Item | Value |
---|---|
geneid | 115825 |
ensemblid | ENSG00000139668.9 |
hgncid | 20482 |
symbol | WDFY2 |
name | WD repeat and FYVE domain containing 2 |
refseq_nuc | NM_052950.4 |
refseq_prot | NP_443182.1 |
ensembl_nuc | ENST00000298125.7 |
ensembl_prot | ENSP00000298125.4 |
mane_status | MANE Select |
chr | chr13 |
start | 51584462 |
end | 51767709 |
strand | + |
ver | v1.2 |
region | chr13:51584462-51767709 |
region5000 | chr13:51579462-51772709 |
regionname0 | WDFY2_chr13_51584462_51767709 |
regionname5000 | WDFY2_chr13_51579462_51772709 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 400 | 271 | 78 | 51 | 98 | 14 | 28 | 76 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
a0002 | 0/0 | 400 | 5 | 0 | 5 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
a0003 | 0/0 | 400 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
a0004 | 0/0 | 400 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
chapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1203 | 226 | 75 | 43 | 73 | 9 | 24 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 | |
c0002 | 0/0 | 1203 | 43 | 1 | 8 | 25 | 5 | 4 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 | |
c0003 | 0/0 | 1203 | 5 | 0 | 5 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 | |
c0004 | 0/0 | 1203 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 | |
c0005 | 0/0 | 1203 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 | |
c0006 | 0/0 | 1203 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 | |
c0007 | 0/0 | 1203 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 8167 | 90 | 27 | 7 | 41 | 5 | 9 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
t0002 | 0/0 | 8154 | 39 | 1 | 8 | 21 | 5 | 4 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
t0003 | 0/0 | 8167 | 36 | 3 | 11 | 14 | 3 | 5 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
t0004 | 0/0 | 8167 | 25 | 10 | 13 | 0 | 0 | 2 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
t0005 | 0/0 | 8167 | 8 | 7 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
t0006 | 0/0 | 8167 | 7 | 0 | 0 | 6 | 0 | 1 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
t0007 | 0/0 | 8167 | 6 | 0 | 5 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
t0008 | 0/0 | 8167 | 6 | 0 | 0 | 6 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
t0009 | 1/0 | 8167 | 5 | 2 | 2 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
t0010 | 0/0 | 8167 | 5 | 5 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
t0011 | 0/0 | 8154 | 4 | 0 | 0 | 4 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
t0012 | 0/0 | 8167 | 3 | 2 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
t0013 | 0/0 | 8167 | 3 | 3 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
t0014 | 0/0 | 8167 | 3 | 0 | 2 | 0 | 0 | 1 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
t0015 | 0/0 | 8167 | 3 | 0 | 2 | 0 | 1 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
t0016 | 0/0 | 8167 | 2 | 2 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
t0017 | 0/0 | 8167 | 2 | 2 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
t0018 | 0/0 | 8167 | 2 | 2 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
t0019 | 0/0 | 8154 | 2 | 0 | 0 | 0 | 0 | 2 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
t0020 | 0/0 | 8167 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
t0021 | 0/0 | 8167 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
t0022 | 0/0 | 8167 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
t0023 | 0/0 | 8167 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
t0024 | 0/0 | 8167 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
t0025 | 0/0 | 8167 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
t0026 | 0/0 | 8167 | 1 | 0 | 0 | 0 | 0 | 1 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
t0027 | 0/0 | 8167 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
t0028 | 0/0 | 8167 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
t0029 | 0/0 | 8167 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
t0030 | 0/0 | 8167 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
t0031 | 0/0 | 8167 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
t0032 | 0/0 | 8167 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
t0033 | 0/0 | 8167 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
t0034 | 0/0 | 8167 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
t0035 | 0/0 | 8167 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
t0036 | 0/0 | 8123 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
t0037 | 0/0 | 8116 | 1 | 0 | 0 | 0 | 0 | 1 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
t0038 | 0/0 | 8167 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
t0039 | 0/0 | 8167 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
t0040 | 0/0 | 8167 | 1 | 0 | 0 | 0 | 0 | 1 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
t0041 | 0/0 | 8167 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
t0042 | 0/0 | 8167 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
t0043 | 0/0 | 8154 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
t0044 | 0/0 | 8154 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
t0045 | 0/0 | 8154 | 1 | 0 | 0 | 0 | 0 | 1 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
t0046 | 0/0 | 8167 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0114 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0117 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1203 | 226 | 75 | 43 | 73 | 9 | 24 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 | |
a0001c0002 | 0/0 | 1203 | 43 | 1 | 8 | 25 | 5 | 4 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 | |
a0001c0006 | 0/0 | 1203 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 | |
a0001c0007 | 0/0 | 1203 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 | |
a0002c0003 | 0/0 | 1203 | 5 | 0 | 5 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 | |
a0003c0004 | 0/0 | 1203 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 | |
a0004c0005 | 0/0 | 1203 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 9369 | 89 | 26 | 7 | 41 | 5 | 9 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
a0001c0001t0002 | 0/0 | 9356 | 2 | 0 | 0 | 1 | 0 | 1 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
a0001c0001t0003 | 0/0 | 9369 | 36 | 3 | 11 | 14 | 3 | 5 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
a0001c0001t0004 | 0/0 | 9369 | 20 | 10 | 8 | 0 | 0 | 2 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
a0001c0001t0005 | 0/0 | 9369 | 8 | 7 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
a0001c0001t0006 | 0/0 | 9369 | 7 | 0 | 0 | 6 | 0 | 1 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
a0001c0001t0007 | 0/0 | 9369 | 6 | 0 | 5 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
a0001c0001t0008 | 0/0 | 9369 | 6 | 0 | 0 | 6 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
a0001c0001t0009 | 1/0 | 9369 | 5 | 2 | 2 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
a0001c0001t0010 | 0/0 | 9369 | 5 | 5 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
a0001c0001t0012 | 0/0 | 9369 | 3 | 2 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
a0001c0001t0013 | 0/0 | 9369 | 3 | 3 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
a0001c0001t0014 | 0/0 | 9369 | 3 | 0 | 2 | 0 | 0 | 1 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
a0001c0001t0015 | 0/0 | 9369 | 3 | 0 | 2 | 0 | 1 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
a0001c0001t0017 | 0/0 | 9369 | 2 | 2 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
a0001c0001t0018 | 0/0 | 9369 | 2 | 2 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
a0001c0001t0019 | 0/0 | 9356 | 2 | 0 | 0 | 0 | 0 | 2 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
a0001c0001t0020 | 0/0 | 9369 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
a0001c0001t0021 | 0/0 | 9369 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
a0001c0001t0023 | 0/0 | 9369 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
a0001c0001t0024 | 0/0 | 9369 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
a0001c0001t0025 | 0/0 | 9369 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
a0001c0001t0026 | 0/0 | 9369 | 1 | 0 | 0 | 0 | 0 | 1 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
a0001c0001t0027 | 0/0 | 9369 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
a0001c0001t0028 | 0/0 | 9369 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
a0001c0001t0029 | 0/0 | 9369 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
a0001c0001t0030 | 0/0 | 9369 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
a0001c0001t0031 | 0/0 | 9369 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
a0001c0001t0032 | 0/0 | 9369 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
a0001c0001t0033 | 0/0 | 9369 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
a0001c0001t0034 | 0/0 | 9369 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
a0001c0001t0035 | 0/0 | 9369 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
a0001c0001t0036 | 0/0 | 9325 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
a0001c0001t0037 | 0/0 | 9318 | 1 | 0 | 0 | 0 | 0 | 1 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
a0001c0001t0038 | 0/0 | 9369 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
a0001c0001t0039 | 0/0 | 9369 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
a0001c0001t0040 | 0/0 | 9369 | 1 | 0 | 0 | 0 | 0 | 1 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
a0001c0001t0041 | 0/0 | 9369 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
a0001c0001t0042 | 0/0 | 9369 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
a0001c0001t0044 | 0/0 | 9356 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
a0001c0001t0046 | 0/0 | 9369 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
a0001c0002t0002 | 0/0 | 9356 | 37 | 1 | 8 | 20 | 5 | 3 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
a0001c0002t0011 | 0/0 | 9356 | 4 | 0 | 0 | 4 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
a0001c0002t0043 | 0/0 | 9356 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
a0001c0002t0045 | 0/0 | 9356 | 1 | 0 | 0 | 0 | 0 | 1 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
a0001c0006t0016 | 0/0 | 9369 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
a0001c0007t0016 | 0/0 | 9369 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
a0002c0003t0004 | 0/0 | 9369 | 5 | 0 | 5 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
a0003c0004t0001 | 0/0 | 9369 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
a0004c0005t0022 | 0/0 | 9369 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | copy fasta | chr13 | 51579462 | 51772709 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0117 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0003g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0003g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0003g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0003g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0003g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0003g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0003g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0003g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0003g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0003g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0003g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0003g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0003g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0004g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0004g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0004g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0004g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0004g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0004g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0004g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0004g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0004g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0004g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0004g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0004g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0004g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0004g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0004g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0004g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0004g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0004g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0004g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0004g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0005g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0005g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0005g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0005g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0005g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0005g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0005g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0005g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0006g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0006g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0006g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0006g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0006g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0006g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0006g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0007g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0007g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0007g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0007g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0007g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0007g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0008g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0008g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0008g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0008g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0008g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0008g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0009g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0009g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0009g0114 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0009g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0009g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0010g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0010g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0010g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0010g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0010g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0012g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0012g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0012g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0013g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0013g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0013g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0014g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0014g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0014g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0015g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0015g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0015g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0017g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0017g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0018g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0018g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0019g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0019g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0020g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0021g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0023g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0024g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0025g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0026g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0027g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0028g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0029g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0030g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0031g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0032g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0033g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0034g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0035g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0036g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0037g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0038g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0039g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0040g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0041g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0042g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0044g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0001t0046g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0002t0002g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0002t0002g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0002t0002g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0002t0002g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0002t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0002t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0002t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0002t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0002t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0002t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0002t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0002t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0002t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0002t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0002t0011g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0002t0011g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0002t0011g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0002t0011g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0002t0043g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0002t0045g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0006t0016g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0001c0007t0016g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0002c0003t0004g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0002c0003t0004g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0002c0003t0004g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0002c0003t0004g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0002c0003t0004g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0003c0004t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
a0004c0005t0022g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0077 | EUR | GBR | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG00099 | hp2 | a0001 | c0001 | t0003 | g0163 | EUR | GBR | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG00140 | hp1 | a0001 | c0001 | t0003 | g0243 | EUR | GBR | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG00140 | hp2 | a0001 | c0002 | t0002 | g0249 | EUR | GBR | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG00280 | hp1 | a0001 | c0001 | t0003 | g0230 | EUR | FIN | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0096 | EUR | FIN | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG00323 | hp1 | a0001 | c0001 | t0015 | g0135 | EUR | FIN | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG00323 | hp2 | a0001 | c0002 | t0002 | g0028 | EUR | FIN | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG00408 | hp1 | a0001 | c0002 | t0011 | g0045 | EAS | CHS | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG00408 | hp2 | a0001 | c0001 | t0039 | g0274 | EAS | CHS | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG00423 | hp1 | a0001 | c0002 | t0011 | g0103 | EAS | CHS | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | CHS | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG00558 | hp1 | a0001 | c0002 | t0002 | g0039 | EAS | CHS | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | CHS | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG00609 | hp1 | a0001 | c0002 | t0011 | g0022 | EAS | CHS | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG00642 | hp1 | a0001 | c0001 | t0003 | g0207 | AMR | PUR | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG00642 | hp2 | a0001 | c0002 | t0002 | g0250 | AMR | PUR | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | CHS | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG00673 | hp2 | a0001 | c0002 | t0002 | g0029 | EAS | CHS | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG00733 | hp1 | a0001 | c0002 | t0002 | g0026 | AMR | PUR | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG00735 | hp1 | a0001 | c0001 | t0003 | g0238 | AMR | PUR | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG00735 | hp2 | a0001 | c0001 | t0004 | g0276 | AMR | PUR | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG01069 | hp2 | a0001 | c0001 | t0003 | g0246 | AMR | PUR | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG01070 | hp1 | a0001 | c0002 | t0002 | g0015 | AMR | PUR | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG01070 | hp2 | a0001 | c0001 | t0003 | g0231 | AMR | PUR | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG01071 | hp1 | a0001 | c0001 | t0003 | g0229 | AMR | PUR | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG01071 | hp2 | a0001 | c0002 | t0002 | g0014 | AMR | PUR | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG01081 | hp1 | a0001 | c0001 | t0015 | g0127 | AMR | PUR | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG01081 | hp2 | a0002 | c0003 | t0004 | g0181 | AMR | PUR | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG01106 | hp1 | a0001 | c0001 | t0005 | g0147 | AMR | PUR | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG01106 | hp2 | a0001 | c0001 | t0004 | g0183 | AMR | PUR | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG01169 | hp1 | a0001 | c0001 | t0009 | g0141 | AMR | PUR | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG01169 | hp2 | a0001 | c0001 | t0003 | g0210 | AMR | PUR | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG01192 | hp1 | a0001 | c0001 | t0023 | g0058 | AMR | PUR | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG01192 | hp2 | a0001 | c0001 | t0014 | g0146 | AMR | PUR | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG01243 | hp1 | a0001 | c0001 | t0009 | g0145 | AMR | PUR | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG01243 | hp2 | a0001 | c0001 | t0012 | g0201 | AMR | PUR | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG01256 | hp1 | a0001 | c0001 | t0007 | g0071 | AMR | CLM | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG01256 | hp2 | a0001 | c0001 | t0015 | g0134 | AMR | CLM | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG01257 | hp1 | a0001 | c0001 | t0003 | g0239 | AMR | CLM | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG01257 | hp2 | a0001 | c0002 | t0002 | g0251 | AMR | CLM | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG01261 | hp2 | a0001 | c0001 | t0004 | g0178 | AMR | CLM | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG01346 | hp1 | a0001 | c0002 | t0002 | g0037 | AMR | CLM | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG01346 | hp2 | a0001 | c0001 | t0021 | g0066 | AMR | CLM | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG01361 | hp1 | a0001 | c0001 | t0007 | g0091 | AMR | CLM | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG01361 | hp2 | a0001 | c0001 | t0004 | g0204 | AMR | CLM | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG01433 | hp1 | a0001 | c0001 | t0007 | g0070 | AMR | CLM | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG01433 | hp2 | a0001 | c0002 | t0002 | g0032 | AMR | CLM | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG01496 | hp1 | a0001 | c0001 | t0003 | g0233 | AMR | CLM | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG01496 | hp2 | a0002 | c0003 | t0004 | g0185 | AMR | CLM | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | IBS | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG01515 | hp2 | a0001 | c0002 | t0002 | g0152 | EUR | IBS | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0078 | EUR | IBS | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG01517 | hp2 | a0001 | c0002 | t0002 | g0151 | EUR | IBS | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | ACB | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG01884 | hp2 | a0004 | c0005 | t0022 | g0150 | AFR | ACB | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG01891 | hp2 | a0001 | c0001 | t0004 | g0189 | AFR | ACB | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG01934 | hp1 | a0001 | c0001 | t0004 | g0192 | AMR | PEL | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG01934 | hp2 | a0001 | c0001 | t0003 | g0218 | AMR | PEL | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG01943 | hp1 | a0001 | c0001 | t0004 | g0193 | AMR | PEL | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG01943 | hp2 | a0001 | c0001 | t0003 | g0240 | AMR | PEL | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PEL | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG01952 | hp2 | a0002 | c0003 | t0004 | g0184 | AMR | PEL | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG01975 | hp1 | a0001 | c0001 | t0007 | g0092 | AMR | PEL | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG01975 | hp2 | a0001 | c0001 | t0042 | g0154 | AMR | PEL | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG01978 | hp1 | a0001 | c0001 | t0004 | g0191 | AMR | PEL | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | PEL | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG01981 | hp1 | a0001 | c0002 | t0002 | g0253 | AMR | PEL | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG01981 | hp2 | a0001 | c0001 | t0027 | g0176 | AMR | PEL | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG01993 | hp1 | a0001 | c0001 | t0003 | g0217 | AMR | PEL | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG01993 | hp2 | a0002 | c0003 | t0004 | g0180 | AMR | PEL | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG02015 | hp1 | a0001 | c0002 | t0002 | g0042 | EAS | KHV | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG02015 | hp2 | a0001 | c0001 | t0006 | g0172 | EAS | KHV | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG02055 | hp2 | a0001 | c0001 | t0005 | g0018 | AFR | ACB | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG02074 | hp2 | a0001 | c0002 | t0002 | g0123 | EAS | KHV | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG02080 | hp2 | a0001 | c0002 | t0002 | g0030 | EAS | KHV | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG02145 | hp1 | a0001 | c0001 | t0013 | g0263 | AFR | ACB | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG02145 | hp2 | a0001 | c0001 | t0004 | g0269 | AFR | ACB | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG02155 | hp1 | a0001 | c0001 | t0003 | g0232 | EAS | CDX | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG02155 | hp2 | a0001 | c0002 | t0002 | g0040 | EAS | CDX | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG02257 | hp2 | a0001 | c0001 | t0030 | g0001 | AFR | ACB | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG02258 | hp1 | a0001 | c0007 | t0016 | g0278 | AFR | ACB | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG02258 | hp2 | a0001 | c0001 | t0004 | g0206 | AFR | ACB | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG02273 | hp1 | a0001 | c0001 | t0004 | g0199 | AMR | PEL | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG02273 | hp2 | a0001 | c0001 | t0007 | g0079 | AMR | PEL | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | PEL | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG02293 | hp2 | a0002 | c0003 | t0004 | g0179 | AMR | PEL | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG02451 | hp1 | a0003 | c0004 | t0001 | g0108 | AFR | ACB | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG02572 | hp1 | a0001 | c0001 | t0031 | g0149 | AFR | GWD | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG02572 | hp2 | a0001 | c0001 | t0033 | g0200 | AFR | GWD | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG02615 | hp1 | a0001 | c0001 | t0004 | g0182 | AFR | GWD | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG02622 | hp1 | a0001 | c0001 | t0032 | g0202 | AFR | GWD | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | GWD | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG02630 | hp2 | a0001 | c0001 | t0004 | g0196 | AFR | GWD | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG02647 | hp1 | a0001 | c0001 | t0010 | g0006 | AFR | GWD | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG02683 | hp1 | a0001 | c0001 | t0026 | g0155 | SAS | PJL | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG02683 | hp2 | a0001 | c0002 | t0002 | g0252 | SAS | PJL | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0259 | SAS | PJL | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG02698 | hp2 | a0001 | c0001 | t0004 | g0188 | SAS | PJL | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG02717 | hp2 | a0001 | c0006 | t0016 | g0277 | AFR | GWD | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG02723 | hp1 | a0001 | c0001 | t0025 | g0168 | AFR | GWD | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG02723 | hp2 | a0001 | c0001 | t0004 | g0198 | AFR | GWD | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG02738 | hp2 | a0001 | c0001 | t0037 | g0219 | SAS | PJL | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG02809 | hp1 | a0001 | c0001 | t0009 | g0111 | AFR | GWD | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG02895 | hp1 | a0001 | c0001 | t0017 | g0161 | AFR | GWD | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG02895 | hp2 | a0001 | c0001 | t0041 | g0156 | AFR | GWD | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG02896 | hp1 | a0001 | c0001 | t0035 | g0195 | AFR | GWD | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG02896 | hp2 | a0001 | c0001 | t0010 | g0002 | AFR | GWD | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG02897 | hp1 | a0001 | c0001 | t0010 | g0003 | AFR | GWD | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG02897 | hp2 | a0001 | c0001 | t0017 | g0162 | AFR | GWD | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG02922 | hp1 | a0001 | c0001 | t0009 | g0113 | AFR | ESN | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG02922 | hp2 | a0001 | c0001 | t0005 | g0017 | AFR | ESN | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | ESN | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG02965 | hp2 | a0001 | c0001 | t0024 | g0009 | AFR | ESN | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG02970 | hp1 | a0001 | c0001 | t0046 | g0109 | AFR | ESN | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ESN | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG02976 | hp1 | a0001 | c0001 | t0018 | g0023 | AFR | ESN | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | ESN | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG03041 | hp1 | a0001 | c0001 | t0013 | g0265 | AFR | GWD | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG03130 | hp1 | a0001 | c0001 | t0004 | g0190 | AFR | ESN | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG03130 | hp2 | a0001 | c0001 | t0010 | g0005 | AFR | ESN | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG03139 | hp1 | a0001 | c0001 | t0018 | g0270 | AFR | ESN | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ESN | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG03195 | hp1 | a0001 | c0001 | t0010 | g0004 | AFR | ESN | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG03195 | hp2 | a0001 | c0001 | t0004 | g0203 | AFR | ESN | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | MSL | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | MSL | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | MSL | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | MSL | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG03453 | hp1 | a0001 | c0001 | t0005 | g0016 | AFR | MSL | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG03453 | hp2 | a0001 | c0001 | t0012 | g0194 | AFR | MSL | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG03486 | hp1 | a0001 | c0001 | t0028 | g0061 | AFR | MSL | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG03486 | hp2 | a0001 | c0001 | t0012 | g0205 | AFR | MSL | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG03491 | hp2 | a0001 | c0001 | t0019 | g0261 | SAS | PJL | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG03492 | hp1 | a0001 | c0001 | t0019 | g0260 | SAS | PJL | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG03516 | hp1 | a0001 | c0001 | t0005 | g0153 | AFR | ESN | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG03516 | hp2 | a0001 | c0001 | t0029 | g0272 | AFR | ESN | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG03540 | hp2 | a0001 | c0001 | t0013 | g0264 | AFR | GWD | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | MSL | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG03579 | hp2 | a0001 | c0001 | t0005 | g0021 | AFR | MSL | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG03710 | hp1 | a0001 | c0001 | t0040 | g0136 | SAS | PJL | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG03831 | hp1 | a0001 | c0001 | t0014 | g0223 | SAS | BEB | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG03831 | hp2 | a0001 | c0001 | t0003 | g0115 | SAS | BEB | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG03834 | hp1 | a0001 | c0001 | t0003 | g0227 | SAS | BEB | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG03834 | hp2 | a0001 | c0002 | t0045 | g0035 | SAS | BEB | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | BEB | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG03927 | hp2 | a0001 | c0001 | t0006 | g0169 | SAS | BEB | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG04115 | hp1 | a0001 | c0001 | t0003 | g0242 | SAS | STU | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG04115 | hp2 | a0001 | c0002 | t0002 | g0033 | SAS | STU | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG04184 | hp1 | a0001 | c0001 | t0004 | g0177 | SAS | BEB | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG04184 | hp2 | a0001 | c0001 | t0003 | g0222 | SAS | BEB | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | STU | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG04199 | hp2 | a0001 | c0002 | t0002 | g0257 | SAS | STU | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG04204 | hp1 | a0001 | c0001 | t0003 | g0220 | SAS | STU | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | STU | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | STU | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | STU | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA18522 | hp1 | a0001 | c0001 | t0004 | g0197 | AFR | YRI | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA18522 | hp2 | a0001 | c0001 | t0003 | g0112 | AFR | YRI | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA18747 | hp1 | a0001 | c0001 | t0006 | g0235 | EAS | CHB | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA18747 | hp2 | a0001 | c0001 | t0003 | g0166 | EAS | CHB | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | YRI | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA18906 | hp2 | a0001 | c0001 | t0034 | g0024 | AFR | YRI | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA18939 | hp1 | a0001 | c0002 | t0002 | g0131 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA18941 | hp1 | a0001 | c0001 | t0008 | g0215 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA18941 | hp2 | a0001 | c0001 | t0006 | g0174 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA18943 | hp1 | a0001 | c0001 | t0006 | g0047 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA18943 | hp2 | a0001 | c0002 | t0002 | g0170 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA18948 | hp1 | a0001 | c0002 | t0002 | g0052 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA18950 | hp1 | a0001 | c0001 | t0003 | g0244 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA18951 | hp1 | a0001 | c0001 | t0008 | g0214 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA18952 | hp1 | a0001 | c0002 | t0002 | g0043 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA18964 | hp1 | a0001 | c0002 | t0002 | g0051 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA18966 | hp2 | a0001 | c0001 | t0003 | g0224 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA18969 | hp1 | a0001 | c0002 | t0002 | g0050 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA18974 | hp2 | a0001 | c0001 | t0003 | g0236 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA18975 | hp1 | a0001 | c0001 | t0003 | g0237 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA18977 | hp2 | a0001 | c0002 | t0002 | g0031 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA18980 | hp1 | a0001 | c0001 | t0003 | g0221 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA18982 | hp2 | a0001 | c0001 | t0003 | g0234 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA18983 | hp2 | a0001 | c0002 | t0002 | g0048 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA18986 | hp1 | a0001 | c0001 | t0003 | g0211 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA18986 | hp2 | a0001 | c0002 | t0043 | g0038 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA18987 | hp1 | a0001 | c0002 | t0002 | g0060 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA18991 | hp1 | a0001 | c0001 | t0006 | g0171 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA18995 | hp2 | a0001 | c0001 | t0003 | g0241 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA18998 | hp1 | a0001 | c0001 | t0008 | g0271 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA19003 | hp1 | a0001 | c0002 | t0002 | g0046 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA19003 | hp2 | a0001 | c0001 | t0038 | g0248 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA19007 | hp1 | a0001 | c0001 | t0008 | g0216 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA19009 | hp1 | a0001 | c0001 | t0007 | g0073 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA19009 | hp2 | a0001 | c0002 | t0002 | g0049 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA19011 | hp1 | a0001 | c0002 | t0011 | g0044 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA19011 | hp2 | a0001 | c0001 | t0008 | g0212 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA19012 | hp1 | a0001 | c0002 | t0002 | g0041 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA19063 | hp1 | a0001 | c0002 | t0002 | g0036 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA19065 | hp1 | a0001 | c0002 | t0002 | g0034 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA19065 | hp2 | a0001 | c0001 | t0006 | g0173 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA19068 | hp1 | a0001 | c0001 | t0003 | g0209 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA19074 | hp1 | a0001 | c0001 | t0044 | g0262 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA19077 | hp2 | a0001 | c0001 | t0003 | g0226 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA19081 | hp2 | a0001 | c0001 | t0003 | g0245 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA19085 | hp1 | a0001 | c0001 | t0008 | g0213 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA20129 | hp1 | a0001 | c0002 | t0002 | g0254 | AFR | ASW | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA20129 | hp2 | a0001 | c0001 | t0004 | g0186 | AFR | ASW | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA20752 | hp1 | a0001 | c0002 | t0002 | g0148 | EUR | TSI | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | TSI | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG01123 | hp1 | a0001 | c0001 | t0014 | g0119 | AMR | CLM | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | ACB | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG02486 | hp1 | a0001 | c0001 | t0005 | g0020 | AFR | ACB | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG02486 | hp2 | a0001 | c0001 | t0003 | g0053 | AFR | ACB | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG02559 | hp1 | a0001 | c0001 | t0005 | g0019 | AFR | ACB | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG02559 | hp2 | a0001 | c0001 | t0020 | g0273 | AFR | ACB | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG06807 | hp1 | a0001 | c0001 | t0003 | g0208 | AFR | USA | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | USA | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA18955 | hp1 | a0001 | c0001 | t0003 | g0225 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
NA18955 | hp2 | a0001 | c0001 | t0036 | g0247 | EAS | JPT | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0117 | REF | REF | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0009 | g0114 | REF | REF | WDFY2_chr13_51579462_51772709 | WDFY2 | chr13 | 51579462 | 51772709 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:51719321 | G | A | 1 | a0003 | 1 | HG02451.hp1 | missense_variant | MODERATE | c.458G>A | p.Arg153Gln | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/12 | 684/9369 | 458/1203 | 153/400 | chr13 | 51719321 | ||
chr13:51739117 | G | A | 1 | a0004 | 1 | HG01884.hp2 | missense_variant | MODERATE | c.667G>A | p.Val223Ile | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/12 | 893/9369 | 667/1203 | 223/400 | chr13 | 51739117 | ||
chr13:51758193 | C | T | 1 | a0002 | 5 | HG01081.hp2 HG01496.hp2 HG01952.hp2 others(2): Show |
missense_variant&splice_region_variant | MODERATE | c.1066C>T | p.Arg356Cys | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 11/12 | 1292/9369 | 1066/1203 | 356/400 | chr13 | 51758193 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:51584744 | G | T | 1 | a0001c0007 | 1 | HG02258.hp1 | synonymous_variant | LOW | c.57G>T | p.Arg19Arg | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/12 | 283/9369 | 57/1203 | 19/400 | chr13 | 51584744 | ||
chr13:51719268 | C | T | 1 | a0001c0006 | 1 | HG02717.hp2 | synonymous_variant | LOW | c.405C>T | p.Asp135Asp | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/12 | 631/9369 | 405/1203 | 135/400 | chr13 | 51719268 | ||
chr13:51739059 | C | T | 1 | a0001c0002 | 43 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(40): Show |
synonymous_variant | LOW | c.609C>T | p.Thr203Thr | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/12 | 835/9369 | 609/1203 | 203/400 | chr13 | 51739059 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:51584576 | G | A | 1 | a0001c0001t0005 | 8 | HG01106.hp1 HG02055.hp2 HG02486.hp1 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-112G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/12 | 112 | chr13 | 51584576 | |||||
chr13:51759812 | C | T | 1 | a0001c0001t0046 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*43C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 12/12 | 43 | chr13 | 51759812 | |||||
chr13:51759819 | TTTAACCC others(6): Show |
T | 7 | a0001c0001t0002a0001c0001t0019a0001c0001t0044others(4): Show | 48 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*54_*66delACCCAAAT others(5): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 12/12 | 54 | INFO_REALIGN_3_PRIME | chr13 | 51759819 | ||||
chr13:51759936 | G | C | 1 | a0001c0001t0012 | 3 | HG01243.hp2 HG03453.hp2 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*167G>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 12/12 | 167 | chr13 | 51759936 | |||||
chr13:51760043 | G | A | 1 | a0001c0001t0020 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*274G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 12/12 | 274 | chr13 | 51760043 | |||||
chr13:51760275 | G | T | 1 | a0001c0001t0042 | 1 | HG01975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*506G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 12/12 | 506 | chr13 | 51760275 | |||||
chr13:51760474 | A | G | 1 | a0001c0001t0041 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*705A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 12/12 | 705 | chr13 | 51760474 | |||||
chr13:51760483 | C | T | 7 | a0001c0001t0003a0001c0001t0008a0001c0001t0036others(4): Show | 47 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*714C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 12/12 | 714 | chr13 | 51760483 | |||||
chr13:51760600 | G | A | 1 | a0001c0001t0021 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*831G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 12/12 | 831 | chr13 | 51760600 | |||||
chr13:51760662 | G | A | 1 | a0004c0005t0022 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*893G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 12/12 | 893 | chr13 | 51760662 | |||||
chr13:51761065 | T | C | 8 | a0001c0001t0002a0001c0001t0019a0001c0001t0044others(5): Show | 49 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*1296T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 12/12 | 1296 | chr13 | 51761065 | |||||
chr13:51761389 | C | T | 1 | a0001c0001t0040 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1620C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 12/12 | 1620 | chr13 | 51761389 | |||||
chr13:51761449 | G | A | 1 | a0004c0005t0022 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1680G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 12/12 | 1680 | chr13 | 51761449 | |||||
chr13:51761629 | C | T | 7 | a0001c0001t0002a0001c0001t0019a0001c0001t0044others(4): Show | 48 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*1860C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 12/12 | 1860 | chr13 | 51761629 | |||||
chr13:51761724 | A | G | 11 | a0001c0001t0004a0001c0001t0005a0001c0001t0012others(8): Show | 44 | HG00735.hp2 HG01081.hp2 HG01106.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*1955A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 12/12 | 1955 | chr13 | 51761724 | |||||
chr13:51761799 | C | T | 1 | a0004c0005t0022 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2030C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 12/12 | 2030 | chr13 | 51761799 | |||||
chr13:51761916 | C | T | 2 | a0001c0001t0010a0001c0001t0030 | 6 | HG02257.hp2 HG02647.hp1 HG02896.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2147C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 12/12 | 2147 | chr13 | 51761916 | |||||
chr13:51762384 | G | A | 1 | a0004c0005t0022 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2615G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 12/12 | 2615 | chr13 | 51762384 | |||||
chr13:51762438 | A | G | 2 | a0001c0001t0020a0001c0001t0029 | 2 | HG02559.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2669A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 12/12 | 2669 | chr13 | 51762438 | |||||
chr13:51762499 | C | T | 1 | a0001c0002t0011 | 4 | HG00408.hp1 HG00423.hp1 HG00609.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2730C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 12/12 | 2730 | chr13 | 51762499 | |||||
chr13:51762825 | C | G | 1 | a0001c0001t0039 | 1 | HG00408.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3056C>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 12/12 | 3056 | chr13 | 51762825 | |||||
chr13:51762894 | C | T | 1 | a0001c0001t0035 | 1 | HG02896.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3125C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 12/12 | 3125 | chr13 | 51762894 | |||||
chr13:51763163 | T | C | 1 | a0001c0001t0023 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3394T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 12/12 | 3394 | chr13 | 51763163 | |||||
chr13:51763313 | G | C | 1 | a0001c0001t0024 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3544G>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 12/12 | 3544 | chr13 | 51763313 | |||||
