geneid | 5074 |
---|---|
ensemblid | ENSG00000177425.11 |
hgncid | 8614 |
symbol | PAWR |
name | pro-apoptotic WT1 regulator |
refseq_nuc | NM_002583.4 |
refseq_prot | NP_002574.2 |
ensembl_nuc | ENST00000328827.9 |
ensembl_prot | ENSP00000328088.4 |
mane_status | MANE Select |
chr | chr12 |
start | 79584879 |
end | 79690964 |
strand | - |
ver | v1.2 |
region | chr12:79584879-79690964 |
region5000 | chr12:79579879-79695964 |
regionname0 | PAWR_chr12_79584879_79690964 |
regionname5000 | PAWR_chr12_79579879_79695964 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 340 | 156 | 17 | 33 | 84 | 2 | 18 | 65 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
a0002 | 0/0 | 340 | 82 | 36 | 8 | 31 | 0 | 7 | 27 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
a0003 | 0/0 | 340 | 11 | 8 | 2 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
a0004 | 0/0 | 340 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
a0005 | 0/0 | 340 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
a0006 | 0/0 | 340 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
a0007 | 0/0 | 340 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 1023 | 107 | 16 | 25 | 53 | 2 | 10 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
c0002 | 0/0 | 1023 | 82 | 36 | 8 | 31 | 0 | 7 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
c0003 | 1/0 | 1023 | 49 | 1 | 8 | 31 | 0 | 8 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
c0004 | 0/0 | 1023 | 8 | 5 | 2 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
c0005 | 0/0 | 1023 | 3 | 3 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
c0006 | 0/0 | 1023 | 3 | 3 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
c0007 | 0/0 | 1023 | 2 | 2 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
c0008 | 0/0 | 1023 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
c0009 | 0/0 | 1023 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 7969 | 62 | 21 | 5 | 30 | 0 | 6 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
t0002 | 0/1 | 7965 | 58 | 1 | 15 | 34 | 1 | 6 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
t0003 | 1/0 | 7969 | 42 | 4 | 9 | 22 | 0 | 6 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
t0004 | 0/0 | 7969 | 30 | 9 | 6 | 11 | 1 | 3 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
t0005 | 0/0 | 7969 | 13 | 10 | 3 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
t0006 | 0/0 | 7968 | 6 | 1 | 3 | 2 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
t0007 | 0/0 | 7969 | 5 | 4 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
t0008 | 0/0 | 7969 | 5 | 0 | 0 | 5 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
t0009 | 0/0 | 7967 | 4 | 3 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
t0010 | 0/0 | 7969 | 3 | 0 | 0 | 3 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
t0011 | 0/0 | 7970 | 3 | 3 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
t0012 | 0/0 | 7970 | 2 | 0 | 0 | 1 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
t0013 | 0/0 | 7969 | 2 | 0 | 0 | 2 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
t0014 | 0/0 | 7969 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
t0015 | 0/0 | 7969 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
t0016 | 0/0 | 7969 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
t0017 | 0/0 | 7970 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
t0018 | 0/0 | 7969 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
t0019 | 0/0 | 7969 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
t0020 | 0/0 | 7969 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
t0021 | 0/0 | 7969 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
t0022 | 0/0 | 7969 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
t0023 | 0/0 | 7969 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
t0024 | 0/0 | 7970 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
t0025 | 0/0 | 7966 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
t0026 | 0/0 | 7966 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
t0027 | 0/0 | 7970 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
t0028 | 0/0 | 7969 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
t0029 | 0/0 | 7965 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
t0030 | 0/0 | 7965 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
t0031 | 0/0 | 7969 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
t0032 | 0/0 | 7969 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
t0033 | 0/0 | 7969 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
t0034 | 0/0 | 7969 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0106 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0130 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1023 | 107 | 16 | 25 | 53 | 2 | 10 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
a0001c0003 | 1/0 | 1023 | 49 | 1 | 8 | 31 | 0 | 8 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
a0002c0002 | 0/0 | 1023 | 82 | 36 | 8 | 31 | 0 | 7 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
a0003c0004 | 0/0 | 1023 | 8 | 5 | 2 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
a0003c0005 | 0/0 | 1023 | 3 | 3 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
a0004c0006 | 0/0 | 1023 | 3 | 3 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
a0005c0007 | 0/0 | 1023 | 2 | 2 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
a0006c0008 | 0/0 | 1023 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
a0007c0009 | 0/0 | 1023 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 0/1 | 8987 | 57 | 1 | 15 | 33 | 1 | 6 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
a0001c0001t0003 | 0/0 | 8991 | 5 | 3 | 0 | 2 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
a0001c0001t0004 | 0/0 | 8991 | 30 | 9 | 6 | 11 | 1 | 3 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
a0001c0001t0006 | 0/0 | 8990 | 6 | 1 | 3 | 2 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
a0001c0001t0010 | 0/0 | 8991 | 3 | 0 | 0 | 3 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
a0001c0001t0016 | 0/0 | 8991 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
a0001c0001t0025 | 0/0 | 8988 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
a0001c0001t0026 | 0/0 | 8988 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
a0001c0001t0029 | 0/0 | 8987 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
a0001c0001t0030 | 0/0 | 8987 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
a0001c0001t0032 | 0/0 | 8991 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
a0001c0003t0002 | 0/0 | 8987 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
a0001c0003t0003 | 1/0 | 8991 | 35 | 1 | 8 | 20 | 0 | 5 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
a0001c0003t0008 | 0/0 | 8991 | 5 | 0 | 0 | 5 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
a0001c0003t0013 | 0/0 | 8991 | 2 | 0 | 0 | 2 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
a0001c0003t0014 | 0/0 | 8991 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
a0001c0003t0023 | 0/0 | 8991 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
a0001c0003t0024 | 0/0 | 8992 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
a0001c0003t0027 | 0/0 | 8992 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
a0001c0003t0028 | 0/0 | 8991 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
a0001c0003t0031 | 0/0 | 8991 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
a0002c0002t0001 | 0/0 | 8991 | 61 | 21 | 5 | 29 | 0 | 6 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
a0002c0002t0005 | 0/0 | 8991 | 13 | 10 | 3 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
a0002c0002t0012 | 0/0 | 8992 | 2 | 0 | 0 | 1 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
a0002c0002t0015 | 0/0 | 8991 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
a0002c0002t0017 | 0/0 | 8992 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
a0002c0002t0018 | 0/0 | 8991 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
a0002c0002t0019 | 0/0 | 8991 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
a0002c0002t0020 | 0/0 | 8991 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
a0002c0002t0021 | 0/0 | 8991 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
a0003c0004t0001 | 0/0 | 8991 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
a0003c0004t0007 | 0/0 | 8991 | 2 | 1 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
a0003c0004t0009 | 0/0 | 8989 | 4 | 3 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
a0003c0004t0022 | 0/0 | 8991 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
a0003c0005t0007 | 0/0 | 8991 | 3 | 3 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
a0004c0006t0011 | 0/0 | 8992 | 3 | 3 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
a0005c0007t0033 | 0/0 | 8991 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
a0005c0007t0034 | 0/0 | 8991 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
a0006c0008t0003 | 0/0 | 8991 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
a0007c0009t0003 | 0/0 | 8991 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | copy fasta | chr12 | 79579879 | 79695964 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0130 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0004g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0004g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0004g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0004g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0004g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0004g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0004g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0004g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0004g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0004g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0004g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0004g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0004g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0004g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0004g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0004g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0004g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0004g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0004g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0004g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0004g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0004g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0004g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0004g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0004g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0004g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0004g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0004g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0004g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0006g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0006g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0006g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0006g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0006g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0006g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0010g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0010g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0010g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0016g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0025g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0026g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0029g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0030g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0032g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0003g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0003g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0003g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0003g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0003g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0003g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0003g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0003g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0003g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0003g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0003g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0003g0106 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0003g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0003g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0003g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0008g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0008g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0008g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0008g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0008g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0013g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0013g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0014g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0023g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0024g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0027g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0028g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0031g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0005g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0005g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0005g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0005g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0005g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0005g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0005g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0005g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0005g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0005g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0005g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0005g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0005g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0012g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0012g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0015g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0017g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0018g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0019g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0020g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0021g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0003c0004t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0003c0004t0007g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0003c0004t0007g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0003c0004t0009g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0003c0004t0009g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0003c0004t0009g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0003c0004t0009g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0003c0004t0022g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0003c0005t0007g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0003c0005t0007g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0003c0005t0007g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0004c0006t0011g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0004c0006t0011g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0004c0006t0011g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0005c0007t0033g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0005c0007t0034g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0006c0008t0003g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0007c0009t0003g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00423 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | CHS | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG00423 | hp2 | a0001 | c0001 | t0004 | g0036 | EAS | CHS | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | CHS | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | CHS | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG00544 | hp1 | a0001 | c0003 | t0003 | g0142 | EAS | CHS | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG00544 | hp2 | a0002 | c0002 | t0001 | g0216 | EAS | CHS | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG00621 | hp1 | a0001 | c0003 | t0003 | g0078 | EAS | CHS | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG00621 | hp2 | a0002 | c0002 | t0001 | g0223 | EAS | CHS | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0105 | AMR | PUR | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG00639 | hp2 | a0002 | c0002 | t0005 | g0182 | AMR | PUR | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | CHS | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG00673 | hp2 | a0002 | c0002 | t0001 | g0236 | EAS | CHS | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0154 | AMR | PUR | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG00741 | hp2 | a0001 | c0003 | t0003 | g0100 | AMR | PUR | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0074 | AMR | PUR | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01069 | hp2 | a0001 | c0003 | t0003 | g0083 | AMR | PUR | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01074 | hp1 | a0001 | c0003 | t0003 | g0087 | AMR | PUR | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01074 | hp2 | a0003 | c0004 | t0009 | g0160 | AMR | PUR | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0059 | AMR | PUR | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01081 | hp2 | a0001 | c0001 | t0004 | g0163 | AMR | PUR | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01099 | hp1 | a0001 | c0003 | t0003 | g0005 | AMR | PUR | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01099 | hp2 | a0001 | c0001 | t0004 | g0035 | AMR | PUR | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01109 | hp1 | a0002 | c0002 | t0005 | g0248 | AMR | PUR | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01109 | hp2 | a0001 | c0001 | t0006 | g0034 | AMR | PUR | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0118 | AMR | PUR | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01168 | hp2 | a0001 | c0001 | t0006 | g0023 | AMR | PUR | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01169 | hp1 | a0006 | c0008 | t0003 | g0098 | AMR | PUR | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0117 | AMR | PUR | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01192 | hp1 | a0002 | c0002 | t0001 | g0171 | AMR | PUR | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0080 | AMR | PUR | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01243 | hp1 | a0003 | c0004 | t0007 | g0168 | AMR | PUR | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0076 | AMR | PUR | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01255 | hp1 | a0001 | c0001 | t0004 | g0020 | AMR | CLM | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0067 | AMR | CLM | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01256 | hp1 | a0002 | c0002 | t0001 | g0222 | AMR | CLM | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01256 | hp2 | a0001 | c0001 | t0006 | g0014 | AMR | CLM | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01257 | hp2 | a0001 | c0001 | t0004 | g0021 | AMR | CLM | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01258 | hp1 | a0001 | c0001 | t0004 | g0022 | AMR | CLM | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01258 | hp2 | a0002 | c0002 | t0001 | g0217 | AMR | CLM | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01261 | hp1 | a0002 | c0002 | t0005 | g0252 | AMR | CLM | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01261 | hp2 | a0001 | c0003 | t0003 | g0096 | AMR | CLM | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01884 | hp1 | a0001 | c0001 | t0004 | g0017 | AFR | ACB | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01884 | hp2 | a0002 | c0002 | t0005 | g0183 | AFR | ACB | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01891 | hp1 | a0001 | c0003 | t0003 | g0103 | AFR | ACB | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01891 | hp2 | a0002 | c0002 | t0001 | g0178 | AFR | ACB | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01928 | hp1 | a0001 | c0003 | t0003 | g0099 | AMR | PEL | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0113 | AMR | PEL | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0061 | AMR | PEL | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01952 | hp2 | a0001 | c0003 | t0003 | g0046 | AMR | PEL | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01975 | hp1 | a0001 | c0001 | t0030 | g0058 | AMR | PEL | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01975 | hp2 | a0002 | c0002 | t0001 | g0208 | AMR | PEL | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0060 | AMR | PEL | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01981 | hp2 | a0001 | c0003 | t0003 | g0079 | AMR | PEL | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01993 | hp1 | a0001 | c0001 | t0004 | g0019 | AMR | PEL | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0123 | AMR | PEL | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | KHV | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02027 | hp2 | a0002 | c0002 | t0001 | g0191 | EAS | KHV | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | KHV | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02040 | hp2 | a0001 | c0001 | t0004 | g0033 | EAS | KHV | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02055 | hp1 | a0001 | c0001 | t0016 | g0012 | AFR | ACB | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02055 | hp2 | a0002 | c0002 | t0005 | g0233 | AFR | ACB | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02056 | hp1 | a0001 | c0001 | t0025 | g0109 | EAS | KHV | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02056 | hp2 | a0001 | c0003 | t0003 | g0146 | EAS | KHV | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02071 | hp1 | a0001 | c0003 | t0003 | g0085 | EAS | KHV | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02071 | hp2 | a0003 | c0004 | t0001 | g0007 | EAS | KHV | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | KHV | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02074 | hp2 | a0001 | c0001 | t0004 | g0024 | EAS | KHV | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02080 | hp1 | a0001 | c0001 | t0004 | g0031 | EAS | KHV | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | KHV | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02145 | hp1 | a0005 | c0007 | t0033 | g0256 | AFR | ACB | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02145 | hp2 | a0002 | c0002 | t0001 | g0232 | AFR | ACB | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02257 | hp1 | a0002 | c0002 | t0017 | g0184 | AFR | ACB | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02257 | hp2 | a0001 | c0001 | t0004 | g0010 | AFR | ACB | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02258 | hp1 | a0004 | c0006 | t0011 | g0240 | AFR | ACB | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02258 | hp2 | a0002 | c0002 | t0001 | g0176 | AFR | ACB | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02300 | hp1 | a0002 | c0002 | t0001 | g0206 | AMR | PEL | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0047 | AMR | PEL | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0071 | AFR | ACB | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02451 | hp2 | a0003 | c0004 | t0022 | g0166 | AFR | ACB | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02523 | hp1 | a0001 | c0003 | t0013 | g0095 | EAS | KHV | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | KHV | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02572 | hp1 | a0002 | c0002 | t0001 | g0170 | AFR | GWD | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02572 | hp2 | a0001 | c0001 | t0003 | g0039 | AFR | GWD | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02602 | hp1 | a0001 | c0003 | t0028 | g0084 | SAS | PJL | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0049 | SAS | PJL | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02615 | hp1 | a0002 | c0002 | t0015 | g0177 | AFR | GWD | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02615 | hp2 | a0001 | c0001 | t0004 | g0018 | AFR | GWD | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02622 | hp1 | a0002 | c0002 | t0001 | g0185 | AFR | GWD | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02622 | hp2 | a0002 | c0002 | t0005 | g0244 | AFR | GWD | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02630 | hp1 | a0002 | c0002 | t0001 | g0229 | AFR | GWD | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02630 | hp2 | a0002 | c0002 | t0005 | g0243 | AFR | GWD | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02647 | hp1 | a0001 | c0001 | t0004 | g0037 | AFR | GWD | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02647 | hp2 | a0002 | c0002 | t0001 | g0253 | AFR | GWD | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02683 | hp1 | a0001 | c0003 | t0003 | g0145 | SAS | PJL | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02683 | hp2 | a0001 | c0001 | t0004 | g0124 | SAS | PJL | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02717 | hp1 | a0002 | c0002 | t0001 | g0228 | AFR | GWD | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02717 | hp2 | a0002 | c0002 | t0005 | g0250 | AFR | GWD | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02886 | hp1 | a0002 | c0002 | t0021 | g0186 | AFR | GWD | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02886 | hp2 | a0002 | c0002 | t0001 | g0215 | AFR | GWD | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02895 | hp1 | a0002 | c0002 | t0001 | g0242 | AFR | GWD | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02895 | hp2 | a0002 | c0002 | t0005 | g0214 | AFR | GWD | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02896 | hp1 | a0003 | c0004 | t0009 | g0158 | AFR | GWD | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02896 | hp2 | a0002 | c0002 | t0005 | g0251 | AFR | GWD | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02922 | hp1 | a0003 | c0004 | t0007 | g0167 | AFR | ESN | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02922 | hp2 | a0003 | c0005 | t0007 | g0165 | AFR | ESN | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02976 | hp1 | a0005 | c0007 | t0034 | g0255 | AFR | ESN | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02976 | hp2 | a0001 | c0001 | t0004 | g0013 | AFR | ESN | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG03041 | hp1 | a0001 | c0001 | t0003 | g0038 | AFR | GWD | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG03041 | hp2 | a0002 | c0002 | t0018 | g0245 | AFR | GWD | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG03139 | hp1 | a0002 | c0002 | t0001 | g0172 | AFR | ESN | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG03139 | hp2 | a0001 | c0001 | t0003 | g0040 | AFR | ESN | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG03195 | hp1 | a0002 | c0002 | t0005 | g0249 | AFR | ESN | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG03195 | hp2 | a0003 | c0004 | t0009 | g0157 | AFR | ESN | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG03209 | hp1 | a0002 | c0002 | t0001 | g0231 | AFR | MSL | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG03209 | hp2 | a0002 | c0002 | t0019 | g0179 | AFR | MSL | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG03225 | hp1 | a0004 | c0006 | t0011 | g0239 | AFR | MSL | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG03225 | hp2 | a0002 | c0002 | t0001 | g0181 | AFR | MSL | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG03453 | hp1 | a0003 | c0005 | t0007 | g0003 | AFR | MSL | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG03453 | hp2 | a0002 | c0002 | t0001 | g0187 | AFR | MSL | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG03486 | hp1 | a0002 | c0002 | t0001 | g0238 | AFR | MSL | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG03486 | hp2 | a0004 | c0006 | t0011 | g0241 | AFR | MSL | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG03490 | hp1 | a0002 | c0002 | t0001 | g0192 | SAS | PJL | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG03490 | hp2 | a0001 | c0003 | t0003 | g0094 | SAS | PJL | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG03491 | hp1 | a0002 | c0002 | t0001 | g0209 | SAS | PJL | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG03491 | hp2 | a0007 | c0009 | t0003 | g0152 | SAS | PJL | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG03516 | hp1 | a0001 | c0001 | t0006 | g0026 | AFR | ESN | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG03516 | hp2 | a0002 | c0002 | t0001 | g0175 | AFR | ESN | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG03654 | hp1 | a0001 | c0001 | t0029 | g0120 | SAS | PJL | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG03654 | hp2 | a0001 | c0001 | t0004 | g0032 | SAS | PJL | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0081 | SAS | STU | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG03688 | hp2 | a0002 | c0002 | t0001 | g0210 | SAS | STU | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG03831 | hp1 | a0002 | c0002 | t0001 | g0169 | SAS | BEB | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG03831 | hp2 | a0001 | c0003 | t0027 | g0135 | SAS | BEB | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0115 | SAS | BEB | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG03834 | hp2 | a0001 | c0001 | t0004 | g0011 | SAS | BEB | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG03927 | hp1 | a0002 | c0002 | t0012 | g0189 | SAS | BEB | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG03927 | hp2 | a0001 | c0003 | t0003 | g0254 | SAS | BEB | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG04115 | hp1 | a0001 | c0003 | t0024 | g0149 | SAS | STU | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG04115 | hp2 | a0002 | c0002 | t0001 | g0225 | SAS | STU | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG04184 | hp1 | a0001 | c0003 | t0003 | g0097 | SAS | BEB | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0045 | SAS | BEB | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0069 | SAS | STU | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG04204 | hp2 | a0002 | c0002 | t0001 | g0195 | SAS | STU | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG04228 | hp1 | a0001 | c0003 | t0003 | g0143 | SAS | STU | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0090 | SAS | STU | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18906 | hp1 | a0002 | c0002 | t0001 | g0230 | AFR | YRI | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18906 | hp2 | a0002 | c0002 | t0001 | g0211 | AFR | YRI | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18939 | hp1 | a0001 | c0003 | t0003 | g0082 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18941 | hp1 | a0001 | c0001 | t0004 | g0128 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18941 | hp2 | a0001 | c0001 | t0026 | g0056 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18942 | hp1 | a0001 | c0001 | t0006 | g0008 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18942 | hp2 | a0001 | c0003 | t0014 | g0162 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18945 | hp1 | a0002 | c0002 | t0001 | g0200 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18945 | hp2 | a0001 | c0001 | t0004 | g0028 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18946 | hp1 | a0001 | c0003 | t0008 | g0136 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18946 | hp2 | a0002 | c0002 | t0001 | g0226 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18952 | hp2 | a0002 | c0002 | t0001 | g0218 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18956 | hp1 | a0002 | c0002 | t0001 | g0201 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18956 | hp2 | a0001 | c0003 | t0003 | g0161 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18957 | hp1 | a0001 | c0003 | t0023 | g0148 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18957 | hp2 | a0001 | c0001 | t0004 | g0125 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18959 | hp2 | a0001 | c0003 | t0031 | g0122 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18960 | hp1 | a0001 | c0003 | t0003 | g0150 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18965 | hp1 | a0001 | c0001 | t0006 | g0025 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18965 | hp2 | a0002 | c0002 | t0001 | g0237 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18966 | hp1 | a0001 | c0001 | t0004 | g0156 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18966 | hp2 | a0001 | c0003 | t0008 | g0138 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18967 | hp1 | a0001 | c0003 | t0003 | g0131 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18967 | hp2 | a0002 | c0002 | t0012 | g0221 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18968 | hp2 | a0001 | c0001 | t0010 | g0127 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18969 | hp1 | a0001 | c0003 | t0003 | g0086 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18972 | hp1 | a0001 | c0003 | t0008 | g0151 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18972 | hp2 | a0002 | c0002 | t0001 | g0213 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18973 | hp2 | a0002 | c0002 | t0001 | g0234 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18982 | hp1 | a0001 | c0001 | t0004 | g0027 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18982 | hp2 | a0001 | c0003 | t0008 | g0137 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18984 | hp1 | a0001 | c0003 | t0008 | g0139 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18984 | hp2 | a0002 | c0002 | t0001 | g0220 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18985 | hp1 | a0001 | c0003 | t0013 | g0041 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18985 | hp2 | a0002 | c0002 | t0001 | g0207 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18987 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18987 | hp2 | a0001 | c0001 | t0010 | g0129 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18992 | hp2 | a0002 | c0002 | t0001 | g0197 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18994 | hp2 | a0002 | c0002 | t0001 | g0204 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18999 | hp1 | a0001 | c0003 | t0003 | g0147 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18999 | hp2 | a0002 | c0002 | t0001 | g0173 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19001 | hp1 | a0001 | c0003 | t0003 | g0104 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19001 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19002 | hp1 | a0001 | c0003 | t0003 | g0132 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19002 | hp2 | a0002 | c0002 | t0001 | g0199 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19003 | hp1 | a0002 | c0002 | t0001 | g0188 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19004 | hp1 | a0002 | c0002 | t0001 | g0212 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19005 | hp1 | a0001 | c0003 | t0003 | g0144 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19005 | hp2 | a0002 | c0002 | t0001 | g0196 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19006 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19006 | hp2 | a0002 | c0002 | t0001 | g0227 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19007 | hp2 | a0001 | c0003 | t0003 | g0101 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19009 | hp1 | a0002 | c0002 | t0001 | g0224 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19056 | hp1 | a0002 | c0002 | t0001 | g0198 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19056 | hp2 | a0001 | c0003 | t0003 | g0140 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19057 | hp1 | a0002 | c0002 | t0001 | g0235 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19060 | hp1 | a0002 | c0002 | t0001 | g0205 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19060 | hp2 | a0001 | c0003 | t0003 | g0102 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19063 | hp2 | a0001 | c0001 | t0004 | g0030 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19065 | hp1 | a0001 | c0003 | t0003 | g0089 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19066 | hp1 | a0002 | c0002 | t0020 | g0194 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19066 | hp2 | a0001 | c0001 | t0004 | g0029 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19074 | hp2 | a0002 | c0002 | t0001 | g0193 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19077 | hp1 | a0002 | c0002 | t0001 | g0202 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19079 | hp1 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19079 | hp2 | a0001 | c0003 | t0002 | g0155 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19080 | hp1 | a0002 | c0002 | t0001 | g0190 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19084 | hp1 | a0001 | c0003 | t0003 | g0141 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19084 | hp2 | a0001 | c0001 | t0003 | g0110 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19085 | hp1 | a0001 | c0001 | t0010 | g0126 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19087 | hp1 | a0001 | c0003 | t0003 | g0133 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19087 | hp2 | a0002 | c0002 | t0001 | g0174 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19090 | hp2 | a0001 | c0003 | t0003 | g0075 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19240 | hp1 | a0002 | c0002 | t0005 | g0247 | AFR | YRI | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19240 | hp2 | a0003 | c0005 | t0007 | g0164 | AFR | YRI | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0057 | EUR | TSI | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA20805 | hp2 | a0001 | c0001 | t0004 | g0015 | EUR | TSI | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02486 | hp1 | a0002 | c0002 | t0005 | g0246 | AFR | ACB | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02486 | hp2 | a0001 | c0001 | t0004 | g0009 | AFR | ACB | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02559 | hp1 | a0001 | c0001 | t0004 | g0001 | AFR | ACB | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02559 | hp2 | a0002 | c0002 | t0001 | g0180 | AFR | ACB | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG03471 | hp1 | a0001 | c0001 | t0004 | g0016 | AFR | MSL | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG03471 | hp2 | a0003 | c0004 | t0009 | g0159 | AFR | MSL | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG06807 | hp1 | a0001 | c0001 | t0032 | g0006 | AFR | USA | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG06807 | hp2 | a0002 | c0002 | t0001 | g0219 | AFR | USA | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA20300 | hp1 | a0001 | c0001 | t0004 | g0002 | AFR | USA | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA20300 | hp2 | a0002 | c0002 | t0001 | g0203 | AFR | USA | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0130 | REF | REF | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
homoSapiens_grch38 | hp1 | a0001 | c0003 | t0003 | g0106 | REF | REF | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:79596633
|
C | A | 1 | a0006 | 1 | HG01169.hp1 | missense_variant | MODERATE | c.709G>T | p.Val237Phe | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 5/7 | 949/8991 | 709/1023 | 237/340 | chr12 | 79596633 | ||
chr12:79621127
|
A | C | 4 | a0002a0003a0004others(1): Show | 98 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(95): Show |
missense_variant | MODERATE | c.597T>G | p.Ile199Met | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/7 | 837/8991 | 597/1023 | 199/340 | chr12 | 79621127 | ||
chr12:79621147
|
T | C | 1 | a0007 | 1 | HG03491.hp2 | missense_variant | MODERATE | c.577A>G | p.Ile193Val | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/7 | 817/8991 | 577/1023 | 193/340 | chr12 | 79621147 | ||
chr12:79689874
|
T | C | 1 | a0005 | 2 | HG02145.hp1 HG02976.hp1 |
missense_variant | MODERATE | c.371A>G | p.Gln124Arg | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/7 | 611/8991 | 371/1023 | 124/340 | chr12 | 79689874 | ||
chr12:79690012
|
G | C | 1 | a0002 | 82 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(79): Show |
missense_variant | MODERATE | c.233C>G | p.Pro78Arg | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/7 | 473/8991 | 233/1023 | 78/340 | chr12 | 79690012 | ||
chr12:79690120
|
G | A | 1 | a0004 | 3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
missense_variant | MODERATE | c.125C>T | p.Pro42Leu | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/7 | 365/8991 | 125/1023 | 42/340 | chr12 | 79690120 | ||
chr12:79690874
|
T | C | 1 | a0005 | 2 | HG02145.hp1 HG02976.hp1 |
splice_region_variant | LOW | c.-150A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 1/7 | chr12 | 79690874 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:79592625
|
C | A | 3 | a0003c0005a0004c0006a0005c0007 | 8 | HG02145.hp1 HG02258.hp1 HG02922.hp2 others(5): Show |
synonymous_variant | LOW | c.1005G>T | p.Val335Val | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 1245/8991 | 1005/1023 | 335/340 | chr12 | 79592625 | ||
chr12:79621127
|
A | T | 1 | a0001c0001 | 107 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(104): Show |
synonymous_variant | LOW | c.597T>A | p.Ile199Ile | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/7 | 837/8991 | 597/1023 | 199/340 | chr12 | 79621127 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:79584919
|
TAA | T | 1 | a0003c0004t0009 | 4 | HG01074.hp2 HG02896.hp1 HG03195.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*7686_*7687delTT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 7686 | chr12 | 79584919 | |||||
