Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5727 |
| ensemblid | ENSG00000185920.19 |
| hgncid | 9585 |
| symbol | PTCH1 |
| name | patched 1 |
| refseq_nuc | NM_000264.5 |
| refseq_prot | NP_000255.2 |
| ensembl_nuc | ENST00000331920.11 |
| ensembl_prot | ENSP00000332353.6 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 95442980 |
| end | 95509266 |
| strand | - |
| ver | v1.2 |
| region | chr9:95442980-95509266 |
| region5000 | chr9:95437980-95514266 |
| regionname0 | PTCH1_chr9_95442980_95509266 |
| regionname5000 | PTCH1_chr9_95437980_95514266 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 1447 | 152 | 53 | 28 | 45 | 8 | 17 | 37 | PTCH1_chr9_95437980_95514266 | PTCH1 | MASAG others(1442): Show |
chr9 | 95437980 | 95514266 |
| a0002 | 0/1 | 1447 | 84 | 18 | 12 | 44 | 4 | 5 | 31 | PTCH1_chr9_95437980_95514266 | PTCH1 | MASAG others(1442): Show |
chr9 | 95437980 | 95514266 |
| a0003 | 0/0 | 1447 | 24 | 9 | 0 | 13 | 0 | 2 | 8 | PTCH1_chr9_95437980_95514266 | PTCH1 | MASAG others(1442): Show |
chr9 | 95437980 | 95514266 |
| a0004 | 0/0 | 1447 | 7 | 0 | 0 | 6 | 0 | 1 | 4 | PTCH1_chr9_95437980_95514266 | PTCH1 | MASAG others(1442): Show |
chr9 | 95437980 | 95514266 |
| a0005 | 0/0 | 1447 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | MASAG others(1442): Show |
chr9 | 95437980 | 95514266 |
| a0006 | 0/0 | 1447 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | MASAG others(1442): Show |
chr9 | 95437980 | 95514266 |
| a0007 | 0/0 | 1447 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | PTCH1_chr9_95437980_95514266 | PTCH1 | MASAG others(1442): Show |
chr9 | 95437980 | 95514266 |
| a0008 | 0/0 | 1447 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | MASAG others(1442): Show |
chr9 | 95437980 | 95514266 |
| a0009 | 0/0 | 1447 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | MASAG others(1442): Show |
chr9 | 95437980 | 95514266 |
| a0010 | 0/0 | 1447 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | MASAG others(1442): Show |
chr9 | 95437980 | 95514266 |
| a0011 | 0/0 | 1447 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | MASAG others(1442): Show |
chr9 | 95437980 | 95514266 |
| a0012 | 0/0 | 1447 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | MASAG others(1442): Show |
chr9 | 95437980 | 95514266 |
| a0013 | 0/0 | 1447 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | MASAG others(1442): Show |
chr9 | 95437980 | 95514266 |
| a0014 | 0/0 | 1447 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | MASAG others(1442): Show |
chr9 | 95437980 | 95514266 |
| a0015 | 0/0 | 1447 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | MASAG others(1442): Show |
chr9 | 95437980 | 95514266 |
| a0016 | 0/0 | 1447 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | MASAG others(1442): Show |
chr9 | 95437980 | 95514266 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002 | 1/0 | 4341 | 65 | 27 | 18 | 8 | 3 | 8 | PTCH1_chr9_95437980_95514266 | PTCH1 | ATGGC others(4336): Show |
chr9 | 95437980 | 95514266 | ||
| a0001c0003 | 0/0 | 4341 | 45 | 19 | 5 | 17 | 2 | 2 | PTCH1_chr9_95437980_95514266 | PTCH1 | ATGGC others(4336): Show |
chr9 | 95437980 | 95514266 | ||
| a0001c0004 | 0/0 | 4341 | 25 | 1 | 2 | 16 | 2 | 4 | PTCH1_chr9_95437980_95514266 | PTCH1 | ATGGC others(4336): Show |
chr9 | 95437980 | 95514266 | ||
| a0001c0007 | 0/0 | 4341 | 4 | 0 | 0 | 3 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | ATGGC others(4336): Show |
chr9 | 95437980 | 95514266 | ||
| a0001c0009 | 0/0 | 4341 | 4 | 1 | 2 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | ATGGC others(4336): Show |
chr9 | 95437980 | 95514266 | ||
| a0001c0013 | 0/0 | 4341 | 2 | 2 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ATGGC others(4336): Show |
chr9 | 95437980 | 95514266 | ||
| a0001c0014 | 0/0 | 4341 | 2 | 1 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ATGGC others(4336): Show |
chr9 | 95437980 | 95514266 | ||
| a0001c0022 | 0/0 | 4341 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | ATGGC others(4336): Show |
chr9 | 95437980 | 95514266 | ||
| a0001c0024 | 0/0 | 4341 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ATGGC others(4336): Show |
chr9 | 95437980 | 95514266 | ||
| a0001c0030 | 0/0 | 4341 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ATGGC others(4336): Show |
chr9 | 95437980 | 95514266 | ||
| a0001c0037 | 0/0 | 4341 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ATGGC others(4336): Show |
chr9 | 95437980 | 95514266 | ||
| a0001c0038 | 0/0 | 4341 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ATGGC others(4336): Show |
chr9 | 95437980 | 95514266 | ||
| a0002c0001 | 0/1 | 4341 | 74 | 15 | 12 | 39 | 3 | 4 | PTCH1_chr9_95437980_95514266 | PTCH1 | ATGGC others(4336): Show |
chr9 | 95437980 | 95514266 | ||
| a0002c0011 | 0/0 | 4341 | 3 | 0 | 0 | 2 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | ATGGC others(4336): Show |
chr9 | 95437980 | 95514266 | ||
| a0002c0017 | 0/0 | 4341 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ATGGC others(4336): Show |
chr9 | 95437980 | 95514266 | ||
| a0002c0019 | 0/0 | 4341 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ATGGC others(4336): Show |
chr9 | 95437980 | 95514266 | ||
| a0002c0020 | 0/0 | 4341 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ATGGC others(4336): Show |
chr9 | 95437980 | 95514266 | ||
| a0002c0029 | 0/0 | 4341 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ATGGC others(4336): Show |
chr9 | 95437980 | 95514266 | ||
| a0002c0032 | 0/0 | 4341 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ATGGC others(4336): Show |
chr9 | 95437980 | 95514266 | ||
| a0002c0035 | 0/0 | 4341 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ATGGC others(4336): Show |
chr9 | 95437980 | 95514266 | ||
| a0002c0036 | 0/0 | 4341 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ATGGC others(4336): Show |
chr9 | 95437980 | 95514266 | ||
| a0003c0005 | 0/0 | 4341 | 20 | 9 | 0 | 9 | 0 | 2 | PTCH1_chr9_95437980_95514266 | PTCH1 | ATGGC others(4336): Show |
chr9 | 95437980 | 95514266 | ||
| a0003c0010 | 0/0 | 4341 | 3 | 0 | 0 | 3 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ATGGC others(4336): Show |
chr9 | 95437980 | 95514266 | ||
| a0003c0031 | 0/0 | 4341 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ATGGC others(4336): Show |
chr9 | 95437980 | 95514266 | ||
| a0004c0006 | 0/0 | 4341 | 6 | 0 | 0 | 5 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | ATGGC others(4336): Show |
chr9 | 95437980 | 95514266 | ||
| a0004c0021 | 0/0 | 4341 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ATGGC others(4336): Show |
chr9 | 95437980 | 95514266 | ||
| a0005c0008 | 0/0 | 4341 | 4 | 4 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ATGGC others(4336): Show |
chr9 | 95437980 | 95514266 | ||
| a0006c0016 | 0/0 | 4341 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ATGGC others(4336): Show |
chr9 | 95437980 | 95514266 | ||
| a0006c0023 | 0/0 | 4341 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ATGGC others(4336): Show |
chr9 | 95437980 | 95514266 | ||
| a0007c0012 | 0/0 | 4341 | 2 | 0 | 0 | 2 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ATGGC others(4336): Show |
chr9 | 95437980 | 95514266 | ||
| a0008c0015 | 0/0 | 4341 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ATGGC others(4336): Show |
chr9 | 95437980 | 95514266 | ||
| a0009c0025 | 0/0 | 4341 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ATGGC others(4336): Show |
chr9 | 95437980 | 95514266 | ||
| a0010c0018 | 0/0 | 4341 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ATGGC others(4336): Show |
chr9 | 95437980 | 95514266 | ||
| a0011c0033 | 0/0 | 4341 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ATGGC others(4336): Show |
chr9 | 95437980 | 95514266 | ||
| a0012c0026 | 0/0 | 4341 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ATGGC others(4336): Show |
chr9 | 95437980 | 95514266 | ||
| a0013c0027 | 0/0 | 4341 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | ATGGC others(4336): Show |
chr9 | 95437980 | 95514266 | ||
| a0014c0039 | 0/0 | 4341 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ATGGC others(4336): Show |
chr9 | 95437980 | 95514266 | ||
| a0015c0028 | 0/0 | 4341 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ATGGC others(4336): Show |
chr9 | 95437980 | 95514266 | ||
| a0016c0034 | 0/0 | 4341 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ATGGC others(4336): Show |
chr9 | 95437980 | 95514266 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001 | 1/0 | 8662 | 15 | 0 | 5 | 3 | 1 | 5 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8657): Show |
chr9 | 95437980 | 95514266 |
| a0001c0002t0002 | 0/0 | 8665 | 3 | 2 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8660): Show |
chr9 | 95437980 | 95514266 |
| a0001c0002t0003 | 0/0 | 8662 | 16 | 2 | 5 | 4 | 2 | 3 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8657): Show |
chr9 | 95437980 | 95514266 |
| a0001c0002t0005 | 0/0 | 8663 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8658): Show |
chr9 | 95437980 | 95514266 |
| a0001c0002t0007 | 0/0 | 8665 | 3 | 3 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8660): Show |
chr9 | 95437980 | 95514266 |
| a0001c0002t0008 | 0/0 | 8666 | 7 | 6 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8661): Show |
chr9 | 95437980 | 95514266 |
| a0001c0002t0009 | 0/0 | 8662 | 3 | 3 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8657): Show |
chr9 | 95437980 | 95514266 |
| a0001c0002t0010 | 0/0 | 8663 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8658): Show |
chr9 | 95437980 | 95514266 |
| a0001c0002t0011 | 0/0 | 8666 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8661): Show |
chr9 | 95437980 | 95514266 |
| a0001c0002t0012 | 0/0 | 8659 | 2 | 0 | 2 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8654): Show |
chr9 | 95437980 | 95514266 |
| a0001c0002t0016 | 0/0 | 8666 | 3 | 2 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8661): Show |
chr9 | 95437980 | 95514266 |
| a0001c0002t0017 | 0/0 | 8663 | 2 | 2 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8658): Show |
chr9 | 95437980 | 95514266 |
| a0001c0002t0020 | 0/0 | 8663 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8658): Show |
chr9 | 95437980 | 95514266 |
| a0001c0002t0022 | 0/0 | 8669 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8664): Show |
chr9 | 95437980 | 95514266 |
| a0001c0002t0023 | 0/0 | 8665 | 2 | 1 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8660): Show |
chr9 | 95437980 | 95514266 |
| a0001c0002t0032 | 0/0 | 8663 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8658): Show |
chr9 | 95437980 | 95514266 |
| a0001c0002t0035 | 0/0 | 8665 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8660): Show |
chr9 | 95437980 | 95514266 |
| a0001c0002t0040 | 0/0 | 8665 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8660): Show |
chr9 | 95437980 | 95514266 |
| a0001c0002t0042 | 0/0 | 8665 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8660): Show |
chr9 | 95437980 | 95514266 |
| a0001c0003t0001 | 0/0 | 8662 | 4 | 0 | 1 | 3 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8657): Show |
chr9 | 95437980 | 95514266 |
| a0001c0003t0002 | 0/0 | 8665 | 2 | 2 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8660): Show |
chr9 | 95437980 | 95514266 |
| a0001c0003t0003 | 0/0 | 8662 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8657): Show |
chr9 | 95437980 | 95514266 |
| a0001c0003t0004 | 0/0 | 8666 | 20 | 1 | 4 | 12 | 1 | 2 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8661): Show |
chr9 | 95437980 | 95514266 |
| a0001c0003t0005 | 0/0 | 8663 | 5 | 4 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8658): Show |
chr9 | 95437980 | 95514266 |
| a0001c0003t0009 | 0/0 | 8662 | 3 | 3 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8657): Show |
chr9 | 95437980 | 95514266 |
| a0001c0003t0012 | 0/0 | 8659 | 2 | 2 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8654): Show |
chr9 | 95437980 | 95514266 |
| a0001c0003t0013 | 0/0 | 8663 | 4 | 4 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8658): Show |
chr9 | 95437980 | 95514266 |
| a0001c0003t0020 | 0/0 | 8663 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8658): Show |
chr9 | 95437980 | 95514266 |
| a0001c0003t0021 | 0/0 | 8663 | 2 | 2 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8658): Show |
chr9 | 95437980 | 95514266 |
| a0001c0003t0037 | 0/0 | 8669 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8664): Show |
chr9 | 95437980 | 95514266 |
| a0001c0004t0001 | 0/0 | 8662 | 5 | 1 | 0 | 1 | 1 | 2 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8657): Show |
chr9 | 95437980 | 95514266 |
| a0001c0004t0002 | 0/0 | 8665 | 14 | 0 | 1 | 10 | 1 | 2 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8660): Show |
chr9 | 95437980 | 95514266 |
| a0001c0004t0007 | 0/0 | 8665 | 3 | 0 | 1 | 2 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8660): Show |
chr9 | 95437980 | 95514266 |
| a0001c0004t0022 | 0/0 | 8669 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8664): Show |
chr9 | 95437980 | 95514266 |
| a0001c0004t0024 | 0/0 | 8665 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8660): Show |
chr9 | 95437980 | 95514266 |
| a0001c0004t0034 | 0/0 | 8665 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8660): Show |
chr9 | 95437980 | 95514266 |
| a0001c0007t0002 | 0/0 | 8665 | 3 | 0 | 0 | 3 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8660): Show |
chr9 | 95437980 | 95514266 |
| a0001c0007t0014 | 0/0 | 8651 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8646): Show |
chr9 | 95437980 | 95514266 |
| a0001c0009t0002 | 0/0 | 8665 | 4 | 1 | 2 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8660): Show |
chr9 | 95437980 | 95514266 |
| a0001c0013t0025 | 0/0 | 8666 | 2 | 2 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8661): Show |
chr9 | 95437980 | 95514266 |
| a0001c0014t0003 | 0/0 | 8662 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8657): Show |
chr9 | 95437980 | 95514266 |
| a0001c0014t0033 | 0/0 | 8663 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8658): Show |
chr9 | 95437980 | 95514266 |
| a0001c0022t0002 | 0/0 | 8665 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8660): Show |
chr9 | 95437980 | 95514266 |
| a0001c0024t0007 | 0/0 | 8665 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8660): Show |
chr9 | 95437980 | 95514266 |
| a0001c0030t0038 | 0/0 | 8669 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8664): Show |
chr9 | 95437980 | 95514266 |
| a0001c0037t0002 | 0/0 | 8665 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8660): Show |
chr9 | 95437980 | 95514266 |
| a0001c0038t0014 | 0/0 | 8651 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8646): Show |
chr9 | 95437980 | 95514266 |
| a0002c0001t0001 | 0/1 | 8662 | 50 | 3 | 10 | 32 | 1 | 3 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8657): Show |
chr9 | 95437980 | 95514266 |
| a0002c0001t0003 | 0/0 | 8662 | 3 | 0 | 2 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8657): Show |
chr9 | 95437980 | 95514266 |
| a0002c0001t0004 | 0/0 | 8666 | 2 | 0 | 0 | 2 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8661): Show |
chr9 | 95437980 | 95514266 |
| a0002c0001t0005 | 0/0 | 8663 | 2 | 2 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8658): Show |
chr9 | 95437980 | 95514266 |
| a0002c0001t0006 | 0/0 | 8663 | 8 | 8 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8658): Show |
chr9 | 95437980 | 95514266 |
| a0002c0001t0018 | 0/0 | 8662 | 2 | 0 | 0 | 0 | 2 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8657): Show |
chr9 | 95437980 | 95514266 |
| a0002c0001t0019 | 0/0 | 8662 | 2 | 0 | 0 | 2 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8657): Show |
chr9 | 95437980 | 95514266 |
| a0002c0001t0026 | 0/0 | 8662 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8657): Show |
chr9 | 95437980 | 95514266 |
| a0002c0001t0027 | 0/0 | 8666 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8661): Show |
chr9 | 95437980 | 95514266 |
| a0002c0001t0028 | 0/0 | 8662 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8657): Show |
chr9 | 95437980 | 95514266 |
| a0002c0001t0029 | 0/0 | 8662 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8657): Show |
chr9 | 95437980 | 95514266 |
| a0002c0001t0041 | 0/0 | 8666 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8661): Show |
chr9 | 95437980 | 95514266 |
| a0002c0011t0002 | 0/0 | 8665 | 3 | 0 | 0 | 2 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8660): Show |
chr9 | 95437980 | 95514266 |
| a0002c0017t0004 | 0/0 | 8666 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8661): Show |
chr9 | 95437980 | 95514266 |
| a0002c0019t0006 | 0/0 | 8663 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8658): Show |
chr9 | 95437980 | 95514266 |
| a0002c0020t0001 | 0/0 | 8662 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8657): Show |
chr9 | 95437980 | 95514266 |
| a0002c0029t0001 | 0/0 | 8662 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8657): Show |
chr9 | 95437980 | 95514266 |
| a0002c0032t0001 | 0/0 | 8662 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8657): Show |
chr9 | 95437980 | 95514266 |
| a0002c0035t0001 | 0/0 | 8662 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8657): Show |
chr9 | 95437980 | 95514266 |
| a0002c0036t0031 | 0/0 | 8663 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8658): Show |
chr9 | 95437980 | 95514266 |
| a0003c0005t0001 | 0/0 | 8662 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8657): Show |
chr9 | 95437980 | 95514266 |
| a0003c0005t0002 | 0/0 | 8665 | 6 | 0 | 0 | 5 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8660): Show |
chr9 | 95437980 | 95514266 |
| a0003c0005t0003 | 0/0 | 8662 | 4 | 4 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8657): Show |
chr9 | 95437980 | 95514266 |
| a0003c0005t0005 | 0/0 | 8663 | 2 | 2 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8658): Show |
chr9 | 95437980 | 95514266 |
| a0003c0005t0007 | 0/0 | 8665 | 2 | 2 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8660): Show |
chr9 | 95437980 | 95514266 |
| a0003c0005t0011 | 0/0 | 8666 | 3 | 0 | 0 | 3 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8661): Show |
chr9 | 95437980 | 95514266 |
| a0003c0005t0024 | 0/0 | 8665 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8660): Show |
chr9 | 95437980 | 95514266 |
| a0003c0005t0036 | 0/0 | 8666 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8661): Show |
chr9 | 95437980 | 95514266 |
| a0003c0010t0015 | 0/0 | 8666 | 2 | 0 | 0 | 2 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8661): Show |
chr9 | 95437980 | 95514266 |
| a0003c0010t0030 | 0/0 | 8663 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8658): Show |
chr9 | 95437980 | 95514266 |
| a0003c0031t0003 | 0/0 | 8662 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8657): Show |
chr9 | 95437980 | 95514266 |
| a0004c0006t0001 | 0/0 | 8662 | 2 | 0 | 0 | 2 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8657): Show |
chr9 | 95437980 | 95514266 |
| a0004c0006t0002 | 0/0 | 8665 | 3 | 0 | 0 | 3 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8660): Show |
chr9 | 95437980 | 95514266 |
| a0004c0006t0005 | 0/0 | 8663 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8658): Show |
chr9 | 95437980 | 95514266 |
| a0004c0021t0015 | 0/0 | 8666 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8661): Show |
chr9 | 95437980 | 95514266 |
| a0005c0008t0010 | 0/0 | 8663 | 4 | 4 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8658): Show |
chr9 | 95437980 | 95514266 |
| a0006c0016t0001 | 0/0 | 8662 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8657): Show |
chr9 | 95437980 | 95514266 |
| a0006c0023t0011 | 0/0 | 8666 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8661): Show |
chr9 | 95437980 | 95514266 |
| a0007c0012t0003 | 0/0 | 8662 | 2 | 0 | 0 | 2 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8657): Show |
chr9 | 95437980 | 95514266 |
| a0008c0015t0001 | 0/0 | 8662 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8657): Show |
chr9 | 95437980 | 95514266 |
| a0009c0025t0003 | 0/0 | 8662 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8657): Show |
chr9 | 95437980 | 95514266 |
| a0010c0018t0014 | 0/0 | 8651 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8646): Show |
chr9 | 95437980 | 95514266 |
| a0011c0033t0005 | 0/0 | 8663 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8658): Show |
chr9 | 95437980 | 95514266 |
| a0012c0026t0039 | 0/0 | 8666 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8661): Show |
chr9 | 95437980 | 95514266 |
| a0013c0027t0001 | 0/0 | 8662 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8657): Show |
chr9 | 95437980 | 95514266 |
| a0014c0039t0001 | 0/0 | 8662 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8657): Show |
chr9 | 95437980 | 95514266 |
| a0015c0028t0002 | 0/0 | 8665 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8660): Show |
chr9 | 95437980 | 95514266 |
| a0016c0034t0003 | 0/0 | 8662 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | ACCCC others(8657): Show |
chr9 | 95437980 | 95514266 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001g0010 | 1/0 | 2 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0003g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0003g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0003g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0003g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0003g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0003g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0003g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0003g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0003g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0003g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0005g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0007g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0007g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0007g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0008g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0008g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0008g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0008g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0008g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0008g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0009g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0009g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0009g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0010g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0011g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0012g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0016g0021 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0016g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0017g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0017g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0020g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0022g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0023g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0023g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0032g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0035g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0040g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0002t0042g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0003g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0004g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0004g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0004g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0004g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0004g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0004g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0004g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0004g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0004g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0004g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0004g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0004g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0004g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0004g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0004g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0004g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0004g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0004g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0004g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0005g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0005g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0005g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0005g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0005g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0009g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0009g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0009g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0012g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0013g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0013g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0013g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0013g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0020g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0021g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0021g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0003t0037g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0004t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0004t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0004t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0004t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0004t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0004t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0004t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0004t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0004t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0004t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0004t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0004t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0004t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0004t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0004t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0004t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0004t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0004t0007g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0004t0007g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0004t0007g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0004t0022g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0004t0024g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0004t0034g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0007t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0007t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0007t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0007t0014g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0009t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0009t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0009t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0009t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0013t0025g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0013t0025g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0014t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0014t0033g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0022t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0024t0007g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0030t0038g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0037t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0001c0038t0014g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0001 