chr13:51763672 | C | G | 1 | a0001c0002t0045 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3903C>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 12/12 | 3903 | chr13 | 51763672 | |||||
chr13:51763703 | C | T | 2 | a0001c0001t0028a0001c0001t0041 | 2 | HG02895.hp2 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3934C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 12/12 | 3934 | chr13 | 51763703 | |||||
chr13:51763743 | A | G | 1 | a0001c0001t0034 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3974A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 12/12 | 3974 | chr13 | 51763743 | |||||
chr13:51763751 | T | C | 1 | a0001c0001t0031 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3982T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 12/12 | 3982 | chr13 | 51763751 | |||||
chr13:51763966 | A | G | 2 | a0001c0001t0007a0001c0001t0027 | 7 | HG01256.hp1 HG01361.hp1 HG01433.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4197A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 12/12 | 4197 | chr13 | 51763966 | |||||
chr13:51764218 | TGCAAGGT others(37): Show |
T | 1 | a0001c0001t0036 | 1 | NA18955.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4450_*4493delGCAA others(40): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 12/12 | 4450 | chr13 | 51764218 | |||||
chr13:51764419 | G | T | 1 | a0001c0001t0026 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4650G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 12/12 | 4650 | chr13 | 51764419 | |||||
chr13:51764587 | C | T | 2 | a0001c0001t0010a0001c0001t0030 | 6 | HG02257.hp2 HG02647.hp1 HG02896.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4818C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 12/12 | 4818 | chr13 | 51764587 | |||||
chr13:51764588 | C | T | 1 | a0001c0001t0027 | 1 | HG01981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4819C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 12/12 | 4819 | chr13 | 51764588 | |||||
chr13:51764674 | A | G | 2 | a0001c0001t0036a0001c0001t0038 | 2 | NA18955.hp2 NA19003.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4905A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 12/12 | 4905 | chr13 | 51764674 | |||||
chr13:51764914 | A | G | 20 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(17): Show | 99 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*5145A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 12/12 | 5145 | chr13 | 51764914 | |||||
chr13:51765007 | C | G | 7 | a0001c0001t0002a0001c0001t0019a0001c0001t0044others(4): Show | 48 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*5238C>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 12/12 | 5238 | chr13 | 51765007 | |||||
chr13:51765087 | C | T | 1 | a0001c0001t0025 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5318C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 12/12 | 5318 | chr13 | 51765087 | |||||
chr13:51765295 | C | T | 1 | a0001c0001t0033 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5526C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 12/12 | 5526 | chr13 | 51765295 | |||||
chr13:51765558 | C | T | 2 | a0001c0001t0010a0001c0001t0030 | 6 | HG02257.hp2 HG02647.hp1 HG02896.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5789C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 12/12 | 5789 | chr13 | 51765558 | |||||
chr13:51765614 | C | G | 7 | a0001c0001t0002a0001c0001t0019a0001c0001t0044others(4): Show | 48 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*5845C>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 12/12 | 5845 | chr13 | 51765614 | |||||
chr13:51766229 | C | T | 1 | a0001c0001t0015 | 3 | HG00323.hp1 HG01081.hp1 HG01256.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6460C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 12/12 | 6460 | chr13 | 51766229 | |||||
chr13:51766263 | C | T | 1 | a0001c0001t0017 | 2 | HG02895.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6494C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 12/12 | 6494 | chr13 | 51766263 | |||||
chr13:51766317 | C | T | 1 | a0001c0001t0006 | 7 | HG02015.hp2 HG03927.hp2 NA18747.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*6548C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 12/12 | 6548 | chr13 | 51766317 | |||||
chr13:51766467 | GCTGAGAA others(44): Show |
G | 1 | a0001c0001t0037 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6699_*6749delCTGA others(47): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 12/12 | 6699 | chr13 | 51766467 | |||||
chr13:51766585 | G | T | 3 | a0001c0001t0005a0001c0001t0018a0001c0001t0031 | 11 | HG01106.hp1 HG02055.hp2 HG02486.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*6816G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 12/12 | 6816 | chr13 | 51766585 | |||||
chr13:51766614 | A | G | 49 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(46): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
3_prime_UTR_variant | MODIFIER | c.*6845A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 12/12 | 6845 | chr13 | 51766614 | |||||
chr13:51766629 | T | G | 1 | a0001c0002t0043 | 1 | NA18986.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6860T>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 12/12 | 6860 | chr13 | 51766629 | |||||
chr13:51766635 | C | A | 1 | a0001c0001t0019 | 2 | HG03491.hp2 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6866C>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 12/12 | 6866 | chr13 | 51766635 | |||||
chr13:51766726 | A | G | 1 | a0001c0001t0030 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6957A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 12/12 | 6957 | chr13 | 51766726 | |||||
chr13:51766751 | G | A | 1 | a0001c0001t0013 | 3 | HG02145.hp1 HG03041.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6982G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 12/12 | 6982 | chr13 | 51766751 | |||||
chr13:51766780 | T | C | 1 | a0001c0001t0044 | 1 | NA19074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7011T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 12/12 | 7011 | chr13 | 51766780 | |||||
chr13:51766832 | G | A | 4 | a0001c0001t0005a0001c0001t0018a0001c0001t0031others(1): Show | 12 | HG01106.hp1 HG02055.hp2 HG02486.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*7063G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 12/12 | 7063 | chr13 | 51766832 | |||||
chr13:51767045 | T | C | 20 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(17): Show | 99 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*7276T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 12/12 | 7276 | chr13 | 51767045 | |||||
chr13:51767179 | T | C | 1 | a0001c0001t0046 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7410T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 12/12 | 7410 | chr13 | 51767179 | |||||
chr13:51767246 | C | T | 2 | a0001c0001t0010a0001c0001t0030 | 6 | HG02257.hp2 HG02647.hp1 HG02896.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*7477C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 12/12 | 7477 | chr13 | 51767246 | |||||
chr13:51767436 | G | A | 1 | a0001c0001t0014 | 3 | HG01123.hp1 HG01192.hp2 HG03831.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7667G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 12/12 | 7667 | chr13 | 51767436 | |||||
chr13:51767652 | C | T | 3 | a0001c0006t0016a0001c0007t0016a0004c0005t0022 | 3 | HG01884.hp2 HG02258.hp1 HG02717.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7883C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 12/12 | 7883 | chr13 | 51767652 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:51584918 | G | A | 6 | a0001c0001t0010g0002a0001c0001t0010g0003a0001c0001t0010g0004others(3): Show | 6 | HG02257.hp2 HG02647.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.137+94G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51584918 | ||||||
chr13:51585018 | C | T | 2 | a0001c0006t0016g0277a0001c0007t0016g0278 | 2 | HG02258.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.137+194C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51585018 | ||||||
chr13:51585033 | C | T | 1 | a0001c0001t0004g0276 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.137+209C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51585033 | ||||||
chr13:51585271 | C | T | 1 | a0001c0001t0001g0275 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.137+447C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51585271 | ||||||
chr13:51585472 | G | A | 1 | a0001c0001t0001g0007 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.137+648G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51585472 | ||||||
chr13:51585553 | A | G | 1 | a0001c0001t0039g0274 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.137+729A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51585553 | ||||||
chr13:51585750 | T | C | 1 | a0001c0001t0001g0008 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.137+926T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51585750 | ||||||
chr13:51585940 | G | T | 2 | a0001c0001t0020g0273a0001c0001t0029g0272 | 2 | HG02559.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.137+1116G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51585940 | ||||||
chr13:51586327 | T | G | 4 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0275others(1): Show | 4 | HG00733.hp2 HG01123.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.137+1503T>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51586327 | ||||||
chr13:51586787 | C | T | 1 | a0001c0001t0008g0271 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.137+1963C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51586787 | ||||||
chr13:51586917 | G | C | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | NA19012.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.137+2093G>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51586917 | ||||||
chr13:51586952 | G | T | 1 | a0001c0001t0018g0270 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.137+2128G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51586952 | ||||||
chr13:51587095 | C | T | 4 | a0001c0001t0001g0266a0001c0001t0001g0267a0001c0001t0001g0268others(1): Show | 4 | HG02109.hp2 HG02145.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.137+2271C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51587095 | ||||||
chr13:51587189 | C | T | 3 | a0001c0001t0013g0263a0001c0001t0013g0264a0001c0001t0013g0265 | 3 | HG02145.hp1 HG03041.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.137+2365C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51587189 | ||||||
chr13:51587515 | A | G | 5 | a0001c0001t0001g0258a0001c0001t0002g0259a0001c0001t0019g0260others(2): Show | 5 | HG01069.hp1 HG02698.hp1 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.137+2691A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51587515 | ||||||
chr13:51587570 | A | G | 1 | a0001c0002t0002g0257 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.137+2746A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51587570 | ||||||
chr13:51587637 | C | T | 1 | a0001c0001t0004g0269 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.137+2813C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51587637 | ||||||
chr13:51587746 | A | G | 2 | a0001c0001t0001g0255a0001c0001t0001g0256 | 2 | HG01978.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.137+2922A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51587746 | ||||||
chr13:51587833 | C | T | 6 | a0001c0002t0002g0249a0001c0002t0002g0250a0001c0002t0002g0251others(3): Show | 6 | HG00140.hp2 HG00642.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.137+3009C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51587833 | ||||||
chr13:51587834 | G | A | 1 | a0001c0001t0030g0001 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.137+3010G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51587834 | ||||||
chr13:51587874 | C | T | 44 | a0001c0001t0001g0228a0001c0001t0003g0207a0001c0001t0003g0208others(41): Show | 44 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.137+3050C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51587874 | ||||||
chr13:51588612 | G | A | 1 | a0001c0002t0002g0249 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.137+3788G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51588612 | ||||||
chr13:51588649 | G | A | 2 | a0001c0002t0002g0014a0001c0002t0002g0015 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.137+3825G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51588649 | ||||||
chr13:51588792 | G | A | 1 | a0001c0006t0016g0277 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.137+3968G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51588792 | ||||||
chr13:51588930 | T | G | 2 | a0001c0001t0003g0207a0001c0001t0003g0208 | 2 | HG00642.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.137+4106T>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51588930 | ||||||
chr13:51589066 | A | G | 32 | a0001c0001t0001g0187a0001c0001t0004g0177a0001c0001t0004g0178others(29): Show | 32 | HG00735.hp2 HG01081.hp2 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.137+4242A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51589066 | ||||||
chr13:51589099 | A | G | 2 | a0001c0001t0020g0273a0001c0001t0029g0272 | 2 | HG02559.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.137+4275A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51589099 | ||||||
chr13:51589314 | G | A | 6 | a0001c0001t0010g0002a0001c0001t0010g0003a0001c0001t0010g0004others(3): Show | 6 | HG02257.hp2 HG02647.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.137+4490G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51589314 | ||||||
chr13:51589316 | G | A | 1 | a0001c0001t0024g0009 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.137+4492G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51589316 | ||||||
chr13:51589398 | C | T | 1 | a0001c0001t0001g0275 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.137+4574C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51589398 | ||||||
chr13:51589403 | T | C | 1 | a0001c0006t0016g0277 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.137+4579T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51589403 | ||||||
chr13:51589682 | T | C | 1 | a0001c0001t0001g0007 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.137+4858T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51589682 | ||||||
chr13:51590053 | T | C | 1 | a0001c0001t0003g0209 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.137+5229T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51590053 | ||||||
chr13:51590159 | A | C | 1 | a0001c0001t0024g0009 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.137+5335A>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51590159 | ||||||
chr13:51590188 | A | T | 13 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0167others(10): Show | 13 | HG00099.hp2 HG02015.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.137+5364A>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51590188 | ||||||
chr13:51590351 | A | G | 6 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159others(3): Show | 6 | HG02630.hp1 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.137+5527A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51590351 | ||||||
chr13:51590461 | A | G | 1 | a0001c0001t0041g0156 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.137+5637A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51590461 | ||||||
chr13:51590771 | A | T | 2 | a0001c0001t0036g0247a0001c0001t0038g0248 | 2 | NA18955.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.137+5947A>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51590771 | ||||||
chr13:51590881 | A | T | 1 | a0001c0001t0026g0155 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.137+6057A>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51590881 | ||||||
chr13:51590936 | G | T | 1 | a0001c0001t0042g0154 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.137+6112G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51590936 | ||||||
chr13:51591020 | A | G | 1 | a0001c0001t0005g0153 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.137+6196A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51591020 | ||||||
chr13:51591267 | A | G | 4 | a0001c0001t0001g0266a0001c0001t0001g0267a0001c0001t0001g0268others(1): Show | 4 | HG02109.hp2 HG02145.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.137+6443A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51591267 | ||||||
chr13:51591396 | T | C | 4 | a0001c0001t0001g0266a0001c0001t0001g0267a0001c0001t0001g0268others(1): Show | 4 | HG02109.hp2 HG02145.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.137+6572T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51591396 | ||||||
chr13:51591442 | G | A | 2 | a0001c0001t0010g0002a0001c0001t0010g0003 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.137+6618G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51591442 | ||||||
chr13:51591573 | A | C | 2 | a0001c0002t0002g0151a0001c0002t0002g0152 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.137+6749A>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51591573 | ||||||
chr13:51591817 | C | T | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.137+6993C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51591817 | ||||||
chr13:51592007 | G | C | 32 | a0001c0001t0001g0187a0001c0001t0004g0177a0001c0001t0004g0178others(29): Show | 32 | HG00735.hp2 HG01081.hp2 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.137+7183G>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51592007 | ||||||
chr13:51592023 | A | G | 1 | a0001c0001t0031g0149 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.137+7199A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51592023 | ||||||
chr13:51592055 | A | T | 1 | a0001c0001t0003g0246 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.137+7231A>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51592055 | ||||||
chr13:51592056 | T | G | 1 | a0001c0001t0003g0246 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.137+7232T>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51592056 | ||||||
chr13:51592062 | T | G | 1 | a0001c0001t0003g0246 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.137+7238T>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51592062 | ||||||
chr13:51592063 | A | T | 1 | a0001c0001t0003g0246 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.137+7239A>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51592063 | ||||||
chr13:51592075 | T | G | 1 | a0001c0001t0003g0246 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.137+7251T>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51592075 | ||||||
chr13:51592077 | G | C | 1 | a0001c0001t0003g0246 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.137+7253G>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51592077 | ||||||
chr13:51592081 | A | T | 1 | a0001c0001t0003g0246 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.137+7257A>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51592081 | ||||||
chr13:51592085 | A | G | 1 | a0001c0001t0003g0246 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.137+7261A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51592085 | ||||||
chr13:51592091 | A | T | 1 | a0001c0001t0003g0246 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.137+7267A>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51592091 | ||||||
chr13:51592098 | A | G | 1 | a0001c0001t0003g0246 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.137+7274A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51592098 | ||||||
chr13:51592102 | C | G | 1 | a0001c0001t0003g0246 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.137+7278C>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51592102 | ||||||
chr13:51592105 | C | T | 1 | a0001c0001t0003g0246 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.137+7281C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51592105 | ||||||
chr13:51592106 | A | T | 1 | a0001c0001t0003g0246 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.137+7282A>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51592106 | ||||||
chr13:51592115 | A | T | 4 | a0001c0001t0001g0266a0001c0001t0001g0267a0001c0001t0001g0268others(1): Show | 4 | HG02109.hp2 HG02145.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.137+7291A>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51592115 | ||||||
chr13:51592136 | G | T | 1 | a0001c0001t0003g0246 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.137+7312G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51592136 | ||||||
chr13:51592141 | A | G | 1 | a0001c0001t0003g0246 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.137+7317A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51592141 | ||||||
chr13:51592143 | A | G | 1 | a0001c0001t0003g0246 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.137+7319A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51592143 | ||||||
chr13:51592144 | A | T | 1 | a0001c0001t0003g0246 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.137+7320A>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51592144 | ||||||
chr13:51592149 | A | T | 1 | a0001c0001t0003g0246 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.137+7325A>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51592149 | ||||||
chr13:51592150 | A | G | 1 | a0001c0001t0003g0246 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.137+7326A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51592150 | ||||||
chr13:51592151 | A | T | 1 | a0001c0001t0003g0246 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.137+7327A>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51592151 | ||||||
chr13:51592152 | A | G | 1 | a0001c0002t0002g0148 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.137+7328A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51592152 | ||||||
chr13:51592152 | A | T | 1 | a0001c0001t0003g0246 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.137+7328A>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51592152 | ||||||
chr13:51592154 | A | G | 1 | a0001c0001t0003g0246 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.137+7330A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51592154 | ||||||
chr13:51592155 | A | T | 1 | a0001c0001t0003g0246 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.137+7331A>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51592155 | ||||||
chr13:51592209 | G | C | 5 | a0001c0001t0001g0258a0001c0001t0002g0259a0001c0001t0019g0260others(2): Show | 5 | HG01069.hp1 HG02698.hp1 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.137+7385G>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51592209 | ||||||
chr13:51592545 | A | G | 1 | a0001c0001t0005g0147 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.137+7721A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51592545 | ||||||
chr13:51592960 | G | A | 169 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(166): Show | 169 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.137+8136G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51592960 | ||||||
chr13:51593045 | T | C | 8 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(5): Show | 8 | HG01106.hp1 HG02055.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.137+8221T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51593045 | ||||||
chr13:51593092 | G | A | 4 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0275others(1): Show | 4 | HG00733.hp2 HG01123.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.137+8268G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51593092 | ||||||
chr13:51593861 | T | C | 1 | a0001c0001t0003g0210 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.137+9037T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51593861 | ||||||
chr13:51594629 | G | A | 4 | a0001c0001t0001g0266a0001c0001t0001g0267a0001c0001t0001g0268others(1): Show | 4 | HG02109.hp2 HG02145.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.137+9805G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51594629 | ||||||
chr13:51594657 | T | G | 176 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(173): Show | 176 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.137+9833T>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51594657 | ||||||
chr13:51594765 | C | T | 2 | a0001c0001t0020g0273a0001c0001t0029g0272 | 2 | HG02559.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.137+9941C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51594765 | ||||||
chr13:51594800 | TCCTGCAG others(2): Show |
T | 11 | a0001c0001t0001g0104a0001c0001t0001g0175a0001c0001t0003g0245others(8): Show | 11 | HG00423.hp1 HG02015.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.137+9996_137+10004 others(12): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr13 | 51594800 | |||||
chr13:51595054 | T | C | 3 | a0001c0001t0013g0263a0001c0001t0013g0264a0001c0001t0013g0265 | 3 | HG02145.hp1 HG03041.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.137+10230T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51595054 | ||||||
chr13:51595198 | C | T | 1 | a0001c0001t0014g0146 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.137+10374C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51595198 | ||||||
chr13:51595497 | G | A | 1 | a0001c0001t0003g0211 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.137+10673G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51595497 | ||||||
chr13:51595568 | A | G | 274 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(271): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.137+10744A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51595568 | ||||||
chr13:51595571 | T | G | 5 | a0001c0001t0008g0212a0001c0001t0008g0213a0001c0001t0008g0214others(2): Show | 5 | NA18941.hp1 NA18951.hp1 NA19007.hp1 others(2): Show |
intron_variant | MODIFIER | c.137+10747T>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51595571 | ||||||
chr13:51596043 | C | T | 1 | a0001c0001t0012g0205 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.137+11219C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51596043 | ||||||
chr13:51596100 | G | A | 2 | a0001c0001t0018g0270a0001c0002t0011g0022 | 2 | HG00609.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.137+11276G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51596100 | ||||||
chr13:51596482 | C | T | 176 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(173): Show | 176 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.137+11658C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51596482 | ||||||
chr13:51596705 | G | T | 1 | a0001c0001t0003g0244 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.137+11881G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51596705 | ||||||
chr13:51596985 | G | A | 9 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(6): Show | 9 | HG01123.hp1 HG01192.hp2 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.137+12161G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51596985 | ||||||
chr13:51597169 | C | T | 2 | a0001c0006t0016g0277a0001c0007t0016g0278 | 2 | HG02258.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.137+12345C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51597169 | ||||||
chr13:51597182 | A | G | 5 | a0001c0001t0001g0258a0001c0001t0002g0259a0001c0001t0019g0260others(2): Show | 5 | HG01069.hp1 HG02698.hp1 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.137+12358A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51597182 | ||||||
chr13:51597390 | G | A | 2 | a0001c0006t0016g0277a0001c0007t0016g0278 | 2 | HG02258.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.137+12566G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51597390 | ||||||
chr13:51597549 | T | G | 1 | a0001c0001t0031g0149 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.137+12725T>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51597549 | ||||||
chr13:51597568 | T | C | 1 | a0001c0001t0008g0271 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.137+12744T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51597568 | ||||||
chr13:51597611 | A | G | 6 | a0001c0001t0010g0002a0001c0001t0010g0003a0001c0001t0010g0004others(3): Show | 6 | HG02257.hp2 HG02647.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.137+12787A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51597611 | ||||||
chr13:51597734 | T | C | 1 | a0001c0001t0018g0023 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.137+12910T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51597734 | ||||||
chr13:51598087 | T | C | 1 | a0001c0001t0026g0155 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.137+13263T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51598087 | ||||||
chr13:51598098 | G | A | 1 | a0001c0001t0029g0272 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.137+13274G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51598098 | ||||||
chr13:51598104 | A | C | 2 | a0001c0006t0016g0277a0001c0007t0016g0278 | 2 | HG02258.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.137+13280A>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51598104 | ||||||
chr13:51598125 | T | C | 11 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(8): Show | 11 | HG01106.hp1 HG02055.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.137+13301T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51598125 | ||||||
chr13:51598130 | T | C | 11 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(8): Show | 11 | HG01106.hp1 HG02055.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.137+13306T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51598130 | ||||||
chr13:51598131 | G | A | 11 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(8): Show | 11 | HG01106.hp1 HG02055.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.137+13307G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51598131 | ||||||
chr13:51598133 | G | A | 11 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(8): Show | 11 | HG01106.hp1 HG02055.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.137+13309G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51598133 | ||||||
chr13:51598134 | C | T | 11 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(8): Show | 11 | HG01106.hp1 HG02055.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.137+13310C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51598134 | ||||||
chr13:51598135 | A | G | 11 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(8): Show | 11 | HG01106.hp1 HG02055.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.137+13311A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51598135 | ||||||
chr13:51598211 | T | C | 2 | a0001c0001t0001g0266a0001c0001t0034g0024 | 2 | HG03579.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.137+13387T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51598211 | ||||||
chr13:51598255 | G | T | 49 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0012others(46): Show | 49 | HG00099.hp1 HG00280.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.137+13431G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51598255 | ||||||
chr13:51598451 | C | T | 46 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(43): Show | 46 | HG00099.hp1 HG00280.hp2 HG01256.hp1 others(43): Show |
intron_variant | MODIFIER | c.137+13627C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51598451 | ||||||
chr13:51598462 | A | C | 81 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(78): Show | 81 | HG00099.hp1 HG00280.hp2 HG01106.hp1 others(78): Show |
intron_variant | MODIFIER | c.137+13638A>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51598462 | ||||||
chr13:51598905 | C | CT | 66 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0013others(63): Show | 66 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.137+14103dupT | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr13 | 51598905 | |||||
chr13:51598905 | C | CTT | 6 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(3): Show | 6 | HG02559.hp2 HG03486.hp1 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.137+14102_137+1410 others(6): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr13 | 51598905 | |||||
chr13:51598971 | T | C | 8 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(5): Show | 8 | HG01192.hp1 HG01884.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.137+14147T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51598971 | ||||||
chr13:51599050 | A | T | 2 | a0001c0006t0016g0277a0001c0007t0016g0278 | 2 | HG02258.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.137+14226A>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51599050 | ||||||
chr13:51599145 | G | T | 1 | a0001c0001t0003g0241 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.137+14321G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51599145 | ||||||
chr13:51599175 | G | A | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG01891.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.137+14351G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51599175 | ||||||
chr13:51599265 | G | A | 1 | a0001c0001t0001g0025 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.137+14441G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51599265 | ||||||
chr13:51599355 | A | C | 1 | a0001c0001t0003g0053 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.137+14531A>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51599355 | ||||||
chr13:51599521 | T | G | 2 | a0001c0001t0001g0124a0001c0002t0002g0123 | 2 | HG02074.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.137+14697T>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51599521 | ||||||
chr13:51599550 | G | C | 49 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0012others(46): Show | 49 | HG00099.hp1 HG00280.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.137+14726G>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51599550 | ||||||
chr13:51599584 | T | C | 8 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(5): Show | 8 | HG01192.hp1 HG01884.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.137+14760T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51599584 | ||||||
chr13:51599658 | T | C | 1 | a0001c0001t0001g0105 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.137+14834T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51599658 | ||||||
chr13:51599900 | A | C | 5 | a0001c0001t0001g0105a0001c0001t0001g0175a0001c0001t0004g0269others(2): Show | 5 | HG02145.hp2 HG02258.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.137+15076A>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51599900 | ||||||
chr13:51599908 | C | A | 1 | a0001c0001t0001g0258 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.137+15084C>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51599908 | ||||||
chr13:51600352 | A | T | 2 | a0001c0001t0010g0005a0001c0001t0010g0006 | 2 | HG02647.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.137+15528A>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51600352 | ||||||
chr13:51600411 | C | G | 2 | a0001c0001t0017g0161a0001c0001t0017g0162 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.137+15587C>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51600411 | ||||||
chr13:51600583 | G | A | 265 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(262): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.137+15759G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51600583 | ||||||
chr13:51600793 | G | C | 2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 2 | HG02109.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.137+15969G>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51600793 | ||||||
chr13:51601321 | T | A | 2 | a0001c0001t0001g0067a0001c0001t0021g0066 | 2 | HG01346.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.137+16497T>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51601321 | ||||||
chr13:51601418 | C | CT | 31 | a0001c0001t0001g0098a0001c0001t0004g0177a0001c0001t0004g0178others(28): Show | 31 | HG00735.hp2 HG01081.hp2 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.137+16608dupT | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr13 | 51601418 | |||||
chr13:51601471 | A | G | 1 | a0001c0001t0001g0064 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.137+16647A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51601471 | ||||||
chr13:51601540 | G | A | 1 | a0001c0001t0004g0188 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.137+16716G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51601540 | ||||||
chr13:51601603 | C | T | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.137+16779C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51601603 | ||||||
chr13:51601674 | C | A | 1 | a0001c0001t0003g0217 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.137+16850C>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51601674 | ||||||
chr13:51601758 | G | A | 4 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0275others(1): Show | 4 | HG00733.hp2 HG01123.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.137+16934G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51601758 | ||||||
chr13:51601787 | C | T | 6 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(3): Show | 6 | HG01261.hp1 HG01978.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.137+16963C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51601787 | ||||||
chr13:51601788 | G | A | 1 | a0001c0002t0002g0026 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.137+16964G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51601788 | ||||||
chr13:51601795 | T | C | 3 | a0001c0001t0003g0218a0001c0001t0003g0242a0001c0001t0037g0219 | 3 | HG01934.hp2 HG02738.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.137+16971T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51601795 | ||||||
chr13:51601838 | T | C | 247 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(244): Show | 247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.137+17014T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51601838 | ||||||
chr13:51601995 | C | G | 1 | a0001c0001t0001g0104 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.137+17171C>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51601995 | ||||||
chr13:51602022 | C | G | 2 | a0001c0001t0010g0002a0001c0001t0010g0003 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.137+17198C>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51602022 | ||||||
chr13:51602059 | A | C | 50 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0012others(47): Show | 50 | HG00099.hp1 HG00280.hp2 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.137+17235A>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51602059 | ||||||
chr13:51602207 | C | T | 2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 2 | HG02109.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.137+17383C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51602207 | ||||||
chr13:51602287 | G | A | 1 | a0001c0007t0016g0278 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.137+17463G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51602287 | ||||||
chr13:51602319 | T | A | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | NA18953.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.137+17495T>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51602319 | ||||||
chr13:51602519 | CAT | C | 3 | a0001c0001t0020g0273a0001c0001t0029g0272a0001c0001t0046g0109 | 3 | HG02559.hp2 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.137+17696_137+1769 others(6): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51602519 | ||||||
chr13:51602748 | C | A | 2 | a0001c0001t0046g0109a0004c0005t0022g0150 | 2 | HG01884.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.137+17924C>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51602748 | ||||||
chr13:51602950 | G | A | 1 | a0001c0001t0018g0270 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.137+18126G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51602950 | ||||||
chr13:51603085 | A | C | 1 | a0001c0001t0004g0269 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.137+18261A>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51603085 | ||||||
chr13:51603130 | G | A | 1 | a0001c0001t0004g0177 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.137+18306G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51603130 | ||||||
chr13:51603141 | A | T | 1 | a0001c0001t0001g0069 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.137+18317A>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51603141 | ||||||
chr13:51603257 | C | T | 6 | a0001c0002t0002g0249a0001c0002t0002g0250a0001c0002t0002g0251others(3): Show | 6 | HG00140.hp2 HG00642.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.137+18433C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51603257 | ||||||
chr13:51603279 | G | A | 1 | a0001c0001t0018g0023 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.137+18455G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51603279 | ||||||
chr13:51603367 | G | A | 2 | a0001c0001t0010g0005a0001c0001t0010g0006 | 2 | HG02647.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.137+18543G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51603367 | ||||||
chr13:51603589 | A | G | 1 | a0001c0001t0001g0122 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.137+18765A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51603589 | ||||||
chr13:51603764 | A | C | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.137+18940A>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51603764 | ||||||
chr13:51604030 | G | C | 48 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0002g0259others(45): Show | 48 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(45): Show |
intron_variant | MODIFIER | c.137+19206G>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51604030 | ||||||
chr13:51604187 | A | G | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.137+19363A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51604187 | ||||||
chr13:51604289 | G | A | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.137+19465G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51604289 | ||||||
chr13:51604466 | A | G | 1 | a0001c0001t0001g0266 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.137+19642A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51604466 | ||||||
chr13:51604477 | A | G | 1 | a0001c0001t0001g0063 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.137+19653A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51604477 | ||||||
chr13:51604670 | A | G | 1 | a0001c0001t0003g0240 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.137+19846A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51604670 | ||||||
chr13:51604715 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.137+19891G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51604715 | ||||||
chr13:51604809 | T | A | 48 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0002g0259others(45): Show | 48 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(45): Show |
intron_variant | MODIFIER | c.137+19985T>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51604809 | ||||||
chr13:51604849 | G | C | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.137+20025G>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51604849 | ||||||
chr13:51605078 | G | A | 31 | a0001c0001t0004g0177a0001c0001t0004g0178a0001c0001t0004g0182others(28): Show | 31 | HG00735.hp2 HG01081.hp2 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.137+20254G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51605078 | ||||||
chr13:51605079 | G | A | 8 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(5): Show | 8 | HG01106.hp1 HG02055.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.137+20255G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51605079 | ||||||
chr13:51605142 | G | C | 2 | a0001c0001t0020g0273a0001c0001t0029g0272 | 2 | HG02559.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.137+20318G>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51605142 | ||||||
chr13:51605546 | A | G | 2 | a0001c0001t0001g0011a0001c0001t0001g0275 | 2 | HG00733.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.137+20722A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51605546 | ||||||
chr13:51605581 | C | T | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.137+20757C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51605581 | ||||||
chr13:51606432 | G | A | 48 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0002g0259others(45): Show | 48 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(45): Show |
intron_variant | MODIFIER | c.137+21608G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51606432 | ||||||
chr13:51606675 | G | C | 4 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159others(1): Show | 4 | HG02630.hp1 HG02965.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.137+21851G>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51606675 | ||||||
chr13:51607224 | T | A | 2 | a0001c0001t0004g0189a0001c0001t0004g0203 | 2 | HG01891.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.137+22400T>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51607224 | ||||||
chr13:51607450 | A | T | 1 | a0001c0001t0003g0239 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.137+22626A>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51607450 | ||||||
chr13:51607473 | G | C | 3 | a0001c0001t0013g0263a0001c0001t0013g0264a0001c0001t0013g0265 | 3 | HG02145.hp1 HG03041.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.137+22649G>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51607473 | ||||||
chr13:51607575 | T | G | 1 | a0001c0001t0003g0245 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.137+22751T>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51607575 | ||||||
chr13:51607589 | A | G | 162 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(159): Show | 162 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.137+22765A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51607589 | ||||||
chr13:51607590 | A | G | 2 | a0001c0001t0010g0002a0001c0001t0010g0003 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.137+22766A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51607590 | ||||||
chr13:51607740 | A | G | 2 | a0001c0001t0001g0137a0001c0001t0040g0136 | 2 | HG03492.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.137+22916A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51607740 | ||||||
chr13:51607786 | C | T | 1 | a0001c0001t0001g0008 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.137+22962C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51607786 | ||||||
chr13:51607790 | A | C | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.137+22966A>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51607790 | ||||||
chr13:51608119 | T | G | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.137+23295T>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51608119 | ||||||
chr13:51608358 | A | G | 1 | a0001c0001t0001g0144 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.137+23534A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51608358 | ||||||
chr13:51608370 | G | C | 1 | a0001c0001t0003g0245 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.137+23546G>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51608370 | ||||||
chr13:51608420 | G | A | 1 | a0001c0001t0001g0027 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.137+23596G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51608420 | ||||||
chr13:51608668 | G | A | 1 | a0003c0004t0001g0108 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.137+23844G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51608668 | ||||||
chr13:51608778 | A | G | 1 | a0002c0003t0004g0185 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.137+23954A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51608778 | ||||||
