Item | Value |
---|---|
geneid | 6433 |
ensemblid | ENSG00000061936.10 |
hgncid | 10790 |
symbol | SFSWAP |
name | splicing factor SWAP |
refseq_nuc | NM_004592.4 |
refseq_prot | NP_004583.2 |
ensembl_nuc | ENST00000261674.9 |
ensembl_prot | ENSP00000261674.4 |
mane_status | MANE Select |
chr | chr12 |
start | 131711090 |
end | 131799738 |
strand | + |
ver | v1.2 |
region | chr12:131711090-131799738 |
region5000 | chr12:131706090-131804738 |
regionname0 | SFSWAP_chr12_131711090_131799738 |
regionname5000 | SFSWAP_chr12_131706090_131804738 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0000 | 0/0 | 0 | 5 | 2 | 1 | 2 | 0 | 0 | 2 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0001 | 0/1 | 951 | 284 | 69 | 69 | 104 | 10 | 31 | 75 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0002 | 1/0 | 951 | 18 | 11 | 1 | 1 | 2 | 2 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0003 | 0/0 | 951 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0004 | 0/0 | 951 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0005 | 0/0 | 951 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0006 | 0/0 | 951 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0007 | 0/0 | 951 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0008 | 0/0 | 951 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0009 | 0/0 | 951 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0010 | 0/0 | 951 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0011 | 0/0 | 951 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0012 | 0/0 | 951 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 2856 | 241 | 52 | 51 | 103 | 8 | 26 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
c0002 | 0/0 | 2856 | 19 | 1 | 13 | 0 | 2 | 3 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
c0003 | 0/0 | 2856 | 14 | 10 | 1 | 1 | 2 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
c0004 | 0/0 | 2856 | 6 | 6 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
c0005 | 0/0 | 2857 | 4 | 1 | 1 | 2 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
c0006 | 0/0 | 2856 | 3 | 3 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
c0007 | 0/0 | 2856 | 2 | 0 | 2 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
c0008 | 0/0 | 2856 | 2 | 0 | 2 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
c0009 | 0/0 | 2856 | 2 | 2 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
c0010 | 0/0 | 2856 | 2 | 0 | 1 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
c0011 | 0/0 | 2856 | 2 | 2 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
c0012 | 0/0 | 2856 | 2 | 2 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
c0013 | 0/0 | 2856 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
c0014 | 0/0 | 2856 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
c0015 | 0/0 | 2856 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
c0016 | 0/0 | 2856 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
c0017 | 0/0 | 2856 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
c0018 | 0/0 | 2856 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
c0019 | 0/0 | 2856 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
c0020 | 0/0 | 2856 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
c0021 | 0/0 | 2856 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
c0022 | 0/0 | 2856 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
c0023 | 0/0 | 2857 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
c0024 | 0/0 | 2856 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
c0025 | 0/0 | 2856 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
c0026 | 1/0 | 2856 | 1 | 0 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
c0027 | 0/0 | 2856 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
c0028 | 0/0 | 2856 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
c0029 | 0/0 | 2856 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
c0030 | 0/0 | 2856 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
c0031 | 0/0 | 2856 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 391 | 244 | 40 | 64 | 104 | 10 | 25 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
t0002 | 0/0 | 391 | 42 | 23 | 5 | 5 | 0 | 9 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
t0003 | 0/0 | 391 | 24 | 22 | 1 | 0 | 1 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
t0004 | 1/0 | 391 | 7 | 1 | 1 | 1 | 1 | 2 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
t0005 | 0/0 | 391 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0029 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0213 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0000c0005 | 0/0 | 2857 | 4 | 1 | 1 | 2 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0000c0023 | 0/0 | 2857 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0001c0001 | 0/1 | 2856 | 241 | 52 | 51 | 103 | 8 | 26 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0001c0002 | 0/0 | 2856 | 19 | 1 | 13 | 0 | 2 | 3 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0001c0004 | 0/0 | 2856 | 6 | 6 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0001c0006 | 0/0 | 2856 | 3 | 3 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0001c0007 | 0/0 | 2856 | 2 | 0 | 2 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0001c0008 | 0/0 | 2856 | 2 | 0 | 2 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0001c0010 | 0/0 | 2856 | 2 | 0 | 1 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0001c0011 | 0/0 | 2856 | 2 | 2 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0001c0012 | 0/0 | 2856 | 2 | 2 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0001c0015 | 0/0 | 2856 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0001c0018 | 0/0 | 2856 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0001c0019 | 0/0 | 2856 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0001c0029 | 0/0 | 2856 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0001c0031 | 0/0 | 2856 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0002c0003 | 0/0 | 2856 | 14 | 10 | 1 | 1 | 2 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0002c0025 | 0/0 | 2856 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0002c0026 | 1/0 | 2856 | 1 | 0 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0002c0027 | 0/0 | 2856 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0002c0028 | 0/0 | 2856 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0003c0009 | 0/0 | 2856 | 2 | 2 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0004c0014 | 0/0 | 2856 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0005c0016 | 0/0 | 2856 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0006c0024 | 0/0 | 2856 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0007c0020 | 0/0 | 2856 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0008c0021 | 0/0 | 2856 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0009c0022 | 0/0 | 2856 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0010c0017 | 0/0 | 2856 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0011c0013 | 0/0 | 2856 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0012c0030 | 0/0 | 2856 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0000c0005t0001 | 0/0 | 3247 | 4 | 1 | 1 | 2 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0000c0023t0001 | 0/0 | 3247 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0001c0001t0001 | 0/1 | 3246 | 196 | 26 | 45 | 98 | 8 | 18 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0001c0001t0002 | 0/0 | 3246 | 33 | 15 | 5 | 5 | 0 | 8 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0001c0001t0003 | 0/0 | 3246 | 10 | 10 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0001c0001t0004 | 0/0 | 3246 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0001c0001t0005 | 0/0 | 3246 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0001c0002t0001 | 0/0 | 3246 | 19 | 1 | 13 | 0 | 2 | 3 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0001c0004t0001 | 0/0 | 3246 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0001c0004t0002 | 0/0 | 3246 | 5 | 5 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0001c0006t0001 | 0/0 | 3246 | 3 | 3 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0001c0007t0001 | 0/0 | 3246 | 2 | 0 | 2 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0001c0008t0001 | 0/0 | 3246 | 2 | 0 | 2 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0001c0010t0001 | 0/0 | 3246 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0001c0010t0004 | 0/0 | 3246 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0001c0011t0002 | 0/0 | 3246 | 2 | 2 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0001c0012t0001 | 0/0 | 3246 | 2 | 2 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0001c0015t0002 | 0/0 | 3246 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0001c0018t0001 | 0/0 | 3246 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0001c0019t0001 | 0/0 | 3246 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0001c0029t0002 | 0/0 | 3246 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0001c0031t0001 | 0/0 | 3246 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0002c0003t0003 | 0/0 | 3246 | 12 | 10 | 1 | 0 | 1 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0002c0003t0004 | 0/0 | 3246 | 2 | 0 | 0 | 1 | 1 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0002c0025t0004 | 0/0 | 3246 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0002c0026t0004 | 1/0 | 3246 | 1 | 0 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0002c0027t0003 | 0/0 | 3246 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0002c0028t0004 | 0/0 | 3246 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0003c0009t0001 | 0/0 | 3246 | 2 | 2 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0004c0014t0001 | 0/0 | 3246 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0005c0016t0001 | 0/0 | 3246 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0006c0024t0001 | 0/0 | 3246 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0007c0020t0001 | 0/0 | 3246 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0008c0021t0003 | 0/0 | 3246 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0009c0022t0001 | 0/0 | 3246 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0010c0017t0001 | 0/0 | 3246 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0011c0013t0001 | 0/0 | 3246 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
a0012c0030t0001 | 0/0 | 3246 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | copy fasta | chr12 | 131706090 | 131804738 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0000c0005t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0000c0005t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0000c0005t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0000c0005t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0000c0023t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0213 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0003g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0003g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0004g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0001t0005g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0002t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0002t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0002t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0002t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0002t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0002t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0002t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0002t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0002t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0002t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0002t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0002t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0002t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0002t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0004t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0004t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0004t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0004t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0004t0002g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0004t0002g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0006t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0006t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0006t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0007t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0007t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0008t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0008t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0010t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0010t0004g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0011t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0011t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0012t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0012t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0015t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0018t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0019t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0029t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0001c0031t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0002c0003t0003g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0002c0003t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0002c0003t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0002c0003t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0002c0003t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0002c0003t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0002c0003t0003g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0002c0003t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0002c0003t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0002c0003t0003g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0002c0003t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0002c0003t0004g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0002c0003t0004g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0002c0025t0004g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0002c0026t0004g0029 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0002c0027t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0002c0028t0004g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0003c0009t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0003c0009t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0004c0014t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0005c0016t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0006c0024t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0007c0020t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0008c0021t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0009c0022t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0010c0017t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0011c0013t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
a0012c0030t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0202 | EUR | GBR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG00099 | hp2 | a0001 | c0002 | t0001 | g0292 | EUR | GBR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG00140 | hp1 | a0001 | c0002 | t0001 | g0286 | EUR | GBR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0226 | EUR | GBR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0206 | EUR | FIN | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0159 | EUR | FIN | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0075 | EUR | FIN | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0223 | EUR | FIN | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | CHS | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | CHS | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | CHS | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | CHS | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | CHS | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | CHS | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0062 | AMR | PUR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG00639 | hp2 | a0001 | c0002 | t0001 | g0293 | AMR | PUR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG00642 | hp1 | a0001 | c0002 | t0001 | g0302 | AMR | PUR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG00642 | hp2 | a0001 | c0001 | t0005 | g0222 | AMR | PUR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | CHS | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG00733 | hp2 | a0001 | c0008 | t0001 | g0235 | AMR | PUR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0304 | AMR | PUR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG00741 | hp1 | a0001 | c0002 | t0001 | g0300 | AMR | PUR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01071 | hp2 | a0001 | c0002 | t0001 | g0283 | AMR | PUR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01074 | hp2 | a0001 | c0002 | t0001 | g0291 | AMR | PUR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01081 | hp2 | a0001 | c0002 | t0001 | g0289 | AMR | PUR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01099 | hp2 | a0001 | c0002 | t0001 | g0295 | AMR | PUR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0085 | AMR | PUR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0096 | AMR | PUR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01168 | hp2 | a0001 | c0007 | t0001 | g0296 | AMR | PUR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01169 | hp1 | a0001 | c0007 | t0001 | g0284 | AMR | PUR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0088 | AMR | PUR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01175 | hp1 | a0001 | c0008 | t0001 | g0236 | AMR | PUR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01175 | hp2 | a0000 | c0005 | t0001 | g0121 | AMR | PUR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01243 | hp2 | a0001 | c0002 | t0001 | g0303 | AMR | PUR | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | CLM | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01257 | hp2 | a0001 | c0002 | t0001 | g0290 | AMR | CLM | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | CLM | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0263 | AMR | CLM | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01261 | hp1 | a0001 | c0010 | t0004 | g0023 | AMR | CLM | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01346 | hp1 | a0001 | c0002 | t0001 | g0294 | AMR | CLM | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | CLM | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01358 | hp1 | a0001 | c0002 | t0001 | g0298 | AMR | CLM | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | CLM | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | CLM | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | CLM | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0070 | EUR | IBS | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0265 | EUR | IBS | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01884 | hp1 | a0001 | c0002 | t0001 | g0297 | AFR | ACB | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0086 | AFR | ACB | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01891 | hp1 | a0003 | c0009 | t0001 | g0052 | AFR | ACB | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01891 | hp2 | a0001 | c0004 | t0002 | g0011 | AFR | ACB | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | PEL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01934 | hp2 | a0002 | c0003 | t0003 | g0033 | AMR | PEL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0277 | AMR | PEL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0057 | AMR | PEL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | PEL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PEL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PEL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PEL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01978 | hp2 | a0005 | c0016 | t0001 | g0214 | AMR | PEL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | PEL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | PEL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PEL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | KHV | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | KHV | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | KHV | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02055 | hp1 | a0001 | c0001 | t0003 | g0039 | AFR | ACB | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | KHV | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02071 | hp1 | a0007 | c0020 | t0001 | g0280 | EAS | KHV | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02129 | hp2 | a0001 | c0010 | t0001 | g0240 | EAS | KHV | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | KHV | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | KHV | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | KHV | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0084 | AFR | ACB | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02145 | hp2 | a0002 | c0003 | t0003 | g0030 | AFR | ACB | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | PEL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | CDX | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | CDX | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | CDX | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | CDX | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02257 | hp1 | a0000 | c0005 | t0001 | g0120 | AFR | ACB | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02257 | hp2 | a0002 | c0027 | t0003 | g0035 | AFR | ACB | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02258 | hp1 | a0001 | c0001 | t0003 | g0031 | AFR | ACB | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02258 | hp2 | a0003 | c0009 | t0001 | g0053 | AFR | ACB | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PEL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02280 | hp1 | a0001 | c0001 | t0003 | g0308 | AFR | ACB | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | PEL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02293 | hp2 | a0001 | c0002 | t0001 | g0287 | AMR | PEL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | PEL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02451 | hp1 | a0001 | c0015 | t0002 | g0008 | AFR | ACB | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02451 | hp2 | a0008 | c0021 | t0003 | g0020 | AFR | ACB | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0093 | AFR | GWD | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02572 | hp2 | a0002 | c0003 | t0003 | g0040 | AFR | GWD | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0282 | SAS | PJL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | GWD | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02630 | hp1 | a0001 | c0004 | t0001 | g0099 | AFR | GWD | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02630 | hp2 | a0001 | c0001 | t0003 | g0036 | AFR | GWD | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0077 | SAS | PJL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02683 | hp2 | a0001 | c0002 | t0001 | g0288 | SAS | PJL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0266 | SAS | PJL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02717 | hp2 | a0001 | c0011 | t0002 | g0080 | AFR | GWD | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02723 | hp1 | a0001 | c0004 | t0002 | g0009 | AFR | GWD | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0310 | SAS | PJL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02809 | hp2 | a0001 | c0001 | t0003 | g0018 | AFR | GWD | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0101 | AFR | GWD | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02886 | hp1 | a0001 | c0001 | t0003 | g0021 | AFR | GWD | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02886 | hp2 | a0001 | c0001 | t0004 | g0305 | AFR | GWD | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0098 | AFR | GWD | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | GWD | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02922 | hp1 | a0001 | c0006 | t0001 | g0016 | AFR | ESN | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | ESN | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ESN | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02965 | hp2 | a0002 | c0003 | t0003 | g0001 | AFR | ESN | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | ESN | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02976 | hp2 | a0002 | c0003 | t0003 | g0001 | AFR | ESN | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03017 | hp2 | a0002 | c0028 | t0004 | g0309 | SAS | PJL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03041 | hp1 | a0001 | c0011 | t0002 | g0081 | AFR | GWD | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03041 | hp2 | a0001 | c0004 | t0002 | g0306 | AFR | GWD | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03098 | hp2 | a0001 | c0012 | t0001 | g0044 | AFR | MSL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | ESN | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03130 | hp2 | a0001 | c0006 | t0001 | g0017 | AFR | ESN | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | ESN | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03139 | hp2 | a0001 | c0012 | t0001 | g0045 | AFR | ESN | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ESN | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03195 | hp2 | a0001 | c0004 | t0002 | g0307 | AFR | ESN | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0091 | AFR | MSL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | MSL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | MSL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03225 | hp2 | a0001 | c0018 | t0001 | g0015 | AFR | MSL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03239 | hp2 | a0009 | c0022 | t0001 | g0125 | SAS | PJL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03453 | hp1 | a0001 | c0031 | t0001 | g0046 | AFR | MSL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0089 | AFR | MSL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03490 | hp1 | a0004 | c0014 | t0001 | g0272 | SAS | PJL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03516 | hp1 | a0001 | c0001 | t0003 | g0038 | AFR | ESN | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | ESN | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03540 | hp1 | a0002 | c0003 | t0003 | g0028 | AFR | GWD | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0092 | AFR | GWD | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0055 | SAS | PJL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | BEB | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | BEB | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | BEB | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | BEB | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0078 | SAS | BEB | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | BEB | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0060 | SAS | BEB | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | BEB | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG04199 | hp1 | a0002 | c0025 | t0004 | g0042 | SAS | STU | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0065 | SAS | STU | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0056 | SAS | STU | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG04204 | hp2 | a0001 | c0002 | t0001 | g0301 | SAS | STU | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG04228 | hp1 | a0001 | c0029 | t0002 | g0059 | SAS | STU | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG04228 | hp2 | a0001 | c0019 | t0001 | g0195 | SAS | STU | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0094 | AFR | YRI | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18522 | hp2 | a0001 | c0001 | t0003 | g0311 | AFR | YRI | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | CHB | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | CHB | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18906 | hp1 | a0002 | c0003 | t0003 | g0027 | AFR | YRI | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0095 | AFR | YRI | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18962 | hp2 | a0006 | c0024 | t0001 | g0131 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18966 | hp1 | a0000 | c0005 | t0001 | g0251 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19009 | hp2 | a0011 | c0013 | t0001 | g0111 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0082 | AFR | LWK | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19030 | hp2 | a0001 | c0006 | t0001 | g0014 | AFR | LWK | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19043 | hp1 | a0002 | c0003 | t0003 | g0026 | AFR | LWK | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | LWK | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19057 | hp1 | a0002 | c0003 | t0004 | g0022 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19072 | hp1 | a0000 | c0005 | t0001 | g0199 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19240 | hp1 | a0001 | c0001 | t0003 | g0025 | AFR | YRI | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | YRI | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | ASW | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ASW | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA20752 | hp1 | a0002 | c0003 | t0003 | g0041 | EUR | TSI | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA20752 | hp2 | a0002 | c0003 | t0004 | g0024 | EUR | TSI | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA20905 | hp1 | a0012 | c0030 | t0001 | g0196 | SAS | GIH | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA20905 | hp2 | a0001 | c0002 | t0001 | g0299 | SAS | GIH | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG01123 | hp2 | a0001 | c0002 | t0001 | g0285 | AMR | CLM | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02109 | hp2 | a0002 | c0003 | t0003 | g0034 | AFR | ACB | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0097 | AFR | ACB | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02486 | hp2 | a0002 | c0003 | t0003 | g0043 | AFR | ACB | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02559 | hp1 | a0000 | c0023 | t0001 | g0051 | AFR | ACB | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0100 | AFR | ACB | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03471 | hp1 | a0001 | c0004 | t0002 | g0010 | AFR | MSL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0087 | AFR | MSL | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG06807 | hp1 | a0010 | c0017 | t0001 | g0209 | AFR | USA | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
HG06807 | hp2 | a0002 | c0003 | t0003 | g0032 | AFR | USA | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA21309 | hp1 | a0001 | c0001 | t0003 | g0037 | AFR | LWK | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | LWK | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0213 | REF | REF | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
homoSapiens_grch38 | hp1 | a0002 | c0026 | t0004 | g0029 | REF | REF | SFSWAP_chr12_131706090_131804738 | SFSWAP | chr12 | 131706090 | 131804738 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:131711375
|
A | G | 1 | a0012 | 1 | NA20905.hp1 | missense_variant | MODERATE | c.146A>G | p.Glu49Gly | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 1/18 | 286/3246 | 146/2856 | 49/951 | chr12 | 131711375 | ||
chr12:131714138
|
G | C | 1 | a0011 | 1 | NA19009.hp2 | missense_variant | MODERATE | c.286G>C | p.Asp96His | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 2/18 | 426/3246 | 286/2856 | 96/951 | chr12 | 131714138 | ||
chr12:131719498
|
G | A | 1 | a0004 | 1 | HG03490.hp1 | missense_variant | MODERATE | c.565G>A | p.Val189Ile | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/18 | 705/3246 | 565/2856 | 189/951 | chr12 | 131719498 | ||
chr12:131753245
|
G | A | 1 | a0005 | 1 | HG01978.hp2 | missense_variant | MODERATE | c.1204G>A | p.Val402Met | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 8/18 | 1344/3246 | 1204/2856 | 402/951 | chr12 | 131753245 | ||
chr12:131753303
|
T | C | 12 | a0000a0001a0003others(9): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
missense_variant | MODERATE | c.1262T>C | p.Leu421Pro | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 8/18 | 1402/3246 | 1262/2856 | 421/951 | chr12 | 131753303 | ||
chr12:131753306
|
C | T | 1 | a0006 | 1 | NA18962.hp2 | missense_variant | MODERATE | c.1265C>T | p.Pro422Leu | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 8/18 | 1405/3246 | 1265/2856 | 422/951 | chr12 | 131753306 | ||
chr12:131755465
|
G | A | 1 | a0010 | 1 | HG06807.hp1 | missense_variant | MODERATE | c.1534G>A | p.Gly512Ser | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 10/18 | 1674/3246 | 1534/2856 | 512/951 | chr12 | 131755465 | ||
chr12:131756537
|
A | G | 2 | a0000a0003 | 3 | HG01891.hp1 HG02258.hp2 HG02559.hp1 |
missense_variant | MODERATE | c.1613A>G | p.Glu538Gly | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/18 | 1753/3246 | 1613/2856 | 538/951 | chr12 | 131756537 | ||
chr12:131778324
|
G | A | 1 | a0007 | 1 | HG02071.hp1 | missense_variant | MODERATE | c.2402G>A | p.Arg801Gln | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/18 | 2542/3246 | 2402/2856 | 801/951 | chr12 | 131778324 | ||
chr12:131797206
|
C | CG | 1 | a0000 | 5 | HG01175.hp2 HG02257.hp1 HG02559.hp1 others(2): Show |
frameshift_variant | HIGH | c.2565dupG | p.Ser856fs | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 16/18 | 2706/3246 | 2566/2856 | 856/951 | INFO_REALIGN_3_PRIME | chr12 | 131797206 | |
chr12:131797317
|
G | A | 1 | a0008 | 1 | HG02451.hp2 | missense_variant | MODERATE | c.2674G>A | p.Val892Ile | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 16/18 | 2814/3246 | 2674/2856 | 892/951 | chr12 | 131797317 | ||
chr12:131797354
|
G | A | 1 | a0009 | 1 | HG03239.hp2 | missense_variant | MODERATE | c.2711G>A | p.Arg904His | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 16/18 | 2851/3246 | 2711/2856 | 904/951 | chr12 | 131797354 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:131711310
|
C | T | 2 | a0001c0012a0001c0031 | 3 | HG03098.hp2 HG03139.hp2 HG03453.hp1 |
synonymous_variant | LOW | c.81C>T | p.Gly27Gly | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 1/18 | 221/3246 | 81/2856 | 27/951 | chr12 | 131711310 | ||
chr12:131719467
|
C | T | 1 | a0001c0029 | 1 | HG04228.hp1 | synonymous_variant | LOW | c.534C>T | p.Ala178Ala | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/18 | 674/3246 | 534/2856 | 178/951 | chr12 | 131719467 | ||
chr12:131725413
|
C | T | 1 | a0001c0011 | 2 | HG02717.hp2 HG03041.hp1 |
synonymous_variant | LOW | c.615C>T | p.Thr205Thr | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 5/18 | 755/3246 | 615/2856 | 205/951 | chr12 | 131725413 | ||
chr12:131725518
|
T | C | 2 | a0001c0004a0001c0015 | 7 | HG01891.hp2 HG02451.hp1 HG02630.hp1 others(4): Show |
synonymous_variant | LOW | c.720T>C | p.Phe240Phe | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 5/18 | 860/3246 | 720/2856 | 240/951 | chr12 | 131725518 | ||
chr12:131753202
|
C | T | 1 | a0002c0028 | 1 | HG03017.hp2 | synonymous_variant | LOW | c.1161C>T | p.Ile387Ile | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 8/18 | 1301/3246 | 1161/2856 | 387/951 | chr12 | 131753202 | ||
chr12:131753205
|
C | T | 2 | a0001c0002a0001c0010 | 21 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(18): Show |
synonymous_variant | LOW | c.1164C>T | p.Asp388Asp | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 8/18 | 1304/3246 | 1164/2856 | 388/951 | chr12 | 131753205 | ||
chr12:131754407
|
C | T | 1 | a0001c0006 | 3 | HG02922.hp1 HG03130.hp2 NA19030.hp2 |
synonymous_variant | LOW | c.1362C>T | p.Pro454Pro | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 9/18 | 1502/3246 | 1362/2856 | 454/951 | chr12 | 131754407 | ||
chr12:131754443
|
T | C | 1 | a0001c0015 | 1 | HG02451.hp1 | synonymous_variant | LOW | c.1398T>C | p.Tyr466Tyr | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 9/18 | 1538/3246 | 1398/2856 | 466/951 | chr12 | 131754443 | ||
chr12:131755464
|
G | T | 1 | a0001c0015 | 1 | HG02451.hp1 | synonymous_variant | LOW | c.1533G>T | p.Gly511Gly | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 10/18 | 1673/3246 | 1533/2856 | 511/951 | chr12 | 131755464 | ||
chr12:131756562
|
C | T | 1 | a0002c0027 | 1 | HG02257.hp2 | synonymous_variant | LOW | c.1638C>T | p.Ala546Ala | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/18 | 1778/3246 | 1638/2856 | 546/951 | chr12 | 131756562 | ||
chr12:131766167
|
G | C | 3 | a0001c0002a0001c0007a0002c0025 | 22 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(19): Show |
synonymous_variant | LOW | c.2001G>C | p.Leu667Leu | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/18 | 2141/3246 | 2001/2856 | 667/951 | chr12 | 131766167 | ||
chr12:131766227
|
G | A | 2 | a0001c0006a0001c0018 | 4 | HG02922.hp1 HG03130.hp2 HG03225.hp2 others(1): Show |
synonymous_variant | LOW | c.2061G>A | p.Ala687Ala | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/18 | 2201/3246 | 2061/2856 | 687/951 | chr12 | 131766227 | ||
chr12:131778169
|
G | A | 1 | a0001c0019 | 1 | HG04228.hp2 | synonymous_variant | LOW | c.2247G>A | p.Pro749Pro | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/18 | 2387/3246 | 2247/2856 | 749/951 | chr12 | 131778169 | ||
chr12:131786568
|
T | C | 28 | a0000c0005a0000c0023a0001c0001others(25): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
synonymous_variant | LOW | c.2514T>C | p.Ser838Ser | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/18 | 2654/3246 | 2514/2856 | 838/951 | chr12 | 131786568 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:131711129
|
A | C | 27 | a0000c0005t0001a0000c0023t0001a0001c0001t0001others(24): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
5_prime_UTR_variant | MODIFIER | c.-101A>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 1/18 | 101 | chr12 | 131711129 | |||||
chr12:131711129
|
A | T | 1 | a0001c0001t0005 | 1 | HG00642.hp2 | 5_prime_UTR_variant | MODIFIER | c.-101A>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 1/18 | 101 | chr12 | 131711129 | |||||
chr12:131799508
|
G | A | 9 | a0001c0001t0002a0001c0001t0003a0001c0004t0002others(6): Show | 66 | HG00639.hp1 HG01106.hp2 HG01167.hp2 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*20G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 18/18 | 20 | chr12 | 131799508 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:131711491
|
C | T | 1 | a0001c0001t0003g0311 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.218+44C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 1/17 | chr12 | 131711491 | ||||||
chr12:131711712
|
A | G | 1 | a0001c0001t0002g0310 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.218+265A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 1/17 | chr12 | 131711712 | ||||||
chr12:131711798
|
C | T | 1 | a0002c0028t0004g0309 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.218+351C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 1/17 | chr12 | 131711798 | ||||||
chr12:131712193
|
T | A | 1 | a0001c0015t0002g0008 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.218+746T>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 1/17 | chr12 | 131712193 | ||||||
chr12:131712284
|
T | G | 3 | a0001c0004t0002g0009a0001c0004t0002g0010a0001c0004t0002g0011 | 3 | HG01891.hp2 HG02723.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.218+837T>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 1/17 | chr12 | 131712284 | ||||||
chr12:131712751
|
C | T | 1 | a0001c0001t0003g0308 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.218+1304C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 1/17 | chr12 | 131712751 | ||||||
chr12:131712752
|
A | G | 6 | a0001c0004t0002g0009a0001c0004t0002g0010a0001c0004t0002g0011others(3): Show | 6 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.218+1305A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 1/17 | chr12 | 131712752 | ||||||
chr12:131713002
|
T | G | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.219-1069T>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 1/17 | chr12 | 131713002 | ||||||
chr12:131713966
|
C | T | 1 | a0001c0001t0004g0305 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.219-105C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 1/17 | chr12 | 131713966 | ||||||
chr12:131714016
|
G | A | 6 | a0001c0004t0002g0009a0001c0004t0002g0010a0001c0004t0002g0011others(3): Show | 6 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.219-55G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 1/17 | chr12 | 131714016 | ||||||
chr12:131714561
|
A | G | 1 | a0001c0001t0001g0304 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.389-261A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 2/17 | chr12 | 131714561 | ||||||
chr12:131714762
|
T | C | 1 | a0001c0001t0003g0311 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.389-60T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 2/17 | chr12 | 131714762 | ||||||
chr12:131715372
|
TG | T | 4 | a0001c0006t0001g0014a0001c0006t0001g0016a0001c0006t0001g0017others(1): Show | 4 | HG02922.hp1 HG03130.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.520+421delG | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 131715372 | |||||
chr12:131715461
|
C | G | 21 | a0001c0002t0001g0283a0001c0002t0001g0285a0001c0002t0001g0286others(18): Show | 21 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.520+508C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 3/17 | chr12 | 131715461 | ||||||
chr12:131715579
|
C | T | 1 | a0001c0001t0002g0282 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.520+626C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 3/17 | chr12 | 131715579 | ||||||
chr12:131715582
|
A | G | 1 | a0001c0001t0001g0281 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.520+629A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 3/17 | chr12 | 131715582 | ||||||
chr12:131715597
|
C | T | 3 | a0001c0004t0002g0009a0001c0004t0002g0010a0001c0004t0002g0011 | 3 | HG01891.hp2 HG02723.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.520+644C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 3/17 | chr12 | 131715597 | ||||||
chr12:131715615
|
C | T | 2 | a0001c0001t0001g0279a0007c0020t0001g0280 | 2 | HG02071.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.520+662C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 3/17 | chr12 | 131715615 | ||||||
chr12:131715617
|
C | T | 191 | a0000c0005t0001g0120a0000c0005t0001g0121a0000c0005t0001g0199others(188): Show | 197 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.520+664C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 3/17 | chr12 | 131715617 | ||||||
chr12:131715681
|
A | T | 6 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275others(3): Show | 6 | HG00741.hp2 HG01167.hp1 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.520+728A>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 3/17 | chr12 | 131715681 | ||||||
chr12:131715749
|
TTTACA | T | 82 | a0000c0005t0001g0120a0000c0005t0001g0121a0001c0001t0001g0002others(79): Show | 83 | HG00280.hp2 HG00597.hp1 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.520+803_520+807del others(5): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr12 | 131715749 | |||||
chr12:131715897
|
A | G | 1 | a0001c0001t0001g0173 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.520+944A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 3/17 | chr12 | 131715897 | ||||||
chr12:131715945
|
C | G | 1 | a0001c0001t0002g0101 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.520+992C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 3/17 | chr12 | 131715945 | ||||||
chr12:131716360
|
G | A | 2 | a0001c0001t0003g0018a0001c0006t0001g0014 | 2 | HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.520+1407G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 3/17 | chr12 | 131716360 | ||||||
chr12:131716571
|
T | A | 1 | a0001c0001t0002g0019 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.520+1618T>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 3/17 | chr12 | 131716571 | ||||||
chr12:131716588
|
C | T | 1 | a0004c0014t0001g0272 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.520+1635C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 3/17 | chr12 | 131716588 | ||||||
chr12:131717057
|
C | T | 3 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0172 | 3 | NA18942.hp1 NA18966.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.520+2104C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 3/17 | chr12 | 131717057 | ||||||
chr12:131717177
|
G | C | 1 | a0001c0001t0001g0174 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.520+2224G>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 3/17 | chr12 | 131717177 | ||||||
chr12:131717242
|
C | T | 1 | a0001c0001t0002g0100 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.521-2212C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 3/17 | chr12 | 131717242 | ||||||
chr12:131717416
|
A | G | 1 | a0001c0004t0001g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.521-2038A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 3/17 | chr12 | 131717416 | ||||||
chr12:131717463
|
A | G | 1 | a0001c0001t0002g0098 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.521-1991A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 3/17 | chr12 | 131717463 | ||||||
chr12:131718117
|
A | G | 56 | a0000c0023t0001g0051a0001c0001t0001g0047a0001c0001t0001g0048others(53): Show | 56 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.521-1337A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 3/17 | chr12 | 131718117 | ||||||