chr12:79585275
|
G | A | 2 | a0005c0007t0033a0005c0007t0034 | 2 | HG02145.hp1 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7332C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 7332 | chr12 | 79585275 | |||||
chr12:79585294
|
G | A | 1 | a0001c0001t0030 | 1 | HG01975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7313C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 7313 | chr12 | 79585294 | |||||
chr12:79585414
|
G | T | 2 | a0005c0007t0033a0005c0007t0034 | 2 | HG02145.hp1 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7193C>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 7193 | chr12 | 79585414 | |||||
chr12:79585415
|
A | T | 2 | a0005c0007t0033a0005c0007t0034 | 2 | HG02145.hp1 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7192T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 7192 | chr12 | 79585415 | |||||
chr12:79585535
|
C | T | 1 | a0002c0002t0020 | 1 | NA19066.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7072G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 7072 | chr12 | 79585535 | |||||
chr12:79585610
|
C | T | 2 | a0005c0007t0033a0005c0007t0034 | 2 | HG02145.hp1 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6997G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 6997 | chr12 | 79585610 | |||||
chr12:79585791
|
G | C | 2 | a0005c0007t0033a0005c0007t0034 | 2 | HG02145.hp1 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6816C>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 6816 | chr12 | 79585791 | |||||
chr12:79586003
|
C | T | 1 | a0001c0001t0025 | 1 | HG02056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6604G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 6604 | chr12 | 79586003 | |||||
chr12:79586043
|
C | T | 1 | a0001c0001t0029 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6564G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 6564 | chr12 | 79586043 | |||||
chr12:79586083
|
C | T | 1 | a0003c0004t0022 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6524G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 6524 | chr12 | 79586083 | |||||
chr12:79586092
|
A | G | 1 | a0003c0004t0022 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6515T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 6515 | chr12 | 79586092 | |||||
chr12:79586139
|
A | C | 4 | a0001c0001t0004a0001c0001t0006a0001c0001t0010others(1): Show | 40 | HG00423.hp2 HG01081.hp2 HG01099.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*6468T>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 6468 | chr12 | 79586139 | |||||
chr12:79586166
|
C | T | 4 | a0001c0001t0004a0001c0001t0006a0001c0001t0010others(1): Show | 40 | HG00423.hp2 HG01081.hp2 HG01099.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*6441G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 6441 | chr12 | 79586166 | |||||
chr12:79586925
|
C | T | 2 | a0005c0007t0033a0005c0007t0034 | 2 | HG02145.hp1 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5682G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 5682 | chr12 | 79586925 | |||||
chr12:79587035
|
G | A | 2 | a0005c0007t0033a0005c0007t0034 | 2 | HG02145.hp1 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5572C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 5572 | chr12 | 79587035 | |||||
chr12:79587262
|
G | A | 1 | a0003c0004t0009 | 4 | HG01074.hp2 HG02896.hp1 HG03195.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5345C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 5345 | chr12 | 79587262 | |||||
chr12:79587908
|
GCTGT | G | 6 | a0001c0001t0002a0001c0001t0025a0001c0001t0026others(3): Show | 62 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*4695_*4698delACAG | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 4695 | chr12 | 79587908 | |||||
chr12:79587948
|
G | C | 2 | a0005c0007t0033a0005c0007t0034 | 2 | HG02145.hp1 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4659C>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 4659 | chr12 | 79587948 | |||||
chr12:79588074
|
C | A | 1 | a0001c0003t0013 | 2 | HG02523.hp1 NA18985.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4533G>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 4533 | chr12 | 79588074 | |||||
chr12:79588199
|
C | T | 1 | a0001c0001t0016 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4408G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 4408 | chr12 | 79588199 | |||||
chr12:79588272
|
A | G | 1 | a0001c0003t0028 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4335T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 4335 | chr12 | 79588272 | |||||
chr12:79588487
|
T | C | 4 | a0001c0001t0004a0001c0001t0006a0001c0001t0010others(1): Show | 40 | HG00423.hp2 HG01081.hp2 HG01099.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*4120A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 4120 | chr12 | 79588487 | |||||
chr12:79588511
|
A | C | 1 | a0001c0001t0032 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4096T>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 4096 | chr12 | 79588511 | |||||
chr12:79588722
|
T | A | 2 | a0005c0007t0033a0005c0007t0034 | 2 | HG02145.hp1 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3885A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 3885 | chr12 | 79588722 | |||||
chr12:79588797
|
C | T | 2 | a0001c0003t0027a0001c0003t0031 | 2 | HG03831.hp2 NA18959.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3810G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 3810 | chr12 | 79588797 | |||||
chr12:79588909
|
G | C | 3 | a0001c0003t0008a0001c0003t0027a0001c0003t0031 | 7 | HG03831.hp2 NA18946.hp1 NA18959.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3698C>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 3698 | chr12 | 79588909 | |||||
chr12:79588916
|
C | T | 2 | a0005c0007t0033a0005c0007t0034 | 2 | HG02145.hp1 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3691G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 3691 | chr12 | 79588916 | |||||
chr12:79589262
|
G | C | 1 | a0005c0007t0034 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3345C>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 3345 | chr12 | 79589262 | |||||
chr12:79589274
|
A | G | 1 | a0003c0004t0009 | 4 | HG01074.hp2 HG02896.hp1 HG03195.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3333T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 3333 | chr12 | 79589274 | |||||
chr12:79589496
|
T | C | 1 | a0002c0002t0021 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3111A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 3111 | chr12 | 79589496 | |||||
chr12:79589527
|
T | G | 1 | a0001c0001t0032 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3080A>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 3080 | chr12 | 79589527 | |||||
chr12:79589734
|
T | C | 1 | a0002c0002t0018 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2873A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 2873 | chr12 | 79589734 | |||||
chr12:79589935
|
C | T | 1 | a0004c0006t0011 | 3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2672G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 2672 | chr12 | 79589935 | |||||
chr12:79590196
|
A | AT | 10 | a0001c0001t0004a0001c0001t0010a0001c0001t0016others(7): Show | 44 | HG00423.hp2 HG01081.hp2 HG01099.hp2 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*2410dupA | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 2410 | chr12 | 79590196 | |||||
chr12:79590246
|
C | G | 1 | a0002c0002t0019 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2361G>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 2361 | chr12 | 79590246 | |||||
chr12:79590389
|
C | T | 3 | a0002c0002t0005a0002c0002t0017a0002c0002t0018 | 15 | HG00639.hp2 HG01109.hp1 HG01261.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2218G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 2218 | chr12 | 79590389 | |||||
chr12:79590447
|
C | T | 1 | a0001c0001t0010 | 3 | NA18968.hp2 NA18987.hp2 NA19085.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2160G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 2160 | chr12 | 79590447 | |||||
chr12:79590515
|
AT | A | 4 | a0001c0001t0004a0001c0001t0006a0001c0001t0010others(1): Show | 40 | HG00423.hp2 HG01081.hp2 HG01099.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*2091delA | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 2091 | chr12 | 79590515 | |||||
chr12:79590539
|
T | C | 1 | a0003c0004t0022 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2068A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 2068 | chr12 | 79590539 | |||||
chr12:79590908
|
T | A | 2 | a0005c0007t0033a0005c0007t0034 | 2 | HG02145.hp1 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1699A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 1699 | chr12 | 79590908 | |||||
chr12:79590919
|
C | T | 10 | a0002c0002t0001a0002c0002t0005a0002c0002t0012others(7): Show | 83 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*1688G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 1688 | chr12 | 79590919 | |||||
chr12:79591014
|
C | T | 4 | a0001c0001t0004a0001c0001t0006a0001c0001t0010others(1): Show | 40 | HG00423.hp2 HG01081.hp2 HG01099.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*1593G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 1593 | chr12 | 79591014 | |||||
chr12:79591146
|
A | G | 1 | a0002c0002t0015 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1461T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 1461 | chr12 | 79591146 | |||||
chr12:79591540
|
C | T | 2 | a0005c0007t0033a0005c0007t0034 | 2 | HG02145.hp1 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1067G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 1067 | chr12 | 79591540 | |||||
chr12:79591616
|
G | A | 1 | a0003c0004t0022 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*991C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 991 | chr12 | 79591616 | |||||
chr12:79591895
|
C | T | 1 | a0001c0003t0023 | 1 | NA18957.hp1 | 3_prime_UTR_variant | MODIFIER | c.*712G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 712 | chr12 | 79591895 | |||||
chr12:79592094
|
A | C | 21 | a0001c0001t0004a0001c0001t0006a0001c0001t0010others(18): Show | 138 | HG00423.hp2 HG00544.hp2 HG00621.hp2 others(135): Show |
3_prime_UTR_variant | MODIFIER | c.*513T>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 513 | chr12 | 79592094 | |||||
chr12:79592224
|
G | T | 1 | a0001c0003t0014 | 1 | NA18942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*383C>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 383 | chr12 | 79592224 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:79592875
|
G | A | 138 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0009others(135): Show | 138 | HG00423.hp2 HG00544.hp2 HG00621.hp2 others(135): Show |
intron_variant | MODIFIER | c.937-182C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 6/6 | chr12 | 79592875 | ||||||
chr12:79592919
|
T | G | 3 | a0004c0006t0011g0239a0004c0006t0011g0240a0004c0006t0011g0241 | 3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.937-226A>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 6/6 | chr12 | 79592919 | ||||||
chr12:79593068
|
T | C | 2 | a0001c0003t0003g0100a0001c0003t0003g0103 | 2 | HG00741.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.937-375A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 6/6 | chr12 | 79593068 | ||||||
chr12:79593069
|
A | G | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.937-376T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 6/6 | chr12 | 79593069 | ||||||
chr12:79593166
|
A | T | 3 | a0003c0005t0007g0003a0003c0005t0007g0164a0003c0005t0007g0165 | 3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.937-473T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 6/6 | chr12 | 79593166 | ||||||
chr12:79593454
|
A | G | 1 | a0003c0004t0022g0166 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.937-761T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 6/6 | chr12 | 79593454 | ||||||
chr12:79593666
|
T | A | 2 | a0003c0004t0007g0167a0003c0004t0007g0168 | 2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.936+663A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 6/6 | chr12 | 79593666 | ||||||
chr12:79593701
|
G | A | 39 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0009others(36): Show | 39 | HG00423.hp2 HG01081.hp2 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.936+628C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 6/6 | chr12 | 79593701 | ||||||
chr12:79593701
|
G | GT | 37 | a0001c0001t0002g0065a0001c0001t0002g0069a0001c0001t0002g0093others(34): Show | 37 | HG00438.hp1 HG00438.hp2 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.936+627dupA | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 6/6 | chr12 | 79593701 | ||||||
chr12:79593701
|
G | T | 1 | a0001c0001t0004g0018 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.936+628C>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 6/6 | chr12 | 79593701 | ||||||
chr12:79593740
|
C | T | 2 | a0001c0001t0002g0114a0001c0001t0025g0109 | 2 | HG02056.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.936+589G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 6/6 | chr12 | 79593740 | ||||||
chr12:79593793
|
C | T | 1 | a0003c0004t0009g0157 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.936+536G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 6/6 | chr12 | 79593793 | ||||||
chr12:79593892
|
C | T | 40 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0009others(37): Show | 40 | HG00423.hp2 HG01081.hp2 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.936+437G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 6/6 | chr12 | 79593892 | ||||||
chr12:79593914
|
G | C | 2 | a0002c0002t0001g0217a0002c0002t0001g0222 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.936+415C>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 6/6 | chr12 | 79593914 | ||||||
chr12:79594048
|
A | G | 2 | a0003c0004t0007g0167a0003c0004t0007g0168 | 2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.936+281T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 6/6 | chr12 | 79594048 | ||||||
chr12:79594234
|
T | C | 2 | a0003c0004t0007g0167a0003c0004t0007g0168 | 2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.936+95A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 6/6 | chr12 | 79594234 | ||||||
chr12:79594567
|
T | C | 1 | a0003c0004t0009g0160 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.832-134A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 5/6 | chr12 | 79594567 | ||||||
chr12:79594700
|
C | CGT | 12 | a0001c0001t0002g0061a0001c0001t0002g0066a0001c0003t0023g0148others(9): Show | 12 | HG01074.hp2 HG01243.hp1 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.832-269_832-268dup others(2): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 5/6 | chr12 | 79594700 | ||||||
chr12:79594700
|
C | CGTGTGTG others(5): Show |
1 | a0005c0007t0034g0255 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.832-279_832-268dup others(12): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 5/6 | chr12 | 79594700 | ||||||
chr12:79594700
|
C | CGTGTGTG others(7): Show |
1 | a0005c0007t0033g0256 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.832-281_832-268dup others(14): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 5/6 | chr12 | 79594700 | ||||||
chr12:79594700
|
CGT | C | 35 | a0001c0001t0002g0112a0001c0001t0002g0115a0001c0001t0004g0001others(32): Show | 35 | HG00423.hp2 HG00438.hp1 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.832-269_832-268del others(2): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 5/6 | chr12 | 79594700 | ||||||
chr12:79594700
|
CGTGTGTG others(5): Show |
C | 83 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0001g0171others(80): Show | 83 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.832-279_832-268del others(12): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 5/6 | chr12 | 79594700 | ||||||
chr12:79594744
|
T | G | 7 | a0001c0001t0004g0031a0001c0001t0004g0033a0001c0001t0004g0125others(4): Show | 7 | HG02040.hp2 HG02080.hp1 NA18941.hp1 others(4): Show |
intron_variant | MODIFIER | c.832-311A>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 5/6 | chr12 | 79594744 | ||||||
chr12:79595114
|
T | C | 1 | a0001c0003t0003g0082 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.832-681A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 5/6 | chr12 | 79595114 | ||||||
chr12:79595393
|
T | C | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.832-960A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 5/6 | chr12 | 79595393 | ||||||
chr12:79595617
|
C | G | 3 | a0003c0005t0007g0003a0003c0005t0007g0164a0003c0005t0007g0165 | 3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.831+894G>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 5/6 | chr12 | 79595617 | ||||||
chr12:79595646
|
A | G | 3 | a0003c0005t0007g0003a0003c0005t0007g0164a0003c0005t0007g0165 | 3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.831+865T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 5/6 | chr12 | 79595646 | ||||||
chr12:79596174
|
C | T | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.831+337G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 5/6 | chr12 | 79596174 | ||||||
chr12:79596295
|
A | G | 2 | a0001c0001t0003g0038a0001c0001t0003g0039 | 2 | HG02572.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.831+216T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 5/6 | chr12 | 79596295 | ||||||
chr12:79596430
|
T | C | 1 | a0001c0001t0002g0047 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.831+81A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 5/6 | chr12 | 79596430 | ||||||
chr12:79596713
|
C | A | 1 | a0003c0004t0022g0166 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.684-55G>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79596713 | ||||||
chr12:79597057
|
C | CT | 7 | a0001c0001t0002g0117a0001c0001t0002g0118a0001c0003t0003g0087others(4): Show | 7 | HG01074.hp1 HG01168.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.684-400dupA | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79597057 | ||||||
chr12:79597144
|
G | A | 1 | a0001c0001t0002g0074 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.684-486C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79597144 | ||||||
chr12:79597354
|
G | A | 3 | a0003c0005t0007g0003a0003c0005t0007g0164a0003c0005t0007g0165 | 3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.684-696C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79597354 | ||||||
chr12:79597426
|
T | C | 1 | a0001c0001t0002g0123 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.684-768A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79597426 | ||||||
chr12:79597711
|
A | G | 3 | a0001c0001t0003g0038a0001c0001t0003g0039a0001c0001t0003g0040 | 3 | HG02572.hp2 HG03041.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.684-1053T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79597711 | ||||||
chr12:79597751
|
A | G | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.684-1093T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79597751 | ||||||
chr12:79597816
|
A | G | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.684-1158T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79597816 | ||||||
chr12:79597880
|
T | C | 1 | a0001c0003t0003g0085 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.684-1222A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79597880 | ||||||
chr12:79597971
|
G | A | 132 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0009others(129): Show | 132 | HG00423.hp2 HG00544.hp2 HG00621.hp2 others(129): Show |
intron_variant | MODIFIER | c.684-1313C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79597971 | ||||||
chr12:79598003
|
A | G | 1 | a0003c0004t0022g0166 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.684-1345T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79598003 | ||||||
chr12:79598017
|
T | C | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.684-1359A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79598017 | ||||||
chr12:79598256
|
T | C | 1 | a0001c0001t0003g0039 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.684-1598A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79598256 | ||||||
chr12:79598413
|
A | G | 2 | a0002c0002t0001g0215a0002c0002t0001g0242 | 2 | HG02886.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.684-1755T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79598413 | ||||||
chr12:79598607
|
A | G | 1 | a0001c0001t0002g0044 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.684-1949T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79598607 | ||||||
chr12:79598851
|
C | T | 4 | a0003c0004t0009g0157a0003c0004t0009g0158a0003c0004t0009g0159others(1): Show | 4 | HG01074.hp2 HG02896.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.684-2193G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79598851 | ||||||
chr12:79599033
|
C | T | 2 | a0001c0001t0002g0117a0001c0001t0002g0118 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.684-2375G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79599033 | ||||||
chr12:79599149
|
T | C | 1 | a0001c0001t0002g0081 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.684-2491A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79599149 | ||||||
chr12:79599162
|
A | G | 1 | a0001c0001t0004g0029 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.684-2504T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79599162 | ||||||
chr12:79599924
|
C | T | 83 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0001g0171others(80): Show | 83 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.684-3266G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79599924 | ||||||
chr12:79599925
|
G | A | 1 | a0001c0001t0002g0112 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.684-3267C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79599925 | ||||||
chr12:79599940
|
A | G | 1 | a0003c0004t0022g0166 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.684-3282T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79599940 | ||||||
chr12:79599992
|
T | A | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.684-3334A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79599992 | ||||||
chr12:79600026
|
G | T | 1 | a0003c0004t0009g0160 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.684-3368C>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79600026 | ||||||
chr12:79600259
|
A | G | 1 | a0002c0002t0001g0220 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.684-3601T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79600259 | ||||||
chr12:79600478
|
G | T | 3 | a0003c0005t0007g0003a0003c0005t0007g0164a0003c0005t0007g0165 | 3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.684-3820C>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79600478 | ||||||
chr12:79600486
|
G | A | 40 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0009others(37): Show | 40 | HG00423.hp2 HG01081.hp2 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.684-3828C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79600486 | ||||||
chr12:79600488
|
G | A | 1 | a0001c0001t0004g0027 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.684-3830C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79600488 | ||||||
chr12:79600535
|
C | T | 1 | a0003c0004t0022g0166 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.684-3877G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79600535 | ||||||
chr12:79600616
|
G | A | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.684-3958C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79600616 | ||||||
chr12:79600648
|
C | CT | 78 | a0001c0001t0002g0065a0001c0001t0002g0067a0001c0001t0002g0081others(75): Show | 78 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.684-3991dupA | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79600648 | ||||||
chr12:79600648
|
C | CTT | 9 | a0002c0002t0001g0170a0002c0002t0001g0190a0002c0002t0001g0191others(6): Show | 9 | HG01256.hp1 HG01261.hp1 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.684-3992_684-3991d others(4): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79600648 | ||||||
chr12:79600648
|
CT | C | 9 | a0001c0001t0006g0023a0003c0004t0007g0167a0003c0004t0007g0168others(6): Show | 9 | HG01074.hp2 HG01168.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.684-3991delA | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79600648 | ||||||
chr12:79600648
|
CTT | C | 6 | a0003c0005t0007g0003a0003c0005t0007g0164a0003c0005t0007g0165others(3): Show | 6 | HG02258.hp1 HG02922.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.684-3992_684-3991d others(4): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79600648 | ||||||
chr12:79600770
|
A | G | 1 | a0001c0003t0003g0100 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.684-4112T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79600770 | ||||||
chr12:79600958
|
A | G | 1 | a0001c0001t0002g0067 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.684-4300T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79600958 | ||||||
chr12:79601207
|
A | AT | 12 | a0001c0001t0002g0050a0001c0001t0002g0055a0001c0001t0002g0076others(9): Show | 12 | HG01243.hp2 HG01981.hp2 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.684-4550dupA | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79601207 | ||||||
chr12:79601207
|
AT | A | 40 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0009others(37): Show | 40 | HG00423.hp2 HG01074.hp1 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.684-4550delA | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79601207 | ||||||
chr12:79601207
|
ATT | A | 19 | a0001c0001t0004g0015a0001c0001t0004g0019a0001c0001t0004g0020others(16): Show | 19 | HG00621.hp2 HG01074.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.684-4551_684-4550d others(4): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79601207 | ||||||
chr12:79601207
|
ATTT | A | 74 | a0001c0001t0006g0014a0002c0002t0001g0169a0002c0002t0001g0172others(71): Show | 74 | HG00544.hp2 HG00639.hp2 HG00673.hp2 others(71): Show |
intron_variant | MODIFIER | c.684-4552_684-4550d others(5): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79601207 | ||||||
chr12:79601551
|
T | G | 1 | a0001c0001t0004g0024 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.684-4893A>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79601551 | ||||||
chr12:79601907
|
G | A | 3 | a0002c0002t0005g0183a0002c0002t0005g0233a0002c0002t0017g0184 | 3 | HG01884.hp2 HG02055.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.684-5249C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79601907 | ||||||
chr12:79601908
|
C | A | 3 | a0002c0002t0005g0183a0002c0002t0005g0233a0002c0002t0017g0184 | 3 | HG01884.hp2 HG02055.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.684-5250G>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79601908 | ||||||
chr12:79601999
|
A | T | 2 | a0002c0002t0001g0176a0002c0002t0001g0180 | 2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.684-5341T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79601999 | ||||||
chr12:79602056
|
A | G | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.684-5398T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79602056 | ||||||
chr12:79602135
|
C | T | 1 | a0003c0005t0007g0165 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.684-5477G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79602135 | ||||||
chr12:79602213
|
G | A | 1 | a0005c0007t0033g0256 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.684-5555C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79602213 | ||||||
chr12:79602348
|
T | G | 1 | a0001c0001t0002g0050 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.684-5690A>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79602348 | ||||||
chr12:79602770
|
A | AT | 10 | a0001c0001t0002g0042a0001c0001t0002g0052a0001c0001t0002g0153others(7): Show | 10 | HG00639.hp2 HG01891.hp2 NA18945.hp2 others(7): Show |
intron_variant | MODIFIER | c.684-6113dupA | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79602770 | ||||||
chr12:79603153
|
G | A | 1 | a0001c0001t0006g0025 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.684-6495C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79603153 | ||||||
chr12:79603314
|
C | G | 98 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0001g0171others(95): Show | 98 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.684-6656G>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79603314 | ||||||
chr12:79603320
|
CAAATAAG others(6): Show |
C | 4 | a0003c0004t0009g0157a0003c0004t0009g0158a0003c0004t0009g0159others(1): Show | 4 | HG01074.hp2 HG02896.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.684-6675_684-6663d others(15): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79603320 | ||||||
chr12:79603367
|
A | G | 2 | a0001c0001t0002g0044a0001c0001t0002g0045 | 2 | HG02523.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.684-6709T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79603367 | ||||||
chr12:79603541
|
C | T | 1 | a0001c0001t0004g0033 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.684-6883G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79603541 | ||||||
chr12:79603584
|
T | C | 2 | a0003c0004t0007g0167a0003c0004t0007g0168 | 2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.684-6926A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79603584 | ||||||
chr12:79603665
|
C | CAATTTTT others(4): Show |
1 | a0005c0007t0033g0256 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.684-7008_684-7007i others(13): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79603665 | ||||||
chr12:79603666
|
T | A | 3 | a0003c0005t0007g0003a0003c0005t0007g0164a0003c0005t0007g0165 | 3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.684-7008A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79603666 | ||||||
chr12:79603667
|
A | AT | 25 | a0001c0001t0002g0044a0001c0001t0002g0051a0001c0001t0002g0052others(22): Show | 25 | HG00423.hp1 HG00438.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.684-7010dupA | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79603667 | ||||||
chr12:79603667
|
A | T | 4 | a0001c0003t0013g0041a0001c0003t0013g0095a0005c0007t0033g0256others(1): Show | 4 | HG02145.hp1 HG02523.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.684-7009T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79603667 | ||||||
chr12:79603667
|
AT | A | 83 | a0001c0001t0002g0004a0001c0001t0002g0073a0001c0001t0004g0009others(80): Show | 83 | HG00544.hp2 HG00621.hp2 HG00673.hp2 others(80): Show |
intron_variant | MODIFIER | c.684-7010delA | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79603667 | ||||||
chr12:79603667
|
ATTTTTTT others(9): Show |
A | 1 | a0001c0001t0029g0120 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.684-7025_684-7010d others(18): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79603667 | ||||||
chr12:79604174
|
T | G | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.684-7516A>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79604174 | ||||||
chr12:79604834
|
TAGAAAAC | T | 3 | a0003c0005t0007g0003a0003c0005t0007g0164a0003c0005t0007g0165 | 3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.684-8183_684-8177d others(9): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79604834 | ||||||
chr12:79604857
|
G | C | 83 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0001g0171others(80): Show | 83 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.684-8199C>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79604857 | ||||||
chr12:79605018
|
C | T | 98 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0001g0171others(95): Show | 98 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.684-8360G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79605018 | ||||||
chr12:79605020
|
G | A | 98 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0001g0171others(95): Show | 98 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.684-8362C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79605020 | ||||||
chr12:79605047
|
GATA | G | 4 | a0002c0002t0001g0172a0002c0002t0001g0212a0002c0002t0001g0213others(1): Show | 4 | HG03139.hp1 HG03209.hp1 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.684-8392_684-8390d others(5): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79605047 | ||||||
chr12:79605060
|
A | ATATAT | 9 | a0003c0004t0009g0157a0003c0004t0009g0158a0003c0004t0009g0159others(6): Show | 9 | HG01074.hp2 HG02145.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.684-8403_684-8402i others(7): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79605060 | ||||||
chr12:79605090
|
T | C | 3 | a0004c0006t0011g0239a0004c0006t0011g0240a0004c0006t0011g0241 | 3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.684-8432A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79605090 | ||||||
chr12:79605529
|
T | A | 59 | a0001c0001t0002g0004a0001c0001t0002g0042a0001c0001t0002g0044others(56): Show | 59 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.683+8046A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79605529 | ||||||
chr12:79605530
|
A | T | 90 | a0001c0001t0006g0008a0002c0002t0001g0169a0002c0002t0001g0170others(87): Show | 90 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(87): Show |
intron_variant | MODIFIER | c.683+8045T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79605530 | ||||||
chr12:79605531
|
A | T | 4 | a0002c0002t0001g0219a0003c0005t0007g0003a0003c0005t0007g0164others(1): Show | 4 | HG02922.hp2 HG03453.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.683+8044T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79605531 | ||||||
chr12:79605620
|
G | A | 3 | a0004c0006t0011g0239a0004c0006t0011g0240a0004c0006t0011g0241 | 3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.683+7955C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79605620 | ||||||
chr12:79605690
|
A | G | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.683+7885T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79605690 | ||||||
chr12:79605758
|
T | C | 1 | a0001c0003t0003g0131 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.683+7817A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79605758 | ||||||
chr12:79605768
|
C | T | 1 | a0002c0002t0005g0250 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.683+7807G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79605768 | ||||||
chr12:79605847
|
C | G | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.683+7728G>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79605847 | ||||||
chr12:79605919
|
C | T | 1 | a0003c0004t0022g0166 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.683+7656G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79605919 | ||||||
chr12:79606058
|
A | C | 1 | a0001c0001t0002g0043 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.683+7517T>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79606058 | ||||||
chr12:79606397
|
T | C | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.683+7178A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79606397 | ||||||
chr12:79606789
|
T | C | 9 | a0003c0004t0009g0157a0003c0004t0009g0158a0003c0004t0009g0159others(6): Show | 9 | HG01074.hp2 HG02145.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.683+6786A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79606789 | ||||||
chr12:79606969
|
C | A | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.683+6606G>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79606969 | ||||||
chr12:79607153
|
G | A | 2 | a0001c0001t0002g0068a0001c0001t0002g0072 | 2 | NA18968.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.683+6422C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79607153 | ||||||
chr12:79607310
|
T | C | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.683+6265A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79607310 | ||||||
chr12:79607423
|
C | T | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.683+6152G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79607423 | ||||||
chr12:79607587
|
G | A | 2 | a0001c0003t0003g0005a0001c0003t0028g0084 | 2 | HG01099.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.683+5988C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79607587 | ||||||
chr12:79607711
|
G | A | 1 | a0001c0001t0004g0009 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.683+5864C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79607711 | ||||||
chr12:79607728
|
CA | C | 68 | a0001c0001t0002g0047a0001c0001t0002g0052a0001c0001t0002g0055others(65): Show | 68 | HG00423.hp2 HG00438.hp2 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.683+5846delT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79607728 | ||||||
chr12:79607734
|
A | T | 40 | a0002c0002t0001g0169a0002c0002t0001g0173a0002c0002t0001g0174others(37): Show | 40 | HG00544.hp2 HG00621.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.683+5841T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79607734 | ||||||
chr12:79607739
|
A | T | 81 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0001g0171others(78): Show | 81 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.683+5836T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79607739 | ||||||
chr12:79607743
|
A | T | 18 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0006g0008others(15): Show | 18 | HG01099.hp1 HG01243.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.683+5832T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79607743 | ||||||
chr12:79607744
|
A | T | 88 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0001g0171others(85): Show | 88 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.683+5831T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79607744 | ||||||
chr12:79607745
|
AT | A | 33 | a0001c0001t0002g0042a0001c0001t0002g0045a0001c0001t0002g0048others(30): Show | 33 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.683+5829delA | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79607745 | ||||||
chr12:79607746
|
T | A | 107 | a0001c0001t0002g0044a0001c0001t0002g0090a0001c0001t0002g0114others(104): Show | 107 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(104): Show |
intron_variant | MODIFIER | c.683+5829A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79607746 | ||||||
chr12:79607878
|
C | T | 1 | a0002c0002t0001g0237 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.683+5697G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79607878 | ||||||
chr12:79607879
|
G | A | 1 | a0002c0002t0019g0179 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.683+5696C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79607879 | ||||||
chr12:79607887
|
C | T | 5 | a0003c0005t0007g0003a0003c0005t0007g0164a0003c0005t0007g0165others(2): Show | 5 | HG02145.hp1 HG02922.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.683+5688G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79607887 | ||||||
chr12:79607894
|
A | G | 2 | a0001c0001t0002g0057a0001c0001t0002g0074 | 2 | HG01069.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.683+5681T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79607894 | ||||||
chr12:79607912
|
G | A | 40 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0009others(37): Show | 40 | HG00423.hp2 HG01081.hp2 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.683+5663C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79607912 | ||||||
chr12:79607980
|
C | T | 1 | a0002c0002t0001g0198 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.683+5595G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79607980 | ||||||
chr12:79607990
|
A | C | 2 | a0001c0003t0003g0079a0001c0003t0003g0102 | 2 | HG01981.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.683+5585T>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79607990 | ||||||
chr12:79608002
|
T | C | 40 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0009others(37): Show | 40 | HG00423.hp2 HG01081.hp2 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.683+5573A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79608002 | ||||||
chr12:79608033
|
G | A | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.683+5542C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79608033 | ||||||
chr12:79608044
|
G | A | 1 | a0001c0001t0032g0006 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.683+5531C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79608044 | ||||||
chr12:79608049
|
C | CA | 12 | a0001c0001t0002g0048a0001c0001t0002g0059a0001c0001t0002g0076others(9): Show | 12 | HG01074.hp2 HG01081.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.683+5525dupT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79608049 | ||||||
chr12:79608326
|
G | A | 142 | a0001c0001t0003g0038a0001c0001t0003g0039a0001c0001t0003g0040others(139): Show | 142 | HG00423.hp2 HG00544.hp2 HG00621.hp2 others(139): Show |
intron_variant | MODIFIER | c.683+5249C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79608326 | ||||||
chr12:79608418
|
G | A | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.683+5157C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79608418 | ||||||
chr12:79608453
|
C | T | 3 | a0001c0001t0002g0051a0001c0001t0002g0093a0001c0001t0002g0119 | 3 | HG00423.hp1 NA18959.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.683+5122G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79608453 | ||||||
chr12:79609008
|
A | G | 9 | a0003c0004t0009g0157a0003c0004t0009g0158a0003c0004t0009g0159others(6): Show | 9 | HG01074.hp2 HG02145.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.683+4567T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79609008 | ||||||
