Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 27253 |
| ensemblid | ENSG00000118946.12 |
| hgncid | 14267 |
| symbol | PCDH17 |
| name | protocadherin 17 |
| refseq_nuc | NM_001040429.3 |
| refseq_prot | NP_001035519.1 |
| ensembl_nuc | ENST00000377918.8 |
| ensembl_prot | ENSP00000367151.3 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 57631744 |
| end | 57729311 |
| strand | + |
| ver | v1.2 |
| region | chr13:57631744-57729311 |
| region5000 | chr13:57626744-57734311 |
| regionname0 | PCDH17_chr13_57631744_57729311 |
| regionname5000 | PCDH17_chr13_57626744_57734311 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1159 | 303 | 70 | 67 | 128 | 11 | 25 | 102 | PCDH17_chr13_57626744_57734311 | PCDH17 | MYLSI others(1154): Show |
chr13 | 57626744 | 57734311 |
| a0002 | 0/0 | 1159 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | MYLSI others(1154): Show |
chr13 | 57626744 | 57734311 |
| a0003 | 0/0 | 1159 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | MYLSI others(1154): Show |
chr13 | 57626744 | 57734311 |
| a0004 | 0/0 | 1159 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | MYLSI others(1154): Show |
chr13 | 57626744 | 57734311 |
| a0005 | 0/0 | 1159 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | MYLSI others(1154): Show |
chr13 | 57626744 | 57734311 |
| a0006 | 0/0 | 1159 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | MYLSI others(1154): Show |
chr13 | 57626744 | 57734311 |
| a0007 | 0/0 | 1159 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | MYLSI others(1154): Show |
chr13 | 57626744 | 57734311 |
| a0008 | 0/0 | 1159 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | MYLSI others(1154): Show |
chr13 | 57626744 | 57734311 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 3477 | 287 | 63 | 66 | 122 | 10 | 24 | PCDH17_chr13_57626744_57734311 | PCDH17 | ATGTA others(3472): Show |
chr13 | 57626744 | 57734311 | ||
| a0001c0002 | 0/0 | 3477 | 4 | 4 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | ATGTA others(3472): Show |
chr13 | 57626744 | 57734311 | ||
| a0001c0003 | 0/0 | 3477 | 3 | 0 | 0 | 2 | 1 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | ATGTA others(3472): Show |
chr13 | 57626744 | 57734311 | ||
| a0001c0004 | 0/0 | 3477 | 2 | 2 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | ATGTA others(3472): Show |
chr13 | 57626744 | 57734311 | ||
| a0001c0005 | 0/0 | 3477 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | ATGTA others(3472): Show |
chr13 | 57626744 | 57734311 | ||
| a0001c0006 | 0/0 | 3477 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | ATGTA others(3472): Show |
chr13 | 57626744 | 57734311 | ||
| a0001c0010 | 0/0 | 3477 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | ATGTA others(3472): Show |
chr13 | 57626744 | 57734311 | ||
| a0001c0011 | 0/0 | 3477 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | ATGTA others(3472): Show |
chr13 | 57626744 | 57734311 | ||
| a0001c0012 | 0/0 | 3477 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | ATGTA others(3472): Show |
chr13 | 57626744 | 57734311 | ||
| a0001c0013 | 0/0 | 3477 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | ATGTA others(3472): Show |
chr13 | 57626744 | 57734311 | ||
| a0001c0016 | 0/0 | 3477 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | ATGTA others(3472): Show |
chr13 | 57626744 | 57734311 | ||
| a0002c0015 | 0/0 | 3477 | 1 | 0 | 0 | 0 | 1 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | ATGTA others(3472): Show |
chr13 | 57626744 | 57734311 | ||
| a0003c0014 | 0/0 | 3477 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | ATGTA others(3472): Show |
chr13 | 57626744 | 57734311 | ||
| a0004c0007 | 0/0 | 3477 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | ATGTA others(3472): Show |
chr13 | 57626744 | 57734311 | ||
| a0005c0009 | 0/0 | 3477 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | ATGTA others(3472): Show |
chr13 | 57626744 | 57734311 | ||
| a0006c0008 | 0/0 | 3477 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | ATGTA others(3472): Show |
chr13 | 57626744 | 57734311 | ||
| a0007c0017 | 0/0 | 3477 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | ATGTA others(3472): Show |
chr13 | 57626744 | 57734311 | ||
| a0008c0018 | 0/0 | 3477 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | ATGTA others(3472): Show |
chr13 | 57626744 | 57734311 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 8297 | 50 | 4 | 15 | 22 | 1 | 8 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8292): Show |
chr13 | 57626744 | 57734311 |
| a0001c0001t0002 | 0/0 | 8300 | 51 | 23 | 7 | 17 | 2 | 2 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8295): Show |
chr13 | 57626744 | 57734311 |
| a0001c0001t0003 | 0/0 | 8299 | 31 | 1 | 18 | 7 | 1 | 4 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8294): Show |
chr13 | 57626744 | 57734311 |
| a0001c0001t0004 | 0/0 | 8298 | 20 | 4 | 5 | 9 | 1 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8293): Show |
chr13 | 57626744 | 57734311 |
| a0001c0001t0005 | 0/0 | 8299 | 13 | 10 | 1 | 2 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8294): Show |
chr13 | 57626744 | 57734311 |
| a0001c0001t0006 | 0/1 | 8298 | 13 | 1 | 4 | 5 | 1 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8293): Show |
chr13 | 57626744 | 57734311 |
| a0001c0001t0007 | 0/0 | 8298 | 12 | 0 | 0 | 10 | 1 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8293): Show |
chr13 | 57626744 | 57734311 |
| a0001c0001t0008 | 0/0 | 8300 | 12 | 1 | 3 | 7 | 1 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8295): Show |
chr13 | 57626744 | 57734311 |
| a0001c0001t0009 | 0/0 | 8301 | 10 | 0 | 5 | 2 | 1 | 2 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8296): Show |
chr13 | 57626744 | 57734311 |
| a0001c0001t0010 | 0/0 | 8298 | 8 | 2 | 2 | 3 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8293): Show |
chr13 | 57626744 | 57734311 |
| a0001c0001t0011 | 0/0 | 8298 | 5 | 0 | 0 | 5 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8293): Show |
chr13 | 57626744 | 57734311 |
| a0001c0001t0012 | 0/0 | 8299 | 5 | 0 | 0 | 5 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8294): Show |
chr13 | 57626744 | 57734311 |
| a0001c0001t0013 | 0/0 | 8299 | 4 | 1 | 0 | 1 | 0 | 2 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8294): Show |
chr13 | 57626744 | 57734311 |
| a0001c0001t0014 | 0/0 | 8298 | 4 | 0 | 0 | 4 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8293): Show |
chr13 | 57626744 | 57734311 |
| a0001c0001t0015 | 0/0 | 8297 | 3 | 3 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8292): Show |
chr13 | 57626744 | 57734311 |
| a0001c0001t0016 | 0/0 | 8297 | 2 | 0 | 0 | 2 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8292): Show |
chr13 | 57626744 | 57734311 |
| a0001c0001t0017 | 0/0 | 8299 | 2 | 0 | 0 | 2 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8294): Show |
chr13 | 57626744 | 57734311 |
| a0001c0001t0018 | 0/0 | 8300 | 2 | 2 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8295): Show |
chr13 | 57626744 | 57734311 |
| a0001c0001t0019 | 0/0 | 8299 | 2 | 0 | 0 | 2 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8294): Show |
chr13 | 57626744 | 57734311 |
| a0001c0001t0020 | 0/0 | 8301 | 2 | 0 | 2 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8296): Show |
chr13 | 57626744 | 57734311 |
| a0001c0001t0021 | 0/0 | 8299 | 2 | 0 | 1 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8294): Show |
chr13 | 57626744 | 57734311 |
| a0001c0001t0022 | 0/0 | 8299 | 2 | 1 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8294): Show |
chr13 | 57626744 | 57734311 |
| a0001c0001t0023 | 0/0 | 8298 | 2 | 0 | 0 | 2 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8293): Show |
chr13 | 57626744 | 57734311 |
| a0001c0001t0024 | 0/0 | 8298 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8293): Show |
chr13 | 57626744 | 57734311 |
| a0001c0001t0025 | 0/0 | 8297 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8292): Show |
chr13 | 57626744 | 57734311 |
| a0001c0001t0026 | 0/0 | 8299 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8294): Show |
chr13 | 57626744 | 57734311 |
| a0001c0001t0027 | 0/0 | 8300 | 1 | 0 | 0 | 0 | 1 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8295): Show |
chr13 | 57626744 | 57734311 |
| a0001c0001t0029 | 0/0 | 8298 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8293): Show |
chr13 | 57626744 | 57734311 |
| a0001c0001t0030 | 0/0 | 8301 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8296): Show |
chr13 | 57626744 | 57734311 |
| a0001c0001t0031 | 0/0 | 8300 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8295): Show |
chr13 | 57626744 | 57734311 |
| a0001c0001t0032 | 1/0 | 8300 | 1 | 0 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8295): Show |
chr13 | 57626744 | 57734311 |
| a0001c0001t0033 | 0/0 | 8301 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8296): Show |
chr13 | 57626744 | 57734311 |
| a0001c0001t0034 | 0/0 | 8299 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8294): Show |
chr13 | 57626744 | 57734311 |
| a0001c0001t0035 | 0/0 | 8300 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8295): Show |
chr13 | 57626744 | 57734311 |
| a0001c0001t0036 | 0/0 | 8298 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8293): Show |
chr13 | 57626744 | 57734311 |
| a0001c0001t0037 | 0/0 | 8300 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8295): Show |
chr13 | 57626744 | 57734311 |
| a0001c0001t0038 | 0/0 | 8300 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8295): Show |
chr13 | 57626744 | 57734311 |
| a0001c0001t0039 | 0/0 | 8301 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8296): Show |
chr13 | 57626744 | 57734311 |
| a0001c0001t0040 | 0/0 | 8301 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8296): Show |
chr13 | 57626744 | 57734311 |
| a0001c0001t0041 | 0/0 | 8300 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8295): Show |
chr13 | 57626744 | 57734311 |
| a0001c0001t0042 | 0/0 | 8298 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8293): Show |
chr13 | 57626744 | 57734311 |
| a0001c0001t0043 | 0/0 | 8301 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8296): Show |
chr13 | 57626744 | 57734311 |
| a0001c0001t0044 | 0/0 | 8298 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8293): Show |
chr13 | 57626744 | 57734311 |
| a0001c0001t0046 | 0/0 | 8301 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8296): Show |
chr13 | 57626744 | 57734311 |
| a0001c0001t0047 | 0/0 | 8299 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8294): Show |
chr13 | 57626744 | 57734311 |
| a0001c0001t0048 | 0/0 | 8298 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8293): Show |
chr13 | 57626744 | 57734311 |
| a0001c0001t0050 | 0/0 | 8299 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8294): Show |
chr13 | 57626744 | 57734311 |
| a0001c0001t0051 | 0/0 | 8300 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8295): Show |
chr13 | 57626744 | 57734311 |
| a0001c0001t0052 | 0/0 | 8298 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8293): Show |
chr13 | 57626744 | 57734311 |
| a0001c0001t0053 | 0/0 | 8297 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8292): Show |
chr13 | 57626744 | 57734311 |
| a0001c0001t0054 | 0/0 | 8299 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8294): Show |
chr13 | 57626744 | 57734311 |
| a0001c0001t0055 | 0/0 | 8298 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8293): Show |
chr13 | 57626744 | 57734311 |
| a0001c0001t0056 | 0/0 | 8298 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8293): Show |
chr13 | 57626744 | 57734311 |
| a0001c0002t0001 | 0/0 | 8297 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8292): Show |
chr13 | 57626744 | 57734311 |
| a0001c0002t0005 | 0/0 | 8299 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8294): Show |
chr13 | 57626744 | 57734311 |
| a0001c0002t0006 | 0/0 | 8298 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8293): Show |
chr13 | 57626744 | 57734311 |
| a0001c0002t0049 | 0/0 | 8297 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8292): Show |
chr13 | 57626744 | 57734311 |
| a0001c0003t0001 | 0/0 | 8297 | 1 | 0 | 0 | 0 | 1 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8292): Show |
chr13 | 57626744 | 57734311 |
| a0001c0003t0002 | 0/0 | 8300 | 2 | 0 | 0 | 2 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8295): Show |
chr13 | 57626744 | 57734311 |
| a0001c0004t0005 | 0/0 | 8299 | 2 | 2 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8294): Show |
chr13 | 57626744 | 57734311 |
| a0001c0005t0028 | 0/0 | 8298 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8293): Show |
chr13 | 57626744 | 57734311 |
| a0001c0006t0003 | 0/0 | 8299 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8294): Show |
chr13 | 57626744 | 57734311 |
| a0001c0010t0001 | 0/0 | 8297 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8292): Show |
chr13 | 57626744 | 57734311 |
| a0001c0011t0001 | 0/0 | 8297 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8292): Show |
chr13 | 57626744 | 57734311 |
| a0001c0012t0001 | 0/0 | 8297 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8292): Show |
chr13 | 57626744 | 57734311 |
| a0001c0013t0016 | 0/0 | 8297 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8292): Show |
chr13 | 57626744 | 57734311 |
| a0001c0016t0005 | 0/0 | 8299 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8294): Show |
chr13 | 57626744 | 57734311 |
| a0002c0015t0003 | 0/0 | 8299 | 1 | 0 | 0 | 0 | 1 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8294): Show |
chr13 | 57626744 | 57734311 |
| a0003c0014t0006 | 0/0 | 8298 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8293): Show |
chr13 | 57626744 | 57734311 |
| a0004c0007t0006 | 0/0 | 8298 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8293): Show |
chr13 | 57626744 | 57734311 |
| a0005c0009t0007 | 0/0 | 8298 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8293): Show |
chr13 | 57626744 | 57734311 |
| a0006c0008t0045 | 0/0 | 8298 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8293): Show |
chr13 | 57626744 | 57734311 |
| a0007c0017t0011 | 0/0 | 8298 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8293): Show |
chr13 | 57626744 | 57734311 |
| a0008c0018t0011 | 0/0 | 8298 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | GCATT others(8293): Show |
chr13 | 57626744 | 57734311 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0002g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0002g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0002g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0003g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0003g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0003g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0003g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0003g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0003g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0004g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0004g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0004g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0004g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0004g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0004g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0004g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0004g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0004g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0004g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0004g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0004g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0004g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0004g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0004g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0004g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0004g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0004g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0005g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0005g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0005g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0005g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0005g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0005g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0005g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0005g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0005g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0005g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0005g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0005g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0005g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0006g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0006g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0006g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0006g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0006g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0006g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0006g0128 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0006g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0006g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0006g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0006g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0006g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0006g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0007g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0007g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0007g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0007g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0007g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0007g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0007g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0007g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0007g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0007g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0007g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0007g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0008g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0008g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0008g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0008g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0008g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0008g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0008g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0008g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0008g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0008g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0009g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0009g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0009g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0009g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0009g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0009g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0009g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0009g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0009g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0009g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0010g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0010g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0010g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0010g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0010g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0010g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0010g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0010g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0011g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0011g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0011g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0011g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0011g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0012g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0012g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0012g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0012g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0012g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0013g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0013g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0013g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0013g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0014g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0014g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0014g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0015g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0015g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0015g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0016g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0016g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0017g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0017g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0018g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0018g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0019g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0019g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0020g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0020g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0021g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0021g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0022g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0022g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0023g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0023g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0024g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0025g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0026g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0027g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0029g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0030g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0031g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0032g0034 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0033g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0034g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0035g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0036g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0037g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0038g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0039g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0040g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0041g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0042g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0043g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0044g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0046g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0047g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0048g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0050g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0051g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0052g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0053g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0054g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0055g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0001t0056g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0002t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0002t0005g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0002t0006g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0002t0049g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0003t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0003t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0003t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0004t0005g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0004t0005g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0005t0028g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0006t0003g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0010t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0011t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0012t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0013t0016g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0001c0016t0005g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0002c0015t0003g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0003c0014t0006g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0004c0007t0006g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0005c0009t0007g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0006c0008t0045g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0007c0017t0011g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| a0008c0018t0011g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0215 | EUR | GBR | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG00140 | hp2 | a0001 | c0001 | t0006 | g0240 | EUR | GBR | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG00280 | hp1 | a0001 | c0003 | t0001 | g0267 | EUR | FIN | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG00280 | hp2 | a0002 | c0015 | t0003 | g0039 | EUR | FIN | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG00323 | hp1 | a0001 | c0001 | t0007 | g0111 | EUR | FIN | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0191 | EUR | FIN | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0288 | EAS | CHS | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG00544 | hp2 | a0001 | c0001 | t0033 | g0237 | EAS | CHS | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG00558 | hp1 | a0001 | c0001 | t0007 | g0156 | EAS | CHS | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG00558 | hp2 | a0001 | c0001 | t0011 | g0150 | EAS | CHS | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0250 | EAS | CHS | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG00597 | hp2 | a0001 | c0001 | t0017 | g0180 | EAS | CHS | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0256 | EAS | CHS | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG00621 | hp2 | a0001 | c0003 | t0002 | g0272 | EAS | CHS | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG00639 | hp1 | a0001 | c0001 | t0022 | g0197 | AMR | PUR | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG00673 | hp1 | a0001 | c0001 | t0029 | g0053 | EAS | CHS | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG00673 | hp2 | a0001 | c0001 | t0007 | g0200 | EAS | CHS | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG00735 | hp2 | a0001 | c0001 | t0009 | g0042 | AMR | PUR | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0213 | AMR | PUR | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG00741 | hp1 | a0001 | c0001 | t0010 | g0223 | AMR | PUR | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG01069 | hp1 | a0001 | c0001 | t0009 | g0025 | AMR | PUR | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG01069 | hp2 | a0003 | c0014 | t0006 | g0184 | AMR | PUR | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0249 | AMR | PUR | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG01081 | hp1 | a0001 | c0001 | t0054 | g0224 | AMR | PUR | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG01081 | hp2 | a0001 | c0001 | t0020 | g0131 | AMR | PUR | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0212 | AMR | PUR | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG01099 | hp2 | a0001 | c0006 | t0003 | g0130 | AMR | PUR | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0066 | AMR | PUR | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG01106 | hp2 | a0001 | c0001 | t0006 | g0132 | AMR | PUR | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0086 | AMR | PUR | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG01109 | hp2 | a0001 | c0001 | t0039 | g0279 | AMR | PUR | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG01168 | hp1 | a0001 | c0001 | t0021 | g0152 | AMR | PUR | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0261 | AMR | PUR | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0052 | AMR | PUR | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0260 | AMR | PUR | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG01175 | hp2 | a0001 | c0001 | t0006 | g0222 | AMR | PUR | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG01192 | hp1 | a0001 | c0001 | t0009 | g0301 | AMR | PUR | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0109 | AMR | PUR | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0278 | AMR | PUR | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG01255 | hp1 | a0001 | c0001 | t0010 | g0097 | AMR | CLM | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG01255 | hp2 | a0001 | c0001 | t0009 | g0027 | AMR | CLM | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG01256 | hp1 | a0001 | c0001 | t0004 | g0005 | AMR | CLM | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0068 | AMR | CLM | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG01257 | hp1 | a0001 | c0001 | t0008 | g0001 | AMR | CLM | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG01258 | hp1 | a0001 | c0001 | t0008 | g0001 | AMR | CLM | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG01258 | hp2 | a0001 | c0001 | t0004 | g0005 | AMR | CLM | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0182 | AMR | CLM | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG01261 | hp2 | a0001 | c0001 | t0009 | g0026 | AMR | CLM | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG01346 | hp2 | a0001 | c0001 | t0020 | g0248 | AMR | CLM | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0280 | AMR | CLM | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0203 | AMR | CLM | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG01496 | hp1 | a0001 | c0001 | t0005 | g0291 | AMR | CLM | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0181 | EUR | IBS | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG01515 | hp2 | a0001 | c0001 | t0027 | g0028 | EUR | IBS | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0236 | AFR | ACB | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0144 | AFR | ACB | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0146 | AFR | ACB | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0099 | AFR | ACB | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0041 | AMR | PEL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0187 | AMR | PEL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0070 | AMR | PEL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0072 | AMR | PEL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0071 | AMR | PEL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG01975 | hp2 | a0001 | c0001 | t0004 | g0136 | AMR | PEL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0069 | AMR | PEL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG01978 | hp2 | a0001 | c0001 | t0006 | g0217 | AMR | PEL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0157 | AMR | PEL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG01981 | hp2 | a0001 | c0001 | t0006 | g0216 | AMR | PEL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG01993 | hp1 | a0001 | c0001 | t0004 | g0241 | AMR | PEL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG02015 | hp1 | a0001 | c0001 | t0007 | g0167 | EAS | KHV | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG02015 | hp2 | a0001 | c0001 | t0011 | g0019 | EAS | KHV | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG02027 | hp1 | a0001 | c0001 | t0008 | g0043 | EAS | KHV | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG02027 | hp2 | a0001 | c0001 | t0005 | g0205 | EAS | KHV | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0202 | AFR | ACB | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG02055 | hp2 | a0001 | c0001 | t0018 | g0061 | AFR | ACB | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG02074 | hp1 | a0001 | c0001 | t0016 | g0271 | EAS | KHV | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG02074 | hp2 | a0001 | c0001 | t0007 | g0199 | EAS | KHV | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG02080 | hp1 | a0001 | c0001 | t0016 | g0276 | EAS | KHV | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG02080 | hp2 | a0001 | c0001 | t0007 | g0084 | EAS | KHV | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG02083 | hp1 | a0001 | c0005 | t0028 | g0037 | EAS | KHV | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG02083 | hp2 | a0001 | c0001 | t0004 | g0273 | EAS | KHV | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG02129 | hp1 | a0001 | c0001 | t0023 | g0229 | EAS | KHV | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG02129 | hp2 | a0001 | c0001 | t0004 | g0112 | EAS | KHV | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG02132 | hp1 | a0001 | c0001 | t0007 | g0268 | EAS | KHV | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG02132 | hp2 | a0001 | c0001 | t0008 | g0022 | EAS | KHV | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG02135 | hp2 | a0001 | c0001 | t0004 | g0168 | EAS | KHV | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PEL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG02148 | hp2 | a0001 | c0001 | t0008 | g0033 | AMR | PEL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG02257 | hp1 | a0001 | c0004 | t0005 | g0060 | AFR | ACB | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG02257 | hp2 | a0001 | c0001 | t0034 | g0246 | AFR | ACB | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG02258 | hp1 | a0001 | c0004 | t0005 | g0059 | AFR | ACB | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0115 | AFR | ACB | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG02280 | hp2 | a0001 | c0001 | t0005 | g0124 | AFR | ACB | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0067 | AMR | PEL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0208 | AMR | PEL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG02451 | hp1 | a0001 | c0001 | t0005 | g0141 | AFR | ACB | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG02451 | hp2 | a0001 | c0001 | t0005 | g0295 | AFR | ACB | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG02572 | hp1 | a0001 | c0001 | t0043 | g0087 | AFR | GWD | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG02572 | hp2 | a0001 | c0001 | t0037 | g0014 | AFR | GWD | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0242 | SAS | PJL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0012 | SAS | PJL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG02615 | hp1 | a0001 | c0001 | t0015 | g0015 | AFR | GWD | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG02615 | hp2 | a0001 | c0001 | t0005 | g0107 | AFR | GWD | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0075 | AFR | GWD | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0145 | AFR | GWD | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0302 | AFR | GWD | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0096 | AFR | GWD | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0135 | AFR | GWD | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0198 | AFR | GWD | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG02735 | hp1 | a0001 | c0001 | t0021 | g0078 | SAS | PJL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0221 | SAS | PJL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG02738 | hp1 | a0001 | c0001 | t0010 | g0190 | SAS | PJL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG02738 | hp2 | a0001 | c0001 | t0007 | g0121 | SAS | PJL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0100 | AFR | GWD | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0137 | AFR | GWD | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0098 | AFR | GWD | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG02818 | hp2 | a0001 | c0001 | t0008 | g0044 | AFR | GWD | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0092 | AFR | GWD | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG02897 | hp1 | a0001 | c0001 | t0010 | g0003 | AFR | GWD | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG02897 | hp2 | a0001 | c0001 | t0041 | g0095 | AFR | GWD | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG02976 | hp1 | a0001 | c0001 | t0005 | g0125 | AFR | ESN | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG02976 | hp2 | a0001 | c0001 | t0042 | g0296 | AFR | ESN | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG03017 | hp2 | a0001 | c0016 | t0005 | g0214 | SAS | PJL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG03041 | hp2 | a0001 | c0002 | t0049 | g0209 | AFR | GWD | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG03098 | hp1 | a0001 | c0001 | t0040 | g0106 | AFR | MSL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG03098 | hp2 | a0001 | c0001 | t0035 | g0062 | AFR | MSL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | ESN | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0143 | AFR | ESN | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG03195 | hp1 | a0001 | c0001 | t0018 | g0179 | AFR | ESN | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG03195 | hp2 | a0001 | c0001 | t0005 | g0139 | AFR | ESN | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0297 | AFR | MSL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0103 | AFR | MSL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | MSL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG03225 | hp2 | a0001 | c0001 | t0005 | g0142 | AFR | MSL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0283 | SAS | PJL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG03453 | hp1 | a0001 | c0001 | t0005 | g0140 | AFR | MSL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG03453 | hp2 | a0001 | c0002 | t0006 | g0210 | AFR | MSL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG03486 | hp1 | a0001 | c0002 | t0005 | g0206 | AFR | MSL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0147 | AFR | MSL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG03491 | hp1 | a0001 | c0001 | t0013 | g0021 | SAS | PJL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG03492 | hp1 | a0001 | c0001 | t0013 | g0029 | SAS | PJL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG03516 | hp1 | a0001 | c0001 | t0013 | g0018 | AFR | ESN | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG03516 | hp2 | a0001 | c0001 | t0015 | g0013 | AFR | ESN | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG03579 | hp1 | a0001 | c0001 | t0005 | g0292 | AFR | MSL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0108 | AFR | MSL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG03669 | hp2 | a0001 | c0001 | t0009 | g0244 | SAS | PJL | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | BEB | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0282 | SAS | BEB | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0243 | SAS | BEB | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG04184 | hp2 | a0001 | c0001 | t0004 | g0123 | SAS | BEB | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG04199 | hp1 | a0004 | c0007 | t0006 | g0193 | SAS | STU | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG04199 | hp2 | a0001 | c0001 | t0009 | g0195 | SAS | STU | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | STU | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | STU | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | YRI | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA18522 | hp2 | a0001 | c0001 | t0044 | g0238 | AFR | YRI | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA18939 | hp1 | a0001 | c0001 | t0014 | g0177 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA18939 | hp2 | a0001 | c0001 | t0017 | g0204 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA18940 | hp1 | a0001 | c0001 | t0010 | g0008 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA18940 | hp2 | a0001 | c0001 | t0051 | g0129 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA18942 | hp1 | a0001 | c0001 | t0012 | g0045 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA18942 | hp2 | a0001 | c0001 | t0012 | g0046 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA18943 | hp2 | a0001 | c0001 | t0011 | g0054 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA18948 | hp2 | a0001 | c0001 | t0013 | g0030 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA18949 | hp2 | a0001 | c0001 | t0008 | g0002 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA18951 | hp1 | a0001 | c0001 | t0004 | g0266 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA18952 | hp1 | a0001 | c0001 | t0014 | g0004 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA18952 | hp2 | a0001 | c0013 | t0016 | g0275 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA18953 | hp1 | a0001 | c0001 | t0014 | g0004 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA18956 | hp1 | a0001 | c0001 | t0038 | g0286 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA18956 | hp2 | a0001 | c0001 | t0052 | g0220 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA18959 | hp2 | a0001 | c0001 | t0047 | g0090 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA18962 | hp1 | a0001 | c0001 | t0004 | g0081 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA18962 | hp2 | a0005 | c0009 | t0007 | g0258 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA18965 | hp2 | a0001 | c0001 | t0014 | g0171 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA18967 | hp1 | a0001 | c0001 | t0009 | g0050 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA18967 | hp2 | a0001 | c0001 | t0003 | g0252 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA18968 | hp2 | a0001 | c0001 | t0004 | g0114 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA18969 | hp2 | a0001 | c0001 | t0008 | g0262 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA18971 | hp1 | a0001 | c0001 | t0048 | g0277 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA18971 | hp2 | a0001 | c0001 | t0025 | g0183 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA18977 | hp1 | a0001 | c0001 | t0007 | g0265 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0165 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA18980 | hp2 | a0001 | c0001 | t0006 | g0094 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA18981 | hp2 | a0001 | c0001 | t0019 | g0178 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA18982 | hp1 | a0001 | c0001 | t0011 | g0020 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA18984 | hp2 | a0001 | c0001 | t0050 | g0122 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA18985 | hp2 | a0001 | c0001 | t0053 | g0074 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA18988 | hp2 | a0001 | c0001 | t0005 | g0270 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA18990 | hp1 | a0001 | c0001 | t0012 | g0038 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0287 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA18992 | hp1 | a0006 | c0008 | t0045 | g0281 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA18992 | hp2 | a0001 | c0011 | t0001 | g0235 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA18993 | hp1 | a0001 | c0001 | t0056 | g0056 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA18993 | hp2 | a0001 | c0001 | t0019 | g0151 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA18994 | hp1 | a0001 | c0001 | t0006 | g0093 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA18998 | hp1 | a0001 | c0001 | t0007 | g0234 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA18999 | hp1 | a0007 | c0017 | t0011 | g0055 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA19000 | hp1 | a0001 | c0010 | t0001 | g0274 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA19000 | hp2 | a0001 | c0001 | t0004 | g0230 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA19001 | hp1 | a0008 | c0018 | t0011 | g0040 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA19001 | hp2 | a0001 | c0001 | t0030 | g0036 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA19004 | hp1 | a0001 | c0001 | t0024 | g0201 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA19009 | hp1 | a0001 | c0001 | t0026 | g0247 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA19009 | hp2 | a0001 | c0001 | t0007 | g0233 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA19010 | hp1 | a0001 | c0001 | t0011 | g0299 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA19010 | hp2 | a0001 | c0001 | t0006 | g0077 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA19011 | hp1 | a0001 | c0001 | t0004 | g0076 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA19011 | hp2 | a0001 | c0001 | t0012 | g0032 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA19012 | hp1 | a0001 | c0001 | t0010 | g0263 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA19012 | hp2 | a0001 | c0001 | t0055 | g0188 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA19030 | hp1 | a0001 | c0001 | t0015 | g0016 | AFR | LWK | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0148 | AFR | LWK | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0300 | AFR | LWK | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA19043 | hp2 | a0001 | c0001 | t0010 | g0294 | AFR | LWK | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA19056 | hp2 | a0001 | c0001 | t0023 | g0231 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA19057 | hp1 | a0001 | c0001 | t0012 | g0047 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0264 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA19058 | hp1 | a0001 | c0001 | t0006 | g0057 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA19060 | hp1 | a0001 | c0001 | t0006 | g0080 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA19060 | hp2 | a0001 | c0001 | t0008 | g0035 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA19062 | hp2 | a0001 | c0001 | t0008 | g0049 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA19064 | hp2 | a0001 | c0001 | t0009 | g0051 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA19066 | hp1 | a0001 | c0003 | t0002 | g0257 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA19074 | hp2 | a0001 | c0001 | t0008 | g0002 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA19083 | hp1 | a0001 | c0001 | t0004 | g0175 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA19086 | hp1 | a0001 | c0001 | t0007 | g0269 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0298 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA19087 | hp2 | a0001 | c0001 | t0010 | g0239 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA20129 | hp1 | a0001 | c0001 | t0022 | g0290 | AFR | ASW | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0293 | AFR | ASW | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA20752 | hp1 | a0001 | c0001 | t0004 | g0065 | EUR | TSI | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA20752 | hp2 | a0001 | c0001 | t0009 | g0024 | EUR | TSI | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA20805 | hp1 | a0001 | c0001 | t0008 | g0023 | EUR | TSI | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0196 | EUR | TSI | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA20905 | hp1 | a0001 | c0001 | t0006 | g0186 | SAS | GIH | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA20905 | hp2 | a0001 | c0001 | t0031 | g0031 | SAS | GIH | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0245 | AMR | CLM | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG02486 | hp1 | a0001 | c0001 | t0036 | g0211 | AFR | ACB | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0104 | AFR | ACB | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0079 | AFR | USA | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0133 | AFR | USA | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA20300 | hp1 | a0001 | c0001 | t0005 | g0126 | AFR | USA | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA20300 | hp2 | a0001 | c0012 | t0001 | g0088 | AFR | USA | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA21309 | hp1 | a0001 | c0001 | t0006 | g0017 | AFR | LWK | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| NA21309 | hp2 | a0001 | c0001 | t0046 | g0091 | AFR | LWK | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0006 | g0128 | REF | REF | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0032 | g0034 | REF | REF | PCDH17_chr13_57626744_57734311 | PCDH17 | chr13 | 57626744 | 57734311 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:57632775 | G | T | 1 | a0008 | 1 | NA19001.hp1 | missense_variant | MODERATE | c.229G>T | p.Val77Leu | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/4 | 1032/8300 | 229/3480 | 77/1159 | chr13 | 57632775 | |||
| chr13:57632992 | C | T | 1 | a0007 | 1 | NA18999.hp1 | missense_variant | MODERATE | c.446C>T | p.Thr149Ile | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/4 | 1249/8300 | 446/3480 | 149/1159 | chr13 | 57632992 | |||
| chr13:57633577 | G | T | 1 | a0002 | 1 | HG00280.hp2 | missense_variant | MODERATE | c.1031G>T | p.Arg344Leu | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/4 | 1834/8300 | 1031/3480 | 344/1159 | chr13 | 57633577 | |||
| chr13:57633964 | C | T | 1 | a0003 | 1 | HG01069.hp2 | missense_variant | MODERATE | c.1418C>T | p.Thr473Ile | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/4 | 2221/8300 | 1418/3480 | 473/1159 | chr13 | 57633964 | |||
| chr13:57666785 | G | A | 1 | a0004 | 1 | HG04199.hp1 | missense_variant | MODERATE | c.2749G>A | p.Ala917Thr | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/4 | 3552/8300 | 2749/3480 | 917/1159 | chr13 | 57666785 | |||
| chr13:57724954 | G | C | 1 | a0006 | 1 | NA18992.hp1 | missense_variant | MODERATE | c.3140G>C | p.Cys1047Ser | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 4/4 | 3943/8300 | 3140/3480 | 1047/1159 | chr13 | 57724954 | |||
| chr13:57725224 | A | G | 1 | a0005 | 1 | NA18962.hp2 | missense_variant | MODERATE | c.3410A>G | p.Glu1137Gly | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 4/4 | 4213/8300 | 3410/3480 | 1137/1159 | chr13 | 57725224 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:57633054 | C | T | 1 | a0001c0004 | 2 | HG02257.hp1 HG02258.hp1 |
synonymous_variant | LOW | c.508C>T | p.Leu170Leu | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/4 | 1311/8300 | 508/3480 | 170/1159 | chr13 | 57633054 | |||
| chr13:57633326 | A | G | 1 | a0001c0016 | 1 | HG03017.hp2 | synonymous_variant | LOW | c.780A>G | p.Thr260Thr | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/4 | 1583/8300 | 780/3480 | 260/1159 | chr13 | 57633326 | |||
| chr13:57633647 | C | A | 1 | a0001c0005 | 1 | HG02083.hp1 | synonymous_variant | LOW | c.1101C>A | p.Pro367Pro | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/4 | 1904/8300 | 1101/3480 | 367/1159 | chr13 | 57633647 | |||
| chr13:57633749 | G | A | 1 | a0001c0006 | 1 | HG01099.hp2 | synonymous_variant | LOW | c.1203G>A | p.Gly401Gly | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/4 | 2006/8300 | 1203/3480 | 401/1159 | chr13 | 57633749 | |||
| chr13:57634136 | G | C | 1 | a0001c0003 | 3 | HG00280.hp1 HG00621.hp2 NA19066.hp1 |
synonymous_variant | LOW | c.1590G>C | p.Thr530Thr | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/4 | 2393/8300 | 1590/3480 | 530/1159 | chr13 | 57634136 | |||
| chr13:57634310 | G | A | 1 | a0001c0002 | 4 | HG02723.hp2 HG03041.hp2 HG03453.hp2 others(1): Show |
synonymous_variant | LOW | c.1764G>A | p.Leu588Leu | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/4 | 2567/8300 | 1764/3480 | 588/1159 | chr13 | 57634310 | |||
| chr13:57634661 | G | T | 1 | a0001c0013 | 1 | NA18952.hp2 | synonymous_variant | LOW | c.2115G>T | p.Ser705Ser | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/4 | 2918/8300 | 2115/3480 | 705/1159 | chr13 | 57634661 | |||
| chr13:57634781 | C | G | 1 | a0001c0012 | 1 | NA20300.hp2 | synonymous_variant | LOW | c.2235C>G | p.Ala745Ala | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/4 | 3038/8300 | 2235/3480 | 745/1159 | chr13 | 57634781 | |||
| chr13:57724694 | A | G | 1 | a0001c0011 | 1 | NA18992.hp2 | synonymous_variant | LOW | c.2880A>G | p.Ala960Ala | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 4/4 | 3683/8300 | 2880/3480 | 960/1159 | chr13 | 57724694 | |||
| chr13:57725003 | C | G | 1 | a0001c0010 | 1 | NA19000.hp1 | synonymous_variant | LOW | c.3189C>G | p.Ala1063Ala | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 4/4 | 3992/8300 | 3189/3480 | 1063/1159 | chr13 | 57725003 | |||
| chr13:57725255 | A | G | 1 | a0006c0008 | 1 | NA18992.hp1 | synonymous_variant | LOW | c.3441A>G | p.Gln1147Gln | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 4/4 | 4244/8300 | 3441/3480 | 1147/1159 | chr13 | 57725255 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:57631780 | G | A | 3 | a0001c0001t0017 a0001c0001t0024 a0001c0001t0025 |
4 | HG00597.hp2 NA18939.hp2 NA18971.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-767G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/4 | 767 | chr13 | 57631780 | ||||||
| chr13:57631787 | GA | G | 59 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(56): Show |
263 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(260): Show |
5_prime_UTR_variant | MODIFIER | c.-750delA | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/4 | 750 | INFO_REALIGN_3_PRIME | chr13 | 57631787 | |||||
| chr13:57631801 | G | C | 2 | a0001c0001t0034 a0001c0001t0035 |
2 | HG02257.hp2 HG03098.hp2 |
5_prime_UTR_variant | MODIFIER | c.-746G>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/4 | 746 | chr13 | 57631801 | ||||||
| chr13:57631803 | T | C | 1 | a0001c0001t0036 | 1 | HG02486.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-744T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/4 | chr13 | 57631803 | |||||||
| chr13:57631875 | A | C | 1 | a0001c0001t0056 | 1 | NA18993.hp1 | 5_prime_UTR_variant | MODIFIER | c.-672A>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/4 | 672 | chr13 | 57631875 | ||||||
| chr13:57632078 | T | C | 2 | a0001c0001t0015 a0001c0001t0037 |
4 | HG02572.hp2 HG02615.hp1 HG03516.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-469T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/4 | 469 | chr13 | 57632078 | ||||||
| chr13:57632389 | C | T | 1 | a0001c0001t0055 | 1 | NA19012.hp2 | 5_prime_UTR_variant | MODIFIER | c.-158C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/4 | 158 | chr13 | 57632389 | ||||||
| chr13:57632485 | C | T | 1 | a0001c0001t0033 | 1 | HG00544.hp2 | 5_prime_UTR_variant | MODIFIER | c.-62C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/4 | 62 | chr13 | 57632485 | ||||||
| chr13:57725300 | G | GA | 37 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(34): Show |
154 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(151): Show |
3_prime_UTR_variant | MODIFIER | c.*17dupA | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 4/4 | 18 | INFO_REALIGN_3_PRIME | chr13 | 57725300 | |||||
| chr13:57725490 | G | A | 1 | a0001c0001t0018 | 2 | HG02055.hp2 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*196G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 4/4 | 196 | chr13 | 57725490 | ||||||
| chr13:57725549 | G | A | 28 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0010 others(25): Show |
107 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*255G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 4/4 | 255 | chr13 | 57725549 | ||||||
| chr13:57726102 | A | G | 5 | a0001c0001t0007 a0001c0001t0023 a0001c0001t0053 others(2): Show |
17 | HG00323.hp1 HG00558.hp1 HG00673.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*808A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 4/4 | 808 | chr13 | 57726102 | ||||||
| chr13:57726159 | T | C | 1 | a0001c0001t0034 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*865T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 4/4 | 865 | chr13 | 57726159 | ||||||
| chr13:57726298 | C | T | 1 | a0001c0001t0046 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1004C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 4/4 | 1004 | chr13 | 57726298 | ||||||
| chr13:57726309 | A | C | 3 | a0001c0001t0024 a0001c0001t0026 a0006c0008t0045 |
3 | NA18992.hp1 NA19004.hp1 NA19009.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1015A>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 4/4 | 1015 | chr13 | 57726309 | ||||||
| chr13:57726625 | G | A | 1 | a0001c0001t0050 | 1 | NA18984.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1331G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 4/4 | 1331 | chr13 | 57726625 | ||||||
| chr13:57726724 | T | C | 2 | a0001c0001t0023 a0001c0001t0053 |
3 | HG02129.hp1 NA18985.hp2 NA19056.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1430T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 4/4 | 1430 | chr13 | 57726724 | ||||||
| chr13:57726737 | C | T | 1 | a0001c0001t0044 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1443C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 4/4 | 1443 | chr13 | 57726737 | ||||||
| chr13:57727204 | A | T | 1 | a0001c0001t0043 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1910A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 4/4 | 1910 | chr13 | 57727204 | ||||||
| chr13:57727438 | T | C | 1 | a0001c0001t0038 | 1 | NA18956.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2144T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 4/4 | 2144 | chr13 | 57727438 | ||||||
| chr13:57727718 | G | C | 7 | a0001c0001t0006 a0001c0001t0013 a0001c0001t0036 others(4): Show |
21 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2424G>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 4/4 | 2424 | chr13 | 57727718 | ||||||
| chr13:57727977 | G | A | 72 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(69): Show |
306 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
3_prime_UTR_variant | MODIFIER | c.*2683G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 4/4 | 2683 | chr13 | 57727977 | ||||||
| chr13:57728010 | A | T | 1 | a0001c0001t0029 | 1 | HG00673.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2716A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 4/4 | 2716 | chr13 | 57728010 | ||||||
| chr13:57728304 | G | T | 1 | a0001c0002t0049 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3010G>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 4/4 | 3010 | chr13 | 57728304 | ||||||
| chr13:57728387 | A | G | 1 | a0001c0001t0014 | 4 | NA18939.hp1 NA18952.hp1 NA18953.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3093A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 4/4 | 3093 | chr13 | 57728387 | ||||||
| chr13:57728478 | T | C | 1 | a0001c0001t0039 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3184T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 4/4 | 3184 | chr13 | 57728478 | ||||||
| chr13:57728517 | T | TA | 7 | a0001c0001t0020 a0001c0001t0030 a0001c0001t0039 others(4): Show |
8 | HG01081.hp2 HG01109.hp2 HG01346.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3246dupA | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 4/4 | 3247 | INFO_REALIGN_3_PRIME | chr13 | 57728517 | |||||
| chr13:57728517 | TA | T | 13 | a0001c0001t0005 a0001c0001t0007 a0001c0001t0010 others(10): Show |
47 | HG00323.hp1 HG00558.hp1 HG00597.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*3246delA | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 4/4 | 3246 | INFO_REALIGN_3_PRIME | chr13 | 57728517 | |||||
| chr13:57728517 | TAA | T | 33 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0006 others(30): Show |
129 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*3245_*3246delAA | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 4/4 | 3245 | INFO_REALIGN_3_PRIME | chr13 | 57728517 | |||||
| chr13:57728703 | G | A | 1 | a0001c0001t0042 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3409G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 4/4 | 3409 | chr13 | 57728703 | ||||||
| chr13:57728707 | G | A | 1 | a0001c0001t0041 | 1 | HG02897.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3413G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 4/4 | 3413 | chr13 | 57728707 | ||||||
| chr13:57728907 | A | G | 1 | a0001c0001t0031 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3613A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 4/4 | 3613 | chr13 | 57728907 | ||||||
| chr13:57728943 | G | A | 4 | a0001c0001t0016 a0001c0001t0048 a0001c0005t0028 others(1): Show |
5 | HG02074.hp1 HG02080.hp1 HG02083.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3649G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 4/4 | 3649 | chr13 | 57728943 | ||||||
| chr13:57728949 | T | C | 1 | a0001c0001t0041 | 1 | HG02897.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3655T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 4/4 | 3655 | chr13 | 57728949 | ||||||
| chr13:57729037 | G | A | 1 | a0001c0001t0044 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3743G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 4/4 | 3743 | chr13 | 57729037 | ||||||
| chr13:57729073 | T | C | 1 | a0001c0001t0040 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3779T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 4/4 | 3779 | chr13 | 57729073 | ||||||
| chr13:57729212 | A | G | 1 | a0001c0001t0018 | 2 | HG02055.hp2 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3918A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 4/4 | 3918 | chr13 | 57729212 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:57635244 | C | T | 1 | a0001c0001t0004g0302 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2565+133C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57635244 | |||||||
| chr13:57636343 | T | A | 2 | a0001c0001t0002g0009 a0001c0001t0002g0010 |
2 | HG03130.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2565+1232T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57636343 | |||||||
| chr13:57636383 | A | G | 1 | a0001c0001t0009g0301 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2565+1272A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57636383 | |||||||
| chr13:57636743 | A | G | 1 | a0001c0001t0002g0300 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2565+1632A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57636743 | |||||||
| chr13:57636779 | A | T | 1 | a0001c0001t0011g0299 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.2565+1668A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57636779 | |||||||
