geneid | 10130 |
---|---|
ensemblid | ENSG00000143870.13 |
hgncid | 30168 |
symbol | PDIA6 |
name | protein disulfide isomerase family A member 6 |
refseq_nuc | NM_005742.4 |
refseq_prot | NP_005733.1 |
ensembl_nuc | ENST00000272227.8 |
ensembl_prot | ENSP00000272227.4 |
mane_status | MANE Select |
chr | chr2 |
start | 10783391 |
end | 10812785 |
strand | - |
ver | v1.2 |
region | chr2:10783391-10812785 |
region5000 | chr2:10778391-10817785 |
regionname0 | PDIA6_chr2_10783391_10812785 |
regionname5000 | PDIA6_chr2_10778391_10817785 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 440 | 255 | 85 | 52 | 81 | 10 | 25 | 63 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
a0002 | 0/0 | 440 | 83 | 7 | 19 | 43 | 2 | 12 | 31 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
a0003 | 0/0 | 440 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
a0004 | 0/0 | 440 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
a0005 | 0/0 | 440 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1323 | 167 | 51 | 31 | 69 | 5 | 9 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
c0002 | 0/0 | 1323 | 79 | 7 | 17 | 41 | 2 | 12 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
c0003 | 0/0 | 1323 | 34 | 3 | 13 | 11 | 3 | 4 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
c0004 | 0/0 | 1323 | 31 | 28 | 3 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
c0005 | 0/0 | 1323 | 21 | 2 | 4 | 1 | 2 | 12 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
c0006 | 0/0 | 1323 | 2 | 0 | 2 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
c0007 | 0/0 | 1323 | 2 | 1 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
c0008 | 0/0 | 1323 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
c0009 | 0/0 | 1323 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
c0010 | 0/0 | 1323 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
c0011 | 0/0 | 1323 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
c0012 | 0/0 | 1323 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
c0013 | 0/0 | 1323 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 957 | 242 | 37 | 55 | 115 | 9 | 24 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
t0002 | 0/0 | 957 | 29 | 26 | 3 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
t0003 | 0/0 | 957 | 21 | 2 | 4 | 1 | 2 | 12 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
t0004 | 0/0 | 956 | 17 | 13 | 4 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
t0005 | 0/0 | 957 | 11 | 9 | 2 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
t0006 | 0/0 | 958 | 5 | 0 | 0 | 3 | 0 | 2 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
t0007 | 0/0 | 957 | 4 | 0 | 0 | 4 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
t0008 | 0/0 | 957 | 3 | 0 | 3 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
t0009 | 0/0 | 957 | 2 | 2 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
t0010 | 0/0 | 957 | 2 | 2 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
t0011 | 0/0 | 957 | 1 | 0 | 0 | 0 | 1 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
t0012 | 0/0 | 957 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
t0013 | 0/0 | 957 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
t0014 | 0/0 | 957 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
t0015 | 0/0 | 958 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
t0016 | 0/0 | 957 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 6 | 0 | 4 | 0 | 0 | 2 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0002 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0003 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0004 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0005 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0006 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0007 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0008 | 1/0 | 3 | 2 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0009 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0010 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0011 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0018 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0021 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0107 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1323 | 167 | 51 | 31 | 69 | 5 | 9 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
a0001c0003 | 0/0 | 1323 | 34 | 3 | 13 | 11 | 3 | 4 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
a0001c0004 | 0/0 | 1323 | 31 | 28 | 3 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
a0001c0005 | 0/0 | 1323 | 21 | 2 | 4 | 1 | 2 | 12 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
a0001c0012 | 0/0 | 1323 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
a0001c0013 | 0/0 | 1323 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
a0002c0002 | 0/0 | 1323 | 79 | 7 | 17 | 41 | 2 | 12 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
a0002c0006 | 0/0 | 1323 | 2 | 0 | 2 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
a0002c0009 | 0/0 | 1323 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
a0002c0011 | 0/0 | 1323 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
a0003c0007 | 0/0 | 1323 | 2 | 1 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
a0004c0008 | 0/0 | 1323 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
a0005c0010 | 0/0 | 1323 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 2279 | 135 | 26 | 25 | 69 | 4 | 9 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
a0001c0001t0004 | 0/0 | 2278 | 17 | 13 | 4 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
a0001c0001t0005 | 0/0 | 2279 | 9 | 8 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
a0001c0001t0009 | 0/0 | 2279 | 2 | 2 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
a0001c0001t0011 | 0/0 | 2279 | 1 | 0 | 0 | 0 | 1 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
a0001c0001t0012 | 0/0 | 2279 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
a0001c0001t0013 | 0/0 | 2279 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
a0001c0001t0014 | 0/0 | 2279 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
a0001c0003t0001 | 0/0 | 2279 | 28 | 3 | 10 | 10 | 3 | 2 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
a0001c0003t0006 | 0/0 | 2280 | 2 | 0 | 0 | 0 | 0 | 2 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
a0001c0003t0008 | 0/0 | 2279 | 3 | 0 | 3 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
a0001c0003t0016 | 0/0 | 2279 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
a0001c0004t0001 | 0/0 | 2279 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
a0001c0004t0002 | 0/0 | 2279 | 27 | 25 | 2 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
a0001c0004t0010 | 0/0 | 2279 | 2 | 2 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
a0001c0004t0015 | 0/0 | 2280 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
a0001c0005t0003 | 0/0 | 2279 | 21 | 2 | 4 | 1 | 2 | 12 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
a0001c0012t0002 | 0/0 | 2279 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
a0001c0013t0002 | 0/0 | 2279 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
a0002c0002t0001 | 0/0 | 2279 | 72 | 7 | 17 | 34 | 2 | 12 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
a0002c0002t0006 | 0/0 | 2280 | 3 | 0 | 0 | 3 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
a0002c0002t0007 | 0/0 | 2279 | 4 | 0 | 0 | 4 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
a0002c0006t0001 | 0/0 | 2279 | 2 | 0 | 2 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
a0002c0009t0001 | 0/0 | 2279 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
a0002c0011t0001 | 0/0 | 2279 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
a0003c0007t0005 | 0/0 | 2279 | 2 | 1 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
a0004c0008t0001 | 0/0 | 2279 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
a0005c0010t0001 | 0/0 | 2279 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | copy fasta | chr2 | 10778391 | 10817785 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 6 | 0 | 4 | 0 | 0 | 2 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0003 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0004 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0005 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0006 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0007 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0008 | 1/0 | 3 | 2 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0107 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0004g0002 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0004g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0004g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0004g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0004g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0004g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0004g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0004g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0004g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0004g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0004g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0004g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0004g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0005g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0005g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0005g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0005g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0005g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0005g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0005g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0005g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0009g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0009g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0011g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0012g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0013g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0001t0014g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0003t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0003t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0003t0001g0021 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0003t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0003t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0003t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0003t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0003t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0003t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0003t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0003t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0003t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0003t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0003t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0003t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0003t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0003t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0003t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0003t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0003t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0003t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0003t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0003t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0003t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0003t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0003t0006g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0003t0006g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0003t0008g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0003t0008g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0003t0016g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0004t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0004t0002g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0004t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0004t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0004t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0004t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0004t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0004t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0004t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0004t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0004t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0004t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0004t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0004t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0004t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0004t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0004t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0004t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0004t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0004t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0004t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0004t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0004t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0004t0002g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0004t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0004t0002g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0004t0002g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0004t0010g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0004t0010g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0004t0015g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0005t0003g0011 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0005t0003g0018 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0005t0003g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0005t0003g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0005t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0005t0003g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0005t0003g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0005t0003g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0005t0003g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0005t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0005t0003g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0005t0003g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0005t0003g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0005t0003g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0005t0003g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0005t0003g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0005t0003g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0005t0003g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0012t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0001c0013t0002g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0006g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0006g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0006g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0007g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0007g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0007g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0002t0007g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0006t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0006t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0009t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0002c0011t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0003c0007t0005g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0003c0007t0005g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0004c0008t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
a0005c0010t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00280 | hp1 | a0001 | c0005 | t0003 | g0011 | EUR | FIN | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | FIN | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG00323 | hp1 | a0001 | c0003 | t0001 | g0245 | EUR | FIN | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG00323 | hp2 | a0001 | c0001 | t0011 | g0066 | EUR | FIN | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | CHS | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG00408 | hp2 | a0002 | c0002 | t0001 | g0167 | EAS | CHS | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG00558 | hp1 | a0002 | c0002 | t0001 | g0168 | EAS | CHS | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG00597 | hp2 | a0001 | c0003 | t0001 | g0235 | EAS | CHS | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG00609 | hp2 | a0001 | c0003 | t0001 | g0234 | EAS | CHS | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG00639 | hp1 | a0001 | c0004 | t0002 | g0288 | AMR | PUR | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG00639 | hp2 | a0001 | c0013 | t0002 | g0278 | AMR | PUR | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG00642 | hp2 | a0002 | c0002 | t0001 | g0184 | AMR | PUR | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG00733 | hp1 | a0001 | c0003 | t0001 | g0249 | AMR | PUR | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG00735 | hp1 | a0002 | c0006 | t0001 | g0253 | AMR | PUR | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG00735 | hp2 | a0002 | c0002 | t0001 | g0185 | AMR | PUR | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG00741 | hp1 | a0002 | c0002 | t0001 | g0200 | AMR | PUR | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG01069 | hp2 | a0001 | c0003 | t0008 | g0022 | AMR | PUR | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG01070 | hp2 | a0001 | c0003 | t0001 | g0204 | AMR | PUR | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG01071 | hp1 | a0001 | c0003 | t0008 | g0022 | AMR | PUR | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG01081 | hp1 | a0002 | c0002 | t0001 | g0177 | AMR | PUR | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG01081 | hp2 | a0002 | c0002 | t0001 | g0156 | AMR | PUR | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG01099 | hp1 | a0001 | c0005 | t0003 | g0018 | AMR | PUR | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG01099 | hp2 | a0001 | c0003 | t0001 | g0236 | AMR | PUR | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG01106 | hp2 | a0002 | c0002 | t0001 | g0163 | AMR | PUR | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG01109 | hp1 | a0001 | c0001 | t0004 | g0043 | AMR | PUR | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG01167 | hp2 | a0001 | c0001 | t0004 | g0041 | AMR | PUR | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG01169 | hp1 | a0001 | c0001 | t0004 | g0040 | AMR | PUR | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG01175 | hp1 | a0002 | c0002 | t0001 | g0221 | AMR | PUR | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG01175 | hp2 | a0001 | c0004 | t0001 | g0279 | AMR | PUR | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG01192 | hp1 | a0002 | c0002 | t0001 | g0225 | AMR | PUR | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG01192 | hp2 | a0001 | c0003 | t0008 | g0252 | AMR | PUR | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG01243 | hp1 | a0001 | c0003 | t0001 | g0250 | AMR | PUR | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG01243 | hp2 | a0001 | c0001 | t0004 | g0045 | AMR | PUR | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG01255 | hp2 | a0001 | c0003 | t0001 | g0248 | AMR | CLM | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG01256 | hp2 | a0001 | c0003 | t0001 | g0019 | AMR | CLM | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG01258 | hp1 | a0002 | c0002 | t0001 | g0159 | AMR | CLM | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG01258 | hp2 | a0001 | c0003 | t0001 | g0019 | AMR | CLM | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG01261 | hp1 | a0001 | c0004 | t0002 | g0284 | AMR | CLM | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | CLM | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG01433 | hp1 | a0002 | c0006 | t0001 | g0215 | AMR | CLM | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG01433 | hp2 | a0001 | c0005 | t0003 | g0147 | AMR | CLM | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG01496 | hp2 | a0003 | c0007 | t0005 | g0063 | AMR | CLM | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG01515 | hp1 | a0001 | c0003 | t0001 | g0021 | EUR | IBS | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG01515 | hp2 | a0002 | c0002 | t0001 | g0189 | EUR | IBS | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0084 | EUR | IBS | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG01517 | hp2 | a0001 | c0003 | t0001 | g0021 | EUR | IBS | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG01884 | hp1 | a0001 | c0004 | t0002 | g0282 | AFR | ACB | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG01884 | hp2 | a0001 | c0001 | t0009 | g0257 | AFR | ACB | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG01928 | hp1 | a0002 | c0002 | t0001 | g0216 | AMR | PEL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG01928 | hp2 | a0001 | c0001 | t0012 | g0098 | AMR | PEL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG01934 | hp1 | a0001 | c0005 | t0003 | g0255 | AMR | PEL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG01934 | hp2 | a0002 | c0002 | t0001 | g0187 | AMR | PEL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG01943 | hp1 | a0001 | c0005 | t0003 | g0138 | AMR | PEL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG01975 | hp1 | a0002 | c0002 | t0001 | g0188 | AMR | PEL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG01975 | hp2 | a0001 | c0003 | t0001 | g0237 | AMR | PEL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG01978 | hp1 | a0002 | c0002 | t0001 | g0176 | AMR | PEL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG01978 | hp2 | a0001 | c0001 | t0005 | g0031 | AMR | PEL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG01981 | hp2 | a0001 | c0003 | t0001 | g0243 | AMR | PEL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02040 | hp1 | a0002 | c0002 | t0007 | g0155 | EAS | KHV | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02040 | hp2 | a0002 | c0002 | t0001 | g0223 | EAS | KHV | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02055 | hp1 | a0001 | c0004 | t0002 | g0287 | AFR | ACB | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02055 | hp2 | a0001 | c0001 | t0013 | g0289 | AFR | ACB | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02071 | hp2 | a0002 | c0011 | t0001 | g0024 | EAS | KHV | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02074 | hp1 | a0001 | c0003 | t0001 | g0239 | EAS | KHV | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02074 | hp2 | a0002 | c0002 | t0001 | g0207 | EAS | KHV | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | KHV | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02083 | hp2 | a0002 | c0002 | t0001 | g0175 | EAS | KHV | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02132 | hp1 | a0002 | c0002 | t0001 | g0217 | EAS | KHV | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02145 | hp1 | a0001 | c0001 | t0004 | g0038 | AFR | ACB | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PEL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02155 | hp1 | a0002 | c0002 | t0001 | g0165 | EAS | CDX | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | CDX | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CDX | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02165 | hp2 | a0002 | c0002 | t0001 | g0166 | EAS | CDX | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02257 | hp2 | a0001 | c0004 | t0002 | g0271 | AFR | ACB | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02258 | hp1 | a0005 | c0010 | t0001 | g0194 | AFR | ACB | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02258 | hp2 | a0002 | c0002 | t0001 | g0198 | AFR | ACB | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | ACB | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | ACB | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02293 | hp1 | a0002 | c0002 | t0001 | g0227 | AMR | PEL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PEL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02300 | hp1 | a0002 | c0002 | t0001 | g0179 | AMR | PEL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02300 | hp2 | a0002 | c0002 | t0001 | g0158 | AMR | PEL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02451 | hp2 | a0001 | c0004 | t0002 | g0275 | AFR | ACB | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02523 | hp1 | a0002 | c0002 | t0001 | g0199 | EAS | KHV | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02523 | hp2 | a0002 | c0002 | t0001 | g0195 | EAS | KHV | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02572 | hp1 | a0001 | c0001 | t0004 | g0039 | AFR | GWD | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02572 | hp2 | a0001 | c0001 | t0005 | g0030 | AFR | GWD | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02602 | hp1 | a0001 | c0003 | t0001 | g0241 | SAS | PJL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02615 | hp1 | a0001 | c0001 | t0004 | g0037 | AFR | GWD | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02615 | hp2 | a0002 | c0002 | t0001 | g0212 | AFR | GWD | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02622 | hp1 | a0003 | c0007 | t0005 | g0062 | AFR | GWD | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02622 | hp2 | a0002 | c0002 | t0001 | g0214 | AFR | GWD | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02630 | hp1 | a0001 | c0004 | t0002 | g0277 | AFR | GWD | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02630 | hp2 | a0001 | c0001 | t0004 | g0002 | AFR | GWD | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02647 | hp2 | a0001 | c0004 | t0002 | g0269 | AFR | GWD | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02698 | hp1 | a0002 | c0002 | t0001 | g0181 | SAS | PJL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02698 | hp2 | a0001 | c0005 | t0003 | g0146 | SAS | PJL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02717 | hp1 | a0001 | c0004 | t0002 | g0023 | AFR | GWD | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02717 | hp2 | a0001 | c0004 | t0002 | g0276 | AFR | GWD | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02723 | hp1 | a0001 | c0004 | t0002 | g0261 | AFR | GWD | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02735 | hp1 | a0001 | c0005 | t0003 | g0018 | SAS | PJL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02735 | hp2 | a0002 | c0002 | t0001 | g0180 | SAS | PJL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02738 | hp1 | a0001 | c0003 | t0006 | g0294 | SAS | PJL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02738 | hp2 | a0002 | c0002 | t0001 | g0233 | SAS | PJL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02809 | hp1 | a0001 | c0004 | t0015 | g0296 | AFR | GWD | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02818 | hp2 | a0001 | c0004 | t0002 | g0281 | AFR | GWD | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02886 | hp2 | a0001 | c0001 | t0004 | g0002 | AFR | GWD | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02896 | hp1 | a0001 | c0004 | t0002 | g0272 | AFR | GWD | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02896 | hp2 | a0001 | c0001 | t0004 | g0002 | AFR | GWD | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02897 | hp1 | a0001 | c0001 | t0004 | g0034 | AFR | GWD | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02897 | hp2 | a0001 | c0004 | t0002 | g0270 | AFR | GWD | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02922 | hp1 | a0001 | c0004 | t0002 | g0283 | AFR | ESN | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02922 | hp2 | a0001 | c0001 | t0004 | g0036 | AFR | ESN | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ESN | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02970 | hp1 | a0001 | c0001 | t0005 | g0027 | AFR | ESN | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02970 | hp2 | a0001 | c0001 | t0014 | g0290 | AFR | ESN | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02976 | hp1 | a0001 | c0001 | t0004 | g0002 | AFR | ESN | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG03017 | hp1 | a0002 | c0002 | t0001 | g0202 | SAS | PJL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG03041 | hp1 | a0001 | c0001 | t0005 | g0025 | AFR | GWD | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG03041 | hp2 | a0001 | c0004 | t0002 | g0268 | AFR | GWD | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG03098 | hp1 | a0001 | c0012 | t0002 | g0274 | AFR | MSL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG03098 | hp2 | a0001 | c0004 | t0002 | g0259 | AFR | MSL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG03195 | hp1 | a0001 | c0005 | t0003 | g0145 | AFR | ESN | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG03195 | hp2 | a0001 | c0001 | t0005 | g0026 | AFR | ESN | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG03209 | hp1 | a0001 | c0001 | t0009 | g0256 | AFR | MSL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG03209 | hp2 | a0001 | c0004 | t0002 | g0265 | AFR | MSL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | MSL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG03225 | hp2 | a0001 | c0004 | t0010 | g0260 | AFR | MSL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG03239 | hp1 | a0001 | c0005 | t0003 | g0141 | SAS | PJL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG03239 | hp2 | a0002 | c0002 | t0001 | g0210 | SAS | PJL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | MSL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG03453 | hp2 | a0002 | c0002 | t0001 | g0193 | AFR | MSL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG03486 | hp2 | a0001 | c0001 | t0005 | g0012 | AFR | MSL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG03490 | hp1 | a0002 | c0002 | t0001 | g0224 | SAS | PJL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG03490 | hp2 | a0001 | c0005 | t0003 | g0150 | SAS | PJL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG03491 | hp1 | a0002 | c0002 | t0001 | g0191 | SAS | PJL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG03491 | hp2 | a0001 | c0005 | t0003 | g0151 | SAS | PJL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG03516 | hp1 | a0001 | c0004 | t0002 | g0285 | AFR | ESN | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG03516 | hp2 | a0001 | c0001 | t0005 | g0012 | AFR | ESN | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG03540 | hp1 | a0001 | c0001 | t0004 | g0002 | AFR | GWD | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG03540 | hp2 | a0001 | c0004 | t0002 | g0286 | AFR | GWD | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG03579 | hp1 | a0001 | c0003 | t0001 | g0229 | AFR | MSL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG03579 | hp2 | a0001 | c0004 | t0002 | g0266 | AFR | MSL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG03654 | hp1 | a0001 | c0005 | t0003 | g0142 | SAS | PJL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG03688 | hp1 | a0001 | c0005 | t0003 | g0148 | SAS | STU | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG03688 | hp2 | a0004 | c0008 | t0001 | g0220 | SAS | STU | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG03704 | hp1 | a0001 | c0005 | t0003 | g0011 | SAS | PJL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG03704 | hp2 | a0002 | c0002 | t0001 | g0201 | SAS | PJL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG03710 | hp1 | a0001 | c0005 | t0003 | g0144 | SAS | PJL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG03831 | hp1 | a0001 | c0005 | t0003 | g0143 | SAS | BEB | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | BEB | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG03834 | hp1 | a0002 | c0002 | t0001 | g0196 | SAS | BEB | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG03834 | hp2 | a0001 | c0003 | t0001 | g0251 | SAS | BEB | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | BEB | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG03927 | hp2 | a0002 | c0002 | t0001 | g0228 | SAS | BEB | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG03942 | hp1 | a0001 | c0005 | t0003 | g0149 | SAS | BEB | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG03942 | hp2 | a0002 | c0002 | t0001 | g0157 | SAS | BEB | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | BEB | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG04184 | hp2 | a0001 | c0003 | t0006 | g0295 | SAS | BEB | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG04204 | hp1 | a0002 | c0002 | t0001 | g0161 | SAS | STU | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | STU | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG04228 | hp1 | a0001 | c0005 | t0003 | g0139 | SAS | STU | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | STU | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | YRI | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | YRI | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | YRI | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA18906 | hp2 | a0001 | c0001 | t0004 | g0044 | AFR | YRI | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA18943 | hp1 | a0001 | c0003 | t0001 | g0246 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA18945 | hp1 | a0001 | c0003 | t0001 | g0020 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA18945 | hp2 | a0002 | c0002 | t0001 | g0162 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA18950 | hp2 | a0002 | c0002 | t0001 | g0160 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA18951 | hp1 | a0002 | c0002 | t0007 | g0152 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA18957 | hp2 | a0001 | c0003 | t0001 | g0244 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA18960 | hp2 | a0002 | c0002 | t0001 | g0170 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA18964 | hp1 | a0002 | c0002 | t0001 | g0178 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA18965 | hp1 | a0002 | c0002 | t0001 | g0208 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA18969 | hp1 | a0002 | c0002 | t0007 | g0154 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA18971 | hp1 | a0002 | c0002 | t0001 | g0183 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA18973 | hp2 | a0001 | c0003 | t0001 | g0242 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA18975 | hp2 | a0001 | c0003 | t0001 | g0238 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA18977 | hp2 | a0002 | c0002 | t0001 | g0209 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA18979 | hp1 | a0002 | c0002 | t0001 | g0171 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA18980 | hp2 | a0002 | c0002 | t0001 | g0226 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA18984 | hp2 | a0002 | c0002 | t0001 | g0173 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA18989 | hp1 | a0002 | c0002 | t0001 | g0172 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA18993 | hp1 | a0002 | c0002 | t0001 | g0169 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA18993 | hp2 | a0002 | c0002 | t0007 | g0153 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA18998 | hp2 | a0002 | c0002 | t0001 | g0203 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA18999 | hp1 | a0002 | c0009 | t0001 | g0192 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA18999 | hp2 | a0002 | c0002 | t0001 | g0230 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA19001 | hp1 | a0002 | c0002 | t0001 | g0231 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA19002 | hp1 | a0002 | c0002 | t0001 | g0206 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA19004 | hp2 | a0002 | c0002 | t0001 | g0186 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA19005 | hp1 | a0001 | c0003 | t0001 | g0020 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA19005 | hp2 | a0001 | c0003 | t0016 | g0297 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA19006 | hp1 | a0002 | c0002 | t0006 | g0292 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA19012 | hp2 | a0002 | c0002 | t0001 | g0174 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA19030 | hp1 | a0001 | c0001 | t0005 | g0029 | AFR | LWK | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA19030 | hp2 | a0001 | c0005 | t0003 | g0254 | AFR | LWK | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA19043 | hp1 | a0001 | c0004 | t0002 | g0280 | AFR | LWK | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | LWK | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA19054 | hp1 | a0001 | c0003 | t0001 | g0240 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA19057 | hp2 | a0002 | c0002 | t0001 | g0213 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA19060 | hp2 | a0002 | c0002 | t0001 | g0218 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA19064 | hp2 | a0002 | c0002 | t0006 | g0293 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA19070 | hp1 | a0001 | c0005 | t0003 | g0140 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA19074 | hp2 | a0002 | c0002 | t0001 | g0182 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA19079 | hp2 | a0002 | c0002 | t0001 | g0219 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA19082 | hp2 | a0002 | c0002 | t0001 | g0205 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA19083 | hp2 | a0002 | c0002 | t0006 | g0291 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA19084 | hp1 | a0002 | c0002 | t0001 | g0197 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA19240 | hp1 | a0002 | c0002 | t0001 | g0222 | AFR | YRI | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA19240 | hp2 | a0001 | c0004 | t0002 | g0262 | AFR | YRI | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA20129 | hp1 | a0001 | c0001 | t0004 | g0035 | AFR | ASW | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA20129 | hp2 | a0001 | c0003 | t0001 | g0137 | AFR | ASW | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | TSI | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA20752 | hp2 | a0001 | c0005 | t0003 | g0011 | EUR | TSI | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0105 | EUR | TSI | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA20805 | hp2 | a0002 | c0002 | t0001 | g0211 | EUR | TSI | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG01123 | hp1 | a0002 | c0002 | t0001 | g0232 | AMR | CLM | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG01123 | hp2 | a0001 | c0003 | t0001 | g0247 | AMR | CLM | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02109 | hp1 | a0002 | c0002 | t0001 | g0190 | AFR | ACB | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02486 | hp1 | a0001 | c0001 | t0004 | g0042 | AFR | ACB | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02486 | hp2 | a0001 | c0004 | t0002 | g0023 | AFR | ACB | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02559 | hp1 | a0001 | c0004 | t0010 | g0267 | AFR | ACB | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG03471 | hp1 | a0001 | c0001 | t0005 | g0032 | AFR | MSL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG03471 | hp2 | a0001 | c0004 | t0002 | g0264 | AFR | MSL | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG06807 | hp1 | a0001 | c0003 | t0001 | g0136 | AFR | USA | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
HG06807 | hp2 | a0001 | c0004 | t0002 | g0273 | AFR | USA | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA20300 | hp1 | a0002 | c0002 | t0001 | g0164 | AFR | USA | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA20300 | hp2 | a0001 | c0004 | t0002 | g0263 | AFR | USA | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | LWK | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | LWK | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0107 | REF | REF | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0008 | REF | REF | PDIA6_chr2_10778391_10817785 | PDIA6 | chr2 | 10778391 | 10817785 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:10784271
|
T | C | 1 | a0003 | 2 | HG01496.hp2 HG02622.hp1 |
missense_variant | MODERATE | c.1310A>G | p.Lys437Arg | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 13/13 | 1399/2279 | 1310/1323 | 437/440 | chr2 | 10784271 | ||
chr2:10784320
|
C | T | 1 | a0005 | 1 | HG02258.hp1 | missense_variant | MODERATE | c.1261G>A | p.Val421Met | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 13/13 | 1350/2279 | 1261/1323 | 421/440 | chr2 | 10784320 | ||
chr2:10790777
|
T | C | 3 | a0002a0004a0005 | 85 | HG00408.hp2 HG00558.hp1 HG00642.hp2 others(82): Show |
missense_variant | MODERATE | c.641A>G | p.Lys214Arg | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 7/13 | 730/2279 | 641/1323 | 214/440 | chr2 | 10790777 | ||
chr2:10802550
|
C | T | 1 | a0004 | 1 | HG03688.hp2 | missense_variant | MODERATE | c.110G>A | p.Arg37Gln | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/13 | 199/2279 | 110/1323 | 37/440 | chr2 | 10802550 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:10785003
|
C | T | 1 | a0001c0013 | 1 | HG00639.hp2 | synonymous_variant | LOW | c.1185G>A | p.Thr395Thr | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 12/13 | 1274/2279 | 1185/1323 | 395/440 | chr2 | 10785003 | ||
chr2:10789812
|
G | A | 2 | a0002c0006a0004c0008 | 3 | HG00735.hp1 HG01433.hp1 HG03688.hp2 |
synonymous_variant | LOW | c.777C>T | p.Ser259Ser | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 8/13 | 866/2279 | 777/1323 | 259/440 | chr2 | 10789812 | ||
chr2:10789857
|
C | T | 1 | a0002c0009 | 1 | NA18999.hp1 | synonymous_variant | LOW | c.732G>A | p.Gln244Gln | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 8/13 | 821/2279 | 732/1323 | 244/440 | chr2 | 10789857 | ||
chr2:10793123
|
C | T | 7 | a0001c0003a0002c0002a0002c0006others(4): Show | 119 | HG00323.hp1 HG00408.hp2 HG00558.hp1 others(116): Show |
synonymous_variant | LOW | c.426G>A | p.Arg142Arg | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 5/13 | 515/2279 | 426/1323 | 142/440 | chr2 | 10793123 | ||
chr2:10793168
|
C | T | 1 | a0001c0012 | 1 | HG03098.hp1 | synonymous_variant | LOW | c.381G>A | p.Ala127Ala | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 5/13 | 470/2279 | 381/1323 | 127/440 | chr2 | 10793168 | ||
chr2:10802561
|
C | T | 7 | a0001c0003a0001c0005a0002c0002others(4): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
synonymous_variant | LOW | c.99G>A | p.Ser33Ser | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/13 | 188/2279 | 99/1323 | 33/440 | chr2 | 10802561 | ||
chr2:10802576
|
G | A | 3 | a0001c0004a0001c0012a0001c0013 | 33 | HG00639.hp1 HG00639.hp2 HG01175.hp2 others(30): Show |
synonymous_variant | LOW | c.84C>T | p.Ile28Ile | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/13 | 173/2279 | 84/1323 | 28/440 | chr2 | 10802576 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:10783455
|
C | T | 8 | a0001c0003t0008a0001c0003t0016a0001c0004t0002others(5): Show | 57 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*803G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 13/13 | 803 | chr2 | 10783455 | |||||
chr2:10783540
|
G | A | 2 | a0001c0001t0005a0003c0007t0005 | 11 | HG01496.hp2 HG01978.hp2 HG02572.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*718C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 13/13 | 718 | chr2 | 10783540 | |||||
chr2:10783565
|
T | C | 1 | a0001c0003t0008 | 3 | HG01069.hp2 HG01071.hp1 HG01192.hp2 |
3_prime_UTR_variant | MODIFIER | c.*693A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 13/13 | 693 | chr2 | 10783565 | |||||
chr2:10783574
|
T | C | 2 | a0001c0001t0005a0003c0007t0005 | 11 | HG01496.hp2 HG01978.hp2 HG02572.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*684A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 13/13 | 684 | chr2 | 10783574 | |||||
chr2:10783695
|
C | T | 5 | a0001c0004t0002a0001c0004t0010a0001c0004t0015others(2): Show | 32 | HG00639.hp1 HG00639.hp2 HG01261.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*563G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 13/13 | 563 | chr2 | 10783695 | |||||
chr2:10783843
|
T | C | 1 | a0002c0002t0007 | 4 | HG02040.hp1 NA18951.hp1 NA18969.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*415A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 13/13 | 415 | chr2 | 10783843 | |||||
chr2:10783865
|
T | C | 5 | a0001c0004t0002a0001c0004t0010a0001c0004t0015others(2): Show | 32 | HG00639.hp1 HG00639.hp2 HG01261.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*393A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 13/13 | 393 | chr2 | 10783865 | |||||
chr2:10783877
|
T | C | 1 | a0001c0004t0010 | 2 | HG02559.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*381A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 13/13 | 381 | chr2 | 10783877 | |||||
chr2:10784006
|
A | G | 1 | a0001c0001t0012 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*252T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 13/13 | 252 | chr2 | 10784006 | |||||
chr2:10784050
|
C | T | 1 | a0001c0001t0009 | 2 | HG01884.hp2 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*208G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 13/13 | 208 | chr2 | 10784050 | |||||
chr2:10784186
|
TG | T | 2 | a0001c0001t0004a0001c0001t0014 | 18 | HG01109.hp1 HG01167.hp2 HG01169.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*71delC | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 13/13 | 71 | chr2 | 10784186 | |||||
chr2:10784209
|
C | T | 1 | a0001c0001t0011 | 1 | HG00323.hp2 | 3_prime_UTR_variant | MODIFIER | c.*49G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 13/13 | 49 | chr2 | 10784209 | |||||
chr2:10812755
|
G | A | 1 | a0001c0001t0013 | 1 | HG02055.hp2 | 5_prime_UTR_variant | MODIFIER | c.-59C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/13 | 59 | chr2 | 10812755 | |||||
chr2:10812767
|
G | A | 1 | a0001c0003t0016 | 1 | NA19005.hp2 | 5_prime_UTR_variant | MODIFIER | c.-71C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/13 | 71 | chr2 | 10812767 | |||||
chr2:10812767
|
G | GC | 4 | a0001c0001t0014a0001c0003t0006a0001c0004t0015others(1): Show | 7 | HG02738.hp1 HG02809.hp1 HG02970.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-72dupG | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/13 | 72 | chr2 | 10812767 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:10784398
|
T | C | 167 | a0001c0001t0001g0120a0001c0001t0009g0256a0001c0001t0009g0257others(164): Show | 175 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(172): Show |
intron_variant | MODIFIER | c.1255-72A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 12/12 | chr2 | 10784398 | ||||||
chr2:10784458
|
C | A | 3 | a0001c0003t0008g0022a0001c0003t0008g0252a0001c0003t0016g0297 | 4 | HG01069.hp2 HG01071.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.1255-132G>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 12/12 | chr2 | 10784458 | ||||||
chr2:10784487
|
C | T | 3 | a0001c0003t0008g0022a0001c0003t0008g0252a0001c0003t0016g0297 | 4 | HG01069.hp2 HG01071.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.1255-161G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 12/12 | chr2 | 10784487 | ||||||
