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 | copy fasta | chr6 | 43071314 | 43166715 |
a0002 | 0/0 | 1070 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
a0003 | 0/1 | 1070 | 8 | 5 | 1 | 1 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
a0004 | 0/0 | 1070 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
a0005 | 0/0 | 1070 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
a0006 | 0/0 | 1070 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
a0007 | 0/0 | 1070 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
a0008 | 0/0 | 1070 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 3213 | 155 | 30 | 29 | 76 | 2 | 17 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
c0002 | 0/0 | 3213 | 78 | 33 | 22 | 12 | 2 | 9 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
c0003 | 0/1 | 3213 | 7 | 4 | 1 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
c0004 | 0/0 | 3213 | 6 | 6 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
c0005 | 0/0 | 3213 | 3 | 0 | 0 | 0 | 0 | 3 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
c0006 | 0/0 | 3213 | 3 | 0 | 0 | 3 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
c0007 | 0/0 | 3213 | 2 | 0 | 0 | 2 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
c0008 | 0/0 | 3213 | 2 | 0 | 0 | 2 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
c0009 | 0/0 | 3213 | 2 | 0 | 2 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
c0010 | 0/0 | 3213 | 2 | 0 | 0 | 2 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
c0011 | 0/0 | 3213 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
c0012 | 0/0 | 3213 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
c0013 | 0/0 | 3213 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
c0014 | 0/0 | 3213 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
c0015 | 0/0 | 3213 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
c0016 | 0/0 | 3213 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
c0017 | 0/0 | 3213 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
c0018 | 0/0 | 3213 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
c0019 | 0/0 | 3213 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
c0020 | 0/0 | 3213 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
c0021 | 0/0 | 3213 | 1 | 0 | 0 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
c0022 | 0/0 | 3213 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 1010 | 162 | 38 | 40 | 59 | 2 | 22 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
t0002 | 0/1 | 1010 | 94 | 29 | 15 | 41 | 2 | 6 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
t0003 | 0/0 | 1010 | 6 | 5 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
t0004 | 0/0 | 1010 | 4 | 4 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
t0005 | 0/0 | 1010 | 2 | 2 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
t0006 | 0/0 | 1010 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
t0007 | 0/0 | 1010 | 1 | 0 | 0 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
t0008 | 0/0 | 1010 | 1 | 0 | 0 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
t0009 | 0/0 | 1010 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0099 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0219 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 3213 | 155 | 30 | 29 | 76 | 2 | 17 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
a0001c0002 | 0/0 | 3213 | 78 | 33 | 22 | 12 | 2 | 9 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
a0001c0005 | 0/0 | 3213 | 3 | 0 | 0 | 0 | 0 | 3 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
a0001c0006 | 0/0 | 3213 | 3 | 0 | 0 | 3 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
a0001c0008 | 0/0 | 3213 | 2 | 0 | 0 | 2 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
a0001c0009 | 0/0 | 3213 | 2 | 0 | 2 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
a0001c0010 | 0/0 | 3213 | 2 | 0 | 0 | 2 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
a0001c0012 | 0/0 | 3213 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
a0001c0015 | 0/0 | 3213 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
a0001c0017 | 0/0 | 3213 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
a0001c0021 | 0/0 | 3213 | 1 | 0 | 0 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
a0001c0022 | 0/0 | 3213 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
a0002c0004 | 0/0 | 3213 | 6 | 6 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
a0002c0014 | 0/0 | 3213 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
a0002c0016 | 0/0 | 3213 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
a0003c0003 | 0/1 | 3213 | 7 | 4 | 1 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
a0003c0018 | 0/0 | 3213 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
a0004c0007 | 0/0 | 3213 | 2 | 0 | 0 | 2 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
a0005c0011 | 0/0 | 3213 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
a0006c0013 | 0/0 | 3213 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
a0007c0020 | 0/0 | 3213 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
a0008c0019 | 0/0 | 3213 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | 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 | copy fasta | chr6 | 43071314 | 43166715 |
a0001c0001t0002 | 0/0 | 4222 | 69 | 13 | 12 | 37 | 2 | 5 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
a0001c0001t0003 | 0/0 | 4222 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
a0001c0001t0004 | 0/0 | 4222 | 2 | 2 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
a0001c0001t0008 | 0/0 | 4222 | 1 | 0 | 0 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
a0001c0002t0001 | 0/0 | 4222 | 62 | 20 | 20 | 12 | 2 | 8 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
a0001c0002t0002 | 0/0 | 4222 | 5 | 4 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
a0001c0002t0003 | 0/0 | 4222 | 5 | 4 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
a0001c0002t0004 | 0/0 | 4222 | 2 | 2 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
a0001c0002t0005 | 0/0 | 4222 | 2 | 2 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
a0001c0002t0007 | 0/0 | 4222 | 1 | 0 | 0 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
a0001c0002t0009 | 0/0 | 4222 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
a0001c0005t0001 | 0/0 | 4222 | 3 | 0 | 0 | 0 | 0 | 3 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
a0001c0006t0001 | 0/0 | 4222 | 3 | 0 | 0 | 3 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
a0001c0008t0001 | 0/0 | 4222 | 2 | 0 | 0 | 2 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
a0001c0009t0001 | 0/0 | 4222 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
a0001c0009t0002 | 0/0 | 4222 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
a0001c0010t0002 | 0/0 | 4222 | 2 | 0 | 0 | 2 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
a0001c0012t0002 | 0/0 | 4222 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
a0001c0015t0001 | 0/0 | 4222 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
a0001c0017t0001 | 0/0 | 4222 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
a0001c0021t0002 | 0/0 | 4222 | 1 | 0 | 0 | 0 | 0 | 1 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
a0001c0022t0001 | 0/0 | 4222 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
a0002c0004t0002 | 0/0 | 4222 | 6 | 6 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
a0002c0014t0002 | 0/0 | 4222 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
a0002c0016t0002 | 0/0 | 4222 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
a0003c0003t0001 | 0/0 | 4222 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
a0003c0003t0002 | 0/1 | 4222 | 6 | 3 | 1 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
a0003c0018t0001 | 0/0 | 4222 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
a0004c0007t0001 | 0/0 | 4222 | 2 | 0 | 0 | 2 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
a0005c0011t0002 | 0/0 | 4222 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
a0006c0013t0001 | 0/0 | 4222 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
a0007c0020t0006 | 0/0 | 4222 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | chr6 | 43071314 | 43166715 |
a0008c0019t0001 | 0/0 | 4222 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | copy fasta | 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 |
a0001c0001t0001g0050 | 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 |
a0001c0001t0001g0096 | 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 |
a0001c0001t0001g0176 | 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 |
a0001c0001t0001g0263 | 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 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 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 |
a0001c0001t0002g0261 | 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 |
a0001c0001t0008g0177 | 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 |
a0001c0002t0001g0095 | 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 |
a0001c0002t0001g0103 | 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 |
a0001c0002t0001g0262 | 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 |
a0001c0002t0002g0104 | 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 |
a0001c0005t0001g0174 | 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 |
a0002c0004t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
a0002c0004t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
a0002c0004t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
a0002c0004t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
a0002c0004t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
a0002c0004t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
a0002c0014t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
a0002c0016t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
a0003c0003t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
a0003c0003t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
a0003c0003t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
a0003c0003t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
a0003c0003t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
a0003c0003t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
a0003c0003t0002g0219 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
a0003c0018t0001g0248 | 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 |
a0005c0011t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
a0006c0013t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
a0007c0020t0006g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
a0008c0019t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 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 | g0261 | 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 | g0262 | 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 | g0050 | 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 | g0104 | 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 | a0003 | 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 | g0053 | 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 | g0103 | AMR | PEL | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0054 | 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 | g0051 | 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 | a0003 | 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 | a0003 | 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 | a0002 | 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 | a0008 | 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 | a0002 | 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 | a0002 | 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 | a0003 | 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 | a0002 | 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 | a0003 | 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 | a0002 | 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 | a0002 | c0014 | t0002 | g0241 | AFR | MSL | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
HG03225 | hp2 | a0002 | 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 | g0174 | 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 | g0177 | 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 | a0007 | 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 | a0003 | 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 | g0095 | 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 | a0006 | c0013 | t0001 | g0063 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0264 | 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 | g0052 | 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 | g0263 | 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 | a0003 | 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 | a0005 | 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 | g0096 | EAS | JPT | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0017 | 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 | g0016 | 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 | g0176 | 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 | a0002 | 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 | hp1 | a0003 | c0003 | t0002 | g0219 | REF | REF | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0099 | REF | REF | PTK7_chr6_43071314_43166715 | PTK7 | chr6 | 43071314 | 43166715 |