| chr13:57636917 | G | T | 52 | a0001c0001t0001g0008 a0001c0001t0001g0253 a0001c0001t0001g0254 others(49): Show |
52 | HG00280.hp1 HG00544.hp1 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.2565+1806G>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57636917 | |||||||
| chr13:57637113 | C | T | 2 | a0001c0001t0002g0249 a0001c0001t0020g0248 |
2 | HG01074.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.2565+2002C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57637113 | |||||||
| chr13:57637469 | A | G | 1 | a0001c0001t0026g0247 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2565+2358A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57637469 | |||||||
| chr13:57638040 | A | C | 1 | a0001c0001t0034g0246 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2565+2929A>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57638040 | |||||||
| chr13:57638272 | T | A | 2 | a0001c0001t0001g0011 a0001c0001t0003g0012 |
2 | HG01361.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.2565+3161T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57638272 | |||||||
| chr13:57638470 | T | C | 4 | a0001c0001t0015g0013 a0001c0001t0015g0015 a0001c0001t0015g0016 others(1): Show |
4 | HG02572.hp2 HG02615.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.2565+3359T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57638470 | |||||||
| chr13:57638507 | C | T | 258 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(255): Show |
262 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.2565+3396C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57638507 | |||||||
| chr13:57639081 | T | C | 1 | a0001c0001t0001g0058 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2565+3970T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57639081 | |||||||
| chr13:57639178 | T | A | 4 | a0001c0001t0001g0058 a0001c0001t0018g0061 a0001c0004t0005g0059 others(1): Show |
4 | HG02055.hp2 HG02257.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.2565+4067T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57639178 | |||||||
| chr13:57639260 | C | G | 1 | a0001c0001t0003g0245 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2565+4149C>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57639260 | |||||||
| chr13:57639358 | A | C | 2 | a0001c0001t0002g0009 a0001c0001t0002g0010 |
2 | HG03130.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2565+4247A>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57639358 | |||||||
| chr13:57639502 | A | T | 1 | a0001c0001t0006g0057 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2565+4391A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57639502 | |||||||
| chr13:57639711 | T | C | 1 | a0001c0001t0002g0300 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2565+4600T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57639711 | |||||||
| chr13:57640395 | A | C | 164 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0058 others(161): Show |
168 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.2565+5284A>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57640395 | |||||||
| chr13:57640611 | C | T | 51 | a0001c0001t0001g0003 a0001c0001t0001g0101 a0001c0001t0001g0102 others(48): Show |
51 | HG00323.hp1 HG01081.hp2 HG01099.hp2 others(48): Show |
intron_variant | MODIFIER | c.2565+5500C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57640611 | |||||||
| chr13:57640617 | G | T | 1 | a0001c0001t0009g0244 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2565+5506G>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57640617 | |||||||
| chr13:57640713 | T | C | 2 | a0001c0001t0034g0246 a0001c0001t0035g0062 |
2 | HG02257.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2565+5602T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57640713 | |||||||
| chr13:57640774 | A | T | 1 | a0001c0001t0009g0244 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2565+5663A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57640774 | |||||||
| chr13:57640794 | A | G | 3 | a0001c0001t0011g0054 a0001c0001t0056g0056 a0007c0017t0011g0055 |
3 | NA18943.hp2 NA18993.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.2565+5683A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57640794 | |||||||
| chr13:57640890 | A | C | 1 | a0001c0001t0003g0298 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.2565+5779A>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57640890 | |||||||
| chr13:57640893 | C | T | 1 | a0001c0001t0002g0297 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2565+5782C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57640893 | |||||||
| chr13:57640894 | G | A | 2 | a0001c0001t0002g0009 a0001c0001t0002g0010 |
2 | HG03130.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2565+5783G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57640894 | |||||||
| chr13:57640918 | A | G | 2 | a0001c0001t0034g0246 a0001c0001t0035g0062 |
2 | HG02257.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2565+5807A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57640918 | |||||||
| chr13:57640924 | A | T | 6 | a0001c0001t0002g0242 a0001c0001t0002g0249 a0001c0001t0003g0243 others(3): Show |
6 | HG00140.hp2 HG01074.hp1 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.2565+5813A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57640924 | |||||||
| chr13:57641008 | G | A | 207 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(204): Show |
211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.2565+5897G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57641008 | |||||||
| chr13:57641142 | G | A | 207 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(204): Show |
211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.2565+6031G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57641142 | |||||||
| chr13:57641558 | GA | G | 24 | a0001c0001t0001g0110 a0001c0001t0001g0113 a0001c0001t0001g0253 others(21): Show |
24 | HG00280.hp2 HG00323.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.2565+6477delA | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57641558 | ||||||
| chr13:57641558 | GAA | G | 8 | a0001c0001t0001g0048 a0001c0001t0002g0115 a0001c0001t0004g0114 others(5): Show |
8 | HG01069.hp2 HG01496.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.2565+6476_2565+647 others(6): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57641558 | ||||||
| chr13:57641558 | GAAA | G | 11 | a0001c0001t0001g0058 a0001c0001t0001g0116 a0001c0001t0001g0117 others(8): Show |
11 | HG00673.hp1 HG01123.hp1 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.2565+6475_2565+647 others(7): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57641558 | ||||||
| chr13:57641558 | GAAAA | G | 9 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0085 others(6): Show |
9 | HG01109.hp1 HG01934.hp2 HG02080.hp2 others(6): Show |
intron_variant | MODIFIER | c.2565+6474_2565+647 others(8): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57641558 | ||||||
| chr13:57641558 | GAAAAA | G | 19 | a0001c0001t0001g0189 a0001c0001t0001g0255 a0001c0001t0001g0259 others(16): Show |
20 | HG00323.hp2 HG00621.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.2565+6473_2565+647 others(9): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57641558 | ||||||
| chr13:57641558 | GAAAAAA | G | 9 | a0001c0001t0001g0192 a0001c0001t0002g0127 a0001c0001t0002g0194 others(6): Show |
9 | HG00735.hp1 HG01074.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.2565+6472_2565+647 others(10): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57641558 | ||||||
| chr13:57641558 | GAAAAAAA | G | 21 | a0001c0001t0001g0008 a0001c0001t0001g0089 a0001c0001t0002g0133 others(18): Show |
21 | HG00140.hp2 HG00280.hp1 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.2565+6471_2565+647 others(11): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57641558 | ||||||
| chr13:57641558 | GAAAAAAA others(1): Show |
G | 14 | a0001c0001t0001g0134 a0001c0001t0001g0138 a0001c0001t0002g0009 others(11): Show |
14 | HG00639.hp1 HG01975.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.2565+6470_2565+647 others(12): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57641558 | ||||||
| chr13:57641558 | GAAAAAAA others(2): Show |
G | 22 | a0001c0001t0002g0202 a0001c0001t0002g0203 a0001c0001t0003g0298 others(19): Show |
22 | HG00621.hp2 HG00673.hp2 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.2565+6469_2565+647 others(13): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57641558 | ||||||
| chr13:57641558 | GAAAAAAA others(3): Show |
G | 15 | a0001c0001t0001g0207 a0001c0001t0001g0215 a0001c0001t0001g0218 others(12): Show |
15 | HG00140.hp1 HG00738.hp1 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.2565+6468_2565+647 others(14): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57641558 | ||||||
| chr13:57641558 | GAAAAAAA others(4): Show |
G | 20 | a0001c0001t0001g0007 a0001c0001t0002g0006 a0001c0001t0002g0143 others(17): Show |
22 | HG00741.hp1 HG00741.hp2 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.2565+6467_2565+647 others(15): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57641558 | ||||||
| chr13:57641558 | GAAAAAAA others(5): Show |
G | 5 | a0001c0001t0001g0227 a0001c0001t0002g0147 a0001c0001t0002g0226 others(2): Show |
5 | HG01074.hp2 HG02897.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.2565+6466_2565+647 others(16): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57641558 | ||||||
| chr13:57641558 | GAAAAAAA others(6): Show |
G | 18 | a0001c0001t0001g0228 a0001c0001t0001g0284 a0001c0001t0001g0289 others(15): Show |
18 | HG00544.hp1 HG02129.hp1 HG02615.hp1 others(15): Show |
intron_variant | MODIFIER | c.2565+6465_2565+647 others(17): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57641558 | ||||||
| chr13:57641558 | GAAAAAAA others(7): Show |
G | 10 | a0001c0001t0002g0096 a0001c0001t0002g0098 a0001c0001t0002g0236 others(7): Show |
10 | HG01255.hp1 HG01496.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.2565+6464_2565+647 others(18): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57641558 | ||||||
| chr13:57641558 | GAAAAAAA others(8): Show |
G | 3 | a0001c0001t0002g0100 a0001c0001t0033g0237 a0001c0001t0044g0238 |
3 | HG00544.hp2 HG02809.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2565+6463_2565+647 others(19): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57641558 | ||||||
| chr13:57641558 | GAAAAAAA others(9): Show |
G | 2 | a0001c0001t0005g0295 a0001c0001t0042g0296 |
2 | HG02451.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2565+6462_2565+647 others(20): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57641558 | ||||||
| chr13:57641571 | A | T | 1 | a0001c0001t0010g0239 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2565+6460A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57641571 | |||||||
| chr13:57641572 | AAAAAAAA others(10): Show |
A | 2 | a0001c0001t0010g0294 a0001c0001t0034g0246 |
2 | HG02257.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2565+6463_2565+647 others(21): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57641572 | ||||||
| chr13:57641573 | A | T | 3 | a0001c0001t0003g0252 a0001c0001t0010g0239 a0001c0003t0002g0257 |
3 | NA18967.hp2 NA19066.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.2565+6462A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57641573 | |||||||
| chr13:57641573 | AAAAAAAA others(9): Show |
A | 1 | a0001c0001t0004g0168 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2565+6464_2565+647 others(20): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57641573 | ||||||
| chr13:57641574 | AAAAAAAA others(8): Show |
A | 24 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0155 others(21): Show |
25 | HG00558.hp1 HG00558.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.2565+6465_2565+647 others(19): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57641574 | ||||||
| chr13:57641574 | AAAAAAAA others(10): Show |
A | 1 | a0001c0004t0005g0059 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2565+6465_2565+648 others(21): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57641574 | ||||||
| chr13:57641575 | A | T | 10 | a0001c0001t0001g0253 a0001c0001t0001g0254 a0001c0001t0002g0075 others(7): Show |
10 | HG01261.hp1 HG01515.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.2565+6464A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57641575 | |||||||
| chr13:57641575 | AAAAAAAA others(7): Show |
A | 2 | a0001c0001t0001g0149 a0001c0001t0019g0151 |
2 | HG01175.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.2565+6466_2565+647 others(18): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57641575 | ||||||
| chr13:57641575 | AAAAAAAA others(9): Show |
A | 2 | a0001c0001t0002g0103 a0001c0001t0002g0108 |
2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2565+6466_2565+648 others(20): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57641575 | ||||||
| chr13:57641575 | AAAAAAAA others(15): Show |
A | 1 | a0001c0001t0004g0109 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2565+6466_2565+648 others(26): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57641575 | ||||||
| chr13:57641576 | AAAAAAAA others(6): Show |
A | 1 | a0001c0001t0002g0251 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2565+6467_2565+647 others(17): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57641576 | ||||||
| chr13:57641576 | AAAAAAAA others(8): Show |
A | 5 | a0001c0001t0001g0158 a0001c0001t0001g0163 a0001c0001t0001g0164 others(2): Show |
5 | HG01346.hp1 HG01433.hp2 HG04204.hp2 others(2): Show |
intron_variant | MODIFIER | c.2565+6467_2565+648 others(19): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57641576 | ||||||
| chr13:57641577 | A | AT | 4 | a0001c0001t0002g0073 a0001c0001t0005g0107 a0001c0001t0017g0180 others(1): Show |
4 | HG00597.hp2 HG02615.hp2 NA18943.hp1 others(1): Show |
intron_variant | MODIFIER | c.2565+6466_2565+646 others(5): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57641577 | |||||||
| chr13:57641577 | A | T | 18 | a0001c0001t0001g0058 a0001c0001t0001g0089 a0001c0001t0001g0253 others(15): Show |
18 | HG00280.hp1 HG01074.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.2565+6466A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57641577 | |||||||
| chr13:57641577 | AAAAAAAA others(5): Show |
A | 1 | a0001c0001t0002g0250 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2565+6468_2565+647 others(16): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57641577 | ||||||
| chr13:57641577 | AAAAAAAA others(9): Show |
A | 2 | a0001c0001t0001g0003 a0001c0001t0010g0003 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2565+6468_2565+648 others(20): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57641577 | ||||||
| chr13:57641578 | AAAAAAAA others(4): Show |
A | 1 | a0001c0001t0001g0105 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2565+6469_2565+647 others(15): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57641578 | ||||||
| chr13:57641578 | AAAAAAAA others(6): Show |
A | 1 | a0001c0001t0002g0104 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2565+6469_2565+648 others(17): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57641578 | ||||||
| chr13:57641578 | AAAAAAAA others(8): Show |
A | 1 | a0001c0001t0001g0169 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2565+6469_2565+648 others(19): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57641578 | ||||||
| chr13:57641579 | A | T | 44 | a0001c0001t0001g0058 a0001c0001t0001g0089 a0001c0001t0001g0102 others(41): Show |
44 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.2565+6468A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57641579 | |||||||
| chr13:57641579 | AAAAAAAA others(3): Show |
A | 1 | a0001c0001t0009g0027 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2565+6470_2565+647 others(14): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57641579 | ||||||
| chr13:57641580 | AAAAAAAA others(12): Show |
A | 1 | a0001c0001t0040g0106 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2565+6471_2565+648 others(23): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57641580 | ||||||
| chr13:57641581 | A | T | 70 | a0001c0001t0001g0058 a0001c0001t0001g0089 a0001c0001t0001g0101 others(67): Show |
71 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.2565+6470A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57641581 | |||||||
| chr13:57641583 | A | T | 101 | a0001c0001t0001g0008 a0001c0001t0001g0058 a0001c0001t0001g0089 others(98): Show |
102 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.2565+6472A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57641583 | |||||||
| chr13:57641585 | A | T | 139 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0058 others(136): Show |
142 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.2565+6474A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57641585 | |||||||
| chr13:57641587 | A | AT | 4 | a0001c0001t0009g0024 a0001c0001t0012g0032 a0001c0001t0026g0247 others(1): Show |
4 | HG01515.hp2 NA19009.hp1 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.2565+6476_2565+647 others(5): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57641587 | |||||||
| chr13:57641587 | A | T | 181 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0048 others(178): Show |
184 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.2565+6476A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57641587 | |||||||
| chr13:57641588 | AT | A | 6 | a0001c0001t0006g0017 a0001c0001t0006g0057 a0001c0001t0008g0001 others(3): Show |
7 | HG01257.hp1 HG03492.hp1 NA18949.hp2 others(4): Show |
intron_variant | MODIFIER | c.2565+6478delT | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57641588 | |||||||
| chr13:57641588 | ATATATAT others(10): Show |
A | 1 | a0001c0001t0003g0072 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2565+6478_2565+649 others(21): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57641588 | |||||||
| chr13:57641589 | T | A | 1 | a0001c0001t0008g0033 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2565+6478T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57641589 | |||||||
| chr13:57641591 | T | A | 1 | a0001c0001t0006g0017 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2565+6480T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57641591 | |||||||
| chr13:57641622 | A | G | 2 | a0001c0001t0003g0260 a0001c0001t0003g0261 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.2565+6511A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57641622 | |||||||
| chr13:57641623 | T | A | 2 | a0001c0001t0003g0260 a0001c0001t0003g0261 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.2565+6512T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57641623 | |||||||
| chr13:57641779 | G | A | 1 | a0001c0001t0002g0278 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2565+6668G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57641779 | |||||||
| chr13:57641995 | A | C | 1 | a0001c0001t0001g0113 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.2565+6884A>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57641995 | |||||||
| chr13:57642060 | G | A | 25 | a0001c0001t0001g0003 a0001c0001t0001g0101 a0001c0001t0001g0102 others(22): Show |
25 | HG00323.hp1 HG01081.hp2 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.2565+6949G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57642060 | |||||||
| chr13:57642186 | C | A | 46 | a0001c0001t0001g0149 a0001c0001t0001g0153 a0001c0001t0001g0154 others(43): Show |
47 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.2565+7075C>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57642186 | |||||||
| chr13:57642330 | T | C | 1 | a0001c0001t0002g0103 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2565+7219T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57642330 | |||||||
| chr13:57642398 | A | G | 5 | a0001c0001t0002g0196 a0001c0001t0003g0187 a0001c0001t0003g0191 others(2): Show |
5 | HG00323.hp2 HG01069.hp2 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.2565+7287A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57642398 | |||||||
| chr13:57642443 | A | G | 1 | a0001c0001t0019g0178 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2565+7332A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57642443 | |||||||
| chr13:57642674 | G | C | 1 | a0001c0001t0016g0271 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2565+7563G>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57642674 | |||||||
| chr13:57643012 | C | T | 2 | a0001c0001t0002g0009 a0001c0001t0002g0010 |
2 | HG03130.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2565+7901C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57643012 | |||||||
| chr13:57643081 | T | C | 1 | a0001c0001t0001g0149 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2565+7970T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57643081 | |||||||
| chr13:57643180 | T | G | 6 | a0001c0001t0002g0242 a0001c0001t0002g0249 a0001c0001t0003g0243 others(3): Show |
6 | HG00140.hp2 HG01074.hp1 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.2565+8069T>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57643180 | |||||||
| chr13:57643277 | G | A | 205 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(202): Show |
209 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.2565+8166G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57643277 | |||||||
| chr13:57643569 | G | A | 99 | a0001c0001t0001g0007 a0001c0001t0001g0149 a0001c0001t0001g0153 others(96): Show |
103 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.2565+8458G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57643569 | |||||||
| chr13:57643724 | T | C | 1 | a0001c0001t0006g0057 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2565+8613T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57643724 | |||||||
| chr13:57643772 | A | C | 1 | a0001c0001t0018g0061 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2565+8661A>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57643772 | |||||||
| chr13:57643953 | A | G | 6 | a0001c0001t0002g0293 a0001c0001t0005g0291 a0001c0001t0005g0292 others(3): Show |
6 | HG01496.hp1 HG02451.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.2565+8842A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57643953 | |||||||
| chr13:57644485 | A | G | 1 | a0001c0001t0018g0061 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2565+9374A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57644485 | |||||||
| chr13:57644512 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2565+9401G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57644512 | |||||||
| chr13:57644526 | T | TA | 57 | a0001c0001t0001g0008 a0001c0001t0001g0189 a0001c0001t0001g0218 others(54): Show |
57 | HG00280.hp1 HG00544.hp1 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.2565+9424dupA | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57644526 | ||||||
| chr13:57644556 | C | G | 2 | a0001c0001t0014g0004 a0001c0001t0014g0177 |
3 | NA18939.hp1 NA18952.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.2565+9445C>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57644556 | |||||||
| chr13:57644593 | C | T | 2 | a0001c0001t0001g0176 a0001c0001t0004g0175 |
2 | NA19066.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.2565+9482C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57644593 | |||||||
| chr13:57644596 | C | T | 25 | a0001c0001t0001g0003 a0001c0001t0001g0101 a0001c0001t0001g0102 others(22): Show |
25 | HG00323.hp1 HG01081.hp2 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.2565+9485C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57644596 | |||||||
| chr13:57644966 | G | A | 3 | a0001c0001t0002g0119 a0001c0001t0002g0120 a0001c0001t0002g0127 |
3 | NA19007.hp2 NA19062.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.2565+9855G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57644966 | |||||||
| chr13:57645165 | C | T | 1 | a0001c0001t0002g0100 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2565+10054C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57645165 | |||||||
| chr13:57646461 | A | C | 51 | a0001c0001t0001g0003 a0001c0001t0001g0101 a0001c0001t0001g0102 others(48): Show |
51 | HG00323.hp1 HG01081.hp2 HG01099.hp2 others(48): Show |
intron_variant | MODIFIER | c.2565+11350A>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57646461 | |||||||
| chr13:57646676 | T | C | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG00639.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.2565+11565T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57646676 | |||||||
| chr13:57646689 | T | C | 1 | a0001c0004t0005g0059 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2565+11578T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57646689 | |||||||
| chr13:57646699 | G | A | 19 | a0001c0001t0001g0011 a0001c0001t0001g0063 a0001c0001t0001g0064 others(16): Show |
19 | HG00639.hp2 HG01106.hp1 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.2565+11588G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57646699 | |||||||
| chr13:57646734 | C | T | 1 | a0001c0001t0003g0282 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2565+11623C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57646734 | |||||||
| chr13:57646764 | T | A | 1 | a0001c0001t0007g0121 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2565+11653T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57646764 | |||||||
| chr13:57646905 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2565+11794C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57646905 | |||||||
| chr13:57646911 | C | A | 1 | a0001c0001t0003g0245 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2565+11800C>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57646911 | |||||||
| chr13:57646922 | T | G | 2 | a0001c0001t0002g0006 a0001c0001t0003g0221 |
3 | HG00741.hp2 HG01192.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.2565+11811T>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57646922 | |||||||
| chr13:57646947 | A | T | 1 | a0001c0001t0003g0221 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2565+11836A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57646947 | |||||||
| chr13:57647541 | C | T | 1 | a0001c0001t0002g0174 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.2565+12430C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57647541 | |||||||
| chr13:57648161 | T | C | 1 | a0001c0001t0011g0150 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2565+13050T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57648161 | |||||||
| chr13:57648190 | A | G | 2 | a0001c0004t0005g0059 a0001c0004t0005g0060 |
2 | HG02257.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.2565+13079A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57648190 | |||||||
| chr13:57648295 | G | T | 10 | a0001c0001t0009g0050 a0001c0001t0009g0051 a0001c0001t0011g0054 others(7): Show |
10 | HG02083.hp1 NA18942.hp2 NA18943.hp2 others(7): Show |
intron_variant | MODIFIER | c.2565+13184G>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57648295 | |||||||
| chr13:57648378 | G | A | 51 | a0001c0001t0001g0003 a0001c0001t0001g0101 a0001c0001t0001g0102 others(48): Show |
51 | HG00323.hp1 HG01081.hp2 HG01099.hp2 others(48): Show |
intron_variant | MODIFIER | c.2565+13267G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57648378 | |||||||
| chr13:57648544 | T | A | 236 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(233): Show |
240 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.2565+13433T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57648544 | |||||||
| chr13:57648673 | T | C | 1 | a0001c0012t0001g0088 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2565+13562T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57648673 | |||||||
| chr13:57648714 | A | G | 2 | a0001c0001t0034g0246 a0001c0001t0035g0062 |
2 | HG02257.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2565+13603A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57648714 | |||||||
| chr13:57649038 | A | G | 1 | a0001c0001t0012g0047 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2565+13927A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57649038 | |||||||
| chr13:57649380 | A | G | 1 | a0001c0001t0001g0058 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2565+14269A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57649380 | |||||||
| chr13:57649583 | A | T | 1 | a0001c0001t0001g0173 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2565+14472A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57649583 | |||||||
| chr13:57649675 | T | C | 51 | a0001c0001t0001g0003 a0001c0001t0001g0101 a0001c0001t0001g0102 others(48): Show |
51 | HG00323.hp1 HG01081.hp2 HG01099.hp2 others(48): Show |
intron_variant | MODIFIER | c.2565+14564T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57649675 | |||||||
| chr13:57649896 | T | C | 1 | a0001c0001t0001g0255 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2565+14785T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57649896 | |||||||
| chr13:57649987 | G | A | 4 | a0001c0001t0001g0058 a0001c0001t0018g0061 a0001c0004t0005g0059 others(1): Show |
4 | HG02055.hp2 HG02257.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.2565+14876G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57649987 | |||||||
| chr13:57650218 | T | TTG | 40 | a0001c0001t0001g0101 a0001c0001t0001g0110 a0001c0001t0001g0113 others(37): Show |
41 | HG00323.hp1 HG00621.hp1 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.2565+15149_2565+15 others(8): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57650218 | ||||||
| chr13:57650218 | T | TTGTG | 47 | a0001c0001t0001g0003 a0001c0001t0001g0102 a0001c0001t0001g0105 others(44): Show |
47 | HG00544.hp1 HG00558.hp1 HG01069.hp2 others(44): Show |
intron_variant | MODIFIER | c.2565+15147_2565+15 others(10): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57650218 | ||||||
| chr13:57650218 | T | TTGTGTG | 43 | a0001c0001t0001g0058 a0001c0001t0001g0176 a0001c0001t0001g0189 others(40): Show |
43 | HG00140.hp2 HG00280.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.2565+15145_2565+15 others(12): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57650218 | ||||||
| chr13:57650218 | T | TTGTGTGT others(1): Show |
55 | a0001c0001t0001g0007 a0001c0001t0001g0138 a0001c0001t0001g0158 others(52): Show |
58 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.2565+15143_2565+15 others(14): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57650218 | ||||||
| chr13:57650218 | T | TTGTGTGT others(3): Show |
10 | a0001c0001t0001g0215 a0001c0001t0002g0278 a0001c0001t0003g0170 others(7): Show |
10 | HG00140.hp1 HG00544.hp2 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.2565+15141_2565+15 others(16): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57650218 | ||||||
| chr13:57650218 | T | TTGTGTGT others(5): Show |
4 | a0001c0001t0001g0172 a0001c0001t0002g0103 a0001c0001t0006g0217 others(1): Show |
4 | HG01978.hp2 HG03209.hp2 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.2565+15139_2565+15 others(18): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57650218 | ||||||