chr13:51608870 | A | C | 1 | a0001c0001t0001g0097 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.137+24046A>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51608870 | ||||||
chr13:51609017 | T | C | 1 | a0001c0001t0046g0109 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.137+24193T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51609017 | ||||||
chr13:51609201 | A | G | 30 | a0001c0001t0004g0177a0001c0001t0004g0178a0001c0001t0004g0182others(27): Show | 30 | HG00735.hp2 HG01081.hp2 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.137+24377A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51609201 | ||||||
chr13:51609427 | G | A | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.137+24603G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51609427 | ||||||
chr13:51609428 | G | T | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.137+24604G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51609428 | ||||||
chr13:51609589 | A | G | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.137+24765A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51609589 | ||||||
chr13:51609601 | A | AC | 78 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0012others(75): Show | 78 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.137+24782dupC | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr13 | 51609601 | |||||
chr13:51609601 | A | ACC | 25 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0068others(22): Show | 25 | HG00323.hp2 HG00423.hp1 HG00673.hp2 others(22): Show |
intron_variant | MODIFIER | c.137+24781_137+2478 others(6): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr13 | 51609601 | |||||
chr13:51609604 | C | G | 1 | a0001c0002t0002g0052 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.137+24780C>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51609604 | ||||||
chr13:51609604 | CCCG | C | 20 | a0001c0001t0004g0177a0001c0001t0004g0182a0001c0001t0004g0188others(17): Show | 20 | HG00735.hp2 HG01081.hp2 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.137+24783_137+2478 others(7): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr13 | 51609604 | |||||
chr13:51609606 | CG | C | 5 | a0001c0001t0004g0178a0001c0001t0013g0265a0001c0001t0029g0272others(2): Show | 5 | HG01261.hp2 HG02572.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.137+24783delG | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51609606 | ||||||
chr13:51609607 | G | C | 141 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(138): Show | 141 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.137+24783G>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51609607 | ||||||
chr13:51609607 | G | GC | 21 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0125others(18): Show | 21 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(18): Show |
intron_variant | MODIFIER | c.137+24790dupC | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr13 | 51609607 | |||||
chr13:51609624 | A | C | 1 | a0001c0001t0001g0143 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.137+24800A>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51609624 | ||||||
chr13:51609722 | A | G | 1 | a0001c0001t0042g0154 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.137+24898A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51609722 | ||||||
chr13:51609966 | A | G | 1 | a0001c0001t0037g0219 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.137+25142A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51609966 | ||||||
chr13:51610013 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.137+25189G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51610013 | ||||||
chr13:51610162 | G | T | 3 | a0001c0001t0009g0141a0001c0001t0009g0145a0001c0001t0042g0154 | 3 | HG01169.hp1 HG01243.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.137+25338G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51610162 | ||||||
chr13:51610240 | G | GT | 53 | a0001c0001t0001g0089a0001c0001t0001g0124a0001c0001t0001g0255others(50): Show | 53 | HG00140.hp1 HG00735.hp2 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.137+25430dupT | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr13 | 51610240 | |||||
chr13:51610254 | T | G | 1 | a0001c0001t0024g0009 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.137+25430T>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51610254 | ||||||
chr13:51610255 | G | T | 237 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0012others(234): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.137+25431G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51610255 | ||||||
chr13:51610256 | G | T | 140 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0012others(137): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.137+25432G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51610256 | ||||||
chr13:51610270 | C | A | 2 | a0001c0001t0046g0109a0004c0005t0022g0150 | 2 | HG01884.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.137+25446C>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51610270 | ||||||
chr13:51610380 | C | T | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.137+25556C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51610380 | ||||||
chr13:51610383 | A | G | 2 | a0001c0001t0010g0002a0001c0001t0010g0003 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.137+25559A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51610383 | ||||||
chr13:51610421 | T | G | 1 | a0001c0001t0003g0163 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.137+25597T>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51610421 | ||||||
chr13:51611051 | T | C | 1 | a0001c0001t0004g0269 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.137+26227T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51611051 | ||||||
chr13:51611062 | C | T | 1 | a0001c0001t0028g0061 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.137+26238C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51611062 | ||||||
chr13:51611294 | A | G | 1 | a0001c0001t0018g0270 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.137+26470A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51611294 | ||||||
chr13:51611371 | G | T | 1 | a0001c0001t0041g0156 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.137+26547G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51611371 | ||||||
chr13:51611609 | T | G | 2 | a0001c0002t0002g0014a0001c0002t0002g0015 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.137+26785T>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51611609 | ||||||
chr13:51611659 | C | T | 4 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0275others(1): Show | 4 | HG00733.hp2 HG01123.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.137+26835C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51611659 | ||||||
chr13:51611719 | A | G | 48 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0002g0259others(45): Show | 48 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(45): Show |
intron_variant | MODIFIER | c.137+26895A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51611719 | ||||||
chr13:51611802 | A | G | 44 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0003g0053others(41): Show | 44 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(41): Show |
intron_variant | MODIFIER | c.137+26978A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51611802 | ||||||
chr13:51612140 | C | A | 1 | a0001c0001t0020g0273 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.137+27316C>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51612140 | ||||||
chr13:51612165 | A | T | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.137+27341A>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51612165 | ||||||
chr13:51612326 | G | A | 1 | a0001c0001t0009g0111 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.137+27502G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51612326 | ||||||
chr13:51612375 | T | G | 6 | a0001c0001t0010g0002a0001c0001t0010g0003a0001c0001t0010g0004others(3): Show | 6 | HG02257.hp2 HG02647.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.137+27551T>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51612375 | ||||||
chr13:51612393 | C | G | 1 | a0001c0001t0046g0109 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.137+27569C>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51612393 | ||||||
chr13:51612474 | G | A | 4 | a0001c0001t0001g0266a0001c0001t0001g0267a0001c0001t0001g0268others(1): Show | 4 | HG02109.hp2 HG02145.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.137+27650G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51612474 | ||||||
chr13:51612488 | A | G | 1 | a0001c0001t0004g0269 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.137+27664A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51612488 | ||||||
chr13:51612568 | C | G | 1 | a0001c0002t0002g0048 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.137+27744C>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51612568 | ||||||
chr13:51612597 | T | C | 2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 2 | HG02109.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.137+27773T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51612597 | ||||||
chr13:51612651 | C | T | 8 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(5): Show | 8 | HG01192.hp1 HG01884.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.137+27827C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51612651 | ||||||
chr13:51612652 | T | C | 1 | a0001c0002t0002g0048 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.137+27828T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51612652 | ||||||
chr13:51612693 | A | G | 1 | a0001c0001t0003g0245 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.137+27869A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51612693 | ||||||
chr13:51612731 | T | C | 1 | a0001c0001t0002g0259 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.137+27907T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51612731 | ||||||
chr13:51612762 | T | C | 3 | a0001c0001t0013g0263a0001c0001t0013g0264a0001c0001t0013g0265 | 3 | HG02145.hp1 HG03041.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.137+27938T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51612762 | ||||||
chr13:51612775 | C | T | 1 | a0001c0001t0001g0266 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.137+27951C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51612775 | ||||||
chr13:51612941 | A | G | 1 | a0001c0001t0001g0010 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.137+28117A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51612941 | ||||||
chr13:51613024 | C | T | 1 | a0001c0001t0001g0088 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.137+28200C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51613024 | ||||||
chr13:51613153 | A | G | 4 | a0001c0001t0004g0182a0001c0001t0004g0197a0001c0001t0004g0198others(1): Show | 4 | HG02572.hp2 HG02615.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.137+28329A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51613153 | ||||||
chr13:51613171 | T | C | 50 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0012others(47): Show | 50 | HG00099.hp1 HG00280.hp2 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.137+28347T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51613171 | ||||||
chr13:51613191 | A | G | 1 | a0001c0001t0031g0149 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.137+28367A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51613191 | ||||||
chr13:51613280 | C | T | 2 | a0001c0006t0016g0277a0001c0007t0016g0278 | 2 | HG02258.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.137+28456C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51613280 | ||||||
chr13:51613556 | C | A | 1 | a0001c0001t0001g0065 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.137+28732C>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51613556 | ||||||
chr13:51613734 | A | G | 1 | a0001c0007t0016g0278 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.137+28910A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51613734 | ||||||
chr13:51613752 | G | A | 30 | a0001c0001t0004g0177a0001c0001t0004g0178a0001c0001t0004g0182others(27): Show | 30 | HG00735.hp2 HG01081.hp2 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.137+28928G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51613752 | ||||||
chr13:51614164 | C | T | 2 | a0001c0001t0034g0024a0001c0001t0037g0219 | 2 | HG02738.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.137+29340C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51614164 | ||||||
chr13:51614172 | C | T | 1 | a0001c0001t0001g0187 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.137+29348C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51614172 | ||||||
chr13:51614186 | C | CA | 58 | a0001c0001t0001g0054a0001c0001t0001g0062a0001c0001t0001g0074others(55): Show | 58 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.137+29386dupA | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr13 | 51614186 | |||||
chr13:51614186 | CA | C | 6 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0087others(3): Show | 6 | HG00733.hp2 HG01123.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.137+29386delA | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr13 | 51614186 | |||||
chr13:51614211 | G | A | 1 | a0001c0002t0002g0037 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.137+29387G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51614211 | ||||||
chr13:51614324 | G | A | 48 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0002g0259others(45): Show | 48 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(45): Show |
intron_variant | MODIFIER | c.137+29500G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51614324 | ||||||
chr13:51614689 | C | T | 3 | a0001c0001t0013g0263a0001c0001t0013g0264a0001c0001t0013g0265 | 3 | HG02145.hp1 HG03041.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.137+29865C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51614689 | ||||||
chr13:51615232 | A | G | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG01891.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.137+30408A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51615232 | ||||||
chr13:51615990 | T | C | 1 | a0001c0002t0002g0026 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.137+31166T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51615990 | ||||||
chr13:51616094 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.137+31270G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51616094 | ||||||
chr13:51616139 | A | G | 1 | a0001c0001t0001g0157 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.137+31315A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51616139 | ||||||
chr13:51616177 | C | T | 1 | a0001c0001t0005g0020 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.137+31353C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51616177 | ||||||
chr13:51617000 | A | C | 1 | a0001c0002t0002g0051 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.137+32176A>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51617000 | ||||||
chr13:51617084 | C | T | 4 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0275others(1): Show | 4 | HG00733.hp2 HG01123.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.137+32260C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51617084 | ||||||
chr13:51617137 | T | C | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.137+32313T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51617137 | ||||||
chr13:51617346 | C | CT | 52 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0012others(49): Show | 52 | HG00099.hp1 HG00280.hp2 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.137+32533dupT | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr13 | 51617346 | |||||
chr13:51617442 | C | T | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.137+32618C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51617442 | ||||||
chr13:51617944 | A | T | 48 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0002g0259others(45): Show | 48 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(45): Show |
intron_variant | MODIFIER | c.137+33120A>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51617944 | ||||||
chr13:51617954 | A | C | 1 | a0003c0004t0001g0108 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.137+33130A>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51617954 | ||||||
chr13:51618032 | T | C | 1 | a0001c0001t0001g0100 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.137+33208T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51618032 | ||||||
chr13:51618259 | G | A | 276 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(273): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.137+33435G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51618259 | ||||||
chr13:51618553 | G | A | 56 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0128others(53): Show | 56 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(53): Show |
intron_variant | MODIFIER | c.137+33729G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51618553 | ||||||
chr13:51618612 | T | C | 1 | a0001c0001t0001g0125 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.137+33788T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51618612 | ||||||
chr13:51618622 | A | T | 1 | a0001c0001t0009g0141 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.137+33798A>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51618622 | ||||||
chr13:51618767 | T | C | 1 | a0001c0001t0004g0190 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.137+33943T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51618767 | ||||||
chr13:51619013 | C | G | 1 | a0001c0001t0001g0086 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.137+34189C>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51619013 | ||||||
chr13:51619200 | C | A | 2 | a0001c0001t0001g0067a0001c0001t0021g0066 | 2 | HG01346.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.137+34376C>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51619200 | ||||||
chr13:51619433 | CA | C | 166 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(163): Show | 166 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.137+34622delA | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr13 | 51619433 | |||||
chr13:51619601 | A | G | 3 | a0001c0001t0013g0263a0001c0001t0013g0264a0001c0001t0013g0265 | 3 | HG02145.hp1 HG03041.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.137+34777A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51619601 | ||||||
chr13:51619790 | A | G | 1 | a0001c0001t0046g0109 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.137+34966A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51619790 | ||||||
chr13:51619969 | A | C | 2 | a0001c0001t0001g0266a0001c0001t0004g0269 | 2 | HG02145.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.137+35145A>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51619969 | ||||||
chr13:51620021 | A | G | 1 | a0001c0001t0004g0206 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.137+35197A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51620021 | ||||||
chr13:51620128 | A | G | 17 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0138others(14): Show | 17 | HG01891.hp1 HG02015.hp2 HG02647.hp2 others(14): Show |
intron_variant | MODIFIER | c.137+35304A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51620128 | ||||||
chr13:51620237 | GT | G | 3 | a0001c0001t0001g0266a0001c0001t0004g0269a0004c0005t0022g0150 | 3 | HG01884.hp2 HG02145.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.137+35414delT | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51620237 | ||||||
chr13:51620491 | T | C | 1 | a0001c0001t0034g0024 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.137+35667T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51620491 | ||||||
chr13:51620571 | C | T | 1 | a0001c0001t0005g0017 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.137+35747C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51620571 | ||||||
chr13:51620582 | G | A | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | NA18953.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.137+35758G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51620582 | ||||||
chr13:51620683 | T | C | 1 | a0001c0001t0001g0144 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.137+35859T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51620683 | ||||||
chr13:51620684 | T | C | 2 | a0001c0001t0017g0161a0001c0001t0017g0162 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.137+35860T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51620684 | ||||||
chr13:51620690 | C | T | 1 | a0001c0006t0016g0277 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.137+35866C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51620690 | ||||||
chr13:51620695 | ACTTTGCT others(15): Show |
A | 1 | a0001c0001t0046g0109 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.137+35877_137+3589 others(26): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr13 | 51620695 | |||||
chr13:51620808 | T | C | 162 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(159): Show | 162 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.137+35984T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51620808 | ||||||
chr13:51620915 | C | T | 1 | a0001c0001t0014g0146 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.137+36091C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51620915 | ||||||
chr13:51621090 | T | G | 2 | a0001c0001t0020g0273a0001c0001t0029g0272 | 2 | HG02559.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.137+36266T>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51621090 | ||||||
chr13:51621179 | T | C | 1 | a0001c0007t0016g0278 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.137+36355T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51621179 | ||||||
chr13:51621584 | T | C | 1 | a0001c0001t0008g0271 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.137+36760T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51621584 | ||||||
chr13:51621601 | T | C | 1 | a0001c0001t0002g0259 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.137+36777T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51621601 | ||||||
chr13:51621621 | T | C | 1 | a0001c0002t0043g0038 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.137+36797T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51621621 | ||||||
chr13:51621757 | A | G | 1 | a0001c0001t0020g0273 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.137+36933A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51621757 | ||||||
chr13:51621778 | A | T | 41 | a0001c0001t0004g0177a0001c0001t0004g0178a0001c0001t0004g0182others(38): Show | 41 | HG00735.hp2 HG01081.hp2 HG01106.hp1 others(38): Show |
intron_variant | MODIFIER | c.137+36954A>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51621778 | ||||||
chr13:51621962 | G | A | 4 | a0001c0001t0001g0228a0001c0001t0003g0210a0001c0001t0003g0229others(1): Show | 4 | HG01069.hp2 HG01071.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.137+37138G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51621962 | ||||||
chr13:51621976 | A | G | 1 | a0001c0001t0005g0021 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.137+37152A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51621976 | ||||||
chr13:51621978 | G | A | 1 | a0001c0001t0024g0009 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.137+37154G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51621978 | ||||||
chr13:51622244 | T | C | 1 | a0001c0001t0018g0023 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.137+37420T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51622244 | ||||||
chr13:51622709 | A | G | 1 | a0001c0001t0001g0025 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.137+37885A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51622709 | ||||||
chr13:51622853 | C | CT | 27 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0062others(24): Show | 27 | HG00280.hp2 HG00673.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.138-37721dupT | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr13 | 51622853 | |||||
chr13:51622853 | CT | C | 13 | a0001c0001t0001g0055a0001c0001t0001g0121a0001c0001t0001g0122others(10): Show | 13 | HG01884.hp2 HG01891.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.138-37721delT | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr13 | 51622853 | |||||
chr13:51622853 | CTTTTTTT others(3): Show |
C | 48 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0002g0259others(45): Show | 48 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(45): Show |
intron_variant | MODIFIER | c.138-37730_138-3772 others(14): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr13 | 51622853 | |||||
chr13:51622927 | G | C | 1 | a0001c0001t0034g0024 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.138-37669G>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51622927 | ||||||
chr13:51623119 | A | G | 1 | a0001c0001t0003g0238 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.138-37477A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51623119 | ||||||
chr13:51623222 | TA | T | 32 | a0001c0001t0004g0177a0001c0001t0004g0178a0001c0001t0004g0182others(29): Show | 32 | HG00735.hp2 HG01081.hp2 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.138-37363delA | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr13 | 51623222 | |||||
chr13:51623300 | T | A | 1 | a0001c0001t0030g0001 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.138-37296T>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51623300 | ||||||
chr13:51623636 | C | G | 1 | a0001c0001t0046g0109 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.138-36960C>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51623636 | ||||||
chr13:51623838 | G | A | 8 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(5): Show | 8 | HG01106.hp1 HG02055.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.138-36758G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51623838 | ||||||
chr13:51623840 | G | GT | 27 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(24): Show | 27 | HG00323.hp1 HG00558.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.138-36742dupT | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr13 | 51623840 | |||||
chr13:51623875 | T | A | 51 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0012others(48): Show | 51 | HG00099.hp1 HG00280.hp2 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.138-36721T>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51623875 | ||||||
chr13:51623928 | C | T | 2 | a0001c0001t0020g0273a0001c0001t0029g0272 | 2 | HG02559.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.138-36668C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51623928 | ||||||
chr13:51624029 | C | T | 1 | a0001c0001t0046g0109 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.138-36567C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51624029 | ||||||
chr13:51624724 | G | A | 3 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0275 | 3 | HG00733.hp2 HG01123.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.138-35872G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51624724 | ||||||
chr13:51625054 | A | G | 5 | a0001c0002t0002g0249a0001c0002t0002g0250a0001c0002t0002g0251others(2): Show | 5 | HG00140.hp2 HG00642.hp2 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.138-35542A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51625054 | ||||||
chr13:51625089 | A | G | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | NA18953.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.138-35507A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51625089 | ||||||
chr13:51625191 | G | C | 2 | a0001c0001t0003g0207a0001c0001t0003g0208 | 2 | HG00642.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.138-35405G>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51625191 | ||||||
chr13:51625635 | C | T | 2 | a0001c0002t0002g0014a0001c0002t0002g0015 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.138-34961C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51625635 | ||||||
chr13:51626130 | TAAATGAG others(1): Show |
T | 4 | a0001c0001t0046g0109a0001c0006t0016g0277a0001c0007t0016g0278others(1): Show | 4 | HG01884.hp2 HG02258.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.138-34457_138-3445 others(12): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr13 | 51626130 | |||||
chr13:51626494 | C | T | 3 | a0001c0001t0013g0263a0001c0001t0013g0264a0001c0001t0013g0265 | 3 | HG02145.hp1 HG03041.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.138-34102C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51626494 | ||||||
chr13:51626707 | A | G | 6 | a0001c0001t0010g0002a0001c0001t0010g0003a0001c0001t0010g0004others(3): Show | 6 | HG02257.hp2 HG02647.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.138-33889A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51626707 | ||||||
chr13:51626868 | A | G | 42 | a0001c0001t0004g0177a0001c0001t0004g0178a0001c0001t0004g0182others(39): Show | 42 | HG00735.hp2 HG01081.hp2 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.138-33728A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51626868 | ||||||
chr13:51626947 | G | A | 1 | a0001c0001t0008g0271 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.138-33649G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51626947 | ||||||
chr13:51627033 | G | A | 1 | a0001c0001t0003g0217 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.138-33563G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51627033 | ||||||
chr13:51627280 | G | A | 1 | a0001c0001t0004g0189 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.138-33316G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51627280 | ||||||
chr13:51627500 | C | G | 1 | a0001c0001t0001g0072 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.138-33096C>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51627500 | ||||||
chr13:51627544 | T | G | 3 | a0001c0001t0001g0139a0001c0001t0001g0143a0001c0001t0026g0155 | 3 | HG02683.hp1 HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.138-33052T>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51627544 | ||||||
chr13:51627662 | G | A | 2 | a0001c0001t0001g0011a0001c0001t0001g0275 | 2 | HG00733.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.138-32934G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51627662 | ||||||
chr13:51627690 | G | A | 1 | a0001c0001t0003g0218 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.138-32906G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51627690 | ||||||
chr13:51627752 | A | G | 1 | a0001c0001t0018g0023 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.138-32844A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51627752 | ||||||
chr13:51628133 | G | T | 2 | a0001c0002t0002g0014a0001c0002t0002g0015 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.138-32463G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51628133 | ||||||
chr13:51628134 | C | T | 2 | a0001c0002t0002g0014a0001c0002t0002g0015 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.138-32462C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51628134 | ||||||
chr13:51628211 | G | A | 1 | a0001c0002t0002g0254 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.138-32385G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51628211 | ||||||
chr13:51628379 | C | T | 2 | a0001c0006t0016g0277a0001c0007t0016g0278 | 2 | HG02258.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.138-32217C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51628379 | ||||||
chr13:51628562 | C | T | 3 | a0001c0001t0001g0104a0001c0001t0001g0160a0001c0006t0016g0277 | 3 | HG02717.hp2 HG03225.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.138-32034C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51628562 | ||||||
chr13:51628612 | A | G | 1 | a0001c0001t0001g0266 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.138-31984A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51628612 | ||||||
chr13:51628619 | C | G | 1 | a0001c0001t0001g0011 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.138-31977C>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51628619 | ||||||
chr13:51628629 | C | T | 1 | a0001c0001t0035g0195 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.138-31967C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51628629 | ||||||
chr13:51628673 | G | A | 2 | a0001c0001t0046g0109a0004c0005t0022g0150 | 2 | HG01884.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.138-31923G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51628673 | ||||||
chr13:51629159 | C | G | 48 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0002g0259others(45): Show | 48 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(45): Show |
intron_variant | MODIFIER | c.138-31437C>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51629159 | ||||||
chr13:51629618 | C | T | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.138-30978C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51629618 | ||||||
chr13:51629660 | A | C | 1 | a0001c0001t0001g0094 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.138-30936A>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51629660 | ||||||
chr13:51629780 | G | A | 1 | a0001c0001t0046g0109 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.138-30816G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51629780 | ||||||
chr13:51629826 | C | CT | 255 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0011others(252): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.138-30755dupT | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr13 | 51629826 | |||||
chr13:51629826 | C | CTT | 14 | a0001c0001t0001g0010a0001c0001t0003g0209a0001c0001t0003g0224others(11): Show | 14 | HG01123.hp2 HG02258.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.138-30756_138-3075 others(6): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr13 | 51629826 | |||||
chr13:51629874 | G | A | 3 | a0001c0001t0013g0263a0001c0001t0013g0264a0001c0001t0013g0265 | 3 | HG02145.hp1 HG03041.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.138-30722G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51629874 | ||||||
chr13:51629882 | A | G | 3 | a0001c0001t0013g0263a0001c0001t0013g0264a0001c0001t0013g0265 | 3 | HG02145.hp1 HG03041.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.138-30714A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51629882 | ||||||
chr13:51629985 | T | G | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.138-30611T>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51629985 | ||||||
chr13:51630427 | T | G | 1 | a0001c0002t0002g0252 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.138-30169T>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51630427 | ||||||
chr13:51630479 | T | A | 1 | a0001c0001t0001g0159 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.138-30117T>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51630479 | ||||||
chr13:51630758 | C | T | 4 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0275others(1): Show | 4 | HG00733.hp2 HG01123.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.138-29838C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51630758 | ||||||
chr13:51631045 | A | G | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.138-29551A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51631045 | ||||||
chr13:51631130 | G | A | 277 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(274): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.138-29466G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51631130 | ||||||
chr13:51631162 | C | T | 1 | a0001c0001t0001g0008 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.138-29434C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51631162 | ||||||
chr13:51631163 | G | A | 1 | a0001c0002t0002g0039 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.138-29433G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51631163 | ||||||
chr13:51631235 | G | A | 1 | a0001c0002t0002g0030 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.138-29361G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51631235 | ||||||
chr13:51631354 | G | A | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.138-29242G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51631354 | ||||||
chr13:51631391 | TA | T | 10 | a0001c0001t0001g0120a0001c0001t0001g0143a0001c0001t0005g0017others(7): Show | 10 | HG00323.hp1 HG01515.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.138-29187delA | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr13 | 51631391 | |||||
chr13:51631514 | A | G | 2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 2 | HG02109.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.138-29082A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51631514 | ||||||
chr13:51631523 | A | G | 1 | a0001c0001t0039g0274 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.138-29073A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51631523 | ||||||
chr13:51631716 | C | T | 1 | a0001c0007t0016g0278 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.138-28880C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51631716 | ||||||
chr13:51631768 | G | A | 125 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0025others(122): Show | 125 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.138-28828G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51631768 | ||||||
chr13:51631808 | C | T | 1 | a0001c0001t0004g0269 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.138-28788C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51631808 | ||||||
chr13:51631816 | A | G | 30 | a0001c0001t0004g0177a0001c0001t0004g0178a0001c0001t0004g0182others(27): Show | 30 | HG00735.hp2 HG01081.hp2 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.138-28780A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51631816 | ||||||
chr13:51631862 | A | G | 2 | a0001c0001t0020g0273a0001c0001t0029g0272 | 2 | HG02559.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.138-28734A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51631862 | ||||||
chr13:51632213 | G | A | 4 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159others(1): Show | 4 | HG02630.hp1 HG02965.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.138-28383G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51632213 | ||||||
chr13:51632280 | G | C | 2 | a0001c0001t0001g0077a0001c0001t0001g0094 | 2 | HG00099.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.138-28316G>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51632280 | ||||||
chr13:51632538 | G | A | 1 | a0001c0001t0001g0025 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.138-28058G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51632538 | ||||||
chr13:51632549 | T | C | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.138-28047T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51632549 | ||||||
chr13:51632576 | A | G | 2 | a0001c0001t0001g0074a0001c0001t0001g0081 | 2 | NA18964.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.138-28020A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51632576 | ||||||
chr13:51632687 | A | G | 1 | a0001c0001t0034g0024 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.138-27909A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51632687 | ||||||
chr13:51632956 | G | T | 1 | a0001c0001t0003g0241 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.138-27640G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51632956 | ||||||
chr13:51632963 | C | T | 1 | a0001c0001t0003g0239 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.138-27633C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51632963 | ||||||
chr13:51633352 | C | A | 44 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0003g0053others(41): Show | 44 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(41): Show |
intron_variant | MODIFIER | c.138-27244C>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51633352 | ||||||
chr13:51633369 | A | C | 3 | a0001c0001t0001g0084a0001c0001t0001g0102a0001c0001t0002g0085 | 3 | NA18977.hp1 NA18983.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.138-27227A>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51633369 | ||||||
chr13:51633450 | C | T | 1 | a0001c0001t0004g0190 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.138-27146C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51633450 | ||||||
chr13:51633597 | G | T | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.138-26999G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51633597 | ||||||
chr13:51634287 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.138-26309G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51634287 | ||||||
chr13:51634510 | A | G | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.138-26086A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51634510 | ||||||
chr13:51634668 | A | G | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.138-25928A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51634668 | ||||||
chr13:51634725 | T | G | 2 | a0001c0001t0018g0270a0001c0001t0046g0109 | 2 | HG02970.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.138-25871T>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51634725 | ||||||
chr13:51635105 | A | AT | 8 | a0001c0001t0003g0115a0001c0001t0003g0209a0001c0001t0003g0224others(5): Show | 8 | HG03831.hp2 HG03834.hp1 NA18950.hp1 others(5): Show |
intron_variant | MODIFIER | c.138-25481dupT | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr13 | 51635105 | |||||
chr13:51635118 | A | G | 1 | a0001c0001t0001g0143 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.138-25478A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51635118 | ||||||
chr13:51635286 | A | G | 48 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0002g0259others(45): Show | 48 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(45): Show |
intron_variant | MODIFIER | c.138-25310A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51635286 | ||||||
chr13:51635472 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.138-25124C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51635472 | ||||||
chr13:51635473 | G | A | 1 | a0001c0002t0011g0103 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.138-25123G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51635473 | ||||||
chr13:51635579 | A | T | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | NA18953.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.138-25017A>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51635579 | ||||||
chr13:51635631 | C | T | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | NA18953.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.138-24965C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51635631 | ||||||
chr13:51635679 | A | T | 3 | a0001c0001t0013g0263a0001c0001t0013g0264a0001c0001t0013g0265 | 3 | HG02145.hp1 HG03041.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.138-24917A>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51635679 | ||||||
chr13:51635719 | G | T | 1 | a0001c0001t0003g0227 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.138-24877G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51635719 | ||||||
chr13:51635753 | C | T | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.138-24843C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51635753 | ||||||
chr13:51636132 | A | G | 41 | a0001c0001t0004g0177a0001c0001t0004g0178a0001c0001t0004g0182others(38): Show | 41 | HG00735.hp2 HG01081.hp2 HG01106.hp1 others(38): Show |
intron_variant | MODIFIER | c.138-24464A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51636132 | ||||||
chr13:51636176 | T | G | 1 | a0001c0001t0004g0178 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.138-24420T>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51636176 | ||||||
chr13:51636271 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.138-24325G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51636271 | ||||||
chr13:51636559 | G | C | 1 | a0001c0001t0008g0215 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.138-24037G>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51636559 | ||||||
chr13:51636637 | G | A | 1 | a0001c0001t0010g0004 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.138-23959G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51636637 | ||||||
chr13:51636682 | A | G | 1 | a0001c0001t0001g0187 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.138-23914A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51636682 | ||||||
chr13:51637151 | A | C | 276 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(273): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.138-23445A>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51637151 | ||||||
chr13:51637155 | A | G | 2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 2 | HG02109.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.138-23441A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51637155 | ||||||
chr13:51637174 | G | A | 1 | a0001c0001t0020g0273 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.138-23422G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51637174 | ||||||
chr13:51637274 | G | A | 1 | a0001c0001t0001g0064 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.138-23322G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51637274 | ||||||
chr13:51637394 | G | T | 1 | a0001c0001t0001g0096 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.138-23202G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51637394 | ||||||
chr13:51637479 | G | A | 2 | a0001c0001t0001g0055a0001c0001t0001g0056 | 2 | HG01884.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.138-23117G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51637479 | ||||||
chr13:51638028 | C | T | 178 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(175): Show | 178 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.138-22568C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51638028 | ||||||
chr13:51638434 | C | T | 1 | a0001c0001t0004g0269 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.138-22162C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51638434 | ||||||
chr13:51638540 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.138-22056C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51638540 | ||||||
chr13:51638547 | T | C | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.138-22049T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51638547 | ||||||
chr13:51638603 | G | A | 1 | a0001c0001t0009g0145 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.138-21993G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51638603 | ||||||
chr13:51638683 | A | G | 1 | a0001c0001t0046g0109 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.138-21913A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51638683 | ||||||
chr13:51638725 | C | T | 1 | a0001c0001t0003g0209 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.138-21871C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51638725 | ||||||
chr13:51638755 | G | A | 1 | a0001c0001t0008g0213 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.138-21841G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51638755 | ||||||
chr13:51639226 | A | G | 2 | a0001c0001t0001g0255a0001c0001t0001g0256 | 2 | HG01978.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.138-21370A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51639226 | ||||||
chr13:51639470 | C | T | 4 | a0001c0002t0011g0022a0001c0002t0011g0044a0001c0002t0011g0045others(1): Show | 4 | HG00408.hp1 HG00423.hp1 HG00609.hp1 others(1): Show |
intron_variant | MODIFIER | c.138-21126C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51639470 | ||||||
chr13:51639694 | C | T | 1 | a0001c0001t0001g0124 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.138-20902C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51639694 | ||||||