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0078 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0003g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0003g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0004g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0004g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0005g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0005g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0006g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0006g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0006g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0006g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0006g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0006g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0018g0007 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0019g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0026g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0027g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0028g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0029g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0001t0041g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0011t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0011t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0011t0002g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0017t0004g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0019t0006g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0020t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0029t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0032t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0035t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0002c0036t0031g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0003c0005t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0003c0005t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0003c0005t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0003c0005t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0003c0005t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0003c0005t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0003c0005t0003g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0003c0005t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0003c0005t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0003c0005t0005g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0003c0005t0005g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0003c0005t0007g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0003c0005t0007g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0003c0005t0011g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0003c0005t0011g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0003c0005t0011g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0003c0005t0024g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0003c0005t0036g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0003c0010t0015g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0003c0010t0030g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0003c0031t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0004c0006t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0004c0006t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0004c0006t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0004c0006t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0004c0006t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0004c0006t0005g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0004c0021t0015g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0005c0008t0010g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0005c0008t0010g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0005c0008t0010g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0006c0016t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0006c0023t0011g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0007c0012t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0007c0012t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0008c0015t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0009c0025t0003g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0010c0018t0014g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0011c0033t0005g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0012c0026t0039g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0013c0027t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0014c0039t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0015c0028t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| a0016c0034t0003g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0003 | g0117 | EUR | GBR | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG00099 | hp2 | a0001 | c0004 | t0001 | g0088 | EUR | GBR | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG00140 | hp1 | a0002 | c0001 | t0001 | g0142 | EUR | GBR | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG00140 | hp2 | a0001 | c0004 | t0002 | g0242 | EUR | GBR | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG00408 | hp1 | a0002 | c0001 | t0001 | g0129 | EAS | CHS | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG00408 | hp2 | a0001 | c0002 | t0002 | g0237 | EAS | CHS | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG00423 | hp1 | a0002 | c0001 | t0001 | g0155 | EAS | CHS | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG00423 | hp2 | a0001 | c0007 | t0002 | g0245 | EAS | CHS | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG00558 | hp1 | a0002 | c0029 | t0001 | g0109 | EAS | CHS | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG00558 | hp2 | a0006 | c0016 | t0001 | g0090 | EAS | CHS | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG00597 | hp1 | a0001 | c0003 | t0004 | g0041 | EAS | CHS | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG00597 | hp2 | a0002 | c0001 | t0001 | g0002 | EAS | CHS | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG00609 | hp1 | a0003 | c0010 | t0030 | g0153 | EAS | CHS | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG00609 | hp2 | a0002 | c0011 | t0002 | g0213 | EAS | CHS | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG00673 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | CHS | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG00673 | hp2 | a0004 | c0021 | t0015 | g0204 | EAS | CHS | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG00738 | hp1 | a0002 | c0001 | t0001 | g0121 | AMR | PUR | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG00738 | hp2 | a0001 | c0003 | t0001 | g0044 | AMR | PUR | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01069 | hp1 | a0001 | c0002 | t0012 | g0005 | AMR | PUR | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01069 | hp2 | a0008 | c0015 | t0001 | g0120 | AMR | PUR | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01071 | hp1 | a0001 | c0002 | t0003 | g0015 | AMR | PUR | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01071 | hp2 | a0001 | c0002 | t0012 | g0005 | AMR | PUR | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01074 | hp1 | a0001 | c0002 | t0003 | g0015 | AMR | PUR | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01074 | hp2 | a0001 | c0002 | t0022 | g0215 | AMR | PUR | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01081 | hp1 | a0001 | c0002 | t0023 | g0194 | AMR | PUR | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01081 | hp2 | a0001 | c0014 | t0033 | g0085 | AMR | PUR | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01099 | hp1 | a0001 | c0003 | t0004 | g0046 | AMR | PUR | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01099 | hp2 | a0002 | c0001 | t0001 | g0011 | AMR | PUR | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0124 | AMR | PUR | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01106 | hp2 | a0002 | c0001 | t0003 | g0074 | AMR | PUR | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0072 | AMR | PUR | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01109 | hp2 | a0001 | c0002 | t0020 | g0175 | AMR | PUR | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01167 | hp1 | a0001 | c0003 | t0004 | g0051 | AMR | PUR | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0116 | AMR | PUR | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01175 | hp1 | a0001 | c0004 | t0007 | g0222 | AMR | PUR | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01175 | hp2 | a0002 | c0001 | t0001 | g0123 | AMR | PUR | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01192 | hp1 | a0002 | c0001 | t0001 | g0011 | AMR | PUR | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01192 | hp2 | a0001 | c0003 | t0004 | g0047 | AMR | PUR | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01243 | hp1 | a0001 | c0002 | t0016 | g0021 | AMR | PUR | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01243 | hp2 | a0001 | c0002 | t0008 | g0179 | AMR | PUR | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01255 | hp1 | a0001 | c0002 | t0003 | g0060 | AMR | CLM | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01255 | hp2 | a0001 | c0003 | t0004 | g0045 | AMR | CLM | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01358 | hp1 | a0001 | c0002 | t0003 | g0148 | AMR | CLM | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01358 | hp2 | a0001 | c0002 | t0040 | g0216 | AMR | CLM | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01361 | hp1 | a0001 | c0009 | t0002 | g0230 | AMR | CLM | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01361 | hp2 | a0002 | c0001 | t0001 | g0128 | AMR | CLM | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0151 | AMR | CLM | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01433 | hp2 | a0002 | c0001 | t0001 | g0115 | AMR | CLM | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01516 | hp1 | a0002 | c0001 | t0018 | g0007 | EUR | IBS | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01516 | hp2 | a0001 | c0002 | t0003 | g0156 | EUR | IBS | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01517 | hp1 | a0002 | c0017 | t0004 | g0043 | EUR | IBS | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01517 | hp2 | a0002 | c0001 | t0018 | g0007 | EUR | IBS | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01884 | hp1 | a0001 | c0002 | t0002 | g0185 | AFR | ACB | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01884 | hp2 | a0003 | c0005 | t0007 | g0193 | AFR | ACB | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01934 | hp1 | a0002 | c0001 | t0001 | g0146 | AMR | PEL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01934 | hp2 | a0001 | c0002 | t0003 | g0159 | AMR | PEL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01952 | hp1 | a0009 | c0025 | t0003 | g0174 | AMR | PEL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01952 | hp2 | a0002 | c0001 | t0003 | g0095 | AMR | PEL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01975 | hp1 | a0002 | c0001 | t0001 | g0076 | AMR | PEL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG01975 | hp2 | a0001 | c0004 | t0002 | g0220 | AMR | PEL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0126 | AMR | PEL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02004 | hp2 | a0002 | c0001 | t0001 | g0077 | AMR | PEL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02015 | hp1 | a0003 | c0005 | t0002 | g0019 | EAS | KHV | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02015 | hp2 | a0001 | c0038 | t0014 | g0250 | EAS | KHV | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02027 | hp1 | a0001 | c0003 | t0004 | g0034 | EAS | KHV | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02027 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | KHV | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02040 | hp1 | a0002 | c0001 | t0029 | g0099 | EAS | KHV | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02040 | hp2 | a0002 | c0001 | t0001 | g0157 | EAS | KHV | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02055 | hp1 | a0001 | c0009 | t0002 | g0231 | AFR | ACB | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02055 | hp2 | a0002 | c0001 | t0001 | g0110 | AFR | ACB | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02056 | hp1 | a0001 | c0003 | t0004 | g0036 | EAS | KHV | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02056 | hp2 | a0003 | c0010 | t0015 | g0018 | EAS | KHV | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02071 | hp1 | a0002 | c0001 | t0019 | g0013 | EAS | KHV | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02071 | hp2 | a0010 | c0018 | t0014 | g0249 | EAS | KHV | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02129 | hp1 | a0006 | c0023 | t0011 | g0211 | EAS | KHV | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02129 | hp2 | a0002 | c0001 | t0001 | g0161 | EAS | KHV | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02135 | hp1 | a0003 | c0005 | t0002 | g0019 | EAS | KHV | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02135 | hp2 | a0001 | c0002 | t0003 | g0149 | EAS | KHV | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02145 | hp1 | a0005 | c0008 | t0010 | g0168 | AFR | ACB | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02145 | hp2 | a0001 | c0003 | t0005 | g0061 | AFR | ACB | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02155 | hp1 | a0001 | c0004 | t0002 | g0221 | EAS | CDX | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02155 | hp2 | a0002 | c0001 | t0001 | g0136 | EAS | CDX | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02257 | hp1 | a0001 | c0002 | t0009 | g0066 | AFR | ACB | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02257 | hp2 | a0002 | c0019 | t0006 | g0103 | AFR | ACB | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02258 | hp1 | a0002 | c0001 | t0028 | g0057 | AFR | ACB | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02258 | hp2 | a0001 | c0003 | t0012 | g0006 | AFR | ACB | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02300 | hp1 | a0001 | c0009 | t0002 | g0229 | AMR | PEL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02300 | hp2 | a0002 | c0001 | t0001 | g0114 | AMR | PEL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02451 | hp1 | a0001 | c0002 | t0035 | g0190 | AFR | ACB | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02451 | hp2 | a0001 | c0003 | t0021 | g0170 | AFR | ACB | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02523 | hp1 | a0004 | c0006 | t0001 | g0176 | EAS | KHV | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02523 | hp2 | a0011 | c0033 | t0005 | g0138 | EAS | KHV | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02572 | hp1 | a0001 | c0030 | t0038 | g0195 | AFR | GWD | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02572 | hp2 | a0005 | c0008 | t0010 | g0167 | AFR | GWD | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02615 | hp1 | a0001 | c0003 | t0009 | g0062 | AFR | GWD | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02615 | hp2 | a0001 | c0002 | t0023 | g0238 | AFR | GWD | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02622 | hp1 | a0001 | c0002 | t0007 | g0189 | AFR | GWD | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02622 | hp2 | a0001 | c0003 | t0002 | g0197 | AFR | GWD | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02630 | hp1 | a0002 | c0001 | t0006 | g0003 | AFR | GWD | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02630 | hp2 | a0001 | c0003 | t0013 | g0053 | AFR | GWD | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02647 | hp1 | a0003 | c0005 | t0005 | g0091 | AFR | GWD | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02647 | hp2 | a0001 | c0003 | t0021 | g0166 | AFR | GWD | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02683 | hp1 | a0001 | c0002 | t0003 | g0160 | SAS | PJL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02683 | hp2 | a0001 | c0022 | t0002 | g0252 | SAS | PJL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02717 | hp1 | a0001 | c0002 | t0003 | g0026 | AFR | GWD | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02717 | hp2 | a0002 | c0036 | t0031 | g0119 | AFR | GWD | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02723 | hp1 | a0001 | c0024 | t0007 | g0188 | AFR | GWD | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02723 | hp2 | a0001 | c0002 | t0032 | g0165 | AFR | GWD | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02735 | hp1 | a0001 | c0002 | t0003 | g0118 | SAS | PJL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02735 | hp2 | a0001 | c0009 | t0002 | g0228 | SAS | PJL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02738 | hp1 | a0001 | c0004 | t0002 | g0241 | SAS | PJL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0139 | SAS | PJL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02809 | hp1 | a0001 | c0002 | t0010 | g0169 | AFR | GWD | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02809 | hp2 | a0002 | c0001 | t0006 | g0079 | AFR | GWD | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02818 | hp1 | a0001 | c0013 | t0025 | g0254 | AFR | GWD | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02818 | hp2 | a0012 | c0026 | t0039 | g0192 | AFR | GWD | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02895 | hp1 | a0001 | c0003 | t0013 | g0054 | AFR | GWD | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02895 | hp2 | a0005 | c0008 | t0010 | g0016 | AFR | GWD | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02897 | hp1 | a0002 | c0001 | t0006 | g0101 | AFR | GWD | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02897 | hp2 | a0005 | c0008 | t0010 | g0016 | AFR | GWD | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02922 | hp1 | a0001 | c0002 | t0008 | g0017 | AFR | ESN | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02922 | hp2 | a0003 | c0005 | t0036 | g0239 | AFR | ESN | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02965 | hp1 | a0002 | c0001 | t0005 | g0071 | AFR | ESN | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02965 | hp2 | a0001 | c0003 | t0020 | g0171 | AFR | ESN | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02970 | hp1 | a0002 | c0001 | t0006 | g0098 | AFR | ESN | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02970 | hp2 | a0003 | c0005 | t0003 | g0008 | AFR | ESN | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02976 | hp1 | a0001 | c0003 | t0009 | g0052 | AFR | ESN | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02976 | hp2 | a0003 | c0005 | t0007 | g0212 | AFR | ESN | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0010 | SAS | PJL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03017 | hp2 | a0002 | c0001 | t0001 | g0158 | SAS | PJL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03041 | hp1 | a0002 | c0001 | t0006 | g0003 | AFR | GWD | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03041 | hp2 | a0001 | c0013 | t0025 | g0255 | AFR | GWD | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03098 | hp1 | a0001 | c0002 | t0011 | g0186 | AFR | MSL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03098 | hp2 | a0001 | c0002 | t0008 | g0181 | AFR | MSL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03130 | hp1 | a0001 | c0002 | t0016 | g0021 | AFR | ESN | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03130 | hp2 | a0003 | c0005 | t0005 | g0087 | AFR | ESN | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03139 | hp1 | a0001 | c0003 | t0013 | g0028 | AFR | ESN | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03139 | hp2 | a0002 | c0001 | t0041 | g0253 | AFR | ESN | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03195 | hp1 | a0003 | c0005 | t0003 | g0081 | AFR | ESN | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03195 | hp2 | a0001 | c0003 | t0005 | g0064 | AFR | ESN | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03225 | hp1 | a0002 | c0001 | t0006 | g0003 | AFR | MSL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03225 | hp2 | a0001 | c0002 | t0003 | g0083 | AFR | MSL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03239 | hp1 | a0002 | c0001 | t0001 | g0150 | SAS | PJL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03239 | hp2 | a0001 | c0004 | t0002 | g0224 | SAS | PJL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03453 | hp1 | a0001 | c0003 | t0009 | g0059 | AFR | MSL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03453 | hp2 | a0001 | c0003 | t0002 | g0198 | AFR | MSL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03486 | hp1 | a0001 | c0002 | t0017 | g0022 | AFR | MSL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03486 | hp2 | a0001 | c0002 | t0042 | g0256 | AFR | MSL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0075 | SAS | PJL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03490 | hp2 | a0001 | c0004 | t0001 | g0009 | SAS | PJL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03491 | hp1 | a0001 | c0002 | t0003 | g0163 | SAS | PJL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0125 | SAS | PJL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03492 | hp1 | a0001 | c0004 | t0001 | g0009 | SAS | PJL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0143 | SAS | PJL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03516 | hp1 | a0001 | c0002 | t0008 | g0017 | AFR | ESN | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03516 | hp2 | a0003 | c0005 | t0003 | g0008 | AFR | ESN | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03540 | hp1 | a0002 | c0001 | t0005 | g0100 | AFR | GWD | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03540 | hp2 | a0001 | c0002 | t0016 | g0244 | AFR | GWD | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03579 | hp1 | a0002 | c0001 | t0001 | g0069 | AFR | MSL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03579 | hp2 | a0001 | c0002 | t0008 | g0182 | AFR | MSL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03704 | hp1 | a0002 | c0011 | t0002 | g0251 | SAS | PJL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03704 | hp2 | a0001 | c0003 | t0004 | g0048 | SAS | PJL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03710 | hp1 | a0003 | c0005 | t0001 | g0154 | SAS | PJL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03710 | hp2 | a0002 | c0001 | t0003 | g0111 | SAS | PJL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG04184 | hp1 | a0001 | c0003 | t0004 | g0092 | SAS | BEB | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG04184 | hp2 | a0004 | c0006 | t0005 | g0089 | SAS | BEB | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG04199 | hp1 | a0001 | c0007 | t0014 | g0248 | SAS | STU | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG04199 | hp2 | a0013 | c0027 | t0001 | g0097 | SAS | STU | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18747 | hp1 | a0002 | c0001 | t0001 | g0105 | EAS | CHB | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18747 | hp2 | a0003 | c0031 | t0003 | g0173 | EAS | CHB | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18906 | hp1 | a0002 | c0035 | t0001 | g0106 | AFR | YRI | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18906 | hp2 | a0001 | c0003 | t0005 | g0065 | AFR | YRI | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18939 | hp1 | a0002 | c0001 | t0001 | g0012 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18939 | hp2 | a0001 | c0003 | t0004 | g0030 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18940 | hp1 | a0002 | c0001 | t0001 | g0108 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18940 | hp2 | a0001 | c0004 | t0007 | g0232 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18943 | hp1 | a0002 | c0011 | t0002 | g0223 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18943 | hp2 | a0001 | c0002 | t0003 | g0014 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18944 | hp1 | a0001 | c0003 | t0004 | g0039 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18944 | hp2 | a0002 | c0001 | t0001 | g0145 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18946 | hp1 | a0001 | c0004 | t0034 | g0217 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18946 | hp2 | a0002 | c0001 | t0001 | g0131 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18949 | hp1 | a0002 | c0001 | t0001 | g0144 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18949 | hp2 | a0004 | c0006 | t0001 | g0172 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18952 | hp1 | a0003 | c0005 | t0002 | g0201 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18952 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18954 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18954 | hp2 | a0002 | c0001 | t0004 | g0135 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18956 | hp1 | a0001 | c0003 | t0004 | g0031 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18956 | hp2 | a0014 | c0039 | t0001 | g0178 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18957 | hp1 | a0002 | c0001 | t0001 | g0112 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18957 | hp2 | a0003 | c0005 | t0011 | g0200 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18962 | hp1 | a0001 | c0004 | t0024 | g0233 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18962 | hp2 | a0001 | c0003 | t0004 | g0035 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18965 | hp1 | a0001 | c0007 | t0002 | g0246 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18965 | hp2 | a0015 | c0028 | t0002 | g0196 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18967 | hp1 | a0001 | c0003 | t0037 | g0236 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18967 | hp2 | a0002 | c0001 | t0001 | g0012 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18968 | hp1 | a0001 | c0003 | t0001 | g0032 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18968 | hp2 | a0003 | c0005 | t0002 | g0210 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18969 | hp1 | a0002 | c0001 | t0001 | g0093 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18969 | hp2 | a0001 | c0004 | t0007 | g0235 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18970 | hp1 | a0002 | c0001 | t0001 | g0140 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18970 | hp2 | a0007 | c0012 | t0003 | g0024 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18971 | hp1 | a0002 | c0001 | t0001 | g0137 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18971 | hp2 | a0001 | c0004 | t0022 | g0240 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18973 | hp1 | a0001 | c0004 | t0002 | g0225 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18973 | hp2 | a0002 | c0032 | t0001 | g0152 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18975 | hp1 | a0002 | c0001 | t0001 | g0134 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18975 | hp2 | a0003 | c0010 | t0015 | g0018 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18977 | hp1 | a0003 | c0005 | t0011 | g0205 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18977 | hp2 | a0002 | c0001 | t0019 | g0013 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18979 | hp1 | a0003 | c0005 | t0011 | g0209 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18979 | hp2 | a0002 | c0001 | t0001 | g0130 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18983 | hp1 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18983 | hp2 | a0001 | c0004 | t0002 | g0020 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18986 | hp1 | a0004 | c0006 | t0002 | g0208 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18986 | hp2 | a0001 | c0003 | t0005 | g0042 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18988 | hp1 | a0007 | c0012 | t0003 | g0025 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18988 | hp2 | a0002 | c0001 | t0027 | g0122 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18991 | hp1 | a0002 | c0001 | t0001 | g0133 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18991 | hp2 | a0001 | c0004 | t0002 | g0227 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18994 | hp1 | a0004 | c0006 | t0002 | g0203 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18994 | hp2 | a0001 | c0004 | t0002 | g0218 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18999 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18999 | hp2 | a0001 | c0004 | t0002 | g0243 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA19000 | hp1 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA19000 | hp2 | a0001 | c0003 | t0004 | g0037 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA19004 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA19004 | hp2 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA19005 | hp1 | a0002 | c0001 | t0001 | g0027 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA19005 | hp2 | a0003 | c0005 | t0002 | g0202 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA19007 | hp1 | a0002 | c0001 | t0001 | g0127 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA19007 | hp2 | a0001 | c0004 | t0002 | g0226 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA19011 | hp1 | a0002 | c0001 | t0001 | g0107 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA19011 | hp2 | a0001 | c0004 | t0001 | g0086 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA19030 | hp1 | a0001 | c0002 | t0007 | g0191 | AFR | LWK | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA19030 | hp2 | a0003 | c0005 | t0003 | g0082 | AFR | LWK | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA19043 | hp1 | a0002 | c0001 | t0006 | g0104 | AFR | LWK | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA19043 | hp2 | a0001 | c0003 | t0005 | g0063 | AFR | LWK | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA19056 | hp1 | a0002 | c0001 | t0004 | g0132 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA19056 | hp2 | a0001 | c0003 | t0004 | g0050 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA19062 | hp1 | a0002 | c0001 | t0026 | g0147 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA19062 | hp2 | a0001 | c0002 | t0003 | g0014 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA19064 | hp1 | a0004 | c0006 | t0002 | g0207 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA19064 | hp2 | a0001 | c0003 | t0004 | g0029 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA19066 | hp1 | a0001 | c0007 | t0002 | g0247 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA19066 | hp2 | a0002 | c0020 | t0001 | g0073 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA19068 | hp1 | a0001 | c0004 | t0002 | g0234 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA19068 | hp2 | a0001 | c0002 | t0001 | g0141 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA19079 | hp1 | a0001 | c0004 | t0002 | g0219 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA19079 | hp2 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA19083 | hp1 | a0003 | c0005 | t0024 | g0206 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA19083 | hp2 | a0002 | c0001 | t0001 | g0162 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA19086 | hp1 | a0001 | c0002 | t0001 | g0080 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA19086 | hp2 | a0001 | c0004 | t0002 | g0020 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA19090 | hp1 | a0001 | c0003 | t0004 | g0040 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA19090 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA19240 | hp1 | a0001 | c0002 | t0008 | g0183 | AFR | YRI | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA19240 | hp2 | a0001 | c0002 | t0009 | g0056 | AFR | YRI | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA20129 | hp1 | a0001 | c0002 | t0008 | g0180 | AFR | ASW | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA20129 | hp2 | a0001 | c0002 | t0007 | g0187 | AFR | ASW | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0164 | EUR | TSI | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA20752 | hp2 | a0001 | c0003 | t0004 | g0033 | EUR | TSI | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA20805 | hp1 | a0001 | c0037 | t0002 | g0214 | EUR | TSI | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA20805 | hp2 | a0001 | c0003 | t0003 | g0067 | EUR | TSI | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA20905 | hp1 | a0002 | c0001 | t0001 | g0001 | SAS | GIH | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA20905 | hp2 | a0003 | c0005 | t0002 | g0199 | SAS | GIH | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02109 | hp1 | a0001 | c0002 | t0009 | g0055 | AFR | ACB | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02109 | hp2 | a0001 | c0003 | t0012 | g0006 | AFR | ACB | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02486 | hp1 | a0001 | c0002 | t0002 | g0184 | AFR | ACB | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02486 | hp2 | a0001 | c0004 | t0001 | g0177 | AFR | ACB | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02559 | hp1 | a0001 | c0003 | t0004 | g0038 | AFR | ACB | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG02559 | hp2 | a0001 | c0002 | t0005 | g0068 | AFR | ACB | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03471 | hp1 | a0002 | c0001 | t0006 | g0102 | AFR | MSL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG03471 | hp2 | a0001 | c0002 | t0017 | g0023 | AFR | MSL | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG06807 | hp1 | a0002 | c0001 | t0001 | g0070 | AFR | USA | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| HG06807 | hp2 | a0001 | c0014 | t0003 | g0084 | AFR | USA | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18955 | hp1 | a0001 | c0003 | t0004 | g0049 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA18955 | hp2 | a0001 | c0002 | t0003 | g0094 | EAS | JPT | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA21309 | hp1 | a0001 | c0003 | t0013 | g0058 | AFR | LWK | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| NA21309 | hp2 | a0016 | c0034 | t0003 | g0113 | AFR | LWK | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| homoSapiens | chm13v2 | a0002 | c0001 | t0001 | g0078 | REF | REF | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0010 | REF | REF | PTCH1_chr9_95437980_95514266 | PTCH1 | chr9 | 95437980 | 95514266 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:95446931 | C | T | 1 | a0015 | 1 | NA18965.hp2 | missense_variant | MODERATE | c.4325G>A | p.Arg1442Gln | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 23/24 | 5230/8662 | 4325/4344 | 1442/1447 | chr9 | 95446931 | |||
| chr9:95446967 | A | G | 1 | a0012 | 1 | HG02818.hp2 | missense_variant | MODERATE | c.4289T>C | p.Ile1430Thr | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 23/24 | 5194/8662 | 4289/4344 | 1430/1447 | chr9 | 95446967 | |||
| chr9:95447108 | G | A | 1 | a0013 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.4148C>T | p.Pro1383Leu | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 23/24 | 5053/8662 | 4148/4344 | 1383/1447 | chr9 | 95447108 | |||
| chr9:95447312 | G | A | 7 | a0002 a0004 a0010 others(4): Show |
95 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(92): Show |
missense_variant | MODERATE | c.3944C>T | p.Pro1315Leu | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 23/24 | 4849/8662 | 3944/4344 | 1315/1447 | chr9 | 95447312 | |||
| chr9:95447349 | G | A | 1 | a0006 | 2 | HG00558.hp2 HG02129.hp1 |
missense_variant | MODERATE | c.3907C>T | p.Arg1303Cys | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 23/24 | 4812/8662 | 3907/4344 | 1303/1447 | chr9 | 95447349 | |||
| chr9:95447411 | G | A | 1 | a0005 | 4 | HG02145.hp1 HG02572.hp2 HG02895.hp2 others(1): Show |
missense_variant | MODERATE | c.3845C>T | p.Pro1282Leu | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 23/24 | 4750/8662 | 3845/4344 | 1282/1447 | chr9 | 95447411 | |||
| chr9:95449107 | C | T | 1 | a0009 | 1 | HG01952.hp1 | missense_variant | MODERATE | c.3766G>A | p.Val1256Met | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 22/24 | 4671/8662 | 3766/4344 | 1256/1447 | chr9 | 95449107 | |||
| chr9:95449290 | T | A | 4 | a0003 a0004 a0006 others(1): Show |
35 | HG00558.hp2 HG00609.hp1 HG00673.hp2 others(32): Show |
missense_variant | MODERATE | c.3583A>T | p.Thr1195Ser | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 22/24 | 4488/8662 | 3583/4344 | 1195/1447 | chr9 | 95449290 | |||
| chr9:95467197 | T | C | 1 | a0010 | 1 | HG02071.hp2 | missense_variant | MODERATE | c.2479A>G | p.Ser827Gly | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/24 | 3384/8662 | 2479/4344 | 827/1447 | chr9 | 95467197 | |||
| chr9:95468779 | G | A | 1 | a0011 | 1 | HG02523.hp2 | missense_variant | MODERATE | c.2222C>T | p.Ala741Val | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 14/24 | 3127/8662 | 2222/4344 | 741/1447 | chr9 | 95468779 | |||
| chr9:95468828 | G | A | 1 | a0016 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.2173C>T | p.Pro725Ser | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 14/24 | 3078/8662 | 2173/4344 | 725/1447 | chr9 | 95468828 | |||
| chr9:95476101 | C | T | 1 | a0008 | 1 | HG01069.hp2 | missense_variant | MODERATE | c.1661G>A | p.Ser554Asn | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/24 | 2566/8662 | 1661/4344 | 554/1447 | chr9 | 95476101 | |||
| chr9:95508253 | C | G | 1 | a0007 | 2 | NA18970.hp2 NA18988.hp1 |
missense_variant | MODERATE | c.109G>C | p.Gly37Arg | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 1/24 | 1014/8662 | 109/4344 | 37/1447 | chr9 | 95508253 | |||
| chr9:95508325 | G | C | 1 | a0014 | 1 | NA18956.hp2 | missense_variant | MODERATE | c.37C>G | p.Arg13Gly | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 1/24 | 942/8662 | 37/4344 | 13/1447 | chr9 | 95508325 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:95447176 | G | A | 2 | a0001c0037 a0002c0029 |
2 | HG00558.hp1 NA20805.hp1 |
synonymous_variant | LOW | c.4080C>T | p.Ser1360Ser | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 23/24 | 4985/8662 | 4080/4344 | 1360/1447 | chr9 | 95447176 | |||
| chr9:95449186 | C | T | 1 | a0001c0024 | 1 | HG02723.hp1 | synonymous_variant | LOW | c.3687G>A | p.Thr1229Thr | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 22/24 | 4592/8662 | 3687/4344 | 1229/1447 | chr9 | 95449186 | |||
| chr9:95449249 | G | A | 1 | a0001c0030 | 1 | HG02572.hp1 | synonymous_variant | LOW | c.3624C>T | p.Ala1208Ala | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 22/24 | 4529/8662 | 3624/4344 | 1208/1447 | chr9 | 95449249 | |||
| chr9:95449306 | G | A | 1 | a0001c0014 | 2 | HG01081.hp2 HG06807.hp2 |
synonymous_variant | LOW | c.3567C>T | p.Gly1189Gly | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 22/24 | 4472/8662 | 3567/4344 | 1189/1447 | chr9 | 95449306 | |||
| chr9:95453540 | G | A | 1 | a0002c0032 | 1 | NA18973.hp2 | synonymous_variant | LOW | c.3387C>T | p.Gly1129Gly | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/24 | 4292/8662 | 3387/4344 | 1129/1447 | chr9 | 95453540 | |||
| chr9:95456387 | G | A | 1 | a0002c0036 | 1 | HG02717.hp2 | synonymous_variant | LOW | c.3195C>T | p.Val1065Val | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 19/24 | 4100/8662 | 3195/4344 | 1065/1447 | chr9 | 95456387 | |||
| chr9:95458040 | A | C | 7 | a0001c0022 a0003c0005 a0003c0010 others(4): Show |
33 | HG00558.hp2 HG00609.hp1 HG00673.hp2 others(30): Show |
synonymous_variant | LOW | c.3141T>G | p.Leu1047Leu | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 18/24 | 4046/8662 | 3141/4344 | 1047/1447 | chr9 | 95458040 | |||
| chr9:95458268 | A | G | 2 | a0003c0010 a0004c0021 |
4 | HG00609.hp1 HG00673.hp2 HG02056.hp2 others(1): Show |
synonymous_variant | LOW | c.2913T>C | p.Tyr971Tyr | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 18/24 | 3818/8662 | 2913/4344 | 971/1447 | chr9 | 95458268 | |||
| chr9:95458271 | C | T | 1 | a0002c0020 | 1 | NA19066.hp2 | synonymous_variant | LOW | c.2910G>A | p.Glu970Glu | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 18/24 | 3815/8662 | 2910/4344 | 970/1447 | chr9 | 95458271 | |||
| chr9:95459688 | C | T | 1 | a0001c0013 | 2 | HG02818.hp1 HG03041.hp2 |
synonymous_variant | LOW | c.2799G>A | p.Ala933Ala | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 17/24 | 3704/8662 | 2799/4344 | 933/1447 | chr9 | 95459688 | |||
| chr9:95468802 | T | C | 3 | a0001c0007 a0001c0038 a0010c0018 |
6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
synonymous_variant | LOW | c.2199A>G | p.Ser733Ser | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 14/24 | 3104/8662 | 2199/4344 | 733/1447 | chr9 | 95468802 | |||
| chr9:95469039 | C | T | 1 | a0002c0019 | 1 | HG02257.hp2 | synonymous_variant | LOW | c.1962G>A | p.Thr654Thr | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 14/24 | 2867/8662 | 1962/4344 | 654/1447 | chr9 | 95469039 | |||
| chr9:95469147 | G | A | 2 | a0002c0035 a0002c0036 |
2 | HG02717.hp2 NA18906.hp1 |
synonymous_variant | LOW | c.1854C>T | p.Cys618Cys | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 14/24 | 2759/8662 | 1854/4344 | 618/1447 | chr9 | 95469147 | |||
| chr9:95476076 | G | A | 4 | a0001c0004 a0001c0009 a0001c0037 others(1): Show |
33 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(30): Show |
synonymous_variant | LOW | c.1686C>T | p.Ala562Ala | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/24 | 2591/8662 | 1686/4344 | 562/1447 | chr9 | 95476076 | |||
| chr9:95476097 | A | G | 6 | a0001c0003 a0001c0007 a0001c0038 others(3): Show |
53 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(50): Show |
synonymous_variant | LOW | c.1665T>C | p.Asn555Asn | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/24 | 2570/8662 | 1665/4344 | 555/1447 | chr9 | 95476097 | |||
| chr9:95481960 | T | C | 1 | a0001c0009 | 4 | HG01361.hp1 HG02055.hp1 HG02300.hp1 others(1): Show |
synonymous_variant | LOW | c.735A>G | p.Thr245Thr | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 5/24 | 1640/8662 | 735/4344 | 245/1447 | chr9 | 95481960 | |||
| chr9:95506597 | C | A | 1 | a0001c0038 | 1 | HG02015.hp2 | splice_region_variant&synonymous_variant | LOW | c.204G>T | p.Gly68Gly | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/24 | 1109/8662 | 204/4344 | 68/1447 | chr9 | 95506597 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:95443161 | C | A | 17 | a0001c0002t0003 a0001c0002t0007 a0001c0002t0035 others(14): Show |
43 | HG00099.hp1 HG01071.hp1 HG01074.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*3232G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 24/24 | 3751 | chr9 | 95443161 | ||||||
| chr9:95443236 | C | T | 3 | a0001c0007t0014 a0001c0038t0014 a0010c0018t0014 |
3 | HG02015.hp2 HG02071.hp2 HG04199.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3157G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 24/24 | 3676 | chr9 | 95443236 | ||||||
| chr9:95443363 | T | C | 33 | a0001c0002t0005 a0001c0002t0008 a0001c0002t0009 others(30): Show |
81 | HG00597.hp1 HG01074.hp2 HG01081.hp1 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*3030A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 24/24 | 3549 | chr9 | 95443363 | ||||||
| chr9:95443397 | TACAA | T | 2 | a0001c0002t0012 a0001c0003t0012 |
4 | HG01069.hp1 HG01071.hp2 HG02109.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2992_*2995delTTGT | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 24/24 | 3511 | chr9 | 95443397 | ||||||
| chr9:95443613 | T | A | 1 | a0002c0001t0029 | 1 | HG02040.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2780A>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 24/24 | 3299 | chr9 | 95443613 | ||||||
| chr9:95443735 | A | C | 1 | a0002c0036t0031 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2658T>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 24/24 | 3177 | chr9 | 95443735 | ||||||
| chr9:95444104 | G | GT | 12 | a0001c0002t0005 a0001c0002t0011 a0001c0003t0005 others(9): Show |
21 | HG00609.hp1 HG00673.hp2 HG02056.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2288dupA | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 24/24 | 2807 | chr9 | 95444104 | ||||||
| chr9:95444117 | T | A | 1 | a0001c0013t0025 | 2 | HG02818.hp1 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2276A>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 24/24 | 2795 | chr9 | 95444117 | ||||||
| chr9:95444117 | TA | T | 3 | a0001c0007t0014 a0002c0001t0006 a0010c0018t0014 |
4 | HG02071.hp2 HG03041.hp1 HG04199.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2275delT | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 24/24 | 2794 | chr9 | 95444117 | ||||||
| chr9:95444118 | A | T | 15 | a0001c0002t0008 a0001c0002t0012 a0001c0002t0016 others(12): Show |
33 | HG01069.hp1 HG01071.hp2 HG01109.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*2275T>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 24/24 | 2794 | chr9 | 95444118 | ||||||
| chr9:95444488 | G | C | 6 | a0001c0002t0008 a0001c0002t0032 a0002c0001t0006 others(3): Show |
19 | HG01243.hp2 HG02257.hp2 HG02630.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1905C>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 24/24 | 2424 | chr9 | 95444488 | ||||||
| chr9:95444491 | ACACACAC others(11): Show |
A | 3 | a0001c0007t0014 a0001c0038t0014 a0010c0018t0014 |
3 | HG02015.hp2 HG02071.hp2 HG04199.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1884_*1901delCGTG others(14): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 24/24 | 2403 | chr9 | 95444491 | ||||||
| chr9:95444509 | G | GCA | 22 | a0001c0002t0005 a0001c0002t0009 a0001c0002t0011 others(19): Show |
55 | HG00597.hp1 HG01074.hp2 HG01081.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*1882_*1883dupTG | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 24/24 | 2402 | chr9 | 95444509 | ||||||
| chr9:95444509 | G | GCACACA | 6 | a0001c0002t0008 a0001c0002t0032 a0002c0001t0006 others(3): Show |
17 | HG01243.hp2 HG02257.hp2 HG02630.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1878_*1883dupTGTG others(2): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 24/24 | 2402 | chr9 | 95444509 | ||||||
| chr9:95444509 | G | GCACACAC others(3): Show |
1 | a0002c0001t0006 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1874_*1883dupTGTG others(6): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 24/24 | 2402 | chr9 | 95444509 | ||||||
| chr9:95444571 | T | G | 1 | a0001c0003t0037 | 1 | NA18967.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1822A>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 24/24 | 2341 | chr9 | 95444571 | ||||||
| chr9:95444684 | C | T | 6 | a0001c0002t0008 a0001c0002t0032 a0002c0001t0006 others(3): Show |
19 | HG01243.hp2 HG02257.hp2 HG02630.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1709G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 24/24 | 2228 | chr9 | 95444684 | ||||||
| chr9:95444685 | G | A | 4 | a0002c0001t0019 a0003c0010t0015 a0003c0010t0030 others(1): Show |
6 | HG00609.hp1 HG00673.hp2 HG02056.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1708C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 24/24 | 2227 | chr9 | 95444685 | ||||||
| chr9:95444691 | G | A | 3 | a0002c0001t0006 a0002c0001t0041 a0002c0019t0006 |
10 | HG02257.hp2 HG02630.hp1 HG02809.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1702C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 24/24 | 2221 | chr9 | 95444691 | ||||||
| chr9:95444777 | T | G | 6 | a0001c0002t0008 a0001c0002t0032 a0002c0001t0006 others(3): Show |
19 | HG01243.hp2 HG02257.hp2 HG02630.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1616A>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 24/24 | 2135 | chr9 | 95444777 | ||||||
| chr9:95444848 | A | G | 3 | a0001c0002t0017 a0001c0003t0021 a0001c0014t0033 |
5 | HG01081.hp2 HG02451.hp2 HG02647.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1545T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 24/24 | 2064 | chr9 | 95444848 | ||||||
| chr9:95444858 | A | G | 3 | a0001c0002t0017 a0001c0003t0021 a0001c0014t0033 |
5 | HG01081.hp2 HG02451.hp2 HG02647.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1535T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 24/24 | 2054 | chr9 | 95444858 | ||||||
| chr9:95445020 | C | G | 7 | a0001c0002t0022 a0001c0003t0004 a0001c0003t0037 others(4): Show |
27 | HG00597.hp1 HG01074.hp2 HG01099.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*1373G>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 24/24 | 1892 | chr9 | 95445020 | ||||||
| chr9:95445039 | A | C | 1 | a0002c0001t0028 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1354T>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 24/24 | 1873 | chr9 | 95445039 | ||||||
| chr9:95445327 | T | G | 2 | a0001c0003t0021 a0001c0014t0033 |
3 | HG01081.hp2 HG02451.hp2 HG02647.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1066A>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 24/24 | 1585 | chr9 | 95445327 | ||||||
| chr9:95445542 | C | G | 1 | a0001c0002t0008 | 7 | HG01243.hp2 HG02922.hp1 HG03098.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*851G>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 24/24 | 1370 | chr9 | 95445542 | ||||||
| chr9:95445592 | G | A | 1 | a0001c0014t0033 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*801C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 24/24 | 1320 | chr9 | 95445592 | ||||||
| chr9:95445606 | G | A | 2 | a0001c0004t0024 a0003c0005t0024 |
2 | NA18962.hp1 NA19083.hp1 |
3_prime_UTR_variant | MODIFIER | c.*787C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 24/24 | 1306 | chr9 | 95445606 | ||||||
| chr9:95445613 | G | A | 3 | a0001c0007t0014 a0001c0038t0014 a0010c0018t0014 |
3 | HG02015.hp2 HG02071.hp2 HG04199.hp1 |
3_prime_UTR_variant | MODIFIER | c.*780C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 24/24 | 1299 | chr9 | 95445613 | ||||||
| chr9:95445644 | G | GAAAT | 3 | a0001c0007t0014 a0001c0038t0014 a0010c0018t0014 |
3 | HG02015.hp2 HG02071.hp2 HG04199.hp1 |
3_prime_UTR_variant | MODIFIER | c.*748_*749insATTT | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 24/24 | 1267 | chr9 | 95445644 | ||||||
| chr9:95445644 | G | GAAGT | 8 | a0001c0002t0022 a0001c0003t0004 a0001c0003t0037 others(5): Show |
28 | HG00597.hp1 HG01074.hp2 HG01099.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*748_*749insACTT | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 24/24 | 1267 | chr9 | 95445644 | ||||||
| chr9:95445728 | C | CA | 20 | a0001c0002t0008 a0001c0002t0010 a0001c0002t0012 others(17): Show |
46 | HG01069.hp1 HG01071.hp2 HG01081.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*664dupT | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | 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 | ENST00000331920.11 | protein_coding | 24/24 | 969 | chr9 | 95445943 | ||||||
| chr9:95446156 | C | G | 9 | a0001c0002t0008 a0001c0002t0012 a0001c0002t0035 others(6): Show |
27 | HG01069.hp1 HG01071.hp2 HG01243.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*237G>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 24/24 | 756 | chr9 | 95446156 | ||||||
| chr9:95446162 | A | G | 1 | a0002c0001t0018 | 2 | HG01516.hp1 HG01517.hp2 |
3_prime_UTR_variant | MODIFIER | c.*231T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | 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 | ENST00000331920.11 | protein_coding | 24/24 | 664 | chr9 | 95446248 | ||||||
| chr9:95446288 | C | T | 1 | a0001c0004t0034 | 1 | NA18946.hp1 | 3_prime_UTR_variant | MODIFIER | c.*105G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 24/24 | 624 | chr9 | 95446288 | ||||||
| chr9:95446308 | C | T | 2 | a0001c0002t0012 a0001c0003t0012 |
4 | HG01069.hp1 HG01071.hp2 HG02109.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*85G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 24/24 | 604 | chr9 | 95446308 | ||||||
| chr9:95508364 | T | TGCC | 40 | a0001c0002t0002 a0001c0002t0007 a0001c0002t0008 others(37): Show |
88 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(85): Show |
5_prime_UTR_variant | MODIFIER | c.-6_-4dupGGC | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 1/24 | 4 | chr9 | 95508364 | ||||||
| chr9:95508628 | G | A | 1 | a0002c0001t0041 | 1 | HG03139.hp2 | 5_prime_UTR_variant | MODIFIER | c.-267C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 1/24 | 267 | chr9 | 95508628 | ||||||
| chr9:95508702 | T | G | 2 | a0001c0002t0042 a0001c0013t0025 |
3 | HG02818.hp1 HG03041.hp2 HG03486.hp2 |
5_prime_UTR_variant | MODIFIER | c.-341A>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 1/24 | 341 | chr9 | 95508702 | ||||||
| chr9:95509256 | G | T | 1 | a0001c0002t0017 | 2 | HG03471.hp2 HG03486.hp1 |
5_prime_UTR_variant | MODIFIER | c.-895C>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 1/24 | 895 | chr9 | 95509256 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:95446437 | G | A | 1 | a0001c0002t0020g0175 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.*2-46C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 23/23 | chr9 | 95446437 | |||||||
| chr9:95446505 | G | A | 5 | a0001c0002t0001g0080 a0001c0002t0001g0096 a0001c0004t0024g0233 others(2): Show |
5 | NA18962.hp1 NA19004.hp2 NA19011.hp1 others(2): Show |
intron_variant | MODIFIER | c.*2-114C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 23/23 | chr9 | 95446505 | |||||||
| chr9:95446508 | G | A | 1 | a0002c0001t0004g0135 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.*2-117C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 23/23 | chr9 | 95446508 | |||||||
| chr9:95446571 | C | T | 1 | a0001c0009t0002g0229 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.*2-180G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 23/23 | chr9 | 95446571 | |||||||
| chr9:95446682 | C | T | 2 | a0001c0002t0022g0215 a0001c0003t0004g0038 |
2 | HG01074.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.*1+229G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 23/23 | chr9 | 95446682 | |||||||
| chr9:95446773 | A | G | 2 | a0001c0002t0008g0183 a0002c0036t0031g0119 |
2 | HG02717.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.*1+138T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 23/23 | chr9 | 95446773 | |||||||
| chr9:95446812 | C | T | 1 | a0002c0001t0001g0127 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.*1+99G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 23/23 | chr9 | 95446812 | |||||||
| chr9:95446874 | T | C | 17 | a0001c0004t0002g0227 a0002c0001t0001g0002 a0002c0001t0001g0012 others(14): Show |
21 | HG00597.hp2 HG02040.hp1 NA18939.hp1 others(18): Show |
intron_variant | MODIFIER | c.*1+37A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 23/23 | chr9 | 95446874 | |||||||
| chr9:95446904 | C | T | 1 | a0002c0001t0001g0134 | 1 | NA18975.hp1 | splice_region_variant&intron_variant | LOW | c.*1+7G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 23/23 | chr9 | 95446904 | |||||||
| chr9:95447460 | G | A | 1 | a0015c0028t0002g0196 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.3805-9C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 22/23 | chr9 | 95447460 | |||||||
| chr9:95447617 | C | T | 8 | a0001c0007t0002g0245 a0001c0007t0002g0246 a0001c0007t0002g0247 others(5): Show |
9 | HG00423.hp2 HG00609.hp1 HG02015.hp2 others(6): Show |
intron_variant | MODIFIER | c.3805-166G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 22/23 | chr9 | 95447617 | |||||||
| chr9:95447648 | A | T | 9 | a0001c0002t0003g0026 a0001c0002t0003g0083 a0001c0002t0007g0187 others(6): Show |
11 | HG01069.hp1 HG01071.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.3805-197T>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 22/23 | chr9 | 95447648 | |||||||
| chr9:95447676 | G | A | 28 | a0001c0002t0003g0026 a0001c0002t0003g0083 a0001c0002t0007g0187 others(25): Show |
33 | HG00423.hp2 HG00609.hp1 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.3805-225C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 22/23 | chr9 | 95447676 | |||||||
| chr9:95447802 | G | A | 1 | a0001c0030t0038g0195 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3805-351C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 22/23 | chr9 | 95447802 | |||||||