chr2:10784559
|
AC | A | 42 | a0001c0003t0008g0022a0001c0003t0008g0252a0001c0003t0016g0297others(39): Show | 47 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(44): Show |
intron_variant | MODIFIER | c.1255-234delG | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 12/12 | chr2 | 10784559 | ||||||
chr2:10784560
|
CT | C | 125 | a0001c0001t0001g0120a0001c0001t0009g0256a0001c0001t0009g0257others(122): Show | 128 | HG00323.hp1 HG00408.hp2 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.1255-235delA | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 12/12 | chr2 | 10784560 | ||||||
chr2:10784567
|
G | A | 46 | a0001c0003t0008g0022a0001c0003t0008g0252a0001c0003t0016g0297others(43): Show | 51 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.1255-241C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 12/12 | chr2 | 10784567 | ||||||
chr2:10784709
|
A | G | 1 | a0001c0001t0001g0090 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1254+225T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 12/12 | chr2 | 10784709 | ||||||
chr2:10785276
|
T | G | 1 | a0001c0004t0002g0271 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1158-246A>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10785276 | ||||||
chr2:10785280
|
C | T | 54 | a0001c0001t0009g0256a0001c0001t0009g0257a0001c0003t0008g0022others(51): Show | 59 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.1158-250G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10785280 | ||||||
chr2:10785435
|
C | G | 54 | a0001c0001t0001g0028a0001c0003t0008g0022a0001c0003t0008g0252others(51): Show | 59 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.1158-405G>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10785435 | ||||||
chr2:10785448
|
C | T | 3 | a0001c0001t0004g0002a0001c0001t0004g0034a0001c0001t0004g0039 | 7 | HG02572.hp1 HG02630.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1158-418G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10785448 | ||||||
chr2:10785619
|
AT | A | 3 | a0001c0001t0005g0012a0001c0001t0005g0025a0001c0001t0005g0029 | 4 | HG03041.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1158-590delA | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10785619 | ||||||
chr2:10785764
|
T | G | 1 | a0001c0001t0004g0037 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1158-734A>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10785764 | ||||||
chr2:10785877
|
C | T | 1 | a0001c0003t0001g0236 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1158-847G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10785877 | ||||||
chr2:10785975
|
A | C | 2 | a0001c0001t0001g0112a0001c0001t0001g0124 | 2 | NA18986.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.1158-945T>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10785975 | ||||||
chr2:10786005
|
C | T | 1 | a0001c0001t0001g0128 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1158-975G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10786005 | ||||||
chr2:10786006
|
A | G | 1 | a0001c0001t0001g0128 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1158-976T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10786006 | ||||||
chr2:10786062
|
C | T | 7 | a0001c0001t0001g0054a0001c0001t0001g0058a0001c0001t0001g0059others(4): Show | 7 | HG02109.hp1 HG02145.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1158-1032G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10786062 | ||||||
chr2:10786097
|
T | C | 1 | a0002c0002t0001g0181 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1158-1067A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10786097 | ||||||
chr2:10786196
|
G | A | 2 | a0001c0001t0009g0256a0001c0001t0009g0257 | 2 | HG01884.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1157+1085C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10786196 | ||||||
chr2:10786248
|
G | A | 1 | a0001c0004t0002g0281 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1157+1033C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10786248 | ||||||
chr2:10786271
|
C | T | 1 | a0001c0005t0003g0138 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1157+1010G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10786271 | ||||||
chr2:10786280
|
G | A | 1 | a0002c0002t0001g0161 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1157+1001C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10786280 | ||||||
chr2:10786291
|
C | T | 1 | a0001c0003t0001g0229 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1157+990G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10786291 | ||||||
chr2:10786318
|
T | C | 88 | a0001c0001t0001g0028a0001c0001t0001g0097a0001c0001t0001g0127others(85): Show | 100 | HG00280.hp1 HG00323.hp1 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.1157+963A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10786318 | ||||||
chr2:10786319
|
G | C | 3 | a0001c0001t0001g0116a0002c0002t0001g0171a0002c0002t0001g0197 | 3 | HG00408.hp1 NA18979.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1157+962C>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10786319 | ||||||
chr2:10786325
|
G | GA | 118 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0047others(115): Show | 122 | HG00408.hp2 HG00558.hp1 HG00639.hp1 others(119): Show |
intron_variant | MODIFIER | c.1157+955dupT | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10786325 | ||||||
chr2:10786404
|
G | A | 26 | a0001c0001t0001g0121a0001c0001t0004g0039a0001c0003t0001g0136others(23): Show | 27 | HG01099.hp1 HG01934.hp1 HG01943.hp1 others(24): Show |
intron_variant | MODIFIER | c.1157+877C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10786404 | ||||||
chr2:10786407
|
G | A | 1 | a0001c0003t0016g0297 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1157+874C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10786407 | ||||||
chr2:10786407
|
G | C | 8 | a0001c0001t0001g0105a0001c0001t0001g0109a0001c0001t0001g0114others(5): Show | 8 | HG01346.hp2 HG02148.hp2 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.1157+874C>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10786407 | ||||||
chr2:10786489
|
A | G | 30 | a0001c0004t0001g0279a0001c0004t0002g0023a0001c0004t0002g0259others(27): Show | 31 | HG00639.hp1 HG01175.hp2 HG01261.hp1 others(28): Show |
intron_variant | MODIFIER | c.1157+792T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10786489 | ||||||
chr2:10786509
|
CTCTCCAC others(16): Show |
C | 46 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0054others(43): Show | 51 | HG00639.hp1 HG00639.hp2 HG01070.hp2 others(48): Show |
intron_variant | MODIFIER | c.1157+749_1157+771d others(25): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10786509 | ||||||
chr2:10786641
|
A | G | 24 | a0001c0001t0001g0091a0001c0003t0001g0019a0001c0003t0001g0020others(21): Show | 27 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(24): Show |
intron_variant | MODIFIER | c.1157+640T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10786641 | ||||||
chr2:10786693
|
C | T | 32 | a0001c0004t0001g0279a0001c0004t0002g0023a0001c0004t0002g0259others(29): Show | 33 | HG00639.hp1 HG00639.hp2 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.1157+588G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10786693 | ||||||
chr2:10786694
|
G | A | 7 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0088others(4): Show | 9 | HG00558.hp2 NA18955.hp2 NA18960.hp1 others(6): Show |
intron_variant | MODIFIER | c.1157+587C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10786694 | ||||||
chr2:10786767
|
G | A | 1 | a0001c0001t0001g0093 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1157+514C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10786767 | ||||||
chr2:10786784
|
A | G | 32 | a0001c0004t0001g0279a0001c0004t0002g0023a0001c0004t0002g0259others(29): Show | 33 | HG00639.hp1 HG00639.hp2 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.1157+497T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10786784 | ||||||
chr2:10786876
|
T | C | 1 | a0001c0001t0001g0074 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1157+405A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10786876 | ||||||
chr2:10786894
|
G | T | 3 | a0001c0001t0001g0111a0001c0001t0001g0116a0001c0001t0001g0123 | 3 | HG00408.hp1 HG01943.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.1157+387C>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10786894 | ||||||
chr2:10786912
|
C | T | 85 | a0002c0002t0001g0156a0002c0002t0001g0157a0002c0002t0001g0158others(82): Show | 85 | HG00408.hp2 HG00558.hp1 HG00642.hp2 others(82): Show |
intron_variant | MODIFIER | c.1157+369G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10786912 | ||||||
chr2:10786918
|
C | T | 32 | a0001c0004t0001g0279a0001c0004t0002g0023a0001c0004t0002g0259others(29): Show | 33 | HG00639.hp1 HG00639.hp2 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.1157+363G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10786918 | ||||||
chr2:10786930
|
A | T | 1 | a0001c0003t0016g0297 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1157+351T>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10786930 | ||||||
chr2:10787077
|
C | T | 1 | a0001c0001t0001g0070 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1157+204G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10787077 | ||||||
chr2:10787092
|
C | A | 6 | a0001c0003t0001g0236a0001c0003t0001g0245a0001c0003t0001g0247others(3): Show | 6 | HG00323.hp1 HG00733.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.1157+189G>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10787092 | ||||||
chr2:10787219
|
T | C | 140 | a0001c0003t0001g0204a0001c0003t0001g0229a0001c0003t0008g0022others(137): Show | 145 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(142): Show |
intron_variant | MODIFIER | c.1157+62A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 11/12 | chr2 | 10787219 | ||||||
chr2:10787463
|
G | A | 1 | a0001c0001t0001g0130 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.999-24C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 10/12 | chr2 | 10787463 | ||||||
chr2:10787475
|
CTT | C | 6 | a0001c0004t0002g0282a0001c0004t0002g0283a0001c0004t0002g0284others(3): Show | 6 | HG01261.hp1 HG01884.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.999-38_999-37delAA | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 10/12 | chr2 | 10787475 | ||||||
chr2:10787526
|
C | T | 1 | a0002c0002t0001g0210 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.999-87G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 10/12 | chr2 | 10787526 | ||||||
chr2:10787611
|
A | G | 21 | a0001c0003t0008g0022a0001c0003t0008g0252a0001c0003t0016g0297others(18): Show | 25 | HG00280.hp1 HG01069.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.999-172T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 10/12 | chr2 | 10787611 | ||||||
chr2:10787792
|
C | A | 1 | a0002c0002t0001g0175 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.999-353G>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 10/12 | chr2 | 10787792 | ||||||
chr2:10787792
|
C | T | 1 | a0001c0001t0001g0055 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.999-353G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 10/12 | chr2 | 10787792 | ||||||
chr2:10787865
|
G | C | 32 | a0001c0004t0001g0279a0001c0004t0002g0023a0001c0004t0002g0259others(29): Show | 33 | HG00639.hp1 HG00639.hp2 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.999-426C>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 10/12 | chr2 | 10787865 | ||||||
chr2:10787918
|
T | A | 1 | a0001c0004t0010g0260 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.999-479A>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 10/12 | chr2 | 10787918 | ||||||
chr2:10787922
|
C | T | 2 | a0001c0003t0001g0136a0001c0003t0001g0137 | 2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.999-483G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 10/12 | chr2 | 10787922 | ||||||
chr2:10787939
|
G | A | 32 | a0001c0004t0001g0279a0001c0004t0002g0023a0001c0004t0002g0259others(29): Show | 33 | HG00639.hp1 HG00639.hp2 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.999-500C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 10/12 | chr2 | 10787939 | ||||||
chr2:10787954
|
T | A | 1 | a0001c0003t0006g0295 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.999-515A>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 10/12 | chr2 | 10787954 | ||||||
chr2:10787956
|
C | T | 87 | a0001c0003t0001g0204a0001c0003t0001g0229a0002c0002t0001g0156others(84): Show | 87 | HG00408.hp2 HG00558.hp1 HG00642.hp2 others(84): Show |
intron_variant | MODIFIER | c.999-517G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 10/12 | chr2 | 10787956 | ||||||
chr2:10788022
|
T | C | 133 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(130): Show | 140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.999-583A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 10/12 | chr2 | 10788022 | ||||||
chr2:10788065
|
C | CAAAAA | 23 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(20): Show | 26 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.998+627_999-627dup others(5): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 10/12 | chr2 | 10788065 | ||||||
chr2:10788065
|
C | CAAAAAA | 6 | a0001c0003t0001g0246a0001c0005t0003g0145a0002c0002t0001g0168others(3): Show | 6 | HG00558.hp1 HG03195.hp1 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.998+626_999-627dup others(6): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 10/12 | chr2 | 10788065 | ||||||
chr2:10788065
|
C | CAAAAAAA | 94 | a0001c0003t0001g0204a0001c0003t0001g0229a0001c0005t0003g0011others(91): Show | 97 | HG00280.hp1 HG00642.hp2 HG00735.hp1 others(94): Show |
intron_variant | MODIFIER | c.998+625_999-627dup others(7): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 10/12 | chr2 | 10788065 | ||||||
chr2:10788065
|
C | CAAAAAAA others(8): Show |
1 | a0001c0003t0016g0297 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.998+617_999-627dup others(15): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 10/12 | chr2 | 10788065 | ||||||
chr2:10788065
|
C | CAAAAAAA others(9): Show |
2 | a0001c0003t0008g0022a0001c0003t0008g0252 | 3 | HG01069.hp2 HG01071.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.999-627_999-626ins others(16): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 10/12 | chr2 | 10788065 | ||||||
chr2:10788081
|
G | A | 87 | a0001c0003t0001g0204a0001c0003t0001g0229a0002c0002t0001g0156others(84): Show | 87 | HG00408.hp2 HG00558.hp1 HG00642.hp2 others(84): Show |
intron_variant | MODIFIER | c.998+616C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 10/12 | chr2 | 10788081 | ||||||
chr2:10788124
|
G | A | 18 | a0001c0005t0003g0011a0001c0005t0003g0018a0001c0005t0003g0138others(15): Show | 21 | HG00280.hp1 HG01099.hp1 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.998+573C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 10/12 | chr2 | 10788124 | ||||||
chr2:10788149
|
A | G | 87 | a0001c0003t0001g0204a0001c0003t0001g0229a0002c0002t0001g0156others(84): Show | 87 | HG00408.hp2 HG00558.hp1 HG00642.hp2 others(84): Show |
intron_variant | MODIFIER | c.998+548T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 10/12 | chr2 | 10788149 | ||||||
chr2:10788261
|
G | T | 133 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(130): Show | 140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.998+436C>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 10/12 | chr2 | 10788261 | ||||||
chr2:10788462
|
C | G | 1 | a0001c0001t0005g0031 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.998+235G>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 10/12 | chr2 | 10788462 | ||||||
chr2:10788484
|
T | C | 133 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(130): Show | 140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.998+213A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 10/12 | chr2 | 10788484 | ||||||
chr2:10788541
|
A | G | 18 | a0001c0005t0003g0011a0001c0005t0003g0018a0001c0005t0003g0138others(15): Show | 21 | HG00280.hp1 HG01099.hp1 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.998+156T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 10/12 | chr2 | 10788541 | ||||||
chr2:10788568
|
G | A | 1 | a0002c0002t0007g0153 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.998+129C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 10/12 | chr2 | 10788568 | ||||||
chr2:10788568
|
G | GA | 97 | a0001c0001t0001g0077a0001c0001t0001g0090a0001c0001t0005g0029others(94): Show | 97 | HG00408.hp2 HG00558.hp1 HG00639.hp1 others(94): Show |
intron_variant | MODIFIER | c.998+128dupT | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 10/12 | chr2 | 10788568 | ||||||
chr2:10788568
|
G | GAA | 41 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(38): Show | 47 | HG00280.hp1 HG00323.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.998+127_998+128dup others(2): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 10/12 | chr2 | 10788568 | ||||||
chr2:10788568
|
GA | G | 9 | a0001c0003t0008g0022a0001c0003t0008g0252a0001c0004t0002g0271others(6): Show | 10 | HG00639.hp2 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.998+128delT | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 10/12 | chr2 | 10788568 | ||||||
chr2:10788584
|
A | C | 87 | a0001c0003t0001g0204a0001c0003t0001g0229a0002c0002t0001g0156others(84): Show | 87 | HG00408.hp2 HG00558.hp1 HG00642.hp2 others(84): Show |
intron_variant | MODIFIER | c.998+113T>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 10/12 | chr2 | 10788584 | ||||||
chr2:10788651
|
A | C | 133 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(130): Show | 140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.998+46T>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 10/12 | chr2 | 10788651 | ||||||
chr2:10788780
|
T | C | 133 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(130): Show | 140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.926-11A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 9/12 | chr2 | 10788780 | ||||||
chr2:10788836
|
A | G | 133 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(130): Show | 140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.925+61T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 9/12 | chr2 | 10788836 | ||||||
chr2:10789007
|
A | G | 133 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(130): Show | 140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.841-26T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 8/12 | chr2 | 10789007 | ||||||
chr2:10789066
|
C | T | 10 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0047others(7): Show | 10 | HG01109.hp2 HG01891.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.841-85G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 8/12 | chr2 | 10789066 | ||||||
chr2:10789191
|
A | G | 76 | a0001c0001t0001g0004a0001c0001t0001g0028a0001c0001t0001g0033others(73): Show | 85 | HG00639.hp2 HG01069.hp1 HG01070.hp2 others(82): Show |
intron_variant | MODIFIER | c.841-210T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 8/12 | chr2 | 10789191 | ||||||
chr2:10789198
|
G | A | 1 | a0001c0001t0001g0049 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.841-217C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 8/12 | chr2 | 10789198 | ||||||
chr2:10789216
|
A | G | 148 | a0001c0001t0001g0009a0001c0001t0001g0078a0001c0001t0001g0094others(145): Show | 161 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.841-235T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 8/12 | chr2 | 10789216 | ||||||
chr2:10789259
|
CACTT | C | 87 | a0001c0003t0001g0204a0001c0003t0001g0229a0001c0004t0002g0285others(84): Show | 87 | HG00408.hp2 HG00558.hp1 HG00642.hp2 others(84): Show |
intron_variant | MODIFIER | c.841-282_841-279del others(4): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 8/12 | chr2 | 10789259 | ||||||
chr2:10789266
|
T | C | 1 | a0001c0001t0001g0117 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.841-285A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 8/12 | chr2 | 10789266 | ||||||
chr2:10789267
|
T | G | 1 | a0002c0002t0006g0292 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.841-286A>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 8/12 | chr2 | 10789267 | ||||||
chr2:10789268
|
G | T | 1 | a0002c0002t0006g0292 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.841-287C>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 8/12 | chr2 | 10789268 | ||||||
chr2:10789289
|
A | G | 18 | a0001c0005t0003g0011a0001c0005t0003g0018a0001c0005t0003g0138others(15): Show | 21 | HG00280.hp1 HG01099.hp1 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.841-308T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 8/12 | chr2 | 10789289 | ||||||
chr2:10789362
|
AT | A | 203 | a0001c0001t0001g0028a0001c0001t0001g0033a0001c0001t0001g0046others(200): Show | 216 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(213): Show |
intron_variant | MODIFIER | c.841-382delA | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 8/12 | chr2 | 10789362 | ||||||
chr2:10789407
|
G | GAAAAC | 114 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(111): Show | 118 | HG00323.hp1 HG00408.hp2 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.840+337_840+341dup others(5): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 8/12 | chr2 | 10789407 | ||||||
chr2:10789407
|
GAAAAC | G | 18 | a0001c0005t0003g0011a0001c0005t0003g0018a0001c0005t0003g0138others(15): Show | 21 | HG00280.hp1 HG01099.hp1 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.840+337_840+341del others(5): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 8/12 | chr2 | 10789407 | ||||||
chr2:10789437
|
C | T | 133 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(130): Show | 140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.840+312G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 8/12 | chr2 | 10789437 | ||||||
chr2:10789476
|
T | C | 165 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(162): Show | 173 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(170): Show |
intron_variant | MODIFIER | c.840+273A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 8/12 | chr2 | 10789476 | ||||||
chr2:10789513
|
A | C | 3 | a0002c0002t0001g0190a0002c0002t0001g0214a0002c0002t0001g0222 | 3 | HG02109.hp1 HG02622.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.840+236T>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 8/12 | chr2 | 10789513 | ||||||
chr2:10789741
|
T | C | 133 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(130): Show | 140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
splice_region_variant&intron_variant | LOW | c.840+8A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 8/12 | chr2 | 10789741 | ||||||
chr2:10789924
|
A | T | 133 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(130): Show | 140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.700-35T>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 7/12 | chr2 | 10789924 | ||||||
chr2:10789980
|
AT | A | 18 | a0001c0001t0001g0004a0001c0001t0001g0028a0001c0001t0001g0050others(15): Show | 22 | HG01069.hp1 HG01978.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.700-92delA | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 7/12 | chr2 | 10789980 | ||||||
chr2:10789980
|