chr13:51639827 | T | C | 1 | a0001c0001t0042g0154 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.138-20769T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51639827 | ||||||
chr13:51640190 | G | A | 1 | a0001c0001t0004g0190 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.138-20406G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51640190 | ||||||
chr13:51640357 | C | T | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.138-20239C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51640357 | ||||||
chr13:51640385 | G | T | 1 | a0001c0001t0001g0101 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.138-20211G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51640385 | ||||||
chr13:51640652 | C | T | 1 | a0001c0001t0046g0109 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.138-19944C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51640652 | ||||||
chr13:51640834 | G | GAAACTCC others(187): Show |
1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.138-19761_138-1976 others(198): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr13 | 51640834 | |||||
chr13:51640886 | C | A | 2 | a0001c0001t0010g0002a0001c0001t0010g0003 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.138-19710C>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51640886 | ||||||
chr13:51641226 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.138-19370C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51641226 | ||||||
chr13:51641543 | C | T | 1 | a0001c0001t0003g0112 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.138-19053C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51641543 | ||||||
chr13:51641592 | C | T | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.138-19004C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51641592 | ||||||
chr13:51641598 | G | A | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.138-18998G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51641598 | ||||||
chr13:51641705 | A | C | 1 | a0001c0001t0001g0063 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.138-18891A>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51641705 | ||||||
chr13:51641741 | A | G | 9 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(6): Show | 9 | HG01192.hp1 HG01884.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.138-18855A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51641741 | ||||||
chr13:51641780 | C | A | 1 | a0001c0001t0004g0206 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.138-18816C>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51641780 | ||||||
chr13:51641783 | G | A | 2 | a0001c0006t0016g0277a0001c0007t0016g0278 | 2 | HG02258.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.138-18813G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51641783 | ||||||
chr13:51641808 | A | G | 1 | a0001c0001t0004g0178 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.138-18788A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51641808 | ||||||
chr13:51641825 | C | CA | 89 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(86): Show | 89 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.138-18742dupA | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr13 | 51641825 | |||||
chr13:51641825 | C | CAA | 15 | a0001c0001t0001g0007a0001c0001t0001g0067a0001c0001t0001g0075others(12): Show | 15 | HG01517.hp1 HG01952.hp1 HG01975.hp1 others(12): Show |
intron_variant | MODIFIER | c.138-18743_138-1874 others(6): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr13 | 51641825 | |||||
chr13:51641825 | CA | C | 19 | a0001c0001t0001g0105a0001c0001t0001g0107a0001c0001t0001g0118others(16): Show | 19 | HG01070.hp1 HG01261.hp1 HG01517.hp2 others(16): Show |
intron_variant | MODIFIER | c.138-18742delA | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr13 | 51641825 | |||||
chr13:51641825 | CAAAAAAA others(5): Show |
C | 4 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0275others(1): Show | 4 | HG00733.hp2 HG01123.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.138-18753_138-1874 others(16): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr13 | 51641825 | |||||
chr13:51641855 | T | A | 1 | a0001c0001t0010g0005 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.138-18741T>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51641855 | ||||||
chr13:51641855 | T | C | 1 | a0001c0001t0005g0021 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.138-18741T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51641855 | ||||||
chr13:51642090 | A | G | 1 | a0001c0001t0018g0270 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.138-18506A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51642090 | ||||||
chr13:51642165 | A | G | 1 | a0001c0001t0004g0189 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.138-18431A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51642165 | ||||||
chr13:51642356 | C | T | 4 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0167others(1): Show | 4 | HG02717.hp1 HG02723.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.138-18240C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51642356 | ||||||
chr13:51642433 | G | A | 1 | a0001c0001t0003g0230 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.138-18163G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51642433 | ||||||
chr13:51642437 | T | A | 6 | a0001c0001t0003g0209a0001c0001t0003g0224a0001c0001t0003g0226others(3): Show | 6 | NA18950.hp1 NA18966.hp2 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.138-18159T>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51642437 | ||||||
chr13:51642588 | C | G | 3 | a0001c0001t0015g0127a0001c0001t0015g0134a0001c0001t0015g0135 | 3 | HG00323.hp1 HG01081.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.138-18008C>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51642588 | ||||||
chr13:51642595 | G | C | 1 | a0001c0001t0026g0155 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.138-18001G>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51642595 | ||||||
chr13:51642676 | C | CT | 30 | a0001c0001t0001g0027a0001c0001t0001g0068a0001c0001t0001g0090others(27): Show | 30 | HG00642.hp1 HG00673.hp2 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.138-17897dupT | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr13 | 51642676 | |||||
chr13:51642676 | CT | C | 12 | a0001c0001t0001g0065a0001c0001t0001g0105a0001c0001t0003g0053others(9): Show | 12 | HG01106.hp1 HG01433.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.138-17897delT | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr13 | 51642676 | |||||
chr13:51642676 | CTTTTTTT others(5): Show |
C | 8 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(5): Show | 8 | HG01192.hp1 HG01884.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.138-17908_138-1789 others(16): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr13 | 51642676 | |||||
chr13:51642865 | A | G | 1 | a0001c0002t0002g0036 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.138-17731A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51642865 | ||||||
chr13:51642892 | G | A | 2 | a0001c0001t0004g0196a0001c0001t0032g0202 | 2 | HG02622.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.138-17704G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51642892 | ||||||
chr13:51642967 | C | T | 4 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0275others(1): Show | 4 | HG00733.hp2 HG01123.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.138-17629C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51642967 | ||||||
chr13:51642968 | G | A | 2 | a0001c0001t0010g0004a0001c0001t0030g0001 | 2 | HG02257.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.138-17628G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51642968 | ||||||
chr13:51643140 | T | G | 1 | a0001c0001t0003g0053 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.138-17456T>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51643140 | ||||||
chr13:51643210 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.138-17386G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51643210 | ||||||
chr13:51643269 | A | C | 1 | a0001c0001t0003g0236 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.138-17327A>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51643269 | ||||||
chr13:51643270 | T | A | 1 | a0001c0001t0003g0236 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.138-17326T>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51643270 | ||||||
chr13:51643300 | G | T | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.138-17296G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51643300 | ||||||
chr13:51643423 | G | A | 1 | a0001c0001t0031g0149 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.138-17173G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51643423 | ||||||
chr13:51643459 | T | C | 1 | a0001c0001t0001g0228 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.138-17137T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51643459 | ||||||
chr13:51643549 | A | G | 8 | a0001c0001t0001g0124a0001c0001t0001g0128a0001c0001t0001g0129others(5): Show | 8 | HG00609.hp2 HG02056.hp2 HG02074.hp2 others(5): Show |
intron_variant | MODIFIER | c.138-17047A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51643549 | ||||||
chr13:51643591 | G | C | 1 | a0001c0001t0029g0272 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.138-17005G>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51643591 | ||||||
chr13:51643870 | G | T | 1 | a0001c0001t0003g0236 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.138-16726G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51643870 | ||||||
chr13:51644111 | CAG | C | 98 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0012others(95): Show | 98 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.138-16482_138-1648 others(6): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr13 | 51644111 | |||||
chr13:51644172 | C | A | 1 | a0001c0001t0003g0218 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.138-16424C>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51644172 | ||||||
chr13:51644310 | C | T | 1 | a0001c0001t0006g0174 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.138-16286C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51644310 | ||||||
chr13:51644460 | T | G | 1 | a0001c0001t0034g0024 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.138-16136T>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51644460 | ||||||
chr13:51644715 | A | T | 2 | a0001c0001t0018g0270a0003c0004t0001g0108 | 2 | HG02451.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.138-15881A>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51644715 | ||||||
chr13:51645012 | C | A | 8 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(5): Show | 8 | HG01192.hp1 HG01884.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.138-15584C>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51645012 | ||||||
chr13:51645070 | A | G | 1 | a0001c0001t0005g0147 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.138-15526A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51645070 | ||||||
chr13:51645210 | G | T | 1 | a0001c0001t0001g0013 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.138-15386G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51645210 | ||||||
chr13:51645368 | A | G | 20 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0062others(17): Show | 20 | HG00280.hp2 HG00673.hp1 NA18950.hp2 others(17): Show |
intron_variant | MODIFIER | c.138-15228A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51645368 | ||||||
chr13:51645472 | G | A | 1 | a0001c0001t0001g0110 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.138-15124G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51645472 | ||||||
chr13:51645603 | A | G | 2 | a0001c0001t0036g0247a0001c0001t0038g0248 | 2 | NA18955.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.138-14993A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51645603 | ||||||
chr13:51645633 | C | T | 4 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0275others(1): Show | 4 | HG00733.hp2 HG01123.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.138-14963C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51645633 | ||||||
chr13:51646143 | G | A | 8 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(5): Show | 8 | HG01192.hp1 HG01884.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.138-14453G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51646143 | ||||||
chr13:51646181 | G | A | 1 | a0001c0001t0001g0081 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.138-14415G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51646181 | ||||||
chr13:51646205 | C | A | 1 | a0001c0001t0029g0272 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.138-14391C>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51646205 | ||||||
chr13:51646256 | G | A | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.138-14340G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51646256 | ||||||
chr13:51646393 | T | C | 2 | a0001c0001t0046g0109a0004c0005t0022g0150 | 2 | HG01884.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.138-14203T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51646393 | ||||||
chr13:51646929 | G | A | 1 | a0001c0001t0003g0225 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.138-13667G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51646929 | ||||||
chr13:51647301 | C | G | 1 | a0001c0001t0004g0189 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.138-13295C>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51647301 | ||||||
chr13:51647455 | G | A | 3 | a0001c0001t0013g0263a0001c0001t0013g0264a0001c0001t0013g0265 | 3 | HG02145.hp1 HG03041.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.138-13141G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51647455 | ||||||
chr13:51647490 | C | T | 1 | a0001c0002t0002g0026 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.138-13106C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51647490 | ||||||
chr13:51647571 | A | G | 2 | a0001c0001t0019g0260a0001c0001t0019g0261 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.138-13025A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51647571 | ||||||
chr13:51647765 | T | TA | 21 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0025others(18): Show | 21 | HG00609.hp2 HG00733.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.138-12809dupA | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr13 | 51647765 | |||||
chr13:51647765 | TA | T | 12 | a0001c0001t0001g0059a0001c0001t0001g0087a0001c0001t0001g0088others(9): Show | 12 | HG00323.hp2 HG01069.hp1 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.138-12809delA | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr13 | 51647765 | |||||
chr13:51647839 | T | C | 1 | a0001c0001t0018g0270 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.138-12757T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51647839 | ||||||
chr13:51648086 | C | T | 48 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0002g0259others(45): Show | 48 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(45): Show |
intron_variant | MODIFIER | c.138-12510C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51648086 | ||||||
chr13:51648139 | G | A | 1 | a0001c0001t0001g0008 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.138-12457G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51648139 | ||||||
chr13:51648150 | G | A | 1 | a0001c0001t0003g0227 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.138-12446G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51648150 | ||||||
chr13:51648187 | A | G | 1 | a0001c0001t0004g0186 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.138-12409A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51648187 | ||||||
chr13:51648234 | A | G | 3 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140 | 3 | HG02647.hp2 HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.138-12362A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51648234 | ||||||
chr13:51648372 | G | T | 1 | a0001c0001t0004g0188 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.138-12224G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51648372 | ||||||
chr13:51648647 | T | TC | 4 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0275others(1): Show | 4 | HG00733.hp2 HG01123.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.138-11948dupC | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr13 | 51648647 | |||||
chr13:51648669 | A | G | 1 | a0003c0004t0001g0108 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.138-11927A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51648669 | ||||||
chr13:51648775 | G | A | 6 | a0001c0001t0010g0002a0001c0001t0010g0003a0001c0001t0010g0004others(3): Show | 6 | HG02257.hp2 HG02647.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.138-11821G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51648775 | ||||||
chr13:51648820 | C | A | 1 | a0001c0001t0004g0178 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.138-11776C>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51648820 | ||||||
chr13:51648929 | T | G | 3 | a0001c0001t0013g0263a0001c0001t0013g0264a0001c0001t0013g0265 | 3 | HG02145.hp1 HG03041.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.138-11667T>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51648929 | ||||||
chr13:51648945 | A | G | 177 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(174): Show | 177 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.138-11651A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51648945 | ||||||
chr13:51649063 | T | C | 247 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(244): Show | 247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.138-11533T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51649063 | ||||||
chr13:51649336 | G | A | 1 | a0001c0001t0004g0206 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.138-11260G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51649336 | ||||||
chr13:51649353 | C | A | 1 | a0001c0001t0001g0275 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.138-11243C>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51649353 | ||||||
chr13:51649423 | CT | C | 10 | a0001c0001t0001g0142a0001c0001t0001g0159a0001c0001t0003g0236others(7): Show | 10 | HG01070.hp1 HG01256.hp2 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.138-11158delT | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr13 | 51649423 | |||||
chr13:51649532 | G | A | 2 | a0001c0001t0018g0270a0003c0004t0001g0108 | 2 | HG02451.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.138-11064G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51649532 | ||||||
chr13:51649575 | C | G | 14 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(11): Show | 14 | HG00323.hp1 HG00558.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.138-11021C>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51649575 | ||||||
chr13:51649583 | A | G | 2 | a0001c0001t0010g0002a0001c0001t0010g0003 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.138-11013A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51649583 | ||||||
chr13:51649788 | G | A | 2 | a0001c0001t0020g0273a0001c0001t0029g0272 | 2 | HG02559.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.138-10808G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51649788 | ||||||
chr13:51650092 | G | A | 1 | a0001c0006t0016g0277 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.138-10504G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51650092 | ||||||
chr13:51650212 | G | C | 2 | a0001c0001t0020g0273a0001c0001t0029g0272 | 2 | HG02559.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.138-10384G>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51650212 | ||||||
chr13:51650214 | T | C | 2 | a0001c0001t0020g0273a0001c0001t0029g0272 | 2 | HG02559.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.138-10382T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51650214 | ||||||
chr13:51650224 | T | G | 1 | a0001c0001t0001g0063 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.138-10372T>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51650224 | ||||||
chr13:51650311 | T | G | 1 | a0001c0001t0001g0158 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.138-10285T>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51650311 | ||||||
chr13:51650491 | A | C | 31 | a0001c0001t0001g0068a0001c0001t0004g0177a0001c0001t0004g0178others(28): Show | 31 | HG00735.hp2 HG01081.hp2 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.138-10105A>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51650491 | ||||||
chr13:51650550 | T | C | 1 | a0001c0001t0004g0269 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.138-10046T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51650550 | ||||||
chr13:51650565 | CTT | C | 4 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159others(1): Show | 4 | HG02630.hp1 HG02965.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.138-10030_138-1002 others(6): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51650565 | ||||||
chr13:51650671 | T | A | 1 | a0001c0001t0001g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.138-9925T>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51650671 | ||||||
chr13:51650743 | C | G | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.138-9853C>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51650743 | ||||||
chr13:51650755 | G | A | 1 | a0001c0001t0004g0206 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.138-9841G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51650755 | ||||||
chr13:51650765 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.138-9831C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51650765 | ||||||
chr13:51650811 | T | C | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.138-9785T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51650811 | ||||||
chr13:51650912 | G | A | 2 | a0001c0001t0004g0196a0001c0001t0032g0202 | 2 | HG02622.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.138-9684G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51650912 | ||||||
chr13:51651096 | C | G | 4 | a0001c0001t0001g0117a0001c0001t0001g0267a0001c0001t0001g0268others(1): Show | 4 | HG01243.hp1 HG02109.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.138-9500C>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51651096 | ||||||
chr13:51651206 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.138-9390G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51651206 | ||||||
chr13:51651283 | C | T | 1 | a0001c0001t0004g0276 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.138-9313C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51651283 | ||||||
chr13:51651399 | T | C | 1 | a0001c0001t0046g0109 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.138-9197T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51651399 | ||||||
chr13:51651823 | T | C | 7 | a0001c0001t0007g0070a0001c0001t0007g0071a0001c0001t0007g0073others(4): Show | 7 | HG01256.hp1 HG01361.hp1 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.138-8773T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51651823 | ||||||
chr13:51651917 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.138-8679C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51651917 | ||||||
chr13:51651919 | C | G | 1 | a0001c0001t0001g0126 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.138-8677C>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51651919 | ||||||
chr13:51652118 | G | T | 1 | a0001c0001t0001g0268 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.138-8478G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51652118 | ||||||
chr13:51652155 | G | A | 1 | a0001c0001t0046g0109 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.138-8441G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51652155 | ||||||
chr13:51652803 | A | G | 1 | a0001c0007t0016g0278 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.138-7793A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51652803 | ||||||
chr13:51652824 | G | C | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.138-7772G>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51652824 | ||||||
chr13:51652895 | G | T | 7 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(4): Show | 7 | HG02055.hp2 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.138-7701G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51652895 | ||||||
chr13:51652917 | T | C | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.138-7679T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51652917 | ||||||
chr13:51652921 | C | G | 1 | a0001c0001t0003g0241 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.138-7675C>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51652921 | ||||||
chr13:51652994 | C | G | 8 | a0001c0001t0007g0070a0001c0001t0010g0002a0001c0001t0010g0003others(5): Show | 8 | HG01192.hp1 HG01433.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.138-7602C>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51652994 | ||||||
chr13:51653202 | A | G | 4 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0275others(1): Show | 4 | HG00733.hp2 HG01123.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.138-7394A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51653202 | ||||||
chr13:51653224 | C | T | 2 | a0001c0001t0017g0161a0001c0001t0017g0162 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.138-7372C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51653224 | ||||||
chr13:51653304 | G | A | 41 | a0001c0001t0004g0177a0001c0001t0004g0178a0001c0001t0004g0182others(38): Show | 41 | HG00735.hp2 HG01081.hp2 HG01106.hp1 others(38): Show |
intron_variant | MODIFIER | c.138-7292G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51653304 | ||||||
chr13:51653419 | G | A | 1 | a0001c0001t0002g0259 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.138-7177G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51653419 | ||||||
chr13:51653429 | A | G | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.138-7167A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51653429 | ||||||
chr13:51653468 | A | G | 1 | a0001c0001t0001g0105 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.138-7128A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51653468 | ||||||
chr13:51653674 | CA | C | 4 | a0001c0001t0001g0266a0001c0001t0001g0267a0001c0001t0001g0268others(1): Show | 4 | HG02109.hp2 HG02145.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.138-6921delA | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51653674 | ||||||
chr13:51653725 | T | C | 1 | a0001c0007t0016g0278 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.138-6871T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51653725 | ||||||
chr13:51653772 | G | C | 1 | a0001c0001t0029g0272 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.138-6824G>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51653772 | ||||||
chr13:51653786 | C | T | 1 | a0001c0001t0001g0095 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.138-6810C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51653786 | ||||||
chr13:51653819 | G | T | 1 | a0001c0002t0002g0026 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.138-6777G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51653819 | ||||||
chr13:51653851 | T | C | 6 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(3): Show | 6 | HG01261.hp1 HG01978.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.138-6745T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51653851 | ||||||
chr13:51653855 | G | T | 1 | a0001c0002t0002g0041 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.138-6741G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51653855 | ||||||
chr13:51653993 | T | C | 5 | a0002c0003t0004g0179a0002c0003t0004g0180a0002c0003t0004g0181others(2): Show | 5 | HG01081.hp2 HG01496.hp2 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.138-6603T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51653993 | ||||||
chr13:51654025 | G | A | 2 | a0001c0006t0016g0277a0001c0007t0016g0278 | 2 | HG02258.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.138-6571G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51654025 | ||||||
chr13:51654055 | G | C | 1 | a0001c0001t0004g0204 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.138-6541G>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51654055 | ||||||
chr13:51654109 | G | A | 1 | a0001c0001t0029g0272 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.138-6487G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51654109 | ||||||
chr13:51654126 | G | A | 1 | a0001c0001t0001g0098 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.138-6470G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51654126 | ||||||
chr13:51654177 | C | T | 8 | a0001c0001t0001g0175a0001c0001t0003g0166a0001c0001t0006g0169others(5): Show | 8 | HG02015.hp2 HG03927.hp2 NA18747.hp2 others(5): Show |
intron_variant | MODIFIER | c.138-6419C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51654177 | ||||||
chr13:51654203 | C | T | 1 | a0001c0001t0003g0222 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.138-6393C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51654203 | ||||||
chr13:51654259 | A | G | 1 | a0001c0002t0002g0251 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.138-6337A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51654259 | ||||||
chr13:51654290 | T | G | 2 | a0001c0001t0046g0109a0004c0005t0022g0150 | 2 | HG01884.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.138-6306T>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51654290 | ||||||
chr13:51654352 | G | T | 54 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0012others(51): Show | 54 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(51): Show |
intron_variant | MODIFIER | c.138-6244G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51654352 | ||||||
chr13:51654530 | C | T | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.138-6066C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51654530 | ||||||
chr13:51654717 | A | G | 1 | a0002c0003t0004g0184 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.138-5879A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51654717 | ||||||
chr13:51654933 | C | T | 8 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(5): Show | 8 | HG01192.hp1 HG01884.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.138-5663C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51654933 | ||||||
chr13:51655284 | G | A | 5 | a0001c0001t0008g0212a0001c0001t0008g0213a0001c0001t0008g0214others(2): Show | 5 | NA18941.hp1 NA18951.hp1 NA19007.hp1 others(2): Show |
intron_variant | MODIFIER | c.138-5312G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51655284 | ||||||
chr13:51655336 | G | C | 1 | a0001c0002t0002g0257 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.138-5260G>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51655336 | ||||||
chr13:51655358 | G | A | 1 | a0001c0001t0015g0134 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.138-5238G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51655358 | ||||||
chr13:51655388 | T | G | 1 | a0001c0001t0003g0231 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.138-5208T>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51655388 | ||||||
chr13:51655444 | A | T | 1 | a0001c0001t0041g0156 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.138-5152A>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51655444 | ||||||
chr13:51655449 | T | G | 1 | a0001c0001t0004g0190 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.138-5147T>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51655449 | ||||||
chr13:51655502 | T | G | 1 | a0001c0002t0002g0254 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.138-5094T>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51655502 | ||||||
chr13:51655684 | T | C | 1 | a0001c0001t0001g0013 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.138-4912T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51655684 | ||||||
chr13:51655745 | C | A | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.138-4851C>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51655745 | ||||||
chr13:51655763 | C | T | 4 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0275others(1): Show | 4 | HG00733.hp2 HG01123.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.138-4833C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51655763 | ||||||
chr13:51656053 | C | CT | 17 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0133others(14): Show | 17 | HG02015.hp2 HG02056.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.138-4526dupT | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr13 | 51656053 | |||||
chr13:51656053 | CT | C | 7 | a0001c0001t0001g0099a0001c0001t0001g0266a0001c0001t0001g0267others(4): Show | 7 | HG02109.hp2 HG02145.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.138-4526delT | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr13 | 51656053 | |||||
chr13:51656163 | C | A | 1 | a0001c0002t0002g0042 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.138-4433C>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51656163 | ||||||
chr13:51656382 | T | G | 62 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0012others(59): Show | 62 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.138-4214T>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51656382 | ||||||
chr13:51656534 | C | T | 2 | a0001c0001t0001g0267a0001c0001t0001g0268 | 2 | HG02109.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.138-4062C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51656534 | ||||||
chr13:51656581 | G | T | 1 | a0001c0001t0046g0109 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.138-4015G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51656581 | ||||||
chr13:51656664 | T | C | 2 | a0001c0001t0001g0077a0001c0001t0001g0094 | 2 | HG00099.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.138-3932T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51656664 | ||||||
chr13:51656733 | T | C | 1 | a0001c0001t0001g0187 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.138-3863T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51656733 | ||||||
chr13:51656761 | C | G | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.138-3835C>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51656761 | ||||||
chr13:51656858 | A | G | 1 | a0001c0001t0034g0024 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.138-3738A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51656858 | ||||||
chr13:51657056 | T | C | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.138-3540T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51657056 | ||||||
chr13:51657458 | A | G | 1 | a0001c0002t0002g0040 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.138-3138A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51657458 | ||||||
chr13:51657612 | A | G | 8 | a0001c0001t0001g0063a0001c0001t0001g0082a0001c0001t0001g0083others(5): Show | 8 | HG00280.hp2 NA18950.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.138-2984A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51657612 | ||||||
chr13:51657624 | C | T | 1 | a0001c0001t0004g0204 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.138-2972C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51657624 | ||||||
chr13:51657633 | T | G | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.138-2963T>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51657633 | ||||||
chr13:51658250 | A | G | 1 | a0001c0001t0034g0024 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.138-2346A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51658250 | ||||||
chr13:51658420 | C | A | 6 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(3): Show | 6 | HG01261.hp1 HG01978.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.138-2176C>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51658420 | ||||||
chr13:51658704 | G | A | 1 | a0001c0001t0046g0109 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.138-1892G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51658704 | ||||||
chr13:51658966 | G | A | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.138-1630G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51658966 | ||||||
chr13:51659108 | G | T | 54 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0012others(51): Show | 54 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(51): Show |
intron_variant | MODIFIER | c.138-1488G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51659108 | ||||||
chr13:51659270 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.138-1326G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51659270 | ||||||
chr13:51659417 | G | A | 2 | a0001c0001t0020g0273a0001c0001t0029g0272 | 2 | HG02559.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.138-1179G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51659417 | ||||||
chr13:51659496 | C | T | 1 | a0001c0001t0004g0203 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.138-1100C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51659496 | ||||||
chr13:51659541 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.138-1055A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51659541 | ||||||
chr13:51659610 | A | G | 1 | a0001c0001t0036g0247 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.138-986A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51659610 | ||||||
chr13:51659619 | C | G | 1 | a0001c0001t0029g0272 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.138-977C>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51659619 | ||||||
chr13:51659904 | T | C | 1 | a0001c0001t0001g0116 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.138-692T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51659904 | ||||||
chr13:51659972 | A | G | 1 | a0001c0001t0018g0270 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.138-624A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51659972 | ||||||
chr13:51660219 | C | T | 2 | a0001c0001t0019g0260a0001c0001t0019g0261 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.138-377C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51660219 | ||||||
chr13:51660487 | G | A | 1 | a0001c0001t0034g0024 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.138-109G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51660487 | ||||||
chr13:51660502 | A | C | 1 | a0001c0001t0046g0109 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.138-94A>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 1/11 | chr13 | 51660502 | ||||||
chr13:51660785 | T | C | 2 | a0001c0002t0002g0042a0001c0002t0002g0052 | 2 | HG02015.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.205+122T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51660785 | ||||||
chr13:51660853 | C | G | 1 | a0001c0001t0004g0269 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.205+190C>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51660853 | ||||||
chr13:51660856 | T | C | 1 | a0001c0001t0001g0187 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.205+193T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51660856 | ||||||
chr13:51660902 | G | T | 2 | a0001c0001t0005g0020a0001c0001t0005g0021 | 2 | HG02486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.205+239G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51660902 | ||||||
chr13:51661296 | T | C | 8 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(5): Show | 8 | HG01192.hp1 HG01884.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.205+633T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51661296 | ||||||
chr13:51661301 | G | T | 1 | a0001c0001t0003g0210 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.205+638G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51661301 | ||||||
chr13:51661525 | T | C | 1 | a0001c0001t0034g0024 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.205+862T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51661525 | ||||||
chr13:51661628 | C | A | 3 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140 | 3 | HG02647.hp2 HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.205+965C>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51661628 | ||||||
chr13:51661671 | A | G | 1 | a0001c0001t0004g0269 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.205+1008A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51661671 | ||||||
chr13:51661771 | C | T | 1 | a0001c0001t0001g0142 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.205+1108C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51661771 | ||||||
chr13:51661806 | C | T | 1 | a0001c0006t0016g0277 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.205+1143C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51661806 | ||||||
chr13:51661882 | C | G | 1 | a0001c0001t0006g0235 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.205+1219C>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51661882 | ||||||
chr13:51662011 | C | G | 1 | a0001c0001t0020g0273 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.205+1348C>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51662011 | ||||||
chr13:51662035 | A | G | 1 | a0001c0001t0001g0099 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.205+1372A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51662035 | ||||||
chr13:51662072 | G | A | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.205+1409G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51662072 | ||||||
chr13:51662190 | C | T | 2 | a0001c0001t0004g0190a0001c0001t0004g0206 | 2 | HG02258.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.205+1527C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51662190 | ||||||
chr13:51662290 | T | C | 1 | a0001c0001t0001g0062 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.205+1627T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51662290 | ||||||
chr13:51662467 | C | T | 1 | a0001c0001t0034g0024 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.205+1804C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51662467 | ||||||
chr13:51662499 | G | A | 1 | a0001c0001t0034g0024 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.205+1836G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51662499 | ||||||
chr13:51662657 | G | A | 4 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159others(1): Show | 4 | HG02630.hp1 HG02965.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.205+1994G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51662657 | ||||||
chr13:51662804 | A | T | 271 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(268): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.205+2141A>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51662804 | ||||||
chr13:51662812 | G | C | 2 | a0001c0001t0017g0161a0001c0001t0017g0162 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.205+2149G>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51662812 | ||||||
chr13:51662846 | G | T | 1 | a0001c0007t0016g0278 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.205+2183G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51662846 | ||||||
chr13:51663067 | C | T | 2 | a0001c0001t0017g0161a0001c0001t0017g0162 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.205+2404C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51663067 | ||||||
chr13:51663081 | G | A | 1 | a0001c0001t0003g0208 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.205+2418G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51663081 | ||||||
chr13:51663168 | C | A | 1 | a0001c0001t0004g0189 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.205+2505C>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51663168 | ||||||
chr13:51663387 | G | A | 1 | a0001c0001t0041g0156 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.205+2724G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51663387 | ||||||
chr13:51663448 | A | T | 1 | a0001c0001t0018g0270 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.205+2785A>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51663448 | ||||||
chr13:51663457 | T | G | 1 | a0001c0001t0046g0109 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.205+2794T>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51663457 | ||||||
chr13:51663655 | C | T | 1 | a0001c0001t0003g0243 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.205+2992C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51663655 | ||||||
chr13:51664173 | A | G | 1 | a0001c0001t0034g0024 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.205+3510A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51664173 | ||||||
chr13:51664336 | T | G | 1 | a0001c0001t0001g0072 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.205+3673T>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51664336 | ||||||
chr13:51664429 | C | A | 7 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(4): Show | 7 | HG02055.hp2 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.205+3766C>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51664429 | ||||||
chr13:51664578 | C | G | 1 | a0001c0001t0009g0141 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.205+3915C>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51664578 | ||||||
chr13:51664672 | A | C | 2 | a0001c0001t0001g0159a0001c0001t0001g0160 | 2 | HG02965.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.205+4009A>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51664672 | ||||||
chr13:51664922 | T | C | 1 | a0001c0001t0001g0105 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.205+4259T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51664922 | ||||||
chr13:51665015 | G | A | 4 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0275others(1): Show | 4 | HG00733.hp2 HG01123.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.205+4352G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51665015 | ||||||
chr13:51665337 | G | C | 1 | a0001c0001t0004g0190 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.205+4674G>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51665337 | ||||||
chr13:51665686 | A | G | 1 | a0001c0001t0001g0129 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.205+5023A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51665686 | ||||||
chr13:51665758 | G | A | 2 | a0001c0001t0004g0196a0001c0001t0032g0202 | 2 | HG02622.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.205+5095G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51665758 | ||||||
chr13:51665893 | C | G | 2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 2 | HG02109.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.205+5230C>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51665893 | ||||||
chr13:51666229 | C | A | 30 | a0001c0001t0004g0177a0001c0001t0004g0178a0001c0001t0004g0182others(27): Show | 30 | HG00735.hp2 HG01081.hp2 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.205+5566C>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51666229 | ||||||
chr13:51666598 | A | G | 1 | a0001c0001t0005g0147 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.205+5935A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51666598 | ||||||
chr13:51666692 | T | C | 1 | a0001c0001t0015g0134 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.205+6029T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51666692 | ||||||
chr13:51666817 | A | G | 2 | a0001c0001t0005g0020a0001c0001t0005g0021 | 2 | HG02486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.205+6154A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51666817 | ||||||
chr13:51667418 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.205+6755G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51667418 | ||||||
chr13:51667879 | C | CT | 19 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(16): Show | 19 | HG01192.hp1 HG01346.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.205+7246dupT | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr13 | 51667879 | |||||