chr12:79609052
|
G | A | 98 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0001g0171others(95): Show | 98 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.683+4523C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79609052 | ||||||
chr12:79609429
|
C | T | 3 | a0003c0005t0007g0003a0003c0005t0007g0164a0003c0005t0007g0165 | 3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.683+4146G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79609429 | ||||||
chr12:79609601
|
A | G | 5 | a0001c0003t0008g0136a0001c0003t0008g0137a0001c0003t0008g0138others(2): Show | 5 | NA18946.hp1 NA18966.hp2 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.683+3974T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79609601 | ||||||
chr12:79609614
|
G | T | 1 | a0001c0003t0003g0143 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.683+3961C>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79609614 | ||||||
chr12:79609647
|
T | C | 1 | a0003c0005t0007g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.683+3928A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79609647 | ||||||
chr12:79609720
|
G | A | 3 | a0003c0005t0007g0003a0003c0005t0007g0164a0003c0005t0007g0165 | 3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.683+3855C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79609720 | ||||||
chr12:79609784
|
C | T | 2 | a0002c0002t0001g0217a0002c0002t0001g0222 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.683+3791G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79609784 | ||||||
chr12:79609790
|
G | A | 4 | a0003c0004t0009g0157a0003c0004t0009g0158a0003c0004t0009g0159others(1): Show | 4 | HG01074.hp2 HG02896.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.683+3785C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79609790 | ||||||
chr12:79609891
|
CT | C | 4 | a0001c0003t0002g0155a0001c0003t0003g0086a0001c0003t0003g0131others(1): Show | 4 | NA18967.hp1 NA18969.hp1 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.683+3683delA | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79609891 | ||||||
chr12:79610086
|
C | T | 1 | a0002c0002t0019g0179 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.683+3489G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79610086 | ||||||
chr12:79610098
|
T | TG | 4 | a0003c0004t0009g0157a0003c0004t0009g0158a0003c0004t0009g0159others(1): Show | 4 | HG01074.hp2 HG02896.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.683+3476dupC | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79610098 | ||||||
chr12:79610208
|
T | C | 1 | a0002c0002t0018g0245 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.683+3367A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79610208 | ||||||
chr12:79610538
|
C | T | 1 | a0001c0003t0003g0102 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.683+3037G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79610538 | ||||||
chr12:79610539
|
G | A | 83 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0001g0171others(80): Show | 83 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.683+3036C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79610539 | ||||||
chr12:79610694
|
G | C | 1 | a0002c0002t0001g0253 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.683+2881C>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79610694 | ||||||
chr12:79610735
|
T | C | 3 | a0002c0002t0001g0172a0002c0002t0001g0212a0002c0002t0001g0213 | 3 | HG03139.hp1 NA18972.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.683+2840A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79610735 | ||||||
chr12:79610762
|
TA | T | 7 | a0001c0001t0002g0004a0001c0001t0002g0119a0001c0001t0004g0027others(4): Show | 7 | HG01257.hp1 HG02922.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.683+2812delT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79610762 | ||||||
chr12:79610808
|
A | C | 3 | a0004c0006t0011g0239a0004c0006t0011g0240a0004c0006t0011g0241 | 3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.683+2767T>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79610808 | ||||||
chr12:79610903
|
C | T | 3 | a0003c0005t0007g0003a0003c0005t0007g0164a0003c0005t0007g0165 | 3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.683+2672G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79610903 | ||||||
chr12:79610922
|
G | A | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.683+2653C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79610922 | ||||||
chr12:79610995
|
A | T | 1 | a0001c0001t0003g0040 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.683+2580T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79610995 | ||||||
chr12:79611019
|
A | G | 2 | a0001c0001t0002g0055a0001c0001t0002g0064 | 2 | HG02027.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.683+2556T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79611019 | ||||||
chr12:79611087
|
T | G | 3 | a0002c0002t0005g0183a0002c0002t0005g0233a0002c0002t0017g0184 | 3 | HG01884.hp2 HG02055.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.683+2488A>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79611087 | ||||||
chr12:79611390
|
C | G | 3 | a0004c0006t0011g0239a0004c0006t0011g0240a0004c0006t0011g0241 | 3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.683+2185G>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79611390 | ||||||
chr12:79611797
|
T | C | 1 | a0002c0002t0001g0172 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.683+1778A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79611797 | ||||||
chr12:79611881
|
A | G | 3 | a0001c0001t0003g0038a0001c0001t0003g0039a0001c0001t0003g0040 | 3 | HG02572.hp2 HG03041.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.683+1694T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79611881 | ||||||
chr12:79611992
|
A | G | 1 | a0002c0002t0001g0211 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.683+1583T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79611992 | ||||||
chr12:79612111
|
G | C | 3 | a0002c0002t0001g0228a0002c0002t0001g0229a0002c0002t0001g0230 | 3 | HG02630.hp1 HG02717.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.683+1464C>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79612111 | ||||||
chr12:79612324
|
CTCTT | C | 3 | a0003c0005t0007g0003a0003c0005t0007g0164a0003c0005t0007g0165 | 3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.683+1247_683+1250d others(6): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79612324 | ||||||
chr12:79612349
|
T | C | 3 | a0003c0005t0007g0003a0003c0005t0007g0164a0003c0005t0007g0165 | 3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.683+1226A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79612349 | ||||||
chr12:79612367
|
A | G | 4 | a0003c0004t0009g0157a0003c0004t0009g0158a0003c0004t0009g0159others(1): Show | 4 | HG01074.hp2 HG02896.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.683+1208T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79612367 | ||||||
chr12:79612477
|
A | C | 4 | a0001c0003t0002g0155a0001c0003t0003g0086a0001c0003t0003g0131others(1): Show | 4 | NA18967.hp1 NA18969.hp1 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.683+1098T>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79612477 | ||||||
chr12:79612570
|
A | G | 2 | a0003c0004t0007g0167a0003c0004t0007g0168 | 2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.683+1005T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79612570 | ||||||
chr12:79612729
|
G | C | 2 | a0001c0001t0004g0009a0001c0001t0004g0010 | 2 | HG02257.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.683+846C>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79612729 | ||||||
chr12:79612738
|
C | T | 3 | a0004c0006t0011g0239a0004c0006t0011g0240a0004c0006t0011g0241 | 3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.683+837G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79612738 | ||||||
chr12:79612866
|
A | G | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.683+709T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79612866 | ||||||
chr12:79612913
|
G | A | 83 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0001g0171others(80): Show | 83 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.683+662C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79612913 | ||||||
chr12:79613236
|
T | C | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.683+339A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79613236 | ||||||
chr12:79613391
|
A | G | 1 | a0002c0002t0001g0231 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.683+184T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79613391 | ||||||
chr12:79613411
|
C | G | 3 | a0003c0005t0007g0003a0003c0005t0007g0164a0003c0005t0007g0165 | 3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.683+164G>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79613411 | ||||||
chr12:79613548
|
A | G | 3 | a0004c0006t0011g0239a0004c0006t0011g0240a0004c0006t0011g0241 | 3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.683+27T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79613548 | ||||||
chr12:79613718
|
G | A | 3 | a0001c0001t0004g0031a0001c0001t0004g0033a0001c0001t0004g0125 | 3 | HG02040.hp2 HG02080.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.649-109C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613718 | ||||||
chr12:79613899
|
T | C | 1 | a0001c0001t0032g0006 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.649-290A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613899 | ||||||
chr12:79613931
|
T | TTATATA | 4 | a0001c0001t0002g0044a0001c0001t0002g0123a0001c0001t0002g0134others(1): Show | 4 | HG00544.hp1 HG00673.hp1 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.649-328_649-323dup others(6): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613931 | ||||||
chr12:79613931
|
T | TTATATAT others(3): Show |
1 | a0001c0003t0003g0102 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.649-332_649-323dup others(10): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613931 | ||||||
chr12:79613931
|
T | TTATATAT others(5): Show |
1 | a0001c0001t0002g0057 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.649-334_649-323dup others(12): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613931 | ||||||
chr12:79613931
|
T | TTATATAT others(7): Show |
1 | a0001c0003t0008g0151 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.649-336_649-323dup others(14): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613931 | ||||||
chr12:79613931
|
T | TTATATAT others(11): Show |
1 | a0001c0003t0003g0089 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.649-340_649-323dup others(18): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613931 | ||||||
chr12:79613931
|
TTATATAT others(15): Show |
T | 1 | a0001c0003t0003g0133 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.649-344_649-323del others(22): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613931 | ||||||
chr12:79613933
|
A | T | 3 | a0001c0001t0003g0038a0001c0001t0003g0039a0001c0001t0003g0040 | 3 | HG02572.hp2 HG03041.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.649-324T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613933 | ||||||
chr12:79613943
|
ATATATAT others(38): Show |
A | 1 | a0001c0001t0002g0072 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.649-379_649-335del others(45): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613943 | ||||||
chr12:79613943
|
ATATATAT others(41): Show |
A | 1 | a0001c0001t0002g0068 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.649-382_649-335del others(48): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613943 | ||||||
chr12:79613943
|
ATATATAT others(48): Show |
A | 4 | a0001c0001t0004g0011a0001c0001t0004g0124a0001c0001t0004g0125others(1): Show | 4 | HG01109.hp2 HG02683.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.649-389_649-335del others(55): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613943 | ||||||
chr12:79613943
|
ATATATAT others(49): Show |
A | 23 | a0001c0001t0004g0001a0001c0001t0004g0009a0001c0001t0004g0010others(20): Show | 23 | HG01081.hp2 HG01099.hp2 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.649-390_649-335del others(56): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613943 | ||||||
chr12:79613943
|
ATATATAT others(50): Show |
A | 2 | a0001c0001t0004g0013a0001c0001t0004g0128 | 2 | HG02976.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.649-391_649-335del others(57): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613943 | ||||||
chr12:79613945
|
ATATATAT others(39): Show |
A | 1 | a0001c0003t0003g0140 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.649-382_649-337del others(46): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613945 | ||||||
chr12:79613945
|
ATATATAT others(40): Show |
A | 1 | a0001c0003t0028g0084 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.649-383_649-337del others(47): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613945 | ||||||
chr12:79613945
|
ATATATAT others(48): Show |
A | 1 | a0001c0001t0004g0036 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.649-391_649-337del others(55): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613945 | ||||||
chr12:79613945
|
ATATATAT others(49): Show |
A | 9 | a0001c0001t0004g0002a0001c0001t0004g0021a0001c0001t0004g0022others(6): Show | 9 | HG01257.hp2 HG01258.hp1 HG02074.hp2 others(6): Show |
intron_variant | MODIFIER | c.649-392_649-337del others(56): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613945 | ||||||
chr12:79613947
|
ATATATAT others(34): Show |
A | 1 | a0002c0002t0001g0225 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.649-379_649-339del others(41): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613947 | ||||||
chr12:79613947
|
ATATATAT others(35): Show |
A | 1 | a0001c0003t0003g0094 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.649-380_649-339del others(42): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613947 | ||||||
chr12:79613947
|
ATATATAT others(38): Show |
A | 1 | a0001c0001t0002g0062 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.649-383_649-339del others(45): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613947 | ||||||
chr12:79613947
|
ATATATAT others(41): Show |
A | 1 | a0001c0001t0002g0071 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.649-386_649-339del others(48): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613947 | ||||||
chr12:79613947
|
ATATATAT others(47): Show |
A | 1 | a0001c0001t0004g0156 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.649-392_649-339del others(54): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613947 | ||||||
chr12:79613949
|
ATATATAT others(31): Show |
A | 1 | a0002c0002t0020g0194 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.649-378_649-341del others(38): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613949 | ||||||
chr12:79613949
|
ATATATAT others(32): Show |
A | 1 | a0002c0002t0001g0218 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.649-379_649-341del others(39): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613949 | ||||||
chr12:79613949
|
ATATATAT others(44): Show |
A | 2 | a0003c0005t0007g0164a0003c0005t0007g0165 | 2 | HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.649-391_649-341del others(51): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613949 | ||||||
chr12:79613951
|
ATATATAT others(29): Show |
A | 1 | a0002c0002t0001g0207 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.649-378_649-343del others(36): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613951 | ||||||
chr12:79613951
|
ATATATAT others(30): Show |
A | 1 | a0001c0001t0002g0111 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.649-379_649-343del others(37): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613951 | ||||||
chr12:79613951
|
ATATATAT others(31): Show |
A | 3 | a0001c0001t0002g0153a0002c0002t0001g0195a0002c0002t0001g0236 | 3 | HG00673.hp2 HG04204.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.649-380_649-343del others(38): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613951 | ||||||
chr12:79613951
|
ATATATAT others(32): Show |
A | 3 | a0001c0001t0002g0107a0001c0001t0002g0116a0002c0002t0001g0198 | 3 | NA18987.hp1 NA18992.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.649-381_649-343del others(39): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613951 | ||||||
chr12:79613951
|
ATATATAT others(33): Show |
A | 1 | a0002c0002t0001g0169 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.649-382_649-343del others(40): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613951 | ||||||
chr12:79613951
|
ATATATAT others(34): Show |
A | 5 | a0001c0003t0003g0100a0002c0002t0001g0174a0002c0002t0001g0192others(2): Show | 5 | HG00741.hp2 HG03490.hp1 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.649-383_649-343del others(41): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613951 | ||||||
chr12:79613951
|
ATATATAT others(35): Show |
A | 1 | a0002c0002t0001g0173 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.649-384_649-343del others(42): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613951 | ||||||
chr12:79613951
|
ATATATAT others(41): Show |
A | 1 | a0003c0004t0007g0168 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.649-390_649-343del others(48): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613951 | ||||||
chr12:79613951
|
ATATATAT others(42): Show |
A | 1 | a0003c0004t0007g0167 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.649-391_649-343del others(49): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613951 | ||||||
chr12:79613953
|
ATATATAT others(28): Show |
A | 1 | a0002c0002t0001g0235 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.649-379_649-345del others(35): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613953 | ||||||
chr12:79613953
|
ATATATAT others(29): Show |
A | 2 | a0002c0002t0001g0216a0002c0002t0019g0179 | 2 | HG00544.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.649-380_649-345del others(36): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613953 | ||||||
chr12:79613953
|
ATATATAT others(31): Show |
A | 1 | a0002c0002t0012g0189 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.649-382_649-345del others(38): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613953 | ||||||
chr12:79613953
|
ATATATAT others(32): Show |
A | 3 | a0002c0002t0001g0191a0002c0002t0005g0249a0002c0002t0005g0252 | 3 | HG01261.hp1 HG02027.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.649-383_649-345del others(39): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613953 | ||||||
chr12:79613953
|
ATATATAT others(34): Show |
A | 5 | a0002c0002t0001g0196a0002c0002t0001g0220a0002c0002t0001g0226others(2): Show | 5 | NA18946.hp2 NA18965.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.649-385_649-345del others(41): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613953 | ||||||
chr12:79613953
|
ATATATAT others(35): Show |
A | 1 | a0002c0002t0001g0215 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.649-386_649-345del others(42): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613953 | ||||||
chr12:79613955
|
ATATATAT others(29): Show |
A | 2 | a0002c0002t0001g0231a0002c0002t0001g0232 | 2 | HG02145.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.649-382_649-347del others(36): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613955 | ||||||
chr12:79613955
|
ATATATAT others(30): Show |
A | 2 | a0002c0002t0001g0178a0002c0002t0001g0229 | 2 | HG01891.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.649-383_649-347del others(37): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613955 | ||||||
chr12:79613955
|
ATATATAT others(31): Show |
A | 2 | a0002c0002t0001g0175a0002c0002t0001g0187 | 2 | HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.649-384_649-347del others(38): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613955 | ||||||
chr12:79613955
|
ATATATAT others(32): Show |
A | 12 | a0001c0001t0032g0006a0002c0002t0001g0170a0002c0002t0001g0193others(9): Show | 12 | HG02572.hp1 HG02630.hp2 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.649-385_649-347del others(39): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613955 | ||||||
chr12:79613955
|
ATATATAT others(33): Show |
A | 2 | a0002c0002t0001g0242a0002c0002t0005g0214 | 2 | HG02895.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.649-386_649-347del others(40): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613955 | ||||||
chr12:79613955
|
ATATATAT others(34): Show |
A | 3 | a0002c0002t0001g0238a0002c0002t0021g0186a0003c0004t0001g0007 | 3 | HG02071.hp2 HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.649-387_649-347del others(41): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613955 | ||||||
chr12:79613957
|
ATATATAT others(26): Show |
A | 1 | a0001c0003t0008g0136 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.649-381_649-349del others(33): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613957 | ||||||
chr12:79613957
|
ATATATAT others(27): Show |
A | 1 | a0001c0001t0026g0056 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.649-382_649-349del others(34): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613957 | ||||||
chr12:79613957
|
ATATATAT others(28): Show |
A | 4 | a0002c0002t0001g0176a0002c0002t0001g0180a0002c0002t0001g0213others(1): Show | 4 | HG02258.hp2 HG02559.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.649-383_649-349del others(35): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613957 | ||||||
chr12:79613957
|
ATATATAT others(29): Show |
A | 4 | a0002c0002t0001g0188a0002c0002t0001g0202a0002c0002t0001g0212others(1): Show | 4 | NA19003.hp1 NA19004.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.649-384_649-349del others(36): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613957 | ||||||
chr12:79613957
|
ATATATAT others(30): Show |
A | 3 | a0002c0002t0001g0228a0002c0002t0001g0230a0002c0002t0005g0182 | 3 | HG00639.hp2 HG02717.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.649-385_649-349del others(37): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613957 | ||||||
chr12:79613957
|
ATATATAT others(31): Show |
A | 1 | a0002c0002t0005g0233 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.649-386_649-349del others(38): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613957 | ||||||
chr12:79613957
|
ATATATAT others(32): Show |
A | 7 | a0002c0002t0001g0171a0002c0002t0001g0185a0002c0002t0005g0183others(4): Show | 7 | HG01192.hp1 HG01884.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.649-387_649-349del others(39): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613957 | ||||||
chr12:79613957
|
ATATATAT others(33): Show |
A | 2 | a0002c0002t0005g0246a0002c0002t0005g0248 | 2 | HG01109.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.649-388_649-349del others(40): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613957 | ||||||
chr12:79613959
|
ATATATAT others(22): Show |
A | 1 | a0001c0001t0002g0115 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.649-379_649-351del others(29): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613959 | ||||||
chr12:79613959
|
ATATATAT others(23): Show |
A | 1 | a0001c0001t0002g0047 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.649-380_649-351del others(30): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613959 | ||||||
chr12:79613959
|
ATATATAT others(27): Show |
A | 1 | a0001c0001t0002g0073 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.649-384_649-351del others(34): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613959 | ||||||
chr12:79613959
|
ATATATAT others(28): Show |
A | 1 | a0002c0002t0001g0253 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.649-385_649-351del others(35): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613959 | ||||||
chr12:79613959
|
ATATATAT others(29): Show |
A | 5 | a0002c0002t0001g0190a0002c0002t0001g0203a0002c0002t0001g0204others(2): Show | 5 | HG00621.hp2 HG02300.hp1 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.649-386_649-351del others(36): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613959 | ||||||
chr12:79613959
|
ATATATAT others(30): Show |
A | 3 | a0002c0002t0001g0181a0002c0002t0001g0208a0002c0002t0017g0184 | 3 | HG01975.hp2 HG02257.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.649-387_649-351del others(37): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613959 | ||||||
chr12:79613959
|
ATATATAT others(31): Show |
A | 1 | a0002c0002t0001g0211 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.649-388_649-351del others(38): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613959 | ||||||
chr12:79613959
|
ATATATAT others(33): Show |
A | 2 | a0002c0002t0001g0217a0002c0002t0001g0222 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.649-390_649-351del others(40): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613959 | ||||||
chr12:79613959
|
ATATATAT others(38): Show |
A | 1 | a0005c0007t0034g0255 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.649-395_649-351del others(45): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613959 | ||||||
chr12:79613961
|
ATATATAT others(24): Show |
A | 1 | a0001c0001t0002g0050 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.649-383_649-353del others(31): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613961 | ||||||
chr12:79613961
|
ATATATAT others(27): Show |
A | 2 | a0001c0003t0003g0085a0002c0002t0001g0205 | 2 | HG02071.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.649-386_649-353del others(34): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613961 | ||||||
chr12:79613961
|
ATATATAT others(28): Show |
A | 1 | a0004c0006t0011g0239 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.649-387_649-353del others(35): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613961 | ||||||
chr12:79613961
|
ATATATAT others(32): Show |
A | 1 | a0002c0002t0005g0247 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.649-391_649-353del others(39): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613961 | ||||||
chr12:79613963
|
ATATATAT others(25): Show |
A | 1 | a0003c0004t0022g0166 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.649-386_649-355del others(32): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613963 | ||||||
chr12:79613963
|
ATATATAT others(26): Show |
A | 1 | a0002c0002t0001g0172 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.649-387_649-355del others(33): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613963 | ||||||
chr12:79613965
|
ATATATAT others(16): Show |
A | 1 | a0001c0001t0002g0045 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.649-379_649-357del others(23): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613965 | ||||||
chr12:79613965
|
ATATATAT others(19): Show |
A | 1 | a0001c0001t0002g0093 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.649-382_649-357del others(26): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613965 | ||||||
chr12:79613965
|
ATATATAT others(24): Show |
A | 2 | a0001c0001t0003g0039a0001c0001t0003g0040 | 2 | HG02572.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.649-387_649-357del others(31): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613965 | ||||||
chr12:79613965
|
ATATATAT others(25): Show |
A | 1 | a0001c0001t0003g0038 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.649-388_649-357del others(32): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613965 | ||||||
chr12:79613967
|
ATATATAT others(12): Show |
A | 1 | a0001c0001t0002g0051 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.649-377_649-359del others(19): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613967 | ||||||
chr12:79613967
|
ATATATAT others(14): Show |
A | 1 | a0001c0001t0002g0052 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.649-379_649-359del others(21): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613967 | ||||||
chr12:79613967
|
ATATATAT others(17): Show |
A | 1 | a0001c0003t0008g0139 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.649-382_649-359del others(24): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613967 | ||||||
chr12:79613969
|
ATATATAT others(15): Show |
A | 1 | a0001c0001t0002g0043 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.649-382_649-361del others(22): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613969 | ||||||
chr12:79613969
|
ATATATAT others(20): Show |
A | 1 | a0001c0001t0002g0088 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.649-387_649-361del others(27): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613969 | ||||||
chr12:79613969
|
ATATATAT others(26): Show |
A | 1 | a0005c0007t0033g0256 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.649-393_649-361del others(33): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613969 | ||||||
chr12:79613973
|
ATATATAT others(7): Show |
A | 2 | a0001c0001t0002g0117a0001c0001t0002g0118 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.649-378_649-365del others(14): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613973 | ||||||
chr12:79613973
|
ATATATAT others(18): Show |
A | 1 | a0003c0004t0009g0160 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.649-389_649-365del others(25): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613973 | ||||||
chr12:79613973
|
ATATATAT others(22): Show |
A | 1 | a0003c0005t0007g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.649-393_649-365del others(29): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613973 | ||||||
chr12:79613975
|
A | T | 1 | a0003c0004t0009g0158 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.649-366T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613975 | ||||||
chr12:79613975
|
ATATATTT others(6): Show |
A | 1 | a0001c0003t0003g0150 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.649-379_649-367del others(13): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613975 | ||||||
chr12:79613975
|
ATATATTT others(8): Show |
A | 1 | a0001c0001t0002g0053 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.649-381_649-367del others(15): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613975 | ||||||
chr12:79613975
|
ATATATTT others(11): Show |
A | 1 | a0001c0003t0024g0149 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.649-384_649-367del others(18): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613975 | ||||||
chr12:79613977
|
A | T | 1 | a0003c0004t0009g0158 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.649-368T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613977 | ||||||
chr12:79613977
|
ATATTTTT others(3): Show |
A | 1 | a0001c0001t0002g0154 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.649-378_649-369del others(10): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613977 | ||||||
chr12:79613977
|
ATATTTTT others(4): Show |
A | 3 | a0001c0001t0002g0061a0001c0001t0029g0120a0001c0001t0030g0058 | 3 | HG01952.hp1 HG01975.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.649-379_649-369del others(11): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613977 | ||||||
chr12:79613977
|
ATATTTTT others(6): Show |
A | 1 | a0001c0001t0002g0090 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.649-381_649-369del others(13): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613977 | ||||||
chr12:79613977
|
ATATTTTT others(8): Show |
A | 1 | a0001c0001t0002g0004 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.649-383_649-369del others(15): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613977 | ||||||
chr12:79613977
|
ATATTTTT others(9): Show |
A | 1 | a0001c0003t0003g0145 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.649-384_649-369del others(16): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613977 | ||||||
chr12:79613979
|
A | T | 2 | a0001c0001t0003g0110a0003c0004t0009g0158 | 2 | HG02896.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.649-370T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613979 | ||||||
chr12:79613979
|
ATTT | A | 5 | a0001c0001t0002g0092a0001c0003t0003g0143a0001c0003t0003g0147others(2): Show | 5 | HG04228.hp1 NA18939.hp2 NA18956.hp2 others(2): Show |
intron_variant | MODIFIER | c.649-373_649-371del others(3): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613979 | ||||||
chr12:79613979
|
ATTTTTTT others(1): Show |
A | 6 | a0001c0001t0002g0055a0001c0001t0002g0105a0001c0001t0002g0114others(3): Show | 6 | HG00639.hp1 HG01074.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.649-378_649-371del others(8): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613979 | ||||||
chr12:79613979
|
ATTTTTTT others(3): Show |
A | 7 | a0001c0001t0002g0064a0001c0001t0002g0108a0001c0001t0002g0112others(4): Show | 7 | HG00438.hp1 HG01891.hp1 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.649-380_649-371del others(10): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613979 | ||||||
chr12:79613979
|
ATTTTTTT others(4): Show |
A | 7 | a0001c0001t0002g0048a0001c0001t0002g0049a0001c0001t0002g0059others(4): Show | 7 | HG01081.hp1 HG01192.hp2 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.649-381_649-371del others(11): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613979 | ||||||
chr12:79613979
|
ATTTTTTT others(5): Show |
A | 2 | a0001c0001t0002g0060a0006c0008t0003g0098 | 2 | HG01169.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.649-382_649-371del others(12): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613979 | ||||||
chr12:79613979
|
ATTTTTTT others(6): Show |
A | 1 | a0003c0004t0009g0159 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.649-383_649-371del others(13): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613979 | ||||||
chr12:79613979
|
ATTTTTTT others(22): Show |
A | 1 | a0001c0003t0003g0005 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.649-399_649-371del others(29): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613979 | ||||||
chr12:79613980
|
T | TA | 4 | a0001c0001t0002g0070a0001c0003t0003g0141a0001c0003t0027g0135others(1): Show | 4 | HG02040.hp1 HG03491.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.649-372_649-371ins others(1): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613980 | ||||||
chr12:79613980
|
T | TATA | 3 | a0001c0001t0002g0067a0001c0003t0003g0082a0001c0003t0003g0104 | 3 | HG01255.hp2 NA18939.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.649-372_649-371ins others(3): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613980 | ||||||
chr12:79613980
|
T | TATATATA others(4): Show |
1 | a0001c0003t0003g0097 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.649-372_649-371ins others(11): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613980 | ||||||
chr12:79613981
|
T | A | 10 | a0001c0001t0002g0044a0001c0001t0002g0057a0001c0001t0002g0063others(7): Show | 10 | HG00544.hp1 HG00673.hp1 HG01993.hp2 others(7): Show |
intron_variant | MODIFIER | c.649-372A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613981 | ||||||
chr12:79613982
|
T | A | 12 | a0001c0001t0002g0070a0001c0001t0002g0077a0001c0001t0002g0091others(9): Show | 12 | HG02040.hp1 HG03491.hp2 HG03831.hp2 others(9): Show |
intron_variant | MODIFIER | c.649-373A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613982 | ||||||
chr12:79613983
|
T | A | 11 | a0001c0001t0002g0044a0001c0001t0002g0057a0001c0001t0002g0063others(8): Show | 11 | HG00544.hp1 HG00673.hp1 HG01993.hp2 others(8): Show |
intron_variant | MODIFIER | c.649-374A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613983 | ||||||
chr12:79613984
|
T | A | 16 | a0001c0001t0002g0070a0001c0001t0002g0077a0001c0001t0002g0091others(13): Show | 16 | HG02040.hp1 HG03491.hp2 HG03831.hp2 others(13): Show |
intron_variant | MODIFIER | c.649-375A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613984 | ||||||
chr12:79613985
|
T | A | 12 | a0001c0001t0002g0044a0001c0001t0002g0057a0001c0001t0002g0063others(9): Show | 12 | HG00544.hp1 HG00673.hp1 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.649-376A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613985 | ||||||
chr12:79613986
|
T | A | 19 | a0001c0001t0002g0066a0001c0001t0002g0070a0001c0001t0002g0077others(16): Show | 19 | HG01069.hp2 HG02040.hp1 HG03491.hp2 others(16): Show |
intron_variant | MODIFIER | c.649-377A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613986 | ||||||
chr12:79613987
|
T | A | 16 | a0001c0001t0002g0044a0001c0001t0002g0057a0001c0001t0002g0063others(13): Show | 16 | HG00544.hp1 HG00673.hp1 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.649-378A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613987 | ||||||
chr12:79613988
|
T | A | 20 | a0001c0001t0002g0065a0001c0001t0002g0066a0001c0001t0002g0070others(17): Show | 20 | HG00438.hp2 HG00621.hp1 HG01928.hp1 others(17): Show |
intron_variant | MODIFIER | c.649-379A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613988 | ||||||
chr12:79613989
|
T | A | 20 | a0001c0001t0002g0044a0001c0001t0002g0055a0001c0001t0002g0057others(17): Show | 20 | HG00639.hp1 HG00673.hp1 HG01069.hp1 others(17): Show |
intron_variant | MODIFIER | c.649-380A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613989 | ||||||
chr12:79613990
|
T | A | 22 | a0001c0001t0002g0065a0001c0001t0002g0070a0001c0001t0002g0077others(19): Show | 22 | HG00438.hp2 HG00621.hp1 HG01928.hp1 others(19): Show |
intron_variant | MODIFIER | c.649-381A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613990 | ||||||
chr12:79613991
|
T | A | 24 | a0001c0001t0002g0044a0001c0001t0002g0055a0001c0001t0002g0063others(21): Show | 24 | HG00438.hp1 HG00639.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.649-382A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613991 | ||||||
chr12:79613992
|
T | A | 20 | a0001c0001t0002g0048a0001c0001t0002g0049a0001c0001t0002g0070others(17): Show | 20 | HG00621.hp1 HG01192.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.649-383A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613992 | ||||||
chr12:79613993
|
T | A | 14 | a0001c0001t0002g0044a0001c0001t0002g0063a0001c0001t0002g0069others(11): Show | 14 | HG00639.hp1 HG00673.hp1 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.649-384A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613993 | ||||||
chr12:79613994
|
T | A | 8 | a0001c0001t0002g0070a0001c0001t0002g0092a0001c0003t0003g0097others(5): Show | 8 | HG02040.hp1 HG03471.hp2 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.649-385A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613994 | ||||||
chr12:79613995
|
T | A | 3 | a0001c0001t0002g0063a0001c0001t0002g0105a0001c0003t0008g0151 | 3 | HG00639.hp1 HG02074.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.649-386A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613995 | ||||||
chr12:79613996
|
T | A | 4 | a0001c0001t0002g0092a0001c0003t0027g0135a0001c0003t0031g0122others(1): Show | 4 | HG03471.hp2 HG03831.hp2 NA18939.hp2 others(1): Show |
intron_variant | MODIFIER | c.649-387A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613996 | ||||||
chr12:79614001
|
T | A | 1 | a0002c0002t0001g0187 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.649-392A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79614001 | ||||||
chr12:79614010
|
T | C | 1 | a0002c0002t0001g0225 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.649-401A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79614010 | ||||||
chr12:79614044
|
C | G | 1 | a0002c0002t0001g0219 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.649-435G>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79614044 | ||||||
chr12:79614063
|
T | C | 1 | a0001c0001t0002g0071 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.649-454A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79614063 | ||||||
chr12:79614088
|
G | A | 1 | a0002c0002t0001g0219 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.649-479C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79614088 | ||||||
chr12:79614103
|
C | T | 1 | a0001c0001t0002g0069 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.649-494G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79614103 | ||||||
chr12:79614312
|
A | ATAGTCTT | 5 | a0003c0005t0007g0003a0003c0005t0007g0164a0003c0005t0007g0165others(2): Show | 5 | HG02145.hp1 HG02922.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.649-710_649-704dup others(7): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79614312 | ||||||
chr12:79614763
|
G | C | 3 | a0002c0002t0001g0228a0002c0002t0001g0229a0002c0002t0001g0230 | 3 | HG02630.hp1 HG02717.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.649-1154C>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79614763 | ||||||
chr12:79614795
|
T | A | 2 | a0003c0004t0007g0167a0003c0004t0007g0168 | 2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.649-1186A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79614795 | ||||||
chr12:79615291
|
C | T | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.649-1682G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79615291 | ||||||
chr12:79615469
|
C | T | 1 | a0002c0002t0001g0231 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.649-1860G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79615469 | ||||||
chr12:79615470
|
G | T | 1 | a0002c0002t0001g0171 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.649-1861C>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79615470 | ||||||
chr12:79615572
|
C | A | 1 | a0002c0002t0001g0175 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.649-1963G>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79615572 | ||||||
chr12:79615657
|
