001c0002t0011g0188 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2700+626T>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 16/23 | chr9 | 95461230 | ||||||
| chr9:95461275
|
C | T | 1 | a0002c0001t0001g0088 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2700+581G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 16/23 | chr9 | 95461275 | ||||||
| chr9:95461394
|
C | T | 1 | a0001c0030t0032g0211 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2700+462G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 16/23 | chr9 | 95461394 | ||||||
| chr9:95461416
|
C | T | 1 | a0002c0001t0002g0131 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2700+440G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 16/23 | chr9 | 95461416 | ||||||
| chr9:95461455
|
G | T | 3 | a0001c0003t0001g0191a0001c0003t0001g0192a0001c0003t0037g0037 | 3 | HG02622.hp2 HG02965.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2700+401C>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 16/23 | chr9 | 95461455 | ||||||
| chr9:95461556
|
A | G | 1 | a0010c0028t0001g0150 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2700+300T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 16/23 | chr9 | 95461556 | ||||||
| chr9:95461560
|
T | C | 1 | a0001c0003t0003g0179 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2700+296A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 16/23 | chr9 | 95461560 | ||||||
| chr9:95461574
|
C | T | 11 | a0001c0003t0004g0196a0001c0003t0004g0198a0001c0003t0004g0199others(8): Show | 11 | HG02145.hp2 HG02615.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.2700+282G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 16/23 | chr9 | 95461574 | ||||||
| chr9:95462061
|
G | A | 1 | a0002c0001t0001g0134 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2558-63C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 15/23 | chr9 | 95462061 | ||||||
| chr9:95462078
|
C | G | 151 | a0001c0002t0002g0214a0001c0002t0002g0261a0001c0002t0003g0235others(148): Show | 159 | HG00140.hp2 HG00423.hp2 HG00558.hp2 others(156): Show |
intron_variant | MODIFIER | c.2558-80G>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 15/23 | chr9 | 95462078 | ||||||
| chr9:95462205
|
G | C | 11 | a0001c0003t0004g0196a0001c0003t0004g0198a0001c0003t0004g0199others(8): Show | 11 | HG02145.hp2 HG02615.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.2558-207C>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 15/23 | chr9 | 95462205 | ||||||
| chr9:95462345
|
G | A | 10 | a0001c0002t0002g0214a0001c0002t0013g0009a0001c0003t0013g0209others(7): Show | 11 | HG01069.hp1 HG01071.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.2558-347C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 15/23 | chr9 | 95462345 | ||||||
| chr9:95462403
|
A | G | 18 | a0001c0004t0001g0012a0001c0004t0001g0231a0001c0004t0001g0237others(15): Show | 19 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(16): Show |
intron_variant | MODIFIER | c.2558-405T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 15/23 | chr9 | 95462403 | ||||||
| chr9:95462429
|
T | C | 1 | a0001c0002t0001g0034 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2558-431A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 15/23 | chr9 | 95462429 | ||||||
| chr9:95462499
|
G | C | 1 | a0004c0006t0027g0025 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2558-501C>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 15/23 | chr9 | 95462499 | ||||||
| chr9:95462521
|
A | T | 1 | a0001c0002t0001g0034 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2558-523T>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 15/23 | chr9 | 95462521 | ||||||
| chr9:95462658
|
G | A | 1 | a0002c0001t0029g0040 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.2558-660C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 15/23 | chr9 | 95462658 | ||||||
| chr9:95462774
|
G | T | 102 | a0001c0002t0002g0214a0001c0002t0002g0261a0001c0002t0003g0235others(99): Show | 107 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(104): Show |
intron_variant | MODIFIER | c.2558-776C>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 15/23 | chr9 | 95462774 | ||||||
| chr9:95462832
|
C | A | 1 | a0001c0002t0005g0204 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2558-834G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 15/23 | chr9 | 95462832 | ||||||
| chr9:95462941
|
G | A | 3 | a0001c0003t0023g0038a0001c0015t0002g0055a0001c0015t0039g0130 | 3 | HG01081.hp2 HG02647.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2558-943C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 15/23 | chr9 | 95462941 | ||||||
| chr9:95462964
|
T | C | 1 | a0008c0018t0001g0154 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.2558-966A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 15/23 | chr9 | 95462964 | ||||||
| chr9:95462966
|
G | A | 1 | a0001c0003t0023g0039 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2558-968C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 15/23 | chr9 | 95462966 | ||||||
| chr9:95462999
|
C | A | 1 | a0001c0002t0005g0207 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2558-1001G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 15/23 | chr9 | 95462999 | ||||||
| chr9:95463007
|
C | T | 1 | a0001c0002t0005g0207 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2558-1009G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 15/23 | chr9 | 95463007 | ||||||
| chr9:95463110
|
G | A | 1 | a0001c0003t0005g0208 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2558-1112C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 15/23 | chr9 | 95463110 | ||||||
| chr9:95463125
|
C | T | 3 | a0004c0006t0002g0022a0004c0006t0027g0025a0004c0016t0002g0024 | 3 | HG02451.hp1 HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.2558-1127G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 15/23 | chr9 | 95463125 | ||||||
| chr9:95463139
|
C | T | 1 | a0001c0002t0001g0085 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2558-1141G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 15/23 | chr9 | 95463139 | ||||||
| chr9:95463170
|
CA | C | 44 | a0001c0002t0002g0214a0001c0002t0013g0009a0001c0002t0040g0230others(41): Show | 47 | HG00140.hp2 HG00609.hp2 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.2558-1173delT | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 15/23 | chr9 | 95463170 | ||||||
| chr9:95463187
|
C | T | 6 | a0001c0008t0012g0014a0001c0008t0012g0017a0001c0008t0012g0018others(3): Show | 6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.2558-1189G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 15/23 | chr9 | 95463187 | ||||||
| chr9:95463260
|
G | A | 12 | a0001c0003t0004g0196a0001c0003t0004g0198a0001c0003t0004g0199others(9): Show | 12 | HG02109.hp2 HG02145.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.2558-1262C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 15/23 | chr9 | 95463260 | ||||||
| chr9:95463332
|
C | T | 1 | a0002c0001t0001g0090 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2558-1334G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 15/23 | chr9 | 95463332 | ||||||
| chr9:95463376
|
C | T | 44 | a0001c0002t0002g0214a0001c0002t0013g0009a0001c0002t0040g0230others(41): Show | 47 | HG00140.hp2 HG00609.hp2 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.2558-1378G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 15/23 | chr9 | 95463376 | ||||||
| chr9:95463401
|
C | T | 51 | a0001c0002t0002g0261a0001c0002t0005g0201a0001c0002t0005g0204others(48): Show | 54 | HG00558.hp2 HG00609.hp1 HG00673.hp2 others(51): Show |
intron_variant | MODIFIER | c.2558-1403G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 15/23 | chr9 | 95463401 | ||||||
| chr9:95463425
|
T | C | 1 | a0001c0009t0001g0249 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2558-1427A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 15/23 | chr9 | 95463425 | ||||||
| chr9:95463538
|
C | T | 2 | a0002c0034t0001g0145a0002c0035t0038g0099 | 2 | HG02717.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2558-1540G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 15/23 | chr9 | 95463538 | ||||||
| chr9:95463591
|
T | A | 1 | a0001c0003t0037g0037 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2558-1593A>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 15/23 | chr9 | 95463591 | ||||||
| chr9:95463681
|
T | C | 1 | a0002c0001t0001g0124 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2558-1683A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 15/23 | chr9 | 95463681 | ||||||
| chr9:95463784
|
G | A | 50 | a0001c0002t0003g0235a0001c0003t0001g0007a0001c0003t0001g0160others(47): Show | 51 | HG00423.hp2 HG00597.hp1 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.2558-1786C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 15/23 | chr9 | 95463784 | ||||||
| chr9:95463885
|
G | A | 2 | a0004c0006t0001g0032a0004c0006t0001g0033 | 2 | HG01884.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.2558-1887C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 15/23 | chr9 | 95463885 | ||||||
| chr9:95463963
|
C | T | 1 | a0004c0016t0002g0024 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2558-1965G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 15/23 | chr9 | 95463963 | ||||||
| chr9:95463969
|
C | T | 2 | a0001c0002t0011g0008a0001c0002t0011g0185 | 3 | HG01243.hp1 HG03130.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2558-1971G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 15/23 | chr9 | 95463969 | ||||||
| chr9:95463985
|
C | T | 7 | a0001c0002t0013g0009a0004c0006t0006g0001a0004c0006t0006g0021others(4): Show | 9 | HG01069.hp1 HG01071.hp2 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.2558-1987G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 15/23 | chr9 | 95463985 | ||||||
| chr9:95463986
|
G | A | 1 | a0002c0001t0001g0088 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2558-1988C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 15/23 | chr9 | 95463986 | ||||||
| chr9:95464025
|
C | T | 44 | a0001c0002t0003g0235a0001c0003t0001g0007a0001c0003t0001g0160others(41): Show | 45 | HG00597.hp1 HG00738.hp2 HG01074.hp2 others(42): Show |
intron_variant | MODIFIER | c.2558-2027G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 15/23 | chr9 | 95464025 | ||||||
| chr9:95464113
|
A | C | 50 | a0001c0002t0003g0235a0001c0003t0001g0007a0001c0003t0001g0160others(47): Show | 51 | HG00423.hp2 HG00597.hp1 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.2558-2115T>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 15/23 | chr9 | 95464113 | ||||||
| chr9:95464262
|
A | G | 1 | a0001c0002t0001g0061 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2558-2264T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 15/23 | chr9 | 95464262 | ||||||
| chr9:95464420
|
T | C | 50 | a0001c0002t0003g0235a0001c0003t0001g0007a0001c0003t0001g0160others(47): Show | 51 | HG00423.hp2 HG00597.hp1 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.2558-2422A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 15/23 | chr9 | 95464420 | ||||||
| chr9:95464748
|
T | C | 2 | a0001c0003t0023g0038a0001c0030t0032g0211 | 2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.2557+2368A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 15/23 | chr9 | 95464748 | ||||||
| chr9:95464876
|
C | T | 2 | a0002c0001t0001g0082a0002c0001t0001g0138 | 2 | HG01175.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.2557+2240G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 15/23 | chr9 | 95464876 | ||||||
| chr9:95464951
|
T | C | 26 | a0001c0024t0001g0227a0003c0005t0001g0011a0003c0005t0001g0140others(23): Show | 28 | HG00558.hp2 HG00609.hp1 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.2557+2165A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 15/23 | chr9 | 95464951 | ||||||
| chr9:95465003
|
G | A | 1 | a0001c0002t0011g0188 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2557+2113C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 15/23 | chr9 | 95465003 | ||||||
| chr9:95465056
|
G | A | 1 | a0001c0002t0011g0188 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2557+2060C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 15/23 | chr9 | 95465056 | ||||||
| chr9:95465133
|
C | T | 50 | a0001c0002t0003g0235a0001c0003t0001g0007a0001c0003t0001g0160others(47): Show | 51 | HG00423.hp2 HG00597.hp1 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.2557+1983G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 15/23 | chr9 | 95465133 | ||||||
| chr9:95465451
|
G | A | 2 | a0001c0002t0020g0035a0001c0002t0020g0042 | 2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2557+1665C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 15/23 | chr9 | 95465451 | ||||||
| chr9:95465479
|
C | T | 2 | a0001c0003t0023g0038a0001c0030t0032g0211 | 2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.2557+1637G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 15/23 | chr9 | 95465479 | ||||||
| chr9:95465505
|
A | G | 1 | a0001c0002t0002g0195 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2557+1611T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 15/23 | chr9 | 95465505 | ||||||
| chr9:95465528
|
G | T | 50 | a0001c0002t0003g0235a0001c0003t0001g0007a0001c0003t0001g0160others(47): Show | 51 | HG00423.hp2 HG00597.hp1 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.2557+1588C>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 15/23 | chr9 | 95465528 | ||||||
| chr9:95465667
|
G | A | 2 | a0001c0002t0001g0073a0001c0002t0001g0074 | 2 | HG00639.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.2557+1449C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 15/23 | chr9 | 95465667 | ||||||
| chr9:95465719
|
A | G | 1 | a0001c0003t0023g0039 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2557+1397T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 15/23 | chr9 | 95465719 | ||||||
| chr9:95465897
|
T | C | 1 | a0002c0001t0001g0125 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2557+1219A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 15/23 | chr9 | 95465897 | ||||||
| chr9:95465943
|
C | T | 48 | a0001c0002t0002g0214a0001c0002t0013g0009a0001c0002t0040g0230others(45): Show | 51 | HG00140.hp2 HG00609.hp2 HG01069.hp1 others(48): Show |
intron_variant | MODIFIER | c.2557+1173G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 15/23 | chr9 | 95465943 | ||||||
| chr9:95466132
|
C | A | 1 | a0001c0003t0023g0039 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2557+984G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 15/23 | chr9 | 95466132 | ||||||
| chr9:95466255
|
C | A | 1 | a0001c0002t0005g0259 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2557+861G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 15/23 | chr9 | 95466255 | ||||||
| chr9:95466379
|
T | G | 1 | a0001c0002t0001g0093 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2557+737A>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 15/23 | chr9 | 95466379 | ||||||
| chr9:95466873
|
C | T | 2 | a0003c0005t0004g0076a0003c0005t0004g0108 | 2 | HG02647.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2557+243G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 15/23 | chr9 | 95466873 | ||||||
| chr9:95466982
|
A | T | 2 | a0001c0002t0001g0093a0013c0033t0002g0118 | 2 | HG01167.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2557+134T>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 15/23 | chr9 | 95466982 | ||||||
| chr9:95467008
|
C | T | 3 | a0001c0003t0001g0191a0001c0003t0001g0192a0001c0003t0037g0037 | 3 | HG02622.hp2 HG02965.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2557+108G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 15/23 | chr9 | 95467008 | ||||||
| chr9:95467015
|
G | A | 50 | a0001c0002t0002g0214a0001c0002t0011g0008a0001c0002t0011g0185others(47): Show | 54 | HG00140.hp2 HG00609.hp2 HG01069.hp1 others(51): Show |
intron_variant | MODIFIER | c.2557+101C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 15/23 | chr9 | 95467015 | ||||||
| chr9:95467084
|
C | T | 3 | a0001c0003t0001g0191a0001c0003t0001g0192a0001c0003t0037g0037 | 3 | HG02622.hp2 HG02965.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2557+32G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 15/23 | chr9 | 95467084 | ||||||
| chr9:95467107
|
C | G | 149 | a0001c0002t0002g0214a0001c0002t0002g0261a0001c0002t0003g0235others(146): Show | 157 | HG00140.hp2 HG00423.hp2 HG00558.hp2 others(154): Show |
intron_variant | MODIFIER | c.2557+9G>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 15/23 | chr9 | 95467107 | ||||||