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 | a0005 | 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 | a0006 | 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 | a0007 | 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 | a0008 | 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 | a0003 | 8 | HG01261.hp2 HG02145.hp2 HG02258.hp2 others(5): 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 | a0002 | 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 |
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 | a0001c0015a0002c0014 | 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 | a0001c0002a0001c0005a0001c0006others(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 | a0003c0018 | 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 |
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 | a0001c0001t0002a0001c0002t0002a0001c0009t0002others(8): Show | 94 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(91): 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 | a0007c0020t0006 | 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 | a0001c0001t0004a0001c0002t0004a0007c0020t0006 | 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 | a0001c0001t0003a0001c0002t0003 | 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 |
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 | a0001c0001t0001g0246a0001c0001t0001g0263a0001c0001t0001g0268others(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 | a0001c0001t0001g0002a0001c0001t0001g0003 | 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 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(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 | a0003c0003t0001g0243 | 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 | a0001c0001t0001g0230a0001c0001t0001g0237a0001c0001t0001g0238others(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 | a0001c0001t0001g0227a0001c0001t0001g0246a0001c0001t0001g0263others(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 | a0001c0009t0001g0062a0001c0009t0002g0061 | 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 | a0001c0001t0001g0064a0001c0001t0001g0065a0006c0013t0001g0063 | 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 | 108 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(105): Show | 108 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(105): 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 | a0001c0001t0001g0246a0001c0001t0001g0263a0001c0001t0001g0268others(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 | a0001c0002t0001g0216a0001c0002t0001g0217a0001c0002t0001g0218 | 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 | 3 | a0001c0001t0001g0220a0001c0001t0002g0221a0003c0003t0002g0219 | 3 | HG02027.hp1 NA18995.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.79+2284G>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43078851 | ||||||
chr6:43079185
|
C | T | 2 | a0001c0001t0002g0059a0001c0001t0002g0060 | 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 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(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 | 7 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0002g0067others(4): Show | 7 | HG01261.hp2 HG03130.hp1 HG03209.hp1 others(4): 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 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0002g0004others(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 | a0003c0003t0001g0243 | 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 | a0001c0001t0001g0006a0002c0004t0002g0007 | 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 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0073others(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 | a0001c0001t0001g0208a0001c0001t0001g0210a0001c0001t0001g0211others(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 | 116 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(113): Show | 116 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(113): 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 | a0001c0001t0001g0220a0001c0001t0002g0221 | 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 | a0001c0001t0001g0230a0001c0001t0001g0237a0001c0001t0001g0238others(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 | a0001c0001t0002g0254a0001c0001t0002g0255a0001c0001t0002g0256 | 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 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0002t0001g0075 | 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 | 67 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(64): Show | 67 | HG00323.hp1 HG00639.hp2 HG00642.hp1 others(64): 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 | a0001c0001t0002g0009a0001c0001t0002g0222a0001c0001t0002g0223others(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 | a0001c0001t0001g0073a0001c0001t0001g0186a0001c0001t0001g0187others(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 | a0001c0001t0002g0179a0001c0002t0001g0180a0001c0002t0001g0181others(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 | 3 | a0001c0001t0001g0220a0001c0001t0002g0221a0003c0003t0002g0219 | 3 | HG02027.hp1 NA18995.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.79+5136C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43081703 | ||||||
chr6:43081723
|
A | G | 195 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(192): Show | 195 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(192): Show |
intron_variant | MODIFIER | c.79+5156A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43081723 | ||||||
chr6:43082066
|
G | T | 3 | a0001c0001t0001g0220a0001c0001t0002g0221a0003c0003t0002g0219 | 3 | HG02027.hp1 NA18995.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.79+5499G>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43082066 | ||||||
chr6:43082751
|
G | A | 3 | a0001c0001t0001g0220a0001c0001t0002g0221a0003c0003t0002g0219 | 3 | HG02027.hp1 NA18995.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.79+6184G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43082751 | ||||||
chr6:43082876
|
G | A | 4 | a0001c0001t0002g0222a0001c0001t0002g0223a0001c0001t0002g0224others(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 | 3 | a0001c0001t0001g0220a0001c0001t0002g0221a0003c0003t0002g0219 | 3 | HG02027.hp1 NA18995.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.79+6446G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43083013 | ||||||
chr6:43083084
|
G | A | 3 | a0001c0001t0001g0220a0001c0001t0002g0221a0003c0003t0002g0219 | 3 | HG02027.hp1 NA18995.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.79+6517G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43083084 | ||||||
chr6:43083086
|
G | A | 141 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(138): Show | 141 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(138): 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 | 3 | a0001c0001t0001g0220a0001c0001t0002g0221a0003c0003t0002g0219 | 3 | HG02027.hp1 NA18995.hp2 homoSapiens_chm13v2.hp1 |
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 | a0001c0002t0005g0137a0001c0002t0005g0138 | 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 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0135others(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 | a0001c0001t0001g0050a0001c0001t0002g0048a0001c0001t0002g0049others(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 | a0003c0003t0002g0178 | 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 | 141 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(138): Show | 141 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(138): 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 | a0002c0004t0002g0007 | 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 | a0001c0001t0001g0073a0001c0001t0001g0186a0001c0001t0001g0187others(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 | a0001c0001t0002g0242a0001c0002t0009g0233 | 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 | 3 | a0001c0001t0001g0220a0001c0001t0002g0221a0003c0003t0002g0219 | 3 | HG02027.hp1 NA18995.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.79+9056A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43085623 | ||||||
chr6:43085664
|
T | C | 1 | a0003c0003t0001g0243 | 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 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(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 | 3 | a0001c0001t0001g0220a0001c0001t0002g0221a0003c0003t0002g0219 | 3 | HG02027.hp1 NA18995.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.79+9320T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43085887 | ||||||
chr6:43085933
|
C | CA | 19 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0085others(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 | a0001c0001t0001g0246a0001c0001t0001g0263a0001c0001t0001g0268others(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 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(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 | 79 | a0001c0001t0001g0066a0001c0001t0001g0073a0001c0001t0001g0132others(76): Show | 79 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(76): 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 | a0001c0001t0002g0234a0001c0001t0002g0242a0001c0002t0009g0233 | 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 | 7 | a0001c0001t0001g0135a0001c0001t0001g0220a0001c0001t0002g0221others(4): Show | 7 | HG02027.hp1 HG02818.hp1 NA18995.hp2 others(4): 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 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0086others(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 | a0001c0002t0001g0168a0001c0002t0001g0169 | 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 | a0001c0001t0002g0222a0001c0001t0002g0223a0001c0001t0002g0224others(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 | ||||||
chr6:43087119
|
G | A | 1 | a0003c0003t0002g0219 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.79+10552G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43087119 | ||||||
chr6:43087746
|
C | T | 5 | a0001c0001t0001g0085a0001c0001t0001g0126a0001c0001t0001g0127others(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 | a0001c0001t0001g0011a0001c0001t0001g0058 | 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 | a0001c0002t0001g0183a0001c0002t0001g0184 | 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 | a0001c0001t0002g0222a0001c0001t0002g0223a0001c0001t0002g0224others(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 | 3 | a0001c0001t0001g0220a0001c0001t0002g0221a0003c0003t0002g0219 | 3 | HG02027.hp1 NA18995.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.79+12080A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43088647 | ||||||
chr6:43088690
|
A | AAAAT | 36 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0071others(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 | a0001c0001t0001g0085a0001c0001t0001g0202a0001c0001t0002g0222others(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 | 4 | a0001c0001t0001g0087a0001c0001t0001g0220a0001c0001t0002g0221others(1): Show | 4 | HG02027.hp1 NA18612.hp2 NA18995.hp2 others(1): Show |
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 | 143 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(140): Show | 143 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(140): 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 | a0001c0001t0001g0011a0001c0001t0001g0058 | 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 | 3 | a0001c0001t0001g0220a0001c0001t0002g0221a0003c0003t0002g0219 | 3 | HG02027.hp1 NA18995.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.79+12887C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43089454 | ||||||
chr6:43089527
|
A | T | 3 | a0001c0001t0001g0220a0001c0001t0002g0221a0003c0003t0002g0219 | 3 | HG02027.hp1 NA18995.hp2 homoSapiens_chm13v2.hp1 |
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 | 143 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(140): Show | 143 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(140): 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 | a0001c0001t0002g0222a0001c0001t0002g0223a0001c0001t0002g0224others(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 | a0001c0001t0002g0222a0001c0001t0002g0223a0001c0001t0002g0224others(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 | a0001c0001t0002g0222a0001c0001t0002g0223a0001c0001t0002g0224others(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 | a0001c0001t0002g0012a0001c0001t0002g0222a0001c0001t0002g0223others(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 | 158 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(155): Show | 158 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(155): 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 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(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 | |||||
chr6:43091154
|
C | CTT | 5 | a0001c0001t0001g0220a0001c0001t0002g0010a0001c0001t0002g0054others(2): Show | 5 | HG01952.hp1 HG02027.hp1 NA18995.hp2 others(2): Show |
intron_variant | MODIFIER | c.79+14604_79+14605d others(4): Show |