G | C | 3 | a0004c0006t0011g0239a0004c0006t0011g0240a0004c0006t0011g0241 | 3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.649-2048C>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79615657 | ||||||
chr12:79615662
|
C | T | 3 | a0004c0006t0011g0239a0004c0006t0011g0240a0004c0006t0011g0241 | 3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.649-2053G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79615662 | ||||||
chr12:79615828
|
G | T | 1 | a0002c0002t0001g0219 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.649-2219C>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79615828 | ||||||
chr12:79615914
|
G | A | 1 | a0001c0003t0003g0089 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.649-2305C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79615914 | ||||||
chr12:79616056
|
C | CA | 86 | a0001c0001t0002g0072a0001c0001t0002g0076a0001c0001t0002g0154others(83): Show | 86 | HG00544.hp2 HG00673.hp2 HG00741.hp1 others(83): Show |
intron_variant | MODIFIER | c.649-2448dupT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79616056 | ||||||
chr12:79616056
|
CA | C | 10 | a0001c0001t0002g0068a0001c0001t0002g0108a0001c0001t0002g0116others(7): Show | 10 | HG01884.hp1 HG02145.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.649-2448delT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79616056 | ||||||
chr12:79616193
|
A | T | 14 | a0003c0004t0007g0167a0003c0004t0007g0168a0003c0004t0009g0157others(11): Show | 14 | HG01074.hp2 HG01243.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.649-2584T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79616193 | ||||||
chr12:79616389
|
A | T | 40 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0009others(37): Show | 40 | HG00423.hp2 HG01081.hp2 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.649-2780T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79616389 | ||||||
chr12:79616428
|
T | G | 5 | a0003c0005t0007g0003a0003c0005t0007g0164a0003c0005t0007g0165others(2): Show | 5 | HG02145.hp1 HG02922.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.649-2819A>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79616428 | ||||||
chr12:79616674
|
G | A | 1 | a0003c0004t0022g0166 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.649-3065C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79616674 | ||||||
chr12:79616676
|
C | T | 3 | a0003c0005t0007g0003a0003c0005t0007g0164a0003c0005t0007g0165 | 3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.649-3067G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79616676 | ||||||
chr12:79616680
|
T | C | 1 | a0002c0002t0020g0194 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.649-3071A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79616680 | ||||||
chr12:79616789
|
C | G | 3 | a0004c0006t0011g0239a0004c0006t0011g0240a0004c0006t0011g0241 | 3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.649-3180G>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79616789 | ||||||
chr12:79616839
|
C | A | 1 | a0003c0004t0009g0159 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.649-3230G>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79616839 | ||||||
chr12:79616861
|
C | T | 1 | a0001c0001t0032g0006 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.649-3252G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79616861 | ||||||
chr12:79617586
|
A | AG | 142 | a0001c0001t0003g0038a0001c0001t0003g0039a0001c0001t0003g0040others(139): Show | 142 | HG00423.hp2 HG00544.hp2 HG00621.hp2 others(139): Show |
intron_variant | MODIFIER | c.648+3489dupC | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79617586 | ||||||
chr12:79617628
|
T | C | 2 | a0003c0004t0007g0167a0003c0004t0007g0168 | 2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.648+3448A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79617628 | ||||||
chr12:79617782
|
T | G | 3 | a0002c0002t0005g0183a0002c0002t0005g0233a0002c0002t0017g0184 | 3 | HG01884.hp2 HG02055.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.648+3294A>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79617782 | ||||||
chr12:79617884
|
G | C | 98 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0001g0171others(95): Show | 98 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.648+3192C>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79617884 | ||||||
chr12:79618032
|
C | A | 3 | a0001c0001t0002g0051a0001c0001t0002g0093a0001c0001t0002g0119 | 3 | HG00423.hp1 NA18959.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.648+3044G>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79618032 | ||||||
chr12:79618130
|
T | C | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.648+2946A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79618130 | ||||||
chr12:79618202
|
G | C | 8 | a0001c0003t0003g0046a0001c0003t0003g0083a0001c0003t0003g0087others(5): Show | 8 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.648+2874C>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79618202 | ||||||
chr12:79618429
|
C | T | 1 | a0001c0003t0003g0005 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.648+2647G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79618429 | ||||||
chr12:79618549
|
T | G | 1 | a0001c0001t0002g0080 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.648+2527A>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79618549 | ||||||
chr12:79618902
|
T | C | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.648+2174A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79618902 | ||||||
chr12:79618963
|
C | T | 2 | a0003c0005t0007g0164a0003c0005t0007g0165 | 2 | HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.648+2113G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79618963 | ||||||
chr12:79619181
|
C | T | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.648+1895G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79619181 | ||||||
chr12:79619252
|
G | A | 2 | a0003c0005t0007g0164a0003c0005t0007g0165 | 2 | HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.648+1824C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79619252 | ||||||
chr12:79619429
|
T | C | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.648+1647A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79619429 | ||||||
chr12:79619479
|
G | A | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.648+1597C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79619479 | ||||||
chr12:79619580
|
G | A | 1 | a0001c0001t0002g0081 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.648+1496C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79619580 | ||||||
chr12:79619588
|
A | G | 3 | a0004c0006t0011g0239a0004c0006t0011g0240a0004c0006t0011g0241 | 3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.648+1488T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79619588 | ||||||
chr12:79619710
|
C | T | 1 | a0001c0001t0004g0033 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.648+1366G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79619710 | ||||||
chr12:79619729
|
G | A | 1 | a0001c0001t0004g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.648+1347C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79619729 | ||||||
chr12:79619878
|
C | T | 1 | a0003c0005t0007g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.648+1198G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79619878 | ||||||
chr12:79619935
|
T | C | 3 | a0003c0005t0007g0003a0003c0005t0007g0164a0003c0005t0007g0165 | 3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.648+1141A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79619935 | ||||||
chr12:79620392
|
G | C | 1 | a0002c0002t0005g0243 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.648+684C>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79620392 | ||||||
chr12:79620408
|
A | G | 83 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0001g0171others(80): Show | 83 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.648+668T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79620408 | ||||||
chr12:79620528
|
C | A | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.648+548G>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79620528 | ||||||
chr12:79620593
|
T | C | 15 | a0002c0002t0001g0188a0002c0002t0001g0190a0002c0002t0001g0191others(12): Show | 15 | HG00621.hp2 HG01975.hp2 HG02027.hp2 others(12): Show |
intron_variant | MODIFIER | c.648+483A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79620593 | ||||||
chr12:79620744
|
A | G | 3 | a0002c0002t0001g0228a0002c0002t0001g0229a0002c0002t0001g0230 | 3 | HG02630.hp1 HG02717.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.648+332T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79620744 | ||||||
chr12:79620979
|
G | T | 1 | a0003c0004t0022g0166 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.648+97C>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79620979 | ||||||
chr12:79621066
|
A | C | 1 | a0001c0003t0003g0143 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.648+10T>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79621066 | ||||||
chr12:79621406
|
C | T | 4 | a0003c0004t0009g0157a0003c0004t0009g0158a0003c0004t0009g0159others(1): Show | 4 | HG01074.hp2 HG02896.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.517-199G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79621406 | ||||||
chr12:79621593
|
A | C | 1 | a0002c0002t0005g0183 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.517-386T>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79621593 | ||||||
chr12:79621756
|
T | C | 3 | a0004c0006t0011g0239a0004c0006t0011g0240a0004c0006t0011g0241 | 3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.517-549A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79621756 | ||||||
chr12:79621779
|
G | T | 83 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0001g0171others(80): Show | 83 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.517-572C>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79621779 | ||||||
chr12:79621793
|
G | A | 205 | a0001c0001t0002g0004a0001c0001t0002g0042a0001c0001t0002g0043others(202): Show | 205 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(202): Show |
intron_variant | MODIFIER | c.517-586C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79621793 | ||||||
chr12:79621813
|
C | T | 98 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0001g0171others(95): Show | 98 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.517-606G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79621813 | ||||||
chr12:79621989
|
T | C | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-782A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79621989 | ||||||
chr12:79622308
|
A | T | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-1101T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79622308 | ||||||
chr12:79622482
|
A | G | 5 | a0003c0005t0007g0003a0003c0005t0007g0164a0003c0005t0007g0165others(2): Show | 5 | HG02145.hp1 HG02922.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.517-1275T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79622482 | ||||||
chr12:79622576
|
T | C | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-1369A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79622576 | ||||||
chr12:79622579
|
T | C | 40 | a0002c0002t0001g0169a0002c0002t0001g0173a0002c0002t0001g0174others(37): Show | 40 | HG00544.hp2 HG00621.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.517-1372A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79622579 | ||||||
chr12:79622632
|
A | G | 1 | a0001c0003t0003g0079 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.517-1425T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79622632 | ||||||
chr12:79622941
|
G | A | 1 | a0003c0004t0022g0166 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.517-1734C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79622941 | ||||||
chr12:79622987
|
T | C | 2 | a0003c0005t0007g0164a0003c0005t0007g0165 | 2 | HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.517-1780A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79622987 | ||||||
chr12:79623068
|
T | C | 2 | a0001c0003t0003g0096a0001c0003t0003g0101 | 2 | HG01261.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.517-1861A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79623068 | ||||||
chr12:79623083
|
C | T | 3 | a0002c0002t0001g0228a0002c0002t0001g0229a0002c0002t0001g0230 | 3 | HG02630.hp1 HG02717.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.517-1876G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79623083 | ||||||
chr12:79623359
|
C | T | 1 | a0001c0001t0004g0033 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.517-2152G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79623359 | ||||||
chr12:79623428
|
G | A | 2 | a0001c0003t0003g0145a0001c0003t0024g0149 | 2 | HG02683.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.517-2221C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79623428 | ||||||
chr12:79623496
|
T | C | 40 | a0002c0002t0001g0169a0002c0002t0001g0173a0002c0002t0001g0174others(37): Show | 40 | HG00544.hp2 HG00621.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.517-2289A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79623496 | ||||||
chr12:79623508
|
G | GTTAC | 141 | a0001c0001t0003g0038a0001c0001t0003g0039a0001c0001t0003g0040others(138): Show | 141 | HG00423.hp2 HG00544.hp2 HG00621.hp2 others(138): Show |
intron_variant | MODIFIER | c.517-2302_517-2301i others(6): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79623508 | ||||||
chr12:79623559
|
T | C | 1 | a0001c0001t0002g0123 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.517-2352A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79623559 | ||||||
chr12:79623634
|
CTT | C | 83 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0001g0171others(80): Show | 83 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.517-2429_517-2428d others(4): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79623634 | ||||||
chr12:79623643
|
A | T | 1 | a0001c0001t0004g0035 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.517-2436T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79623643 | ||||||
chr12:79623903
|
G | C | 1 | a0003c0004t0022g0166 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.517-2696C>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79623903 | ||||||
chr12:79623946
|
G | C | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-2739C>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79623946 | ||||||
chr12:79624056
|
G | A | 1 | a0001c0001t0004g0028 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.517-2849C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79624056 | ||||||
chr12:79624197
|
G | A | 1 | a0003c0004t0001g0007 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.517-2990C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79624197 | ||||||
chr12:79624288
|
C | A | 2 | a0003c0004t0007g0167a0003c0004t0007g0168 | 2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.517-3081G>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79624288 | ||||||
chr12:79624352
|
G | A | 1 | a0003c0004t0022g0166 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.517-3145C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79624352 | ||||||
chr12:79624635
|
A | G | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-3428T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79624635 | ||||||
chr12:79624700
|
G | A | 3 | a0002c0002t0001g0185a0002c0002t0001g0238a0002c0002t0021g0186 | 3 | HG02622.hp1 HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.517-3493C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79624700 | ||||||
chr12:79625063
|
T | C | 3 | a0004c0006t0011g0239a0004c0006t0011g0240a0004c0006t0011g0241 | 3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.517-3856A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79625063 | ||||||
chr12:79625133
|
G | A | 1 | a0002c0002t0001g0232 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.517-3926C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79625133 | ||||||
chr12:79625134
|
C | A | 1 | a0002c0002t0001g0232 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.517-3927G>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79625134 | ||||||
chr12:79625214
|
A | G | 1 | a0001c0003t0013g0041 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.517-4007T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79625214 | ||||||
chr12:79625305
|
C | T | 1 | a0002c0002t0001g0181 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.517-4098G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79625305 | ||||||
chr12:79625352
|
A | T | 1 | a0003c0004t0022g0166 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.517-4145T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79625352 | ||||||
chr12:79625559
|
C | T | 1 | a0001c0001t0004g0018 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.517-4352G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79625559 | ||||||
chr12:79625560
|
G | A | 2 | a0001c0001t0002g0055a0001c0001t0002g0064 | 2 | HG02027.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.517-4353C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79625560 | ||||||
chr12:79625593
|
G | A | 1 | a0003c0004t0022g0166 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.517-4386C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79625593 | ||||||
chr12:79625647
|
T | C | 62 | a0001c0001t0002g0004a0001c0001t0002g0042a0001c0001t0002g0043others(59): Show | 62 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.517-4440A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79625647 | ||||||
chr12:79625674
|
G | A | 1 | a0002c0002t0001g0187 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.517-4467C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79625674 | ||||||
chr12:79625675
|
C | A | 1 | a0002c0002t0001g0187 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.517-4468G>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79625675 | ||||||
chr12:79625681
|
G | A | 1 | a0003c0004t0009g0159 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.517-4474C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79625681 | ||||||
chr12:79625721
|
A | G | 1 | a0001c0001t0006g0023 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.517-4514T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79625721 | ||||||
chr12:79625744
|
C | T | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-4537G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79625744 | ||||||
chr12:79625769
|
G | A | 1 | a0001c0001t0002g0076 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.517-4562C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79625769 | ||||||
chr12:79625777
|
G | A | 2 | a0001c0003t0013g0041a0001c0003t0013g0095 | 2 | HG02523.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.517-4570C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79625777 | ||||||
chr12:79625848
|
C | T | 4 | a0002c0002t0005g0246a0002c0002t0005g0247a0002c0002t0005g0248others(1): Show | 4 | HG01109.hp1 HG02486.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.517-4641G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79625848 | ||||||
chr12:79625849
|
G | A | 1 | a0003c0004t0022g0166 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.517-4642C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79625849 | ||||||
chr12:79625870
|
A | C | 98 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0001g0171others(95): Show | 98 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.517-4663T>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79625870 | ||||||
chr12:79625874
|
G | C | 2 | a0001c0001t0002g0055a0001c0001t0002g0064 | 2 | HG02027.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.517-4667C>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79625874 | ||||||
chr12:79625928
|
T | G | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-4721A>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79625928 | ||||||
chr12:79625931
|
G | A | 1 | a0001c0003t0003g0079 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.517-4724C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79625931 | ||||||
chr12:79626049
|
A | G | 1 | a0001c0001t0002g0073 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.517-4842T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79626049 | ||||||
chr12:79626089
|
G | A | 15 | a0001c0001t0002g0042a0001c0001t0002g0044a0001c0001t0002g0045others(12): Show | 15 | HG00438.hp1 HG01928.hp2 HG02056.hp1 others(12): Show |
intron_variant | MODIFIER | c.517-4882C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79626089 | ||||||
chr12:79626162
|
T | C | 3 | a0004c0006t0011g0239a0004c0006t0011g0240a0004c0006t0011g0241 | 3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.517-4955A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79626162 | ||||||
chr12:79626162
|
T | TAAAAAAA others(17): Show |
1 | a0005c0007t0034g0255 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.517-4956_517-4955i others(26): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79626162 | ||||||
chr12:79626163
|
T | A | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-4956A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79626163 | ||||||
chr12:79626163
|
T | TA | 30 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0009others(27): Show | 30 | HG00423.hp2 HG01099.hp2 HG01261.hp2 others(27): Show |
intron_variant | MODIFIER | c.517-4957dupT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79626163 | ||||||
chr12:79626163
|
T | TAAAAAAA others(9): Show |
2 | a0003c0005t0007g0164a0003c0005t0007g0165 | 2 | HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.517-4972_517-4957d others(18): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79626163 | ||||||
chr12:79626163
|
TA | T | 62 | a0001c0001t0002g0004a0001c0001t0002g0042a0001c0001t0002g0043others(59): Show | 62 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.517-4957delT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79626163 | ||||||
chr12:79626163
|
TAAAAAAA | T | 82 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0001g0171others(79): Show | 82 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.517-4963_517-4957d others(9): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79626163 | ||||||
chr12:79626220
|
A | G | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-5013T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79626220 | ||||||
chr12:79626266
|
T | C | 1 | a0003c0005t0007g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.517-5059A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79626266 | ||||||
chr12:79626420
|
C | T | 2 | a0002c0002t0001g0217a0002c0002t0001g0222 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.517-5213G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79626420 | ||||||
chr12:79626447
|
T | G | 255 | a0001c0001t0002g0004a0001c0001t0002g0042a0001c0001t0002g0043others(252): Show | 255 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(252): Show |
intron_variant | MODIFIER | c.517-5240A>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79626447 | ||||||
chr12:79626554
|
C | T | 1 | a0002c0002t0001g0209 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.517-5347G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79626554 | ||||||
chr12:79626579
|
CT | C | 40 | a0002c0002t0001g0169a0002c0002t0001g0173a0002c0002t0001g0174others(37): Show | 40 | HG00544.hp2 HG00621.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.517-5373delA | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79626579 | ||||||
chr12:79626590
|
T | A | 1 | a0001c0001t0002g0154 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.517-5383A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79626590 | ||||||
chr12:79626789
|
T | C | 1 | a0001c0001t0002g0071 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.517-5582A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79626789 | ||||||
chr12:79626801
|
C | T | 1 | a0001c0003t0028g0084 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.517-5594G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79626801 | ||||||
chr12:79626956
|
G | A | 3 | a0001c0001t0002g0051a0001c0001t0002g0093a0001c0001t0002g0119 | 3 | HG00423.hp1 NA18959.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.517-5749C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79626956 | ||||||
chr12:79626989
|
T | C | 1 | a0003c0005t0007g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.517-5782A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79626989 | ||||||
chr12:79626997
|
T | C | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-5790A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79626997 | ||||||
chr12:79627052
|
G | A | 1 | a0001c0001t0002g0048 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.517-5845C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79627052 | ||||||
chr12:79627059
|
T | C | 1 | a0005c0007t0034g0255 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.517-5852A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79627059 | ||||||
chr12:79627102
|
C | T | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-5895G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79627102 | ||||||
chr12:79627150
|
C | T | 3 | a0003c0005t0007g0003a0003c0005t0007g0164a0003c0005t0007g0165 | 3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.517-5943G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79627150 | ||||||
chr12:79627187
|
C | G | 3 | a0004c0006t0011g0239a0004c0006t0011g0240a0004c0006t0011g0241 | 3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.517-5980G>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79627187 | ||||||
chr12:79627254
|
G | T | 3 | a0004c0006t0011g0239a0004c0006t0011g0240a0004c0006t0011g0241 | 3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.517-6047C>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79627254 | ||||||
chr12:79627275
|
C | T | 83 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0001g0171others(80): Show | 83 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.517-6068G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79627275 | ||||||
chr12:79627276
|
G | A | 2 | a0001c0001t0004g0001a0001c0001t0004g0002 | 2 | HG02559.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.517-6069C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79627276 | ||||||
chr12:79627386
|
C | T | 3 | a0003c0005t0007g0003a0003c0005t0007g0164a0003c0005t0007g0165 | 3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.517-6179G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79627386 | ||||||
chr12:79627417
|
G | A | 1 | a0006c0008t0003g0098 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.517-6210C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79627417 | ||||||
chr12:79627486
|
A | G | 2 | a0002c0002t0001g0226a0002c0002t0012g0221 | 2 | NA18946.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.517-6279T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79627486 | ||||||
chr12:79627501
|
C | G | 1 | a0001c0001t0004g0011 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.517-6294G>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79627501 | ||||||
chr12:79627899
|
C | T | 2 | a0001c0003t0003g0150a0001c0003t0023g0148 | 2 | NA18957.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.517-6692G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79627899 | ||||||
chr12:79627978
|
C | A | 1 | a0002c0002t0012g0189 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.517-6771G>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79627978 | ||||||
chr12:79628053
|
A | G | 5 | a0003c0005t0007g0003a0003c0005t0007g0164a0003c0005t0007g0165others(2): Show | 5 | HG02145.hp1 HG02922.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.517-6846T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79628053 | ||||||
chr12:79628176
|
T | C | 1 | a0002c0002t0001g0218 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.517-6969A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79628176 | ||||||
chr12:79628190
|
C | G | 1 | a0002c0002t0001g0172 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.517-6983G>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79628190 | ||||||
chr12:79628259
|
C | T | 1 | a0002c0002t0005g0246 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.517-7052G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79628259 | ||||||
chr12:79628662
|
T | TA | 5 | a0003c0005t0007g0003a0003c0005t0007g0164a0003c0005t0007g0165others(2): Show | 5 | HG02145.hp1 HG02922.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.517-7456dupT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79628662 | ||||||
chr12:79628677
|
C | T | 1 | a0001c0003t0008g0137 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.517-7470G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79628677 | ||||||
chr12:79628735
|
G | A | 3 | a0004c0006t0011g0239a0004c0006t0011g0240a0004c0006t0011g0241 | 3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.517-7528C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79628735 | ||||||
chr12:79629001
|
G | A | 1 | a0001c0001t0029g0120 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.517-7794C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79629001 | ||||||
chr12:79629035
|
C | T | 3 | a0004c0006t0011g0239a0004c0006t0011g0240a0004c0006t0011g0241 | 3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.517-7828G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79629035 | ||||||
chr12:79629330
|
G | A | 83 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0001g0171others(80): Show | 83 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.517-8123C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79629330 | ||||||
chr12:79629344
|
T | A | 2 | a0002c0002t0005g0246a0002c0002t0005g0248 | 2 | HG01109.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.517-8137A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79629344 | ||||||
chr12:79629449
|
T | C | 1 | a0002c0002t0001g0211 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.517-8242A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79629449 | ||||||
chr12:79629734
|
G | T | 1 | a0003c0004t0022g0166 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.517-8527C>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79629734 | ||||||
chr12:79629943
|
T | C | 1 | a0002c0002t0001g0219 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.517-8736A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79629943 | ||||||
chr12:79629959
|
C | T | 1 | a0002c0002t0001g0200 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.517-8752G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79629959 | ||||||
chr12:79630074
|
TA | T | 3 | a0001c0001t0004g0011a0001c0001t0004g0035a0001c0001t0004g0124 | 3 | HG01099.hp2 HG02683.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.517-8868delT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79630074 | ||||||
chr12:79630240
|
A | G | 98 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0001g0171others(95): Show | 98 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.517-9033T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79630240 | ||||||
chr12:79630315
|
A | T | 62 | a0001c0001t0002g0004a0001c0001t0002g0042a0001c0001t0002g0043others(59): Show | 62 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.517-9108T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79630315 | ||||||
chr12:79630315
|
ATT | A | 97 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0001g0171others(94): Show | 97 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(94): Show |
intron_variant | MODIFIER | c.517-9110_517-9109d others(4): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79630315 | ||||||
chr12:79630317
|
T | A | 1 | a0003c0004t0001g0007 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.517-9110A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79630317 | ||||||
chr12:79630368
|
C | T | 3 | a0003c0005t0007g0003a0003c0005t0007g0164a0003c0005t0007g0165 | 3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.517-9161G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79630368 | ||||||
chr12:79630454
|
T | C | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-9247A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79630454 | ||||||
chr12:79630634
|
T | C | 1 | a0001c0001t0006g0026 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.517-9427A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79630634 | ||||||
chr12:79630660
|
C | T | 4 | a0003c0004t0009g0157a0003c0004t0009g0158a0003c0004t0009g0159others(1): Show | 4 | HG01074.hp2 HG02896.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.517-9453G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79630660 | ||||||
chr12:79630858
|
CA | C | 30 | a0001c0001t0002g0062a0001c0003t0003g0082a0002c0002t0001g0170others(27): Show | 30 | HG00639.hp2 HG01109.hp1 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.517-9652delT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79630858 | ||||||
chr12:79631005
|
T | A | 40 | a0002c0002t0001g0169a0002c0002t0001g0173a0002c0002t0001g0174others(37): Show | 40 | HG00544.hp2 HG00621.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.517-9798A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79631005 | ||||||
chr12:79631021
|
A | T | 7 | a0002c0002t0001g0193a0002c0002t0001g0199a0002c0002t0001g0200others(4): Show | 7 | HG00673.hp2 NA18945.hp1 NA18952.hp2 others(4): Show |
intron_variant | MODIFIER | c.517-9814T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79631021 | ||||||
chr12:79631291
|
G | A | 138 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0009others(135): Show | 138 | HG00423.hp2 HG00544.hp2 HG00621.hp2 others(135): Show |
intron_variant | MODIFIER | c.517-10084C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79631291 | ||||||
chr12:79631434
|
A | C | 1 | a0001c0001t0002g0047 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.517-10227T>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79631434 | ||||||
chr12:79631646
|
G | A | 1 | a0001c0001t0002g0057 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.517-10439C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79631646 | ||||||
chr12:79631740
|
A | G | 1 | a0001c0001t0004g0037 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.517-10533T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79631740 | ||||||
chr12:79631742
|
T | C | 4 | a0003c0004t0009g0157a0003c0004t0009g0158a0003c0004t0009g0159others(1): Show | 4 | HG01074.hp2 HG02896.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.517-10535A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79631742 | ||||||
chr12:79631931
|
G | A | 1 | a0006c0008t0003g0098 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.517-10724C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79631931 | ||||||
chr12:79632013
|
A | G | 3 | a0004c0006t0011g0239a0004c0006t0011g0240a0004c0006t0011g0241 | 3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.517-10806T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632013 | ||||||
chr12:79632089
|
T | C | 2 | a0003c0005t0007g0164a0003c0005t0007g0165 | 2 | HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.517-10882A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632089 | ||||||
chr12:79632132
|
C | CA | 10 | a0001c0001t0002g0063a0001c0001t0002g0066a0001c0001t0002g0091others(7): Show | 10 | HG00423.hp2 HG02074.hp1 HG03139.hp2 others(7): Show |
intron_variant | MODIFIER | c.517-10926dupT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632132 | ||||||
chr12:79632132
|
C | CAAAAAAA others(6): Show |
1 | a0003c0005t0007g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.517-10938_517-1092 others(17): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632132 | ||||||
chr12:79632132
|
C | CAAAAAAA others(7): Show |
2 | a0003c0005t0007g0164a0003c0005t0007g0165 | 2 | HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.517-10939_517-1092 others(18): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632132 | ||||||
chr12:79632132
|
CA | C | 86 | a0001c0001t0004g0028a0002c0002t0001g0169a0002c0002t0001g0170others(83): Show | 86 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(83): Show |
intron_variant | MODIFIER | c.517-10926delT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632132 | ||||||
chr12:79632151
|
A | G | 7 | a0001c0001t0002g0068a0001c0001t0002g0070a0001c0001t0002g0072others(4): Show | 7 | HG02040.hp1 NA18941.hp2 NA18960.hp2 others(4): Show |
intron_variant | MODIFIER | c.517-10944T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632151 | ||||||
chr12:79632174
|
A | G | 3 | a0004c0006t0011g0239a0004c0006t0011g0240a0004c0006t0011g0241 | 3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.517-10967T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632174 | ||||||
chr12:79632179
|
A | T | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-10972T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632179 | ||||||
chr12:79632257
|
A | ACAAAT | 5 | a0003c0005t0007g0003a0003c0005t0007g0164a0003c0005t0007g0165others(2): Show | 5 | HG02145.hp1 HG02922.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.517-11051_517-1105 others(9): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632257 | ||||||
chr12:79632288
|
A | AATATATA others(7): Show |
3 | a0001c0001t0004g0019a0001c0001t0006g0014a0001c0001t0006g0034 | 3 | HG01109.hp2 HG01256.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.517-11095_517-1108 others(18): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632288 | ||||||
chr12:79632288
|
AATATATA others(19): Show |
A | 1 | a0002c0002t0001g0195 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.517-11107_517-1108 others(30): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632288 | ||||||
chr12:79632288
|
AATATATA others(21): Show |
A | 1 | a0003c0004t0007g0168 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.517-11109_517-1108 others(32): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632288 | ||||||
chr12:79632288
|
AATATATA others(23): Show |
A | 1 | a0003c0004t0007g0167 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.517-11111_517-1108 others(34): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632288 | ||||||
chr12:79632288
|
AATATATA others(31): Show |
A | 5 | a0002c0002t0001g0175a0003c0004t0009g0157a0003c0004t0009g0158others(2): Show | 5 | HG01074.hp2 HG02896.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.517-11119_517-1108 others(42): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632288 | ||||||
chr12:79632288
|
AATATATA others(33): Show |
A | 2 | a0003c0005t0007g0164a0003c0005t0007g0165 | 2 | HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.517-11121_517-1108 others(44): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632288 | ||||||
chr12:79632288
|
AATATATA others(35): Show |
A | 1 | a0002c0002t0001g0230 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.517-11123_517-1108 others(46): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632288 | ||||||
chr12:79632288
|
AATATATA others(37): Show |
A | 5 | a0002c0002t0005g0182a0003c0004t0022g0166a0004c0006t0011g0239others(2): Show | 5 | HG00639.hp2 HG02258.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.517-11125_517-1108 others(48): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632288 | ||||||
chr12:79632290
|
TATATACA others(15): Show |
T | 3 | a0002c0002t0001g0170a0002c0002t0001g0172a0002c0002t0001g0253 | 3 | HG02572.hp1 HG02647.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.517-11105_517-1108 others(26): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632290 | ||||||
chr12:79632292
|
T | A | 1 | a0002c0002t0001g0212 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.517-11085A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632292 | ||||||
chr12:79632292
|
TATACATA others(9): Show |
T | 11 | a0001c0001t0002g0090a0002c0002t0001g0173a0002c0002t0001g0174others(8): Show | 11 | HG01261.hp1 HG02486.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.517-11101_517-1108 others(20): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632292 | ||||||
chr12:79632292
|
TATACATA others(13): Show |
T | 2 | a0002c0002t0001g0191a0002c0002t0017g0184 | 2 | HG02027.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.517-11105_517-1108 others(24): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632292 | ||||||
chr12:79632294
|
TACATATA others(7): Show |
T | 10 | a0002c0002t0001g0178a0002c0002t0001g0188a0002c0002t0001g0202others(7): Show | 10 | HG00621.hp2 HG01891.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.517-11101_517-1108 others(18): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632294 | ||||||
chr12:79632294
|
TACATATA others(11): Show |
T | 11 | a0002c0002t0001g0171a0002c0002t0001g0185a0002c0002t0001g0187others(8): Show | 11 | HG01109.hp1 HG01192.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.517-11105_517-1108 others(22): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632294 | ||||||
chr12:79632296
|
C | CAT | 25 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0009others(22): Show | 25 | HG00423.hp2 HG01081.hp2 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.517-11091_517-1109 others(6): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632296 | ||||||
chr12:79632296
|
C | CATATATA others(11): Show |
3 | a0001c0001t0004g0013a0001c0001t0004g0016a0001c0001t0004g0018 | 3 | HG02615.hp2 HG02976.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.517-11090_517-1108 others(22): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632296 | ||||||
chr12:79632296
|
C | CATATATA others(25): Show |
3 | a0001c0001t0004g0031a0001c0001t0004g0124a0001c0001t0004g0125 | 3 | HG02080.hp1 HG02683.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.517-11090_517-1108 others(36): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632296 | ||||||