chr12:131718264
|
T | C | 1 | a0001c0001t0001g0012 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.521-1190T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 3/17 | chr12 | 131718264 | ||||||
chr12:131718389
|
C | T | 1 | a0001c0001t0001g0271 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.521-1065C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 3/17 | chr12 | 131718389 | ||||||
chr12:131718599
|
G | A | 6 | a0001c0004t0002g0009a0001c0004t0002g0010a0001c0004t0002g0011others(3): Show | 6 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.521-855G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 3/17 | chr12 | 131718599 | ||||||
chr12:131718688
|
C | T | 4 | a0001c0001t0002g0019a0001c0012t0001g0044a0001c0012t0001g0045others(1): Show | 4 | HG03098.hp2 HG03139.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.521-766C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 3/17 | chr12 | 131718688 | ||||||
chr12:131718971
|
A | G | 1 | a0001c0001t0003g0311 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.521-483A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 3/17 | chr12 | 131718971 | ||||||
chr12:131718986
|
A | G | 3 | a0001c0004t0002g0009a0001c0004t0002g0010a0001c0004t0002g0011 | 3 | HG01891.hp2 HG02723.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.521-468A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 3/17 | chr12 | 131718986 | ||||||
chr12:131719043
|
T | G | 91 | a0000c0023t0001g0051a0001c0001t0001g0012a0001c0001t0001g0013others(88): Show | 91 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.521-411T>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 3/17 | chr12 | 131719043 | ||||||
chr12:131719129
|
C | T | 4 | a0001c0006t0001g0014a0001c0006t0001g0016a0001c0006t0001g0017others(1): Show | 4 | HG02922.hp1 HG03130.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.521-325C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 3/17 | chr12 | 131719129 | ||||||
chr12:131719130
|
G | A | 3 | a0001c0012t0001g0044a0001c0012t0001g0045a0001c0031t0001g0046 | 3 | HG03098.hp2 HG03139.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.521-324G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 3/17 | chr12 | 131719130 | ||||||
chr12:131719258
|
C | T | 2 | a0001c0001t0001g0168a0001c0001t0001g0169 | 2 | NA19074.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.521-196C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 3/17 | chr12 | 131719258 | ||||||
chr12:131719278
|
A | C | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.521-176A>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 3/17 | chr12 | 131719278 | ||||||
chr12:131719294
|
G | A | 1 | a0001c0001t0001g0279 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.521-160G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 3/17 | chr12 | 131719294 | ||||||
chr12:131719366
|
A | C | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.521-88A>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 3/17 | chr12 | 131719366 | ||||||
chr12:131719568
|
C | T | 16 | a0001c0001t0001g0090a0001c0001t0002g0084a0001c0001t0002g0085others(13): Show | 16 | HG01106.hp2 HG01167.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.606+29C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/17 | chr12 | 131719568 | ||||||
chr12:131719663
|
G | T | 1 | a0001c0001t0001g0083 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.606+124G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/17 | chr12 | 131719663 | ||||||
chr12:131719843
|
G | A | 1 | a0001c0001t0001g0176 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.606+304G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/17 | chr12 | 131719843 | ||||||
chr12:131719949
|
T | G | 281 | a0000c0005t0001g0120a0000c0005t0001g0121a0000c0005t0001g0199others(278): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.606+410T>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/17 | chr12 | 131719949 | ||||||
chr12:131720126
|
A | C | 1 | a0001c0001t0001g0270 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.606+587A>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/17 | chr12 | 131720126 | ||||||
chr12:131720441
|
G | A | 1 | a0001c0001t0001g0047 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.606+902G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/17 | chr12 | 131720441 | ||||||
chr12:131720563
|
A | G | 173 | a0000c0005t0001g0120a0000c0005t0001g0121a0000c0023t0001g0051others(170): Show | 174 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.606+1024A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/17 | chr12 | 131720563 | ||||||
chr12:131720585
|
C | G | 1 | a0001c0006t0001g0014 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.606+1046C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/17 | chr12 | 131720585 | ||||||
chr12:131720589
|
A | G | 1 | a0001c0002t0001g0303 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.606+1050A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/17 | chr12 | 131720589 | ||||||
chr12:131720984
|
G | A | 1 | a0008c0021t0003g0020 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.606+1445G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/17 | chr12 | 131720984 | ||||||
chr12:131721598
|
A | T | 19 | a0001c0001t0001g0090a0001c0001t0002g0082a0001c0001t0002g0084others(16): Show | 19 | HG01106.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.606+2059A>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/17 | chr12 | 131721598 | ||||||
chr12:131721599
|
T | A | 2 | a0001c0001t0001g0048a0001c0001t0001g0049 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.606+2060T>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/17 | chr12 | 131721599 | ||||||
chr12:131721731
|
G | C | 6 | a0001c0004t0002g0009a0001c0004t0002g0010a0001c0004t0002g0011others(3): Show | 6 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.606+2192G>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/17 | chr12 | 131721731 | ||||||
chr12:131721765
|
G | A | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.606+2226G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/17 | chr12 | 131721765 | ||||||
chr12:131722044
|
T | C | 83 | a0000c0005t0001g0120a0000c0005t0001g0121a0001c0001t0001g0002others(80): Show | 84 | HG00280.hp2 HG00597.hp1 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.606+2505T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/17 | chr12 | 131722044 | ||||||
chr12:131722396
|
T | C | 1 | a0001c0001t0002g0084 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.606+2857T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/17 | chr12 | 131722396 | ||||||
chr12:131722434
|
G | A | 3 | a0001c0012t0001g0044a0001c0012t0001g0045a0001c0031t0001g0046 | 3 | HG03098.hp2 HG03139.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.606+2895G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/17 | chr12 | 131722434 | ||||||
chr12:131722590
|
A | C | 83 | a0000c0005t0001g0120a0000c0005t0001g0121a0001c0001t0001g0002others(80): Show | 84 | HG00280.hp2 HG00597.hp1 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.607-2815A>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/17 | chr12 | 131722590 | ||||||
chr12:131722624
|
C | A | 56 | a0000c0023t0001g0051a0001c0001t0001g0047a0001c0001t0001g0048others(53): Show | 56 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.607-2781C>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/17 | chr12 | 131722624 | ||||||
chr12:131722854
|
C | T | 2 | a0001c0001t0001g0267a0001c0001t0001g0268 | 2 | HG01934.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.607-2551C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/17 | chr12 | 131722854 | ||||||
chr12:131722897
|
T | C | 1 | a0007c0020t0001g0280 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.607-2508T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/17 | chr12 | 131722897 | ||||||
chr12:131722917
|
C | G | 6 | a0001c0001t0001g0175a0001c0001t0001g0262a0001c0001t0001g0263others(3): Show | 6 | HG01257.hp1 HG01258.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.607-2488C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/17 | chr12 | 131722917 | ||||||
chr12:131722989
|
C | T | 83 | a0000c0005t0001g0120a0000c0005t0001g0121a0001c0001t0001g0002others(80): Show | 84 | HG00280.hp2 HG00597.hp1 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.607-2416C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/17 | chr12 | 131722989 | ||||||
chr12:131723104
|
T | C | 3 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104 | 3 | HG02004.hp2 HG02148.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.607-2301T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/17 | chr12 | 131723104 | ||||||
chr12:131723135
|
T | A | 3 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0002g0050 | 3 | HG01258.hp1 HG02818.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.607-2270T>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/17 | chr12 | 131723135 | ||||||
chr12:131723146
|
TTCA | T | 3 | a0000c0023t0001g0051a0003c0009t0001g0052a0003c0009t0001g0053 | 3 | HG01891.hp1 HG02258.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.607-2254_607-2252d others(5): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 131723146 | |||||
chr12:131723279
|
C | G | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.607-2126C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/17 | chr12 | 131723279 | ||||||
chr12:131723557
|
G | A | 1 | a0001c0001t0003g0021 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.607-1848G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/17 | chr12 | 131723557 | ||||||
chr12:131724273
|
G | T | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.607-1132G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/17 | chr12 | 131724273 | ||||||
chr12:131724972
|
C | A | 7 | a0001c0004t0001g0099a0001c0004t0002g0009a0001c0004t0002g0010others(4): Show | 7 | HG01891.hp2 HG02451.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.607-433C>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/17 | chr12 | 131724972 | ||||||
chr12:131725110
|
A | G | 1 | a0001c0001t0001g0167 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.607-295A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/17 | chr12 | 131725110 | ||||||
chr12:131725236
|
T | A | 7 | a0001c0004t0001g0099a0001c0004t0002g0009a0001c0004t0002g0010others(4): Show | 7 | HG01891.hp2 HG02451.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.607-169T>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/17 | chr12 | 131725236 | ||||||
chr12:131725294
|
A | G | 1 | a0001c0001t0001g0304 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.607-111A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/17 | chr12 | 131725294 | ||||||
chr12:131725381
|
G | A | 1 | a0001c0002t0001g0283 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.607-24G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/17 | chr12 | 131725381 | ||||||
chr12:131725387
|
ATG | A | 108 | a0000c0005t0001g0199a0000c0005t0001g0251a0001c0001t0001g0003others(105): Show | 113 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.607-12_607-11delGT | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr12 | 131725387 | |||||
chr12:131725684
|
G | A | 6 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(3): Show | 6 | HG02040.hp2 HG03834.hp2 NA18970.hp2 others(3): Show |
intron_variant | MODIFIER | c.832+54G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 5/17 | chr12 | 131725684 | ||||||
chr12:131725924
|
G | T | 3 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0166 | 3 | NA18960.hp1 NA19084.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.832+294G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 5/17 | chr12 | 131725924 | ||||||
chr12:131726078
|
G | T | 1 | a0001c0001t0001g0278 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.832+448G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 5/17 | chr12 | 131726078 | ||||||
chr12:131726175
|
T | TAC | 83 | a0000c0005t0001g0120a0000c0005t0001g0121a0001c0001t0001g0002others(80): Show | 84 | HG00280.hp2 HG00597.hp1 HG00673.hp2 others(81): Show |
intron_variant | MODIFIER | c.832+559_832+560dup others(2): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr12 | 131726175 | |||||
chr12:131726177
|
C | T | 1 | a0001c0001t0001g0261 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.832+547C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 5/17 | chr12 | 131726177 | ||||||
chr12:131726202
|
AT | A | 109 | a0000c0005t0001g0199a0000c0005t0001g0251a0001c0001t0001g0003others(106): Show | 114 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.832+585delT | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr12 | 131726202 | |||||
chr12:131726223
|
G | A | 1 | a0001c0001t0002g0019 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.832+593G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 5/17 | chr12 | 131726223 | ||||||
chr12:131726224
|
A | G | 1 | a0001c0001t0002g0019 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.832+594A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 5/17 | chr12 | 131726224 | ||||||
chr12:131726257
|
G | A | 2 | a0001c0004t0002g0306a0001c0004t0002g0307 | 2 | HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.832+627G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 5/17 | chr12 | 131726257 | ||||||
chr12:131726356
|
C | T | 3 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0079 | 3 | HG02622.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.833-584C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 5/17 | chr12 | 131726356 | ||||||
chr12:131726420
|
G | A | 6 | a0001c0004t0002g0009a0001c0004t0002g0010a0001c0004t0002g0011others(3): Show | 6 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.833-520G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 5/17 | chr12 | 131726420 | ||||||
chr12:131726475
|
G | T | 1 | a0001c0001t0001g0160 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.833-465G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 5/17 | chr12 | 131726475 | ||||||
chr12:131726671
|
G | GA | 10 | a0001c0001t0001g0013a0001c0001t0001g0112a0001c0001t0001g0113others(7): Show | 10 | HG01106.hp2 HG01243.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.833-261dupA | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr12 | 131726671 | |||||
chr12:131726697
|
C | T | 21 | a0001c0002t0001g0283a0001c0002t0001g0285a0001c0002t0001g0286others(18): Show | 21 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.833-243C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 5/17 | chr12 | 131726697 | ||||||
chr12:131727347
|
C | T | 1 | a0001c0001t0001g0159 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.945+295C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 6/17 | chr12 | 131727347 | ||||||
chr12:131727466
|
C | T | 19 | a0000c0005t0001g0251a0001c0001t0001g0005a0001c0001t0001g0006others(16): Show | 22 | HG00558.hp2 HG02015.hp2 HG02040.hp1 others(19): Show |
intron_variant | MODIFIER | c.945+414C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 6/17 | chr12 | 131727466 | ||||||
chr12:131727553
|
G | T | 5 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0243others(2): Show | 5 | HG01358.hp2 HG01952.hp1 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.945+501G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 6/17 | chr12 | 131727553 | ||||||
chr12:131727705
|
A | G | 1 | a0001c0001t0001g0110 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.946-588A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 6/17 | chr12 | 131727705 | ||||||
chr12:131727978
|
A | G | 21 | a0001c0002t0001g0283a0001c0002t0001g0285a0001c0002t0001g0286others(18): Show | 21 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.946-315A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 6/17 | chr12 | 131727978 | ||||||
chr12:131728271
|
G | T | 2 | a0001c0001t0001g0267a0001c0001t0001g0268 | 2 | HG01934.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.946-22G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 6/17 | chr12 | 131728271 | ||||||
chr12:131728563
|
G | A | 47 | a0000c0005t0001g0199a0000c0005t0001g0251a0001c0001t0001g0003others(44): Show | 52 | HG00558.hp2 HG00597.hp2 HG00738.hp1 others(49): Show |
intron_variant | MODIFIER | c.1081+135G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131728563 | ||||||
chr12:131728669
|
G | A | 1 | a0001c0002t0001g0285 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1081+241G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131728669 | ||||||
chr12:131728816
|
C | T | 3 | a0001c0001t0001g0012a0001c0001t0001g0013a0002c0003t0003g0043 | 3 | HG01243.hp1 HG02486.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1081+388C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131728816 | ||||||
chr12:131728846
|
C | T | 4 | a0001c0006t0001g0014a0001c0006t0001g0016a0001c0006t0001g0017others(1): Show | 4 | HG02922.hp1 HG03130.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1081+418C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131728846 | ||||||
chr12:131729028
|
C | T | 58 | a0000c0023t0001g0051a0001c0001t0001g0047a0001c0001t0001g0048others(55): Show | 58 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.1081+600C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131729028 | ||||||
chr12:131729163
|
G | A | 1 | a0001c0001t0001g0278 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1081+735G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131729163 | ||||||
chr12:131729337
|
T | C | 227 | a0000c0005t0001g0120a0000c0005t0001g0121a0000c0005t0001g0199others(224): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.1081+909T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131729337 | ||||||
chr12:131729516
|
G | A | 1 | a0001c0001t0002g0019 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1081+1088G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131729516 | ||||||
chr12:131729599
|
A | G | 1 | a0001c0004t0001g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1081+1171A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131729599 | ||||||
chr12:131729643
|
G | C | 1 | a0001c0001t0001g0167 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1081+1215G>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131729643 | ||||||
chr12:131729668
|
G | A | 1 | a0001c0004t0001g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1081+1240G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131729668 | ||||||
chr12:131729943
|
C | T | 226 | a0000c0005t0001g0120a0000c0005t0001g0121a0000c0005t0001g0199others(223): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.1081+1515C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131729943 | ||||||
chr12:131730029
|
A | G | 51 | a0000c0005t0001g0199a0000c0005t0001g0251a0001c0001t0001g0003others(48): Show | 56 | HG00558.hp2 HG00597.hp2 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.1081+1601A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131730029 | ||||||
chr12:131730043
|
A | G | 1 | a0001c0001t0002g0078 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1081+1615A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131730043 | ||||||
chr12:131730140
|
G | A | 1 | a0001c0001t0001g0181 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1081+1712G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131730140 | ||||||
chr12:131730255
|
C | A | 192 | a0000c0005t0001g0120a0000c0005t0001g0121a0000c0005t0001g0199others(189): Show | 198 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.1081+1827C>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131730255 | ||||||
chr12:131730318
|
G | T | 1 | a0001c0001t0002g0077 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1081+1890G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131730318 | ||||||
chr12:131730344
|
T | C | 6 | a0001c0004t0002g0009a0001c0004t0002g0010a0001c0004t0002g0011others(3): Show | 6 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1081+1916T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131730344 | ||||||
chr12:131730355
|
G | A | 6 | a0001c0004t0002g0009a0001c0004t0002g0010a0001c0004t0002g0011others(3): Show | 6 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1081+1927G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131730355 | ||||||
chr12:131730426
|
G | A | 1 | a0001c0001t0001g0261 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1081+1998G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131730426 | ||||||
chr12:131730494
|
C | T | 1 | a0001c0001t0003g0021 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1081+2066C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131730494 | ||||||
chr12:131730630
|
G | T | 1 | a0001c0001t0002g0076 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1081+2202G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131730630 | ||||||
chr12:131730648
|
C | G | 1 | a0001c0001t0002g0076 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1081+2220C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131730648 | ||||||
chr12:131731022
|
C | A | 6 | a0001c0004t0002g0009a0001c0004t0002g0010a0001c0004t0002g0011others(3): Show | 6 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1081+2594C>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131731022 | ||||||
chr12:131731174
|
A | T | 1 | a0001c0001t0001g0158 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1081+2746A>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131731174 | ||||||
chr12:131731175
|
T | A | 1 | a0001c0001t0001g0158 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1081+2747T>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131731175 | ||||||
chr12:131731176
|
A | T | 1 | a0001c0001t0001g0158 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1081+2748A>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131731176 | ||||||
chr12:131731222
|
G | A | 1 | a0001c0002t0001g0286 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1081+2794G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131731222 | ||||||
chr12:131731235
|
G | A | 19 | a0001c0001t0001g0090a0001c0001t0002g0082a0001c0001t0002g0084others(16): Show | 19 | HG01106.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.1081+2807G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131731235 | ||||||
chr12:131731316
|
A | G | 307 | a0000c0005t0001g0120a0000c0005t0001g0121a0000c0005t0001g0199others(304): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.1081+2888A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131731316 | ||||||
chr12:131731799
|
A | G | 68 | a0001c0001t0001g0002a0001c0001t0001g0105a0001c0001t0001g0106others(65): Show | 69 | HG00280.hp2 HG00597.hp1 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.1081+3371A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131731799 | ||||||
chr12:131731824
|
T | C | 1 | a0001c0001t0001g0002 | 2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.1081+3396T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131731824 | ||||||