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 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0132others(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 | a0001c0001t0001g0013a0001c0001t0002g0044a0001c0001t0002g0047others(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 | a0002c0016t0002g0225 | 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 | a0001c0001t0002g0008a0001c0001t0002g0010a0001c0001t0002g0015others(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 | a0007c0020t0006g0226 | 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 | a0001c0001t0002g0222a0001c0001t0002g0223a0001c0001t0002g0224others(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 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0022others(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 | a0001c0001t0001g0006a0001c0001t0001g0124a0001c0001t0001g0230others(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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0080others(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 | a0001c0001t0002g0222a0001c0001t0002g0223a0001c0001t0002g0224others(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 | a0001c0001t0001g0170a0001c0001t0001g0172a0001c0001t0001g0173 | 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 | a0001c0001t0001g0037a0001c0001t0002g0036 | 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 | a0003c0003t0002g0162a0003c0003t0002g0163a0003c0003t0002g0178 | 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 | a0001c0001t0001g0119a0001c0001t0002g0009a0001c0001t0002g0222others(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 | a0001c0001t0002g0234a0001c0001t0002g0242a0001c0002t0009g0233 | 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 | a0001c0001t0001g0011a0001c0001t0001g0058 | 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 | a0001c0001t0002g0222a0001c0001t0002g0223a0001c0001t0002g0224others(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 | a0001c0001t0002g0214a0001c0002t0003g0148a0001c0002t0003g0149others(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 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(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 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0072others(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 | a0001c0002t0001g0250a0001c0002t0001g0251 | 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 | a0001c0001t0001g0186a0001c0002t0001g0198 | 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 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(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 | a0001c0001t0001g0230a0001c0002t0002g0231a0001c0017t0001g0232 | 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 | a0001c0001t0001g0066a0001c0001t0001g0072a0001c0001t0001g0073others(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 | a0001c0001t0001g0022a0001c0001t0001g0037a0001c0001t0001g0050others(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 | a0001c0001t0001g0230a0001c0001t0002g0234a0001c0001t0002g0242others(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 |
151 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(148): Show | 151 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(148): 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 | a0003c0003t0002g0121 | 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 | a0001c0001t0001g0230a0001c0002t0002g0231a0001c0012t0002g0229others(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 | a0001c0001t0002g0059a0001c0001t0002g0060 | 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 | 151 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(148): Show | 151 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(148): 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 | a0003c0003t0002g0121 | 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 | a0001c0001t0002g0222a0001c0001t0002g0223a0001c0001t0002g0224others(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 | ||||||
chr6:43098100
|
G | T | 1 | a0003c0003t0002g0219 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.79+21533G>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43098100 | ||||||
chr6:43098175
|
A | G | 75 | a0001c0001t0001g0066a0001c0001t0001g0072a0001c0001t0001g0073others(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 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(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 | a0001c0001t0002g0012a0001c0001t0002g0020a0001c0021t0002g0019 | 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 | 151 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(148): Show | 151 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(148): 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 | a0007c0020t0006g0226 | 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 | a0001c0001t0002g0179a0001c0002t0001g0180a0001c0002t0001g0181 | 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 | a0002c0016t0002g0225 | 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 | 66 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0022others(63): Show | 66 | HG00323.hp1 HG00597.hp2 HG00642.hp1 others(63): 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 | a0001c0001t0001g0013a0001c0001t0002g0005a0001c0001t0002g0033others(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 | a0001c0001t0001g0187a0001c0001t0001g0199a0001c0001t0001g0200others(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 | |||||
chr6:43099306
|
C | T | 1 | a0003c0003t0002g0219 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.79+22739C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43099306 | ||||||
chr6:43099409
|
T | A | 5 | a0001c0001t0001g0230a0001c0002t0002g0231a0001c0012t0002g0229others(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 | a0001c0002t0002g0249a0001c0002t0004g0228a0002c0004t0002g0239others(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 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(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 | a0001c0001t0002g0012a0001c0001t0002g0020a0001c0021t0002g0019 | 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 | a0003c0018t0001g0248 | 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 | a0001c0001t0001g0066a0001c0001t0001g0072a0001c0001t0001g0073others(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 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(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 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(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 | 159 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(156): Show | 159 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(156): 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 | 159 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(156): Show | 159 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(156): 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 | a0001c0001t0001g0066a0001c0001t0001g0072a0001c0001t0001g0073others(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 | a0001c0001t0001g0238a0002c0004t0002g0235 | 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 | a0001c0001t0002g0222a0001c0001t0002g0223a0001c0001t0002g0224others(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 | a0002c0004t0002g0024a0002c0004t0002g0025 | 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 | a0001c0001t0001g0119a0001c0001t0002g0067a0001c0001t0002g0082others(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 |
3 | a0001c0001t0001g0220a0001c0001t0002g0221a0003c0003t0002g0219 | 3 | HG02027.hp1 NA18995.hp2 homoSapiens_chm13v2.hp1 |
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 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(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 | a0003c0003t0001g0243 | 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 | 151 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(148): Show | 151 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(148): 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 | 76 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(73): Show | 76 | HG00323.hp1 HG00597.hp2 HG00639.hp2 others(73): 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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0086 | 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 | a0001c0001t0002g0222a0001c0001t0002g0223a0001c0001t0002g0224others(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 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0037others(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 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(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 | a0001c0001t0002g0234a0001c0001t0002g0242a0001c0002t0009g0233 | 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 | a0001c0008t0001g0107a0001c0008t0001g0108 | 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 | 3 | a0001c0001t0001g0220a0001c0001t0002g0221a0003c0003t0002g0219 | 3 | HG02027.hp1 NA18995.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.79+26031A>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43102598 | ||||||
chr6:43102600
|
C | CA | 9 | a0001c0001t0001g0069a0001c0001t0001g0073a0001c0001t0001g0220others(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 | a0001c0001t0002g0222a0001c0001t0002g0223a0001c0001t0002g0224 | 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 | a0001c0001t0001g0011a0001c0001t0001g0058 | 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 | a0001c0001t0001g0230a0001c0001t0001g0246a0001c0001t0001g0263others(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 | a0001c0001t0001g0066a0001c0001t0001g0072a0001c0001t0001g0073others(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 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(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 | a0001c0001t0002g0082a0001c0001t0002g0083a0001c0001t0002g0116others(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 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(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 | a0003c0003t0001g0243 | 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 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(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 | a0003c0018t0001g0248 | 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 | a0007c0020t0006g0226 | 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 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(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 | a0001c0001t0001g0066a0001c0001t0001g0072a0001c0001t0001g0073others(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 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0194others(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 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(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 | a0001c0001t0001g0072a0001c0001t0001g0132 | 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 | a0002c0004t0002g0046 | 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 | a0001c0015t0001g0240a0002c0014t0002g0241 | 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 | a0001c0001t0001g0238a0001c0001t0004g0269a0002c0004t0002g0235others(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 | a0003c0003t0001g0243 | 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 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0135others(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 | 118 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(115): Show | 118 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(115): 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 | a0001c0001t0001g0119a0001c0001t0001g0192a0001c0001t0001g0220others(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 | a0001c0001t0001g0092a0001c0001t0001g0153a0001c0001t0001g0154others(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 | 3 | a0001c0001t0001g0220a0001c0001t0002g0221a0003c0003t0002g0219 | 3 | HG02027.hp1 NA18995.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.80-23111C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43105866 | ||||||
chr6:43105913
|
T | C | 3 | a0001c0001t0001g0220a0001c0001t0002g0221a0003c0003t0002g0219 | 3 | HG02027.hp1 NA18995.hp2 homoSapiens_chm13v2.hp1 |