ATTT | A | 68 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(65): Show | 74 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.700-94_700-92delAA others(1): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 7/12 | chr2 | 10789980 | ||||||
chr2:10789980
|
ATTTT | A | 64 | a0001c0003t0001g0136a0001c0003t0001g0137a0001c0003t0008g0022others(61): Show | 65 | HG00642.hp2 HG00735.hp1 HG00735.hp2 others(62): Show |
intron_variant | MODIFIER | c.700-95_700-92delAA others(2): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 7/12 | chr2 | 10789980 | ||||||
chr2:10790025
|
C | T | 1 | a0001c0001t0005g0032 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.700-136G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 7/12 | chr2 | 10790025 | ||||||
chr2:10790071
|
T | C | 1 | a0001c0005t0003g0145 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.700-182A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 7/12 | chr2 | 10790071 | ||||||
chr2:10790082
|
A | G | 133 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(130): Show | 140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.700-193T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 7/12 | chr2 | 10790082 | ||||||
chr2:10790126
|
A | G | 133 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(130): Show | 140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.700-237T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 7/12 | chr2 | 10790126 | ||||||
chr2:10790140
|
G | A | 133 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(130): Show | 140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.700-251C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 7/12 | chr2 | 10790140 | ||||||
chr2:10790141
|
G | A | 133 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(130): Show | 140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.700-252C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 7/12 | chr2 | 10790141 | ||||||
chr2:10790167
|
C | T | 2 | a0001c0004t0002g0282a0001c0004t0002g0283 | 2 | HG01884.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.700-278G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 7/12 | chr2 | 10790167 | ||||||
chr2:10790235
|
GTGT | G | 10 | a0001c0004t0002g0259a0001c0004t0002g0261a0001c0004t0002g0262others(7): Show | 10 | HG00639.hp1 HG02559.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.700-349_700-347del others(3): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 7/12 | chr2 | 10790235 | ||||||
chr2:10790309
|
T | G | 133 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(130): Show | 140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.699+410A>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 7/12 | chr2 | 10790309 | ||||||
chr2:10790515
|
C | T | 1 | a0001c0001t0001g0052 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.699+204G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 7/12 | chr2 | 10790515 | ||||||
chr2:10790645
|
A | G | 1 | a0002c0002t0007g0153 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.699+74T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 7/12 | chr2 | 10790645 | ||||||
chr2:10790875
|
A | G | 133 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(130): Show | 140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.585-42T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 6/12 | chr2 | 10790875 | ||||||
chr2:10790920
|
G | A | 133 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(130): Show | 140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.585-87C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 6/12 | chr2 | 10790920 | ||||||
chr2:10790937
|
T | C | 133 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(130): Show | 140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.585-104A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 6/12 | chr2 | 10790937 | ||||||
chr2:10790968
|
T | A | 6 | a0001c0004t0002g0282a0001c0004t0002g0283a0001c0004t0002g0284others(3): Show | 6 | HG01261.hp1 HG01884.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.585-135A>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 6/12 | chr2 | 10790968 | ||||||
chr2:10790972
|
A | G | 2 | a0001c0003t0001g0136a0001c0003t0001g0137 | 2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.585-139T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 6/12 | chr2 | 10790972 | ||||||
chr2:10791150
|
CT | C | 134 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(131): Show | 141 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.585-318delA | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 6/12 | chr2 | 10791150 | ||||||
chr2:10791176
|
T | C | 25 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(22): Show | 28 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.585-343A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 6/12 | chr2 | 10791176 | ||||||
chr2:10791259
|
T | A | 1 | a0001c0001t0001g0113 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.585-426A>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 6/12 | chr2 | 10791259 | ||||||
chr2:10791309
|
A | C | 23 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(20): Show | 26 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.585-476T>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 6/12 | chr2 | 10791309 | ||||||
chr2:10791677
|
G | A | 2 | a0001c0001t0001g0073a0001c0001t0001g0086 | 2 | HG02027.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.584+118C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 6/12 | chr2 | 10791677 | ||||||
chr2:10791956
|
T | C | 133 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(130): Show | 140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.454-31A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 5/12 | chr2 | 10791956 | ||||||
chr2:10792081
|
C | A | 133 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(130): Show | 140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.454-156G>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 5/12 | chr2 | 10792081 | ||||||
chr2:10792098
|
T | C | 6 | a0001c0004t0002g0282a0001c0004t0002g0283a0001c0004t0002g0284others(3): Show | 6 | HG01261.hp1 HG01884.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.454-173A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 5/12 | chr2 | 10792098 | ||||||
chr2:10792174
|
T | C | 134 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(131): Show | 141 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.454-249A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 5/12 | chr2 | 10792174 | ||||||
chr2:10792314
|
C | T | 133 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(130): Show | 140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.454-389G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 5/12 | chr2 | 10792314 | ||||||
chr2:10792431
|
C | T | 1 | a0002c0002t0001g0195 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.454-506G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 5/12 | chr2 | 10792431 | ||||||
chr2:10792552
|
C | T | 1 | a0001c0001t0001g0096 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.453+544G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 5/12 | chr2 | 10792552 | ||||||
chr2:10792622
|
T | C | 133 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(130): Show | 140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.453+474A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 5/12 | chr2 | 10792622 | ||||||
chr2:10792639
|
C | T | 23 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(20): Show | 26 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.453+457G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 5/12 | chr2 | 10792639 | ||||||
chr2:10792735
|
A | AAT | 133 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(130): Show | 140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.453+359_453+360dup others(2): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 5/12 | chr2 | 10792735 | ||||||
chr2:10792796
|
C | T | 1 | a0001c0004t0002g0275 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.453+300G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 5/12 | chr2 | 10792796 | ||||||
chr2:10792808
|
A | G | 133 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(130): Show | 140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.453+288T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 5/12 | chr2 | 10792808 | ||||||
chr2:10792863
|
G | A | 87 | a0001c0003t0001g0204a0001c0003t0001g0229a0002c0002t0001g0156others(84): Show | 87 | HG00408.hp2 HG00558.hp1 HG00642.hp2 others(84): Show |
intron_variant | MODIFIER | c.453+233C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 5/12 | chr2 | 10792863 | ||||||
chr2:10792898
|
C | T | 21 | a0001c0003t0008g0022a0001c0003t0008g0252a0001c0003t0016g0297others(18): Show | 25 | HG00280.hp1 HG01069.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.453+198G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 5/12 | chr2 | 10792898 | ||||||
chr2:10792913
|
G | A | 1 | a0001c0001t0005g0031 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.453+183C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 5/12 | chr2 | 10792913 | ||||||
chr2:10792950
|
T | C | 6 | a0001c0004t0002g0282a0001c0004t0002g0283a0001c0004t0002g0284others(3): Show | 6 | HG01261.hp1 HG01884.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.453+146A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 5/12 | chr2 | 10792950 | ||||||
chr2:10793037
|
G | A | 32 | a0001c0004t0001g0279a0001c0004t0002g0023a0001c0004t0002g0259others(29): Show | 33 | HG00639.hp1 HG00639.hp2 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.453+59C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 5/12 | chr2 | 10793037 | ||||||
chr2:10793069
|
T | A | 21 | a0001c0003t0008g0022a0001c0003t0008g0252a0001c0003t0016g0297others(18): Show | 25 | HG00280.hp1 HG01069.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.453+27A>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 5/12 | chr2 | 10793069 | ||||||
chr2:10793220
|
T | TAGGC | 86 | a0001c0004t0002g0276a0001c0004t0002g0281a0002c0002t0001g0156others(83): Show | 86 | HG00408.hp2 HG00558.hp1 HG00642.hp2 others(83): Show |
intron_variant | MODIFIER | c.347-22_347-19dupGC others(2): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10793220 | ||||||
chr2:10793264
|
C | T | 2 | a0001c0005t0003g0254a0001c0005t0003g0255 | 2 | HG01934.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.347-62G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10793264 | ||||||
chr2:10793265
|
G | C | 1 | a0002c0002t0001g0161 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.347-63C>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10793265 | ||||||
chr2:10793294
|
C | T | 1 | a0001c0001t0001g0093 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.347-92G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10793294 | ||||||
chr2:10793295
|
G | A | 166 | a0001c0001t0001g0093a0001c0003t0001g0019a0001c0003t0001g0020others(163): Show | 174 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(171): Show |
intron_variant | MODIFIER | c.347-93C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10793295 | ||||||
chr2:10793296
|
G | C | 1 | a0001c0001t0001g0093 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.347-94C>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10793296 | ||||||
chr2:10793367
|
T | C | 87 | a0001c0003t0001g0204a0001c0003t0001g0229a0002c0002t0001g0156others(84): Show | 87 | HG00408.hp2 HG00558.hp1 HG00642.hp2 others(84): Show |
intron_variant | MODIFIER | c.347-165A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10793367 | ||||||
chr2:10793375
|
A | G | 133 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(130): Show | 140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.347-173T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10793375 | ||||||
chr2:10793556
|
A | G | 133 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(130): Show | 140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.347-354T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10793556 | ||||||
chr2:10793697
|
C | T | 2 | a0001c0003t0001g0234a0001c0003t0001g0235 | 2 | HG00597.hp2 HG00609.hp2 |
intron_variant | MODIFIER | c.347-495G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10793697 | ||||||
chr2:10793698
|
G | A | 133 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(130): Show | 140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.347-496C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10793698 | ||||||
chr2:10793774
|
A | G | 1 | a0001c0001t0001g0074 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.347-572T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10793774 | ||||||
chr2:10793795
|
A | G | 165 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(162): Show | 173 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(170): Show |
intron_variant | MODIFIER | c.347-593T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10793795 | ||||||
chr2:10793886
|
A | G | 133 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(130): Show | 140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.347-684T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10793886 | ||||||
chr2:10793941
|
C | T | 1 | a0001c0004t0002g0280 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.347-739G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10793941 | ||||||
chr2:10794075
|
GA | G | 11 | a0002c0002t0001g0160a0002c0002t0001g0162a0002c0002t0001g0169others(8): Show | 11 | HG02083.hp2 NA18945.hp2 NA18950.hp2 others(8): Show |
intron_variant | MODIFIER | c.347-874delT | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10794075 | ||||||
chr2:10794088
|
AACATATG others(7): Show |
A | 112 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(109): Show | 115 | HG00323.hp1 HG00408.hp2 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.347-900_347-887del others(14): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10794088 | ||||||
chr2:10794211
|
A | G | 133 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(130): Show | 140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.347-1009T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10794211 | ||||||
chr2:10794218
|
C | T | 2 | a0001c0001t0004g0035a0001c0001t0004g0042 | 2 | HG02486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.347-1016G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10794218 | ||||||
chr2:10794394
|
T | C | 32 | a0001c0004t0001g0279a0001c0004t0002g0023a0001c0004t0002g0259others(29): Show | 33 | HG00639.hp1 HG00639.hp2 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.347-1192A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10794394 | ||||||
chr2:10794400
|
C | T | 1 | a0001c0001t0005g0032 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.347-1198G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10794400 | ||||||
chr2:10794405
|
C | T | 133 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(130): Show | 140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.347-1203G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10794405 | ||||||
chr2:10794432
|
C | T | 133 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(130): Show | 140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.347-1230G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10794432 | ||||||
chr2:10794433
|
G | A | 1 | a0001c0001t0001g0114 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.347-1231C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10794433 | ||||||
chr2:10794448
|
G | GA | 25 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0068others(22): Show | 26 | HG00639.hp1 HG00639.hp2 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.347-1247dupT | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10794448 | ||||||
chr2:10794448
|
G | GAA | 6 | a0001c0004t0001g0279a0001c0004t0002g0261a0001c0004t0002g0263others(3): Show | 6 | HG01175.hp2 HG02559.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.347-1248_347-1247d others(4): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10794448 | ||||||
chr2:10794460
|
AAAT | A | 133 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(130): Show | 140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.347-1261_347-1259d others(5): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10794460 | ||||||
chr2:10794462
|
AT | A | 4 | a0001c0001t0001g0057a0001c0001t0001g0078a0001c0001t0001g0094others(1): Show | 4 | HG00323.hp2 HG01106.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.347-1261delA | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10794462 | ||||||
chr2:10794468
|
C | CT | 17 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0089others(14): Show | 17 | HG00558.hp2 HG00639.hp1 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.347-1267dupA | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10794468 | ||||||
chr2:10794468
|
C | CTT | 10 | a0001c0001t0004g0040a0001c0004t0002g0259a0001c0004t0002g0266others(7): Show | 10 | HG01169.hp1 HG01261.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.347-1268_347-1267d others(4): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10794468 | ||||||
chr2:10794468
|
CTTTTTT | C | 130 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(127): Show | 137 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.347-1272_347-1267d others(8): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10794468 | ||||||
chr2:10794468
|
CTTTTTTT others(4): Show |
C | 15 | a0001c0004t0002g0023a0001c0004t0002g0268a0001c0004t0002g0269others(12): Show | 16 | HG00639.hp2 HG02257.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.347-1277_347-1267d others(13): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10794468 | ||||||
chr2:10794472
|
T | C | 1 | a0001c0001t0001g0129 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.347-1270A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10794472 | ||||||
chr2:10794495
|
T | C | 1 | a0001c0001t0013g0289 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.347-1293A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10794495 | ||||||
chr2:10794514
|
C | G | 21 | a0001c0003t0008g0022a0001c0003t0008g0252a0001c0003t0016g0297others(18): Show | 25 | HG00280.hp1 HG01069.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.347-1312G>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10794514 | ||||||
chr2:10794538
|
C | A | 2 | a0001c0003t0001g0136a0001c0003t0001g0137 | 2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.347-1336G>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10794538 | ||||||
chr2:10794625
|
C | G | 2 | a0001c0003t0001g0136a0001c0003t0001g0137 | 2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.347-1423G>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10794625 | ||||||
chr2:10794626
|
T | G | 2 | a0001c0003t0001g0136a0001c0003t0001g0137 | 2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.347-1424A>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10794626 | ||||||
chr2:10794828
|
G | T | 2 | a0001c0003t0001g0136a0001c0003t0001g0137 | 2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.347-1626C>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10794828 | ||||||
chr2:10795013
|
G | A | 4 | a0002c0002t0001g0156a0002c0002t0001g0157a0002c0002t0001g0158others(1): Show | 4 | HG01081.hp2 HG01258.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.347-1811C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10795013 | ||||||
chr2:10795098
|
T | C | 133 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(130): Show | 140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.347-1896A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10795098 | ||||||
chr2:10795119
|
C | T | 1 | a0001c0004t0002g0263 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.347-1917G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10795119 | ||||||
chr2:10795187
|
G | A | 1 | a0001c0004t0010g0260 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.346+1894C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10795187 | ||||||
chr2:10795402
|
C | T | 112 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(109): Show | 115 | HG00323.hp1 HG00408.hp2 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.346+1679G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10795402 | ||||||
chr2:10795488
|
CAGACGA | C | 131 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(128): Show | 138 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.346+1587_346+1592d others(8): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10795488 | ||||||
chr2:10795504
|
C | T | 3 | a0001c0003t0008g0022a0001c0003t0008g0252a0001c0003t0016g0297 | 4 | HG01069.hp2 HG01071.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.346+1577G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10795504 | ||||||
chr2:10795669
|
C | T | 2 | a0001c0004t0002g0272a0001c0004t0015g0296 | 2 | HG02809.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.346+1412G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10795669 | ||||||
chr2:10795735
|
C | T | 133 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(130): Show | 140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.346+1346G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10795735 | ||||||
chr2:10795825
|
C | T | 294 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(291): Show | 337 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(334): Show |
intron_variant | MODIFIER | c.346+1256G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10795825 | ||||||
chr2:10795963
|
T | C | 2 | a0001c0001t0009g0256a0001c0001t0009g0257 | 2 | HG01884.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.346+1118A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10795963 | ||||||
chr2:10795966
|
A | G | 110 | a0001c0003t0001g0136a0001c0003t0001g0137a0001c0003t0001g0204others(107): Show | 114 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.346+1115T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10795966 | ||||||
chr2:10795996
|
A | C | 21 | a0001c0003t0008g0022a0001c0003t0008g0252a0001c0003t0016g0297others(18): Show | 25 | HG00280.hp1 HG01069.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.346+1085T>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10795996 | ||||||
chr2:10796060
|
C | CT | 52 | a0001c0001t0001g0004a0001c0001t0001g0028a0001c0001t0001g0033others(49): Show | 60 | HG00639.hp1 HG01069.hp1 HG01109.hp1 others(57): Show |
intron_variant | MODIFIER | c.346+1020dupA | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10796060 | ||||||
chr2:10796060
|
C | CTT | 7 | a0001c0001t0005g0031a0001c0004t0001g0279a0001c0004t0002g0261others(4): Show | 7 | HG01175.hp2 HG01978.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.346+1019_346+1020d others(4): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10796060 | ||||||
chr2:10796060
|
CTTTTTTT others(1): Show |
C | 133 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(130): Show | 140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.346+1013_346+1020d others(10): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10796060 | ||||||
chr2:10796069
|
T | G | 2 | a0001c0005t0003g0254a0001c0005t0003g0255 | 2 | HG01934.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.346+1012A>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10796069 | ||||||
chr2:10796072
|
T | C | 133 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(130): Show | 140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.346+1009A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10796072 | ||||||