| chr9:95447888 | G | A | 8 | a0001c0002t0005g0068 a0003c0005t0005g0087 a0003c0005t0007g0193 others(5): Show |
8 | HG01884.hp2 HG02559.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.3805-437C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 22/23 | chr9 | 95447888 | |||||||
| chr9:95448223 | C | T | 2 | a0001c0002t0009g0055 a0001c0002t0009g0056 |
2 | HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3805-772G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 22/23 | chr9 | 95448223 | |||||||
| chr9:95448224 | G | A | 1 | a0001c0002t0008g0183 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3805-773C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 22/23 | chr9 | 95448224 | |||||||
| chr9:95448227 | C | T | 1 | a0001c0002t0007g0191 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3805-776G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 22/23 | chr9 | 95448227 | |||||||
| chr9:95448659 | G | T | 59 | a0001c0002t0007g0191 a0001c0002t0009g0055 a0001c0002t0009g0056 others(56): Show |
60 | HG00423.hp2 HG00597.hp1 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.3804+410C>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 22/23 | chr9 | 95448659 | |||||||
| chr9:95448730 | G | GA | 33 | a0001c0003t0004g0034 a0003c0005t0001g0154 a0003c0005t0002g0019 others(30): Show |
36 | HG00558.hp2 HG00609.hp1 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.3804+338dupT | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 22/23 | chr9 | 95448730 | |||||||
| chr9:95449438 | C | A | 2 | a0001c0003t0002g0197 a0001c0003t0002g0198 |
2 | HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.3550-115G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 21/23 | chr9 | 95449438 | |||||||
| chr9:95449661 | G | A | 1 | a0001c0003t0001g0004 | 2 | NA18954.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.3549+180C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 21/23 | chr9 | 95449661 | |||||||
| chr9:95449678 | C | G | 1 | a0001c0009t0002g0228 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.3549+163G>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 21/23 | chr9 | 95449678 | |||||||
| chr9:95449706 | C | T | 6 | a0001c0007t0002g0245 a0001c0007t0002g0246 a0001c0007t0002g0247 others(3): Show |
6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.3549+135G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 21/23 | chr9 | 95449706 | |||||||
| chr9:95449803 | C | A | 2 | a0001c0013t0025g0254 a0001c0013t0025g0255 |
2 | HG02818.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.3549+38G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 21/23 | chr9 | 95449803 | |||||||
| chr9:95450027 | C | T | 1 | a0001c0003t0004g0034 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.3450-87G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/23 | chr9 | 95450027 | |||||||
| chr9:95450072 | A | C | 2 | a0001c0003t0002g0197 a0001c0003t0002g0198 |
2 | HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.3450-132T>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/23 | chr9 | 95450072 | |||||||
| chr9:95450238 | A | G | 1 | a0002c0035t0001g0106 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3450-298T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/23 | chr9 | 95450238 | |||||||
| chr9:95450270 | C | T | 8 | a0001c0002t0007g0191 a0001c0002t0009g0055 a0001c0002t0009g0056 others(5): Show |
8 | HG01952.hp1 HG02109.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.3450-330G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/23 | chr9 | 95450270 | |||||||
| chr9:95450326 | C | T | 29 | a0001c0002t0022g0215 a0001c0003t0001g0004 a0001c0003t0001g0032 others(26): Show |
30 | HG00597.hp1 HG00738.hp2 HG01074.hp2 others(27): Show |
intron_variant | MODIFIER | c.3450-386G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/23 | chr9 | 95450326 | |||||||
| chr9:95450788 | G | C | 3 | a0001c0003t0005g0061 a0001c0003t0009g0062 a0009c0025t0003g0174 |
3 | HG01952.hp1 HG02145.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.3450-848C>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/23 | chr9 | 95450788 | |||||||
| chr9:95451004 | A | AG | 31 | a0001c0002t0020g0175 a0001c0002t0040g0216 a0001c0004t0001g0009 others(28): Show |
33 | HG00099.hp2 HG00140.hp2 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.3450-1065dupC | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/23 | chr9 | 95451004 | |||||||
| chr9:95451071 | T | G | 2 | a0001c0014t0003g0084 a0001c0014t0033g0085 |
2 | HG01081.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.3450-1131A>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/23 | chr9 | 95451071 | |||||||
| chr9:95451404 | G | C | 1 | a0001c0003t0013g0058 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3450-1464C>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/23 | chr9 | 95451404 | |||||||
| chr9:95451446 | C | G | 30 | a0001c0002t0040g0216 a0001c0004t0001g0009 a0001c0004t0001g0086 others(27): Show |
32 | HG00099.hp2 HG00140.hp2 HG01175.hp1 others(29): Show |
intron_variant | MODIFIER | c.3450-1506G>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/23 | chr9 | 95451446 | |||||||
| chr9:95451478 | G | A | 1 | a0001c0004t0001g0177 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3450-1538C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/23 | chr9 | 95451478 | |||||||
| chr9:95451627 | T | C | 2 | a0001c0002t0009g0055 a0001c0002t0009g0056 |
2 | HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3450-1687A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/23 | chr9 | 95451627 | |||||||
| chr9:95452085 | A | G | 30 | a0001c0002t0040g0216 a0001c0004t0001g0009 a0001c0004t0001g0086 others(27): Show |
32 | HG00099.hp2 HG00140.hp2 HG01175.hp1 others(29): Show |
intron_variant | MODIFIER | c.3449+1393T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/23 | chr9 | 95452085 | |||||||
| chr9:95452328 | G | GAC | 6 | a0001c0002t0001g0125 a0001c0002t0001g0143 a0001c0002t0003g0060 others(3): Show |
6 | HG01255.hp1 HG02451.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.3449+1148_3449+114 others(6): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/23 | chr9 | 95452328 | |||||||
| chr9:95452328 | G | GACACAC | 12 | a0001c0002t0002g0184 a0001c0002t0007g0191 a0001c0002t0008g0017 others(9): Show |
15 | HG01069.hp1 HG01071.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.3449+1144_3449+114 others(10): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/23 | chr9 | 95452328 | |||||||
| chr9:95452328 | G | GACACACA others(1): Show |
8 | a0001c0002t0002g0185 a0001c0002t0003g0026 a0001c0002t0003g0083 others(5): Show |
8 | HG01358.hp2 HG01884.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.3449+1142_3449+114 others(12): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/23 | chr9 | 95452328 | |||||||
| chr9:95452328 | G | GACACACA others(3): Show |
33 | a0001c0002t0009g0066 a0001c0002t0017g0022 a0001c0002t0017g0023 others(30): Show |
35 | HG00099.hp2 HG00140.hp2 HG01175.hp1 others(32): Show |
intron_variant | MODIFIER | c.3449+1140_3449+114 others(14): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/23 | chr9 | 95452328 | |||||||
| chr9:95452328 | G | GACACACA others(5): Show |
12 | a0001c0003t0004g0039 a0001c0003t0004g0047 a0001c0003t0005g0061 others(9): Show |
12 | HG00423.hp2 HG01192.hp2 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.3449+1138_3449+114 others(16): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/23 | chr9 | 95452328 | |||||||
| chr9:95452328 | G | GACACACA others(7): Show |
10 | a0001c0002t0009g0055 a0001c0002t0009g0056 a0001c0002t0011g0186 others(7): Show |
10 | HG02027.hp1 HG02109.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.3449+1136_3449+114 others(18): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/23 | chr9 | 95452328 | |||||||
| chr9:95452328 | G | GACACACA others(9): Show |
25 | a0001c0002t0032g0165 a0001c0003t0001g0004 a0001c0003t0001g0032 others(22): Show |
26 | HG00738.hp2 HG01099.hp1 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.3449+1134_3449+114 others(20): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/23 | chr9 | 95452328 | |||||||
| chr9:95452328 | G | GACACACA others(11): Show |
5 | a0001c0003t0004g0040 a0001c0004t0022g0240 a0001c0007t0014g0248 others(2): Show |
5 | HG01517.hp1 HG02015.hp2 HG04199.hp1 others(2): Show |
intron_variant | MODIFIER | c.3449+1132_3449+114 others(22): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/23 | chr9 | 95452328 | |||||||
| chr9:95452328 | G | GACACACA others(13): Show |
1 | a0001c0003t0005g0042 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.3449+1130_3449+114 others(24): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/23 | chr9 | 95452328 | |||||||
| chr9:95452328 | G | GACACACA others(15): Show |
1 | a0001c0003t0004g0041 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.3449+1128_3449+114 others(26): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/23 | chr9 | 95452328 | |||||||
| chr9:95452328 | GAC | G | 82 | a0001c0002t0001g0075 a0001c0002t0002g0237 a0001c0002t0010g0169 others(79): Show |
98 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.3449+1148_3449+114 others(6): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/23 | chr9 | 95452328 | |||||||
| chr9:95452356 | C | CACACACA others(6): Show |
1 | a0001c0002t0022g0215 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.3449+1121_3449+112 others(17): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/23 | chr9 | 95452356 | |||||||
| chr9:95452357 | A | ACACACAC others(12): Show |
1 | a0001c0003t0037g0236 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.3449+1120_3449+112 others(23): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/23 | chr9 | 95452357 | |||||||
| chr9:95452376 | G | A | 1 | a0001c0002t0003g0083 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3449+1102C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/23 | chr9 | 95452376 | |||||||
| chr9:95452476 | C | T | 41 | a0001c0002t0002g0184 a0001c0002t0002g0185 a0001c0002t0003g0026 others(38): Show |
45 | HG00099.hp2 HG00140.hp2 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.3449+1002G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/23 | chr9 | 95452476 | |||||||
| chr9:95452903 | T | C | 29 | a0001c0002t0022g0215 a0001c0003t0001g0004 a0001c0003t0001g0032 others(26): Show |
30 | HG00597.hp1 HG00738.hp2 HG01074.hp2 others(27): Show |
intron_variant | MODIFIER | c.3449+575A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/23 | chr9 | 95452903 | |||||||
| chr9:95453024 | C | T | 53 | a0001c0002t0002g0184 a0001c0002t0002g0185 a0001c0002t0003g0026 others(50): Show |
59 | HG00099.hp2 HG00140.hp2 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.3449+454G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/23 | chr9 | 95453024 | |||||||
| chr9:95453046 | T | C | 6 | a0001c0002t0008g0017 a0001c0002t0008g0179 a0001c0002t0008g0180 others(3): Show |
7 | HG01243.hp2 HG02922.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.3449+432A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/23 | chr9 | 95453046 | |||||||
| chr9:95453113 | C | A | 1 | a0003c0005t0003g0082 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3449+365G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/23 | chr9 | 95453113 | |||||||
| chr9:95453114 | G | A | 1 | a0001c0003t0004g0030 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.3449+364C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/23 | chr9 | 95453114 | |||||||
| chr9:95453141 | T | A | 2 | a0001c0002t0016g0021 a0001c0002t0016g0244 |
3 | HG01243.hp1 HG03130.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.3449+337A>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/23 | chr9 | 95453141 | |||||||
| chr9:95453244 | G | A | 1 | a0001c0009t0002g0230 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.3449+234C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/23 | chr9 | 95453244 | |||||||
| chr9:95453349 | T | C | 40 | a0001c0002t0022g0215 a0001c0003t0001g0004 a0001c0003t0001g0032 others(37): Show |
41 | HG00597.hp1 HG00738.hp2 HG01074.hp2 others(38): Show |
intron_variant | MODIFIER | c.3449+129A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 20/23 | chr9 | 95453349 | |||||||
| chr9:95453686 | C | G | 32 | a0003c0005t0001g0154 a0003c0005t0002g0019 a0003c0005t0002g0199 others(29): Show |
35 | HG00558.hp2 HG00609.hp1 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.3307-66G>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 19/23 | chr9 | 95453686 | |||||||
| chr9:95453772 | C | A | 1 | a0002c0001t0001g0133 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3307-152G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 19/23 | chr9 | 95453772 | |||||||
| chr9:95453772 | C | T | 6 | a0001c0002t0009g0055 a0001c0002t0009g0056 a0001c0002t0009g0066 others(3): Show |
6 | HG01952.hp1 HG02109.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.3307-152G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 19/23 | chr9 | 95453772 | |||||||
| chr9:95453991 | T | C | 6 | a0001c0002t0008g0017 a0001c0002t0008g0179 a0001c0002t0008g0180 others(3): Show |
7 | HG01243.hp2 HG02922.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.3307-371A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 19/23 | chr9 | 95453991 | |||||||
| chr9:95454363 | A | G | 6 | a0001c0007t0002g0245 a0001c0007t0002g0246 a0001c0007t0002g0247 others(3): Show |
6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.3307-743T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 19/23 | chr9 | 95454363 | |||||||
| chr9:95454594 | A | G | 155 | a0001c0002t0002g0184 a0001c0002t0002g0185 a0001c0002t0003g0026 others(152): Show |
166 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.3307-974T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 19/23 | chr9 | 95454594 | |||||||
| chr9:95454804 | C | G | 1 | a0001c0002t0042g0256 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3307-1184G>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 19/23 | chr9 | 95454804 | |||||||
| chr9:95455066 | A | G | 97 | a0001c0002t0007g0191 a0001c0002t0009g0055 a0001c0002t0009g0056 others(94): Show |
102 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.3306+1210T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 19/23 | chr9 | 95455066 | |||||||
| chr9:95455226 | C | T | 3 | a0001c0002t0001g0125 a0001c0002t0001g0143 a0002c0001t0001g0158 |
3 | HG03017.hp2 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.3306+1050G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 19/23 | chr9 | 95455226 | |||||||
| chr9:95455299 | T | C | 155 | a0001c0002t0002g0184 a0001c0002t0002g0185 a0001c0002t0003g0026 others(152): Show |
166 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.3306+977A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 19/23 | chr9 | 95455299 | |||||||
| chr9:95455328 | G | A | 2 | a0001c0002t0001g0151 a0001c0002t0003g0015 |
3 | HG01071.hp1 HG01074.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.3306+948C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 19/23 | chr9 | 95455328 | |||||||
| chr9:95455442 | C | G | 9 | a0001c0003t0005g0063 a0001c0003t0005g0064 a0001c0003t0005g0065 others(6): Show |
9 | HG02630.hp2 HG02895.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.3306+834G>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 19/23 | chr9 | 95455442 | |||||||
| chr9:95455462 | C | T | 2 | a0001c0002t0002g0184 a0001c0002t0002g0185 |
2 | HG01884.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.3306+814G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 19/23 | chr9 | 95455462 | |||||||
| chr9:95455495 | T | C | 2 | a0001c0013t0025g0254 a0001c0013t0025g0255 |
2 | HG02818.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.3306+781A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 19/23 | chr9 | 95455495 | |||||||
| chr9:95455507 | A | G | 3 | a0001c0003t0021g0166 a0001c0014t0003g0084 a0001c0014t0033g0085 |
3 | HG01081.hp2 HG02647.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.3306+769T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 19/23 | chr9 | 95455507 | |||||||
| chr9:95455728 | T | G | 2 | a0001c0002t0012g0005 a0001c0003t0012g0006 |
4 | HG01069.hp1 HG01071.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.3306+548A>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 19/23 | chr9 | 95455728 | |||||||
| chr9:95455759 | C | T | 8 | a0001c0002t0009g0055 a0001c0002t0009g0056 a0001c0002t0009g0066 others(5): Show |
8 | HG01952.hp1 HG02109.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.3306+517G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 19/23 | chr9 | 95455759 | |||||||
| chr9:95455760 | G | A | 2 | a0001c0013t0025g0254 a0001c0013t0025g0255 |
2 | HG02818.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.3306+516C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 19/23 | chr9 | 95455760 | |||||||
| chr9:95455960 | G | A | 2 | a0002c0035t0001g0106 a0002c0036t0031g0119 |
2 | HG02717.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3306+316C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 19/23 | chr9 | 95455960 | |||||||
| chr9:95456030 | C | T | 1 | a0003c0005t0002g0210 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.3306+246G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 19/23 | chr9 | 95456030 | |||||||
| chr9:95456160 | G | A | 2 | a0001c0013t0025g0254 a0001c0013t0025g0255 |
2 | HG02818.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.3306+116C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 19/23 | chr9 | 95456160 | |||||||
| chr9:95456192 | G | GC | 156 | a0001c0002t0002g0184 a0001c0002t0002g0185 a0001c0002t0003g0026 others(153): Show |
167 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.3306+83dupG | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 19/23 | chr9 | 95456192 | |||||||
| chr9:95456418 | A | G | 2 | a0001c0002t0001g0125 a0001c0002t0001g0143 |
2 | HG03491.hp2 HG03492.hp2 |
splice_region_variant&intron_variant | LOW | c.3169-5T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 18/23 | chr9 | 95456418 | |||||||
| chr9:95456710 | G | A | 1 | a0003c0005t0007g0212 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3169-297C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 18/23 | chr9 | 95456710 | |||||||
| chr9:95456755 | C | T | 2 | a0001c0013t0025g0254 a0001c0013t0025g0255 |
2 | HG02818.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.3169-342G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 18/23 | chr9 | 95456755 | |||||||
| chr9:95456761 | T | TCA | 8 | a0001c0007t0002g0245 a0001c0007t0002g0246 a0001c0007t0002g0247 others(5): Show |
8 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.3169-350_3169-349d others(4): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 18/23 | chr9 | 95456761 | |||||||
| chr9:95456984 | G | A | 1 | a0002c0020t0001g0073 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.3169-571C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 18/23 | chr9 | 95456984 | |||||||
| chr9:95457009 | C | T | 4 | a0001c0002t0003g0014 a0001c0002t0003g0148 a0001c0002t0003g0149 others(1): Show |
5 | HG01358.hp1 HG01934.hp2 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.3169-596G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 18/23 | chr9 | 95457009 | |||||||
| chr9:95457022 | C | G | 1 | a0001c0002t0023g0194 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3169-609G>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 18/23 | chr9 | 95457022 | |||||||
| chr9:95457565 | T | C | 3 | a0002c0001t0001g0012 a0002c0001t0001g0093 a0002c0001t0001g0133 |
4 | NA18939.hp1 NA18967.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.3168+448A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 18/23 | chr9 | 95457565 | |||||||
| chr9:95457667 | T | C | 1 | a0002c0001t0001g0150 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3168+346A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 18/23 | chr9 | 95457667 | |||||||
| chr9:95457755 | G | A | 3 | a0002c0001t0001g0076 a0002c0001t0001g0077 a0002c0001t0018g0007 |
4 | HG01516.hp1 HG01517.hp2 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.3168+258C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 18/23 | chr9 | 95457755 | |||||||
| chr9:95457777 | G | C | 1 | a0001c0002t0007g0191 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3168+236C>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 18/23 | chr9 | 95457777 | |||||||
| chr9:95457780 | C | T | 1 | a0003c0005t0007g0193 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3168+233G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 18/23 | chr9 | 95457780 | |||||||
| chr9:95457793 | C | T | 1 | a0002c0001t0003g0111 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.3168+220G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 18/23 | chr9 | 95457793 | |||||||
| chr9:95458432 | T | C | 2 | a0001c0013t0025g0254 a0001c0013t0025g0255 |
2 | HG02818.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2888-139A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 17/23 | chr9 | 95458432 | |||||||
| chr9:95458564 | C | T | 2 | a0001c0002t0002g0184 a0001c0002t0002g0185 |
2 | HG01884.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.2888-271G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 17/23 | chr9 | 95458564 | |||||||
| chr9:95458576 | AT | A | 6 | a0001c0007t0002g0245 a0001c0007t0002g0246 a0001c0007t0002g0247 others(3): Show |
6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.2888-284delA | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 17/23 | chr9 | 95458576 | |||||||
| chr9:95458939 | C | T | 2 | a0001c0002t0017g0022 a0001c0002t0017g0023 |
2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2888-646G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 17/23 | chr9 | 95458939 | |||||||
| chr9:95459017 | G | A | 1 | a0001c0002t0001g0096 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.2887+583C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 17/23 | chr9 | 95459017 | |||||||
| chr9:95459272 | C | T | 3 | a0003c0010t0015g0018 a0003c0010t0030g0153 a0004c0021t0015g0204 |
4 | HG00609.hp1 HG00673.hp2 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.2887+328G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 17/23 | chr9 | 95459272 | |||||||
| chr9:95459306 | C | T | 1 | a0001c0003t0013g0058 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2887+294G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 17/23 | chr9 | 95459306 | |||||||
| chr9:95459340 | G | A | 1 | a0001c0014t0033g0085 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2887+260C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 17/23 | chr9 | 95459340 | |||||||
| chr9:95459418 | G | A | 6 | a0001c0007t0002g0245 a0001c0007t0002g0246 a0001c0007t0002g0247 others(3): Show |
6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.2887+182C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 17/23 | chr9 | 95459418 | |||||||
| chr9:95459512 | G | A | 1 | a0002c0001t0001g0136 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2887+88C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 17/23 | chr9 | 95459512 | |||||||
| chr9:95459563 | T | C | 3 | a0001c0002t0016g0021 a0001c0002t0016g0244 a0001c0002t0020g0175 |
4 | HG01109.hp2 HG01243.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.2887+37A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 17/23 | chr9 | 95459563 | |||||||
| chr9:95459579 | T | C | 155 | a0001c0002t0002g0184 a0001c0002t0002g0185 a0001c0002t0003g0026 others(152): Show |
166 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.2887+21A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 17/23 | chr9 | 95459579 | |||||||
| chr9:95459891 | T | C | 2 | a0001c0002t0003g0118 a0001c0002t0003g0163 |
2 | HG02735.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.2704-108A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 16/23 | chr9 | 95459891 | |||||||
| chr9:95460072 | A | G | 1 | a0001c0002t0023g0194 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2704-289T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 16/23 | chr9 | 95460072 | |||||||
| chr9:95460145 | C | T | 3 | a0002c0001t0001g0012 a0002c0001t0001g0093 a0002c0001t0001g0133 |
4 | NA18939.hp1 NA18967.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.2704-362G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 16/23 | chr9 | 95460145 | |||||||
| chr9:95460298 | G | A | 4 | a0001c0002t0010g0169 a0005c0008t0010g0016 a0005c0008t0010g0167 others(1): Show |
5 | HG02145.hp1 HG02572.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2704-515C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 16/23 | chr9 | 95460298 | |||||||
| chr9:95460299 | T | G | 1 | a0002c0001t0003g0111 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2704-516A>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 16/23 | chr9 | 95460299 | |||||||
| chr9:95460349 | G | A | 1 | a0009c0025t0003g0174 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2704-566C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 16/23 | chr9 | 95460349 | |||||||
| chr9:95460365 | C | T | 1 | a0001c0002t0002g0237 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2704-582G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 16/23 | chr9 | 95460365 | |||||||
| chr9:95460369 | C | T | 34 | a0001c0022t0002g0252 a0003c0005t0001g0154 a0003c0005t0002g0019 others(31): Show |
37 | HG00558.hp2 HG00609.hp1 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.2704-586G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 16/23 | chr9 | 95460369 | |||||||
| chr9:95460371 | C | T | 1 | a0001c0030t0038g0195 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2704-588G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 16/23 | chr9 | 95460371 | |||||||
| chr9:95460383 | C | T | 40 | a0001c0002t0002g0184 a0001c0002t0002g0185 a0001c0002t0003g0026 others(37): Show |
45 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.2704-600G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 16/23 | chr9 | 95460383 | |||||||
| chr9:95460404 | G | A | 3 | a0001c0002t0009g0055 a0001c0002t0009g0056 a0009c0025t0003g0174 |
3 | HG01952.hp1 HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2704-621C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 16/23 | chr9 | 95460404 | |||||||
| chr9:95460416 | T | C | 1 | a0001c0003t0004g0045 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2704-633A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 16/23 | chr9 | 95460416 | |||||||
| chr9:95460467 | C | T | 6 | a0001c0007t0002g0245 a0001c0007t0002g0246 a0001c0007t0002g0247 others(3): Show |
6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.2704-684G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 16/23 | chr9 | 95460467 | |||||||
| chr9:95460505 | T | G | 1 | a0002c0001t0006g0102 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2704-722A>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 16/23 | chr9 | 95460505 | |||||||
| chr9:95460510 | A | G | 2 | a0001c0002t0009g0055 a0001c0002t0009g0056 |
2 | HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2704-727T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 16/23 | chr9 | 95460510 | |||||||
| chr9:95460527 | C | T | 1 | a0001c0003t0020g0171 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2704-744G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 16/23 | chr9 | 95460527 | |||||||
| chr9:95460588 | G | C | 1 | a0001c0002t0022g0215 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2704-805C>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 16/23 | chr9 | 95460588 | |||||||
| chr9:95460646 | A | C | 1 | a0001c0004t0002g0220 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2704-863T>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 16/23 | chr9 | 95460646 | |||||||
| chr9:95460751 | G | C | 1 | a0002c0036t0031g0119 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2704-968C>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 16/23 | chr9 | 95460751 | |||||||