chr13:51667879 | C | CTTTTTTT | 6 | a0001c0001t0001g0266a0001c0001t0004g0188a0001c0001t0004g0197others(3): Show | 6 | HG02698.hp2 HG02723.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.205+7240_205+7246d others(9): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr13 | 51667879 | |||||
chr13:51667879 | C | CTTTTTTT others(1): Show |
11 | a0001c0001t0004g0178a0001c0001t0004g0182a0001c0001t0005g0019others(8): Show | 11 | HG01081.hp2 HG01261.hp2 HG01993.hp2 others(8): Show |
intron_variant | MODIFIER | c.205+7239_205+7246d others(10): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr13 | 51667879 | |||||
chr13:51667879 | C | CTTTTTTT others(2): Show |
13 | a0001c0001t0004g0191a0001c0001t0004g0193a0001c0001t0004g0199others(10): Show | 13 | HG01106.hp1 HG01243.hp2 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.205+7238_205+7246d others(11): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr13 | 51667879 | |||||
chr13:51667879 | C | CTTTTTTT others(3): Show |
3 | a0001c0001t0004g0183a0001c0001t0004g0186a0001c0001t0004g0190 | 3 | HG01106.hp2 HG03130.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.205+7237_205+7246d others(12): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr13 | 51667879 | |||||
chr13:51667879 | C | CTTTTTTT others(4): Show |
2 | a0001c0001t0004g0189a0001c0001t0004g0276 | 2 | HG00735.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.205+7236_205+7246d others(13): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr13 | 51667879 | |||||
chr13:51667879 | C | CTTTTTTT others(7): Show |
1 | a0001c0001t0004g0192 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.205+7233_205+7246d others(16): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr13 | 51667879 | |||||
chr13:51667879 | C | CTTTTTTT others(8): Show |
1 | a0001c0001t0004g0203 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.205+7232_205+7246d others(17): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr13 | 51667879 | |||||
chr13:51667879 | CT | C | 81 | a0001c0001t0001g0010a0001c0001t0001g0067a0001c0001t0001g0076others(78): Show | 81 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.205+7246delT | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr13 | 51667879 | |||||
chr13:51667879 | CTT | C | 7 | a0001c0001t0001g0011a0001c0001t0003g0231a0001c0001t0038g0248others(4): Show | 7 | HG00408.hp2 HG00609.hp1 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.205+7245_205+7246d others(4): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr13 | 51667879 | |||||
chr13:51667879 | CTTTTTTT others(3): Show |
C | 13 | a0001c0001t0001g0133a0001c0001t0008g0212a0001c0001t0019g0260others(10): Show | 13 | HG00323.hp2 HG00408.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.205+7237_205+7246d others(12): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr13 | 51667879 | |||||
chr13:51667879 | CTTTTTTT others(4): Show |
C | 36 | a0001c0001t0002g0259a0001c0001t0003g0053a0001c0001t0018g0270others(33): Show | 36 | HG00140.hp2 HG00423.hp1 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.205+7236_205+7246d others(13): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr13 | 51667879 | |||||
chr13:51667879 | CTTTTTTT others(5): Show |
C | 1 | a0001c0002t0002g0152 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.205+7235_205+7246d others(14): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr13 | 51667879 | |||||
chr13:51667879 | CTTTTTTT others(6): Show |
C | 1 | a0001c0006t0016g0277 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.205+7234_205+7246d others(15): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr13 | 51667879 | |||||
chr13:51667945 | G | A | 11 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(8): Show | 11 | HG01106.hp1 HG02055.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.206-7225G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51667945 | ||||||
chr13:51667992 | C | T | 1 | a0001c0001t0001g0083 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.206-7178C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51667992 | ||||||
chr13:51668017 | A | G | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.206-7153A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51668017 | ||||||
chr13:51668037 | G | A | 1 | a0001c0006t0016g0277 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.206-7133G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51668037 | ||||||
chr13:51668150 | A | G | 2 | a0001c0001t0010g0005a0001c0001t0010g0006 | 2 | HG02647.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.206-7020A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51668150 | ||||||
chr13:51668179 | C | T | 1 | a0001c0001t0020g0273 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.206-6991C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51668179 | ||||||
chr13:51668180 | G | A | 6 | a0001c0001t0010g0002a0001c0001t0010g0003a0001c0001t0010g0004others(3): Show | 6 | HG02257.hp2 HG02647.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.206-6990G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51668180 | ||||||
chr13:51668301 | C | T | 3 | a0001c0001t0003g0053a0001c0002t0002g0037a0001c0002t0002g0148 | 3 | HG01346.hp1 HG02486.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.206-6869C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51668301 | ||||||
chr13:51668341 | G | A | 2 | a0001c0001t0018g0270a0001c0001t0031g0149 | 2 | HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.206-6829G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51668341 | ||||||
chr13:51668527 | C | T | 11 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(8): Show | 11 | HG01106.hp1 HG02055.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.206-6643C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51668527 | ||||||
chr13:51668594 | A | G | 4 | a0001c0001t0001g0266a0001c0001t0001g0267a0001c0001t0001g0268others(1): Show | 4 | HG02109.hp2 HG02145.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.206-6576A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51668594 | ||||||
chr13:51669378 | G | T | 4 | a0001c0001t0001g0266a0001c0001t0001g0267a0001c0001t0001g0268others(1): Show | 4 | HG02109.hp2 HG02145.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.206-5792G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51669378 | ||||||
chr13:51669687 | G | A | 1 | a0001c0002t0002g0257 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.206-5483G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51669687 | ||||||
chr13:51670000 | C | T | 2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 2 | HG02109.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.206-5170C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51670000 | ||||||
chr13:51670005 | C | G | 1 | a0001c0001t0004g0189 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.206-5165C>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51670005 | ||||||
chr13:51670234 | A | G | 1 | a0001c0001t0001g0072 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.206-4936A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51670234 | ||||||
chr13:51670488 | T | C | 1 | a0001c0001t0007g0073 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.206-4682T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51670488 | ||||||
chr13:51670489 | G | GCA | 35 | a0001c0001t0001g0068a0001c0001t0001g0075a0001c0001t0001g0076others(32): Show | 35 | HG00099.hp1 HG00423.hp1 HG01256.hp1 others(32): Show |
intron_variant | MODIFIER | c.206-4634_206-4633d others(4): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr13 | 51670489 | |||||
chr13:51670489 | G | GCACA | 9 | a0001c0001t0001g0063a0001c0001t0001g0072a0001c0001t0001g0078others(6): Show | 9 | HG01069.hp1 HG01517.hp1 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.206-4636_206-4633d others(6): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr13 | 51670489 | |||||
chr13:51670489 | G | GCACACA | 4 | a0001c0001t0001g0100a0001c0001t0007g0079a0001c0001t0019g0260others(1): Show | 4 | HG02273.hp2 HG03491.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.206-4638_206-4633d others(8): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr13 | 51670489 | |||||
chr13:51670489 | G | GCACACAC others(3): Show |
1 | a0001c0001t0007g0092 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.206-4642_206-4633d others(12): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr13 | 51670489 | |||||
chr13:51670489 | G | GCACACAC others(9): Show |
1 | a0001c0001t0001g0121 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.206-4648_206-4633d others(18): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr13 | 51670489 | |||||
chr13:51670489 | G | GCGCGCAC others(3): Show |
1 | a0001c0001t0005g0021 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.206-4680_206-4679i others(12): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr13 | 51670489 | |||||
chr13:51670489 | GCA | G | 83 | a0001c0001t0001g0025a0001c0001t0001g0062a0001c0001t0001g0064others(80): Show | 83 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.206-4634_206-4633d others(4): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr13 | 51670489 | |||||
chr13:51670489 | GCACA | G | 44 | a0001c0001t0001g0082a0001c0001t0001g0118a0001c0001t0001g0130others(41): Show | 44 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.206-4636_206-4633d others(6): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr13 | 51670489 | |||||
chr13:51670489 | GCACACA | G | 17 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(14): Show | 17 | HG01106.hp2 HG01192.hp1 HG01256.hp2 others(14): Show |
intron_variant | MODIFIER | c.206-4638_206-4633d others(8): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr13 | 51670489 | |||||
chr13:51670489 | GCACACAC others(3): Show |
G | 3 | a0001c0001t0001g0054a0001c0001t0003g0222a0001c0006t0016g0277 | 3 | HG02717.hp2 HG03209.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.206-4642_206-4633d others(12): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr13 | 51670489 | |||||
chr13:51670489 | GCACACAC others(5): Show |
G | 2 | a0001c0001t0001g0133a0001c0001t0009g0141 | 2 | HG01169.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.206-4644_206-4633d others(14): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr13 | 51670489 | |||||
chr13:51670489 | GCACACAC others(19): Show |
G | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.206-4658_206-4633d others(28): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr13 | 51670489 | |||||
chr13:51670491 | A | G | 4 | a0001c0001t0005g0016a0001c0001t0005g0018a0001c0001t0005g0019others(1): Show | 4 | HG02055.hp2 HG02559.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.206-4679A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51670491 | ||||||
chr13:51670493 | A | G | 3 | a0001c0001t0005g0018a0001c0001t0005g0019a0001c0001t0005g0153 | 3 | HG02055.hp2 HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.206-4677A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51670493 | ||||||
chr13:51670495 | A | G | 3 | a0001c0001t0005g0018a0001c0001t0005g0019a0001c0001t0005g0147 | 3 | HG01106.hp1 HG02055.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.206-4675A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51670495 | ||||||
chr13:51670497 | A | G | 1 | a0001c0001t0005g0147 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.206-4673A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51670497 | ||||||
chr13:51670536 | C | CACAG | 4 | a0001c0001t0012g0194a0001c0001t0012g0201a0002c0003t0004g0181others(1): Show | 4 | HG01081.hp2 HG01243.hp2 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.206-4633_206-4632i others(6): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr13 | 51670536 | |||||
chr13:51670536 | C | CAG | 3 | a0001c0001t0004g0177a0002c0003t0004g0179a0002c0003t0004g0184 | 3 | HG01952.hp2 HG02293.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.206-4632_206-4631d others(4): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr13 | 51670536 | |||||
chr13:51670536 | C | G | 22 | a0001c0001t0004g0178a0001c0001t0004g0182a0001c0001t0004g0183others(19): Show | 22 | HG00735.hp2 HG01106.hp2 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.206-4634C>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51670536 | ||||||
chr13:51670617 | C | T | 4 | a0001c0001t0004g0182a0001c0001t0004g0197a0001c0001t0004g0198others(1): Show | 4 | HG02572.hp2 HG02615.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.206-4553C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51670617 | ||||||
chr13:51670737 | A | T | 177 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(174): Show | 177 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.206-4433A>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51670737 | ||||||
chr13:51670966 | C | T | 2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 2 | HG02109.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.206-4204C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51670966 | ||||||
chr13:51671056 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.206-4114C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51671056 | ||||||
chr13:51671181 | TGTGA | T | 6 | a0001c0001t0010g0002a0001c0001t0010g0003a0001c0001t0010g0004others(3): Show | 6 | HG02257.hp2 HG02647.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.206-3986_206-3983d others(6): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr13 | 51671181 | |||||
chr13:51671196 | C | T | 1 | a0001c0001t0004g0269 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.206-3974C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51671196 | ||||||
chr13:51671291 | A | G | 41 | a0001c0001t0004g0177a0001c0001t0004g0178a0001c0001t0004g0182others(38): Show | 41 | HG00735.hp2 HG01081.hp2 HG01106.hp1 others(38): Show |
intron_variant | MODIFIER | c.206-3879A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51671291 | ||||||
chr13:51671605 | CATATTAG others(1): Show |
C | 3 | a0001c0001t0013g0263a0001c0001t0013g0264a0001c0001t0013g0265 | 3 | HG02145.hp1 HG03041.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.206-3564_206-3557d others(10): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51671605 | ||||||
chr13:51671653 | T | G | 2 | a0001c0001t0008g0215a0001c0001t0008g0216 | 2 | NA18941.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.206-3517T>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51671653 | ||||||
chr13:51671776 | C | CT | 32 | a0001c0001t0001g0072a0001c0001t0001g0125a0001c0001t0001g0133others(29): Show | 32 | HG00423.hp2 HG00642.hp1 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.206-3369dupT | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr13 | 51671776 | |||||
chr13:51671776 | CT | C | 13 | a0001c0001t0001g0059a0001c0001t0001g0064a0001c0001t0001g0105others(10): Show | 13 | HG02145.hp1 HG02258.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.206-3369delT | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr13 | 51671776 | |||||
chr13:51671776 | CTTTTTTT others(10): Show |
C | 6 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(3): Show | 6 | HG01261.hp1 HG01978.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.206-3385_206-3369d others(19): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr13 | 51671776 | |||||
chr13:51671837 | G | A | 54 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0012others(51): Show | 54 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(51): Show |
intron_variant | MODIFIER | c.206-3333G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51671837 | ||||||
chr13:51671944 | C | T | 1 | a0001c0001t0046g0109 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.206-3226C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51671944 | ||||||
chr13:51671994 | G | A | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.206-3176G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51671994 | ||||||
chr13:51672027 | G | A | 4 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0275others(1): Show | 4 | HG00733.hp2 HG01123.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.206-3143G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51672027 | ||||||
chr13:51672240 | G | T | 1 | a0001c0001t0004g0178 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.206-2930G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51672240 | ||||||
chr13:51672334 | T | C | 6 | a0001c0001t0010g0002a0001c0001t0010g0003a0001c0001t0010g0004others(3): Show | 6 | HG02257.hp2 HG02647.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.206-2836T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51672334 | ||||||
chr13:51672495 | G | A | 1 | a0001c0001t0046g0109 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.206-2675G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51672495 | ||||||
chr13:51672636 | C | T | 1 | a0001c0001t0003g0053 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.206-2534C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51672636 | ||||||
chr13:51672694 | C | T | 1 | a0001c0001t0003g0222 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.206-2476C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51672694 | ||||||
chr13:51672788 | T | A | 2 | a0001c0006t0016g0277a0001c0007t0016g0278 | 2 | HG02258.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.206-2382T>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51672788 | ||||||
chr13:51672921 | A | G | 3 | a0001c0002t0002g0032a0001c0002t0002g0151a0001c0002t0002g0152 | 3 | HG01433.hp2 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.206-2249A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51672921 | ||||||
chr13:51673060 | C | T | 1 | a0001c0001t0037g0219 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.206-2110C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51673060 | ||||||
chr13:51673082 | T | G | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.206-2088T>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51673082 | ||||||
chr13:51673167 | G | A | 1 | a0001c0001t0001g0010 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.206-2003G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51673167 | ||||||
chr13:51673588 | G | T | 2 | a0001c0006t0016g0277a0001c0007t0016g0278 | 2 | HG02258.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.206-1582G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51673588 | ||||||
chr13:51673621 | A | G | 1 | a0001c0001t0024g0009 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.206-1549A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51673621 | ||||||
chr13:51674019 | T | C | 1 | a0001c0001t0015g0134 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.206-1151T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51674019 | ||||||
chr13:51674169 | G | A | 3 | a0001c0001t0002g0259a0001c0001t0019g0260a0001c0001t0019g0261 | 3 | HG02698.hp1 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.206-1001G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51674169 | ||||||
chr13:51674476 | G | C | 1 | a0001c0001t0001g0090 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.206-694G>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51674476 | ||||||
chr13:51674527 | A | C | 1 | a0001c0001t0001g0072 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.206-643A>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51674527 | ||||||
chr13:51674633 | C | A | 2 | a0001c0001t0001g0116a0001c0001t0001g0118 | 2 | HG01261.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.206-537C>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51674633 | ||||||
chr13:51674806 | A | G | 1 | a0001c0001t0018g0023 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.206-364A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51674806 | ||||||
chr13:51675002 | G | A | 8 | a0001c0001t0003g0211a0001c0001t0003g0221a0001c0001t0003g0225others(5): Show | 8 | HG02155.hp1 NA18950.hp1 NA18955.hp1 others(5): Show |
intron_variant | MODIFIER | c.206-168G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51675002 | ||||||
chr13:51675008 | G | A | 1 | a0001c0006t0016g0277 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.206-162G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 2/11 | chr13 | 51675008 | ||||||
chr13:51675483 | G | A | 1 | a0001c0001t0001g0124 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.279+240G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51675483 | ||||||
chr13:51675512 | A | G | 1 | a0001c0001t0034g0024 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.279+269A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51675512 | ||||||
chr13:51675644 | A | T | 1 | a0001c0001t0018g0270 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.279+401A>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51675644 | ||||||
chr13:51676172 | A | G | 1 | a0001c0001t0001g0128 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.279+929A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51676172 | ||||||
chr13:51676278 | A | G | 4 | a0001c0001t0001g0266a0001c0001t0001g0267a0001c0001t0001g0268others(1): Show | 4 | HG02109.hp2 HG02145.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.279+1035A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51676278 | ||||||
chr13:51676319 | C | T | 4 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0167others(1): Show | 4 | HG02717.hp1 HG02723.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.279+1076C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51676319 | ||||||
chr13:51676370 | A | G | 1 | a0001c0001t0001g0099 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.279+1127A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51676370 | ||||||
chr13:51676804 | A | C | 6 | a0001c0001t0010g0002a0001c0001t0010g0003a0001c0001t0010g0004others(3): Show | 6 | HG02257.hp2 HG02647.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.279+1561A>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51676804 | ||||||
chr13:51676980 | G | A | 2 | a0001c0001t0001g0067a0001c0001t0021g0066 | 2 | HG01346.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.279+1737G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51676980 | ||||||
chr13:51677053 | G | A | 1 | a0001c0001t0003g0225 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.279+1810G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51677053 | ||||||
chr13:51677125 | A | G | 1 | a0001c0006t0016g0277 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.279+1882A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51677125 | ||||||
chr13:51677256 | C | A | 3 | a0001c0001t0013g0263a0001c0001t0013g0264a0001c0001t0013g0265 | 3 | HG02145.hp1 HG03041.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.279+2013C>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51677256 | ||||||
chr13:51677434 | G | T | 1 | a0001c0001t0001g0105 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.279+2191G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51677434 | ||||||
chr13:51678041 | C | T | 1 | a0001c0002t0002g0026 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.279+2798C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51678041 | ||||||
chr13:51678382 | T | C | 1 | a0001c0001t0024g0009 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.279+3139T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51678382 | ||||||
chr13:51678657 | A | G | 1 | a0001c0001t0001g0099 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.279+3414A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51678657 | ||||||
chr13:51678710 | G | T | 4 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0275others(1): Show | 4 | HG00733.hp2 HG01123.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.279+3467G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51678710 | ||||||
chr13:51678906 | A | G | 4 | a0001c0001t0046g0109a0001c0006t0016g0277a0001c0007t0016g0278others(1): Show | 4 | HG01884.hp2 HG02258.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.279+3663A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51678906 | ||||||
chr13:51678956 | G | A | 1 | a0001c0001t0001g0266 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.279+3713G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51678956 | ||||||
chr13:51679240 | A | G | 2 | a0001c0001t0006g0047a0001c0001t0006g0173 | 2 | NA18943.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.279+3997A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51679240 | ||||||
chr13:51679281 | A | G | 1 | a0001c0002t0002g0123 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.279+4038A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51679281 | ||||||
chr13:51679307 | T | G | 1 | a0002c0003t0004g0184 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.279+4064T>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51679307 | ||||||
chr13:51679519 | G | T | 62 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0012others(59): Show | 62 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.279+4276G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51679519 | ||||||
chr13:51679681 | A | G | 6 | a0001c0001t0010g0002a0001c0001t0010g0003a0001c0001t0010g0004others(3): Show | 6 | HG02257.hp2 HG02647.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.279+4438A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51679681 | ||||||
chr13:51679956 | G | T | 1 | a0001c0001t0037g0219 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.279+4713G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51679956 | ||||||
chr13:51680098 | G | A | 1 | a0001c0001t0003g0053 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.279+4855G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51680098 | ||||||
chr13:51680162 | C | T | 62 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0012others(59): Show | 62 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.279+4919C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51680162 | ||||||
chr13:51680268 | A | G | 1 | a0001c0001t0003g0225 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.279+5025A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51680268 | ||||||
chr13:51680616 | G | A | 1 | a0001c0006t0016g0277 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.279+5373G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51680616 | ||||||
chr13:51680712 | G | A | 1 | a0003c0004t0001g0108 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.279+5469G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51680712 | ||||||
chr13:51680719 | A | C | 1 | a0001c0001t0001g0059 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.279+5476A>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51680719 | ||||||
chr13:51680736 | G | A | 1 | a0001c0001t0003g0112 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.279+5493G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51680736 | ||||||
chr13:51681110 | C | T | 4 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0275others(1): Show | 4 | HG00733.hp2 HG01123.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.279+5867C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51681110 | ||||||
chr13:51681185 | T | C | 274 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(271): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.279+5942T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51681185 | ||||||
chr13:51681338 | C | T | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.279+6095C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51681338 | ||||||
chr13:51681488 | C | T | 2 | a0001c0001t0003g0166a0001c0001t0006g0169 | 2 | HG03927.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.279+6245C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51681488 | ||||||
chr13:51681499 | C | A | 2 | a0001c0001t0003g0207a0001c0001t0003g0208 | 2 | HG00642.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.279+6256C>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51681499 | ||||||
chr13:51681656 | A | G | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.279+6413A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51681656 | ||||||
chr13:51681741 | A | G | 8 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(5): Show | 8 | HG01192.hp1 HG01884.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.279+6498A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51681741 | ||||||
chr13:51682109 | C | A | 1 | a0001c0001t0025g0168 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.279+6866C>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51682109 | ||||||
chr13:51682537 | G | T | 1 | a0001c0001t0001g0126 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.279+7294G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51682537 | ||||||
chr13:51682813 | A | C | 1 | a0001c0001t0046g0109 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.279+7570A>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51682813 | ||||||
chr13:51682901 | G | A | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.279+7658G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51682901 | ||||||
chr13:51682955 | A | C | 2 | a0001c0006t0016g0277a0001c0007t0016g0278 | 2 | HG02258.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.279+7712A>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51682955 | ||||||
chr13:51683125 | T | A | 1 | a0001c0001t0034g0024 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.279+7882T>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51683125 | ||||||
chr13:51683165 | T | G | 1 | a0001c0001t0001g0054 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.279+7922T>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51683165 | ||||||
chr13:51683434 | C | T | 2 | a0001c0006t0016g0277a0001c0007t0016g0278 | 2 | HG02258.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.279+8191C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51683434 | ||||||
chr13:51683838 | G | C | 1 | a0001c0001t0001g0105 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.279+8595G>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51683838 | ||||||
chr13:51683882 | A | T | 1 | a0001c0001t0028g0061 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.279+8639A>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51683882 | ||||||
chr13:51683946 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.279+8703C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51683946 | ||||||
chr13:51683971 | A | T | 1 | a0001c0001t0042g0154 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.279+8728A>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51683971 | ||||||
chr13:51684368 | GT | G | 8 | a0001c0001t0010g0002a0001c0001t0010g0003a0001c0001t0010g0004others(5): Show | 8 | HG02257.hp2 HG02647.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.279+9141delT | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr13 | 51684368 | |||||
chr13:51684448 | C | G | 2 | a0001c0001t0020g0273a0001c0001t0029g0272 | 2 | HG02559.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.279+9205C>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51684448 | ||||||
chr13:51684509 | G | C | 1 | a0001c0001t0024g0009 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.279+9266G>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51684509 | ||||||
chr13:51684900 | C | G | 5 | a0001c0001t0003g0210a0001c0001t0003g0229a0001c0001t0003g0231others(2): Show | 5 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+9657C>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51684900 | ||||||
chr13:51684901 | G | A | 1 | a0001c0001t0001g0095 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.279+9658G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51684901 | ||||||
chr13:51684980 | T | C | 2 | a0001c0001t0020g0273a0001c0001t0029g0272 | 2 | HG02559.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.279+9737T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51684980 | ||||||
chr13:51685373 | C | T | 2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 2 | HG02109.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.279+10130C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51685373 | ||||||
chr13:51685623 | ATCT | A | 3 | a0001c0001t0013g0263a0001c0001t0013g0264a0001c0001t0013g0265 | 3 | HG02145.hp1 HG03041.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.279+10383_279+1038 others(7): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr13 | 51685623 | |||||
chr13:51685816 | C | G | 4 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0275others(1): Show | 4 | HG00733.hp2 HG01123.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.279+10573C>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51685816 | ||||||
chr13:51685839 | C | T | 1 | a0001c0006t0016g0277 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.279+10596C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51685839 | ||||||
chr13:51686065 | G | A | 2 | a0001c0006t0016g0277a0001c0007t0016g0278 | 2 | HG02258.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.279+10822G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51686065 | ||||||
chr13:51686117 | T | A | 1 | a0001c0001t0046g0109 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.279+10874T>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51686117 | ||||||
chr13:51686164 | A | G | 2 | a0001c0006t0016g0277a0001c0007t0016g0278 | 2 | HG02258.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.279+10921A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51686164 | ||||||
chr13:51686262 | C | G | 179 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(176): Show | 179 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.279+11019C>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51686262 | ||||||
chr13:51686331 | C | T | 4 | a0001c0001t0002g0259a0001c0001t0019g0260a0001c0001t0019g0261others(1): Show | 4 | HG02698.hp1 HG03491.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.279+11088C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51686331 | ||||||
chr13:51686953 | T | C | 1 | a0001c0001t0003g0217 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.279+11710T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51686953 | ||||||
chr13:51687026 | C | T | 1 | a0001c0001t0003g0240 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.279+11783C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51687026 | ||||||
chr13:51687125 | A | G | 30 | a0001c0001t0004g0177a0001c0001t0004g0178a0001c0001t0004g0182others(27): Show | 30 | HG00735.hp2 HG01081.hp2 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.279+11882A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51687125 | ||||||
chr13:51687255 | A | G | 4 | a0001c0001t0002g0259a0001c0001t0019g0260a0001c0001t0019g0261others(1): Show | 4 | HG02698.hp1 HG03491.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.279+12012A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51687255 | ||||||
chr13:51688203 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.279+12960C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51688203 | ||||||
chr13:51688300 | G | A | 1 | a0001c0001t0001g0268 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.279+13057G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51688300 | ||||||
chr13:51688301 | C | T | 2 | a0001c0001t0004g0196a0001c0001t0032g0202 | 2 | HG02622.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.279+13058C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51688301 | ||||||
chr13:51688542 | T | G | 1 | a0001c0001t0001g0120 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.279+13299T>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51688542 | ||||||
chr13:51688595 | G | A | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.279+13352G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51688595 | ||||||
chr13:51688638 | C | G | 1 | a0001c0001t0001g0187 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.279+13395C>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51688638 | ||||||
chr13:51688958 | G | A | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.279+13715G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51688958 | ||||||
chr13:51688967 | A | G | 265 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(262): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.279+13724A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51688967 | ||||||
chr13:51689366 | C | T | 177 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(174): Show | 177 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.279+14123C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51689366 | ||||||
chr13:51689393 | G | A | 177 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(174): Show | 177 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.279+14150G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51689393 | ||||||
chr13:51689525 | A | G | 1 | a0003c0004t0001g0108 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.280-14071A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51689525 | ||||||
chr13:51689563 | G | C | 1 | a0001c0001t0007g0070 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.280-14033G>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51689563 | ||||||
chr13:51689698 | A | G | 44 | a0001c0001t0003g0053a0001c0002t0002g0014a0001c0002t0002g0015others(41): Show | 44 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(41): Show |
intron_variant | MODIFIER | c.280-13898A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51689698 | ||||||
chr13:51689712 | T | A | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.280-13884T>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51689712 | ||||||
chr13:51689726 | T | G | 1 | a0001c0001t0034g0024 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.280-13870T>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51689726 | ||||||
chr13:51689727 | C | G | 1 | a0001c0001t0034g0024 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.280-13869C>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51689727 | ||||||
chr13:51689728 | C | A | 1 | a0001c0001t0034g0024 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.280-13868C>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51689728 | ||||||
chr13:51690008 | C | A | 6 | a0001c0001t0001g0065a0001c0001t0001g0074a0001c0001t0001g0081others(3): Show | 6 | HG00423.hp2 NA18964.hp2 NA18991.hp2 others(3): Show |
intron_variant | MODIFIER | c.280-13588C>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51690008 | ||||||
chr13:51690161 | T | A | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.280-13435T>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51690161 | ||||||
chr13:51690196 | A | AT | 5 | a0001c0002t0002g0148a0001c0002t0011g0022a0001c0002t0011g0044others(2): Show | 5 | HG00408.hp1 HG00423.hp1 HG00609.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-13392dupT | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr13 | 51690196 | |||||
chr13:51690197 | T | A | 1 | a0001c0001t0031g0149 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.280-13399T>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51690197 | ||||||
chr13:51690197 | T | TA | 267 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(264): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.280-13399_280-1339 others(5): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51690197 | ||||||
chr13:51690198 | T | A | 1 | a0003c0004t0001g0108 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.280-13398T>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51690198 | ||||||
chr13:51690199 | T | A | 1 | a0001c0001t0031g0149 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.280-13397T>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51690199 | ||||||
chr13:51690247 | A | G | 48 | a0001c0001t0002g0259a0001c0001t0003g0053a0001c0001t0019g0260others(45): Show | 48 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(45): Show |
intron_variant | MODIFIER | c.280-13349A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51690247 | ||||||
chr13:51690291 | T | A | 4 | a0001c0002t0011g0022a0001c0002t0011g0044a0001c0002t0011g0045others(1): Show | 4 | HG00408.hp1 HG00423.hp1 HG00609.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-13305T>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51690291 | ||||||
chr13:51690291 | T | C | 165 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(162): Show | 165 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.280-13305T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51690291 | ||||||
chr13:51690325 | C | T | 1 | a0001c0001t0029g0272 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.280-13271C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51690325 | ||||||
chr13:51690345 | C | G | 1 | a0001c0002t0002g0041 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.280-13251C>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51690345 | ||||||
chr13:51690372 | A | G | 2 | a0001c0001t0001g0138a0001c0001t0001g0140 | 2 | HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.280-13224A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51690372 | ||||||
chr13:51690518 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.280-13078C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51690518 | ||||||
chr13:51690644 | C | A | 1 | a0001c0007t0016g0278 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.280-12952C>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51690644 | ||||||
chr13:51690645 | G | T | 3 | a0001c0001t0013g0263a0001c0001t0013g0264a0001c0001t0013g0265 | 3 | HG02145.hp1 HG03041.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.280-12951G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51690645 | ||||||
chr13:51690654 | A | G | 1 | a0001c0002t0002g0251 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.280-12942A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51690654 | ||||||
chr13:51690680 | G | A | 1 | a0001c0001t0003g0241 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.280-12916G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51690680 | ||||||
chr13:51690701 | G | A | 2 | a0001c0006t0016g0277a0001c0007t0016g0278 | 2 | HG02258.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.280-12895G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51690701 | ||||||
chr13:51690823 | G | T | 1 | a0001c0007t0016g0278 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.280-12773G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51690823 | ||||||
chr13:51690834 | A | T | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.280-12762A>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51690834 | ||||||
chr13:51690914 | A | T | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.280-12682A>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51690914 | ||||||
chr13:51690972 | T | C | 14 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(11): Show | 14 | HG00323.hp1 HG00558.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.280-12624T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51690972 | ||||||
chr13:51691210 | G | A | 1 | a0001c0001t0005g0019 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.280-12386G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51691210 | ||||||
chr13:51691444 | C | T | 179 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(176): Show | 179 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.280-12152C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51691444 | ||||||
chr13:51691459 | T | C | 1 | a0001c0002t0002g0039 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.280-12137T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51691459 | ||||||
chr13:51691478 | C | G | 1 | a0001c0001t0001g0010 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.280-12118C>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51691478 | ||||||
chr13:51691541 | G | A | 11 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(8): Show | 11 | HG01106.hp1 HG01433.hp2 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.280-12055G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51691541 | ||||||
chr13:51691564 | T | C | 1 | a0001c0001t0001g0159 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.280-12032T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51691564 | ||||||
chr13:51691677 | C | G | 1 | a0001c0001t0029g0272 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.280-11919C>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51691677 | ||||||
chr13:51691698 | G | A | 2 | a0001c0001t0046g0109a0004c0005t0022g0150 | 2 | HG01884.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.280-11898G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51691698 | ||||||
chr13:51691764 | T | C | 1 | a0001c0001t0007g0070 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.280-11832T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51691764 | ||||||
chr13:51691804 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.280-11792C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51691804 | ||||||
chr13:51691805 | G | A | 2 | a0001c0001t0005g0016a0001c0001t0005g0017 | 2 | HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.280-11791G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51691805 | ||||||
chr13:51691839 | T | A | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.280-11757T>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51691839 | ||||||
chr13:51691870 | C | T | 1 | a0001c0001t0031g0149 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.280-11726C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51691870 | ||||||
chr13:51692054 | A | C | 1 | a0001c0001t0001g0105 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.280-11542A>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51692054 | ||||||
chr13:51692055 | C | A | 1 | a0001c0001t0001g0105 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.280-11541C>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51692055 | ||||||
chr13:51692090 | G | T | 1 | a0001c0001t0001g0105 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.280-11506G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51692090 | ||||||
chr13:51692194 | T | G | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.280-11402T>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51692194 | ||||||
chr13:51692317 | A | T | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.280-11279A>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51692317 | ||||||
chr13:51692318 | T | A | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.280-11278T>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51692318 | ||||||
chr13:51692350 | T | G | 1 | a0001c0001t0003g0236 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.280-11246T>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51692350 | ||||||
chr13:51692356 | G | A | 1 | a0001c0002t0002g0250 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.280-11240G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51692356 | ||||||
chr13:51692358 | A | G | 2 | a0001c0001t0046g0109a0004c0005t0022g0150 | 2 | HG01884.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.280-11238A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51692358 | ||||||
chr13:51692362 | C | A | 2 | a0001c0001t0001g0057a0001c0001t0001g0059 | 2 | HG02615.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.280-11234C>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51692362 | ||||||
chr13:51692405 | G | T | 2 | a0001c0001t0003g0115a0001c0001t0003g0227 | 2 | HG03831.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.280-11191G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51692405 | ||||||
chr13:51692494 | A | G | 1 | a0001c0001t0001g0086 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.280-11102A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51692494 | ||||||
chr13:51692588 | C | T | 1 | a0001c0001t0031g0149 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.280-11008C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51692588 | ||||||
chr13:51692634 | A | G | 1 | a0001c0001t0009g0145 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.280-10962A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51692634 | ||||||
