Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5754 |
| ensemblid | ENSG00000112655.16 |
| hgncid | 9618 |
| symbol | PTK7 |
| name | protein tyrosine kinase 7 (inactive) |
| refseq_nuc | NM_002821.5 |
| refseq_prot | NP_002812.2 |
| ensembl_nuc | ENST00000230419.9 |
| ensembl_prot | ENSP00000230419.4 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 43076314 |
| end | 43161715 |
| strand | + |
| ver | v1.2 |
| region | chr6:43076314-43161715 |
| region5000 | chr6:43071314-43166715 |
| regionname0 | PTK7_chr6_43076314_43161715 |
| regionname5000 | PTK7_chr6_43071314_43166715 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 1070 | 250 | 65 | 55 | 95 | 4 | 30 | 73 | PTK7_chr6_43071314_43166715 | PTK7 | MGAAR others(1065): Show |
chr6 | 43071314 | 43166715 |
| a0002 | 0/1 | 1070 | 8 | 5 | 1 | 1 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | MGAAR others(1065): Show |
chr6 | 43071314 | 43166715 |
| a0003 | 0/0 | 1070 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | MGAAR others(1065): Show |
chr6 | 43071314 | 43166715 |
| a0004 | 0/0 | 1070 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | PTK7_chr6_43071314_43166715 | PTK7 | MGAAR others(1065): Show |
chr6 | 43071314 | 43166715 |
| a0005 | 0/0 | 1070 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | MGAAR others(1065): Show |
chr6 | 43071314 | 43166715 |
| a0006 | 0/0 | 1070 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | MGAAR others(1065): Show |
chr6 | 43071314 | 43166715 |
| a0007 | 0/0 | 1070 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | MGAAR others(1065): Show |
chr6 | 43071314 | 43166715 |
| a0008 | 0/0 | 1070 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | MGAAR others(1065): Show |
chr6 | 43071314 | 43166715 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 3210 | 155 | 30 | 29 | 76 | 2 | 17 | PTK7_chr6_43071314_43166715 | PTK7 | ATGGG others(3205): Show |
chr6 | 43071314 | 43166715 | ||
| a0001c0002 | 0/0 | 3210 | 78 | 33 | 22 | 12 | 2 | 9 | PTK7_chr6_43071314_43166715 | PTK7 | ATGGG others(3205): Show |
chr6 | 43071314 | 43166715 | ||
| a0001c0005 | 0/0 | 3210 | 3 | 0 | 0 | 0 | 0 | 3 | PTK7_chr6_43071314_43166715 | PTK7 | ATGGG others(3205): Show |
chr6 | 43071314 | 43166715 | ||
| a0001c0006 | 0/0 | 3210 | 3 | 0 | 0 | 3 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | ATGGG others(3205): Show |
chr6 | 43071314 | 43166715 | ||
| a0001c0008 | 0/0 | 3210 | 2 | 0 | 0 | 2 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | ATGGG others(3205): Show |
chr6 | 43071314 | 43166715 | ||
| a0001c0009 | 0/0 | 3210 | 2 | 0 | 2 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | ATGGG others(3205): Show |
chr6 | 43071314 | 43166715 | ||
| a0001c0010 | 0/0 | 3210 | 2 | 0 | 0 | 2 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | ATGGG others(3205): Show |
chr6 | 43071314 | 43166715 | ||
| a0001c0012 | 0/0 | 3210 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | ATGGG others(3205): Show |
chr6 | 43071314 | 43166715 | ||
| a0001c0015 | 0/0 | 3210 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | ATGGG others(3205): Show |
chr6 | 43071314 | 43166715 | ||
| a0001c0017 | 0/0 | 3210 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | ATGGG others(3205): Show |
chr6 | 43071314 | 43166715 | ||
| a0001c0021 | 0/0 | 3210 | 1 | 0 | 0 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | ATGGG others(3205): Show |
chr6 | 43071314 | 43166715 | ||
| a0001c0022 | 0/0 | 3210 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | ATGGG others(3205): Show |
chr6 | 43071314 | 43166715 | ||
| a0002c0003 | 0/1 | 3210 | 7 | 4 | 1 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | ATGGG others(3205): Show |
chr6 | 43071314 | 43166715 | ||
| a0002c0018 | 0/0 | 3210 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | ATGGG others(3205): Show |
chr6 | 43071314 | 43166715 | ||
| a0003c0004 | 0/0 | 3210 | 6 | 6 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | ATGGG others(3205): Show |
chr6 | 43071314 | 43166715 | ||
| a0003c0014 | 0/0 | 3210 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | ATGGG others(3205): Show |
chr6 | 43071314 | 43166715 | ||
| a0003c0016 | 0/0 | 3210 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | ATGGG others(3205): Show |
chr6 | 43071314 | 43166715 | ||
| a0004c0007 | 0/0 | 3210 | 2 | 0 | 0 | 2 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | ATGGG others(3205): Show |
chr6 | 43071314 | 43166715 | ||
| a0005c0019 | 0/0 | 3210 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | ATGGG others(3205): Show |
chr6 | 43071314 | 43166715 | ||
| a0006c0020 | 0/0 | 3210 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | ATGGG others(3205): Show |
chr6 | 43071314 | 43166715 | ||
| a0007c0013 | 0/0 | 3210 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | ATGGG others(3205): Show |
chr6 | 43071314 | 43166715 | ||
| a0008c0011 | 0/0 | 3210 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | ATGGG others(3205): Show |
chr6 | 43071314 | 43166715 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 4222 | 82 | 14 | 17 | 39 | 0 | 11 | PTK7_chr6_43071314_43166715 | PTK7 | ACTGG others(4217): Show |
chr6 | 43071314 | 43166715 |
| a0001c0001t0002 | 0/0 | 4222 | 69 | 13 | 12 | 37 | 2 | 5 | PTK7_chr6_43071314_43166715 | PTK7 | ACTGG others(4217): Show |
chr6 | 43071314 | 43166715 |
| a0001c0001t0003 | 0/0 | 4222 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | ACTGG others(4217): Show |
chr6 | 43071314 | 43166715 |
| a0001c0001t0004 | 0/0 | 4222 | 2 | 2 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | ACTGG others(4217): Show |
chr6 | 43071314 | 43166715 |
| a0001c0001t0008 | 0/0 | 4222 | 1 | 0 | 0 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | ACTGG others(4217): Show |
chr6 | 43071314 | 43166715 |
| a0001c0002t0001 | 0/0 | 4222 | 62 | 20 | 20 | 12 | 2 | 8 | PTK7_chr6_43071314_43166715 | PTK7 | ACTGG others(4217): Show |
chr6 | 43071314 | 43166715 |
| a0001c0002t0002 | 0/0 | 4222 | 5 | 4 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | ACTGG others(4217): Show |
chr6 | 43071314 | 43166715 |
| a0001c0002t0003 | 0/0 | 4222 | 5 | 4 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | ACTGG others(4217): Show |
chr6 | 43071314 | 43166715 |
| a0001c0002t0004 | 0/0 | 4222 | 2 | 2 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | ACTGG others(4217): Show |
chr6 | 43071314 | 43166715 |
| a0001c0002t0005 | 0/0 | 4222 | 2 | 2 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | ACTGG others(4217): Show |
chr6 | 43071314 | 43166715 |
| a0001c0002t0007 | 0/0 | 4222 | 1 | 0 | 0 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | ACTGG others(4217): Show |
chr6 | 43071314 | 43166715 |
| a0001c0002t0009 | 0/0 | 4222 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | ACTGG others(4217): Show |
chr6 | 43071314 | 43166715 |
| a0001c0005t0001 | 0/0 | 4222 | 3 | 0 | 0 | 0 | 0 | 3 | PTK7_chr6_43071314_43166715 | PTK7 | ACTGG others(4217): Show |
chr6 | 43071314 | 43166715 |
| a0001c0006t0001 | 0/0 | 4222 | 3 | 0 | 0 | 3 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | ACTGG others(4217): Show |
chr6 | 43071314 | 43166715 |
| a0001c0008t0001 | 0/0 | 4222 | 2 | 0 | 0 | 2 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | ACTGG others(4217): Show |
chr6 | 43071314 | 43166715 |
| a0001c0009t0001 | 0/0 | 4222 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | ACTGG others(4217): Show |
chr6 | 43071314 | 43166715 |
| a0001c0009t0002 | 0/0 | 4222 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | ACTGG others(4217): Show |
chr6 | 43071314 | 43166715 |
| a0001c0010t0002 | 0/0 | 4222 | 2 | 0 | 0 | 2 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | ACTGG others(4217): Show |
chr6 | 43071314 | 43166715 |
| a0001c0012t0002 | 0/0 | 4222 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | ACTGG others(4217): Show |
chr6 | 43071314 | 43166715 |
| a0001c0015t0001 | 0/0 | 4222 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | ACTGG others(4217): Show |
chr6 | 43071314 | 43166715 |
| a0001c0017t0001 | 0/0 | 4222 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | ACTGG others(4217): Show |
chr6 | 43071314 | 43166715 |
| a0001c0021t0002 | 0/0 | 4222 | 1 | 0 | 0 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | ACTGG others(4217): Show |
chr6 | 43071314 | 43166715 |
| a0001c0022t0001 | 0/0 | 4222 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | ACTGG others(4217): Show |
chr6 | 43071314 | 43166715 |
| a0002c0003t0001 | 0/0 | 4222 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | ACTGG others(4217): Show |
chr6 | 43071314 | 43166715 |
| a0002c0003t0002 | 0/1 | 4222 | 6 | 3 | 1 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | ACTGG others(4217): Show |
chr6 | 43071314 | 43166715 |
| a0002c0018t0001 | 0/0 | 4222 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | ACTGG others(4217): Show |
chr6 | 43071314 | 43166715 |
| a0003c0004t0002 | 0/0 | 4222 | 6 | 6 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | ACTGG others(4217): Show |
chr6 | 43071314 | 43166715 |
| a0003c0014t0002 | 0/0 | 4222 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | ACTGG others(4217): Show |
chr6 | 43071314 | 43166715 |
| a0003c0016t0002 | 0/0 | 4222 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | ACTGG others(4217): Show |
chr6 | 43071314 | 43166715 |
| a0004c0007t0001 | 0/0 | 4222 | 2 | 0 | 0 | 2 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | ACTGG others(4217): Show |
chr6 | 43071314 | 43166715 |
| a0005c0019t0001 | 0/0 | 4222 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | ACTGG others(4217): Show |
chr6 | 43071314 | 43166715 |
| a0006c0020t0006 | 0/0 | 4222 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | ACTGG others(4217): Show |
chr6 | 43071314 | 43166715 |
| a0007c0013t0001 | 0/0 | 4222 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | ACTGG others(4217): Show |
chr6 | 43071314 | 43166715 |
| a0008c0011t0002 | 0/0 | 4222 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | ACTGG others(4217): Show |
chr6 | 43071314 | 43166715 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0099 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0002g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0002g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0002g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0002g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0002g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0002g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0003g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0004g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0004g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0001t0008g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0003g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0003g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0004g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0004g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0005g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0005g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0007g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0002t0009g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0005t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0005t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0005t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0006t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0006t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0006t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0008t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0008t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0009t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0009t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0010t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0010t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0012t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0015t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0017t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0021t0002g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0001c0022t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0002c0003t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0002c0003t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0002c0003t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0002c0003t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0002c0003t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0002c0003t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0002c0003t0002g0219 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0002c0018t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0003c0004t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0003c0004t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0003c0004t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0003c0004t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0003c0004t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0003c0004t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0003c0014t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0003c0016t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0004c0007t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0004c0007t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0005c0019t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0006c0020t0006g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0007c0013t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| a0008c0011t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0043 | EUR | FIN | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG00323 | hp2 | a0001 | c0002 | t0001 | g0207 | EUR | FIN | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0264 | EAS | CHS | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | CHS | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0123 | EAS | CHS | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0151 | EAS | CHS | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | CHS | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0265 | EAS | CHS | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG00609 | hp2 | a0001 | c0010 | t0002 | g0093 | EAS | CHS | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0217 | AMR | PUR | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0023 | AMR | PUR | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0060 | AMR | PUR | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG00733 | hp1 | a0001 | c0009 | t0002 | g0061 | AMR | PUR | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0144 | AMR | PUR | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG00741 | hp2 | a0001 | c0017 | t0001 | g0232 | AMR | PUR | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0216 | AMR | PUR | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0218 | AMR | PUR | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0145 | AMR | PUR | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0169 | AMR | PUR | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0261 | AMR | PUR | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0114 | AMR | PUR | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG01169 | hp1 | a0001 | c0002 | t0003 | g0147 | AMR | PUR | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0059 | AMR | PUR | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0165 | AMR | CLM | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | CLM | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG01258 | hp1 | a0001 | c0002 | t0002 | g0103 | AMR | CLM | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0168 | AMR | CLM | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0041 | AMR | CLM | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG01261 | hp2 | a0002 | c0003 | t0002 | g0070 | AMR | CLM | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | CLM | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0102 | AMR | CLM | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG01358 | hp2 | a0001 | c0002 | t0001 | g0215 | AMR | CLM | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0105 | AMR | CLM | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | CLM | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | CLM | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0054 | AMR | CLM | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0158 | AFR | ACB | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0234 | AFR | ACB | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG01891 | hp2 | a0001 | c0002 | t0003 | g0014 | AFR | ACB | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0049 | AMR | PEL | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0191 | AMR | PEL | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0055 | AMR | PEL | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG01943 | hp2 | a0001 | c0002 | t0001 | g0104 | AMR | PEL | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0050 | AMR | PEL | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG01952 | hp2 | a0001 | c0009 | t0001 | g0062 | AMR | PEL | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG01975 | hp2 | a0001 | c0002 | t0001 | g0089 | AMR | PEL | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0112 | AMR | PEL | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0052 | AMR | PEL | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0039 | AMR | PEL | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0125 | AMR | PEL | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | KHV | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | KHV | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | KHV | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | ACB | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | ACB | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0272 | EAS | KHV | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG02071 | hp1 | a0001 | c0010 | t0002 | g0045 | EAS | KHV | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0257 | EAS | KHV | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG02135 | hp2 | a0001 | c0006 | t0001 | g0084 | EAS | KHV | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG02145 | hp1 | a0001 | c0015 | t0001 | g0240 | AFR | ACB | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG02145 | hp2 | a0002 | c0018 | t0001 | g0248 | AFR | ACB | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG02148 | hp1 | a0001 | c0002 | t0001 | g0113 | AMR | PEL | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0048 | AMR | PEL | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | ACB | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG02258 | hp2 | a0002 | c0003 | t0002 | g0178 | AFR | ACB | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | ACB | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG02280 | hp2 | a0001 | c0002 | t0001 | g0180 | AFR | ACB | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0129 | AMR | PEL | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0214 | AFR | ACB | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0042 | AFR | GWD | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG02572 | hp2 | a0001 | c0002 | t0001 | g0140 | AFR | GWD | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG02615 | hp1 | a0003 | c0004 | t0002 | g0046 | AFR | GWD | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0252 | AFR | GWD | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0047 | AFR | GWD | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG02622 | hp2 | a0005 | c0019 | t0001 | g0141 | AFR | GWD | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0183 | AFR | GWD | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG02630 | hp2 | a0003 | c0004 | t0002 | g0007 | AFR | GWD | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0109 | SAS | PJL | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0136 | AFR | GWD | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0122 | SAS | PJL | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG02809 | hp1 | a0001 | c0001 | t0004 | g0269 | AFR | GWD | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG02809 | hp2 | a0001 | c0012 | t0002 | g0229 | AFR | GWD | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG02818 | hp1 | a0001 | c0002 | t0002 | g0249 | AFR | GWD | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG02818 | hp2 | a0003 | c0004 | t0002 | g0235 | AFR | GWD | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG02895 | hp1 | a0001 | c0002 | t0009 | g0233 | AFR | GWD | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG02895 | hp2 | a0001 | c0002 | t0005 | g0138 | AFR | GWD | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG02897 | hp1 | a0001 | c0002 | t0005 | g0137 | AFR | GWD | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG02922 | hp1 | a0001 | c0002 | t0002 | g0026 | AFR | ESN | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0181 | AFR | ESN | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG02965 | hp1 | a0002 | c0003 | t0002 | g0163 | AFR | ESN | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0035 | AFR | ESN | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0146 | AFR | ESN | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0222 | AFR | ESN | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0251 | AFR | ESN | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG02976 | hp2 | a0003 | c0004 | t0002 | g0239 | AFR | ESN | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0195 | SAS | PJL | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0032 | AFR | GWD | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | MSL | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0034 | AFR | MSL | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG03130 | hp1 | a0002 | c0003 | t0001 | g0243 | AFR | ESN | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0223 | AFR | ESN | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG03139 | hp1 | a0001 | c0002 | t0001 | g0250 | AFR | ESN | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | ESN | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG03195 | hp1 | a0003 | c0004 | t0002 | g0025 | AFR | ESN | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0224 | AFR | ESN | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG03209 | hp1 | a0001 | c0002 | t0004 | g0228 | AFR | MSL | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG03209 | hp2 | a0001 | c0002 | t0001 | g0056 | AFR | MSL | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG03225 | hp1 | a0003 | c0014 | t0002 | g0241 | AFR | MSL | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG03225 | hp2 | a0003 | c0016 | t0002 | g0225 | AFR | MSL | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0245 | SAS | PJL | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG03492 | hp2 | a0001 | c0005 | t0001 | g0156 | SAS | PJL | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0142 | AFR | ESN | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0201 | AFR | ESN | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0242 | AFR | GWD | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0044 | AFR | GWD | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG03579 | hp2 | a0001 | c0002 | t0003 | g0148 | AFR | MSL | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0020 | SAS | PJL | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0152 | SAS | PJL | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | STU | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0244 | SAS | STU | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG03704 | hp1 | a0001 | c0021 | t0002 | g0019 | SAS | PJL | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG03704 | hp2 | a0001 | c0005 | t0001 | g0177 | SAS | PJL | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0161 | SAS | PJL | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | BEB | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG03834 | hp2 | a0001 | c0001 | t0008 | g0176 | SAS | BEB | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG04115 | hp1 | a0001 | c0002 | t0007 | g0115 | SAS | STU | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0175 | SAS | STU | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0031 | SAS | BEB | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0074 | SAS | BEB | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | STU | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0143 | SAS | STU | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0029 | SAS | STU | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0260 | SAS | STU | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0268 | SAS | STU | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0012 | SAS | STU | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA18522 | hp1 | a0001 | c0002 | t0002 | g0253 | AFR | YRI | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA18522 | hp2 | a0006 | c0020 | t0006 | g0226 | AFR | YRI | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | CHB | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | CHB | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA18906 | hp1 | a0001 | c0002 | t0004 | g0139 | AFR | YRI | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA18906 | hp2 | a0001 | c0002 | t0002 | g0231 | AFR | YRI | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA18943 | hp1 | a0002 | c0003 | t0002 | g0121 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA18944 | hp1 | a0001 | c0008 | t0001 | g0108 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0198 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA18954 | hp1 | a0001 | c0002 | t0001 | g0090 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0110 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA18975 | hp1 | a0007 | c0013 | t0001 | g0063 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA18977 | hp2 | a0001 | c0002 | t0001 | g0091 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0075 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA18984 | hp2 | a0001 | c0002 | t0001 | g0196 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA18992 | hp2 | a0001 | c0002 | t0001 | g0134 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0106 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA18998 | hp1 | a0001 | c0006 | t0001 | g0078 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA18999 | hp1 | a0001 | c0008 | t0001 | g0107 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA19003 | hp2 | a0004 | c0007 | t0001 | g0131 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA19012 | hp2 | a0001 | c0006 | t0001 | g0081 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0185 | AFR | LWK | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0236 | AFR | LWK | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0203 | AFR | LWK | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA19043 | hp2 | a0002 | c0003 | t0002 | g0162 | AFR | LWK | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA19065 | hp2 | a0008 | c0011 | t0002 | g0040 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA19080 | hp2 | a0001 | c0002 | t0001 | g0159 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA19081 | hp2 | a0004 | c0007 | t0001 | g0130 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA19240 | hp1 | a0001 | c0002 | t0003 | g0149 | AFR | YRI | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0247 | AFR | YRI | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | ASW | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | ASW | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0258 | EUR | TSI | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0179 | EUR | TSI | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | GIH | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA20905 | hp2 | a0001 | c0005 | t0001 | g0157 | SAS | GIH | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | CLM | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG01123 | hp2 | a0001 | c0022 | t0001 | g0155 | AMR | CLM | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG02109 | hp1 | a0001 | c0002 | t0003 | g0150 | AFR | ACB | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | ACB | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0182 | AFR | ACB | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0033 | AFR | ACB | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG06807 | hp1 | a0003 | c0004 | t0002 | g0024 | AFR | USA | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0184 | AFR | USA | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0120 | AFR | USA | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0267 | AFR | USA | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| homoSapiens | chm13v2 | a0002 | c0003 | t0002 | g0219 | REF | REF | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0099 | REF | REF | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:43129805 | G | A | 1 | a0008 | 1 | NA19065.hp2 | missense_variant | MODERATE | c.446G>A | p.Arg149His | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 3/20 | 621/4222 | 446/3213 | 149/1070 | chr6 | 43129805 | |||
| chr6:43130322 | G | A | 1 | a0004 | 2 | NA19003.hp2 NA19081.hp2 |
missense_variant | MODERATE | c.563G>A | p.Arg188Gln | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 4/20 | 738/4222 | 563/3213 | 188/1070 | chr6 | 43130322 | |||
| chr6:43130655 | G | A | 1 | a0007 | 1 | NA18975.hp1 | missense_variant | MODERATE | c.806G>A | p.Arg269His | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 5/20 | 981/4222 | 806/3213 | 269/1070 | chr6 | 43130655 | |||
| chr6:43132493 | C | T | 1 | a0006 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.1034C>T | p.Pro345Leu | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 7/20 | 1209/4222 | 1034/3213 | 345/1070 | chr6 | 43132493 | |||
| chr6:43132518 | C | G | 1 | a0005 | 1 | HG02622.hp2 | missense_variant | MODERATE | c.1059C>G | p.Ser353Arg | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 7/20 | 1234/4222 | 1059/3213 | 353/1070 | chr6 | 43132518 | |||
| chr6:43144529 | C | T | 1 | a0002 | 7 | HG01261.hp2 HG02145.hp2 HG02258.hp2 others(4): Show |
missense_variant | MODERATE | c.2330C>T | p.Ala777Val | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 15/20 | 2505/4222 | 2330/3213 | 777/1070 | chr6 | 43144529 | |||
| chr6:43160781 | G | A | 1 | a0003 | 8 | HG02615.hp1 HG02630.hp2 HG02818.hp2 others(5): Show |
missense_variant | MODERATE | c.3113G>A | p.Arg1038Gln | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 20/20 | 3288/4222 | 3113/3213 | 1038/1070 | chr6 | 43160781 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:43076566 | C | T | 1 | a0001c0022 | 1 | HG01123.hp2 | splice_region_variant&synonymous_variant | LOW | c.78C>T | p.Gly26Gly | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/20 | 253/4222 | 78/3213 | 26/1070 | chr6 | 43076566 | |||
| chr6:43130257 | G | A | 1 | a0001c0012 | 1 | HG02809.hp2 | synonymous_variant | LOW | c.498G>A | p.Gly166Gly | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 4/20 | 673/4222 | 498/3213 | 166/1070 | chr6 | 43130257 | |||
| chr6:43130263 | C | G | 1 | a0001c0012 | 1 | HG02809.hp2 | synonymous_variant | LOW | c.504C>G | p.Pro168Pro | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 4/20 | 679/4222 | 504/3213 | 168/1070 | chr6 | 43130263 | |||
| chr6:43130557 | A | G | 1 | a0001c0006 | 3 | HG02135.hp2 NA18998.hp1 NA19012.hp2 |
synonymous_variant | LOW | c.708A>G | p.Val236Val | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 5/20 | 883/4222 | 708/3213 | 236/1070 | chr6 | 43130557 | |||
| chr6:43132019 | C | T | 1 | a0001c0021 | 1 | HG03704.hp1 | synonymous_variant | LOW | c.816C>T | p.Pro272Pro | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 6/20 | 991/4222 | 816/3213 | 272/1070 | chr6 | 43132019 | |||
| chr6:43132106 | C | T | 1 | a0001c0010 | 2 | HG00609.hp2 HG02071.hp1 |
synonymous_variant | LOW | c.903C>T | p.Cys301Cys | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 6/20 | 1078/4222 | 903/3213 | 301/1070 | chr6 | 43132106 | |||
| chr6:43132536 | G | A | 2 | a0001c0015 a0003c0014 |
2 | HG02145.hp1 HG03225.hp1 |
synonymous_variant | LOW | c.1077G>A | p.Ala359Ala | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 7/20 | 1252/4222 | 1077/3213 | 359/1070 | chr6 | 43132536 | |||
| chr6:43132635 | C | T | 1 | a0001c0009 | 2 | HG00733.hp1 HG01952.hp2 |
synonymous_variant | LOW | c.1176C>T | p.His392His | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 7/20 | 1351/4222 | 1176/3213 | 392/1070 | chr6 | 43132635 | |||
| chr6:43139249 | G | A | 1 | a0001c0008 | 2 | NA18944.hp1 NA18999.hp1 |
synonymous_variant | LOW | c.1476G>A | p.Ala492Ala | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 9/20 | 1651/4222 | 1476/3213 | 492/1070 | chr6 | 43139249 | |||
| chr6:43142013 | G | A | 4 | a0001c0002 a0001c0005 a0001c0006 others(1): Show |
85 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(82): Show |
synonymous_variant | LOW | c.1851G>A | p.Gly617Gly | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 12/20 | 2026/4222 | 1851/3213 | 617/1070 | chr6 | 43142013 | |||
| chr6:43142211 | C | T | 1 | a0002c0018 | 1 | HG02145.hp2 | synonymous_variant | LOW | c.1959C>T | p.Asp653Asp | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 13/20 | 2134/4222 | 1959/3213 | 653/1070 | chr6 | 43142211 | |||
| chr6:43142265 | C | T | 1 | a0001c0005 | 3 | HG03492.hp2 HG03704.hp2 NA20905.hp2 |
synonymous_variant | LOW | c.2013C>T | p.Asn671Asn | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 13/20 | 2188/4222 | 2013/3213 | 671/1070 | chr6 | 43142265 | |||
| chr6:43145252 | G | A | 1 | a0001c0017 | 1 | HG00741.hp2 | synonymous_variant | LOW | c.2460G>A | p.Glu820Glu | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 16/20 | 2635/4222 | 2460/3213 | 820/1070 | chr6 | 43145252 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:43076433 | A | G | 1 | a0001c0002t0005 | 2 | HG02895.hp2 HG02897.hp1 |
5_prime_UTR_variant | MODIFIER | c.-56A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/20 | 56 | chr6 | 43076433 | ||||||
| chr6:43161114 | T | C | 11 | a0001c0001t0002 a0001c0002t0002 a0001c0009t0002 others(8): Show |
93 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*233T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 20/20 | 233 | chr6 | 43161114 | ||||||
| chr6:43161127 | T | G | 1 | a0006c0020t0006 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*246T>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 20/20 | 246 | chr6 | 43161127 | ||||||
| chr6:43161346 | C | G | 3 | a0001c0001t0004 a0001c0002t0004 a0006c0020t0006 |
5 | HG02809.hp1 HG03209.hp1 NA18522.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*465C>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 20/20 | 465 | chr6 | 43161346 | ||||||
| chr6:43161385 | C | T | 1 | a0001c0002t0009 | 1 | HG02895.hp1 | 3_prime_UTR_variant | MODIFIER | c.*504C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 20/20 | 504 | chr6 | 43161385 | ||||||
| chr6:43161425 | T | C | 1 | a0001c0002t0007 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*544T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 20/20 | 544 | chr6 | 43161425 | ||||||
| chr6:43161595 | G | A | 2 | a0001c0001t0003 a0001c0002t0003 |
6 | HG01169.hp1 HG01891.hp2 HG02109.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*714G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 20/20 | 714 | chr6 | 43161595 | ||||||
| chr6:43161698 | A | T | 1 | a0001c0001t0008 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*817A>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 20/20 | 817 | chr6 | 43161698 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:43076762 | C | T | 1 | a0001c0001t0002g0272 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.79+195C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43076762 | |||||||
| chr6:43076868 | T | C | 1 | a0001c0001t0002g0001 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.79+301T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43076868 | |||||||
| chr6:43076882 | A | G | 26 | a0001c0001t0001g0246 a0001c0001t0001g0262 a0001c0001t0001g0268 others(23): Show |
26 | HG00423.hp2 HG00609.hp1 HG01099.hp1 others(23): Show |
intron_variant | MODIFIER | c.79+315A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43076882 | |||||||
| chr6:43076902 | G | A | 2 | a0001c0001t0001g0002 a0001c0001t0001g0003 |