| chr9:95467109
|
G | A | 2 | a0001c0004t0002g0250a0001c0004t0002g0252 | 2 | NA18940.hp2 NA18969.hp2 |
splice_region_variant&intron_variant | LOW | c.2557+7C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 15/23 | chr9 | 95467109 | ||||||
| chr9:95467527
|
T | G | 1 | a0001c0003t0037g0037 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2248-102A>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 14/23 | chr9 | 95467527 | ||||||
| chr9:95467714
|
G | A | 1 | a0001c0030t0032g0211 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2248-289C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 14/23 | chr9 | 95467714 | ||||||
| chr9:95468078
|
T | C | 1 | a0001c0030t0032g0211 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2248-653A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 14/23 | chr9 | 95468078 | ||||||
| chr9:95468210
|
G | A | 1 | a0002c0001t0001g0092 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2247+541C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 14/23 | chr9 | 95468210 | ||||||
| chr9:95468263
|
C | T | 28 | a0001c0002t0003g0235a0001c0003t0001g0007a0001c0003t0001g0160others(25): Show | 29 | HG00597.hp1 HG00738.hp2 HG01074.hp2 others(26): Show |
intron_variant | MODIFIER | c.2247+488G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 14/23 | chr9 | 95468263 | ||||||
| chr9:95468556
|
C | T | 1 | a0002c0001t0001g0137 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2247+195G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 14/23 | chr9 | 95468556 | ||||||
| chr9:95468613
|
A | G | 1 | a0001c0003t0003g0170 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2247+138T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 14/23 | chr9 | 95468613 | ||||||
| chr9:95468623
|
T | C | 1 | a0001c0030t0032g0211 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2247+128A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 14/23 | chr9 | 95468623 | ||||||
| chr9:95468625
|
T | C | 45 | a0001c0002t0003g0235a0001c0003t0001g0007a0001c0003t0001g0160others(42): Show | 46 | HG00597.hp1 HG00738.hp2 HG01074.hp2 others(43): Show |
intron_variant | MODIFIER | c.2247+126A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 14/23 | chr9 | 95468625 | ||||||
| chr9:95468632
|
C | T | 1 | a0006c0010t0007g0013 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2247+119G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 14/23 | chr9 | 95468632 | ||||||
| chr9:95468638
|
C | T | 1 | a0001c0030t0032g0211 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2247+113G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 14/23 | chr9 | 95468638 | ||||||
| chr9:95468642
|
AT | A | 143 | a0001c0002t0002g0214a0001c0002t0002g0261a0001c0002t0003g0235others(140): Show | 151 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(148): Show |
intron_variant | MODIFIER | c.2247+108delA | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 14/23 | chr9 | 95468642 | ||||||
| chr9:95468642
|
ATT | A | 6 | a0001c0008t0012g0014a0001c0008t0012g0017a0001c0008t0012g0018others(3): Show | 6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.2247+107_2247+108d others(4): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 14/23 | chr9 | 95468642 | ||||||
| chr9:95468726
|
A | G | 40 | a0001c0002t0003g0235a0001c0003t0001g0007a0001c0003t0001g0160others(37): Show | 41 | HG00597.hp1 HG00738.hp2 HG01074.hp2 others(38): Show |
intron_variant | MODIFIER | c.2247+25T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 14/23 | chr9 | 95468726 | ||||||
| chr9:95469321
|
ACCTGGTT others(5): Show |
A | 1 | a0002c0001t0001g0043 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1845-180_1845-169d others(14): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 13/23 | chr9 | 95469321 | ||||||
| chr9:95469347
|
A | G | 1 | a0002c0001t0001g0053 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1845-194T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 13/23 | chr9 | 95469347 | ||||||
| chr9:95469553
|
C | T | 1 | a0004c0006t0002g0026 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1844+260G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 13/23 | chr9 | 95469553 | ||||||
| chr9:95469626
|
G | A | 50 | a0001c0002t0002g0214a0001c0002t0011g0008a0001c0002t0011g0185others(47): Show | 54 | HG00140.hp2 HG00609.hp2 HG01069.hp1 others(51): Show |
intron_variant | MODIFIER | c.1844+187C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 13/23 | chr9 | 95469626 | ||||||
| chr9:95470257
|
T | C | 1 | a0006c0010t0007g0013 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1726-326A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 12/23 | chr9 | 95470257 | ||||||
| chr9:95470263
|
T | G | 2 | a0001c0004t0001g0257a0002c0013t0001g0241 | 2 | NA18943.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.1726-332A>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 12/23 | chr9 | 95470263 | ||||||
| chr9:95470322
|
T | C | 1 | a0004c0006t0002g0022 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1726-391A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 12/23 | chr9 | 95470322 | ||||||
| chr9:95470343
|
T | A | 14 | a0001c0002t0002g0261a0001c0002t0005g0201a0001c0002t0005g0204others(11): Show | 15 | HG01952.hp1 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.1726-412A>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 12/23 | chr9 | 95470343 | ||||||
| chr9:95470410
|
C | A | 3 | a0003c0005t0004g0076a0003c0005t0004g0108a0009c0026t0002g0190 | 3 | HG01952.hp1 HG02647.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1726-479G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 12/23 | chr9 | 95470410 | ||||||
| chr9:95470472
|
A | G | 51 | a0001c0002t0003g0235a0001c0003t0001g0007a0001c0003t0001g0160others(48): Show | 52 | HG00423.hp2 HG00597.hp1 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.1726-541T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 12/23 | chr9 | 95470472 | ||||||
| chr9:95470528
|
A | G | 1 | a0002c0001t0029g0040 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1726-597T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 12/23 | chr9 | 95470528 | ||||||
| chr9:95470533
|
G | A | 2 | a0001c0002t0011g0008a0001c0002t0011g0185 | 3 | HG01243.hp1 HG03130.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1726-602C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 12/23 | chr9 | 95470533 | ||||||
| chr9:95470791
|
G | A | 2 | a0001c0002t0020g0035a0001c0002t0020g0042 | 2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1726-860C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 12/23 | chr9 | 95470791 | ||||||
| chr9:95470812
|
C | T | 1 | a0004c0006t0027g0025 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1726-881G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 12/23 | chr9 | 95470812 | ||||||
| chr9:95470908
|
C | T | 1 | a0004c0006t0006g0001 | 2 | HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1726-977G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 12/23 | chr9 | 95470908 | ||||||
| chr9:95470916
|
C | A | 6 | a0001c0008t0012g0014a0001c0008t0012g0017a0001c0008t0012g0018others(3): Show | 6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1726-985G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 12/23 | chr9 | 95470916 | ||||||
| chr9:95470927
|
C | A | 1 | a0001c0002t0001g0034 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1726-996G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 12/23 | chr9 | 95470927 | ||||||
| chr9:95471036
|
T | C | 4 | a0001c0002t0007g0036a0006c0010t0007g0013a0006c0010t0007g0263others(1): Show | 5 | HG02145.hp1 HG02572.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1726-1105A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 12/23 | chr9 | 95471036 | ||||||
| chr9:95471082
|
C | CA | 47 | a0001c0002t0002g0261a0001c0002t0005g0201a0001c0002t0005g0204others(44): Show | 50 | HG00558.hp2 HG00609.hp1 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.1726-1152dupT | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 12/23 | chr9 | 95471082 | ||||||
| chr9:95471082
|
CAAAAAAA others(5): Show |
C | 45 | a0001c0002t0003g0235a0001c0003t0001g0007a0001c0003t0001g0160others(42): Show | 46 | HG00597.hp1 HG00738.hp2 HG01074.hp2 others(43): Show |
intron_variant | MODIFIER | c.1726-1163_1726-115 others(16): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 12/23 | chr9 | 95471082 | ||||||
| chr9:95471154
|
A | T | 1 | a0002c0001t0001g0143 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1726-1223T>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 12/23 | chr9 | 95471154 | ||||||
| chr9:95471227
|
G | A | 12 | a0001c0003t0004g0196a0001c0003t0004g0198a0001c0003t0004g0199others(9): Show | 12 | HG02109.hp2 HG02145.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.1726-1296C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 12/23 | chr9 | 95471227 | ||||||
| chr9:95471242
|
G | A | 1 | a0001c0003t0008g0194 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1726-1311C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 12/23 | chr9 | 95471242 | ||||||
| chr9:95471815
|
A | G | 149 | a0001c0002t0002g0214a0001c0002t0002g0261a0001c0002t0003g0235others(146): Show | 157 | HG00140.hp2 HG00423.hp2 HG00558.hp2 others(154): Show |
intron_variant | MODIFIER | c.1726-1884T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 12/23 | chr9 | 95471815 | ||||||
| chr9:95471836
|
C | T | 1 | a0002c0001t0001g0092 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1726-1905G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 12/23 | chr9 | 95471836 | ||||||
| chr9:95471855
|
A | G | 1 | a0001c0002t0002g0261 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1726-1924T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 12/23 | chr9 | 95471855 | ||||||
| chr9:95471998
|
T | C | 1 | a0002c0001t0001g0135 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1726-2067A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 12/23 | chr9 | 95471998 | ||||||
| chr9:95472101
|
AAC | A | 12 | a0001c0003t0004g0196a0001c0003t0004g0198a0001c0003t0004g0199others(9): Show | 12 | HG02109.hp2 HG02145.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.1726-2172_1726-217 others(6): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 12/23 | chr9 | 95472101 | ||||||
| chr9:95472105
|
C | CA | 6 | a0001c0008t0012g0014a0001c0008t0012g0017a0001c0008t0012g0018others(3): Show | 6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1726-2175dupT | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 12/23 | chr9 | 95472105 | ||||||
| chr9:95472105
|
CAG | C | 48 | a0001c0002t0002g0261a0001c0002t0005g0201a0001c0002t0005g0204others(45): Show | 51 | HG00558.hp2 HG00609.hp1 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.1726-2176_1726-217 others(6): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 12/23 | chr9 | 95472105 | ||||||
| chr9:95472281
|
C | T | 48 | a0001c0002t0002g0214a0001c0002t0013g0009a0001c0002t0040g0230others(45): Show | 51 | HG00140.hp2 HG00609.hp2 HG01069.hp1 others(48): Show |
intron_variant | MODIFIER | c.1726-2350G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 12/23 | chr9 | 95472281 | ||||||
| chr9:95472310
|
G | C | 3 | a0001c0014t0021g0212a0001c0014t0021g0213a0004c0006t0004g0027 | 3 | HG02818.hp1 HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1726-2379C>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 12/23 | chr9 | 95472310 | ||||||
| chr9:95472368
|
GT | G | 50 | a0001c0002t0002g0214a0001c0002t0011g0008a0001c0002t0011g0185others(47): Show | 54 | HG00140.hp2 HG00609.hp2 HG01069.hp1 others(51): Show |
intron_variant | MODIFIER | c.1726-2438delA | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 12/23 | chr9 | 95472368 | ||||||
| chr9:95472503
|
C | T | 2 | a0001c0003t0001g0191a0001c0003t0001g0192 | 2 | HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1726-2572G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 12/23 | chr9 | 95472503 | ||||||
| chr9:95472621
|
C | T | 48 | a0001c0002t0002g0214a0001c0002t0013g0009a0001c0002t0040g0230others(45): Show | 51 | HG00140.hp2 HG00609.hp2 HG01069.hp1 others(48): Show |
intron_variant | MODIFIER | c.1726-2690G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 12/23 | chr9 | 95472621 | ||||||
| chr9:95472663
|
C | T | 1 | a0001c0003t0023g0038 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1726-2732G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 12/23 | chr9 | 95472663 | ||||||
| chr9:95472669
|
C | A | 3 | a0001c0014t0021g0212a0001c0014t0021g0213a0004c0006t0004g0027 | 3 | HG02818.hp1 HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1726-2738G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 12/23 | chr9 | 95472669 | ||||||
| chr9:95472829
|
C | T | 1 | a0001c0002t0002g0261 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1726-2898G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 12/23 | chr9 | 95472829 | ||||||
| chr9:95472966
|
T | C | 4 | a0001c0002t0007g0036a0006c0010t0007g0013a0006c0010t0007g0263others(1): Show | 5 | HG02145.hp1 HG02572.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1726-3035A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 12/23 | chr9 | 95472966 | ||||||
| chr9:95473028
|
T | C | 51 | a0001c0002t0003g0235a0001c0003t0001g0007a0001c0003t0001g0160others(48): Show | 52 | HG00423.hp2 HG00597.hp1 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.1725+3006A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 12/23 | chr9 | 95473028 | ||||||
| chr9:95473218
|
T | A | 1 | a0001c0002t0005g0207 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1725+2816A>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 12/23 | chr9 | 95473218 | ||||||
| chr9:95473447
|
G | A | 3 | a0003c0005t0002g0079a0003c0005t0002g0128a0003c0005t0002g0129 | 3 | HG03195.hp1 HG03516.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1725+2587C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 12/23 | chr9 | 95473447 | ||||||
| chr9:95473542
|
A | AT | 11 | a0001c0002t0001g0156a0001c0002t0011g0008a0001c0002t0011g0185others(8): Show | 12 | HG01106.hp1 HG01175.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.1725+2491dupA | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 12/23 | chr9 | 95473542 | ||||||
| chr9:95473542
|
AT | A | 90 | a0001c0002t0001g0153a0001c0002t0002g0067a0001c0002t0002g0126others(87): Show | 94 | HG00140.hp2 HG00597.hp1 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.1725+2491delA | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 12/23 | chr9 | 95473542 | ||||||
| chr9:95473542
|
ATT | A | 8 | a0001c0004t0001g0242a0001c0008t0012g0014a0001c0008t0012g0017others(5): Show | 8 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.1725+2490_1725+249 others(6): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 12/23 | chr9 | 95473542 | ||||||
| chr9:95473577
|
T | C | 51 | a0001c0002t0003g0235a0001c0003t0001g0007a0001c0003t0001g0160others(48): Show | 52 | HG00423.hp2 HG00597.hp1 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.1725+2457A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 12/23 | chr9 | 95473577 | ||||||
| chr9:95473596
|
G | C | 3 | a0001c0014t0021g0212a0001c0014t0021g0213a0004c0006t0004g0027 | 3 | HG02818.hp1 HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1725+2438C>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 12/23 | chr9 | 95473596 | ||||||
| chr9:95473603
|
A | G | 51 | a0001c0002t0003g0235a0001c0003t0001g0007a0001c0003t0001g0160others(48): Show | 52 | HG00423.hp2 HG00597.hp1 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.1725+2431T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 12/23 | chr9 | 95473603 | ||||||
| chr9:95473637
|
C | T | 2 | a0004c0006t0001g0032a0004c0006t0001g0033 | 2 | HG01884.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1725+2397G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 12/23 | chr9 | 95473637 | ||||||
| chr9:95473821
|
C | T | 2 | a0001c0003t0003g0110a0001c0003t0031g0253 | 2 | HG04184.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.1725+2213G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 12/23 | chr9 | 95473821 | ||||||
| chr9:95473873
|
G | C | 3 | a0003c0012t0002g0184a0003c0012t0002g0186a0003c0012t0002g0187 | 3 | NA18747.hp2 NA18970.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.1725+2161C>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 12/23 | chr9 | 95473873 | ||||||
| chr9:95473879
|
T | C | 1 | a0001c0015t0002g0055 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1725+2155A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 12/23 | chr9 | 95473879 | ||||||
| chr9:95473920
|