chr12:79632296
|
C | CATATATA others(55): Show |
1 | a0001c0001t0004g0033 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.517-11090_517-1108 others(66): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632296 | ||||||
chr12:79632296
|
C | T | 46 | a0002c0002t0001g0169a0002c0002t0001g0176a0002c0002t0001g0180others(43): Show | 46 | HG00544.hp2 HG00673.hp2 HG01256.hp1 others(43): Show |
intron_variant | MODIFIER | c.517-11089G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632296 | ||||||
chr12:79632296
|
CATATATA others(15): Show |
C | 1 | a0001c0003t0003g0086 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.517-11111_517-1109 others(26): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632296 | ||||||
chr12:79632296
|
CATATATA others(17): Show |
C | 1 | a0001c0003t0003g0079 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.517-11113_517-1109 others(28): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632296 | ||||||
chr12:79632296
|
CATATATA others(19): Show |
C | 2 | a0001c0001t0003g0040a0001c0003t0003g0085 | 2 | HG02071.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.517-11115_517-1109 others(30): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632296 | ||||||
chr12:79632296
|
CATATATA others(21): Show |
C | 2 | a0001c0001t0003g0038a0001c0001t0003g0039 | 2 | HG02572.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.517-11117_517-1109 others(32): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632296 | ||||||
chr12:79632296
|
CATATATA others(25): Show |
C | 2 | a0001c0001t0002g0049a0001c0001t0016g0012 | 2 | HG02055.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.517-11121_517-1109 others(36): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632296 | ||||||
chr12:79632296
|
CATATATA others(39): Show |
C | 2 | a0001c0001t0002g0068a0001c0001t0002g0072 | 2 | NA18968.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.517-11135_517-1109 others(50): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632296 | ||||||
chr12:79632298
|
TATATATA others(7): Show |
T | 17 | a0001c0001t0002g0004a0001c0001t0002g0042a0001c0001t0002g0043others(14): Show | 17 | HG00741.hp1 HG01243.hp2 HG01257.hp1 others(14): Show |
intron_variant | MODIFIER | c.517-11105_517-1109 others(18): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632298 | ||||||
chr12:79632300
|
TATATATA others(5): Show |
T | 43 | a0001c0001t0002g0055a0001c0001t0002g0059a0001c0001t0002g0060others(40): Show | 43 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.517-11105_517-1109 others(16): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632300 | ||||||
chr12:79632302
|
TATATACA others(3): Show |
T | 13 | a0001c0001t0002g0047a0001c0001t0002g0048a0001c0003t0003g0078others(10): Show | 13 | HG00621.hp1 HG01069.hp2 HG02300.hp1 others(10): Show |
intron_variant | MODIFIER | c.517-11105_517-1109 others(14): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632302 | ||||||
chr12:79632302
|
TATATACA others(38): Show |
T | 1 | a0002c0002t0001g0197 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.517-11140_517-1109 others(49): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632302 | ||||||
chr12:79632303
|
ATATACAT others(52): Show |
A | 1 | a0003c0005t0007g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.517-11155_517-1109 others(63): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632303 | ||||||
chr12:79632304
|
TATACATA others(1): Show |
T | 8 | a0001c0001t0002g0057a0001c0001t0002g0121a0001c0003t0027g0135others(5): Show | 8 | HG02145.hp2 HG02886.hp1 HG03831.hp2 others(5): Show |
intron_variant | MODIFIER | c.517-11105_517-1109 others(12): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632304 | ||||||
chr12:79632304
|
TATACATA others(40): Show |
T | 1 | a0002c0002t0001g0219 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.517-11144_517-1109 others(51): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632304 | ||||||
chr12:79632306
|
TACATAC | T | 9 | a0001c0001t0002g0074a0001c0001t0002g0080a0001c0003t0003g0097others(6): Show | 9 | HG01069.hp1 HG01192.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.517-11105_517-1110 others(10): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632306 | ||||||
chr12:79632307
|
ACATACAT others(55): Show |
A | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-11162_517-1110 others(66): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632307 | ||||||
chr12:79632308
|
C | T | 63 | a0001c0001t0002g0051a0001c0001t0002g0053a0001c0001t0002g0069others(60): Show | 63 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(60): Show |
intron_variant | MODIFIER | c.517-11101G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632308 | ||||||
chr12:79632310
|
T | C | 4 | a0001c0001t0004g0010a0001c0001t0004g0028a0001c0001t0004g0030others(1): Show | 4 | HG02257.hp2 NA18945.hp2 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.517-11103A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632310 | ||||||
chr12:79632312
|
C | CATATATA others(5): Show |
2 | a0001c0001t0002g0134a0001c0003t0003g0075 | 2 | HG00673.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.517-11117_517-1110 others(16): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632312 | ||||||
chr12:79632312
|
C | T | 63 | a0001c0001t0002g0077a0001c0001t0004g0001a0001c0001t0004g0002others(60): Show | 63 | HG00423.hp2 HG00621.hp2 HG01081.hp2 others(60): Show |
intron_variant | MODIFIER | c.517-11105G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632312 | ||||||
chr12:79632312
|
CAT | C | 5 | a0001c0001t0002g0069a0001c0003t0003g0100a0001c0003t0003g0146others(2): Show | 5 | HG00741.hp2 HG02056.hp2 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.517-11107_517-1110 others(6): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632312 | ||||||
chr12:79632312
|
CATAT | C | 4 | a0001c0003t0003g0102a0001c0003t0003g0103a0001c0003t0003g0145others(1): Show | 4 | HG01169.hp1 HG01891.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.517-11109_517-1110 others(8): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632312 | ||||||
chr12:79632316
|
T | TATATATA others(1): Show |
3 | a0001c0001t0004g0015a0001c0001t0004g0032a0001c0001t0006g0026 | 3 | HG03516.hp1 HG03654.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.517-11110_517-1110 others(12): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632316 | ||||||
chr12:79632318
|
T | C | 5 | a0001c0001t0002g0074a0001c0001t0002g0080a0001c0003t0003g0097others(2): Show | 5 | HG01069.hp1 HG01192.hp2 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.517-11111A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632318 | ||||||
chr12:79632318
|
T | TATATACA others(15): Show |
1 | a0001c0001t0004g0037 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.517-11112_517-1111 others(26): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632318 | ||||||
chr12:79632320
|
T | C | 3 | a0001c0001t0002g0057a0001c0001t0002g0121a0001c0003t0027g0135 | 3 | HG03831.hp2 NA19003.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.517-11113A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632320 | ||||||
chr12:79632322
|
T | C | 8 | a0001c0001t0002g0047a0001c0001t0002g0048a0001c0003t0003g0078others(5): Show | 8 | HG00621.hp1 HG01069.hp2 HG02300.hp2 others(5): Show |
intron_variant | MODIFIER | c.517-11115A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632322 | ||||||
chr12:79632324
|
T | C | 46 | a0001c0001t0002g0055a0001c0001t0002g0059a0001c0001t0002g0060others(43): Show | 46 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.517-11117A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632324 | ||||||
chr12:79632324
|
T | TATATATA others(13): Show |
1 | a0001c0001t0002g0153 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.517-11118_517-1111 others(24): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632324 | ||||||
chr12:79632326
|
T | C | 20 | a0001c0001t0002g0004a0001c0001t0002g0042a0001c0001t0002g0043others(17): Show | 20 | HG00741.hp1 HG01243.hp2 HG01257.hp1 others(17): Show |
intron_variant | MODIFIER | c.517-11119A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632326 | ||||||
chr12:79632326
|
T | TATATATA others(11): Show |
3 | a0001c0001t0002g0107a0001c0001t0002g0111a0001c0001t0002g0116 | 3 | NA18987.hp1 NA18992.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.517-11120_517-1111 others(22): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632326 | ||||||
chr12:79632328
|
T | C | 3 | a0001c0001t0002g0090a0001c0001t0002g0117a0001c0001t0002g0118 | 3 | HG01168.hp1 HG01169.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.517-11121A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632328 | ||||||
chr12:79632330
|
T | G | 4 | a0003c0004t0009g0157a0003c0004t0009g0158a0003c0004t0009g0159others(1): Show | 4 | HG01074.hp2 HG02896.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.517-11123A>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632330 | ||||||
chr12:79632332
|
T | A | 4 | a0003c0004t0009g0157a0003c0004t0009g0158a0003c0004t0009g0159others(1): Show | 4 | HG01074.hp2 HG02896.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.517-11125A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632332 | ||||||
chr12:79632334
|
T | C | 2 | a0001c0001t0016g0012a0001c0003t0003g0086 | 2 | HG02055.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.517-11127A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632334 | ||||||
chr12:79632338
|
T | C | 12 | a0001c0001t0003g0040a0001c0001t0004g0011a0001c0001t0004g0031others(9): Show | 12 | HG01099.hp2 HG02040.hp2 HG02071.hp1 others(9): Show |
intron_variant | MODIFIER | c.517-11131A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632338 | ||||||
chr12:79632339
|
A | T | 1 | a0002c0002t0001g0192 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.517-11132T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632339 | ||||||
chr12:79632340
|
T | C | 3 | a0001c0001t0002g0069a0001c0001t0003g0038a0001c0001t0003g0039 | 3 | HG02572.hp2 HG03041.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.517-11133A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632340 | ||||||
chr12:79632341
|
A | T | 1 | a0002c0002t0001g0192 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.517-11134T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632341 | ||||||
chr12:79632341
|
ATATATAT others(15): Show |
A | 5 | a0001c0003t0002g0155a0001c0003t0003g0131a0001c0003t0003g0132others(2): Show | 5 | HG00544.hp1 NA18967.hp1 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.517-11156_517-1113 others(26): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632341 | ||||||
chr12:79632343
|
A | T | 1 | a0002c0002t0001g0192 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.517-11136T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632343 | ||||||
chr12:79632344
|
T | C | 2 | a0001c0001t0002g0117a0001c0001t0002g0118 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.517-11137A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632344 | ||||||
chr12:79632345
|
A | T | 1 | a0002c0002t0001g0192 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.517-11138T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632345 | ||||||
chr12:79632346
|
T | TATATATA others(4): Show |
2 | a0001c0001t0002g0117a0001c0001t0002g0118 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.517-11140_517-1113 others(15): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632346 | ||||||
chr12:79632346
|
TA | T | 8 | a0002c0002t0001g0176a0002c0002t0001g0188a0002c0002t0001g0191others(5): Show | 8 | HG02027.hp2 HG02258.hp2 HG02300.hp1 others(5): Show |
intron_variant | MODIFIER | c.517-11140delT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632346 | ||||||
chr12:79632347
|
A | T | 2 | a0002c0002t0001g0180a0002c0002t0001g0192 | 2 | HG02559.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.517-11140T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632347 | ||||||
chr12:79632348
|
T | C | 1 | a0001c0003t0003g0147 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.517-11141A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632348 | ||||||
chr12:79632348
|
TA | T | 5 | a0002c0002t0001g0195a0002c0002t0001g0208a0002c0002t0001g0209others(2): Show | 5 | HG01975.hp2 HG02071.hp2 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.517-11142delT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632348 | ||||||
chr12:79632348
|
TATATATA others(6): Show |
T | 1 | a0001c0001t0002g0114 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.517-11154_517-1114 others(17): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632348 | ||||||
chr12:79632349
|
A | T | 23 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0001g0176others(20): Show | 23 | HG01256.hp1 HG01258.hp2 HG02027.hp2 others(20): Show |
intron_variant | MODIFIER | c.517-11142T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632349 | ||||||
chr12:79632349
|
ATATATAT others(6): Show |
A | 2 | a0001c0001t0002g0092a0001c0001t0003g0110 | 2 | NA18939.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.517-11155_517-1114 others(17): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632349 | ||||||
chr12:79632349
|
ATATATAT others(7): Show |
A | 1 | a0001c0001t0002g0108 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.517-11156_517-1114 others(18): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632349 | ||||||
chr12:79632350
|
TA | T | 3 | a0002c0002t0001g0171a0002c0002t0001g0199a0002c0002t0001g0223 | 3 | HG00621.hp2 HG01192.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.517-11144delT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632350 | ||||||
chr12:79632350
|
TATATATA others(4): Show |
T | 2 | a0001c0003t0003g0099a0001c0003t0008g0139 | 2 | HG01928.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.517-11154_517-1114 others(15): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632350 | ||||||
chr12:79632351
|
A | T | 46 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0001g0173others(43): Show | 46 | HG00544.hp2 HG00673.hp2 HG01256.hp1 others(43): Show |
intron_variant | MODIFIER | c.517-11144T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632351 | ||||||
chr12:79632351
|
ATATATAT others(5): Show |
A | 2 | a0001c0001t0002g0051a0001c0001t0029g0120 | 2 | HG00423.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.517-11156_517-1114 others(16): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632351 | ||||||
chr12:79632352
|
TATATATA others(2): Show |
T | 4 | a0001c0003t0008g0136a0001c0003t0008g0137a0001c0003t0008g0138others(1): Show | 4 | NA18946.hp1 NA18966.hp2 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.517-11154_517-1114 others(13): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632352 | ||||||
chr12:79632353
|
A | G | 1 | a0001c0001t0004g0013 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.517-11146T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632353 | ||||||
chr12:79632353
|
A | T | 75 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0001g0171others(72): Show | 75 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.517-11146T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632353 | ||||||
chr12:79632353
|
ATATATAT others(3): Show |
A | 3 | a0001c0001t0002g0053a0001c0001t0002g0119a0001c0003t0003g0046 | 3 | HG01952.hp2 HG02080.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.517-11156_517-1114 others(14): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632353 | ||||||
chr12:79632355
|
A | T | 83 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0001g0171others(80): Show | 83 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.517-11148T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632355 | ||||||
chr12:79632357
|
A | T | 85 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0001g0171others(82): Show | 85 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.517-11150T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632357 | ||||||
chr12:79632359
|
A | T | 87 | a0001c0001t0004g0017a0002c0002t0001g0169a0002c0002t0001g0170others(84): Show | 87 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.517-11152T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632359 | ||||||
chr12:79632361
|
A | AT | 7 | a0001c0001t0004g0010a0001c0001t0004g0019a0001c0001t0004g0027others(4): Show | 7 | HG01993.hp1 HG02257.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.517-11155dupA | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632361 | ||||||
chr12:79632361
|
A | T | 120 | a0001c0001t0002g0043a0001c0001t0002g0090a0001c0001t0002g0123others(117): Show | 120 | HG00423.hp2 HG00544.hp2 HG00621.hp1 others(117): Show |
intron_variant | MODIFIER | c.517-11154T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632361 | ||||||
chr12:79632363
|
T | A | 4 | a0001c0003t0003g0096a0004c0006t0011g0239a0004c0006t0011g0240others(1): Show | 4 | HG01261.hp2 HG02258.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.517-11156A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632363 | ||||||
chr12:79632377
|
A | T | 1 | a0001c0003t0003g0133 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.517-11170T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632377 | ||||||
chr12:79632428
|
G | A | 1 | a0001c0001t0004g0011 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.517-11221C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632428 | ||||||
chr12:79632545
|
A | C | 5 | a0003c0005t0007g0003a0003c0005t0007g0164a0003c0005t0007g0165others(2): Show | 5 | HG02145.hp1 HG02922.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.517-11338T>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632545 | ||||||
chr12:79632772
|
C | T | 1 | a0001c0001t0002g0048 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.517-11565G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632772 | ||||||
chr12:79632773
|
C | G | 3 | a0002c0002t0001g0228a0002c0002t0001g0229a0002c0002t0001g0230 | 3 | HG02630.hp1 HG02717.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.517-11566G>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632773 | ||||||
chr12:79632855
|
C | T | 2 | a0001c0001t0004g0001a0001c0001t0004g0002 | 2 | HG02559.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.517-11648G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632855 | ||||||
chr12:79632882
|
C | A | 3 | a0003c0005t0007g0003a0003c0005t0007g0164a0003c0005t0007g0165 | 3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.517-11675G>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632882 | ||||||
chr12:79633126
|
A | AAAAC | 4 | a0002c0002t0001g0225a0004c0006t0011g0239a0004c0006t0011g0240others(1): Show | 4 | HG02258.hp1 HG03225.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.517-11923_517-1192 others(8): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79633126 | ||||||
chr12:79633187
|
T | G | 3 | a0003c0005t0007g0003a0003c0005t0007g0164a0003c0005t0007g0165 | 3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.517-11980A>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79633187 | ||||||
chr12:79633260
|
T | C | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-12053A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79633260 | ||||||
chr12:79633514
|
G | GT | 4 | a0003c0004t0009g0157a0003c0004t0009g0158a0003c0004t0009g0159others(1): Show | 4 | HG01074.hp2 HG02896.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.517-12308dupA | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79633514 | ||||||
chr12:79633514
|
G | T | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-12307C>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79633514 | ||||||
chr12:79633526
|
T | C | 1 | a0001c0003t0003g0089 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.517-12319A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79633526 | ||||||
chr12:79633716
|
C | T | 2 | a0003c0004t0007g0167a0003c0004t0007g0168 | 2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.517-12509G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79633716 | ||||||
chr12:79633955
|
C | T | 3 | a0003c0005t0007g0003a0003c0005t0007g0164a0003c0005t0007g0165 | 3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.517-12748G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79633955 | ||||||
chr12:79633973
|
A | G | 1 | a0001c0001t0006g0008 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.517-12766T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79633973 | ||||||
chr12:79633974
|
G | A | 3 | a0002c0002t0001g0185a0002c0002t0001g0238a0002c0002t0021g0186 | 3 | HG02622.hp1 HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.517-12767C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79633974 | ||||||
chr12:79634061
|
G | C | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-12854C>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79634061 | ||||||
chr12:79634664
|
A | AAGAAAC | 138 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0009others(135): Show | 138 | HG00423.hp2 HG00544.hp2 HG00621.hp2 others(135): Show |
intron_variant | MODIFIER | c.517-13458_517-1345 others(10): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79634664 | ||||||
chr12:79634958
|
C | T | 98 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0001g0171others(95): Show | 98 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.517-13751G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79634958 | ||||||
chr12:79634966
|
C | A | 1 | a0001c0003t0003g0078 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.517-13759G>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79634966 | ||||||
chr12:79635032
|
C | T | 1 | a0002c0002t0020g0194 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.517-13825G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79635032 | ||||||
chr12:79635150
|
A | G | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-13943T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79635150 | ||||||
chr12:79635464
|
T | C | 4 | a0003c0004t0009g0157a0003c0004t0009g0158a0003c0004t0009g0159others(1): Show | 4 | HG01074.hp2 HG02896.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.517-14257A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79635464 | ||||||
chr12:79635643
|
G | A | 3 | a0003c0005t0007g0003a0003c0005t0007g0164a0003c0005t0007g0165 | 3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.517-14436C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79635643 | ||||||
chr12:79635736
|
T | G | 83 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0001g0171others(80): Show | 83 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.517-14529A>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79635736 | ||||||
chr12:79636338
|
C | CAT | 98 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0001g0171others(95): Show | 98 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.517-15132_517-1513 others(6): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79636338 | ||||||
chr12:79636656
|
C | T | 3 | a0004c0006t0011g0239a0004c0006t0011g0240a0004c0006t0011g0241 | 3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.517-15449G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79636656 | ||||||
chr12:79636666
|
T | C | 2 | a0002c0002t0001g0217a0002c0002t0001g0222 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.517-15459A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79636666 | ||||||
chr12:79636699
|
C | T | 2 | a0001c0001t0002g0055a0001c0001t0002g0064 | 2 | HG02027.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.517-15492G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79636699 | ||||||
chr12:79636927
|
T | C | 83 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0001g0171others(80): Show | 83 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.517-15720A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79636927 | ||||||
chr12:79636939
|
T | C | 2 | a0003c0004t0007g0167a0003c0004t0007g0168 | 2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.517-15732A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79636939 | ||||||
chr12:79637191
|
G | C | 4 | a0002c0002t0001g0172a0002c0002t0001g0211a0002c0002t0001g0212others(1): Show | 4 | HG03139.hp1 NA18906.hp2 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.517-15984C>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79637191 | ||||||
chr12:79637446
|
C | T | 1 | a0001c0003t0014g0162 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.517-16239G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79637446 | ||||||
chr12:79637489
|
T | TAAGCCAA others(9): Show |
1 | a0002c0002t0001g0218 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.517-16298_517-1628 others(20): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79637489 | ||||||
chr12:79637541
|
T | TAAAAAAA others(317): Show |
2 | a0003c0004t0009g0159a0003c0004t0009g0160 | 2 | HG01074.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.517-16335_517-1633 others(328): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79637541 | ||||||
chr12:79637541
|
T | TAAAAAAA others(319): Show |
1 | a0003c0004t0009g0158 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.517-16335_517-1633 others(330): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79637541 | ||||||
chr12:79637541
|
T | TAAAAAAA others(320): Show |
1 | a0003c0004t0009g0157 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.517-16335_517-1633 others(331): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79637541 | ||||||
chr12:79637541
|
TA | T | 92 | a0001c0001t0004g0027a0002c0002t0001g0169a0002c0002t0001g0170others(89): Show | 92 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(89): Show |
intron_variant | MODIFIER | c.517-16335delT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79637541 | ||||||
chr12:79637649
|
A | T | 2 | a0003c0004t0007g0167a0003c0004t0007g0168 | 2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.517-16442T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79637649 | ||||||
chr12:79637656
|
C | T | 1 | a0004c0006t0011g0241 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.517-16449G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79637656 | ||||||
chr12:79637977
|
A | G | 1 | a0001c0003t0003g0079 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.517-16770T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79637977 | ||||||
chr12:79638138
|
C | CA | 14 | a0002c0002t0005g0182a0002c0002t0005g0183a0002c0002t0005g0233others(11): Show | 14 | HG00639.hp2 HG01109.hp1 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.517-16932dupT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638138 | ||||||
chr12:79638288
|
T | G | 2 | a0001c0001t0002g0108a0001c0001t0002g0113 | 2 | HG01928.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.517-17081A>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638288 | ||||||
chr12:79638466
|
T | C | 1 | a0003c0005t0007g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.517-17259A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638466 | ||||||
chr12:79638757
|
C | A | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-17550G>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638757 | ||||||
chr12:79638790
|
G | GGT | 69 | a0001c0001t0002g0004a0001c0001t0002g0042a0001c0001t0002g0044others(66): Show | 69 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.517-17585_517-1758 others(6): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638790 | ||||||
chr12:79638790
|
G | GGTGT | 4 | a0001c0001t0002g0053a0001c0001t0002g0080a0001c0001t0002g0130others(1): Show | 4 | HG01192.hp2 HG02080.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.517-17587_517-1758 others(8): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638790 | ||||||
chr12:79638790
|
G | GT | 7 | a0001c0001t0002g0074a0001c0001t0004g0036a0001c0003t0002g0155others(4): Show | 7 | HG00423.hp2 HG01069.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.517-17584_517-1758 others(5): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638790 | ||||||
chr12:79638790
|
GGT | G | 88 | a0001c0003t0003g0046a0001c0003t0003g0083a0002c0002t0001g0169others(85): Show | 88 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.517-17585_517-1758 others(6): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638790 | ||||||
chr12:79638790
|
GGTGTGTG others(3): Show |
G | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-17593_517-1758 others(14): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638790 | ||||||
chr12:79638794
|
T | G | 18 | a0002c0002t0001g0170a0002c0002t0001g0171a0002c0002t0001g0181others(15): Show | 18 | HG00639.hp2 HG01109.hp1 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.517-17587A>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638794 | ||||||
chr12:79638810
|
T | C | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-17603A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638810 | ||||||
chr12:79638863
|
C | CAT | 6 | a0001c0001t0002g0092a0001c0003t0003g0082a0001c0003t0008g0151others(3): Show | 6 | HG00673.hp2 HG02602.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.517-17658_517-1765 others(6): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638863 | ||||||
chr12:79638863
|
C | CATAT | 10 | a0001c0001t0002g0055a0001c0001t0002g0081a0001c0001t0002g0105others(7): Show | 10 | HG00544.hp2 HG00639.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.517-17660_517-1765 others(8): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638863 | ||||||
chr12:79638863
|
C | CATATAT | 5 | a0001c0001t0004g0036a0001c0003t0002g0155a0002c0002t0001g0188others(2): Show | 5 | HG00423.hp2 HG01169.hp1 NA19003.hp1 others(2): Show |
intron_variant | MODIFIER | c.517-17662_517-1765 others(10): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638863 | ||||||
chr12:79638863
|
C | CATATATA others(1): Show |
12 | a0001c0001t0002g0071a0001c0001t0002g0080a0001c0001t0002g0117others(9): Show | 12 | HG00639.hp2 HG01168.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.517-17664_517-1765 others(12): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638863 | ||||||
chr12:79638863
|
C | CATATATA others(3): Show |
11 | a0001c0001t0002g0042a0001c0001t0002g0048a0001c0001t0002g0049others(8): Show | 11 | HG00438.hp1 HG01099.hp2 HG02602.hp2 others(8): Show |
intron_variant | MODIFIER | c.517-17666_517-1765 others(14): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638863 | ||||||
chr12:79638863
|
C | CATATATA others(5): Show |
6 | a0001c0001t0002g0051a0001c0001t0002g0070a0001c0001t0002g0072others(3): Show | 6 | HG00423.hp1 HG02040.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.517-17668_517-1765 others(16): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638863 | ||||||
chr12:79638863
|
C | CATATATA others(7): Show |
4 | a0001c0001t0002g0074a0001c0001t0002g0114a0001c0001t0002g0123others(1): Show | 4 | HG00741.hp1 HG01069.hp1 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.517-17670_517-1765 others(18): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638863 | ||||||
chr12:79638863
|
C | CATATATA others(9): Show |
1 | a0001c0001t0002g0063 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.517-17672_517-1765 others(20): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638863 | ||||||
chr12:79638863
|
C | CATATATA others(17): Show |
1 | a0001c0001t0002g0057 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.517-17680_517-1765 others(28): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638863 | ||||||
chr12:79638868
|
ATATATAT others(34): Show |
A | 4 | a0002c0002t0001g0172a0002c0002t0001g0211a0002c0002t0001g0212others(1): Show | 4 | HG03139.hp1 NA18906.hp2 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.517-17702_517-1766 others(45): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638868 | ||||||
chr12:79638876
|
A | ATATATAT others(11): Show |
1 | a0001c0001t0002g0153 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.517-17670_517-1766 others(22): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638876 | ||||||
chr12:79638878
|
A | ATATATAT others(9): Show |
1 | a0001c0001t0002g0116 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.517-17672_517-1767 others(20): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638878 | ||||||
chr12:79638878
|
ATATATAT others(31): Show |
A | 3 | a0003c0005t0007g0003a0003c0005t0007g0164a0003c0005t0007g0165 | 3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.517-17709_517-1767 others(42): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638878 | ||||||
chr12:79638880
|
ATATATAT others(17): Show |
A | 1 | a0003c0004t0009g0159 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.517-17697_517-1767 others(28): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638880 | ||||||
chr12:79638880
|
ATATATAT others(18): Show |
A | 2 | a0003c0004t0009g0157a0003c0004t0009g0160 | 2 | HG01074.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.517-17698_517-1767 others(29): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638880 | ||||||
chr12:79638880
|
ATATATAT others(19): Show |
A | 1 | a0003c0004t0009g0158 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.517-17699_517-1767 others(30): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638880 | ||||||
chr12:79638890
|
ATATATAT others(7): Show |
A | 1 | a0003c0004t0022g0166 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.517-17697_517-1768 others(18): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638890 | ||||||
chr12:79638892
|
A | T | 1 | a0001c0003t0014g0162 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.517-17685T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638892 | ||||||
chr12:79638894
|
A | G | 2 | a0001c0001t0002g0107a0001c0001t0002g0111 | 2 | NA18992.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.517-17687T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638894 | ||||||
chr12:79638894
|
A | T | 2 | a0001c0001t0004g0024a0001c0003t0014g0162 | 2 | HG02074.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.517-17687T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638894 | ||||||
chr12:79638896
|
A | ATAT | 5 | a0001c0001t0004g0013a0001c0001t0004g0015a0001c0001t0004g0020others(2): Show | 5 | HG01255.hp1 HG01981.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.517-17690_517-1768 others(7): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638896 | ||||||
chr12:79638896
|
A | ATATATAT others(4): Show |
3 | a0001c0001t0002g0113a0001c0001t0003g0054a0001c0001t0026g0056 | 3 | HG01928.hp2 NA18941.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.517-17690_517-1768 others(15): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638896 | ||||||
chr12:79638896
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0002g0093 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.517-17690_517-1768 others(17): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638896 | ||||||
chr12:79638896
|
A | ATATATAT others(8): Show |
1 | a0001c0003t0027g0135 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.517-17690_517-1768 others(19): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638896 | ||||||
chr12:79638896
|
A | ATATATAT others(9): Show |
1 | a0001c0001t0002g0047 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.517-17690_517-1768 others(20): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638896 | ||||||
chr12:79638896
|
A | ATATATAT others(9): Show |
1 | a0001c0001t0004g0029 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.517-17690_517-1768 others(20): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638896 | ||||||
chr12:79638896
|
A | ATATATAT others(5): Show |
1 | a0001c0003t0031g0122 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.517-17690_517-1768 others(16): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638896 | ||||||
chr12:79638896
|
A | ATATATAT others(3): Show |
1 | a0001c0001t0002g0062 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.517-17690_517-1768 others(14): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638896 | ||||||
chr12:79638896
|
A | ATATATAT others(5): Show |
1 | a0001c0001t0004g0124 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.517-17690_517-1768 others(16): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638896 | ||||||
chr12:79638896
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0004g0128 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.517-17690_517-1768 others(17): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638896 | ||||||
chr12:79638896
|
A | ATATATAT others(3): Show |
2 | a0001c0001t0010g0126a0001c0003t0003g0085 | 2 | HG02071.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.517-17690_517-1768 others(14): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638896 | ||||||
chr12:79638896
|
A | ATATATAT others(5): Show |
1 | a0001c0001t0006g0008 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.517-17690_517-1768 others(16): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638896 | ||||||
chr12:79638896
|
A | ATATATAT others(6): Show |
2 | a0001c0001t0010g0127a0001c0001t0010g0129 | 2 | NA18968.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.517-17690_517-1768 others(17): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638896 | ||||||
chr12:79638896
|
A | ATATATAT others(9): Show |
1 | a0001c0001t0004g0009 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.517-17690_517-1768 others(20): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638896 | ||||||
chr12:79638896
|
A | ATATTT | 5 | a0001c0001t0004g0010a0001c0001t0006g0026a0001c0003t0003g0075others(2): Show | 5 | HG01074.hp1 HG02257.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.517-17690_517-1768 others(9): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638896 | ||||||
chr12:79638896
|
A | ATATTTTT others(5): Show |
1 | a0001c0001t0004g0011 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.517-17690_517-1768 others(16): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638896 | ||||||
chr12:79638896
|
A | ATATTTTT others(12): Show |
1 | a0005c0007t0034g0255 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.517-17690_517-1768 others(23): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638896 | ||||||
chr12:79638896
|
A | T | 5 | a0001c0001t0003g0039a0001c0001t0003g0040a0001c0001t0004g0024others(2): Show | 5 | HG02074.hp2 HG02572.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.517-17689T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638896 | ||||||
chr12:79638896
|
AT | A | 11 | a0002c0002t0001g0181a0002c0002t0001g0185a0002c0002t0001g0193others(8): Show | 11 | HG02622.hp1 HG03225.hp2 HG03491.hp1 others(8): Show |
intron_variant | MODIFIER | c.517-17690delA | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638896 | ||||||
chr12:79638896
|
ATT | A | 7 | a0001c0001t0002g0053a0002c0002t0001g0180a0002c0002t0001g0199others(4): Show | 7 | HG02080.hp2 HG02559.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.517-17691_517-1769 others(6): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638896 | ||||||
chr12:79638896
|
ATTT | A | 14 | a0002c0002t0001g0169a0002c0002t0001g0192a0002c0002t0001g0217others(11): Show | 14 | HG01109.hp1 HG01256.hp1 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.517-17692_517-1769 others(7): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638896 | ||||||
chr12:79638896
|
ATTTTT | A | 9 | a0001c0001t0004g0031a0001c0001t0006g0023a0002c0002t0001g0176others(6): Show | 9 | HG01168.hp2 HG01243.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.517-17694_517-1769 others(9): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638896 | ||||||
chr12:79638896
|
ATTTTTT | A | 5 | a0001c0001t0004g0033a0002c0002t0001g0171a0002c0002t0001g0232others(2): Show | 5 | HG01192.hp1 HG02040.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.517-17695_517-1769 others(10): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638896 | ||||||
chr12:79638896
|
ATTTTTTT others(1): Show |
A | 5 | a0001c0001t0004g0022a0002c0002t0001g0187a0002c0002t0001g0228others(2): Show | 5 | HG01258.hp1 HG02630.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.517-17697_517-1769 others(12): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638896 | ||||||
chr12:79638896
|
ATTTTTTT others(5): Show |
A | 1 | a0002c0002t0001g0219 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.517-17701_517-1769 others(16): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638896 | ||||||
chr12:79638897
|
T | TA | 9 | a0001c0001t0002g0067a0001c0001t0002g0073a0001c0003t0024g0149others(6): Show | 9 | HG01255.hp2 HG02071.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.517-17691_517-1769 others(5): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638897 | ||||||
chr12:79638897
|
T | TATA | 10 | a0001c0001t0004g0018a0001c0003t0003g0078a0002c0002t0001g0190others(7): Show | 10 | HG00621.hp1 HG01975.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.517-17691_517-1769 others(7): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638897 | ||||||
chr12:79638897
|
T | TATATA | 4 | a0001c0003t0003g0086a0001c0003t0003g0089a0002c0002t0001g0197others(1): Show | 4 | HG02300.hp1 NA18969.hp1 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.517-17691_517-1769 others(9): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638897 | ||||||
chr12:79638897
|
T | TATATATA | 9 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0066others(6): Show | 9 | HG00621.hp2 HG01952.hp1 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.517-17691_517-1769 others(11): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638897 | ||||||
chr12:79638897
|
T | TATATATA others(2): Show |