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 | a0001c0001t0002g0101a0001c0002t0001g0089a0001c0002t0001g0091others(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 | a0001c0001t0001g0085a0001c0001t0002g0272 | 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 | a0007c0020t0006g0226 | 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 | a0001c0001t0001g0069a0001c0001t0001g0071a0001c0001t0001g0199others(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 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(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 | a0001c0001t0001g0187a0001c0001t0001g0190a0001c0001t0001g0194 | 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 | a0001c0001t0001g0230a0001c0001t0001g0246a0001c0001t0001g0263others(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 | a0007c0020t0006g0226 | 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 | a0001c0001t0002g0222a0001c0001t0002g0223a0001c0001t0002g0224others(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 | 117 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(114): Show | 117 | HG00323.hp1 HG00544.hp1 HG00597.hp2 others(114): 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 | a0001c0001t0001g0230a0001c0001t0001g0246a0001c0001t0001g0263others(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 | a0003c0003t0002g0121 | 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 | a0007c0020t0006g0226 | 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 | a0001c0001t0001g0200a0001c0001t0001g0202a0001c0001t0001g0204others(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 | a0001c0001t0002g0027a0001c0001t0002g0028a0001c0001t0002g0059others(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 | a0001c0001t0001g0066a0001c0001t0001g0072a0001c0001t0001g0100others(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 | 25 | a0001c0001t0001g0013a0001c0001t0001g0064a0001c0001t0001g0065others(22): Show | 25 | HG00609.hp2 HG00741.hp2 HG01928.hp1 others(22): 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 | a0001c0001t0002g0222a0001c0001t0002g0223a0001c0001t0002g0224others(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 | a0001c0001t0001g0077a0001c0001t0001g0200a0001c0001t0001g0204others(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 | a0001c0001t0001g0069a0001c0001t0001g0124a0001c0001t0001g0133others(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 | a0001c0001t0001g0013a0001c0001t0002g0005a0001c0001t0002g0033others(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 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(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 | 97 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(94): Show | 97 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(94): 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 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0002t0001g0145others(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 | a0001c0001t0002g0041a0001c0001t0002g0057a0001c0001t0002g0082others(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 | a0001c0008t0001g0107a0001c0008t0001g0108 | 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 | 92 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(89): Show | 92 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(89): 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 | a0001c0001t0002g0010a0001c0001t0002g0030a0001c0001t0002g0036others(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 | 270 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(267): Show | 270 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(267): Show |
intron_variant | MODIFIER | c.80-18741T>C | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43110236 | ||||||
chr6:43110328
|
T | C | 96 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(93): Show | 96 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(93): 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 | a0001c0001t0001g0058a0001c0001t0001g0119a0001c0001t0002g0234others(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 | a0001c0001t0004g0269a0008c0019t0001g0141 | 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 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(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 | a0007c0020t0006g0226 | 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 | 153 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(150): Show | 153 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(150): 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 | a0001c0001t0001g0212a0001c0001t0001g0213 | 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 | a0007c0020t0006g0226 | 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 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(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 | a0001c0001t0001g0268a0001c0002t0001g0031 | 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 | a0001c0001t0001g0246a0001c0001t0001g0263a0001c0001t0001g0268others(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 | a0001c0001t0002g0234a0001c0001t0002g0242a0001c0002t0009g0233 | 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 | a0007c0020t0006g0226 | 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 | 108 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(105): Show | 108 | HG00323.hp1 HG00544.hp1 HG00597.hp2 others(105): 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 | a0001c0001t0002g0048a0001c0001t0002g0057a0001c0001t0002g0256others(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 | a0001c0001t0001g0246a0001c0001t0001g0263a0001c0001t0001g0268others(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 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0066others(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 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(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 | a0001c0001t0002g0222a0001c0001t0002g0223a0001c0001t0002g0224others(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 | 28 | a0001c0001t0001g0194a0001c0001t0001g0246a0001c0001t0001g0263others(25): Show | 28 | HG00423.hp2 HG01099.hp1 HG01891.hp1 others(25): 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 | a0007c0020t0006g0226 | 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 | a0001c0001t0001g0202a0001c0001t0001g0204a0001c0001t0001g0206others(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 | a0001c0001t0002g0234a0001c0001t0002g0242a0001c0002t0009g0233 | 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 | a0001c0001t0002g0059a0001c0001t0002g0060 | 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 | a0001c0001t0002g0021a0001c0001t0002g0265 | 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 | a0001c0001t0001g0200a0001c0001t0001g0202a0001c0001t0001g0204others(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 | 153 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(150): Show | 153 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(150): 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 | a0007c0020t0006g0226 | 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 | a0007c0020t0006g0226 | 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 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(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 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(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 | a0001c0001t0001g0230a0001c0002t0002g0231a0001c0012t0002g0229others(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 | a0001c0001t0002g0234a0001c0001t0002g0242a0001c0002t0009g0233 | 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 | a0001c0001t0001g0119a0001c0001t0002g0010a0001c0001t0002g0067others(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 | a0007c0020t0006g0226 | 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 | a0001c0001t0002g0222a0001c0001t0002g0223a0001c0001t0002g0224 | 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 | a0001c0001t0002g0234a0001c0001t0002g0242a0001c0002t0009g0233 | 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 | a0001c0001t0002g0222a0001c0001t0002g0223a0001c0001t0002g0224 | 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 | ||||||
chr6:43114913
|
G | A | 1 | a0003c0003t0002g0219 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.80-14064G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43114913 | ||||||
chr6:43114915
|
G | A | 1 | a0007c0020t0006g0226 | 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 | 133 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(130): Show | 133 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(130): 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 | a0001c0001t0001g0160a0001c0002t0001g0152a0001c0002t0001g0161others(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 | a0007c0020t0006g0226 | 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 | a0007c0020t0006g0226 | 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 | a0002c0004t0002g0235 | 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 | a0001c0001t0002g0234a0001c0001t0002g0242a0001c0002t0009g0233others(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 | a0001c0001t0001g0200a0001c0001t0001g0202a0001c0001t0001g0204others(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 | a0007c0020t0006g0226 | 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 | a0007c0020t0006g0226 | 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 | a0001c0001t0001g0069a0001c0001t0001g0077a0001c0001t0001g0127others(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 | 15 | a0001c0001t0001g0194a0001c0001t0001g0199a0001c0001t0001g0200others(12): Show | 15 | HG02027.hp1 HG02055.hp1 HG02055.hp2 others(12): 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 | a0001c0001t0001g0064a0001c0001t0001g0066a0001c0001t0001g0072others(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 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(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 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(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 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(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 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0202others(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 | a0001c0002t0001g0090a0001c0002t0001g0106 | 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 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0037others(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 | a0008c0019t0001g0141 | 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 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0202others(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 | a0001c0001t0001g0100a0001c0001t0001g0220 | 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 | a0001c0001t0001g0050a0001c0001t0001g0079a0001c0001t0001g0080others(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 | a0001c0001t0001g0204a0001c0006t0001g0084a0003c0003t0001g0243 | 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 | a0001c0001t0001g0200a0001c0001t0001g0202a0001c0001t0001g0205others(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 | a0001c0001t0001g0199a0001c0002t0001g0203a0003c0018t0001g0248 | 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 | a0007c0020t0006g0226 | 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 | a0001c0001t0001g0197a0001c0001t0002g0042a0001c0002t0001g0031 | 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 | a0001c0001t0001g0013a0001c0001t0001g0037a0001c0001t0001g0066others(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 | a0001c0001t0001g0097a0001c0001t0001g0100a0001c0001t0001g0187others(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 | a0001c0001t0001g0073a0001c0001t0001g0220a0001c0001t0002g0016others(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 | a0001c0001t0001g0098a0001c0002t0001g0114a0005c0011t0002g0040 | 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 | a0001c0002t0001g0056a0001c0015t0001g0240a0002c0014t0002g0241 | 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 | a0001c0001t0001g0154a0001c0002t0001g0145a0001c0002t0001g0146others(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 | a0001c0001t0001g0153a0001c0001t0001g0160a0001c0002t0001g0136others(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 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0135others(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 | a0001c0002t0001g0074a0001c0002t0003g0148a0002c0016t0002g0225 | 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 | a0001c0001t0001g0167a0001c0002t0001g0109a0001c0002t0001g0122others(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 | a0001c0001t0001g0188a0001c0012t0002g0229 | 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 | |||||
chr6:43116643
|
TGTGTGTG others(3): Show |
T | 1 | a0003c0003t0002g0219 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.80-12332_80-12323d others(12): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43116643 | |||||