| chr13:57650218 | TTG | T | 45 | a0001c0001t0001g0048 a0001c0001t0001g0089 a0001c0001t0001g0155 others(42): Show |
46 | HG00280.hp2 HG00735.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.2565+15149_2565+15 others(8): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57650218 | ||||||
| chr13:57650218 | TTGTG | T | 13 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0002g0075 others(10): Show |
13 | HG01168.hp1 HG01192.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.2565+15147_2565+15 others(10): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57650218 | ||||||
| chr13:57650218 | TTGTGTG | T | 16 | a0001c0001t0001g0011 a0001c0001t0001g0063 a0001c0001t0001g0064 others(13): Show |
16 | HG00639.hp2 HG01106.hp1 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.2565+15145_2565+15 others(12): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57650218 | ||||||
| chr13:57650218 | TTGTGTGT others(1): Show |
T | 4 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0003g0079 others(1): Show |
4 | HG02735.hp1 HG03017.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.2565+15143_2565+15 others(14): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57650218 | ||||||
| chr13:57650218 | TTGTGTGT others(11): Show |
T | 1 | a0001c0001t0039g0279 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2565+15133_2565+15 others(24): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57650218 | ||||||
| chr13:57650311 | G | C | 56 | a0001c0001t0001g0008 a0001c0001t0001g0218 a0001c0001t0001g0253 others(53): Show |
56 | HG00280.hp1 HG00544.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.2565+15200G>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57650311 | |||||||
| chr13:57650986 | C | T | 55 | a0001c0001t0001g0008 a0001c0001t0001g0218 a0001c0001t0001g0253 others(52): Show |
55 | HG00280.hp1 HG00544.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.2566-15482C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57650986 | |||||||
| chr13:57651007 | A | G | 26 | a0001c0001t0001g0105 a0001c0001t0001g0138 a0001c0001t0002g0103 others(23): Show |
26 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.2566-15461A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57651007 | |||||||
| chr13:57651036 | A | T | 18 | a0001c0001t0001g0011 a0001c0001t0001g0063 a0001c0001t0001g0064 others(15): Show |
18 | HG00639.hp2 HG01106.hp1 HG01256.hp2 others(15): Show |
intron_variant | MODIFIER | c.2566-15432A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57651036 | |||||||
| chr13:57651304 | A | G | 1 | a0001c0001t0006g0217 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2566-15164A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57651304 | |||||||
| chr13:57651356 | G | GT | 17 | a0001c0001t0002g0098 a0001c0001t0003g0041 a0001c0001t0004g0099 others(14): Show |
17 | HG00673.hp1 HG00735.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.2566-15089dupT | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57651356 | ||||||
| chr13:57651356 | GT | G | 188 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(185): Show |
192 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.2566-15089delT | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57651356 | ||||||
| chr13:57651359 | T | G | 1 | a0001c0001t0010g0263 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2566-15109T>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57651359 | |||||||
| chr13:57651369 | T | G | 1 | a0001c0001t0001g0113 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.2566-15099T>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57651369 | |||||||
| chr13:57651476 | T | A | 1 | a0001c0001t0001g0158 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2566-14992T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57651476 | |||||||
| chr13:57651483 | A | G | 3 | a0001c0001t0002g0006 a0001c0001t0003g0221 a0001c0001t0010g0239 |
4 | HG00741.hp2 HG01192.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.2566-14985A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57651483 | |||||||
| chr13:57651568 | T | G | 217 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(214): Show |
221 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.2566-14900T>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57651568 | |||||||
| chr13:57651574 | G | A | 17 | a0001c0001t0001g0008 a0001c0001t0001g0218 a0001c0001t0002g0225 others(14): Show |
17 | HG00621.hp1 HG02027.hp2 HG02074.hp1 others(14): Show |
intron_variant | MODIFIER | c.2566-14894G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57651574 | |||||||
| chr13:57651612 | A | G | 1 | a0001c0001t0012g0046 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2566-14856A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57651612 | |||||||
| chr13:57651707 | C | A | 1 | a0001c0001t0003g0170 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2566-14761C>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57651707 | |||||||
| chr13:57651837 | ATAT | A | 4 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0034g0246 others(1): Show |
4 | HG02257.hp2 HG03098.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.2566-14623_2566-14 others(9): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57651837 | ||||||
| chr13:57651954 | A | G | 1 | a0001c0001t0002g0075 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2566-14514A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57651954 | |||||||
| chr13:57652033 | C | G | 2 | a0001c0001t0034g0246 a0001c0001t0035g0062 |
2 | HG02257.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2566-14435C>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57652033 | |||||||
| chr13:57652207 | A | G | 1 | a0001c0001t0007g0111 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2566-14261A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57652207 | |||||||
| chr13:57652284 | C | CA | 58 | a0001c0001t0001g0003 a0001c0001t0001g0058 a0001c0001t0001g0101 others(55): Show |
58 | HG00323.hp1 HG01081.hp2 HG01099.hp2 others(55): Show |
intron_variant | MODIFIER | c.2566-14166dupA | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57652284 | ||||||
| chr13:57652284 | C | CAA | 165 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(162): Show |
169 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.2566-14167_2566-14 others(8): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57652284 | ||||||
| chr13:57652284 | C | CAAA | 15 | a0001c0001t0001g0149 a0001c0001t0001g0159 a0001c0001t0001g0228 others(12): Show |
15 | HG01109.hp2 HG01175.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.2566-14168_2566-14 others(9): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57652284 | ||||||
| chr13:57652567 | C | A | 1 | a0001c0001t0001g0058 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2566-13901C>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57652567 | |||||||
| chr13:57652610 | A | G | 18 | a0001c0001t0001g0011 a0001c0001t0001g0063 a0001c0001t0001g0064 others(15): Show |
18 | HG00639.hp2 HG01106.hp1 HG01256.hp2 others(15): Show |
intron_variant | MODIFIER | c.2566-13858A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57652610 | |||||||
| chr13:57652766 | G | A | 2 | a0001c0001t0002g0009 a0001c0001t0002g0010 |
2 | HG03130.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2566-13702G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57652766 | |||||||
| chr13:57652785 | A | G | 1 | a0001c0001t0035g0062 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2566-13683A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57652785 | |||||||
| chr13:57652808 | G | A | 51 | a0001c0001t0001g0003 a0001c0001t0001g0101 a0001c0001t0001g0102 others(48): Show |
51 | HG00323.hp1 HG01081.hp2 HG01099.hp2 others(48): Show |
intron_variant | MODIFIER | c.2566-13660G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57652808 | |||||||
| chr13:57652913 | C | G | 1 | a0001c0001t0002g0118 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2566-13555C>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57652913 | |||||||
| chr13:57652989 | A | G | 26 | a0001c0001t0001g0105 a0001c0001t0001g0138 a0001c0001t0002g0103 others(23): Show |
26 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.2566-13479A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57652989 | |||||||
| chr13:57653157 | T | A | 18 | a0001c0001t0001g0011 a0001c0001t0001g0063 a0001c0001t0001g0064 others(15): Show |
18 | HG00639.hp2 HG01106.hp1 HG01256.hp2 others(15): Show |
intron_variant | MODIFIER | c.2566-13311T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57653157 | |||||||
| chr13:57653325 | AC | A | 3 | a0001c0001t0018g0061 a0001c0004t0005g0059 a0001c0004t0005g0060 |
3 | HG02055.hp2 HG02257.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.2566-13141delC | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57653325 | ||||||
| chr13:57653441 | A | G | 1 | a0001c0001t0006g0094 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2566-13027A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57653441 | |||||||
| chr13:57653442 | T | C | 1 | a0001c0001t0004g0136 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2566-13026T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57653442 | |||||||
| chr13:57653611 | G | A | 5 | a0001c0001t0002g0283 a0001c0001t0003g0280 a0001c0001t0003g0282 others(2): Show |
5 | HG01109.hp2 HG01361.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.2566-12857G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57653611 | |||||||
| chr13:57653618 | G | T | 1 | a0001c0001t0011g0020 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2566-12850G>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57653618 | |||||||
| chr13:57654202 | A | T | 164 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0058 others(161): Show |
168 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.2566-12266A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57654202 | |||||||
| chr13:57654319 | A | G | 1 | a0001c0001t0001g0158 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2566-12149A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57654319 | |||||||
| chr13:57654361 | A | G | 10 | a0001c0001t0001g0289 a0001c0001t0002g0185 a0001c0001t0002g0250 others(7): Show |
10 | HG00544.hp1 HG00597.hp1 NA18945.hp2 others(7): Show |
intron_variant | MODIFIER | c.2566-12107A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57654361 | |||||||
| chr13:57654401 | GT | G | 30 | a0001c0001t0001g0105 a0001c0001t0001g0138 a0001c0001t0002g0103 others(27): Show |
30 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.2566-12057delT | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57654401 | ||||||
| chr13:57654401 | GTT | G | 25 | a0001c0001t0001g0003 a0001c0001t0001g0101 a0001c0001t0001g0102 others(22): Show |
25 | HG00323.hp1 HG01081.hp2 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.2566-12058_2566-12 others(8): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57654401 | ||||||
| chr13:57654660 | C | T | 19 | a0001c0001t0001g0011 a0001c0001t0001g0063 a0001c0001t0001g0064 others(16): Show |
19 | HG00639.hp2 HG01106.hp1 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.2566-11808C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57654660 | |||||||
| chr13:57654936 | T | C | 236 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(233): Show |
240 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.2566-11532T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57654936 | |||||||
| chr13:57654982 | GTTGGGGA others(9): Show |
G | 1 | a0001c0001t0017g0204 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.2566-11483_2566-11 others(22): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57654982 | ||||||
| chr13:57655211 | G | GC | 217 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(214): Show |
221 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.2566-11257_2566-11 others(7): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57655211 | |||||||
| chr13:57655426 | A | G | 2 | a0001c0001t0034g0246 a0001c0001t0035g0062 |
2 | HG02257.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2566-11042A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57655426 | |||||||
| chr13:57655826 | G | A | 1 | a0001c0001t0023g0229 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2566-10642G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57655826 | |||||||
| chr13:57655868 | T | TA | 256 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(253): Show |
260 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.2566-10593dupA | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57655868 | ||||||
| chr13:57656079 | GA | G | 55 | a0001c0001t0001g0008 a0001c0001t0001g0218 a0001c0001t0001g0253 others(52): Show |
55 | HG00280.hp1 HG00544.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.2566-10381delA | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57656079 | ||||||
| chr13:57656089 | G | A | 55 | a0001c0001t0001g0008 a0001c0001t0001g0218 a0001c0001t0001g0253 others(52): Show |
55 | HG00280.hp1 HG00544.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.2566-10379G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57656089 | |||||||
| chr13:57656347 | G | A | 1 | a0001c0001t0034g0246 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2566-10121G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57656347 | |||||||
| chr13:57656440 | T | C | 51 | a0001c0001t0001g0003 a0001c0001t0001g0101 a0001c0001t0001g0102 others(48): Show |
51 | HG00323.hp1 HG01081.hp2 HG01099.hp2 others(48): Show |
intron_variant | MODIFIER | c.2566-10028T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57656440 | |||||||
| chr13:57656562 | G | A | 1 | a0002c0015t0003g0039 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2566-9906G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57656562 | |||||||
| chr13:57656890 | A | C | 164 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0058 others(161): Show |
168 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.2566-9578A>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57656890 | |||||||
| chr13:57657139 | G | A | 2 | a0001c0001t0001g0159 a0001c0001t0002g0174 |
2 | NA19002.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.2566-9329G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57657139 | |||||||
| chr13:57657185 | A | C | 2 | a0001c0001t0034g0246 a0001c0001t0035g0062 |
2 | HG02257.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2566-9283A>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57657185 | |||||||
| chr13:57657452 | A | T | 1 | a0001c0001t0034g0246 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2566-9016A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57657452 | |||||||
| chr13:57657470 | TTA | T | 4 | a0001c0001t0001g0058 a0001c0001t0018g0061 a0001c0004t0005g0059 others(1): Show |
4 | HG02055.hp2 HG02257.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.2566-8996_2566-899 others(6): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57657470 | ||||||
| chr13:57657524 | A | G | 1 | a0001c0001t0002g0075 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2566-8944A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57657524 | |||||||
| chr13:57657642 | T | C | 1 | a0001c0001t0017g0180 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2566-8826T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57657642 | |||||||
| chr13:57657678 | G | C | 2 | a0001c0001t0001g0105 a0001c0001t0002g0104 |
2 | HG02486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2566-8790G>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57657678 | |||||||
| chr13:57657811 | T | G | 3 | a0001c0001t0006g0057 a0001c0001t0008g0002 a0001c0001t0008g0033 |
4 | HG02148.hp2 NA18949.hp2 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.2566-8657T>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57657811 | |||||||
| chr13:57658300 | G | A | 1 | a0001c0005t0028g0037 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2566-8168G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57658300 | |||||||
| chr13:57658355 | G | C | 3 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0021g0078 |
3 | HG02735.hp1 HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.2566-8113G>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57658355 | |||||||
| chr13:57658426 | C | A | 1 | a0001c0001t0002g0009 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2566-8042C>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57658426 | |||||||
| chr13:57658640 | G | A | 25 | a0001c0001t0001g0003 a0001c0001t0001g0101 a0001c0001t0001g0102 others(22): Show |
25 | HG00323.hp1 HG01081.hp2 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.2566-7828G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57658640 | |||||||
| chr13:57658764 | G | GTTTGT | 26 | a0001c0001t0001g0003 a0001c0001t0001g0058 a0001c0001t0001g0089 others(23): Show |
26 | HG00597.hp1 HG01109.hp1 HG01255.hp1 others(23): Show |
intron_variant | MODIFIER | c.2566-7674_2566-767 others(9): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57658764 | ||||||
| chr13:57658764 | G | GTTTGTTT others(3): Show |
4 | a0001c0001t0001g0110 a0001c0001t0001g0113 a0001c0001t0005g0124 others(1): Show |
4 | HG02257.hp2 HG02280.hp2 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.2566-7679_2566-767 others(14): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57658764 | ||||||
| chr13:57658764 | G | GTTTGTTT others(8): Show |
37 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0105 others(34): Show |
37 | HG00323.hp1 HG01081.hp2 HG01099.hp2 others(34): Show |
intron_variant | MODIFIER | c.2566-7684_2566-767 others(19): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57658764 | ||||||
| chr13:57658764 | G | GTTTGTTT others(13): Show |
8 | a0001c0001t0001g0138 a0001c0001t0002g0103 a0001c0001t0002g0108 others(5): Show |
8 | HG01243.hp1 HG01975.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.2566-7689_2566-767 others(24): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57658764 | ||||||
| chr13:57658764 | G | GTTTGTTT others(18): Show |
1 | a0001c0001t0004g0112 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2566-7694_2566-767 others(29): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57658764 | ||||||
| chr13:57658883 | G | A | 1 | a0001c0001t0018g0061 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2566-7585G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57658883 | |||||||
| chr13:57658911 | C | T | 1 | a0001c0001t0003g0071 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2566-7557C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57658911 | |||||||
| chr13:57659021 | A | T | 2 | a0001c0004t0005g0059 a0001c0004t0005g0060 |
2 | HG02257.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.2566-7447A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57659021 | |||||||
| chr13:57659103 | T | TTG | 13 | a0001c0001t0001g0058 a0001c0001t0002g0006 a0001c0001t0002g0010 others(10): Show |
14 | HG00741.hp2 HG01192.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.2566-7337_2566-733 others(6): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57659103 | ||||||
| chr13:57659103 | T | TTGTG | 11 | a0001c0001t0002g0009 a0001c0001t0002g0066 a0001c0001t0002g0181 others(8): Show |
11 | HG00738.hp1 HG00741.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.2566-7339_2566-733 others(8): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57659103 | ||||||
| chr13:57659103 | T | TTGTGTG | 70 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0085 others(67): Show |
73 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.2566-7341_2566-733 others(10): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57659103 | ||||||
| chr13:57659103 | T | TTGTGTGT others(1): Show |
40 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0082 others(37): Show |
40 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.2566-7343_2566-733 others(12): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57659103 | ||||||
| chr13:57659103 | T | TTGTGTGT others(3): Show |
39 | a0001c0001t0001g0008 a0001c0001t0001g0218 a0001c0001t0001g0253 others(36): Show |
39 | HG00280.hp1 HG00544.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.2566-7345_2566-733 others(14): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57659103 | ||||||
| chr13:57659103 | T | TTGTGTGT others(5): Show |
2 | a0001c0001t0022g0290 a0001c0001t0048g0277 |
2 | NA18971.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2566-7347_2566-733 others(16): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57659103 | ||||||
| chr13:57659103 | T | TTGTGTGT others(7): Show |
1 | a0001c0001t0003g0282 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2566-7349_2566-733 others(18): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57659103 | ||||||
| chr13:57659103 | TTG | T | 4 | a0001c0001t0002g0086 a0001c0001t0002g0283 a0001c0001t0011g0020 others(1): Show |
4 | HG01109.hp1 HG03239.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.2566-7337_2566-733 others(6): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57659103 | ||||||
| chr13:57659103 | TTGTGTG | T | 4 | a0001c0001t0015g0013 a0001c0001t0015g0015 a0001c0001t0015g0016 others(1): Show |
4 | HG02572.hp2 HG02615.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.2566-7341_2566-733 others(10): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57659103 | ||||||
| chr13:57659131 | G | A | 1 | a0001c0001t0004g0302 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2566-7337G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57659131 | |||||||
| chr13:57659131 | G | GTA | 7 | a0001c0001t0001g0138 a0001c0001t0002g0103 a0001c0001t0002g0108 others(4): Show |
7 | HG02723.hp1 HG02809.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.2566-7334_2566-733 others(6): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57659131 | ||||||
| chr13:57659131 | G | GTGTA | 39 | a0001c0001t0001g0003 a0001c0001t0001g0101 a0001c0001t0001g0102 others(36): Show |
39 | HG00323.hp1 HG01081.hp2 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.2566-7336_2566-733 others(8): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57659131 | ||||||
| chr13:57659131 | G | GTGTGTA | 4 | a0001c0001t0001g0105 a0001c0001t0002g0104 a0001c0001t0002g0115 others(1): Show |
4 | HG02280.hp1 HG02486.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2566-7336_2566-733 others(10): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57659131 | ||||||
| chr13:57659167 | A | G | 21 | a0001c0001t0001g0089 a0001c0001t0002g0073 a0001c0001t0002g0086 others(18): Show |
21 | HG01109.hp1 HG01255.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.2566-7301A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57659167 | |||||||
| chr13:57659188 | T | C | 20 | a0001c0001t0001g0011 a0001c0001t0001g0063 a0001c0001t0001g0064 others(17): Show |
20 | HG00140.hp2 HG00639.hp2 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.2566-7280T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57659188 | |||||||
| chr13:57659633 | C | G | 2 | a0001c0001t0034g0246 a0001c0001t0035g0062 |
2 | HG02257.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2566-6835C>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57659633 | |||||||
| chr13:57659897 | G | A | 4 | a0001c0001t0001g0058 a0001c0001t0018g0061 a0001c0004t0005g0059 others(1): Show |
4 | HG02055.hp2 HG02257.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.2566-6571G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57659897 | |||||||
| chr13:57659961 | G | A | 22 | a0001c0001t0001g0089 a0001c0001t0002g0073 a0001c0001t0002g0086 others(19): Show |
22 | HG01109.hp1 HG01255.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.2566-6507G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57659961 | |||||||
| chr13:57659961 | G | C | 1 | a0001c0002t0049g0209 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2566-6507G>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57659961 | |||||||
| chr13:57660030 | C | T | 236 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(233): Show |
240 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.2566-6438C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57660030 | |||||||
| chr13:57660092 | A | C | 40 | a0001c0001t0001g0007 a0001c0001t0001g0192 a0001c0001t0001g0207 others(37): Show |
42 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.2566-6376A>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57660092 | |||||||
| chr13:57660251 | T | TA | 21 | a0001c0001t0001g0089 a0001c0001t0002g0073 a0001c0001t0002g0086 others(18): Show |
21 | HG01109.hp1 HG01255.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.2566-6213dupA | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57660251 | ||||||
| chr13:57660369 | G | A | 1 | a0001c0001t0008g0033 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2566-6099G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57660369 | |||||||
| chr13:57660396 | T | G | 1 | a0001c0001t0001g0058 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2566-6072T>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57660396 | |||||||
| chr13:57661064 | C | T | 1 | a0001c0001t0014g0171 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2566-5404C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57661064 | |||||||
| chr13:57661065 | G | A | 1 | a0001c0001t0001g0089 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.2566-5403G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57661065 | |||||||
| chr13:57661069 | G | A | 100 | a0001c0001t0001g0007 a0001c0001t0001g0149 a0001c0001t0001g0153 others(97): Show |
104 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.2566-5399G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57661069 | |||||||
| chr13:57661368 | T | C | 1 | a0001c0001t0002g0103 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2566-5100T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57661368 | |||||||
| chr13:57661466 | T | C | 1 | a0001c0001t0039g0279 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2566-5002T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57661466 | |||||||
| chr13:57661579 | T | A | 2 | a0001c0001t0002g0073 a0001c0001t0053g0074 |
2 | NA18943.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.2566-4889T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57661579 | |||||||
| chr13:57661587 | T | A | 53 | a0001c0001t0001g0003 a0001c0001t0001g0101 a0001c0001t0001g0102 others(50): Show |
53 | HG00323.hp1 HG01081.hp2 HG01099.hp2 others(50): Show |
intron_variant | MODIFIER | c.2566-4881T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57661587 | |||||||
| chr13:57661658 | A | G | 1 | a0001c0001t0003g0245 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2566-4810A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57661658 | |||||||
| chr13:57661812 | C | T | 236 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(233): Show |
240 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.2566-4656C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57661812 | |||||||
| chr13:57661845 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2566-4623G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57661845 | |||||||
| chr13:57661876 | G | A | 53 | a0001c0001t0001g0008 a0001c0001t0001g0218 a0001c0001t0001g0253 others(50): Show |
53 | HG00280.hp1 HG00544.hp1 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.2566-4592G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57661876 | |||||||
| chr13:57661894 | G | A | 1 | a0001c0001t0004g0302 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2566-4574G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57661894 | |||||||
| chr13:57661903 | T | C | 1 | a0001c0001t0004g0266 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.2566-4565T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57661903 | |||||||
| chr13:57661963 | G | A | 21 | a0001c0001t0001g0089 a0001c0001t0002g0073 a0001c0001t0002g0086 others(18): Show |
21 | HG01109.hp1 HG01255.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.2566-4505G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57661963 | |||||||
| chr13:57662194 | G | A | 1 | a0001c0001t0002g0115 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2566-4274G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57662194 | |||||||
| chr13:57662359 | A | G | 2 | a0001c0001t0002g0009 a0001c0001t0002g0010 |
2 | HG03130.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2566-4109A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57662359 | |||||||
| chr13:57662574 | CACAA | C | 53 | a0001c0001t0001g0008 a0001c0001t0001g0218 a0001c0001t0001g0253 others(50): Show |
53 | HG00280.hp1 HG00544.hp1 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.2566-3890_2566-388 others(8): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57662574 | ||||||
| chr13:57662761 | A | G | 108 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0149 others(105): Show |
112 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.2566-3707A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57662761 | |||||||
| chr13:57662878 | T | C | 3 | a0001c0001t0003g0187 a0001c0001t0003g0191 a0003c0014t0006g0184 |
3 | HG00323.hp2 HG01069.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.2566-3590T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57662878 | |||||||
| chr13:57662960 | C | T | 236 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(233): Show |
240 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.2566-3508C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57662960 | |||||||
| chr13:57663002 | A | T | 2 | a0001c0001t0002g0009 a0001c0001t0002g0010 |
2 | HG03130.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2566-3466A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57663002 | |||||||
| chr13:57663101 | A | T | 1 | a0001c0001t0029g0053 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2566-3367A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57663101 | |||||||
| chr13:57663381 | G | A | 19 | a0001c0001t0001g0011 a0001c0001t0001g0063 a0001c0001t0001g0064 others(16): Show |
19 | HG00639.hp2 HG01106.hp1 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.2566-3087G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57663381 | |||||||
| chr13:57663517 | T | C | 4 | a0001c0001t0001g0058 a0001c0001t0018g0061 a0001c0004t0005g0059 others(1): Show |
4 | HG02055.hp2 HG02257.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.2566-2951T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57663517 | |||||||
| chr13:57663605 | G | A | 1 | a0001c0001t0013g0018 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2566-2863G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57663605 | |||||||
| chr13:57663963 | G | T | 1 | a0001c0001t0052g0220 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2566-2505G>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57663963 | |||||||
| chr13:57664087 | A | G | 1 | a0001c0001t0011g0299 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.2566-2381A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57664087 | |||||||
| chr13:57664283 | C | G | 54 | a0001c0001t0001g0008 a0001c0001t0001g0218 a0001c0001t0001g0253 others(51): Show |