chr12:131731849
|
C | T | 1 | a0002c0003t0003g0043 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1081+3421C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131731849 | ||||||
chr12:131731901
|
C | CT | 85 | a0000c0005t0001g0120a0000c0005t0001g0121a0001c0001t0001g0002others(82): Show | 86 | HG00280.hp2 HG00597.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.1081+3499dupT | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131731901 | |||||
chr12:131731901
|
C | CTT | 27 | a0001c0001t0001g0122a0001c0001t0001g0153a0001c0001t0001g0154others(24): Show | 27 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.1081+3498_1081+349 others(6): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131731901 | |||||
chr12:131731901
|
CT | C | 87 | a0000c0005t0001g0251a0001c0001t0001g0003a0001c0001t0001g0004others(84): Show | 92 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(89): Show |
intron_variant | MODIFIER | c.1081+3499delT | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131731901 | |||||
chr12:131732013
|
G | A | 1 | a0001c0001t0001g0164 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1081+3585G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131732013 | ||||||
chr12:131732148
|
G | A | 21 | a0001c0002t0001g0283a0001c0002t0001g0285a0001c0002t0001g0286others(18): Show | 21 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.1081+3720G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131732148 | ||||||
chr12:131732163
|
G | A | 1 | a0001c0001t0002g0100 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1081+3735G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131732163 | ||||||
chr12:131732199
|
G | A | 6 | a0001c0004t0002g0009a0001c0004t0002g0010a0001c0004t0002g0011others(3): Show | 6 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1081+3771G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131732199 | ||||||
chr12:131732608
|
C | T | 1 | a0003c0009t0001g0053 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1081+4180C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131732608 | ||||||
chr12:131732902
|
ACT | A | 82 | a0000c0005t0001g0120a0000c0005t0001g0121a0001c0001t0001g0002others(79): Show | 83 | HG00280.hp2 HG00597.hp1 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.1081+4478_1081+447 others(6): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131732902 | |||||
chr12:131732930
|
C | T | 1 | a0001c0001t0001g0179 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1081+4502C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131732930 | ||||||
chr12:131732950
|
G | A | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | HG03209.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1081+4522G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131732950 | ||||||
chr12:131732988
|
G | C | 225 | a0000c0005t0001g0120a0000c0005t0001g0121a0000c0005t0001g0199others(222): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.1081+4560G>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131732988 | ||||||
chr12:131733190
|
G | T | 1 | a0001c0001t0001g0230 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1081+4762G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131733190 | ||||||
chr12:131733225
|
G | A | 108 | a0000c0005t0001g0199a0000c0005t0001g0251a0001c0001t0001g0003others(105): Show | 113 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.1081+4797G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131733225 | ||||||
chr12:131733296
|
C | T | 1 | a0001c0001t0003g0311 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1081+4868C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131733296 | ||||||
chr12:131733333
|
C | T | 2 | a0001c0001t0001g0074a0001c0001t0001g0075 | 2 | HG00323.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.1081+4905C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131733333 | ||||||
chr12:131733396
|
C | T | 1 | a0001c0002t0001g0283 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1081+4968C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131733396 | ||||||
chr12:131733408
|
A | G | 1 | a0001c0001t0003g0018 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1081+4980A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131733408 | ||||||
chr12:131733442
|
G | A | 56 | a0000c0023t0001g0051a0001c0001t0001g0047a0001c0001t0001g0048others(53): Show | 56 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.1081+5014G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131733442 | ||||||
chr12:131733470
|
C | T | 1 | a0001c0001t0003g0039 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1081+5042C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131733470 | ||||||
chr12:131733497
|
A | C | 22 | a0001c0002t0001g0283a0001c0002t0001g0285a0001c0002t0001g0286others(19): Show | 22 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.1081+5069A>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131733497 | ||||||
chr12:131733639
|
A | C | 1 | a0001c0004t0001g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1081+5211A>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131733639 | ||||||
chr12:131733773
|
G | A | 50 | a0000c0005t0001g0199a0000c0005t0001g0251a0001c0001t0001g0003others(47): Show | 55 | HG00558.hp2 HG00597.hp2 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.1081+5345G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131733773 | ||||||
chr12:131733907
|
C | T | 6 | a0001c0004t0002g0009a0001c0004t0002g0010a0001c0004t0002g0011others(3): Show | 6 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1081+5479C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131733907 | ||||||
chr12:131734030
|
A | G | 1 | a0001c0001t0001g0266 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1081+5602A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131734030 | ||||||
chr12:131734041
|
C | G | 4 | a0001c0001t0002g0019a0001c0012t0001g0044a0001c0012t0001g0045others(1): Show | 4 | HG03098.hp2 HG03139.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1081+5613C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131734041 | ||||||
chr12:131734176
|
A | G | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1081+5748A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131734176 | ||||||
chr12:131734192
|
G | A | 6 | a0001c0004t0002g0009a0001c0004t0002g0010a0001c0004t0002g0011others(3): Show | 6 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1081+5764G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131734192 | ||||||
chr12:131734482
|
G | A | 1 | a0009c0022t0001g0125 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1081+6054G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131734482 | ||||||
chr12:131734535
|
C | A | 1 | a0001c0001t0002g0064 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1081+6107C>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131734535 | ||||||
chr12:131734541
|
CAT | C | 8 | a0001c0001t0001g0181a0001c0001t0002g0084a0001c0001t0002g0091others(5): Show | 8 | HG02145.hp1 HG02572.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1081+6114_1081+611 others(6): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131734541 | ||||||
chr12:131734655
|
G | A | 1 | a0001c0001t0001g0126 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1081+6227G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131734655 | ||||||
chr12:131734788
|
TCTCCCTG others(75): Show |
T | 1 | a0001c0001t0001g0201 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1081+6362_1081+644 others(86): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131734788 | |||||
chr12:131734872
|
C | A | 1 | a0001c0001t0001g0201 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1081+6444C>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131734872 | ||||||
chr12:131734882
|
A | G | 25 | a0000c0023t0001g0051a0001c0001t0001g0047a0001c0001t0001g0048others(22): Show | 25 | HG00323.hp1 HG00733.hp1 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.1081+6454A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131734882 | ||||||
chr12:131734898
|
C | T | 1 | a0001c0001t0001g0239 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1081+6470C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131734898 | ||||||
chr12:131734923
|
A | AG | 10 | a0001c0001t0001g0073a0001c0001t0001g0124a0001c0001t0001g0158others(7): Show | 10 | HG00639.hp1 HG01934.hp1 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.1081+6502dupG | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131734923 | |||||
chr12:131735209
|
C | T | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1081+6781C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131735209 | ||||||
chr12:131735245
|
C | T | 2 | a0001c0001t0001g0257a0001c0001t0001g0258 | 2 | NA18986.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1081+6817C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131735245 | ||||||
chr12:131735247
|
G | A | 54 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0177others(51): Show | 54 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(51): Show |
intron_variant | MODIFIER | c.1081+6819G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131735247 | ||||||
chr12:131735249
|
G | A | 2 | a0001c0001t0002g0019a0001c0004t0001g0099 | 2 | HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1081+6821G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131735249 | ||||||
chr12:131735262
|
T | G | 56 | a0000c0023t0001g0051a0001c0001t0001g0047a0001c0001t0001g0048others(53): Show | 56 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.1081+6834T>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131735262 | ||||||
chr12:131735425
|
T | G | 1 | a0000c0023t0001g0051 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1081+6997T>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131735425 | ||||||
chr12:131735545
|
G | A | 1 | a0001c0006t0001g0014 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1081+7117G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131735545 | ||||||
chr12:131735561
|
G | A | 1 | a0001c0001t0001g0115 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1081+7133G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131735561 | ||||||
chr12:131735684
|
C | G | 6 | a0001c0004t0002g0009a0001c0004t0002g0010a0001c0004t0002g0011others(3): Show | 6 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1081+7256C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131735684 | ||||||
chr12:131735750
|
G | A | 18 | a0001c0001t0001g0061a0001c0001t0002g0050a0001c0001t0002g0054others(15): Show | 18 | HG00639.hp1 HG01943.hp2 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.1081+7322G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131735750 | ||||||
chr12:131735802
|
T | C | 56 | a0000c0023t0001g0051a0001c0001t0001g0047a0001c0001t0001g0048others(53): Show | 56 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.1081+7374T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131735802 | ||||||
chr12:131735840
|
T | G | 24 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0002t0001g0283others(21): Show | 24 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.1081+7412T>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131735840 | ||||||
chr12:131736039
|
C | T | 3 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104 | 3 | HG02004.hp2 HG02148.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1081+7611C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131736039 | ||||||
chr12:131736287
|
G | A | 2 | a0001c0004t0002g0306a0001c0004t0002g0307 | 2 | HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1081+7859G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131736287 | ||||||
chr12:131736311
|
A | C | 1 | a0001c0006t0001g0014 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1081+7883A>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131736311 | ||||||
chr12:131736401
|
A | T | 62 | a0000c0023t0001g0051a0001c0001t0001g0047a0001c0001t0001g0048others(59): Show | 62 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.1081+7973A>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131736401 | ||||||
chr12:131736414
|
A | G | 4 | a0001c0001t0001g0194a0001c0006t0001g0016a0001c0019t0001g0195others(1): Show | 4 | HG02735.hp1 HG02922.hp1 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.1081+7986A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131736414 | ||||||
chr12:131736488
|
G | A | 1 | a0001c0001t0002g0086 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1081+8060G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131736488 | ||||||
chr12:131736514
|
C | T | 62 | a0000c0023t0001g0051a0001c0001t0001g0047a0001c0001t0001g0048others(59): Show | 62 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.1081+8086C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131736514 | ||||||
chr12:131736570
|
G | A | 1 | a0001c0001t0002g0064 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1081+8142G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131736570 | ||||||
chr12:131736583
|
G | A | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1081+8155G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131736583 | ||||||
chr12:131736690
|
CAT | C | 16 | a0001c0001t0001g0090a0001c0001t0002g0084a0001c0001t0002g0085others(13): Show | 16 | HG01106.hp2 HG01167.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.1081+8264_1081+826 others(6): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131736690 | |||||
chr12:131736718
|
T | C | 6 | a0001c0004t0002g0009a0001c0004t0002g0010a0001c0004t0002g0011others(3): Show | 6 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1081+8290T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131736718 | ||||||
chr12:131736751
|
G | A | 4 | a0001c0001t0002g0019a0001c0012t0001g0044a0001c0012t0001g0045others(1): Show | 4 | HG03098.hp2 HG03139.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1081+8323G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131736751 | ||||||
chr12:131736822
|
A | G | 303 | a0000c0005t0001g0120a0000c0005t0001g0121a0000c0005t0001g0199others(300): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.1081+8394A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131736822 | ||||||
chr12:131737126
|
G | T | 1 | a0001c0001t0001g0047 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1081+8698G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131737126 | ||||||
chr12:131737147
|
G | A | 2 | a0001c0004t0002g0306a0001c0004t0002g0307 | 2 | HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1081+8719G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131737147 | ||||||
chr12:131737236
|
G | A | 1 | a0001c0001t0001g0202 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1081+8808G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131737236 | ||||||
chr12:131737259
|
G | T | 83 | a0000c0005t0001g0120a0000c0005t0001g0121a0001c0001t0001g0002others(80): Show | 84 | HG00280.hp2 HG00597.hp1 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.1081+8831G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131737259 | ||||||
chr12:131737526
|
A | G | 1 | a0001c0001t0001g0256 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1081+9098A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131737526 | ||||||
chr12:131737674
|
G | A | 51 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0177others(48): Show | 51 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(48): Show |
intron_variant | MODIFIER | c.1081+9246G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131737674 | ||||||
chr12:131737731
|
C | T | 1 | a0001c0001t0001g0179 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1081+9303C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131737731 | ||||||
chr12:131737743
|
T | C | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1081+9315T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131737743 | ||||||
chr12:131738283
|
A | G | 2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | NA18990.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1081+9855A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131738283 | ||||||
chr12:131738288
|
G | A | 6 | a0001c0004t0002g0009a0001c0004t0002g0010a0001c0004t0002g0011others(3): Show | 6 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1081+9860G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131738288 | ||||||
chr12:131738562
|
G | A | 1 | a0001c0004t0001g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1081+10134G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131738562 | ||||||
chr12:131738629
|
T | G | 1 | a0002c0003t0003g0032 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1081+10201T>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131738629 | ||||||
chr12:131738799
|
G | A | 1 | a0001c0001t0001g0203 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1081+10371G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131738799 | ||||||
chr12:131738885
|
C | CT | 44 | a0000c0005t0001g0199a0000c0005t0001g0251a0001c0001t0001g0003others(41): Show | 47 | HG00558.hp2 HG00597.hp2 HG00738.hp1 others(44): Show |
intron_variant | MODIFIER | c.1081+10481dupT | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131738885 | |||||
chr12:131738885
|
C | CTT | 7 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0174others(4): Show | 9 | HG02109.hp1 HG02717.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1081+10480_1081+10 others(8): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131738885 | |||||
chr12:131738885
|
C | CTTTTTTT others(4): Show |
14 | a0001c0001t0001g0116a0001c0001t0001g0231a0001c0001t0001g0271others(11): Show | 14 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.1081+10471_1081+10 others(17): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131738885 | |||||
chr12:131738885
|
C | CTTTTTTT others(5): Show |
45 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(42): Show | 45 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(42): Show |
intron_variant | MODIFIER | c.1081+10470_1081+10 others(18): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131738885 | |||||
chr12:131738885
|
C | CTTTTTTT others(6): Show |
50 | a0000c0005t0001g0120a0000c0005t0001g0121a0001c0001t0001g0002others(47): Show | 51 | HG00609.hp2 HG00642.hp1 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.1081+10469_1081+10 others(19): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131738885 | |||||
chr12:131738885
|
C | CTTTTTTT others(7): Show |
30 | a0001c0001t0001g0102a0001c0001t0001g0107a0001c0001t0001g0108others(27): Show | 30 | HG00323.hp2 HG00609.hp1 HG00673.hp2 others(27): Show |
intron_variant | MODIFIER | c.1081+10468_1081+10 others(20): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131738885 | |||||
chr12:131738885
|
C | CTTTTTTT others(8): Show |
10 | a0001c0001t0001g0103a0001c0001t0001g0109a0001c0001t0001g0144others(7): Show | 10 | HG00140.hp2 HG00280.hp2 HG02004.hp2 others(7): Show |
intron_variant | MODIFIER | c.1081+10467_1081+10 others(21): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131738885 | |||||
chr12:131738885
|
C | CTTTTTTT others(9): Show |
7 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0149others(4): Show | 7 | HG02602.hp2 HG02630.hp1 HG02698.hp1 others(4): Show |
intron_variant | MODIFIER | c.1081+10466_1081+10 others(22): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131738885 | |||||
chr12:131738885
|
C | CTTTTTTT others(10): Show |
3 | a0001c0001t0001g0104a0001c0001t0001g0164a0001c0001t0001g0228 | 3 | HG02148.hp1 NA18941.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.1081+10465_1081+10 others(23): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131738885 | |||||
chr12:131738885
|
C | CTTTTTTT others(11): Show |
4 | a0001c0001t0001g0166a0001c0001t0001g0277a0001c0004t0002g0306others(1): Show | 4 | HG01943.hp1 HG03041.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1081+10464_1081+10 others(24): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131738885 | |||||
chr12:131738885
|
C | CTTTTTTT others(16): Show |
1 | a0001c0001t0001g0151 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1081+10459_1081+10 others(29): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131738885 | |||||
chr12:131738885
|
CTTT | C | 53 | a0000c0023t0001g0051a0001c0001t0001g0047a0001c0001t0001g0048others(50): Show | 53 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.1081+10479_1081+10 others(9): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131738885 | |||||
chr12:131738885
|
CTTTTTTT others(8): Show |
C | 4 | a0001c0001t0002g0019a0001c0012t0001g0044a0001c0012t0001g0045others(1): Show | 4 | HG03098.hp2 HG03139.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1081+10467_1081+10 others(21): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131738885 | |||||
chr12:131738933
|
A | G | 1 | a0001c0006t0001g0016 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1081+10505A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131738933 | ||||||
chr12:131738948
|
C | T | 1 | a0001c0004t0001g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1081+10520C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131738948 | ||||||
chr12:131738975
|
C | CCTCAACC others(7): Show |
292 | a0000c0005t0001g0120a0000c0005t0001g0121a0000c0005t0001g0199others(289): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.1081+10552_1081+10 others(20): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131738975 | |||||
chr12:131739033
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1081+10605C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131739033 | ||||||
chr12:131739128
|
T | G | 82 | a0000c0005t0001g0120a0000c0005t0001g0121a0001c0001t0001g0002others(79): Show | 83 | HG00280.hp2 HG00609.hp1 HG00673.hp2 others(80): Show |
intron_variant | MODIFIER | c.1081+10700T>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131739128 | ||||||
chr12:131739238
|
A | G | 6 | a0001c0004t0002g0009a0001c0004t0002g0010a0001c0004t0002g0011others(3): Show | 6 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1081+10810A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131739238 | ||||||
chr12:131739281
|
A | G | 2 | a0001c0001t0001g0221a0001c0001t0005g0222 | 2 | HG00642.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.1081+10853A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131739281 | ||||||
chr12:131739335
|
G | C | 56 | a0000c0023t0001g0051a0001c0001t0001g0047a0001c0001t0001g0048others(53): Show | 56 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.1081+10907G>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131739335 | ||||||
chr12:131739486
|
A | G | 49 | a0000c0005t0001g0199a0000c0005t0001g0251a0001c0001t0001g0003others(46): Show | 54 | HG00558.hp2 HG00597.hp2 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.1081+11058A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131739486 | ||||||
chr12:131739499
|