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 | a0001c0001t0002g0023a0001c0001t0002g0029a0001c0001t0002g0101others(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 | a0001c0001t0002g0254a0001c0001t0002g0255 | 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 | a0001c0001t0004g0269a0001c0017t0001g0232 | 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 | a0001c0001t0001g0064a0001c0001t0001g0127a0001c0001t0001g0172others(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 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0230others(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 | a0001c0001t0001g0002a0001c0001t0001g0087a0001c0001t0001g0094others(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 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0013others(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 | a0001c0001t0001g0126a0001c0001t0001g0263a0001c0001t0002g0264others(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 | a0001c0001t0001g0200a0001c0001t0001g0202a0001c0001t0001g0204others(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 | a0001c0001t0001g0160a0001c0001t0002g0214a0001c0002t0001g0152others(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 | a0001c0001t0001g0011a0001c0001t0001g0050a0001c0001t0001g0058others(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 | 118 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0037others(115): Show | 118 | HG00323.hp1 HG00323.hp2 HG00597.hp1 others(115): 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 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0202others(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 | a0003c0003t0001g0243 | 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 | 181 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(178): Show | 181 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(178): 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 | a0008c0019t0001g0141 | 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 | a0001c0001t0001g0230a0001c0002t0002g0231a0001c0017t0001g0232 | 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 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0202others(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 | a0002c0004t0002g0046 | 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 | a0001c0002t0001g0074a0001c0002t0001g0109a0001c0002t0001g0122others(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 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(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 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0160others(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 | a0001c0001t0001g0066a0001c0001t0001g0199a0001c0001t0001g0200others(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 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(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 | a0001c0001t0001g0246a0001c0001t0001g0263a0001c0001t0001g0268others(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 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(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 | a0001c0001t0001g0077a0001c0001t0001g0212a0001c0001t0001g0213others(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 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0202others(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 | a0001c0001t0001g0119a0001c0001t0002g0008a0001c0001t0002g0015others(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 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(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 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0202others(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 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0202others(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 | a0001c0001t0001g0003a0001c0001t0001g0064a0001c0001t0001g0100others(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 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0086others(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 | a0001c0001t0001g0188a0001c0001t0001g0193a0001c0010t0002g0093 | 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 | a0001c0001t0001g0073a0001c0002t0001g0191a0001c0009t0002g0061 | 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 | a0001c0001t0001g0213a0001c0002t0001g0102a0001c0002t0001g0113others(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 | a0001c0001t0001g0160a0001c0001t0001g0204a0001c0002t0001g0152 | 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 | a0001c0002t0001g0185a0001c0002t0003g0148a0001c0002t0003g0149 | 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 | a0001c0001t0001g0170a0001c0001t0003g0201a0001c0002t0001g0161 | 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 | a0001c0002t0001g0183a0001c0002t0001g0184 | 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 | a0003c0003t0001g0243 | 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 | a0001c0002t0001g0252a0001c0002t0001g0262 | 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 | a0001c0001t0001g0246a0001c0002t0002g0253 | 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 | a0001c0002t0001g0207a0001c0002t0001g0216a0001c0002t0001g0217others(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 | a0001c0001t0001g0263a0001c0001t0001g0270a0001c0001t0002g0256others(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 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0002t0001g0146 | 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 | a0001c0001t0001g0153a0001c0001t0001g0154 | 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 | a0001c0001t0002g0264a0001c0001t0002g0271a0001c0002t0001g0196 | 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 | a0001c0001t0001g0202a0001c0002t0001g0090a0001c0002t0001g0109others(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 | a0001c0002t0001g0034a0001c0002t0001g0180a0001c0002t0001g0181others(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 | a0001c0002t0001g0151a0001c0002t0001g0159a0001c0022t0001g0155 | 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 | a0001c0001t0001g0199a0001c0012t0002g0229 | 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 | a0001c0001t0002g0254a0001c0001t0002g0259a0001c0002t0001g0258others(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 | a0001c0001t0002g0083a0001c0001t0002g0118a0001c0001t0002g0265others(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 | a0001c0015t0001g0240a0002c0014t0002g0241 | 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 | a0001c0002t0001g0106a0001c0002t0001g0136a0001c0006t0001g0078 | 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 | a0001c0001t0001g0200a0001c0002t0001g0142a0001c0002t0001g0143 | 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 | a0001c0002t0001g0250a0001c0002t0001g0251 | 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 | a0001c0001t0002g0012a0001c0001t0002g0209a0001c0001t0002g0255others(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 | a0001c0001t0002g0032a0001c0001t0002g0036a0001c0001t0002g0057others(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 | a0001c0002t0001g0089a0001c0015t0001g0240a0002c0014t0002g0241others(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 | a0001c0001t0001g0230a0001c0001t0001g0238a0001c0002t0001g0129others(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 | a0001c0001t0001g0166a0001c0001t0001g0205a0001c0002t0001g0074others(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 | a0001c0001t0002g0242a0001c0002t0009g0233 | 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 | 5 | a0001c0001t0002g0020a0001c0001t0002g0041a0001c0001t0002g0053others(2): Show | 5 | HG01261.hp1 HG01496.hp2 HG01943.hp1 others(2): 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 | a0001c0001t0001g0006a0001c0001t0001g0119a0001c0001t0002g0027others(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 | a0001c0001t0001g0058a0001c0001t0002g0039 | 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 | a0001c0001t0001g0204a0001c0001t0002g0175a0001c0002t0001g0089others(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 | a0001c0001t0001g0126a0001c0002t0001g0110a0007c0020t0006g0226 | 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 | a0001c0001t0001g0022a0001c0001t0001g0066a0001c0001t0001g0072others(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 | a0001c0001t0001g0065a0001c0001t0001g0076a0001c0001t0001g0098others(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 | a0001c0001t0001g0087a0001c0002t0001g0134a0001c0002t0001g0182others(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 | a0001c0001t0001g0206a0001c0006t0001g0084a0003c0003t0002g0162others(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 | a0001c0001t0002g0223a0001c0001t0002g0224 | 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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0037others(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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0022others(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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0022others(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 | a0001c0001t0001g0003a0001c0001t0001g0022a0001c0001t0001g0068others(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 | a0001c0001t0001g0022a0001c0001t0001g0072a0001c0001t0001g0208others(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 | a0001c0001t0001g0037a0001c0001t0002g0001a0001c0001t0002g0009others(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 | a0001c0001t0001g0022a0001c0001t0001g0072a0001c0001t0001g0208others(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 | a0001c0015t0001g0240a0002c0014t0002g0241 | 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 | a0001c0001t0001g0050a0001c0001t0002g0028a0001c0001t0002g0029others(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 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0008others(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 | a0001c0001t0002g0223a0001c0001t0002g0224 | 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 | a0001c0001t0002g0222a0001c0001t0002g0223a0001c0001t0002g0224 | 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 | a0001c0015t0001g0240a0002c0014t0002g0241 | 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 | a0001c0015t0001g0240a0002c0014t0002g0241 | 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 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0058others(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 | a0001c0015t0001g0240a0002c0014t0002g0241 | 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 | a0001c0002t0001g0252a0001c0002t0002g0253 | 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 | a0001c0001t0002g0195a0001c0001t0002g0214a0001c0002t0001g0123others(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 | 39 | a0001c0001t0001g0094a0001c0001t0001g0199a0001c0001t0001g0200others(36): Show | 39 | HG00423.hp2 HG01099.hp1 HG01891.hp1 others(36): 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 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(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 | a0001c0002t0001g0250a0001c0002t0001g0251a0008c0019t0001g0141 | 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 | a0001c0002t0001g0250a0001c0002t0001g0251a0008c0019t0001g0141 | 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 | a0001c0001t0001g0037a0001c0001t0001g0098a0001c0001t0001g0153others(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 | a0001c0002t0001g0250a0001c0002t0001g0251a0008c0019t0001g0141 | 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 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0202others(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 | a0003c0018t0001g0248 | 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 | a0001c0001t0001g0119a0001c0001t0002g0010a0001c0001t0002g0067others(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 | a0001c0001t0001g0230a0001c0001t0004g0269a0001c0002t0002g0231others(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 | a0006c0013t0001g0063 | 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 | a0001c0002t0001g0250a0001c0002t0001g0251 | 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 | a0001c0001t0001g0230a0001c0001t0002g0222a0001c0001t0002g0223others(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 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(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 | a0001c0001t0001g0200a0001c0001t0001g0205 | 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 | a0001c0001t0002g0234a0001c0001t0002g0242a0001c0002t0009g0233 | 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 | a0001c0001t0001g0003a0001c0001t0001g0073a0001c0001t0001g0133others(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 | 67 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0085others(64): Show | 67 | HG00323.hp2 HG00597.hp1 HG00639.hp1 others(64): 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 | a0001c0001t0001g0013a0001c0001t0001g0050a0001c0001t0001g0199others(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 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0037others(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 | a0001c0001t0001g0200a0001c0001t0001g0202a0001c0001t0001g0204others(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 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0135others(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 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(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 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0202others(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 | ||||||
chr6:43121572
|
T | TCTGCAGC others(10): Show |
1 | a0003c0003t0002g0219 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.80-7404_80-7388dup others(17): Show |
PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr6 | 43121572 | |||||
chr6:43121691
|