A | G | 40 | a0001c0002t0003g0235a0001c0003t0001g0007a0001c0003t0001g0160others(37): Show | 41 | HG00597.hp1 HG00738.hp2 HG01074.hp2 others(38): Show |
intron_variant | MODIFIER | c.1725+2114T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 12/23 | chr9 | 95473920 | ||||||
| chr9:95474027
|
C | T | 3 | a0004c0006t0006g0001a0004c0006t0006g0030a0004c0006t0006g0031 | 4 | HG02922.hp1 HG03098.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1725+2007G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 12/23 | chr9 | 95474027 | ||||||
| chr9:95474115
|
A | G | 2 | a0001c0002t0011g0008a0001c0002t0011g0185 | 3 | HG01243.hp1 HG03130.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1725+1919T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 12/23 | chr9 | 95474115 | ||||||
| chr9:95474204
|
C | A | 1 | a0001c0004t0003g0255 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1725+1830G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 12/23 | chr9 | 95474204 | ||||||
| chr9:95474382
|
C | T | 28 | a0001c0002t0003g0235a0001c0003t0001g0007a0001c0003t0001g0160others(25): Show | 29 | HG00597.hp1 HG00738.hp2 HG01074.hp2 others(26): Show |
intron_variant | MODIFIER | c.1725+1652G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 12/23 | chr9 | 95474382 | ||||||
| chr9:95474583
|
C | T | 44 | a0001c0003t0001g0007a0001c0003t0001g0160a0001c0003t0001g0166others(41): Show | 45 | HG00597.hp1 HG00738.hp2 HG01099.hp1 others(42): Show |
intron_variant | MODIFIER | c.1725+1451G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 12/23 | chr9 | 95474583 | ||||||
| chr9:95474760
|
A | G | 1 | a0001c0002t0013g0009 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1725+1274T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 12/23 | chr9 | 95474760 | ||||||
| chr9:95474818
|
A | G | 1 | a0002c0001t0001g0006 | 2 | HG01099.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1725+1216T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 12/23 | chr9 | 95474818 | ||||||
| chr9:95474883
|
G | A | 14 | a0001c0002t0002g0261a0001c0002t0005g0201a0001c0002t0005g0204others(11): Show | 15 | HG01952.hp1 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.1725+1151C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 12/23 | chr9 | 95474883 | ||||||
| chr9:95475038
|
T | C | 5 | a0004c0006t0006g0001a0004c0006t0006g0028a0004c0006t0006g0029others(2): Show | 6 | HG01243.hp2 HG02922.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1725+996A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 12/23 | chr9 | 95475038 | ||||||
| chr9:95475169
|
C | T | 1 | a0002c0001t0001g0152 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1725+865G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 12/23 | chr9 | 95475169 | ||||||
| chr9:95475171
|
T | C | 2 | a0001c0003t0003g0177a0001c0003t0034g0068 | 2 | NA20752.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1725+863A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 12/23 | chr9 | 95475171 | ||||||
| chr9:95475280
|
C | T | 1 | a0002c0001t0003g0151 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1725+754G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 12/23 | chr9 | 95475280 | ||||||
| chr9:95475514
|
A | G | 140 | a0001c0002t0002g0214a0001c0002t0002g0261a0001c0002t0003g0235others(137): Show | 148 | HG00140.hp2 HG00423.hp2 HG00558.hp2 others(145): Show |
intron_variant | MODIFIER | c.1725+520T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 12/23 | chr9 | 95475514 | ||||||
| chr9:95475701
|
A | G | 1 | a0002c0001t0028g0105 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1725+333T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 12/23 | chr9 | 95475701 | ||||||
| chr9:95475737
|
T | G | 1 | a0001c0002t0013g0009 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1725+297A>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 12/23 | chr9 | 95475737 | ||||||
| chr9:95475770
|
T | C | 2 | a0001c0002t0011g0008a0001c0002t0011g0185 | 3 | HG01243.hp1 HG03130.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1725+264A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 12/23 | chr9 | 95475770 | ||||||
| chr9:95475995
|
C | T | 1 | a0002c0001t0001g0137 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1725+39G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 12/23 | chr9 | 95475995 | ||||||
| chr9:95476217
|
C | G | 1 | a0001c0030t0032g0211 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1600-58G>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 11/23 | chr9 | 95476217 | ||||||
| chr9:95476219
|
G | C | 1 | a0001c0030t0032g0211 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1600-60C>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 11/23 | chr9 | 95476219 | ||||||
| chr9:95476566
|
T | C | 1 | a0001c0002t0005g0207 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1599+193A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 11/23 | chr9 | 95476566 | ||||||
| chr9:95476578
|
T | C | 26 | a0001c0024t0001g0227a0003c0005t0001g0011a0003c0005t0001g0140others(23): Show | 28 | HG00558.hp2 HG00609.hp1 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.1599+181A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 11/23 | chr9 | 95476578 | ||||||
| chr9:95476631
|
G | A | 1 | a0012c0032t0004g0089 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1599+128C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 11/23 | chr9 | 95476631 | ||||||
| chr9:95476684
|
A | G | 1 | a0001c0002t0001g0034 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1599+75T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 11/23 | chr9 | 95476684 | ||||||
| chr9:95476865
|
A | G | 48 | a0001c0002t0002g0261a0001c0002t0005g0201a0001c0002t0005g0204others(45): Show | 51 | HG00558.hp2 HG00609.hp1 HG00673.hp2 others(48): Show |
splice_region_variant&intron_variant | LOW | c.1501-8T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 10/23 | chr9 | 95476865 | ||||||
| chr9:95476908
|
G | C | 29 | a0001c0002t0001g0034a0001c0002t0001g0083a0001c0002t0001g0144others(26): Show | 29 | HG00140.hp1 HG00408.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.1501-51C>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 10/23 | chr9 | 95476908 | ||||||
| chr9:95477144
|
C | T | 1 | a0002c0013t0001g0233 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1501-287G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 10/23 | chr9 | 95477144 | ||||||
| chr9:95477151
|
A | C | 1 | a0001c0003t0023g0038 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1501-294T>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 10/23 | chr9 | 95477151 | ||||||
| chr9:95477221
|
G | A | 44 | a0001c0003t0001g0007a0001c0003t0001g0160a0001c0003t0001g0166others(41): Show | 45 | HG00597.hp1 HG00738.hp2 HG01099.hp1 others(42): Show |
intron_variant | MODIFIER | c.1500+326C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 10/23 | chr9 | 95477221 | ||||||
| chr9:95477448
|
G | A | 39 | a0001c0003t0001g0007a0001c0003t0001g0160a0001c0003t0001g0166others(36): Show | 40 | HG00597.hp1 HG00738.hp2 HG01099.hp1 others(37): Show |
intron_variant | MODIFIER | c.1500+99C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 10/23 | chr9 | 95477448 | ||||||
| chr9:95477752
|
T | G | 3 | a0001c0014t0021g0212a0001c0014t0021g0213a0004c0006t0004g0027 | 3 | HG02818.hp1 HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1345-50A>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 9/23 | chr9 | 95477752 | ||||||
| chr9:95477828
|
T | C | 1 | a0002c0021t0009g0047 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1345-126A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 9/23 | chr9 | 95477828 | ||||||
| chr9:95477838
|
G | A | 149 | a0001c0002t0002g0214a0001c0002t0002g0261a0001c0002t0003g0235others(146): Show | 157 | HG00140.hp2 HG00423.hp2 HG00558.hp2 others(154): Show |
intron_variant | MODIFIER | c.1345-136C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 9/23 | chr9 | 95477838 | ||||||
| chr9:95478387
|
G | A | 3 | a0001c0003t0005g0208a0001c0003t0005g0210a0001c0003t0013g0209 | 3 | HG02109.hp2 HG02976.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1213-201C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 8/23 | chr9 | 95478387 | ||||||
| chr9:95478398
|
G | T | 3 | a0003c0005t0001g0223a0007c0019t0001g0109a0007c0025t0004g0224 | 3 | HG00558.hp2 HG02129.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.1213-212C>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 8/23 | chr9 | 95478398 | ||||||
| chr9:95478431
|
G | C | 1 | a0001c0008t0012g0018 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1213-245C>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 8/23 | chr9 | 95478431 | ||||||
| chr9:95478551
|
T | A | 1 | a0001c0002t0001g0112 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1213-365A>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 8/23 | chr9 | 95478551 | ||||||
| chr9:95478654
|
C | A | 1 | a0003c0012t0002g0186 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1212+346G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 8/23 | chr9 | 95478654 | ||||||
| chr9:95478788
|
T | C | 1 | a0009c0026t0002g0190 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1212+212A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 8/23 | chr9 | 95478788 | ||||||
| chr9:95478857
|
G | A | 6 | a0001c0008t0012g0014a0001c0008t0012g0017a0001c0008t0012g0018others(3): Show | 6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1212+143C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 8/23 | chr9 | 95478857 | ||||||
| chr9:95478960
|
T | C | 1 | a0001c0003t0023g0038 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1212+40A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 8/23 | chr9 | 95478960 | ||||||
| chr9:95478967
|
C | T | 2 | a0002c0001t0001g0084a0002c0001t0001g0134 | 2 | NA18946.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.1212+33G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 8/23 | chr9 | 95478967 | ||||||
| chr9:95479317
|
T | C | 1 | a0004c0006t0001g0033 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1065-170A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 7/23 | chr9 | 95479317 | ||||||
| chr9:95479322
|
G | A | 1 | a0001c0003t0023g0038 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1065-175C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 7/23 | chr9 | 95479322 | ||||||
| chr9:95479670
|
G | A | 1 | a0009c0026t0002g0190 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1064+299C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 7/23 | chr9 | 95479670 | ||||||
| chr9:95479817
|
A | G | 1 | a0001c0003t0023g0039 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1064+152T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 7/23 | chr9 | 95479817 | ||||||
| chr9:95479830
|
A | G | 49 | a0001c0002t0002g0214a0001c0002t0003g0235a0001c0002t0013g0009others(46): Show | 52 | HG00140.hp2 HG00609.hp2 HG01069.hp1 others(49): Show |
intron_variant | MODIFIER | c.1064+139T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 7/23 | chr9 | 95479830 | ||||||
| chr9:95479895
|
T | C | 14 | a0001c0002t0002g0261a0001c0002t0005g0201a0001c0002t0005g0204others(11): Show | 15 | HG01952.hp1 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.1064+74A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 7/23 | chr9 | 95479895 | ||||||
| chr9:95480193
|
T | G | 1 | a0004c0006t0002g0022 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.943-103A>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 6/23 | chr9 | 95480193 | ||||||
| chr9:95480265
|
C | G | 1 | a0001c0002t0005g0259 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.942+125G>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 6/23 | chr9 | 95480265 | ||||||
| chr9:95480315
|
A | G | 1 | a0013c0033t0002g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.942+75T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 6/23 | chr9 | 95480315 | ||||||
| chr9:95480643
|
A | G | 49 | a0001c0002t0002g0214a0001c0002t0003g0235a0001c0002t0013g0009others(46): Show | 52 | HG00140.hp2 HG00609.hp2 HG01069.hp1 others(49): Show |
intron_variant | MODIFIER | c.744-55T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 5/23 | chr9 | 95480643 | ||||||
| chr9:95480702
|
G | A | 150 | a0001c0002t0002g0214a0001c0002t0002g0261a0001c0002t0003g0235others(147): Show | 158 | HG00140.hp2 HG00423.hp2 HG00558.hp2 others(155): Show |
intron_variant | MODIFIER | c.744-114C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 5/23 | chr9 | 95480702 | ||||||
| chr9:95480792
|
C | T | 1 | a0003c0005t0002g0225 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.744-204G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 5/23 | chr9 | 95480792 | ||||||
| chr9:95480875
|
A | G | 1 | a0001c0002t0002g0261 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.744-287T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 5/23 | chr9 | 95480875 | ||||||
| chr9:95480905
|
A | C | 49 | a0001c0003t0001g0007a0001c0003t0001g0160a0001c0003t0001g0166others(46): Show | 50 | HG00423.hp2 HG00597.hp1 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.744-317T>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 5/23 | chr9 | 95480905 | ||||||
| chr9:95480907
|
A | AT | 48 | a0001c0002t0002g0214a0001c0002t0003g0235a0001c0002t0011g0008others(45): Show | 52 | HG00140.hp2 HG00609.hp2 HG01069.hp1 others(49): Show |
intron_variant | MODIFIER | c.744-320dupA | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 5/23 | chr9 | 95480907 | ||||||
| chr9:95480907
|
AT | A | 81 | a0001c0002t0001g0034a0001c0002t0001g0061a0001c0002t0001g0085others(78): Show | 87 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.744-320delA | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 5/23 | chr9 | 95480907 | ||||||
| chr9:95480921
|
A | T | 2 | a0001c0002t0001g0073a0001c0002t0001g0074 | 2 | HG00639.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.744-333T>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 5/23 | chr9 | 95480921 | ||||||
| chr9:95481103
|
A | G | 49 | a0001c0003t0001g0007a0001c0003t0001g0160a0001c0003t0001g0166others(46): Show | 50 | HG00423.hp2 HG00597.hp1 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.744-515T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 5/23 | chr9 | 95481103 | ||||||
| chr9:95481143
|
G | A | 1 | a0001c0003t0023g0038 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.744-555C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 5/23 | chr9 | 95481143 | ||||||
| chr9:95481259
|
T | C | 1 | a0001c0003t0003g0174 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.744-671A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 5/23 | chr9 | 95481259 | ||||||
| chr9:95481465
|
G | C | 3 | a0001c0004t0001g0244a0001c0004t0001g0245a0001c0004t0041g0265 | 3 | NA18991.hp2 NA19007.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.743+484C>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 5/23 | chr9 | 95481465 | ||||||
| chr9:95481586
|
C | T | 27 | a0001c0003t0001g0007a0001c0003t0001g0160a0001c0003t0001g0166others(24): Show | 28 | HG00597.hp1 HG00738.hp2 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.743+363G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 5/23 | chr9 | 95481586 | ||||||
| chr9:95481638
|
G | A | 1 | a0001c0003t0005g0208 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.743+311C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 5/23 | chr9 | 95481638 | ||||||
| chr9:95482266
|
G | A | 2 | a0001c0002t0005g0204a0001c0002t0005g0205 | 2 | HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.582-63C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 3/23 | chr9 | 95482266 | ||||||
| chr9:95482301
|
G | T | 1 | a0001c0002t0002g0214 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.582-98C>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 3/23 | chr9 | 95482301 | ||||||
| chr9:95482326
|
C | T | 1 | a0002c0001t0001g0098 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.582-123G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 3/23 | chr9 | 95482326 | ||||||
| chr9:95482329
|
G | A | 1 | a0002c0001t0035g0113 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.582-126C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 3/23 | chr9 | 95482329 | ||||||
| chr9:95482338
|
T | C | 3 | a0001c0008t0012g0014a0001c0008t0012g0017a0001c0008t0012g0018 | 3 | HG00423.hp2 NA18965.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.582-135A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 3/23 | chr9 | 95482338 | ||||||
| chr9:95482537
|
G | A | 2 | a0004c0006t0001g0032a0004c0006t0001g0033 | 2 | HG01884.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.582-334C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 3/23 | chr9 | 95482537 | ||||||