2 | HG00642.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.79+335G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43076902 | |||||||
| chr6:43076922 | A | T | 1 | a0001c0001t0001g0245 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.79+355A>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43076922 | |||||||
| chr6:43077199 | C | T | 1 | a0001c0001t0001g0244 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.79+632C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43077199 | |||||||
| chr6:43077219 | G | A | 58 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(55): Show |
58 | HG00323.hp1 HG00597.hp2 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.79+652G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43077219 | |||||||
| chr6:43077231 | G | A | 1 | a0001c0001t0002g0004 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.79+664G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43077231 | |||||||
| chr6:43077301 | G | A | 1 | a0001c0001t0001g0246 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.79+734G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43077301 | |||||||
| chr6:43077617 | G | T | 1 | a0002c0003t0001g0243 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.79+1050G>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43077617 | |||||||
| chr6:43077724 | G | T | 41 | a0001c0001t0001g0230 a0001c0001t0001g0237 a0001c0001t0001g0238 others(38): Show |
41 | HG00423.hp2 HG00609.hp1 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.79+1157G>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43077724 | |||||||
| chr6:43077831 | C | G | 27 | a0001c0001t0001g0227 a0001c0001t0001g0246 a0001c0001t0001g0262 others(24): Show |
27 | HG00423.hp2 HG00609.hp1 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.79+1264C>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43077831 | |||||||
| chr6:43078133 | C | T | 1 | a0001c0001t0002g0242 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.79+1566C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43078133 | |||||||
| chr6:43078389 | G | A | 2 | a0001c0009t0001g0062 a0001c0009t0002g0061 |
2 | HG00733.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.79+1822G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43078389 | |||||||
| chr6:43078469 | G | A | 3 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0007c0013t0001g0063 |
3 | NA18951.hp1 NA18975.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.79+1902G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43078469 | |||||||
| chr6:43078526 | A | AG | 107 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(104): Show |
107 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(104): Show |
intron_variant | MODIFIER | c.79+1963dupG | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43078526 | ||||||
| chr6:43078534 | C | T | 19 | a0001c0001t0001g0246 a0001c0001t0001g0262 a0001c0001t0001g0268 others(16): Show |
19 | HG00423.hp2 HG00609.hp1 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.79+1967C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43078534 | |||||||
| chr6:43078550 | C | T | 3 | a0001c0002t0001g0216 a0001c0002t0001g0217 a0001c0002t0001g0218 |
3 | HG00639.hp1 HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.79+1983C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43078550 | |||||||
| chr6:43078749 | G | A | 1 | a0001c0001t0002g0001 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.79+2182G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43078749 | |||||||
| chr6:43078851 | G | C | 2 | a0001c0001t0001g0220 a0001c0001t0002g0221 |
2 | HG02027.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.79+2284G>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43078851 | |||||||
| chr6:43079185 | C | T | 2 | a0001c0001t0002g0059 a0001c0001t0002g0060 |
2 | HG00642.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.79+2618C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43079185 | |||||||
| chr6:43079321 | G | A | 1 | a0001c0001t0001g0066 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.79+2754G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43079321 | |||||||
| chr6:43079399 | G | A | 1 | a0001c0001t0002g0005 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.79+2832G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43079399 | |||||||
| chr6:43079410 | TGATCGTG others(34): Show |
T | 59 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(56): Show |
59 | HG00323.hp1 HG00597.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.79+2871_79+2911del others(41): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43079410 | ||||||
| chr6:43079561 | A | T | 1 | a0001c0001t0001g0058 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.79+2994A>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43079561 | |||||||
| chr6:43079655 | A | G | 1 | a0001c0002t0001g0215 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.79+3088A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43079655 | |||||||
| chr6:43079878 | A | G | 1 | a0001c0001t0002g0214 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.79+3311A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43079878 | |||||||
| chr6:43079896 | C | CA | 6 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0002g0067 others(3): Show |
6 | HG01261.hp2 HG03130.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.79+3345dupA | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43079896 | ||||||
| chr6:43079896 | CA | C | 6 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0002g0004 others(3): Show |
6 | HG00544.hp1 HG02145.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.79+3345delA | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43079896 | ||||||
| chr6:43079932 | G | A | 1 | a0002c0003t0001g0243 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.79+3365G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43079932 | |||||||
| chr6:43080049 | C | A | 2 | a0001c0001t0001g0006 a0003c0004t0002g0007 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.79+3482C>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43080049 | |||||||
| chr6:43080049 | C | CA | 13 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(10): Show |
13 | HG00741.hp2 HG01433.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.79+3502dupA | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43080049 | ||||||
| chr6:43080049 | CA | C | 8 | a0001c0001t0001g0208 a0001c0001t0001g0210 a0001c0001t0001g0211 others(5): Show |
8 | HG00323.hp2 HG03209.hp2 NA18962.hp1 others(5): Show |
intron_variant | MODIFIER | c.79+3502delA | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43080049 | ||||||
| chr6:43080209 | A | G | 115 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(112): Show |
115 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(112): Show |
intron_variant | MODIFIER | c.79+3642A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43080209 | |||||||
| chr6:43080265 | T | C | 2 | a0001c0001t0001g0220 a0001c0001t0002g0221 |
2 | HG02027.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.79+3698T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43080265 | |||||||
| chr6:43080276 | C | T | 41 | a0001c0001t0001g0230 a0001c0001t0001g0237 a0001c0001t0001g0238 others(38): Show |
41 | HG00423.hp2 HG00609.hp1 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.79+3709C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43080276 | |||||||
| chr6:43080937 | G | A | 3 | a0001c0001t0002g0254 a0001c0001t0002g0255 a0001c0001t0002g0256 |
3 | NA18944.hp2 NA18951.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.79+4370G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43080937 | |||||||
| chr6:43080954 | T | C | 1 | a0001c0001t0002g0008 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.79+4387T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43080954 | |||||||
| chr6:43080954 | T | TAC | 3 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0002t0001g0075 |
3 | NA18950.hp2 NA18982.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.79+4409_79+4410dup others(2): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43080954 | ||||||
| chr6:43080954 | T | TACAC | 66 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(63): Show |
66 | HG00323.hp1 HG00639.hp2 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.79+4407_79+4410dup others(4): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43080954 | ||||||
| chr6:43080954 | T | TACACAC | 8 | a0001c0001t0002g0009 a0001c0001t0002g0222 a0001c0001t0002g0223 others(5): Show |
8 | HG00597.hp2 HG02145.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.79+4405_79+4410dup others(6): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43080954 | ||||||
| chr6:43080954 | TACAC | T | 57 | a0001c0001t0001g0073 a0001c0001t0001g0186 a0001c0001t0001g0187 others(54): Show |
57 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.79+4407_79+4410del others(4): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43080954 | ||||||
| chr6:43081200 | C | T | 1 | a0001c0002t0001g0056 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.79+4633C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43081200 | |||||||
| chr6:43081605 | A | C | 7 | a0001c0001t0002g0179 a0001c0002t0001g0180 a0001c0002t0001g0181 others(4): Show |
7 | HG02280.hp2 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.79+5038A>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43081605 | |||||||
| chr6:43081703 | C | T | 2 | a0001c0001t0001g0220 a0001c0001t0002g0221 |
2 | HG02027.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.79+5136C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43081703 | |||||||
| chr6:43081723 | A | G | 194 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(191): Show |
194 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(191): Show |
intron_variant | MODIFIER | c.79+5156A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43081723 | |||||||
| chr6:43082066 | G | T | 2 | a0001c0001t0001g0220 a0001c0001t0002g0221 |
2 | HG02027.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.79+5499G>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43082066 | |||||||
| chr6:43082751 | G | A | 2 | a0001c0001t0001g0220 a0001c0001t0002g0221 |
2 | HG02027.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.79+6184G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43082751 | |||||||
| chr6:43082876 | G | A | 4 | a0001c0001t0002g0222 a0001c0001t0002g0223 a0001c0001t0002g0224 others(1): Show |
4 | HG02970.hp2 HG03130.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.79+6309G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43082876 | |||||||
| chr6:43083013 | G | A | 2 | a0001c0001t0001g0220 a0001c0001t0002g0221 |
2 | HG02027.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.79+6446G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43083013 | |||||||
| chr6:43083084 | G | A | 2 | a0001c0001t0001g0220 a0001c0001t0002g0221 |
2 | HG02027.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.79+6517G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43083084 | |||||||
| chr6:43083086 | G | A | 140 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(137): Show |
140 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.79+6519G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43083086 | |||||||
| chr6:43083128 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.79+6561G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43083128 | |||||||
| chr6:43083162 | A | G | 2 | a0001c0001t0001g0220 a0001c0001t0002g0221 |
2 | HG02027.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.79+6595A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43083162 | |||||||
| chr6:43083224 | T | C | 1 | a0001c0002t0001g0136 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.79+6657T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43083224 | |||||||
| chr6:43083530 | G | A | 2 | a0001c0002t0005g0137 a0001c0002t0005g0138 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.79+6963G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43083530 | |||||||
| chr6:43083559 | C | T | 5 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0135 others(2): Show |
5 | NA18950.hp2 NA18982.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.79+6992C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43083559 | |||||||
| chr6:43083801 | A | G | 8 | a0001c0001t0001g0051 a0001c0001t0002g0048 a0001c0001t0002g0049 others(5): Show |
8 | HG01175.hp1 HG01496.hp2 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.79+7234A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43083801 | |||||||
| chr6:43083844 | A | G | 1 | a0002c0003t0002g0178 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.79+7277A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43083844 | |||||||
| chr6:43083876 | A | G | 140 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(137): Show |
140 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.79+7309A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43083876 | |||||||
| chr6:43084023 | G | A | 1 | a0001c0001t0001g0002 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.79+7456G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43084023 | |||||||
| chr6:43084229 | C | A | 1 | a0001c0002t0004g0139 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.79+7662C>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43084229 | |||||||
| chr6:43084268 | C | T | 1 | a0003c0004t0002g0007 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.79+7701C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43084268 | |||||||
| chr6:43084426 | A | G | 62 | a0001c0001t0001g0073 a0001c0001t0001g0186 a0001c0001t0001g0187 others(59): Show |
62 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.79+7859A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43084426 | |||||||
| chr6:43084625 | T | C | 2 | a0001c0001t0002g0242 a0001c0002t0009g0233 |
2 | HG02895.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.79+8058T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43084625 | |||||||
| chr6:43085051 | A | C | 1 | a0001c0001t0002g0047 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.79+8484A>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43085051 | |||||||
| chr6:43085341 | C | T | 1 | a0001c0002t0002g0253 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.79+8774C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43085341 | |||||||
| chr6:43085374 | G | A | 1 | a0001c0001t0001g0199 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.79+8807G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43085374 | |||||||
| chr6:43085384 | G | A | 1 | a0001c0002t0001g0247 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.79+8817G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43085384 | |||||||
| chr6:43085416 | T | A | 1 | a0001c0001t0002g0009 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.79+8849T>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43085416 | |||||||
| chr6:43085606 | C | T | 1 | a0001c0002t0001g0198 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.79+9039C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43085606 | |||||||
| chr6:43085623 | A | G | 2 | a0001c0001t0001g0220 a0001c0001t0002g0221 |
2 | HG02027.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.79+9056A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43085623 | |||||||
| chr6:43085664 | T | C | 1 | a0002c0003t0001g0243 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.79+9097T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43085664 | |||||||
| chr6:43085714 | A | G | 58 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(55): Show |
58 | HG00323.hp1 HG00597.hp2 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.79+9147A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43085714 | |||||||
| chr6:43085746 | C | T | 1 | a0001c0001t0001g0133 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.79+9179C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43085746 | |||||||
| chr6:43085802 | G | T | 1 | a0001c0001t0001g0199 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.79+9235G>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43085802 | |||||||
| chr6:43085887 | T | C | 2 | a0001c0001t0001g0220 a0001c0001t0002g0221 |
2 | HG02027.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.79+9320T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43085887 | |||||||
| chr6:43085933 | C | CA | 19 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0085 others(16): Show |
19 | HG01261.hp2 HG02027.hp2 HG02135.hp2 others(16): Show |
intron_variant | MODIFIER | c.79+9387dupA | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43085933 | ||||||
| chr6:43085933 | CA | C | 24 | a0001c0001t0001g0246 a0001c0001t0001g0262 a0001c0001t0001g0268 others(21): Show |
24 | HG00423.hp2 HG00609.hp1 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.79+9387delA | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43085933 | ||||||
| chr6:43085953 | A | AT | 60 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(57): Show |
60 | HG00323.hp1 HG00597.hp2 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.79+9386_79+9387ins others(1): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43085953 | |||||||
| chr6:43085953 | A | T | 78 | a0001c0001t0001g0066 a0001c0001t0001g0073 a0001c0001t0001g0132 others(75): Show |
78 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.79+9386A>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43085953 | |||||||
| chr6:43086097 | C | T | 1 | a0001c0001t0001g0002 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.79+9530C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43086097 | |||||||
| chr6:43086309 | T | C | 1 | a0001c0001t0002g0010 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.79+9742T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43086309 | |||||||
| chr6:43086346 | C | T | 1 | a0001c0001t0001g0211 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.79+9779C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43086346 | |||||||
| chr6:43086369 | C | T | 3 | a0001c0001t0002g0234 a0001c0001t0002g0242 a0001c0002t0009g0233 |
3 | HG01891.hp1 HG02895.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.79+9802C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43086369 | |||||||
| chr6:43086416 | C | CT | 6 | a0001c0001t0001g0135 a0001c0001t0001g0220 a0001c0001t0002g0221 others(3): Show |
6 | HG02027.hp1 HG02818.hp1 NA18995.hp2 others(3): Show |
intron_variant | MODIFIER | c.79+9863dupT | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43086416 | ||||||
| chr6:43086416 | CT | C | 32 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0086 others(29): Show |
32 | HG00544.hp1 HG00639.hp1 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.79+9863delT | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43086416 | ||||||
| chr6:43086469 | C | T | 1 | a0001c0017t0001g0232 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.79+9902C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43086469 | |||||||
| chr6:43086769 | A | C | 1 | a0001c0002t0001g0129 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.79+10202A>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43086769 | |||||||
| chr6:43086894 | A | G | 2 | a0001c0002t0001g0168 a0001c0002t0001g0169 |
2 | HG01074.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.79+10327A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43086894 | |||||||
| chr6:43086902 | A | G | 4 | a0001c0001t0002g0222 a0001c0001t0002g0223 a0001c0001t0002g0224 others(1): Show |
4 | HG02970.hp2 HG03130.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.79+10335A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43086902 | |||||||
| chr6:43086908 | G | A | 1 | a0001c0006t0001g0078 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.79+10341G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43086908 | |||||||
| chr6:43086983 | C | T | 1 | a0001c0001t0001g0227 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.79+10416C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43086983 | |||||||
| chr6:43087746 | C | T | 5 | a0001c0001t0001g0085 a0001c0001t0001g0126 a0001c0001t0001g0127 others(2): Show |
5 | HG00423.hp1 HG02056.hp1 NA18943.hp2 others(2): Show |
intron_variant | MODIFIER | c.79+11179C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43087746 | |||||||
| chr6:43087856 | T | C | 1 | a0001c0001t0001g0244 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.79+11289T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43087856 | |||||||
| chr6:43087858 | T | C | 2 | a0001c0001t0001g0011 a0001c0001t0001g0058 |
2 | HG03834.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.79+11291T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43087858 | |||||||
| chr6:43088374 | A | G | 2 | a0001c0002t0001g0183 a0001c0002t0001g0184 |
2 | HG02630.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.79+11807A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43088374 | |||||||
| chr6:43088395 | A | G | 4 | a0001c0001t0002g0222 a0001c0001t0002g0223 a0001c0001t0002g0224 others(1): Show |
4 | HG02970.hp2 HG03130.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.79+11828A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43088395 | |||||||
| chr6:43088647 | A | G | 2 | a0001c0001t0001g0220 a0001c0001t0002g0221 |
2 | HG02027.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.79+12080A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43088647 | |||||||
| chr6:43088690 | A | AAAAT | 36 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0071 others(33): Show |
36 | HG00423.hp1 HG00544.hp2 HG00733.hp2 others(33): Show |
intron_variant | MODIFIER | c.79+12163_79+12166d others(6): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43088690 | ||||||
| chr6:43088690 | AAAAT | A | 9 | a0001c0001t0001g0085 a0001c0001t0001g0202 a0001c0001t0002g0222 others(6): Show |
9 | HG00741.hp1 HG02083.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.79+12163_79+12166d others(6): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43088690 | ||||||
| chr6:43088690 | AAAATAAA others(1): Show |
A | 3 | a0001c0001t0001g0087 a0001c0001t0001g0220 a0001c0001t0002g0221 |
3 | HG02027.hp1 NA18612.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.79+12159_79+12166d others(10): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43088690 | ||||||
| chr6:43088831 | T | G | 1 | a0001c0001t0002g0214 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.79+12264T>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43088831 | |||||||
| chr6:43088923 | T | C | 142 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(139): Show |
142 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.79+12356T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43088923 | |||||||
| chr6:43088951 | G | A | 1 | a0001c0001t0001g0199 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.79+12384G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43088951 | |||||||
| chr6:43089061 | T | G | 2 | a0001c0001t0001g0011 a0001c0001t0001g0058 |
2 | HG03834.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.79+12494T>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43089061 | |||||||
| chr6:43089454 | C | T | 2 | a0001c0001t0001g0220 a0001c0001t0002g0221 |
2 | HG02027.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.79+12887C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43089454 | |||||||
| chr6:43089527 | A | T | 2 | a0001c0001t0001g0220 a0001c0001t0002g0221 |
2 | HG02027.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.79+12960A>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43089527 | |||||||
| chr6:43089555 | A | G | 1 | a0001c0001t0001g0071 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.79+12988A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43089555 | |||||||
| chr6:43089843 | A | G | 142 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(139): Show |
142 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.79+13276A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43089843 | |||||||
| chr6:43090172 | G | T | 5 | a0001c0001t0002g0222 a0001c0001t0002g0223 a0001c0001t0002g0224 others(2): Show |
5 | HG02809.hp1 HG02970.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.79+13605G>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43090172 | |||||||
| chr6:43090547 | G | T | 5 | a0001c0001t0002g0222 a0001c0001t0002g0223 a0001c0001t0002g0224 others(2): Show |
5 | HG02809.hp1 HG02970.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.79+13980G>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43090547 | |||||||
| chr6:43090563 | A | G | 5 | a0001c0001t0002g0222 a0001c0001t0002g0223 a0001c0001t0002g0224 others(2): Show |
5 | HG02809.hp1 HG02970.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.79+13996A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43090563 | |||||||
| chr6:43090601 | G | A | 1 | a0001c0002t0001g0182 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.79+14034G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43090601 | |||||||
| chr6:43090649 | G | A | 1 | a0001c0002t0001g0145 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.79+14082G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43090649 | |||||||
| chr6:43090722 | C | T | 1 | a0001c0002t0001g0120 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.79+14155C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43090722 | |||||||
| chr6:43090819 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.79+14252G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43090819 | |||||||
| chr6:43090894 | T | G | 7 | a0001c0001t0002g0012 a0001c0001t0002g0222 a0001c0001t0002g0223 others(4): Show |
7 | HG02809.hp2 HG02970.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.79+14327T>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43090894 | |||||||
| chr6:43090998 | C | G | 157 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(154): Show |
157 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(154): Show |
intron_variant | MODIFIER | c.79+14431C>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43090998 | |||||||
| chr6:43091146 | G | C | 1 | a0001c0001t0002g0012 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.79+14579G>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43091146 | |||||||
| chr6:43091154 | C | CT | 68 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(65): Show |
68 | HG00323.hp1 HG00597.hp2 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.79+14605dupT | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43091154 | ||||||
| chr6:43091304 | G | T | 1 | a0001c0002t0001g0125 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.79+14737G>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43091304 | |||||||
| chr6:43091623 | C | T | 66 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0132 others(63): Show |
66 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.79+15056C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43091623 | |||||||
| chr6:43092049 | G | A | 1 | a0001c0001t0002g0005 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.79+15482G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43092049 | |||||||
| chr6:43092156 | C | T | 1 | a0001c0002t0001g0247 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.79+15589C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43092156 | |||||||
| chr6:43092208 | C | G | 1 | a0001c0002t0002g0249 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.79+15641C>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43092208 | |||||||
| chr6:43092232 | G | C | 4 | a0001c0001t0001g0013 a0001c0001t0002g0044 a0001c0001t0002g0047 others(1): Show |
4 | HG01891.hp2 HG02622.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.79+15665G>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43092232 | |||||||
| chr6:43092330 | C | T | 1 | a0003c0016t0002g0225 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.79+15763C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43092330 | |||||||
| chr6:43092523 | T | C | 6 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0015 others(3): Show |
6 | NA18968.hp2 NA18999.hp2 NA19002.hp2 others(3): Show |
intron_variant | MODIFIER | c.79+15956T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43092523 | |||||||
| chr6:43092791 | T | C | 1 | a0006c0020t0006g0226 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.79+16224T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43092791 | |||||||
| chr6:43092950 | C | A | 1 | a0001c0002t0001g0146 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.79+16383C>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43092950 | |||||||
| chr6:43093036 | T | C | 5 | a0001c0001t0002g0222 a0001c0001t0002g0223 a0001c0001t0002g0224 others(2): Show |
5 | HG02809.hp1 HG02970.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.79+16469T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43093036 | |||||||
| chr6:43093056 | G | A | 1 | a0001c0001t0001g0211 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.79+16489G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43093056 | |||||||
| chr6:43093183 | C | CT | 116 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0022 others(113): Show |
116 | HG00423.hp2 HG00544.hp1 HG00597.hp2 others(113): Show |
intron_variant | MODIFIER | c.79+16639dupT | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43093183 | ||||||
| chr6:43093183 | C | CTT | 33 | a0001c0001t0001g0006 a0001c0001t0001g0124 a0001c0001t0001g0230 others(30): Show |
33 | HG00323.hp1 HG00741.hp2 HG01261.hp1 others(30): Show |
intron_variant | MODIFIER | c.79+16638_79+16639d others(4): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43093183 | ||||||
| chr6:43093183 | CT | C | 7 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0080 others(4): Show |
7 | HG00642.hp2 HG01081.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.79+16639delT | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43093183 | ||||||
| chr6:43093211 | C | T | 5 | a0001c0001t0002g0222 a0001c0001t0002g0223 a0001c0001t0002g0224 others(2): Show |
5 | HG02809.hp1 HG02970.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.79+16644C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43093211 | |||||||
| chr6:43093249 | G | C | 3 | a0001c0001t0001g0170 a0001c0001t0001g0172 a0001c0001t0001g0173 |
3 | HG01069.hp2 HG01099.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.79+16682G>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43093249 | |||||||
| chr6:43093371 | T | G | 1 | a0001c0001t0001g0088 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.79+16804T>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43093371 | |||||||
| chr6:43093476 | C | G | 2 | a0001c0001t0001g0037 a0001c0001t0002g0036 |
2 | NA18969.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.79+16909C>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43093476 | |||||||
| chr6:43093505 | A | T | 1 | a0001c0001t0001g0238 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.79+16938A>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43093505 | |||||||
| chr6:43093784 | G | T | 3 | a0002c0003t0002g0162 a0002c0003t0002g0163 a0002c0003t0002g0178 |
3 | HG02258.hp2 HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.79+17217G>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43093784 | |||||||
| chr6:43093796 | G | A | 1 | a0001c0002t0001g0182 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.79+17229G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43093796 | |||||||
| chr6:43094019 | G | A | 1 | a0001c0002t0001g0258 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.79+17452G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43094019 | |||||||
| chr6:43094467 | A | AT | 8 | a0001c0001t0001g0119 a0001c0001t0002g0009 a0001c0001t0002g0222 others(5): Show |
8 | HG00597.hp2 HG02056.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.79+17916dupT | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43094467 | ||||||
| chr6:43094488 | C | T | 1 | a0001c0001t0001g0037 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.79+17921C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43094488 | |||||||
| chr6:43094503 | C | T | 1 | a0001c0002t0001g0196 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.79+17936C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43094503 | |||||||
| chr6:43094562 | T | C | 3 | a0001c0001t0002g0234 a0001c0001t0002g0242 a0001c0002t0009g0233 |
3 | HG01891.hp1 HG02895.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.79+17995T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43094562 | |||||||
| chr6:43094660 | A | C | 1 | a0001c0001t0001g0197 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.79+18093A>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43094660 | |||||||
| chr6:43094700 | G | T | 1 | a0001c0001t0004g0269 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.79+18133G>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43094700 | |||||||
| chr6:43094720 | C | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0058 |
2 | HG03834.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.79+18153C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43094720 | |||||||
| chr6:43094724 | C | T | 1 | a0001c0002t0001g0140 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.79+18157C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43094724 | |||||||
| chr6:43094769 | C | T | 1 | a0001c0002t0001g0267 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.79+18202C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43094769 | |||||||
| chr6:43094774 | G | A | 5 | a0001c0001t0002g0222 a0001c0001t0002g0223 a0001c0001t0002g0224 others(2): Show |
5 | HG02809.hp1 HG02970.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.79+18207G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43094774 | |||||||
| chr6:43094906 | G | A | 1 | a0001c0001t0001g0268 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.79+18339G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43094906 | |||||||
| chr6:43095080 | C | G | 1 | a0001c0001t0001g0072 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.79+18513C>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43095080 | |||||||
| chr6:43095177 | T | A | 4 | a0001c0001t0002g0214 a0001c0002t0003g0148 a0001c0002t0003g0149 others(1): Show |
4 | HG02109.hp1 HG02451.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.79+18610T>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43095177 | |||||||
| chr6:43095197 | T | TA | 70 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(67): Show |
70 | HG00597.hp2 HG00639.hp2 HG00642.hp1 others(67): Show |
intron_variant | MODIFIER | c.79+18654dupA | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43095197 | ||||||
| chr6:43095197 | TA | T | 72 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0072 others(69): Show |
72 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.79+18654delA | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43095197 | ||||||
| chr6:43095262 | C | T | 1 | a0001c0002t0001g0161 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.79+18695C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43095262 | |||||||
| chr6:43095344 | C | T | 1 | a0001c0002t0003g0014 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.79+18777C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43095344 | |||||||
| chr6:43095626 | G | A | 2 | a0001c0002t0001g0250 a0001c0002t0001g0251 |
2 | HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.79+19059G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43095626 | |||||||
| chr6:43095677 | T | G | 2 | a0001c0001t0001g0186 a0001c0002t0001g0198 |
2 | NA18947.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.79+19110T>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43095677 | |||||||
| chr6:43095732 | T | G | 1 | a0001c0001t0002g0009 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.79+19165T>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43095732 | |||||||
| chr6:43095778 | A | C | 68 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(65): Show |
68 | HG00323.hp1 HG00597.hp2 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.79+19211A>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43095778 | |||||||
| chr6:43095923 | C | T | 1 | a0001c0001t0002g0272 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.79+19356C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43095923 | |||||||