chr13:51692790 | G | A | 62 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0012others(59): Show | 62 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.280-10806G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51692790 | ||||||
chr13:51693063 | C | T | 2 | a0001c0002t0002g0014a0001c0002t0002g0015 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.280-10533C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51693063 | ||||||
chr13:51693133 | T | A | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.280-10463T>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51693133 | ||||||
chr13:51693197 | A | C | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.280-10399A>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51693197 | ||||||
chr13:51693208 | T | A | 1 | a0001c0001t0029g0272 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.280-10388T>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51693208 | ||||||
chr13:51693322 | T | C | 2 | a0001c0006t0016g0277a0001c0007t0016g0278 | 2 | HG02258.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.280-10274T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51693322 | ||||||
chr13:51693436 | A | T | 6 | a0001c0001t0010g0002a0001c0001t0010g0003a0001c0001t0010g0004others(3): Show | 6 | HG02257.hp2 HG02647.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.280-10160A>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51693436 | ||||||
chr13:51693490 | G | T | 1 | a0001c0001t0018g0270 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.280-10106G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51693490 | ||||||
chr13:51693667 | G | C | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.280-9929G>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51693667 | ||||||
chr13:51693673 | G | A | 44 | a0001c0001t0003g0053a0001c0002t0002g0014a0001c0002t0002g0015others(41): Show | 44 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(41): Show |
intron_variant | MODIFIER | c.280-9923G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51693673 | ||||||
chr13:51693804 | T | A | 1 | a0001c0001t0034g0024 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.280-9792T>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51693804 | ||||||
chr13:51693863 | A | G | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.280-9733A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51693863 | ||||||
chr13:51694015 | T | G | 1 | a0001c0001t0003g0225 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.280-9581T>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51694015 | ||||||
chr13:51694156 | C | T | 2 | a0001c0001t0046g0109a0004c0005t0022g0150 | 2 | HG01884.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.280-9440C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51694156 | ||||||
chr13:51694170 | T | G | 1 | a0001c0001t0001g0157 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.280-9426T>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51694170 | ||||||
chr13:51694182 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.280-9414C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51694182 | ||||||
chr13:51694199 | T | G | 4 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0275others(1): Show | 4 | HG00733.hp2 HG01123.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-9397T>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51694199 | ||||||
chr13:51694248 | C | G | 1 | a0001c0001t0034g0024 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.280-9348C>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51694248 | ||||||
chr13:51694411 | T | G | 1 | a0001c0001t0026g0155 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.280-9185T>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51694411 | ||||||
chr13:51694425 | T | A | 1 | a0001c0001t0001g0105 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.280-9171T>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51694425 | ||||||
chr13:51694427 | T | C | 4 | a0001c0001t0002g0259a0001c0001t0019g0260a0001c0001t0019g0261others(1): Show | 4 | HG02698.hp1 HG03491.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-9169T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51694427 | ||||||
chr13:51694473 | G | T | 3 | a0001c0001t0013g0263a0001c0001t0013g0264a0001c0001t0013g0265 | 3 | HG02145.hp1 HG03041.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.280-9123G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51694473 | ||||||
chr13:51694539 | G | T | 2 | a0001c0002t0002g0042a0001c0002t0002g0052 | 2 | HG02015.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.280-9057G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51694539 | ||||||
chr13:51694587 | C | T | 2 | a0001c0001t0001g0105a0003c0004t0001g0108 | 2 | HG02451.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.280-9009C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51694587 | ||||||
chr13:51694661 | T | C | 272 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(269): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.280-8935T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51694661 | ||||||
chr13:51694773 | G | A | 1 | a0001c0001t0009g0141 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.280-8823G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51694773 | ||||||
chr13:51694781 | C | T | 1 | a0001c0001t0009g0141 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.280-8815C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51694781 | ||||||
chr13:51694783 | A | C | 1 | a0001c0001t0009g0141 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.280-8813A>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51694783 | ||||||
chr13:51694783 | A | G | 2 | a0001c0001t0019g0260a0001c0001t0019g0261 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.280-8813A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51694783 | ||||||
chr13:51694811 | A | C | 1 | a0001c0001t0009g0141 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.280-8785A>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51694811 | ||||||
chr13:51694825 | G | A | 1 | a0001c0001t0009g0141 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.280-8771G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51694825 | ||||||
chr13:51694827 | C | T | 1 | a0001c0001t0009g0141 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.280-8769C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51694827 | ||||||
chr13:51694837 | G | T | 1 | a0001c0001t0020g0273 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.280-8759G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51694837 | ||||||
chr13:51694847 | A | G | 1 | a0001c0001t0009g0141 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.280-8749A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51694847 | ||||||
chr13:51694851 | T | C | 1 | a0001c0001t0009g0141 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.280-8745T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51694851 | ||||||
chr13:51694867 | G | C | 1 | a0001c0001t0009g0141 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.280-8729G>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51694867 | ||||||
chr13:51694868 | G | T | 1 | a0001c0001t0009g0141 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.280-8728G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51694868 | ||||||
chr13:51694877 | G | A | 1 | a0001c0001t0009g0141 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.280-8719G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51694877 | ||||||
chr13:51694886 | T | C | 1 | a0001c0001t0009g0141 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.280-8710T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51694886 | ||||||
chr13:51694887 | G | A | 1 | a0001c0001t0009g0141 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.280-8709G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51694887 | ||||||
chr13:51694888 | T | C | 1 | a0001c0001t0009g0141 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.280-8708T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51694888 | ||||||
chr13:51694908 | C | T | 1 | a0001c0001t0009g0141 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.280-8688C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51694908 | ||||||
chr13:51694914 | C | T | 1 | a0001c0001t0009g0141 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.280-8682C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51694914 | ||||||
chr13:51694915 | A | G | 1 | a0001c0001t0009g0141 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.280-8681A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51694915 | ||||||
chr13:51694925 | A | T | 1 | a0001c0001t0009g0141 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.280-8671A>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51694925 | ||||||
chr13:51694928 | C | A | 1 | a0001c0001t0009g0141 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.280-8668C>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51694928 | ||||||
chr13:51694940 | C | A | 1 | a0001c0001t0009g0141 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.280-8656C>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51694940 | ||||||
chr13:51694953 | C | G | 1 | a0001c0001t0001g0069 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.280-8643C>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51694953 | ||||||
chr13:51694970 | G | A | 1 | a0001c0001t0004g0203 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.280-8626G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51694970 | ||||||
chr13:51695002 | G | A | 12 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0167others(9): Show | 12 | HG02015.hp2 HG02717.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.280-8594G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51695002 | ||||||
chr13:51695011 | A | G | 1 | a0001c0001t0029g0272 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.280-8585A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51695011 | ||||||
chr13:51695014 | C | A | 54 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0012others(51): Show | 54 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(51): Show |
intron_variant | MODIFIER | c.280-8582C>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51695014 | ||||||
chr13:51695034 | A | T | 2 | a0001c0001t0017g0161a0001c0001t0017g0162 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.280-8562A>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51695034 | ||||||
chr13:51695055 | A | G | 2 | a0001c0001t0020g0273a0001c0001t0029g0272 | 2 | HG02559.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.280-8541A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51695055 | ||||||
chr13:51695105 | A | C | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.280-8491A>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51695105 | ||||||
chr13:51695121 | G | C | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.280-8475G>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51695121 | ||||||
chr13:51695135 | C | T | 3 | a0001c0001t0013g0263a0001c0001t0013g0264a0001c0001t0013g0265 | 3 | HG02145.hp1 HG03041.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.280-8461C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51695135 | ||||||
chr13:51695254 | C | T | 1 | a0001c0001t0013g0264 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.280-8342C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51695254 | ||||||
chr13:51695398 | A | C | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.280-8198A>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51695398 | ||||||
chr13:51695399 | C | A | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.280-8197C>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51695399 | ||||||
chr13:51695400 | A | G | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.280-8196A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51695400 | ||||||
chr13:51695471 | C | G | 5 | a0002c0003t0004g0179a0002c0003t0004g0180a0002c0003t0004g0181others(2): Show | 5 | HG01081.hp2 HG01496.hp2 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.280-8125C>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51695471 | ||||||
chr13:51695565 | A | G | 4 | a0001c0001t0046g0109a0001c0006t0016g0277a0001c0007t0016g0278others(1): Show | 4 | HG01884.hp2 HG02258.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.280-8031A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51695565 | ||||||
chr13:51695568 | T | C | 2 | a0001c0001t0010g0004a0001c0001t0030g0001 | 2 | HG02257.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.280-8028T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51695568 | ||||||
chr13:51695569 | G | A | 2 | a0001c0001t0010g0004a0001c0001t0030g0001 | 2 | HG02257.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.280-8027G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51695569 | ||||||
chr13:51695595 | G | T | 1 | a0001c0001t0004g0203 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.280-8001G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51695595 | ||||||
chr13:51695695 | A | G | 8 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(5): Show | 8 | HG01192.hp1 HG01884.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.280-7901A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51695695 | ||||||
chr13:51695846 | G | C | 2 | a0001c0001t0003g0236a0001c0001t0028g0061 | 2 | HG03486.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.280-7750G>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51695846 | ||||||
chr13:51695904 | T | C | 2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 2 | HG02109.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.280-7692T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51695904 | ||||||
chr13:51695910 | C | T | 50 | a0001c0001t0002g0259a0001c0001t0003g0053a0001c0001t0010g0005others(47): Show | 50 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(47): Show |
intron_variant | MODIFIER | c.280-7686C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51695910 | ||||||
chr13:51695964 | G | A | 1 | a0001c0001t0001g0266 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.280-7632G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51695964 | ||||||
chr13:51695986 | C | T | 1 | a0001c0002t0002g0026 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.280-7610C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51695986 | ||||||
chr13:51696094 | C | G | 1 | a0001c0001t0034g0024 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.280-7502C>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51696094 | ||||||
chr13:51696394 | C | G | 2 | a0001c0001t0004g0183a0001c0001t0004g0276 | 2 | HG00735.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.280-7202C>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51696394 | ||||||
chr13:51696486 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.280-7110G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51696486 | ||||||
chr13:51696700 | A | G | 3 | a0001c0001t0001g0076a0001c0001t0001g0089a0001c0001t0001g0100 | 3 | HG03491.hp1 HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.280-6896A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51696700 | ||||||
chr13:51697097 | G | A | 1 | a0001c0001t0004g0186 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.280-6499G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51697097 | ||||||
chr13:51697442 | G | A | 1 | a0001c0002t0045g0035 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.280-6154G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51697442 | ||||||
chr13:51697458 | C | T | 1 | a0001c0001t0020g0273 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.280-6138C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51697458 | ||||||
chr13:51697632 | C | CA | 7 | a0001c0001t0001g0104a0001c0001t0001g0126a0001c0001t0001g0266others(4): Show | 7 | HG00558.hp2 HG01257.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.280-5948dupA | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr13 | 51697632 | |||||
chr13:51697649 | T | A | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.280-5947T>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51697649 | ||||||
chr13:51698247 | G | A | 2 | a0001c0001t0001g0267a0001c0001t0001g0268 | 2 | HG02109.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.280-5349G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51698247 | ||||||
chr13:51698357 | A | G | 3 | a0001c0001t0013g0263a0001c0001t0013g0264a0001c0001t0013g0265 | 3 | HG02145.hp1 HG03041.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.280-5239A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51698357 | ||||||
chr13:51698491 | A | G | 54 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0012others(51): Show | 54 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(51): Show |
intron_variant | MODIFIER | c.280-5105A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51698491 | ||||||
chr13:51698556 | G | A | 4 | a0001c0002t0011g0022a0001c0002t0011g0044a0001c0002t0011g0045others(1): Show | 4 | HG00408.hp1 HG00423.hp1 HG00609.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-5040G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51698556 | ||||||
chr13:51698556 | G | C | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.280-5040G>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51698556 | ||||||
chr13:51698725 | T | A | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.280-4871T>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51698725 | ||||||
chr13:51698802 | T | G | 2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 2 | HG02109.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.280-4794T>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51698802 | ||||||
chr13:51698840 | A | G | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.280-4756A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51698840 | ||||||
chr13:51699063 | C | A | 1 | a0001c0001t0046g0109 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.280-4533C>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51699063 | ||||||
chr13:51699202 | C | T | 12 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0167others(9): Show | 12 | HG02015.hp2 HG02717.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.280-4394C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51699202 | ||||||
chr13:51699364 | G | A | 1 | a0001c0002t0002g0252 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.280-4232G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51699364 | ||||||
chr13:51699486 | G | A | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.280-4110G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51699486 | ||||||
chr13:51699516 | A | G | 1 | a0001c0001t0009g0141 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.280-4080A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51699516 | ||||||
chr13:51699673 | AAT | A | 4 | a0001c0001t0002g0259a0001c0001t0019g0260a0001c0001t0019g0261others(1): Show | 4 | HG02698.hp1 HG03491.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-3921_280-3920d others(4): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr13 | 51699673 | |||||
chr13:51699684 | A | G | 1 | a0001c0001t0001g0077 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.280-3912A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51699684 | ||||||
chr13:51699726 | G | T | 1 | a0001c0002t0045g0035 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.280-3870G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51699726 | ||||||
chr13:51699909 | A | C | 3 | a0001c0001t0003g0053a0001c0002t0002g0037a0001c0002t0002g0148 | 3 | HG01346.hp1 HG02486.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.280-3687A>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51699909 | ||||||
chr13:51700452 | A | G | 10 | a0001c0002t0002g0029a0001c0002t0002g0030a0001c0002t0002g0031others(7): Show | 10 | HG00673.hp2 HG02015.hp1 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.280-3144A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51700452 | ||||||
chr13:51700484 | A | G | 1 | a0001c0001t0001g0128 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.280-3112A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51700484 | ||||||
chr13:51700550 | A | G | 1 | a0001c0001t0009g0141 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.280-3046A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51700550 | ||||||
chr13:51700573 | T | C | 1 | a0001c0001t0008g0214 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.280-3023T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51700573 | ||||||
chr13:51700607 | G | A | 175 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(172): Show | 175 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.280-2989G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51700607 | ||||||
chr13:51700808 | A | G | 48 | a0001c0001t0002g0259a0001c0001t0003g0053a0001c0001t0019g0260others(45): Show | 48 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(45): Show |
intron_variant | MODIFIER | c.280-2788A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51700808 | ||||||
chr13:51700828 | G | A | 1 | a0001c0001t0001g0007 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.280-2768G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51700828 | ||||||
chr13:51700859 | C | T | 4 | a0001c0001t0001g0266a0001c0001t0001g0267a0001c0001t0001g0268others(1): Show | 4 | HG02109.hp2 HG02145.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-2737C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51700859 | ||||||
chr13:51701010 | A | C | 1 | a0001c0001t0031g0149 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.280-2586A>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51701010 | ||||||
chr13:51701247 | GTGTGGTG others(9): Show |
G | 1 | a0001c0001t0046g0109 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.280-2345_280-2330d others(18): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr13 | 51701247 | |||||
chr13:51701289 | G | A | 4 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0167others(1): Show | 4 | HG02717.hp1 HG02723.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.280-2307G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51701289 | ||||||
chr13:51701385 | G | A | 3 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140 | 3 | HG02647.hp2 HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.280-2211G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51701385 | ||||||
chr13:51701520 | C | CA | 19 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(16): Show | 19 | HG00735.hp1 HG01192.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.280-2057dupA | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr13 | 51701520 | |||||
chr13:51701520 | C | CAA | 98 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0012others(95): Show | 98 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.280-2058_280-2057d others(4): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr13 | 51701520 | |||||
chr13:51701520 | CA | C | 10 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0124others(7): Show | 10 | HG00609.hp2 HG02074.hp1 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.280-2057delA | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr13 | 51701520 | |||||
chr13:51701743 | G | C | 1 | a0001c0001t0012g0205 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.280-1853G>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51701743 | ||||||
chr13:51701982 | G | A | 3 | a0001c0001t0003g0229a0001c0001t0003g0246a0001c0001t0040g0136 | 3 | HG01069.hp2 HG01071.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.280-1614G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51701982 | ||||||
chr13:51702086 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.280-1510C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51702086 | ||||||
chr13:51702491 | T | G | 2 | a0001c0001t0015g0127a0001c0001t0015g0135 | 2 | HG00323.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.280-1105T>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51702491 | ||||||
chr13:51702600 | A | G | 1 | a0001c0001t0009g0113 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.280-996A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51702600 | ||||||
chr13:51702651 | G | A | 28 | a0001c0001t0004g0177a0001c0001t0004g0178a0001c0001t0004g0182others(25): Show | 28 | HG00735.hp2 HG01081.hp2 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.280-945G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51702651 | ||||||
chr13:51702882 | T | G | 41 | a0001c0001t0004g0177a0001c0001t0004g0178a0001c0001t0004g0182others(38): Show | 41 | HG00735.hp2 HG01081.hp2 HG01106.hp1 others(38): Show |
intron_variant | MODIFIER | c.280-714T>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51702882 | ||||||
chr13:51702918 | G | T | 5 | a0002c0003t0004g0179a0002c0003t0004g0180a0002c0003t0004g0181others(2): Show | 5 | HG01081.hp2 HG01496.hp2 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.280-678G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51702918 | ||||||
chr13:51702931 | G | T | 5 | a0002c0003t0004g0179a0002c0003t0004g0180a0002c0003t0004g0181others(2): Show | 5 | HG01081.hp2 HG01496.hp2 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.280-665G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51702931 | ||||||
chr13:51703096 | T | C | 1 | a0001c0006t0016g0277 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.280-500T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51703096 | ||||||
chr13:51703256 | G | A | 3 | a0001c0002t0002g0032a0001c0002t0002g0151a0001c0002t0002g0152 | 3 | HG01433.hp2 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.280-340G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51703256 | ||||||
chr13:51703309 | A | G | 1 | a0003c0004t0001g0108 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.280-287A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51703309 | ||||||
chr13:51703322 | G | A | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.280-274G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51703322 | ||||||
chr13:51703406 | T | C | 2 | a0001c0001t0010g0002a0001c0001t0010g0003 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.280-190T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51703406 | ||||||
chr13:51703451 | G | A | 1 | a0001c0001t0020g0273 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.280-145G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51703451 | ||||||
chr13:51703500 | G | A | 1 | a0001c0006t0016g0277 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.280-96G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51703500 | ||||||
chr13:51703557 | G | T | 48 | a0001c0001t0002g0259a0001c0001t0003g0053a0001c0001t0019g0260others(45): Show | 48 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(45): Show |
intron_variant | MODIFIER | c.280-39G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 3/11 | chr13 | 51703557 | ||||||
chr13:51703727 | A | G | 1 | a0001c0001t0004g0193 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.334+77A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51703727 | ||||||
chr13:51703735 | T | C | 1 | a0001c0001t0046g0109 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.334+85T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51703735 | ||||||
chr13:51703929 | G | A | 1 | a0001c0001t0005g0019 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.334+279G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51703929 | ||||||
chr13:51704423 | G | A | 179 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(176): Show | 179 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.334+773G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51704423 | ||||||
chr13:51704597 | C | T | 8 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(5): Show | 8 | HG01106.hp1 HG02055.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.334+947C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51704597 | ||||||
chr13:51704737 | A | G | 2 | a0001c0006t0016g0277a0001c0007t0016g0278 | 2 | HG02258.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.334+1087A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51704737 | ||||||
chr13:51704972 | T | C | 8 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(5): Show | 8 | HG01192.hp1 HG01884.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.334+1322T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51704972 | ||||||
chr13:51705002 | A | C | 1 | a0001c0001t0010g0004 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.334+1352A>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51705002 | ||||||
chr13:51705093 | C | G | 1 | a0001c0001t0001g0266 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.334+1443C>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51705093 | ||||||
chr13:51705094 | T | G | 1 | a0001c0001t0001g0266 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.334+1444T>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51705094 | ||||||
chr13:51705530 | C | T | 2 | a0001c0001t0006g0171a0001c0001t0006g0174 | 2 | NA18941.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.334+1880C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51705530 | ||||||
chr13:51705571 | G | GT | 6 | a0001c0001t0001g0266a0001c0001t0001g0267a0001c0001t0001g0268others(3): Show | 6 | HG01884.hp2 HG02109.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.334+1932dupT | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr13 | 51705571 | |||||
chr13:51705664 | C | T | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.334+2014C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51705664 | ||||||
chr13:51705674 | G | A | 2 | a0001c0006t0016g0277a0001c0007t0016g0278 | 2 | HG02258.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.334+2024G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51705674 | ||||||
chr13:51706007 | A | G | 1 | a0001c0001t0035g0195 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.334+2357A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51706007 | ||||||
chr13:51706111 | C | T | 1 | a0001c0001t0007g0092 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.334+2461C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51706111 | ||||||
chr13:51706240 | C | T | 2 | a0001c0001t0017g0161a0001c0001t0017g0162 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.334+2590C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51706240 | ||||||
chr13:51706291 | G | C | 1 | a0002c0003t0004g0185 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.334+2641G>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51706291 | ||||||
chr13:51706463 | G | A | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.334+2813G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51706463 | ||||||
chr13:51706690 | G | A | 1 | a0001c0001t0007g0092 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.334+3040G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51706690 | ||||||
chr13:51707165 | G | A | 1 | a0001c0002t0002g0257 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.334+3515G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51707165 | ||||||
chr13:51707190 | C | T | 1 | a0001c0001t0003g0208 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.334+3540C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51707190 | ||||||
chr13:51707298 | A | G | 54 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0012others(51): Show | 54 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(51): Show |
intron_variant | MODIFIER | c.334+3648A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51707298 | ||||||
chr13:51707302 | G | A | 1 | a0001c0001t0039g0274 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.334+3652G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51707302 | ||||||
chr13:51707303 | C | T | 3 | a0001c0001t0013g0263a0001c0001t0013g0264a0001c0001t0013g0265 | 3 | HG02145.hp1 HG03041.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.334+3653C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51707303 | ||||||
chr13:51707348 | G | A | 1 | a0001c0001t0004g0203 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.334+3698G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51707348 | ||||||
chr13:51707832 | G | T | 1 | a0001c0001t0004g0206 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.334+4182G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51707832 | ||||||
chr13:51707939 | C | CT | 47 | a0001c0001t0001g0027a0001c0001t0001g0105a0001c0001t0001g0107others(44): Show | 47 | HG00323.hp2 HG00423.hp1 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.334+4321dupT | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr13 | 51707939 | |||||
chr13:51707939 | C | CTT | 27 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0126others(24): Show | 27 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(24): Show |
intron_variant | MODIFIER | c.334+4320_334+4321d others(4): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr13 | 51707939 | |||||
chr13:51707939 | C | CTTT | 33 | a0001c0001t0001g0059a0001c0001t0001g0106a0001c0001t0001g0120others(30): Show | 33 | HG00280.hp1 HG00323.hp1 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.334+4319_334+4321d others(5): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr13 | 51707939 | |||||
chr13:51707939 | C | CTTTT | 21 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0118others(18): Show | 21 | HG01243.hp2 HG01261.hp1 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.334+4318_334+4321d others(6): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr13 | 51707939 | |||||
chr13:51707939 | C | CTTTTT | 8 | a0001c0001t0001g0057a0001c0001t0001g0121a0001c0001t0001g0144others(5): Show | 8 | HG01192.hp1 HG01891.hp2 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.334+4317_334+4321d others(7): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr13 | 51707939 | |||||
chr13:51707939 | C | CTTTTTT | 6 | a0001c0001t0001g0054a0001c0001t0001g0122a0001c0001t0003g0226others(3): Show | 6 | HG01891.hp1 HG02622.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.334+4316_334+4321d others(8): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr13 | 51707939 | |||||
chr13:51707939 | C | CTTTTTTT others(4): Show |
1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.334+4311_334+4321d others(13): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr13 | 51707939 | |||||
chr13:51707939 | C | CTTTTTTT others(5): Show |
1 | a0001c0001t0001g0266 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.334+4310_334+4321d others(14): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr13 | 51707939 | |||||
chr13:51707939 | CT | C | 7 | a0001c0001t0001g0139a0001c0001t0044g0262a0001c0002t0002g0131others(4): Show | 7 | HG00642.hp2 HG01257.hp2 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.334+4321delT | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr13 | 51707939 | |||||
chr13:51707939 | CTT | C | 22 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0013others(19): Show | 22 | HG00673.hp1 HG01192.hp2 HG01361.hp1 others(19): Show |
intron_variant | MODIFIER | c.334+4320_334+4321d others(4): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr13 | 51707939 | |||||
chr13:51707939 | CTTT | C | 31 | a0001c0001t0001g0012a0001c0001t0001g0063a0001c0001t0001g0065others(28): Show | 31 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(28): Show |
intron_variant | MODIFIER | c.334+4319_334+4321d others(5): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr13 | 51707939 | |||||
chr13:51707939 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0004g0269 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.334+4312_334+4321d others(12): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr13 | 51707939 | |||||
chr13:51707939 | CTTTTTTT others(4): Show |
C | 4 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0275others(1): Show | 4 | HG00733.hp2 HG01123.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.334+4311_334+4321d others(13): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr13 | 51707939 | |||||
chr13:51707939 | CTTTTTTT others(5): Show |
C | 7 | a0001c0001t0003g0234a0001c0001t0010g0002a0001c0001t0010g0003others(4): Show | 7 | HG02257.hp2 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.334+4310_334+4321d others(14): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr13 | 51707939 | |||||
chr13:51707939 | CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0046g0109 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.334+4309_334+4321d others(15): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr13 | 51707939 | |||||
chr13:51707975 | G | T | 1 | a0001c0001t0001g0077 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.334+4325G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51707975 | ||||||
chr13:51708072 | A | G | 10 | a0001c0002t0002g0029a0001c0002t0002g0030a0001c0002t0002g0031others(7): Show | 10 | HG00673.hp2 HG02015.hp1 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.334+4422A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51708072 | ||||||
chr13:51708120 | G | C | 1 | a0001c0001t0046g0109 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.334+4470G>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51708120 | ||||||
chr13:51708323 | C | G | 1 | a0001c0001t0004g0177 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.334+4673C>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51708323 | ||||||
chr13:51708326 | TA | T | 266 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(263): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.334+4692delA | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr13 | 51708326 | |||||
chr13:51708340 | A | T | 1 | a0001c0001t0001g0175 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.334+4690A>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51708340 | ||||||
chr13:51708342 | AT | A | 3 | a0001c0001t0001g0084a0001c0001t0001g0102a0001c0001t0002g0085 | 3 | NA18977.hp1 NA18983.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.334+4693delT | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51708342 | ||||||
chr13:51708382 | G | T | 2 | a0001c0006t0016g0277a0001c0007t0016g0278 | 2 | HG02258.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.334+4732G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51708382 | ||||||
chr13:51708581 | TA | T | 43 | a0001c0001t0003g0115a0001c0001t0003g0163a0001c0001t0003g0166others(40): Show | 43 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(40): Show |
intron_variant | MODIFIER | c.334+4942delA | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr13 | 51708581 | |||||
chr13:51708960 | C | T | 4 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0275others(1): Show | 4 | HG00733.hp2 HG01123.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.334+5310C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51708960 | ||||||
chr13:51708977 | C | T | 1 | a0001c0001t0001g0144 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.334+5327C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51708977 | ||||||
chr13:51709021 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.334+5371C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51709021 | ||||||
chr13:51709164 | C | T | 48 | a0001c0001t0002g0259a0001c0001t0003g0053a0001c0001t0019g0260others(45): Show | 48 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(45): Show |
intron_variant | MODIFIER | c.334+5514C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51709164 | ||||||
chr13:51709426 | C | G | 1 | a0001c0001t0046g0109 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.334+5776C>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51709426 | ||||||
chr13:51709453 | G | A | 7 | a0001c0001t0001g0075a0001c0001t0001g0084a0001c0001t0001g0087others(4): Show | 7 | HG01257.hp1 NA18969.hp2 NA18977.hp1 others(4): Show |
intron_variant | MODIFIER | c.334+5803G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51709453 | ||||||
chr13:51709453 | G | C | 3 | a0001c0001t0036g0247a0001c0001t0038g0248a0001c0001t0039g0274 | 3 | HG00408.hp2 NA18955.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.334+5803G>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51709453 | ||||||
chr13:51709563 | G | C | 2 | a0001c0001t0003g0211a0001c0001t0003g0234 | 2 | NA18982.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.334+5913G>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51709563 | ||||||
chr13:51709648 | T | C | 1 | a0001c0001t0003g0222 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.334+5998T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51709648 | ||||||
chr13:51709651 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.334+6001C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51709651 | ||||||
chr13:51709813 | A | C | 1 | a0001c0001t0001g0142 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.334+6163A>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51709813 | ||||||
chr13:51709922 | C | G | 1 | a0001c0001t0001g0139 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.334+6272C>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51709922 | ||||||
chr13:51709978 | A | C | 1 | a0001c0006t0016g0277 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.334+6328A>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51709978 | ||||||
chr13:51709979 | C | A | 1 | a0001c0006t0016g0277 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.334+6329C>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51709979 | ||||||
chr13:51709987 | A | G | 48 | a0001c0001t0002g0259a0001c0001t0003g0053a0001c0001t0019g0260others(45): Show | 48 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(45): Show |
intron_variant | MODIFIER | c.334+6337A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51709987 | ||||||
chr13:51710029 | A | C | 2 | a0001c0001t0001g0011a0001c0001t0001g0275 | 2 | HG00733.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.334+6379A>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51710029 | ||||||
chr13:51710055 | C | T | 1 | a0001c0001t0042g0154 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.334+6405C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51710055 | ||||||
chr13:51710104 | T | C | 1 | a0001c0001t0001g0008 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.334+6454T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51710104 | ||||||
chr13:51710107 | T | A | 2 | a0001c0001t0010g0005a0001c0001t0010g0006 | 2 | HG02647.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.334+6457T>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51710107 | ||||||
chr13:51710118 | C | T | 4 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0275others(1): Show | 4 | HG00733.hp2 HG01123.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.334+6468C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51710118 | ||||||
chr13:51710136 | C | T | 2 | a0001c0001t0001g0137a0001c0001t0001g0228 | 2 | HG03492.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.334+6486C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51710136 | ||||||
chr13:51710150 | C | T | 1 | a0001c0001t0023g0058 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.334+6500C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51710150 | ||||||
chr13:51710156 | C | A | 2 | a0001c0001t0001g0104a0001c0001t0001g0125 | 2 | HG00423.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.334+6506C>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51710156 | ||||||
chr13:51710190 | A | G | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.334+6540A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51710190 | ||||||
chr13:51710356 | C | G | 1 | a0001c0001t0001g0120 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.334+6706C>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51710356 | ||||||
chr13:51710554 | A | C | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.334+6904A>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51710554 | ||||||
chr13:51710606 | A | C | 3 | a0001c0001t0001g0266a0001c0001t0001g0267a0001c0001t0001g0268 | 3 | HG02109.hp2 HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.334+6956A>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51710606 | ||||||
chr13:51710862 | C | T | 4 | a0001c0001t0003g0210a0001c0001t0003g0229a0001c0001t0003g0246others(1): Show | 4 | HG01069.hp2 HG01071.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.334+7212C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51710862 | ||||||
chr13:51710868 | G | A | 1 | a0001c0001t0024g0009 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.334+7218G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51710868 | ||||||
chr13:51710871 | A | G | 4 | a0001c0001t0003g0210a0001c0001t0003g0229a0001c0001t0003g0246others(1): Show | 4 | HG01069.hp2 HG01071.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.334+7221A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51710871 | ||||||
chr13:51710908 | T | C | 1 | a0001c0001t0001g0095 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.334+7258T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51710908 | ||||||
chr13:51710935 | CTACTT | C | 8 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(5): Show | 8 | HG01192.hp1 HG01884.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.334+7288_334+7292d others(7): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr13 | 51710935 | |||||
chr13:51711019 | C | T | 1 | a0001c0001t0034g0024 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.334+7369C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51711019 | ||||||
chr13:51711020 | G | A | 4 | a0001c0001t0001g0266a0001c0001t0001g0267a0001c0001t0001g0268others(1): Show | 4 | HG02109.hp2 HG02145.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.334+7370G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51711020 | ||||||
chr13:51711199 | T | C | 4 | a0001c0001t0001g0266a0001c0001t0001g0267a0001c0001t0001g0268others(1): Show | 4 | HG02109.hp2 HG02145.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.334+7549T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51711199 | ||||||
chr13:51711211 | G | A | 30 | a0001c0001t0004g0177a0001c0001t0004g0178a0001c0001t0004g0182others(27): Show | 30 | HG00735.hp2 HG01081.hp2 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.334+7561G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51711211 | ||||||
chr13:51711403 | C | G | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.334+7753C>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51711403 | ||||||
chr13:51711539 | A | G | 1 | a0001c0001t0009g0141 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.335-7659A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51711539 | ||||||
chr13:51711770 | C | T | 1 | a0001c0001t0001g0187 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.335-7428C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51711770 | ||||||
chr13:51711892 | A | G | 4 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0275others(1): Show | 4 | HG00733.hp2 HG01123.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.335-7306A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51711892 | ||||||
chr13:51711932 | A | G | 1 | a0001c0007t0016g0278 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.335-7266A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51711932 | ||||||
chr13:51711955 | T | A | 169 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(166): Show | 169 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.335-7243T>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51711955 | ||||||
chr13:51712123 | C | A | 8 | a0001c0002t0002g0043a0001c0002t0002g0046a0001c0002t0002g0048others(5): Show | 8 | HG02074.hp2 NA18943.hp2 NA18952.hp1 others(5): Show |
intron_variant | MODIFIER | c.335-7075C>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51712123 | ||||||
chr13:51712125 | G | T | 8 | a0001c0002t0002g0043a0001c0002t0002g0046a0001c0002t0002g0048others(5): Show | 8 | HG02074.hp2 NA18943.hp2 NA18952.hp1 others(5): Show |