| chr9:95482675
|
C | G | 1 | a0002c0001t0001g0052 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.582-472G>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 3/23 | chr9 | 95482675 | ||||||
| chr9:95482696
|
C | T | 49 | a0001c0003t0001g0007a0001c0003t0001g0160a0001c0003t0001g0166others(46): Show | 50 | HG00423.hp2 HG00597.hp1 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.582-493G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 3/23 | chr9 | 95482696 | ||||||
| chr9:95482726
|
A | G | 1 | a0002c0001t0002g0131 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.582-523T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 3/23 | chr9 | 95482726 | ||||||
| chr9:95482744
|
A | G | 27 | a0001c0003t0001g0007a0001c0003t0001g0160a0001c0003t0001g0166others(24): Show | 28 | HG00597.hp1 HG00738.hp2 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.582-541T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 3/23 | chr9 | 95482744 | ||||||
| chr9:95483093
|
A | G | 1 | a0001c0002t0011g0185 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.582-890T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 3/23 | chr9 | 95483093 | ||||||
| chr9:95483109
|
G | GA | 49 | a0001c0003t0001g0007a0001c0003t0001g0160a0001c0003t0001g0166others(46): Show | 50 | HG00423.hp2 HG00597.hp1 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.582-907dupT | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 3/23 | chr9 | 95483109 | ||||||
| chr9:95483264
|
C | CA | 7 | a0004c0006t0002g0023a0004c0006t0006g0001a0004c0006t0006g0021others(4): Show | 8 | HG01243.hp2 HG02922.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.582-1062dupT | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 3/23 | chr9 | 95483264 | ||||||
| chr9:95483264
|
CAA | C | 43 | a0001c0003t0001g0007a0001c0003t0001g0160a0001c0003t0001g0166others(40): Show | 44 | HG00597.hp1 HG00738.hp2 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.582-1063_582-1062d others(4): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 3/23 | chr9 | 95483264 | ||||||
| chr9:95483373
|
A | G | 1 | a0001c0003t0003g0170 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.582-1170T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 3/23 | chr9 | 95483373 | ||||||
| chr9:95483410
|
GA | G | 20 | a0001c0002t0005g0201a0001c0002t0005g0204a0001c0002t0005g0205others(17): Show | 22 | HG00738.hp2 HG01243.hp1 HG01952.hp1 others(19): Show |
intron_variant | MODIFIER | c.582-1208delT | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 3/23 | chr9 | 95483410 | ||||||
| chr9:95483425
|
A | AG | 6 | a0001c0008t0012g0014a0001c0008t0012g0017a0001c0008t0012g0018others(3): Show | 6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.582-1223_582-1222i others(3): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 3/23 | chr9 | 95483425 | ||||||
| chr9:95483434
|
A | G | 13 | a0001c0003t0004g0196a0001c0003t0004g0198a0001c0003t0004g0199others(10): Show | 13 | HG02109.hp2 HG02145.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.582-1231T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 3/23 | chr9 | 95483434 | ||||||
| chr9:95483573
|
T | C | 51 | a0001c0002t0002g0214a0001c0002t0003g0235a0001c0002t0011g0008others(48): Show | 55 | HG00140.hp2 HG00609.hp2 HG01069.hp1 others(52): Show |
intron_variant | MODIFIER | c.582-1370A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 3/23 | chr9 | 95483573 | ||||||
| chr9:95483607
|
C | T | 1 | a0003c0005t0002g0128 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.582-1404G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 3/23 | chr9 | 95483607 | ||||||
| chr9:95483692
|
A | G | 51 | a0001c0002t0002g0214a0001c0002t0003g0235a0001c0002t0011g0008others(48): Show | 55 | HG00140.hp2 HG00609.hp2 HG01069.hp1 others(52): Show |
intron_variant | MODIFIER | c.582-1489T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 3/23 | chr9 | 95483692 | ||||||
| chr9:95483697
|
T | C | 1 | a0001c0002t0005g0201 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.582-1494A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 3/23 | chr9 | 95483697 | ||||||
| chr9:95483748
|
C | T | 1 | a0001c0003t0003g0174 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.582-1545G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 3/23 | chr9 | 95483748 | ||||||
| chr9:95483772
|
T | G | 22 | a0001c0024t0001g0227a0003c0005t0001g0011a0003c0005t0001g0140others(19): Show | 24 | HG00558.hp2 HG00609.hp1 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.582-1569A>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 3/23 | chr9 | 95483772 | ||||||
| chr9:95483862
|
T | C | 3 | a0002c0001t0001g0149a0002c0001t0018g0077a0002c0001t0018g0102 | 3 | HG02071.hp1 NA18956.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.582-1659A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 3/23 | chr9 | 95483862 | ||||||
| chr9:95484110
|
C | T | 2 | a0001c0002t0001g0144a0011c0027t0001g0142 | 2 | HG02738.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.581+1575G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 3/23 | chr9 | 95484110 | ||||||
| chr9:95484121
|
A | G | 1 | a0001c0003t0023g0039 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.581+1564T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 3/23 | chr9 | 95484121 | ||||||
| chr9:95484236
|
T | C | 2 | a0001c0002t0011g0188a0001c0003t0023g0038 | 2 | HG01109.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.581+1449A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 3/23 | chr9 | 95484236 | ||||||
| chr9:95484472
|
C | A | 2 | a0001c0002t0001g0144a0011c0027t0001g0142 | 2 | HG02738.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.581+1213G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 3/23 | chr9 | 95484472 | ||||||
| chr9:95484544
|
C | T | 1 | a0001c0003t0004g0198 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.581+1141G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 3/23 | chr9 | 95484544 | ||||||
| chr9:95484615
|
G | C | 1 | a0005c0007t0004g0158 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.581+1070C>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 3/23 | chr9 | 95484615 | ||||||
| chr9:95484922
|
C | T | 40 | a0001c0003t0001g0007a0001c0003t0001g0160a0001c0003t0001g0166others(37): Show | 41 | HG00597.hp1 HG00738.hp2 HG01099.hp1 others(38): Show |
intron_variant | MODIFIER | c.581+763G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 3/23 | chr9 | 95484922 | ||||||
| chr9:95484943
|
C | T | 3 | a0001c0014t0021g0212a0001c0014t0021g0213a0004c0006t0004g0027 | 3 | HG02818.hp1 HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.581+742G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 3/23 | chr9 | 95484943 | ||||||
| chr9:95485004
|
G | A | 1 | a0002c0013t0001g0258 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.581+681C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 3/23 | chr9 | 95485004 | ||||||
| chr9:95485148
|
G | C | 1 | a0002c0001t0001g0065 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.581+537C>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 3/23 | chr9 | 95485148 | ||||||
| chr9:95485261
|
C | T | 2 | a0001c0002t0020g0035a0001c0002t0020g0042 | 2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.581+424G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 3/23 | chr9 | 95485261 | ||||||
| chr9:95485508
|
C | T | 40 | a0001c0003t0001g0007a0001c0003t0001g0160a0001c0003t0001g0166others(37): Show | 41 | HG00597.hp1 HG00738.hp2 HG01099.hp1 others(38): Show |
intron_variant | MODIFIER | c.581+177G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 3/23 | chr9 | 95485508 | ||||||
| chr9:95486046
|
A | G | 40 | a0001c0003t0001g0007a0001c0003t0001g0160a0001c0003t0001g0166others(37): Show | 41 | HG00597.hp1 HG00738.hp2 HG01099.hp1 others(38): Show |
intron_variant | MODIFIER | c.392-172T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95486046 | ||||||
| chr9:95486105
|
A | G | 49 | a0001c0003t0001g0007a0001c0003t0001g0160a0001c0003t0001g0166others(46): Show | 50 | HG00423.hp2 HG00597.hp1 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.392-231T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95486105 | ||||||
| chr9:95486149
|
G | GA | 43 | a0001c0003t0001g0007a0001c0003t0001g0160a0001c0003t0001g0166others(40): Show | 44 | HG00597.hp1 HG00738.hp2 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.392-276_392-275ins others(1): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95486149 | ||||||
| chr9:95486353
|
C | A | 149 | a0001c0002t0002g0214a0001c0002t0002g0261a0001c0002t0003g0235others(146): Show | 157 | HG00140.hp2 HG00423.hp2 HG00558.hp2 others(154): Show |
intron_variant | MODIFIER | c.392-479G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95486353 | ||||||
| chr9:95486514
|
C | A | 1 | a0001c0003t0005g0208 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.392-640G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95486514 | ||||||
| chr9:95486570
|
G | A | 1 | a0001c0004t0003g0255 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.392-696C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95486570 | ||||||
| chr9:95487173
|
A | G | 1 | a0001c0003t0008g0193 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.392-1299T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95487173 | ||||||
| chr9:95487218
|
G | A | 1 | a0002c0013t0001g0258 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.392-1344C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95487218 | ||||||
| chr9:95487267
|
T | C | 1 | a0001c0002t0001g0034 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.392-1393A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95487267 | ||||||
| chr9:95487316
|
T | C | 1 | a0002c0001t0001g0136 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.392-1442A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95487316 | ||||||
| chr9:95487377
|
A | G | 1 | a0002c0020t0003g0178 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.392-1503T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95487377 | ||||||
| chr9:95487681
|
C | T | 34 | a0001c0002t0003g0235a0001c0002t0040g0230a0001c0004t0001g0012others(31): Show | 35 | HG00140.hp2 HG00609.hp2 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.392-1807G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95487681 | ||||||
| chr9:95487824
|
A | G | 1 | a0001c0003t0008g0194 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.392-1950T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95487824 | ||||||
| chr9:95487904
|
T | C | 2 | a0001c0003t0001g0191a0001c0003t0001g0192 | 2 | HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.392-2030A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95487904 | ||||||
| chr9:95487931
|
A | C | 15 | a0001c0002t0002g0261a0001c0002t0005g0201a0001c0002t0005g0204others(12): Show | 16 | HG01109.hp2 HG01952.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.392-2057T>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95487931 | ||||||
| chr9:95488105
|
A | G | 2 | a0001c0002t0005g0207a0001c0030t0032g0211 | 2 | HG01081.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.392-2231T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95488105 | ||||||
| chr9:95488293
|
C | G | 2 | a0001c0002t0005g0204a0001c0002t0005g0205 | 2 | HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.392-2419G>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95488293 | ||||||
| chr9:95488392
|
T | C | 27 | a0001c0003t0001g0007a0001c0003t0001g0160a0001c0003t0001g0166others(24): Show | 28 | HG00597.hp1 HG00738.hp2 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.392-2518A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95488392 | ||||||
| chr9:95488415
|
A | G | 6 | a0001c0008t0012g0014a0001c0008t0012g0017a0001c0008t0012g0018others(3): Show | 6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.392-2541T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95488415 | ||||||
| chr9:95488669
|
A | G | 2 | a0001c0002t0005g0207a0001c0030t0032g0211 | 2 | HG01081.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.392-2795T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95488669 | ||||||
| chr9:95488674
|
A | G | 6 | a0001c0008t0012g0014a0001c0008t0012g0017a0001c0008t0012g0018others(3): Show | 6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.392-2800T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95488674 | ||||||
| chr9:95488902
|
A | G | 6 | a0001c0008t0012g0014a0001c0008t0012g0017a0001c0008t0012g0018others(3): Show | 6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.392-3028T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95488902 | ||||||
| chr9:95489097
|
A | G | 15 | a0001c0002t0002g0261a0001c0002t0005g0201a0001c0002t0005g0204others(12): Show | 16 | HG01109.hp2 HG01952.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.392-3223T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95489097 | ||||||
| chr9:95489230
|
T | C | 6 | a0001c0008t0012g0014a0001c0008t0012g0017a0001c0008t0012g0018others(3): Show | 6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.392-3356A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95489230 | ||||||
| chr9:95489340
|
GT | G | 3 | a0003c0012t0002g0184a0003c0012t0002g0186a0003c0012t0002g0187 | 3 | NA18747.hp2 NA18970.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.392-3467delA | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95489340 | ||||||
| chr9:95489357
|
C | T | 1 | a0001c0030t0032g0211 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.392-3483G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95489357 | ||||||
| chr9:95489381
|
C | T | 1 | a0001c0002t0001g0254 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.392-3507G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95489381 | ||||||
| chr9:95489426
|
G | A | 2 | a0001c0003t0001g0191a0001c0003t0001g0192 | 2 | HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.392-3552C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95489426 | ||||||
| chr9:95489539
|
C | T | 3 | a0001c0014t0021g0212a0001c0014t0021g0213a0004c0006t0004g0027 | 3 | HG02818.hp1 HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.392-3665G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95489539 | ||||||
| chr9:95489602
|
T | G | 1 | a0007c0025t0004g0224 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.392-3728A>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95489602 | ||||||
| chr9:95489692
|
C | T | 2 | a0001c0003t0001g0191a0001c0003t0001g0192 | 2 | HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.392-3818G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95489692 | ||||||
| chr9:95489796
|
T | C | 1 | a0002c0001t0001g0056 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.392-3922A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95489796 | ||||||
| chr9:95489802
|
A | AT | 21 | a0001c0002t0002g0214a0001c0002t0005g0259a0001c0002t0013g0009others(18): Show | 23 | HG01069.hp1 HG01071.hp2 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.392-3929dupA | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95489802 | ||||||
| chr9:95489917
|
A | C | 1 | a0001c0002t0001g0061 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.392-4043T>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95489917 | ||||||
| chr9:95489967
|
A | AT | 6 | a0001c0008t0012g0014a0001c0008t0012g0017a0001c0008t0012g0018others(3): Show | 6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.392-4094dupA | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95489967 | ||||||
| chr9:95490031
|
T | C | 53 | a0001c0002t0002g0214a0001c0002t0003g0235a0001c0002t0011g0008others(50): Show | 57 | HG00140.hp2 HG00609.hp2 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.392-4157A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95490031 | ||||||
| chr9:95490036
|
T | C | 3 | a0001c0003t0005g0208a0001c0003t0005g0210a0001c0003t0013g0209 | 3 | HG02109.hp2 HG02976.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.392-4162A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95490036 | ||||||
| chr9:95490044
|
C | T | 1 | a0001c0003t0023g0038 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.392-4170G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95490044 | ||||||
| chr9:95490270
|
C | T | 1 | a0011c0027t0001g0142 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.392-4396G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95490270 | ||||||
| chr9:95490519
|