6 | a0001c0001t0002g0043a0001c0001t0002g0044a0001c0001t0002g0052others(3): Show | 6 | HG01081.hp1 HG02523.hp1 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.517-17691_517-1769 others(13): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638897 | ||||||
chr12:79638897
|
T | TATATATA others(4): Show |
5 | a0001c0001t0002g0068a0001c0001t0002g0091a0001c0001t0002g0134others(2): Show | 5 | HG00673.hp1 HG01069.hp2 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.517-17691_517-1769 others(15): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638897 | ||||||
chr12:79638897
|
T | TATATATA others(10): Show |
2 | a0001c0001t0002g0107a0001c0001t0002g0111 | 2 | NA18992.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.517-17691_517-1769 others(21): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638897 | ||||||
chr12:79638897
|
T | TATATATA others(16): Show |
1 | a0001c0001t0002g0045 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.517-17691_517-1769 others(27): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638897 | ||||||
chr12:79638898
|
T | A | 34 | a0001c0001t0002g0042a0001c0001t0002g0048a0001c0001t0002g0055others(31): Show | 34 | HG00423.hp2 HG00544.hp2 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.517-17691A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638898 | ||||||
chr12:79638899
|
T | A | 38 | a0001c0001t0002g0043a0001c0001t0002g0052a0001c0001t0002g0061others(35): Show | 38 | HG00621.hp2 HG00673.hp1 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.517-17692A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638899 | ||||||
chr12:79638900
|
T | A | 26 | a0001c0001t0002g0048a0001c0001t0002g0055a0001c0001t0002g0081others(23): Show | 26 | HG00423.hp2 HG00544.hp2 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.517-17693A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638900 | ||||||
chr12:79638901
|
T | A | 39 | a0001c0001t0002g0073a0001c0001t0002g0134a0002c0002t0001g0169others(36): Show | 39 | HG00621.hp2 HG00673.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.517-17694A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638901 | ||||||
chr12:79638901
|
T | C | 1 | a0001c0001t0002g0053 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.517-17694A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638901 | ||||||
chr12:79638902
|
T | A | 22 | a0001c0001t0002g0048a0001c0001t0004g0125a0001c0003t0023g0148others(19): Show | 22 | HG00544.hp2 HG00639.hp2 HG00673.hp2 others(19): Show |
intron_variant | MODIFIER | c.517-17695A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638902 | ||||||
chr12:79638903
|
T | A | 33 | a0001c0001t0004g0031a0002c0002t0001g0169a0002c0002t0001g0176others(30): Show | 33 | HG01109.hp1 HG01243.hp1 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.517-17696A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638903 | ||||||
chr12:79638904
|
T | A | 23 | a0001c0001t0002g0048a0001c0001t0004g0033a0001c0001t0004g0125others(20): Show | 23 | HG00544.hp2 HG00639.hp2 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.517-17697A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638904 | ||||||
chr12:79638905
|
T | A | 28 | a0001c0001t0004g0021a0002c0002t0001g0176a0002c0002t0001g0178others(25): Show | 28 | HG01109.hp1 HG01257.hp2 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.517-17698A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638905 | ||||||
chr12:79638906
|
T | A | 21 | a0001c0001t0002g0048a0001c0001t0004g0022a0002c0002t0001g0170others(18): Show | 21 | HG01192.hp1 HG01258.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.517-17699A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638906 | ||||||
chr12:79638907
|
T | A | 19 | a0002c0002t0001g0175a0002c0002t0001g0176a0002c0002t0001g0178others(16): Show | 19 | HG01109.hp1 HG01261.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.517-17700A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638907 | ||||||
chr12:79638908
|
T | A | 12 | a0001c0001t0002g0048a0002c0002t0001g0170a0002c0002t0001g0171others(9): Show | 12 | HG01192.hp1 HG01884.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.517-17701A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638908 | ||||||
chr12:79638909
|
T | A | 11 | a0002c0002t0001g0175a0002c0002t0001g0176a0002c0002t0001g0181others(8): Show | 11 | HG01261.hp1 HG02258.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.517-17702A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638909 | ||||||
chr12:79638910
|
T | A | 9 | a0001c0001t0002g0048a0002c0002t0001g0170a0002c0002t0001g0180others(6): Show | 9 | HG02145.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.517-17703A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638910 | ||||||
chr12:79638911
|
T | A | 2 | a0002c0002t0001g0175a0002c0002t0018g0245 | 2 | HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.517-17704A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638911 | ||||||
chr12:79638912
|
T | A | 3 | a0002c0002t0001g0219a0002c0002t0001g0230a0002c0002t0001g0232 | 3 | HG02145.hp2 HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.517-17705A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638912 | ||||||
chr12:79638914
|
T | A | 1 | a0002c0002t0001g0219 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.517-17707A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638914 | ||||||
chr12:79638916
|
T | A | 1 | a0002c0002t0001g0219 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.517-17709A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638916 | ||||||
chr12:79638918
|
T | A | 1 | a0002c0002t0001g0219 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.517-17711A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638918 | ||||||
chr12:79639027
|
C | T | 1 | a0001c0001t0003g0038 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.517-17820G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639027 | ||||||
chr12:79639049
|
G | A | 1 | a0001c0001t0025g0109 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.517-17842C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639049 | ||||||
chr12:79639078
|
A | G | 1 | a0002c0002t0001g0190 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.517-17871T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639078 | ||||||
chr12:79639133
|
G | A | 3 | a0003c0005t0007g0003a0003c0005t0007g0164a0003c0005t0007g0165 | 3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.517-17926C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639133 | ||||||
chr12:79639177
|
C | A | 3 | a0001c0001t0003g0038a0001c0001t0003g0039a0001c0001t0003g0040 | 3 | HG02572.hp2 HG03041.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.517-17970G>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639177 | ||||||
chr12:79639322
|
C | A | 1 | a0002c0002t0001g0187 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.517-18115G>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639322 | ||||||
chr12:79639536
|
A | C | 1 | a0002c0002t0001g0197 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.517-18329T>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639536 | ||||||
chr12:79639567
|
T | C | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-18360A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639567 | ||||||
chr12:79639694
|
G | A | 4 | a0001c0001t0004g0027a0001c0001t0004g0028a0001c0001t0004g0030others(1): Show | 4 | NA18945.hp2 NA18966.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.517-18487C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639694 | ||||||
chr12:79639811
|
A | ATTCCTT | 75 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0001g0172others(72): Show | 75 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.517-18610_517-1860 others(10): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639811 | ||||||
chr12:79639811
|
A | ATTCCTTT others(5): Show |
1 | a0002c0002t0001g0171 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.517-18616_517-1860 others(16): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639811 | ||||||
chr12:79639811
|
ATTCCTT | A | 7 | a0001c0001t0004g0035a0001c0001t0004g0124a0003c0004t0007g0167others(4): Show | 7 | HG01099.hp2 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.517-18610_517-1860 others(10): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639811 | ||||||
chr12:79639831
|
T | C | 1 | a0002c0002t0001g0207 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.517-18624A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639831 | ||||||
chr12:79639831
|
T | TCCTTTTC others(47): Show |
1 | a0002c0002t0001g0242 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.517-18625_517-1862 others(58): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639831 | ||||||
chr12:79639832
|
C | T | 60 | a0001c0001t0002g0004a0001c0001t0002g0042a0001c0001t0002g0043others(57): Show | 60 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.517-18625G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639832 | ||||||
chr12:79639833
|
C | CATTCCTA others(23): Show |
1 | a0002c0002t0005g0183 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.517-18656_517-1862 others(34): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639833 | ||||||
chr12:79639833
|
C | CATTCCTA others(41): Show |
1 | a0002c0002t0018g0245 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.517-18674_517-1862 others(52): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639833 | ||||||
chr12:79639833
|
C | CTTTCCTA others(53): Show |
1 | a0002c0002t0001g0253 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.517-18627_517-1862 others(64): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639833 | ||||||
chr12:79639833
|
C | T | 61 | a0001c0001t0002g0004a0001c0001t0002g0042a0001c0001t0002g0043others(58): Show | 61 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.517-18626G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639833 | ||||||
chr12:79639833
|
CATTCCT | C | 42 | a0001c0003t0002g0155a0001c0003t0003g0005a0001c0003t0003g0046others(39): Show | 42 | HG00544.hp1 HG00621.hp1 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.517-18632_517-1862 others(10): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639833 | ||||||
chr12:79639833
|
CATTCCTA others(5): Show |
C | 7 | a0001c0001t0003g0038a0001c0001t0003g0039a0001c0001t0003g0040others(4): Show | 7 | HG01256.hp1 HG01258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.517-18638_517-1862 others(16): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639833 | ||||||
chr12:79639833
|
CATTCCTA others(11): Show |
C | 43 | a0001c0001t0002g0116a0001c0001t0004g0001a0001c0001t0004g0002others(40): Show | 43 | HG00423.hp2 HG01081.hp2 HG01099.hp2 others(40): Show |
intron_variant | MODIFIER | c.517-18644_517-1862 others(22): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639833 | ||||||
chr12:79639834
|
A | T | 1 | a0002c0002t0001g0215 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.517-18627T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639834 | ||||||
chr12:79639837
|
C | T | 1 | a0002c0002t0001g0215 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.517-18630G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639837 | ||||||
chr12:79639838
|
C | T | 2 | a0001c0001t0002g0113a0001c0001t0003g0054 | 2 | HG01928.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.517-18631G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639838 | ||||||
chr12:79639839
|
T | C | 9 | a0002c0002t0001g0207a0002c0002t0001g0215a0002c0002t0001g0231others(6): Show | 9 | HG01261.hp1 HG02630.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.517-18632A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639839 | ||||||
chr12:79639840
|
A | T | 1 | a0002c0002t0001g0237 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.517-18633T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639840 | ||||||
chr12:79639845
|
T | C | 9 | a0002c0002t0001g0207a0002c0002t0001g0225a0002c0002t0001g0231others(6): Show | 9 | HG01261.hp1 HG02630.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.517-18638A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639845 | ||||||
chr12:79639851
|
T | C | 10 | a0002c0002t0001g0207a0002c0002t0001g0218a0002c0002t0001g0225others(7): Show | 10 | HG01261.hp1 HG02630.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.517-18644A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639851 | ||||||
chr12:79639857
|
T | C | 8 | a0002c0002t0001g0225a0002c0002t0001g0231a0002c0002t0001g0242others(5): Show | 8 | HG01261.hp1 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.517-18650A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639857 | ||||||
chr12:79639863
|
T | C | 8 | a0002c0002t0001g0225a0002c0002t0001g0231a0002c0002t0001g0242others(5): Show | 8 | HG01261.hp1 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.517-18656A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639863 | ||||||
chr12:79639863
|
TATTCCTA others(21): Show |
T | 6 | a0003c0005t0007g0003a0003c0005t0007g0164a0003c0005t0007g0165others(3): Show | 6 | HG02258.hp1 HG02922.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.517-18684_517-1865 others(32): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639863 | ||||||
chr12:79639869
|
T | C | 8 | a0002c0002t0001g0225a0002c0002t0001g0231a0002c0002t0001g0242others(5): Show | 8 | HG01261.hp1 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.517-18662A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639869 | ||||||
chr12:79639869
|
TATTCCTA others(10): Show |
T | 3 | a0001c0001t0002g0081a0005c0007t0033g0256a0005c0007t0034g0255 | 3 | HG02145.hp1 HG02976.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.517-18679_517-1866 others(21): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639869 | ||||||
chr12:79639874
|
CT | C | 35 | a0002c0002t0001g0169a0002c0002t0001g0173a0002c0002t0001g0174others(32): Show | 35 | HG00544.hp2 HG00621.hp2 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.517-18668delA | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639874 | ||||||
chr12:79639874
|
CTATTCCT | C | 5 | a0002c0002t0001g0228a0002c0002t0001g0229a0002c0002t0001g0230others(2): Show | 5 | HG01243.hp1 HG02630.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.517-18674_517-1866 others(11): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639874 | ||||||
chr12:79639875
|
T | C | 8 | a0002c0002t0001g0198a0002c0002t0001g0225a0002c0002t0001g0231others(5): Show | 8 | HG01261.hp1 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.517-18668A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639875 | ||||||
chr12:79639875
|
TATTCCTA others(4): Show |
T | 1 | a0001c0003t0008g0136 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.517-18679_517-1866 others(15): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639875 | ||||||
chr12:79639879
|
C | CCATT | 8 | a0002c0002t0001g0175a0002c0002t0001g0198a0002c0002t0001g0205others(5): Show | 8 | HG02895.hp1 HG03516.hp2 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.517-18673_517-1867 others(8): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639879 | ||||||
chr12:79639879
|
C | CCATTCCA others(212): Show |
1 | a0002c0002t0001g0207 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.517-18673_517-1867 others(223): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639879 | ||||||
chr12:79639879
|
C | CCATTCCA others(262): Show |
1 | a0002c0002t0001g0218 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.517-18673_517-1867 others(273): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639879 | ||||||
chr12:79639879
|
C | CCCATTCC others(57): Show |
1 | a0002c0002t0005g0250 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.517-18673_517-1867 others(68): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639879 | ||||||
chr12:79639879
|
C | CCCATTCC others(64): Show |
2 | a0002c0002t0001g0231a0002c0002t0019g0179 | 2 | HG03209.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.517-18673_517-1867 others(75): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639879 | ||||||
chr12:79639879
|
C | CCCATTCC others(82): Show |
1 | a0002c0002t0001g0225 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.517-18673_517-1867 others(93): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639879 | ||||||
chr12:79639879
|
C | CCCATTCC others(51): Show |
1 | a0002c0002t0005g0252 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.517-18673_517-1867 others(62): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639879 | ||||||
chr12:79639879
|
C | CCCATTCC others(45): Show |
1 | a0002c0002t0005g0249 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.517-18673_517-1867 others(56): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639879 | ||||||
chr12:79639879
|
C | CCCATTCC others(39): Show |
1 | a0002c0002t0005g0243 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.517-18673_517-1867 others(50): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639879 | ||||||
chr12:79639880
|
CT | C | 35 | a0002c0002t0001g0169a0002c0002t0001g0173a0002c0002t0001g0174others(32): Show | 35 | HG00544.hp2 HG00621.hp2 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.517-18674delA | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639880 | ||||||
chr12:79639881
|
T | C | 17 | a0002c0002t0001g0175a0002c0002t0001g0198a0002c0002t0001g0205others(14): Show | 17 | HG01261.hp1 HG02630.hp2 HG02717.hp2 others(14): Show |
intron_variant | MODIFIER | c.517-18674A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639881 | ||||||
chr12:79639881
|
T | TATTCCAT others(3): Show |
4 | a0002c0002t0001g0185a0002c0002t0001g0187a0002c0002t0001g0237others(1): Show | 4 | HG02622.hp1 HG02886.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.517-18684_517-1867 others(14): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639881 | ||||||
chr12:79639881
|
T | TATTCCTA others(24): Show |
1 | a0002c0002t0001g0181 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.517-18675_517-1867 others(35): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639881 | ||||||
chr12:79639881
|
T | TATTCCTA others(22): Show |
1 | a0002c0002t0005g0244 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.517-18675_517-1867 others(33): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639881 | ||||||
chr12:79639881
|
T | TATTCCTA others(32): Show |
1 | a0002c0002t0001g0238 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.517-18675_517-1867 others(43): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639881 | ||||||
chr12:79639881
|
T | TATTCCTA others(23): Show |
1 | a0002c0002t0015g0177 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.517-18675_517-1867 others(34): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639881 | ||||||
chr12:79639881
|
T | TATTCCTA others(28): Show |
1 | a0002c0002t0001g0178 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.517-18675_517-1867 others(39): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639881 | ||||||
chr12:79639881
|
T | TATTCCTA others(33): Show |
1 | a0002c0002t0017g0184 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.517-18675_517-1867 others(44): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639881 | ||||||
chr12:79639881
|
T | TATTCCTA others(39): Show |
1 | a0002c0002t0001g0176 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.517-18675_517-1867 others(50): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639881 | ||||||
chr12:79639881
|
T | TATTCCTA others(45): Show |
1 | a0002c0002t0001g0171 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.517-18675_517-1867 others(56): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639881 | ||||||
chr12:79639881
|
T | TATTCCTA others(55): Show |
1 | a0002c0002t0001g0180 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.517-18675_517-1867 others(66): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639881 | ||||||
chr12:79639881
|
T | TATTCCTA others(63): Show |
1 | a0002c0002t0005g0182 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.517-18675_517-1867 others(74): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639881 | ||||||
chr12:79639881
|
T | TATTCCTA others(70): Show |
2 | a0002c0002t0001g0232a0002c0002t0005g0233 | 2 | HG02055.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.517-18675_517-1867 others(81): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639881 | ||||||
chr12:79639881
|
T | TATTCCTA others(75): Show |
1 | a0002c0002t0005g0246 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.517-18675_517-1867 others(86): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639881 | ||||||
chr12:79639881
|
T | TATTCCTA others(85): Show |
1 | a0002c0002t0005g0251 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.517-18675_517-1867 others(96): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639881 | ||||||
chr12:79639881
|
T | TATTCCTA others(86): Show |
1 | a0002c0002t0005g0248 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.517-18675_517-1867 others(97): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639881 | ||||||
chr12:79639881
|
T | TATTCCTA others(97): Show |
1 | a0002c0002t0001g0170 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.517-18675_517-1867 others(108): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639881 | ||||||
chr12:79639881
|
T | TATTCCTA others(108): Show |
1 | a0002c0002t0005g0247 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.517-18675_517-1867 others(119): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639881 | ||||||
chr12:79639881
|
TATTCC | T | 63 | a0001c0001t0002g0004a0001c0001t0002g0042a0001c0001t0002g0043others(60): Show | 63 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.517-18679_517-1867 others(9): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639881 | ||||||
chr12:79639881
|
TATTCCAT others(3): Show |
T | 1 | a0001c0001t0025g0109 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.517-18684_517-1867 others(14): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639881 | ||||||
chr12:79639911
|
C | CATTCCAT others(8): Show |
1 | a0002c0002t0001g0253 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.517-18705_517-1870 others(19): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639911 | ||||||
chr12:79639911
|
C | T | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-18704G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639911 | ||||||
chr12:79639916
|
T | C | 5 | a0001c0003t0003g0094a0002c0002t0001g0231a0002c0002t0005g0182others(2): Show | 5 | HG00639.hp2 HG02055.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.517-18709A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639916 | ||||||
chr12:79639975
|
TCTAAGCG others(10): Show |
T | 1 | a0002c0002t0005g0247 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.517-18785_517-1876 others(21): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639975 | ||||||
chr12:79639982
|
G | A | 2 | a0003c0005t0007g0164a0003c0005t0007g0165 | 2 | HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.517-18775C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639982 | ||||||
chr12:79640022
|
A | G | 2 | a0002c0002t0001g0217a0002c0002t0001g0222 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.517-18815T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79640022 | ||||||
chr12:79640183
|
C | A | 98 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0001g0171others(95): Show | 98 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.517-18976G>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79640183 | ||||||
chr12:79640191
|
C | T | 1 | a0001c0003t0003g0089 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.517-18984G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79640191 | ||||||
chr12:79640434
|
C | T | 1 | a0003c0004t0009g0159 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.517-19227G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79640434 | ||||||
chr12:79640565
|
ACT | A | 83 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0001g0171others(80): Show | 83 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.517-19360_517-1935 others(6): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79640565 | ||||||
chr12:79640642
|
G | A | 1 | a0001c0001t0002g0069 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.517-19435C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79640642 | ||||||
chr12:79640703
|
T | C | 3 | a0002c0002t0001g0185a0002c0002t0001g0238a0002c0002t0021g0186 | 3 | HG02622.hp1 HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.517-19496A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79640703 | ||||||
chr12:79640738
|
C | T | 4 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(1): Show | 4 | HG01081.hp1 HG01952.hp1 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.517-19531G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79640738 | ||||||
chr12:79640972
|
T | C | 4 | a0003c0004t0009g0157a0003c0004t0009g0158a0003c0004t0009g0159others(1): Show | 4 | HG01074.hp2 HG02896.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.517-19765A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79640972 | ||||||
chr12:79640974
|
G | A | 3 | a0003c0005t0007g0003a0003c0005t0007g0164a0003c0005t0007g0165 | 3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.517-19767C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79640974 | ||||||
chr12:79641257
|
G | A | 4 | a0003c0004t0009g0157a0003c0004t0009g0158a0003c0004t0009g0159others(1): Show | 4 | HG01074.hp2 HG02896.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.517-20050C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79641257 | ||||||
chr12:79641289
|
A | T | 40 | a0002c0002t0001g0169a0002c0002t0001g0173a0002c0002t0001g0174others(37): Show | 40 | HG00544.hp2 HG00621.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.517-20082T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79641289 | ||||||
chr12:79641582
|
C | T | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-20375G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79641582 | ||||||
chr12:79641631
|
G | A | 1 | a0002c0002t0005g0182 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.517-20424C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79641631 | ||||||
chr12:79641697
|
C | A | 255 | a0001c0001t0002g0004a0001c0001t0002g0042a0001c0001t0002g0043others(252): Show | 255 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(252): Show |
intron_variant | MODIFIER | c.517-20490G>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79641697 | ||||||
chr12:79641845
|
CA | C | 54 | a0001c0001t0002g0049a0001c0001t0002g0051a0001c0001t0002g0055others(51): Show | 54 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.517-20639delT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79641845 | ||||||
chr12:79641845
|
CAA | C | 86 | a0001c0001t0002g0004a0001c0001t0002g0042a0001c0001t0002g0043others(83): Show | 86 | HG00438.hp1 HG00438.hp2 HG00639.hp1 others(83): Show |
intron_variant | MODIFIER | c.517-20640_517-2063 others(6): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79641845 | ||||||
chr12:79641845
|
CAAAA | C | 14 | a0002c0002t0001g0169a0002c0002t0001g0174a0002c0002t0001g0191others(11): Show | 14 | HG00673.hp2 HG01074.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.517-20642_517-2063 others(8): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79641845 | ||||||
chr12:79641845
|
CAAAAA | C | 44 | a0002c0002t0001g0170a0002c0002t0001g0173a0002c0002t0001g0188others(41): Show | 44 | HG00544.hp2 HG00621.hp2 HG01243.hp1 others(41): Show |
intron_variant | MODIFIER | c.517-20643_517-2063 others(9): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79641845 | ||||||
chr12:79641845
|
CAAAAAA | C | 37 | a0002c0002t0001g0171a0002c0002t0001g0172a0002c0002t0001g0175others(34): Show | 37 | HG00639.hp2 HG01109.hp1 HG01192.hp1 others(34): Show |
intron_variant | MODIFIER | c.517-20644_517-2063 others(10): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79641845 | ||||||
chr12:79642030
|
C | T | 1 | a0002c0002t0001g0253 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.517-20823G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79642030 | ||||||
chr12:79642167
|
C | T | 4 | a0003c0004t0009g0157a0003c0004t0009g0158a0003c0004t0009g0159others(1): Show | 4 | HG01074.hp2 HG02896.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.517-20960G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79642167 | ||||||
chr12:79642185
|
T | A | 3 | a0003c0005t0007g0003a0003c0005t0007g0164a0003c0005t0007g0165 | 3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.517-20978A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79642185 | ||||||
chr12:79642252
|
T | C | 1 | a0002c0002t0001g0198 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.517-21045A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79642252 | ||||||
chr12:79642378
|
AT | A | 3 | a0004c0006t0011g0239a0004c0006t0011g0240a0004c0006t0011g0241 | 3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.517-21172delA | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79642378 | ||||||
chr12:79642553
|
T | C | 1 | a0001c0001t0004g0033 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.517-21346A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79642553 | ||||||
chr12:79642595
|
G | A | 1 | a0001c0003t0003g0097 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.517-21388C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79642595 | ||||||
chr12:79642742
|
C | T | 1 | a0001c0003t0003g0075 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.517-21535G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79642742 | ||||||
chr12:79642743
|
A | G | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-21536T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79642743 | ||||||
chr12:79642770
|
G | A | 83 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0001g0171others(80): Show | 83 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.517-21563C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79642770 | ||||||
chr12:79642844
|
G | A | 1 | a0002c0002t0001g0219 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.517-21637C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79642844 | ||||||
chr12:79642915
|
GA | G | 3 | a0003c0005t0007g0003a0003c0005t0007g0164a0003c0005t0007g0165 | 3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.517-21709delT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79642915 | ||||||
chr12:79643021
|
T | C | 83 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0001g0171others(80): Show | 83 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.517-21814A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79643021 | ||||||
chr12:79643041
|
C | T | 4 | a0003c0004t0009g0157a0003c0004t0009g0158a0003c0004t0009g0159others(1): Show | 4 | HG01074.hp2 HG02896.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.517-21834G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79643041 | ||||||
chr12:79643137
|
T | C | 3 | a0003c0005t0007g0003a0003c0005t0007g0164a0003c0005t0007g0165 | 3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.517-21930A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79643137 | ||||||
chr12:79643168
|
G | A | 3 | a0003c0005t0007g0003a0003c0005t0007g0164a0003c0005t0007g0165 | 3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.517-21961C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79643168 | ||||||
chr12:79643211
|
A | G | 4 | a0003c0004t0009g0157a0003c0004t0009g0158a0003c0004t0009g0159others(1): Show | 4 | HG01074.hp2 HG02896.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.517-22004T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79643211 | ||||||
chr12:79643445
|
C | A | 1 | a0002c0002t0001g0187 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.517-22238G>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79643445 | ||||||
chr12:79643996
|
G | A | 1 | a0003c0004t0022g0166 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.517-22789C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79643996 | ||||||
chr12:79644350
|
C | T | 5 | a0003c0005t0007g0003a0003c0005t0007g0164a0003c0005t0007g0165others(2): Show | 5 | HG02145.hp1 HG02922.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.517-23143G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79644350 | ||||||
chr12:79644659
|
T | C | 1 | a0002c0002t0001g0187 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.517-23452A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79644659 | ||||||
chr12:79644665
|
TAGCAAAA others(3): Show |
T | 1 | a0001c0001t0002g0116 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.517-23468_517-2345 others(14): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79644665 | ||||||
chr12:79644746
|
C | T | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-23539G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79644746 | ||||||
chr12:79644806
|
G | T | 2 | a0003c0004t0009g0159a0003c0004t0009g0160 | 2 | HG01074.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.517-23599C>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79644806 | ||||||
chr12:79644872
|
G | A | 1 | a0002c0002t0001g0198 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.517-23665C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79644872 | ||||||
chr12:79645007
|
AAAG | A | 5 | a0002c0002t0001g0185a0002c0002t0001g0238a0002c0002t0021g0186others(2): Show | 5 | HG02145.hp1 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.517-23803_517-2380 others(7): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79645007 | ||||||
chr12:79645036
|
C | CCA | 11 | a0001c0001t0002g0107a0001c0001t0002g0111a0001c0003t0003g0005others(8): Show | 11 | HG00621.hp1 HG01074.hp2 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.517-23831_517-2383 others(6): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79645036 | ||||||
chr12:79645036
|
C | CCACA | 4 | a0001c0001t0002g0123a0001c0001t0002g0153a0001c0003t0023g0148others(1): Show | 4 | HG01993.hp2 HG02145.hp1 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.517-23833_517-2383 others(8): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79645036 | ||||||
chr12:79645036
|
C | CCACACAC others(1): Show |
42 | a0002c0002t0001g0169a0002c0002t0001g0172a0002c0002t0001g0173others(39): Show | 42 | HG00544.hp2 HG00621.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.517-23837_517-2383 others(12): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79645036 | ||||||
chr12:79645036
|
C | CCACACAC others(3): Show |
38 | a0001c0001t0004g0031a0001c0001t0004g0033a0001c0001t0004g0125others(35): Show | 38 | HG01109.hp1 HG01192.hp1 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.517-23839_517-2383 others(14): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79645036 | ||||||
chr12:79645036
|
C | CCACACAC others(5): Show |
40 | a0001c0001t0002g0116a0001c0001t0004g0001a0001c0001t0004g0002others(37): Show | 40 | HG00423.hp2 HG00639.hp2 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.517-23841_517-2383 others(16): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79645036 | ||||||
chr12:79645036
|
C | CCACACAC others(7): Show |
7 | a0001c0001t0004g0019a0001c0001t0004g0032a0001c0001t0004g0163others(4): Show | 7 | HG01081.hp2 HG01168.hp2 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.517-23843_517-2383 others(18): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79645036 | ||||||
chr12:79645036
|
C | CCACACAC others(9): Show |
1 | a0001c0001t0004g0024 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.517-23845_517-2383 others(20): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79645036 | ||||||
chr12:79645036
|
C | CCACACAC others(11): Show |
1 | a0002c0002t0001g0175 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.517-23847_517-2383 others(22): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79645036 | ||||||
chr12:79645068
|
A | ACACACAC others(6): Show |
1 | a0001c0001t0004g0156 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.517-23862_517-2386 others(17): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79645068 | ||||||
chr12:79645069
|
A | C | 47 | a0001c0001t0002g0116a0001c0001t0004g0001a0001c0001t0004g0002others(44): Show | 47 | HG00423.hp2 HG01081.hp2 HG01099.hp2 others(44): Show |
intron_variant | MODIFIER | c.517-23862T>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79645069 | ||||||
chr12:79645070
|
A | C | 1 | a0001c0001t0004g0156 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.517-23863T>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79645070 | ||||||
chr12:79645084
|
T | C | 1 | a0002c0002t0001g0219 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.517-23877A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79645084 | ||||||
chr12:79645399
|
G | A | 40 | a0002c0002t0001g0169a0002c0002t0001g0173a0002c0002t0001g0174others(37): Show | 40 | HG00544.hp2 HG00621.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.517-24192C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79645399 | ||||||
chr12:79645524
|
C | G | 2 | a0002c0002t0001g0231a0002c0002t0019g0179 | 2 | HG03209.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.517-24317G>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79645524 | ||||||
chr12:79645562
|
G | A | 2 | a0003c0004t0009g0157a0003c0004t0009g0158 | 2 | HG02896.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.517-24355C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79645562 | ||||||
chr12:79645652
|
T | A | 3 | a0002c0002t0001g0185a0002c0002t0001g0238a0002c0002t0021g0186 | 3 | HG02622.hp1 HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.517-24445A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79645652 | ||||||
chr12:79645673
|
T | C | 3 | a0002c0002t0001g0228a0002c0002t0001g0229a0002c0002t0001g0230 | 3 | HG02630.hp1 HG02717.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.517-24466A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79645673 | ||||||
chr12:79645967
|
T | A | 1 | a0002c0002t0001g0219 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.517-24760A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79645967 | ||||||
chr12:79646062
|
T | C | 5 | a0001c0003t0002g0155a0001c0003t0003g0086a0001c0003t0003g0131others(2): Show | 5 | HG00544.hp1 NA18967.hp1 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.517-24855A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79646062 | ||||||
chr12:79646138
|
ATCTTAAA others(4): Show |
A | 1 | a0002c0002t0001g0198 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.517-24942_517-2493 others(15): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79646138 | ||||||
chr12:79646165
|
C | T | 5 | a0003c0005t0007g0003a0003c0005t0007g0164a0003c0005t0007g0165others(2): Show | 5 | HG02145.hp1 HG02922.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.517-24958G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79646165 | ||||||
chr12:79646314
|
T | C | 2 | a0003c0004t0007g0167a0003c0004t0007g0168 | 2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.517-25107A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79646314 | ||||||
chr12:79646354
|
T | G | 10 | a0001c0001t0004g0015a0001c0001t0004g0019a0001c0001t0004g0020others(7): Show | 10 | HG01081.hp2 HG01109.hp2 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.517-25147A>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79646354 | ||||||
chr12:79646384
|
T | A | 1 | a0001c0003t0023g0148 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.517-25177A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79646384 | ||||||
chr12:79646391
|
T | C | 1 | a0001c0001t0006g0026 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.517-25184A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79646391 | ||||||
chr12:79646506
|
T | C | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-25299A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79646506 | ||||||
chr12:79646552
|
T | C | 3 | a0002c0002t0001g0228a0002c0002t0001g0229a0002c0002t0001g0230 | 3 | HG02630.hp1 HG02717.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.517-25345A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79646552 | ||||||
chr12:79646704
|
G | C | 1 | a0001c0001t0006g0023 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.517-25497C>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79646704 | ||||||
chr12:79646710
|
C | A | 2 | a0001c0003t0003g0145a0001c0003t0024g0149 | 2 | HG02683.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.517-25503G>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79646710 | ||||||
chr12:79646742
|
T | C | 1 | a0002c0002t0001g0229 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.517-25535A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79646742 | ||||||
chr12:79646848
|
C | A | 40 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0009others(37): Show | 40 | HG00423.hp2 HG01081.hp2 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.517-25641G>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79646848 | ||||||
chr12:79646866
|
C | T | 1 | a0002c0002t0001g0253 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.517-25659G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79646866 | ||||||
chr12:79646948
|
C | T | 1 | a0003c0005t0007g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.517-25741G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79646948 | ||||||
chr12:79647173
|
CA | C | 95 | a0001c0001t0004g0013a0002c0002t0001g0169a0002c0002t0001g0170others(92): Show | 95 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.517-25967delT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79647173 | ||||||
chr12:79647243
|
T | C | 1 | a0001c0001t0002g0115 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.517-26036A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79647243 | ||||||
chr12:79647759
|
A | G | 37 | a0002c0002t0001g0170a0002c0002t0001g0171a0002c0002t0001g0172others(34): Show | 37 | HG00639.hp2 HG01109.hp1 HG01192.hp1 others(34): Show |