| chr6:43096080 | A | G | 3 | a0001c0001t0001g0230 a0001c0002t0002g0231 a0001c0017t0001g0232 |
3 | HG00741.hp2 HG02055.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.79+19513A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43096080 | |||||||
| chr6:43096108 | G | C | 75 | a0001c0001t0001g0066 a0001c0001t0001g0072 a0001c0001t0001g0073 others(72): Show |
75 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.79+19541G>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43096108 | |||||||
| chr6:43096315 | G | A | 25 | a0001c0001t0001g0022 a0001c0001t0001g0037 a0001c0001t0001g0051 others(22): Show |
25 | HG00323.hp1 HG00597.hp2 HG01175.hp1 others(22): Show |
intron_variant | MODIFIER | c.79+19748G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43096315 | |||||||
| chr6:43096423 | G | T | 9 | a0001c0001t0001g0230 a0001c0001t0002g0234 a0001c0001t0002g0242 others(6): Show |
9 | HG00741.hp2 HG01891.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.79+19856G>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43096423 | |||||||
| chr6:43096753 | C | T | 1 | a0001c0001t0004g0269 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.79+20186C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43096753 | |||||||
| chr6:43096957 | G | GGGCCGTG others(26): Show |
150 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(147): Show |
150 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.79+20392_79+20424d others(35): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43096957 | ||||||
| chr6:43096999 | A | G | 1 | a0001c0001t0001g0160 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.79+20432A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43096999 | |||||||
| chr6:43097102 | C | T | 1 | a0001c0010t0002g0045 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.79+20535C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43097102 | |||||||
| chr6:43097136 | G | A | 1 | a0002c0003t0002g0121 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.79+20569G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43097136 | |||||||
| chr6:43097232 | C | T | 6 | a0001c0001t0001g0230 a0001c0002t0002g0231 a0001c0012t0002g0229 others(3): Show |
6 | HG00741.hp2 HG02055.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.79+20665C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43097232 | |||||||
| chr6:43097245 | C | A | 2 | a0001c0001t0002g0059 a0001c0001t0002g0060 |
2 | HG00642.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.79+20678C>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43097245 | |||||||
| chr6:43097591 | T | C | 150 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(147): Show |
150 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.79+21024T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43097591 | |||||||
| chr6:43097653 | C | G | 1 | a0001c0012t0002g0229 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.79+21086C>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43097653 | |||||||
| chr6:43097678 | C | T | 1 | a0002c0003t0002g0121 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.79+21111C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43097678 | |||||||
| chr6:43097688 | T | C | 1 | a0001c0002t0001g0089 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.79+21121T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43097688 | |||||||
| chr6:43097821 | G | C | 5 | a0001c0001t0002g0222 a0001c0001t0002g0223 a0001c0001t0002g0224 others(2): Show |
5 | HG02809.hp1 HG02970.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.79+21254G>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43097821 | |||||||
| chr6:43098175 | A | G | 75 | a0001c0001t0001g0066 a0001c0001t0001g0072 a0001c0001t0001g0073 others(72): Show |
75 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.79+21608A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43098175 | |||||||
| chr6:43098386 | C | T | 73 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(70): Show |
73 | HG00323.hp1 HG00597.hp2 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.79+21819C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43098386 | |||||||
| chr6:43098400 | G | C | 3 | a0001c0001t0002g0012 a0001c0001t0002g0020 a0001c0021t0002g0019 |
3 | HG03669.hp1 HG03704.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.79+21833G>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43098400 | |||||||
| chr6:43098773 | A | AAGC | 150 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(147): Show |
150 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.79+22208_79+22210d others(5): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43098773 | ||||||
| chr6:43098818 | A | G | 1 | a0001c0001t0001g0069 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.79+22251A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43098818 | |||||||
| chr6:43098870 | G | T | 1 | a0001c0001t0001g0166 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.79+22303G>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43098870 | |||||||
| chr6:43098920 | A | T | 1 | a0006c0020t0006g0226 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.79+22353A>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43098920 | |||||||
| chr6:43099109 | C | T | 3 | a0001c0001t0002g0179 a0001c0002t0001g0180 a0001c0002t0001g0181 |
3 | HG02280.hp2 HG02922.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.79+22542C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43099109 | |||||||
| chr6:43099132 | T | A | 1 | a0003c0016t0002g0225 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.79+22565T>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43099132 | |||||||
| chr6:43099235 | C | CT | 65 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0022 others(62): Show |
65 | HG00323.hp1 HG00597.hp2 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.79+22683dupT | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43099235 | ||||||
| chr6:43099235 | C | CTTTT | 9 | a0001c0001t0001g0013 a0001c0001t0002g0005 a0001c0001t0002g0033 others(6): Show |
9 | HG01891.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.79+22680_79+22683d others(6): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43099235 | ||||||
| chr6:43099235 | CT | C | 9 | a0001c0001t0001g0187 a0001c0001t0001g0199 a0001c0001t0001g0200 others(6): Show |
9 | HG01167.hp2 HG02109.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.79+22683delT | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43099235 | ||||||
| chr6:43099409 | T | A | 5 | a0001c0001t0001g0230 a0001c0002t0002g0231 a0001c0012t0002g0229 others(2): Show |
5 | HG00741.hp2 HG02055.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.79+22842T>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43099409 | |||||||
| chr6:43099463 | G | C | 4 | a0001c0002t0002g0249 a0001c0002t0004g0228 a0002c0018t0001g0248 others(1): Show |
4 | HG02145.hp2 HG02818.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.79+22896G>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43099463 | |||||||
| chr6:43099590 | G | A | 1 | a0001c0001t0004g0269 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.79+23023G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43099590 | |||||||
| chr6:43099749 | G | A | 73 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(70): Show |
73 | HG00323.hp1 HG00597.hp2 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.79+23182G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43099749 | |||||||
| chr6:43099857 | T | C | 3 | a0001c0001t0002g0012 a0001c0001t0002g0020 a0001c0021t0002g0019 |
3 | HG03669.hp1 HG03704.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.79+23290T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43099857 | |||||||
| chr6:43100033 | G | A | 1 | a0001c0001t0001g0127 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.79+23466G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43100033 | |||||||
| chr6:43100171 | C | G | 1 | a0002c0018t0001g0248 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.79+23604C>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43100171 | |||||||
| chr6:43100226 | A | G | 1 | a0001c0001t0001g0199 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.79+23659A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43100226 | |||||||
| chr6:43100382 | CA | C | 41 | a0001c0001t0001g0066 a0001c0001t0001g0072 a0001c0001t0001g0073 others(38): Show |
41 | HG00544.hp1 HG00639.hp1 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.79+23830delA | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43100382 | ||||||
| chr6:43100406 | G | GT | 67 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(64): Show |
67 | HG00323.hp1 HG00597.hp2 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.79+23846dupT | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43100406 | ||||||
| chr6:43100414 | A | T | 78 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(75): Show |
78 | HG00323.hp1 HG00597.hp2 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.79+23847A>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43100414 | |||||||
| chr6:43100445 | C | CT | 158 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(155): Show |
158 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(155): Show |
intron_variant | MODIFIER | c.79+23887dupT | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43100445 | ||||||
| chr6:43100545 | G | GT | 158 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(155): Show |
158 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(155): Show |
intron_variant | MODIFIER | c.79+23979dupT | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43100545 | ||||||
| chr6:43100574 | G | C | 1 | a0001c0001t0002g0116 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.79+24007G>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43100574 | |||||||
| chr6:43100632 | G | T | 35 | a0001c0001t0001g0066 a0001c0001t0001g0072 a0001c0001t0001g0073 others(32): Show |
35 | HG00544.hp1 HG00639.hp1 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.79+24065G>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43100632 | |||||||
| chr6:43100724 | C | G | 2 | a0001c0001t0001g0238 a0003c0004t0002g0235 |
2 | HG01255.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.79+24157C>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43100724 | |||||||
| chr6:43100747 | T | C | 5 | a0001c0001t0002g0222 a0001c0001t0002g0223 a0001c0001t0002g0224 others(2): Show |
5 | HG02809.hp1 HG02970.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.79+24180T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43100747 | |||||||
| chr6:43100932 | G | A | 2 | a0003c0004t0002g0024 a0003c0004t0002g0025 |
2 | HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.79+24365G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43100932 | |||||||
| chr6:43101033 | G | A | 9 | a0001c0001t0001g0119 a0001c0001t0002g0067 a0001c0001t0002g0082 others(6): Show |
9 | HG02027.hp2 HG02056.hp2 NA18947.hp2 others(6): Show |
intron_variant | MODIFIER | c.79+24466G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43101033 | |||||||
| chr6:43101225 | A | AAAAAGAA others(6): Show |
2 | a0001c0001t0001g0220 a0001c0001t0002g0221 |
2 | HG02027.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.79+24661_79+24662i others(15): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43101225 | ||||||
| chr6:43101225 | A | AAAAG | 71 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(68): Show |
71 | HG00323.hp1 HG00597.hp2 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.79+24676_79+24679d others(6): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43101225 | ||||||
| chr6:43101283 | T | C | 1 | a0002c0003t0001g0243 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.79+24716T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43101283 | |||||||
| chr6:43101475 | C | T | 1 | a0001c0001t0001g0186 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.79+24908C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43101475 | |||||||
| chr6:43101506 | T | C | 150 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(147): Show |
150 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.79+24939T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43101506 | |||||||
| chr6:43101563 | T | G | 1 | a0001c0002t0001g0203 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.79+24996T>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43101563 | |||||||
| chr6:43101606 | A | G | 75 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(72): Show |
75 | HG00323.hp1 HG00597.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.79+25039A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43101606 | |||||||
| chr6:43101609 | A | G | 1 | a0001c0001t0002g0032 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.79+25042A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43101609 | |||||||
| chr6:43101664 | A | G | 1 | a0001c0001t0002g0060 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.79+25097A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43101664 | |||||||
| chr6:43101709 | T | C | 3 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0086 |
3 | HG00642.hp2 HG01081.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.79+25142T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43101709 | |||||||
| chr6:43101772 | T | G | 5 | a0001c0001t0002g0222 a0001c0001t0002g0223 a0001c0001t0002g0224 others(2): Show |
5 | HG02809.hp1 HG02970.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.79+25205T>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43101772 | |||||||
| chr6:43101779 | C | T | 50 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0037 others(47): Show |
50 | HG00323.hp1 HG00597.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.79+25212C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43101779 | |||||||
| chr6:43101930 | T | C | 1 | a0001c0001t0004g0269 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.79+25363T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43101930 | |||||||
| chr6:43101987 | G | C | 1 | a0001c0001t0001g0079 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.79+25420G>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43101987 | |||||||
| chr6:43102135 | C | T | 1 | a0001c0001t0002g0234 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.79+25568C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43102135 | |||||||
| chr6:43102152 | A | G | 1 | a0001c0002t0001g0129 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.79+25585A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43102152 | |||||||
| chr6:43102292 | G | A | 68 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(65): Show |
68 | HG00323.hp1 HG00597.hp2 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.79+25725G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43102292 | |||||||
| chr6:43102293 | C | T | 3 | a0001c0001t0002g0234 a0001c0001t0002g0242 a0001c0002t0009g0233 |
3 | HG01891.hp1 HG02895.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.79+25726C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43102293 | |||||||
| chr6:43102349 | C | T | 1 | a0001c0002t0001g0109 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.79+25782C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43102349 | |||||||
| chr6:43102558 | C | T | 2 | a0001c0008t0001g0107 a0001c0008t0001g0108 |
2 | NA18944.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.79+25991C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43102558 | |||||||
| chr6:43102598 | A | C | 2 | a0001c0001t0001g0220 a0001c0001t0002g0221 |
2 | HG02027.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.79+26031A>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43102598 | |||||||
| chr6:43102600 | C | CA | 9 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0220 others(6): Show |
9 | HG02027.hp1 HG02135.hp1 HG02300.hp2 others(6): Show |
intron_variant | MODIFIER | c.79+26042dupA | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43102600 | ||||||
| chr6:43102887 | T | C | 1 | a0001c0012t0002g0229 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.80-26090T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43102887 | |||||||
| chr6:43102949 | A | T | 3 | a0001c0001t0002g0222 a0001c0001t0002g0223 a0001c0001t0002g0224 |
3 | HG02970.hp2 HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.80-26028A>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43102949 | |||||||
| chr6:43103190 | T | C | 2 | a0001c0001t0001g0011 a0001c0001t0001g0058 |
2 | HG03834.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.80-25787T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43103190 | |||||||
| chr6:43103456 | G | GGT | 42 | a0001c0001t0001g0230 a0001c0001t0001g0246 a0001c0001t0001g0262 others(39): Show |
42 | HG00423.hp2 HG00609.hp1 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.80-25500_80-25499d others(4): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43103456 | ||||||
| chr6:43103456 | G | GGTGT | 41 | a0001c0001t0001g0066 a0001c0001t0001g0072 a0001c0001t0001g0073 others(38): Show |
41 | HG00544.hp1 HG00639.hp1 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.80-25502_80-25499d others(6): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43103456 | ||||||
| chr6:43103456 | G | GGTGTGT | 61 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(58): Show |
61 | HG00323.hp1 HG00597.hp2 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.80-25504_80-25499d others(8): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43103456 | ||||||
| chr6:43103456 | G | GGTGTGTG others(1): Show |
7 | a0001c0001t0002g0082 a0001c0001t0002g0083 a0001c0001t0002g0116 others(4): Show |
7 | HG02027.hp2 HG04184.hp1 NA18947.hp2 others(4): Show |
intron_variant | MODIFIER | c.80-25506_80-25499d others(10): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43103456 | ||||||
| chr6:43103552 | C | T | 68 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(65): Show |
68 | HG00323.hp1 HG00597.hp2 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.80-25425C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43103552 | |||||||
| chr6:43103609 | G | A | 1 | a0001c0002t0001g0267 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.80-25368G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43103609 | |||||||
| chr6:43103642 | C | T | 1 | a0002c0003t0001g0243 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.80-25335C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43103642 | |||||||
| chr6:43103800 | T | G | 72 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(69): Show |
72 | HG00323.hp1 HG00597.hp2 HG00642.hp1 others(69): Show |
intron_variant | MODIFIER | c.80-25177T>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43103800 | |||||||
| chr6:43104092 | A | G | 1 | a0002c0018t0001g0248 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.80-24885A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43104092 | |||||||
| chr6:43104123 | A | G | 1 | a0001c0001t0002g0032 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.80-24854A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43104123 | |||||||
| chr6:43104409 | A | T | 1 | a0006c0020t0006g0226 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.80-24568A>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43104409 | |||||||
| chr6:43104479 | A | G | 69 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(66): Show |
69 | HG00323.hp1 HG00597.hp2 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.80-24498A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43104479 | |||||||
| chr6:43104525 | C | G | 1 | a0001c0001t0002g0020 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.80-24452C>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43104525 | |||||||
| chr6:43104535 | T | C | 1 | a0001c0001t0002g0020 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.80-24442T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43104535 | |||||||
| chr6:43104808 | C | CT | 70 | a0001c0001t0001g0066 a0001c0001t0001g0072 a0001c0001t0001g0073 others(67): Show |
70 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.80-24147dupT | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43104808 | ||||||
| chr6:43104808 | C | CTT | 12 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 others(9): Show |
12 | HG00741.hp2 HG02055.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.80-24148_80-24147d others(4): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43104808 | ||||||
| chr6:43104808 | CT | C | 63 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(60): Show |
63 | HG00323.hp1 HG00597.hp2 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.80-24147delT | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43104808 | ||||||
| chr6:43104847 | C | G | 1 | a0001c0001t0001g0088 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.80-24130C>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43104847 | |||||||
| chr6:43104993 | A | T | 1 | a0001c0002t0001g0140 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.80-23984A>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43104993 | |||||||
| chr6:43105002 | G | A | 2 | a0001c0001t0001g0072 a0001c0001t0001g0132 |
2 | NA18612.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.80-23975G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43105002 | |||||||
| chr6:43105013 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.80-23964G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43105013 | |||||||
| chr6:43105058 | G | A | 1 | a0003c0004t0002g0046 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.80-23919G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43105058 | |||||||
| chr6:43105124 | T | A | 2 | a0001c0015t0001g0240 a0003c0014t0002g0241 |
2 | HG02145.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.80-23853T>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43105124 | |||||||
| chr6:43105125 | A | T | 4 | a0001c0001t0001g0238 a0001c0001t0004g0269 a0002c0003t0001g0243 others(1): Show |
4 | HG01255.hp2 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-23852A>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43105125 | |||||||
| chr6:43105126 | A | T | 1 | a0002c0003t0001g0243 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.80-23851A>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43105126 | |||||||
| chr6:43105347 | G | A | 10 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0135 others(7): Show |
10 | HG02135.hp2 NA18950.hp2 NA18954.hp1 others(7): Show |
intron_variant | MODIFIER | c.80-23630G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43105347 | |||||||
| chr6:43105450 | C | CA | 117 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(114): Show |
117 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.80-23507dupA | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43105450 | ||||||
| chr6:43105450 | C | CAA | 40 | a0001c0001t0001g0119 a0001c0001t0001g0192 a0001c0001t0001g0220 others(37): Show |
40 | HG00423.hp2 HG01099.hp1 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.80-23508_80-23507d others(4): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43105450 | ||||||
| chr6:43105450 | CA | C | 24 | a0001c0001t0001g0092 a0001c0001t0001g0153 a0001c0001t0001g0154 others(21): Show |
24 | HG00741.hp1 HG01074.hp1 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.80-23507delA | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43105450 | ||||||
| chr6:43105653 | A | T | 1 | a0001c0001t0002g0256 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.80-23324A>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43105653 | |||||||
| chr6:43105865 | C | A | 1 | a0001c0002t0001g0090 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.80-23112C>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43105865 | |||||||
| chr6:43105866 | C | T | 2 | a0001c0001t0001g0220 a0001c0001t0002g0221 |
2 | HG02027.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.80-23111C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43105866 | |||||||
| chr6:43105913 | T | C | 2 | a0001c0001t0001g0220 a0001c0001t0002g0221 |
2 | HG02027.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.80-23064T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43105913 | |||||||
| chr6:43106139 | C | T | 1 | a0001c0002t0001g0091 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.80-22838C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43106139 | |||||||
| chr6:43106457 | A | G | 12 | a0001c0001t0002g0101 a0001c0002t0001g0089 a0001c0002t0001g0091 others(9): Show |
12 | HG00544.hp2 HG01258.hp1 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.80-22520A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43106457 | |||||||
| chr6:43106536 | C | T | 2 | a0001c0001t0001g0085 a0001c0001t0002g0272 |
2 | HG02056.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.80-22441C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43106536 | |||||||
| chr6:43106608 | G | A | 1 | a0006c0020t0006g0226 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.80-22369G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43106608 | |||||||
| chr6:43106650 | C | CT | 19 | a0001c0001t0001g0069 a0001c0001t0001g0071 a0001c0001t0001g0199 others(16): Show |
19 | HG01167.hp1 HG01258.hp1 HG01346.hp2 others(16): Show |
intron_variant | MODIFIER | c.80-22306dupT | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43106650 | ||||||
| chr6:43106650 | CT | C | 111 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(108): Show |
111 | HG00323.hp1 HG00544.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.80-22306delT | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43106650 | ||||||
| chr6:43106652 | T | C | 1 | a0001c0001t0001g0211 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.80-22325T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43106652 | |||||||
| chr6:43106708 | C | T | 3 | a0001c0001t0001g0187 a0001c0001t0001g0190 a0001c0001t0001g0194 |
3 | HG01167.hp2 HG01169.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.80-22269C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43106708 | |||||||
| chr6:43106839 | C | T | 1 | a0001c0001t0001g0199 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.80-22138C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43106839 | |||||||
| chr6:43106842 | C | T | 34 | a0001c0001t0001g0230 a0001c0001t0001g0246 a0001c0001t0001g0262 others(31): Show |
34 | HG00423.hp2 HG00609.hp1 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.80-22135C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43106842 | |||||||
| chr6:43106869 | GCCTCCCA others(301): Show |
G | 1 | a0006c0020t0006g0226 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.80-22071_80-21764d others(2): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43106869 | ||||||
| chr6:43106914 | CCTCTT | C | 5 | a0001c0001t0002g0222 a0001c0001t0002g0223 a0001c0001t0002g0224 others(2): Show |
5 | HG02809.hp1 HG02970.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.80-22061_80-22057d others(7): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43106914 | ||||||
| chr6:43106926 | AT | A | 116 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(113): Show |
116 | HG00323.hp1 HG00544.hp1 HG00597.hp2 others(113): Show |
intron_variant | MODIFIER | c.80-22037delT | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43106926 | ||||||
| chr6:43106926 | ATT | A | 31 | a0001c0001t0001g0230 a0001c0001t0001g0246 a0001c0001t0001g0262 others(28): Show |
31 | HG00423.hp2 HG00741.hp2 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.80-22038_80-22037d others(4): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43106926 | ||||||
| chr6:43106928 | T | TTTTTTTT others(260): Show |
1 | a0002c0003t0002g0121 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.80-21995_80-21994i others(269): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43106928 | ||||||
| chr6:43106987 | A | C | 1 | a0001c0002t0004g0139 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.80-21990A>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43106987 | |||||||
| chr6:43107158 | A | T | 1 | a0001c0001t0002g0195 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.80-21819A>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43107158 | |||||||
| chr6:43107218 | C | G | 1 | a0001c0012t0002g0229 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.80-21759C>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43107218 | |||||||
| chr6:43107549 | T | A | 1 | a0006c0020t0006g0226 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.80-21428T>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43107549 | |||||||
| chr6:43107744 | C | T | 7 | a0001c0001t0001g0200 a0001c0001t0001g0202 a0001c0001t0001g0204 others(4): Show |
7 | HG02109.hp2 HG02258.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.80-21233C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43107744 | |||||||
| chr6:43107844 | C | T | 1 | a0001c0001t0004g0236 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.80-21133C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43107844 | |||||||
| chr6:43107875 | G | A | 1 | a0001c0001t0002g0028 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.80-21102G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43107875 | |||||||
| chr6:43107979 | C | T | 4 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0059 others(1): Show |
4 | HG00642.hp1 HG01175.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.80-20998C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43107979 | |||||||
| chr6:43108015 | GATT | G | 41 | a0001c0001t0001g0066 a0001c0001t0001g0072 a0001c0001t0001g0100 others(38): Show |
41 | HG00544.hp1 HG00733.hp2 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.80-20955_80-20953d others(5): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43108015 | ||||||
| chr6:43108094 | C | CT | 24 | a0001c0001t0001g0013 a0001c0001t0001g0064 a0001c0001t0001g0065 others(21): Show |
24 | HG00609.hp2 HG00741.hp2 HG01928.hp1 others(21): Show |
intron_variant | MODIFIER | c.80-20864dupT | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43108094 | ||||||
| chr6:43108094 | C | CTT | 5 | a0001c0001t0002g0222 a0001c0001t0002g0223 a0001c0001t0002g0224 others(2): Show |
5 | HG02970.hp2 HG03130.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.80-20865_80-20864d others(4): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43108094 | ||||||
| chr6:43108094 | CT | C | 14 | a0001c0001t0001g0077 a0001c0001t0001g0200 a0001c0001t0001g0204 others(11): Show |
14 | HG01496.hp2 HG01891.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.80-20864delT | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43108094 | ||||||
| chr6:43108287 | G | A | 4 | a0001c0001t0001g0069 a0001c0001t0001g0124 a0001c0001t0001g0133 others(1): Show |
4 | NA18978.hp2 NA19002.hp1 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.80-20690G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43108287 | |||||||
| chr6:43108545 | G | T | 7 | a0001c0001t0001g0013 a0001c0001t0002g0005 a0001c0001t0002g0033 others(4): Show |
7 | HG02486.hp2 HG02572.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.80-20432G>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43108545 | |||||||
| chr6:43108547 | A | T | 1 | a0001c0001t0001g0199 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.80-20430A>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43108547 | |||||||
| chr6:43108590 | C | T | 66 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(63): Show |
66 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.80-20387C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43108590 | |||||||
| chr6:43108602 | G | A | 1 | a0001c0002t0002g0249 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.80-20375G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43108602 | |||||||
| chr6:43108639 | C | T | 1 | a0001c0002t0001g0182 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.80-20338C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43108639 | |||||||
| chr6:43108653 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.80-20324C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43108653 | |||||||
| chr6:43108818 | G | A | 96 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(93): Show |
96 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(93): Show |
intron_variant | MODIFIER | c.80-20159G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43108818 | |||||||
| chr6:43109295 | C | T | 1 | a0001c0002t0001g0196 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.80-19682C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43109295 | |||||||
| chr6:43109404 | CT | C | 7 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0002t0001g0145 others(4): Show |
7 | HG01074.hp1 HG01123.hp2 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.80-19571delT | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43109404 | ||||||
| chr6:43109701 | C | CT | 6 | a0001c0001t0002g0041 a0001c0001t0002g0057 a0001c0001t0002g0082 others(3): Show |
6 | HG01261.hp1 HG02145.hp2 NA18944.hp1 others(3): Show |
intron_variant | MODIFIER | c.80-19261dupT | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43109701 | ||||||
| chr6:43109735 | G | A | 1 | a0001c0015t0001g0240 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.80-19242G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43109735 | |||||||
| chr6:43109896 | C | T | 2 | a0001c0008t0001g0107 a0001c0008t0001g0108 |
2 | NA18944.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.80-19081C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43109896 | |||||||
| chr6:43109905 | A | T | 1 | a0001c0002t0001g0196 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.80-19072A>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43109905 | |||||||
| chr6:43109997 | C | CT | 91 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(88): Show |
91 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.80-18963dupT | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43109997 | ||||||
| chr6:43109997 | C | CTT | 8 | a0001c0001t0002g0010 a0001c0001t0002g0030 a0001c0001t0002g0036 others(5): Show |
8 | HG02027.hp2 HG02976.hp1 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.80-18964_80-18963d others(4): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43109997 | ||||||
| chr6:43110168 | T | C | 1 | a0001c0001t0002g0265 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.80-18809T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43110168 | |||||||
| chr6:43110212 | G | C | 1 | a0001c0001t0001g0199 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.80-18765G>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43110212 | |||||||
| chr6:43110236 | T | C | 269 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(266): Show |
269 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(266): Show |
intron_variant | MODIFIER | c.80-18741T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43110236 | |||||||
| chr6:43110328 | T | C | 95 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(92): Show |
95 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.80-18649T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43110328 | |||||||
| chr6:43110381 | G | GT | 5 | a0001c0001t0001g0058 a0001c0001t0001g0119 a0001c0001t0002g0234 others(2): Show |
5 | HG01891.hp1 HG02056.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.80-18586dupT | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43110381 | ||||||
| chr6:43110389 | T | G | 2 | a0001c0001t0004g0269 a0005c0019t0001g0141 |
2 | HG02622.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.80-18588T>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43110389 | |||||||
| chr6:43110407 | GTTTTGT | G | 66 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(63): Show |
66 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.80-18552_80-18547d others(8): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43110407 | ||||||
| chr6:43110428 | T | C | 1 | a0001c0001t0001g0092 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.80-18549T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43110428 | |||||||
| chr6:43110461 | G | A | 1 | a0006c0020t0006g0226 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.80-18516G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43110461 | |||||||