T | TCACA | 10 | a0001c0002t0020g0035a0001c0003t0023g0038a0003c0005t0001g0175others(7): Show | 11 | HG00609.hp1 HG02056.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.392-4646_392-4645i others(6): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95490519 | ||||||
| chr9:95490519
|
T | TCACACA | 15 | a0001c0002t0005g0259a0001c0030t0032g0211a0003c0005t0001g0011others(12): Show | 17 | HG00558.hp2 HG00673.hp2 HG02015.hp1 others(14): Show |
intron_variant | MODIFIER | c.392-4646_392-4645i others(8): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95490519 | ||||||
| chr9:95490519
|
T | TCACACAC others(1): Show |
10 | a0001c0002t0002g0261a0001c0002t0005g0201a0001c0002t0005g0205others(7): Show | 10 | HG02109.hp1 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.392-4646_392-4645i others(10): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95490519 | ||||||
| chr9:95490519
|
T | TCACACAC others(3): Show |
4 | a0001c0002t0005g0204a0003c0005t0004g0215a0003c0012t0002g0187others(1): Show | 4 | HG03098.hp1 NA18979.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.392-4646_392-4645i others(12): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95490519 | ||||||
| chr9:95490519
|
T | TCACACAC others(5): Show |
4 | a0001c0002t0005g0207a0003c0005t0004g0076a0003c0005t0004g0108others(1): Show | 4 | HG01081.hp1 HG01952.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.392-4646_392-4645i others(14): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95490519 | ||||||
| chr9:95490519
|
T | TCACACAC others(7): Show |
1 | a0001c0014t0021g0213 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.392-4646_392-4645i others(16): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95490519 | ||||||
| chr9:95490520
|
G | C | 47 | a0001c0002t0002g0261a0001c0002t0005g0201a0001c0002t0005g0204others(44): Show | 50 | HG00558.hp2 HG00609.hp1 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.392-4646C>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95490520 | ||||||
| chr9:95490520
|
G | GAC | 19 | a0001c0002t0002g0041a0001c0002t0002g0111a0001c0003t0001g0007others(16): Show | 20 | HG02135.hp2 HG02559.hp1 HG02630.hp2 others(17): Show |
intron_variant | MODIFIER | c.392-4648_392-4647d others(4): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95490520 | ||||||
| chr9:95490520
|
G | GACAC | 14 | a0001c0003t0001g0191a0001c0003t0001g0192a0001c0003t0003g0170others(11): Show | 14 | HG00597.hp1 HG02109.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.392-4650_392-4647d others(6): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95490520 | ||||||
| chr9:95490520
|
G | GACACAC | 9 | a0001c0003t0003g0110a0001c0003t0003g0161a0001c0003t0003g0162others(6): Show | 9 | HG01167.hp1 HG02027.hp1 HG03453.hp1 others(6): Show |
intron_variant | MODIFIER | c.392-4652_392-4647d others(8): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95490520 | ||||||
| chr9:95490520
|
G | GACACACA others(1): Show |
5 | a0001c0003t0001g0160a0001c0003t0003g0164a0001c0003t0003g0179others(2): Show | 5 | HG00738.hp2 HG01255.hp2 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.392-4654_392-4647d others(10): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95490520 | ||||||
| chr9:95490520
|
G | GACACACA others(3): Show |
5 | a0001c0003t0003g0172a0001c0003t0003g0180a0001c0003t0003g0181others(2): Show | 5 | HG01099.hp1 HG01192.hp2 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.392-4656_392-4647d others(12): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95490520 | ||||||
| chr9:95490520
|
GAC | G | 44 | a0001c0002t0003g0235a0001c0002t0011g0185a0001c0002t0013g0009others(41): Show | 47 | HG00140.hp2 HG00558.hp1 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.392-4648_392-4647d others(4): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95490520 | ||||||
| chr9:95490520
|
GACAC | G | 4 | a0001c0002t0001g0073a0001c0002t0001g0074a0001c0002t0011g0008others(1): Show | 5 | HG00639.hp1 HG01109.hp1 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.392-4650_392-4647d others(6): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95490520 | ||||||
| chr9:95490520
|
GACACAC | G | 6 | a0001c0008t0012g0014a0001c0008t0012g0017a0001c0008t0012g0018others(3): Show | 6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.392-4652_392-4647d others(8): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95490520 | ||||||
| chr9:95490520
|
GACACACA others(5): Show |
G | 7 | a0001c0002t0001g0061a0002c0001t0001g0056a0002c0001t0001g0062others(4): Show | 7 | HG01106.hp2 HG01123.hp2 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.392-4658_392-4647d others(14): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95490520 | ||||||
| chr9:95490529
|
A | ACC | 9 | a0002c0001t0004g0094a0002c0001t0009g0080a0002c0001t0009g0095others(6): Show | 9 | HG02257.hp2 HG02630.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.392-4656_392-4655i others(4): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95490529 | ||||||
| chr9:95490558
|
A | C | 3 | a0001c0024t0001g0227a0014c0017t0022g0020a0016c0039t0022g0262 | 3 | HG02683.hp2 HG02723.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.392-4684T>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95490558 | ||||||
| chr9:95490565
|
G | A | 150 | a0001c0002t0002g0214a0001c0002t0002g0261a0001c0002t0003g0235others(147): Show | 158 | HG00140.hp2 HG00423.hp2 HG00558.hp2 others(155): Show |
intron_variant | MODIFIER | c.392-4691C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95490565 | ||||||
| chr9:95490617
|
C | CA | 7 | a0001c0002t0002g0005a0001c0002t0002g0041a0001c0002t0002g0067others(4): Show | 8 | HG01358.hp1 HG01934.hp1 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.392-4744dupT | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95490617 | ||||||
| chr9:95490668
|
A | G | 53 | a0001c0002t0002g0261a0001c0002t0005g0201a0001c0002t0005g0204others(50): Show | 56 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.392-4794T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95490668 | ||||||
| chr9:95490759
|
C | G | 9 | a0002c0001t0004g0094a0002c0001t0009g0080a0002c0001t0009g0095others(6): Show | 9 | HG02257.hp2 HG02630.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.392-4885G>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95490759 | ||||||
| chr9:95490929
|
C | T | 6 | a0001c0008t0012g0014a0001c0008t0012g0017a0001c0008t0012g0018others(3): Show | 6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.392-5055G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95490929 | ||||||
| chr9:95490957
|
C | T | 1 | a0001c0003t0003g0183 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.392-5083G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95490957 | ||||||
| chr9:95491121
|
T | C | 5 | a0001c0002t0005g0204a0001c0002t0005g0205a0003c0005t0004g0076others(2): Show | 5 | HG01952.hp1 HG02109.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.392-5247A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95491121 | ||||||
| chr9:95491194
|
G | A | 44 | a0001c0003t0001g0007a0001c0003t0001g0160a0001c0003t0001g0166others(41): Show | 45 | HG00597.hp1 HG00738.hp2 HG01099.hp1 others(42): Show |
intron_variant | MODIFIER | c.392-5320C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95491194 | ||||||
| chr9:95491208
|
C | T | 14 | a0001c0002t0005g0204a0001c0002t0005g0205a0001c0002t0007g0036others(11): Show | 15 | HG01109.hp2 HG01952.hp1 HG02056.hp1 others(12): Show |
intron_variant | MODIFIER | c.392-5334G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95491208 | ||||||
| chr9:95491243
|
C | T | 1 | a0002c0001t0035g0113 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.392-5369G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95491243 | ||||||
| chr9:95491254
|
G | A | 1 | a0003c0005t0002g0206 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.392-5380C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95491254 | ||||||
| chr9:95491380
|
G | A | 1 | a0001c0002t0005g0207 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.392-5506C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95491380 | ||||||
| chr9:95491381
|
G | A | 1 | a0001c0002t0013g0009 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.392-5507C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95491381 | ||||||
| chr9:95491469
|
C | T | 1 | a0003c0005t0004g0108 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.392-5595G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95491469 | ||||||
| chr9:95491554
|
T | C | 1 | a0001c0003t0037g0037 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.392-5680A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95491554 | ||||||
| chr9:95491776
|
C | T | 2 | a0002c0001t0017g0046a0010c0028t0001g0150 | 2 | NA18965.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.392-5902G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95491776 | ||||||
| chr9:95491903
|
T | C | 1 | a0002c0001t0001g0138 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.392-6029A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95491903 | ||||||
| chr9:95491936
|
T | C | 2 | a0001c0002t0002g0107a0001c0002t0002g0139 | 2 | HG01071.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.392-6062A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95491936 | ||||||
| chr9:95491947
|
C | T | 1 | a0011c0027t0001g0142 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.392-6073G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95491947 | ||||||
| chr9:95492017
|
A | T | 1 | a0001c0002t0005g0201 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.392-6143T>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95492017 | ||||||
| chr9:95492040
|
G | A | 1 | a0002c0031t0001g0091 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.392-6166C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95492040 | ||||||
| chr9:95492096
|
C | T | 2 | a0001c0003t0001g0191a0001c0003t0001g0192 | 2 | HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.392-6222G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95492096 | ||||||
| chr9:95492190
|
A | G | 2 | a0001c0002t0020g0035a0001c0002t0020g0042 | 2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.392-6316T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95492190 | ||||||
| chr9:95492244
|
C | A | 106 | a0001c0002t0002g0214a0001c0002t0002g0261a0001c0002t0003g0235others(103): Show | 113 | HG00140.hp2 HG00423.hp2 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.392-6370G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95492244 | ||||||
| chr9:95492328
|
G | C | 6 | a0001c0008t0012g0014a0001c0008t0012g0017a0001c0008t0012g0018others(3): Show | 6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.392-6454C>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95492328 | ||||||
| chr9:95492337
|
T | C | 4 | a0001c0002t0007g0036a0006c0010t0007g0013a0006c0010t0007g0263others(1): Show | 5 | HG02145.hp1 HG02572.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.392-6463A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95492337 | ||||||
| chr9:95492571
|
A | G | 1 | a0009c0026t0002g0190 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.392-6697T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95492571 | ||||||
| chr9:95492713
|
G | A | 1 | a0004c0006t0006g0001 | 2 | HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.392-6839C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95492713 | ||||||
| chr9:95492821
|
A | AG | 150 | a0001c0002t0002g0214a0001c0002t0002g0261a0001c0002t0003g0235others(147): Show | 158 | HG00140.hp2 HG00423.hp2 HG00558.hp2 others(155): Show |
intron_variant | MODIFIER | c.392-6948_392-6947i others(3): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95492821 | ||||||
| chr9:95493156
|
T | C | 31 | a0001c0002t0005g0201a0001c0002t0005g0259a0001c0002t0020g0035others(28): Show | 33 | HG00558.hp2 HG00609.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.392-7282A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95493156 | ||||||
| chr9:95493244
|
G | A | 1 | a0002c0001t0001g0124 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.392-7370C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95493244 | ||||||
| chr9:95493256
|
A | C | 2 | a0001c0002t0005g0207a0001c0030t0032g0211 | 2 | HG01081.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.392-7382T>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95493256 | ||||||
| chr9:95493337
|
C | G | 1 | a0003c0005t0004g0216 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.392-7463G>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95493337 | ||||||
| chr9:95493545
|
A | C | 1 | a0004c0006t0006g0028 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.392-7671T>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95493545 | ||||||
| chr9:95493746
|
T | C | 1 | a0001c0002t0007g0036 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.392-7872A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95493746 | ||||||
| chr9:95493750
|
C | T | 1 | a0001c0003t0008g0194 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.392-7876G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95493750 | ||||||
| chr9:95493801
|
C | CA | 18 | a0001c0003t0001g0191a0001c0003t0001g0192a0001c0003t0004g0196others(15): Show | 18 | HG01884.hp2 HG02109.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.392-7928dupT | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95493801 | ||||||
| chr9:95493801
|
C | CAA | 25 | a0001c0003t0001g0007a0001c0003t0001g0160a0001c0003t0001g0166others(22): Show | 26 | HG00597.hp1 HG00738.hp2 HG01099.hp1 others(23): Show |
intron_variant | MODIFIER | c.392-7929_392-7928d others(4): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95493801 | ||||||
| chr9:95493899
|
G | A | 2 | a0001c0015t0002g0055a0001c0015t0039g0130 | 2 | HG01081.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.392-8025C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95493899 | ||||||
| chr9:95493953
|
T | G | 2 | a0001c0002t0002g0104a0002c0001t0002g0054 | 2 | HG01516.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.392-8079A>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95493953 | ||||||
| chr9:95494027
|
G | A | 43 | a0001c0003t0001g0007a0001c0003t0001g0160a0001c0003t0001g0166others(40): Show | 44 | HG00597.hp1 HG00738.hp2 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.392-8153C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95494027 | ||||||
| chr9:95494046
|
C | T | 3 | a0003c0005t0002g0079a0003c0005t0002g0128a0003c0005t0002g0129 | 3 | HG03195.hp1 HG03516.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.392-8172G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95494046 | ||||||
| chr9:95494076
|
A | AACCGCAC others(3): Show |
1 | a0001c0003t0008g0193 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.392-8212_392-8203d others(12): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95494076 | ||||||
| chr9:95494076
|
AACCGCAC others(3): Show |
A | 5 | a0001c0002t0002g0214a0001c0003t0023g0038a0001c0014t0021g0212others(2): Show | 5 | HG02647.hp2 HG02818.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.392-8212_392-8203d others(12): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95494076 | ||||||
| chr9:95494131
|
C | T | 1 | a0001c0002t0020g0035 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.392-8257G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95494131 | ||||||
| chr9:95494139
|
C | T | 1 | a0002c0013t0001g0233 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.392-8265G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95494139 | ||||||
| chr9:95494158
|
T | A | 18 | a0001c0002t0011g0008a0001c0002t0011g0185a0001c0002t0013g0009others(15): Show | 21 | HG01069.hp1 HG01071.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.392-8284A>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95494158 | ||||||
| chr9:95494164
|
G | A | 3 | a0001c0003t0001g0191a0001c0003t0001g0192a0003c0005t0002g0206 | 3 | HG01884.hp2 HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.392-8290C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95494164 | ||||||
| chr9:95494333
|
C | T | 4 | a0001c0002t0007g0036a0006c0010t0007g0013a0006c0010t0007g0263others(1): Show | 5 | HG02145.hp1 HG02572.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.392-8459G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95494333 | ||||||
| chr9:95494438
|
C | G | 14 | a0001c0002t0013g0009a0004c0006t0001g0032a0004c0006t0001g0033others(11): Show | 16 | HG01069.hp1 HG01071.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.392-8564G>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95494438 | ||||||
| chr9:95494769
|
T | C | 1 | a0001c0002t0001g0148 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.392-8895A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95494769 | ||||||