| chr9:95461155 | A | G | 6 | a0001c0002t0008g0017 a0001c0002t0008g0179 a0001c0002t0008g0180 others(3): Show |
7 | HG01243.hp2 HG02922.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.2703+701T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 16/23 | chr9 | 95461155 | |||||||
| chr9:95461179 | T | C | 2 | a0001c0002t0032g0165 a0012c0026t0039g0192 |
2 | HG02723.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.2703+677A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 16/23 | chr9 | 95461179 | |||||||
| chr9:95461230 | A | T | 1 | a0001c0002t0020g0175 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2703+626T>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 16/23 | chr9 | 95461230 | |||||||
| chr9:95461275 | C | T | 1 | a0002c0001t0001g0136 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2703+581G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 16/23 | chr9 | 95461275 | |||||||
| chr9:95461394 | C | T | 1 | a0001c0030t0038g0195 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2703+462G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 16/23 | chr9 | 95461394 | |||||||
| chr9:95461416 | C | T | 1 | a0002c0001t0003g0111 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2703+440G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 16/23 | chr9 | 95461416 | |||||||
| chr9:95461455 | G | T | 3 | a0001c0003t0002g0197 a0001c0003t0002g0198 a0001c0003t0020g0171 |
3 | HG02622.hp2 HG02965.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2703+401C>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 16/23 | chr9 | 95461455 | |||||||
| chr9:95461556 | A | G | 1 | a0015c0028t0002g0196 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2703+300T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 16/23 | chr9 | 95461556 | |||||||
| chr9:95461560 | T | C | 1 | a0001c0003t0004g0045 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2703+296A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 16/23 | chr9 | 95461560 | |||||||
| chr9:95461574 | C | T | 11 | a0001c0003t0005g0061 a0001c0003t0005g0063 a0001c0003t0005g0064 others(8): Show |
11 | HG02145.hp2 HG02615.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.2703+282G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 16/23 | chr9 | 95461574 | |||||||
| chr9:95462061 | G | A | 1 | a0002c0001t0001g0131 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2561-63C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95462061 | |||||||
| chr9:95462078 | C | G | 155 | a0001c0002t0002g0184 a0001c0002t0002g0185 a0001c0002t0003g0026 others(152): Show |
166 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.2561-80G>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95462078 | |||||||
| chr9:95462205 | G | C | 11 | a0001c0003t0005g0061 a0001c0003t0005g0063 a0001c0003t0005g0064 others(8): Show |
11 | HG02145.hp2 HG02615.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.2561-207C>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95462205 | |||||||
| chr9:95462345 | G | A | 11 | a0001c0002t0002g0184 a0001c0002t0002g0185 a0001c0002t0003g0026 others(8): Show |
13 | HG01069.hp1 HG01071.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.2561-347C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95462345 | |||||||
| chr9:95462403 | A | G | 19 | a0001c0004t0001g0086 a0001c0004t0002g0020 a0001c0004t0002g0218 others(16): Show |
20 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(17): Show |
intron_variant | MODIFIER | c.2561-405T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95462403 | |||||||
| chr9:95462429 | T | C | 1 | a0001c0002t0001g0141 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2561-431A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95462429 | |||||||
| chr9:95462499 | G | C | 1 | a0001c0002t0035g0190 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2561-501C>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95462499 | |||||||
| chr9:95462521 | A | T | 1 | a0001c0002t0001g0141 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2561-523T>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95462521 | |||||||
| chr9:95462658 | G | A | 1 | a0002c0001t0027g0122 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.2561-660C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95462658 | |||||||
| chr9:95462774 | G | T | 104 | a0001c0002t0003g0026 a0001c0002t0003g0083 a0001c0002t0007g0187 others(101): Show |
110 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(107): Show |
intron_variant | MODIFIER | c.2561-776C>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95462774 | |||||||
| chr9:95462832 | C | A | 1 | a0001c0002t0009g0056 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2561-834G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95462832 | |||||||
| chr9:95462941 | G | A | 3 | a0001c0003t0021g0166 a0001c0014t0003g0084 a0001c0014t0033g0085 |
3 | HG01081.hp2 HG02647.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2561-943C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95462941 | |||||||
| chr9:95462964 | T | C | 1 | a0008c0015t0001g0120 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.2561-966A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95462964 | |||||||
| chr9:95462966 | G | A | 1 | a0001c0003t0021g0170 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2561-968C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95462966 | |||||||
| chr9:95462999 | C | A | 1 | a0001c0002t0023g0194 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2561-1001G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95462999 | |||||||
| chr9:95463007 | C | T | 1 | a0001c0002t0023g0194 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2561-1009G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95463007 | |||||||
| chr9:95463110 | G | A | 1 | a0001c0003t0009g0052 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2561-1112C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95463110 | |||||||
| chr9:95463125 | C | T | 3 | a0001c0002t0007g0189 a0001c0002t0035g0190 a0001c0024t0007g0188 |
3 | HG02451.hp1 HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.2561-1127G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95463125 | |||||||
| chr9:95463170 | CA | C | 47 | a0001c0002t0002g0184 a0001c0002t0002g0185 a0001c0002t0003g0026 others(44): Show |
51 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.2561-1173delT | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95463170 | |||||||
| chr9:95463187 | C | T | 6 | a0001c0007t0002g0245 a0001c0007t0002g0246 a0001c0007t0002g0247 others(3): Show |
6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.2561-1189G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95463187 | |||||||
| chr9:95463260 | G | A | 12 | a0001c0003t0005g0061 a0001c0003t0005g0063 a0001c0003t0005g0064 others(9): Show |
13 | HG02109.hp2 HG02145.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.2561-1262C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95463260 | |||||||
| chr9:95463376 | C | T | 47 | a0001c0002t0002g0184 a0001c0002t0002g0185 a0001c0002t0003g0026 others(44): Show |
51 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.2561-1378G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95463376 | |||||||
| chr9:95463401 | C | T | 52 | a0001c0002t0007g0191 a0001c0002t0009g0055 a0001c0002t0009g0056 others(49): Show |
56 | HG00558.hp2 HG00609.hp1 HG00673.hp2 others(53): Show |
intron_variant | MODIFIER | c.2561-1403G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95463401 | |||||||
| chr9:95463425 | T | C | 1 | a0001c0009t0002g0231 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2561-1427A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95463425 | |||||||
| chr9:95463538 | C | T | 2 | a0002c0035t0001g0106 a0002c0036t0031g0119 |
2 | HG02717.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2561-1540G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95463538 | |||||||
| chr9:95463591 | T | A | 1 | a0001c0003t0020g0171 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2561-1593A>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95463591 | |||||||
| chr9:95463681 | T | C | 1 | a0002c0001t0001g0155 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2561-1683A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95463681 | |||||||
| chr9:95463784 | G | A | 50 | a0001c0002t0022g0215 a0001c0003t0001g0004 a0001c0003t0001g0032 others(47): Show |
52 | HG00423.hp2 HG00597.hp1 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.2561-1786C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95463784 | |||||||
| chr9:95463885 | G | A | 2 | a0001c0002t0002g0184 a0001c0002t0002g0185 |
2 | HG01884.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.2561-1887C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95463885 | |||||||
| chr9:95463963 | C | T | 1 | a0001c0024t0007g0188 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2561-1965G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95463963 | |||||||
| chr9:95463969 | C | T | 2 | a0001c0002t0016g0021 a0001c0002t0016g0244 |
3 | HG01243.hp1 HG03130.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2561-1971G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95463969 | |||||||
| chr9:95463985 | C | T | 7 | a0001c0002t0008g0017 a0001c0002t0008g0179 a0001c0002t0008g0180 others(4): Show |
9 | HG01069.hp1 HG01071.hp2 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.2561-1987G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95463985 | |||||||
| chr9:95463986 | G | A | 1 | a0002c0001t0001g0136 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2561-1988C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95463986 | |||||||
| chr9:95464025 | C | T | 44 | a0001c0002t0022g0215 a0001c0003t0001g0004 a0001c0003t0001g0032 others(41): Show |
46 | HG00597.hp1 HG00738.hp2 HG01074.hp2 others(43): Show |
intron_variant | MODIFIER | c.2561-2027G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95464025 | |||||||
| chr9:95464113 | A | C | 50 | a0001c0002t0022g0215 a0001c0003t0001g0004 a0001c0003t0001g0032 others(47): Show |
52 | HG00423.hp2 HG00597.hp1 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.2561-2115T>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95464113 | |||||||
| chr9:95464262 | A | G | 1 | a0001c0002t0001g0075 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2561-2264T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95464262 | |||||||
| chr9:95464420 | T | C | 50 | a0001c0002t0022g0215 a0001c0003t0001g0004 a0001c0003t0001g0032 others(47): Show |
52 | HG00423.hp2 HG00597.hp1 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.2561-2422A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95464420 | |||||||
| chr9:95464748 | T | C | 2 | a0001c0003t0021g0166 a0001c0030t0038g0195 |
2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.2560+2368A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95464748 | |||||||
| chr9:95464876 | C | T | 2 | a0002c0001t0001g0123 a0002c0001t0001g0150 |
2 | HG01175.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.2560+2240G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95464876 | |||||||
| chr9:95464951 | T | C | 27 | a0001c0022t0002g0252 a0003c0005t0001g0154 a0003c0005t0002g0019 others(24): Show |
29 | HG00558.hp2 HG00609.hp1 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.2560+2165A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95464951 | |||||||
| chr9:95465003 | G | A | 1 | a0001c0002t0020g0175 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2560+2113C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95465003 | |||||||
| chr9:95465056 | G | A | 1 | a0001c0002t0020g0175 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2560+2060C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95465056 | |||||||
| chr9:95465133 | C | T | 50 | a0001c0002t0022g0215 a0001c0003t0001g0004 a0001c0003t0001g0032 others(47): Show |
52 | HG00423.hp2 HG00597.hp1 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.2560+1983G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95465133 | |||||||
| chr9:95465451 | G | A | 2 | a0001c0002t0017g0022 a0001c0002t0017g0023 |
2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2560+1665C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95465451 | |||||||
| chr9:95465479 | C | T | 2 | a0001c0003t0021g0166 a0001c0030t0038g0195 |
2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.2560+1637G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95465479 | |||||||
| chr9:95465505 | A | G | 1 | a0001c0002t0003g0060 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2560+1611T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95465505 | |||||||
| chr9:95465528 | G | T | 50 | a0001c0002t0022g0215 a0001c0003t0001g0004 a0001c0003t0001g0032 others(47): Show |
52 | HG00423.hp2 HG00597.hp1 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.2560+1588C>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95465528 | |||||||
| chr9:95465667 | G | A | 1 | a0001c0002t0001g0072 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2560+1449C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95465667 | |||||||
| chr9:95465719 | A | G | 1 | a0001c0003t0021g0170 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2560+1397T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95465719 | |||||||
| chr9:95465897 | T | C | 1 | a0002c0001t0001g0157 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2560+1219A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95465897 | |||||||
| chr9:95465943 | C | T | 51 | a0001c0002t0002g0184 a0001c0002t0002g0185 a0001c0002t0003g0026 others(48): Show |
56 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.2560+1173G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95465943 | |||||||
| chr9:95466132 | C | A | 1 | a0001c0003t0021g0170 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2560+984G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95466132 | |||||||
| chr9:95466255 | C | A | 1 | a0001c0002t0023g0238 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2560+861G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95466255 | |||||||
| chr9:95466379 | T | G | 1 | a0001c0002t0001g0116 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2560+737A>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95466379 | |||||||
| chr9:95466873 | C | T | 2 | a0003c0005t0005g0087 a0003c0005t0005g0091 |
2 | HG02647.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2560+243G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95466873 | |||||||
| chr9:95466982 | A | T | 3 | a0001c0002t0001g0116 a0002c0001t0001g0115 a0016c0034t0003g0113 |
3 | HG01167.hp2 HG01433.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2560+134T>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95466982 | |||||||
| chr9:95467008 | C | T | 3 | a0001c0003t0002g0197 a0001c0003t0002g0198 a0001c0003t0020g0171 |
3 | HG02622.hp2 HG02965.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2560+108G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95467008 | |||||||
| chr9:95467015 | G | A | 53 | a0001c0002t0002g0184 a0001c0002t0002g0185 a0001c0002t0003g0026 others(50): Show |
59 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.2560+101C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95467015 | |||||||
| chr9:95467084 | C | T | 3 | a0001c0003t0002g0197 a0001c0003t0002g0198 a0001c0003t0020g0171 |
3 | HG02622.hp2 HG02965.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2560+32G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95467084 | |||||||
| chr9:95467107 | C | G | 153 | a0001c0002t0002g0184 a0001c0002t0002g0185 a0001c0002t0003g0026 others(150): Show |
164 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.2560+9G>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95467107 | |||||||
| chr9:95467109 | G | A | 2 | a0001c0004t0007g0232 a0001c0004t0007g0235 |
2 | NA18940.hp2 NA18969.hp2 |
splice_region_variant&intron_variant | LOW | c.2560+7C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 15/23 | chr9 | 95467109 | |||||||
| chr9:95467527 | T | G | 1 | a0001c0003t0020g0171 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2251-102A>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 14/23 | chr9 | 95467527 | |||||||
| chr9:95467714 | G | A | 1 | a0001c0030t0038g0195 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2251-289C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 14/23 | chr9 | 95467714 | |||||||
| chr9:95468078 | T | C | 1 | a0001c0030t0038g0195 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2251-653A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 14/23 | chr9 | 95468078 | |||||||
| chr9:95468210 | G | A | 1 | a0002c0001t0001g0161 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2250+541C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 14/23 | chr9 | 95468210 | |||||||
| chr9:95468263 | C | T | 28 | a0001c0002t0022g0215 a0001c0003t0001g0004 a0001c0003t0001g0032 others(25): Show |
29 | HG00597.hp1 HG00738.hp2 HG01074.hp2 others(26): Show |
intron_variant | MODIFIER | c.2250+488G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 14/23 | chr9 | 95468263 | |||||||
| chr9:95468556 | C | T | 1 | a0002c0001t0001g0146 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2250+195G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 14/23 | chr9 | 95468556 | |||||||
| chr9:95468613 | A | G | 1 | a0001c0003t0004g0040 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2250+138T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 14/23 | chr9 | 95468613 | |||||||
| chr9:95468623 | T | C | 1 | a0001c0030t0038g0195 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2250+128A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 14/23 | chr9 | 95468623 | |||||||
| chr9:95468625 | T | C | 45 | a0001c0002t0022g0215 a0001c0003t0001g0004 a0001c0003t0001g0032 others(42): Show |
47 | HG00597.hp1 HG00738.hp2 HG01074.hp2 others(44): Show |
intron_variant | MODIFIER | c.2250+126A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 14/23 | chr9 | 95468625 | |||||||
| chr9:95468632 | C | T | 1 | a0005c0008t0010g0016 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2250+119G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 14/23 | chr9 | 95468632 | |||||||
| chr9:95468638 | C | T | 1 | a0001c0030t0038g0195 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2250+113G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 14/23 | chr9 | 95468638 | |||||||
| chr9:95468642 | AT | A | 148 | a0001c0002t0002g0184 a0001c0002t0002g0185 a0001c0002t0003g0026 others(145): Show |
159 | HG00099.hp2 HG00140.hp2 HG00558.hp2 others(156): Show |
intron_variant | MODIFIER | c.2250+108delA | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 14/23 | chr9 | 95468642 | |||||||
| chr9:95468642 | ATT | A | 6 | a0001c0007t0002g0245 a0001c0007t0002g0246 a0001c0007t0002g0247 others(3): Show |
6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.2250+107_2250+108d others(4): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 14/23 | chr9 | 95468642 | |||||||
| chr9:95468726 | A | G | 40 | a0001c0002t0022g0215 a0001c0003t0001g0004 a0001c0003t0001g0032 others(37): Show |
42 | HG00597.hp1 HG00738.hp2 HG01074.hp2 others(39): Show |
intron_variant | MODIFIER | c.2250+25T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 14/23 | chr9 | 95468726 | |||||||
| chr9:95469321 | ACCTGGTT others(5): Show |
A | 1 | a0002c0001t0001g0129 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1848-180_1848-169d others(14): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 13/23 | chr9 | 95469321 | |||||||
| chr9:95469553 | C | T | 2 | a0001c0002t0003g0026 a0001c0002t0003g0083 |
2 | HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1847+260G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 13/23 | chr9 | 95469553 | |||||||
| chr9:95469626 | G | A | 53 | a0001c0002t0002g0184 a0001c0002t0002g0185 a0001c0002t0003g0026 others(50): Show |
59 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.1847+187C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 13/23 | chr9 | 95469626 | |||||||
| chr9:95470257 | T | C | 1 | a0005c0008t0010g0016 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1729-326A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95470257 | |||||||
| chr9:95470263 | T | G | 2 | a0001c0004t0002g0243 a0002c0011t0002g0223 |
2 | NA18943.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.1729-332A>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95470263 | |||||||
| chr9:95470322 | T | C | 1 | a0001c0002t0007g0189 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1729-391A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95470322 | |||||||
| chr9:95470343 | T | A | 14 | a0001c0002t0007g0191 a0001c0002t0009g0055 a0001c0002t0009g0056 others(11): Show |
15 | HG01952.hp1 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.1729-412A>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95470343 | |||||||
| chr9:95470410 | C | A | 3 | a0003c0005t0005g0087 a0003c0005t0005g0091 a0009c0025t0003g0174 |
3 | HG01952.hp1 HG02647.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1729-479G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95470410 | |||||||
| chr9:95470472 | A | G | 51 | a0001c0002t0022g0215 a0001c0003t0001g0004 a0001c0003t0001g0032 others(48): Show |
53 | HG00423.hp2 HG00597.hp1 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.1729-541T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95470472 | |||||||
| chr9:95470528 | A | G | 1 | a0002c0001t0027g0122 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1729-597T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95470528 | |||||||
| chr9:95470533 | G | A | 2 | a0001c0002t0016g0021 a0001c0002t0016g0244 |
3 | HG01243.hp1 HG03130.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1729-602C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95470533 | |||||||
| chr9:95470791 | G | A | 2 | a0001c0002t0017g0022 a0001c0002t0017g0023 |
2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1729-860C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95470791 | |||||||
| chr9:95470812 | C | T | 1 | a0001c0002t0035g0190 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1729-881G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95470812 | |||||||
| chr9:95470908 | C | T | 1 | a0001c0002t0008g0017 | 2 | HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1729-977G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95470908 | |||||||
| chr9:95470916 | C | A | 6 | a0001c0007t0002g0245 a0001c0007t0002g0246 a0001c0007t0002g0247 others(3): Show |
6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1729-985G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95470916 | |||||||
| chr9:95470927 | C | A | 1 | a0001c0002t0001g0141 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1729-996G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95470927 | |||||||
| chr9:95471036 | T | C | 4 | a0001c0002t0010g0169 a0005c0008t0010g0016 a0005c0008t0010g0167 others(1): Show |
5 | HG02145.hp1 HG02572.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1729-1105A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95471036 | |||||||
| chr9:95471082 | C | CA | 48 | a0001c0002t0007g0191 a0001c0002t0009g0055 a0001c0002t0009g0056 others(45): Show |
51 | HG00558.hp2 HG00609.hp1 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.1729-1152dupT | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95471082 | |||||||
| chr9:95471082 | CAAAAAAA others(5): Show |
C | 45 | a0001c0002t0022g0215 a0001c0003t0001g0004 a0001c0003t0001g0032 others(42): Show |
47 | HG00597.hp1 HG00738.hp2 HG01074.hp2 others(44): Show |
intron_variant | MODIFIER | c.1729-1163_1729-115 others(16): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95471082 | |||||||
| chr9:95471154 | A | T | 1 | a0002c0001t0001g0114 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1729-1223T>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95471154 | |||||||
| chr9:95471227 | G | A | 12 | a0001c0003t0005g0061 a0001c0003t0005g0063 a0001c0003t0005g0064 others(9): Show |
13 | HG02109.hp2 HG02145.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1729-1296C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95471227 | |||||||
| chr9:95471242 | G | A | 1 | a0001c0003t0013g0058 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1729-1311C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95471242 | |||||||
| chr9:95471815 | A | G | 153 | a0001c0002t0002g0184 a0001c0002t0002g0185 a0001c0002t0003g0026 others(150): Show |
164 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.1729-1884T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95471815 | |||||||
| chr9:95471836 | C | T | 1 | a0002c0001t0001g0161 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1729-1905G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95471836 | |||||||
| chr9:95471855 | A | G | 1 | a0001c0002t0007g0191 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1729-1924T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95471855 | |||||||
| chr9:95471998 | T | C | 1 | a0002c0001t0001g0137 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1729-2067A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95471998 | |||||||
| chr9:95472101 | AAC | A | 12 | a0001c0003t0005g0061 a0001c0003t0005g0063 a0001c0003t0005g0064 others(9): Show |
13 | HG02109.hp2 HG02145.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1729-2172_1729-217 others(6): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95472101 | |||||||
| chr9:95472105 | C | CA | 6 | a0001c0007t0002g0245 a0001c0007t0002g0246 a0001c0007t0002g0247 others(3): Show |
6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1729-2175dupT | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95472105 | |||||||
| chr9:95472105 | CAG | C | 49 | a0001c0002t0007g0191 a0001c0002t0009g0055 a0001c0002t0009g0056 others(46): Show |
52 | HG00558.hp2 HG00609.hp1 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.1729-2176_1729-217 others(6): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95472105 | |||||||
| chr9:95472281 | C | T | 51 | a0001c0002t0002g0184 a0001c0002t0002g0185 a0001c0002t0003g0026 others(48): Show |
56 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.1729-2350G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95472281 | |||||||
| chr9:95472310 | G | C | 3 | a0001c0002t0011g0186 a0001c0013t0025g0254 a0001c0013t0025g0255 |
3 | HG02818.hp1 HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1729-2379C>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95472310 | |||||||
| chr9:95472368 | GT | G | 53 | a0001c0002t0002g0184 a0001c0002t0002g0185 a0001c0002t0003g0026 others(50): Show |
59 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.1729-2438delA | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95472368 | |||||||
| chr9:95472503 | C | T | 2 | a0001c0003t0002g0197 a0001c0003t0002g0198 |
2 | HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1729-2572G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95472503 | |||||||
| chr9:95472621 | C | T | 51 | a0001c0002t0002g0184 a0001c0002t0002g0185 a0001c0002t0003g0026 others(48): Show |
56 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.1729-2690G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95472621 | |||||||
| chr9:95472663 | C | T | 1 | a0001c0003t0021g0166 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1729-2732G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95472663 | |||||||
| chr9:95472669 | C | A | 3 | a0001c0002t0011g0186 a0001c0013t0025g0254 a0001c0013t0025g0255 |
3 | HG02818.hp1 HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1729-2738G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95472669 | |||||||
| chr9:95472829 | C | T | 1 | a0001c0002t0007g0191 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1729-2898G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95472829 | |||||||