T | G | 1 | a0001c0001t0001g0226 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1081+11071T>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131739499 | ||||||
chr12:131739536
|
C | CT | 47 | a0001c0001t0001g0002a0001c0001t0001g0113a0001c0001t0001g0124others(44): Show | 48 | HG00597.hp2 HG00609.hp1 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.1081+11136dupT | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131739536 | |||||
chr12:131739536
|
CT | C | 23 | a0001c0001t0001g0012a0001c0001t0001g0105a0001c0001t0001g0106others(20): Show | 23 | HG02027.hp1 HG02486.hp1 HG02559.hp2 others(20): Show |
intron_variant | MODIFIER | c.1081+11136delT | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131739536 | |||||
chr12:131739536
|
CTT | C | 29 | a0001c0001t0001g0047a0001c0001t0001g0061a0001c0001t0001g0072others(26): Show | 29 | HG00639.hp1 HG01106.hp2 HG01123.hp1 others(26): Show |
intron_variant | MODIFIER | c.1081+11135_1081+11 others(8): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131739536 | |||||
chr12:131739536
|
CTTT | C | 19 | a0000c0023t0001g0051a0001c0001t0001g0048a0001c0001t0001g0063others(16): Show | 19 | HG00323.hp1 HG00733.hp1 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.1081+11134_1081+11 others(9): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131739536 | |||||
chr12:131739536
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0002g0019 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1081+11127_1081+11 others(16): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131739536 | |||||
chr12:131739536
|
CTTTTTTT others(4): Show |
C | 3 | a0001c0012t0001g0044a0001c0012t0001g0045a0001c0031t0001g0046 | 3 | HG03098.hp2 HG03139.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1081+11126_1081+11 others(17): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131739536 | |||||
chr12:131739536
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0001g0259 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1081+11125_1081+11 others(18): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131739536 | |||||
chr12:131739536
|
CTTTTTTT others(7): Show |
C | 9 | a0000c0005t0001g0120a0000c0005t0001g0121a0001c0001t0001g0115others(6): Show | 9 | HG01175.hp2 HG01496.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1081+11123_1081+11 others(20): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131739536 | |||||
chr12:131739536
|
CTTTTTTT others(8): Show |
C | 1 | a0001c0001t0001g0114 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1081+11122_1081+11 others(21): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131739536 | |||||
chr12:131739622
|
T | C | 83 | a0000c0005t0001g0120a0000c0005t0001g0121a0001c0001t0001g0002others(80): Show | 84 | HG00280.hp2 HG00597.hp1 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.1081+11194T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131739622 | ||||||
chr12:131739634
|
C | T | 1 | a0001c0001t0001g0143 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1081+11206C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131739634 | ||||||
chr12:131739700
|
C | T | 6 | a0001c0004t0002g0009a0001c0004t0002g0010a0001c0004t0002g0011others(3): Show | 6 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1081+11272C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131739700 | ||||||
chr12:131739707
|
G | A | 6 | a0001c0004t0002g0009a0001c0004t0002g0010a0001c0004t0002g0011others(3): Show | 6 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1081+11279G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131739707 | ||||||
chr12:131739735
|
G | C | 56 | a0000c0023t0001g0051a0001c0001t0001g0047a0001c0001t0001g0048others(53): Show | 56 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.1081+11307G>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131739735 | ||||||
chr12:131739834
|
C | T | 2 | a0000c0023t0001g0051a0003c0009t0001g0053 | 2 | HG02258.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1081+11406C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131739834 | ||||||
chr12:131739882
|
G | A | 3 | a0001c0004t0002g0009a0001c0004t0002g0010a0001c0004t0002g0011 | 3 | HG01891.hp2 HG02723.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1081+11454G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131739882 | ||||||
chr12:131740048
|
G | T | 108 | a0000c0005t0001g0199a0000c0005t0001g0251a0001c0001t0001g0003others(105): Show | 113 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.1081+11620G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131740048 | ||||||
chr12:131740062
|
G | T | 51 | a0000c0005t0001g0199a0000c0005t0001g0251a0001c0001t0001g0003others(48): Show | 56 | HG00558.hp2 HG00597.hp2 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.1081+11634G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131740062 | ||||||
chr12:131740230
|
T | A | 21 | a0001c0002t0001g0283a0001c0002t0001g0285a0001c0002t0001g0286others(18): Show | 21 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.1081+11802T>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131740230 | ||||||
chr12:131740245
|
A | C | 7 | a0001c0004t0001g0099a0001c0004t0002g0009a0001c0004t0002g0010others(4): Show | 7 | HG01891.hp2 HG02451.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1081+11817A>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131740245 | ||||||
chr12:131740438
|
T | G | 83 | a0000c0005t0001g0120a0000c0005t0001g0121a0001c0001t0001g0002others(80): Show | 84 | HG00280.hp2 HG00597.hp1 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.1081+12010T>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131740438 | ||||||
chr12:131740459
|
A | G | 1 | a0001c0001t0001g0275 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1081+12031A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131740459 | ||||||
chr12:131740531
|
C | T | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1081+12103C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131740531 | ||||||
chr12:131740671
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1081+12243G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131740671 | ||||||
chr12:131740837
|
C | T | 1 | a0001c0001t0001g0238 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1082-12286C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131740837 | ||||||
chr12:131740966
|
C | CT | 132 | a0000c0005t0001g0120a0000c0005t0001g0121a0001c0001t0001g0002others(129): Show | 133 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.1082-12133dupT | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131740966 | |||||
chr12:131740966
|
C | CTT | 7 | a0001c0001t0001g0122a0001c0001t0001g0136a0001c0001t0001g0146others(4): Show | 7 | HG00642.hp1 HG01952.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.1082-12134_1082-12 others(8): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131740966 | |||||
chr12:131740966
|
C | CTTTTTTT others(3): Show |
1 | a0001c0001t0001g0110 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1082-12149_1082-12 others(16): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131740966 | |||||
chr12:131740966
|
CT | C | 50 | a0000c0005t0001g0251a0001c0001t0001g0003a0001c0001t0001g0004others(47): Show | 55 | HG00558.hp2 HG00597.hp2 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.1082-12133delT | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131740966 | |||||
chr12:131740966
|
CTTTTTTT | C | 8 | a0001c0001t0001g0012a0001c0001t0001g0175a0001c0001t0001g0234others(5): Show | 8 | HG01257.hp1 HG01258.hp2 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.1082-12139_1082-12 others(13): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131740966 | |||||
chr12:131740967
|
T | TTTTTTTT others(11): Show |
1 | a0001c0001t0001g0198 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1082-12148_1082-12 others(24): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131740967 | |||||
chr12:131740973
|
T | C | 4 | a0001c0001t0002g0054a0001c0001t0002g0058a0001c0001t0002g0091others(1): Show | 4 | HG02027.hp1 HG03209.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1082-12150T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131740973 | ||||||
chr12:131741218
|
G | A | 21 | a0001c0002t0001g0283a0001c0002t0001g0285a0001c0002t0001g0286others(18): Show | 21 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.1082-11905G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131741218 | ||||||
chr12:131741237
|
A | T | 1 | a0001c0001t0002g0019 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1082-11886A>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131741237 | ||||||
chr12:131741259
|
C | T | 3 | a0001c0012t0001g0044a0001c0012t0001g0045a0001c0031t0001g0046 | 3 | HG03098.hp2 HG03139.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1082-11864C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131741259 | ||||||
chr12:131741398
|
G | A | 2 | a0001c0001t0001g0103a0001c0001t0001g0104 | 2 | HG02004.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.1082-11725G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131741398 | ||||||
chr12:131741505
|
C | T | 63 | a0000c0005t0001g0120a0000c0005t0001g0121a0001c0001t0001g0114others(60): Show | 63 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.1082-11618C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131741505 | ||||||
chr12:131741601
|
G | T | 56 | a0000c0023t0001g0051a0001c0001t0001g0047a0001c0001t0001g0048others(53): Show | 56 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.1082-11522G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131741601 | ||||||
chr12:131741644
|
C | CA | 17 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0090others(14): Show | 17 | HG01243.hp1 HG01261.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.1082-11463dupA | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131741644 | |||||
chr12:131741687
|
G | A | 4 | a0001c0001t0002g0019a0001c0012t0001g0044a0001c0012t0001g0045others(1): Show | 4 | HG03098.hp2 HG03139.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1082-11436G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131741687 | ||||||
chr12:131741720
|
G | A | 3 | a0001c0012t0001g0044a0001c0012t0001g0045a0001c0031t0001g0046 | 3 | HG03098.hp2 HG03139.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1082-11403G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131741720 | ||||||
chr12:131741924
|
C | T | 1 | a0001c0002t0001g0303 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1082-11199C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131741924 | ||||||
chr12:131742013
|
A | T | 281 | a0000c0005t0001g0120a0000c0005t0001g0121a0000c0005t0001g0199others(278): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.1082-11110A>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131742013 | ||||||
chr12:131742263
|
G | A | 1 | a0001c0002t0001g0301 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1082-10860G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131742263 | ||||||
chr12:131742297
|
A | G | 2 | a0001c0001t0001g0124a0001c0001t0001g0157 | 2 | HG01978.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1082-10826A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131742297 | ||||||
chr12:131742440
|
T | C | 3 | a0001c0012t0001g0044a0001c0012t0001g0045a0001c0031t0001g0046 | 3 | HG03098.hp2 HG03139.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1082-10683T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131742440 | ||||||
chr12:131742513
|
G | A | 2 | a0001c0001t0001g0257a0001c0001t0001g0258 | 2 | NA18986.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1082-10610G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131742513 | ||||||
chr12:131742528
|
G | T | 1 | a0002c0003t0003g0043 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1082-10595G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131742528 | ||||||
chr12:131742593
|
A | G | 1 | a0001c0001t0001g0253 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1082-10530A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131742593 | ||||||
chr12:131742633
|
CT | C | 23 | a0001c0001t0001g0153a0001c0001t0002g0310a0001c0002t0001g0283others(20): Show | 23 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.1082-10476delT | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131742633 | |||||
chr12:131742661
|
G | A | 18 | a0000c0023t0001g0051a0001c0001t0001g0048a0001c0001t0001g0049others(15): Show | 18 | HG00323.hp1 HG00733.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.1082-10462G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131742661 | ||||||
chr12:131742664
|
G | T | 6 | a0001c0004t0002g0009a0001c0004t0002g0010a0001c0004t0002g0011others(3): Show | 6 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1082-10459G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131742664 | ||||||
chr12:131742683
|
C | A | 1 | a0001c0001t0002g0062 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1082-10440C>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131742683 | ||||||
chr12:131743208
|
G | A | 83 | a0000c0005t0001g0120a0000c0005t0001g0121a0001c0001t0001g0002others(80): Show | 84 | HG00280.hp2 HG00597.hp1 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.1082-9915G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131743208 | ||||||
chr12:131743223
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1082-9900C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131743223 | ||||||
chr12:131743303
|
C | T | 1 | a0001c0001t0001g0258 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1082-9820C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131743303 | ||||||
chr12:131743446
|
A | G | 83 | a0000c0005t0001g0120a0000c0005t0001g0121a0001c0001t0001g0002others(80): Show | 84 | HG00280.hp2 HG00597.hp1 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.1082-9677A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131743446 | ||||||
chr12:131743504
|
G | A | 4 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0004t0002g0306others(1): Show | 4 | HG01243.hp1 HG03041.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1082-9619G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131743504 | ||||||
chr12:131743516
|
C | T | 1 | a0001c0001t0001g0138 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1082-9607C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131743516 | ||||||
chr12:131743560
|
G | A | 5 | a0001c0001t0003g0031a0001c0001t0003g0308a0001c0001t0004g0305others(2): Show | 5 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1082-9563G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131743560 | ||||||
chr12:131743929
|
C | T | 1 | a0001c0002t0001g0283 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1082-9194C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131743929 | ||||||
chr12:131744068
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1082-9055G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131744068 | ||||||
chr12:131744177
|
C | T | 2 | a0001c0002t0001g0287a0001c0002t0001g0288 | 2 | HG02293.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.1082-8946C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131744177 | ||||||
chr12:131744446
|
C | G | 56 | a0000c0023t0001g0051a0001c0001t0001g0047a0001c0001t0001g0048others(53): Show | 56 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.1082-8677C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131744446 | ||||||
chr12:131744713
|
A | G | 1 | a0001c0004t0001g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1082-8410A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131744713 | ||||||
chr12:131744788
|
A | G | 55 | a0000c0023t0001g0051a0001c0001t0001g0047a0001c0001t0001g0048others(52): Show | 55 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.1082-8335A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131744788 | ||||||
chr12:131744807
|
A | G | 1 | a0001c0029t0002g0059 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1082-8316A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131744807 | ||||||
chr12:131744912
|
T | G | 3 | a0001c0001t0001g0233a0001c0008t0001g0235a0001c0008t0001g0236 | 3 | HG00733.hp2 HG01175.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.1082-8211T>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131744912 | ||||||
chr12:131744962
|
G | A | 1 | a0001c0001t0001g0047 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1082-8161G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131744962 | ||||||
chr12:131745018
|
A | T | 1 | a0001c0001t0001g0161 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1082-8105A>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131745018 | ||||||
chr12:131745195
|
G | A | 56 | a0000c0023t0001g0051a0001c0001t0001g0047a0001c0001t0001g0048others(53): Show | 56 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.1082-7928G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131745195 | ||||||
chr12:131745430
|
G | T | 1 | a0001c0001t0001g0070 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1082-7693G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131745430 | ||||||
chr12:131745557
|
G | A | 1 | a0002c0003t0004g0022 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1082-7566G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131745557 | ||||||
chr12:131745630
|
G | A | 4 | a0001c0001t0001g0147a0001c0001t0001g0164a0001c0001t0001g0165others(1): Show | 4 | NA18960.hp1 NA19065.hp1 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.1082-7493G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131745630 | ||||||
chr12:131745754
|
C | CT | 11 | a0001c0001t0001g0112a0001c0001t0001g0153a0001c0001t0001g0194others(8): Show | 11 | HG00741.hp1 HG01099.hp2 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.1082-7356dupT | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131745754 | |||||
chr12:131745947
|
G | C | 4 | a0001c0001t0002g0019a0001c0012t0001g0044a0001c0012t0001g0045others(1): Show | 4 | HG03098.hp2 HG03139.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1082-7176G>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131745947 | ||||||
chr12:131745960
|
C | T | 2 | a0001c0001t0001g0257a0001c0001t0001g0258 | 2 | NA18986.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1082-7163C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131745960 | ||||||
chr12:131746082
|
C | T | 81 | a0000c0005t0001g0120a0000c0005t0001g0121a0001c0001t0001g0002others(78): Show | 82 | HG00280.hp2 HG00597.hp1 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.1082-7041C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131746082 | ||||||
chr12:131746312
|
C | G | 108 | a0000c0005t0001g0199a0000c0005t0001g0251a0001c0001t0001g0003others(105): Show | 113 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.1082-6811C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131746312 | ||||||
chr12:131746319
|
G | A | 2 | a0001c0001t0001g0160a0003c0009t0001g0052 | 2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1082-6804G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131746319 | ||||||
chr12:131746376
|
G | T | 4 | a0001c0006t0001g0014a0001c0006t0001g0016a0001c0006t0001g0017others(1): Show | 4 | HG02922.hp1 HG03130.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1082-6747G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131746376 | ||||||
chr12:131746691
|
A | G | 1 | a0001c0001t0001g0047 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1082-6432A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131746691 | ||||||
chr12:131746704
|
A | G | 1 | a0001c0001t0001g0047 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1082-6419A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131746704 | ||||||
chr12:131746827
|
G | A | 1 | a0001c0002t0001g0301 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1082-6296G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131746827 | ||||||
chr12:131746875
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1082-6248C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131746875 | ||||||
chr12:131746921
|
G | A | 1 | a0001c0002t0001g0292 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1082-6202G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131746921 | ||||||
chr12:131746931
|
G | C | 51 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0172others(48): Show | 51 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(48): Show |
intron_variant | MODIFIER | c.1082-6192G>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131746931 | ||||||
chr12:131746932
|
G | A | 3 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0172 | 3 | NA18942.hp1 NA18966.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.1082-6191G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131746932 | ||||||
chr12:131746955
|
T | G | 1 | a0001c0001t0003g0021 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1082-6168T>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131746955 | ||||||
chr12:131746961
|
G | A | 1 | a0001c0001t0001g0130 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1082-6162G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131746961 | ||||||
chr12:131746964
|
T | C | 2 | a0001c0001t0001g0074a0001c0001t0001g0130 | 2 | HG03239.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1082-6159T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131746964 | ||||||
chr12:131746972
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1082-6151C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131746972 | ||||||
chr12:131746976
|
T | C | 1 | a0001c0001t0001g0130 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1082-6147T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131746976 | ||||||
chr12:131747021
|
A | G | 1 | a0001c0001t0001g0171 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1082-6102A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131747021 | ||||||
chr12:131747023
|
C | G | 1 | a0001c0001t0001g0171 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1082-6100C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131747023 | ||||||
chr12:131747036
|
A | G | 64 | a0000c0005t0001g0199a0000c0005t0001g0251a0001c0001t0001g0003others(61): Show | 70 | HG00558.hp2 HG00597.hp2 HG00738.hp1 others(67): Show |
intron_variant | MODIFIER | c.1082-6087A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131747036 | ||||||
chr12:131747083
|
A | G | 1 | a0001c0001t0001g0149 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1082-6040A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131747083 | ||||||
chr12:131747103
|
C | CAAAAAAA others(2): Show |
61 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0047others(58): Show | 61 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.1082-6012_1082-600 others(13): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131747103 | |||||
chr12:131747103
|
C | CAAAAAAA others(3): Show |