| chr9:95494827
|
C | T | 1 | a0003c0005t0002g0079 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.392-8953G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95494827 | ||||||
| chr9:95494886
|
T | C | 1 | a0002c0001t0001g0125 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.392-9012A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95494886 | ||||||
| chr9:95495012
|
C | T | 1 | a0001c0030t0032g0211 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.392-9138G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95495012 | ||||||
| chr9:95495023
|
C | T | 33 | a0001c0002t0003g0235a0001c0002t0040g0230a0001c0004t0001g0012others(30): Show | 34 | HG00140.hp2 HG00609.hp2 HG01074.hp2 others(31): Show |
intron_variant | MODIFIER | c.392-9149G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95495023 | ||||||
| chr9:95495054
|
G | A | 1 | a0003c0005t0002g0206 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.392-9180C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95495054 | ||||||
| chr9:95495214
|
C | T | 1 | a0001c0002t0001g0112 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.392-9340G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95495214 | ||||||
| chr9:95495237
|
A | C | 2 | a0001c0003t0003g0177a0001c0003t0034g0068 | 2 | NA20752.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.392-9363T>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95495237 | ||||||
| chr9:95495427
|
C | CT | 16 | a0001c0002t0002g0111a0001c0002t0005g0204a0001c0002t0005g0205others(13): Show | 16 | HG01952.hp2 HG02109.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.392-9554dupA | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95495427 | ||||||
| chr9:95495441
|
A | T | 4 | a0001c0002t0020g0035a0001c0002t0020g0042a0014c0017t0022g0020others(1): Show | 4 | HG02723.hp2 HG02818.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.392-9567T>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95495441 | ||||||
| chr9:95495524
|
G | A | 1 | a0001c0002t0033g0157 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.392-9650C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95495524 | ||||||
| chr9:95495560
|
C | T | 149 | a0001c0002t0002g0214a0001c0002t0002g0261a0001c0002t0003g0235others(146): Show | 157 | HG00140.hp2 HG00423.hp2 HG00558.hp2 others(154): Show |
intron_variant | MODIFIER | c.392-9686G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95495560 | ||||||
| chr9:95495646
|
A | G | 2 | a0001c0002t0011g0008a0001c0002t0011g0185 | 3 | HG01243.hp1 HG03130.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.392-9772T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95495646 | ||||||
| chr9:95495753
|
T | TG | 8 | a0001c0003t0004g0196a0001c0003t0004g0198a0001c0003t0004g0199others(5): Show | 8 | HG02145.hp2 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.392-9880dupC | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95495753 | ||||||
| chr9:95496084
|
T | C | 1 | a0001c0003t0004g0199 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.392-10210A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95496084 | ||||||
| chr9:95496128
|
C | A | 1 | a0001c0003t0030g0173 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.392-10254G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95496128 | ||||||
| chr9:95496199
|
C | G | 1 | a0003c0005t0001g0223 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.391+10208G>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95496199 | ||||||
| chr9:95496537
|
T | TA | 20 | a0001c0002t0005g0259a0001c0024t0001g0227a0002c0001t0009g0260others(17): Show | 22 | HG00673.hp2 HG02015.hp1 HG02056.hp2 others(19): Show |
intron_variant | MODIFIER | c.391+9869dupT | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95496537 | ||||||
| chr9:95496979
|
G | A | 2 | a0001c0002t0005g0207a0001c0030t0032g0211 | 2 | HG01081.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.391+9428C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95496979 | ||||||
| chr9:95497421
|
T | G | 131 | a0001c0002t0001g0254a0001c0002t0002g0147a0001c0002t0002g0195others(128): Show | 138 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.391+8986A>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95497421 | ||||||
| chr9:95497489
|
CT | C | 131 | a0001c0002t0001g0254a0001c0002t0002g0147a0001c0002t0002g0195others(128): Show | 138 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.391+8917delA | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95497489 | ||||||
| chr9:95497951
|
C | T | 2 | a0001c0002t0001g0073a0001c0002t0001g0074 | 2 | HG00639.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.391+8456G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95497951 | ||||||
| chr9:95497967
|
G | A | 8 | a0001c0002t0007g0036a0001c0003t0023g0038a0001c0003t0023g0039others(5): Show | 9 | HG01884.hp2 HG02145.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.391+8440C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95497967 | ||||||
| chr9:95498232
|
G | A | 131 | a0001c0002t0001g0254a0001c0002t0002g0147a0001c0002t0002g0195others(128): Show | 138 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.391+8175C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95498232 | ||||||
| chr9:95498273
|
T | C | 8 | a0001c0002t0011g0008a0001c0002t0011g0185a0001c0002t0011g0188others(5): Show | 9 | HG01109.hp2 HG01243.hp1 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.391+8134A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95498273 | ||||||
| chr9:95498656
|
T | C | 2 | a0001c0014t0021g0212a0001c0014t0021g0213 | 2 | HG02818.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.391+7751A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95498656 | ||||||
| chr9:95498729
|
G | T | 2 | a0001c0014t0021g0212a0001c0014t0021g0213 | 2 | HG02818.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.391+7678C>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95498729 | ||||||
| chr9:95498750
|
C | A | 17 | a0001c0002t0002g0261a0004c0006t0001g0032a0004c0006t0001g0033others(14): Show | 18 | HG01243.hp2 HG01884.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.391+7657G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95498750 | ||||||
| chr9:95499108
|
C | T | 1 | a0001c0004t0001g0229 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.391+7299G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95499108 | ||||||
| chr9:95499519
|
G | C | 4 | a0001c0002t0007g0036a0006c0010t0007g0013a0006c0010t0007g0263others(1): Show | 5 | HG02145.hp1 HG02572.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.391+6888C>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95499519 | ||||||
| chr9:95499783
|
C | G | 1 | a0004c0006t0002g0023 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.391+6624G>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95499783 | ||||||
| chr9:95499896
|
G | A | 42 | a0001c0002t0002g0195a0001c0002t0005g0204a0001c0002t0005g0205others(39): Show | 44 | HG00597.hp1 HG00738.hp2 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.391+6511C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95499896 | ||||||
| chr9:95499908
|
C | G | 5 | a0001c0015t0002g0055a0001c0015t0039g0130a0003c0005t0002g0079others(2): Show | 5 | HG01081.hp2 HG03195.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.391+6499G>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95499908 | ||||||
| chr9:95499941
|
G | A | 45 | a0001c0002t0002g0195a0001c0002t0005g0204a0001c0002t0005g0205others(42): Show | 47 | HG00597.hp1 HG00738.hp2 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.391+6466C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95499941 | ||||||
| chr9:95500002
|
C | A | 2 | a0014c0017t0022g0020a0016c0039t0022g0262 | 2 | HG02723.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.391+6405G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95500002 | ||||||
| chr9:95500035
|
G | A | 1 | a0001c0002t0002g0126 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.391+6372C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95500035 | ||||||
| chr9:95500116
|
G | A | 1 | a0004c0006t0006g0031 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.391+6291C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95500116 | ||||||
| chr9:95500213
|
A | G | 1 | a0002c0001t0002g0060 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.391+6194T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95500213 | ||||||
| chr9:95500350
|
T | C | 3 | a0001c0008t0015g0015a0001c0037t0024g0016a0015c0038t0015g0019 | 3 | HG02015.hp2 HG02071.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.391+6057A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95500350 | ||||||
| chr9:95500353
|
C | T | 1 | a0001c0004t0001g0256 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.391+6054G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95500353 | ||||||
| chr9:95500453
|
A | G | 61 | a0001c0002t0001g0254a0001c0002t0002g0147a0001c0002t0003g0235others(58): Show | 65 | HG00140.hp2 HG00408.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.391+5954T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95500453 | ||||||
| chr9:95500551
|
A | G | 132 | a0001c0002t0001g0254a0001c0002t0002g0147a0001c0002t0002g0195others(129): Show | 139 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.391+5856T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95500551 | ||||||
| chr9:95500575
|
C | T | 1 | a0001c0002t0001g0153 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.391+5832G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95500575 | ||||||
| chr9:95500654
|
G | A | 1 | a0001c0004t0003g0255 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.391+5753C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95500654 | ||||||
| chr9:95500747
|
C | T | 16 | a0004c0006t0001g0032a0004c0006t0001g0033a0004c0006t0002g0022others(13): Show | 17 | HG01243.hp2 HG01884.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.391+5660G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95500747 | ||||||
| chr9:95500838
|
T | C | 2 | a0001c0003t0023g0039a0001c0003t0037g0037 | 2 | HG02451.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.391+5569A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95500838 | ||||||
| chr9:95500856
|
A | C | 17 | a0001c0002t0002g0261a0004c0006t0001g0032a0004c0006t0001g0033others(14): Show | 18 | HG01243.hp2 HG01884.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.391+5551T>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95500856 | ||||||
| chr9:95500950
|
C | T | 2 | a0001c0002t0020g0035a0001c0002t0020g0042 | 2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.391+5457G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95500950 | ||||||
| chr9:95500961
|
G | A | 1 | a0001c0002t0004g0071 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.391+5446C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95500961 | ||||||
| chr9:95501063
|
T | C | 1 | a0001c0002t0002g0261 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.391+5344A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95501063 | ||||||
| chr9:95501174
|
C | A | 16 | a0001c0024t0001g0227a0003c0005t0001g0011a0003c0005t0001g0175others(13): Show | 18 | HG00673.hp2 HG02015.hp1 HG02056.hp2 others(15): Show |
intron_variant | MODIFIER | c.391+5233G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95501174 | ||||||
| chr9:95501375
|
G | C | 3 | a0001c0002t0002g0141a0001c0003t0034g0068a0002c0001t0036g0127 | 3 | HG00639.hp2 HG02683.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.391+5032C>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95501375 | ||||||
| chr9:95501539
|
T | TA | 98 | a0001c0002t0001g0254a0001c0002t0002g0147a0001c0002t0002g0195others(95): Show | 104 | HG00140.hp2 HG00408.hp2 HG00597.hp1 others(101): Show |
intron_variant | MODIFIER | c.391+4867dupT | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95501539 | ||||||
| chr9:95501539
|
TA | T | 7 | a0001c0002t0001g0093a0001c0002t0001g0106a0001c0002t0002g0107others(4): Show | 7 | HG01069.hp2 HG01074.hp1 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.391+4867delT | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95501539 | ||||||
| chr9:95501539
|
TAAA | T | 18 | a0001c0002t0002g0261a0001c0002t0004g0071a0004c0006t0001g0032others(15): Show | 19 | HG01243.hp2 HG01884.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.391+4865_391+4867d others(5): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95501539 | ||||||
| chr9:95501588
|
G | A | 16 | a0004c0006t0001g0032a0004c0006t0001g0033a0004c0006t0002g0022others(13): Show | 17 | HG01243.hp2 HG01884.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.391+4819C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95501588 | ||||||
| chr9:95501985
|
A | G | 1 | a0003c0005t0001g0228 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.391+4422T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95501985 | ||||||
| chr9:95502055
|
G | C | 3 | a0001c0003t0004g0198a0001c0003t0004g0199a0001c0003t0004g0200 | 3 | HG03195.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.391+4352C>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95502055 | ||||||
| chr9:95502090
|
A | G | 8 | a0001c0002t0011g0008a0001c0002t0011g0185a0001c0002t0011g0188others(5): Show | 9 | HG01109.hp2 HG01243.hp1 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.391+4317T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95502090 | ||||||
| chr9:95502236
|
G | A | 2 | a0003c0005t0001g0223a0007c0025t0004g0224 | 2 | HG02129.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.391+4171C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95502236 | ||||||
| chr9:95502466
|
C | A | 3 | a0002c0001t0014g0057a0002c0001t0014g0058a0002c0001t0014g0059 | 3 | HG01123.hp2 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.391+3941G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95502466 | ||||||
| chr9:95502660
|
A | C | 45 | a0001c0002t0002g0195a0001c0002t0005g0204a0001c0002t0005g0205others(42): Show | 47 | HG00597.hp1 HG00738.hp2 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.391+3747T>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95502660 | ||||||
| chr9:95502666
|
A | C | 16 | a0001c0024t0001g0227a0003c0005t0001g0011a0003c0005t0001g0175others(13): Show | 18 | HG00673.hp2 HG02015.hp1 HG02056.hp2 others(15): Show |
intron_variant | MODIFIER | c.391+3741T>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95502666 | ||||||
| chr9:95502722
|
C | A | 17 | a0001c0002t0002g0261a0004c0006t0001g0032a0004c0006t0001g0033others(14): Show | 18 | HG01243.hp2 HG01884.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.391+3685G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95502722 | ||||||
| chr9:95502869
|
G | A | 1 | a0001c0004t0001g0229 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.391+3538C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95502869 | ||||||
| chr9:95502894
|
C | T | 1 | a0002c0001t0028g0105 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.391+3513G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95502894 | ||||||
| chr9:95502907
|
G | A | 2 | a0001c0003t0008g0202a0001c0003t0008g0203 | 2 | HG02630.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.391+3500C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95502907 | ||||||
| chr9:95502936
|
C | T | 6 | a0004c0006t0006g0001a0004c0006t0006g0021a0004c0006t0006g0028others(3): Show | 7 | HG01243.hp2 HG02922.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.391+3471G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95502936 | ||||||
| chr9:95503243
|
G | A | 1 | a0001c0004t0001g0256 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.391+3164C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95503243 | ||||||
| chr9:95503380
|
C | A | 3 | a0001c0002t0002g0214a0001c0014t0021g0212a0001c0014t0021g0213 | 3 | HG02818.hp1 HG03041.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.391+3027G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95503380 | ||||||
| chr9:95503405
|
G | A | 1 | a0001c0002t0005g0201 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.391+3002C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95503405 | ||||||
| chr9:95503498
|
C | T | 132 | a0001c0002t0001g0254a0001c0002t0002g0147a0001c0002t0002g0195others(129): Show | 139 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.391+2909G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95503498 | ||||||
| chr9:95503551
|
G | T | 1 | a0001c0003t0003g0183 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.391+2856C>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95503551 | ||||||