| chr9:95472966 | T | C | 4 | a0001c0002t0010g0169 a0005c0008t0010g0016 a0005c0008t0010g0167 others(1): Show |
5 | HG02145.hp1 HG02572.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1729-3035A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95472966 | |||||||
| chr9:95473028 | T | C | 51 | a0001c0002t0022g0215 a0001c0003t0001g0004 a0001c0003t0001g0032 others(48): Show |
53 | HG00423.hp2 HG00597.hp1 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.1728+3006A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95473028 | |||||||
| chr9:95473218 | T | A | 1 | a0001c0002t0023g0194 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1728+2816A>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95473218 | |||||||
| chr9:95473447 | G | A | 3 | a0003c0005t0003g0008 a0003c0005t0003g0081 a0003c0005t0003g0082 |
4 | HG02970.hp2 HG03195.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1728+2587C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95473447 | |||||||
| chr9:95473542 | A | AT | 14 | a0001c0002t0001g0124 a0001c0002t0001g0151 a0001c0002t0016g0021 others(11): Show |
15 | HG01106.hp1 HG01175.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.1728+2491dupA | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95473542 | |||||||
| chr9:95473542 | AT | A | 93 | a0001c0002t0001g0080 a0001c0002t0002g0184 a0001c0002t0002g0185 others(90): Show |
99 | HG00099.hp2 HG00140.hp2 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.1728+2491delA | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95473542 | |||||||
| chr9:95473542 | ATT | A | 8 | a0001c0004t0002g0224 a0001c0007t0002g0245 a0001c0007t0002g0246 others(5): Show |
8 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.1728+2490_1728+249 others(6): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95473542 | |||||||
| chr9:95473577 | T | C | 51 | a0001c0002t0022g0215 a0001c0003t0001g0004 a0001c0003t0001g0032 others(48): Show |
53 | HG00423.hp2 HG00597.hp1 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.1728+2457A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95473577 | |||||||
| chr9:95473596 | G | C | 3 | a0001c0002t0011g0186 a0001c0013t0025g0254 a0001c0013t0025g0255 |
3 | HG02818.hp1 HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1728+2438C>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95473596 | |||||||
| chr9:95473603 | A | G | 51 | a0001c0002t0022g0215 a0001c0003t0001g0004 a0001c0003t0001g0032 others(48): Show |
53 | HG00423.hp2 HG00597.hp1 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.1728+2431T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95473603 | |||||||
| chr9:95473637 | C | T | 2 | a0001c0002t0002g0184 a0001c0002t0002g0185 |
2 | HG01884.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1728+2397G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95473637 | |||||||
| chr9:95473821 | C | T | 2 | a0001c0003t0004g0092 a0001c0003t0037g0236 |
2 | HG04184.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.1728+2213G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95473821 | |||||||
| chr9:95473873 | G | C | 3 | a0003c0031t0003g0173 a0007c0012t0003g0024 a0007c0012t0003g0025 |
3 | NA18747.hp2 NA18970.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.1728+2161C>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95473873 | |||||||
| chr9:95473879 | T | C | 1 | a0001c0014t0003g0084 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1728+2155A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95473879 | |||||||
| chr9:95473920 | A | G | 40 | a0001c0002t0022g0215 a0001c0003t0001g0004 a0001c0003t0001g0032 others(37): Show |
42 | HG00597.hp1 HG00738.hp2 HG01074.hp2 others(39): Show |
intron_variant | MODIFIER | c.1728+2114T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95473920 | |||||||
| chr9:95474027 | C | T | 3 | a0001c0002t0008g0017 a0001c0002t0008g0181 a0001c0002t0008g0182 |
4 | HG02922.hp1 HG03098.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1728+2007G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95474027 | |||||||
| chr9:95474115 | A | G | 2 | a0001c0002t0016g0021 a0001c0002t0016g0244 |
3 | HG01243.hp1 HG03130.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1728+1919T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95474115 | |||||||
| chr9:95474204 | C | A | 1 | a0001c0004t0022g0240 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1728+1830G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95474204 | |||||||
| chr9:95474382 | C | T | 28 | a0001c0002t0022g0215 a0001c0003t0001g0004 a0001c0003t0001g0032 others(25): Show |
29 | HG00597.hp1 HG00738.hp2 HG01074.hp2 others(26): Show |
intron_variant | MODIFIER | c.1728+1652G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95474382 | |||||||
| chr9:95474583 | C | T | 44 | a0001c0003t0001g0004 a0001c0003t0001g0032 a0001c0003t0001g0044 others(41): Show |
46 | HG00597.hp1 HG00738.hp2 HG01099.hp1 others(43): Show |
intron_variant | MODIFIER | c.1728+1451G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95474583 | |||||||
| chr9:95474760 | A | G | 1 | a0001c0002t0012g0005 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1728+1274T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95474760 | |||||||
| chr9:95474818 | A | G | 1 | a0002c0001t0001g0011 | 2 | HG01099.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1728+1216T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95474818 | |||||||
| chr9:95474883 | G | A | 14 | a0001c0002t0007g0191 a0001c0002t0009g0055 a0001c0002t0009g0056 others(11): Show |
15 | HG01952.hp1 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.1728+1151C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95474883 | |||||||
| chr9:95475038 | T | C | 5 | a0001c0002t0008g0017 a0001c0002t0008g0179 a0001c0002t0008g0180 others(2): Show |
6 | HG01243.hp2 HG02922.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1728+996A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95475038 | |||||||
| chr9:95475169 | C | T | 1 | a0002c0001t0001g0121 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1728+865G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95475169 | |||||||
| chr9:95475171 | T | C | 2 | a0001c0003t0003g0067 a0001c0003t0004g0033 |
2 | NA20752.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1728+863A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95475171 | |||||||
| chr9:95475280 | C | T | 1 | a0002c0001t0004g0132 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1728+754G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95475280 | |||||||
| chr9:95475514 | A | G | 144 | a0001c0002t0002g0184 a0001c0002t0002g0185 a0001c0002t0003g0026 others(141): Show |
155 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(152): Show |
intron_variant | MODIFIER | c.1728+520T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95475514 | |||||||
| chr9:95475701 | A | G | 1 | a0002c0001t0006g0079 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1728+333T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95475701 | |||||||
| chr9:95475737 | T | G | 1 | a0001c0002t0012g0005 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1728+297A>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95475737 | |||||||
| chr9:95475770 | T | C | 2 | a0001c0002t0016g0021 a0001c0002t0016g0244 |
3 | HG01243.hp1 HG03130.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1728+264A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95475770 | |||||||
| chr9:95475995 | C | T | 1 | a0002c0001t0001g0146 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1728+39G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 12/23 | chr9 | 95475995 | |||||||
| chr9:95476217 | C | G | 1 | a0001c0030t0038g0195 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1603-58G>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 11/23 | chr9 | 95476217 | |||||||
| chr9:95476219 | G | C | 1 | a0001c0030t0038g0195 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1603-60C>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 11/23 | chr9 | 95476219 | |||||||
| chr9:95476328 | C | T | 1 | a0002c0001t0001g0158 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1603-169G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 11/23 | chr9 | 95476328 | |||||||
| chr9:95476566 | T | C | 1 | a0001c0002t0023g0194 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1602+193A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 11/23 | chr9 | 95476566 | |||||||
| chr9:95476578 | T | C | 27 | a0001c0022t0002g0252 a0003c0005t0001g0154 a0003c0005t0002g0019 others(24): Show |
29 | HG00558.hp2 HG00609.hp1 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.1602+181A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 11/23 | chr9 | 95476578 | |||||||
| chr9:95476631 | G | A | 1 | a0011c0033t0005g0138 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1602+128C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 11/23 | chr9 | 95476631 | |||||||
| chr9:95476684 | A | G | 1 | a0001c0002t0001g0141 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1602+75T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 11/23 | chr9 | 95476684 | |||||||
| chr9:95476865 | A | G | 49 | a0001c0002t0007g0191 a0001c0002t0009g0055 a0001c0002t0009g0056 others(46): Show |
52 | HG00558.hp2 HG00609.hp1 HG00673.hp2 others(49): Show |
splice_region_variant&intron_variant | LOW | c.1504-8T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 10/23 | chr9 | 95476865 | |||||||
| chr9:95476908 | G | C | 27 | a0001c0002t0001g0124 a0001c0002t0001g0125 a0001c0002t0001g0126 others(24): Show |
27 | HG00140.hp1 HG00408.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.1504-51C>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 10/23 | chr9 | 95476908 | |||||||
| chr9:95477144 | C | T | 1 | a0002c0011t0002g0213 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1504-287G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 10/23 | chr9 | 95477144 | |||||||
| chr9:95477151 | A | C | 1 | a0001c0003t0021g0166 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1504-294T>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 10/23 | chr9 | 95477151 | |||||||
| chr9:95477221 | G | A | 44 | a0001c0003t0001g0004 a0001c0003t0001g0032 a0001c0003t0001g0044 others(41): Show |
46 | HG00597.hp1 HG00738.hp2 HG01099.hp1 others(43): Show |
intron_variant | MODIFIER | c.1503+326C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 10/23 | chr9 | 95477221 | |||||||
| chr9:95477448 | G | A | 39 | a0001c0003t0001g0004 a0001c0003t0001g0032 a0001c0003t0001g0044 others(36): Show |
41 | HG00597.hp1 HG00738.hp2 HG01099.hp1 others(38): Show |
intron_variant | MODIFIER | c.1503+99C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 10/23 | chr9 | 95477448 | |||||||
| chr9:95477752 | T | G | 3 | a0001c0002t0011g0186 a0001c0013t0025g0254 a0001c0013t0025g0255 |
3 | HG02818.hp1 HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1348-50A>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 9/23 | chr9 | 95477752 | |||||||
| chr9:95477828 | T | C | 1 | a0002c0019t0006g0103 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1348-126A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 9/23 | chr9 | 95477828 | |||||||
| chr9:95477838 | G | A | 153 | a0001c0002t0002g0184 a0001c0002t0002g0185 a0001c0002t0003g0026 others(150): Show |
164 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.1348-136C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 9/23 | chr9 | 95477838 | |||||||
| chr9:95478387 | G | A | 3 | a0001c0003t0009g0052 a0001c0003t0009g0059 a0001c0003t0012g0006 |
4 | HG02109.hp2 HG02258.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1216-201C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 8/23 | chr9 | 95478387 | |||||||
| chr9:95478398 | G | T | 3 | a0003c0005t0002g0210 a0006c0016t0001g0090 a0006c0023t0011g0211 |
3 | HG00558.hp2 HG02129.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.1216-212C>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 8/23 | chr9 | 95478398 | |||||||
| chr9:95478431 | G | C | 1 | a0001c0007t0002g0247 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1216-245C>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 8/23 | chr9 | 95478431 | |||||||
| chr9:95478551 | T | A | 1 | a0001c0002t0001g0096 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1216-365A>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 8/23 | chr9 | 95478551 | |||||||
| chr9:95478654 | C | A | 1 | a0007c0012t0003g0024 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1215+346G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 8/23 | chr9 | 95478654 | |||||||
| chr9:95478788 | T | C | 1 | a0009c0025t0003g0174 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1215+212A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 8/23 | chr9 | 95478788 | |||||||
| chr9:95478857 | G | A | 6 | a0001c0007t0002g0245 a0001c0007t0002g0246 a0001c0007t0002g0247 others(3): Show |
6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1215+143C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 8/23 | chr9 | 95478857 | |||||||
| chr9:95478960 | T | C | 1 | a0001c0003t0021g0166 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1215+40A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 8/23 | chr9 | 95478960 | |||||||
| chr9:95478967 | C | T | 2 | a0002c0001t0001g0130 a0002c0001t0001g0131 |
2 | NA18946.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.1215+33G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 8/23 | chr9 | 95478967 | |||||||
| chr9:95479317 | T | C | 1 | a0001c0002t0002g0185 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1068-170A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 7/23 | chr9 | 95479317 | |||||||
| chr9:95479322 | G | A | 1 | a0001c0003t0021g0166 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1068-175C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 7/23 | chr9 | 95479322 | |||||||
| chr9:95479670 | G | A | 1 | a0009c0025t0003g0174 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1067+299C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 7/23 | chr9 | 95479670 | |||||||
| chr9:95479817 | A | G | 1 | a0001c0003t0021g0170 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1067+152T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 7/23 | chr9 | 95479817 | |||||||
| chr9:95479830 | A | G | 52 | a0001c0002t0002g0184 a0001c0002t0002g0185 a0001c0002t0003g0026 others(49): Show |
57 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.1067+139T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 7/23 | chr9 | 95479830 | |||||||
| chr9:95479895 | T | C | 14 | a0001c0002t0007g0191 a0001c0002t0009g0055 a0001c0002t0009g0056 others(11): Show |
15 | HG01952.hp1 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.1067+74A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 7/23 | chr9 | 95479895 | |||||||
| chr9:95480193 | T | G | 1 | a0001c0002t0007g0189 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.946-103A>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 6/23 | chr9 | 95480193 | |||||||
| chr9:95480265 | C | G | 1 | a0001c0002t0023g0238 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.945+125G>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 6/23 | chr9 | 95480265 | |||||||
| chr9:95480315 | A | G | 1 | a0016c0034t0003g0113 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.945+75T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 6/23 | chr9 | 95480315 | |||||||
| chr9:95480643 | A | G | 52 | a0001c0002t0002g0184 a0001c0002t0002g0185 a0001c0002t0003g0026 others(49): Show |
57 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.747-55T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 5/23 | chr9 | 95480643 | |||||||
| chr9:95480702 | G | A | 154 | a0001c0002t0002g0184 a0001c0002t0002g0185 a0001c0002t0003g0026 others(151): Show |
165 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.747-114C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 5/23 | chr9 | 95480702 | |||||||
| chr9:95480792 | C | T | 1 | a0003c0005t0007g0212 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.747-204G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 5/23 | chr9 | 95480792 | |||||||
| chr9:95480875 | A | G | 1 | a0001c0002t0007g0191 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.747-287T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 5/23 | chr9 | 95480875 | |||||||
| chr9:95480905 | A | C | 49 | a0001c0003t0001g0004 a0001c0003t0001g0032 a0001c0003t0001g0044 others(46): Show |
51 | HG00423.hp2 HG00597.hp1 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.747-317T>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 5/23 | chr9 | 95480905 | |||||||
| chr9:95480907 | A | AT | 51 | a0001c0002t0002g0184 a0001c0002t0002g0185 a0001c0002t0003g0026 others(48): Show |
57 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.747-320dupA | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 5/23 | chr9 | 95480907 | |||||||
| chr9:95480907 | AT | A | 69 | a0001c0002t0001g0075 a0001c0002t0001g0141 a0001c0002t0002g0237 others(66): Show |
83 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.747-320delA | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 5/23 | chr9 | 95480907 | |||||||
| chr9:95480921 | A | T | 1 | a0001c0002t0001g0072 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.747-333T>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 5/23 | chr9 | 95480921 | |||||||
| chr9:95481103 | A | G | 49 | a0001c0003t0001g0004 a0001c0003t0001g0032 a0001c0003t0001g0044 others(46): Show |
51 | HG00423.hp2 HG00597.hp1 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.747-515T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 5/23 | chr9 | 95481103 | |||||||
| chr9:95481143 | G | A | 1 | a0001c0003t0021g0166 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.747-555C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 5/23 | chr9 | 95481143 | |||||||
| chr9:95481259 | T | C | 1 | a0001c0003t0004g0034 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.747-671A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 5/23 | chr9 | 95481259 | |||||||
| chr9:95481465 | G | C | 3 | a0001c0004t0002g0226 a0001c0004t0002g0227 a0001c0004t0002g0234 |
3 | NA18991.hp2 NA19007.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.746+484C>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 5/23 | chr9 | 95481465 | |||||||
| chr9:95481586 | C | T | 27 | a0001c0003t0001g0004 a0001c0003t0001g0032 a0001c0003t0001g0044 others(24): Show |
28 | HG00597.hp1 HG00738.hp2 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.746+363G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 5/23 | chr9 | 95481586 | |||||||
| chr9:95481638 | G | A | 1 | a0001c0003t0009g0052 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.746+311C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 5/23 | chr9 | 95481638 | |||||||
| chr9:95482266 | G | A | 2 | a0001c0002t0009g0055 a0001c0002t0009g0056 |
2 | HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.585-63C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 3/23 | chr9 | 95482266 | |||||||
| chr9:95482301 | G | T | 1 | a0001c0002t0042g0256 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.585-98C>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 3/23 | chr9 | 95482301 | |||||||
| chr9:95482326 | C | T | 1 | a0002c0001t0001g0112 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.585-123G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 3/23 | chr9 | 95482326 | |||||||
| chr9:95482329 | G | A | 1 | a0002c0001t0029g0099 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.585-126C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 3/23 | chr9 | 95482329 | |||||||
| chr9:95482338 | T | C | 3 | a0001c0007t0002g0245 a0001c0007t0002g0246 a0001c0007t0002g0247 |
3 | HG00423.hp2 NA18965.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.585-135A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 3/23 | chr9 | 95482338 | |||||||
| chr9:95482537 | G | A | 2 | a0001c0002t0002g0184 a0001c0002t0002g0185 |
2 | HG01884.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.585-334C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 3/23 | chr9 | 95482537 | |||||||
| chr9:95482696 | C | T | 49 | a0001c0003t0001g0004 a0001c0003t0001g0032 a0001c0003t0001g0044 others(46): Show |
51 | HG00423.hp2 HG00597.hp1 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.585-493G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 3/23 | chr9 | 95482696 | |||||||
| chr9:95482726 | A | G | 1 | a0002c0001t0003g0111 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.585-523T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 3/23 | chr9 | 95482726 | |||||||
| chr9:95482744 | A | G | 27 | a0001c0003t0001g0004 a0001c0003t0001g0032 a0001c0003t0001g0044 others(24): Show |
28 | HG00597.hp1 HG00738.hp2 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.585-541T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 3/23 | chr9 | 95482744 | |||||||
| chr9:95483093 | A | G | 1 | a0001c0002t0016g0244 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.585-890T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 3/23 | chr9 | 95483093 | |||||||
| chr9:95483109 | G | GA | 49 | a0001c0003t0001g0004 a0001c0003t0001g0032 a0001c0003t0001g0044 others(46): Show |
51 | HG00423.hp2 HG00597.hp1 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.585-907dupT | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 3/23 | chr9 | 95483109 | |||||||
| chr9:95483264 | C | CA | 7 | a0001c0002t0007g0187 a0001c0002t0008g0017 a0001c0002t0008g0179 others(4): Show |
8 | HG01243.hp2 HG02922.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.585-1062dupT | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 3/23 | chr9 | 95483264 | |||||||
| chr9:95483264 | CAA | C | 43 | a0001c0003t0001g0004 a0001c0003t0001g0032 a0001c0003t0001g0044 others(40): Show |
45 | HG00597.hp1 HG00738.hp2 HG01099.hp1 others(42): Show |
intron_variant | MODIFIER | c.585-1063_585-1062d others(4): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 3/23 | chr9 | 95483264 | |||||||
| chr9:95483373 | A | G | 1 | a0001c0003t0004g0040 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.585-1170T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 3/23 | chr9 | 95483373 | |||||||
| chr9:95483410 | GA | G | 20 | a0001c0002t0009g0055 a0001c0002t0009g0056 a0001c0002t0009g0066 others(17): Show |
22 | HG00738.hp2 HG01243.hp1 HG01952.hp1 others(19): Show |
intron_variant | MODIFIER | c.585-1208delT | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 3/23 | chr9 | 95483410 | |||||||
| chr9:95483425 | A | AG | 6 | a0001c0007t0002g0245 a0001c0007t0002g0246 a0001c0007t0002g0247 others(3): Show |
6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.585-1223_585-1222i others(3): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 3/23 | chr9 | 95483425 | |||||||
| chr9:95483434 | A | G | 13 | a0001c0003t0005g0061 a0001c0003t0005g0063 a0001c0003t0005g0064 others(10): Show |
14 | HG02109.hp2 HG02145.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.585-1231T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 3/23 | chr9 | 95483434 | |||||||
| chr9:95483573 | T | C | 54 | a0001c0002t0002g0184 a0001c0002t0002g0185 a0001c0002t0003g0026 others(51): Show |
60 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.585-1370A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 3/23 | chr9 | 95483573 | |||||||
| chr9:95483607 | C | T | 1 | a0003c0005t0003g0082 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.585-1404G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 3/23 | chr9 | 95483607 | |||||||
| chr9:95483692 | A | G | 54 | a0001c0002t0002g0184 a0001c0002t0002g0185 a0001c0002t0003g0026 others(51): Show |
60 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.585-1489T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 3/23 | chr9 | 95483692 | |||||||
| chr9:95483697 | T | C | 1 | a0001c0002t0009g0066 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.585-1494A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 3/23 | chr9 | 95483697 | |||||||
| chr9:95483748 | C | T | 1 | a0001c0003t0004g0034 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.585-1545G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 3/23 | chr9 | 95483748 | |||||||
| chr9:95483772 | T | G | 23 | a0001c0022t0002g0252 a0003c0005t0001g0154 a0003c0005t0002g0019 others(20): Show |
25 | HG00558.hp2 HG00609.hp1 HG00673.hp2 others(22): Show |
intron_variant | MODIFIER | c.585-1569A>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 3/23 | chr9 | 95483772 | |||||||
| chr9:95483862 | T | C | 2 | a0002c0001t0019g0013 a0014c0039t0001g0178 |
3 | HG02071.hp1 NA18956.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.585-1659A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 3/23 | chr9 | 95483862 | |||||||
| chr9:95484110 | C | T | 2 | a0001c0002t0001g0139 a0013c0027t0001g0097 |
2 | HG02738.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.584+1575G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 3/23 | chr9 | 95484110 | |||||||
| chr9:95484121 | A | G | 1 | a0001c0003t0021g0170 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.584+1564T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 3/23 | chr9 | 95484121 | |||||||
| chr9:95484236 | T | C | 2 | a0001c0002t0020g0175 a0001c0003t0021g0166 |
2 | HG01109.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.584+1449A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 3/23 | chr9 | 95484236 | |||||||
| chr9:95484472 | C | A | 2 | a0001c0002t0001g0139 a0013c0027t0001g0097 |
2 | HG02738.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.584+1213G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 3/23 | chr9 | 95484472 | |||||||
| chr9:95484544 | C | T | 1 | a0001c0003t0005g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.584+1141G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 3/23 | chr9 | 95484544 | |||||||
| chr9:95484615 | G | C | 1 | a0004c0006t0005g0089 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.584+1070C>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 3/23 | chr9 | 95484615 | |||||||
| chr9:95484922 | C | T | 40 | a0001c0003t0001g0004 a0001c0003t0001g0032 a0001c0003t0001g0044 others(37): Show |
42 | HG00597.hp1 HG00738.hp2 HG01099.hp1 others(39): Show |
intron_variant | MODIFIER | c.584+763G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 3/23 | chr9 | 95484922 | |||||||
| chr9:95484943 | C | T | 3 | a0001c0002t0011g0186 a0001c0013t0025g0254 a0001c0013t0025g0255 |
3 | HG02818.hp1 HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.584+742G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 3/23 | chr9 | 95484943 | |||||||
| chr9:95485004 | G | A | 1 | a0002c0011t0002g0251 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.584+681C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 3/23 | chr9 | 95485004 | |||||||
| chr9:95485148 | G | C | 1 | a0002c0001t0001g0140 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.584+537C>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 3/23 | chr9 | 95485148 | |||||||
| chr9:95485261 | C | T | 2 | a0001c0002t0017g0022 a0001c0002t0017g0023 |
2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.584+424G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 3/23 | chr9 | 95485261 | |||||||
| chr9:95485508 | C | T | 40 | a0001c0003t0001g0004 a0001c0003t0001g0032 a0001c0003t0001g0044 others(37): Show |
42 | HG00597.hp1 HG00738.hp2 HG01099.hp1 others(39): Show |
intron_variant | MODIFIER | c.584+177G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 3/23 | chr9 | 95485508 | |||||||
| chr9:95486046 | A | G | 40 | a0001c0003t0001g0004 a0001c0003t0001g0032 a0001c0003t0001g0044 others(37): Show |
42 | HG00597.hp1 HG00738.hp2 HG01099.hp1 others(39): Show |
intron_variant | MODIFIER | c.395-172T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95486046 | |||||||
| chr9:95486105 | A | G | 49 | a0001c0003t0001g0004 a0001c0003t0001g0032 a0001c0003t0001g0044 others(46): Show |