54 | HG00280.hp1 HG00544.hp1 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.2566-2185C>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57664283 | |||||||
| chr13:57664325 | A | G | 1 | a0001c0003t0002g0272 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2566-2143A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57664325 | |||||||
| chr13:57664408 | C | G | 1 | a0001c0003t0002g0272 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2566-2060C>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57664408 | |||||||
| chr13:57664411 | A | G | 1 | a0001c0001t0022g0197 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2566-2057A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57664411 | |||||||
| chr13:57664726 | A | G | 56 | a0001c0001t0001g0003 a0001c0001t0001g0101 a0001c0001t0001g0102 others(53): Show |
56 | HG00323.hp1 HG01081.hp2 HG01099.hp2 others(53): Show |
intron_variant | MODIFIER | c.2566-1742A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57664726 | |||||||
| chr13:57664818 | A | T | 1 | a0001c0001t0006g0094 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2566-1650A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57664818 | |||||||
| chr13:57664965 | T | C | 1 | a0001c0001t0010g0239 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2566-1503T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57664965 | |||||||
| chr13:57665113 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2566-1355G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57665113 | |||||||
| chr13:57665146 | A | T | 2 | a0001c0001t0012g0032 a0001c0001t0012g0045 |
2 | NA18942.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.2566-1322A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57665146 | |||||||
| chr13:57665172 | T | TG | 47 | a0001c0001t0001g0003 a0001c0001t0001g0101 a0001c0001t0001g0102 others(44): Show |
47 | HG00323.hp1 HG01081.hp2 HG01099.hp2 others(44): Show |
intron_variant | MODIFIER | c.2566-1288dupG | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57665172 | ||||||
| chr13:57665206 | C | CACTT | 218 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(215): Show |
222 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.2566-1260_2566-125 others(8): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 57665206 | ||||||
| chr13:57665265 | G | GA | 260 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(257): Show |
264 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.2566-1203_2566-120 others(5): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57665265 | |||||||
| chr13:57665339 | C | T | 1 | a0001c0001t0018g0179 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2566-1129C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57665339 | |||||||
| chr13:57665555 | C | T | 53 | a0001c0001t0001g0008 a0001c0001t0001g0218 a0001c0001t0001g0253 others(50): Show |
53 | HG00280.hp1 HG00544.hp1 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.2566-913C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57665555 | |||||||
| chr13:57665762 | A | G | 5 | a0001c0001t0036g0211 a0001c0002t0001g0198 a0001c0002t0005g0206 others(2): Show |
5 | HG02486.hp1 HG02723.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.2566-706A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57665762 | |||||||
| chr13:57665879 | G | C | 218 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(215): Show |
222 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.2566-589G>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 1/3 | chr13 | 57665879 | |||||||
| chr13:57667052 | C | T | 237 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(234): Show |
241 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.2797+219C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57667052 | |||||||
| chr13:57667086 | T | C | 19 | a0001c0001t0001g0011 a0001c0001t0001g0063 a0001c0001t0001g0064 others(16): Show |
19 | HG00140.hp2 HG00639.hp2 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.2797+253T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57667086 | |||||||
| chr13:57667108 | T | C | 1 | a0001c0001t0004g0114 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2797+275T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57667108 | |||||||
| chr13:57667514 | A | G | 2 | a0001c0001t0034g0246 a0001c0001t0035g0062 |
2 | HG02257.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2797+681A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57667514 | |||||||
| chr13:57667554 | G | A | 1 | a0001c0001t0002g0092 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2797+721G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57667554 | |||||||
| chr13:57667687 | A | G | 1 | a0001c0001t0001g0113 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.2797+854A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57667687 | |||||||
| chr13:57667769 | TTA | T | 258 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(255): Show |
262 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.2797+945_2797+946d others(4): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57667769 | ||||||
| chr13:57667812 | G | A | 1 | a0001c0001t0002g0236 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2797+979G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57667812 | |||||||
| chr13:57667880 | CTTAT | C | 97 | a0001c0001t0001g0007 a0001c0001t0001g0149 a0001c0001t0001g0153 others(94): Show |
101 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.2797+1052_2797+105 others(8): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57667880 | ||||||
| chr13:57667895 | T | A | 2 | a0001c0001t0002g0100 a0001c0001t0008g0044 |
2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.2797+1062T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57667895 | |||||||
| chr13:57667900 | A | T | 1 | a0001c0001t0013g0030 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2797+1067A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57667900 | |||||||
| chr13:57668022 | G | C | 1 | a0001c0001t0001g0058 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2797+1189G>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57668022 | |||||||
| chr13:57668167 | G | T | 1 | a0001c0001t0013g0018 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2797+1334G>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57668167 | |||||||
| chr13:57668331 | G | A | 1 | a0001c0001t0003g0221 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2797+1498G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57668331 | |||||||
| chr13:57668404 | T | C | 27 | a0001c0001t0001g0003 a0001c0001t0001g0101 a0001c0001t0001g0102 others(24): Show |
27 | HG00323.hp1 HG01081.hp2 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.2797+1571T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57668404 | |||||||
| chr13:57668566 | A | T | 216 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(213): Show |
220 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.2797+1733A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57668566 | |||||||
| chr13:57668801 | A | G | 1 | a0001c0001t0002g0146 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2797+1968A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57668801 | |||||||
| chr13:57668998 | C | T | 1 | a0001c0001t0002g0009 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2797+2165C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57668998 | |||||||
| chr13:57669016 | G | A | 2 | a0001c0001t0002g0096 a0001c0001t0002g0098 |
2 | HG02630.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.2797+2183G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57669016 | |||||||
| chr13:57669388 | T | C | 1 | a0001c0001t0044g0238 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2797+2555T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57669388 | |||||||
| chr13:57669434 | G | A | 266 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(263): Show |
270 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.2797+2601G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57669434 | |||||||
| chr13:57669753 | A | G | 1 | a0001c0001t0002g0100 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2797+2920A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57669753 | |||||||
| chr13:57670332 | C | T | 4 | a0001c0001t0001g0058 a0001c0001t0018g0061 a0001c0004t0005g0059 others(1): Show |
4 | HG02055.hp2 HG02257.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.2797+3499C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57670332 | |||||||
| chr13:57670350 | T | C | 1 | a0001c0001t0007g0156 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2797+3517T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57670350 | |||||||
| chr13:57670745 | T | C | 1 | a0001c0001t0002g0115 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2797+3912T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57670745 | |||||||
| chr13:57670869 | G | A | 1 | a0001c0001t0002g0219 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.2797+4036G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57670869 | |||||||
| chr13:57671007 | G | T | 1 | a0001c0001t0002g0300 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2797+4174G>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57671007 | |||||||
| chr13:57671017 | C | A | 150 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0149 others(147): Show |
154 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.2797+4184C>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57671017 | |||||||
| chr13:57671041 | C | G | 4 | a0001c0001t0001g0058 a0001c0001t0018g0061 a0001c0004t0005g0059 others(1): Show |
4 | HG02055.hp2 HG02257.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.2797+4208C>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57671041 | |||||||
| chr13:57671048 | T | C | 1 | a0001c0001t0001g0048 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2797+4215T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57671048 | |||||||
| chr13:57671087 | C | G | 27 | a0001c0001t0001g0003 a0001c0001t0001g0101 a0001c0001t0001g0102 others(24): Show |
27 | HG00323.hp1 HG01081.hp2 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.2797+4254C>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57671087 | |||||||
| chr13:57671267 | T | C | 54 | a0001c0001t0001g0003 a0001c0001t0001g0101 a0001c0001t0001g0102 others(51): Show |
54 | HG00323.hp1 HG01081.hp2 HG01099.hp2 others(51): Show |
intron_variant | MODIFIER | c.2797+4434T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57671267 | |||||||
| chr13:57671394 | A | G | 2 | a0001c0001t0002g0009 a0001c0001t0002g0010 |
2 | HG03130.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2797+4561A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57671394 | |||||||
| chr13:57671544 | A | G | 54 | a0001c0001t0001g0003 a0001c0001t0001g0101 a0001c0001t0001g0102 others(51): Show |
54 | HG00323.hp1 HG01081.hp2 HG01099.hp2 others(51): Show |
intron_variant | MODIFIER | c.2797+4711A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57671544 | |||||||
| chr13:57671820 | G | A | 4 | a0001c0001t0001g0058 a0001c0001t0018g0061 a0001c0004t0005g0059 others(1): Show |
4 | HG02055.hp2 HG02257.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.2797+4987G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57671820 | |||||||
| chr13:57671878 | C | T | 260 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(257): Show |
264 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.2797+5045C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57671878 | |||||||
| chr13:57672027 | C | T | 2 | a0001c0001t0034g0246 a0001c0001t0035g0062 |
2 | HG02257.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2797+5194C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57672027 | |||||||
| chr13:57672028 | T | G | 1 | a0001c0001t0007g0200 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2797+5195T>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57672028 | |||||||
| chr13:57672338 | T | C | 1 | a0001c0001t0011g0019 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2797+5505T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57672338 | |||||||
| chr13:57672346 | G | A | 1 | a0001c0001t0007g0234 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.2797+5513G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57672346 | |||||||
| chr13:57672670 | C | T | 1 | a0001c0001t0018g0179 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2797+5837C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57672670 | |||||||
| chr13:57672846 | G | A | 54 | a0001c0001t0001g0008 a0001c0001t0001g0218 a0001c0001t0001g0253 others(51): Show |
54 | HG00280.hp1 HG00544.hp1 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.2797+6013G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57672846 | |||||||
| chr13:57672868 | A | G | 4 | a0001c0001t0015g0013 a0001c0001t0015g0015 a0001c0001t0015g0016 others(1): Show |
4 | HG02572.hp2 HG02615.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.2797+6035A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57672868 | |||||||
| chr13:57672909 | T | C | 1 | a0001c0001t0002g0115 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2797+6076T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57672909 | |||||||
| chr13:57673140 | G | T | 96 | a0001c0001t0001g0007 a0001c0001t0001g0149 a0001c0001t0001g0153 others(93): Show |
100 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.2797+6307G>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57673140 | |||||||
| chr13:57673313 | C | T | 1 | a0001c0001t0002g0075 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2797+6480C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57673313 | |||||||
| chr13:57673381 | G | C | 2 | a0001c0001t0004g0175 a0001c0011t0001g0235 |
2 | NA18992.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.2797+6548G>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57673381 | |||||||
| chr13:57673502 | C | T | 52 | a0001c0001t0001g0003 a0001c0001t0001g0101 a0001c0001t0001g0102 others(49): Show |
52 | HG00323.hp1 HG01099.hp2 HG01123.hp1 others(49): Show |
intron_variant | MODIFIER | c.2797+6669C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57673502 | |||||||
| chr13:57673620 | T | C | 22 | a0001c0001t0001g0089 a0001c0001t0002g0073 a0001c0001t0002g0086 others(19): Show |
22 | HG01109.hp1 HG01255.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.2797+6787T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57673620 | |||||||
| chr13:57673710 | G | T | 50 | a0001c0001t0001g0003 a0001c0001t0001g0101 a0001c0001t0001g0102 others(47): Show |
50 | HG00323.hp1 HG01099.hp2 HG01123.hp1 others(47): Show |
intron_variant | MODIFIER | c.2797+6877G>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57673710 | |||||||
| chr13:57673762 | T | C | 1 | a0001c0001t0018g0061 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2797+6929T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57673762 | |||||||
| chr13:57673830 | T | C | 54 | a0001c0001t0001g0218 a0001c0001t0001g0253 a0001c0001t0001g0254 others(51): Show |
54 | HG00280.hp1 HG00544.hp1 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.2797+6997T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57673830 | |||||||
| chr13:57673883 | ATCTCGGT others(8): Show |
A | 32 | a0001c0001t0001g0058 a0001c0001t0001g0105 a0001c0001t0001g0138 others(29): Show |
32 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.2797+7054_2797+706 others(19): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57673883 | ||||||
| chr13:57673990 | A | C | 142 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(139): Show |
147 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.2797+7157A>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57673990 | |||||||
| chr13:57674034 | A | C | 1 | a0001c0001t0002g0219 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.2797+7201A>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57674034 | |||||||
| chr13:57674288 | G | A | 3 | a0001c0001t0015g0013 a0001c0001t0015g0015 a0001c0001t0037g0014 |
3 | HG02572.hp2 HG02615.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2797+7455G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57674288 | |||||||
| chr13:57674458 | G | A | 7 | a0001c0001t0002g0092 a0001c0001t0002g0096 a0001c0001t0002g0098 others(4): Show |
7 | HG01255.hp1 HG01891.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.2797+7625G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57674458 | |||||||
| chr13:57674488 | C | T | 1 | a0001c0003t0002g0272 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2797+7655C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57674488 | |||||||
| chr13:57674598 | G | A | 117 | a0001c0001t0001g0008 a0001c0001t0001g0048 a0001c0001t0001g0058 others(114): Show |
119 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(116): Show |
intron_variant | MODIFIER | c.2797+7765G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57674598 | |||||||
| chr13:57674655 | C | T | 44 | a0001c0001t0001g0003 a0001c0001t0001g0085 a0001c0001t0001g0102 others(41): Show |
44 | HG01099.hp2 HG01109.hp2 HG01175.hp2 others(41): Show |
intron_variant | MODIFIER | c.2797+7822C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57674655 | |||||||
| chr13:57674681 | A | G | 1 | a0001c0012t0001g0088 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2797+7848A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57674681 | |||||||
| chr13:57674903 | G | A | 2 | a0001c0001t0007g0111 a0001c0001t0054g0224 |
2 | HG00323.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.2797+8070G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57674903 | |||||||
| chr13:57675293 | C | T | 1 | a0001c0001t0002g0293 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2797+8460C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57675293 | |||||||
| chr13:57675296 | A | G | 18 | a0001c0001t0002g0278 a0001c0001t0006g0017 a0001c0001t0006g0077 others(15): Show |
18 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.2797+8463A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57675296 | |||||||
| chr13:57675339 | A | G | 1 | a0001c0001t0004g0135 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2797+8506A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57675339 | |||||||
| chr13:57675396 | G | A | 2 | a0001c0001t0001g0155 a0001c0001t0021g0152 |
2 | HG00738.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.2797+8563G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57675396 | |||||||
| chr13:57675723 | G | C | 17 | a0001c0001t0002g0278 a0001c0001t0006g0017 a0001c0001t0006g0077 others(14): Show |
17 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.2797+8890G>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57675723 | |||||||
| chr13:57676086 | AT | A | 3 | a0001c0001t0004g0168 a0001c0001t0004g0230 a0001c0005t0028g0037 |
3 | HG02083.hp1 HG02135.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.2797+9255delT | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57676086 | ||||||
| chr13:57676100 | T | C | 1 | a0001c0001t0001g0011 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2797+9267T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57676100 | |||||||
| chr13:57676188 | TG | T | 110 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(107): Show |
111 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.2797+9357delG | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57676188 | ||||||
| chr13:57676930 | C | T | 1 | a0001c0012t0001g0088 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2797+10097C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57676930 | |||||||
| chr13:57677306 | T | C | 2 | a0001c0001t0018g0061 a0001c0001t0018g0179 |
2 | HG02055.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2797+10473T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57677306 | |||||||
| chr13:57677461 | C | A | 3 | a0001c0001t0024g0201 a0001c0001t0026g0247 a0006c0008t0045g0281 |
3 | NA18992.hp1 NA19004.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.2797+10628C>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57677461 | |||||||
| chr13:57677575 | G | A | 2 | a0001c0001t0002g0006 a0001c0001t0003g0221 |
3 | HG00741.hp2 HG01192.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.2797+10742G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57677575 | |||||||
| chr13:57677763 | A | C | 2 | a0001c0001t0018g0061 a0001c0001t0018g0179 |
2 | HG02055.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2797+10930A>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57677763 | |||||||
| chr13:57677853 | C | T | 126 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
127 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.2797+11020C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57677853 | |||||||
| chr13:57678144 | C | CAT | 60 | a0001c0001t0002g0066 a0001c0001t0002g0092 a0001c0001t0002g0096 others(57): Show |
61 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.2797+11328_2797+11 others(8): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57678144 | ||||||
| chr13:57678144 | C | CATAT | 19 | a0001c0001t0002g0278 a0001c0001t0006g0017 a0001c0001t0006g0057 others(16): Show |
19 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.2797+11326_2797+11 others(10): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57678144 | ||||||
| chr13:57678444 | G | A | 1 | a0003c0014t0006g0184 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.2797+11611G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57678444 | |||||||
| chr13:57678667 | G | A | 260 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(257): Show |
265 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.2797+11834G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57678667 | |||||||
| chr13:57678808 | A | T | 1 | a0001c0001t0014g0171 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2797+11975A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57678808 | |||||||
| chr13:57678823 | T | A | 1 | a0001c0001t0025g0183 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.2797+11990T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57678823 | |||||||
| chr13:57678933 | C | T | 2 | a0001c0001t0006g0077 a0001c0001t0006g0080 |
2 | NA19010.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.2797+12100C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57678933 | |||||||
| chr13:57678935 | T | A | 2 | a0001c0001t0006g0077 a0001c0001t0006g0080 |
2 | NA19010.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.2797+12102T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57678935 | |||||||
| chr13:57679279 | G | A | 1 | a0001c0001t0043g0087 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2797+12446G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57679279 | |||||||
| chr13:57679283 | A | G | 1 | a0001c0001t0002g0278 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2797+12450A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57679283 | |||||||
| chr13:57679320 | C | T | 1 | a0001c0001t0004g0081 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2797+12487C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57679320 | |||||||
| chr13:57679360 | CA | C | 199 | a0001c0001t0001g0008 a0001c0001t0001g0058 a0001c0001t0001g0063 others(196): Show |
203 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.2797+12539delA | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57679360 | ||||||
| chr13:57679360 | CAA | C | 43 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(40): Show |
44 | HG00597.hp2 HG01074.hp2 HG01169.hp1 others(41): Show |
intron_variant | MODIFIER | c.2797+12538_2797+12 others(8): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57679360 | ||||||
| chr13:57679487 | A | G | 3 | a0001c0001t0004g0168 a0001c0001t0004g0230 a0001c0005t0028g0037 |
3 | HG02083.hp1 HG02135.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.2797+12654A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57679487 | |||||||
| chr13:57679508 | A | G | 1 | a0001c0001t0023g0229 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2797+12675A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57679508 | |||||||
| chr13:57679599 | C | T | 2 | a0001c0001t0004g0230 a0001c0005t0028g0037 |
2 | HG02083.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.2797+12766C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57679599 | |||||||
| chr13:57679733 | T | A | 8 | a0001c0001t0001g0192 a0001c0001t0003g0012 a0001c0001t0007g0084 others(5): Show |
8 | HG00323.hp1 HG00558.hp1 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.2797+12900T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57679733 | |||||||
| chr13:57679822 | A | G | 2 | a0001c0001t0007g0233 a0001c0001t0007g0234 |
2 | NA18998.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.2797+12989A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57679822 | |||||||
| chr13:57679843 | G | A | 1 | a0001c0001t0002g0278 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2797+13010G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57679843 | |||||||
| chr13:57679962 | T | G | 11 | a0001c0001t0001g0058 a0001c0001t0001g0102 a0001c0001t0004g0302 others(8): Show |
11 | HG01943.hp2 HG02258.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.2797+13129T>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57679962 | |||||||
| chr13:57680003 | A | T | 1 | a0001c0001t0001g0149 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2797+13170A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57680003 | |||||||
| chr13:57680139 | C | CAT | 57 | a0001c0001t0002g0066 a0001c0001t0002g0092 a0001c0001t0002g0096 others(54): Show |
58 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.2797+13320_2797+13 others(8): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57680139 | ||||||
| chr13:57680178 | A | G | 3 | a0001c0001t0001g0138 a0001c0001t0010g0097 a0001c0001t0010g0294 |
3 | HG01255.hp1 HG03041.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2797+13345A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57680178 | |||||||
| chr13:57680206 | A | G | 1 | a0001c0001t0022g0290 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2797+13373A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57680206 | |||||||
| chr13:57680254 | G | T | 1 | a0001c0003t0002g0257 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.2797+13421G>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57680254 | |||||||
| chr13:57680446 | G | A | 42 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(39): Show |
43 | HG00597.hp2 HG01074.hp2 HG01169.hp1 others(40): Show |
intron_variant | MODIFIER | c.2797+13613G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57680446 | |||||||
| chr13:57680496 | T | C | 71 | a0001c0001t0002g0006 a0001c0001t0002g0073 a0001c0001t0002g0118 others(68): Show |
74 | HG00673.hp2 HG00741.hp2 HG01069.hp2 others(71): Show |
intron_variant | MODIFIER | c.2797+13663T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57680496 | |||||||
| chr13:57680554 | C | A | 8 | a0001c0001t0001g0192 a0001c0001t0003g0012 a0001c0001t0007g0084 others(5): Show |
8 | HG00323.hp1 HG00558.hp1 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.2797+13721C>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57680554 | |||||||
| chr13:57680561 | A | G | 1 | a0001c0001t0040g0106 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2797+13728A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57680561 | |||||||
| chr13:57680639 | A | C | 58 | a0001c0001t0001g0008 a0001c0001t0001g0063 a0001c0001t0001g0064 others(55): Show |
58 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.2797+13806A>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57680639 | |||||||
| chr13:57680767 | A | T | 5 | a0001c0001t0002g0104 a0001c0001t0002g0147 a0001c0001t0037g0014 others(2): Show |
5 | HG02257.hp1 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2797+13934A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57680767 | |||||||
| chr13:57680975 | T | A | 19 | a0001c0001t0002g0278 a0001c0001t0006g0017 a0001c0001t0006g0057 others(16): Show |
19 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.2797+14142T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57680975 | |||||||
| chr13:57681041 | G | A | 2 | a0001c0001t0002g0225 a0001c0001t0005g0270 |
2 | NA18988.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.2797+14208G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57681041 | |||||||
| chr13:57681130 | G | A | 1 | a0001c0001t0015g0016 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2797+14297G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57681130 | |||||||
| chr13:57681870 | G | A | 1 | a0001c0001t0003g0282 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2797+15037G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57681870 | |||||||
| chr13:57681944 | G | A | 2 | a0001c0001t0005g0124 a0001c0001t0005g0125 |
2 | HG02280.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2797+15111G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57681944 | |||||||
| chr13:57682257 | G | A | 6 | a0001c0001t0002g0104 a0001c0001t0002g0147 a0001c0001t0037g0014 others(3): Show |
6 | HG02257.hp1 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.2797+15424G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57682257 | |||||||
| chr13:57682346 | A | G | 1 | a0001c0001t0001g0105 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2797+15513A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57682346 | |||||||
| chr13:57682627 | G | A | 1 | a0001c0001t0010g0239 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2797+15794G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57682627 | |||||||
| chr13:57682646 | G | A | 1 | a0001c0001t0006g0217 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2797+15813G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57682646 | |||||||
| chr13:57682746 | C | T | 3 | a0001c0001t0001g0138 a0001c0001t0010g0097 a0001c0001t0010g0294 |
3 | HG01255.hp1 HG03041.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2797+15913C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57682746 | |||||||
| chr13:57682827 | C | T | 1 | a0001c0001t0002g0133 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2797+15994C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57682827 | |||||||
| chr13:57682893 | T | C | 18 | a0001c0001t0006g0017 a0001c0001t0006g0057 a0001c0001t0006g0077 others(15): Show |
18 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.2797+16060T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57682893 | |||||||
| chr13:57683031 | C | T | 243 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(240): Show |
248 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.2797+16198C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57683031 | |||||||
| chr13:57683131 | A | G | 57 | a0001c0001t0002g0066 a0001c0001t0002g0092 a0001c0001t0002g0096 others(54): Show |
58 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.2797+16298A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57683131 | |||||||
| chr13:57683180 | A | G | 1 | a0001c0001t0001g0048 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2797+16347A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57683180 | |||||||