| chr9:95503619
|
A | G | 45 | a0001c0002t0002g0195a0001c0002t0005g0204a0001c0002t0005g0205others(42): Show | 47 | HG00597.hp1 HG00738.hp2 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.391+2788T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95503619 | ||||||
| chr9:95503732
|
TAGGGCCG others(322): Show |
T | 140 | a0001c0002t0001g0254a0001c0002t0002g0147a0001c0002t0002g0195others(137): Show | 148 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.391+2346_391+2674d others(2): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95503732 | ||||||
| chr9:95504022
|
C | CA | 6 | a0001c0002t0001g0144a0001c0015t0002g0055a0002c0001t0001g0006others(3): Show | 7 | HG00408.hp1 HG01099.hp2 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.391+2384dupT | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95504022 | ||||||
| chr9:95504022
|
C | CAAAAAAA others(6): Show |
1 | a0002c0034t0001g0145 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.391+2372_391+2384d others(15): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95504022 | ||||||
| chr9:95504022
|
CA | C | 34 | a0001c0002t0001g0106a0001c0002t0001g0112a0001c0002t0002g0041others(31): Show | 34 | HG00423.hp1 HG00558.hp1 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.391+2384delT | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95504022 | ||||||
| chr9:95504022
|
CAA | C | 28 | a0001c0002t0001g0074a0001c0002t0001g0093a0001c0002t0001g0156others(25): Show | 30 | HG01106.hp1 HG01109.hp1 HG01123.hp1 others(27): Show |
intron_variant | MODIFIER | c.391+2383_391+2384d others(4): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95504022 | ||||||
| chr9:95504022
|
CAAA | C | 24 | a0001c0002t0001g0073a0001c0002t0001g0083a0001c0002t0001g0085others(21): Show | 24 | HG00639.hp1 HG01069.hp2 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.391+2382_391+2384d others(5): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95504022 | ||||||
| chr9:95504022
|
CAAAAAAA others(4): Show |
C | 1 | a0002c0001t0003g0151 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.391+2374_391+2384d others(13): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95504022 | ||||||
| chr9:95504022
|
CAAAAAAA others(10): Show |
C | 1 | a0003c0005t0002g0079 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.391+2368_391+2384d others(19): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95504022 | ||||||
| chr9:95504022
|
CAAAAAAA others(11): Show |
C | 2 | a0001c0002t0020g0042a0001c0004t0001g0078 | 2 | HG03471.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.391+2367_391+2384d others(20): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95504022 | ||||||
| chr9:95504022
|
CAAAAAAA others(12): Show |
C | 2 | a0001c0002t0020g0035a0002c0001t0018g0077 | 2 | HG02071.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.391+2366_391+2384d others(21): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95504022 | ||||||
| chr9:95504022
|
CAAAAAAA others(14): Show |
C | 1 | a0003c0005t0004g0076 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.391+2364_391+2384d others(23): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95504022 | ||||||
| chr9:95504056
|
A | C | 2 | a0001c0002t0020g0035a0001c0002t0020g0042 | 2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.391+2351T>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95504056 | ||||||
| chr9:95504061
|
A | T | 2 | a0001c0002t0020g0035a0001c0002t0020g0042 | 2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.391+2346T>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95504061 | ||||||
| chr9:95504088
|
A | G | 132 | a0001c0002t0001g0254a0001c0002t0002g0147a0001c0002t0002g0195others(129): Show | 139 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.391+2319T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95504088 | ||||||
| chr9:95504380
|
G | A | 6 | a0001c0008t0012g0014a0001c0008t0012g0017a0001c0008t0012g0018others(3): Show | 6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.391+2027C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95504380 | ||||||
| chr9:95504573
|
T | A | 46 | a0001c0002t0002g0195a0001c0002t0005g0201a0001c0002t0005g0204others(43): Show | 48 | HG00597.hp1 HG00738.hp2 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.391+1834A>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95504573 | ||||||
| chr9:95505066
|
G | A | 1 | a0015c0038t0015g0019 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.391+1341C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95505066 | ||||||
| chr9:95505141
|
G | A | 24 | a0001c0002t0002g0261a0001c0002t0007g0036a0001c0003t0023g0038others(21): Show | 26 | HG01243.hp2 HG01884.hp1 HG02145.hp1 others(23): Show |
intron_variant | MODIFIER | c.391+1266C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95505141 | ||||||
| chr9:95505266
|
C | T | 2 | a0001c0003t0008g0202a0001c0003t0008g0203 | 2 | HG02630.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.391+1141G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95505266 | ||||||
| chr9:95505300
|
G | A | 1 | a0001c0030t0032g0211 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.391+1107C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95505300 | ||||||
| chr9:95505359
|
G | A | 1 | a0002c0001t0001g0146 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.391+1048C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95505359 | ||||||
| chr9:95505361
|
A | T | 7 | a0001c0002t0001g0061a0002c0001t0001g0056a0002c0001t0001g0062others(4): Show | 7 | HG01106.hp2 HG01123.hp2 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.391+1046T>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95505361 | ||||||
| chr9:95505464
|
T | G | 140 | a0001c0002t0001g0254a0001c0002t0002g0147a0001c0002t0002g0195others(137): Show | 148 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.391+943A>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95505464 | ||||||
| chr9:95505488
|
G | A | 1 | a0004c0006t0006g0021 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.391+919C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95505488 | ||||||
| chr9:95505833
|
T | C | 1 | a0001c0003t0003g0183 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.391+574A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95505833 | ||||||
| chr9:95505881
|
G | T | 6 | a0004c0006t0006g0001a0004c0006t0006g0021a0004c0006t0006g0028others(3): Show | 7 | HG01243.hp2 HG02922.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.391+526C>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95505881 | ||||||
| chr9:95505918
|
C | A | 1 | a0001c0004t0001g0257 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.391+489G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95505918 | ||||||
| chr9:95505983
|
C | T | 1 | a0002c0022t0001g0075 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.391+424G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95505983 | ||||||
| chr9:95506114
|
G | A | 6 | a0001c0008t0012g0014a0001c0008t0012g0017a0001c0008t0012g0018others(3): Show | 6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.391+293C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95506114 | ||||||
| chr9:95506192
|
C | G | 1 | a0001c0003t0005g0208 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.391+215G>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95506192 | ||||||
| chr9:95506195
|
G | T | 6 | a0001c0008t0012g0014a0001c0008t0012g0017a0001c0008t0012g0018others(3): Show | 6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.391+212C>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95506195 | ||||||
| chr9:95506336
|
T | C | 2 | a0001c0002t0011g0008a0001c0002t0011g0185 | 3 | HG01243.hp1 HG03130.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.391+71A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 2/23 | chr9 | 95506336 | ||||||
| chr9:95506656
|
A | ACGCCCGC others(11): Show |
24 | a0001c0003t0001g0007a0001c0003t0001g0160a0001c0003t0001g0166others(21): Show | 25 | HG00597.hp1 HG00738.hp2 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.199-75_199-58dupGG others(16): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95506656 | ||||||
| chr9:95506816
|
G | A | 6 | a0001c0008t0012g0014a0001c0008t0012g0017a0001c0008t0012g0018others(3): Show | 6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.199-217C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95506816 | ||||||
| chr9:95507136
|
CG | C | 85 | a0001c0002t0001g0254a0001c0002t0002g0214a0001c0002t0002g0261others(82): Show | 90 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.199-538delC | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95507136 | ||||||
| chr9:95507156
|
C | T | 2 | a0001c0002t0001g0073a0001c0002t0001g0074 | 2 | HG00639.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.199-557G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95507156 | ||||||
| chr9:95507208
|
G | C | 1 | a0001c0002t0001g0148 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.199-609C>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95507208 | ||||||
| chr9:95507381
|
G | A | 3 | a0004c0006t0002g0022a0004c0006t0027g0025a0004c0016t0002g0024 | 3 | HG02451.hp1 HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.199-782C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95507381 | ||||||
| chr9:95507433
|
T | A | 1 | a0002c0013t0001g0258 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.199-834A>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95507433 | ||||||
| chr9:95507655
|
A | C | 1 | a0001c0003t0003g0161 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.199-1056T>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95507655 | ||||||
| chr9:95507757
|
T | C | 4 | a0004c0006t0002g0022a0004c0006t0002g0023a0004c0006t0027g0025others(1): Show | 4 | HG02451.hp1 HG02622.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.199-1158A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95507757 | ||||||
| chr9:95507764
|
C | T | 4 | a0001c0002t0004g0071a0002c0001t0001g0069a0002c0001t0001g0072others(1): Show | 4 | HG02559.hp2 HG02965.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.199-1165G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95507764 | ||||||
| chr9:95507792
|
A | T | 1 | a0001c0003t0034g0068 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.199-1193T>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95507792 | ||||||
| chr9:95507886
|
A | G | 131 | a0001c0002t0001g0254a0001c0002t0002g0195a0001c0002t0002g0214others(128): Show | 138 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.199-1287T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95507886 | ||||||
| chr9:95507889
|
A | G | 141 | a0001c0002t0001g0254a0001c0002t0002g0195a0001c0002t0002g0214others(138): Show | 149 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.199-1290T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95507889 | ||||||
| chr9:95507905
|
T | TAC | 13 | a0001c0002t0005g0207a0001c0002t0007g0036a0001c0002t0020g0035others(10): Show | 14 | HG01081.hp1 HG01884.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.199-1308_199-1307d others(4): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95507905 | ||||||
| chr9:95507905
|
T | TACAC | 124 | a0001c0002t0001g0254a0001c0002t0002g0195a0001c0002t0002g0214others(121): Show | 131 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.199-1310_199-1307d others(6): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95507905 | ||||||
| chr9:95507905
|
T | TACACAC | 3 | a0001c0002t0005g0201a0001c0003t0004g0200a0001c0024t0001g0227 | 3 | HG02257.hp1 HG02683.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.199-1312_199-1307d others(8): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95507905 | ||||||
| chr9:95508034
|
TGTGA | T | 49 | a0001c0002t0002g0195a0001c0002t0002g0214a0001c0002t0002g0261others(46): Show | 51 | HG00597.hp1 HG00738.hp2 HG01069.hp1 others(48): Show |
intron_variant | MODIFIER | c.199-1439_199-1436d others(6): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95508034 | ||||||
| chr9:95508038
|
AGTGAGTG others(1): Show |
A | 62 | a0001c0002t0001g0254a0001c0002t0003g0235a0001c0002t0005g0259others(59): Show | 66 | HG00140.hp2 HG00408.hp2 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.199-1447_199-1440d others(10): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95508038 | ||||||
| chr9:95508040
|
TGA | T | 14 | a0004c0006t0001g0032a0004c0006t0001g0033a0004c0006t0002g0022others(11): Show | 15 | HG01243.hp2 HG01884.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.199-1443_199-1442d others(4): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95508040 | ||||||
| chr9:95508042
|
A | T | 7 | a0001c0002t0002g0067a0001c0008t0012g0014a0001c0008t0012g0017others(4): Show | 7 | HG00423.hp2 HG01358.hp1 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.199-1443T>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95508042 | ||||||
| chr9:95508060
|
A | T | 17 | a0001c0002t0002g0261a0002c0001t0001g0063a0004c0006t0001g0032others(14): Show | 18 | HG01243.hp2 HG01884.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.199-1461T>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95508060 | ||||||
| chr9:95508253
|
C | G | 2 | a0003c0012t0002g0186a0003c0012t0002g0187 | 2 | NA18970.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.199-1654G>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95508253 | ||||||
| chr9:95508325
|
G | C | 1 | a0002c0001t0001g0149 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.199-1726C>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95508325 | ||||||
| chr9:95508364
|
T | TGCC | 84 | a0001c0002t0001g0254a0001c0002t0002g0214a0001c0002t0002g0261others(81): Show | 89 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.199-1768_199-1766d others(5): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95508364 | ||||||
| chr9:95508628
|
G | A | 1 | a0002c0001t0009g0260 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.199-2029C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95508628 | ||||||
| chr9:95508702
|
T | G | 3 | a0001c0002t0002g0214a0001c0014t0021g0212a0001c0014t0021g0213 | 3 | HG02818.hp1 HG03041.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.199-2103A>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95508702 | ||||||
| chr9:95509160
|
C | T | 1 | a0002c0001t0007g0066 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.199-2561G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95509160 | ||||||
| chr9:95509256
|
G | T | 2 | a0001c0002t0020g0035a0001c0002t0020g0042 | 2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.199-2657C>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95509256 | ||||||
| chr9:95509397
|
T | A | 1 | a0001c0002t0005g0205 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.199-2798A>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95509397 | ||||||
| chr9:95509474
|
G | A | 1 | a0004c0006t0002g0022 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.199-2875C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95509474 | ||||||
| chr9:95509615
|
GCA | G | 6 | a0002c0001t0001g0051a0002c0001t0001g0052a0002c0001t0001g0053others(3): Show | 6 | NA18960.hp1 NA18960.hp2 NA18969.hp1 others(3): Show |
intron_variant | MODIFIER | c.199-3018_199-3017d others(4): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95509615 | ||||||
| chr9:95509724
|
C | T | 7 | a0001c0002t0001g0061a0002c0001t0001g0056a0002c0001t0001g0062others(4): Show | 7 | HG01106.hp2 HG01123.hp2 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.199-3125G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95509724 | ||||||
| chr9:95509742
|
C | G | 1 | a0004c0006t0002g0022 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.199-3143G>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95509742 | ||||||
| chr9:95510002
|
T | TA | 29 | a0001c0002t0001g0254a0001c0002t0003g0235a0001c0003t0031g0253others(26): Show | 30 | HG00140.hp2 HG00408.hp2 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.199-3404dupT | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95510002 | ||||||
| chr9:95510002
|
TA | T | 15 | a0001c0002t0002g0214a0001c0002t0020g0035a0001c0002t0020g0042others(12): Show | 15 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.199-3404delT | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95510002 | ||||||
| chr9:95510012
|
A | C | 1 | a0002c0001t0002g0054 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.199-3413T>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95510012 | ||||||
| chr9:95510182
|