51 | HG00423.hp2 HG00597.hp1 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.395-231T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95486105 | |||||||
| chr9:95486149 | G | GA | 43 | a0001c0003t0001g0004 a0001c0003t0001g0032 a0001c0003t0001g0044 others(40): Show |
45 | HG00597.hp1 HG00738.hp2 HG01099.hp1 others(42): Show |
intron_variant | MODIFIER | c.395-276_395-275ins others(1): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95486149 | |||||||
| chr9:95486353 | C | A | 153 | a0001c0002t0002g0184 a0001c0002t0002g0185 a0001c0002t0003g0026 others(150): Show |
164 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.395-479G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95486353 | |||||||
| chr9:95486514 | C | A | 1 | a0001c0003t0009g0052 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.395-640G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95486514 | |||||||
| chr9:95486570 | G | A | 1 | a0001c0004t0022g0240 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.395-696C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95486570 | |||||||
| chr9:95487173 | A | G | 1 | a0001c0003t0013g0028 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.395-1299T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95487173 | |||||||
| chr9:95487218 | G | A | 1 | a0002c0011t0002g0251 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.395-1344C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95487218 | |||||||
| chr9:95487267 | T | C | 1 | a0001c0002t0001g0141 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.395-1393A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95487267 | |||||||
| chr9:95487316 | T | C | 1 | a0002c0001t0001g0142 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.395-1442A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95487316 | |||||||
| chr9:95487377 | A | G | 1 | a0002c0017t0004g0043 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.395-1503T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95487377 | |||||||
| chr9:95487681 | C | T | 36 | a0001c0002t0022g0215 a0001c0002t0040g0216 a0001c0004t0001g0009 others(33): Show |
39 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.395-1807G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95487681 | |||||||
| chr9:95487824 | A | G | 1 | a0001c0003t0013g0058 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.395-1950T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95487824 | |||||||
| chr9:95487904 | T | C | 2 | a0001c0003t0002g0197 a0001c0003t0002g0198 |
2 | HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.395-2030A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95487904 | |||||||
| chr9:95487931 | A | C | 15 | a0001c0002t0007g0191 a0001c0002t0009g0055 a0001c0002t0009g0056 others(12): Show |
16 | HG01109.hp2 HG01952.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.395-2057T>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95487931 | |||||||
| chr9:95488105 | A | G | 2 | a0001c0002t0023g0194 a0001c0030t0038g0195 |
2 | HG01081.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.395-2231T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95488105 | |||||||
| chr9:95488293 | C | G | 2 | a0001c0002t0009g0055 a0001c0002t0009g0056 |
2 | HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.395-2419G>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95488293 | |||||||
| chr9:95488392 | T | C | 27 | a0001c0003t0001g0004 a0001c0003t0001g0032 a0001c0003t0001g0044 others(24): Show |
28 | HG00597.hp1 HG00738.hp2 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.395-2518A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95488392 | |||||||
| chr9:95488415 | A | G | 6 | a0001c0007t0002g0245 a0001c0007t0002g0246 a0001c0007t0002g0247 others(3): Show |
6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.395-2541T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95488415 | |||||||
| chr9:95488669 | A | G | 2 | a0001c0002t0023g0194 a0001c0030t0038g0195 |
2 | HG01081.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.395-2795T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95488669 | |||||||
| chr9:95488674 | A | G | 6 | a0001c0007t0002g0245 a0001c0007t0002g0246 a0001c0007t0002g0247 others(3): Show |
6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.395-2800T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95488674 | |||||||
| chr9:95488902 | A | G | 6 | a0001c0007t0002g0245 a0001c0007t0002g0246 a0001c0007t0002g0247 others(3): Show |
6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.395-3028T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95488902 | |||||||
| chr9:95489097 | A | G | 15 | a0001c0002t0007g0191 a0001c0002t0009g0055 a0001c0002t0009g0056 others(12): Show |
16 | HG01109.hp2 HG01952.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.395-3223T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95489097 | |||||||
| chr9:95489230 | T | C | 6 | a0001c0007t0002g0245 a0001c0007t0002g0246 a0001c0007t0002g0247 others(3): Show |
6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.395-3356A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95489230 | |||||||
| chr9:95489340 | GT | G | 3 | a0003c0031t0003g0173 a0007c0012t0003g0024 a0007c0012t0003g0025 |
3 | NA18747.hp2 NA18970.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.395-3467delA | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95489340 | |||||||
| chr9:95489357 | C | T | 1 | a0001c0030t0038g0195 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.395-3483G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95489357 | |||||||
| chr9:95489381 | C | T | 1 | a0001c0002t0002g0237 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.395-3507G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95489381 | |||||||
| chr9:95489426 | G | A | 2 | a0001c0003t0002g0197 a0001c0003t0002g0198 |
2 | HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.395-3552C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95489426 | |||||||
| chr9:95489539 | C | T | 3 | a0001c0002t0011g0186 a0001c0013t0025g0254 a0001c0013t0025g0255 |
3 | HG02818.hp1 HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.395-3665G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95489539 | |||||||
| chr9:95489602 | T | G | 1 | a0006c0023t0011g0211 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.395-3728A>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95489602 | |||||||
| chr9:95489692 | C | T | 2 | a0001c0003t0002g0197 a0001c0003t0002g0198 |
2 | HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.395-3818G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95489692 | |||||||
| chr9:95489796 | T | C | 1 | a0002c0001t0001g0077 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.395-3922A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95489796 | |||||||
| chr9:95489802 | A | AT | 22 | a0001c0002t0002g0184 a0001c0002t0002g0185 a0001c0002t0003g0026 others(19): Show |
24 | HG01069.hp1 HG01071.hp2 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.395-3929dupA | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95489802 | |||||||
| chr9:95489917 | A | C | 1 | a0001c0002t0001g0075 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.395-4043T>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95489917 | |||||||
| chr9:95489967 | A | AT | 6 | a0001c0007t0002g0245 a0001c0007t0002g0246 a0001c0007t0002g0247 others(3): Show |
6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.395-4094dupA | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95489967 | |||||||
| chr9:95490031 | T | C | 56 | a0001c0002t0002g0184 a0001c0002t0002g0185 a0001c0002t0003g0026 others(53): Show |
62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.395-4157A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95490031 | |||||||
| chr9:95490036 | T | C | 3 | a0001c0003t0009g0052 a0001c0003t0009g0059 a0001c0003t0012g0006 |
4 | HG02109.hp2 HG02258.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.395-4162A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95490036 | |||||||
| chr9:95490044 | C | T | 1 | a0001c0003t0021g0166 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.395-4170G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95490044 | |||||||
| chr9:95490270 | C | T | 1 | a0013c0027t0001g0097 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.395-4396G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95490270 | |||||||
| chr9:95490519 | T | TCACA | 10 | a0001c0002t0017g0022 a0001c0003t0021g0166 a0003c0005t0002g0199 others(7): Show |
11 | HG00609.hp1 HG02056.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.395-4646_395-4645i others(6): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95490519 | |||||||
| chr9:95490519 | T | TCACACA | 16 | a0001c0002t0023g0238 a0001c0030t0038g0195 a0003c0005t0001g0154 others(13): Show |
18 | HG00558.hp2 HG00673.hp2 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.395-4646_395-4645i others(8): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95490519 | |||||||
| chr9:95490519 | T | TCACACAC others(1): Show |
10 | a0001c0002t0007g0191 a0001c0002t0009g0055 a0001c0002t0009g0066 others(7): Show |
10 | HG02109.hp1 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.395-4646_395-4645i others(10): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95490519 | |||||||
| chr9:95490519 | T | TCACACAC others(3): Show |
4 | a0001c0002t0009g0056 a0001c0002t0011g0186 a0003c0005t0011g0209 others(1): Show |
4 | HG03098.hp1 NA18979.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.395-4646_395-4645i others(12): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95490519 | |||||||
| chr9:95490519 | T | TCACACAC others(5): Show |
4 | a0001c0002t0023g0194 a0003c0005t0005g0087 a0003c0005t0005g0091 others(1): Show |
4 | HG01081.hp1 HG01952.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.395-4646_395-4645i others(14): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95490519 | |||||||
| chr9:95490519 | T | TCACACAC others(7): Show |
1 | a0001c0013t0025g0255 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.395-4646_395-4645i others(16): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95490519 | |||||||
| chr9:95490520 | G | C | 48 | a0001c0002t0007g0191 a0001c0002t0009g0055 a0001c0002t0009g0056 others(45): Show |
51 | HG00558.hp2 HG00609.hp1 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.395-4646C>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95490520 | |||||||
| chr9:95490520 | G | GAC | 19 | a0001c0002t0001g0143 a0001c0002t0003g0094 a0001c0002t0003g0149 others(16): Show |
20 | HG02135.hp2 HG02559.hp1 HG02630.hp2 others(17): Show |
intron_variant | MODIFIER | c.395-4648_395-4647d others(4): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95490520 | |||||||
| chr9:95490520 | G | GACAC | 14 | a0001c0003t0002g0197 a0001c0003t0002g0198 a0001c0003t0003g0067 others(11): Show |
15 | HG00597.hp1 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.395-4650_395-4647d others(6): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95490520 | |||||||
| chr9:95490520 | G | GACACAC | 9 | a0001c0003t0004g0029 a0001c0003t0004g0030 a0001c0003t0004g0031 others(6): Show |
9 | HG01167.hp1 HG02027.hp1 HG03453.hp1 others(6): Show |
intron_variant | MODIFIER | c.395-4652_395-4647d others(8): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95490520 | |||||||
| chr9:95490520 | G | GACACACA others(1): Show |
5 | a0001c0003t0001g0044 a0001c0003t0004g0036 a0001c0003t0004g0045 others(2): Show |
5 | HG00738.hp2 HG01255.hp2 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.395-4654_395-4647d others(10): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95490520 | |||||||
| chr9:95490520 | G | GACACACA others(3): Show |
5 | a0001c0003t0004g0046 a0001c0003t0004g0047 a0001c0003t0004g0048 others(2): Show |
5 | HG01099.hp1 HG01192.hp2 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.395-4656_395-4647d others(12): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95490520 | |||||||
| chr9:95490520 | GAC | G | 47 | a0001c0002t0002g0184 a0001c0002t0002g0185 a0001c0002t0003g0026 others(44): Show |
52 | HG00140.hp2 HG00558.hp1 HG01069.hp1 others(49): Show |
intron_variant | MODIFIER | c.395-4648_395-4647d others(4): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95490520 | |||||||
| chr9:95490520 | GACAC | G | 4 | a0001c0002t0001g0072 a0001c0002t0016g0021 a0001c0004t0001g0088 others(1): Show |
5 | HG00099.hp2 HG01109.hp1 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.395-4650_395-4647d others(6): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95490520 | |||||||
| chr9:95490520 | GACACAC | G | 6 | a0001c0007t0002g0245 a0001c0007t0002g0246 a0001c0007t0002g0247 others(3): Show |
6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.395-4652_395-4647d others(8): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95490520 | |||||||
| chr9:95490520 | GACACACA others(5): Show |
G | 5 | a0001c0002t0001g0075 a0002c0001t0001g0076 a0002c0001t0001g0077 others(2): Show |
6 | HG01106.hp2 HG01516.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.395-4658_395-4647d others(14): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95490520 | |||||||
| chr9:95490529 | A | ACC | 10 | a0002c0001t0005g0100 a0002c0001t0006g0003 a0002c0001t0006g0079 others(7): Show |
12 | HG02257.hp2 HG02258.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.395-4656_395-4655i others(4): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95490529 | |||||||
| chr9:95490558 | A | C | 3 | a0001c0002t0032g0165 a0001c0022t0002g0252 a0012c0026t0039g0192 |
3 | HG02683.hp2 HG02723.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.395-4684T>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95490558 | |||||||
| chr9:95490565 | G | A | 154 | a0001c0002t0002g0184 a0001c0002t0002g0185 a0001c0002t0003g0026 others(151): Show |
165 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.395-4691C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95490565 | |||||||
| chr9:95490617 | C | CA | 7 | a0001c0002t0003g0014 a0001c0002t0003g0148 a0001c0002t0003g0149 others(4): Show |
8 | HG01358.hp1 HG01934.hp1 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.395-4744dupT | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95490617 | |||||||
| chr9:95490668 | A | G | 54 | a0001c0002t0007g0191 a0001c0002t0009g0055 a0001c0002t0009g0056 others(51): Show |
57 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.395-4794T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95490668 | |||||||
| chr9:95490759 | C | G | 10 | a0002c0001t0005g0100 a0002c0001t0006g0003 a0002c0001t0006g0079 others(7): Show |
12 | HG02257.hp2 HG02258.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.395-4885G>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95490759 | |||||||
| chr9:95490929 | C | T | 6 | a0001c0007t0002g0245 a0001c0007t0002g0246 a0001c0007t0002g0247 others(3): Show |
6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.395-5055G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95490929 | |||||||
| chr9:95490957 | C | T | 1 | a0001c0003t0004g0051 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.395-5083G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95490957 | |||||||
| chr9:95491121 | T | C | 5 | a0001c0002t0009g0055 a0001c0002t0009g0056 a0003c0005t0005g0087 others(2): Show |
5 | HG01952.hp1 HG02109.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.395-5247A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95491121 | |||||||
| chr9:95491194 | G | A | 44 | a0001c0003t0001g0004 a0001c0003t0001g0032 a0001c0003t0001g0044 others(41): Show |
46 | HG00597.hp1 HG00738.hp2 HG01099.hp1 others(43): Show |
intron_variant | MODIFIER | c.395-5320C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95491194 | |||||||
| chr9:95491208 | C | T | 14 | a0001c0002t0009g0055 a0001c0002t0009g0056 a0001c0002t0010g0169 others(11): Show |
15 | HG01109.hp2 HG01952.hp1 HG02056.hp1 others(12): Show |
intron_variant | MODIFIER | c.395-5334G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95491208 | |||||||
| chr9:95491243 | C | T | 1 | a0002c0001t0029g0099 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.395-5369G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95491243 | |||||||
| chr9:95491254 | G | A | 1 | a0003c0005t0007g0193 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.395-5380C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95491254 | |||||||
| chr9:95491380 | G | A | 1 | a0001c0002t0023g0194 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.395-5506C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95491380 | |||||||
| chr9:95491381 | G | A | 1 | a0001c0002t0012g0005 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.395-5507C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95491381 | |||||||
| chr9:95491469 | C | T | 1 | a0003c0005t0005g0087 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.395-5595G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95491469 | |||||||
| chr9:95491477 | C | T | 1 | a0002c0001t0006g0098 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.395-5603G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95491477 | |||||||
| chr9:95491554 | T | C | 1 | a0001c0003t0020g0171 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.395-5680A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95491554 | |||||||
| chr9:95491776 | C | T | 1 | a0015c0028t0002g0196 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.395-5902G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95491776 | |||||||
| chr9:95491903 | T | C | 1 | a0002c0001t0001g0150 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.395-6029A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95491903 | |||||||
| chr9:95491936 | T | C | 2 | a0001c0002t0001g0151 a0001c0002t0003g0015 |
3 | HG01071.hp1 HG01074.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.395-6062A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95491936 | |||||||
| chr9:95491947 | C | T | 1 | a0013c0027t0001g0097 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.395-6073G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95491947 | |||||||
| chr9:95492017 | A | T | 1 | a0001c0002t0009g0066 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.395-6143T>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95492017 | |||||||
| chr9:95492040 | G | A | 1 | a0002c0032t0001g0152 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.395-6166C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95492040 | |||||||
| chr9:95492096 | C | T | 2 | a0001c0003t0002g0197 a0001c0003t0002g0198 |
2 | HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.395-6222G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95492096 | |||||||
| chr9:95492190 | A | G | 2 | a0001c0002t0017g0022 a0001c0002t0017g0023 |
2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.395-6316T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95492190 | |||||||
| chr9:95492244 | C | A | 110 | a0001c0002t0002g0184 a0001c0002t0002g0185 a0001c0002t0003g0026 others(107): Show |
119 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.395-6370G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95492244 | |||||||
| chr9:95492328 | G | C | 6 | a0001c0007t0002g0245 a0001c0007t0002g0246 a0001c0007t0002g0247 others(3): Show |
6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.395-6454C>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95492328 | |||||||
| chr9:95492337 | T | C | 4 | a0001c0002t0010g0169 a0005c0008t0010g0016 a0005c0008t0010g0167 others(1): Show |
5 | HG02145.hp1 HG02572.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.395-6463A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95492337 | |||||||
| chr9:95492571 | A | G | 1 | a0009c0025t0003g0174 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.395-6697T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95492571 | |||||||
| chr9:95492713 | G | A | 1 | a0001c0002t0008g0017 | 2 | HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.395-6839C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95492713 | |||||||
| chr9:95492821 | A | AG | 154 | a0001c0002t0002g0184 a0001c0002t0002g0185 a0001c0002t0003g0026 others(151): Show |
165 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.395-6948_395-6947i others(3): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95492821 | |||||||
| chr9:95493156 | T | C | 32 | a0001c0002t0009g0066 a0001c0002t0017g0022 a0001c0002t0017g0023 others(29): Show |
34 | HG00558.hp2 HG00609.hp1 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.395-7282A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95493156 | |||||||
| chr9:95493244 | G | A | 1 | a0002c0001t0001g0155 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.395-7370C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95493244 | |||||||
| chr9:95493256 | A | C | 2 | a0001c0002t0023g0194 a0001c0030t0038g0195 |
2 | HG01081.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.395-7382T>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95493256 | |||||||
| chr9:95493337 | C | G | 1 | a0003c0005t0011g0200 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.395-7463G>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95493337 | |||||||
| chr9:95493545 | A | C | 1 | a0001c0002t0008g0179 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.395-7671T>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95493545 | |||||||
| chr9:95493746 | T | C | 1 | a0001c0002t0010g0169 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.395-7872A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95493746 | |||||||
| chr9:95493750 | C | T | 1 | a0001c0003t0013g0058 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.395-7876G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95493750 | |||||||
| chr9:95493801 | C | CA | 18 | a0001c0003t0002g0197 a0001c0003t0002g0198 a0001c0003t0005g0061 others(15): Show |
19 | HG01884.hp2 HG02109.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.395-7928dupT | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95493801 | |||||||
| chr9:95493801 | C | CAA | 25 | a0001c0003t0001g0004 a0001c0003t0001g0032 a0001c0003t0001g0044 others(22): Show |
26 | HG00597.hp1 HG00738.hp2 HG01099.hp1 others(23): Show |
intron_variant | MODIFIER | c.395-7929_395-7928d others(4): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95493801 | |||||||
| chr9:95493899 | G | A | 2 | a0001c0014t0003g0084 a0001c0014t0033g0085 |
2 | HG01081.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.395-8025C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95493899 | |||||||
| chr9:95493953 | T | G | 2 | a0001c0002t0003g0156 a0002c0001t0003g0095 |
2 | HG01516.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.395-8079A>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95493953 | |||||||
| chr9:95494027 | G | A | 43 | a0001c0003t0001g0004 a0001c0003t0001g0032 a0001c0003t0001g0044 others(40): Show |
45 | HG00597.hp1 HG00738.hp2 HG01099.hp1 others(42): Show |
intron_variant | MODIFIER | c.395-8153C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95494027 | |||||||
| chr9:95494046 | C | T | 3 | a0003c0005t0003g0008 a0003c0005t0003g0081 a0003c0005t0003g0082 |
4 | HG02970.hp2 HG03195.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.395-8172G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95494046 | |||||||
| chr9:95494076 | A | AACCGCAC others(3): Show |
1 | a0001c0003t0013g0028 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.395-8212_395-8203d others(12): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95494076 | |||||||
| chr9:95494076 | AACCGCAC others(3): Show |
A | 5 | a0001c0002t0011g0186 a0001c0002t0042g0256 a0001c0003t0021g0166 others(2): Show |
5 | HG02647.hp2 HG02818.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.395-8212_395-8203d others(12): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95494076 | |||||||
| chr9:95494131 | C | T | 1 | a0001c0002t0017g0022 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.395-8257G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95494131 | |||||||
| chr9:95494139 | C | T | 1 | a0002c0011t0002g0213 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.395-8265G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95494139 | |||||||
| chr9:95494158 | T | A | 19 | a0001c0002t0002g0184 a0001c0002t0002g0185 a0001c0002t0003g0026 others(16): Show |
22 | HG01069.hp1 HG01071.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.395-8284A>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95494158 | |||||||
| chr9:95494164 | G | A | 3 | a0001c0003t0002g0197 a0001c0003t0002g0198 a0003c0005t0007g0193 |
3 | HG01884.hp2 HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.395-8290C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95494164 | |||||||
| chr9:95494333 | C | T | 4 | a0001c0002t0010g0169 a0005c0008t0010g0016 a0005c0008t0010g0167 others(1): Show |
5 | HG02145.hp1 HG02572.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.395-8459G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95494333 | |||||||
| chr9:95494438 | C | G | 15 | a0001c0002t0002g0184 a0001c0002t0002g0185 a0001c0002t0003g0026 others(12): Show |
17 | HG01069.hp1 HG01071.hp2 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.395-8564G>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95494438 | |||||||
| chr9:95494769 | T | C | 1 | a0001c0002t0001g0164 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.395-8895A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95494769 | |||||||
| chr9:95494827 | C | T | 1 | a0003c0005t0003g0081 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.395-8953G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95494827 | |||||||
| chr9:95494886 | T | C | 1 | a0002c0001t0001g0157 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.395-9012A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95494886 | |||||||
| chr9:95495012 | C | T | 1 | a0001c0030t0038g0195 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.395-9138G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95495012 | |||||||
| chr9:95495023 | C | T | 34 | a0001c0002t0022g0215 a0001c0002t0040g0216 a0001c0004t0001g0009 others(31): Show |
37 | HG00140.hp2 HG00609.hp2 HG01074.hp2 others(34): Show |
intron_variant | MODIFIER | c.395-9149G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95495023 | |||||||
| chr9:95495054 | G | A | 1 | a0003c0005t0007g0193 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.395-9180C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95495054 | |||||||
| chr9:95495214 | C | T | 1 | a0001c0002t0001g0096 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.395-9340G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95495214 | |||||||
| chr9:95495237 | A | C | 2 | a0001c0003t0003g0067 a0001c0003t0004g0033 |
2 | NA20752.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.395-9363T>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95495237 | |||||||
| chr9:95495427 | C | CT | 17 | a0001c0002t0003g0094 a0001c0002t0009g0055 a0001c0002t0009g0056 others(14): Show |
17 | HG01952.hp2 HG02109.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.395-9554dupA | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95495427 | |||||||
| chr9:95495441 | A | T | 4 | a0001c0002t0017g0022 a0001c0002t0017g0023 a0001c0002t0032g0165 others(1): Show |
4 | HG02723.hp2 HG02818.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.395-9567T>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95495441 | |||||||
| chr9:95495502 | G | A | 1 | a0002c0001t0001g0158 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.395-9628C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95495502 | |||||||
| chr9:95495560 | C | T | 154 | a0001c0002t0002g0184 a0001c0002t0002g0185 a0001c0002t0003g0026 others(151): Show |
165 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.395-9686G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95495560 | |||||||