| chr13:57683281 | A | G | 19 | a0001c0001t0002g0278 a0001c0001t0006g0017 a0001c0001t0006g0057 others(16): Show |
19 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.2797+16448A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57683281 | |||||||
| chr13:57683293 | C | T | 108 | a0001c0001t0002g0006 a0001c0001t0002g0066 a0001c0001t0002g0073 others(105): Show |
111 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.2797+16460C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57683293 | |||||||
| chr13:57683384 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2797+16551G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57683384 | |||||||
| chr13:57683422 | C | G | 18 | a0001c0001t0006g0017 a0001c0001t0006g0057 a0001c0001t0006g0077 others(15): Show |
18 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.2797+16589C>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57683422 | |||||||
| chr13:57683533 | T | A | 262 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(259): Show |
267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.2797+16700T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57683533 | |||||||
| chr13:57683645 | C | T | 1 | a0001c0001t0043g0087 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2797+16812C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57683645 | |||||||
| chr13:57683686 | C | T | 1 | a0001c0001t0001g0159 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.2797+16853C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57683686 | |||||||
| chr13:57683687 | G | A | 6 | a0001c0001t0002g0104 a0001c0001t0002g0147 a0001c0001t0037g0014 others(3): Show |
6 | HG02257.hp1 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.2797+16854G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57683687 | |||||||
| chr13:57683717 | C | T | 1 | a0001c0001t0002g0010 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2797+16884C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57683717 | |||||||
| chr13:57683777 | C | T | 18 | a0001c0001t0006g0017 a0001c0001t0006g0057 a0001c0001t0006g0077 others(15): Show |
18 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.2797+16944C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57683777 | |||||||
| chr13:57683823 | C | T | 18 | a0001c0001t0006g0017 a0001c0001t0006g0057 a0001c0001t0006g0077 others(15): Show |
18 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.2797+16990C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57683823 | |||||||
| chr13:57683878 | A | G | 1 | a0001c0001t0015g0016 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2797+17045A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57683878 | |||||||
| chr13:57683960 | G | A | 106 | a0001c0001t0002g0006 a0001c0001t0002g0066 a0001c0001t0002g0073 others(103): Show |
109 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(106): Show |
intron_variant | MODIFIER | c.2797+17127G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57683960 | |||||||
| chr13:57683962 | A | C | 1 | a0001c0001t0006g0077 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2797+17129A>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57683962 | |||||||
| chr13:57683995 | AG | A | 18 | a0001c0001t0006g0017 a0001c0001t0006g0057 a0001c0001t0006g0077 others(15): Show |
18 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.2797+17166delG | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57683995 | ||||||
| chr13:57684014 | G | A | 18 | a0001c0001t0006g0017 a0001c0001t0006g0057 a0001c0001t0006g0077 others(15): Show |
18 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.2797+17181G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57684014 | |||||||
| chr13:57684086 | C | T | 1 | a0001c0001t0036g0211 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2797+17253C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57684086 | |||||||
| chr13:57684333 | A | T | 3 | a0001c0001t0002g0300 a0001c0001t0041g0095 a0001c0001t0043g0087 |
3 | HG02572.hp1 HG02897.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2797+17500A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57684333 | |||||||
| chr13:57684335 | C | A | 3 | a0001c0001t0002g0300 a0001c0001t0041g0095 a0001c0001t0043g0087 |
3 | HG02572.hp1 HG02897.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2797+17502C>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57684335 | |||||||
| chr13:57684566 | A | G | 18 | a0001c0001t0006g0017 a0001c0001t0006g0057 a0001c0001t0006g0077 others(15): Show |
18 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.2797+17733A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57684566 | |||||||
| chr13:57684638 | T | G | 3 | a0001c0001t0004g0099 a0001c0001t0005g0141 a0001c0001t0042g0296 |
3 | HG01891.hp2 HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2797+17805T>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57684638 | |||||||
| chr13:57685084 | G | C | 2 | a0001c0001t0002g0010 a0001c0001t0002g0236 |
2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2797+18251G>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57685084 | |||||||
| chr13:57685141 | G | C | 1 | a0001c0001t0025g0183 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.2797+18308G>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57685141 | |||||||
| chr13:57685358 | C | A | 152 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(149): Show |
153 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.2797+18525C>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57685358 | |||||||
| chr13:57686031 | G | A | 8 | a0001c0001t0001g0192 a0001c0001t0003g0012 a0001c0001t0007g0084 others(5): Show |
8 | HG00323.hp1 HG00558.hp1 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.2797+19198G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57686031 | |||||||
| chr13:57686090 | G | GA | 36 | a0001c0001t0002g0066 a0001c0001t0002g0119 a0001c0001t0002g0120 others(33): Show |
37 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.2797+19267dupA | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57686090 | ||||||
| chr13:57686145 | A | G | 110 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(107): Show |
111 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.2797+19312A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57686145 | |||||||
| chr13:57686298 | C | G | 8 | a0001c0001t0001g0058 a0001c0001t0004g0302 a0001c0001t0005g0107 others(5): Show |
8 | HG02258.hp2 HG02280.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.2797+19465C>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57686298 | |||||||
| chr13:57686302 | C | T | 18 | a0001c0001t0006g0017 a0001c0001t0006g0057 a0001c0001t0006g0077 others(15): Show |
18 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.2797+19469C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57686302 | |||||||
| chr13:57686436 | T | C | 1 | a0001c0001t0005g0126 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2797+19603T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57686436 | |||||||
| chr13:57686594 | A | C | 3 | a0001c0001t0001g0138 a0001c0001t0010g0097 a0001c0001t0010g0294 |
3 | HG01255.hp1 HG03041.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2797+19761A>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57686594 | |||||||
| chr13:57686614 | C | T | 2 | a0001c0001t0002g0010 a0001c0001t0002g0236 |
2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2797+19781C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57686614 | |||||||
| chr13:57686707 | A | G | 1 | a0005c0009t0007g0258 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2797+19874A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57686707 | |||||||
| chr13:57686896 | G | A | 20 | a0001c0001t0002g0092 a0001c0001t0002g0096 a0001c0001t0002g0098 others(17): Show |
20 | HG01496.hp1 HG01891.hp1 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.2797+20063G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57686896 | |||||||
| chr13:57686957 | G | A | 1 | a0001c0001t0003g0282 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2797+20124G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57686957 | |||||||
| chr13:57687070 | A | G | 2 | a0001c0001t0018g0061 a0001c0001t0018g0179 |
2 | HG02055.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2797+20237A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57687070 | |||||||
| chr13:57687109 | C | T | 5 | a0001c0001t0006g0057 a0001c0001t0006g0093 a0001c0001t0006g0094 others(2): Show |
5 | NA18948.hp2 NA18959.hp2 NA18980.hp2 others(2): Show |
intron_variant | MODIFIER | c.2797+20276C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57687109 | |||||||
| chr13:57687431 | A | G | 1 | a0001c0001t0008g0023 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2797+20598A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57687431 | |||||||
| chr13:57687525 | T | C | 1 | a0002c0015t0003g0039 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2797+20692T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57687525 | |||||||
| chr13:57687551 | T | A | 2 | a0001c0001t0007g0233 a0001c0001t0007g0234 |
2 | NA18998.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.2797+20718T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57687551 | |||||||
| chr13:57687783 | A | G | 262 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(259): Show |
267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.2797+20950A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57687783 | |||||||
| chr13:57687833 | T | C | 5 | a0001c0001t0013g0018 a0001c0001t0034g0246 a0001c0001t0036g0211 others(2): Show |
5 | HG02257.hp2 HG02486.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.2797+21000T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57687833 | |||||||
| chr13:57687872 | A | T | 2 | a0001c0001t0002g0010 a0001c0001t0002g0236 |
2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2797+21039A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57687872 | |||||||
| chr13:57687888 | G | C | 1 | a0001c0001t0002g0148 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2797+21055G>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57687888 | |||||||
| chr13:57687892 | C | T | 2 | a0001c0001t0018g0061 a0001c0001t0018g0179 |
2 | HG02055.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2797+21059C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57687892 | |||||||
| chr13:57687942 | C | G | 2 | a0001c0001t0002g0010 a0001c0001t0002g0236 |
2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2797+21109C>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57687942 | |||||||
| chr13:57687956 | T | C | 18 | a0001c0001t0001g0192 a0001c0001t0002g0009 a0001c0001t0002g0010 others(15): Show |
18 | HG00323.hp1 HG00558.hp1 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.2797+21123T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57687956 | |||||||
| chr13:57687982 | G | C | 6 | a0001c0001t0002g0104 a0001c0001t0002g0147 a0001c0001t0037g0014 others(3): Show |
6 | HG02257.hp1 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.2797+21149G>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57687982 | |||||||
| chr13:57688182 | C | G | 2 | a0001c0001t0018g0061 a0001c0001t0018g0179 |
2 | HG02055.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2797+21349C>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57688182 | |||||||
| chr13:57688351 | T | C | 1 | a0001c0001t0030g0036 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2797+21518T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57688351 | |||||||
| chr13:57688505 | C | A | 2 | a0001c0001t0018g0061 a0001c0001t0018g0179 |
2 | HG02055.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2797+21672C>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57688505 | |||||||
| chr13:57688811 | A | G | 19 | a0001c0001t0002g0278 a0001c0001t0006g0017 a0001c0001t0006g0057 others(16): Show |
19 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.2797+21978A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57688811 | |||||||
| chr13:57688860 | A | G | 9 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0075 others(6): Show |
9 | HG01109.hp1 HG01884.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.2797+22027A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57688860 | |||||||
| chr13:57688879 | A | G | 5 | a0001c0001t0002g0104 a0001c0001t0002g0147 a0001c0001t0037g0014 others(2): Show |
5 | HG02257.hp1 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2797+22046A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57688879 | |||||||
| chr13:57689013 | A | T | 1 | a0001c0001t0001g0164 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2797+22180A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57689013 | |||||||
| chr13:57689056 | G | C | 52 | a0001c0001t0002g0006 a0001c0001t0002g0073 a0001c0001t0002g0118 others(49): Show |
55 | HG00673.hp2 HG00741.hp2 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.2797+22223G>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57689056 | |||||||
| chr13:57689063 | C | T | 1 | a0001c0001t0016g0271 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2797+22230C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57689063 | |||||||
| chr13:57689070 | T | G | 1 | a0001c0001t0010g0239 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2797+22237T>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57689070 | |||||||
| chr13:57689156 | A | G | 88 | a0001c0001t0002g0006 a0001c0001t0002g0066 a0001c0001t0002g0073 others(85): Show |
92 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.2797+22323A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57689156 | |||||||
| chr13:57689200 | A | C | 1 | a0001c0001t0056g0056 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.2797+22367A>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57689200 | |||||||
| chr13:57689328 | G | A | 52 | a0001c0001t0002g0006 a0001c0001t0002g0073 a0001c0001t0002g0118 others(49): Show |
55 | HG00673.hp2 HG00741.hp2 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.2797+22495G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57689328 | |||||||
| chr13:57689357 | C | T | 1 | a0001c0001t0002g0236 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2797+22524C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57689357 | |||||||
| chr13:57689430 | G | T | 1 | a0001c0001t0044g0238 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2797+22597G>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57689430 | |||||||
| chr13:57689468 | T | A | 6 | a0001c0001t0002g0104 a0001c0001t0002g0147 a0001c0001t0037g0014 others(3): Show |
6 | HG02257.hp1 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.2797+22635T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57689468 | |||||||
| chr13:57689673 | A | G | 1 | a0001c0001t0002g0075 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2797+22840A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57689673 | |||||||
| chr13:57689868 | A | T | 2 | a0001c0001t0007g0233 a0001c0001t0007g0234 |
2 | NA18998.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.2797+23035A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57689868 | |||||||
| chr13:57689881 | T | C | 2 | a0001c0001t0018g0061 a0001c0001t0018g0179 |
2 | HG02055.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2797+23048T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57689881 | |||||||
| chr13:57689926 | T | C | 19 | a0001c0001t0002g0278 a0001c0001t0006g0017 a0001c0001t0006g0057 others(16): Show |
19 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.2797+23093T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57689926 | |||||||
| chr13:57689994 | G | A | 2 | a0001c0001t0018g0061 a0001c0001t0018g0179 |
2 | HG02055.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2797+23161G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57689994 | |||||||
| chr13:57690087 | A | C | 55 | a0001c0001t0002g0066 a0001c0001t0002g0092 a0001c0001t0002g0096 others(52): Show |
56 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.2797+23254A>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57690087 | |||||||
| chr13:57690116 | A | ATT | 19 | a0001c0001t0002g0278 a0001c0001t0006g0017 a0001c0001t0006g0057 others(16): Show |
19 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.2797+23284_2797+23 others(8): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57690116 | ||||||
| chr13:57690118 | A | C | 19 | a0001c0001t0002g0278 a0001c0001t0006g0017 a0001c0001t0006g0057 others(16): Show |
19 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.2797+23285A>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57690118 | |||||||
| chr13:57690329 | T | C | 128 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(125): Show |
129 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.2797+23496T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57690329 | |||||||
| chr13:57690373 | A | G | 1 | a0001c0001t0006g0240 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2797+23540A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57690373 | |||||||
| chr13:57690451 | T | G | 2 | a0001c0001t0002g0073 a0001c0001t0002g0118 |
2 | NA18943.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.2797+23618T>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57690451 | |||||||
| chr13:57690475 | G | C | 2 | a0001c0001t0005g0107 a0001c0001t0005g0142 |
2 | HG02615.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2797+23642G>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57690475 | |||||||
| chr13:57690545 | T | C | 261 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(258): Show |
266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.2797+23712T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57690545 | |||||||
| chr13:57690591 | C | A | 19 | a0001c0001t0002g0278 a0001c0001t0006g0017 a0001c0001t0006g0057 others(16): Show |
19 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.2797+23758C>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57690591 | |||||||
| chr13:57690618 | C | T | 2 | a0001c0001t0018g0061 a0001c0001t0018g0179 |
2 | HG02055.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2797+23785C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57690618 | |||||||
| chr13:57690845 | G | A | 18 | a0001c0001t0006g0017 a0001c0001t0006g0057 a0001c0001t0006g0077 others(15): Show |
18 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.2797+24012G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57690845 | |||||||
| chr13:57690927 | T | G | 18 | a0001c0001t0006g0017 a0001c0001t0006g0057 a0001c0001t0006g0077 others(15): Show |
18 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.2797+24094T>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57690927 | |||||||
| chr13:57690950 | T | A | 18 | a0001c0001t0006g0017 a0001c0001t0006g0057 a0001c0001t0006g0077 others(15): Show |
18 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.2797+24117T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57690950 | |||||||
| chr13:57690972 | T | C | 1 | a0001c0001t0002g0185 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2797+24139T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57690972 | |||||||
| chr13:57691272 | A | G | 1 | a0001c0001t0016g0271 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2797+24439A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57691272 | |||||||
| chr13:57691301 | T | G | 1 | a0001c0001t0025g0183 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.2797+24468T>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57691301 | |||||||
| chr13:57691462 | G | A | 261 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(258): Show |
266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.2797+24629G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57691462 | |||||||
| chr13:57691786 | T | C | 18 | a0001c0001t0006g0017 a0001c0001t0006g0057 a0001c0001t0006g0077 others(15): Show |
18 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.2797+24953T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57691786 | |||||||
| chr13:57691843 | T | C | 2 | a0001c0001t0018g0061 a0001c0001t0018g0179 |
2 | HG02055.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2797+25010T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57691843 | |||||||
| chr13:57692042 | T | G | 1 | a0001c0001t0008g0044 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2797+25209T>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57692042 | |||||||
| chr13:57692088 | C | T | 243 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(240): Show |
248 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.2797+25255C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57692088 | |||||||
| chr13:57692188 | G | A | 7 | a0001c0001t0002g0104 a0001c0001t0002g0147 a0001c0001t0034g0246 others(4): Show |
7 | HG02257.hp1 HG02257.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.2797+25355G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57692188 | |||||||
| chr13:57692347 | T | A | 9 | a0001c0001t0001g0192 a0001c0001t0002g0278 a0001c0001t0003g0012 others(6): Show |
9 | HG00323.hp1 HG00558.hp1 HG00735.hp1 others(6): Show |
intron_variant | MODIFIER | c.2797+25514T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57692347 | |||||||
| chr13:57692406 | C | G | 1 | a0001c0001t0004g0302 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2797+25573C>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57692406 | |||||||
| chr13:57692480 | C | G | 35 | a0001c0001t0002g0066 a0001c0001t0002g0119 a0001c0001t0002g0120 others(32): Show |
36 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.2797+25647C>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57692480 | |||||||
| chr13:57692527 | A | G | 16 | a0001c0001t0002g0092 a0001c0001t0002g0096 a0001c0001t0002g0098 others(13): Show |
16 | HG01891.hp1 HG02280.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.2797+25694A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57692527 | |||||||
| chr13:57692554 | G | T | 18 | a0001c0001t0006g0017 a0001c0001t0006g0057 a0001c0001t0006g0077 others(15): Show |
18 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.2797+25721G>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57692554 | |||||||
| chr13:57692700 | A | T | 2 | a0001c0001t0007g0084 a0001c0001t0007g0156 |
2 | HG00558.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.2797+25867A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57692700 | |||||||
| chr13:57692738 | T | G | 1 | a0001c0001t0043g0087 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2797+25905T>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57692738 | |||||||
| chr13:57692809 | G | A | 19 | a0001c0001t0002g0278 a0001c0001t0006g0017 a0001c0001t0006g0057 others(16): Show |
19 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.2797+25976G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57692809 | |||||||
| chr13:57692937 | A | G | 1 | a0001c0001t0044g0238 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2797+26104A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57692937 | |||||||
| chr13:57693023 | C | A | 19 | a0001c0001t0002g0278 a0001c0001t0006g0017 a0001c0001t0006g0057 others(16): Show |
19 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.2797+26190C>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57693023 | |||||||
| chr13:57693141 | A | T | 57 | a0001c0001t0001g0003 a0001c0001t0002g0066 a0001c0001t0002g0092 others(54): Show |
58 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.2797+26308A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57693141 | |||||||
| chr13:57693143 | G | A | 18 | a0001c0001t0006g0017 a0001c0001t0006g0057 a0001c0001t0006g0077 others(15): Show |
18 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.2797+26310G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57693143 | |||||||
| chr13:57693186 | A | G | 5 | a0001c0001t0003g0068 a0001c0001t0003g0069 a0001c0001t0003g0070 others(2): Show |
5 | HG01256.hp2 HG01943.hp1 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.2797+26353A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57693186 | |||||||
| chr13:57693214 | CT | C | 300 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(297): Show |
305 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.2797+26391delT | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57693214 | ||||||
| chr13:57693229 | T | C | 3 | a0001c0001t0004g0099 a0001c0001t0005g0141 a0001c0001t0042g0296 |
3 | HG01891.hp2 HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2797+26396T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57693229 | |||||||
| chr13:57693277 | A | G | 2 | a0001c0001t0018g0061 a0001c0001t0018g0179 |
2 | HG02055.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2797+26444A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57693277 | |||||||
| chr13:57693278 | A | T | 2 | a0001c0001t0004g0175 a0001c0001t0012g0032 |
2 | NA19011.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.2797+26445A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57693278 | |||||||
| chr13:57693279 | T | A | 18 | a0001c0001t0006g0017 a0001c0001t0006g0057 a0001c0001t0006g0077 others(15): Show |
18 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.2797+26446T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57693279 | |||||||
| chr13:57693295 | T | C | 4 | a0001c0001t0001g0058 a0001c0001t0001g0102 a0001c0001t0010g0239 others(1): Show |
4 | HG01943.hp2 HG02258.hp2 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.2797+26462T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57693295 | |||||||
| chr13:57693307 | C | T | 4 | a0001c0001t0001g0058 a0001c0001t0001g0102 a0001c0001t0010g0239 others(1): Show |
4 | HG01943.hp2 HG02258.hp2 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.2797+26474C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57693307 | |||||||
| chr13:57693315 | C | CAT | 13 | a0001c0001t0001g0169 a0001c0001t0001g0189 a0001c0001t0001g0192 others(10): Show |
13 | HG00639.hp1 HG00735.hp1 HG01123.hp2 others(10): Show |
intron_variant | MODIFIER | c.2797+26511_2797+26 others(8): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57693315 | ||||||
| chr13:57693315 | C | CATAT | 6 | a0001c0001t0001g0173 a0001c0001t0002g0278 a0001c0001t0011g0019 others(3): Show |
6 | HG00280.hp1 HG01243.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.2797+26509_2797+26 others(10): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57693315 | ||||||
| chr13:57693315 | C | CATATAT | 8 | a0001c0001t0001g0063 a0001c0001t0001g0161 a0001c0001t0002g0146 others(5): Show |
8 | HG00639.hp2 HG01255.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.2797+26507_2797+26 others(12): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57693315 | ||||||
| chr13:57693315 | C | CATATATA others(1): Show |
19 | a0001c0001t0001g0003 a0001c0001t0002g0143 a0001c0001t0002g0242 others(16): Show |
19 | HG01109.hp2 HG01496.hp1 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.2797+26505_2797+26 others(14): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57693315 | ||||||
| chr13:57693315 | C | CATATATA others(3): Show |
14 | a0001c0001t0002g0006 a0001c0001t0002g0119 a0001c0001t0002g0127 others(11): Show |
16 | HG00741.hp2 HG01192.hp2 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.2797+26503_2797+26 others(16): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57693315 | ||||||
| chr13:57693315 | C | CATATATA others(5): Show |
16 | a0001c0001t0002g0096 a0001c0001t0002g0115 a0001c0001t0002g0118 others(13): Show |
16 | HG00673.hp2 HG01993.hp1 HG02074.hp2 others(13): Show |
intron_variant | MODIFIER | c.2797+26501_2797+26 others(18): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57693315 | ||||||
| chr13:57693315 | C | CATATATA others(7): Show |
19 | a0001c0001t0002g0066 a0001c0001t0002g0073 a0001c0001t0002g0098 others(16): Show |
19 | HG01074.hp1 HG01081.hp2 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.2797+26499_2797+26 others(20): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57693315 | ||||||
| chr13:57693315 | C | CATATATA others(9): Show |
26 | a0001c0001t0002g0092 a0001c0001t0002g0120 a0001c0001t0002g0137 others(23): Show |
27 | HG01069.hp1 HG01257.hp1 HG01258.hp1 others(24): Show |
intron_variant | MODIFIER | c.2797+26497_2797+26 others(22): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57693315 | ||||||
| chr13:57693315 | C | CATATATA others(11): Show |
13 | a0001c0001t0002g0133 a0001c0001t0002g0148 a0001c0001t0002g0160 others(10): Show |
14 | HG00544.hp2 HG00621.hp2 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.2797+26495_2797+26 others(24): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57693315 | ||||||
| chr13:57693315 | C | CATATATA others(13): Show |
5 | a0001c0001t0002g0174 a0001c0001t0002g0288 a0001c0001t0002g0293 others(2): Show |
5 | HG00544.hp1 HG01099.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.2797+26493_2797+26 others(26): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57693315 | ||||||
| chr13:57693315 | C | CATATATA others(15): Show |
4 | a0001c0001t0002g0194 a0001c0001t0002g0250 a0001c0001t0007g0268 others(1): Show |
4 | HG00597.hp1 HG00735.hp2 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.2797+26491_2797+26 others(28): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57693315 | ||||||
| chr13:57693315 | C | CATATATA others(17): Show |
1 | a0001c0001t0012g0038 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2797+26489_2797+26 others(30): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57693315 | ||||||
| chr13:57693315 | CAT | C | 28 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0048 others(25): Show |
29 | HG00280.hp2 HG00597.hp2 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.2797+26511_2797+26 others(8): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57693315 | ||||||
| chr13:57693315 | CATAT | C | 11 | a0001c0001t0006g0017 a0001c0001t0006g0132 a0001c0001t0006g0186 others(8): Show |
11 | HG00140.hp2 HG01106.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.2797+26509_2797+26 others(10): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57693315 | ||||||
| chr13:57693315 | CATATAT | C | 7 | a0001c0001t0006g0057 a0001c0001t0006g0077 a0001c0001t0006g0080 others(4): Show |
7 | NA18948.hp2 NA18959.hp2 NA18980.hp2 others(4): Show |
intron_variant | MODIFIER | c.2797+26507_2797+26 others(12): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57693315 | ||||||
| chr13:57693342 | A | C | 1 | a0001c0001t0006g0132 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2797+26509A>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57693342 | |||||||
| chr13:57693476 | G | C | 2 | a0001c0004t0005g0059 a0001c0004t0005g0060 |
2 | HG02257.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.2797+26643G>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57693476 | |||||||
| chr13:57693520 | G | A | 9 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0075 others(6): Show |
9 | HG01109.hp1 HG01884.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.2797+26687G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57693520 | |||||||
| chr13:57693522 | G | A | 18 | a0001c0001t0006g0017 a0001c0001t0006g0057 a0001c0001t0006g0077 others(15): Show |