chr2:10796128
|
A | G | 133 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(130): Show | 140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.346+953T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10796128 | ||||||
chr2:10796146
|
C | T | 28 | a0001c0004t0001g0279a0001c0004t0002g0023a0001c0004t0002g0261others(25): Show | 29 | HG00639.hp1 HG00639.hp2 HG01175.hp2 others(26): Show |
intron_variant | MODIFIER | c.346+935G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10796146 | ||||||
chr2:10796156
|
C | T | 87 | a0001c0003t0001g0204a0001c0003t0001g0229a0002c0002t0001g0156others(84): Show | 87 | HG00408.hp2 HG00558.hp1 HG00642.hp2 others(84): Show |
intron_variant | MODIFIER | c.346+925G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10796156 | ||||||
chr2:10796197
|
T | G | 133 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(130): Show | 140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.346+884A>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10796197 | ||||||
chr2:10796254
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.346+827G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10796254 | ||||||
chr2:10796270
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.346+811C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10796270 | ||||||
chr2:10796300
|
G | A | 1 | a0002c0002t0001g0193 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.346+781C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10796300 | ||||||
chr2:10796333
|
A | G | 1 | a0002c0002t0001g0167 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.346+748T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10796333 | ||||||
chr2:10796341
|
T | C | 137 | a0001c0001t0001g0103a0001c0001t0001g0121a0001c0001t0001g0127others(134): Show | 144 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.346+740A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10796341 | ||||||
chr2:10796343
|
A | G | 142 | a0001c0001t0001g0103a0001c0001t0001g0121a0001c0001t0001g0127others(139): Show | 149 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.346+738T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10796343 | ||||||
chr2:10796438
|
G | A | 137 | a0001c0001t0001g0057a0001c0001t0001g0121a0001c0001t0001g0122others(134): Show | 144 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.346+643C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10796438 | ||||||
chr2:10796443
|
C | T | 138 | a0001c0001t0001g0057a0001c0001t0001g0121a0001c0001t0001g0122others(135): Show | 145 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.346+638G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10796443 | ||||||
chr2:10796500
|
TA | T | 38 | a0001c0001t0001g0053a0001c0001t0001g0055a0001c0001t0001g0074others(35): Show | 46 | HG00280.hp1 HG00323.hp2 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.346+580delT | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10796500 | ||||||
chr2:10796583
|
T | A | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.346+498A>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10796583 | ||||||
chr2:10796679
|
G | C | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.346+402C>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10796679 | ||||||
chr2:10796698
|
C | CAG | 134 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(131): Show | 141 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.346+381_346+382dup others(2): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10796698 | ||||||
chr2:10796853
|
C | T | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.346+228G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10796853 | ||||||
chr2:10796854
|
A | T | 1 | a0001c0001t0011g0066 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.346+227T>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10796854 | ||||||
chr2:10796863
|
T | C | 1 | a0001c0004t0002g0265 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.346+218A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10796863 | ||||||
chr2:10796911
|
T | G | 111 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(108): Show | 114 | HG00323.hp1 HG00408.hp2 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.346+170A>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10796911 | ||||||
chr2:10796939
|
T | C | 86 | a0001c0003t0001g0204a0001c0003t0001g0229a0002c0002t0001g0156others(83): Show | 86 | HG00408.hp2 HG00558.hp1 HG00642.hp2 others(83): Show |
intron_variant | MODIFIER | c.346+142A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10796939 | ||||||
chr2:10796969
|
T | A | 23 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(20): Show | 26 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.346+112A>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 4/12 | chr2 | 10796969 | ||||||
chr2:10797283
|
C | T | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.220-76G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 3/12 | chr2 | 10797283 | ||||||
chr2:10797465
|
A | C | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.219+235T>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 3/12 | chr2 | 10797465 | ||||||
chr2:10797500
|
A | G | 1 | a0001c0004t0010g0267 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.219+200T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 3/12 | chr2 | 10797500 | ||||||
chr2:10797561
|
G | A | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.219+139C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 3/12 | chr2 | 10797561 | ||||||
chr2:10797579
|
C | T | 4 | a0001c0001t0001g0028a0001c0001t0005g0012a0001c0001t0005g0025others(1): Show | 5 | HG02257.hp1 HG03041.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.219+121G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 3/12 | chr2 | 10797579 | ||||||
chr2:10797629
|
G | GAATATGG others(24): Show |
1 | a0002c0002t0001g0156 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.219+40_219+70dupTT others(29): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 3/12 | chr2 | 10797629 | ||||||
chr2:10797854
|
T | C | 23 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(20): Show | 26 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.162-97A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10797854 | ||||||
chr2:10797917
|
T | G | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.162-160A>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10797917 | ||||||
chr2:10797953
|
AGGAG | A | 15 | a0001c0001t0001g0053a0001c0001t0004g0002a0001c0001t0004g0034others(12): Show | 19 | HG01109.hp1 HG01167.hp2 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.162-200_162-197del others(4): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10797953 | ||||||
chr2:10798053
|
G | A | 1 | a0001c0003t0001g0247 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.162-296C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10798053 | ||||||
chr2:10798054
|
T | C | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.162-297A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10798054 | ||||||
chr2:10798055
|
G | A | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.162-298C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10798055 | ||||||
chr2:10798102
|
C | T | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.162-345G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10798102 | ||||||
chr2:10798136
|
G | T | 1 | a0001c0001t0005g0027 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.162-379C>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10798136 | ||||||
chr2:10798401
|
C | T | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.162-644G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10798401 | ||||||
chr2:10798546
|
C | A | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.162-789G>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10798546 | ||||||
chr2:10798568
|
CCA | C | 80 | a0001c0003t0001g0204a0001c0003t0001g0235a0001c0003t0001g0238others(77): Show | 80 | HG00408.hp2 HG00558.hp1 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.162-813_162-812del others(2): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10798568 | ||||||
chr2:10798569
|
CA | C | 6 | a0001c0003t0001g0229a0002c0002t0001g0165a0002c0002t0001g0172others(3): Show | 6 | HG02040.hp2 HG02155.hp1 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.162-813delT | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10798569 | ||||||
chr2:10798570
|
A | C | 46 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(43): Show | 53 | HG00280.hp1 HG00323.hp1 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.162-813T>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10798570 | ||||||
chr2:10798572
|
CCAA | C | 20 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(17): Show | 23 | HG00323.hp1 HG00609.hp2 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.162-818_162-816del others(3): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10798572 | ||||||
chr2:10798573
|
C | CA | 52 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(49): Show | 67 | HG00280.hp2 HG00323.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.162-817dupT | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10798573 | ||||||
chr2:10798573
|
CA | C | 11 | a0001c0001t0001g0004a0001c0001t0001g0054a0001c0001t0001g0058others(8): Show | 15 | HG00673.hp1 HG02145.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.162-817delT | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10798573 | ||||||
chr2:10798573
|
CAAAA | C | 21 | a0001c0003t0008g0022a0001c0003t0008g0252a0001c0003t0016g0297others(18): Show | 25 | HG00280.hp1 HG01069.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.162-820_162-817del others(4): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10798573 | ||||||
chr2:10798574
|
A | C | 80 | a0001c0003t0001g0204a0001c0003t0001g0235a0001c0003t0001g0238others(77): Show | 80 | HG00408.hp2 HG00558.hp1 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.162-817T>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10798574 | ||||||
chr2:10798578
|
A | C | 1 | a0001c0005t0003g0146 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.162-821T>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10798578 | ||||||
chr2:10798850
|
A | G | 164 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(161): Show | 172 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.162-1093T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10798850 | ||||||
chr2:10798890
|
T | C | 164 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(161): Show | 172 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.162-1133A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10798890 | ||||||
chr2:10798991
|
C | T | 25 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(22): Show | 28 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.162-1234G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10798991 | ||||||
chr2:10799035
|
AAG | A | 112 | a0001c0001t0005g0030a0001c0003t0001g0019a0001c0003t0001g0020others(109): Show | 115 | HG00323.hp1 HG00408.hp2 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.162-1280_162-1279d others(4): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10799035 | ||||||
chr2:10799115
|
A | G | 25 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(22): Show | 28 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.162-1358T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10799115 | ||||||
chr2:10799187
|
G | C | 1 | a0001c0001t0001g0050 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.162-1430C>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10799187 | ||||||
chr2:10799199
|
G | GTTTATT | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.162-1448_162-1443d others(8): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10799199 | ||||||
chr2:10799264
|
A | G | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.162-1507T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10799264 | ||||||
chr2:10799313
|
A | G | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.162-1556T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10799313 | ||||||
chr2:10799433
|
T | C | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.162-1676A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10799433 | ||||||
chr2:10799534
|
G | A | 2 | a0001c0005t0003g0018a0001c0005t0003g0146 | 3 | HG01099.hp1 HG02698.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.162-1777C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10799534 | ||||||
chr2:10799601
|
G | C | 2 | a0001c0001t0004g0045a0001c0001t0014g0290 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.162-1844C>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10799601 | ||||||
chr2:10799642
|
G | A | 1 | a0001c0001t0013g0289 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.162-1885C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10799642 | ||||||
chr2:10799659
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.162-1902C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10799659 | ||||||
chr2:10799785
|
A | G | 164 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(161): Show | 172 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.162-2028T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10799785 | ||||||
chr2:10799912
|
GA | G | 72 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(69): Show | 91 | HG00280.hp1 HG00280.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.162-2156delT | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10799912 | ||||||
chr2:10799919
|
A | G | 1 | a0001c0001t0001g0101 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.162-2162T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10799919 | ||||||
chr2:10799994
|
GA | G | 16 | a0001c0004t0002g0023a0001c0004t0002g0268a0001c0004t0002g0269others(13): Show | 17 | HG00639.hp2 HG02257.hp2 HG02300.hp1 others(14): Show |
intron_variant | MODIFIER | c.162-2238delT | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10799994 | ||||||
chr2:10799995
|
A | G | 131 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(128): Show | 138 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.162-2238T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10799995 | ||||||
chr2:10799996
|
A | G | 1 | a0002c0002t0001g0179 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.162-2239T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10799996 | ||||||
chr2:10800152
|
C | A | 15 | a0001c0004t0002g0023a0001c0004t0002g0268a0001c0004t0002g0269others(12): Show | 16 | HG00639.hp2 HG02257.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.161+2347G>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10800152 | ||||||
chr2:10800218
|
C | T | 1 | a0001c0001t0001g0130 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.161+2281G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10800218 | ||||||
chr2:10800283
|
C | T | 1 | a0001c0004t0001g0279 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.161+2216G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10800283 | ||||||
chr2:10800354
|
C | T | 1 | a0001c0003t0016g0297 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.161+2145G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10800354 | ||||||
chr2:10800355
|
T | C | 1 | a0001c0004t0002g0263 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.161+2144A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10800355 | ||||||
chr2:10800356
|
A | G | 1 | a0001c0001t0001g0087 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.161+2143T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10800356 | ||||||
chr2:10800370
|
T | C | 1 | a0001c0001t0001g0126 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.161+2129A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10800370 | ||||||
chr2:10800475
|
C | G | 23 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(20): Show | 26 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.161+2024G>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10800475 | ||||||
chr2:10800512
|
T | C | 6 | a0001c0001t0001g0099a0001c0001t0001g0105a0001c0001t0001g0107others(3): Show | 6 | HG01346.hp2 HG02148.hp2 HG03654.hp2 others(3): Show |
intron_variant | MODIFIER | c.161+1987A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10800512 | ||||||
chr2:10800528
|
GT | G | 130 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(127): Show | 137 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.161+1970delA | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10800528 | ||||||
chr2:10800539
|
C | T | 2 | a0001c0001t0004g0040a0001c0001t0004g0041 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.161+1960G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10800539 | ||||||
chr2:10800574
|
ATTTTGAT | A | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.161+1918_161+1924d others(9): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10800574 | ||||||
chr2:10800592
|
A | T | 1 | a0002c0002t0001g0206 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.161+1907T>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10800592 | ||||||
chr2:10800731
|
G | A | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.161+1768C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10800731 | ||||||
chr2:10800830
|
C | T | 2 | a0001c0001t0001g0073a0001c0001t0001g0086 | 2 | HG02027.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.161+1669G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10800830 | ||||||
chr2:10800853
|
T | C | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.161+1646A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10800853 | ||||||
chr2:10801017
|
A | G | 7 | a0001c0004t0002g0023a0001c0004t0002g0268a0001c0004t0002g0269others(4): Show | 8 | HG02451.hp2 HG02486.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.161+1482T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10801017 | ||||||
chr2:10801046
|
A | G | 1 | a0001c0005t0003g0147 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.161+1453T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10801046 | ||||||
chr2:10801123
|
A | G | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.161+1376T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10801123 | ||||||
chr2:10801139
|
C | T | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.161+1360G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10801139 | ||||||
chr2:10801143
|
G | A | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.161+1356C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10801143 | ||||||
chr2:10801175
|
G | A | 23 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(20): Show | 26 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.161+1324C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10801175 | ||||||
chr2:10801186
|
G | A | 1 | a0001c0004t0001g0279 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.161+1313C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10801186 | ||||||
chr2:10801262
|
T | G | 2 | a0001c0001t0004g0040a0001c0001t0004g0041 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.161+1237A>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10801262 | ||||||
chr2:10801272
|
T | TCTCTCAA others(5): Show |
1 | a0002c0002t0001g0179 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.161+1215_161+1226d others(14): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10801272 | ||||||
chr2:10801359
|
T | C | 2 | a0001c0001t0001g0049a0001c0001t0001g0050 | 2 | HG02109.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.161+1140A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10801359 | ||||||
chr2:10801394
|
T | G | 1 | a0001c0001t0001g0080 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.161+1105A>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10801394 | ||||||
chr2:10801412
|
T | C | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.161+1087A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10801412 | ||||||
chr2:10801495
|
A | C | 2 | a0001c0004t0002g0259a0001c0004t0002g0266 | 2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.161+1004T>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10801495 | ||||||
chr2:10801551
|
C | T | 32 | a0001c0004t0001g0279a0001c0004t0002g0023a0001c0004t0002g0259others(29): Show | 33 | HG00639.hp1 HG00639.hp2 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.161+948G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10801551 | ||||||
chr2:10801574
|
T | C | 2 | a0001c0003t0008g0022a0001c0003t0008g0252 | 3 | HG01069.hp2 HG01071.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.161+925A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10801574 | ||||||
chr2:10801597
|
T | C | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.161+902A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10801597 | ||||||
chr2:10801618
|
A | G | 200 | a0001c0001t0001g0028a0001c0001t0001g0033a0001c0001t0001g0046others(197): Show | 213 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(210): Show |
intron_variant | MODIFIER | c.161+881T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10801618 | ||||||
chr2:10802011
|
T | C | 7 | a0001c0004t0002g0023a0001c0004t0002g0268a0001c0004t0002g0269others(4): Show | 8 | HG02451.hp2 HG02486.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.161+488A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10802011 | ||||||
chr2:10802012
|
G | GT | 5 | a0001c0003t0001g0229a0001c0003t0001g0235a0002c0002t0001g0203others(2): Show | 5 | HG00597.hp2 HG03579.hp1 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.161+486dupA | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10802012 | ||||||
chr2:10802207
|
T | C | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.161+292A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10802207 | ||||||
chr2:10802228
|
G | A | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.161+271C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10802228 | ||||||
chr2:10802266
|
A | G | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.161+233T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10802266 | ||||||
chr2:10802285
|
G | T | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.161+214C>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10802285 | ||||||
chr2:10802310
|
C | T | 1 | a0002c0002t0001g0159 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.161+189G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10802310 | ||||||
chr2:10802394
|
C | T | 25 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(22): Show | 28 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.161+105G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10802394 | ||||||
chr2:10802441
|
G | A | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.161+58C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10802441 | ||||||
chr2:10802445
|
T | C | 1 | a0001c0001t0001g0064 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.161+54A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 2/12 | chr2 | 10802445 | ||||||
chr2:10802689
|
G | C | 6 | a0001c0004t0002g0282a0001c0004t0002g0283a0001c0004t0002g0284others(3): Show | 6 | HG01261.hp1 HG01884.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.20-49C>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10802689 | ||||||
chr2:10802864
|
T | C | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.20-224A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10802864 | ||||||
chr2:10802874
|