intron_variant | MODIFIER | c.517-26552T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79647759 | ||||||
chr12:79647812
|
A | G | 3 | a0004c0006t0011g0239a0004c0006t0011g0240a0004c0006t0011g0241 | 3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.517-26605T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79647812 | ||||||
chr12:79647852
|
A | G | 1 | a0001c0001t0032g0006 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.517-26645T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79647852 | ||||||
chr12:79647929
|
A | G | 3 | a0002c0002t0001g0169a0002c0002t0001g0209a0002c0002t0001g0210 | 3 | HG03491.hp1 HG03688.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.517-26722T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79647929 | ||||||
chr12:79648076
|
T | C | 1 | a0002c0002t0001g0181 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.517-26869A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79648076 | ||||||
chr12:79648189
|
A | G | 1 | a0001c0001t0010g0129 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.517-26982T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79648189 | ||||||
chr12:79648195
|
T | A | 2 | a0003c0004t0007g0167a0003c0004t0007g0168 | 2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.517-26988A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79648195 | ||||||
chr12:79648318
|
A | G | 1 | a0001c0003t0003g0079 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.517-27111T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79648318 | ||||||
chr12:79648363
|
G | A | 1 | a0001c0001t0002g0045 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.517-27156C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79648363 | ||||||
chr12:79648468
|
C | T | 3 | a0003c0005t0007g0003a0003c0005t0007g0164a0003c0005t0007g0165 | 3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.517-27261G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79648468 | ||||||
chr12:79648554
|
G | A | 3 | a0003c0005t0007g0003a0003c0005t0007g0164a0003c0005t0007g0165 | 3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.517-27347C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79648554 | ||||||
chr12:79648557
|
G | A | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-27350C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79648557 | ||||||
chr12:79648563
|
G | A | 3 | a0004c0006t0011g0239a0004c0006t0011g0240a0004c0006t0011g0241 | 3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.517-27356C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79648563 | ||||||
chr12:79648617
|
T | TA | 81 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0009others(78): Show | 81 | HG00423.hp2 HG00639.hp2 HG01074.hp2 others(78): Show |
intron_variant | MODIFIER | c.517-27411dupT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79648617 | ||||||
chr12:79648617
|
T | TAA | 16 | a0001c0001t0004g0011a0001c0001t0004g0031a0001c0001t0004g0033others(13): Show | 16 | HG01975.hp2 HG02040.hp2 HG02080.hp1 others(13): Show |
intron_variant | MODIFIER | c.517-27412_517-2741 others(6): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79648617 | ||||||
chr12:79648617
|
T | TAAA | 34 | a0001c0001t0004g0035a0002c0002t0001g0169a0002c0002t0001g0173others(31): Show | 34 | HG00544.hp2 HG00621.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.517-27413_517-2741 others(7): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79648617 | ||||||
chr12:79648617
|
TA | T | 9 | a0001c0001t0002g0057a0001c0001t0002g0071a0001c0001t0002g0092others(6): Show | 9 | HG02145.hp1 HG02451.hp1 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.517-27411delT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79648617 | ||||||
chr12:79648721
|
C | T | 1 | a0003c0004t0022g0166 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.517-27514G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79648721 | ||||||
chr12:79648738
|
A | G | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-27531T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79648738 | ||||||
chr12:79648757
|
C | T | 2 | a0003c0004t0007g0167a0003c0004t0007g0168 | 2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.517-27550G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79648757 | ||||||
chr12:79648793
|
G | GA | 13 | a0001c0001t0002g0071a0002c0002t0001g0169a0002c0002t0001g0187others(10): Show | 13 | HG02071.hp2 HG02145.hp2 HG02300.hp1 others(10): Show |
intron_variant | MODIFIER | c.517-27587dupT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79648793 | ||||||
chr12:79648794
|
A | G | 3 | a0003c0005t0007g0003a0003c0005t0007g0164a0003c0005t0007g0165 | 3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.517-27587T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79648794 | ||||||
chr12:79648804
|
AT | A | 3 | a0003c0004t0022g0166a0003c0005t0007g0164a0003c0005t0007g0165 | 3 | HG02451.hp2 HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.517-27598delA | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79648804 | ||||||
chr12:79648805
|
T | A | 95 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0001g0171others(92): Show | 95 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.517-27598A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79648805 | ||||||
chr12:79648922
|
T | C | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-27715A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79648922 | ||||||
chr12:79649333
|
A | T | 2 | a0003c0005t0007g0164a0003c0005t0007g0165 | 2 | HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.517-28126T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79649333 | ||||||
chr12:79649380
|
C | A | 98 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0001g0171others(95): Show | 98 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.517-28173G>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79649380 | ||||||
chr12:79649596
|
G | A | 3 | a0003c0005t0007g0003a0003c0005t0007g0164a0003c0005t0007g0165 | 3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.517-28389C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79649596 | ||||||
chr12:79649897
|
T | G | 9 | a0003c0004t0009g0157a0003c0004t0009g0158a0003c0004t0009g0159others(6): Show | 9 | HG01074.hp2 HG02145.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.517-28690A>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79649897 | ||||||
chr12:79650015
|
A | T | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-28808T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79650015 | ||||||
chr12:79650147
|
C | G | 9 | a0003c0004t0009g0157a0003c0004t0009g0158a0003c0004t0009g0159others(6): Show | 9 | HG01074.hp2 HG02145.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.517-28940G>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79650147 | ||||||
chr12:79650305
|
G | GC | 3 | a0003c0005t0007g0003a0003c0005t0007g0164a0003c0005t0007g0165 | 3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.517-29099dupG | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79650305 | ||||||
chr12:79650387
|
C | T | 63 | a0001c0001t0002g0004a0001c0001t0002g0042a0001c0001t0002g0043others(60): Show | 63 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.517-29180G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79650387 | ||||||
chr12:79650631
|
C | T | 3 | a0003c0005t0007g0003a0003c0005t0007g0164a0003c0005t0007g0165 | 3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.517-29424G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79650631 | ||||||
chr12:79650714
|
T | TA | 86 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0009others(83): Show | 86 | HG00423.hp2 HG00544.hp2 HG00621.hp2 others(83): Show |
intron_variant | MODIFIER | c.517-29508dupT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79650714 | ||||||
chr12:79650714
|
T | TAA | 17 | a0001c0001t0004g0015a0001c0001t0004g0019a0001c0001t0004g0020others(14): Show | 17 | HG01074.hp2 HG01081.hp2 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.517-29509_517-2950 others(6): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79650714 | ||||||
chr12:79650714
|
TA | T | 63 | a0001c0001t0002g0004a0001c0001t0002g0042a0001c0001t0002g0043others(60): Show | 63 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.517-29508delT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79650714 | ||||||
chr12:79650785
|
A | G | 2 | a0003c0004t0007g0167a0003c0004t0007g0168 | 2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.517-29578T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79650785 | ||||||
chr12:79650825
|
T | C | 1 | a0002c0002t0001g0219 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.517-29618A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79650825 | ||||||
chr12:79651209
|
C | T | 1 | a0001c0001t0004g0031 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.517-30002G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79651209 | ||||||
chr12:79651291
|
G | A | 1 | a0002c0002t0001g0219 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.517-30084C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79651291 | ||||||
chr12:79651397
|
G | A | 2 | a0001c0001t0002g0112a0001c0001t0002g0115 | 2 | HG00438.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.517-30190C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79651397 | ||||||
chr12:79651687
|
G | C | 2 | a0003c0004t0007g0167a0003c0004t0007g0168 | 2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.517-30480C>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79651687 | ||||||
chr12:79651712
|
G | A | 3 | a0003c0005t0007g0003a0003c0005t0007g0164a0003c0005t0007g0165 | 3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.517-30505C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79651712 | ||||||
chr12:79651713
|
G | A | 83 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0001g0171others(80): Show | 83 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.517-30506C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79651713 | ||||||
chr12:79651713
|
G | T | 3 | a0004c0006t0011g0239a0004c0006t0011g0240a0004c0006t0011g0241 | 3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.517-30506C>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79651713 | ||||||
chr12:79651752
|
T | C | 2 | a0003c0005t0007g0164a0003c0005t0007g0165 | 2 | HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.517-30545A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79651752 | ||||||
chr12:79651755
|
G | A | 2 | a0002c0002t0001g0212a0002c0002t0001g0213 | 2 | NA18972.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.517-30548C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79651755 | ||||||
chr12:79651805
|
C | T | 3 | a0003c0005t0007g0003a0003c0005t0007g0164a0003c0005t0007g0165 | 3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.517-30598G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79651805 | ||||||
chr12:79651836
|
G | A | 1 | a0002c0002t0001g0238 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.517-30629C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79651836 | ||||||
chr12:79651981
|
G | A | 1 | a0002c0002t0001g0238 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.517-30774C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79651981 | ||||||
chr12:79652085
|
G | A | 1 | a0001c0001t0002g0113 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.517-30878C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79652085 | ||||||
chr12:79652232
|
G | A | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-31025C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79652232 | ||||||
chr12:79652509
|
G | C | 83 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0001g0171others(80): Show | 83 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.517-31302C>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79652509 | ||||||
chr12:79652544
|
C | T | 83 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0001g0171others(80): Show | 83 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.517-31337G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79652544 | ||||||
chr12:79652576
|
A | C | 2 | a0003c0005t0007g0164a0003c0005t0007g0165 | 2 | HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.517-31369T>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79652576 | ||||||
chr12:79652689
|
T | C | 1 | a0001c0001t0002g0130 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.517-31482A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79652689 | ||||||
chr12:79653041
|
A | G | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-31834T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79653041 | ||||||
chr12:79653057
|
T | G | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-31850A>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79653057 | ||||||
chr12:79653080
|
G | A | 1 | a0003c0005t0007g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.517-31873C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79653080 | ||||||
chr12:79653087
|
G | A | 16 | a0001c0003t0002g0155a0001c0003t0003g0075a0001c0003t0003g0086others(13): Show | 16 | HG00544.hp1 HG02056.hp2 HG03491.hp2 others(13): Show |
intron_variant | MODIFIER | c.517-31880C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79653087 | ||||||
chr12:79653186
|
C | T | 2 | a0002c0002t0001g0178a0002c0002t0001g0253 | 2 | HG01891.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.517-31979G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79653186 | ||||||
chr12:79653287
|
T | C | 138 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0009others(135): Show | 138 | HG00423.hp2 HG00544.hp2 HG00621.hp2 others(135): Show |
intron_variant | MODIFIER | c.517-32080A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79653287 | ||||||
chr12:79653362
|
G | A | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-32155C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79653362 | ||||||
chr12:79653430
|
T | C | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-32223A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79653430 | ||||||
chr12:79653443
|
A | C | 7 | a0001c0003t0003g0075a0001c0003t0003g0133a0001c0003t0003g0144others(4): Show | 7 | HG02056.hp2 NA18957.hp1 NA18960.hp1 others(4): Show |
intron_variant | MODIFIER | c.517-32236T>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79653443 | ||||||
chr12:79653519
|
G | T | 1 | a0002c0002t0001g0187 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.517-32312C>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79653519 | ||||||
chr12:79653543
|
G | A | 1 | a0007c0009t0003g0152 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.517-32336C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79653543 | ||||||
chr12:79653583
|
G | A | 5 | a0002c0002t0001g0191a0002c0002t0001g0196a0002c0002t0001g0197others(2): Show | 5 | HG02027.hp2 HG02071.hp2 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.517-32376C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79653583 | ||||||
chr12:79653605
|
G | A | 1 | a0002c0002t0001g0207 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.517-32398C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79653605 | ||||||
chr12:79653657
|
T | C | 1 | a0001c0003t0003g0254 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.517-32450A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79653657 | ||||||
chr12:79653843
|
T | C | 1 | a0001c0001t0004g0030 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.517-32636A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79653843 | ||||||
chr12:79654015
|
T | A | 1 | a0001c0001t0002g0114 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.517-32808A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79654015 | ||||||
chr12:79654032
|
A | G | 1 | a0001c0001t0032g0006 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.517-32825T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79654032 | ||||||
chr12:79654202
|
G | C | 1 | a0001c0001t0002g0123 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.517-32995C>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79654202 | ||||||
chr12:79654420
|
C | CT | 142 | a0001c0001t0003g0038a0001c0001t0003g0039a0001c0001t0003g0040others(139): Show | 142 | HG00423.hp2 HG00544.hp2 HG00621.hp2 others(139): Show |
intron_variant | MODIFIER | c.517-33214dupA | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79654420 | ||||||
chr12:79654698
|
C | T | 63 | a0001c0001t0002g0004a0001c0001t0002g0042a0001c0001t0002g0043others(60): Show | 63 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.517-33491G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79654698 | ||||||
chr12:79654733
|
G | C | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-33526C>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79654733 | ||||||
chr12:79654774
|
T | C | 3 | a0004c0006t0011g0239a0004c0006t0011g0240a0004c0006t0011g0241 | 3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.517-33567A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79654774 | ||||||
chr12:79654795
|
C | T | 1 | a0001c0003t0003g0082 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.517-33588G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79654795 | ||||||
chr12:79654843
|
T | C | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-33636A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79654843 | ||||||
chr12:79655017
|
G | A | 1 | a0001c0003t0003g0131 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.517-33810C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79655017 | ||||||
chr12:79655042
|
G | A | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-33835C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79655042 | ||||||
chr12:79655070
|
A | G | 3 | a0004c0006t0011g0239a0004c0006t0011g0240a0004c0006t0011g0241 | 3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.517-33863T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79655070 | ||||||
chr12:79655109
|
T | A | 98 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0001g0171others(95): Show | 98 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.517-33902A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79655109 | ||||||
chr12:79655122
|
T | C | 2 | a0002c0002t0001g0231a0002c0002t0019g0179 | 2 | HG03209.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.517-33915A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79655122 | ||||||
chr12:79655245
|
G | T | 1 | a0001c0001t0032g0006 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.517-34038C>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79655245 | ||||||
chr12:79655387
|
C | T | 3 | a0002c0002t0001g0185a0002c0002t0001g0238a0002c0002t0021g0186 | 3 | HG02622.hp1 HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.517-34180G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79655387 | ||||||
chr12:79655410
|
T | C | 1 | a0001c0003t0003g0101 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.517-34203A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79655410 | ||||||
chr12:79655477
|
A | G | 3 | a0002c0002t0001g0228a0002c0002t0001g0229a0002c0002t0001g0230 | 3 | HG02630.hp1 HG02717.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.516+34252T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79655477 | ||||||
chr12:79655611
|
C | T | 3 | a0003c0005t0007g0003a0003c0005t0007g0164a0003c0005t0007g0165 | 3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.516+34118G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79655611 | ||||||
chr12:79655820
|
T | C | 37 | a0002c0002t0001g0170a0002c0002t0001g0171a0002c0002t0001g0172others(34): Show | 37 | HG00639.hp2 HG01109.hp1 HG01192.hp1 others(34): Show |
intron_variant | MODIFIER | c.516+33909A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79655820 | ||||||
chr12:79655966
|
A | G | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.516+33763T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79655966 | ||||||
chr12:79656135
|
C | T | 1 | a0001c0003t0003g0140 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.516+33594G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79656135 | ||||||
chr12:79656185
|
A | G | 83 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0001g0171others(80): Show | 83 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.516+33544T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79656185 | ||||||
chr12:79656420
|
C | T | 10 | a0002c0002t0001g0188a0002c0002t0001g0190a0002c0002t0001g0202others(7): Show | 10 | HG00621.hp2 HG01975.hp2 HG02300.hp1 others(7): Show |
intron_variant | MODIFIER | c.516+33309G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79656420 | ||||||
chr12:79656654
|
T | G | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.516+33075A>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79656654 | ||||||
chr12:79657420
|
T | TA | 7 | a0001c0001t0032g0006a0003c0004t0009g0157a0003c0004t0009g0158others(4): Show | 7 | HG01074.hp2 HG02145.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.516+32308dupT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79657420 | ||||||
chr12:79657421
|
A | T | 35 | a0002c0002t0001g0169a0002c0002t0001g0188a0002c0002t0001g0190others(32): Show | 35 | HG00621.hp2 HG00673.hp2 HG01975.hp2 others(32): Show |
intron_variant | MODIFIER | c.516+32308T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79657421 | ||||||
chr12:79657552
|
G | A | 3 | a0004c0006t0011g0239a0004c0006t0011g0240a0004c0006t0011g0241 | 3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.516+32177C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79657552 | ||||||
chr12:79657562
|
C | T | 1 | a0001c0001t0004g0015 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.516+32167G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79657562 | ||||||
chr12:79657563
|
G | A | 1 | a0001c0003t0013g0095 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.516+32166C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79657563 | ||||||
chr12:79657635
|
C | T | 1 | a0002c0002t0001g0227 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.516+32094G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79657635 | ||||||
chr12:79657663
|
G | A | 2 | a0003c0004t0007g0167a0003c0004t0007g0168 | 2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.516+32066C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79657663 | ||||||
chr12:79657749
|
G | A | 4 | a0002c0002t0001g0230a0003c0005t0007g0003a0003c0005t0007g0164others(1): Show | 4 | HG02922.hp2 HG03453.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.516+31980C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79657749 | ||||||
chr12:79657875
|
T | C | 1 | a0001c0001t0006g0026 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.516+31854A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79657875 | ||||||
chr12:79658020
|
T | C | 3 | a0002c0002t0001g0228a0002c0002t0001g0229a0002c0002t0001g0230 | 3 | HG02630.hp1 HG02717.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.516+31709A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79658020 | ||||||
chr12:79658224
|
T | C | 3 | a0001c0001t0002g0051a0001c0001t0002g0093a0001c0003t0031g0122 | 3 | HG00423.hp1 NA18959.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.516+31505A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79658224 | ||||||
chr12:79658436
|
T | C | 1 | a0005c0007t0033g0256 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.516+31293A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79658436 | ||||||
chr12:79658541
|
A | G | 2 | a0001c0003t0003g0145a0001c0003t0024g0149 | 2 | HG02683.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.516+31188T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79658541 | ||||||
chr12:79658770
|
T | C | 40 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0009others(37): Show | 40 | HG00423.hp2 HG01081.hp2 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.516+30959A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79658770 | ||||||
chr12:79658789
|
G | A | 2 | a0003c0004t0007g0167a0003c0004t0007g0168 | 2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.516+30940C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79658789 | ||||||
chr12:79658792
|
T | C | 1 | a0001c0003t0003g0085 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.516+30937A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79658792 | ||||||
chr12:79658880
|
T | G | 2 | a0002c0002t0005g0183a0002c0002t0017g0184 | 2 | HG01884.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.516+30849A>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79658880 | ||||||
chr12:79659019
|
T | C | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.516+30710A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79659019 | ||||||
chr12:79659043
|
A | G | 2 | a0003c0004t0007g0167a0003c0004t0007g0168 | 2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.516+30686T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79659043 | ||||||
chr12:79659141
|
C | T | 2 | a0001c0001t0002g0073a0001c0001t0026g0056 | 2 | NA18941.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.516+30588G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79659141 | ||||||
chr12:79659158
|
G | A | 2 | a0002c0002t0001g0215a0002c0002t0005g0214 | 2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.516+30571C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79659158 | ||||||
chr12:79659165
|
C | T | 3 | a0001c0001t0003g0038a0001c0001t0003g0039a0001c0001t0003g0040 | 3 | HG02572.hp2 HG03041.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.516+30564G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79659165 | ||||||
chr12:79659166
|
G | A | 4 | a0003c0004t0009g0157a0003c0004t0009g0158a0003c0004t0009g0159others(1): Show | 4 | HG01074.hp2 HG02896.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.516+30563C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79659166 | ||||||
chr12:79659169
|
C | T | 2 | a0002c0002t0001g0176a0002c0002t0001g0180 | 2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.516+30560G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79659169 | ||||||
chr12:79659218
|
C | A | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.516+30511G>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79659218 | ||||||
chr12:79659255
|
C | T | 4 | a0003c0004t0009g0157a0003c0004t0009g0158a0003c0004t0009g0159others(1): Show | 4 | HG01074.hp2 HG02896.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.516+30474G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79659255 | ||||||
chr12:79659297
|
GA | G | 5 | a0002c0002t0001g0219a0003c0004t0009g0157a0003c0004t0009g0158others(2): Show | 5 | HG01074.hp2 HG02896.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.516+30431delT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79659297 | ||||||
chr12:79659311
|
T | C | 1 | a0002c0002t0001g0208 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.516+30418A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79659311 | ||||||
chr12:79659442
|
T | C | 3 | a0003c0005t0007g0003a0003c0005t0007g0164a0003c0005t0007g0165 | 3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.516+30287A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79659442 | ||||||
chr12:79660170
|
T | C | 1 | a0007c0009t0003g0152 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.516+29559A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79660170 | ||||||
chr12:79660185
|
A | T | 3 | a0003c0005t0007g0003a0003c0005t0007g0164a0003c0005t0007g0165 | 3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.516+29544T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79660185 | ||||||
chr12:79660254
|
A | G | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.516+29475T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79660254 | ||||||
chr12:79660358
|
C | T | 2 | a0002c0002t0001g0215a0002c0002t0005g0214 | 2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.516+29371G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79660358 | ||||||
chr12:79660540
|
C | T | 1 | a0001c0001t0002g0042 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.516+29189G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79660540 | ||||||
chr12:79660583
|
C | CT | 48 | a0001c0001t0002g0055a0001c0001t0002g0116a0001c0001t0003g0054others(45): Show | 48 | HG00544.hp2 HG00621.hp2 HG00673.hp2 others(45): Show |
intron_variant | MODIFIER | c.516+29145dupA | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79660583 | ||||||
chr12:79660583
|
CT | C | 5 | a0001c0001t0002g0115a0001c0001t0002g0123a0002c0002t0005g0251others(2): Show | 5 | HG01993.hp2 HG02145.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.516+29145delA | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79660583 | ||||||
chr12:79660906
|
A | G | 1 | a0001c0001t0004g0024 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.516+28823T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79660906 | ||||||
chr12:79660911
|
T | C | 9 | a0003c0004t0009g0157a0003c0004t0009g0158a0003c0004t0009g0159others(6): Show | 9 | HG01074.hp2 HG02145.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.516+28818A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79660911 | ||||||
chr12:79661040
|
G | C | 1 | a0001c0003t0003g0078 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.516+28689C>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79661040 | ||||||
chr12:79661148
|
C | A | 2 | a0001c0003t0003g0079a0001c0003t0003g0102 | 2 | HG01981.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.516+28581G>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79661148 | ||||||
chr12:79661206
|
G | A | 1 | a0004c0006t0011g0240 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.516+28523C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79661206 | ||||||
chr12:79661248
|
C | CA | 40 | a0001c0001t0002g0072a0001c0001t0002g0153a0001c0001t0004g0024others(37): Show | 40 | HG00423.hp2 HG00639.hp2 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.516+28480dupT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79661248 | ||||||
chr12:79661248
|
C | CAA | 9 | a0001c0001t0002g0116a0001c0003t0003g0079a0002c0002t0001g0178others(6): Show | 9 | HG01891.hp2 HG01981.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.516+28479_516+2848 others(6): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79661248 | ||||||
chr12:79661248
|
CA | C | 5 | a0001c0001t0002g0047a0001c0001t0002g0074a0001c0001t0004g0128others(2): Show | 5 | HG01069.hp1 HG01069.hp2 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.516+28480delT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79661248 | ||||||
chr12:79661347
|
T | C | 30 | a0001c0001t0002g0119a0001c0003t0002g0155a0001c0003t0003g0075others(27): Show | 30 | HG00544.hp1 HG02056.hp2 HG02071.hp1 others(27): Show |
intron_variant | MODIFIER | c.516+28382A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79661347 | ||||||
chr12:79661355
|
A | G | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.516+28374T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79661355 | ||||||
chr12:79661403
|
C | A | 3 | a0003c0005t0007g0003a0003c0005t0007g0164a0003c0005t0007g0165 | 3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.516+28326G>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79661403 | ||||||
chr12:79661452
|
A | G | 98 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0001g0171others(95): Show | 98 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.516+28277T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79661452 | ||||||
chr12:79661900
|
G | C | 3 | a0004c0006t0011g0239a0004c0006t0011g0240a0004c0006t0011g0241 | 3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.516+27829C>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79661900 | ||||||
chr12:79661986
|
A | G | 98 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0001g0171others(95): Show | 98 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.516+27743T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79661986 | ||||||
chr12:79662191
|
A | G | 98 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0001g0171others(95): Show | 98 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.516+27538T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79662191 | ||||||
chr12:79662201
|
C | CA | 65 | a0001c0001t0002g0081a0001c0001t0002g0116a0001c0001t0006g0034others(62): Show | 65 | HG00544.hp2 HG00673.hp2 HG01074.hp2 others(62): Show |
intron_variant | MODIFIER | c.516+27527dupT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79662201 | ||||||
chr12:79662201
|
C | CAA | 30 | a0002c0002t0001g0171a0002c0002t0001g0185a0002c0002t0001g0188others(27): Show | 30 | HG00621.hp2 HG00639.hp2 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.516+27526_516+2752 others(6): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79662201 | ||||||
chr12:79662201
|
CA | C | 9 | a0001c0001t0002g0004a0001c0001t0003g0038a0001c0001t0003g0039others(6): Show | 9 | HG01257.hp1 HG02040.hp2 HG02080.hp1 others(6): Show |
intron_variant | MODIFIER | c.516+27527delT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79662201 | ||||||
chr12:79662246
|
C | T | 2 | a0002c0002t0001g0215a0002c0002t0005g0214 | 2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.516+27483G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79662246 | ||||||
chr12:79662334
|
C | G | 1 | a0003c0005t0007g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.516+27395G>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79662334 | ||||||
chr12:79662453
|
C | A | 1 | a0001c0001t0002g0073 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.516+27276G>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79662453 | ||||||
chr12:79662523
|
A | G | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.516+27206T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79662523 | ||||||
chr12:79662648
|
A | G | 3 | a0004c0006t0011g0239a0004c0006t0011g0240a0004c0006t0011g0241 | 3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.516+27081T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79662648 | ||||||
chr12:79662761
|
T | C | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.516+26968A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79662761 | ||||||
chr12:79662813
|
T | G | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.516+26916A>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79662813 | ||||||
chr12:79663355
|
T | C | 28 | a0002c0002t0001g0170a0002c0002t0001g0171a0002c0002t0001g0175others(25): Show | 28 | HG00639.hp2 HG01109.hp1 HG01192.hp1 others(25): Show |
intron_variant | MODIFIER | c.516+26374A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79663355 | ||||||
chr12:79663583
|
C | A | 3 | a0003c0005t0007g0003a0003c0005t0007g0164a0003c0005t0007g0165 | 3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.516+26146G>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79663583 | ||||||
chr12:79663601
|
A | T | 3 | a0003c0005t0007g0003a0003c0005t0007g0164a0003c0005t0007g0165 | 3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.516+26128T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79663601 | ||||||
chr12:79663770
|
C | CA | 7 | a0001c0001t0002g0081a0001c0001t0002g0118a0001c0001t0004g0001others(4): Show | 7 | HG01168.hp1 HG02559.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.516+25958dupT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79663770 | ||||||
chr12:79664009
|
T | C | 5 | a0003c0005t0007g0003a0003c0005t0007g0164a0003c0005t0007g0165others(2): Show | 5 | HG02145.hp1 HG02922.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.516+25720A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79664009 | ||||||
chr12:79664131
|
T | A | 1 | a0002c0002t0001g0175 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.516+25598A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79664131 | ||||||
chr12:79664132
|
C | T | 1 | a0002c0002t0001g0175 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.516+25597G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79664132 | ||||||
chr12:79664137
|
A | C | 3 | a0004c0006t0011g0239a0004c0006t0011g0240a0004c0006t0011g0241 | 3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.516+25592T>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79664137 | ||||||
chr12:79664365
|
C | G | 2 | a0001c0001t0002g0119a0001c0003t0027g0135 | 2 | HG03831.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.516+25364G>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79664365 | ||||||
chr12:79664411
|
C | G | 1 | a0003c0004t0022g0166 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.516+25318G>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79664411 | ||||||
chr12:79664554
|
G | C | 3 | a0004c0006t0011g0239a0004c0006t0011g0240a0004c0006t0011g0241 | 3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.516+25175C>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79664554 | ||||||
chr12:79664658
|
C | CG | 107 | a0001c0001t0002g0004a0001c0001t0002g0042a0001c0001t0002g0043others(104): Show | 107 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.516+25070dupC | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79664658 | ||||||
chr12:79664658
|
C | CGG | 49 | a0001c0001t0002g0052a0001c0001t0002g0053a0001c0001t0004g0036others(46): Show | 49 | HG00423.hp2 HG00621.hp2 HG01256.hp1 others(46): Show |
intron_variant | MODIFIER | c.516+25069_516+2507 others(6): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79664658 | ||||||
chr12:79664658
|
C | CGGG | 25 | a0002c0002t0001g0171a0002c0002t0001g0180a0002c0002t0001g0181others(22): Show | 25 | HG00544.hp2 HG00639.hp2 HG00673.hp2 others(22): Show |
intron_variant | MODIFIER | c.516+25068_516+2507 others(7): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79664658 | ||||||
chr12:79664658
|
C | CGGGG | 16 | a0002c0002t0001g0170a0002c0002t0001g0175a0002c0002t0001g0176others(13): Show | 16 | HG01261.hp1 HG01891.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.516+25067_516+2507 others(8): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79664658 | ||||||
chr12:79664658
|
C | CGGGGGGG others(3): Show |
1 | a0003c0005t0007g0165 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.516+25070_516+2507 others(14): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79664658 | ||||||
chr12:79664658
|
C | CGGGGGGG others(4): Show |
2 | a0003c0005t0007g0003a0003c0005t0007g0164 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.516+25070_516+2507 others(15): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79664658 | ||||||
chr12:79664662
|
G | T | 2 | a0003c0004t0007g0167a0003c0004t0007g0168 | 2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.516+25067C>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79664662 | ||||||
chr12:79665417
|
T | C | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.516+24312A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79665417 | ||||||
chr12:79665498
|
A | G | 40 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0009others(37): Show | 40 | HG00423.hp2 HG01081.hp2 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.516+24231T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79665498 | ||||||
chr12:79665541
|
A | T | 2 | a0003c0004t0007g0167a0003c0004t0007g0168 | 2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.516+24188T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79665541 | ||||||
chr12:79665651
|
T | C | 3 | a0004c0006t0011g0239a0004c0006t0011g0240a0004c0006t0011g0241 | 3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.516+24078A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79665651 | ||||||
chr12:79665661
|
A | G | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.516+24068T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79665661 | ||||||
chr12:79665679
|
T | C | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.516+24050A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79665679 | ||||||
chr12:79665848
|
T | C | 1 | a0001c0001t0002g0076 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.516+23881A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79665848 | ||||||
chr12:79665850
|
T | C | 3 | a0004c0006t0011g0239a0004c0006t0011g0240a0004c0006t0011g0241 | 3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.516+23879A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79665850 | ||||||
chr12:79665994
|
C | G | 3 | a0003c0005t0007g0003a0003c0005t0007g0164a0003c0005t0007g0165 | 3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.516+23735G>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79665994 | ||||||
chr12:79666125
|
A | G | 1 | a0001c0003t0003g0143 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.516+23604T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79666125 | ||||||
chr12:79666700
|
T | C | 1 | a0001c0001t0003g0040 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.516+23029A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79666700 | ||||||
chr12:79666818
|
A | G | 83 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0001g0171others(80): Show | 83 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.516+22911T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79666818 | ||||||
chr12:79666833
|
T | C | 2 | a0002c0002t0001g0226a0002c0002t0012g0221 | 2 | NA18946.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.516+22896A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79666833 | ||||||
chr12:79666985
|
T | C | 2 | a0001c0001t0004g0009a0001c0001t0004g0010 | 2 | HG02257.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.516+22744A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79666985 | ||||||
chr12:79667295
|
C | G | 1 | a0003c0004t0022g0166 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.516+22434G>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79667295 | ||||||