20 | a0000c0023t0001g0051a0001c0001t0001g0066a0001c0001t0001g0090others(17): Show | 20 | HG01074.hp2 HG01106.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.1082-6013_1082-600 others(14): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131747103 | |||||
chr12:131747103
|
C | CAAAAAAA others(4): Show |
5 | a0001c0001t0002g0097a0001c0004t0001g0099a0001c0004t0002g0011others(2): Show | 5 | HG01891.hp2 HG02486.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1082-6014_1082-600 others(15): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131747103 | |||||
chr12:131747138
|
A | C | 97 | a0000c0023t0001g0051a0001c0001t0001g0012a0001c0001t0001g0013others(94): Show | 97 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.1082-5985A>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131747138 | ||||||
chr12:131747140
|
C | T | 14 | a0001c0001t0002g0095a0001c0001t0003g0018a0001c0001t0003g0025others(11): Show | 14 | HG01891.hp2 HG02258.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1082-5983C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131747140 | ||||||
chr12:131747167
|
T | C | 169 | a0000c0005t0001g0120a0000c0023t0001g0051a0001c0001t0001g0002others(166): Show | 170 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.1082-5956T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131747167 | ||||||
chr12:131747212
|
G | A | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1082-5911G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131747212 | ||||||
chr12:131747477
|
G | A | 2 | a0001c0004t0002g0306a0001c0004t0002g0307 | 2 | HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1082-5646G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131747477 | ||||||
chr12:131747615
|
T | C | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1082-5508T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131747615 | ||||||
chr12:131747743
|
G | A | 1 | a0001c0001t0001g0258 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1082-5380G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131747743 | ||||||
chr12:131747826
|
T | A | 1 | a0001c0004t0001g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1082-5297T>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131747826 | ||||||
chr12:131747830
|
G | A | 3 | a0001c0012t0001g0044a0001c0012t0001g0045a0001c0031t0001g0046 | 3 | HG03098.hp2 HG03139.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1082-5293G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131747830 | ||||||
chr12:131748218
|
C | CT | 182 | a0000c0005t0001g0199a0000c0005t0001g0251a0000c0023t0001g0051others(179): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.1082-4890dupT | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131748218 | |||||
chr12:131748218
|
C | CTT | 86 | a0000c0005t0001g0120a0000c0005t0001g0121a0001c0001t0001g0002others(83): Show | 87 | HG00280.hp2 HG00597.hp1 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.1082-4891_1082-489 others(6): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131748218 | |||||
chr12:131748218
|
CT | C | 7 | a0001c0004t0001g0099a0001c0004t0002g0009a0001c0004t0002g0010others(4): Show | 7 | HG01891.hp2 HG02451.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1082-4890delT | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131748218 | |||||
chr12:131748258
|
C | G | 1 | a0001c0004t0001g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1082-4865C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131748258 | ||||||
chr12:131748425
|
G | T | 7 | a0001c0004t0001g0099a0001c0004t0002g0009a0001c0004t0002g0010others(4): Show | 7 | HG01891.hp2 HG02451.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1082-4698G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131748425 | ||||||
chr12:131748490
|
T | C | 2 | a0001c0004t0002g0306a0001c0004t0002g0307 | 2 | HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1082-4633T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131748490 | ||||||
chr12:131748512
|
A | C | 1 | a0001c0004t0001g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1082-4611A>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131748512 | ||||||
chr12:131748598
|
A | C | 83 | a0000c0005t0001g0120a0000c0005t0001g0121a0001c0001t0001g0002others(80): Show | 84 | HG00280.hp2 HG00597.hp1 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.1082-4525A>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131748598 | ||||||
chr12:131748797
|
C | T | 1 | a0012c0030t0001g0196 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1082-4326C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131748797 | ||||||
chr12:131748914
|
A | T | 1 | a0001c0004t0001g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1082-4209A>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131748914 | ||||||
chr12:131748946
|
A | G | 1 | a0001c0004t0001g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1082-4177A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131748946 | ||||||
chr12:131749021
|
A | G | 1 | a0001c0001t0002g0082 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1082-4102A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131749021 | ||||||
chr12:131749062
|
A | C | 56 | a0000c0023t0001g0051a0001c0001t0001g0047a0001c0001t0001g0048others(53): Show | 56 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.1082-4061A>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131749062 | ||||||
chr12:131749113
|
T | A | 2 | a0001c0001t0001g0116a0001c0001t0001g0118 | 2 | HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1082-4010T>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131749113 | ||||||
chr12:131749144
|
C | A | 1 | a0001c0001t0001g0132 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1082-3979C>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131749144 | ||||||
chr12:131749174
|
C | T | 1 | a0001c0001t0001g0220 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1082-3949C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131749174 | ||||||
chr12:131749257
|
G | A | 1 | a0001c0002t0001g0283 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1082-3866G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131749257 | ||||||
chr12:131749287
|
G | T | 7 | a0001c0004t0001g0099a0001c0004t0002g0009a0001c0004t0002g0010others(4): Show | 7 | HG01891.hp2 HG02451.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1082-3836G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131749287 | ||||||
chr12:131749310
|
C | T | 1 | a0001c0001t0003g0021 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1082-3813C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131749310 | ||||||
chr12:131749313
|
C | G | 1 | a0001c0001t0002g0100 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1082-3810C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131749313 | ||||||
chr12:131749667
|
A | T | 1 | a0001c0015t0002g0008 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1082-3456A>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131749667 | ||||||
chr12:131749739
|
G | T | 2 | a0001c0001t0001g0070a0001c0001t0001g0083 | 2 | HG00733.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1082-3384G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131749739 | ||||||
chr12:131749836
|
A | C | 1 | a0001c0001t0003g0308 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1082-3287A>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131749836 | ||||||
chr12:131750055
|
C | T | 1 | a0001c0001t0002g0084 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1082-3068C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131750055 | ||||||
chr12:131750157
|
C | T | 1 | a0001c0001t0003g0039 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1082-2966C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131750157 | ||||||
chr12:131750277
|
C | G | 1 | a0001c0011t0002g0081 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1082-2846C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131750277 | ||||||
chr12:131750373
|
G | A | 21 | a0001c0002t0001g0283a0001c0002t0001g0285a0001c0002t0001g0286others(18): Show | 21 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.1082-2750G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131750373 | ||||||
chr12:131750481
|
G | A | 1 | a0001c0004t0001g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1082-2642G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131750481 | ||||||
chr12:131750519
|
T | TC | 51 | a0000c0005t0001g0199a0000c0005t0001g0251a0001c0001t0001g0003others(48): Show | 56 | HG00558.hp2 HG00597.hp2 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.1082-2602dupC | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131750519 | |||||
chr12:131750540
|
G | A | 1 | a0001c0002t0001g0286 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1082-2583G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131750540 | ||||||
chr12:131750553
|
G | A | 6 | a0001c0001t0003g0018a0001c0001t0003g0025a0001c0001t0003g0031others(3): Show | 6 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1082-2570G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131750553 | ||||||
chr12:131750891
|
TGG | T | 24 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0002t0001g0283others(21): Show | 24 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.1082-2231_1082-223 others(6): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131750891 | ||||||
chr12:131750895
|
AT | A | 24 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0002t0001g0283others(21): Show | 24 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.1082-2226delT | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr12 | 131750895 | |||||
chr12:131750897
|
T | C | 24 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0002t0001g0283others(21): Show | 24 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.1082-2226T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131750897 | ||||||
chr12:131750921
|
A | G | 6 | a0001c0004t0002g0009a0001c0004t0002g0010a0001c0004t0002g0011others(3): Show | 6 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1082-2202A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131750921 | ||||||
chr12:131750927
|
G | T | 1 | a0002c0003t0003g0026 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1082-2196G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131750927 | ||||||
chr12:131750947
|
T | G | 1 | a0001c0004t0001g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1082-2176T>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131750947 | ||||||
chr12:131751072
|
G | T | 1 | a0002c0003t0003g0043 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1082-2051G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131751072 | ||||||
chr12:131751127
|
G | C | 1 | a0001c0001t0001g0281 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1082-1996G>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131751127 | ||||||
chr12:131751314
|
C | T | 51 | a0000c0005t0001g0199a0000c0005t0001g0251a0001c0001t0001g0003others(48): Show | 56 | HG00558.hp2 HG00597.hp2 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.1082-1809C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131751314 | ||||||
chr12:131751349
|
C | T | 18 | a0000c0023t0001g0051a0001c0001t0001g0048a0001c0001t0001g0049others(15): Show | 18 | HG00323.hp1 HG00733.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.1082-1774C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131751349 | ||||||
chr12:131751398
|
G | A | 6 | a0001c0004t0002g0009a0001c0004t0002g0010a0001c0004t0002g0011others(3): Show | 6 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1082-1725G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131751398 | ||||||
chr12:131751413
|
G | T | 7 | a0001c0001t0001g0149a0001c0004t0002g0009a0001c0004t0002g0010others(4): Show | 7 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1082-1710G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131751413 | ||||||
chr12:131751445
|
G | A | 3 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0010t0004g0023 | 3 | HG01243.hp1 HG01261.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1082-1678G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131751445 | ||||||
chr12:131751604
|
C | A | 3 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0179 | 3 | HG01243.hp1 HG03098.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.1082-1519C>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131751604 | ||||||
chr12:131751687
|
A | C | 1 | a0001c0001t0002g0019 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1082-1436A>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131751687 | ||||||
chr12:131751873
|
C | G | 1 | a0001c0001t0001g0264 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1082-1250C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131751873 | ||||||
chr12:131751961
|
G | A | 21 | a0001c0002t0001g0283a0001c0002t0001g0285a0001c0002t0001g0286others(18): Show | 21 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.1082-1162G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131751961 | ||||||
chr12:131752057
|
C | T | 1 | a0001c0001t0002g0019 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1082-1066C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131752057 | ||||||
chr12:131752104
|
A | G | 4 | a0001c0001t0002g0019a0001c0012t0001g0044a0001c0012t0001g0045others(1): Show | 4 | HG03098.hp2 HG03139.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1082-1019A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131752104 | ||||||
chr12:131752291
|
C | T | 1 | a0001c0002t0001g0301 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1082-832C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131752291 | ||||||
chr12:131752392
|
G | A | 1 | a0001c0001t0002g0092 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1082-731G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131752392 | ||||||
chr12:131752478
|
C | G | 1 | a0001c0029t0002g0059 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1082-645C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131752478 | ||||||
chr12:131752788
|
C | A | 3 | a0001c0002t0001g0292a0001c0002t0001g0293a0001c0002t0001g0297 | 3 | HG00099.hp2 HG00639.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.1082-335C>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131752788 | ||||||
chr12:131752790
|
C | T | 11 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0108others(8): Show | 11 | HG02040.hp2 HG02056.hp2 HG03834.hp1 others(8): Show |
intron_variant | MODIFIER | c.1082-333C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131752790 | ||||||
chr12:131753057
|
G | A | 3 | a0001c0012t0001g0044a0001c0012t0001g0045a0001c0031t0001g0046 | 3 | HG03098.hp2 HG03139.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1082-66G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 7/17 | chr12 | 131753057 | ||||||
chr12:131753424
|
C | T | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1322+61C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 8/17 | chr12 | 131753424 | ||||||
chr12:131753501
|
A | G | 1 | a0001c0011t0002g0081 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1322+138A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 8/17 | chr12 | 131753501 | ||||||
chr12:131753580
|
T | A | 19 | a0001c0001t0001g0090a0001c0001t0002g0082a0001c0001t0002g0084others(16): Show | 19 | HG01106.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.1322+217T>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 8/17 | chr12 | 131753580 | ||||||
chr12:131753580
|
T | C | 4 | a0001c0006t0001g0014a0001c0006t0001g0016a0001c0006t0001g0017others(1): Show | 4 | HG02922.hp1 HG03130.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1322+217T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 8/17 | chr12 | 131753580 | ||||||
chr12:131753609
|
T | C | 1 | a0001c0001t0001g0230 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1322+246T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 8/17 | chr12 | 131753609 | ||||||
chr12:131753683
|
T | C | 1 | a0001c0001t0001g0258 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1322+320T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 8/17 | chr12 | 131753683 | ||||||
chr12:131753714
|
A | C | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1322+351A>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 8/17 | chr12 | 131753714 | ||||||
chr12:131753834
|
C | G | 2 | a0001c0001t0001g0267a0001c0001t0001g0268 | 2 | HG01934.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1322+471C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 8/17 | chr12 | 131753834 | ||||||
chr12:131753852
|
C | T | 1 | a0001c0001t0003g0021 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1322+489C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 8/17 | chr12 | 131753852 | ||||||
chr12:131753893
|
C | T | 1 | a0001c0001t0001g0265 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1323-475C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 8/17 | chr12 | 131753893 | ||||||
chr12:131753979
|
C | G | 1 | a0001c0001t0001g0149 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1323-389C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 8/17 | chr12 | 131753979 | ||||||
chr12:131754061
|
A | G | 1 | a0001c0010t0001g0240 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1323-307A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 8/17 | chr12 | 131754061 | ||||||
chr12:131754288
|
C | T | 1 | a0001c0001t0001g0228 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1323-80C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 8/17 | chr12 | 131754288 | ||||||
chr12:131754301
|
C | G | 2 | a0001c0001t0001g0138a0001c0001t0002g0050 | 2 | NA18979.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.1323-67C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 8/17 | chr12 | 131754301 | ||||||
chr12:131754562
|
T | A | 1 | a0001c0001t0001g0194 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1454+63T>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 9/17 | chr12 | 131754562 | ||||||
chr12:131754627
|
C | CT | 91 | a0000c0005t0001g0120a0000c0005t0001g0121a0000c0023t0001g0051others(88): Show | 92 | HG00280.hp1 HG00280.hp2 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.1454+152dupT | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr12 | 131754627 | |||||
chr12:131754627
|
C | CTT | 86 | a0000c0005t0001g0199a0000c0005t0001g0251a0001c0001t0001g0003others(83): Show | 91 | HG00140.hp1 HG00558.hp2 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.1454+151_1454+152d others(4): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr12 | 131754627 | |||||
chr12:131754627
|
C | CTTT | 18 | a0001c0001t0001g0012a0001c0001t0001g0090a0001c0001t0001g0180others(15): Show | 18 | HG00099.hp2 HG00639.hp2 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.1454+150_1454+152d others(5): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr12 | 131754627 | |||||
chr12:131754658
|
G | T | 1 | a0001c0001t0001g0239 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1454+159G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 9/17 | chr12 | 131754658 | ||||||
chr12:131754678
|
G | A | 1 | a0001c0002t0001g0303 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1454+179G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 9/17 | chr12 | 131754678 | ||||||
chr12:131754779
|
G | A | 1 | a0001c0002t0001g0299 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1454+280G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 9/17 | chr12 | 131754779 | ||||||
chr12:131754781
|
G | A | 1 | a0001c0001t0001g0225 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1454+282G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 9/17 | chr12 | 131754781 | ||||||
chr12:131754786
|
A | G | 1 | a0001c0001t0001g0102 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1454+287A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 9/17 | chr12 | 131754786 | ||||||
chr12:131754820
|
A | G | 1 | a0001c0001t0001g0278 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1454+321A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 9/17 | chr12 | 131754820 | ||||||
chr12:131754934
|
A | G | 81 | a0000c0005t0001g0120a0000c0005t0001g0121a0001c0001t0001g0002others(78): Show | 82 | HG00280.hp2 HG00597.hp1 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.1454+435A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 9/17 | chr12 | 131754934 | ||||||
chr12:131754997
|
T | A | 73 | a0000c0005t0001g0120a0000c0005t0001g0121a0001c0001t0001g0002others(70): Show | 74 | HG00280.hp2 HG00597.hp1 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.1455-389T>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 9/17 | chr12 | 131754997 | ||||||
chr12:131755191
|
C | T | 42 | a0000c0005t0001g0199a0000c0005t0001g0251a0001c0001t0001g0003others(39): Show | 46 | HG00558.hp2 HG00597.hp2 HG01358.hp2 others(43): Show |
intron_variant | MODIFIER | c.1455-195C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 9/17 | chr12 | 131755191 | ||||||
chr12:131755209
|
G | A | 21 | a0000c0023t0001g0051a0001c0001t0001g0047a0001c0001t0001g0048others(18): Show | 21 | HG00323.hp1 HG00733.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.1455-177G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 9/17 | chr12 | 131755209 | ||||||
chr12:131755353
|
T | G | 14 | a0001c0001t0002g0084a0001c0001t0002g0085a0001c0001t0002g0086others(11): Show | 14 | HG01106.hp2 HG01167.hp2 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.1455-33T>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 9/17 | chr12 | 131755353 | ||||||
chr12:131755528
|
G | A | 7 | a0001c0001t0003g0018a0001c0004t0002g0009a0001c0004t0002g0010others(4): Show | 7 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1548+49G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 10/17 | chr12 | 131755528 | ||||||
chr12:131755656
|
A | C | 3 | a0001c0001t0002g0019a0001c0012t0001g0044a0001c0012t0001g0045 | 3 | HG03098.hp2 HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1548+177A>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 10/17 | chr12 | 131755656 | ||||||
chr12:131755728
|
A | C | 3 | a0001c0001t0002g0019a0001c0012t0001g0044a0001c0012t0001g0045 | 3 | HG03098.hp2 HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1548+249A>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 10/17 | chr12 | 131755728 | ||||||
chr12:131755796
|
C | T | 106 | a0000c0005t0001g0120a0000c0005t0001g0121a0001c0001t0001g0002others(103): Show | 107 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.1548+317C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 10/17 | chr12 | 131755796 | ||||||
chr12:131755891
|
A | G | 7 | a0001c0001t0003g0018a0001c0004t0002g0009a0001c0004t0002g0010others(4): Show | 7 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1548+412A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 10/17 | chr12 | 131755891 | ||||||
chr12:131755900
|
T | C | 1 | a0001c0001t0001g0176 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1548+421T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 10/17 | chr12 | 131755900 | ||||||