C | T | 32 | a0001c0004t0001g0279a0001c0004t0002g0023a0001c0004t0002g0259others(29): Show | 33 | HG00639.hp1 HG00639.hp2 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.20-234G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10802874 | ||||||
chr2:10802937
|
A | G | 1 | a0001c0004t0002g0266 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.20-297T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10802937 | ||||||
chr2:10803005
|
G | C | 2 | a0001c0001t0001g0049a0001c0001t0001g0050 | 2 | HG02109.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.20-365C>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10803005 | ||||||
chr2:10803029
|
G | A | 3 | a0001c0004t0002g0276a0001c0004t0002g0281a0002c0002t0001g0189 | 3 | HG01515.hp2 HG02717.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.20-389C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10803029 | ||||||
chr2:10803100
|
G | A | 1 | a0002c0002t0001g0169 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.20-460C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10803100 | ||||||
chr2:10803130
|
T | C | 23 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(20): Show | 26 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.20-490A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10803130 | ||||||
chr2:10803237
|
A | C | 23 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(20): Show | 26 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.20-597T>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10803237 | ||||||
chr2:10803291
|
G | A | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.20-651C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10803291 | ||||||
chr2:10803298
|
C | T | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.20-658G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10803298 | ||||||
chr2:10803505
|
C | CACATTAT others(2): Show |
132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.20-874_20-866dupTG others(7): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10803505 | ||||||
chr2:10803536
|
A | G | 18 | a0001c0005t0003g0011a0001c0005t0003g0018a0001c0005t0003g0138others(15): Show | 21 | HG00280.hp1 HG01099.hp1 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.20-896T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10803536 | ||||||
chr2:10803589
|
C | A | 2 | a0003c0007t0005g0062a0003c0007t0005g0063 | 2 | HG01496.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.20-949G>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10803589 | ||||||
chr2:10803675
|
A | AACTG | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.20-1036_20-1035ins others(4): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10803675 | ||||||
chr2:10803689
|
T | C | 1 | a0002c0002t0001g0223 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.20-1049A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10803689 | ||||||
chr2:10803756
|
A | G | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.20-1116T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10803756 | ||||||
chr2:10803789
|
A | G | 3 | a0002c0002t0001g0168a0002c0002t0001g0170a0002c0002t0001g0219 | 3 | HG00558.hp1 NA18960.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.20-1149T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10803789 | ||||||
chr2:10803823
|
T | G | 290 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(287): Show | 333 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(330): Show |
intron_variant | MODIFIER | c.20-1183A>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10803823 | ||||||
chr2:10803824
|
A | G | 1 | a0002c0002t0006g0292 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.20-1184T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10803824 | ||||||
chr2:10803878
|
G | A | 1 | a0001c0001t0001g0101 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.20-1238C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10803878 | ||||||
chr2:10803889
|
G | A | 1 | a0002c0002t0001g0219 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.20-1249C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10803889 | ||||||
chr2:10803909
|
G | T | 1 | a0002c0002t0006g0292 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.20-1269C>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10803909 | ||||||
chr2:10803911
|
G | GT | 10 | a0001c0001t0001g0015a0001c0001t0001g0053a0001c0001t0001g0072others(7): Show | 11 | HG01261.hp2 HG02071.hp2 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.20-1272dupA | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10803911 | ||||||
chr2:10803911
|
G | GTTTTTTT others(1): Show |
21 | a0002c0002t0001g0156a0002c0002t0001g0157a0002c0002t0001g0159others(18): Show | 21 | HG01081.hp2 HG01192.hp1 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.20-1279_20-1272dup others(8): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10803911 | ||||||
chr2:10803911
|
G | GTTTTTTT others(2): Show |
64 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(61): Show | 67 | HG00323.hp1 HG00408.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.20-1280_20-1272dup others(9): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10803911 | ||||||
chr2:10803911
|
G | GTTTTTTT others(3): Show |
18 | a0001c0003t0001g0239a0001c0003t0001g0243a0001c0003t0006g0294others(15): Show | 18 | HG01981.hp2 HG02074.hp1 HG02738.hp1 others(15): Show |
intron_variant | MODIFIER | c.20-1281_20-1272dup others(10): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10803911 | ||||||
chr2:10803911
|
G | GTTTTTTT others(4): Show |
4 | a0001c0003t0001g0136a0001c0003t0001g0137a0001c0003t0001g0238others(1): Show | 4 | HG06807.hp1 NA18945.hp2 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.20-1282_20-1272dup others(11): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10803911 | ||||||
chr2:10803911
|
G | GTTTTTTT others(5): Show |
9 | a0001c0003t0016g0297a0001c0005t0003g0018a0001c0005t0003g0138others(6): Show | 10 | HG01099.hp1 HG01943.hp1 HG02698.hp2 others(7): Show |
intron_variant | MODIFIER | c.20-1283_20-1272dup others(12): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10803911 | ||||||
chr2:10803911
|
G | GTTTTTTT others(6): Show |
9 | a0001c0003t0008g0022a0001c0003t0008g0252a0001c0005t0003g0011others(6): Show | 12 | HG00280.hp1 HG01069.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.20-1284_20-1272dup others(13): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10803911 | ||||||
chr2:10803911
|
G | GTTTTTTT others(7): Show |
2 | a0001c0005t0003g0139a0001c0005t0003g0143 | 2 | HG03831.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.20-1285_20-1272dup others(14): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10803911 | ||||||
chr2:10803911
|
G | T | 1 | a0002c0002t0006g0292 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.20-1271C>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10803911 | ||||||
chr2:10803965
|
T | C | 1 | a0001c0001t0001g0126 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.20-1325A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10803965 | ||||||
chr2:10804027
|
A | G | 1 | a0001c0003t0001g0236 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.20-1387T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10804027 | ||||||
chr2:10804028
|
C | G | 1 | a0001c0003t0001g0236 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.20-1388G>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10804028 | ||||||
chr2:10804041
|
C | T | 1 | a0001c0001t0001g0107 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.20-1401G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10804041 | ||||||
chr2:10804076
|
T | G | 31 | a0001c0004t0002g0023a0001c0004t0002g0259a0001c0004t0002g0261others(28): Show | 32 | HG00639.hp1 HG00639.hp2 HG01261.hp1 others(29): Show |
intron_variant | MODIFIER | c.20-1436A>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10804076 | ||||||
chr2:10804098
|
T | C | 1 | a0001c0001t0001g0068 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.20-1458A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10804098 | ||||||
chr2:10804159
|
C | T | 3 | a0001c0003t0008g0022a0001c0003t0008g0252a0001c0003t0016g0297 | 4 | HG01069.hp2 HG01071.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.20-1519G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10804159 | ||||||
chr2:10804199
|
T | C | 2 | a0001c0003t0008g0022a0001c0003t0008g0252 | 3 | HG01069.hp2 HG01071.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.20-1559A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10804199 | ||||||
chr2:10804223
|
T | A | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.20-1583A>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10804223 | ||||||
chr2:10804275
|
C | G | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.20-1635G>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10804275 | ||||||
chr2:10804285
|
T | C | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.20-1645A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10804285 | ||||||
chr2:10804354
|
T | G | 1 | a0002c0002t0006g0292 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.20-1714A>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10804354 | ||||||
chr2:10804355
|
G | T | 1 | a0002c0002t0006g0292 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.20-1715C>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10804355 | ||||||
chr2:10804356
|
T | G | 1 | a0002c0002t0006g0292 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.20-1716A>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10804356 | ||||||
chr2:10804369
|
C | T | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.20-1729G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10804369 | ||||||
chr2:10804370
|
A | G | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.20-1730T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10804370 | ||||||
chr2:10804396
|
G | C | 164 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(161): Show | 172 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.20-1756C>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10804396 | ||||||
chr2:10804429
|
T | A | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.20-1789A>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10804429 | ||||||
chr2:10804440
|
ATTGCTT | A | 130 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(127): Show | 137 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.20-1806_20-1801del others(6): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10804440 | ||||||
chr2:10804441
|
T | G | 2 | a0002c0002t0001g0218a0002c0002t0006g0291 | 2 | NA19060.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.20-1801A>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10804441 | ||||||
chr2:10804452
|
T | C | 1 | a0002c0002t0006g0291 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.20-1812A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10804452 | ||||||
chr2:10804484
|
A | ATATGCGG others(51): Show |
1 | a0002c0002t0006g0291 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.20-1845_20-1844ins others(58): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10804484 | ||||||
chr2:10804485
|
C | T | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.20-1845G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10804485 | ||||||
chr2:10804487
|
G | T | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.20-1847C>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10804487 | ||||||
chr2:10804490
|
A | G | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.20-1850T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10804490 | ||||||
chr2:10804555
|
T | A | 1 | a0002c0002t0001g0184 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.20-1915A>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10804555 | ||||||
chr2:10804651
|
G | A | 21 | a0001c0003t0008g0022a0001c0003t0008g0252a0001c0003t0016g0297others(18): Show | 25 | HG00280.hp1 HG01069.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.20-2011C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10804651 | ||||||
chr2:10804713
|
T | G | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.20-2073A>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10804713 | ||||||
chr2:10804726
|
T | G | 1 | a0001c0004t0001g0279 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.20-2086A>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10804726 | ||||||
chr2:10804780
|
G | A | 8 | a0001c0004t0002g0271a0001c0004t0002g0272a0001c0004t0002g0273others(5): Show | 8 | HG00639.hp2 HG02257.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.20-2140C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10804780 | ||||||
chr2:10804784
|
T | C | 109 | a0001c0003t0001g0136a0001c0003t0001g0137a0001c0003t0001g0204others(106): Show | 113 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.20-2144A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10804784 | ||||||
chr2:10804881
|
C | A | 10 | a0001c0004t0002g0259a0001c0004t0002g0261a0001c0004t0002g0262others(7): Show | 10 | HG00639.hp1 HG02559.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.20-2241G>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10804881 | ||||||
chr2:10804968
|
C | CTGTT | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.20-2329_20-2328ins others(4): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10804968 | ||||||
chr2:10805040
|
A | G | 6 | a0001c0005t0003g0011a0001c0005t0003g0018a0001c0005t0003g0140others(3): Show | 9 | HG00280.hp1 HG01099.hp1 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.20-2400T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10805040 | ||||||
chr2:10805083
|
T | C | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.20-2443A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10805083 | ||||||
chr2:10805156
|
C | G | 1 | a0001c0001t0001g0071 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.20-2516G>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10805156 | ||||||
chr2:10805246
|
G | A | 33 | a0001c0004t0002g0023a0001c0004t0002g0268a0001c0004t0002g0269others(30): Show | 37 | HG00280.hp1 HG00639.hp2 HG01099.hp1 others(34): Show |
intron_variant | MODIFIER | c.20-2606C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10805246 | ||||||
chr2:10805321
|
A | G | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.20-2681T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10805321 | ||||||
chr2:10805363
|
C | T | 2 | a0001c0003t0008g0022a0001c0003t0008g0252 | 3 | HG01069.hp2 HG01071.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.20-2723G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10805363 | ||||||
chr2:10805387
|
A | G | 2 | a0001c0001t0001g0048a0001c0001t0001g0051 | 2 | HG02451.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.20-2747T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10805387 | ||||||
chr2:10805429
|
TGGAGAAA others(17): Show |
T | 1 | a0002c0002t0001g0186 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.20-2813_20-2790del others(24): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10805429 | ||||||
chr2:10805435
|
A | C | 131 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(128): Show | 138 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.20-2795T>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10805435 | ||||||
chr2:10805453
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.20-2813G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10805453 | ||||||
chr2:10805502
|
C | T | 4 | a0001c0001t0001g0014a0001c0001t0001g0069a0001c0001t0001g0070others(1): Show | 5 | HG02027.hp1 HG02071.hp1 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.20-2862G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10805502 | ||||||
chr2:10805544
|
A | G | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.20-2904T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10805544 | ||||||
chr2:10805580
|
A | G | 1 | a0001c0001t0001g0068 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.20-2940T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10805580 | ||||||
chr2:10805610
|
T | C | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.20-2970A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10805610 | ||||||
chr2:10805688
|
A | T | 1 | a0001c0001t0001g0068 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.20-3048T>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10805688 | ||||||
chr2:10805695
|
T | C | 2 | a0001c0001t0009g0256a0001c0001t0009g0257 | 2 | HG01884.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.20-3055A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10805695 | ||||||
chr2:10805792
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.20-3152G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10805792 | ||||||
chr2:10805803
|
T | C | 133 | a0001c0001t0001g0067a0001c0003t0001g0019a0001c0003t0001g0020others(130): Show | 140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.20-3163A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10805803 | ||||||
chr2:10805826
|
C | T | 21 | a0001c0003t0008g0022a0001c0003t0008g0252a0001c0003t0016g0297others(18): Show | 25 | HG00280.hp1 HG01069.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.20-3186G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10805826 | ||||||
chr2:10805867
|
A | C | 1 | a0002c0002t0001g0225 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.20-3227T>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10805867 | ||||||
chr2:10805868
|
C | A | 1 | a0002c0002t0001g0225 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.20-3228G>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10805868 | ||||||
chr2:10805915
|
T | TG | 7 | a0001c0001t0005g0031a0001c0004t0001g0279a0001c0005t0003g0149others(4): Show | 7 | HG00735.hp2 HG01175.hp2 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.20-3276dupC | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10805915 | ||||||
chr2:10805915
|
TGGGGGGA | T | 25 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(22): Show | 28 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.20-3282_20-3276del others(7): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10805915 | ||||||
chr2:10805922
|
A | AG | 8 | a0001c0001t0001g0084a0001c0003t0008g0252a0001c0005t0003g0254others(5): Show | 8 | HG01192.hp2 HG01517.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.20-3283dupC | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10805922 | ||||||
chr2:10805929
|
A | G | 1 | a0002c0002t0001g0231 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.20-3289T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10805929 | ||||||
chr2:10805994
|
G | GGCACATG others(29): Show |
132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.20-3355_20-3354ins others(36): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10805994 | ||||||
chr2:10806025
|
T | TA | 27 | a0001c0001t0001g0007a0001c0001t0001g0016a0001c0001t0001g0081others(24): Show | 33 | HG00408.hp1 HG00597.hp1 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.20-3386dupT | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806025 | ||||||
chr2:10806025
|
TA | T | 9 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0047others(6): Show | 9 | HG00733.hp2 HG01884.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.20-3386delT | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806025 | ||||||
chr2:10806025
|
TAA | T | 7 | a0001c0001t0001g0048a0001c0001t0001g0051a0001c0001t0001g0052others(4): Show | 7 | HG01109.hp2 HG02055.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.20-3387_20-3386del others(2): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806025 | ||||||
chr2:10806025
|
TAAA | T | 13 | a0001c0003t0001g0136a0001c0003t0001g0137a0002c0002t0001g0162others(10): Show | 13 | HG00408.hp2 HG02040.hp1 HG02165.hp2 others(10): Show |
intron_variant | MODIFIER | c.20-3388_20-3386del others(3): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806025 | ||||||
chr2:10806025
|
TAAAA | T | 65 | a0001c0003t0001g0204a0001c0003t0001g0229a0002c0002t0001g0156others(62): Show | 65 | HG00558.hp1 HG00642.hp2 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.20-3389_20-3386del others(4): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806025 | ||||||
chr2:10806025
|
TAAAAAA | T | 20 | a0001c0003t0008g0022a0001c0003t0008g0252a0001c0003t0016g0297others(17): Show | 24 | HG00280.hp1 HG01069.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.20-3391_20-3386del others(6): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806025 | ||||||
chr2:10806040
|
A | C | 1 | a0002c0002t0006g0291 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.20-3400T>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806040 | ||||||
chr2:10806041
|
AAAAC | A | 22 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(19): Show | 25 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(22): Show |
intron_variant | MODIFIER | c.20-3405_20-3402del others(4): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806041 | ||||||
chr2:10806042
|
A | C | 11 | a0001c0004t0002g0259a0001c0004t0002g0261a0001c0004t0002g0262others(8): Show | 11 | HG00639.hp1 HG02559.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.20-3402T>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806042 | ||||||
chr2:10806046
|
G | A | 106 | a0001c0003t0001g0136a0001c0003t0001g0137a0001c0003t0001g0204others(103): Show | 110 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.20-3406C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806046 | ||||||
chr2:10806046
|
G | C | 25 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(22): Show | 28 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.20-3406C>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806046 | ||||||
chr2:10806179
|
G | A | 3 | a0001c0001t0001g0017a0001c0001t0001g0104a0001c0001t0001g0106 | 4 | NA18960.hp1 NA18972.hp2 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.20-3539C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806179 | ||||||
chr2:10806288
|
G | A | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.20-3648C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806288 | ||||||
chr2:10806330
|
A | C | 1 | a0002c0002t0001g0156 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.20-3690T>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806330 | ||||||
chr2:10806330
|
A | G | 130 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(127): Show | 137 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.20-3690T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806330 | ||||||
chr2:10806367
|
C | CA | 5 | a0001c0001t0001g0013a0001c0001t0001g0061a0001c0001t0001g0119others(2): Show | 6 | HG06807.hp1 NA18973.hp1 NA19002.hp2 others(3): Show |
intron_variant | MODIFIER | c.20-3728dupT | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806367 | ||||||
chr2:10806367
|
CA | C | 93 | a0001c0001t0001g0050a0001c0001t0001g0106a0001c0003t0001g0204others(90): Show | 94 | HG00558.hp1 HG00639.hp2 HG00642.hp2 others(91): Show |
intron_variant | MODIFIER | c.20-3728delT | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806367 | ||||||
chr2:10806400
|
G | C | 16 | a0001c0005t0003g0011a0001c0005t0003g0018a0001c0005t0003g0138others(13): Show | 19 | HG00280.hp1 HG01099.hp1 HG01433.hp2 others(16): Show |
intron_variant | MODIFIER | c.20-3760C>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806400 | ||||||
chr2:10806421
|
C | T | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.20-3781G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806421 | ||||||
chr2:10806458
|