18 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.2797+26689G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57693522 | |||||||
| chr13:57693704 | A | G | 6 | a0001c0001t0002g0104 a0001c0001t0002g0147 a0001c0001t0037g0014 others(3): Show |
6 | HG02257.hp1 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.2797+26871A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57693704 | |||||||
| chr13:57693871 | G | A | 1 | a0001c0001t0001g0011 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2797+27038G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57693871 | |||||||
| chr13:57693935 | G | GTAGGTAC others(7): Show |
1 | a0001c0001t0006g0132 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2797+27103_2797+27 others(20): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57693935 | ||||||
| chr13:57693966 | G | GT | 7 | a0001c0001t0003g0252 a0001c0001t0003g0264 a0001c0001t0003g0298 others(4): Show |
7 | HG02027.hp1 HG02132.hp2 NA18967.hp2 others(4): Show |
intron_variant | MODIFIER | c.2797+27145dupT | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57693966 | ||||||
| chr13:57693988 | G | A | 52 | a0001c0001t0002g0006 a0001c0001t0002g0073 a0001c0001t0002g0118 others(49): Show |
55 | HG00673.hp2 HG00741.hp2 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.2797+27155G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57693988 | |||||||
| chr13:57694228 | A | G | 1 | a0001c0001t0056g0056 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.2797+27395A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57694228 | |||||||
| chr13:57694240 | T | G | 1 | a0001c0001t0005g0295 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2797+27407T>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57694240 | |||||||
| chr13:57694487 | A | G | 1 | a0001c0001t0009g0195 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2797+27654A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57694487 | |||||||
| chr13:57694784 | A | T | 116 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(113): Show |
117 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.2797+27951A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57694784 | |||||||
| chr13:57694818 | G | A | 1 | a0001c0001t0007g0121 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2797+27985G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57694818 | |||||||
| chr13:57694912 | T | C | 1 | a0001c0001t0001g0189 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2797+28079T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57694912 | |||||||
| chr13:57694919 | G | C | 1 | a0001c0001t0004g0241 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2797+28086G>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57694919 | |||||||
| chr13:57695040 | A | C | 1 | a0001c0001t0021g0078 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2797+28207A>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57695040 | |||||||
| chr13:57695332 | T | A | 1 | a0001c0001t0003g0245 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2797+28499T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57695332 | |||||||
| chr13:57695340 | A | G | 8 | a0001c0001t0001g0192 a0001c0001t0003g0012 a0001c0001t0007g0084 others(5): Show |
8 | HG00323.hp1 HG00558.hp1 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.2797+28507A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57695340 | |||||||
| chr13:57695366 | T | C | 5 | a0001c0001t0002g0104 a0001c0001t0002g0147 a0001c0001t0037g0014 others(2): Show |
5 | HG02257.hp1 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2797+28533T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57695366 | |||||||
| chr13:57695421 | GAGAA | G | 261 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(258): Show |
266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.2797+28614_2797+28 others(10): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57695421 | ||||||
| chr13:57695540 | T | C | 1 | a0001c0001t0011g0054 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.2797+28707T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57695540 | |||||||
| chr13:57695629 | C | T | 112 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(109): Show |
113 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.2797+28796C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57695629 | |||||||
| chr13:57695636 | C | T | 1 | a0001c0001t0003g0070 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.2797+28803C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57695636 | |||||||
| chr13:57695667 | G | T | 1 | a0001c0001t0001g0159 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.2797+28834G>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57695667 | |||||||
| chr13:57695997 | A | G | 1 | a0001c0001t0003g0071 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2798-28615A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57695997 | |||||||
| chr13:57696049 | G | A | 7 | a0001c0001t0004g0302 a0001c0001t0005g0107 a0001c0001t0005g0124 others(4): Show |
7 | HG02280.hp2 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.2798-28563G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57696049 | |||||||
| chr13:57696090 | T | C | 88 | a0001c0001t0002g0006 a0001c0001t0002g0066 a0001c0001t0002g0073 others(85): Show |
92 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.2798-28522T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57696090 | |||||||
| chr13:57696103 | A | C | 2 | a0001c0001t0006g0077 a0001c0001t0006g0080 |
2 | NA19010.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.2798-28509A>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57696103 | |||||||
| chr13:57696113 | G | A | 1 | a0001c0001t0002g0250 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2798-28499G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57696113 | |||||||
| chr13:57696138 | A | G | 1 | a0001c0001t0046g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2798-28474A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57696138 | |||||||
| chr13:57696452 | A | G | 2 | a0001c0001t0002g0225 a0001c0001t0005g0270 |
2 | NA18988.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.2798-28160A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57696452 | |||||||
| chr13:57696524 | C | T | 24 | a0001c0001t0002g0278 a0001c0001t0006g0017 a0001c0001t0006g0057 others(21): Show |
24 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.2798-28088C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57696524 | |||||||
| chr13:57696526 | C | CA | 24 | a0001c0001t0002g0278 a0001c0001t0006g0017 a0001c0001t0006g0057 others(21): Show |
24 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.2798-28078dupA | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57696526 | ||||||
| chr13:57696583 | G | A | 24 | a0001c0001t0002g0278 a0001c0001t0006g0017 a0001c0001t0006g0057 others(21): Show |
24 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.2798-28029G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57696583 | |||||||
| chr13:57696587 | C | G | 1 | a0001c0001t0043g0087 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2798-28025C>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57696587 | |||||||
| chr13:57696594 | T | C | 1 | a0001c0001t0009g0024 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2798-28018T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57696594 | |||||||
| chr13:57696602 | A | G | 15 | a0001c0001t0002g0066 a0001c0001t0002g0181 a0001c0001t0002g0196 others(12): Show |
16 | HG00735.hp2 HG00738.hp1 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.2798-28010A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57696602 | |||||||
| chr13:57696633 | A | G | 1 | a0001c0001t0044g0238 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2798-27979A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57696633 | |||||||
| chr13:57696681 | A | G | 2 | a0001c0001t0002g0006 a0001c0001t0003g0221 |
3 | HG00741.hp2 HG01192.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.2798-27931A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57696681 | |||||||
| chr13:57696722 | C | T | 7 | a0001c0001t0004g0302 a0001c0001t0005g0107 a0001c0001t0005g0124 others(4): Show |
7 | HG02280.hp2 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.2798-27890C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57696722 | |||||||
| chr13:57696870 | A | G | 24 | a0001c0001t0002g0278 a0001c0001t0006g0017 a0001c0001t0006g0057 others(21): Show |
24 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.2798-27742A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57696870 | |||||||
| chr13:57697048 | A | G | 2 | a0001c0001t0024g0201 a0001c0001t0026g0247 |
2 | NA19004.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.2798-27564A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57697048 | |||||||
| chr13:57697192 | G | C | 7 | a0001c0001t0004g0302 a0001c0001t0005g0107 a0001c0001t0005g0124 others(4): Show |
7 | HG02280.hp2 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.2798-27420G>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57697192 | |||||||
| chr13:57697218 | A | T | 262 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(259): Show |
267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.2798-27394A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57697218 | |||||||
| chr13:57697245 | T | G | 1 | a0001c0001t0002g0148 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2798-27367T>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57697245 | |||||||
| chr13:57697327 | A | G | 1 | a0001c0001t0003g0245 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2798-27285A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57697327 | |||||||
| chr13:57697485 | T | G | 2 | a0001c0001t0018g0061 a0001c0001t0018g0179 |
2 | HG02055.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2798-27127T>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57697485 | |||||||
| chr13:57697495 | A | G | 9 | a0001c0001t0006g0017 a0001c0001t0006g0186 a0001c0001t0006g0216 others(6): Show |
9 | HG00140.hp2 HG01069.hp2 HG01978.hp2 others(6): Show |
intron_variant | MODIFIER | c.2798-27117A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57697495 | |||||||
| chr13:57697591 | T | TCTC | 24 | a0001c0001t0002g0278 a0001c0001t0006g0017 a0001c0001t0006g0057 others(21): Show |
24 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.2798-27019_2798-27 others(9): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57697591 | ||||||
| chr13:57697594 | G | T | 2 | a0001c0001t0018g0061 a0001c0001t0018g0179 |
2 | HG02055.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2798-27018G>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57697594 | |||||||
| chr13:57697726 | A | C | 24 | a0001c0001t0002g0278 a0001c0001t0006g0017 a0001c0001t0006g0057 others(21): Show |
24 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.2798-26886A>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57697726 | |||||||
| chr13:57697774 | AT | A | 6 | a0001c0001t0002g0104 a0001c0001t0002g0147 a0001c0001t0037g0014 others(3): Show |
6 | HG02257.hp1 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.2798-26826delT | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57697774 | ||||||
| chr13:57697850 | G | A | 24 | a0001c0001t0002g0278 a0001c0001t0006g0017 a0001c0001t0006g0057 others(21): Show |
24 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.2798-26762G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57697850 | |||||||
| chr13:57697862 | C | T | 1 | a0006c0008t0045g0281 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.2798-26750C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57697862 | |||||||
| chr13:57697936 | C | A | 126 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
127 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.2798-26676C>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57697936 | |||||||
| chr13:57697980 | C | T | 24 | a0001c0001t0002g0278 a0001c0001t0006g0017 a0001c0001t0006g0057 others(21): Show |
24 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.2798-26632C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57697980 | |||||||
| chr13:57698035 | A | G | 24 | a0001c0001t0002g0278 a0001c0001t0006g0017 a0001c0001t0006g0057 others(21): Show |
24 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.2798-26577A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57698035 | |||||||
| chr13:57698287 | A | T | 259 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(256): Show |
264 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.2798-26325A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57698287 | |||||||
| chr13:57698686 | AC | A | 148 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(145): Show |
149 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.2798-25925delC | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57698686 | |||||||
| chr13:57698708 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2798-25904G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57698708 | |||||||
| chr13:57698927 | A | G | 24 | a0001c0001t0002g0278 a0001c0001t0006g0017 a0001c0001t0006g0057 others(21): Show |
24 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.2798-25685A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57698927 | |||||||
| chr13:57698970 | G | C | 24 | a0001c0001t0002g0278 a0001c0001t0006g0017 a0001c0001t0006g0057 others(21): Show |
24 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.2798-25642G>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57698970 | |||||||
| chr13:57698971 | C | A | 1 | a0001c0001t0046g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2798-25641C>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57698971 | |||||||
| chr13:57699075 | C | CTTTT | 24 | a0001c0001t0002g0278 a0001c0001t0006g0017 a0001c0001t0006g0057 others(21): Show |
24 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.2798-25537_2798-25 others(10): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57699075 | |||||||
| chr13:57699076 | A | G | 24 | a0001c0001t0002g0278 a0001c0001t0006g0017 a0001c0001t0006g0057 others(21): Show |
24 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.2798-25536A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57699076 | |||||||
| chr13:57699078 | T | C | 24 | a0001c0001t0002g0278 a0001c0001t0006g0017 a0001c0001t0006g0057 others(21): Show |
24 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.2798-25534T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57699078 | |||||||
| chr13:57699087 | T | C | 1 | a0001c0001t0011g0020 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2798-25525T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57699087 | |||||||
| chr13:57699152 | T | G | 24 | a0001c0001t0002g0278 a0001c0001t0006g0017 a0001c0001t0006g0057 others(21): Show |
24 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.2798-25460T>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57699152 | |||||||
| chr13:57699249 | A | G | 1 | a0001c0001t0002g0009 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2798-25363A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57699249 | |||||||
| chr13:57699270 | G | A | 24 | a0001c0001t0002g0278 a0001c0001t0006g0017 a0001c0001t0006g0057 others(21): Show |
24 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.2798-25342G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57699270 | |||||||
| chr13:57699413 | G | A | 1 | a0001c0001t0044g0238 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2798-25199G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57699413 | |||||||
| chr13:57699434 | A | G | 1 | a0001c0001t0003g0280 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2798-25178A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57699434 | |||||||
| chr13:57699603 | G | A | 24 | a0001c0001t0002g0278 a0001c0001t0006g0017 a0001c0001t0006g0057 others(21): Show |
24 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.2798-25009G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57699603 | |||||||
| chr13:57699666 | T | A | 25 | a0001c0001t0002g0278 a0001c0001t0006g0017 a0001c0001t0006g0057 others(22): Show |
25 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.2798-24946T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57699666 | |||||||
| chr13:57699699 | T | C | 2 | a0001c0001t0003g0256 a0001c0001t0008g0049 |
2 | HG00621.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.2798-24913T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57699699 | |||||||
| chr13:57699743 | C | G | 6 | a0001c0001t0002g0104 a0001c0001t0002g0147 a0001c0001t0037g0014 others(3): Show |
6 | HG02257.hp1 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.2798-24869C>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57699743 | |||||||
| chr13:57699751 | G | A | 24 | a0001c0001t0002g0278 a0001c0001t0006g0017 a0001c0001t0006g0057 others(21): Show |
24 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.2798-24861G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57699751 | |||||||
| chr13:57699765 | A | G | 24 | a0001c0001t0002g0278 a0001c0001t0006g0017 a0001c0001t0006g0057 others(21): Show |
24 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.2798-24847A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57699765 | |||||||
| chr13:57699779 | T | C | 24 | a0001c0001t0002g0278 a0001c0001t0006g0017 a0001c0001t0006g0057 others(21): Show |
24 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.2798-24833T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57699779 | |||||||
| chr13:57699814 | A | T | 3 | a0001c0001t0006g0186 a0001c0001t0006g0216 a0001c0001t0006g0217 |
3 | HG01978.hp2 HG01981.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.2798-24798A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57699814 | |||||||
| chr13:57700038 | T | C | 24 | a0001c0001t0002g0278 a0001c0001t0006g0017 a0001c0001t0006g0057 others(21): Show |
24 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.2798-24574T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57700038 | |||||||
| chr13:57700145 | A | G | 24 | a0001c0001t0002g0278 a0001c0001t0006g0017 a0001c0001t0006g0057 others(21): Show |
24 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.2798-24467A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57700145 | |||||||
| chr13:57700313 | C | A | 1 | a0001c0001t0003g0280 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2798-24299C>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57700313 | |||||||
| chr13:57700321 | C | CT | 13 | a0001c0001t0001g0173 a0001c0001t0003g0041 a0001c0001t0003g0187 others(10): Show |
13 | HG00323.hp2 HG01433.hp2 HG01515.hp2 others(10): Show |
intron_variant | MODIFIER | c.2798-24275dupT | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57700321 | ||||||
| chr13:57700321 | CT | C | 29 | a0001c0001t0001g0082 a0001c0001t0001g0254 a0001c0001t0002g0092 others(26): Show |
29 | HG01496.hp1 HG01891.hp1 HG01943.hp1 others(26): Show |
intron_variant | MODIFIER | c.2798-24275delT | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57700321 | ||||||
| chr13:57700379 | C | T | 150 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(147): Show |
151 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.2798-24233C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57700379 | |||||||
| chr13:57700380 | G | A | 6 | a0001c0001t0004g0081 a0001c0001t0012g0046 a0001c0001t0012g0047 others(3): Show |
6 | NA18942.hp2 NA18962.hp1 NA18993.hp1 others(3): Show |
intron_variant | MODIFIER | c.2798-24232G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57700380 | |||||||
| chr13:57700402 | A | T | 259 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(256): Show |
264 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.2798-24210A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57700402 | |||||||
| chr13:57700464 | G | A | 1 | a0001c0006t0003g0130 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2798-24148G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57700464 | |||||||
| chr13:57700466 | G | T | 2 | a0001c0001t0018g0061 a0001c0001t0018g0179 |
2 | HG02055.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2798-24146G>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57700466 | |||||||
| chr13:57700659 | T | C | 259 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(256): Show |
264 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.2798-23953T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57700659 | |||||||
| chr13:57700806 | A | G | 1 | a0001c0003t0002g0272 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2798-23806A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57700806 | |||||||
| chr13:57700909 | C | A | 259 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(256): Show |
264 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.2798-23703C>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57700909 | |||||||
| chr13:57700915 | A | G | 1 | a0001c0012t0001g0088 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2798-23697A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57700915 | |||||||
| chr13:57701004 | A | G | 88 | a0001c0001t0002g0006 a0001c0001t0002g0066 a0001c0001t0002g0073 others(85): Show |
92 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.2798-23608A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57701004 | |||||||
| chr13:57701033 | A | G | 5 | a0001c0001t0005g0139 a0001c0001t0005g0291 a0001c0001t0005g0292 others(2): Show |
5 | HG01496.hp1 HG02451.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.2798-23579A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57701033 | |||||||
| chr13:57701040 | T | C | 1 | a0001c0001t0001g0169 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2798-23572T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57701040 | |||||||
| chr13:57701267 | C | CGTTT | 5 | a0001c0001t0002g0104 a0001c0001t0002g0147 a0001c0001t0037g0014 others(2): Show |
5 | HG02257.hp1 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2798-23324_2798-23 others(10): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57701267 | ||||||
| chr13:57701539 | T | TG | 300 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(297): Show |
306 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.2798-23073_2798-23 others(7): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57701539 | |||||||
| chr13:57701652 | G | A | 3 | a0001c0001t0001g0138 a0001c0001t0010g0097 a0001c0001t0010g0294 |
3 | HG01255.hp1 HG03041.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2798-22960G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57701652 | |||||||
| chr13:57701793 | G | T | 1 | a0001c0001t0003g0287 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.2798-22819G>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57701793 | |||||||
| chr13:57701872 | T | C | 2 | a0001c0001t0002g0086 a0001c0001t0002g0100 |
2 | HG01109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2798-22740T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57701872 | |||||||
| chr13:57701925 | G | A | 1 | a0001c0001t0002g0108 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2798-22687G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57701925 | |||||||
| chr13:57702231 | G | A | 259 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(256): Show |
264 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.2798-22381G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57702231 | |||||||
| chr13:57702295 | T | C | 15 | a0001c0001t0001g0003 a0001c0001t0001g0105 a0001c0001t0002g0185 others(12): Show |
15 | HG00597.hp2 HG02027.hp2 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.2798-22317T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57702295 | |||||||
| chr13:57702447 | G | A | 3 | a0001c0001t0002g0010 a0001c0001t0002g0075 a0001c0001t0002g0236 |
3 | HG01884.hp1 HG02622.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2798-22165G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57702447 | |||||||
| chr13:57703044 | T | A | 23 | a0001c0001t0006g0017 a0001c0001t0006g0057 a0001c0001t0006g0077 others(20): Show |
23 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.2798-21568T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57703044 | |||||||
| chr13:57703172 | C | A | 259 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(256): Show |
264 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.2798-21440C>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57703172 | |||||||
| chr13:57703279 | A | T | 3 | a0001c0001t0002g0010 a0001c0001t0002g0075 a0001c0001t0002g0236 |
3 | HG01884.hp1 HG02622.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2798-21333A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57703279 | |||||||
| chr13:57703405 | G | A | 1 | a0001c0001t0007g0167 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2798-21207G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57703405 | |||||||
| chr13:57703708 | C | T | 4 | a0001c0001t0005g0107 a0001c0001t0005g0126 a0001c0001t0005g0140 others(1): Show |
4 | HG02615.hp2 HG03225.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2798-20904C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57703708 | |||||||
| chr13:57703741 | T | A | 6 | a0001c0001t0002g0009 a0001c0001t0002g0086 a0001c0001t0002g0100 others(3): Show |
6 | HG01109.hp1 HG02572.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2798-20871T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57703741 | |||||||
| chr13:57703791 | A | C | 1 | a0001c0001t0003g0187 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2798-20821A>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57703791 | |||||||
| chr13:57704087 | G | A | 259 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(256): Show |
264 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.2798-20525G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57704087 | |||||||
| chr13:57704146 | T | C | 1 | a0001c0001t0015g0016 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2798-20466T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57704146 | |||||||
| chr13:57704277 | A | T | 1 | a0001c0001t0002g0009 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2798-20335A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57704277 | |||||||
| chr13:57704337 | C | G | 1 | a0001c0001t0024g0201 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.2798-20275C>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57704337 | |||||||
| chr13:57704386 | G | T | 1 | a0001c0001t0007g0121 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2798-20226G>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57704386 | |||||||
| chr13:57704393 | A | G | 292 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(289): Show |
298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.2798-20219A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57704393 | |||||||
| chr13:57704440 | T | A | 1 | a0001c0001t0004g0112 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2798-20172T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57704440 | |||||||
| chr13:57704853 | A | T | 1 | a0001c0001t0011g0020 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2798-19759A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57704853 | |||||||
| chr13:57704896 | A | G | 1 | a0001c0001t0002g0075 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2798-19716A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57704896 | |||||||
| chr13:57705051 | C | T | 1 | a0001c0001t0001g0007 | 2 | NA18969.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.2798-19561C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57705051 | |||||||
| chr13:57705260 | G | C | 259 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(256): Show |
264 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.2798-19352G>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57705260 | |||||||
| chr13:57705654 | A | G | 68 | a0001c0001t0002g0006 a0001c0001t0002g0066 a0001c0001t0002g0073 others(65): Show |
70 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.2798-18958A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57705654 | |||||||
| chr13:57705933 | T | G | 1 | a0001c0001t0002g0300 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2798-18679T>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57705933 | |||||||
| chr13:57706010 | A | C | 259 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(256): Show |
264 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.2798-18602A>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57706010 | |||||||
| chr13:57706015 | TA | T | 12 | a0001c0001t0001g0102 a0001c0001t0001g0159 a0001c0001t0003g0068 others(9): Show |
12 | HG01069.hp1 HG01256.hp2 HG01943.hp1 others(9): Show |
intron_variant | MODIFIER | c.2798-18581delA | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57706015 | ||||||
| chr13:57706341 | C | A | 2 | a0001c0001t0018g0061 a0001c0001t0018g0179 |
2 | HG02055.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2798-18271C>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57706341 | |||||||
| chr13:57706447 | T | C | 7 | a0001c0001t0004g0302 a0001c0001t0005g0107 a0001c0001t0005g0124 others(4): Show |
7 | HG02280.hp2 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.2798-18165T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57706447 | |||||||
| chr13:57706618 | C | A | 1 | a0001c0001t0044g0238 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2798-17994C>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57706618 | |||||||
| chr13:57706751 | C | T | 86 | a0001c0001t0002g0006 a0001c0001t0002g0066 a0001c0001t0002g0073 others(83): Show |
90 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.2798-17861C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57706751 | |||||||
| chr13:57707334 | C | CGT | 28 | a0001c0001t0001g0058 a0001c0001t0001g0102 a0001c0001t0001g0116 others(25): Show |
28 | HG00323.hp1 HG00558.hp1 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.2798-17241_2798-17 others(8): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57707334 | ||||||
| chr13:57707334 | C | CGTGT | 30 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0063 others(27): Show |
30 | HG00140.hp1 HG00639.hp2 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.2798-17243_2798-17 others(10): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57707334 | ||||||
| chr13:57707334 | C | CGTGTGT | 43 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0085 others(40): Show |
44 | HG00280.hp1 HG00558.hp2 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.2798-17245_2798-17 others(12): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57707334 | ||||||
| chr13:57707334 | C | CGTGTGTG others(1): Show |
14 | a0001c0001t0001g0048 a0001c0001t0001g0169 a0001c0001t0001g0228 others(11): Show |
14 | HG00323.hp2 HG00597.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.2798-17247_2798-17 others(14): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57707334 | ||||||
| chr13:57707334 | C | CGTGTGTG others(3): Show |
2 | a0001c0001t0001g0138 a0001c0001t0010g0097 |
2 | HG01255.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2798-17249_2798-17 others(16): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57707334 | ||||||