C | T | 63 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0135others(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 | a0001c0001t0001g0230a0001c0002t0002g0231a0001c0017t0001g0232 | 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 | a0001c0001t0001g0006a0002c0004t0002g0007 | 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 | a0001c0001t0002g0234a0001c0001t0002g0242a0001c0002t0009g0233 | 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 | a0002c0016t0002g0225 | 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 | a0001c0002t0003g0014a0001c0002t0003g0148a0001c0002t0003g0149others(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 | a0001c0002t0001g0180a0001c0002t0001g0181 | 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 | a0002c0016t0002g0225a0003c0003t0002g0162a0003c0003t0002g0163others(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 | a0001c0001t0001g0094a0001c0001t0001g0199a0001c0001t0001g0200others(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 | a0001c0001t0001g0202a0001c0001t0001g0204a0001c0001t0001g0206others(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 | 65 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0085others(62): Show | 65 | HG00323.hp2 HG00597.hp1 HG00639.hp1 others(62): 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 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(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 | a0001c0001t0002g0021a0001c0001t0002g0265 | 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 | a0001c0001t0001g0199a0001c0001t0001g0246a0001c0001t0001g0263others(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 | a0001c0002t0001g0168a0001c0002t0001g0169 | 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 | a0001c0001t0002g0005a0001c0001t0002g0042 | 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 | a0001c0002t0001g0091a0001c0012t0002g0229 | 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 | a0001c0001t0001g0065a0006c0013t0001g0063 | 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 | a0001c0002t0004g0228a0002c0004t0002g0239 | 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 | a0001c0002t0001g0143a0001c0002t0001g0144a0001c0002t0001g0165others(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 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(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 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(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 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(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 | a0001c0002t0001g0183a0001c0002t0001g0184 | 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 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(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 | a0001c0001t0001g0200a0001c0001t0001g0202a0001c0001t0001g0204others(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 | a0001c0002t0001g0095a0001c0002t0001g0110 | 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 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(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 | a0001c0001t0001g0199a0003c0003t0001g0243a0007c0020t0006g0226others(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 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(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 | a0001c0001t0001g0200a0001c0001t0001g0205 | 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 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(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 | a0001c0001t0001g0199a0008c0019t0001g0141 | 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 | a0007c0020t0006g0226 | 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 | a0001c0001t0001g0200a0001c0001t0001g0202a0001c0001t0001g0204others(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 | a0001c0001t0001g0199a0003c0003t0001g0243a0007c0020t0006g0226others(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 | a0003c0003t0001g0243 | 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 | a0001c0001t0001g0094a0001c0001t0001g0096 | 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 | a0001c0001t0001g0200a0001c0001t0001g0202a0001c0001t0001g0204others(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 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(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 | a0001c0001t0001g0199a0003c0003t0001g0243a0007c0020t0006g0226others(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 | a0001c0001t0001g0199a0001c0001t0002g0055a0001c0001t0002g0242others(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 | a0007c0020t0006g0226 | 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 | a0001c0001t0002g0234a0001c0001t0002g0242a0001c0002t0009g0233others(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 | 155 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(152): Show | 155 | HG00323.hp1 HG00323.hp2 HG00597.hp1 others(152): Show |
intron_variant | MODIFIER | c.80-887G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 1/19 | chr6 | 43128090 | ||||||
chr6:43128329
|
G | A | 150 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(147): Show | 150 | HG00323.hp1 HG00323.hp2 HG00597.hp1 others(147): 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 | 78 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0135others(75): Show | 78 | HG00323.hp2 HG00597.hp1 HG00639.hp1 others(75): 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 | 155 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(152): Show | 155 | HG00323.hp1 HG00323.hp2 HG00597.hp1 others(152): 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 | a0001c0002t0003g0014a0001c0002t0003g0148a0001c0002t0003g0150 | 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 | a0001c0001t0001g0199a0003c0003t0001g0243a0007c0020t0006g0226others(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 | a0007c0020t0006g0226 | 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 | a0001c0001t0001g0199a0003c0003t0001g0243a0007c0020t0006g0226others(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 | a0001c0002t0001g0122a0001c0002t0001g0207 | 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 | a0001c0001t0001g0200a0001c0001t0001g0202a0001c0001t0001g0204others(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 | a0001c0002t0001g0145a0001c0002t0004g0139a0003c0003t0002g0070 | 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 | a0008c0019t0001g0141 | 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 | 11 | a0001c0001t0001g0230a0001c0001t0002g0222a0001c0001t0002g0223others(8): Show | 11 | HG00741.hp2 HG02055.hp2 HG02145.hp2 others(8): 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 | a0001c0002t0002g0026a0001c0002t0002g0231 | 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 | a0001c0001t0001g0003a0001c0001t0001g0050a0001c0001t0001g0092others(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 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0037others(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 | a0001c0001t0001g0071a0001c0001t0001g0172a0001c0001t0001g0200others(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 | a0001c0001t0002g0016a0001c0001t0002g0018a0001c0001t0002g0048others(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 | a0001c0001t0001g0065a0001c0001t0001g0077a0001c0001t0001g0085others(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 | a0001c0001t0001g0097a0001c0001t0001g0111a0001c0001t0001g0171others(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 | a0001c0001t0001g0079a0001c0001t0001g0094a0001c0001t0001g0096others(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 | a0001c0002t0001g0142a0001c0002t0002g0026a0001c0002t0002g0231others(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 | a0001c0001t0002g0222a0001c0001t0002g0223a0001c0001t0002g0224others(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 | 4 | a0001c0001t0001g0238a0003c0003t0002g0070a0003c0003t0002g0121others(1): Show | 4 | HG01255.hp2 HG01261.hp2 NA18943.hp1 others(1): Show |
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 | a0001c0001t0001g0204a0001c0001t0003g0201a0001c0002t0001g0203 | 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 | a0001c0002t0004g0228a0002c0004t0002g0235a0002c0004t0002g0239 | 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 | a0007c0020t0006g0226 | 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 | a0008c0019t0001g0141 | 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 | a0003c0003t0001g0243 | 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 | 3 | a0003c0003t0002g0070a0003c0003t0002g0121a0003c0003t0002g0219 | 3 | HG01261.hp2 NA18943.hp1 homoSapiens_chm13v2.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 | a0001c0002t0001g0151a0001c0002t0001g0159 | 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 | 22 | a0001c0001t0001g0166a0001c0001t0001g0200a0001c0001t0001g0202others(19): Show | 22 | HG00741.hp2 HG01261.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.813-254G>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 5/19 | chr6 | 43131762 | ||||||
chr6:43131869
|
C | G | 39 | a0001c0001t0001g0166a0001c0001t0001g0200a0001c0001t0001g0202others(36): Show | 39 | HG00423.hp2 HG01099.hp1 HG01261.hp2 others(36): 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 | a0001c0015t0001g0240a0002c0014t0002g0241 | 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 | a0001c0015t0001g0240a0002c0014t0002g0241 | 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 | a0003c0003t0002g0070 | 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 | 18 | a0001c0002t0001g0031a0001c0002t0001g0196a0001c0002t0001g0198others(15): Show | 18 | HG01099.hp1 HG01261.hp2 HG02145.hp2 others(15): 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 | a0001c0002t0001g0089a0001c0002t0001g0102a0001c0002t0001g0103others(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 | 9 | a0001c0001t0002g0234a0001c0001t0002g0242a0001c0012t0002g0229others(6): Show | 9 | HG01261.hp2 HG01891.hp1 HG02145.hp2 others(6): 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 | a0007c0020t0006g0226 | 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 | 170 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(167): Show | 170 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(167): 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 | a0001c0015t0001g0240a0002c0014t0002g0241 | 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 | 197 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(194): Show | 197 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(194): 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 | a0001c0001t0002g0234a0001c0001t0002g0242a0001c0012t0002g0229others(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 | a0007c0020t0006g0226 | 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 | a0001c0012t0002g0229a0003c0018t0001g0248 | 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 | a0001c0001t0001g0167a0001c0002t0001g0074a0001c0002t0001g0109others(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 | a0001c0001t0001g0097a0001c0001t0004g0269a0001c0002t0001g0091others(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 | 3 | a0003c0003t0002g0070a0003c0003t0002g0121a0003c0003t0002g0219 | 3 | HG01261.hp2 NA18943.hp1 homoSapiens_chm13v2.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 | a0001c0002t0001g0031a0001c0002t0001g0196a0001c0002t0001g0198others(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 | 7 | a0001c0015t0001g0240a0002c0014t0002g0241a0003c0003t0001g0243others(4): Show | 7 | HG01261.hp2 HG02145.hp1 HG02622.hp2 others(4): 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 | a0008c0019t0001g0141 | 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 | a0001c0001t0001g0073a0001c0001t0001g0192 | 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 | a0001c0001t0002g0234a0001c0001t0002g0242 | 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 | 23 | a0001c0001t0002g0234a0001c0001t0002g0242a0001c0002t0001g0031others(20): Show | 23 | HG01099.hp1 HG01261.hp2 HG01891.hp1 others(20): 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 | a0007c0020t0006g0226 | 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 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0077others(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 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(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 | a0001c0001t0002g0234a0001c0001t0002g0242a0001c0012t0002g0229others(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 | a0001c0001t0001g0064a0001c0001t0001g0080 | 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 | a0007c0020t0006g0226 | 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 | a0001c0002t0004g0139a0003c0003t0001g0243a0008c0019t0001g0141 | 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 | 3 | a0003c0003t0002g0070a0003c0003t0002g0121a0003c0003t0002g0219 | 3 | HG01261.hp2 NA18943.hp1 homoSapiens_chm13v2.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 | a0007c0020t0006g0226 | 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 | 7 | a0001c0015t0001g0240a0002c0014t0002g0241a0003c0003t0001g0243others(4): Show | 7 | HG01261.hp2 HG02145.hp1 HG02622.hp2 others(4): 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 | a0001c0002t0001g0031a0001c0002t0001g0196a0001c0002t0001g0198others(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 | a0001c0001t0001g0166a0001c0001t0001g0199a0001c0001t0001g0202others(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 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(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 | 165 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(162): Show | 165 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(162): 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 | a0001c0001t0002g0035a0001c0001t0002g0214 | 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 | a0001c0002t0001g0196a0001c0002t0001g0198 | 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 | 195 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(192): Show | 195 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(192): 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 | a0001c0001t0001g0167a0001c0001t0002g0234a0003c0003t0001g0243 | 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 | a0001c0002t0001g0112a0001c0002t0001g0114a0001c0002t0001g0129others(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 | a0001c0002t0001g0152a0001c0002t0001g0161 | 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 | 11 | a0001c0001t0002g0234a0001c0001t0002g0242a0001c0015t0001g0240others(8): Show | 11 | HG01261.hp2 HG01891.hp1 HG02145.hp1 others(8): 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 | a0001c0001t0002g0054 | 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 | 105 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(102): Show | 105 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(102): 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 | 105 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(102): Show | 105 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(102): 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 | a0001c0015t0001g0240a0002c0014t0002g0241 | 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 | 8 | a0001c0015t0001g0240a0002c0014t0002g0241a0003c0003t0001g0243others(5): Show | 8 | HG01261.hp2 HG02145.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1618+859C>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 10/19 | chr6 | 43140384 | ||||||