chr12:131756114
|
A | G | 140 | a0000c0005t0001g0120a0000c0005t0001g0121a0000c0023t0001g0051others(137): Show | 141 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.1549-359A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 10/17 | chr12 | 131756114 | ||||||
chr12:131756119
|
A | G | 80 | a0000c0005t0001g0120a0000c0005t0001g0121a0001c0001t0001g0002others(77): Show | 81 | HG00280.hp2 HG00597.hp1 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.1549-354A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 10/17 | chr12 | 131756119 | ||||||
chr12:131756196
|
C | CAAAGAAA others(335): Show |
1 | a0001c0012t0001g0045 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1549-261_1549-260i others(344): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr12 | 131756196 | |||||
chr12:131756218
|
G | C | 1 | a0001c0015t0002g0008 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1549-255G>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 10/17 | chr12 | 131756218 | ||||||
chr12:131756249
|
G | A | 1 | a0001c0031t0001g0046 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1549-224G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 10/17 | chr12 | 131756249 | ||||||
chr12:131756392
|
C | CAT | 141 | a0000c0005t0001g0120a0000c0005t0001g0121a0000c0023t0001g0051others(138): Show | 142 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.1549-77_1549-76dup others(2): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr12 | 131756392 | |||||
chr12:131756684
|
A | G | 309 | a0000c0005t0001g0120a0000c0005t0001g0121a0000c0005t0001g0199others(306): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.1720+40A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131756684 | ||||||
chr12:131756757
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1720+113C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131756757 | ||||||
chr12:131756817
|
C | T | 6 | a0001c0001t0001g0135a0001c0001t0001g0147a0001c0001t0001g0151others(3): Show | 6 | HG00597.hp1 HG02155.hp1 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.1720+173C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131756817 | ||||||
chr12:131756819
|
C | T | 1 | a0001c0001t0001g0271 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1720+175C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131756819 | ||||||
chr12:131756820
|
G | A | 2 | a0001c0004t0002g0306a0001c0004t0002g0307 | 2 | HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1720+176G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131756820 | ||||||
chr12:131757106
|
T | C | 309 | a0000c0005t0001g0120a0000c0005t0001g0121a0000c0005t0001g0199others(306): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.1720+462T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131757106 | ||||||
chr12:131757232
|
G | C | 1 | a0001c0031t0001g0046 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1720+588G>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131757232 | ||||||
chr12:131757267
|
T | G | 1 | a0001c0001t0001g0187 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1720+623T>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131757267 | ||||||
chr12:131757319
|
G | A | 2 | a0001c0001t0001g0267a0001c0001t0001g0268 | 2 | HG01934.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1720+675G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131757319 | ||||||
chr12:131757503
|
C | A | 1 | a0001c0001t0002g0064 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1720+859C>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131757503 | ||||||
chr12:131757600
|
G | C | 21 | a0000c0023t0001g0051a0001c0001t0001g0047a0001c0001t0001g0048others(18): Show | 21 | HG00323.hp1 HG00733.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.1720+956G>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131757600 | ||||||
chr12:131757702
|
T | C | 1 | a0001c0006t0001g0014 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1720+1058T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131757702 | ||||||
chr12:131757714
|
G | A | 105 | a0000c0005t0001g0120a0000c0005t0001g0121a0001c0001t0001g0002others(102): Show | 106 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.1720+1070G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131757714 | ||||||
chr12:131757739
|
G | A | 2 | a0001c0001t0002g0057a0001c0001t0002g0062 | 2 | HG00639.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.1720+1095G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131757739 | ||||||
chr12:131757907
|
G | A | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1720+1263G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131757907 | ||||||
chr12:131758007
|
G | C | 1 | a0001c0002t0001g0286 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1720+1363G>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131758007 | ||||||
chr12:131758065
|
C | T | 3 | a0001c0008t0001g0235a0001c0008t0001g0236a0001c0031t0001g0046 | 3 | HG00733.hp2 HG01175.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1720+1421C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131758065 | ||||||
chr12:131758623
|
G | T | 1 | a0001c0004t0001g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1720+1979G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131758623 | ||||||
chr12:131758712
|
C | T | 1 | a0001c0001t0002g0019 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1720+2068C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131758712 | ||||||
chr12:131758776
|
T | G | 21 | a0000c0023t0001g0051a0001c0001t0001g0047a0001c0001t0001g0048others(18): Show | 21 | HG00323.hp1 HG00733.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.1720+2132T>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131758776 | ||||||
chr12:131759019
|
G | A | 1 | a0001c0001t0001g0265 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1720+2375G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131759019 | ||||||
chr12:131759383
|
T | C | 106 | a0000c0005t0001g0120a0000c0005t0001g0121a0001c0001t0001g0002others(103): Show | 107 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.1720+2739T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131759383 | ||||||
chr12:131759499
|
G | A | 80 | a0000c0005t0001g0120a0000c0005t0001g0121a0001c0001t0001g0002others(77): Show | 81 | HG00280.hp2 HG00597.hp1 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.1720+2855G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131759499 | ||||||
chr12:131759570
|
C | T | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1720+2926C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131759570 | ||||||
chr12:131759615
|
C | G | 1 | a0001c0001t0002g0019 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1720+2971C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131759615 | ||||||
chr12:131759641
|
T | TA | 36 | a0001c0001t0001g0061a0001c0001t0002g0050a0001c0001t0002g0054others(33): Show | 36 | HG00639.hp1 HG01106.hp2 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.1720+3007dupA | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr12 | 131759641 | |||||
chr12:131759718
|
C | T | 2 | a0001c0001t0002g0076a0001c0001t0003g0021 | 2 | HG02165.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1720+3074C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131759718 | ||||||
chr12:131759766
|
T | C | 1 | a0001c0029t0002g0059 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1720+3122T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131759766 | ||||||
chr12:131759797
|
G | A | 3 | a0001c0008t0001g0235a0001c0008t0001g0236a0001c0031t0001g0046 | 3 | HG00733.hp2 HG01175.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1720+3153G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131759797 | ||||||
chr12:131759853
|
A | G | 11 | a0001c0001t0001g0265a0001c0002t0001g0285a0001c0002t0001g0287others(8): Show | 11 | HG00741.hp1 HG01099.hp2 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.1720+3209A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131759853 | ||||||
chr12:131760015
|
A | G | 1 | a0002c0028t0004g0309 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1720+3371A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131760015 | ||||||
chr12:131760120
|
A | G | 2 | a0001c0001t0001g0103a0001c0001t0001g0104 | 2 | HG02004.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.1720+3476A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131760120 | ||||||
chr12:131760256
|
C | T | 9 | a0001c0002t0001g0283a0001c0002t0001g0286a0001c0002t0001g0289others(6): Show | 9 | HG00140.hp1 HG00642.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.1720+3612C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131760256 | ||||||
chr12:131760309
|
T | C | 2 | a0001c0001t0001g0179a0001c0001t0001g0207 | 2 | HG01074.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.1720+3665T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131760309 | ||||||
chr12:131760383
|
T | C | 2 | a0001c0001t0001g0267a0001c0001t0001g0268 | 2 | HG01934.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1720+3739T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131760383 | ||||||
chr12:131760481
|
A | T | 5 | a0001c0002t0001g0283a0001c0002t0001g0286a0001c0002t0001g0289others(2): Show | 5 | HG00140.hp1 HG00642.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.1720+3837A>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131760481 | ||||||
chr12:131760869
|
C | G | 6 | a0001c0001t0001g0047a0001c0004t0002g0009a0001c0004t0002g0010others(3): Show | 6 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1721-3587C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131760869 | ||||||
chr12:131760987
|
G | A | 1 | a0001c0006t0001g0014 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1721-3469G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131760987 | ||||||
chr12:131761007
|
A | G | 2 | a0001c0012t0001g0044a0001c0012t0001g0045 | 2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1721-3449A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131761007 | ||||||
chr12:131761011
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1721-3445G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131761011 | ||||||
chr12:131761097
|
C | T | 6 | a0001c0004t0002g0009a0001c0004t0002g0010a0001c0004t0002g0011others(3): Show | 6 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1721-3359C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131761097 | ||||||
chr12:131761176
|
T | C | 1 | a0001c0001t0003g0021 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1721-3280T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131761176 | ||||||
chr12:131761360
|
C | T | 4 | a0001c0006t0001g0014a0001c0006t0001g0016a0001c0006t0001g0017others(1): Show | 4 | HG02922.hp1 HG03130.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1721-3096C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131761360 | ||||||
chr12:131761380
|
C | T | 3 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0265 | 3 | HG01257.hp1 HG01258.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1721-3076C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131761380 | ||||||
chr12:131761436
|
G | C | 130 | a0000c0005t0001g0120a0000c0005t0001g0121a0001c0001t0001g0002others(127): Show | 131 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.1721-3020G>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131761436 | ||||||
chr12:131761548
|
G | T | 18 | a0000c0023t0001g0051a0001c0001t0001g0048a0001c0001t0001g0049others(15): Show | 18 | HG00323.hp1 HG00733.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.1721-2908G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131761548 | ||||||
chr12:131761613
|
G | A | 1 | a0001c0001t0001g0275 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1721-2843G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131761613 | ||||||
chr12:131761638
|
C | T | 2 | a0001c0012t0001g0044a0001c0012t0001g0045 | 2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1721-2818C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131761638 | ||||||
chr12:131761756
|
C | T | 250 | a0000c0005t0001g0120a0000c0005t0001g0121a0000c0005t0001g0199others(247): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.1721-2700C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131761756 | ||||||
chr12:131761862
|
C | T | 1 | a0001c0001t0001g0069 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1721-2594C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131761862 | ||||||
chr12:131761955
|
T | A | 26 | a0001c0002t0001g0283a0001c0002t0001g0285a0001c0002t0001g0286others(23): Show | 26 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.1721-2501T>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131761955 | ||||||
chr12:131761998
|
C | T | 1 | a0001c0006t0001g0014 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1721-2458C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131761998 | ||||||
chr12:131762202
|
C | T | 21 | a0000c0023t0001g0051a0001c0001t0001g0047a0001c0001t0001g0048others(18): Show | 21 | HG00323.hp1 HG00733.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.1721-2254C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131762202 | ||||||
chr12:131762371
|
A | G | 250 | a0000c0005t0001g0120a0000c0005t0001g0121a0000c0005t0001g0199others(247): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.1721-2085A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131762371 | ||||||
chr12:131762613
|
A | G | 4 | a0001c0004t0002g0009a0001c0004t0002g0010a0001c0004t0002g0011others(1): Show | 4 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1721-1843A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131762613 | ||||||
chr12:131762637
|
G | T | 1 | a0001c0001t0002g0101 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1721-1819G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131762637 | ||||||
chr12:131762650
|
A | G | 2 | a0001c0012t0001g0044a0001c0012t0001g0045 | 2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1721-1806A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131762650 | ||||||
chr12:131762709
|
C | G | 18 | a0001c0001t0001g0061a0001c0001t0002g0050a0001c0001t0002g0054others(15): Show | 18 | HG00639.hp1 HG01943.hp2 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.1721-1747C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131762709 | ||||||
chr12:131762900
|
A | G | 1 | a0001c0001t0001g0213 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1721-1556A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131762900 | ||||||
chr12:131762966
|
C | T | 5 | a0001c0001t0001g0066a0001c0001t0001g0068a0001c0001t0001g0069others(2): Show | 5 | HG01123.hp1 HG01261.hp2 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1721-1490C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131762966 | ||||||
chr12:131763146
|
C | T | 1 | a0001c0001t0002g0060 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1721-1310C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131763146 | ||||||
chr12:131763176
|
A | G | 3 | a0001c0008t0001g0235a0001c0008t0001g0236a0001c0031t0001g0046 | 3 | HG00733.hp2 HG01175.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1721-1280A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131763176 | ||||||
chr12:131763223
|
C | T | 49 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0177others(46): Show | 49 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(46): Show |
intron_variant | MODIFIER | c.1721-1233C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131763223 | ||||||
chr12:131763409
|
C | G | 3 | a0001c0002t0001g0292a0001c0002t0001g0293a0001c0002t0001g0297 | 3 | HG00099.hp2 HG00639.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.1721-1047C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131763409 | ||||||
chr12:131763587
|
C | T | 293 | a0000c0005t0001g0120a0000c0005t0001g0121a0000c0005t0001g0199others(290): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.1721-869C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131763587 | ||||||
chr12:131763636
|
CA | C | 5 | a0000c0005t0001g0251a0001c0001t0001g0006a0001c0001t0001g0250others(2): Show | 6 | HG02015.hp2 HG03490.hp2 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.1721-819delA | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131763636 | ||||||
chr12:131763703
|
T | A | 2 | a0001c0001t0001g0267a0001c0001t0001g0268 | 2 | HG01934.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1721-753T>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131763703 | ||||||
chr12:131763757
|
A | G | 2 | a0001c0001t0001g0267a0001c0001t0001g0268 | 2 | HG01934.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1721-699A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131763757 | ||||||
chr12:131763790
|
A | G | 1 | a0001c0001t0002g0084 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1721-666A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131763790 | ||||||
chr12:131763815
|
A | AT | 27 | a0000c0023t0001g0051a0001c0001t0001g0049a0001c0001t0001g0063others(24): Show | 27 | HG00323.hp1 HG00733.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.1721-624dupT | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr12 | 131763815 | |||||
chr12:131763815
|
AT | A | 11 | a0000c0005t0001g0199a0001c0001t0001g0113a0001c0001t0001g0114others(8): Show | 11 | HG00099.hp2 HG01106.hp1 HG02129.hp2 others(8): Show |
intron_variant | MODIFIER | c.1721-624delT | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr12 | 131763815 | |||||
chr12:131764098
|
C | G | 1 | a0001c0001t0001g0163 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1721-358C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131764098 | ||||||
chr12:131764306
|
C | T | 2 | a0001c0012t0001g0044a0001c0012t0001g0045 | 2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1721-150C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131764306 | ||||||
chr12:131764334
|
G | C | 3 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0265 | 3 | HG01257.hp1 HG01258.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1721-122G>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 11/17 | chr12 | 131764334 | ||||||
chr12:131764898
|
G | A | 1 | a0001c0002t0001g0287 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1951+212G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 12/17 | chr12 | 131764898 | ||||||
chr12:131764943
|
T | C | 108 | a0000c0005t0001g0120a0000c0005t0001g0121a0000c0005t0001g0199others(105): Show | 109 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.1951+257T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 12/17 | chr12 | 131764943 | ||||||
chr12:131764952
|
A | G | 5 | a0001c0001t0001g0066a0001c0001t0001g0068a0001c0001t0001g0069others(2): Show | 5 | HG01123.hp1 HG01261.hp2 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1951+266A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 12/17 | chr12 | 131764952 | ||||||
chr12:131765042
|
A | G | 1 | a0001c0001t0001g0105 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1951+356A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 12/17 | chr12 | 131765042 | ||||||
chr12:131765250
|
C | G | 1 | a0001c0001t0001g0112 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1951+564C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 12/17 | chr12 | 131765250 | ||||||
chr12:131765251
|
A | G | 2 | a0001c0012t0001g0044a0001c0012t0001g0045 | 2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1951+565A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 12/17 | chr12 | 131765251 | ||||||
chr12:131765269
|
G | A | 1 | a0001c0001t0001g0002 | 2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.1951+583G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 12/17 | chr12 | 131765269 | ||||||
chr12:131765463
|
A | G | 1 | a0001c0001t0001g0239 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1952-655A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 12/17 | chr12 | 131765463 | ||||||
chr12:131765668
|
C | G | 22 | a0001c0002t0001g0283a0001c0002t0001g0285a0001c0002t0001g0286others(19): Show | 22 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.1952-450C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 12/17 | chr12 | 131765668 | ||||||
chr12:131765815
|
T | TCTC | 250 | a0000c0005t0001g0120a0000c0005t0001g0121a0000c0005t0001g0199others(247): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.1952-303_1952-302i others(5): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 12/17 | chr12 | 131765815 | ||||||
chr12:131765967
|
T | C | 1 | a0002c0003t0003g0041 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1952-151T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 12/17 | chr12 | 131765967 | ||||||
chr12:131766043
|
C | T | 1 | a0003c0009t0001g0052 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1952-75C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 12/17 | chr12 | 131766043 | ||||||
chr12:131766104
|
G | C | 1 | a0001c0001t0001g0112 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1952-14G>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 12/17 | chr12 | 131766104 | ||||||
chr12:131766326
|
A | G | 1 | a0001c0001t0001g0176 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.2142+18A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131766326 | ||||||
chr12:131766521
|
C | A | 1 | a0001c0001t0001g0243 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2142+213C>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131766521 | ||||||
chr12:131766532
|
G | T | 1 | a0003c0009t0001g0052 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2142+224G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131766532 | ||||||
chr12:131766637
|
A | G | 1 | a0001c0001t0001g0212 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2142+329A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131766637 | ||||||
chr12:131766712
|
G | A | 1 | a0001c0004t0001g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2142+404G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131766712 | ||||||
chr12:131766954
|
TGTGTCCG others(56): Show |
T | 51 | a0000c0005t0001g0251a0001c0001t0001g0003a0001c0001t0001g0004others(48): Show | 56 | HG00558.hp2 HG00597.hp2 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.2142+860_2142+922d others(65): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr12 | 131766954 | |||||
chr12:131767014
|
A | T | 6 | a0001c0001t0001g0193a0001c0001t0001g0241a0001c0001t0001g0242others(3): Show | 6 | HG01358.hp2 HG01952.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.2142+706A>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131767014 | ||||||
chr12:131767017
|
C | T | 7 | a0001c0001t0001g0193a0001c0001t0001g0241a0001c0001t0001g0242others(4): Show | 7 | HG01358.hp2 HG01952.hp1 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.2142+709C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131767017 | ||||||