| chr6:43110474 | G | A | 1 | a0001c0002t0001g0075 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.80-18503G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43110474 | |||||||
| chr6:43110653 | A | G | 152 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(149): Show |
152 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(149): Show |
intron_variant | MODIFIER | c.80-18324A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43110653 | |||||||
| chr6:43110662 | G | A | 2 | a0001c0001t0001g0212 a0001c0001t0001g0213 |
2 | HG00544.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.80-18315G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43110662 | |||||||
| chr6:43110709 | C | T | 1 | a0006c0020t0006g0226 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.80-18268C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43110709 | |||||||
| chr6:43110718 | A | G | 96 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(93): Show |
96 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(93): Show |
intron_variant | MODIFIER | c.80-18259A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43110718 | |||||||
| chr6:43110943 | G | A | 1 | a0001c0002t0001g0185 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.80-18034G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43110943 | |||||||
| chr6:43110982 | C | G | 2 | a0001c0001t0001g0268 a0001c0002t0001g0031 |
2 | HG04184.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.80-17995C>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43110982 | |||||||
| chr6:43111263 | C | T | 1 | a0001c0001t0001g0238 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.80-17714C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43111263 | |||||||
| chr6:43111594 | T | C | 28 | a0001c0001t0001g0246 a0001c0001t0001g0262 a0001c0001t0001g0268 others(25): Show |
28 | HG00423.hp2 HG01099.hp1 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.80-17383T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43111594 | |||||||
| chr6:43111596 | C | G | 3 | a0001c0001t0002g0234 a0001c0001t0002g0242 a0001c0002t0009g0233 |
3 | HG01891.hp1 HG02895.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.80-17381C>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43111596 | |||||||
| chr6:43111806 | C | T | 1 | a0006c0020t0006g0226 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.80-17171C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43111806 | |||||||
| chr6:43111837 | C | CT | 107 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(104): Show |
107 | HG00323.hp1 HG00544.hp1 HG00597.hp2 others(104): Show |
intron_variant | MODIFIER | c.80-17123dupT | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43111837 | ||||||
| chr6:43111837 | C | CTT | 6 | a0001c0001t0002g0048 a0001c0001t0002g0057 a0001c0001t0002g0256 others(3): Show |
6 | HG02145.hp1 HG02148.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.80-17124_80-17123d others(4): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43111837 | ||||||
| chr6:43111837 | C | CTTT | 23 | a0001c0001t0001g0246 a0001c0001t0001g0262 a0001c0001t0001g0268 others(20): Show |
23 | HG00423.hp2 HG01099.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.80-17125_80-17123d others(5): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43111837 | ||||||
| chr6:43111882 | G | A | 1 | a0001c0001t0004g0269 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.80-17095G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43111882 | |||||||
| chr6:43111961 | C | T | 1 | a0001c0001t0002g0032 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.80-17016C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43111961 | |||||||
| chr6:43112242 | T | TTTTA | 28 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0066 others(25): Show |
28 | HG00544.hp1 HG00642.hp2 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.80-16694_80-16691d others(6): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43112242 | ||||||
| chr6:43112242 | TTTTA | T | 80 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(77): Show |
80 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.80-16694_80-16691d others(6): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43112242 | ||||||
| chr6:43112242 | TTTTATTT others(1): Show |
T | 7 | a0001c0001t0002g0222 a0001c0001t0002g0223 a0001c0001t0002g0224 others(4): Show |
7 | HG02145.hp1 HG02970.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.80-16698_80-16691d others(10): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43112242 | ||||||
| chr6:43112242 | TTTTATTT others(5): Show |
T | 27 | a0001c0001t0001g0194 a0001c0001t0001g0246 a0001c0001t0001g0262 others(24): Show |
27 | HG00423.hp2 HG01099.hp1 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.80-16702_80-16691d others(14): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43112242 | ||||||
| chr6:43112439 | C | T | 1 | a0006c0020t0006g0226 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.80-16538C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43112439 | |||||||
| chr6:43112459 | T | C | 1 | a0001c0001t0001g0212 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.80-16518T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43112459 | |||||||
| chr6:43112710 | G | A | 5 | a0001c0001t0001g0202 a0001c0001t0001g0204 a0001c0001t0001g0206 others(2): Show |
5 | HG02109.hp2 HG02258.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.80-16267G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43112710 | |||||||
| chr6:43112713 | C | T | 3 | a0001c0001t0002g0234 a0001c0001t0002g0242 a0001c0002t0009g0233 |
3 | HG01891.hp1 HG02895.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.80-16264C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43112713 | |||||||
| chr6:43112746 | C | G | 2 | a0001c0001t0002g0059 a0001c0001t0002g0060 |
2 | HG00642.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.80-16231C>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43112746 | |||||||
| chr6:43112813 | A | C | 2 | a0001c0001t0002g0021 a0001c0001t0002g0265 |
2 | HG00609.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.80-16164A>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43112813 | |||||||
| chr6:43112813 | A | G | 1 | a0001c0001t0002g0082 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.80-16164A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43112813 | |||||||
| chr6:43112941 | G | A | 7 | a0001c0001t0001g0200 a0001c0001t0001g0202 a0001c0001t0001g0204 others(4): Show |
7 | HG02109.hp2 HG02258.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.80-16036G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43112941 | |||||||
| chr6:43112964 | G | A | 1 | a0001c0001t0001g0205 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.80-16013G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43112964 | |||||||
| chr6:43113003 | C | T | 152 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(149): Show |
152 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(149): Show |
intron_variant | MODIFIER | c.80-15974C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43113003 | |||||||
| chr6:43113012 | G | A | 1 | a0001c0001t0004g0269 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.80-15965G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43113012 | |||||||
| chr6:43113172 | C | G | 1 | a0006c0020t0006g0226 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.80-15805C>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43113172 | |||||||
| chr6:43113220 | C | T | 1 | a0006c0020t0006g0226 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.80-15757C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43113220 | |||||||
| chr6:43113248 | G | C | 96 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(93): Show |
96 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(93): Show |
intron_variant | MODIFIER | c.80-15729G>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43113248 | |||||||
| chr6:43113311 | T | C | 67 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(64): Show |
67 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.80-15666T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43113311 | |||||||
| chr6:43113615 | A | G | 4 | a0001c0001t0001g0230 a0001c0002t0002g0231 a0001c0012t0002g0229 others(1): Show |
4 | HG00741.hp2 HG02055.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-15362A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43113615 | |||||||
| chr6:43113709 | C | T | 3 | a0001c0001t0002g0234 a0001c0001t0002g0242 a0001c0002t0009g0233 |
3 | HG01891.hp1 HG02895.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.80-15268C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43113709 | |||||||
| chr6:43113780 | G | A | 1 | a0001c0001t0002g0234 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.80-15197G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43113780 | |||||||
| chr6:43113842 | A | G | 1 | a0001c0001t0002g0018 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.80-15135A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43113842 | |||||||
| chr6:43113940 | C | T | 11 | a0001c0001t0001g0119 a0001c0001t0002g0010 a0001c0001t0002g0067 others(8): Show |
11 | HG02027.hp2 HG02056.hp2 NA18947.hp2 others(8): Show |
intron_variant | MODIFIER | c.80-15037C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43113940 | |||||||
| chr6:43114069 | G | T | 1 | a0001c0001t0002g0195 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.80-14908G>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43114069 | |||||||
| chr6:43114075 | A | G | 1 | a0001c0002t0001g0145 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.80-14902A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43114075 | |||||||
| chr6:43114124 | T | G | 1 | a0006c0020t0006g0226 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.80-14853T>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43114124 | |||||||
| chr6:43114168 | T | C | 1 | a0001c0001t0002g0214 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.80-14809T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43114168 | |||||||
| chr6:43114250 | A | G | 3 | a0001c0001t0002g0222 a0001c0001t0002g0223 a0001c0001t0002g0224 |
3 | HG02970.hp2 HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.80-14727A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43114250 | |||||||
| chr6:43114257 | T | A | 3 | a0001c0001t0002g0234 a0001c0001t0002g0242 a0001c0002t0009g0233 |
3 | HG01891.hp1 HG02895.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.80-14720T>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43114257 | |||||||
| chr6:43114352 | G | C | 1 | a0001c0001t0001g0193 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.80-14625G>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43114352 | |||||||
| chr6:43114356 | C | G | 1 | a0001c0002t0001g0134 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.80-14621C>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43114356 | |||||||
| chr6:43114456 | C | T | 1 | a0001c0002t0001g0074 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.80-14521C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43114456 | |||||||
| chr6:43114465 | C | T | 3 | a0001c0001t0002g0222 a0001c0001t0002g0223 a0001c0001t0002g0224 |
3 | HG02970.hp2 HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.80-14512C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43114465 | |||||||
| chr6:43114610 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.80-14367C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43114610 | |||||||
| chr6:43114840 | G | A | 1 | a0001c0002t0001g0260 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.80-14137G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43114840 | |||||||
| chr6:43114915 | G | A | 1 | a0006c0020t0006g0226 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.80-14062G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43114915 | |||||||
| chr6:43115022 | A | G | 1 | a0001c0002t0003g0147 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.80-13955A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43115022 | |||||||
| chr6:43115042 | C | CA | 132 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(129): Show |
132 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(129): Show |
intron_variant | MODIFIER | c.80-13922dupA | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43115042 | ||||||
| chr6:43115042 | CA | C | 7 | a0001c0001t0001g0160 a0001c0002t0001g0152 a0001c0002t0001g0161 others(4): Show |
7 | HG01071.hp1 HG01074.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.80-13922delA | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43115042 | ||||||
| chr6:43115202 | T | C | 1 | a0006c0020t0006g0226 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.80-13775T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43115202 | |||||||
| chr6:43115259 | A | G | 1 | a0001c0001t0001g0205 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.80-13718A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43115259 | |||||||
| chr6:43115313 | A | G | 1 | a0006c0020t0006g0226 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.80-13664A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43115313 | |||||||
| chr6:43115586 | C | T | 1 | a0003c0004t0002g0235 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.80-13391C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43115586 | |||||||
| chr6:43115589 | A | C | 5 | a0001c0001t0002g0234 a0001c0001t0002g0242 a0001c0002t0009g0233 others(2): Show |
5 | HG01891.hp1 HG02145.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.80-13388A>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43115589 | |||||||
| chr6:43115626 | A | C | 1 | a0001c0002t0001g0123 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.80-13351A>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43115626 | |||||||
| chr6:43115663 | G | A | 7 | a0001c0001t0001g0200 a0001c0001t0001g0202 a0001c0001t0001g0204 others(4): Show |
7 | HG02109.hp2 HG02258.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.80-13314G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43115663 | |||||||
| chr6:43115711 | A | G | 1 | a0006c0020t0006g0226 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.80-13266A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43115711 | |||||||
| chr6:43115842 | T | C | 1 | a0006c0020t0006g0226 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.80-13135T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43115842 | |||||||
| chr6:43115889 | C | T | 1 | a0001c0002t0001g0258 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.80-13088C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43115889 | |||||||
| chr6:43115927 | C | CA | 9 | a0001c0001t0001g0069 a0001c0001t0001g0077 a0001c0001t0001g0127 others(6): Show |
9 | HG00544.hp2 HG00741.hp1 HG02148.hp1 others(6): Show |
intron_variant | MODIFIER | c.80-13030dupA | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43115927 | ||||||
| chr6:43115947 | A | AAAGG | 14 | a0001c0001t0001g0194 a0001c0001t0001g0199 a0001c0001t0001g0200 others(11): Show |
14 | HG02027.hp1 HG02055.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.80-13030_80-13029i others(6): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43115947 | |||||||
| chr6:43115947 | A | AAGG | 47 | a0001c0001t0001g0064 a0001c0001t0001g0066 a0001c0001t0001g0072 others(44): Show |
47 | HG00544.hp1 HG00609.hp1 HG00733.hp2 others(44): Show |
intron_variant | MODIFIER | c.80-13030_80-13029i others(5): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43115947 | |||||||
| chr6:43115947 | A | AGG | 88 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(85): Show |
88 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.80-13029_80-13028d others(4): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43115947 | ||||||
| chr6:43115947 | A | G | 1 | a0001c0001t0002g0047 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.80-13030A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43115947 | |||||||
| chr6:43116036 | A | G | 105 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(102): Show |
105 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(102): Show |
intron_variant | MODIFIER | c.80-12941A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43116036 | |||||||
| chr6:43116258 | A | G | 107 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(104): Show |
107 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(104): Show |
intron_variant | MODIFIER | c.80-12719A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43116258 | |||||||
| chr6:43116303 | G | C | 11 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0202 others(8): Show |
11 | HG02109.hp2 HG02145.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.80-12674G>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43116303 | |||||||
| chr6:43116309 | G | A | 1 | a0001c0001t0001g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.80-12668G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43116309 | |||||||
| chr6:43116358 | C | T | 2 | a0001c0002t0001g0090 a0001c0002t0001g0106 |
2 | NA18954.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.80-12619C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43116358 | |||||||
| chr6:43116361 | C | T | 59 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0037 others(56): Show |
59 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.80-12616C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43116361 | |||||||
| chr6:43116400 | C | T | 1 | a0005c0019t0001g0141 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.80-12577C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43116400 | |||||||
| chr6:43116548 | C | T | 11 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0202 others(8): Show |
11 | HG02109.hp2 HG02145.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.80-12429C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43116548 | |||||||
| chr6:43116573 | T | C | 2 | a0001c0001t0001g0100 a0001c0001t0001g0220 |
2 | HG02015.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.80-12404T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43116573 | |||||||
| chr6:43116602 | GT | G | 5 | a0001c0001t0001g0051 a0001c0001t0001g0079 a0001c0001t0001g0080 others(2): Show |
5 | HG01175.hp1 HG02083.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.80-12372delT | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43116602 | ||||||
| chr6:43116603 | TTTGTG | T | 3 | a0001c0001t0001g0204 a0001c0006t0001g0084 a0002c0003t0001g0243 |
3 | HG02135.hp2 HG02258.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.80-12372_80-12368d others(7): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43116603 | ||||||
| chr6:43116603 | TTTGTGTG | T | 5 | a0001c0001t0001g0200 a0001c0001t0001g0202 a0001c0001t0001g0205 others(2): Show |
5 | HG02109.hp2 HG02280.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.80-12372_80-12366d others(9): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43116603 | ||||||
| chr6:43116603 | TTTGTGTG others(4): Show |
T | 3 | a0001c0001t0001g0199 a0001c0002t0001g0203 a0002c0018t0001g0248 |
3 | HG02145.hp2 NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.80-12372_80-12362d others(13): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43116603 | ||||||
| chr6:43116603 | TTTGTGTG others(8): Show |
T | 1 | a0006c0020t0006g0226 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.80-12372_80-12358d others(17): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43116603 | ||||||
| chr6:43116604 | T | G | 1 | a0001c0001t0001g0003 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.80-12373T>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43116604 | |||||||
| chr6:43116604 | T | TG | 3 | a0001c0001t0001g0197 a0001c0001t0002g0042 a0001c0002t0001g0031 |
3 | HG01884.hp1 HG02572.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.80-12373_80-12372i others(3): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43116604 | |||||||
| chr6:43116604 | T | TTG | 19 | a0001c0001t0001g0013 a0001c0001t0001g0037 a0001c0001t0001g0066 others(16): Show |
19 | HG00423.hp1 HG01433.hp1 HG01433.hp2 others(16): Show |
intron_variant | MODIFIER | c.80-12326_80-12325d others(4): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43116604 | ||||||
| chr6:43116604 | T | TTGTG | 14 | a0001c0001t0001g0097 a0001c0001t0001g0100 a0001c0001t0001g0187 others(11): Show |
14 | HG00323.hp1 HG01167.hp2 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.80-12328_80-12325d others(6): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43116604 | ||||||
| chr6:43116604 | T | TTGTGTG | 4 | a0001c0001t0001g0073 a0001c0001t0001g0220 a0001c0001t0002g0017 others(1): Show |
4 | HG01261.hp1 HG02027.hp1 HG02135.hp1 others(1): Show |
intron_variant | MODIFIER | c.80-12330_80-12325d others(8): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43116604 | ||||||
| chr6:43116604 | T | TTGTGTGT others(1): Show |
3 | a0001c0001t0001g0098 a0001c0002t0001g0114 a0008c0011t0002g0040 |
3 | HG01167.hp1 HG02300.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.80-12332_80-12325d others(10): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43116604 | ||||||
| chr6:43116604 | TTGTG | T | 3 | a0001c0002t0001g0056 a0001c0015t0001g0240 a0003c0014t0002g0241 |
3 | HG02145.hp1 HG03209.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.80-12328_80-12325d others(6): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43116604 | ||||||
| chr6:43116604 | TTGTGTG | T | 7 | a0001c0001t0001g0154 a0001c0002t0001g0145 a0001c0002t0001g0146 others(4): Show |
7 | HG01074.hp1 HG01261.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.80-12330_80-12325d others(8): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43116604 | ||||||
| chr6:43116604 | TTGTGTGT others(1): Show |
T | 12 | a0001c0001t0001g0153 a0001c0001t0001g0160 a0001c0002t0001g0136 others(9): Show |
12 | HG01071.hp1 HG01123.hp2 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.80-12332_80-12325d others(10): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43116604 | ||||||
| chr6:43116604 | TTGTGTGT others(3): Show |
T | 33 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0135 others(30): Show |
33 | HG00597.hp1 HG00639.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.80-12334_80-12325d others(12): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43116604 | ||||||
| chr6:43116604 | TTGTGTGT others(5): Show |
T | 3 | a0001c0002t0001g0074 a0001c0002t0003g0148 a0003c0016t0002g0225 |
3 | HG03225.hp2 HG03579.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.80-12336_80-12325d others(14): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43116604 | ||||||
| chr6:43116604 | TTGTGTGT others(7): Show |
T | 7 | a0001c0001t0001g0167 a0001c0002t0001g0109 a0001c0002t0001g0122 others(4): Show |
7 | HG00323.hp2 HG01169.hp1 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.80-12338_80-12325d others(16): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43116604 | ||||||
| chr6:43116637 | TGTGTGTG others(9): Show |
T | 1 | a0001c0010t0002g0045 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.80-12338_80-12323d others(18): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43116637 | ||||||
| chr6:43116641 | TGTGTGTG others(5): Show |
T | 2 | a0001c0001t0001g0188 a0001c0012t0002g0229 |
2 | HG01123.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.80-12334_80-12323d others(14): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43116641 | ||||||
| chr6:43116645 | TGTGTGTG others(5): Show |
T | 1 | a0001c0001t0001g0246 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.80-12330_80-12319d others(14): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43116645 | ||||||
| chr6:43116647 | T | C | 1 | a0001c0017t0001g0232 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.80-12330T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43116647 | |||||||
| chr6:43116647 | TGTGTGC | T | 5 | a0001c0001t0002g0023 a0001c0001t0002g0029 a0001c0001t0002g0101 others(2): Show |
5 | HG00639.hp2 HG02615.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.80-12328_80-12323d others(8): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43116647 | ||||||
| chr6:43116647 | TGTGTGCG others(3): Show |
T | 2 | a0001c0001t0002g0254 a0001c0001t0002g0255 |
2 | NA18944.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.80-12328_80-12319d others(12): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43116647 | ||||||
| chr6:43116649 | T | C | 2 | a0001c0001t0004g0269 a0001c0017t0001g0232 |
2 | HG00741.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.80-12328T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43116649 | |||||||
| chr6:43116649 | TGTGC | T | 19 | a0001c0001t0001g0064 a0001c0001t0001g0127 a0001c0001t0001g0172 others(16): Show |
19 | HG01069.hp2 HG01081.hp1 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.80-12326_80-12323d others(6): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43116649 | ||||||
| chr6:43116651 | T | C | 12 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0230 others(9): Show |
12 | HG00323.hp2 HG00597.hp1 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.80-12326T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43116651 | |||||||
| chr6:43116651 | TGC | T | 14 | a0001c0001t0001g0002 a0001c0001t0001g0087 a0001c0001t0001g0094 others(11): Show |
14 | HG00609.hp2 HG00642.hp2 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.80-12319_80-12318d others(4): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43116651 | ||||||
| chr6:43116653 | C | T | 97 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(94): Show |
97 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.80-12324C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43116653 | |||||||
| chr6:43116655 | C | CCGCGCTG others(4): Show |
1 | a0001c0001t0001g0230 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.80-12322_80-12321i others(13): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43116655 | |||||||
| chr6:43116655 | C | T | 9 | a0001c0001t0001g0126 a0001c0001t0001g0262 a0001c0001t0002g0263 others(6): Show |
9 | HG01099.hp1 HG02615.hp2 HG04204.hp2 others(6): Show |
intron_variant | MODIFIER | c.80-12322C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43116655 | |||||||
| chr6:43116656 | GCGCA | G | 24 | a0001c0001t0001g0200 a0001c0001t0001g0202 a0001c0001t0001g0204 others(21): Show |
24 | HG00423.hp2 HG01891.hp1 HG02015.hp2 others(21): Show |
intron_variant | MODIFIER | c.80-12308_80-12305d others(6): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43116656 | ||||||
| chr6:43116657 | C | T | 1 | a0001c0002t0001g0260 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.80-12320C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43116657 | |||||||
| chr6:43116658 | G | A | 18 | a0001c0001t0001g0160 a0001c0001t0002g0214 a0001c0002t0001g0152 others(15): Show |
18 | HG01071.hp1 HG01074.hp2 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.80-12319G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43116658 | |||||||
| chr6:43116658 | GCA | G | 35 | a0001c0001t0001g0011 a0001c0001t0001g0051 a0001c0001t0001g0058 others(32): Show |
35 | HG00597.hp2 HG00642.hp1 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.80-12317_80-12316d others(4): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43116658 | ||||||
| chr6:43116660 | A | G | 117 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0037 others(114): Show |
117 | HG00323.hp1 HG00323.hp2 HG00597.hp1 others(114): Show |
intron_variant | MODIFIER | c.80-12317A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43116660 | |||||||
| chr6:43116714 | G | A | 11 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0202 others(8): Show |
11 | HG02109.hp2 HG02145.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.80-12263G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43116714 | |||||||
| chr6:43116927 | G | A | 1 | a0001c0002t0001g0203 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.80-12050G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43116927 | |||||||
| chr6:43116944 | C | T | 1 | a0002c0003t0001g0243 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.80-12033C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43116944 | |||||||
| chr6:43117009 | G | A | 180 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(177): Show |
180 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.80-11968G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43117009 | |||||||
| chr6:43117076 | G | A | 1 | a0005c0019t0001g0141 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.80-11901G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43117076 | |||||||
| chr6:43117127 | G | A | 3 | a0001c0001t0001g0230 a0001c0002t0002g0231 a0001c0017t0001g0232 |
3 | HG00741.hp2 HG02055.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.80-11850G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43117127 | |||||||
| chr6:43117212 | T | G | 11 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0202 others(8): Show |
11 | HG02109.hp2 HG02145.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.80-11765T>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43117212 | |||||||
| chr6:43117352 | C | T | 1 | a0003c0004t0002g0046 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.80-11625C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43117352 | |||||||
| chr6:43117455 | T | C | 1 | a0001c0001t0001g0268 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.80-11522T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43117455 | |||||||
| chr6:43117601 | G | A | 4 | a0001c0002t0001g0074 a0001c0002t0001g0109 a0001c0002t0001g0122 others(1): Show |
4 | HG00323.hp2 HG02698.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-11376G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43117601 | |||||||
| chr6:43117631 | C | T | 68 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(65): Show |
68 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.80-11346C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43117631 | |||||||
| chr6:43117640 | G | A | 31 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0160 others(28): Show |
31 | HG01071.hp1 HG01074.hp1 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.80-11337G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43117640 | |||||||
| chr6:43117674 | G | A | 1 | a0001c0001t0001g0087 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.80-11303G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43117674 | |||||||
| chr6:43117763 | T | C | 1 | a0001c0001t0002g0117 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.80-11214T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43117763 | |||||||
| chr6:43117934 | C | CA | 15 | a0001c0001t0001g0066 a0001c0001t0001g0199 a0001c0001t0001g0200 others(12): Show |
15 | HG02109.hp2 HG02145.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.80-11032dupA | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43117934 | ||||||
| chr6:43117980 | G | A | 68 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(65): Show |
68 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.80-10997G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43117980 | |||||||
| chr6:43117990 | A | G | 28 | a0001c0001t0001g0246 a0001c0001t0001g0262 a0001c0001t0001g0268 others(25): Show |
28 | HG00423.hp2 HG01099.hp1 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.80-10987A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43117990 | |||||||
| chr6:43118044 | A | G | 79 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(76): Show |
79 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.80-10933A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43118044 | |||||||
| chr6:43118102 | C | CT | 40 | a0001c0001t0001g0077 a0001c0001t0001g0212 a0001c0001t0001g0213 others(37): Show |
40 | HG00423.hp2 HG00544.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.80-10855dupT | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43118102 | ||||||
| chr6:43118102 | C | CTT | 11 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0202 others(8): Show |
11 | HG02109.hp2 HG02258.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.80-10856_80-10855d others(4): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43118102 | ||||||
| chr6:43118102 | CTTTT | C | 12 | a0001c0001t0001g0119 a0001c0001t0002g0008 a0001c0001t0002g0015 others(9): Show |
12 | HG00323.hp1 HG01261.hp1 HG01993.hp1 others(9): Show |
intron_variant | MODIFIER | c.80-10858_80-10855d others(6): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43118102 | ||||||
| chr6:43118102 | CTTTTT | C | 56 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(53): Show |
56 | HG00597.hp2 HG00609.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.80-10859_80-10855d others(7): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43118102 | ||||||
| chr6:43118155 | A | G | 1 | a0001c0001t0002g0043 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.80-10822A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43118155 | |||||||
| chr6:43118388 | T | C | 1 | a0001c0001t0001g0085 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.80-10589T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43118388 | |||||||
| chr6:43118398 | G | A | 1 | a0001c0002t0001g0143 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.80-10579G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43118398 | |||||||
| chr6:43118405 | C | T | 1 | a0001c0001t0001g0199 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.80-10572C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43118405 | |||||||
| chr6:43118436 | T | C | 1 | a0001c0001t0002g0265 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.80-10541T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43118436 | |||||||
| chr6:43118441 | C | T | 11 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0202 others(8): Show |
11 | HG02109.hp2 HG02145.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.80-10536C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43118441 | |||||||
| chr6:43118517 | C | T | 9 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0202 others(6): Show |
9 | HG02109.hp2 HG02258.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.80-10460C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43118517 | |||||||
| chr6:43118620 | C | CCT | 14 | a0001c0001t0001g0003 a0001c0001t0001g0064 a0001c0001t0001g0100 others(11): Show |
14 | HG01081.hp2 HG01167.hp2 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.80-10318_80-10317d others(4): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43118620 | ||||||
| chr6:43118620 | C | CCTCT | 6 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0086 others(3): Show |
6 | HG00423.hp1 HG01169.hp2 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.80-10320_80-10317d others(6): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43118620 | ||||||
| chr6:43118620 | C | CCTCTCT | 3 | a0001c0001t0001g0188 a0001c0001t0001g0193 a0001c0010t0002g0093 |
3 | HG00609.hp2 HG01123.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.80-10322_80-10317d others(8): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43118620 | ||||||
| chr6:43118620 | C | CCTCTCTC others(1): Show |
3 | a0001c0001t0001g0073 a0001c0002t0001g0191 a0001c0009t0002g0061 |
3 | HG00733.hp1 HG01928.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.80-10324_80-10317d others(10): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43118620 | ||||||
| chr6:43118620 | CCT | C | 6 | a0001c0001t0001g0213 a0001c0002t0001g0102 a0001c0002t0001g0113 others(3): Show |
6 | HG01346.hp2 HG02148.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.80-10318_80-10317d others(4): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43118620 | ||||||
| chr6:43118620 | CCTCTCT | C | 3 | a0001c0001t0001g0160 a0001c0001t0001g0204 a0001c0002t0001g0152 |
3 | HG01071.hp1 HG02258.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.80-10322_80-10317d others(8): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43118620 | ||||||
| chr6:43118620 | CCTCTCTC others(1): Show |
C | 3 | a0001c0002t0001g0185 a0001c0002t0003g0148 a0001c0002t0003g0149 |
3 | HG03579.hp2 NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.80-10324_80-10317d others(10): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43118620 | ||||||
| chr6:43118620 | CCTCTCTC others(3): Show |
C | 3 | a0001c0001t0001g0170 a0001c0001t0003g0201 a0001c0002t0001g0161 |