intron_variant | MODIFIER | c.335-7073G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51712125 | ||||||
chr13:51712312 | G | A | 1 | a0001c0001t0007g0079 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.335-6886G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51712312 | ||||||
chr13:51712355 | A | G | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | NA18953.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.335-6843A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51712355 | ||||||
chr13:51712630 | A | G | 41 | a0001c0001t0004g0177a0001c0001t0004g0178a0001c0001t0004g0182others(38): Show | 41 | HG00735.hp2 HG01081.hp2 HG01106.hp1 others(38): Show |
intron_variant | MODIFIER | c.335-6568A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51712630 | ||||||
chr13:51712682 | C | T | 2 | a0001c0001t0001g0067a0001c0001t0021g0066 | 2 | HG01346.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.335-6516C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51712682 | ||||||
chr13:51712688 | C | G | 2 | a0001c0001t0036g0247a0001c0001t0038g0248 | 2 | NA18955.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.335-6510C>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51712688 | ||||||
chr13:51712856 | A | G | 62 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0012others(59): Show | 62 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.335-6342A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51712856 | ||||||
chr13:51713013 | C | A | 1 | a0001c0001t0001g0130 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.335-6185C>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51713013 | ||||||
chr13:51713310 | C | G | 10 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0124others(7): Show | 10 | HG00609.hp2 HG02056.hp2 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.335-5888C>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51713310 | ||||||
chr13:51713611 | G | A | 42 | a0001c0001t0004g0177a0001c0001t0004g0178a0001c0001t0004g0182others(39): Show | 42 | HG00735.hp2 HG01081.hp2 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.335-5587G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51713611 | ||||||
chr13:51713644 | G | A | 1 | a0001c0001t0046g0109 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.335-5554G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51713644 | ||||||
chr13:51713714 | G | A | 1 | a0001c0001t0030g0001 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.335-5484G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51713714 | ||||||
chr13:51713846 | C | CA | 37 | a0001c0001t0001g0093a0001c0001t0001g0137a0001c0001t0001g0228others(34): Show | 37 | HG00735.hp2 HG01081.hp2 HG01106.hp2 others(34): Show |
intron_variant | MODIFIER | c.335-5332dupA | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr13 | 51713846 | |||||
chr13:51713846 | C | CAA | 7 | a0001c0001t0001g0255a0001c0001t0004g0196a0001c0001t0010g0005others(4): Show | 7 | HG01884.hp2 HG01952.hp2 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.335-5333_335-5332d others(4): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr13 | 51713846 | |||||
chr13:51713846 | CA | C | 9 | a0001c0001t0001g0138a0001c0001t0001g0267a0001c0001t0001g0268others(6): Show | 9 | HG01081.hp1 HG02109.hp2 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.335-5332delA | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr13 | 51713846 | |||||
chr13:51713976 | C | T | 2 | a0001c0001t0001g0159a0001c0001t0001g0160 | 2 | HG02965.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.335-5222C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51713976 | ||||||
chr13:51714146 | CAT | C | 3 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140 | 3 | HG02647.hp2 HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.335-5049_335-5048d others(4): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr13 | 51714146 | |||||
chr13:51714213 | C | CA | 7 | a0001c0001t0002g0259a0001c0001t0007g0079a0001c0001t0007g0092others(4): Show | 7 | HG01975.hp1 HG02273.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.335-4973dupA | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr13 | 51714213 | |||||
chr13:51714352 | T | C | 2 | a0001c0001t0046g0109a0004c0005t0022g0150 | 2 | HG01884.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.335-4846T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51714352 | ||||||
chr13:51714437 | G | A | 1 | a0001c0001t0003g0232 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.335-4761G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51714437 | ||||||
chr13:51714438 | C | G | 1 | a0001c0002t0002g0049 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.335-4760C>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51714438 | ||||||
chr13:51714705 | C | T | 4 | a0001c0001t0046g0109a0001c0006t0016g0277a0001c0007t0016g0278others(1): Show | 4 | HG01884.hp2 HG02258.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.335-4493C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51714705 | ||||||
chr13:51714940 | G | C | 1 | a0001c0001t0007g0070 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.335-4258G>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51714940 | ||||||
chr13:51714995 | G | A | 1 | a0001c0002t0002g0040 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.335-4203G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51714995 | ||||||
chr13:51716129 | A | G | 2 | a0001c0001t0004g0196a0001c0001t0032g0202 | 2 | HG02622.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.335-3069A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51716129 | ||||||
chr13:51716173 | G | A | 179 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(176): Show | 179 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.335-3025G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51716173 | ||||||
chr13:51716210 | G | A | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.335-2988G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51716210 | ||||||
chr13:51716414 | C | T | 1 | a0001c0001t0005g0021 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.335-2784C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51716414 | ||||||
chr13:51716459 | G | A | 1 | a0001c0001t0001g0007 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.335-2739G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51716459 | ||||||
chr13:51716508 | C | T | 8 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(5): Show | 8 | HG01192.hp1 HG01884.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.335-2690C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51716508 | ||||||
chr13:51716553 | C | T | 1 | a0001c0001t0046g0109 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.335-2645C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51716553 | ||||||
chr13:51716609 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.335-2589C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51716609 | ||||||
chr13:51716692 | C | CA | 127 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0012others(124): Show | 127 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.335-2486dupA | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr13 | 51716692 | |||||
chr13:51716692 | C | CAA | 55 | a0001c0001t0001g0013a0001c0001t0001g0080a0001c0001t0001g0090others(52): Show | 55 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(52): Show |
intron_variant | MODIFIER | c.335-2487_335-2486d others(4): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr13 | 51716692 | |||||
chr13:51716777 | G | GA | 8 | a0001c0001t0001g0013a0001c0001t0001g0118a0001c0001t0004g0178others(5): Show | 8 | HG00735.hp2 HG01106.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.335-2405dupA | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr13 | 51716777 | |||||
chr13:51716777 | GA | G | 56 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0054others(53): Show | 56 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(53): Show |
intron_variant | MODIFIER | c.335-2405delA | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr13 | 51716777 | |||||
chr13:51717231 | T | G | 1 | a0001c0001t0003g0112 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.335-1967T>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51717231 | ||||||
chr13:51717290 | G | GT | 13 | a0001c0001t0004g0198a0001c0001t0005g0016a0001c0001t0005g0017others(10): Show | 13 | HG01106.hp1 HG02055.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.335-1900dupT | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr13 | 51717290 | |||||
chr13:51717292 | T | G | 1 | a0001c0001t0001g0160 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.335-1906T>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51717292 | ||||||
chr13:51717488 | A | C | 1 | a0001c0001t0009g0145 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.335-1710A>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51717488 | ||||||
chr13:51717668 | A | T | 1 | a0003c0004t0001g0108 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.335-1530A>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51717668 | ||||||
chr13:51718403 | C | G | 1 | a0001c0002t0045g0035 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.335-795C>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51718403 | ||||||
chr13:51718485 | C | T | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.335-713C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51718485 | ||||||
chr13:51718488 | G | A | 2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 2 | HG02109.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.335-710G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51718488 | ||||||
chr13:51718559 | T | TAC | 57 | a0001c0001t0001g0025a0001c0001t0001g0055a0001c0001t0001g0056others(54): Show | 57 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(54): Show |
intron_variant | MODIFIER | c.335-596_335-595dup others(2): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr13 | 51718559 | |||||
chr13:51718559 | T | TACAC | 43 | a0001c0001t0001g0012a0001c0001t0001g0062a0001c0001t0001g0067others(40): Show | 43 | HG00099.hp1 HG00673.hp1 HG01106.hp2 others(40): Show |
intron_variant | MODIFIER | c.335-598_335-595dup others(4): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr13 | 51718559 | |||||
chr13:51718559 | T | TACACAC | 13 | a0001c0001t0001g0013a0001c0001t0001g0063a0001c0001t0001g0081others(10): Show | 13 | HG00280.hp2 HG01081.hp2 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.335-600_335-595dup others(6): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr13 | 51718559 | |||||
chr13:51718559 | T | TACACACA others(1): Show |
3 | a0001c0001t0001g0074a0001c0001t0001g0104a0001c0001t0001g0125 | 3 | HG00423.hp2 NA18964.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.335-602_335-595dup others(8): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr13 | 51718559 | |||||
chr13:51718559 | T | TACACACA others(3): Show |
1 | a0001c0001t0005g0147 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.335-604_335-595dup others(10): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr13 | 51718559 | |||||
chr13:51718559 | TAC | T | 32 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0105others(29): Show | 32 | HG00323.hp2 HG00642.hp2 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.335-596_335-595del others(2): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr13 | 51718559 | |||||
chr13:51718559 | TACAC | T | 27 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0120others(24): Show | 27 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(24): Show |
intron_variant | MODIFIER | c.335-598_335-595del others(4): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr13 | 51718559 | |||||
chr13:51718559 | TACACAC | T | 4 | a0001c0001t0001g0137a0001c0001t0001g0157a0001c0001t0001g0158others(1): Show | 4 | HG02630.hp1 HG03139.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.335-600_335-595del others(6): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr13 | 51718559 | |||||
chr13:51718559 | TACACACA others(3): Show |
T | 6 | a0001c0001t0010g0002a0001c0001t0010g0003a0001c0001t0010g0004others(3): Show | 6 | HG02257.hp2 HG02647.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.335-604_335-595del others(10): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr13 | 51718559 | |||||
chr13:51718559 | TACACACA others(5): Show |
T | 1 | a0001c0001t0001g0130 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.335-606_335-595del others(12): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr13 | 51718559 | |||||
chr13:51719030 | A | G | 2 | a0001c0006t0016g0277a0001c0007t0016g0278 | 2 | HG02258.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.335-168A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 4/11 | chr13 | 51719030 | ||||||
chr13:51719373 | C | T | 54 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0012others(51): Show | 54 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(51): Show |
intron_variant | MODIFIER | c.485+25C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51719373 | ||||||
chr13:51719396 | T | C | 266 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(263): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.485+48T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51719396 | ||||||
chr13:51719505 | T | C | 54 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0012others(51): Show | 54 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(51): Show |
intron_variant | MODIFIER | c.485+157T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51719505 | ||||||
chr13:51719552 | A | C | 3 | a0001c0001t0020g0273a0001c0001t0029g0272a0001c0006t0016g0277 | 3 | HG02559.hp2 HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.485+204A>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51719552 | ||||||
chr13:51719700 | C | T | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.485+352C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51719700 | ||||||
chr13:51719701 | A | T | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.485+353A>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51719701 | ||||||
chr13:51719702 | G | T | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.485+354G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51719702 | ||||||
chr13:51719703 | A | T | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.485+355A>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51719703 | ||||||
chr13:51719705 | G | T | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.485+357G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51719705 | ||||||
chr13:51719712 | A | T | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.485+364A>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51719712 | ||||||
chr13:51719713 | C | T | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.485+365C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51719713 | ||||||
chr13:51719715 | C | A | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.485+367C>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51719715 | ||||||
chr13:51719717 | T | A | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.485+369T>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51719717 | ||||||
chr13:51719719 | G | A | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.485+371G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51719719 | ||||||
chr13:51719723 | C | T | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.485+375C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51719723 | ||||||
chr13:51719724 | C | T | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.485+376C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51719724 | ||||||
chr13:51719731 | G | A | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.485+383G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51719731 | ||||||
chr13:51719733 | G | A | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.485+385G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51719733 | ||||||
chr13:51719734 | A | T | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.485+386A>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51719734 | ||||||
chr13:51719736 | C | A | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.485+388C>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51719736 | ||||||
chr13:51719740 | C | A | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.485+392C>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51719740 | ||||||
chr13:51719741 | C | A | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.485+393C>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51719741 | ||||||
chr13:51719742 | C | T | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.485+394C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51719742 | ||||||
chr13:51719743 | A | T | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.485+395A>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51719743 | ||||||
chr13:51719746 | G | T | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.485+398G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51719746 | ||||||
chr13:51719747 | G | A | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.485+399G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51719747 | ||||||
chr13:51719748 | T | A | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.485+400T>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51719748 | ||||||
chr13:51719749 | G | A | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.485+401G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51719749 | ||||||
chr13:51719750 | C | T | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.485+402C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51719750 | ||||||
chr13:51719751 | C | T | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.485+403C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51719751 | ||||||
chr13:51719753 | G | T | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.485+405G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51719753 | ||||||
chr13:51719754 | G | T | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.485+406G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51719754 | ||||||
chr13:51719755 | G | A | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.485+407G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51719755 | ||||||
chr13:51719757 | G | A | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.485+409G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51719757 | ||||||
chr13:51719760 | G | T | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.485+412G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51719760 | ||||||
chr13:51719763 | C | T | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.485+415C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51719763 | ||||||
chr13:51719764 | C | A | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.485+416C>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51719764 | ||||||
chr13:51719767 | A | T | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.485+419A>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51719767 | ||||||
chr13:51719768 | G | T | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.485+420G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51719768 | ||||||
chr13:51719769 | G | A | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.485+421G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51719769 | ||||||
chr13:51719776 | G | A | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.485+428G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51719776 | ||||||
chr13:51719777 | T | A | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.485+429T>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51719777 | ||||||
chr13:51719779 | C | T | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.485+431C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51719779 | ||||||
chr13:51719781 | G | T | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.485+433G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51719781 | ||||||
chr13:51719790 | A | G | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.485+442A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51719790 | ||||||
chr13:51719791 | G | T | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.485+443G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51719791 | ||||||
chr13:51719792 | T | A | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.485+444T>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51719792 | ||||||
chr13:51719797 | G | T | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.485+449G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51719797 | ||||||
chr13:51719798 | A | T | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.485+450A>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51719798 | ||||||
chr13:51719799 | G | T | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.485+451G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51719799 | ||||||
chr13:51719806 | C | A | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.485+458C>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51719806 | ||||||
chr13:51719807 | C | T | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.485+459C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51719807 | ||||||
chr13:51719808 | ATGCCAGG others(5): Show |
A | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.485+461_485+472del others(12): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51719808 | ||||||
chr13:51719822 | G | T | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.485+474G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51719822 | ||||||
chr13:51719824 | G | A | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.485+476G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51719824 | ||||||
chr13:51719825 | G | T | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.485+477G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51719825 | ||||||
chr13:51719826 | G | T | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.485+478G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51719826 | ||||||
chr13:51719827 | T | C | 1 | a0001c0001t0004g0197 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.485+479T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51719827 | ||||||
chr13:51719828 | G | A | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.485+480G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51719828 | ||||||
chr13:51719830 | G | A | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.485+482G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51719830 | ||||||
chr13:51719831 | C | A | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.485+483C>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51719831 | ||||||
chr13:51719833 | G | A | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.485+485G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51719833 | ||||||
chr13:51719834 | G | A | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.485+486G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51719834 | ||||||
chr13:51719836 | A | T | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.485+488A>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51719836 | ||||||
chr13:51719838 | C | A | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.485+490C>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51719838 | ||||||
chr13:51719839 | T | A | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.485+491T>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51719839 | ||||||
chr13:51719841 | C | A | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.485+493C>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51719841 | ||||||
chr13:51719845 | G | T | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.485+497G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51719845 | ||||||
chr13:51719850 | G | A | 4 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0275others(1): Show | 4 | HG00733.hp2 HG01123.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.485+502G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51719850 | ||||||
chr13:51719850 | G | T | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.485+502G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51719850 | ||||||
chr13:51720208 | T | G | 1 | a0001c0001t0029g0272 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.485+860T>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51720208 | ||||||
chr13:51720660 | T | G | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.485+1312T>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51720660 | ||||||
chr13:51720684 | T | G | 1 | a0001c0001t0046g0109 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.485+1336T>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51720684 | ||||||
chr13:51720786 | A | T | 1 | a0001c0001t0003g0225 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.485+1438A>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51720786 | ||||||
chr13:51720839 | T | A | 1 | a0001c0001t0031g0149 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.485+1491T>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51720839 | ||||||
chr13:51720890 | C | G | 1 | a0001c0001t0001g0095 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.485+1542C>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51720890 | ||||||
chr13:51720942 | T | TTC | 15 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0160others(12): Show | 15 | HG00733.hp2 HG01123.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.485+1622_485+1623d others(4): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr13 | 51720942 | |||||
chr13:51720942 | T | TTCTC | 10 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(7): Show | 10 | HG01192.hp1 HG01884.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.485+1620_485+1623d others(6): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr13 | 51720942 | |||||
chr13:51720942 | TTC | T | 37 | a0001c0001t0001g0266a0001c0001t0003g0211a0001c0001t0003g0221others(34): Show | 37 | HG00408.hp1 HG00423.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.485+1622_485+1623d others(4): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr13 | 51720942 | |||||
chr13:51720942 | TTCTC | T | 48 | a0001c0001t0001g0144a0001c0001t0001g0267a0001c0001t0002g0259others(45): Show | 48 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.485+1620_485+1623d others(6): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr13 | 51720942 | |||||
chr13:51720942 | TTCTCTC | T | 12 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0004g0182others(9): Show | 12 | HG01243.hp2 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.485+1618_485+1623d others(8): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr13 | 51720942 | |||||
chr13:51720942 | TTCTCTCT others(5): Show |
T | 1 | a0001c0006t0016g0277 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.485+1612_485+1623d others(14): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr13 | 51720942 | |||||
chr13:51720980 | C | A | 1 | a0001c0002t0002g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.485+1632C>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51720980 | ||||||
chr13:51721023 | T | A | 2 | a0001c0001t0003g0166a0001c0001t0006g0169 | 2 | HG03927.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.485+1675T>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51721023 | ||||||
chr13:51721047 | G | C | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.485+1699G>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51721047 | ||||||
chr13:51721182 | A | C | 178 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(175): Show | 178 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.485+1834A>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51721182 | ||||||
chr13:51721194 | A | G | 2 | a0001c0001t0003g0207a0001c0001t0003g0208 | 2 | HG00642.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.485+1846A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51721194 | ||||||
chr13:51721350 | G | T | 1 | a0001c0001t0001g0165 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.485+2002G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51721350 | ||||||
chr13:51721409 | C | T | 8 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(5): Show | 8 | HG01192.hp1 HG01884.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.485+2061C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51721409 | ||||||
chr13:51721850 | C | T | 1 | a0001c0001t0007g0079 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.485+2502C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51721850 | ||||||
chr13:51721931 | G | T | 54 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0012others(51): Show | 54 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(51): Show |
intron_variant | MODIFIER | c.485+2583G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51721931 | ||||||
chr13:51722054 | G | T | 2 | a0001c0001t0004g0190a0001c0001t0004g0206 | 2 | HG02258.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.485+2706G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51722054 | ||||||
chr13:51722213 | C | T | 8 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(5): Show | 8 | HG01106.hp1 HG02055.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.485+2865C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51722213 | ||||||
chr13:51722690 | T | C | 2 | a0001c0001t0020g0273a0001c0001t0029g0272 | 2 | HG02559.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.485+3342T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51722690 | ||||||
chr13:51722709 | C | G | 2 | a0001c0001t0046g0109a0004c0005t0022g0150 | 2 | HG01884.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.485+3361C>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51722709 | ||||||
chr13:51722727 | G | A | 277 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(274): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.485+3379G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51722727 | ||||||
chr13:51723167 | A | C | 1 | a0001c0001t0034g0024 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.485+3819A>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51723167 | ||||||
chr13:51723168 | A | G | 4 | a0001c0001t0001g0266a0001c0001t0001g0267a0001c0001t0001g0268others(1): Show | 4 | HG02109.hp2 HG02145.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.485+3820A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51723168 | ||||||
chr13:51723295 | A | G | 1 | a0001c0002t0002g0030 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.485+3947A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51723295 | ||||||
chr13:51723614 | G | T | 13 | a0001c0001t0003g0115a0001c0001t0003g0209a0001c0001t0003g0224others(10): Show | 13 | HG03831.hp2 HG03834.hp1 NA18941.hp1 others(10): Show |
intron_variant | MODIFIER | c.486-4064G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51723614 | ||||||
chr13:51723652 | G | T | 2 | a0001c0001t0003g0166a0001c0001t0006g0169 | 2 | HG03927.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.486-4026G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51723652 | ||||||
chr13:51724231 | C | CT | 26 | a0001c0001t0001g0008a0001c0001t0001g0098a0001c0001t0001g0102others(23): Show | 26 | HG00323.hp1 HG01081.hp1 HG01346.hp1 others(23): Show |
intron_variant | MODIFIER | c.486-3424dupT | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr13 | 51724231 | |||||
chr13:51724231 | CT | C | 18 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0001g0093others(15): Show | 18 | HG02145.hp1 HG02615.hp1 HG02647.hp1 others(15): Show |
intron_variant | MODIFIER | c.486-3424delT | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr13 | 51724231 | |||||
chr13:51724244 | T | C | 1 | a0001c0001t0004g0203 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.486-3434T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51724244 | ||||||
chr13:51724263 | G | T | 1 | a0001c0001t0046g0109 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.486-3415G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51724263 | ||||||
chr13:51724293 | A | G | 1 | a0001c0001t0026g0155 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.486-3385A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51724293 | ||||||
chr13:51724379 | A | T | 3 | a0001c0001t0013g0263a0001c0001t0013g0264a0001c0001t0013g0265 | 3 | HG02145.hp1 HG03041.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.486-3299A>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51724379 | ||||||
chr13:51724393 | G | A | 1 | a0001c0001t0004g0198 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.486-3285G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51724393 | ||||||
chr13:51724539 | A | G | 8 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(5): Show | 8 | HG01106.hp1 HG02055.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.486-3139A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51724539 | ||||||
chr13:51724804 | G | C | 1 | a0001c0001t0003g0112 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.486-2874G>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51724804 | ||||||
chr13:51724908 | A | G | 2 | a0001c0001t0046g0109a0004c0005t0022g0150 | 2 | HG01884.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.486-2770A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51724908 | ||||||
chr13:51724994 | G | T | 1 | a0002c0003t0004g0180 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.486-2684G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51724994 | ||||||
chr13:51725208 | G | A | 2 | a0001c0006t0016g0277a0001c0007t0016g0278 | 2 | HG02258.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.486-2470G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51725208 | ||||||
chr13:51725396 | T | C | 1 | a0001c0001t0004g0206 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.486-2282T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51725396 | ||||||
chr13:51725452 | C | T | 1 | a0001c0002t0002g0049 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.486-2226C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51725452 | ||||||
chr13:51725676 | A | G | 1 | a0001c0001t0001g0027 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.486-2002A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51725676 | ||||||
chr13:51725751 | C | T | 1 | a0002c0003t0004g0181 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.486-1927C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51725751 | ||||||
chr13:51725886 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.486-1792G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51725886 | ||||||
chr13:51726144 | C | T | 1 | a0001c0001t0001g0117 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.486-1534C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51726144 | ||||||
chr13:51726220 | G | A | 1 | a0001c0001t0020g0273 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.486-1458G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51726220 | ||||||
chr13:51726248 | TA | T | 47 | a0001c0001t0002g0259a0001c0001t0019g0260a0001c0001t0019g0261others(44): Show | 47 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(44): Show |
intron_variant | MODIFIER | c.486-1428delA | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr13 | 51726248 | |||||
chr13:51726614 | T | G | 1 | a0001c0001t0001g0110 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.486-1064T>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51726614 | ||||||
chr13:51726711 | G | A | 62 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0012others(59): Show | 62 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.486-967G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51726711 | ||||||
chr13:51726711 | G | T | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.486-967G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51726711 | ||||||
chr13:51726857 | C | A | 1 | a0001c0001t0018g0023 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.486-821C>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51726857 | ||||||
chr13:51727175 | C | T | 1 | a0001c0001t0024g0009 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.486-503C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51727175 | ||||||
chr13:51727397 | C | A | 1 | a0001c0001t0001g0080 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.486-281C>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51727397 | ||||||
chr13:51727503 | C | A | 1 | a0001c0001t0001g0010 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.486-175C>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51727503 | ||||||
chr13:51727529 | A | G | 2 | a0001c0001t0046g0109a0004c0005t0022g0150 | 2 | HG01884.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.486-149A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51727529 | ||||||
chr13:51727547 | G | A | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.486-131G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51727547 | ||||||
chr13:51727634 | C | T | 1 | a0001c0001t0007g0079 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.486-44C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51727634 | ||||||
chr13:51727675 | C | T | 2 | a0001c0001t0046g0109a0004c0005t0022g0150 | 2 | HG01884.hp2 HG02970.hp1 |
splice_region_variant&intron_variant | LOW | c.486-3C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 5/11 | chr13 | 51727675 | ||||||
chr13:51728000 | A | G | 11 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(8): Show | 11 | HG01106.hp1 HG02055.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.598+210A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51728000 | ||||||
chr13:51728275 | A | G | 1 | a0001c0006t0016g0277 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.598+485A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51728275 | ||||||
chr13:51728494 | A | G | 53 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0124others(50): Show | 53 | HG00609.hp2 HG00735.hp2 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.598+704A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51728494 | ||||||
chr13:51728625 | C | A | 1 | a0001c0001t0004g0203 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.598+835C>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51728625 | ||||||
chr13:51728630 | T | A | 2 | a0001c0001t0046g0109a0004c0005t0022g0150 | 2 | HG01884.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.598+840T>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51728630 | ||||||
chr13:51728871 | G | T | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG01891.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.598+1081G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51728871 | ||||||
chr13:51728967 | T | C | 2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 2 | HG02109.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.598+1177T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51728967 | ||||||
chr13:51729003 | T | C | 129 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0012others(126): Show | 129 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.598+1213T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51729003 | ||||||
chr13:51729075 | C | T | 3 | a0001c0001t0001g0084a0001c0001t0001g0102a0001c0001t0002g0085 | 3 | NA18977.hp1 NA18983.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.598+1285C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51729075 | ||||||
chr13:51729206 | G | A | 1 | a0001c0001t0001g0007 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.598+1416G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51729206 | ||||||
chr13:51729208 | T | A | 1 | a0001c0006t0016g0277 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.598+1418T>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51729208 | ||||||
chr13:51729411 | T | TAA | 47 | a0001c0001t0002g0259a0001c0001t0019g0260a0001c0001t0019g0261others(44): Show | 47 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(44): Show |
intron_variant | MODIFIER | c.598+1636_598+1637d others(4): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr13 | 51729411 | |||||
chr13:51729411 | TA | T | 9 | a0001c0001t0001g0069a0001c0001t0001g0116a0001c0001t0001g0266others(6): Show | 9 | HG02109.hp2 HG02145.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.598+1637delA | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr13 | 51729411 | |||||
chr13:51729428 | C | A | 2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 2 | HG02109.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.598+1638C>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51729428 | ||||||
chr13:51729452 | A | T | 3 | a0001c0001t0013g0263a0001c0001t0013g0264a0001c0001t0013g0265 | 3 | HG02145.hp1 HG03041.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.598+1662A>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51729452 | ||||||
chr13:51729520 | CCTTCCTC others(36): Show |
C | 1 | a0002c0003t0004g0185 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.598+1771_598+1813d others(45): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr13 | 51729520 | |||||
chr13:51729603 | C | T | 1 | a0001c0001t0003g0218 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.598+1813C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51729603 | ||||||
chr13:51729831 | A | C | 1 | a0001c0001t0001g0143 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.598+2041A>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51729831 | ||||||
chr13:51729909 | A | G | 3 | a0001c0001t0013g0263a0001c0001t0013g0264a0001c0001t0013g0265 | 3 | HG02145.hp1 HG03041.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.598+2119A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51729909 | ||||||
chr13:51730058 | C | T | 3 | a0001c0001t0001g0076a0001c0001t0001g0089a0001c0001t0001g0100 | 3 | HG03491.hp1 HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.598+2268C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51730058 | ||||||
chr13:51730157 | G | A | 1 | a0001c0001t0001g0072 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.598+2367G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51730157 | ||||||
chr13:51730300 | G | A | 1 | a0001c0002t0002g0148 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.598+2510G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51730300 | ||||||
chr13:51730314 | C | T | 2 | a0001c0001t0010g0002a0001c0001t0010g0003 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.598+2524C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51730314 | ||||||
chr13:51730681 | G | A | 1 | a0001c0001t0003g0241 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.598+2891G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51730681 | ||||||
chr13:51730701 | T | G | 47 | a0001c0001t0002g0259a0001c0001t0019g0260a0001c0001t0019g0261others(44): Show | 47 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(44): Show |
intron_variant | MODIFIER | c.598+2911T>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51730701 | ||||||
chr13:51730761 | A | G | 4 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0275others(1): Show | 4 | HG00733.hp2 HG01123.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.598+2971A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51730761 | ||||||
chr13:51730984 | G | T | 1 | a0001c0001t0018g0270 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.598+3194G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51730984 | ||||||
chr13:51731174 | C | G | 1 | a0001c0001t0001g0065 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.598+3384C>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51731174 | ||||||
chr13:51731328 | T | C | 43 | a0001c0002t0002g0014a0001c0002t0002g0015a0001c0002t0002g0026others(40): Show | 43 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(40): Show |
intron_variant | MODIFIER | c.598+3538T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51731328 | ||||||
chr13:51731338 | A | G | 1 | a0001c0001t0046g0109 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.598+3548A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51731338 | ||||||
chr13:51731353 | C | T | 1 | a0001c0002t0002g0043 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.598+3563C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51731353 | ||||||
chr13:51731516 | G | A | 1 | a0001c0001t0035g0195 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.598+3726G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51731516 | ||||||
chr13:51731700 | A | C | 2 | a0001c0002t0002g0014a0001c0002t0002g0015 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.598+3910A>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51731700 | ||||||
chr13:51731855 | C | T | 1 | a0001c0001t0007g0091 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.598+4065C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51731855 | ||||||
chr13:51731892 | G | A | 3 | a0001c0001t0015g0127a0001c0001t0015g0134a0001c0001t0015g0135 | 3 | HG00323.hp1 HG01081.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.598+4102G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51731892 | ||||||
chr13:51732046 | C | T | 1 | a0003c0004t0001g0108 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.598+4256C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51732046 | ||||||
chr13:51732117 | T | C | 8 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(5): Show | 8 | HG01106.hp1 HG02055.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.598+4327T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51732117 | ||||||
chr13:51732155 | G | A | 2 | a0001c0001t0001g0057a0001c0001t0001g0059 | 2 | HG02615.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.598+4365G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51732155 | ||||||
chr13:51732276 | G | T | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.598+4486G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51732276 | ||||||
chr13:51732291 | C | T | 2 | a0001c0001t0001g0057a0001c0001t0001g0059 | 2 | HG02615.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.598+4501C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51732291 | ||||||
chr13:51732390 | G | A | 1 | a0001c0001t0034g0024 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.598+4600G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51732390 | ||||||
chr13:51732643 | C | T | 1 | a0001c0002t0002g0028 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.598+4853C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51732643 | ||||||
chr13:51732794 | C | G | 1 | a0001c0001t0046g0109 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.598+5004C>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51732794 | ||||||
chr13:51732798 | A | G | 2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 2 | HG02109.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.598+5008A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51732798 | ||||||
chr13:51732860 | A | G | 4 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0275others(1): Show | 4 | HG00733.hp2 HG01123.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.598+5070A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51732860 | ||||||
chr13:51733279 | C | T | 1 | a0001c0001t0003g0237 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.598+5489C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51733279 | ||||||
chr13:51733361 | T | G | 1 | a0001c0001t0004g0198 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.598+5571T>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51733361 | ||||||
chr13:51733473 | T | C | 3 | a0001c0001t0013g0263a0001c0001t0013g0264a0001c0001t0013g0265 | 3 | HG02145.hp1 HG03041.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.599-5576T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51733473 | ||||||
chr13:51733506 | C | T | 1 | a0001c0001t0003g0232 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.599-5543C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51733506 | ||||||