chr6:43140452
|
C | CA | 16 | a0001c0001t0001g0011a0001c0001t0002g0008a0001c0001t0002g0039others(13): Show | 16 | HG01261.hp2 HG01891.hp1 HG01993.hp1 others(13): 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 | a0001c0001t0001g0006a0001c0001t0001g0037a0001c0001t0001g0058others(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 | a0001c0001t0001g0094a0001c0001t0001g0211a0001c0002t0001g0089others(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 | a0001c0001t0002g0051a0003c0018t0001g0248 | 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 | a0001c0002t0001g0031a0001c0002t0001g0034a0001c0002t0001g0056others(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 | a0001c0001t0001g0166a0001c0001t0001g0199a0001c0001t0001g0200others(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 | 106 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(103): Show | 106 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(103): 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 | a0001c0001t0004g0269a0001c0015t0001g0240a0002c0014t0002g0241others(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 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(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 | a0008c0019t0001g0141 | 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 | a0003c0003t0002g0162a0003c0003t0002g0163a0003c0003t0002g0178 | 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 | 195 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(192): Show | 195 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(192): 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 | 3 | a0003c0003t0002g0070a0003c0003t0002g0121a0003c0003t0002g0219 | 3 | HG01261.hp2 NA18943.hp1 homoSapiens_chm13v2.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 | a0003c0003t0001g0243a0003c0003t0002g0162a0003c0003t0002g0163others(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 | a0001c0001t0001g0013a0001c0001t0002g0005a0001c0001t0002g0033others(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 | a0001c0001t0001g0166a0001c0001t0001g0199a0001c0001t0001g0200others(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 | a0001c0002t0001g0262 | 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 | a0001c0001t0001g0006a0001c0001t0001g0166a0001c0001t0001g0199others(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 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0037others(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 | 8 | a0003c0003t0001g0243a0003c0003t0002g0070a0003c0003t0002g0121others(5): Show | 8 | HG01261.hp2 HG02145.hp2 HG02258.hp2 others(5): 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 | a0001c0001t0001g0006a0001c0001t0001g0230a0001c0002t0001g0136others(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 |
3 | a0003c0003t0002g0070a0003c0003t0002g0121a0003c0003t0002g0219 | 3 | HG01261.hp2 NA18943.hp1 homoSapiens_chm13v2.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 | a0001c0001t0001g0166a0001c0001t0001g0199a0001c0001t0001g0200others(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 | a0001c0001t0002g0017 | 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 | 270 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(267): Show | 270 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(267): 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 | a0001c0001t0001g0166a0001c0001t0001g0199a0001c0001t0001g0200others(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 | a0001c0001t0001g0011a0001c0001t0001g0058 | 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 | a0001c0002t0001g0180a0001c0002t0001g0181 | 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 | a0001c0001t0001g0068a0001c0002t0001g0143a0001c0002t0001g0144others(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 | a0001c0001t0001g0013a0001c0001t0001g0238 | 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 | a0001c0001t0001g0006a0001c0001t0001g0230a0001c0002t0001g0136others(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 | a0001c0001t0001g0098a0001c0002t0001g0075a0001c0002t0001g0089others(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 | a0001c0001t0002g0044a0001c0001t0002g0222a0001c0001t0002g0223others(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 | a0001c0001t0001g0006a0001c0001t0001g0230a0001c0002t0001g0136others(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 | a0003c0018t0001g0248 | 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 | 194 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0037others(191): Show | 194 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(191): 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 | a0003c0018t0001g0248 | 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 | 4 | a0001c0002t0002g0104a0003c0003t0002g0070a0003c0003t0002g0121others(1): Show | 4 | HG01258.hp1 HG01261.hp2 NA18943.hp1 others(1): Show |
intron_variant | MODIFIER | c.2721+1232G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43147930 | ||||||
chr6:43147932
|
C | A | 121 | a0001c0001t0001g0006a0001c0001t0001g0068a0001c0001t0001g0098others(118): Show | 121 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(118): 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 | a0001c0001t0001g0068a0001c0001t0001g0098a0001c0001t0001g0167others(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 | a0001c0001t0001g0006a0001c0001t0001g0230a0001c0002t0001g0136others(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 | a0001c0001t0002g0044a0001c0001t0002g0222a0001c0001t0002g0223others(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 | a0001c0002t0005g0137a0001c0002t0005g0138 | 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 | a0001c0001t0001g0011a0001c0001t0001g0037a0001c0001t0001g0058others(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 | 194 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0037others(191): Show | 194 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(191): 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 | a0001c0001t0001g0006a0001c0001t0001g0230a0001c0017t0001g0232 | 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 | a0001c0001t0002g0012a0001c0001t0002g0020a0001c0021t0002g0019 | 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 | a0001c0001t0001g0098a0001c0002t0001g0075a0001c0002t0001g0089others(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 | a0001c0001t0001g0006a0001c0001t0001g0068a0001c0001t0001g0076others(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 | a0001c0001t0001g0011a0001c0001t0001g0037a0001c0001t0001g0058others(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 | a0001c0001t0001g0069a0001c0001t0001g0124a0001c0001t0001g0133others(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 | a0008c0019t0001g0141 | 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 | a0001c0005t0001g0156a0001c0005t0001g0157a0001c0005t0001g0174 | 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 | a0001c0001t0001g0013a0001c0001t0001g0069a0001c0001t0001g0077others(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 | 17 | a0001c0001t0001g0011a0001c0001t0001g0050a0001c0001t0001g0073others(14): Show | 17 | HG01123.hp1 HG01175.hp1 HG01258.hp1 others(14): 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 | a0001c0001t0001g0058a0001c0001t0002g0044a0001c0001t0002g0223others(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 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0015others(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 | a0001c0001t0001g0037a0001c0001t0002g0004a0001c0001t0002g0005others(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 | a0001c0001t0002g0042a0001c0001t0002g0067a0001c0001t0002g0255others(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 | a0001c0001t0002g0048a0001c0002t0001g0191a0001c0006t0001g0081 | 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 | a0001c0005t0001g0157a0001c0005t0001g0174 | 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 | a0001c0001t0001g0230a0001c0002t0001g0136a0001c0017t0001g0232others(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 | a0001c0001t0001g0006a0001c0001t0002g0023a0001c0001t0002g0029 | 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 | a0001c0001t0001g0166a0001c0001t0001g0199a0001c0001t0001g0202others(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 | a0001c0002t0001g0056a0001c0002t0001g0134a0001c0002t0001g0151others(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 | a0001c0002t0001g0074a0001c0002t0001g0075a0001c0002t0001g0089others(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 | a0001c0001t0001g0098a0001c0001t0002g0234a0001c0001t0002g0242others(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 | 101 | a0001c0001t0001g0011a0001c0001t0001g0037a0001c0001t0001g0058others(98): Show | 101 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(98): 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 | a0001c0001t0001g0068a0001c0006t0001g0078a0001c0006t0001g0081others(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 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0037others(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 | a0001c0001t0001g0068a0001c0002t0001g0143a0001c0002t0001g0144others(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 | a0001c0001t0001g0011a0001c0001t0001g0037a0001c0001t0001g0058others(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 | a0001c0001t0001g0098a0001c0001t0001g0167a0001c0002t0001g0056others(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 | a0001c0001t0001g0006a0001c0001t0001g0230a0001c0002t0001g0136others(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 | a0001c0002t0001g0122a0001c0002t0001g0207 | 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 | a0001c0001t0002g0254a0001c0001t0002g0255 | 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 | 98 | a0001c0001t0001g0068a0001c0001t0001g0098a0001c0001t0001g0166others(95): Show | 98 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(95): 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 | a0001c0001t0001g0003a0001c0001t0001g0128a0001c0001t0001g0133others(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 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0037others(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 | a0001c0001t0001g0166a0001c0001t0001g0199a0001c0001t0001g0200others(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 | a0001c0001t0001g0006a0001c0001t0001g0230a0001c0017t0001g0232 | 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 | a0003c0003t0001g0243 | 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 | a0001c0001t0004g0236a0001c0001t0004g0269a0001c0002t0004g0139others(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 | a0001c0001t0001g0006a0001c0001t0001g0230a0001c0002t0001g0056others(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 | 34 | a0001c0001t0001g0050a0001c0001t0001g0071a0001c0001t0001g0073others(31): Show | 34 | HG00323.hp2 HG01123.hp1 HG01175.hp1 others(31): 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 | a0001c0001t0001g0064a0001c0001t0001g0211a0001c0002t0001g0142others(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 | a0001c0002t0001g0183a0002c0004t0002g0025 | 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 | a0001c0001t0001g0002a0001c0001t0001g0068a0001c0001t0001g0069others(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 | a0001c0001t0001g0006a0001c0001t0001g0160a0001c0001t0001g0193others(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 | a0001c0001t0001g0230a0001c0001t0002g0004a0001c0001t0002g0028others(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 | a0001c0001t0001g0011a0001c0001t0001g0058a0001c0001t0002g0001others(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 | a0001c0001t0001g0037a0001c0001t0002g0036 | 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 | a0001c0002t0001g0056a0001c0002t0001g0203 | 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 | a0001c0001t0001g0166a0001c0001t0001g0199a0001c0001t0001g0202others(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 | a0001c0001t0001g0270a0004c0007t0001g0131 | 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 | a0001c0001t0002g0044a0001c0001t0002g0222a0001c0001t0002g0223others(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 | a0008c0019t0001g0141 | 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 | a0001c0001t0001g0006a0001c0001t0001g0230a0001c0002t0001g0056others(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 | a0001c0002t0001g0103 | 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 | a0001c0001t0001g0011a0001c0001t0001g0058a0001c0001t0001g0085others(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 |