3 | HG01358.hp1 HG03516.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.80-10326_80-10317d others(12): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43118620 | ||||||
| chr6:43118620 | CCTCTCTC others(11): Show |
C | 2 | a0001c0002t0001g0183 a0001c0002t0001g0184 |
2 | HG02630.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.80-10334_80-10317d others(20): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43118620 | ||||||
| chr6:43118636 | T | C | 1 | a0001c0001t0002g0117 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.80-10341T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43118636 | |||||||
| chr6:43118645 | CTCTCTCT others(13): Show |
C | 1 | a0001c0001t0002g0234 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.80-10330_80-10311d others(22): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43118645 | ||||||
| chr6:43118645 | CTCTCTCT others(21): Show |
C | 1 | a0002c0003t0001g0243 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.80-10330_80-10303d others(30): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43118645 | ||||||
| chr6:43118647 | CTCTCTCT others(9): Show |
C | 2 | a0001c0002t0001g0252 a0001c0002t0001g0261 |
2 | HG01099.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.80-10328_80-10313d others(18): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43118647 | ||||||
| chr6:43118647 | CTCTCTCT others(11): Show |
C | 2 | a0001c0001t0001g0246 a0001c0002t0002g0253 |
2 | NA18522.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.80-10328_80-10311d others(20): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43118647 | ||||||
| chr6:43118647 | CTCTCTCT others(13): Show |
C | 1 | a0001c0001t0002g0257 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.80-10328_80-10309d others(22): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43118647 | ||||||
| chr6:43118649 | CTCTCTCT others(5): Show |
C | 4 | a0001c0002t0001g0207 a0001c0002t0001g0216 a0001c0002t0001g0217 others(1): Show |
4 | HG00323.hp2 HG00639.hp1 HG01069.hp1 others(1): Show |
intron_variant | MODIFIER | c.80-10326_80-10315d others(14): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43118649 | ||||||
| chr6:43118649 | CTCTCTCT others(11): Show |
C | 6 | a0001c0001t0001g0262 a0001c0001t0001g0270 a0001c0001t0002g0256 others(3): Show |
6 | HG00423.hp2 HG04184.hp1 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.80-10326_80-10309d others(20): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43118649 | ||||||
| chr6:43118649 | CTCTCTCT others(13): Show |
C | 1 | a0001c0001t0002g0021 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.80-10326_80-10307d others(22): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43118649 | ||||||
| chr6:43118651 | CTCTCTCT others(3): Show |
C | 3 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0002t0001g0146 |
3 | HG01069.hp2 HG01099.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.80-10324_80-10315d others(12): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43118651 | ||||||
| chr6:43118651 | CTCTCTCT others(5): Show |
C | 1 | a0001c0002t0001g0122 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.80-10324_80-10313d others(14): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43118651 | ||||||
| chr6:43118651 | CTCTCTCT others(7): Show |
C | 2 | a0001c0001t0001g0153 a0001c0001t0001g0154 |
2 | HG01975.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.80-10324_80-10311d others(16): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43118651 | ||||||
| chr6:43118651 | CTCTCTCT others(9): Show |
C | 1 | a0001c0002t0001g0145 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.80-10324_80-10309d others(18): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43118651 | ||||||
| chr6:43118651 | CTCTCTCT others(11): Show |
C | 3 | a0001c0001t0002g0263 a0001c0001t0002g0271 a0001c0002t0001g0196 |
3 | NA18975.hp2 NA18984.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.80-10324_80-10307d others(20): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43118651 | ||||||
| chr6:43118653 | CTCTCTCT others(1): Show |
C | 7 | a0001c0001t0001g0202 a0001c0002t0001g0090 a0001c0002t0001g0109 others(4): Show |
7 | HG01358.hp2 HG01884.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.80-10322_80-10315d others(10): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43118653 | ||||||
| chr6:43118653 | CTCTCTCT others(3): Show |
C | 6 | a0001c0002t0001g0034 a0001c0002t0001g0180 a0001c0002t0001g0181 others(3): Show |
6 | HG02280.hp2 HG02922.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.80-10322_80-10313d others(12): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43118653 | ||||||
| chr6:43118653 | CTCTCTCT others(5): Show |
C | 3 | a0001c0002t0001g0151 a0001c0002t0001g0159 a0001c0022t0001g0155 |
3 | HG00597.hp1 HG01123.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.80-10322_80-10311d others(14): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43118653 | ||||||
| chr6:43118653 | CTCTCTCT others(9): Show |
C | 2 | a0001c0001t0001g0199 a0001c0012t0002g0229 |
2 | HG02809.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.80-10322_80-10307d others(18): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43118653 | ||||||
| chr6:43118653 | CTCTCTCT others(11): Show |
C | 4 | a0001c0001t0002g0254 a0001c0001t0002g0259 a0001c0002t0001g0258 others(1): Show |
4 | HG02015.hp2 HG04204.hp2 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.80-10322_80-10305d others(20): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43118653 | ||||||
| chr6:43118653 | CTCTCTCT others(13): Show |
C | 4 | a0001c0001t0002g0083 a0001c0001t0002g0118 a0001c0001t0002g0265 others(1): Show |
4 | HG00609.hp1 HG02027.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-10322_80-10303d others(22): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43118653 | ||||||
| chr6:43118653 | CTCTCTCT others(17): Show |
C | 1 | a0001c0001t0002g0164 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.80-10322_80-10299d others(26): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43118653 | ||||||
| chr6:43118655 | C | A | 2 | a0001c0015t0001g0240 a0003c0014t0002g0241 |
2 | HG02145.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.80-10322C>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43118655 | |||||||
| chr6:43118655 | CTCTCTAT others(1): Show |
C | 3 | a0001c0002t0001g0106 a0001c0002t0001g0136 a0001c0006t0001g0078 |
3 | HG02717.hp1 NA18995.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.80-10320_80-10313d others(10): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43118655 | ||||||
| chr6:43118655 | CTCTCTAT others(3): Show |
C | 3 | a0001c0001t0001g0200 a0001c0002t0001g0142 a0001c0002t0001g0143 |
3 | HG03098.hp1 HG03516.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.80-10320_80-10311d others(12): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43118655 | ||||||
| chr6:43118655 | CTCTCTAT others(7): Show |
C | 2 | a0001c0002t0001g0250 a0001c0002t0001g0251 |
2 | HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.80-10320_80-10307d others(16): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43118655 | ||||||
| chr6:43118655 | CTCTCTAT others(11): Show |
C | 5 | a0001c0001t0002g0012 a0001c0001t0002g0209 a0001c0001t0002g0255 others(2): Show |
5 | HG03704.hp1 HG04228.hp2 NA18944.hp2 others(2): Show |
intron_variant | MODIFIER | c.80-10320_80-10303d others(20): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43118655 | ||||||
| chr6:43118655 | CTCTCTAT others(13): Show |
C | 8 | a0001c0001t0002g0032 a0001c0001t0002g0036 a0001c0001t0002g0057 others(5): Show |
8 | HG02071.hp1 HG02630.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.80-10320_80-10301d others(22): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43118655 | ||||||
| chr6:43118655 | CTCTCTAT others(15): Show |
C | 1 | a0001c0001t0002g0030 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.80-10320_80-10299d others(24): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43118655 | ||||||
| chr6:43118655 | CTCTCTAT others(17): Show |
C | 1 | a0001c0001t0001g0011 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.80-10320_80-10297d others(26): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43118655 | ||||||
| chr6:43118657 | C | A | 4 | a0001c0002t0001g0089 a0001c0015t0001g0240 a0003c0014t0002g0241 others(1): Show |
4 | HG01975.hp2 HG02145.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.80-10320C>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43118657 | |||||||
| chr6:43118657 | CTCTATAT others(1): Show |
C | 4 | a0001c0001t0001g0230 a0001c0001t0001g0238 a0001c0002t0001g0129 others(1): Show |
4 | HG01255.hp2 HG02055.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-10318_80-10311d others(10): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43118657 | ||||||
| chr6:43118657 | CTCTATAT others(3): Show |
C | 8 | a0001c0001t0001g0166 a0001c0001t0001g0205 a0001c0002t0001g0074 others(5): Show |
8 | HG00741.hp1 HG00741.hp2 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.80-10318_80-10309d others(12): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43118657 | ||||||
| chr6:43118657 | CTCTATAT others(7): Show |
C | 2 | a0001c0001t0002g0242 a0001c0002t0009g0233 |
2 | HG02895.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.80-10318_80-10305d others(16): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43118657 | ||||||
| chr6:43118657 | CTCTATAT others(11): Show |
C | 4 | a0001c0001t0002g0020 a0001c0001t0002g0041 a0001c0001t0002g0054 others(1): Show |
4 | HG01261.hp1 HG01496.hp2 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.80-10318_80-10301d others(20): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43118657 | ||||||
| chr6:43118657 | CTCTATAT others(13): Show |
C | 9 | a0001c0001t0001g0006 a0001c0001t0001g0119 a0001c0001t0002g0027 others(6): Show |
9 | HG00323.hp1 HG02056.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.80-10318_80-10299d others(22): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43118657 | ||||||
| chr6:43118657 | CTCTATAT others(17): Show |
C | 2 | a0001c0001t0001g0058 a0001c0001t0002g0039 |
2 | HG01993.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.80-10318_80-10295d others(26): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43118657 | ||||||
| chr6:43118659 | C | A | 16 | a0001c0001t0001g0204 a0001c0001t0002g0175 a0001c0002t0001g0089 others(13): Show |
16 | HG01167.hp1 HG01346.hp2 HG01943.hp2 others(13): Show |
intron_variant | MODIFIER | c.80-10318C>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43118659 | |||||||
| chr6:43118659 | C | CTA | 3 | a0001c0001t0001g0126 a0001c0002t0001g0110 a0006c0020t0006g0226 |
3 | NA18522.hp2 NA18943.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.80-10290_80-10289d others(4): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43118659 | ||||||
| chr6:43118659 | CTA | C | 13 | a0001c0001t0001g0022 a0001c0001t0001g0066 a0001c0001t0001g0072 others(10): Show |
13 | HG01258.hp1 HG01993.hp2 HG02083.hp1 others(10): Show |
intron_variant | MODIFIER | c.80-10290_80-10289d others(4): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43118659 | ||||||
| chr6:43118659 | CTATA | C | 12 | a0001c0001t0001g0065 a0001c0001t0001g0076 a0001c0001t0001g0098 others(9): Show |
12 | HG01074.hp2 HG02145.hp2 HG02300.hp1 others(9): Show |
intron_variant | MODIFIER | c.80-10292_80-10289d others(6): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43118659 | ||||||
| chr6:43118659 | CTATATA | C | 6 | a0001c0001t0001g0087 a0001c0002t0001g0134 a0001c0002t0001g0182 others(3): Show |
6 | HG01169.hp1 HG02486.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.80-10294_80-10289d others(8): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43118659 | ||||||
| chr6:43118659 | CTATATAT others(1): Show |
C | 4 | a0001c0001t0001g0206 a0001c0006t0001g0084 a0002c0003t0002g0162 others(1): Show |
4 | HG02135.hp2 HG02280.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.80-10296_80-10289d others(10): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43118659 | ||||||
| chr6:43118659 | CTATATAT others(3): Show |
C | 1 | a0001c0002t0004g0139 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.80-10298_80-10289d others(12): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43118659 | ||||||
| chr6:43118659 | CTATATAT others(7): Show |
C | 2 | a0001c0001t0002g0223 a0001c0001t0002g0224 |
2 | HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.80-10302_80-10289d others(16): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43118659 | ||||||
| chr6:43118659 | CTATATAT others(9): Show |
C | 1 | a0001c0001t0002g0222 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.80-10304_80-10289d others(18): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43118659 | ||||||
| chr6:43118661 | A | C | 63 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0037 others(60): Show |
63 | HG00609.hp2 HG00639.hp2 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.80-10316A>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43118661 | |||||||
| chr6:43118663 | A | C | 44 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0022 others(41): Show |
44 | HG00642.hp2 HG00733.hp1 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.80-10314A>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43118663 | |||||||
| chr6:43118665 | A | C | 40 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0022 others(37): Show |
40 | HG00642.hp2 HG01081.hp2 HG01496.hp1 others(37): Show |
intron_variant | MODIFIER | c.80-10312A>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43118665 | |||||||
| chr6:43118667 | A | C | 24 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0068 others(21): Show |
24 | HG01081.hp2 HG01952.hp2 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.80-10310A>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43118667 | |||||||
| chr6:43118667 | ATATATAT others(15): Show |
A | 1 | a0001c0001t0001g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.80-10302_80-10281d others(24): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43118667 | ||||||
| chr6:43118669 | A | C | 10 | a0001c0001t0001g0022 a0001c0001t0001g0072 a0001c0001t0001g0208 others(7): Show |
10 | HG02135.hp2 HG02486.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.80-10308A>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43118669 | |||||||
| chr6:43118669 | ATATATAT others(13): Show |
A | 13 | a0001c0001t0001g0037 a0001c0001t0002g0001 a0001c0001t0002g0009 others(10): Show |
13 | HG00597.hp2 HG00639.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.80-10300_80-10281d others(22): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43118669 | ||||||
| chr6:43118671 | A | C | 6 | a0001c0001t0001g0022 a0001c0001t0001g0072 a0001c0001t0001g0208 others(3): Show |
6 | HG03209.hp1 NA18956.hp1 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.80-10306A>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43118671 | |||||||
| chr6:43118671 | A | G | 2 | a0001c0015t0001g0240 a0003c0014t0002g0241 |
2 | HG02145.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.80-10306A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43118671 | |||||||
| chr6:43118671 | ATATATAT others(11): Show |
A | 10 | a0001c0001t0001g0051 a0001c0001t0002g0028 a0001c0001t0002g0029 others(7): Show |
10 | HG00642.hp1 HG01175.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.80-10298_80-10281d others(20): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43118671 | ||||||
| chr6:43118673 | A | C | 1 | a0001c0002t0004g0228 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.80-10304A>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43118673 | |||||||
| chr6:43118673 | ATATATAT others(9): Show |
A | 9 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0008 others(6): Show |
9 | HG01981.hp2 HG02922.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.80-10296_80-10281d others(18): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43118673 | ||||||
| chr6:43118675 | A | C | 2 | a0001c0001t0002g0223 a0001c0001t0002g0224 |
2 | HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.80-10302A>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43118675 | |||||||
| chr6:43118677 | A | C | 3 | a0001c0001t0002g0222 a0001c0001t0002g0223 a0001c0001t0002g0224 |
3 | HG02970.hp2 HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.80-10300A>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43118677 | |||||||
| chr6:43118679 | A | G | 2 | a0001c0015t0001g0240 a0003c0014t0002g0241 |
2 | HG02145.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.80-10298A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43118679 | |||||||
| chr6:43118683 | A | ATATGTCT others(11): Show |
2 | a0001c0015t0001g0240 a0003c0014t0002g0241 |
2 | HG02145.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.80-10291_80-10290i others(20): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43118683 | ||||||
| chr6:43118689 | G | A | 37 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0058 others(34): Show |
37 | HG00323.hp1 HG00609.hp1 HG01261.hp1 others(34): Show |
intron_variant | MODIFIER | c.80-10288G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43118689 | |||||||
| chr6:43118690 | T | C | 2 | a0001c0015t0001g0240 a0003c0014t0002g0241 |
2 | HG02145.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.80-10287T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43118690 | |||||||
| chr6:43118696 | T | C | 2 | a0001c0002t0001g0252 a0001c0002t0002g0253 |
2 | HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.80-10281T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43118696 | |||||||
| chr6:43118749 | A | ATG | 6 | a0001c0001t0002g0195 a0001c0001t0002g0214 a0001c0002t0001g0123 others(3): Show |
6 | HG00544.hp2 HG00741.hp2 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.80-10204_80-10203d others(4): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43118749 | ||||||
| chr6:43118749 | ATG | A | 38 | a0001c0001t0001g0094 a0001c0001t0001g0199 a0001c0001t0001g0200 others(35): Show |
38 | HG00423.hp2 HG01099.hp1 HG01891.hp1 others(35): Show |
intron_variant | MODIFIER | c.80-10204_80-10203d others(4): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43118749 | ||||||
| chr6:43118749 | ATGTGTG | A | 69 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(66): Show |
69 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.80-10208_80-10203d others(8): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43118749 | ||||||
| chr6:43118773 | G | A | 3 | a0001c0002t0001g0250 a0001c0002t0001g0251 a0005c0019t0001g0141 |
3 | HG02622.hp2 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.80-10204G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43118773 | |||||||
| chr6:43118775 | AT | A | 3 | a0001c0002t0001g0250 a0001c0002t0001g0251 a0005c0019t0001g0141 |
3 | HG02622.hp2 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.80-10201delT | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43118775 | |||||||
| chr6:43118778 | A | AT | 33 | a0001c0001t0001g0037 a0001c0001t0001g0098 a0001c0001t0001g0153 others(30): Show |
33 | HG01071.hp1 HG01074.hp1 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.80-10186dupT | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43118778 | ||||||
| chr6:43118778 | A | T | 3 | a0001c0002t0001g0250 a0001c0002t0001g0251 a0005c0019t0001g0141 |
3 | HG02622.hp2 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.80-10199A>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43118778 | |||||||
| chr6:43118889 | C | T | 11 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0202 others(8): Show |
11 | HG02109.hp2 HG02145.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.80-10088C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43118889 | |||||||
| chr6:43118904 | G | A | 1 | a0002c0018t0001g0248 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.80-10073G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43118904 | |||||||
| chr6:43118922 | C | T | 11 | a0001c0001t0001g0119 a0001c0001t0002g0010 a0001c0001t0002g0067 others(8): Show |
11 | HG02027.hp2 HG02056.hp2 NA18947.hp2 others(8): Show |
intron_variant | MODIFIER | c.80-10055C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43118922 | |||||||
| chr6:43119155 | G | A | 4 | a0001c0001t0001g0230 a0001c0001t0004g0269 a0001c0002t0002g0231 others(1): Show |
4 | HG00741.hp2 HG02055.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.80-9822G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43119155 | |||||||
| chr6:43119177 | G | A | 1 | a0001c0001t0002g0032 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.80-9800G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43119177 | |||||||
| chr6:43119245 | T | C | 1 | a0001c0009t0002g0061 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.80-9732T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43119245 | |||||||
| chr6:43119422 | G | A | 1 | a0001c0001t0001g0066 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.80-9555G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43119422 | |||||||
| chr6:43119430 | A | G | 1 | a0001c0002t0007g0115 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.80-9547A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43119430 | |||||||
| chr6:43119568 | G | A | 1 | a0007c0013t0001g0063 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.80-9409G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43119568 | |||||||
| chr6:43119573 | C | T | 2 | a0001c0002t0001g0250 a0001c0002t0001g0251 |
2 | HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.80-9404C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43119573 | |||||||
| chr6:43119683 | C | T | 1 | a0001c0015t0001g0240 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.80-9294C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43119683 | |||||||
| chr6:43119735 | A | G | 1 | a0001c0001t0002g0030 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.80-9242A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43119735 | |||||||
| chr6:43119940 | C | T | 1 | a0001c0002t0002g0026 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.80-9037C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43119940 | |||||||
| chr6:43120262 | C | A | 7 | a0001c0001t0001g0230 a0001c0001t0002g0222 a0001c0001t0002g0223 others(4): Show |
7 | HG00741.hp2 HG02055.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.80-8715C>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43120262 | |||||||
| chr6:43120283 | A | G | 1 | a0001c0001t0002g0027 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.80-8694A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43120283 | |||||||
| chr6:43120356 | A | G | 1 | a0001c0002t0001g0258 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.80-8621A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43120356 | |||||||
| chr6:43120438 | G | A | 1 | a0001c0002t0001g0102 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.80-8539G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43120438 | |||||||
| chr6:43120457 | A | G | 81 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(78): Show |
81 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.80-8520A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43120457 | |||||||
| chr6:43120534 | C | T | 2 | a0001c0001t0001g0200 a0001c0001t0001g0205 |
2 | HG03098.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.80-8443C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43120534 | |||||||
| chr6:43120659 | C | T | 1 | a0001c0001t0001g0270 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.80-8318C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43120659 | |||||||
| chr6:43120668 | G | A | 1 | a0001c0001t0001g0076 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.80-8309G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43120668 | |||||||
| chr6:43120846 | G | T | 3 | a0001c0001t0002g0234 a0001c0001t0002g0242 a0001c0002t0009g0233 |
3 | HG01891.hp1 HG02895.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.80-8131G>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43120846 | |||||||
| chr6:43121056 | G | GT | 16 | a0001c0001t0001g0003 a0001c0001t0001g0073 a0001c0001t0001g0133 others(13): Show |
16 | HG01081.hp2 HG01255.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.80-7901dupT | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43121056 | ||||||
| chr6:43121056 | GT | G | 66 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0085 others(63): Show |
66 | HG00323.hp2 HG00597.hp1 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.80-7901delT | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43121056 | ||||||
| chr6:43121056 | GTT | G | 14 | a0001c0001t0001g0013 a0001c0001t0001g0051 a0001c0001t0001g0199 others(11): Show |
14 | HG01169.hp1 HG01175.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.80-7902_80-7901del others(2): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43121056 | ||||||
| chr6:43121056 | GTTT | G | 58 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0037 others(55): Show |
58 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.80-7903_80-7901del others(3): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43121056 | ||||||
| chr6:43121056 | GTTTT | G | 8 | a0001c0001t0001g0200 a0001c0001t0001g0202 a0001c0001t0001g0204 others(5): Show |
8 | HG02109.hp2 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.80-7904_80-7901del others(4): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43121056 | ||||||
| chr6:43121145 | G | A | 15 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0135 others(12): Show |
15 | HG00741.hp1 HG01255.hp1 HG02135.hp2 others(12): Show |
intron_variant | MODIFIER | c.80-7832G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43121145 | |||||||
| chr6:43121240 | A | G | 80 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(77): Show |
80 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.80-7737A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43121240 | |||||||
| chr6:43121255 | G | C | 10 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0202 others(7): Show |
10 | HG02109.hp2 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.80-7722G>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43121255 | |||||||
| chr6:43121302 | G | A | 1 | a0001c0001t0001g0244 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.80-7675G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43121302 | |||||||
| chr6:43121691 | C | T | 63 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0135 others(60): Show |
63 | HG00323.hp2 HG00597.hp1 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.80-7286C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43121691 | |||||||
| chr6:43121847 | G | A | 3 | a0001c0001t0001g0230 a0001c0002t0002g0231 a0001c0017t0001g0232 |
3 | HG00741.hp2 HG02055.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.80-7130G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43121847 | |||||||
| chr6:43121943 | C | T | 2 | a0001c0001t0001g0006 a0003c0004t0002g0007 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.80-7034C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43121943 | |||||||
| chr6:43122051 | A | G | 3 | a0001c0001t0002g0234 a0001c0001t0002g0242 a0001c0002t0009g0233 |
3 | HG01891.hp1 HG02895.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.80-6926A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43122051 | |||||||
| chr6:43122185 | G | A | 1 | a0003c0016t0002g0225 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.80-6792G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43122185 | |||||||
| chr6:43122273 | G | C | 1 | a0001c0002t0001g0134 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.80-6704G>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43122273 | |||||||
| chr6:43122366 | T | TGGGTCAG others(12): Show |
4 | a0001c0002t0003g0014 a0001c0002t0003g0148 a0001c0002t0003g0149 others(1): Show |
4 | HG01891.hp2 HG02109.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-6610_80-6592dup others(19): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43122366 | ||||||
| chr6:43122394 | C | T | 2 | a0001c0002t0001g0180 a0001c0002t0001g0181 |
2 | HG02280.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.80-6583C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43122394 | |||||||
| chr6:43122533 | C | A | 4 | a0002c0003t0002g0162 a0002c0003t0002g0163 a0002c0003t0002g0178 others(1): Show |
4 | HG02258.hp2 HG02965.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-6444C>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43122533 | |||||||
| chr6:43122562 | G | A | 1 | a0001c0001t0002g0023 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.80-6415G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43122562 | |||||||
| chr6:43122606 | C | CT | 11 | a0001c0001t0001g0094 a0001c0001t0001g0199 a0001c0001t0001g0200 others(8): Show |
11 | HG02622.hp2 HG03017.hp1 HG03098.hp1 others(8): Show |
intron_variant | MODIFIER | c.80-6352dupT | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43122606 | ||||||
| chr6:43122606 | C | CTT | 5 | a0001c0001t0001g0202 a0001c0001t0001g0204 a0001c0001t0001g0206 others(2): Show |
5 | HG02109.hp2 HG02145.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.80-6353_80-6352dup others(2): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43122606 | ||||||
| chr6:43122606 | CT | C | 64 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0085 others(61): Show |
64 | HG00323.hp2 HG00597.hp1 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.80-6352delT | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43122606 | ||||||
| chr6:43122694 | T | A | 69 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(66): Show |
69 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.80-6283T>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43122694 | |||||||
| chr6:43122902 | C | T | 2 | a0001c0001t0002g0021 a0001c0001t0002g0265 |
2 | HG00609.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.80-6075C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43122902 | |||||||
| chr6:43123016 | C | T | 29 | a0001c0001t0001g0199 a0001c0001t0001g0246 a0001c0001t0001g0262 others(26): Show |
29 | HG00423.hp2 HG01099.hp1 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.80-5961C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43123016 | |||||||
| chr6:43123346 | G | A | 2 | a0001c0002t0001g0168 a0001c0002t0001g0169 |
2 | HG01074.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.80-5631G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43123346 | |||||||
| chr6:43123372 | A | G | 2 | a0001c0001t0002g0005 a0001c0001t0002g0042 |
2 | HG02572.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.80-5605A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43123372 | |||||||
| chr6:43123522 | G | A | 2 | a0001c0002t0001g0091 a0001c0012t0002g0229 |
2 | HG02809.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.80-5455G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43123522 | |||||||
| chr6:43123572 | C | T | 1 | a0001c0002t0001g0252 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.80-5405C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43123572 | |||||||
| chr6:43123608 | G | T | 2 | a0001c0001t0001g0065 a0007c0013t0001g0063 |
2 | NA18975.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.80-5369G>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43123608 | |||||||
| chr6:43123978 | G | A | 2 | a0001c0002t0004g0228 a0003c0004t0002g0239 |
2 | HG02976.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.80-4999G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43123978 | |||||||
| chr6:43124204 | C | A | 5 | a0001c0002t0001g0143 a0001c0002t0001g0144 a0001c0002t0001g0165 others(2): Show |
5 | HG00741.hp1 HG01255.hp1 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.80-4773C>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43124204 | |||||||
| chr6:43124266 | G | A | 1 | a0001c0001t0002g0116 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.80-4711G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43124266 | |||||||
| chr6:43124439 | G | A | 68 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(65): Show |
68 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.80-4538G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43124439 | |||||||
| chr6:43124577 | G | A | 68 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(65): Show |
68 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.80-4400G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43124577 | |||||||
| chr6:43124888 | A | G | 1 | a0001c0001t0002g0023 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.80-4089A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43124888 | |||||||
| chr6:43124912 | C | T | 68 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(65): Show |
68 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.80-4065C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43124912 | |||||||
| chr6:43124994 | G | A | 2 | a0001c0002t0001g0183 a0001c0002t0001g0184 |
2 | HG02630.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.80-3983G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43124994 | |||||||
| chr6:43125729 | A | C | 68 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(65): Show |
68 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.80-3248A>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43125729 | |||||||
| chr6:43126010 | G | A | 14 | a0001c0001t0001g0200 a0001c0001t0001g0202 a0001c0001t0001g0204 others(11): Show |
14 | HG00741.hp2 HG02055.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.80-2967G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43126010 | |||||||
| chr6:43126049 | A | G | 1 | a0001c0021t0002g0019 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.80-2928A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43126049 | |||||||
| chr6:43126118 | G | A | 1 | a0001c0001t0001g0193 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.80-2859G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43126118 | |||||||
| chr6:43126170 | A | G | 1 | a0001c0002t0001g0091 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.80-2807A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43126170 | |||||||
| chr6:43126213 | G | A | 1 | a0001c0002t0003g0149 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.80-2764G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43126213 | |||||||
| chr6:43126243 | C | A | 2 | a0001c0002t0001g0096 a0001c0002t0001g0110 |
2 | NA18962.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.80-2734C>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43126243 | |||||||
| chr6:43126252 | G | A | 68 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(65): Show |
68 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.80-2725G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43126252 | |||||||
| chr6:43126319 | G | A | 4 | a0001c0001t0001g0199 a0002c0003t0001g0243 a0005c0019t0001g0141 others(1): Show |
4 | HG02622.hp2 HG03130.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-2658G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43126319 | |||||||
| chr6:43126339 | T | C | 1 | a0001c0002t0002g0231 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.80-2638T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43126339 | |||||||
| chr6:43126406 | T | C | 77 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(74): Show |
77 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.80-2571T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43126406 | |||||||
| chr6:43126526 | A | T | 2 | a0001c0001t0001g0200 a0001c0001t0001g0205 |
2 | HG03098.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.80-2451A>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43126526 | |||||||
| chr6:43126617 | G | A | 68 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(65): Show |
68 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.80-2360G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43126617 | |||||||
| chr6:43126740 | C | T | 2 | a0001c0001t0001g0199 a0005c0019t0001g0141 |
2 | HG02622.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.80-2237C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43126740 | |||||||
| chr6:43126878 | A | G | 1 | a0006c0020t0006g0226 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.80-2099A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43126878 | |||||||