chr13:51733740 | C | T | 1 | a0001c0001t0003g0245 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.599-5309C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51733740 | ||||||
chr13:51733847 | A | G | 3 | a0001c0002t0002g0032a0001c0002t0002g0151a0001c0002t0002g0152 | 3 | HG01433.hp2 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.599-5202A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51733847 | ||||||
chr13:51733967 | C | A | 49 | a0001c0001t0002g0259a0001c0001t0019g0260a0001c0001t0019g0261others(46): Show | 49 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(46): Show |
intron_variant | MODIFIER | c.599-5082C>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51733967 | ||||||
chr13:51734097 | G | A | 8 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(5): Show | 8 | HG01192.hp1 HG01884.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.599-4952G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51734097 | ||||||
chr13:51734240 | T | C | 1 | a0001c0001t0018g0023 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.599-4809T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51734240 | ||||||
chr13:51734561 | G | A | 1 | a0001c0001t0018g0270 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.599-4488G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51734561 | ||||||
chr13:51734586 | A | G | 1 | a0001c0001t0001g0105 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.599-4463A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51734586 | ||||||
chr13:51734703 | G | A | 1 | a0001c0001t0003g0163 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.599-4346G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51734703 | ||||||
chr13:51734922 | G | A | 1 | a0001c0001t0006g0169 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.599-4127G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51734922 | ||||||
chr13:51734925 | T | C | 14 | a0001c0001t0001g0065a0001c0001t0001g0074a0001c0001t0001g0081others(11): Show | 14 | HG00423.hp2 HG01256.hp1 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.599-4124T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51734925 | ||||||
chr13:51734940 | C | T | 47 | a0001c0001t0002g0259a0001c0001t0019g0260a0001c0001t0019g0261others(44): Show | 47 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(44): Show |
intron_variant | MODIFIER | c.599-4109C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51734940 | ||||||
chr13:51734965 | G | A | 1 | a0001c0002t0002g0254 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.599-4084G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51734965 | ||||||
chr13:51735291 | A | G | 1 | a0001c0001t0003g0211 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.599-3758A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51735291 | ||||||
chr13:51735535 | G | A | 1 | a0001c0001t0046g0109 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.599-3514G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51735535 | ||||||
chr13:51735799 | C | T | 8 | a0001c0002t0002g0043a0001c0002t0002g0046a0001c0002t0002g0048others(5): Show | 8 | HG02074.hp2 NA18943.hp2 NA18952.hp1 others(5): Show |
intron_variant | MODIFIER | c.599-3250C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51735799 | ||||||
chr13:51736178 | G | A | 1 | a0001c0002t0002g0131 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.599-2871G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51736178 | ||||||
chr13:51736213 | T | C | 2 | a0001c0006t0016g0277a0001c0007t0016g0278 | 2 | HG02258.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.599-2836T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51736213 | ||||||
chr13:51736237 | A | G | 1 | a0001c0001t0004g0269 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.599-2812A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51736237 | ||||||
chr13:51736245 | G | T | 6 | a0001c0001t0010g0002a0001c0001t0010g0003a0001c0001t0010g0004others(3): Show | 6 | HG02257.hp2 HG02647.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.599-2804G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51736245 | ||||||
chr13:51736249 | G | A | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.599-2800G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51736249 | ||||||
chr13:51736405 | A | G | 2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 2 | HG02109.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.599-2644A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51736405 | ||||||
chr13:51736595 | C | T | 4 | a0001c0001t0004g0182a0001c0001t0004g0197a0001c0001t0004g0198others(1): Show | 4 | HG02572.hp2 HG02615.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.599-2454C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51736595 | ||||||
chr13:51736642 | G | A | 2 | a0001c0001t0010g0002a0001c0001t0010g0003 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.599-2407G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51736642 | ||||||
chr13:51736647 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.599-2402C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51736647 | ||||||
chr13:51736700 | C | G | 1 | a0001c0007t0016g0278 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.599-2349C>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51736700 | ||||||
chr13:51736738 | G | A | 1 | a0001c0001t0001g0266 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.599-2311G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51736738 | ||||||
chr13:51737120 | C | T | 1 | a0001c0001t0040g0136 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.599-1929C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51737120 | ||||||
chr13:51737253 | G | A | 1 | a0003c0004t0001g0108 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.599-1796G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51737253 | ||||||
chr13:51737345 | G | C | 48 | a0001c0001t0002g0259a0001c0001t0019g0260a0001c0001t0019g0261others(45): Show | 48 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(45): Show |
intron_variant | MODIFIER | c.599-1704G>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51737345 | ||||||
chr13:51737450 | A | G | 6 | a0001c0001t0001g0077a0001c0001t0001g0094a0001c0001t0001g0258others(3): Show | 6 | HG00099.hp1 HG01069.hp1 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.599-1599A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51737450 | ||||||
chr13:51737551 | T | TA | 43 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0012others(40): Show | 43 | HG00099.hp1 HG00280.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.599-1467dupA | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr13 | 51737551 | |||||
chr13:51737551 | T | TAA | 13 | a0001c0001t0001g0072a0001c0001t0001g0088a0001c0001t0001g0090others(10): Show | 13 | HG01081.hp2 HG02258.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.599-1468_599-1467d others(4): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr13 | 51737551 | |||||
chr13:51737551 | T | TAAA | 11 | a0001c0001t0001g0125a0001c0001t0004g0178a0001c0001t0004g0203others(8): Show | 11 | HG00423.hp2 HG01243.hp2 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.599-1469_599-1467d others(5): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr13 | 51737551 | |||||
chr13:51737551 | T | TAAAA | 6 | a0001c0001t0004g0183a0001c0001t0004g0189a0001c0001t0004g0269others(3): Show | 6 | HG00735.hp2 HG01106.hp2 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.599-1470_599-1467d others(6): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr13 | 51737551 | |||||
chr13:51737551 | TA | T | 90 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0025others(87): Show | 90 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.599-1467delA | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr13 | 51737551 | |||||
chr13:51737551 | TAA | T | 7 | a0001c0001t0001g0126a0001c0001t0001g0139a0001c0001t0001g0157others(4): Show | 7 | HG00558.hp2 HG02896.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.599-1468_599-1467d others(4): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr13 | 51737551 | |||||
chr13:51737551 | TAAAA | T | 40 | a0001c0001t0002g0259a0001c0001t0019g0260a0001c0001t0044g0262others(37): Show | 40 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(37): Show |
intron_variant | MODIFIER | c.599-1470_599-1467d others(6): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr13 | 51737551 | |||||
chr13:51737551 | TAAAAA | T | 7 | a0001c0001t0019g0261a0001c0002t0002g0028a0001c0002t0002g0034others(4): Show | 7 | HG00323.hp2 HG03491.hp2 NA18948.hp1 others(4): Show |
intron_variant | MODIFIER | c.599-1471_599-1467d others(7): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr13 | 51737551 | |||||
chr13:51737551 | TAAAAAAA others(5): Show |
T | 2 | a0001c0001t0001g0110a0002c0003t0004g0184 | 2 | HG01952.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.599-1478_599-1467d others(14): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr13 | 51737551 | |||||
chr13:51737551 | TAAAAAAA others(6): Show |
T | 3 | a0001c0001t0017g0161a0001c0001t0020g0273a0001c0001t0029g0272 | 3 | HG02559.hp2 HG02895.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.599-1479_599-1467d others(15): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr13 | 51737551 | |||||
chr13:51737551 | TAAAAAAA others(7): Show |
T | 1 | a0001c0001t0017g0162 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.599-1480_599-1467d others(16): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr13 | 51737551 | |||||
chr13:51737551 | TAAAAAAA others(9): Show |
T | 7 | a0001c0001t0004g0177a0001c0001t0004g0188a0001c0001t0004g0191others(4): Show | 7 | HG01361.hp2 HG01934.hp1 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.599-1482_599-1467d others(18): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr13 | 51737551 | |||||
chr13:51737551 | TAAAAAAA others(11): Show |
T | 1 | a0001c0001t0003g0238 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.599-1484_599-1467d others(20): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr13 | 51737551 | |||||
chr13:51737820 | T | C | 47 | a0001c0001t0002g0259a0001c0001t0019g0260a0001c0001t0019g0261others(44): Show | 47 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(44): Show |
intron_variant | MODIFIER | c.599-1229T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51737820 | ||||||
chr13:51737821 | G | A | 10 | a0001c0002t0002g0029a0001c0002t0002g0030a0001c0002t0002g0031others(7): Show | 10 | HG00673.hp2 HG02015.hp1 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.599-1228G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51737821 | ||||||
chr13:51738038 | TGAGA | T | 47 | a0001c0001t0002g0259a0001c0001t0019g0260a0001c0001t0019g0261others(44): Show | 47 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(44): Show |
intron_variant | MODIFIER | c.599-1008_599-1005d others(6): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr13 | 51738038 | |||||
chr13:51738080 | T | G | 1 | a0001c0007t0016g0278 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.599-969T>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51738080 | ||||||
chr13:51738161 | A | G | 47 | a0001c0001t0002g0259a0001c0001t0019g0260a0001c0001t0019g0261others(44): Show | 47 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(44): Show |
intron_variant | MODIFIER | c.599-888A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51738161 | ||||||
chr13:51738162 | T | C | 1 | a0001c0001t0001g0059 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.599-887T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51738162 | ||||||
chr13:51738248 | ATTG | A | 2 | a0001c0001t0028g0061a0001c0001t0041g0156 | 2 | HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.599-798_599-796del others(3): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr13 | 51738248 | |||||
chr13:51738394 | T | G | 3 | a0001c0001t0001g0266a0001c0001t0001g0267a0001c0001t0001g0268 | 3 | HG02109.hp2 HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.599-655T>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 6/11 | chr13 | 51738394 | ||||||
chr13:51739230 | C | T | 3 | a0001c0001t0001g0008a0001c0001t0001g0067a0001c0001t0021g0066 | 3 | HG01346.hp2 HG01952.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.725+55C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51739230 | ||||||
chr13:51739412 | G | A | 2 | a0001c0001t0001g0074a0001c0001t0001g0081 | 2 | NA18964.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.725+237G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51739412 | ||||||
chr13:51739494 | G | A | 174 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(171): Show | 174 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.725+319G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51739494 | ||||||
chr13:51739595 | T | TCA | 3 | a0001c0001t0002g0259a0001c0001t0019g0260a0001c0001t0019g0261 | 3 | HG02698.hp1 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.725+423_725+424dup others(2): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr13 | 51739595 | |||||
chr13:51740164 | A | G | 6 | a0001c0001t0010g0002a0001c0001t0010g0003a0001c0001t0010g0004others(3): Show | 6 | HG02257.hp2 HG02647.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.725+989A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51740164 | ||||||
chr13:51740182 | C | G | 2 | a0001c0001t0020g0273a0001c0001t0029g0272 | 2 | HG02559.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.725+1007C>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51740182 | ||||||
chr13:51740347 | G | A | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.725+1172G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51740347 | ||||||
chr13:51740393 | A | C | 2 | a0001c0006t0016g0277a0001c0007t0016g0278 | 2 | HG02258.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.725+1218A>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51740393 | ||||||
chr13:51740473 | T | C | 3 | a0001c0001t0001g0076a0001c0001t0001g0089a0001c0001t0001g0100 | 3 | HG03491.hp1 HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.725+1298T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51740473 | ||||||
chr13:51740653 | G | A | 1 | a0001c0001t0046g0109 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.725+1478G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51740653 | ||||||
chr13:51740713 | CA | C | 46 | a0001c0001t0004g0177a0001c0001t0004g0178a0001c0001t0004g0182others(43): Show | 46 | HG00735.hp2 HG01081.hp2 HG01106.hp1 others(43): Show |
intron_variant | MODIFIER | c.725+1554delA | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr13 | 51740713 | |||||
chr13:51740730 | G | A | 3 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118 | 3 | HG01261.hp1 HG04228.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.725+1555G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51740730 | ||||||
chr13:51740810 | A | G | 1 | a0001c0001t0029g0272 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.725+1635A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51740810 | ||||||
chr13:51741368 | C | T | 6 | a0001c0001t0010g0002a0001c0001t0010g0003a0001c0001t0010g0004others(3): Show | 6 | HG02257.hp2 HG02647.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.725+2193C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51741368 | ||||||
chr13:51741370 | G | A | 1 | a0001c0001t0034g0024 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.725+2195G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51741370 | ||||||
chr13:51741514 | G | A | 2 | a0001c0001t0001g0138a0001c0001t0001g0139 | 2 | HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.725+2339G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51741514 | ||||||
chr13:51741520 | G | A | 1 | a0001c0002t0002g0123 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.725+2345G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51741520 | ||||||
chr13:51742058 | C | T | 2 | a0001c0001t0020g0273a0001c0001t0029g0272 | 2 | HG02559.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.725+2883C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51742058 | ||||||
chr13:51742438 | C | CA | 53 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0012others(50): Show | 53 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.725+3274dupA | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr13 | 51742438 | |||||
chr13:51742463 | G | A | 47 | a0001c0001t0002g0259a0001c0001t0019g0260a0001c0001t0019g0261others(44): Show | 47 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(44): Show |
intron_variant | MODIFIER | c.725+3288G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51742463 | ||||||
chr13:51742512 | C | T | 2 | a0001c0001t0010g0005a0001c0001t0010g0006 | 2 | HG02647.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.725+3337C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51742512 | ||||||
chr13:51742762 | A | C | 275 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(272): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.725+3587A>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51742762 | ||||||
chr13:51743036 | G | A | 8 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(5): Show | 8 | HG01192.hp1 HG01884.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.725+3861G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51743036 | ||||||
chr13:51743179 | A | T | 1 | a0001c0001t0001g0266 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.725+4004A>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51743179 | ||||||
chr13:51743216 | G | A | 1 | a0003c0004t0001g0108 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.725+4041G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51743216 | ||||||
chr13:51743222 | A | G | 43 | a0001c0002t0002g0014a0001c0002t0002g0015a0001c0002t0002g0026others(40): Show | 43 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(40): Show |
intron_variant | MODIFIER | c.725+4047A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51743222 | ||||||
chr13:51743504 | C | T | 30 | a0001c0001t0004g0177a0001c0001t0004g0178a0001c0001t0004g0182others(27): Show | 30 | HG00735.hp2 HG01081.hp2 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.725+4329C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51743504 | ||||||
chr13:51743524 | G | A | 8 | a0001c0002t0002g0043a0001c0002t0002g0046a0001c0002t0002g0048others(5): Show | 8 | HG02074.hp2 NA18943.hp2 NA18952.hp1 others(5): Show |
intron_variant | MODIFIER | c.725+4349G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51743524 | ||||||
chr13:51743579 | C | G | 3 | a0001c0001t0013g0263a0001c0001t0013g0264a0001c0001t0013g0265 | 3 | HG02145.hp1 HG03041.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.725+4404C>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51743579 | ||||||
chr13:51743760 | G | A | 1 | a0001c0001t0003g0239 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.725+4585G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51743760 | ||||||
chr13:51743789 | C | A | 1 | a0001c0001t0012g0194 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.725+4614C>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51743789 | ||||||
chr13:51743805 | A | C | 1 | a0001c0002t0043g0038 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.725+4630A>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51743805 | ||||||
chr13:51743876 | A | G | 1 | a0001c0001t0003g0225 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.725+4701A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51743876 | ||||||
chr13:51744386 | A | G | 3 | a0001c0001t0015g0127a0001c0001t0015g0134a0001c0001t0015g0135 | 3 | HG00323.hp1 HG01081.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.725+5211A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51744386 | ||||||
chr13:51744387 | C | A | 6 | a0001c0001t0010g0002a0001c0001t0010g0003a0001c0001t0010g0004others(3): Show | 6 | HG02257.hp2 HG02647.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.725+5212C>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51744387 | ||||||
chr13:51744479 | T | G | 1 | a0001c0001t0003g0112 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.725+5304T>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51744479 | ||||||
chr13:51744482 | G | A | 1 | a0001c0007t0016g0278 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.725+5307G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51744482 | ||||||
chr13:51745286 | G | T | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.726-6024G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51745286 | ||||||
chr13:51745292 | A | G | 1 | a0001c0007t0016g0278 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.726-6018A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51745292 | ||||||
chr13:51745382 | A | G | 6 | a0001c0001t0008g0212a0001c0001t0008g0213a0001c0001t0008g0214others(3): Show | 6 | NA18941.hp1 NA18951.hp1 NA18998.hp1 others(3): Show |
intron_variant | MODIFIER | c.726-5928A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51745382 | ||||||
chr13:51745542 | C | T | 91 | a0001c0001t0001g0096a0001c0001t0002g0259a0001c0001t0004g0177others(88): Show | 91 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.726-5768C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51745542 | ||||||
chr13:51745588 | C | T | 42 | a0001c0001t0004g0177a0001c0001t0004g0178a0001c0001t0004g0182others(39): Show | 42 | HG00735.hp2 HG01081.hp2 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.726-5722C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51745588 | ||||||
chr13:51745693 | C | T | 30 | a0001c0001t0004g0177a0001c0001t0004g0178a0001c0001t0004g0182others(27): Show | 30 | HG00735.hp2 HG01081.hp2 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.726-5617C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51745693 | ||||||
chr13:51745738 | T | TA | 20 | a0001c0001t0001g0027a0001c0001t0001g0107a0001c0001t0001g0122others(17): Show | 20 | HG00642.hp1 HG01106.hp1 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.726-5545dupA | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr13 | 51745738 | |||||
chr13:51745738 | TA | T | 84 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(81): Show | 84 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.726-5545delA | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr13 | 51745738 | |||||
chr13:51745738 | TAA | T | 50 | a0001c0001t0001g0013a0001c0001t0001g0072a0001c0001t0001g0097others(47): Show | 50 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(47): Show |
intron_variant | MODIFIER | c.726-5546_726-5545d others(4): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr13 | 51745738 | |||||
chr13:51745738 | TAAAAAAA others(8): Show |
T | 1 | a0001c0001t0034g0024 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.726-5559_726-5545d others(17): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr13 | 51745738 | |||||
chr13:51745752 | A | C | 1 | a0001c0002t0043g0038 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.726-5558A>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51745752 | ||||||
chr13:51745802 | T | C | 35 | a0001c0001t0004g0177a0001c0001t0004g0178a0001c0001t0004g0182others(32): Show | 35 | HG00735.hp2 HG01081.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.726-5508T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51745802 | ||||||
chr13:51745804 | T | C | 54 | a0001c0001t0002g0259a0001c0001t0007g0070a0001c0001t0007g0071others(51): Show | 54 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.726-5506T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51745804 | ||||||
chr13:51745829 | A | G | 1 | a0001c0001t0009g0111 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.726-5481A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51745829 | ||||||
chr13:51745898 | C | A | 1 | a0001c0001t0003g0241 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.726-5412C>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51745898 | ||||||
chr13:51745961 | CTTTTTCT others(7): Show |
C | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.726-5343_726-5330d others(16): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr13 | 51745961 | |||||
chr13:51745973 | C | CT | 15 | a0001c0001t0001g0027a0001c0001t0001g0116a0001c0001t0001g0117others(12): Show | 15 | HG00323.hp1 HG00558.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.726-5316dupT | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr13 | 51745973 | |||||
chr13:51745973 | C | T | 1 | a0001c0001t0003g0112 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.726-5337C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51745973 | ||||||
chr13:51745973 | CT | C | 102 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0012others(99): Show | 102 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.726-5316delT | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr13 | 51745973 | |||||
chr13:51745973 | CTT | C | 53 | a0001c0001t0002g0259a0001c0001t0007g0070a0001c0001t0007g0071others(50): Show | 53 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.726-5317_726-5316d others(4): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr13 | 51745973 | |||||
chr13:51745978 | T | C | 1 | a0001c0001t0008g0214 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.726-5332T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51745978 | ||||||
chr13:51745979 | T | C | 1 | a0001c0001t0020g0273 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.726-5331T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51745979 | ||||||
chr13:51746161 | T | C | 42 | a0001c0001t0004g0177a0001c0001t0004g0178a0001c0001t0004g0182others(39): Show | 42 | HG00735.hp2 HG01081.hp2 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.726-5149T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51746161 | ||||||
chr13:51746173 | G | C | 1 | a0001c0001t0018g0023 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.726-5137G>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51746173 | ||||||
chr13:51746251 | C | T | 3 | a0001c0001t0003g0224a0001c0001t0003g0226a0001c0001t0003g0237 | 3 | NA18966.hp2 NA18975.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.726-5059C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51746251 | ||||||
chr13:51746703 | C | T | 3 | a0001c0001t0013g0263a0001c0001t0013g0264a0001c0001t0013g0265 | 3 | HG02145.hp1 HG03041.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.726-4607C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51746703 | ||||||
chr13:51746711 | AAC | A | 3 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0275 | 3 | HG00733.hp2 HG01123.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.726-4597_726-4596d others(4): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr13 | 51746711 | |||||
chr13:51746784 | T | C | 1 | a0001c0001t0018g0023 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.726-4526T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51746784 | ||||||
chr13:51747333 | T | G | 4 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0275others(1): Show | 4 | HG00733.hp2 HG01123.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.726-3977T>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51747333 | ||||||
chr13:51747453 | C | T | 3 | a0001c0001t0036g0247a0001c0001t0038g0248a0001c0001t0039g0274 | 3 | HG00408.hp2 NA18955.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.726-3857C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51747453 | ||||||
chr13:51747577 | G | A | 2 | a0001c0006t0016g0277a0001c0007t0016g0278 | 2 | HG02258.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.726-3733G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51747577 | ||||||
chr13:51747618 | G | T | 42 | a0001c0001t0004g0177a0001c0001t0004g0178a0001c0001t0004g0182others(39): Show | 42 | HG00735.hp2 HG01081.hp2 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.726-3692G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51747618 | ||||||
chr13:51748048 | C | G | 47 | a0001c0001t0002g0259a0001c0001t0019g0260a0001c0001t0019g0261others(44): Show | 47 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(44): Show |
intron_variant | MODIFIER | c.726-3262C>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51748048 | ||||||
chr13:51748107 | C | CA | 3 | a0001c0001t0001g0057a0001c0001t0001g0059a0001c0001t0023g0058 | 3 | HG01192.hp1 HG02615.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.726-3202dupA | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr13 | 51748107 | |||||
chr13:51748190 | C | T | 2 | a0001c0001t0001g0133a0004c0005t0022g0150 | 2 | HG01884.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.726-3120C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51748190 | ||||||
chr13:51748229 | C | T | 4 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0275others(1): Show | 4 | HG00733.hp2 HG01123.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.726-3081C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51748229 | ||||||
chr13:51748230 | G | A | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.726-3080G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51748230 | ||||||
chr13:51748354 | A | T | 2 | a0001c0006t0016g0277a0001c0007t0016g0278 | 2 | HG02258.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.726-2956A>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51748354 | ||||||
chr13:51748419 | T | C | 2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 2 | HG02109.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.726-2891T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51748419 | ||||||
chr13:51748496 | G | T | 8 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(5): Show | 8 | HG01106.hp1 HG02055.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.726-2814G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51748496 | ||||||
chr13:51748570 | A | G | 1 | a0001c0001t0003g0210 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.726-2740A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51748570 | ||||||
chr13:51748746 | A | T | 1 | a0001c0001t0001g0008 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.726-2564A>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51748746 | ||||||
chr13:51748785 | C | CAAAACTG others(313): Show |
1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.726-2510_726-2509i others(322): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr13 | 51748785 | |||||
chr13:51748972 | A | G | 1 | a0001c0001t0001g0068 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.726-2338A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51748972 | ||||||
chr13:51749181 | T | C | 11 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(8): Show | 11 | HG01106.hp1 HG02055.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.726-2129T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51749181 | ||||||
chr13:51749209 | A | T | 4 | a0001c0002t0011g0022a0001c0002t0011g0044a0001c0002t0011g0045others(1): Show | 4 | HG00408.hp1 HG00423.hp1 HG00609.hp1 others(1): Show |
intron_variant | MODIFIER | c.726-2101A>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51749209 | ||||||
chr13:51749291 | A | G | 1 | a0001c0001t0001g0096 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.726-2019A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51749291 | ||||||
chr13:51749466 | T | A | 47 | a0001c0001t0002g0259a0001c0001t0019g0260a0001c0001t0019g0261others(44): Show | 47 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(44): Show |
intron_variant | MODIFIER | c.726-1844T>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51749466 | ||||||
chr13:51749638 | G | T | 2 | a0001c0001t0001g0267a0001c0001t0001g0268 | 2 | HG02109.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.726-1672G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51749638 | ||||||
chr13:51749749 | C | A | 1 | a0001c0001t0004g0269 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.726-1561C>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51749749 | ||||||
chr13:51749752 | A | T | 1 | a0001c0001t0004g0269 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.726-1558A>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51749752 | ||||||
chr13:51749753 | G | C | 1 | a0001c0001t0004g0269 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.726-1557G>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51749753 | ||||||
chr13:51749754 | A | T | 1 | a0001c0001t0004g0269 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.726-1556A>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51749754 | ||||||
chr13:51749757 | T | G | 1 | a0001c0001t0004g0269 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.726-1553T>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51749757 | ||||||
chr13:51749765 | G | T | 1 | a0001c0001t0004g0269 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.726-1545G>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51749765 | ||||||
chr13:51750289 | C | T | 1 | a0001c0001t0044g0262 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.726-1021C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51750289 | ||||||
chr13:51750410 | A | G | 1 | a0001c0001t0001g0083 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.726-900A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51750410 | ||||||
chr13:51750411 | C | T | 1 | a0001c0001t0003g0209 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.726-899C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51750411 | ||||||
chr13:51750509 | T | A | 1 | a0001c0001t0006g0169 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.726-801T>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51750509 | ||||||
chr13:51750537 | C | CA | 205 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0012others(202): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.726-759dupA | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr13 | 51750537 | |||||
chr13:51750537 | C | CAA | 56 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0117others(53): Show | 56 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(53): Show |
intron_variant | MODIFIER | c.726-760_726-759dup others(2): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr13 | 51750537 | |||||
chr13:51750577 | T | C | 2 | a0001c0006t0016g0277a0001c0007t0016g0278 | 2 | HG02258.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.726-733T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51750577 | ||||||
chr13:51751048 | C | G | 3 | a0001c0002t0002g0032a0001c0002t0002g0151a0001c0002t0002g0152 | 3 | HG01433.hp2 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.726-262C>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51751048 | ||||||
chr13:51751149 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.726-161C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51751149 | ||||||
chr13:51751211 | G | A | 2 | a0001c0001t0006g0047a0001c0001t0006g0173 | 2 | NA18943.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.726-99G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51751211 | ||||||
chr13:51751256 | G | A | 1 | a0001c0001t0004g0203 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.726-54G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 7/11 | chr13 | 51751256 | ||||||
chr13:51752019 | C | T | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.831+604C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 8/11 | chr13 | 51752019 | ||||||
chr13:51752029 | A | G | 2 | a0001c0001t0001g0074a0001c0001t0001g0081 | 2 | NA18964.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.831+614A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 8/11 | chr13 | 51752029 | ||||||
chr13:51752203 | A | G | 1 | a0001c0007t0016g0278 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.831+788A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 8/11 | chr13 | 51752203 | ||||||
chr13:51752218 | A | C | 2 | a0001c0001t0020g0273a0001c0001t0029g0272 | 2 | HG02559.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.831+803A>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 8/11 | chr13 | 51752218 | ||||||
chr13:51752336 | G | A | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.831+921G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 8/11 | chr13 | 51752336 | ||||||
chr13:51752341 | A | G | 92 | a0001c0001t0002g0259a0001c0001t0004g0177a0001c0001t0004g0178others(89): Show | 92 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.831+926A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 8/11 | chr13 | 51752341 | ||||||
chr13:51752476 | G | A | 3 | a0001c0001t0013g0263a0001c0001t0013g0264a0001c0001t0013g0265 | 3 | HG02145.hp1 HG03041.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.831+1061G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 8/11 | chr13 | 51752476 | ||||||
chr13:51752884 | G | A | 47 | a0001c0001t0002g0259a0001c0001t0019g0260a0001c0001t0019g0261others(44): Show | 47 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(44): Show |
intron_variant | MODIFIER | c.831+1469G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 8/11 | chr13 | 51752884 | ||||||
chr13:51752941 | C | T | 1 | a0001c0001t0001g0144 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.831+1526C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 8/11 | chr13 | 51752941 | ||||||
chr13:51753095 | G | A | 65 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0012others(62): Show | 65 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.831+1680G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 8/11 | chr13 | 51753095 | ||||||
chr13:51753240 | C | G | 54 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0012others(51): Show | 54 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(51): Show |
intron_variant | MODIFIER | c.831+1825C>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 8/11 | chr13 | 51753240 | ||||||
chr13:51753261 | C | T | 1 | a0001c0001t0001g0088 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.831+1846C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 8/11 | chr13 | 51753261 | ||||||
chr13:51753352 | C | G | 1 | a0001c0001t0034g0024 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.831+1937C>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 8/11 | chr13 | 51753352 | ||||||
chr13:51753930 | C | CA | 10 | a0001c0001t0004g0178a0001c0001t0004g0183a0001c0001t0004g0189others(7): Show | 10 | HG00735.hp2 HG01081.hp2 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.832-1415dupA | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr13 | 51753930 | |||||
chr13:51754090 | CA | C | 132 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0012others(129): Show | 132 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.832-1248delA | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr13 | 51754090 | |||||
chr13:51754189 | G | C | 1 | a0001c0001t0046g0109 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.832-1169G>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 8/11 | chr13 | 51754189 | ||||||
chr13:51754225 | A | G | 94 | a0001c0001t0002g0085a0001c0001t0002g0259a0001c0001t0004g0177others(91): Show | 94 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.832-1133A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 8/11 | chr13 | 51754225 | ||||||
chr13:51754549 | G | C | 1 | a0002c0003t0004g0181 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.832-809G>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 8/11 | chr13 | 51754549 | ||||||
chr13:51754708 | T | A | 49 | a0001c0001t0002g0085a0001c0001t0002g0259a0001c0001t0019g0260others(46): Show | 49 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(46): Show |
intron_variant | MODIFIER | c.832-650T>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 8/11 | chr13 | 51754708 | ||||||
chr13:51754730 | T | C | 4 | a0001c0001t0002g0259a0001c0001t0019g0260a0001c0001t0019g0261others(1): Show | 4 | HG02698.hp1 HG03491.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.832-628T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 8/11 | chr13 | 51754730 | ||||||
chr13:51755051 | C | T | 1 | a0001c0001t0034g0024 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.832-307C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 8/11 | chr13 | 51755051 | ||||||
chr13:51755085 | T | C | 9 | a0001c0002t0002g0029a0001c0002t0002g0031a0001c0002t0002g0034others(6): Show | 9 | HG00673.hp2 HG02015.hp1 HG02155.hp2 others(6): Show |
intron_variant | MODIFIER | c.832-273T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 8/11 | chr13 | 51755085 | ||||||
chr13:51755512 | C | A | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.933+53C>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 9/11 | chr13 | 51755512 | ||||||
chr13:51755622 | C | T | 43 | a0001c0001t0004g0177a0001c0001t0004g0178a0001c0001t0004g0182others(40): Show | 43 | HG00735.hp2 HG01081.hp2 HG01106.hp1 others(40): Show |
intron_variant | MODIFIER | c.933+163C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 9/11 | chr13 | 51755622 | ||||||
chr13:51755695 | G | A | 94 | a0001c0001t0002g0085a0001c0001t0002g0259a0001c0001t0004g0177others(91): Show | 94 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.933+236G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 9/11 | chr13 | 51755695 | ||||||
chr13:51755805 | C | G | 3 | a0001c0001t0014g0119a0001c0001t0014g0146a0001c0001t0014g0223 | 3 | HG01123.hp1 HG01192.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.933+346C>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 9/11 | chr13 | 51755805 | ||||||
chr13:51755849 | C | G | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.933+390C>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 9/11 | chr13 | 51755849 | ||||||
chr13:51756060 | C | G | 4 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0275others(1): Show | 4 | HG00733.hp2 HG01123.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.934-272C>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 9/11 | chr13 | 51756060 | ||||||
chr13:51756104 | G | C | 48 | a0001c0001t0002g0085a0001c0001t0002g0259a0001c0001t0019g0260others(45): Show | 48 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(45): Show |
intron_variant | MODIFIER | c.934-228G>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 9/11 | chr13 | 51756104 | ||||||
chr13:51756132 | T | C | 48 | a0001c0001t0002g0085a0001c0001t0002g0259a0001c0001t0019g0260others(45): Show | 48 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(45): Show |
intron_variant | MODIFIER | c.934-200T>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 9/11 | chr13 | 51756132 | ||||||
chr13:51756861 | G | A | 1 | a0001c0001t0004g0203 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1064+399G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 10/11 | chr13 | 51756861 | ||||||
chr13:51756875 | C | T | 1 | a0001c0001t0004g0196 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1064+413C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 10/11 | chr13 | 51756875 | ||||||
chr13:51756955 | C | T | 1 | a0001c0001t0004g0206 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1064+493C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 10/11 | chr13 | 51756955 | ||||||
chr13:51757202 | T | A | 27 | a0001c0001t0003g0163a0001c0001t0003g0166a0001c0001t0003g0207others(24): Show | 27 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(24): Show |
intron_variant | MODIFIER | c.1064+740T>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 10/11 | chr13 | 51757202 | ||||||
chr13:51757457 | G | GAA | 6 | a0001c0002t0002g0249a0001c0002t0002g0250a0001c0002t0002g0251others(3): Show | 6 | HG00140.hp2 HG00642.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1065-725_1065-724d others(4): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr13 | 51757457 | |||||
chr13:51757461 | A | AAG | 86 | a0001c0001t0002g0085a0001c0001t0002g0259a0001c0001t0004g0177others(83): Show | 86 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.1065-730_1065-729i others(4): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr13 | 51757461 | |||||
chr13:51757833 | CT | C | 43 | a0001c0001t0004g0177a0001c0001t0004g0178a0001c0001t0004g0182others(40): Show | 43 | HG00735.hp2 HG01081.hp2 HG01106.hp1 others(40): Show |
intron_variant | MODIFIER | c.1065-346delT | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr13 | 51757833 | |||||
chr13:51758017 | AT | A | 64 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0012others(61): Show | 64 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.1065-165delT | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr13 | 51758017 | |||||
chr13:51758095 | C | T | 1 | a0001c0001t0003g0211 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1065-97C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 10/11 | chr13 | 51758095 | ||||||
chr13:51758407 | C | T | 1 | a0001c0001t0004g0269 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1173+107C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 11/11 | chr13 | 51758407 | ||||||
chr13:51758552 | T | TA | 7 | a0001c0001t0001g0107a0001c0001t0001g0266a0001c0001t0001g0267others(4): Show | 7 | HG02109.hp1 HG02109.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1173+272dupA | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr13 | 51758552 | |||||
chr13:51758552 | TA | T | 105 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0012others(102): Show | 105 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.1173+272delA | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr13 | 51758552 | |||||
chr13:51758552 | TAA | T | 8 | a0001c0001t0001g0097a0001c0001t0005g0016a0001c0001t0005g0017others(5): Show | 8 | HG02055.hp2 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1173+271_1173+272d others(4): Show |
WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr13 | 51758552 | |||||
chr13:51758609 | A | G | 48 | a0001c0001t0002g0085a0001c0001t0002g0259a0001c0001t0019g0260others(45): Show | 48 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(45): Show |
intron_variant | MODIFIER | c.1173+309A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 11/11 | chr13 | 51758609 | ||||||
chr13:51758621 | C | T | 1 | a0001c0001t0003g0218 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1173+321C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 11/11 | chr13 | 51758621 | ||||||
chr13:51758867 | C | T | 1 | a0004c0005t0022g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1173+567C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 11/11 | chr13 | 51758867 | ||||||
chr13:51758921 | C | T | 48 | a0001c0001t0002g0085a0001c0001t0002g0259a0001c0001t0019g0260others(45): Show | 48 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(45): Show |
intron_variant | MODIFIER | c.1173+621C>T | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 11/11 | chr13 | 51758921 | ||||||
chr13:51758953 | C | A | 1 | a0001c0001t0018g0023 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1173+653C>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 11/11 | chr13 | 51758953 | ||||||
chr13:51759067 | G | C | 1 | a0001c0001t0033g0200 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1174-673G>C | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 11/11 | chr13 | 51759067 | ||||||
chr13:51759085 | G | A | 2 | a0001c0001t0019g0260a0001c0001t0019g0261 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1174-655G>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 11/11 | chr13 | 51759085 | ||||||
chr13:51759147 | C | A | 48 | a0001c0001t0002g0085a0001c0001t0002g0259a0001c0001t0019g0260others(45): Show | 48 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(45): Show |
intron_variant | MODIFIER | c.1174-593C>A | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 11/11 | chr13 | 51759147 | ||||||
chr13:51759503 | T | G | 1 | a0003c0004t0001g0108 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1174-237T>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 11/11 | chr13 | 51759503 | ||||||
chr13:51759628 | A | G | 1 | a0001c0001t0018g0270 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1174-112A>G | WDFY2 | ENSG00000139668.9 | transcript | ENST00000298125.7 | protein_coding | 11/11 | chr13 | 51759628 |