chr12:79667299
|
G | T | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.516+22430C>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79667299 | ||||||
chr12:79667506
|
CTG | C | 4 | a0003c0004t0009g0157a0003c0004t0009g0158a0003c0004t0009g0159others(1): Show | 4 | HG01074.hp2 HG02896.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.516+22221_516+2222 others(6): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79667506 | ||||||
chr12:79667576
|
T | C | 3 | a0004c0006t0011g0239a0004c0006t0011g0240a0004c0006t0011g0241 | 3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.516+22153A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79667576 | ||||||
chr12:79667601
|
A | C | 1 | a0002c0002t0012g0189 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.516+22128T>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79667601 | ||||||
chr12:79667632
|
T | G | 2 | a0001c0001t0010g0127a0002c0002t0005g0251 | 2 | HG02896.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.516+22097A>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79667632 | ||||||
chr12:79667713
|
G | A | 2 | a0003c0004t0007g0167a0003c0004t0007g0168 | 2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.516+22016C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79667713 | ||||||
chr12:79667846
|
T | C | 2 | a0001c0001t0002g0077a0001c0001t0002g0134 | 2 | HG00673.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.516+21883A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79667846 | ||||||
chr12:79667863
|
G | A | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.516+21866C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79667863 | ||||||
chr12:79667925
|
C | T | 1 | a0001c0001t0004g0036 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.516+21804G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79667925 | ||||||
chr12:79667942
|
T | C | 3 | a0004c0006t0011g0239a0004c0006t0011g0240a0004c0006t0011g0241 | 3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.516+21787A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79667942 | ||||||
chr12:79668081
|
T | C | 6 | a0001c0001t0004g0027a0001c0001t0004g0028a0001c0001t0004g0029others(3): Show | 6 | NA18942.hp1 NA18945.hp2 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.516+21648A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79668081 | ||||||
chr12:79668104
|
T | C | 3 | a0003c0005t0007g0003a0003c0005t0007g0164a0003c0005t0007g0165 | 3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.516+21625A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79668104 | ||||||
chr12:79668376
|
T | C | 98 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0001g0171others(95): Show | 98 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.516+21353A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79668376 | ||||||
chr12:79668450
|
A | G | 238 | a0001c0001t0002g0004a0001c0001t0002g0042a0001c0001t0002g0043others(235): Show | 238 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(235): Show |
intron_variant | MODIFIER | c.516+21279T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79668450 | ||||||
chr12:79668458
|
C | G | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.516+21271G>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79668458 | ||||||
chr12:79668545
|
T | C | 40 | a0002c0002t0001g0169a0002c0002t0001g0173a0002c0002t0001g0174others(37): Show | 40 | HG00544.hp2 HG00621.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.516+21184A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79668545 | ||||||
chr12:79668581
|
C | T | 1 | a0001c0001t0004g0125 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.516+21148G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79668581 | ||||||
chr12:79668765
|
T | TGCTCACC | 4 | a0001c0001t0004g0128a0001c0001t0010g0126a0001c0001t0010g0127others(1): Show | 4 | NA18941.hp1 NA18968.hp2 NA18987.hp2 others(1): Show |
intron_variant | MODIFIER | c.516+20957_516+2096 others(11): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79668765 | ||||||
chr12:79669231
|
G | C | 1 | a0001c0001t0032g0006 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.516+20498C>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79669231 | ||||||
chr12:79669271
|
T | C | 11 | a0002c0002t0001g0242a0002c0002t0005g0243a0002c0002t0005g0244others(8): Show | 11 | HG01109.hp1 HG01261.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.516+20458A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79669271 | ||||||
chr12:79669335
|
A | G | 1 | a0005c0007t0034g0255 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.516+20394T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79669335 | ||||||
chr12:79669494
|
A | T | 4 | a0003c0004t0009g0157a0003c0004t0009g0158a0003c0004t0009g0159others(1): Show | 4 | HG01074.hp2 HG02896.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.516+20235T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79669494 | ||||||
chr12:79669517
|
C | T | 3 | a0001c0001t0010g0126a0001c0001t0010g0127a0001c0001t0010g0129 | 3 | NA18968.hp2 NA18987.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.516+20212G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79669517 | ||||||
chr12:79670058
|
G | A | 1 | a0001c0001t0004g0011 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.516+19671C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79670058 | ||||||
chr12:79670212
|
A | C | 1 | a0001c0003t0003g0089 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.516+19517T>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79670212 | ||||||
chr12:79670355
|
C | A | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.516+19374G>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79670355 | ||||||
chr12:79670465
|
GA | G | 28 | a0001c0001t0002g0051a0001c0003t0031g0122a0002c0002t0001g0170others(25): Show | 28 | HG00423.hp1 HG00639.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.516+19263delT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79670465 | ||||||
chr12:79670586
|
A | T | 98 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0001g0171others(95): Show | 98 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.516+19143T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79670586 | ||||||
chr12:79670702
|
G | A | 1 | a0001c0001t0002g0080 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.516+19027C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79670702 | ||||||
chr12:79670732
|
A | T | 1 | a0003c0004t0022g0166 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.516+18997T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79670732 | ||||||
chr12:79670873
|
AG | A | 3 | a0002c0002t0001g0218a0005c0007t0033g0256a0005c0007t0034g0255 | 3 | HG02145.hp1 HG02976.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.516+18855delC | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79670873 | ||||||
chr12:79670877
|
G | T | 95 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0001g0171others(92): Show | 95 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.516+18852C>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79670877 | ||||||
chr12:79671053
|
C | G | 1 | a0001c0001t0002g0088 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.516+18676G>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79671053 | ||||||
chr12:79671086
|
T | C | 5 | a0003c0005t0007g0003a0003c0005t0007g0164a0003c0005t0007g0165others(2): Show | 5 | HG02145.hp1 HG02922.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.516+18643A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79671086 | ||||||
chr12:79671123
|
T | TA | 9 | a0001c0001t0002g0081a0002c0002t0001g0218a0002c0002t0001g0219others(6): Show | 9 | HG01074.hp2 HG02145.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.516+18605dupT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79671123 | ||||||
chr12:79671123
|
TA | T | 9 | a0001c0001t0002g0004a0001c0001t0002g0049a0001c0001t0002g0050others(6): Show | 9 | HG01074.hp1 HG01256.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.516+18605delT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79671123 | ||||||
chr12:79671160
|
C | T | 83 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0001g0171others(80): Show | 83 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.516+18569G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79671160 | ||||||
chr12:79671406
|
T | C | 2 | a0003c0004t0007g0167a0003c0004t0007g0168 | 2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.516+18323A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79671406 | ||||||
chr12:79671418
|
G | A | 1 | a0001c0001t0002g0047 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.516+18311C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79671418 | ||||||
chr12:79671536
|
T | G | 40 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0009others(37): Show | 40 | HG00423.hp2 HG01081.hp2 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.516+18193A>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79671536 | ||||||
chr12:79671636
|
C | T | 4 | a0003c0004t0009g0157a0003c0004t0009g0158a0003c0004t0009g0159others(1): Show | 4 | HG01074.hp2 HG02896.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.516+18093G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79671636 | ||||||
chr12:79671699
|
T | C | 1 | a0001c0003t0003g0104 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.516+18030A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79671699 | ||||||
chr12:79671726
|
A | G | 7 | a0001c0003t0002g0155a0001c0003t0003g0086a0001c0003t0003g0131others(4): Show | 7 | HG00544.hp1 NA18967.hp1 NA18969.hp1 others(4): Show |
intron_variant | MODIFIER | c.516+18003T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79671726 | ||||||
chr12:79672005
|
T | C | 3 | a0002c0002t0001g0228a0002c0002t0001g0229a0002c0002t0001g0230 | 3 | HG02630.hp1 HG02717.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.516+17724A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79672005 | ||||||
chr12:79672095
|
G | A | 2 | a0003c0004t0007g0167a0003c0004t0007g0168 | 2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.516+17634C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79672095 | ||||||
chr12:79672142
|
C | T | 1 | a0001c0001t0029g0120 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.516+17587G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79672142 | ||||||
chr12:79672165
|
C | T | 4 | a0003c0004t0009g0157a0003c0004t0009g0158a0003c0004t0009g0159others(1): Show | 4 | HG01074.hp2 HG02896.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.516+17564G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79672165 | ||||||
chr12:79672177
|
G | A | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.516+17552C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79672177 | ||||||
chr12:79672299
|
A | T | 3 | a0003c0005t0007g0003a0003c0005t0007g0164a0003c0005t0007g0165 | 3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.516+17430T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79672299 | ||||||
chr12:79672400
|
C | T | 98 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0001g0171others(95): Show | 98 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.516+17329G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79672400 | ||||||
chr12:79672657
|
TTGTG | T | 2 | a0003c0004t0007g0167a0003c0004t0007g0168 | 2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.516+17068_516+1707 others(8): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79672657 | ||||||
chr12:79672918
|
A | G | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.516+16811T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79672918 | ||||||
chr12:79673213
|
G | A | 4 | a0003c0004t0009g0157a0003c0004t0009g0158a0003c0004t0009g0159others(1): Show | 4 | HG01074.hp2 HG02896.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.516+16516C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79673213 | ||||||
chr12:79673218
|
T | C | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.516+16511A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79673218 | ||||||
chr12:79673358
|
C | T | 1 | a0002c0002t0001g0211 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.516+16371G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79673358 | ||||||
chr12:79673507
|
A | G | 1 | a0001c0001t0002g0119 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.516+16222T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79673507 | ||||||
chr12:79673802
|
C | T | 1 | a0001c0001t0002g0048 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.516+15927G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79673802 | ||||||
chr12:79674250
|
C | T | 4 | a0003c0004t0009g0157a0003c0004t0009g0158a0003c0004t0009g0159others(1): Show | 4 | HG01074.hp2 HG02896.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.516+15479G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79674250 | ||||||
chr12:79674388
|
TA | T | 58 | a0001c0001t0004g0013a0002c0002t0001g0169a0002c0002t0001g0173others(55): Show | 58 | HG00544.hp2 HG00621.hp2 HG00673.hp2 others(55): Show |
intron_variant | MODIFIER | c.516+15340delT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79674388 | ||||||
chr12:79674389
|
A | T | 1 | a0001c0003t0003g0005 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.516+15340T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79674389 | ||||||
chr12:79674423
|
C | T | 1 | a0003c0005t0007g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.516+15306G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79674423 | ||||||
chr12:79674575
|
G | C | 1 | a0001c0001t0032g0006 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.516+15154C>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79674575 | ||||||
chr12:79674729
|
C | T | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.516+15000G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79674729 | ||||||
chr12:79674783
|
C | T | 1 | a0001c0003t0003g0085 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.516+14946G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79674783 | ||||||
chr12:79674909
|
C | T | 7 | a0001c0001t0002g0119a0001c0003t0008g0136a0001c0003t0008g0137others(4): Show | 7 | HG03831.hp2 NA18946.hp1 NA18959.hp1 others(4): Show |
intron_variant | MODIFIER | c.516+14820G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79674909 | ||||||
chr12:79675001
|
G | A | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.516+14728C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79675001 | ||||||
chr12:79675115
|
T | C | 255 | a0001c0001t0002g0004a0001c0001t0002g0042a0001c0001t0002g0043others(252): Show | 255 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(252): Show |
intron_variant | MODIFIER | c.516+14614A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79675115 | ||||||
chr12:79675452
|
C | T | 1 | a0003c0004t0022g0166 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.516+14277G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79675452 | ||||||
chr12:79675619
|
C | T | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.516+14110G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79675619 | ||||||
chr12:79675882
|
T | C | 3 | a0003c0005t0007g0003a0003c0005t0007g0164a0003c0005t0007g0165 | 3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.516+13847A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79675882 | ||||||
chr12:79675990
|
G | A | 6 | a0003c0004t0009g0157a0003c0004t0009g0158a0003c0004t0009g0159others(3): Show | 6 | HG01074.hp2 HG02145.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.516+13739C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79675990 | ||||||
chr12:79676023
|
C | T | 1 | a0002c0002t0001g0175 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.516+13706G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79676023 | ||||||
chr12:79676030
|
A | G | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.516+13699T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79676030 | ||||||
chr12:79676236
|
T | A | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.516+13493A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79676236 | ||||||
chr12:79676240
|
G | C | 1 | a0001c0003t0008g0151 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.516+13489C>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79676240 | ||||||
chr12:79676380
|
T | G | 1 | a0005c0007t0033g0256 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.516+13349A>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79676380 | ||||||
chr12:79676434
|
TTAAA | T | 2 | a0001c0001t0002g0043a0001c0001t0002g0130 | 2 | NA19080.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.516+13291_516+1329 others(8): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79676434 | ||||||
chr12:79676505
|
A | G | 2 | a0003c0004t0007g0167a0003c0004t0007g0168 | 2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.516+13224T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79676505 | ||||||
chr12:79676659
|
C | T | 1 | a0001c0003t0028g0084 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.516+13070G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79676659 | ||||||
chr12:79676754
|
C | T | 2 | a0001c0003t0003g0046a0001c0003t0003g0083 | 2 | HG01069.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.516+12975G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79676754 | ||||||
chr12:79676758
|
C | T | 4 | a0003c0004t0009g0157a0003c0004t0009g0158a0003c0004t0009g0159others(1): Show | 4 | HG01074.hp2 HG02896.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.516+12971G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79676758 | ||||||
chr12:79677022
|
T | C | 1 | a0007c0009t0003g0152 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.516+12707A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79677022 | ||||||
chr12:79677157
|
A | T | 1 | a0001c0001t0002g0043 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.516+12572T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79677157 | ||||||
chr12:79677216
|
A | G | 3 | a0004c0006t0011g0239a0004c0006t0011g0240a0004c0006t0011g0241 | 3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.516+12513T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79677216 | ||||||
chr12:79677419
|
T | C | 1 | a0001c0001t0002g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.516+12310A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79677419 | ||||||
chr12:79677861
|
A | C | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.516+11868T>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79677861 | ||||||
chr12:79677873
|
A | G | 4 | a0003c0004t0009g0157a0003c0004t0009g0158a0003c0004t0009g0159others(1): Show | 4 | HG01074.hp2 HG02896.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.516+11856T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79677873 | ||||||
chr12:79677911
|
C | T | 1 | a0001c0001t0002g0047 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.516+11818G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79677911 | ||||||
chr12:79677944
|
T | C | 4 | a0003c0004t0009g0157a0003c0004t0009g0158a0003c0004t0009g0159others(1): Show | 4 | HG01074.hp2 HG02896.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.516+11785A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79677944 | ||||||
chr12:79678072
|
T | C | 4 | a0001c0001t0004g0031a0001c0001t0004g0033a0001c0001t0004g0125others(1): Show | 4 | HG02040.hp2 HG02080.hp1 NA18952.hp2 others(1): Show |
intron_variant | MODIFIER | c.516+11657A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79678072 | ||||||
chr12:79678175
|
G | A | 82 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0001g0171others(79): Show | 82 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.516+11554C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79678175 | ||||||
chr12:79678357
|
C | T | 1 | a0001c0003t0003g0082 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.516+11372G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79678357 | ||||||
chr12:79678609
|
A | C | 1 | a0001c0003t0014g0162 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.516+11120T>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79678609 | ||||||
chr12:79678663
|
C | G | 3 | a0003c0005t0007g0003a0003c0005t0007g0164a0003c0005t0007g0165 | 3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.516+11066G>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79678663 | ||||||
chr12:79678853
|
G | A | 3 | a0003c0005t0007g0003a0003c0005t0007g0164a0003c0005t0007g0165 | 3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.516+10876C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79678853 | ||||||
chr12:79678868
|
A | AT | 142 | a0001c0001t0002g0088a0001c0001t0002g0090a0001c0001t0002g0091others(139): Show | 142 | HG00423.hp2 HG00544.hp1 HG00639.hp1 others(139): Show |
intron_variant | MODIFIER | c.516+10860dupA | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79678868 | ||||||
chr12:79678868
|
A | ATT | 101 | a0001c0001t0002g0004a0001c0001t0002g0043a0001c0001t0002g0044others(98): Show | 101 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.516+10859_516+1086 others(6): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79678868 | ||||||
chr12:79679052
|
T | C | 4 | a0003c0004t0009g0157a0003c0004t0009g0158a0003c0004t0009g0159others(1): Show | 4 | HG01074.hp2 HG02896.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.516+10677A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79679052 | ||||||
chr12:79679088
|
C | A | 1 | a0007c0009t0003g0152 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.516+10641G>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79679088 | ||||||
chr12:79679613
|
A | C | 1 | a0001c0001t0004g0011 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.516+10116T>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79679613 | ||||||
chr12:79679622
|
C | A | 2 | a0002c0002t0001g0170a0002c0002t0001g0171 | 2 | HG01192.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.516+10107G>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79679622 | ||||||
chr12:79679623
|
C | T | 4 | a0003c0004t0009g0157a0003c0004t0009g0158a0003c0004t0009g0159others(1): Show | 4 | HG01074.hp2 HG02896.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.516+10106G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79679623 | ||||||
chr12:79679634
|
A | G | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.516+10095T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79679634 | ||||||
chr12:79679897
|
G | A | 1 | a0001c0001t0004g0033 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.516+9832C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79679897 | ||||||
chr12:79679918
|
A | G | 41 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0009others(38): Show | 41 | HG00423.hp2 HG01081.hp2 HG01099.hp2 others(38): Show |
intron_variant | MODIFIER | c.516+9811T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79679918 | ||||||
chr12:79679960
|
A | G | 1 | a0002c0002t0001g0238 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.516+9769T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79679960 | ||||||
chr12:79679995
|
T | C | 3 | a0004c0006t0011g0239a0004c0006t0011g0240a0004c0006t0011g0241 | 3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.516+9734A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79679995 | ||||||
chr12:79680014
|
G | A | 14 | a0001c0001t0002g0042a0001c0001t0002g0044a0001c0001t0002g0045others(11): Show | 14 | HG00438.hp1 HG01928.hp2 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.516+9715C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79680014 | ||||||
chr12:79680020
|
C | T | 31 | a0002c0002t0001g0170a0002c0002t0001g0171a0002c0002t0001g0175others(28): Show | 31 | HG00639.hp2 HG01109.hp1 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.516+9709G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79680020 | ||||||
chr12:79680094
|
A | G | 1 | a0002c0002t0001g0219 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.516+9635T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79680094 | ||||||
chr12:79680127
|
A | G | 82 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0001g0171others(79): Show | 82 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.516+9602T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79680127 | ||||||
chr12:79680274
|
C | T | 1 | a0002c0002t0001g0219 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.516+9455G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79680274 | ||||||
chr12:79680305
|
C | G | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.516+9424G>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79680305 | ||||||
chr12:79680405
|
A | G | 5 | a0003c0005t0007g0003a0003c0005t0007g0164a0003c0005t0007g0165others(2): Show | 5 | HG02145.hp1 HG02922.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.516+9324T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79680405 | ||||||
chr12:79680941
|
C | T | 1 | a0002c0002t0001g0172 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.516+8788G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79680941 | ||||||
chr12:79681028
|
T | C | 1 | a0001c0001t0032g0006 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.516+8701A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79681028 | ||||||
chr12:79681042
|
G | C | 1 | a0002c0002t0001g0219 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.516+8687C>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79681042 | ||||||
chr12:79681045
|
G | C | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.516+8684C>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79681045 | ||||||
chr12:79681126
|
A | AGGGAGGG others(3): Show |
2 | a0003c0004t0007g0167a0003c0004t0007g0168 | 2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.516+8593_516+8602d others(12): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79681126 | ||||||
chr12:79681137
|
G | A | 1 | a0001c0001t0032g0006 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.516+8592C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79681137 | ||||||
chr12:79681145
|
TGGGGA | T | 3 | a0001c0001t0003g0038a0001c0001t0003g0039a0001c0001t0003g0040 | 3 | HG02572.hp2 HG03041.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.516+8579_516+8583d others(7): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79681145 | ||||||
chr12:79681688
|
A | C | 1 | a0001c0003t0003g0046 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.516+8041T>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79681688 | ||||||
chr12:79681695
|
C | CT | 4 | a0002c0002t0001g0242a0002c0002t0005g0243a0003c0004t0007g0167others(1): Show | 4 | HG01243.hp1 HG02630.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.516+8033dupA | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79681695 | ||||||
chr12:79681789
|
G | A | 1 | a0001c0001t0006g0034 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.516+7940C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79681789 | ||||||
chr12:79681981
|
T | C | 2 | a0001c0001t0002g0117a0001c0001t0002g0118 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.516+7748A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79681981 | ||||||
chr12:79682161
|
A | G | 5 | a0003c0005t0007g0003a0003c0005t0007g0164a0003c0005t0007g0165others(2): Show | 5 | HG02145.hp1 HG02922.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.516+7568T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79682161 | ||||||
chr12:79682221
|
G | A | 2 | a0001c0001t0002g0117a0001c0001t0002g0118 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.516+7508C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79682221 | ||||||
chr12:79682286
|
G | A | 1 | a0001c0001t0002g0119 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.516+7443C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79682286 | ||||||
chr12:79682504
|
T | C | 1 | a0002c0002t0001g0236 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.516+7225A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79682504 | ||||||
chr12:79682638
|
T | C | 83 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0001g0171others(80): Show | 83 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.516+7091A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79682638 | ||||||
chr12:79682946
|
A | G | 2 | a0001c0001t0004g0009a0001c0001t0004g0010 | 2 | HG02257.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.516+6783T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79682946 | ||||||
chr12:79683593
|
C | G | 3 | a0003c0005t0007g0003a0003c0005t0007g0164a0003c0005t0007g0165 | 3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.516+6136G>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79683593 | ||||||
chr12:79683605
|
C | CT | 5 | a0002c0002t0001g0173a0002c0002t0001g0174a0003c0004t0009g0157others(2): Show | 5 | HG02896.hp1 HG02976.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.516+6123dupA | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79683605 | ||||||
chr12:79683605
|
CT | C | 11 | a0001c0001t0002g0121a0001c0001t0004g0035a0001c0001t0010g0129others(8): Show | 11 | HG01074.hp2 HG01099.hp2 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.516+6123delA | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79683605 | ||||||
chr12:79683621
|
T | A | 1 | a0001c0001t0002g0154 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.516+6108A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79683621 | ||||||
chr12:79683692
|
G | A | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.516+6037C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79683692 | ||||||
chr12:79683752
|
C | A | 1 | a0001c0003t0031g0122 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.516+5977G>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79683752 | ||||||
chr12:79683895
|
G | A | 4 | a0001c0001t0004g0128a0001c0001t0010g0126a0001c0001t0010g0127others(1): Show | 4 | NA18941.hp1 NA18968.hp2 NA18987.hp2 others(1): Show |
intron_variant | MODIFIER | c.516+5834C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79683895 | ||||||
chr12:79683930
|
G | A | 2 | a0003c0004t0007g0167a0003c0004t0007g0168 | 2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.516+5799C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79683930 | ||||||
chr12:79684084
|
C | T | 2 | a0001c0001t0002g0044a0001c0001t0002g0045 | 2 | HG02523.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.516+5645G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79684084 | ||||||
chr12:79684183
|
A | T | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.516+5546T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79684183 | ||||||
chr12:79684292
|
TA | T | 9 | a0002c0002t0001g0172a0003c0004t0009g0157a0003c0004t0009g0158others(6): Show | 9 | HG01074.hp2 HG02145.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.516+5436delT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79684292 | ||||||
chr12:79684303
|
T | A | 1 | a0001c0001t0002g0123 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.516+5426A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79684303 | ||||||
chr12:79684448
|
T | C | 1 | a0003c0004t0022g0166 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.516+5281A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79684448 | ||||||
chr12:79684540
|
G | A | 1 | a0001c0003t0002g0155 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.516+5189C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79684540 | ||||||
chr12:79684614
|
C | T | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.516+5115G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79684614 | ||||||
chr12:79684636
|
G | GA | 4 | a0002c0002t0001g0223a0002c0002t0001g0224a0002c0002t0001g0225others(1): Show | 4 | HG00621.hp2 HG04115.hp2 NA18946.hp2 others(1): Show |
intron_variant | MODIFIER | c.516+5092dupT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79684636 | ||||||
chr12:79684644
|
C | G | 97 | a0002c0002t0001g0170a0002c0002t0001g0171a0002c0002t0001g0172others(94): Show | 97 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(94): Show |
intron_variant | MODIFIER | c.516+5085G>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79684644 | ||||||
chr12:79684856
|
G | A | 1 | a0001c0001t0004g0036 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.516+4873C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79684856 | ||||||
chr12:79685182
|
A | G | 2 | a0002c0002t0001g0170a0002c0002t0001g0171 | 2 | HG01192.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.516+4547T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79685182 | ||||||
chr12:79685268
|
G | A | 141 | a0001c0001t0003g0038a0001c0001t0003g0039a0001c0001t0003g0040others(138): Show | 141 | HG00423.hp2 HG00544.hp2 HG00621.hp2 others(138): Show |
intron_variant | MODIFIER | c.516+4461C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79685268 | ||||||
chr12:79685304
|
T | C | 1 | a0003c0004t0022g0166 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.516+4425A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79685304 | ||||||
chr12:79685350
|
A | G | 1 | a0001c0001t0002g0043 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.516+4379T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79685350 | ||||||
chr12:79685525
|
G | A | 1 | a0004c0006t0011g0241 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.516+4204C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79685525 | ||||||
chr12:79685546
|
T | C | 1 | a0002c0002t0001g0227 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.516+4183A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79685546 | ||||||
chr12:79685803
|
G | A | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.516+3926C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79685803 | ||||||
chr12:79685961
|
C | A | 1 | a0003c0004t0022g0166 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.516+3768G>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79685961 | ||||||
chr12:79686441
|
C | G | 3 | a0003c0005t0007g0003a0003c0005t0007g0164a0003c0005t0007g0165 | 3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.516+3288G>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79686441 | ||||||
chr12:79686463
|
T | C | 1 | a0002c0002t0001g0230 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.516+3266A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79686463 | ||||||
chr12:79686782
|
T | C | 1 | a0003c0004t0022g0166 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.516+2947A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79686782 | ||||||
chr12:79686811
|
A | G | 1 | a0001c0001t0002g0042 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.516+2918T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79686811 | ||||||
chr12:79686838
|
T | C | 83 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0001g0171others(80): Show | 83 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.516+2891A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79686838 | ||||||
chr12:79687174
|
G | A | 3 | a0003c0005t0007g0003a0003c0005t0007g0164a0003c0005t0007g0165 | 3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.516+2555C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79687174 | ||||||
chr12:79687214
|
C | T | 1 | a0001c0003t0013g0041 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.516+2515G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79687214 | ||||||
chr12:79687301
|
A | G | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.516+2428T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79687301 | ||||||
chr12:79687391
|
A | T | 1 | a0003c0004t0022g0166 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.516+2338T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79687391 | ||||||
chr12:79687409
|
A | C | 1 | a0001c0001t0006g0008 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.516+2320T>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79687409 | ||||||
chr12:79687589
|
T | C | 3 | a0004c0006t0011g0239a0004c0006t0011g0240a0004c0006t0011g0241 | 3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.516+2140A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79687589 | ||||||
chr12:79687601
|
T | C | 3 | a0002c0002t0001g0228a0002c0002t0001g0229a0002c0002t0001g0230 | 3 | HG02630.hp1 HG02717.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.516+2128A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79687601 | ||||||
chr12:79687615
|
T | A | 1 | a0002c0002t0001g0231 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.516+2114A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79687615 | ||||||
chr12:79687846
|
G | A | 1 | a0001c0001t0004g0037 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.516+1883C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79687846 | ||||||
chr12:79688029
|
C | T | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.516+1700G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79688029 | ||||||
chr12:79688200
|
C | A | 1 | a0002c0002t0001g0232 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.516+1529G>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79688200 | ||||||
chr12:79688227
|
T | TA | 41 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0009others(38): Show | 41 | HG00423.hp2 HG01081.hp2 HG01099.hp2 others(38): Show |
intron_variant | MODIFIER | c.516+1501dupT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79688227 | ||||||
chr12:79688321
|
A | G | 3 | a0001c0001t0003g0038a0001c0001t0003g0039a0001c0001t0003g0040 | 3 | HG02572.hp2 HG03041.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.516+1408T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79688321 | ||||||
chr12:79688467
|
T | TA | 28 | a0001c0001t0002g0130a0001c0001t0002g0134a0001c0001t0002g0153others(25): Show | 28 | HG00544.hp1 HG00673.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.516+1261dupT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79688467 | ||||||
chr12:79688467
|
TA | T | 113 | a0001c0001t0002g0004a0001c0001t0004g0001a0001c0001t0004g0002others(110): Show | 113 | HG00423.hp2 HG00544.hp2 HG00621.hp2 others(110): Show |
intron_variant | MODIFIER | c.516+1261delT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79688467 | ||||||
chr12:79688708
|
T | A | 4 | a0003c0004t0009g0157a0003c0004t0009g0158a0003c0004t0009g0159others(1): Show | 4 | HG01074.hp2 HG02896.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.516+1021A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79688708 | ||||||
chr12:79688935
|
C | G | 1 | a0005c0007t0034g0255 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.516+794G>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79688935 | ||||||
chr12:79688985
|
T | TAAC | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.516+741_516+743dup others(3): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79688985 | ||||||
chr12:79689126
|
G | A | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.516+603C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79689126 | ||||||
chr12:79689355
|
TGTC | T | 3 | a0003c0005t0007g0003a0003c0005t0007g0164a0003c0005t0007g0165 | 3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.516+371_516+373del others(3): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79689355 | ||||||
chr12:79689397
|
ACAGCCAA others(16): Show |
A | 2 | a0001c0003t0003g0161a0001c0003t0014g0162 | 2 | NA18942.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.516+309_516+331del others(23): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79689397 | ||||||
chr12:79689512
|
C | G | 82 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0001g0171others(79): Show | 82 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.516+217G>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79689512 | ||||||
chr12:79689524
|
G | A | 1 | a0002c0002t0001g0238 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.516+205C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79689524 | ||||||
chr12:79689644
|
C | T | 2 | a0001c0001t0004g0001a0001c0001t0004g0002 | 2 | HG02559.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.516+85G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79689644 | ||||||
chr12:79690423
|
G | A | 11 | a0002c0002t0001g0242a0002c0002t0005g0243a0002c0002t0005g0244others(8): Show | 11 | HG01109.hp1 HG01261.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.-147-32C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 1/6 | chr12 | 79690423 | ||||||
chr12:79690570
|
C | A | 1 | a0001c0001t0004g0163 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-147-179G>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 1/6 | chr12 | 79690570 | ||||||
chr12:79690596
|
G | A | 1 | a0002c0002t0001g0253 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-147-205C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 1/6 | chr12 | 79690596 | ||||||
chr12:79690648
|
A | G | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-148+224T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 1/6 | chr12 | 79690648 | ||||||
chr12:79690683
|
T | C | 92 | a0002c0002t0001g0169a0002c0002t0001g0170a0002c0002t0001g0171others(89): Show | 92 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(89): Show |
intron_variant | MODIFIER | c.-148+189A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 1/6 | chr12 | 79690683 | ||||||
chr12:79690726
|
T | C | 1 | a0001c0003t0003g0254 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-148+146A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 1/6 | chr12 | 79690726 | ||||||
chr12:79690729
|
A | G | 2 | a0005c0007t0033g0256a0005c0007t0034g0255 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-148+143T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 1/6 | chr12 | 79690729 |