| chr6:43126926 | A | G | 14 | a0001c0001t0001g0200 a0001c0001t0001g0202 a0001c0001t0001g0204 others(11): Show |
14 | HG00741.hp2 HG02055.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.80-2051A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43126926 | |||||||
| chr6:43127230 | G | A | 4 | a0001c0001t0001g0199 a0002c0003t0001g0243 a0005c0019t0001g0141 others(1): Show |
4 | HG02622.hp2 HG03130.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-1747G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43127230 | |||||||
| chr6:43127247 | G | A | 1 | a0001c0001t0004g0269 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.80-1730G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43127247 | |||||||
| chr6:43127483 | G | A | 1 | a0002c0003t0001g0243 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.80-1494G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43127483 | |||||||
| chr6:43127651 | C | T | 1 | a0001c0002t0001g0074 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.80-1326C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43127651 | |||||||
| chr6:43127657 | C | T | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | NA19070.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.80-1320C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43127657 | |||||||
| chr6:43127701 | G | A | 14 | a0001c0001t0001g0200 a0001c0001t0001g0202 a0001c0001t0001g0204 others(11): Show |
14 | HG00741.hp2 HG02055.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.80-1276G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43127701 | |||||||
| chr6:43127704 | C | T | 68 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(65): Show |
68 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.80-1273C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43127704 | |||||||
| chr6:43127884 | G | C | 4 | a0001c0001t0001g0199 a0002c0003t0001g0243 a0005c0019t0001g0141 others(1): Show |
4 | HG02622.hp2 HG03130.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-1093G>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43127884 | |||||||
| chr6:43127928 | C | CA | 7 | a0001c0001t0001g0199 a0001c0001t0002g0055 a0001c0001t0002g0242 others(4): Show |
7 | HG01943.hp1 HG02622.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.80-1037dupA | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43127928 | ||||||
| chr6:43128035 | A | T | 1 | a0006c0020t0006g0226 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.80-942A>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43128035 | |||||||
| chr6:43128053 | G | A | 5 | a0001c0001t0002g0234 a0001c0001t0002g0242 a0001c0002t0009g0233 others(2): Show |
5 | HG01891.hp1 HG02145.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.80-924G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43128053 | |||||||
| chr6:43128090 | G | A | 154 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(151): Show |
154 | HG00323.hp1 HG00323.hp2 HG00597.hp1 others(151): Show |
intron_variant | MODIFIER | c.80-887G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43128090 | |||||||
| chr6:43128329 | G | A | 149 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(146): Show |
149 | HG00323.hp1 HG00323.hp2 HG00597.hp1 others(146): Show |
intron_variant | MODIFIER | c.80-648G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43128329 | |||||||
| chr6:43128381 | T | C | 1 | a0001c0001t0002g0195 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.80-596T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43128381 | |||||||
| chr6:43128461 | T | C | 77 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0135 others(74): Show |
77 | HG00323.hp2 HG00597.hp1 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.80-516T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43128461 | |||||||
| chr6:43128471 | A | C | 1 | a0001c0001t0001g0193 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.80-506A>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43128471 | |||||||
| chr6:43128555 | T | C | 154 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(151): Show |
154 | HG00323.hp1 HG00323.hp2 HG00597.hp1 others(151): Show |
intron_variant | MODIFIER | c.80-422T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43128555 | |||||||
| chr6:43128614 | G | A | 3 | a0001c0002t0003g0014 a0001c0002t0003g0148 a0001c0002t0003g0150 |
3 | HG01891.hp2 HG02109.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.80-363G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43128614 | |||||||
| chr6:43128703 | T | A | 4 | a0001c0001t0001g0199 a0002c0003t0001g0243 a0005c0019t0001g0141 others(1): Show |
4 | HG02622.hp2 HG03130.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-274T>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43128703 | |||||||
| chr6:43128732 | C | T | 1 | a0001c0001t0002g0023 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.80-245C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43128732 | |||||||
| chr6:43128752 | T | G | 1 | a0006c0020t0006g0226 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.80-225T>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43128752 | |||||||
| chr6:43128767 | A | G | 4 | a0001c0001t0001g0199 a0002c0003t0001g0243 a0005c0019t0001g0141 others(1): Show |
4 | HG02622.hp2 HG03130.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-210A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43128767 | |||||||
| chr6:43128855 | C | T | 1 | a0001c0001t0004g0269 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.80-122C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43128855 | |||||||
| chr6:43128871 | G | A | 2 | a0001c0002t0001g0122 a0001c0002t0001g0207 |
2 | HG00323.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.80-106G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43128871 | |||||||
| chr6:43129367 | C | T | 1 | a0001c0002t0001g0182 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.367+103C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 2/19 | chr6 | 43129367 | |||||||
| chr6:43129509 | G | A | 14 | a0001c0001t0001g0200 a0001c0001t0001g0202 a0001c0001t0001g0204 others(11): Show |
14 | HG00741.hp2 HG02055.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.368-218G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 2/19 | chr6 | 43129509 | |||||||
| chr6:43129705 | G | C | 3 | a0001c0002t0001g0145 a0001c0002t0004g0139 a0002c0003t0002g0070 |
3 | HG01074.hp1 HG01261.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.368-22G>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 2/19 | chr6 | 43129705 | |||||||
| chr6:43129868 | C | T | 1 | a0005c0019t0001g0141 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.470+39C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 3/19 | chr6 | 43129868 | |||||||
| chr6:43129992 | G | A | 1 | a0004c0007t0001g0131 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.470+163G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 3/19 | chr6 | 43129992 | |||||||
| chr6:43130444 | G | A | 10 | a0001c0001t0001g0230 a0001c0001t0002g0222 a0001c0001t0002g0223 others(7): Show |
10 | HG00741.hp2 HG02055.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.661+24G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 4/19 | chr6 | 43130444 | |||||||
| chr6:43130913 | C | T | 1 | a0001c0002t0001g0267 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.812+252C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 5/19 | chr6 | 43130913 | |||||||
| chr6:43131007 | G | A | 2 | a0001c0002t0002g0026 a0001c0002t0002g0231 |
2 | HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.812+346G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 5/19 | chr6 | 43131007 | |||||||
| chr6:43131029 | T | TCA | 37 | a0001c0001t0001g0003 a0001c0001t0001g0051 a0001c0001t0001g0092 others(34): Show |
37 | HG00544.hp2 HG00642.hp1 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.812+416_812+417dup others(2): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 43131029 | ||||||
| chr6:43131029 | T | TCACA | 40 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0037 others(37): Show |
40 | HG00544.hp1 HG00733.hp2 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.812+414_812+417dup others(4): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 43131029 | ||||||
| chr6:43131029 | T | TCACACA | 19 | a0001c0001t0001g0071 a0001c0001t0001g0172 a0001c0001t0001g0200 others(16): Show |
19 | HG00597.hp2 HG00609.hp1 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.812+412_812+417dup others(6): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 43131029 | ||||||
| chr6:43131029 | T | TCACACAC others(1): Show |
10 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0048 others(7): Show |
10 | HG01884.hp2 HG02148.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.812+410_812+417dup others(8): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 43131029 | ||||||
| chr6:43131029 | T | TCACACAC others(3): Show |
1 | a0001c0001t0002g0015 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.812+408_812+417dup others(10): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 43131029 | ||||||
| chr6:43131029 | TCA | T | 39 | a0001c0001t0001g0065 a0001c0001t0001g0077 a0001c0001t0001g0085 others(36): Show |
39 | HG00423.hp2 HG01099.hp1 HG01123.hp1 others(36): Show |
intron_variant | MODIFIER | c.812+416_812+417del others(2): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 43131029 | ||||||
| chr6:43131029 | TCACA | T | 26 | a0001c0001t0001g0097 a0001c0001t0001g0111 a0001c0001t0001g0171 others(23): Show |
26 | HG00323.hp1 HG00609.hp2 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.812+414_812+417del others(4): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 43131029 | ||||||
| chr6:43131029 | TCACACA | T | 9 | a0001c0001t0001g0079 a0001c0001t0001g0094 a0001c0001t0001g0095 others(6): Show |
9 | HG02055.hp2 HG02572.hp2 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.812+412_812+417del others(6): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 43131029 | ||||||
| chr6:43131029 | TCACACAC others(1): Show |
T | 5 | a0001c0002t0001g0142 a0001c0002t0002g0026 a0001c0002t0002g0231 others(2): Show |
5 | HG00741.hp2 HG02145.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.812+410_812+417del others(8): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 43131029 | ||||||
| chr6:43131029 | TCACACAC others(3): Show |
T | 1 | a0001c0001t0002g0057 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.812+408_812+417del others(10): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 43131029 | ||||||
| chr6:43131029 | TCACACAC others(5): Show |
T | 4 | a0001c0001t0002g0222 a0001c0001t0002g0223 a0001c0001t0002g0224 others(1): Show |
4 | HG02970.hp2 HG03130.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.812+406_812+417del others(12): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 43131029 | ||||||
| chr6:43131029 | TCACACAC others(7): Show |
T | 3 | a0001c0001t0001g0238 a0002c0003t0002g0070 a0002c0003t0002g0121 |
3 | HG01255.hp2 HG01261.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.812+404_812+417del others(14): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 43131029 | ||||||
| chr6:43131029 | TCACACAC others(21): Show |
T | 3 | a0001c0001t0001g0204 a0001c0001t0003g0201 a0001c0002t0001g0203 |
3 | HG02258.hp1 HG03516.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.812+390_812+417del others(28): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 43131029 | ||||||
| chr6:43131029 | TCACACAC others(23): Show |
T | 3 | a0001c0002t0004g0228 a0003c0004t0002g0235 a0003c0004t0002g0239 |
3 | HG02818.hp2 HG02976.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.812+388_812+417del others(30): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 43131029 | ||||||
| chr6:43131031 | A | C | 1 | a0006c0020t0006g0226 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.812+370A>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 5/19 | chr6 | 43131031 | |||||||
| chr6:43131033 | A | C | 1 | a0005c0019t0001g0141 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.812+372A>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 5/19 | chr6 | 43131033 | |||||||
| chr6:43131035 | A | C | 1 | a0002c0003t0001g0243 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.812+374A>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 5/19 | chr6 | 43131035 | |||||||
| chr6:43131061 | A | G | 2 | a0002c0003t0002g0070 a0002c0003t0002g0121 |
2 | HG01261.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.812+400A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 5/19 | chr6 | 43131061 | |||||||
| chr6:43131108 | G | T | 2 | a0001c0002t0001g0151 a0001c0002t0001g0159 |
2 | HG00597.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.812+447G>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 5/19 | chr6 | 43131108 | |||||||
| chr6:43131762 | G | T | 21 | a0001c0001t0001g0166 a0001c0001t0001g0200 a0001c0001t0001g0202 others(18): Show |
21 | HG00741.hp2 HG01261.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.813-254G>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 5/19 | chr6 | 43131762 | |||||||
| chr6:43131869 | C | G | 38 | a0001c0001t0001g0166 a0001c0001t0001g0200 a0001c0001t0001g0202 others(35): Show |
38 | HG00423.hp2 HG01099.hp1 HG01261.hp2 others(35): Show |
intron_variant | MODIFIER | c.813-147C>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 5/19 | chr6 | 43131869 | |||||||
| chr6:43131899 | GTTCCTGG others(4): Show |
G | 2 | a0001c0015t0001g0240 a0003c0014t0002g0241 |
2 | HG02145.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.813-111_813-101del others(11): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr6 | 43131899 | ||||||
| chr6:43132361 | A | G | 2 | a0001c0015t0001g0240 a0003c0014t0002g0241 |
2 | HG02145.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.962-60A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 6/19 | chr6 | 43132361 | |||||||
| chr6:43132418 | C | T | 1 | a0002c0003t0002g0070 | 1 | HG01261.hp2 | splice_region_variant&intron_variant | LOW | c.962-3C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 6/19 | chr6 | 43132418 | |||||||
| chr6:43132799 | T | G | 17 | a0001c0002t0001g0031 a0001c0002t0001g0196 a0001c0002t0001g0198 others(14): Show |
17 | HG01099.hp1 HG01261.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.1228+112T>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 7/19 | chr6 | 43132799 | |||||||
| chr6:43132823 | A | G | 8 | a0001c0002t0001g0089 a0001c0002t0001g0102 a0001c0002t0001g0104 others(5): Show |
8 | HG01258.hp1 HG01346.hp2 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.1228+136A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 7/19 | chr6 | 43132823 | |||||||
| chr6:43132925 | C | T | 1 | a0001c0002t0001g0134 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1228+238C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 7/19 | chr6 | 43132925 | |||||||
| chr6:43132994 | C | T | 1 | a0001c0002t0001g0074 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1228+307C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 7/19 | chr6 | 43132994 | |||||||
| chr6:43133217 | ATTAC | A | 8 | a0001c0001t0002g0234 a0001c0001t0002g0242 a0001c0012t0002g0229 others(5): Show |
8 | HG01261.hp2 HG01891.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1228+534_1228+537d others(6): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr6 | 43133217 | ||||||
| chr6:43133467 | G | C | 1 | a0006c0020t0006g0226 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1228+780G>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 7/19 | chr6 | 43133467 | |||||||
| chr6:43133532 | C | G | 169 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(166): Show |
169 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(166): Show |
intron_variant | MODIFIER | c.1228+845C>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 7/19 | chr6 | 43133532 | |||||||
| chr6:43133548 | G | A | 1 | a0001c0001t0001g0268 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1228+861G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 7/19 | chr6 | 43133548 | |||||||
| chr6:43133756 | C | T | 1 | a0001c0001t0002g0118 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1228+1069C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 7/19 | chr6 | 43133756 | |||||||
| chr6:43133861 | A | G | 2 | a0001c0015t0001g0240 a0003c0014t0002g0241 |
2 | HG02145.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1228+1174A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 7/19 | chr6 | 43133861 | |||||||
| chr6:43133932 | T | C | 196 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(193): Show |
196 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(193): Show |
intron_variant | MODIFIER | c.1228+1245T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 7/19 | chr6 | 43133932 | |||||||
| chr6:43133996 | C | T | 4 | a0001c0001t0002g0234 a0001c0001t0002g0242 a0001c0012t0002g0229 others(1): Show |
4 | HG01891.hp1 HG02145.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1228+1309C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 7/19 | chr6 | 43133996 | |||||||
| chr6:43134036 | A | T | 1 | a0001c0012t0002g0229 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1228+1349A>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 7/19 | chr6 | 43134036 | |||||||
| chr6:43134195 | C | T | 1 | a0001c0002t0001g0215 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1228+1508C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 7/19 | chr6 | 43134195 | |||||||
| chr6:43134228 | G | A | 1 | a0006c0020t0006g0226 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1228+1541G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 7/19 | chr6 | 43134228 | |||||||
| chr6:43134286 | G | T | 1 | a0001c0012t0002g0229 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1228+1599G>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 7/19 | chr6 | 43134286 | |||||||
| chr6:43134304 | G | A | 1 | a0001c0002t0001g0146 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1228+1617G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 7/19 | chr6 | 43134304 | |||||||
| chr6:43134314 | T | A | 1 | a0001c0001t0001g0268 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1228+1627T>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 7/19 | chr6 | 43134314 | |||||||
| chr6:43134334 | C | T | 2 | a0001c0012t0002g0229 a0002c0018t0001g0248 |
2 | HG02145.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1228+1647C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 7/19 | chr6 | 43134334 | |||||||
| chr6:43134488 | A | G | 15 | a0001c0001t0001g0167 a0001c0002t0001g0074 a0001c0002t0001g0109 others(12): Show |
15 | HG00323.hp2 HG01074.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.1228+1801A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 7/19 | chr6 | 43134488 | |||||||
| chr6:43134782 | GA | G | 7 | a0001c0001t0001g0097 a0001c0001t0004g0269 a0001c0002t0001g0091 others(4): Show |
7 | HG02622.hp2 HG02809.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1228+2112delA | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr6 | 43134782 | ||||||
| chr6:43135206 | G | C | 1 | a0001c0001t0002g0257 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1228+2519G>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 7/19 | chr6 | 43135206 | |||||||
| chr6:43135664 | T | A | 2 | a0002c0003t0002g0070 a0002c0003t0002g0121 |
2 | HG01261.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.1228+2977T>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 7/19 | chr6 | 43135664 | |||||||
| chr6:43135847 | G | A | 11 | a0001c0002t0001g0031 a0001c0002t0001g0196 a0001c0002t0001g0198 others(8): Show |
11 | HG01099.hp1 HG02615.hp2 HG02976.hp1 others(8): Show |
intron_variant | MODIFIER | c.1229-3002G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 7/19 | chr6 | 43135847 | |||||||
| chr6:43135880 | C | T | 6 | a0001c0015t0001g0240 a0002c0003t0001g0243 a0002c0003t0002g0070 others(3): Show |
6 | HG01261.hp2 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1229-2969C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 7/19 | chr6 | 43135880 | |||||||
| chr6:43135911 | G | A | 1 | a0005c0019t0001g0141 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1229-2938G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 7/19 | chr6 | 43135911 | |||||||
| chr6:43135971 | C | T | 2 | a0001c0001t0001g0073 a0001c0001t0001g0192 |
2 | HG02071.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.1229-2878C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 7/19 | chr6 | 43135971 | |||||||
| chr6:43136003 | C | T | 1 | a0001c0001t0002g0118 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1229-2846C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 7/19 | chr6 | 43136003 | |||||||
| chr6:43136017 | G | A | 2 | a0001c0001t0002g0234 a0001c0001t0002g0242 |
2 | HG01891.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1229-2832G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 7/19 | chr6 | 43136017 | |||||||
| chr6:43136174 | CA | C | 22 | a0001c0001t0002g0234 a0001c0001t0002g0242 a0001c0002t0001g0031 others(19): Show |
22 | HG01099.hp1 HG01261.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.1229-2664delA | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr6 | 43136174 | ||||||
| chr6:43136199 | G | A | 1 | a0006c0020t0006g0226 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1229-2650G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 7/19 | chr6 | 43136199 | |||||||
| chr6:43136250 | G | A | 1 | a0001c0002t0001g0143 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1229-2599G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 7/19 | chr6 | 43136250 | |||||||
| chr6:43136334 | C | CA | 9 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0077 others(6): Show |
9 | HG01255.hp2 HG01952.hp2 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.1229-2501dupA | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr6 | 43136334 | ||||||
| chr6:43136334 | CA | C | 183 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(180): Show |
183 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.1229-2501delA | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr6 | 43136334 | ||||||
| chr6:43136449 | C | T | 4 | a0001c0001t0002g0234 a0001c0001t0002g0242 a0001c0012t0002g0229 others(1): Show |
4 | HG01891.hp1 HG02145.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1229-2400C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 7/19 | chr6 | 43136449 | |||||||
| chr6:43136471 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1229-2378G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 7/19 | chr6 | 43136471 | |||||||
| chr6:43136504 | C | T | 2 | a0001c0001t0001g0064 a0001c0001t0001g0080 |
2 | HG03688.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.1229-2345C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 7/19 | chr6 | 43136504 | |||||||
| chr6:43136722 | C | G | 1 | a0006c0020t0006g0226 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1229-2127C>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 7/19 | chr6 | 43136722 | |||||||
| chr6:43136934 | G | A | 3 | a0001c0002t0004g0139 a0002c0003t0001g0243 a0005c0019t0001g0141 |
3 | HG02622.hp2 HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1229-1915G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 7/19 | chr6 | 43136934 | |||||||
| chr6:43137021 | T | G | 2 | a0002c0003t0002g0070 a0002c0003t0002g0121 |
2 | HG01261.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.1229-1828T>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 7/19 | chr6 | 43137021 | |||||||
| chr6:43137027 | C | G | 1 | a0006c0020t0006g0226 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1229-1822C>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 7/19 | chr6 | 43137027 | |||||||
| chr6:43137030 | C | T | 6 | a0001c0015t0001g0240 a0002c0003t0001g0243 a0002c0003t0002g0070 others(3): Show |
6 | HG01261.hp2 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1229-1819C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 7/19 | chr6 | 43137030 | |||||||
| chr6:43137371 | G | A | 1 | a0001c0001t0002g0010 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1229-1478G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 7/19 | chr6 | 43137371 | |||||||
| chr6:43137598 | C | T | 12 | a0001c0002t0001g0031 a0001c0002t0001g0196 a0001c0002t0001g0198 others(9): Show |
12 | HG01099.hp1 HG02615.hp2 HG02976.hp1 others(9): Show |
intron_variant | MODIFIER | c.1229-1251C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 7/19 | chr6 | 43137598 | |||||||
| chr6:43137830 | G | A | 9 | a0001c0001t0001g0166 a0001c0001t0001g0199 a0001c0001t0001g0202 others(6): Show |
9 | HG02109.hp2 HG02258.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1229-1019G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 7/19 | chr6 | 43137830 | |||||||
| chr6:43137850 | A | G | 154 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(151): Show |
154 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.1229-999A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 7/19 | chr6 | 43137850 | |||||||
| chr6:43137868 | G | A | 1 | a0001c0001t0004g0269 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1229-981G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 7/19 | chr6 | 43137868 | |||||||
| chr6:43137869 | T | C | 164 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(161): Show |
164 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.1229-980T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 7/19 | chr6 | 43137869 | |||||||
| chr6:43137968 | G | A | 2 | a0001c0001t0002g0035 a0001c0001t0002g0214 |
2 | HG02451.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1229-881G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 7/19 | chr6 | 43137968 | |||||||
| chr6:43138056 | G | A | 2 | a0001c0002t0001g0196 a0001c0002t0001g0198 |
2 | NA18947.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.1229-793G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 7/19 | chr6 | 43138056 | |||||||
| chr6:43138180 | GT | G | 194 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(191): Show |
194 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(191): Show |
intron_variant | MODIFIER | c.1229-661delT | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr6 | 43138180 | ||||||
| chr6:43138232 | G | GTGCAGT | 3 | a0001c0001t0001g0167 a0001c0001t0002g0234 a0002c0003t0001g0243 |
3 | HG01891.hp1 HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1229-616_1229-611d others(8): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr6 | 43138232 | ||||||
| chr6:43138342 | A | T | 1 | a0001c0002t0001g0074 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1229-507A>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 7/19 | chr6 | 43138342 | |||||||
| chr6:43138488 | C | T | 7 | a0001c0002t0001g0112 a0001c0002t0001g0114 a0001c0002t0001g0129 others(4): Show |
7 | HG01074.hp2 HG01167.hp1 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1229-361C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 7/19 | chr6 | 43138488 | |||||||
| chr6:43138675 | T | A | 2 | a0001c0002t0001g0152 a0001c0002t0001g0161 |
2 | HG03669.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1229-174T>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 7/19 | chr6 | 43138675 | |||||||
| chr6:43138679 | A | T | 10 | a0001c0001t0002g0234 a0001c0001t0002g0242 a0001c0015t0001g0240 others(7): Show |
10 | HG01261.hp2 HG01891.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1229-170A>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 7/19 | chr6 | 43138679 | |||||||
| chr6:43138688 | G | T | 1 | a0001c0002t0003g0149 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1229-161G>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 7/19 | chr6 | 43138688 | |||||||
| chr6:43139086 | G | A | 1 | a0001c0002t0001g0074 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1363-50G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 8/19 | chr6 | 43139086 | |||||||
| chr6:43139351 | G | A | 1 | a0001c0001t0002g0050 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1499-55G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 9/19 | chr6 | 43139351 | |||||||
| chr6:43139762 | C | T | 1 | a0001c0002t0001g0114 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1618+237C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 10/19 | chr6 | 43139762 | |||||||
| chr6:43139847 | C | G | 1 | a0001c0012t0002g0229 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1618+322C>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 10/19 | chr6 | 43139847 | |||||||
| chr6:43139880 | G | A | 1 | a0001c0001t0001g0087 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1618+355G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 10/19 | chr6 | 43139880 | |||||||
| chr6:43140006 | T | C | 104 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(101): Show |
104 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(101): Show |
intron_variant | MODIFIER | c.1618+481T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 10/19 | chr6 | 43140006 | |||||||
| chr6:43140150 | T | C | 1 | a0001c0001t0002g0257 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1618+625T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 10/19 | chr6 | 43140150 | |||||||
| chr6:43140205 | G | T | 104 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(101): Show |
104 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(101): Show |
intron_variant | MODIFIER | c.1618+680G>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 10/19 | chr6 | 43140205 | |||||||
| chr6:43140286 | T | C | 2 | a0001c0015t0001g0240 a0003c0014t0002g0241 |
2 | HG02145.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1618+761T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 10/19 | chr6 | 43140286 | |||||||
| chr6:43140384 | C | T | 7 | a0001c0015t0001g0240 a0002c0003t0001g0243 a0002c0003t0002g0070 others(4): Show |
7 | HG01261.hp2 HG02145.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1618+859C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 10/19 | chr6 | 43140384 | |||||||
| chr6:43140452 | C | CA | 15 | a0001c0001t0001g0011 a0001c0001t0002g0008 a0001c0001t0002g0039 others(12): Show |
15 | HG01261.hp2 HG01891.hp1 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.1618+944dupA | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr6 | 43140452 | ||||||
| chr6:43140452 | C | CAA | 88 | a0001c0001t0001g0006 a0001c0001t0001g0037 a0001c0001t0001g0058 others(85): Show |
88 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.1618+943_1618+944d others(4): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr6 | 43140452 | ||||||
| chr6:43140452 | CA | C | 7 | a0001c0001t0001g0094 a0001c0001t0001g0211 a0001c0002t0001g0089 others(4): Show |
7 | HG01975.hp2 HG01993.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1618+944delA | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr6 | 43140452 | ||||||
| chr6:43140470 | T | A | 1 | a0001c0005t0001g0156 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1618+945T>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 10/19 | chr6 | 43140470 | |||||||
| chr6:43140533 | G | T | 1 | a0001c0001t0002g0272 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1618+1008G>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 10/19 | chr6 | 43140533 | |||||||
| chr6:43140668 | G | A | 1 | a0001c0002t0001g0123 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1619-1000G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 10/19 | chr6 | 43140668 | |||||||
| chr6:43140829 | A | T | 2 | a0001c0001t0002g0052 a0002c0018t0001g0248 |
2 | HG01981.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.1619-839A>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 10/19 | chr6 | 43140829 | |||||||
| chr6:43140834 | T | G | 1 | a0001c0002t0001g0215 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1619-834T>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 10/19 | chr6 | 43140834 | |||||||
| chr6:43141206 | A | T | 90 | a0001c0002t0001g0031 a0001c0002t0001g0034 a0001c0002t0001g0056 others(87): Show |
90 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.1619-462A>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 10/19 | chr6 | 43141206 | |||||||
| chr6:43141393 | G | A | 1 | a0001c0001t0002g0195 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1619-275G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 10/19 | chr6 | 43141393 | |||||||
| chr6:43141869 | G | A | 11 | a0001c0001t0001g0166 a0001c0001t0001g0199 a0001c0001t0001g0200 others(8): Show |
11 | HG02109.hp2 HG02258.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1768+52G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 11/19 | chr6 | 43141869 | |||||||
| chr6:43142317 | T | G | 105 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(102): Show |
105 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(102): Show |
intron_variant | MODIFIER | c.2047+18T>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 13/19 | chr6 | 43142317 | |||||||
| chr6:43142426 | C | T | 1 | a0001c0001t0002g0118 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2047+127C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 13/19 | chr6 | 43142426 | |||||||
| chr6:43142466 | A | G | 4 | a0001c0001t0004g0269 a0001c0015t0001g0240 a0003c0014t0002g0241 others(1): Show |
4 | HG02145.hp1 HG02809.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2047+167A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 13/19 | chr6 | 43142466 | |||||||
| chr6:43142502 | G | GGT | 91 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(88): Show |
91 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.2047+220_2047+221d others(4): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr6 | 43142502 | ||||||
| chr6:43142524 | G | C | 1 | a0005c0019t0001g0141 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2047+225G>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 13/19 | chr6 | 43142524 | |||||||
| chr6:43142656 | G | T | 1 | a0001c0001t0001g0246 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2047+357G>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 13/19 | chr6 | 43142656 | |||||||
| chr6:43142711 | G | C | 3 | a0002c0003t0002g0162 a0002c0003t0002g0163 a0002c0003t0002g0178 |
3 | HG02258.hp2 HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2047+412G>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 13/19 | chr6 | 43142711 | |||||||
| chr6:43142986 | C | T | 1 | a0001c0012t0002g0229 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2048-431C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 13/19 | chr6 | 43142986 | |||||||
| chr6:43142987 | C | G | 1 | a0001c0012t0002g0229 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2048-430C>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 13/19 | chr6 | 43142987 | |||||||
| chr6:43143652 | G | A | 1 | a0001c0002t0001g0114 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2251+32G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 14/19 | chr6 | 43143652 | |||||||
| chr6:43143707 | T | C | 194 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(191): Show |
194 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(191): Show |
intron_variant | MODIFIER | c.2251+87T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 14/19 | chr6 | 43143707 | |||||||
| chr6:43143739 | G | T | 1 | a0001c0001t0001g0238 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2251+119G>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 14/19 | chr6 | 43143739 | |||||||
| chr6:43143788 | G | A | 2 | a0002c0003t0002g0070 a0002c0003t0002g0121 |
2 | HG01261.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.2251+168G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 14/19 | chr6 | 43143788 | |||||||
| chr6:43143914 | C | T | 5 | a0002c0003t0001g0243 a0002c0003t0002g0162 a0002c0003t0002g0163 others(2): Show |
5 | HG02145.hp2 HG02258.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.2251+294C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 14/19 | chr6 | 43143914 | |||||||
| chr6:43143915 | G | A | 1 | a0001c0001t0001g0133 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.2251+295G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 14/19 | chr6 | 43143915 | |||||||
| chr6:43144320 | G | C | 11 | a0001c0001t0001g0013 a0001c0001t0002g0005 a0001c0001t0002g0033 others(8): Show |