13 | a0001c0001t0001g0166a0001c0001t0001g0199a0001c0001t0001g0200others(10): Show | 13 | HG01258.hp1 HG01261.hp2 HG01891.hp1 others(10): 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 | a0001c0001t0001g0094a0001c0001t0001g0096 | 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 | 9 | a0001c0001t0002g0234a0001c0001t0002g0242a0001c0002t0002g0104others(6): Show | 9 | HG01258.hp1 HG01261.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.2722-4493C>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43154324 | ||||||
chr6:43154381
|
C | G | 16 | a0001c0001t0001g0006a0001c0001t0001g0230a0001c0001t0002g0234others(13): Show | 16 | HG00741.hp2 HG01258.hp1 HG01261.hp2 others(13): 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 | a0001c0002t0001g0145a0001c0002t0001g0267 | 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 | a0003c0003t0002g0162a0003c0003t0002g0163a0003c0003t0002g0178 | 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 | 270 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(267): Show | 270 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(267): 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 | a0001c0001t0001g0166a0001c0001t0001g0199a0001c0001t0001g0200others(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 | a0001c0001t0001g0073a0001c0001t0001g0087a0001c0001t0001g0097others(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 | a0001c0001t0004g0236a0001c0001t0004g0269a0001c0002t0004g0139others(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 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(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 | a0001c0001t0002g0012a0001c0001t0002g0020a0001c0021t0002g0019 | 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 | a0001c0001t0001g0166a0001c0001t0001g0199a0001c0001t0001g0200others(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 | a0001c0002t0002g0104 | 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 | a0003c0003t0002g0162a0003c0003t0002g0163a0003c0003t0002g0178 | 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 | 4 | a0001c0002t0002g0104a0003c0003t0002g0070a0003c0003t0002g0121others(1): Show | 4 | HG01258.hp1 HG01261.hp2 NA18943.hp1 others(1): Show |
intron_variant | MODIFIER | c.2722-3280G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43155537 | ||||||
chr6:43155578
|
A | AG | 67 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(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 | 93 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0230others(90): Show | 93 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(90): 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 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0008others(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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0073others(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 | a0001c0001t0001g0200a0001c0001t0001g0202a0001c0001t0001g0204others(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 | 67 | a0001c0001t0001g0098a0001c0001t0001g0160a0001c0001t0001g0173others(64): Show | 67 | HG00544.hp2 HG00597.hp1 HG00639.hp1 others(64): 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 | a0001c0001t0001g0167a0001c0001t0002g0035a0001c0001t0002g0043others(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 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(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 | a0001c0001t0002g0021a0001c0001t0002g0028a0001c0001t0002g0179others(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 | a0001c0002t0004g0139a0007c0020t0006g0226 | 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 | a0001c0001t0001g0166a0001c0001t0001g0199a0001c0001t0001g0200others(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 | a0003c0003t0002g0162a0003c0003t0002g0163a0003c0003t0002g0178 | 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 | 82 | a0001c0001t0001g0076a0001c0001t0001g0085a0001c0001t0002g0001others(79): Show | 82 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(79): 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 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0230others(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 | a0003c0003t0002g0162a0003c0003t0002g0163a0003c0003t0002g0178 | 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 | 80 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(77): Show | 80 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(77): 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 | a0001c0001t0002g0117a0001c0001t0002g0261a0001c0001t0002g0264others(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 | a0001c0001t0001g0200a0001c0001t0001g0202a0001c0001t0002g0015others(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 | a0001c0001t0001g0119a0001c0001t0001g0194a0001c0001t0002g0175others(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 | 109 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0166others(106): Show | 109 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(106): Show |
intron_variant | MODIFIER | c.2722-1649G>T | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43157168 | ||||||
chr6:43157169
|
T | G | 6 | a0001c0001t0002g0234a0001c0001t0002g0242a0001c0002t0002g0104others(3): Show | 6 | HG01258.hp1 HG01261.hp2 HG01891.hp1 others(3): 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 | a0001c0001t0001g0186a0001c0010t0002g0045 | 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 | a0001c0001t0002g0044a0001c0001t0002g0222a0001c0001t0002g0223others(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 | a0001c0002t0001g0143a0001c0002t0001g0165a0001c0002t0001g0191others(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 | a0001c0001t0002g0028a0001c0001t0002g0038a0001c0001t0002g0082others(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 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0008others(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 | a0001c0001t0001g0199a0001c0001t0001g0227a0001c0001t0002g0047others(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 | a0001c0002t0001g0250a0001c0002t0001g0251 | 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 | a0001c0001t0001g0167a0001c0001t0001g0172a0001c0001t0001g0176others(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 | a0001c0001t0001g0098a0001c0002t0001g0089a0001c0002t0001g0102others(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 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0008g0177others(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 | a0001c0001t0001g0066a0001c0001t0001g0173a0001c0002t0001g0074others(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 | a0001c0002t0001g0095a0001c0002t0001g0114a0001c0002t0007g0115 | 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 | 3 | a0003c0003t0002g0070a0003c0003t0002g0121a0003c0003t0002g0219 | 3 | HG01261.hp2 NA18943.hp1 homoSapiens_chm13v2.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 | a0001c0002t0002g0104 | 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 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0170others(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 | a0001c0001t0004g0236a0001c0001t0004g0269 | 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 | a0001c0001t0001g0166a0001c0001t0001g0202a0001c0001t0001g0204others(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 | a0001c0001t0001g0200a0001c0001t0001g0205 | 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 | a0003c0018t0001g0248 | 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 | a0003c0003t0002g0162a0003c0003t0002g0163a0003c0003t0002g0178 | 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 | a0001c0001t0002g0101a0001c0001t0002g0175a0001c0001t0002g0195others(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 | a0001c0001t0002g0005a0001c0001t0002g0032a0001c0001t0002g0033others(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 | a0003c0018t0001g0248 | 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 | a0003c0018t0001g0248 | 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 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0006t0001g0081 | 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 | a0001c0001t0002g0012a0001c0001t0002g0035a0001c0001t0002g0057others(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 | a0003c0018t0001g0248 | 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 | a0001c0001t0001g0073a0001c0001t0001g0079a0001c0008t0001g0107others(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 | a0001c0001t0001g0073a0001c0001t0001g0079a0001c0001t0001g0172others(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 | a0001c0001t0001g0066a0001c0001t0001g0073a0001c0001t0001g0079others(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 | a0001c0001t0001g0003a0001c0001t0001g0080a0001c0001t0001g0244 | 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 | a0001c0001t0001g0263a0001c0002t0001g0262 | 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 | a0001c0001t0001g0068a0001c0001t0001g0193 | 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 | a0001c0001t0001g0220a0001c0002t0001g0247 | 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 | a0001c0001t0001g0011a0001c0001t0001g0071 | 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 | a0001c0001t0001g0050 | 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 | a0001c0001t0001g0096a0001c0001t0001g0100a0006c0013t0001g0063 | 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 | a0008c0019t0001g0141 | 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 | a0001c0001t0001g0077a0001c0001t0001g0135 | 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 | a0001c0001t0001g0064a0001c0001t0001g0211 | 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 | a0001c0001t0001g0066a0001c0001t0001g0073a0001c0001t0001g0079others(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 | a0001c0001t0002g0224a0001c0002t0001g0056a0001c0002t0001g0203others(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 | a0001c0001t0002g0224a0001c0002t0001g0056a0001c0002t0001g0203others(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 | a0001c0002t0001g0056a0001c0002t0001g0203a0002c0004t0002g0007others(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 | a0002c0004t0002g0046 | 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 | a0001c0002t0001g0056a0001c0002t0001g0203a0002c0004t0002g0007others(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 | a0002c0004t0002g0235 | 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 | a0001c0002t0001g0056a0001c0002t0001g0203a0002c0004t0002g0239 | 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 | a0001c0001t0004g0236a0001c0001t0004g0269a0001c0002t0004g0228others(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 | a0001c0001t0001g0006a0001c0002t0001g0056 | 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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0068others(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 | a0001c0001t0001g0006a0001c0002t0001g0056 | 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 | a0001c0002t0001g0196a0001c0002t0001g0198a0001c0002t0001g0247others(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 | a0003c0018t0001g0248 | 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 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0230others(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 | 26 | a0001c0001t0002g0044a0001c0001t0002g0222a0001c0001t0002g0223others(23): Show | 26 | HG01258.hp1 HG01261.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.2722-794G>A | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 17/19 | chr6 | 43158023 | ||||||
chr6:43158223
|
C | T | 27 | a0001c0001t0002g0044a0001c0001t0002g0222a0001c0001t0002g0223others(24): Show | 27 | HG01099.hp1 HG01258.hp1 HG01261.hp2 others(24): 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 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0230others(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 | a0001c0001t0001g0166a0001c0001t0001g0199a0001c0001t0001g0200others(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 | a0003c0018t0001g0248 | 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 | 25 | a0001c0001t0002g0044a0001c0001t0002g0222a0001c0001t0002g0223others(22): Show | 25 | HG01258.hp1 HG01261.hp2 HG01891.hp1 others(22): 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 | a0001c0002t0001g0196a0001c0002t0001g0198a0001c0002t0001g0247others(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 | a0001c0001t0001g0100a0001c0001t0001g0220 | 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 | a0001c0001t0001g0166a0001c0001t0001g0199a0001c0001t0001g0200others(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 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0230others(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 | a0001c0002t0001g0151a0001c0002t0001g0159 | 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 | a0003c0003t0002g0162a0003c0003t0002g0163a0003c0003t0002g0178 | 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 | a0003c0003t0002g0162a0003c0003t0002g0163a0003c0003t0002g0178 | 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 | 95 | a0001c0001t0001g0167a0001c0001t0002g0001a0001c0001t0002g0004others(92): Show | 95 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.3053-25A>G | PTK7 | ENSG00000112655.16 | transcript | ENST00000230419.9 | protein_coding | 19/19 | chr6 | 43160696 |