| chr9:95495646 | A | G | 2 | a0001c0002t0016g0021 a0001c0002t0016g0244 |
3 | HG01243.hp1 HG03130.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.395-9772T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95495646 | |||||||
| chr9:95495753 | T | TG | 8 | a0001c0003t0005g0061 a0001c0003t0005g0063 a0001c0003t0005g0064 others(5): Show |
8 | HG02145.hp2 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.395-9880dupC | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95495753 | |||||||
| chr9:95496084 | T | C | 1 | a0001c0003t0005g0064 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.395-10210A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95496084 | |||||||
| chr9:95496128 | C | A | 1 | a0001c0003t0004g0050 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.395-10254G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95496128 | |||||||
| chr9:95496199 | C | G | 1 | a0003c0005t0002g0210 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.394+10208G>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95496199 | |||||||
| chr9:95496537 | T | TA | 21 | a0001c0002t0023g0238 a0001c0022t0002g0252 a0002c0001t0041g0253 others(18): Show |
23 | HG00673.hp2 HG02015.hp1 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.394+9869dupT | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95496537 | |||||||
| chr9:95496979 | G | A | 2 | a0001c0002t0023g0194 a0001c0030t0038g0195 |
2 | HG01081.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.394+9428C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95496979 | |||||||
| chr9:95497421 | T | G | 133 | a0001c0002t0002g0184 a0001c0002t0002g0185 a0001c0002t0002g0237 others(130): Show |
141 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.394+8986A>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95497421 | |||||||
| chr9:95497489 | CT | C | 133 | a0001c0002t0002g0184 a0001c0002t0002g0185 a0001c0002t0002g0237 others(130): Show |
141 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.394+8917delA | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95497489 | |||||||
| chr9:95497951 | C | T | 1 | a0001c0002t0001g0072 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.394+8456G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95497951 | |||||||
| chr9:95497967 | G | A | 8 | a0001c0002t0010g0169 a0001c0003t0020g0171 a0001c0003t0021g0166 others(5): Show |
9 | HG01884.hp2 HG02145.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.394+8440C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95497967 | |||||||
| chr9:95498232 | G | A | 133 | a0001c0002t0002g0184 a0001c0002t0002g0185 a0001c0002t0002g0237 others(130): Show |
141 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.394+8175C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95498232 | |||||||
| chr9:95498273 | T | C | 8 | a0001c0002t0016g0021 a0001c0002t0016g0244 a0001c0002t0020g0175 others(5): Show |
9 | HG01109.hp2 HG01243.hp1 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.394+8134A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95498273 | |||||||
| chr9:95498656 | T | C | 2 | a0001c0013t0025g0254 a0001c0013t0025g0255 |
2 | HG02818.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.394+7751A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95498656 | |||||||
| chr9:95498729 | G | T | 2 | a0001c0013t0025g0254 a0001c0013t0025g0255 |
2 | HG02818.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.394+7678C>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95498729 | |||||||
| chr9:95498750 | C | A | 17 | a0001c0002t0002g0184 a0001c0002t0002g0185 a0001c0002t0003g0026 others(14): Show |
18 | HG01243.hp2 HG01884.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.394+7657G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95498750 | |||||||
| chr9:95499108 | C | T | 1 | a0001c0004t0002g0241 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.394+7299G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95499108 | |||||||
| chr9:95499519 | G | C | 4 | a0001c0002t0010g0169 a0005c0008t0010g0016 a0005c0008t0010g0167 others(1): Show |
5 | HG02145.hp1 HG02572.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.394+6888C>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95499519 | |||||||
| chr9:95499783 | C | G | 1 | a0001c0002t0007g0187 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.394+6624G>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95499783 | |||||||
| chr9:95499896 | G | A | 43 | a0001c0002t0003g0060 a0001c0002t0009g0055 a0001c0002t0009g0056 others(40): Show |
46 | HG00597.hp1 HG00738.hp2 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.394+6511C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95499896 | |||||||
| chr9:95499908 | C | G | 6 | a0001c0002t0003g0083 a0001c0014t0003g0084 a0001c0014t0033g0085 others(3): Show |
7 | HG01081.hp2 HG02970.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.394+6499G>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95499908 | |||||||
| chr9:95499941 | G | A | 46 | a0001c0002t0003g0060 a0001c0002t0009g0055 a0001c0002t0009g0056 others(43): Show |
49 | HG00597.hp1 HG00738.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.394+6466C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95499941 | |||||||
| chr9:95500002 | C | A | 2 | a0001c0002t0032g0165 a0012c0026t0039g0192 |
2 | HG02723.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.394+6405G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95500002 | |||||||
| chr9:95500035 | G | A | 1 | a0001c0002t0003g0159 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.394+6372C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95500035 | |||||||
| chr9:95500116 | G | A | 1 | a0001c0002t0008g0182 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.394+6291C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95500116 | |||||||
| chr9:95500213 | A | G | 1 | a0002c0001t0003g0074 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.394+6194T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95500213 | |||||||
| chr9:95500350 | T | C | 3 | a0001c0007t0014g0248 a0001c0038t0014g0250 a0010c0018t0014g0249 |
3 | HG02015.hp2 HG02071.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.394+6057A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95500350 | |||||||
| chr9:95500353 | C | T | 1 | a0001c0004t0002g0242 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.394+6054G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95500353 | |||||||
| chr9:95500453 | A | G | 62 | a0001c0002t0002g0237 a0001c0002t0003g0163 a0001c0002t0016g0021 others(59): Show |
66 | HG00140.hp2 HG00408.hp2 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.394+5954T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95500453 | |||||||
| chr9:95500551 | A | G | 134 | a0001c0002t0002g0184 a0001c0002t0002g0185 a0001c0002t0002g0237 others(131): Show |
142 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.394+5856T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95500551 | |||||||
| chr9:95500575 | C | T | 1 | a0001c0002t0001g0080 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.394+5832G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95500575 | |||||||
| chr9:95500654 | G | A | 1 | a0001c0004t0022g0240 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.394+5753C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95500654 | |||||||
| chr9:95500747 | C | T | 16 | a0001c0002t0002g0184 a0001c0002t0002g0185 a0001c0002t0003g0026 others(13): Show |
17 | HG01243.hp2 HG01884.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.394+5660G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95500747 | |||||||
| chr9:95500838 | T | C | 2 | a0001c0003t0020g0171 a0001c0003t0021g0170 |
2 | HG02451.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.394+5569A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95500838 | |||||||
| chr9:95500856 | A | C | 17 | a0001c0002t0002g0184 a0001c0002t0002g0185 a0001c0002t0003g0026 others(14): Show |
18 | HG01243.hp2 HG01884.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.394+5551T>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95500856 | |||||||
| chr9:95500950 | C | T | 2 | a0001c0002t0017g0022 a0001c0002t0017g0023 |
2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.394+5457G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95500950 | |||||||
| chr9:95500961 | G | A | 1 | a0001c0002t0005g0068 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.394+5446C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95500961 | |||||||
| chr9:95501063 | T | C | 1 | a0001c0002t0007g0191 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.394+5344A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95501063 | |||||||
| chr9:95501174 | C | A | 17 | a0001c0022t0002g0252 a0003c0005t0002g0019 a0003c0005t0002g0199 others(14): Show |
19 | HG00673.hp2 HG02015.hp1 HG02056.hp2 others(16): Show |
intron_variant | MODIFIER | c.394+5233G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95501174 | |||||||
| chr9:95501375 | G | C | 2 | a0001c0002t0003g0160 a0001c0003t0003g0067 |
2 | HG02683.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.394+5032C>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95501375 | |||||||
| chr9:95501539 | T | TA | 100 | a0001c0002t0002g0237 a0001c0002t0003g0060 a0001c0002t0003g0163 others(97): Show |
107 | HG00140.hp2 HG00408.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.394+4867dupT | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95501539 | |||||||
| chr9:95501539 | TAAA | T | 18 | a0001c0002t0002g0184 a0001c0002t0002g0185 a0001c0002t0003g0026 others(15): Show |
19 | HG01243.hp2 HG01884.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.394+4865_394+4867d others(5): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95501539 | |||||||
| chr9:95501588 | G | A | 16 | a0001c0002t0002g0184 a0001c0002t0002g0185 a0001c0002t0003g0026 others(13): Show |
17 | HG01243.hp2 HG01884.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.394+4819C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95501588 | |||||||
| chr9:95501985 | A | G | 1 | a0003c0005t0002g0199 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.394+4422T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95501985 | |||||||
| chr9:95502055 | G | C | 3 | a0001c0003t0005g0063 a0001c0003t0005g0064 a0001c0003t0005g0065 |
3 | HG03195.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.394+4352C>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95502055 | |||||||
| chr9:95502090 | A | G | 8 | a0001c0002t0016g0021 a0001c0002t0016g0244 a0001c0002t0020g0175 others(5): Show |
9 | HG01109.hp2 HG01243.hp1 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.394+4317T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95502090 | |||||||
| chr9:95502236 | G | A | 2 | a0003c0005t0002g0210 a0006c0023t0011g0211 |
2 | HG02129.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.394+4171C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95502236 | |||||||
| chr9:95502466 | C | A | 1 | a0002c0001t0018g0007 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.394+3941G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95502466 | |||||||
| chr9:95502660 | A | C | 46 | a0001c0002t0003g0060 a0001c0002t0009g0055 a0001c0002t0009g0056 others(43): Show |
49 | HG00597.hp1 HG00738.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.394+3747T>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95502660 | |||||||
| chr9:95502666 | A | C | 17 | a0001c0022t0002g0252 a0003c0005t0002g0019 a0003c0005t0002g0199 others(14): Show |
19 | HG00673.hp2 HG02015.hp1 HG02056.hp2 others(16): Show |
intron_variant | MODIFIER | c.394+3741T>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95502666 | |||||||
| chr9:95502722 | C | A | 17 | a0001c0002t0002g0184 a0001c0002t0002g0185 a0001c0002t0003g0026 others(14): Show |
18 | HG01243.hp2 HG01884.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.394+3685G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95502722 | |||||||
| chr9:95502869 | G | A | 1 | a0001c0004t0002g0241 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.394+3538C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95502869 | |||||||
| chr9:95502894 | C | T | 1 | a0002c0001t0006g0079 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.394+3513G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95502894 | |||||||
| chr9:95502907 | G | A | 2 | a0001c0003t0013g0053 a0001c0003t0013g0054 |
2 | HG02630.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.394+3500C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95502907 | |||||||
| chr9:95502936 | C | T | 6 | a0001c0002t0008g0017 a0001c0002t0008g0179 a0001c0002t0008g0180 others(3): Show |
7 | HG01243.hp2 HG02922.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.394+3471G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95502936 | |||||||
| chr9:95503243 | G | A | 1 | a0001c0004t0002g0242 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.394+3164C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95503243 | |||||||
| chr9:95503380 | C | A | 3 | a0001c0002t0042g0256 a0001c0013t0025g0254 a0001c0013t0025g0255 |
3 | HG02818.hp1 HG03041.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.394+3027G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95503380 | |||||||
| chr9:95503405 | G | A | 1 | a0001c0002t0009g0066 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.394+3002C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95503405 | |||||||
| chr9:95503498 | C | T | 134 | a0001c0002t0002g0184 a0001c0002t0002g0185 a0001c0002t0002g0237 others(131): Show |
142 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.394+2909G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95503498 | |||||||
| chr9:95503551 | G | T | 1 | a0001c0003t0004g0051 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.394+2856C>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95503551 | |||||||
| chr9:95503619 | A | G | 46 | a0001c0002t0003g0060 a0001c0002t0009g0055 a0001c0002t0009g0056 others(43): Show |
49 | HG00597.hp1 HG00738.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.394+2788T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95503619 | |||||||
| chr9:95503732 | TAGGGCCG others(322): Show |
T | 142 | a0001c0002t0002g0184 a0001c0002t0002g0185 a0001c0002t0002g0237 others(139): Show |
151 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(148): Show |
intron_variant | MODIFIER | c.394+2346_394+2674d others(2): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95503732 | |||||||
| chr9:95504022 | C | CA | 6 | a0001c0002t0001g0139 a0001c0014t0003g0084 a0002c0001t0001g0011 others(3): Show |
7 | HG00408.hp1 HG01099.hp2 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.394+2384dupT | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95504022 | |||||||
| chr9:95504022 | C | CAAAAAAA others(6): Show |
1 | a0002c0035t0001g0106 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.394+2372_394+2384d others(15): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95504022 | |||||||
| chr9:95504022 | CA | C | 33 | a0001c0002t0001g0096 a0001c0002t0001g0151 a0001c0002t0003g0015 others(30): Show |
33 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.394+2384delT | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95504022 | |||||||
| chr9:95504022 | CAA | C | 32 | a0001c0002t0001g0010 a0001c0002t0001g0072 a0001c0002t0001g0116 others(29): Show |
35 | HG00099.hp1 HG01106.hp1 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.394+2383_394+2384d others(4): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95504022 | |||||||
| chr9:95504022 | CAAA | C | 17 | a0001c0002t0001g0125 a0001c0002t0001g0126 a0002c0001t0001g0001 others(14): Show |
17 | HG01069.hp2 HG01175.hp2 HG02004.hp1 others(14): Show |
intron_variant | MODIFIER | c.394+2382_394+2384d others(5): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95504022 | |||||||
| chr9:95504022 | CAAAAAAA others(4): Show |
C | 1 | a0002c0001t0004g0132 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.394+2374_394+2384d others(13): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95504022 | |||||||
| chr9:95504022 | CAAAAAAA others(9): Show |
C | 2 | a0001c0002t0001g0143 a0001c0004t0001g0009 |
2 | HG03492.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.394+2369_394+2384d others(18): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95504022 | |||||||
| chr9:95504022 | CAAAAAAA others(10): Show |
C | 1 | a0003c0005t0003g0081 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.394+2368_394+2384d others(19): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95504022 | |||||||
| chr9:95504022 | CAAAAAAA others(11): Show |
C | 3 | a0001c0002t0017g0023 a0001c0004t0001g0009 a0001c0004t0001g0088 |
3 | HG00099.hp2 HG03471.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.394+2367_394+2384d others(20): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95504022 | |||||||
| chr9:95504022 | CAAAAAAA others(12): Show |
C | 2 | a0001c0002t0017g0022 a0002c0001t0019g0013 |
2 | HG02071.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.394+2366_394+2384d others(21): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95504022 | |||||||
| chr9:95504022 | CAAAAAAA others(14): Show |
C | 1 | a0003c0005t0005g0091 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.394+2364_394+2384d others(23): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95504022 | |||||||
| chr9:95504056 | A | C | 2 | a0001c0002t0017g0022 a0001c0002t0017g0023 |
2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.394+2351T>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95504056 | |||||||
| chr9:95504061 | A | T | 2 | a0001c0002t0017g0022 a0001c0002t0017g0023 |
2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.394+2346T>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95504061 | |||||||
| chr9:95504088 | A | G | 134 | a0001c0002t0002g0184 a0001c0002t0002g0185 a0001c0002t0002g0237 others(131): Show |
142 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.394+2319T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95504088 | |||||||
| chr9:95504380 | G | A | 6 | a0001c0007t0002g0245 a0001c0007t0002g0246 a0001c0007t0002g0247 others(3): Show |
6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.394+2027C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95504380 | |||||||
| chr9:95504573 | T | A | 47 | a0001c0002t0003g0060 a0001c0002t0009g0055 a0001c0002t0009g0056 others(44): Show |
50 | HG00597.hp1 HG00738.hp2 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.394+1834A>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95504573 | |||||||
| chr9:95505066 | G | A | 1 | a0010c0018t0014g0249 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.394+1341C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95505066 | |||||||
| chr9:95505141 | G | A | 24 | a0001c0002t0002g0184 a0001c0002t0002g0185 a0001c0002t0003g0026 others(21): Show |
26 | HG01243.hp2 HG01884.hp1 HG02145.hp1 others(23): Show |
intron_variant | MODIFIER | c.394+1266C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95505141 | |||||||
| chr9:95505266 | C | T | 2 | a0001c0003t0013g0053 a0001c0003t0013g0054 |
2 | HG02630.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.394+1141G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95505266 | |||||||
| chr9:95505300 | G | A | 1 | a0001c0030t0038g0195 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.394+1107C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95505300 | |||||||
| chr9:95505359 | G | A | 1 | a0002c0001t0001g0162 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.394+1048C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95505359 | |||||||
| chr9:95505361 | A | T | 5 | a0001c0002t0001g0075 a0002c0001t0001g0076 a0002c0001t0001g0077 others(2): Show |
6 | HG01106.hp2 HG01516.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.394+1046T>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95505361 | |||||||
| chr9:95505464 | T | G | 142 | a0001c0002t0002g0184 a0001c0002t0002g0185 a0001c0002t0002g0237 others(139): Show |
151 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(148): Show |
intron_variant | MODIFIER | c.394+943A>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95505464 | |||||||
| chr9:95505488 | G | A | 1 | a0001c0002t0008g0183 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.394+919C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95505488 | |||||||
| chr9:95505833 | T | C | 1 | a0001c0003t0004g0051 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.394+574A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95505833 | |||||||
| chr9:95505881 | G | T | 6 | a0001c0002t0008g0017 a0001c0002t0008g0179 a0001c0002t0008g0180 others(3): Show |
7 | HG01243.hp2 HG02922.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.394+526C>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95505881 | |||||||
| chr9:95505918 | C | A | 1 | a0001c0004t0002g0243 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.394+489G>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95505918 | |||||||
| chr9:95505983 | C | T | 1 | a0002c0020t0001g0073 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.394+424G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95505983 | |||||||
| chr9:95506114 | G | A | 6 | a0001c0007t0002g0245 a0001c0007t0002g0246 a0001c0007t0002g0247 others(3): Show |
6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.394+293C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95506114 | |||||||
| chr9:95506192 | C | G | 1 | a0001c0003t0009g0052 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.394+215G>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95506192 | |||||||
| chr9:95506195 | G | T | 6 | a0001c0007t0002g0245 a0001c0007t0002g0246 a0001c0007t0002g0247 others(3): Show |
6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.394+212C>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95506195 | |||||||
| chr9:95506336 | T | C | 2 | a0001c0002t0016g0021 a0001c0002t0016g0244 |
3 | HG01243.hp1 HG03130.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.394+71A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 2/23 | chr9 | 95506336 | |||||||
| chr9:95506656 | A | ACGCCCGC others(11): Show |
24 | a0001c0003t0001g0004 a0001c0003t0001g0032 a0001c0003t0001g0044 others(21): Show |
25 | HG00597.hp1 HG00738.hp2 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.202-75_202-58dupGG others(16): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 1/23 | chr9 | 95506656 | |||||||
| chr9:95506816 | G | A | 6 | a0001c0007t0002g0245 a0001c0007t0002g0246 a0001c0007t0002g0247 others(3): Show |
6 | HG00423.hp2 HG02015.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.202-217C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 1/23 | chr9 | 95506816 | |||||||
| chr9:95507136 | CG | C | 86 | a0001c0002t0002g0184 a0001c0002t0002g0185 a0001c0002t0002g0237 others(83): Show |
91 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.202-538delC | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 1/23 | chr9 | 95507136 | |||||||
| chr9:95507156 | C | T | 1 | a0001c0002t0001g0072 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.202-557G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 1/23 | chr9 | 95507156 | |||||||
| chr9:95507208 | G | C | 1 | a0001c0002t0001g0164 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.202-609C>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 1/23 | chr9 | 95507208 | |||||||
| chr9:95507381 | G | A | 3 | a0001c0002t0007g0189 a0001c0002t0035g0190 a0001c0024t0007g0188 |
3 | HG02451.hp1 HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.201+780C>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 1/23 | chr9 | 95507381 | |||||||
| chr9:95507433 | T | A | 1 | a0002c0011t0002g0251 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.201+728A>T | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 1/23 | chr9 | 95507433 | |||||||
| chr9:95507655 | A | C | 1 | a0001c0003t0004g0029 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.201+506T>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 1/23 | chr9 | 95507655 | |||||||
| chr9:95507757 | T | C | 4 | a0001c0002t0007g0187 a0001c0002t0007g0189 a0001c0002t0035g0190 others(1): Show |
4 | HG02451.hp1 HG02622.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.201+404A>G | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 1/23 | chr9 | 95507757 | |||||||
| chr9:95507764 | C | T | 4 | a0001c0002t0005g0068 a0002c0001t0001g0069 a0002c0001t0001g0070 others(1): Show |
4 | HG02559.hp2 HG02965.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.201+397G>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 1/23 | chr9 | 95507764 | |||||||
| chr9:95507792 | A | T | 1 | a0001c0003t0003g0067 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.201+369T>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 1/23 | chr9 | 95507792 | |||||||
| chr9:95507886 | A | G | 133 | a0001c0002t0002g0184 a0001c0002t0002g0185 a0001c0002t0002g0237 others(130): Show |
141 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.201+275T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 1/23 | chr9 | 95507886 | |||||||
| chr9:95507889 | A | G | 143 | a0001c0002t0002g0184 a0001c0002t0002g0185 a0001c0002t0002g0237 others(140): Show |
152 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(149): Show |
intron_variant | MODIFIER | c.201+272T>C | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 1/23 | chr9 | 95507889 | |||||||
| chr9:95507905 | T | TAC | 13 | a0001c0002t0010g0169 a0001c0002t0017g0022 a0001c0002t0017g0023 others(10): Show |
14 | HG01081.hp1 HG01884.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.201+254_201+255dup others(2): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 1/23 | chr9 | 95507905 | |||||||
| chr9:95507905 | T | TACAC | 126 | a0001c0002t0002g0184 a0001c0002t0002g0185 a0001c0002t0002g0237 others(123): Show |
134 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.201+252_201+255dup others(4): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 1/23 | chr9 | 95507905 | |||||||
| chr9:95507905 | T | TACACAC | 3 | a0001c0002t0009g0066 a0001c0003t0005g0065 a0001c0022t0002g0252 |
3 | HG02257.hp1 HG02683.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.201+250_201+255dup others(6): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 1/23 | chr9 | 95507905 | |||||||
| chr9:95508034 | TGTGA | T | 50 | a0001c0002t0003g0060 a0001c0002t0007g0191 a0001c0002t0009g0055 others(47): Show |
53 | HG00597.hp1 HG00738.hp2 HG01069.hp1 others(50): Show |
intron_variant | MODIFIER | c.201+123_201+126del others(4): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 1/23 | chr9 | 95508034 | |||||||
| chr9:95508038 | AGTGAGTG others(1): Show |
A | 63 | a0001c0002t0002g0237 a0001c0002t0016g0021 a0001c0002t0016g0244 others(60): Show |
67 | HG00140.hp2 HG00408.hp2 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.201+115_201+122del others(8): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 1/23 | chr9 | 95508038 | |||||||
| chr9:95508040 | TGA | T | 14 | a0001c0002t0002g0184 a0001c0002t0002g0185 a0001c0002t0003g0026 others(11): Show |
15 | HG01243.hp2 HG01884.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.201+119_201+120del others(2): Show |
PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 1/23 | chr9 | 95508040 | |||||||
| chr9:95508042 | A | T | 7 | a0001c0002t0003g0148 a0001c0007t0002g0245 a0001c0007t0002g0246 others(4): Show |
7 | HG00423.hp2 HG01358.hp1 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.201+119T>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 1/23 | chr9 | 95508042 | |||||||
| chr9:95508060 | A | T | 17 | a0001c0002t0002g0184 a0001c0002t0002g0185 a0001c0002t0003g0026 others(14): Show |
18 | HG01243.hp2 HG01884.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.201+101T>A | PTCH1 | ENSG00000185920.19 | transcript | ENST00000331920.11 | protein_coding | 1/23 | chr9 | 95508060 |