11 | HG02451.hp2 HG02486.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.2252-131G>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 14/19 | chr6 | 43144320 | |||||||
| chr6:43144382 | G | C | 8 | a0001c0001t0001g0166 a0001c0001t0001g0199 a0001c0001t0001g0200 others(5): Show |
8 | HG02109.hp2 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.2252-69G>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 14/19 | chr6 | 43144382 | |||||||
| chr6:43144428 | G | A | 1 | a0001c0002t0001g0261 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2252-23G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 14/19 | chr6 | 43144428 | |||||||
| chr6:43144644 | C | T | 100 | a0001c0001t0001g0006 a0001c0001t0001g0166 a0001c0001t0001g0199 others(97): Show |
100 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.2407+38C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 15/19 | chr6 | 43144644 | |||||||
| chr6:43144674 | A | G | 83 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0037 others(80): Show |
83 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.2407+68A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 15/19 | chr6 | 43144674 | |||||||
| chr6:43144801 | C | T | 1 | a0001c0001t0001g0132 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2407+195C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 15/19 | chr6 | 43144801 | |||||||
| chr6:43144813 | T | G | 7 | a0002c0003t0001g0243 a0002c0003t0002g0070 a0002c0003t0002g0121 others(4): Show |
7 | HG01261.hp2 HG02145.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.2407+207T>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 15/19 | chr6 | 43144813 | |||||||
| chr6:43145018 | C | A | 1 | a0001c0012t0002g0229 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2408-182C>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 15/19 | chr6 | 43145018 | |||||||
| chr6:43145033 | C | G | 1 | a0001c0001t0002g0047 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2408-167C>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 15/19 | chr6 | 43145033 | |||||||
| chr6:43145723 | C | T | 5 | a0001c0001t0001g0006 a0001c0001t0001g0230 a0001c0002t0001g0136 others(2): Show |
5 | HG00741.hp2 HG02055.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.2640+291C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 16/19 | chr6 | 43145723 | |||||||
| chr6:43145905 | A | AGAGCTGC others(19): Show |
2 | a0002c0003t0002g0070 a0002c0003t0002g0121 |
2 | HG01261.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.2640+474_2640+499d others(28): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr6 | 43145905 | ||||||
| chr6:43145920 | T | C | 1 | a0001c0002t0001g0185 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2640+488T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 16/19 | chr6 | 43145920 | |||||||
| chr6:43146126 | G | A | 10 | a0001c0001t0001g0166 a0001c0001t0001g0199 a0001c0001t0001g0200 others(7): Show |
10 | HG02109.hp2 HG02145.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.2641-492G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 16/19 | chr6 | 43146126 | |||||||
| chr6:43146294 | T | C | 1 | a0001c0001t0002g0234 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2641-324T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 16/19 | chr6 | 43146294 | |||||||
| chr6:43146434 | G | A | 1 | a0001c0001t0002g0016 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.2641-184G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 16/19 | chr6 | 43146434 | |||||||
| chr6:43146473 | C | CT | 269 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(266): Show |
269 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(266): Show |
intron_variant | MODIFIER | c.2641-143dupT | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr6 | 43146473 | ||||||
| chr6:43146706 | C | T | 10 | a0001c0001t0001g0166 a0001c0001t0001g0199 a0001c0001t0001g0200 others(7): Show |
10 | HG02109.hp2 HG02145.hp1 HG02258.hp1 others(7): Show |
splice_region_variant&intron_variant | LOW | c.2721+8C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43146706 | |||||||
| chr6:43146835 | C | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0058 |
2 | HG03834.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.2721+137C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43146835 | |||||||
| chr6:43146930 | T | C | 2 | a0001c0002t0001g0180 a0001c0002t0001g0181 |
2 | HG02280.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.2721+232T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43146930 | |||||||
| chr6:43146964 | G | A | 11 | a0001c0001t0001g0068 a0001c0002t0001g0143 a0001c0002t0001g0144 others(8): Show |
11 | HG00741.hp1 HG01255.hp1 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.2721+266G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43146964 | |||||||
| chr6:43147024 | T | A | 2 | a0001c0001t0001g0013 a0001c0001t0001g0238 |
2 | HG01255.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2721+326T>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43147024 | |||||||
| chr6:43147192 | T | C | 5 | a0001c0001t0001g0006 a0001c0001t0001g0230 a0001c0002t0001g0136 others(2): Show |
5 | HG00741.hp2 HG02055.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.2721+494T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43147192 | |||||||
| chr6:43147221 | A | C | 16 | a0001c0001t0001g0098 a0001c0002t0001g0075 a0001c0002t0001g0089 others(13): Show |
16 | HG00544.hp2 HG01346.hp2 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.2721+523A>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43147221 | |||||||
| chr6:43147271 | C | T | 18 | a0001c0001t0002g0044 a0001c0001t0002g0222 a0001c0001t0002g0223 others(15): Show |
18 | HG02572.hp2 HG02615.hp2 HG02922.hp1 others(15): Show |
intron_variant | MODIFIER | c.2721+573C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43147271 | |||||||
| chr6:43147309 | G | A | 4 | a0001c0001t0001g0006 a0001c0001t0001g0230 a0001c0002t0001g0136 others(1): Show |
4 | HG00741.hp2 HG02055.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2721+611G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43147309 | |||||||
| chr6:43147444 | C | G | 1 | a0002c0018t0001g0248 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2721+746C>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43147444 | |||||||
| chr6:43147482 | A | G | 193 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0037 others(190): Show |
193 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(190): Show |
intron_variant | MODIFIER | c.2721+784A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43147482 | |||||||
| chr6:43147604 | A | G | 1 | a0001c0001t0001g0153 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2721+906A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43147604 | |||||||
| chr6:43147899 | G | A | 1 | a0002c0018t0001g0248 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2721+1201G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43147899 | |||||||
| chr6:43147930 | G | A | 3 | a0001c0002t0002g0103 a0002c0003t0002g0070 a0002c0003t0002g0121 |
3 | HG01258.hp1 HG01261.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.2721+1232G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43147930 | |||||||
| chr6:43147932 | C | A | 120 | a0001c0001t0001g0006 a0001c0001t0001g0068 a0001c0001t0001g0098 others(117): Show |
120 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(117): Show |
intron_variant | MODIFIER | c.2721+1234C>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43147932 | |||||||
| chr6:43147935 | C | T | 87 | a0001c0001t0001g0068 a0001c0001t0001g0098 a0001c0001t0001g0167 others(84): Show |
87 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.2721+1237C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43147935 | |||||||
| chr6:43148124 | A | G | 5 | a0001c0001t0001g0006 a0001c0001t0001g0230 a0001c0002t0001g0136 others(2): Show |
5 | HG00741.hp2 HG02055.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.2721+1426A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43148124 | |||||||
| chr6:43148255 | A | AGGGAG | 19 | a0001c0001t0002g0044 a0001c0001t0002g0222 a0001c0001t0002g0223 others(16): Show |
19 | HG02572.hp2 HG02615.hp2 HG02922.hp1 others(16): Show |
intron_variant | MODIFIER | c.2721+1566_2721+157 others(9): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43148255 | ||||||
| chr6:43148266 | G | C | 1 | a0001c0001t0001g0244 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2721+1568G>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43148266 | |||||||
| chr6:43148549 | G | A | 2 | a0001c0002t0005g0137 a0001c0002t0005g0138 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2721+1851G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43148549 | |||||||
| chr6:43148761 | A | T | 172 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0058 others(169): Show |
172 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(169): Show |
intron_variant | MODIFIER | c.2721+2063A>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43148761 | |||||||
| chr6:43148768 | T | TA | 193 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0037 others(190): Show |
193 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(190): Show |
intron_variant | MODIFIER | c.2721+2078dupA | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43148768 | ||||||
| chr6:43148861 | C | A | 3 | a0001c0001t0001g0006 a0001c0001t0001g0230 a0001c0017t0001g0232 |
3 | HG00741.hp2 HG02055.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2721+2163C>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43148861 | |||||||
| chr6:43149007 | C | G | 3 | a0001c0001t0002g0012 a0001c0001t0002g0020 a0001c0021t0002g0019 |
3 | HG03669.hp1 HG03704.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2721+2309C>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43149007 | |||||||
| chr6:43149013 | C | T | 9 | a0001c0001t0001g0098 a0001c0002t0001g0075 a0001c0002t0001g0089 others(6): Show |
9 | HG01346.hp2 HG01433.hp1 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.2721+2315C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43149013 | |||||||
| chr6:43149059 | CA | C | 104 | a0001c0001t0001g0006 a0001c0001t0001g0068 a0001c0001t0001g0076 others(101): Show |
104 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(101): Show |
intron_variant | MODIFIER | c.2721+2383delA | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43149059 | ||||||
| chr6:43149059 | CAA | C | 64 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0058 others(61): Show |
64 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.2721+2382_2721+238 others(6): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43149059 | ||||||
| chr6:43149078 | A | G | 5 | a0001c0001t0001g0069 a0001c0001t0001g0124 a0001c0001t0001g0133 others(2): Show |
5 | HG03540.hp1 NA18978.hp2 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.2721+2380A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43149078 | |||||||
| chr6:43149144 | G | A | 1 | a0005c0019t0001g0141 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2721+2446G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43149144 | |||||||
| chr6:43149307 | G | A | 1 | a0001c0001t0004g0269 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2721+2609G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43149307 | |||||||
| chr6:43149603 | A | C | 1 | a0001c0012t0002g0229 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2721+2905A>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43149603 | |||||||
| chr6:43149810 | A | C | 1 | a0001c0002t0002g0249 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2721+3112A>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43149810 | |||||||
| chr6:43150064 | G | A | 1 | a0001c0002t0001g0143 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2721+3366G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43150064 | |||||||
| chr6:43150069 | TGATAA | T | 3 | a0001c0005t0001g0156 a0001c0005t0001g0157 a0001c0005t0001g0177 |
3 | HG03492.hp2 HG03704.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.2721+3375_2721+337 others(9): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43150069 | ||||||
| chr6:43150113 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2721+3415G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43150113 | |||||||
| chr6:43150461 | CTGGAAAG others(8): Show |
C | 1 | a0001c0002t0001g0161 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2721+3765_2721+377 others(19): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43150461 | ||||||
| chr6:43150787 | C | CT | 21 | a0001c0001t0001g0013 a0001c0001t0001g0069 a0001c0001t0001g0077 others(18): Show |
21 | HG00423.hp1 HG00544.hp1 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.2721+4118dupT | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43150787 | ||||||
| chr6:43150787 | C | CTT | 16 | a0001c0001t0001g0011 a0001c0001t0001g0051 a0001c0001t0001g0073 others(13): Show |
16 | HG01123.hp1 HG01175.hp1 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.2721+4117_2721+411 others(6): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43150787 | ||||||
| chr6:43150787 | C | CTTT | 14 | a0001c0001t0001g0058 a0001c0001t0002g0044 a0001c0001t0002g0223 others(11): Show |
14 | HG01261.hp2 HG02145.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.2721+4116_2721+411 others(7): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43150787 | ||||||
| chr6:43150787 | C | CTTTTTTT | 21 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0015 others(18): Show |
21 | HG00597.hp2 HG00609.hp2 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.2721+4112_2721+411 others(11): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43150787 | ||||||
| chr6:43150787 | C | CTTTTTTT others(1): Show |
34 | a0001c0001t0001g0037 a0001c0001t0002g0004 a0001c0001t0002g0005 others(31): Show |
34 | HG00609.hp1 HG00642.hp1 HG01175.hp2 others(31): Show |
intron_variant | MODIFIER | c.2721+4111_2721+411 others(12): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43150787 | ||||||
| chr6:43150787 | C | CTTTTTTT others(2): Show |
6 | a0001c0001t0002g0042 a0001c0001t0002g0067 a0001c0001t0002g0255 others(3): Show |
6 | HG00423.hp2 HG02572.hp1 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.2721+4110_2721+411 others(13): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43150787 | ||||||
| chr6:43150787 | C | CTTTTTTT others(3): Show |
3 | a0001c0001t0002g0048 a0001c0002t0001g0191 a0001c0006t0001g0081 |
3 | HG01928.hp2 HG02148.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.2721+4109_2721+411 others(14): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43150787 | ||||||
| chr6:43150787 | C | CTTTTTTT others(4): Show |
1 | a0001c0001t0002g0259 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2721+4108_2721+411 others(15): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43150787 | ||||||
| chr6:43150787 | C | CTTTTTTT others(5): Show |
2 | a0001c0005t0001g0157 a0001c0005t0001g0177 |
2 | HG03704.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.2721+4107_2721+411 others(16): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43150787 | ||||||
| chr6:43150787 | C | CTTTTTTT others(6): Show |
1 | a0001c0005t0001g0156 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.2721+4106_2721+411 others(17): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43150787 | ||||||
| chr6:43150787 | C | CTTTTTTT others(7): Show |
1 | a0001c0001t0002g0272 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2721+4105_2721+411 others(18): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43150787 | ||||||
| chr6:43150787 | C | CTTTTTTT others(8): Show |
1 | a0001c0006t0001g0084 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2721+4104_2721+411 others(19): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43150787 | ||||||
| chr6:43150787 | C | CTTTTTTT others(9): Show |
1 | a0001c0001t0002g0032 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2721+4103_2721+411 others(20): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43150787 | ||||||
| chr6:43150787 | C | CTTTTTTT others(16): Show |
1 | a0001c0001t0001g0068 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.2721+4096_2721+411 others(27): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43150787 | ||||||
| chr6:43150787 | C | CTTTTTTT others(22): Show |
1 | a0001c0002t0001g0165 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2721+4090_2721+411 others(33): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43150787 | ||||||
| chr6:43150787 | C | CTTTTTTT others(23): Show |
1 | a0001c0006t0001g0078 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.2721+4118_2721+411 others(34): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43150787 | ||||||
| chr6:43150787 | C | CTTTTTTT others(33): Show |
1 | a0001c0002t0001g0144 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2721+4118_2721+411 others(44): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43150787 | ||||||
| chr6:43150805 | TTTTTTTT others(5): Show |
T | 1 | a0001c0012t0002g0229 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2721+4108_2721+411 others(16): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43150805 | |||||||
| chr6:43150806 | TTTTTTTT others(4): Show |
T | 4 | a0001c0001t0001g0230 a0001c0002t0001g0136 a0001c0017t0001g0232 others(1): Show |
4 | HG00741.hp2 HG02055.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.2721+4109_2721+411 others(15): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43150806 | |||||||
| chr6:43150807 | TTTTTTTT others(3): Show |
T | 3 | a0001c0001t0001g0006 a0001c0001t0002g0023 a0001c0001t0002g0029 |
3 | HG00639.hp2 HG02717.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.2721+4110_2721+411 others(14): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43150807 | |||||||
| chr6:43150811 | TTTTTTC | T | 6 | a0001c0001t0001g0166 a0001c0001t0001g0199 a0001c0001t0001g0202 others(3): Show |
6 | HG02109.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.2721+4114_2721+411 others(10): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43150811 | |||||||
| chr6:43150813 | TTTTC | T | 10 | a0001c0002t0001g0056 a0001c0002t0001g0134 a0001c0002t0001g0151 others(7): Show |
10 | HG00597.hp1 HG00639.hp1 HG01069.hp1 others(7): Show |
intron_variant | MODIFIER | c.2721+4116_2721+411 others(8): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43150813 | |||||||
| chr6:43150815 | TTC | T | 33 | a0001c0002t0001g0074 a0001c0002t0001g0075 a0001c0002t0001g0089 others(30): Show |
33 | HG00323.hp2 HG00544.hp2 HG01074.hp1 others(30): Show |
intron_variant | MODIFIER | c.2721+4118_2721+411 others(6): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43150815 | |||||||
| chr6:43150816 | TC | T | 21 | a0001c0001t0001g0098 a0001c0001t0002g0234 a0001c0001t0002g0242 others(18): Show |
21 | HG01358.hp2 HG01433.hp1 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.2721+4121delC | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43150816 | ||||||
| chr6:43150817 | C | T | 100 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0058 others(97): Show |
100 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.2721+4119C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43150817 | |||||||
| chr6:43150818 | C | T | 4 | a0001c0001t0001g0068 a0001c0006t0001g0078 a0001c0006t0001g0081 others(1): Show |
4 | HG02135.hp2 NA18998.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.2721+4120C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43150818 | |||||||
| chr6:43150825 | A | G | 178 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0037 others(175): Show |
178 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.2721+4127A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43150825 | |||||||
| chr6:43150876 | C | T | 11 | a0001c0001t0001g0068 a0001c0002t0001g0143 a0001c0002t0001g0144 others(8): Show |
11 | HG00741.hp1 HG01255.hp1 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.2721+4178C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43150876 | |||||||
| chr6:43150894 | G | A | 174 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0058 others(171): Show |
174 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(171): Show |
intron_variant | MODIFIER | c.2721+4196G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43150894 | |||||||
| chr6:43150914 | C | T | 57 | a0001c0001t0001g0098 a0001c0001t0001g0167 a0001c0002t0001g0056 others(54): Show |
57 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.2721+4216C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43150914 | |||||||
| chr6:43150915 | G | A | 1 | a0001c0001t0001g0126 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.2721+4217G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43150915 | |||||||
| chr6:43150925 | C | G | 1 | a0001c0001t0002g0265 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2721+4227C>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43150925 | |||||||
| chr6:43150925 | C | T | 5 | a0001c0001t0001g0006 a0001c0001t0001g0230 a0001c0002t0001g0136 others(2): Show |
5 | HG00741.hp2 HG02055.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.2721+4227C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43150925 | |||||||
| chr6:43150998 | T | C | 2 | a0001c0002t0001g0122 a0001c0002t0001g0207 |
2 | HG00323.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.2721+4300T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43150998 | |||||||
| chr6:43151136 | A | G | 2 | a0001c0001t0002g0254 a0001c0001t0002g0255 |
2 | NA18944.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.2721+4438A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43151136 | |||||||
| chr6:43151211 | C | CT | 97 | a0001c0001t0001g0068 a0001c0001t0001g0098 a0001c0001t0001g0166 others(94): Show |
97 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.2721+4527dupT | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43151211 | ||||||
| chr6:43151534 | G | GT | 9 | a0001c0001t0001g0003 a0001c0001t0001g0128 a0001c0001t0001g0133 others(6): Show |
9 | HG00423.hp1 HG01081.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.2721+4850dupT | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43151534 | ||||||
| chr6:43151534 | GT | G | 168 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0037 others(165): Show |
168 | HG00323.hp1 HG00323.hp2 HG00544.hp2 others(165): Show |
intron_variant | MODIFIER | c.2721+4850delT | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43151534 | ||||||
| chr6:43151542 | T | G | 8 | a0001c0001t0001g0166 a0001c0001t0001g0199 a0001c0001t0001g0200 others(5): Show |
8 | HG02109.hp2 HG02145.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.2721+4844T>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43151542 | |||||||
| chr6:43151685 | C | A | 1 | a0001c0002t0001g0247 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2721+4987C>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43151685 | |||||||
| chr6:43151840 | C | T | 1 | a0001c0001t0001g0022 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2721+5142C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43151840 | |||||||
| chr6:43151867 | G | A | 3 | a0001c0001t0001g0006 a0001c0001t0001g0230 a0001c0017t0001g0232 |
3 | HG00741.hp2 HG02055.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2721+5169G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43151867 | |||||||
| chr6:43151879 | C | T | 1 | a0001c0001t0004g0236 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2721+5181C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43151879 | |||||||
| chr6:43151913 | C | T | 1 | a0001c0017t0001g0232 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2721+5215C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43151913 | |||||||
| chr6:43152111 | T | C | 1 | a0002c0003t0001g0243 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2721+5413T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43152111 | |||||||
| chr6:43152190 | TTAGTTGA others(4): Show |
T | 1 | a0001c0002t0001g0218 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.2721+5495_2721+550 others(15): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43152190 | ||||||
| chr6:43152530 | G | A | 5 | a0001c0001t0004g0236 a0001c0001t0004g0269 a0001c0002t0004g0139 others(2): Show |
5 | HG02809.hp1 HG03209.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.2721+5832G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43152530 | |||||||
| chr6:43152713 | G | A | 7 | a0001c0001t0001g0006 a0001c0001t0001g0230 a0001c0002t0001g0056 others(4): Show |
7 | HG00741.hp2 HG02055.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.2721+6015G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43152713 | |||||||
| chr6:43152734 | T | TTTATG | 33 | a0001c0001t0001g0051 a0001c0001t0001g0071 a0001c0001t0001g0073 others(30): Show |
33 | HG00323.hp2 HG01123.hp1 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.2722-6026_2722-602 others(9): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43152734 | ||||||
| chr6:43152734 | T | TTTATGTT others(3): Show |
10 | a0001c0001t0001g0064 a0001c0001t0001g0211 a0001c0002t0001g0142 others(7): Show |
10 | HG00597.hp1 HG01069.hp1 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.2722-6031_2722-602 others(14): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43152734 | ||||||
| chr6:43152734 | T | TTTATGTT others(8): Show |
2 | a0001c0002t0001g0183 a0003c0004t0002g0025 |
2 | HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2722-6036_2722-602 others(19): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43152734 | ||||||
| chr6:43152734 | TTTATG | T | 70 | a0001c0001t0001g0002 a0001c0001t0001g0068 a0001c0001t0001g0069 others(67): Show |
70 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(67): Show |
intron_variant | MODIFIER | c.2722-6026_2722-602 others(9): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43152734 | ||||||
| chr6:43152734 | TTTATGTT others(3): Show |
T | 20 | a0001c0001t0001g0006 a0001c0001t0001g0160 a0001c0001t0001g0193 others(17): Show |
20 | HG01071.hp1 HG01169.hp1 HG01346.hp2 others(17): Show |
intron_variant | MODIFIER | c.2722-6031_2722-602 others(14): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43152734 | ||||||
| chr6:43152734 | TTTATGTT others(8): Show |
T | 12 | a0001c0001t0001g0230 a0001c0001t0002g0004 a0001c0001t0002g0028 others(9): Show |
12 | HG00733.hp1 HG00741.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.2722-6036_2722-602 others(19): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43152734 | ||||||
| chr6:43152734 | TTTATGTT others(13): Show |
T | 65 | a0001c0001t0001g0011 a0001c0001t0001g0058 a0001c0001t0002g0001 others(62): Show |
65 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.2722-6041_2722-602 others(24): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43152734 | ||||||
| chr6:43152734 | TTTATGTT others(18): Show |
T | 2 | a0001c0001t0001g0037 a0001c0001t0002g0036 |
2 | NA18969.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.2722-6046_2722-602 others(29): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43152734 | ||||||
| chr6:43152783 | T | C | 2 | a0001c0002t0001g0056 a0001c0002t0001g0203 |
2 | HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2722-6034T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43152783 | |||||||
| chr6:43152822 | G | T | 1 | a0001c0002t0001g0267 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2722-5995G>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43152822 | |||||||
| chr6:43152839 | G | T | 1 | a0001c0012t0002g0229 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2722-5978G>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43152839 | |||||||
| chr6:43152974 | TG | T | 5 | a0001c0001t0001g0166 a0001c0001t0001g0199 a0001c0001t0001g0202 others(2): Show |
5 | HG02109.hp2 HG02258.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.2722-5839delG | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43152974 | ||||||
| chr6:43152982 | C | T | 2 | a0001c0001t0001g0270 a0004c0007t0001g0131 |
2 | NA18980.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.2722-5835C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43152982 | |||||||
| chr6:43153104 | TTTTA | T | 17 | a0001c0001t0002g0044 a0001c0001t0002g0222 a0001c0001t0002g0223 others(14): Show |
17 | HG02572.hp2 HG02615.hp2 HG02922.hp1 others(14): Show |
intron_variant | MODIFIER | c.2722-5693_2722-569 others(8): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43153104 | ||||||
| chr6:43153215 | A | G | 1 | a0005c0019t0001g0141 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2722-5602A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43153215 | |||||||
| chr6:43153362 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2722-5455C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43153362 | |||||||
| chr6:43153408 | C | T | 7 | a0001c0001t0001g0006 a0001c0001t0001g0230 a0001c0002t0001g0056 others(4): Show |
7 | HG00741.hp2 HG02055.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.2722-5409C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43153408 | |||||||
| chr6:43153465 | A | G | 1 | a0001c0002t0004g0228 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2722-5352A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43153465 | |||||||
| chr6:43153496 | A | G | 1 | a0001c0001t0001g0211 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2722-5321A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43153496 | |||||||
| chr6:43153701 | T | G | 1 | a0001c0002t0001g0104 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2722-5116T>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43153701 | |||||||
| chr6:43153812 | G | A | 1 | a0001c0002t0001g0106 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.2722-5005G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43153812 | |||||||
| chr6:43154162 | C | CTAAA | 7 | a0001c0001t0001g0011 a0001c0001t0001g0058 a0001c0001t0001g0085 others(4): Show |
7 | HG01928.hp2 HG02258.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.2722-4630_2722-462 others(8): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43154162 | ||||||
| chr6:43154162 | C | CTAAATAA others(5): Show |
12 | a0001c0001t0001g0166 a0001c0001t0001g0199 a0001c0001t0001g0200 others(9): Show |
12 | HG01258.hp1 HG01261.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.2722-4638_2722-462 others(16): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43154162 | ||||||
| chr6:43154162 | C | CTAAATAA others(9): Show |
1 | a0001c0001t0002g0242 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2722-4642_2722-462 others(20): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43154162 | ||||||
| chr6:43154273 | A | T | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | NA19070.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.2722-4544A>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43154273 | |||||||
| chr6:43154324 | C | A | 8 | a0001c0001t0002g0234 a0001c0001t0002g0242 a0001c0002t0002g0103 others(5): Show |
8 | HG01258.hp1 HG01261.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.2722-4493C>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43154324 | |||||||
| chr6:43154381 | C | G | 15 | a0001c0001t0001g0006 a0001c0001t0001g0230 a0001c0001t0002g0234 others(12): Show |
15 | HG00741.hp2 HG01258.hp1 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.2722-4436C>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43154381 | |||||||
| chr6:43154439 | G | A | 2 | a0001c0002t0001g0145 a0001c0002t0001g0267 |
2 | HG01074.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2722-4378G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43154439 | |||||||
| chr6:43154575 | G | T | 3 | a0002c0003t0002g0162 a0002c0003t0002g0163 a0002c0003t0002g0178 |
3 | HG02258.hp2 HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2722-4242G>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43154575 | |||||||
| chr6:43154599 | A | G | 1 | a0001c0001t0001g0210 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.2722-4218A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43154599 | |||||||
| chr6:43154631 | G | C | 269 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(266): Show |
269 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(266): Show |
intron_variant | MODIFIER | c.2722-4186G>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43154631 | |||||||
| chr6:43154706 | G | C | 8 | a0001c0001t0001g0166 a0001c0001t0001g0199 a0001c0001t0001g0200 others(5): Show |
8 | HG02109.hp2 HG02145.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.2722-4111G>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43154706 | |||||||
| chr6:43154920 | C | G | 5 | a0001c0001t0001g0073 a0001c0001t0001g0087 a0001c0001t0001g0097 others(2): Show |
5 | HG02071.hp2 HG02135.hp1 NA18612.hp2 others(2): Show |
intron_variant | MODIFIER | c.2722-3897C>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43154920 | |||||||
| chr6:43155014 | T | A | 5 | a0001c0001t0004g0236 a0001c0001t0004g0269 a0001c0002t0004g0139 others(2): Show |
5 | HG02809.hp1 HG03209.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.2722-3803T>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43155014 | |||||||
| chr6:43155033 | G | A | 66 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(63): Show |
66 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.2722-3784G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43155033 | |||||||
| chr6:43155166 | A | G | 3 | a0001c0001t0002g0012 a0001c0001t0002g0020 a0001c0021t0002g0019 |
3 | HG03669.hp1 HG03704.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2722-3651A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43155166 | |||||||
| chr6:43155191 | T | A | 1 | a0001c0017t0001g0232 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2722-3626T>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43155191 | |||||||
| chr6:43155261 | A | C | 8 | a0001c0001t0001g0166 a0001c0001t0001g0199 a0001c0001t0001g0200 others(5): Show |
8 | HG02109.hp2 HG02145.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.2722-3556A>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43155261 | |||||||
| chr6:43155314 | A | G | 1 | a0001c0002t0002g0103 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.2722-3503A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43155314 | |||||||
| chr6:43155470 | G | A | 3 | a0002c0003t0002g0162 a0002c0003t0002g0163 a0002c0003t0002g0178 |
3 | HG02258.hp2 HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2722-3347G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43155470 | |||||||
| chr6:43155504 | C | T | 1 | a0001c0002t0002g0249 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2722-3313C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43155504 | |||||||
| chr6:43155537 | G | A | 3 | a0001c0002t0002g0103 a0002c0003t0002g0070 a0002c0003t0002g0121 |
3 | HG01258.hp1 HG01261.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.2722-3280G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43155537 | |||||||
| chr6:43155578 | A | AG | 67 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(64): Show |
67 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.2722-3238dupG | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43155578 | ||||||
| chr6:43155645 | C | CA | 92 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0230 others(89): Show |
92 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.2722-3159dupA | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43155645 | ||||||
| chr6:43155954 | C | T | 61 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0008 others(58): Show |
61 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.2722-2863C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43155954 | |||||||
| chr6:43156106 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2722-2711G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43156106 | |||||||
| chr6:43156228 | C | CA | 12 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0073 others(9): Show |
12 | HG00642.hp2 HG01081.hp2 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.2722-2563dupA | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43156228 | ||||||
| chr6:43156228 | C | CAA | 6 | a0001c0001t0001g0200 a0001c0001t0001g0202 a0001c0001t0001g0204 others(3): Show |
6 | HG02109.hp2 HG02145.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.2722-2564_2722-256 others(6): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43156228 | ||||||