T | TA | 101 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(98): Show | 105 | HG00323.hp1 HG00408.hp2 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.20-3819dupT | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806458 | ||||||
chr2:10806458
|
TA | T | 16 | a0001c0001t0001g0049a0001c0001t0001g0057a0001c0001t0004g0002others(13): Show | 20 | HG01109.hp1 HG01167.hp2 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.20-3819delT | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806458 | ||||||
chr2:10806477
|
T | TTAGAAAG others(2980): Show |
1 | a0001c0003t0006g0295 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.20-3838_20-3837ins others(2987): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806477 | ||||||
chr2:10806505
|
A | G | 9 | a0001c0001t0001g0028a0001c0001t0005g0012a0001c0001t0005g0025others(6): Show | 10 | HG01978.hp2 HG02257.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.20-3865T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806505 | ||||||
chr2:10806563
|
C | A | 6 | a0001c0004t0002g0282a0001c0004t0002g0283a0001c0004t0002g0284others(3): Show | 6 | HG01261.hp1 HG01884.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.20-3923G>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806563 | ||||||
chr2:10806567
|
C | G | 21 | a0001c0003t0008g0022a0001c0003t0008g0252a0001c0003t0016g0297others(18): Show | 25 | HG00280.hp1 HG01069.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.20-3927G>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806567 | ||||||
chr2:10806622
|
T | TAAAGAGA others(238): Show |
1 | a0001c0003t0001g0229 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.20-3983_20-3982ins others(245): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806622 | ||||||
chr2:10806622
|
T | TAAAGAGA others(221): Show |
1 | a0002c0002t0001g0182 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.20-3983_20-3982ins others(228): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806622 | ||||||
chr2:10806622
|
T | TAAAGAGA others(222): Show |
1 | a0001c0003t0001g0204 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.20-3983_20-3982ins others(229): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806622 | ||||||
chr2:10806628
|
C | A | 4 | a0001c0003t0001g0204a0001c0003t0001g0229a0002c0002t0001g0182others(1): Show | 4 | HG01070.hp2 HG01192.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.20-3988G>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CAA | 26 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(23): Show | 29 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.20-3989_20-3988ins others(2): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CAAAAGAA others(192): Show |
1 | a0002c0002t0001g0203 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(199): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CAAAGAAA others(184): Show |
1 | a0002c0006t0001g0253 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(191): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CAAAGAAA others(180): Show |
1 | a0002c0006t0001g0215 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(187): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CAAAGAAA others(163): Show |
1 | a0004c0008t0001g0220 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(170): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CAAAGAAA others(248): Show |
1 | a0002c0002t0007g0152 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(255): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CAAAGAAA others(199): Show |
1 | a0005c0010t0001g0194 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(206): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CAAAGAAA others(179): Show |
1 | a0002c0002t0001g0195 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(186): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CAAAGAAA others(179): Show |
1 | a0002c0002t0001g0202 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(186): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CAAAGAAA others(155): Show |
1 | a0002c0002t0001g0221 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(162): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CAAAGAAA others(163): Show |
1 | a0002c0002t0001g0159 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(170): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CAAAGAAA others(580): Show |
1 | a0002c0002t0001g0227 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(587): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CAAAGAAA others(464): Show |
1 | a0002c0002t0001g0160 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(471): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CAAAGAAA others(526): Show |
1 | a0002c0002t0001g0186 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(533): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CAAAGAAA others(438): Show |
1 | a0002c0002t0001g0217 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(445): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CAAAGAAA others(449): Show |
1 | a0002c0002t0001g0158 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(456): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CAAAGAAA others(298): Show |
1 | a0002c0002t0001g0211 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(305): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CAAAGAAA others(322): Show |
1 | a0002c0002t0001g0162 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(329): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CAAAGAAA others(254): Show |
1 | a0002c0002t0001g0223 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(261): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CAAAGAAA others(246): Show |
1 | a0002c0002t0001g0206 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(253): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CAAAGAAA others(337): Show |
1 | a0002c0002t0001g0165 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(344): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CAAAGAAA others(210): Show |
2 | a0002c0002t0001g0230a0002c0009t0001g0192 | 2 | NA18999.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.20-3989_20-3988ins others(217): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CAAAGAAA others(373): Show |
1 | a0002c0002t0001g0171 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(380): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CAAAGAAA others(229): Show |
1 | a0002c0002t0001g0181 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(236): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CAAAGAAA others(202): Show |
1 | a0002c0002t0001g0198 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(209): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CAAAGAAA others(198): Show |
1 | a0002c0002t0001g0231 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(205): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CAAAGAAA others(288): Show |
1 | a0002c0002t0001g0169 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(295): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CAAAGAAA others(209): Show |
1 | a0002c0002t0001g0209 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(216): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CAAAGAAA others(366): Show |
1 | a0002c0002t0001g0168 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(373): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CAAAGAAA others(206): Show |
1 | a0002c0002t0001g0173 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(213): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CAAAGAAA others(186): Show |
1 | a0002c0002t0001g0193 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(193): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CAAAGAAA others(254): Show |
1 | a0002c0002t0001g0207 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(261): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CAAAGAAA others(190): Show |
1 | a0002c0002t0001g0189 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(197): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CAAAGAAA others(628): Show |
1 | a0002c0002t0001g0156 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(635): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CAAAGAAA others(228): Show |
1 | a0002c0002t0001g0199 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(235): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CAAAGAAA others(453): Show |
1 | a0002c0002t0001g0216 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(460): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CAAAGAAA others(222): Show |
1 | a0002c0002t0001g0167 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(229): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CAAAGAAA others(533): Show |
1 | a0002c0002t0001g0218 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(540): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CAAAGAAA others(154): Show |
1 | a0002c0002t0001g0232 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(161): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CAAAGAAA others(142): Show |
1 | a0002c0002t0001g0200 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(149): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CAAAGAAA others(233): Show |
1 | a0002c0002t0001g0201 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(240): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CAAAGAAA others(204): Show |
1 | a0002c0002t0001g0224 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(211): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CAAAGAAA others(238): Show |
1 | a0002c0002t0001g0170 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(245): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CAAAGAAA others(309): Show |
1 | a0002c0002t0001g0166 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(316): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CAAAGAAA others(175): Show |
1 | a0002c0002t0001g0184 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(182): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CAAAGAAA others(555): Show |
1 | a0002c0002t0001g0210 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(562): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CAAAGAAA others(464): Show |
1 | a0002c0002t0001g0185 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(471): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CAAAGAAA others(413): Show |
1 | a0002c0002t0001g0157 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(420): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CAAAGAAA others(178): Show |
1 | a0002c0002t0001g0196 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(185): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CAAAGAAA others(236): Show |
1 | a0002c0002t0001g0179 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(243): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CAAAGAAA others(186): Show |
1 | a0002c0002t0001g0176 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(193): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CAAAGAAA others(182): Show |
1 | a0002c0002t0001g0172 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(189): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CAAAGAAA others(166): Show |
1 | a0002c0002t0001g0178 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(173): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CAAAGAAA others(186): Show |
1 | a0002c0002t0001g0205 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(193): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CAAAGAAA others(201): Show |
1 | a0002c0002t0001g0164 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(208): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CAAAGAAA others(194): Show |
1 | a0002c0002t0001g0163 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(201): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CAAAGAAA others(414): Show |
1 | a0002c0002t0006g0291 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(421): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CAAAGAAG others(508): Show |
1 | a0002c0002t0001g0183 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(515): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CAAAGACA others(194): Show |
1 | a0002c0002t0001g0188 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(201): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CAAAGACA others(430): Show |
1 | a0002c0002t0001g0175 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(437): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CAAGAAAA others(441): Show |
1 | a0002c0002t0001g0228 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(448): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CAAGAAAG others(174): Show |
1 | a0002c0002t0001g0219 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(181): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CAAGAAAG others(600): Show |
1 | a0002c0002t0001g0191 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(607): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CAAGAAAG others(367): Show |
1 | a0002c0002t0001g0197 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(374): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CAGAAAGA others(340): Show |
1 | a0002c0002t0006g0293 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(347): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CAGACAGA others(33): Show |
1 | a0001c0005t0003g0145 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(40): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CAGACAGA others(33): Show |
2 | a0001c0005t0003g0138a0001c0005t0003g0254 | 2 | HG01943.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.20-3989_20-3988ins others(40): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CAGACAGA others(37): Show |
8 | a0001c0005t0003g0011a0001c0005t0003g0018a0001c0005t0003g0140others(5): Show | 11 | HG00280.hp1 HG01099.hp1 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.20-3989_20-3988ins others(44): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CAGACAGA others(41): Show |
4 | a0001c0003t0016g0297a0001c0005t0003g0141a0001c0005t0003g0142others(1): Show | 4 | HG03239.hp1 HG03490.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.20-3989_20-3988ins others(48): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CAGACAGA others(45): Show |
3 | a0001c0005t0003g0143a0001c0005t0003g0144a0001c0005t0003g0255 | 3 | HG01934.hp1 HG03710.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.20-3989_20-3988ins others(52): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CAGACAGA others(29): Show |
2 | a0001c0003t0008g0022a0001c0003t0008g0252 | 3 | HG01069.hp2 HG01071.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.20-3989_20-3988ins others(36): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CAGACAGA others(41): Show |
1 | a0001c0005t0003g0139 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(48): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CAGACAGA others(144): Show |
1 | a0002c0002t0001g0177 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(151): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CGAAAGAA others(224): Show |
1 | a0002c0002t0001g0213 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(231): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CGAAAGAA others(298): Show |
1 | a0002c0002t0006g0292 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(305): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CGAAAGAA others(484): Show |
1 | a0002c0002t0007g0155 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(491): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CGAAAGAA others(387): Show |
1 | a0002c0002t0001g0187 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(394): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CGAAAGAA others(255): Show |
1 | a0002c0002t0001g0174 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(262): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CGAAAGAA others(212): Show |
1 | a0002c0002t0001g0214 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(219): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CGAAAGAA others(211): Show |
1 | a0002c0002t0001g0190 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(218): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CGAAAGAA others(215): Show |
1 | a0002c0002t0001g0208 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(222): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CGAAAGAA others(203): Show |
1 | a0002c0002t0001g0212 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(210): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CGAAAGAA others(204): Show |
1 | a0002c0002t0001g0180 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(211): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CGAAAGAA others(231): Show |
1 | a0002c0002t0007g0154 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(238): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CGAAAGAA others(227): Show |
1 | a0002c0002t0007g0153 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(234): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CGAAAGAA others(113): Show |
2 | a0001c0003t0001g0136a0001c0003t0001g0137 | 2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.20-3989_20-3988ins others(120): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806628
|
C | CGAAGGAA others(190): Show |
1 | a0002c0002t0001g0222 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.20-3989_20-3988ins others(197): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806628 | ||||||
chr2:10806648
|
A | AAGAAAGA others(289): Show |
1 | a0002c0002t0001g0226 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.20-4009_20-4008ins others(296): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806648 | ||||||
chr2:10806648
|
A | AAGAAAGA others(255): Show |
1 | a0002c0002t0001g0225 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.20-4009_20-4008ins others(262): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806648 | ||||||
chr2:10806648
|
A | AAGAAAGA others(461): Show |
1 | a0002c0002t0001g0233 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.20-4009_20-4008ins others(468): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806648 | ||||||
chr2:10806648
|
A | AAGAAGGA others(86): Show |
1 | a0001c0003t0006g0294 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.20-4009_20-4008ins others(93): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806648 | ||||||
chr2:10806648
|
A | AAGAAGGA others(98): Show |
5 | a0001c0003t0001g0019a0001c0003t0001g0236a0001c0003t0001g0237others(2): Show | 6 | HG01099.hp2 HG01256.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.20-4009_20-4008ins others(105): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806648 | ||||||
chr2:10806648
|
A | AAGAAGGA others(94): Show |
6 | a0001c0003t0001g0238a0001c0003t0001g0239a0001c0003t0001g0240others(3): Show | 6 | HG01123.hp2 HG02074.hp1 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.20-4009_20-4008ins others(101): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806648 | ||||||
chr2:10806648
|
A | AAGAAGGA others(90): Show |
5 | a0001c0003t0001g0021a0001c0003t0001g0242a0001c0003t0001g0248others(2): Show | 6 | HG00733.hp1 HG01255.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.20-4009_20-4008ins others(97): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806648 | ||||||
chr2:10806648
|
A | AAGAAGGA others(86): Show |
1 | a0001c0003t0006g0295 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.20-4009_20-4008ins others(93): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806648 | ||||||
chr2:10806648
|
A | AAGAAGGA others(98): Show |
2 | a0001c0003t0001g0020a0001c0003t0001g0245 | 3 | HG00323.hp1 NA18945.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.20-4009_20-4008ins others(105): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806648 | ||||||
chr2:10806648
|
A | AAGAAGGA others(90): Show |
1 | a0001c0003t0001g0250 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.20-4009_20-4008ins others(97): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806648 | ||||||
chr2:10806648
|
A | AAGAAGGA others(82): Show |
1 | a0001c0003t0001g0235 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.20-4009_20-4008ins others(89): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806648 | ||||||
chr2:10806648
|
A | AAGAAGGA others(102): Show |
1 | a0001c0003t0001g0234 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.20-4009_20-4008ins others(109): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806648 | ||||||
chr2:10806648
|
A | C | 84 | a0001c0003t0001g0136a0001c0003t0001g0137a0001c0003t0001g0204others(81): Show | 84 | HG00408.hp2 HG00558.hp1 HG00642.hp2 others(81): Show |
intron_variant | MODIFIER | c.20-4008T>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806648 | ||||||
chr2:10806650
|
A | AGAAAGAA others(586): Show |
1 | a0002c0002t0001g0161 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.20-4011_20-4010ins others(593): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806650 | ||||||
chr2:10806650
|
A | G | 131 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(128): Show | 138 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.20-4010T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806650 | ||||||
chr2:10806695
|
T | C | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.20-4055A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806695 | ||||||
chr2:10806758
|
A | T | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.20-4118T>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806758 | ||||||
chr2:10806860
|
C | T | 23 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(20): Show | 26 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.20-4220G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806860 | ||||||
chr2:10806863
|
G | C | 1 | a0002c0002t0001g0227 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.20-4223C>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806863 | ||||||
chr2:10806865
|
C | A | 1 | a0002c0002t0001g0156 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.20-4225G>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806865 | ||||||
chr2:10806866
|
G | A | 9 | a0001c0001t0001g0028a0001c0001t0005g0012a0001c0001t0005g0025others(6): Show | 10 | HG01978.hp2 HG02257.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.20-4226C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806866 | ||||||
chr2:10806876
|
A | G | 164 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(161): Show | 172 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.20-4236T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806876 | ||||||
chr2:10806909
|
C | T | 1 | a0001c0001t0005g0032 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.20-4269G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806909 | ||||||
chr2:10806920
|
G | A | 1 | a0002c0002t0001g0202 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.20-4280C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806920 | ||||||
chr2:10806993
|
T | C | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.20-4353A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10806993 | ||||||
chr2:10807044
|
T | G | 1 | a0001c0001t0001g0059 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.20-4404A>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10807044 | ||||||
chr2:10807046
|
A | G | 1 | a0002c0002t0001g0157 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.20-4406T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10807046 | ||||||