T | C | 54 | a0001c0002t0001g0254a0001c0002t0003g0235a0001c0002t0005g0259others(51): Show | 57 | HG00140.hp2 HG00408.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.199-3583A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95510182 | ||||||
| chr9:95510209
|
T | G | 1 | a0002c0001t0001g0152 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.199-3610A>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95510209 | ||||||
| chr9:95510348
|
G | C | 141 | a0001c0002t0001g0254a0001c0002t0002g0195a0001c0002t0002g0214others(138): Show | 149 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.199-3749C>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95510348 | ||||||
| chr9:95510545
|
C | T | 3 | a0002c0001t0001g0051a0002c0001t0001g0052a0002c0001t0001g0053 | 3 | NA18960.hp1 NA18960.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.199-3946G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95510545 | ||||||
| chr9:95510587
|
C | T | 2 | a0001c0002t0020g0035a0001c0002t0020g0042 | 2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.199-3988G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95510587 | ||||||
| chr9:95510672
|
T | C | 3 | a0001c0002t0005g0207a0001c0030t0032g0211a0003c0005t0002g0206 | 3 | HG01081.hp1 HG01884.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.199-4073A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95510672 | ||||||
| chr9:95510742
|
GAAGA | G | 17 | a0001c0002t0002g0195a0001c0002t0005g0201a0001c0002t0005g0204others(14): Show | 18 | HG01069.hp1 HG01071.hp2 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.199-4147_199-4144d others(6): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95510742 | ||||||
| chr9:95510843
|
G | T | 1 | a0004c0006t0002g0022 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.199-4244C>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95510843 | ||||||
| chr9:95510906
|
G | T | 6 | a0001c0008t0012g0014a0001c0008t0012g0017a0001c0008t0012g0018others(3): Show | 6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.199-4307C>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95510906 | ||||||
| chr9:95511023
|
T | G | 26 | a0001c0003t0001g0007a0001c0003t0001g0160a0001c0003t0001g0166others(23): Show | 27 | HG00597.hp1 HG00738.hp2 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.199-4424A>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95511023 | ||||||
| chr9:95511124
|
C | T | 1 | a0001c0003t0003g0165 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.199-4525G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95511124 | ||||||
| chr9:95511125
|
C | T | 2 | a0002c0001t0001g0049a0002c0001t0001g0050 | 2 | NA18967.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.199-4526G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95511125 | ||||||
| chr9:95511137
|
C | T | 1 | a0001c0004t0001g0229 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.199-4538G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95511137 | ||||||
| chr9:95511398
|
G | A | 1 | a0001c0002t0001g0153 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.199-4799C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95511398 | ||||||
| chr9:95511429
|
C | G | 1 | a0002c0001t0001g0048 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.199-4830G>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95511429 | ||||||
| chr9:95511435
|
C | G | 2 | a0001c0014t0021g0212a0001c0014t0021g0213 | 2 | HG02818.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.199-4836G>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95511435 | ||||||
| chr9:95511509
|
G | A | 60 | a0001c0002t0001g0254a0001c0002t0003g0235a0001c0002t0005g0259others(57): Show | 64 | HG00140.hp2 HG00408.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.199-4910C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95511509 | ||||||
| chr9:95511512
|
C | T | 1 | a0004c0006t0004g0027 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.199-4913G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95511512 | ||||||
| chr9:95511525
|
C | T | 1 | a0001c0002t0005g0207 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.199-4926G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95511525 | ||||||
| chr9:95511595
|
C | T | 2 | a0001c0002t0005g0259a0002c0001t0009g0260 | 2 | HG02615.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.199-4996G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95511595 | ||||||
| chr9:95511743
|
A | G | 1 | a0002c0021t0009g0047 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.198+4880T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95511743 | ||||||
| chr9:95511752
|
A | C | 1 | a0002c0001t0017g0046 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.198+4871T>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95511752 | ||||||
| chr9:95512004
|
T | C | 2 | a0001c0002t0020g0035a0001c0002t0020g0042 | 2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.198+4619A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95512004 | ||||||
| chr9:95512123
|
C | T | 1 | a0002c0001t0001g0045 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.198+4500G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95512123 | ||||||
| chr9:95512135
|
C | A | 1 | a0004c0006t0002g0026 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.198+4488G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95512135 | ||||||
| chr9:95512527
|
C | T | 1 | a0002c0001t0026g0044 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.198+4096G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95512527 | ||||||
| chr9:95512815
|
C | G | 60 | a0001c0002t0001g0254a0001c0002t0003g0235a0001c0002t0005g0259others(57): Show | 64 | HG00140.hp2 HG00408.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.198+3808G>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95512815 | ||||||
| chr9:95512904
|
T | C | 1 | a0001c0003t0003g0174 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.198+3719A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95512904 | ||||||
| chr9:95512992
|
T | A | 3 | a0001c0002t0002g0214a0001c0014t0021g0212a0001c0014t0021g0213 | 3 | HG02818.hp1 HG03041.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.198+3631A>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95512992 | ||||||
| chr9:95513507
|
C | T | 26 | a0001c0003t0001g0007a0001c0003t0001g0160a0001c0003t0001g0166others(23): Show | 27 | HG00597.hp1 HG00738.hp2 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.198+3116G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95513507 | ||||||
| chr9:95513742
|
G | A | 8 | a0001c0002t0007g0036a0001c0003t0023g0038a0001c0003t0023g0039others(5): Show | 9 | HG02145.hp1 HG02451.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.198+2881C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95513742 | ||||||
| chr9:95513746
|
C | T | 1 | a0002c0001t0001g0043 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.198+2877G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95513746 | ||||||
| chr9:95513823
|
C | G | 32 | a0001c0002t0001g0254a0001c0002t0003g0235a0001c0002t0040g0230others(29): Show | 33 | HG00140.hp2 HG00408.hp2 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.198+2800G>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95513823 | ||||||
| chr9:95513899
|
T | C | 1 | a0002c0013t0001g0258 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.198+2724A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95513899 | ||||||
| chr9:95514089
|
G | T | 60 | a0001c0002t0001g0254a0001c0002t0003g0235a0001c0002t0005g0259others(57): Show | 64 | HG00140.hp2 HG00408.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.198+2534C>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95514089 | ||||||
| chr9:95514092
|
T | A | 60 | a0001c0002t0001g0254a0001c0002t0003g0235a0001c0002t0005g0259others(57): Show | 64 | HG00140.hp2 HG00408.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.198+2531A>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95514092 | ||||||
| chr9:95514195
|
A | AT | 4 | a0001c0003t0003g0161a0001c0003t0003g0162a0001c0003t0003g0163others(1): Show | 4 | HG02056.hp1 NA18956.hp1 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.198+2427dupA | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95514195 | ||||||
| chr9:95514321
|
C | G | 16 | a0001c0002t0002g0261a0004c0006t0001g0032a0004c0006t0001g0033others(13): Show | 17 | HG01243.hp2 HG01884.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.198+2302G>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95514321 | ||||||
| chr9:95514471
|
C | T | 131 | a0001c0002t0001g0254a0001c0002t0002g0195a0001c0002t0002g0214others(128): Show | 138 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.198+2152G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95514471 | ||||||
| chr9:95514621
|
G | GGT | 3 | a0001c0002t0002g0041a0001c0002t0020g0042a0002c0001t0029g0040 | 3 | HG02135.hp2 HG03471.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.198+2000_198+2001d others(4): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95514621 | ||||||
| chr9:95514621
|
G | GGTGT | 9 | a0001c0002t0007g0036a0001c0003t0023g0038a0001c0003t0023g0039others(6): Show | 10 | HG02145.hp1 HG02451.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.198+1998_198+2001d others(6): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95514621 | ||||||
| chr9:95514621
|
GGT | G | 5 | a0001c0002t0001g0155a0001c0002t0001g0156a0001c0002t0020g0035others(2): Show | 5 | HG01069.hp2 HG01106.hp1 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.198+2000_198+2001d others(4): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95514621 | ||||||
| chr9:95514647
|
T | A | 1 | a0005c0007t0004g0158 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.198+1976A>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95514647 | ||||||
| chr9:95514647
|
T | TGTGA | 11 | a0001c0002t0002g0261a0003c0005t0001g0228a0004c0006t0001g0032others(8): Show | 12 | HG01243.hp2 HG01884.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.198+1975_198+1976i others(6): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95514647 | ||||||
| chr9:95514647
|
T | TGTGAGA | 32 | a0001c0002t0001g0254a0001c0002t0003g0235a0001c0002t0040g0230others(29): Show | 33 | HG00140.hp2 HG00408.hp2 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.198+1975_198+1976i others(8): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95514647 | ||||||
| chr9:95514647
|
T | TGTGTGA | 28 | a0001c0002t0005g0204a0001c0002t0005g0205a0001c0002t0005g0259others(25): Show | 30 | HG00423.hp2 HG00673.hp2 HG01952.hp1 others(27): Show |
intron_variant | MODIFIER | c.198+1975_198+1976i others(8): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95514647 | ||||||
| chr9:95514647
|
T | TGTGTGAG others(1): Show |
6 | a0001c0003t0003g0179a0001c0003t0003g0180a0001c0003t0003g0181others(3): Show | 6 | HG01099.hp1 HG01167.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.198+1975_198+1976i others(10): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95514647 | ||||||
| chr9:95514647
|
T | TGTGTGTG others(1): Show |
28 | a0001c0002t0011g0008a0001c0002t0011g0188a0001c0003t0001g0007others(25): Show | 30 | HG00597.hp1 HG01109.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.198+1975_198+1976i others(10): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95514647 | ||||||
| chr9:95514647
|
T | TGTGTGTG others(3): Show |
5 | a0001c0002t0005g0207a0001c0003t0005g0208a0001c0003t0005g0210others(2): Show | 5 | HG01081.hp1 HG02109.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.198+1975_198+1976i others(12): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95514647 | ||||||
| chr9:95514647
|
T | TGTGTGTG others(5): Show |
1 | a0001c0002t0002g0214 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.198+1975_198+1976i others(14): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95514647 | ||||||
| chr9:95514647
|
T | TGTGTGTG others(3): Show |
13 | a0001c0002t0002g0195a0001c0002t0005g0201a0001c0002t0011g0185others(10): Show | 14 | HG01069.hp1 HG01071.hp2 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.198+1975_198+1976i others(12): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95514647 | ||||||
| chr9:95514647
|
T | TGTGTGTG others(5): Show |
1 | a0003c0005t0002g0206 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.198+1975_198+1976i others(14): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95514647 | ||||||
| chr9:95514647
|
T | TGTGTGTG others(11): Show |
2 | a0001c0014t0021g0212a0001c0014t0021g0213 | 2 | HG02818.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.198+1975_198+1976i others(20): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95514647 | ||||||
| chr9:95514649
|
A | T | 8 | a0001c0002t0007g0036a0001c0003t0023g0038a0001c0003t0023g0039others(5): Show | 9 | HG02145.hp1 HG02451.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.198+1974T>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95514649 | ||||||
| chr9:95514651
|
A | T | 5 | a0001c0002t0007g0036a0006c0010t0007g0013a0006c0010t0007g0263others(2): Show | 6 | HG02145.hp1 HG02572.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.198+1972T>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95514651 | ||||||
| chr9:95514702
|
AT | A | 3 | a0001c0002t0002g0214a0001c0014t0021g0212a0001c0014t0021g0213 | 3 | HG02818.hp1 HG03041.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.198+1920delA | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95514702 | ||||||
| chr9:95514993
|
G | C | 14 | a0004c0006t0001g0032a0004c0006t0001g0033a0004c0006t0002g0022others(11): Show | 15 | HG01243.hp2 HG01884.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.198+1630C>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95514993 | ||||||
| chr9:95515031
|
C | T | 1 | a0001c0002t0002g0261 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.198+1592G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95515031 | ||||||
| chr9:95515085
|
AGTACCAC others(1): Show |
A | 50 | a0001c0002t0001g0254a0001c0002t0003g0235a0001c0002t0005g0259others(47): Show | 53 | HG00140.hp2 HG00408.hp2 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.198+1530_198+1537d others(10): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95515085 | ||||||
| chr9:95515106
|
G | T | 1 | a0001c0002t0020g0035 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.198+1517C>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95515106 | ||||||
| chr9:95515234
|
G | C | 6 | a0001c0008t0012g0014a0001c0008t0012g0017a0001c0008t0012g0018others(3): Show | 6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.198+1389C>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95515234 | ||||||
| chr9:95515331
|
T | C | 8 | a0001c0002t0011g0008a0001c0002t0011g0185a0001c0002t0011g0188others(5): Show | 9 | HG01109.hp2 HG01243.hp1 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.198+1292A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95515331 | ||||||
| chr9:95515366
|
A | G | 1 | a0001c0003t0004g0159 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.198+1257T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95515366 | ||||||
| chr9:95515509
|
C | T | 1 | a0001c0002t0001g0034 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.198+1114G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95515509 | ||||||
| chr9:95515720
|
C | A | 2 | a0001c0002t0005g0259a0002c0001t0009g0260 | 2 | HG02615.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.198+903G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95515720 | ||||||
| chr9:95515984
|
C | T | 1 | a0001c0002t0002g0261 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.198+639G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95515984 | ||||||
| chr9:95516045
|
G | A | 1 | a0001c0002t0002g0261 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.198+578C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95516045 | ||||||
| chr9:95516050
|
C | G | 131 | a0001c0002t0001g0254a0001c0002t0002g0195a0001c0002t0002g0214others(128): Show | 138 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.198+573G>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95516050 | ||||||
| chr9:95516131
|
C | T | 34 | a0001c0002t0011g0008a0001c0002t0011g0185a0001c0002t0011g0188others(31): Show | 36 | HG00597.hp1 HG00738.hp2 HG01099.hp1 others(33): Show |
intron_variant | MODIFIER | c.198+492G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95516131 | ||||||
| chr9:95516362
|
C | A | 131 | a0001c0002t0001g0254a0001c0002t0002g0195a0001c0002t0002g0214others(128): Show | 138 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.198+261G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000437951.6 | protein_coding | 1/23 | chr9 | 95516362 |