| chr13:57707334 | C | CGTGTGTG others(5): Show |
1 | a0001c0001t0001g0254 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.2798-17251_2798-17 others(18): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57707334 | ||||||
| chr13:57707334 | CGT | C | 49 | a0001c0001t0002g0075 a0001c0001t0002g0086 a0001c0001t0002g0100 others(46): Show |
50 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(47): Show |
intron_variant | MODIFIER | c.2798-17241_2798-17 others(8): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57707334 | ||||||
| chr13:57707334 | CGTGT | C | 74 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0066 others(71): Show |
77 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.2798-17243_2798-17 others(10): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57707334 | ||||||
| chr13:57707334 | CGTGTGT | C | 16 | a0001c0001t0002g0092 a0001c0001t0002g0096 a0001c0001t0002g0098 others(13): Show |
16 | HG01891.hp1 HG02280.hp1 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.2798-17245_2798-17 others(12): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57707334 | ||||||
| chr13:57707334 | CGTGTGTG others(1): Show |
C | 6 | a0001c0001t0004g0123 a0001c0001t0005g0139 a0001c0001t0005g0291 others(3): Show |
6 | HG01496.hp1 HG02451.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.2798-17247_2798-17 others(14): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57707334 | ||||||
| chr13:57707334 | CGTGTGTG others(3): Show |
C | 1 | a0001c0001t0015g0015 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2798-17249_2798-17 others(16): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57707334 | ||||||
| chr13:57707560 | A | G | 3 | a0001c0001t0014g0004 a0001c0001t0014g0171 a0001c0001t0014g0177 |
4 | NA18939.hp1 NA18952.hp1 NA18953.hp1 others(1): Show |
intron_variant | MODIFIER | c.2798-17052A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57707560 | |||||||
| chr13:57707810 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2798-16802C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57707810 | |||||||
| chr13:57707870 | C | A | 4 | a0001c0001t0005g0107 a0001c0001t0005g0126 a0001c0001t0005g0140 others(1): Show |
4 | HG02615.hp2 HG03225.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2798-16742C>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57707870 | |||||||
| chr13:57707901 | T | A | 106 | a0001c0001t0002g0006 a0001c0001t0002g0066 a0001c0001t0002g0073 others(103): Show |
110 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(107): Show |
intron_variant | MODIFIER | c.2798-16711T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57707901 | |||||||
| chr13:57708132 | A | G | 1 | a0001c0001t0008g0023 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2798-16480A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57708132 | |||||||
| chr13:57708156 | A | G | 1 | a0001c0001t0003g0282 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2798-16456A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57708156 | |||||||
| chr13:57708306 | G | C | 1 | a0001c0001t0002g0010 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2798-16306G>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57708306 | |||||||
| chr13:57708389 | T | C | 8 | a0001c0001t0001g0192 a0001c0001t0003g0012 a0001c0001t0007g0084 others(5): Show |
8 | HG00323.hp1 HG00558.hp1 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.2798-16223T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57708389 | |||||||
| chr13:57708518 | G | C | 2 | a0001c0001t0018g0061 a0001c0001t0018g0179 |
2 | HG02055.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2798-16094G>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57708518 | |||||||
| chr13:57708578 | G | A | 114 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(111): Show |
115 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.2798-16034G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57708578 | |||||||
| chr13:57708597 | T | G | 1 | a0001c0001t0003g0282 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2798-16015T>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57708597 | |||||||
| chr13:57708832 | T | C | 95 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(92): Show |
96 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.2798-15780T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57708832 | |||||||
| chr13:57709031 | C | T | 1 | a0001c0001t0002g0185 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2798-15581C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57709031 | |||||||
| chr13:57709075 | A | T | 2 | a0001c0001t0007g0233 a0001c0001t0007g0234 |
2 | NA18998.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.2798-15537A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57709075 | |||||||
| chr13:57709110 | A | AAT | 113 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(110): Show |
114 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.2798-15489_2798-15 others(8): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57709110 | ||||||
| chr13:57709443 | T | C | 1 | a0001c0001t0003g0187 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2798-15169T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57709443 | |||||||
| chr13:57709925 | T | C | 1 | a0001c0001t0001g0110 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.2798-14687T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57709925 | |||||||
| chr13:57710251 | T | C | 1 | a0001c0001t0044g0238 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2798-14361T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57710251 | |||||||
| chr13:57710425 | A | T | 1 | a0001c0001t0024g0201 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.2798-14187A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57710425 | |||||||
| chr13:57710478 | T | A | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
97 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.2798-14134T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57710478 | |||||||
| chr13:57710554 | A | T | 20 | a0001c0001t0002g0092 a0001c0001t0002g0096 a0001c0001t0002g0098 others(17): Show |
20 | HG01496.hp1 HG01891.hp1 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.2798-14058A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57710554 | |||||||
| chr13:57710595 | A | G | 1 | a0001c0001t0046g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2798-14017A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57710595 | |||||||
| chr13:57710611 | C | G | 1 | a0001c0001t0001g0102 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2798-14001C>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57710611 | |||||||
| chr13:57710612 | G | A | 1 | a0001c0001t0009g0024 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2798-14000G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57710612 | |||||||
| chr13:57710663 | GATTGGTT others(5): Show |
G | 1 | a0001c0001t0046g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2798-13946_2798-13 others(18): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57710663 | ||||||
| chr13:57710767 | T | C | 24 | a0001c0001t0002g0278 a0001c0001t0006g0017 a0001c0001t0006g0057 others(21): Show |
24 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.2798-13845T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57710767 | |||||||
| chr13:57710889 | C | T | 1 | a0001c0001t0002g0196 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2798-13723C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57710889 | |||||||
| chr13:57710974 | A | C | 1 | a0001c0001t0006g0057 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2798-13638A>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57710974 | |||||||
| chr13:57711006 | G | C | 95 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(92): Show |
96 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.2798-13606G>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57711006 | |||||||
| chr13:57711203 | C | G | 3 | a0001c0001t0001g0138 a0001c0001t0010g0097 a0001c0001t0010g0294 |
3 | HG01255.hp1 HG03041.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2798-13409C>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57711203 | |||||||
| chr13:57711213 | C | A | 6 | a0001c0001t0002g0009 a0001c0001t0002g0086 a0001c0001t0002g0100 others(3): Show |
6 | HG01109.hp1 HG02572.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2798-13399C>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57711213 | |||||||
| chr13:57711318 | A | T | 16 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0082 others(13): Show |
16 | HG00140.hp1 HG00639.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.2798-13294A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57711318 | |||||||
| chr13:57711395 | C | T | 1 | a0001c0001t0047g0090 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2798-13217C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57711395 | |||||||
| chr13:57711664 | A | G | 1 | a0001c0001t0002g0147 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2798-12948A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57711664 | |||||||
| chr13:57711774 | GAAT | G | 23 | a0001c0001t0006g0017 a0001c0001t0006g0057 a0001c0001t0006g0077 others(20): Show |
23 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.2798-12830_2798-12 others(9): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57711774 | ||||||
| chr13:57711782 | A | G | 88 | a0001c0001t0002g0006 a0001c0001t0002g0066 a0001c0001t0002g0073 others(85): Show |
92 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.2798-12830A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57711782 | |||||||
| chr13:57711801 | A | C | 1 | a0001c0001t0024g0201 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.2798-12811A>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57711801 | |||||||
| chr13:57711851 | A | G | 68 | a0001c0001t0002g0006 a0001c0001t0002g0066 a0001c0001t0002g0073 others(65): Show |
70 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.2798-12761A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57711851 | |||||||
| chr13:57711861 | T | A | 1 | a0001c0001t0001g0169 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2798-12751T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57711861 | |||||||
| chr13:57711868 | G | A | 1 | a0001c0001t0003g0012 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2798-12744G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57711868 | |||||||
| chr13:57712015 | G | T | 1 | a0001c0003t0002g0257 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.2798-12597G>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57712015 | |||||||
| chr13:57712040 | C | T | 1 | a0001c0001t0001g0011 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2798-12572C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57712040 | |||||||
| chr13:57712521 | C | T | 1 | a0001c0001t0044g0238 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2798-12091C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57712521 | |||||||
| chr13:57712679 | A | G | 1 | a0001c0001t0004g0136 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2798-11933A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57712679 | |||||||
| chr13:57713279 | A | T | 7 | a0001c0001t0004g0302 a0001c0001t0005g0107 a0001c0001t0005g0124 others(4): Show |
7 | HG02280.hp2 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.2798-11333A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57713279 | |||||||
| chr13:57713484 | G | T | 5 | a0001c0001t0002g0225 a0001c0001t0004g0076 a0001c0001t0005g0205 others(2): Show |
5 | HG02027.hp2 NA18942.hp1 NA18988.hp2 others(2): Show |
intron_variant | MODIFIER | c.2798-11128G>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57713484 | |||||||
| chr13:57713804 | G | A | 2 | a0001c0001t0015g0013 a0001c0001t0015g0015 |
2 | HG02615.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2798-10808G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57713804 | |||||||
| chr13:57714227 | T | C | 1 | a0001c0001t0002g0236 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2798-10385T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57714227 | |||||||
| chr13:57714368 | T | C | 259 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(256): Show |
264 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.2798-10244T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57714368 | |||||||
| chr13:57714704 | G | A | 1 | a0001c0001t0002g0185 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2798-9908G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57714704 | |||||||
| chr13:57714746 | T | C | 200 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(197): Show |
205 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.2798-9866T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57714746 | |||||||
| chr13:57714788 | G | A | 7 | a0001c0001t0002g0104 a0001c0001t0002g0147 a0001c0001t0034g0246 others(4): Show |
7 | HG02257.hp1 HG02257.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.2798-9824G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57714788 | |||||||
| chr13:57714924 | A | T | 1 | a0001c0001t0002g0297 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2798-9688A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57714924 | |||||||
| chr13:57714994 | A | G | 1 | a0004c0007t0006g0193 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2798-9618A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57714994 | |||||||
| chr13:57714998 | T | C | 1 | a0001c0001t0003g0068 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.2798-9614T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57714998 | |||||||
| chr13:57715026 | G | A | 1 | a0001c0001t0004g0175 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.2798-9586G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57715026 | |||||||
| chr13:57715096 | G | A | 10 | a0001c0001t0004g0081 a0001c0001t0012g0038 a0001c0001t0012g0046 others(7): Show |
10 | NA18942.hp2 NA18962.hp1 NA18990.hp1 others(7): Show |
intron_variant | MODIFIER | c.2798-9516G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57715096 | |||||||
| chr13:57715153 | A | G | 1 | a0005c0009t0007g0258 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2798-9459A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57715153 | |||||||
| chr13:57715211 | A | G | 1 | a0001c0011t0001g0235 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.2798-9401A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57715211 | |||||||
| chr13:57715402 | GAGTGTGT others(38): Show |
G | 1 | a0001c0001t0005g0141 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2798-9206_2798-916 others(49): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57715402 | ||||||
| chr13:57715452 | T | A | 17 | a0001c0001t0001g0192 a0001c0001t0002g0009 a0001c0001t0002g0010 others(14): Show |
17 | HG00323.hp1 HG00558.hp1 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.2798-9160T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57715452 | |||||||
| chr13:57715546 | A | T | 7 | a0001c0001t0004g0302 a0001c0001t0005g0107 a0001c0001t0005g0124 others(4): Show |
7 | HG02280.hp2 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.2798-9066A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57715546 | |||||||
| chr13:57715641 | C | A | 29 | a0001c0001t0004g0302 a0001c0001t0005g0107 a0001c0001t0005g0124 others(26): Show |
29 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.2798-8971C>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57715641 | |||||||
| chr13:57715671 | T | G | 3 | a0001c0001t0004g0099 a0001c0001t0005g0141 a0001c0001t0042g0296 |
3 | HG01891.hp2 HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2798-8941T>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57715671 | |||||||
| chr13:57715910 | T | G | 3 | a0001c0001t0002g0092 a0001c0001t0002g0096 a0001c0001t0002g0098 |
3 | HG02630.hp2 HG02818.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.2798-8702T>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57715910 | |||||||
| chr13:57715947 | T | G | 5 | a0001c0001t0002g0103 a0001c0001t0002g0108 a0001c0001t0002g0133 others(2): Show |
5 | HG02622.hp2 HG02809.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.2798-8665T>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57715947 | |||||||
| chr13:57715957 | A | G | 5 | a0001c0001t0004g0099 a0001c0001t0004g0135 a0001c0001t0004g0144 others(2): Show |
5 | HG01884.hp2 HG01891.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.2798-8655A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57715957 | |||||||
| chr13:57716349 | G | A | 1 | a0001c0001t0001g0110 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.2798-8263G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57716349 | |||||||
| chr13:57716427 | T | A | 1 | a0001c0001t0030g0036 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2798-8185T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57716427 | |||||||
| chr13:57717024 | G | T | 1 | a0001c0001t0008g0023 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2798-7588G>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57717024 | |||||||
| chr13:57717097 | T | C | 1 | a0001c0001t0007g0111 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2798-7515T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57717097 | |||||||
| chr13:57717192 | A | G | 69 | a0001c0001t0002g0006 a0001c0001t0002g0066 a0001c0001t0002g0073 others(66): Show |
71 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.2798-7420A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57717192 | |||||||
| chr13:57717214 | G | A | 1 | a0001c0001t0007g0121 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2798-7398G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57717214 | |||||||
| chr13:57717487 | G | A | 260 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(257): Show |
265 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.2798-7125G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57717487 | |||||||
| chr13:57717528 | C | T | 18 | a0001c0001t0006g0017 a0001c0001t0006g0057 a0001c0001t0006g0077 others(15): Show |
18 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.2798-7084C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57717528 | |||||||
| chr13:57717564 | C | T | 7 | a0001c0001t0001g0192 a0001c0001t0003g0012 a0001c0001t0007g0084 others(4): Show |
7 | HG00323.hp1 HG00558.hp1 HG00735.hp1 others(4): Show |
intron_variant | MODIFIER | c.2798-7048C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57717564 | |||||||
| chr13:57717658 | G | A | 17 | a0001c0001t0001g0192 a0001c0001t0002g0009 a0001c0001t0002g0010 others(14): Show |
17 | HG00323.hp1 HG00558.hp1 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.2798-6954G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57717658 | |||||||
| chr13:57717661 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2798-6951G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57717661 | |||||||
| chr13:57717742 | G | A | 5 | a0001c0001t0005g0139 a0001c0001t0005g0291 a0001c0001t0005g0292 others(2): Show |
5 | HG01496.hp1 HG02451.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.2798-6870G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57717742 | |||||||
| chr13:57717772 | A | C | 1 | a0001c0001t0006g0077 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2798-6840A>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57717772 | |||||||
| chr13:57718073 | A | C | 1 | a0001c0001t0017g0180 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2798-6539A>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57718073 | |||||||
| chr13:57718146 | A | G | 2 | a0001c0001t0013g0021 a0001c0001t0013g0029 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2798-6466A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57718146 | |||||||
| chr13:57718182 | C | T | 1 | a0001c0001t0034g0246 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2798-6430C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57718182 | |||||||
| chr13:57718725 | A | G | 1 | a0001c0001t0015g0016 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2798-5887A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57718725 | |||||||
| chr13:57719037 | T | G | 2 | a0001c0001t0002g0086 a0001c0001t0002g0100 |
2 | HG01109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2798-5575T>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57719037 | |||||||
| chr13:57719153 | C | T | 1 | a0001c0001t0002g0009 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2798-5459C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57719153 | |||||||
| chr13:57719400 | T | C | 7 | a0001c0001t0001g0192 a0001c0001t0003g0012 a0001c0001t0007g0084 others(4): Show |
7 | HG00323.hp1 HG00558.hp1 HG00735.hp1 others(4): Show |
intron_variant | MODIFIER | c.2798-5212T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57719400 | |||||||
| chr13:57719475 | C | T | 4 | a0001c0001t0003g0212 a0001c0001t0003g0213 a0001c0001t0008g0001 others(1): Show |
5 | HG00738.hp1 HG01069.hp1 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.2798-5137C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57719475 | |||||||
| chr13:57719724 | A | G | 3 | a0001c0001t0001g0253 a0001c0001t0001g0255 a0001c0001t0001g0259 |
3 | NA18945.hp1 NA18984.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.2798-4888A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57719724 | |||||||
| chr13:57719863 | T | A | 3 | a0001c0001t0003g0212 a0001c0001t0003g0213 a0001c0001t0008g0001 |
4 | HG00738.hp1 HG01099.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.2798-4749T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57719863 | |||||||
| chr13:57720234 | A | C | 7 | a0001c0001t0004g0302 a0001c0001t0005g0107 a0001c0001t0005g0124 others(4): Show |
7 | HG02280.hp2 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.2798-4378A>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57720234 | |||||||
| chr13:57720239 | C | A | 2 | a0001c0001t0018g0061 a0001c0001t0018g0179 |
2 | HG02055.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2798-4373C>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57720239 | |||||||
| chr13:57720493 | T | C | 5 | a0001c0001t0002g0104 a0001c0001t0002g0147 a0001c0001t0037g0014 others(2): Show |
5 | HG02257.hp1 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2798-4119T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57720493 | |||||||
| chr13:57720495 | A | G | 21 | a0001c0001t0002g0092 a0001c0001t0002g0096 a0001c0001t0002g0098 others(18): Show |
21 | HG01243.hp2 HG01496.hp1 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.2798-4117A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57720495 | |||||||
| chr13:57720676 | A | C | 2 | a0001c0001t0018g0061 a0001c0001t0018g0179 |
2 | HG02055.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2798-3936A>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57720676 | |||||||
| chr13:57720721 | T | A | 1 | a0001c0001t0005g0141 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2798-3891T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57720721 | |||||||
| chr13:57720722 | A | T | 1 | a0001c0001t0005g0141 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2798-3890A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57720722 | |||||||
| chr13:57720773 | T | TGGGGGGG others(38): Show |
1 | a0001c0001t0005g0141 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2798-3837_2798-383 others(49): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57720773 | ||||||
| chr13:57720869 | A | G | 1 | a0001c0001t0003g0245 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2798-3743A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57720869 | |||||||
| chr13:57721369 | T | C | 1 | a0001c0001t0034g0246 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2798-3243T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57721369 | |||||||
| chr13:57721373 | GTATATAT others(4): Show |
G | 3 | a0001c0001t0002g0092 a0001c0001t0002g0096 a0001c0001t0002g0098 |
3 | HG02630.hp2 HG02818.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.2798-3233_2798-322 others(15): Show |
PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57721373 | ||||||
| chr13:57721391 | C | A | 1 | a0001c0001t0003g0067 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2798-3221C>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57721391 | |||||||
| chr13:57721474 | C | T | 1 | a0001c0001t0015g0016 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2798-3138C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57721474 | |||||||
| chr13:57721492 | A | G | 2 | a0001c0001t0002g0086 a0001c0001t0002g0100 |
2 | HG01109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2798-3120A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57721492 | |||||||
| chr13:57721579 | C | A | 1 | a0001c0001t0001g0189 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2798-3033C>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57721579 | |||||||
| chr13:57721975 | G | C | 1 | a0001c0001t0023g0229 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2798-2637G>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57721975 | |||||||
| chr13:57722071 | T | C | 111 | a0001c0001t0002g0006 a0001c0001t0002g0066 a0001c0001t0002g0073 others(108): Show |
115 | HG00323.hp1 HG00544.hp1 HG00544.hp2 others(112): Show |
intron_variant | MODIFIER | c.2798-2541T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57722071 | |||||||
| chr13:57722084 | T | A | 1 | a0001c0001t0002g0148 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2798-2528T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57722084 | |||||||
| chr13:57722089 | A | T | 2 | a0001c0001t0018g0061 a0001c0001t0018g0179 |
2 | HG02055.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2798-2523A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57722089 | |||||||
| chr13:57722118 | G | A | 1 | a0001c0001t0006g0240 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2798-2494G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57722118 | |||||||
| chr13:57722145 | C | T | 1 | a0005c0009t0007g0258 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2798-2467C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57722145 | |||||||
| chr13:57722340 | A | G | 2 | a0001c0001t0016g0276 a0001c0005t0028g0037 |
2 | HG02080.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.2798-2272A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57722340 | |||||||
| chr13:57722355 | T | C | 1 | a0001c0011t0001g0235 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.2798-2257T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57722355 | |||||||
| chr13:57722456 | T | C | 1 | a0001c0001t0002g0194 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.2798-2156T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57722456 | |||||||
| chr13:57722588 | A | T | 21 | a0001c0001t0006g0017 a0001c0001t0006g0057 a0001c0001t0006g0077 others(18): Show |
21 | HG00140.hp2 HG01069.hp2 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.2798-2024A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57722588 | |||||||
| chr13:57722602 | C | T | 1 | a0001c0001t0004g0112 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2798-2010C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57722602 | |||||||
| chr13:57722741 | G | A | 7 | a0001c0001t0001g0218 a0001c0001t0001g0253 a0001c0001t0001g0255 others(4): Show |
7 | NA18945.hp1 NA18984.hp1 NA18988.hp1 others(4): Show |
intron_variant | MODIFIER | c.2798-1871G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57722741 | |||||||
| chr13:57722963 | A | T | 1 | a0001c0001t0034g0246 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2798-1649A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57722963 | |||||||
| chr13:57723025 | C | T | 6 | a0001c0001t0005g0139 a0001c0001t0005g0141 a0001c0001t0005g0291 others(3): Show |
6 | HG01496.hp1 HG02451.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.2798-1587C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57723025 | |||||||
| chr13:57723033 | C | T | 3 | a0001c0001t0014g0004 a0001c0001t0014g0171 a0001c0001t0014g0177 |
4 | NA18939.hp1 NA18952.hp1 NA18953.hp1 others(1): Show |
intron_variant | MODIFIER | c.2798-1579C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57723033 | |||||||
| chr13:57723133 | A | G | 1 | a0001c0001t0044g0238 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2798-1479A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57723133 | |||||||
| chr13:57723267 | T | TA | 253 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(250): Show |
258 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.2798-1340dupA | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 57723267 | ||||||
| chr13:57723419 | A | T | 6 | a0001c0001t0005g0139 a0001c0001t0005g0141 a0001c0001t0005g0291 others(3): Show |
6 | HG01496.hp1 HG02451.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.2798-1193A>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57723419 | |||||||
| chr13:57723420 | A | G | 1 | a0001c0001t0001g0154 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2798-1192A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57723420 | |||||||
| chr13:57723422 | G | A | 38 | a0001c0001t0002g0225 a0001c0001t0002g0297 a0001c0001t0004g0005 others(35): Show |
40 | HG00597.hp2 HG01243.hp1 HG01256.hp1 others(37): Show |
intron_variant | MODIFIER | c.2798-1190G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57723422 | |||||||
| chr13:57723682 | C | A | 254 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(251): Show |
259 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.2798-930C>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57723682 | |||||||
| chr13:57723907 | C | T | 1 | a0001c0001t0002g0300 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2798-705C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57723907 | |||||||
| chr13:57723909 | T | A | 1 | a0001c0001t0008g0033 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2798-703T>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57723909 | |||||||
| chr13:57723937 | C | T | 1 | a0001c0001t0001g0172 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2798-675C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57723937 | |||||||
| chr13:57723973 | T | C | 3 | a0001c0001t0002g0104 a0001c0001t0002g0147 a0001c0001t0037g0014 |
3 | HG02486.hp2 HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2798-639T>C | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57723973 | |||||||
| chr13:57724029 | G | A | 1 | a0001c0001t0006g0077 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2798-583G>A | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57724029 | |||||||
| chr13:57724043 | C | T | 1 | a0001c0001t0002g0236 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2798-569C>T | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57724043 | |||||||
| chr13:57724277 | A | G | 106 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(103): Show |
107 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.2798-335A>G | PCDH17 | ENSG00000118946.12 | transcript | ENST00000377918.8 | protein_coding | 3/3 | chr13 | 57724277 |