chr2:10807134
|
A | G | 2 | a0001c0001t0009g0256a0001c0001t0009g0257 | 2 | HG01884.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.20-4494T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10807134 | ||||||
chr2:10807250
|
C | T | 1 | a0001c0004t0002g0271 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.20-4610G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10807250 | ||||||
chr2:10807258
|
G | T | 1 | a0001c0003t0001g0137 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.20-4618C>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10807258 | ||||||
chr2:10807393
|
A | G | 1 | a0001c0001t0001g0128 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.20-4753T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10807393 | ||||||
chr2:10807675
|
A | G | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.19+5003T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10807675 | ||||||
chr2:10807731
|
T | C | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.19+4947A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10807731 | ||||||
chr2:10807799
|
A | G | 2 | a0001c0003t0001g0204a0001c0003t0001g0229 | 2 | HG01070.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.19+4879T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10807799 | ||||||
chr2:10807814
|
A | T | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.19+4864T>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10807814 | ||||||
chr2:10807867
|
C | A | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.19+4811G>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10807867 | ||||||
chr2:10807926
|
T | A | 11 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0047others(8): Show | 11 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.19+4752A>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10807926 | ||||||
chr2:10807964
|
A | G | 23 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(20): Show | 26 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.19+4714T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10807964 | ||||||
chr2:10808015
|
A | G | 18 | a0001c0005t0003g0011a0001c0005t0003g0018a0001c0005t0003g0138others(15): Show | 21 | HG00280.hp1 HG01099.hp1 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.19+4663T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10808015 | ||||||
chr2:10808157
|
A | C | 2 | a0003c0007t0005g0062a0003c0007t0005g0063 | 2 | HG01496.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.19+4521T>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10808157 | ||||||
chr2:10808283
|
G | A | 131 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(128): Show | 138 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.19+4395C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10808283 | ||||||
chr2:10808283
|
G | C | 1 | a0001c0001t0001g0047 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.19+4395C>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10808283 | ||||||
chr2:10808284
|
A | C | 1 | a0001c0001t0001g0082 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.19+4394T>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10808284 | ||||||
chr2:10808422
|
C | A | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.19+4256G>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10808422 | ||||||
chr2:10808446
|
AC | A | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.19+4231delG | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10808446 | ||||||
chr2:10808460
|
A | T | 15 | a0001c0005t0003g0011a0001c0005t0003g0018a0001c0005t0003g0138others(12): Show | 18 | HG00280.hp1 HG01099.hp1 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.19+4218T>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10808460 | ||||||
chr2:10808488
|
G | A | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.19+4190C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10808488 | ||||||
chr2:10808600
|
G | A | 1 | a0001c0004t0002g0264 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.19+4078C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10808600 | ||||||
chr2:10808705
|
T | C | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.19+3973A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10808705 | ||||||
chr2:10808736
|
A | G | 10 | a0001c0004t0002g0259a0001c0004t0002g0261a0001c0004t0002g0262others(7): Show | 10 | HG00639.hp1 HG02559.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.19+3942T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10808736 | ||||||
chr2:10808848
|
C | T | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.19+3830G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10808848 | ||||||
chr2:10808870
|
G | C | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.19+3808C>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10808870 | ||||||
chr2:10808882
|
G | C | 1 | a0001c0004t0001g0279 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.19+3796C>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10808882 | ||||||
chr2:10809052
|
G | A | 1 | a0001c0004t0002g0265 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.19+3626C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809052 | ||||||
chr2:10809053
|
C | A | 6 | a0001c0004t0002g0271a0001c0004t0002g0272a0001c0004t0002g0273others(3): Show | 6 | HG00639.hp2 HG02257.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.19+3625G>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809053 | ||||||
chr2:10809054
|
C | G | 6 | a0001c0004t0002g0271a0001c0004t0002g0272a0001c0004t0002g0273others(3): Show | 6 | HG00639.hp2 HG02257.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.19+3624G>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809054 | ||||||
chr2:10809075
|
C | T | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.19+3603G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809075 | ||||||
chr2:10809088
|
C | T | 6 | a0001c0004t0002g0282a0001c0004t0002g0283a0001c0004t0002g0284others(3): Show | 6 | HG01261.hp1 HG01884.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.19+3590G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809088 | ||||||
chr2:10809105
|
G | A | 1 | a0001c0001t0001g0105 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.19+3573C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809105 | ||||||
chr2:10809165
|
T | C | 10 | a0001c0004t0002g0259a0001c0004t0002g0261a0001c0004t0002g0262others(7): Show | 10 | HG00639.hp1 HG02559.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.19+3513A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809165 | ||||||
chr2:10809206
|
T | G | 1 | a0001c0005t0003g0146 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.19+3472A>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809206 | ||||||
chr2:10809241
|
T | C | 1 | a0002c0002t0001g0228 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.19+3437A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809241 | ||||||
chr2:10809304
|
A | G | 131 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(128): Show | 138 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.19+3374T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809304 | ||||||
chr2:10809393
|
A | G | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.19+3285T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809393 | ||||||
chr2:10809447
|
C | T | 14 | a0001c0001t0004g0002a0001c0001t0004g0034a0001c0001t0004g0035others(11): Show | 18 | HG01109.hp1 HG01167.hp2 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.19+3231G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809447 | ||||||
chr2:10809463
|
G | A | 2 | a0001c0003t0008g0022a0001c0003t0008g0252 | 3 | HG01069.hp2 HG01071.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.19+3215C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809463 | ||||||
chr2:10809488
|
C | T | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.19+3190G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809488 | ||||||
chr2:10809494
|
G | A | 1 | a0002c0002t0001g0202 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.19+3184C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809494 | ||||||
chr2:10809495
|
G | A | 86 | a0001c0003t0001g0204a0001c0003t0001g0229a0002c0002t0001g0156others(83): Show | 86 | HG00408.hp2 HG00558.hp1 HG00642.hp2 others(83): Show |
intron_variant | MODIFIER | c.19+3183C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809495 | ||||||
chr2:10809510
|
T | C | 131 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(128): Show | 138 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.19+3168A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809510 | ||||||
chr2:10809554
|
G | A | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.19+3124C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809554 | ||||||
chr2:10809556
|
T | C | 111 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(108): Show | 114 | HG00323.hp1 HG00408.hp2 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.19+3122A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809556 | ||||||
chr2:10809645
|
C | CA | 14 | a0001c0001t0001g0033a0001c0001t0001g0048a0001c0001t0001g0065others(11): Show | 14 | HG00323.hp2 HG01261.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.19+3032dupT | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809645 | ||||||
chr2:10809645
|
C | CAA | 38 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0013others(35): Show | 46 | HG00280.hp2 HG00609.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.19+3031_19+3032dup others(2): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809645 | ||||||
chr2:10809645
|
C | CAAA | 41 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(38): Show | 55 | HG00558.hp2 HG00642.hp1 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.19+3030_19+3032dup others(3): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809645 | ||||||
chr2:10809645
|
C | CAAAA | 35 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0010others(32): Show | 47 | HG00408.hp1 HG00597.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.19+3029_19+3032dup others(4): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809645 | ||||||
chr2:10809645
|
C | CAAAAA | 20 | a0001c0001t0001g0060a0001c0001t0001g0120a0001c0001t0001g0121others(17): Show | 20 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.19+3028_19+3032dup others(5): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809645 | ||||||
chr2:10809645
|
C | CAAAAAA | 6 | a0001c0001t0001g0128a0001c0001t0005g0025a0001c0001t0005g0026others(3): Show | 6 | HG00733.hp1 HG01243.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.19+3027_19+3032dup others(6): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809645 | ||||||
chr2:10809645
|
C | CAAAAAAA | 6 | a0001c0001t0001g0028a0001c0001t0005g0012a0001c0001t0005g0027others(3): Show | 7 | HG01978.hp2 HG02257.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.19+3026_19+3032dup others(7): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809645 | ||||||
chr2:10809645
|
C | CAAAAAAA others(3): Show |
1 | a0001c0001t0005g0032 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.19+3023_19+3032dup others(10): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809645 | ||||||
chr2:10809645
|
C | CAAAAAAA others(4): Show |
1 | a0001c0004t0002g0280 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.19+3022_19+3032dup others(11): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809645 | ||||||
chr2:10809645
|
CAAA | C | 14 | a0001c0005t0003g0011a0001c0005t0003g0018a0001c0005t0003g0138others(11): Show | 17 | HG00280.hp1 HG01099.hp1 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.19+3030_19+3032del others(3): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809645 | ||||||
chr2:10809645
|
CAAAAAAA | C | 12 | a0001c0001t0004g0002a0001c0001t0004g0034a0001c0001t0004g0035others(9): Show | 16 | HG01167.hp2 HG01169.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.19+3026_19+3032del others(7): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809645 | ||||||
chr2:10809645
|
CAAAAAAA others(1): Show |
C | 8 | a0001c0004t0002g0259a0001c0004t0002g0261a0001c0004t0002g0262others(5): Show | 8 | HG00639.hp1 HG02723.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.19+3025_19+3032del others(8): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809645 | ||||||
chr2:10809668
|
A | AAC | 27 | a0001c0003t0001g0204a0002c0002t0001g0203a0002c0002t0001g0205others(24): Show | 27 | HG01070.hp2 HG01175.hp1 HG01192.hp1 others(24): Show |
intron_variant | MODIFIER | c.19+3009_19+3010ins others(2): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809668 | ||||||
chr2:10809668
|
A | AC | 49 | a0002c0002t0001g0157a0002c0002t0001g0158a0002c0002t0001g0159others(46): Show | 49 | HG00408.hp2 HG00558.hp1 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.19+3009_19+3010ins others(1): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809668 | ||||||
chr2:10809668
|
A | C | 4 | a0002c0002t0001g0156a0002c0002t0001g0161a0002c0002t0006g0291others(1): Show | 4 | HG01081.hp2 HG04204.hp1 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.19+3010T>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809668 | ||||||
chr2:10809672
|
A | T | 1 | a0002c0002t0001g0160 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.19+3006T>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809672 | ||||||
chr2:10809761
|
C | G | 1 | a0001c0001t0001g0033 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.19+2917G>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809761 | ||||||
chr2:10809788
|
T | C | 1 | a0001c0004t0002g0281 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.19+2890A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809788 | ||||||
chr2:10809889
|
T | A | 1 | a0002c0002t0001g0233 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.19+2789A>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809889 | ||||||
chr2:10809985
|
ATGAC | A | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.19+2689_19+2692del others(4): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809985 | ||||||
chr2:10809990
|
T | A | 2 | a0001c0003t0001g0136a0001c0003t0001g0137 | 2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.19+2688A>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10809990 | ||||||
chr2:10810010
|
T | C | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.19+2668A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10810010 | ||||||
chr2:10810111
|
G | A | 5 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(2): Show | 5 | NA18950.hp1 NA18975.hp1 NA18978.hp1 others(2): Show |
intron_variant | MODIFIER | c.19+2567C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10810111 | ||||||
chr2:10810158
|
G | C | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.19+2520C>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10810158 | ||||||
chr2:10810404
|
A | G | 2 | a0001c0001t0001g0013a0001c0001t0001g0061 | 3 | NA18973.hp1 NA19002.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.19+2274T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10810404 | ||||||
chr2:10810489
|
T | C | 9 | a0001c0001t0001g0028a0001c0001t0005g0012a0001c0001t0005g0025others(6): Show | 10 | HG01978.hp2 HG02257.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.19+2189A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10810489 | ||||||
chr2:10810510
|
T | C | 1 | a0001c0005t0003g0151 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.19+2168A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10810510 | ||||||
chr2:10810539
|
T | C | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.19+2139A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10810539 | ||||||
chr2:10810542
|
T | G | 2 | a0001c0003t0008g0022a0001c0003t0008g0252 | 3 | HG01069.hp2 HG01071.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.19+2136A>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10810542 | ||||||
chr2:10810809
|
A | G | 2 | a0001c0003t0001g0234a0001c0003t0001g0235 | 2 | HG00597.hp2 HG00609.hp2 |
intron_variant | MODIFIER | c.19+1869T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10810809 | ||||||
chr2:10810878
|
G | C | 1 | a0001c0003t0001g0251 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.19+1800C>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10810878 | ||||||
chr2:10810992
|
T | A | 18 | a0001c0005t0003g0011a0001c0005t0003g0018a0001c0005t0003g0138others(15): Show | 21 | HG00280.hp1 HG01099.hp1 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.19+1686A>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10810992 | ||||||
chr2:10811035
|
G | T | 95 | a0001c0001t0001g0028a0001c0001t0005g0012a0001c0001t0005g0025others(92): Show | 96 | HG00408.hp2 HG00558.hp1 HG00642.hp2 others(93): Show |
intron_variant | MODIFIER | c.19+1643C>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10811035 | ||||||
chr2:10811036
|
A | C | 95 | a0001c0001t0001g0028a0001c0001t0005g0012a0001c0001t0005g0025others(92): Show | 96 | HG00408.hp2 HG00558.hp1 HG00642.hp2 others(93): Show |
intron_variant | MODIFIER | c.19+1642T>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10811036 | ||||||
chr2:10811042
|
C | T | 4 | a0002c0002t0001g0156a0002c0002t0001g0157a0002c0002t0001g0158others(1): Show | 4 | HG01081.hp2 HG01258.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.19+1636G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10811042 | ||||||
chr2:10811043
|
A | G | 207 | a0001c0001t0001g0004a0001c0001t0001g0028a0001c0001t0001g0033others(204): Show | 223 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(220): Show |
intron_variant | MODIFIER | c.19+1635T>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10811043 | ||||||
chr2:10811070
|
T | A | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.19+1608A>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10811070 | ||||||
chr2:10811123
|
A | C | 4 | a0002c0002t0007g0152a0002c0002t0007g0153a0002c0002t0007g0154others(1): Show | 4 | HG02040.hp1 NA18951.hp1 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.19+1555T>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10811123 | ||||||
chr2:10811361
|
C | A | 2 | a0001c0003t0001g0136a0001c0003t0001g0137 | 2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.19+1317G>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10811361 | ||||||
chr2:10811476
|
G | A | 1 | a0001c0003t0016g0297 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.19+1202C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10811476 | ||||||
chr2:10811501
|
AACAGAAA others(7): Show |
A | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.19+1163_19+1176del others(14): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10811501 | ||||||
chr2:10811577
|
G | C | 6 | a0001c0004t0002g0282a0001c0004t0002g0283a0001c0004t0002g0284others(3): Show | 6 | HG01261.hp1 HG01884.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.19+1101C>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10811577 | ||||||
chr2:10811669
|
G | A | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.19+1009C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10811669 | ||||||
chr2:10811687
|
G | C | 1 | a0001c0004t0002g0288 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.19+991C>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10811687 | ||||||
chr2:10811785
|
C | G | 130 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(127): Show | 137 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.19+893G>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10811785 | ||||||
chr2:10812099
|
G | C | 1 | a0001c0003t0001g0021 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.19+579C>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10812099 | ||||||
chr2:10812100
|
G | C | 1 | a0001c0003t0001g0021 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.19+578C>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10812100 | ||||||
chr2:10812124
|
G | T | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.19+554C>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10812124 | ||||||
chr2:10812147
|
T | C | 1 | a0001c0001t0001g0134 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.19+531A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10812147 | ||||||
chr2:10812167
|
T | C | 1 | a0001c0001t0001g0135 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.19+511A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10812167 | ||||||
chr2:10812231
|
T | G | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.19+447A>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10812231 | ||||||
chr2:10812238
|
T | C | 2 | a0001c0003t0008g0022a0001c0003t0008g0252 | 3 | HG01069.hp2 HG01071.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.19+440A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10812238 | ||||||
chr2:10812246
|
G | A | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.19+432C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10812246 | ||||||
chr2:10812265
|
A | T | 207 | a0001c0001t0001g0004a0001c0001t0001g0028a0001c0001t0001g0033others(204): Show | 223 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(220): Show |
intron_variant | MODIFIER | c.19+413T>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10812265 | ||||||
chr2:10812309
|
C | A | 1 | a0002c0006t0001g0253 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.19+369G>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10812309 | ||||||
chr2:10812321
|
G | A | 164 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(161): Show | 172 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.19+357C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10812321 | ||||||
chr2:10812343
|
T | TCCGGGAA others(14): Show |
18 | a0001c0005t0003g0011a0001c0005t0003g0018a0001c0005t0003g0138others(15): Show | 21 | HG00280.hp1 HG01099.hp1 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.19+334_19+335insGG others(19): Show |
PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10812343 | ||||||
chr2:10812354
|
A | T | 132 | a0001c0003t0001g0019a0001c0003t0001g0020a0001c0003t0001g0021others(129): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.19+324T>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10812354 | ||||||
chr2:10812522
|
C | G | 1 | a0002c0011t0001g0024 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.19+156G>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10812522 | ||||||
chr2:10812522
|
C | T | 16 | a0001c0005t0003g0011a0001c0005t0003g0018a0001c0005t0003g0138others(13): Show | 19 | HG00280.hp1 HG01099.hp1 HG01433.hp2 others(16): Show |
intron_variant | MODIFIER | c.19+156G>A | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10812522 | ||||||
chr2:10812589
|
G | A | 32 | a0001c0004t0001g0279a0001c0004t0002g0023a0001c0004t0002g0259others(29): Show | 33 | HG00639.hp1 HG00639.hp2 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.19+89C>T | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10812589 | ||||||
chr2:10812653
|
C | G | 2 | a0001c0003t0001g0136a0001c0003t0001g0137 | 2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.19+25G>C | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10812653 | ||||||
chr2:10812664
|
T | C | 167 | a0001c0001t0001g0258a0001c0001t0009g0256a0001c0001t0009g0257others(164): Show | 175 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(172): Show |
intron_variant | MODIFIER | c.19+14A>G | PDIA6 | ENSG00000143870.13 | transcript | ENST00000272227.8 | protein_coding | 1/12 | chr2 | 10812664 |