| chr6:43156228 | CA | C | 66 | a0001c0001t0001g0098 a0001c0001t0001g0160 a0001c0001t0001g0173 others(63): Show |
66 | HG00544.hp2 HG00597.hp1 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.2722-2563delA | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43156228 | ||||||
| chr6:43156228 | CAA | C | 32 | a0001c0001t0001g0167 a0001c0001t0002g0035 a0001c0001t0002g0043 others(29): Show |
32 | HG00323.hp1 HG00323.hp2 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.2722-2564_2722-256 others(6): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43156228 | ||||||
| chr6:43156228 | CAAA | C | 68 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(65): Show |
68 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.2722-2565_2722-256 others(7): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43156228 | ||||||
| chr6:43156228 | CAAAA | C | 6 | a0001c0001t0002g0021 a0001c0001t0002g0028 a0001c0001t0002g0179 others(3): Show |
6 | HG02615.hp1 HG02809.hp2 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.2722-2566_2722-256 others(8): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43156228 | ||||||
| chr6:43156258 | TTAAAA | T | 2 | a0001c0002t0004g0139 a0006c0020t0006g0226 |
2 | NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2722-2556_2722-255 others(9): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43156258 | ||||||
| chr6:43156556 | C | T | 1 | a0001c0002t0001g0191 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.2722-2261C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43156556 | |||||||
| chr6:43156691 | A | C | 1 | a0001c0001t0002g0057 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2722-2126A>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43156691 | |||||||
| chr6:43156726 | T | A | 8 | a0001c0001t0001g0166 a0001c0001t0001g0199 a0001c0001t0001g0200 others(5): Show |
8 | HG02109.hp2 HG02145.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.2722-2091T>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43156726 | |||||||
| chr6:43156851 | C | T | 1 | a0001c0001t0001g0237 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2722-1966C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43156851 | |||||||
| chr6:43156906 | C | T | 3 | a0002c0003t0002g0162 a0002c0003t0002g0163 a0002c0003t0002g0178 |
3 | HG02258.hp2 HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2722-1911C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43156906 | |||||||
| chr6:43156936 | GA | G | 81 | a0001c0001t0001g0076 a0001c0001t0001g0085 a0001c0001t0002g0001 others(78): Show |
81 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.2722-1867delA | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43156936 | ||||||
| chr6:43156936 | GAA | G | 8 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0230 others(5): Show |
8 | HG00741.hp2 HG01255.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.2722-1868_2722-186 others(6): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43156936 | ||||||
| chr6:43156966 | G | A | 3 | a0002c0003t0002g0162 a0002c0003t0002g0163 a0002c0003t0002g0178 |
3 | HG02258.hp2 HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2722-1851G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43156966 | |||||||
| chr6:43156982 | C | T | 79 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(76): Show |
79 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.2722-1835C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43156982 | |||||||
| chr6:43157166 | TG | T | 6 | a0001c0001t0002g0117 a0001c0001t0002g0263 a0001c0001t0002g0264 others(3): Show |
6 | HG00423.hp2 HG02056.hp1 NA18950.hp1 others(3): Show |
intron_variant | MODIFIER | c.2722-1649delG | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43157166 | ||||||
| chr6:43157167 | G | GT | 14 | a0001c0001t0001g0200 a0001c0001t0001g0202 a0001c0001t0002g0015 others(11): Show |
14 | HG01928.hp1 HG02109.hp2 HG02148.hp2 others(11): Show |
intron_variant | MODIFIER | c.2722-1650_2722-164 others(5): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43157167 | |||||||
| chr6:43157168 | G | GT | 8 | a0001c0001t0001g0119 a0001c0001t0001g0194 a0001c0001t0002g0175 others(5): Show |
8 | HG00597.hp1 HG00741.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.2722-1634dupT | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43157168 | ||||||
| chr6:43157168 | G | T | 108 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0166 others(105): Show |
108 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(105): Show |
intron_variant | MODIFIER | c.2722-1649G>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43157168 | |||||||
| chr6:43157169 | T | G | 5 | a0001c0001t0002g0234 a0001c0001t0002g0242 a0001c0002t0002g0103 others(2): Show |
5 | HG01258.hp1 HG01261.hp2 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.2722-1648T>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43157169 | |||||||
| chr6:43157172 | T | G | 1 | a0001c0002t0001g0145 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2722-1645T>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43157172 | |||||||
| chr6:43157183 | T | C | 2 | a0001c0001t0001g0186 a0001c0010t0002g0045 |
2 | HG02071.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.2722-1634T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43157183 | |||||||
| chr6:43157302 | C | T | 8 | a0001c0001t0002g0044 a0001c0001t0002g0222 a0001c0001t0002g0223 others(5): Show |
8 | HG02615.hp2 HG02922.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.2722-1515C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43157302 | |||||||
| chr6:43157326 | CTA | C | 6 | a0001c0002t0001g0143 a0001c0002t0001g0165 a0001c0002t0001g0191 others(3): Show |
6 | HG01255.hp1 HG01928.hp2 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.2722-1453_2722-145 others(6): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43157326 | ||||||
| chr6:43157326 | CTATATAT others(1): Show |
C | 6 | a0001c0001t0002g0028 a0001c0001t0002g0038 a0001c0001t0002g0082 others(3): Show |
6 | HG02027.hp2 NA18947.hp2 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.2722-1459_2722-145 others(12): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43157326 | ||||||
| chr6:43157326 | CTATATAT others(3): Show |
C | 27 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0008 others(24): Show |
27 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.2722-1461_2722-145 others(14): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43157326 | ||||||
| chr6:43157326 | CTATATAT others(5): Show |
C | 5 | a0001c0001t0001g0199 a0001c0001t0001g0227 a0001c0001t0002g0047 others(2): Show |
5 | HG01496.hp2 HG02622.hp1 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.2722-1463_2722-145 others(16): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43157326 | ||||||
| chr6:43157326 | CTATATAT others(7): Show |
C | 2 | a0001c0002t0001g0250 a0001c0002t0001g0251 |
2 | HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2722-1465_2722-145 others(18): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43157326 | ||||||
| chr6:43157326 | CTATATAT others(9): Show |
C | 8 | a0001c0001t0001g0167 a0001c0001t0001g0172 a0001c0001t0001g0174 others(5): Show |
8 | HG01074.hp2 HG01099.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.2722-1467_2722-145 others(20): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43157326 | ||||||
| chr6:43157326 | CTATATAT others(11): Show |
C | 15 | a0001c0001t0001g0098 a0001c0002t0001g0089 a0001c0002t0001g0102 others(12): Show |
15 | HG01169.hp1 HG01346.hp2 HG01433.hp1 others(12): Show |
intron_variant | MODIFIER | c.2722-1469_2722-145 others(22): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43157326 | ||||||
| chr6:43157341 | TATATATA others(10): Show |
T | 5 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0008g0176 others(2): Show |
5 | HG01074.hp1 HG01123.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.2722-1475_2722-145 others(21): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43157341 | |||||||
| chr6:43157341 | TATATATA others(12): Show |
T | 1 | a0001c0002t0001g0110 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2722-1475_2722-145 others(23): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43157341 | |||||||
| chr6:43157343 | TATATATA others(10): Show |
T | 23 | a0001c0001t0001g0066 a0001c0001t0001g0173 a0001c0002t0001g0074 others(20): Show |
23 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.2722-1473_2722-145 others(21): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43157343 | |||||||
| chr6:43157343 | TATATATA others(12): Show |
T | 3 | a0001c0002t0001g0096 a0001c0002t0001g0114 a0001c0002t0007g0115 |
3 | HG01167.hp1 HG04115.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.2722-1473_2722-145 others(23): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43157343 | |||||||
| chr6:43157343 | TATATATA others(26): Show |
T | 2 | a0002c0003t0002g0070 a0002c0003t0002g0121 |
2 | HG01261.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.2722-1473_2722-144 others(37): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43157343 | |||||||
| chr6:43157344 | ATATATAT others(26): Show |
A | 1 | a0001c0002t0002g0103 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.2722-1471_2722-143 others(37): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43157344 | ||||||
| chr6:43157345 | TATATATA others(4): Show |
T | 1 | a0001c0001t0001g0073 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2722-1471_2722-146 others(15): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43157345 | |||||||
| chr6:43157345 | TATATATA others(6): Show |
T | 1 | a0001c0002t0004g0228 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2722-1471_2722-145 others(17): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43157345 | |||||||
| chr6:43157345 | TATATATA others(10): Show |
T | 12 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0170 others(9): Show |
12 | HG01167.hp2 HG01169.hp2 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.2722-1471_2722-145 others(21): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43157345 | |||||||
| chr6:43157347 | TATATATA others(4): Show |
T | 1 | a0001c0001t0002g0272 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2722-1469_2722-145 others(15): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43157347 | |||||||
| chr6:43157347 | TATATATA others(6): Show |
T | 2 | a0001c0001t0004g0236 a0001c0001t0004g0269 |
2 | HG02809.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2722-1469_2722-145 others(17): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43157347 | |||||||
| chr6:43157349 | TATATATA others(4): Show |
T | 16 | a0001c0001t0001g0166 a0001c0001t0001g0202 a0001c0001t0001g0204 others(13): Show |
16 | HG00423.hp2 HG00642.hp1 HG01928.hp1 others(13): Show |
intron_variant | MODIFIER | c.2722-1467_2722-145 others(15): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43157349 | |||||||
| chr6:43157349 | TATATATA others(6): Show |
T | 2 | a0001c0001t0001g0200 a0001c0001t0001g0205 |
2 | HG03098.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2722-1467_2722-145 others(17): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43157349 | |||||||
| chr6:43157350 | A | T | 1 | a0002c0018t0001g0248 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2722-1467A>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43157350 | |||||||
| chr6:43157350 | ATATATAT others(22): Show |
A | 3 | a0002c0003t0002g0162 a0002c0003t0002g0163 a0002c0003t0002g0178 |
3 | HG02258.hp2 HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2722-1465_2722-143 others(33): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43157350 | ||||||
| chr6:43157351 | TATATATA others(2): Show |
T | 4 | a0001c0001t0002g0101 a0001c0001t0002g0175 a0001c0001t0002g0195 others(1): Show |
4 | HG03017.hp1 HG04115.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.2722-1465_2722-145 others(13): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43157351 | |||||||
| chr6:43157351 | TATATATA others(4): Show |
T | 10 | a0001c0001t0002g0005 a0001c0001t0002g0032 a0001c0001t0002g0033 others(7): Show |
10 | HG01943.hp1 HG01952.hp1 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.2722-1465_2722-145 others(15): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43157351 | |||||||
| chr6:43157352 | A | T | 1 | a0002c0018t0001g0248 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2722-1465A>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43157352 | |||||||
| chr6:43157352 | ATATATAT others(15): Show |
A | 1 | a0001c0001t0002g0242 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2722-1463_2722-144 others(26): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43157352 | ||||||
| chr6:43157354 | A | T | 1 | a0002c0018t0001g0248 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2722-1463A>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43157354 | |||||||
| chr6:43157354 | ATATATAT others(4): Show |
A | 1 | a0001c0001t0002g0214 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2722-1461_2722-145 others(15): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43157354 | ||||||
| chr6:43157354 | ATATATAT others(13): Show |
A | 1 | a0001c0002t0001g0136 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2722-1461_2722-144 others(24): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43157354 | ||||||
| chr6:43157354 | ATATATAT others(16): Show |
A | 1 | a0001c0001t0002g0234 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2722-1461_2722-143 others(27): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43157354 | ||||||
| chr6:43157355 | TATA | T | 3 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0006t0001g0081 |
3 | HG00544.hp1 NA18981.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.2722-1461_2722-145 others(7): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43157355 | |||||||
| chr6:43157355 | TATATATA | T | 4 | a0001c0001t0002g0012 a0001c0001t0002g0035 a0001c0001t0002g0057 others(1): Show |
4 | HG02965.hp2 HG03704.hp1 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.2722-1461_2722-145 others(11): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43157355 | |||||||
| chr6:43157356 | A | T | 1 | a0002c0018t0001g0248 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2722-1461A>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43157356 | |||||||
| chr6:43157356 | ATATATAT others(11): Show |
A | 1 | a0001c0001t0001g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2722-1459_2722-144 others(22): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43157356 | ||||||
| chr6:43157358 | A | T | 5 | a0001c0001t0001g0073 a0001c0001t0001g0079 a0001c0008t0001g0107 others(2): Show |
5 | HG02135.hp1 HG02145.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.2722-1459A>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43157358 | |||||||
| chr6:43157358 | ATATATAT others(11): Show |
A | 1 | a0001c0001t0001g0238 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2722-1457_2722-144 others(22): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43157358 | ||||||
| chr6:43157360 | A | T | 36 | a0001c0001t0001g0073 a0001c0001t0001g0079 a0001c0001t0001g0172 others(33): Show |
36 | HG00544.hp1 HG00733.hp1 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.2722-1457A>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43157360 | |||||||
| chr6:43157360 | ATATATTT others(9): Show |
A | 1 | a0001c0001t0001g0230 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2722-1455_2722-144 others(20): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43157360 | ||||||
| chr6:43157361 | T | A | 1 | a0001c0012t0002g0229 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2722-1456T>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43157361 | |||||||
| chr6:43157362 | A | T | 134 | a0001c0001t0001g0066 a0001c0001t0001g0073 a0001c0001t0001g0079 others(131): Show |
134 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.2722-1455A>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43157362 | |||||||
| chr6:43157362 | ATATTTTT others(3): Show |
A | 1 | a0001c0012t0002g0229 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2722-1453_2722-144 others(14): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43157362 | ||||||
| chr6:43157362 | ATATTTTT others(4): Show |
A | 1 | a0001c0017t0001g0232 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2722-1453_2722-144 others(15): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43157362 | ||||||
| chr6:43157364 | A | ATATATAT others(36): Show |
1 | a0001c0001t0001g0208 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.2722-1452_2722-145 others(47): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43157364 | ||||||
| chr6:43157364 | A | ATATATAT others(22): Show |
1 | a0001c0001t0001g0086 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2722-1452_2722-145 others(33): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43157364 | ||||||
| chr6:43157364 | A | ATATATAT others(25): Show |
1 | a0004c0007t0001g0131 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2722-1452_2722-145 others(36): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43157364 | ||||||
| chr6:43157364 | A | ATATATAT others(24): Show |
1 | a0001c0001t0001g0072 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.2722-1452_2722-145 others(35): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43157364 | ||||||
| chr6:43157364 | A | ATATATAT others(18): Show |
1 | a0004c0007t0001g0130 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.2722-1452_2722-145 others(29): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43157364 | ||||||
| chr6:43157364 | A | ATATATAT others(20): Show |
1 | a0001c0001t0001g0270 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2722-1452_2722-145 others(31): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43157364 | ||||||
| chr6:43157364 | A | ATATATAT others(24): Show |
1 | a0001c0001t0001g0128 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2722-1452_2722-145 others(35): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43157364 | ||||||
| chr6:43157364 | A | ATATATAT others(28): Show |
1 | a0001c0001t0001g0126 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.2722-1452_2722-145 others(39): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43157364 | ||||||
| chr6:43157364 | A | ATATATAT others(17): Show |
1 | a0001c0001t0001g0058 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2722-1452_2722-145 others(28): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43157364 | ||||||
| chr6:43157364 | A | ATATATAT others(21): Show |
1 | a0001c0001t0001g0119 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2722-1452_2722-145 others(32): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43157364 | ||||||
| chr6:43157364 | A | ATATATAT others(23): Show |
1 | a0001c0001t0001g0127 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.2722-1452_2722-145 others(34): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43157364 | ||||||
| chr6:43157364 | A | ATATATAT others(13): Show |
1 | a0001c0001t0001g0085 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.2722-1452_2722-145 others(24): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43157364 | ||||||
| chr6:43157364 | A | ATATATAT others(14): Show |
1 | a0001c0001t0001g0092 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2722-1452_2722-145 others(25): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43157364 | ||||||
| chr6:43157364 | A | ATATATAT others(16): Show |
1 | a0001c0001t0001g0132 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2722-1452_2722-145 others(27): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43157364 | ||||||
| chr6:43157364 | A | ATATATAT others(22): Show |
1 | a0001c0001t0001g0037 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2722-1452_2722-145 others(33): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43157364 | ||||||
| chr6:43157364 | A | ATATATAT others(11): Show |
3 | a0001c0001t0001g0003 a0001c0001t0001g0080 a0001c0001t0001g0244 |
3 | HG01081.hp2 HG03688.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.2722-1452_2722-145 others(22): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43157364 | ||||||
| chr6:43157364 | A | ATATATAT others(12): Show |
2 | a0001c0001t0001g0262 a0001c0002t0001g0261 |
2 | HG01099.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.2722-1452_2722-145 others(23): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43157364 | ||||||
| chr6:43157364 | A | ATATATAT others(15): Show |
2 | a0001c0001t0001g0068 a0001c0001t0001g0193 |
2 | NA19004.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.2722-1452_2722-145 others(26): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43157364 | ||||||
| chr6:43157364 | A | ATATATAT others(17): Show |
1 | a0001c0001t0001g0192 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2722-1452_2722-145 others(28): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43157364 | ||||||
| chr6:43157364 | A | ATATATAT others(8): Show |
1 | a0001c0002t0001g0196 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.2722-1452_2722-145 others(19): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43157364 | ||||||
| chr6:43157364 | A | ATATATAT others(9): Show |
1 | a0001c0001t0001g0002 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2722-1452_2722-145 others(20): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43157364 | ||||||
| chr6:43157364 | A | ATATATAT others(10): Show |
1 | a0001c0002t0001g0034 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2722-1452_2722-145 others(21): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43157364 | ||||||
| chr6:43157364 | A | ATATATAT others(12): Show |
2 | a0001c0001t0001g0220 a0001c0002t0001g0247 |
2 | HG02027.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2722-1452_2722-145 others(23): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43157364 | ||||||
| chr6:43157364 | A | ATATATAT others(13): Show |
2 | a0001c0001t0001g0011 a0001c0001t0001g0071 |
2 | HG01433.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.2722-1452_2722-145 others(24): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43157364 | ||||||
| chr6:43157364 | A | ATATATAT others(15): Show |
1 | a0001c0001t0001g0197 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2722-1452_2722-145 others(26): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43157364 | ||||||
| chr6:43157364 | A | ATATATAT others(17): Show |
1 | a0001c0001t0001g0094 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.2722-1452_2722-145 others(28): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43157364 | ||||||
| chr6:43157364 | A | ATATATAT others(6): Show |
1 | a0001c0001t0001g0111 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2722-1452_2722-145 others(17): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43157364 | ||||||
| chr6:43157364 | A | ATATATAT others(7): Show |
1 | a0001c0001t0001g0268 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2722-1452_2722-145 others(18): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43157364 | ||||||
| chr6:43157364 | A | ATATATAT others(8): Show |
1 | a0001c0001t0001g0069 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2722-1452_2722-145 others(19): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43157364 | ||||||
| chr6:43157364 | A | ATATATAT others(9): Show |
1 | a0001c0002t0001g0198 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2722-1452_2722-145 others(20): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43157364 | ||||||
| chr6:43157364 | A | ATATATAT others(12): Show |
1 | a0001c0001t0001g0133 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.2722-1452_2722-145 others(23): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43157364 | ||||||
| chr6:43157364 | A | ATATATAT others(13): Show |
1 | a0001c0001t0001g0051 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2722-1452_2722-145 others(24): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43157364 | ||||||
| chr6:43157364 | A | ATATATAT others(14): Show |
3 | a0001c0001t0001g0095 a0001c0001t0001g0100 a0007c0013t0001g0063 |
3 | HG02015.hp1 NA18975.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.2722-1452_2722-145 others(25): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43157364 | ||||||
| chr6:43157364 | A | ATATATAT others(5): Show |
1 | a0001c0002t0001g0142 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2722-1452_2722-145 others(16): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43157364 | ||||||
| chr6:43157364 | A | ATATATAT others(7): Show |
1 | a0001c0001t0001g0065 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2722-1452_2722-145 others(18): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43157364 | ||||||
| chr6:43157364 | A | ATATATAT others(10): Show |
1 | a0001c0002t0001g0140 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2722-1452_2722-145 others(21): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43157364 | ||||||
| chr6:43157364 | A | ATATATAT others(11): Show |
1 | a0001c0001t0001g0087 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2722-1452_2722-145 others(22): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43157364 | ||||||
| chr6:43157364 | A | ATATATAT others(13): Show |
1 | a0001c0001t0001g0171 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2722-1452_2722-145 others(24): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43157364 | ||||||
| chr6:43157364 | A | ATATATAT others(6): Show |
1 | a0005c0019t0001g0141 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2722-1452_2722-145 others(17): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43157364 | ||||||
| chr6:43157364 | A | ATATATAT others(7): Show |
1 | a0001c0001t0001g0246 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2722-1452_2722-145 others(18): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43157364 | ||||||
| chr6:43157364 | A | ATATATAT others(8): Show |
1 | a0001c0001t0001g0076 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2722-1452_2722-145 others(19): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43157364 | ||||||
| chr6:43157364 | A | ATATATAT others(10): Show |
2 | a0001c0001t0001g0077 a0001c0001t0001g0135 |
2 | NA18950.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.2722-1452_2722-145 others(21): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43157364 | ||||||
| chr6:43157364 | A | ATATATAT others(14): Show |
1 | a0001c0002t0001g0031 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2722-1452_2722-145 others(25): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43157364 | ||||||
| chr6:43157364 | A | ATATATTT others(6): Show |
1 | a0001c0001t0001g0022 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2722-1452_2722-145 others(17): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43157364 | ||||||
| chr6:43157364 | A | ATATATTT others(9): Show |
1 | a0001c0009t0001g0062 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2722-1452_2722-145 others(20): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43157364 | ||||||
| chr6:43157364 | A | ATATTTTT others(8): Show |
2 | a0001c0001t0001g0064 a0001c0001t0001g0211 |
2 | NA18951.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.2722-1452_2722-145 others(19): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43157364 | ||||||
| chr6:43157364 | A | T | 174 | a0001c0001t0001g0066 a0001c0001t0001g0073 a0001c0001t0001g0079 others(171): Show |
174 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(171): Show |
intron_variant | MODIFIER | c.2722-1453A>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43157364 | |||||||
| chr6:43157364 | ATTTTTTT others(3): Show |
A | 1 | a0001c0001t0001g0006 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2722-1451_2722-144 others(14): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr6 | 43157364 | ||||||
| chr6:43157366 | T | A | 11 | a0001c0001t0002g0224 a0001c0002t0001g0056 a0001c0002t0001g0203 others(8): Show |
11 | HG02615.hp1 HG02630.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.2722-1451T>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43157366 | |||||||
| chr6:43157368 | T | A | 11 | a0001c0001t0002g0224 a0001c0002t0001g0056 a0001c0002t0001g0203 others(8): Show |
11 | HG02615.hp1 HG02630.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.2722-1449T>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43157368 | |||||||
| chr6:43157370 | T | A | 10 | a0001c0002t0001g0056 a0001c0002t0001g0203 a0003c0004t0002g0007 others(7): Show |
10 | HG02615.hp1 HG02630.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.2722-1447T>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43157370 | |||||||
| chr6:43157371 | T | TATATATA others(7): Show |
1 | a0003c0004t0002g0046 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2722-1446_2722-144 others(18): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43157371 | |||||||
| chr6:43157372 | T | A | 10 | a0001c0002t0001g0056 a0001c0002t0001g0203 a0003c0004t0002g0007 others(7): Show |
10 | HG02615.hp1 HG02630.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.2722-1445T>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43157372 | |||||||
| chr6:43157373 | T | TATATATA others(4): Show |
1 | a0003c0004t0002g0235 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2722-1444_2722-144 others(15): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43157373 | |||||||
| chr6:43157374 | T | A | 3 | a0001c0002t0001g0056 a0001c0002t0001g0203 a0003c0004t0002g0239 |
3 | HG02976.hp2 HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2722-1443T>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43157374 | |||||||
| chr6:43157374 | T | C | 1 | a0001c0001t0002g0164 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2722-1443T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43157374 | |||||||
| chr6:43157375 | T | C | 5 | a0001c0001t0004g0236 a0001c0001t0004g0269 a0001c0002t0004g0228 others(2): Show |
5 | HG02809.hp1 HG03209.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.2722-1442T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43157375 | |||||||
| chr6:43157376 | C | A | 2 | a0001c0001t0001g0006 a0001c0002t0001g0056 |
2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2722-1441C>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43157376 | |||||||
| chr6:43157376 | C | T | 42 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0013 others(39): Show |
42 | HG00642.hp2 HG00741.hp2 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.2722-1441C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43157376 | |||||||
| chr6:43157377 | T | C | 10 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0068 others(7): Show |
10 | HG00642.hp2 HG01081.hp2 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.2722-1440T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43157377 | |||||||
| chr6:43157378 | T | A | 2 | a0001c0001t0001g0006 a0001c0002t0001g0056 |
2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2722-1439T>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43157378 | |||||||
| chr6:43157378 | T | C | 5 | a0001c0002t0001g0196 a0001c0002t0001g0198 a0001c0002t0001g0247 others(2): Show |
5 | HG02976.hp1 HG03139.hp1 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.2722-1439T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43157378 | |||||||
| chr6:43157384 | T | C | 1 | a0001c0001t0002g0214 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2722-1433T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43157384 | |||||||
| chr6:43157418 | C | T | 1 | a0002c0018t0001g0248 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2722-1399C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43157418 | |||||||
| chr6:43157709 | C | T | 8 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0230 others(5): Show |
8 | HG00741.hp2 HG01255.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.2722-1108C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43157709 | |||||||
| chr6:43158023 | G | A | 25 | a0001c0001t0002g0044 a0001c0001t0002g0222 a0001c0001t0002g0223 others(22): Show |
25 | HG01258.hp1 HG01261.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.2722-794G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43158023 | |||||||
| chr6:43158223 | C | T | 26 | a0001c0001t0002g0044 a0001c0001t0002g0222 a0001c0001t0002g0223 others(23): Show |
26 | HG01099.hp1 HG01258.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.2722-594C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43158223 | |||||||
| chr6:43158235 | C | G | 8 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0230 others(5): Show |
8 | HG00741.hp2 HG01255.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.2722-582C>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43158235 | |||||||
| chr6:43158251 | A | T | 1 | a0001c0001t0002g0272 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2722-566A>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43158251 | |||||||
| chr6:43158281 | A | G | 8 | a0001c0001t0001g0166 a0001c0001t0001g0199 a0001c0001t0001g0200 others(5): Show |
8 | HG02109.hp2 HG02145.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.2722-536A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43158281 | |||||||
| chr6:43158473 | A | G | 1 | a0002c0018t0001g0248 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2722-344A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43158473 | |||||||
| chr6:43158557 | C | T | 24 | a0001c0001t0002g0044 a0001c0001t0002g0222 a0001c0001t0002g0223 others(21): Show |
24 | HG01258.hp1 HG01261.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.2722-260C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43158557 | |||||||
| chr6:43159249 | C | G | 5 | a0001c0002t0001g0196 a0001c0002t0001g0198 a0001c0002t0001g0247 others(2): Show |
5 | HG04204.hp2 NA18947.hp1 NA18984.hp2 others(2): Show |
intron_variant | MODIFIER | c.2873+281C>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 18/19 | chr6 | 43159249 | |||||||
| chr6:43159550 | T | A | 2 | a0001c0001t0001g0100 a0001c0001t0001g0220 |
2 | HG02015.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.2874-238T>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 18/19 | chr6 | 43159550 | |||||||
| chr6:43159630 | A | C | 9 | a0001c0001t0001g0166 a0001c0001t0001g0199 a0001c0001t0001g0200 others(6): Show |
9 | HG02109.hp2 HG02145.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.2874-158A>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 18/19 | chr6 | 43159630 | |||||||
| chr6:43160073 | G | A | 1 | a0001c0001t0001g0237 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.3052+107G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 19/19 | chr6 | 43160073 | |||||||
| chr6:43160178 | C | T | 8 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0230 others(5): Show |
8 | HG00741.hp2 HG01255.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.3052+212C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 19/19 | chr6 | 43160178 | |||||||
| chr6:43160240 | C | G | 1 | a0001c0001t0002g0047 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3052+274C>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 19/19 | chr6 | 43160240 | |||||||
| chr6:43160364 | C | T | 2 | a0001c0002t0001g0151 a0001c0002t0001g0159 |
2 | HG00597.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.3053-357C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 19/19 | chr6 | 43160364 | |||||||
| chr6:43160430 | A | G | 3 | a0002c0003t0002g0162 a0002c0003t0002g0163 a0002c0003t0002g0178 |
3 | HG02258.hp2 HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3053-291A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 19/19 | chr6 | 43160430 | |||||||
| chr6:43160531 | C | T | 1 | a0001c0002t0004g0228 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3053-190C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 19/19 | chr6 | 43160531 | |||||||
| chr6:43160551 | G | A | 3 | a0002c0003t0002g0162 a0002c0003t0002g0163 a0002c0003t0002g0178 |
3 | HG02258.hp2 HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3053-170G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 19/19 | chr6 | 43160551 | |||||||
| chr6:43160696 | A | G | 94 | a0001c0001t0001g0167 a0001c0001t0002g0001 a0001c0001t0002g0004 others(91): Show |
94 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.3053-25A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 19/19 | chr6 | 43160696 |