chr12:131767019
|
T | C | 1 | a0001c0001t0003g0311 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2142+711T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131767019 | ||||||
chr12:131767143
|
C | T | 4 | a0001c0002t0001g0292a0001c0002t0001g0293a0001c0002t0001g0297others(1): Show | 4 | HG00099.hp2 HG00639.hp2 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.2142+835C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131767143 | ||||||
chr12:131767186
|
C | A | 1 | a0001c0001t0001g0047 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2142+878C>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131767186 | ||||||
chr12:131767212
|
C | T | 2 | a0001c0004t0002g0306a0001c0004t0002g0307 | 2 | HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2142+904C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131767212 | ||||||
chr12:131767238
|
A | G | 250 | a0000c0005t0001g0120a0000c0005t0001g0121a0000c0005t0001g0199others(247): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.2142+930A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131767238 | ||||||
chr12:131767842
|
G | T | 1 | a0001c0001t0001g0266 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2142+1534G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131767842 | ||||||
chr12:131767965
|
T | A | 1 | a0001c0001t0001g0154 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.2142+1657T>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131767965 | ||||||
chr12:131768027
|
G | A | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2142+1719G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131768027 | ||||||
chr12:131768030
|
A | G | 2 | a0001c0012t0001g0044a0001c0012t0001g0045 | 2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2142+1722A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131768030 | ||||||
chr12:131768118
|
T | C | 28 | a0000c0023t0001g0051a0001c0001t0001g0047a0001c0001t0001g0048others(25): Show | 28 | HG00323.hp1 HG00733.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.2142+1810T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131768118 | ||||||
chr12:131768230
|
G | A | 4 | a0001c0006t0001g0014a0001c0006t0001g0016a0001c0006t0001g0017others(1): Show | 4 | HG02922.hp1 HG03130.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2142+1922G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131768230 | ||||||
chr12:131768237
|
C | T | 1 | a0002c0003t0004g0022 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2142+1929C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131768237 | ||||||
chr12:131768517
|
G | A | 290 | a0000c0005t0001g0120a0000c0005t0001g0121a0000c0005t0001g0199others(287): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.2142+2209G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131768517 | ||||||
chr12:131768568
|
C | G | 17 | a0000c0023t0001g0051a0001c0001t0001g0047a0001c0001t0001g0048others(14): Show | 17 | HG00323.hp1 HG00733.hp1 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.2142+2260C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131768568 | ||||||
chr12:131768573
|
G | A | 2 | a0001c0012t0001g0044a0001c0012t0001g0045 | 2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2142+2265G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131768573 | ||||||
chr12:131768600
|
C | T | 4 | a0001c0006t0001g0014a0001c0006t0001g0016a0001c0006t0001g0017others(1): Show | 4 | HG02922.hp1 HG03130.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2142+2292C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131768600 | ||||||
chr12:131768631
|
C | T | 18 | a0000c0023t0001g0051a0001c0001t0001g0048a0001c0001t0001g0049others(15): Show | 18 | HG00323.hp1 HG00733.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.2142+2323C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131768631 | ||||||
chr12:131768680
|
C | T | 21 | a0000c0023t0001g0051a0001c0001t0001g0047a0001c0001t0001g0048others(18): Show | 21 | HG00323.hp1 HG00733.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.2142+2372C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131768680 | ||||||
chr12:131768681
|
G | C | 2 | a0001c0001t0001g0279a0007c0020t0001g0280 | 2 | HG02071.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.2142+2373G>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131768681 | ||||||
chr12:131768820
|
C | T | 22 | a0000c0023t0001g0051a0001c0001t0001g0047a0001c0001t0001g0048others(19): Show | 22 | HG00323.hp1 HG00733.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.2142+2512C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131768820 | ||||||
chr12:131768824
|
G | T | 2 | a0002c0003t0003g0041a0002c0028t0004g0309 | 2 | HG03017.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.2142+2516G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131768824 | ||||||
chr12:131768955
|
G | A | 1 | a0001c0001t0001g0176 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.2142+2647G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131768955 | ||||||
chr12:131769020
|
G | A | 1 | a0001c0004t0001g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2142+2712G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131769020 | ||||||
chr12:131769055
|
A | C | 2 | a0001c0001t0002g0077a0001c0001t0002g0282 | 2 | HG02602.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.2142+2747A>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131769055 | ||||||
chr12:131769113
|
C | T | 1 | a0009c0022t0001g0125 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2142+2805C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131769113 | ||||||
chr12:131769126
|
C | CA | 252 | a0000c0005t0001g0120a0000c0005t0001g0121a0000c0005t0001g0199others(249): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.2142+2829dupA | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr12 | 131769126 | |||||
chr12:131769309
|
G | A | 1 | a0001c0001t0001g0191 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2142+3001G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131769309 | ||||||
chr12:131769437
|
A | G | 1 | a0001c0001t0001g0144 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2142+3129A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131769437 | ||||||
chr12:131769441
|
C | T | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2142+3133C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131769441 | ||||||
chr12:131769448
|
T | C | 1 | a0001c0001t0001g0155 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.2142+3140T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131769448 | ||||||
chr12:131769458
|
C | G | 4 | a0000c0005t0001g0121a0001c0001t0001g0116a0001c0001t0001g0118others(1): Show | 4 | HG01175.hp2 HG02280.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.2142+3150C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131769458 | ||||||
chr12:131769604
|
A | ATTTAT | 3 | a0001c0001t0002g0019a0001c0012t0001g0044a0001c0012t0001g0045 | 3 | HG03098.hp2 HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2142+3309_2142+331 others(9): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr12 | 131769604 | |||||
chr12:131769634
|
G | A | 2 | a0001c0004t0002g0306a0001c0004t0002g0307 | 2 | HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2142+3326G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131769634 | ||||||
chr12:131769720
|
G | A | 21 | a0000c0023t0001g0051a0001c0001t0001g0047a0001c0001t0001g0048others(18): Show | 21 | HG00323.hp1 HG00733.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.2142+3412G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131769720 | ||||||
chr12:131769754
|
G | C | 1 | a0001c0001t0003g0021 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2142+3446G>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131769754 | ||||||
chr12:131769787
|
C | T | 1 | a0001c0015t0002g0008 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2142+3479C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131769787 | ||||||
chr12:131769853
|
T | C | 3 | a0001c0001t0002g0019a0001c0012t0001g0044a0001c0012t0001g0045 | 3 | HG03098.hp2 HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2142+3545T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131769853 | ||||||
chr12:131769883
|
A | G | 1 | a0001c0001t0002g0076 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2142+3575A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131769883 | ||||||
chr12:131770045
|
T | C | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2142+3737T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131770045 | ||||||
chr12:131770235
|
G | A | 21 | a0000c0023t0001g0051a0001c0001t0001g0047a0001c0001t0001g0048others(18): Show | 21 | HG00323.hp1 HG00733.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.2142+3927G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131770235 | ||||||
chr12:131770276
|
A | G | 250 | a0000c0005t0001g0120a0000c0005t0001g0121a0000c0005t0001g0199others(247): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.2142+3968A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131770276 | ||||||
chr12:131770369
|
C | T | 1 | a0001c0001t0001g0073 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.2142+4061C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131770369 | ||||||
chr12:131770391
|
T | C | 1 | a0001c0004t0001g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2142+4083T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131770391 | ||||||
chr12:131770622
|
A | AT | 248 | a0000c0005t0001g0120a0000c0005t0001g0121a0000c0005t0001g0199others(245): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.2142+4321dupT | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr12 | 131770622 | |||||
chr12:131770906
|
C | A | 1 | a0001c0001t0001g0225 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2142+4598C>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131770906 | ||||||
chr12:131770911
|
G | T | 4 | a0001c0004t0001g0099a0001c0008t0001g0235a0001c0008t0001g0236others(1): Show | 4 | HG00733.hp2 HG01175.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.2142+4603G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131770911 | ||||||
chr12:131771048
|
C | T | 1 | a0002c0003t0003g0043 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2142+4740C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131771048 | ||||||
chr12:131771064
|
G | A | 2 | a0001c0001t0001g0136a0001c0001t0001g0153 | 2 | NA18939.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.2142+4756G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131771064 | ||||||
chr12:131771387
|
A | G | 1 | a0001c0001t0001g0137 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2142+5079A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131771387 | ||||||
chr12:131771650
|
C | CT | 7 | a0001c0001t0002g0084a0001c0001t0002g0091a0001c0001t0002g0092others(4): Show | 7 | HG01934.hp2 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.2142+5364dupT | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr12 | 131771650 | |||||
chr12:131771650
|
CT | C | 104 | a0000c0005t0001g0251a0001c0001t0001g0003a0001c0001t0001g0004others(101): Show | 108 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.2142+5364delT | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr12 | 131771650 | |||||
chr12:131771650
|
CTT | C | 126 | a0000c0005t0001g0120a0000c0005t0001g0121a0000c0023t0001g0051others(123): Show | 128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.2142+5363_2142+536 others(6): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr12 | 131771650 | |||||
chr12:131771711
|
T | TAGCGCGA others(4): Show |
1 | a0001c0001t0001g0262 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.2142+5404_2142+541 others(15): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr12 | 131771711 | |||||
chr12:131771715
|
G | A | 3 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0079 | 3 | HG02622.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2142+5407G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131771715 | ||||||
chr12:131771723
|
G | A | 7 | a0001c0001t0002g0019a0001c0004t0002g0009a0001c0004t0002g0010others(4): Show | 7 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.2142+5415G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131771723 | ||||||
chr12:131771729
|
A | G | 1 | a0001c0001t0001g0218 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2142+5421A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131771729 | ||||||
chr12:131771802
|
A | G | 1 | a0001c0015t0002g0008 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2142+5494A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131771802 | ||||||
chr12:131771812
|
G | A | 7 | a0001c0001t0002g0019a0001c0004t0002g0009a0001c0004t0002g0010others(4): Show | 7 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.2142+5504G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131771812 | ||||||
chr12:131771820
|
G | A | 3 | a0001c0001t0001g0139a0001c0001t0001g0183a0001c0001t0001g0184 | 3 | NA18995.hp2 NA19003.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.2142+5512G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131771820 | ||||||
chr12:131771931
|
G | A | 2 | a0001c0008t0001g0235a0001c0008t0001g0236 | 2 | HG00733.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.2142+5623G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131771931 | ||||||
chr12:131771949
|
C | G | 22 | a0001c0002t0001g0283a0001c0002t0001g0285a0001c0002t0001g0286others(19): Show | 22 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.2142+5641C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131771949 | ||||||
chr12:131771957
|
G | A | 1 | a0001c0001t0001g0047 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2142+5649G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131771957 | ||||||
chr12:131772026
|
A | G | 11 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0002g0019others(8): Show | 11 | HG01243.hp1 HG01891.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.2142+5718A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131772026 | ||||||
chr12:131772036
|
G | C | 1 | a0001c0006t0001g0017 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2142+5728G>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131772036 | ||||||
chr12:131772051
|
C | T | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2142+5743C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131772051 | ||||||
chr12:131772166
|
C | T | 1 | a0001c0001t0002g0076 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2142+5858C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131772166 | ||||||
chr12:131772189
|
C | G | 1 | a0001c0001t0002g0019 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2143-5876C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131772189 | ||||||
chr12:131772279
|
T | C | 1 | a0001c0004t0001g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2143-5786T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131772279 | ||||||
chr12:131772325
|
A | G | 1 | a0001c0001t0001g0160 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2143-5740A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131772325 | ||||||
chr12:131772442
|
A | G | 303 | a0000c0005t0001g0120a0000c0005t0001g0121a0000c0005t0001g0199others(300): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.2143-5623A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131772442 | ||||||
chr12:131772473
|
G | A | 1 | a0001c0015t0002g0008 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2143-5592G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131772473 | ||||||
chr12:131772618
|
C | T | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2143-5447C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131772618 | ||||||
chr12:131772619
|
G | A | 21 | a0000c0023t0001g0051a0001c0001t0001g0047a0001c0001t0001g0048others(18): Show | 21 | HG00323.hp1 HG00733.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.2143-5446G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131772619 | ||||||
chr12:131772630
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2143-5435G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131772630 | ||||||
chr12:131772805
|
T | C | 37 | a0001c0001t0001g0061a0001c0001t0002g0050a0001c0001t0002g0054others(34): Show | 37 | HG00639.hp1 HG01106.hp2 HG01167.hp2 others(34): Show |
intron_variant | MODIFIER | c.2143-5260T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131772805 | ||||||
chr12:131772811
|
G | A | 21 | a0000c0023t0001g0051a0001c0001t0001g0047a0001c0001t0001g0048others(18): Show | 21 | HG00323.hp1 HG00733.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.2143-5254G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131772811 | ||||||
chr12:131773110
|
G | A | 1 | a0001c0001t0001g0002 | 2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.2143-4955G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131773110 | ||||||
chr12:131773201
|
A | G | 291 | a0000c0005t0001g0120a0000c0005t0001g0121a0000c0005t0001g0199others(288): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.2143-4864A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131773201 | ||||||
chr12:131773225
|
G | T | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2143-4840G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131773225 | ||||||
chr12:131773232
|
C | T | 1 | a0001c0015t0002g0008 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2143-4833C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131773232 | ||||||
chr12:131773309
|
G | C | 21 | a0000c0023t0001g0051a0001c0001t0001g0047a0001c0001t0001g0048others(18): Show | 21 | HG00323.hp1 HG00733.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.2143-4756G>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131773309 | ||||||
chr12:131773400
|
T | TA | 9 | a0001c0001t0003g0036a0001c0001t0003g0037a0001c0001t0003g0038others(6): Show | 10 | HG02055.hp1 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.2143-4664dupA | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr12 | 131773400 | |||||
chr12:131773410
|
G | GCTCACTG others(4): Show |
3 | a0000c0023t0001g0051a0003c0009t0001g0052a0003c0009t0001g0053 | 3 | HG01891.hp1 HG02258.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.2143-4652_2143-464 others(15): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr12 | 131773410 | |||||
chr12:131773748
|
T | C | 2 | a0001c0001t0001g0145a0001c0001t0001g0158 | 2 | NA18941.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.2143-4317T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131773748 | ||||||
chr12:131773883
|
G | A | 1 | a0001c0001t0001g0133 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.2143-4182G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131773883 | ||||||
chr12:131773889
|
G | A | 7 | a0001c0001t0002g0019a0001c0004t0002g0009a0001c0004t0002g0010others(4): Show | 7 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.2143-4176G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131773889 | ||||||
chr12:131774204
|
G | T | 21 | a0000c0023t0001g0051a0001c0001t0001g0047a0001c0001t0001g0048others(18): Show | 21 | HG00323.hp1 HG00733.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.2143-3861G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131774204 | ||||||
chr12:131774254
|
A | G | 1 | a0001c0015t0002g0008 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2143-3811A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131774254 | ||||||
chr12:131774315
|
A | G | 250 | a0000c0005t0001g0120a0000c0005t0001g0121a0000c0005t0001g0199others(247): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.2143-3750A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131774315 | ||||||
chr12:131774513
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.2143-3552G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131774513 | ||||||
chr12:131774536
|
G | A | 1 | a0002c0003t0003g0033 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2143-3529G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131774536 | ||||||
chr12:131774567
|
G | A | 1 | a0001c0001t0001g0145 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2143-3498G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131774567 | ||||||
chr12:131774749
|
AC | A | 22 | a0001c0002t0001g0283a0001c0002t0001g0285a0001c0002t0001g0286others(19): Show | 22 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.2143-3314delC | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr12 | 131774749 | |||||
chr12:131774877
|
T | C | 1 | a0009c0022t0001g0125 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2143-3188T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131774877 | ||||||
chr12:131774959
|
G | A | 5 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0243others(2): Show | 5 | HG01358.hp2 HG01952.hp1 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.2143-3106G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131774959 | ||||||
chr12:131774962
|
A | T | 1 | a0001c0004t0001g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2143-3103A>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131774962 | ||||||
chr12:131774963
|
G | T | 1 | a0001c0004t0001g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2143-3102G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131774963 | ||||||
chr12:131775005
|
G | A | 1 | a0001c0004t0001g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2143-3060G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131775005 | ||||||
chr12:131775133
|
C | A | 1 | a0001c0001t0001g0276 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2143-2932C>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131775133 | ||||||
chr12:131775258
|
G | A | 4 | a0001c0006t0001g0014a0001c0006t0001g0016a0001c0006t0001g0017others(1): Show | 4 | HG02922.hp1 HG03130.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2143-2807G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131775258 | ||||||
chr12:131775284
|
C | T | 3 | a0001c0008t0001g0235a0001c0008t0001g0236a0001c0031t0001g0046 | 3 | HG00733.hp2 HG01175.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2143-2781C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131775284 | ||||||
chr12:131775297
|
T | C | 1 | a0002c0003t0003g0032 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2143-2768T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131775297 | ||||||
chr12:131775363
|
C | T | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2143-2702C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131775363 | ||||||
chr12:131775381
|
C | G | 36 | a0001c0001t0001g0061a0001c0001t0002g0050a0001c0001t0002g0054others(33): Show | 36 | HG00639.hp1 HG01106.hp2 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.2143-2684C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131775381 | ||||||
chr12:131775401
|
C | T | 37 | a0001c0001t0001g0061a0001c0001t0002g0050a0001c0001t0002g0054others(34): Show | 37 | HG00639.hp1 HG01106.hp2 HG01167.hp2 others(34): Show |
intron_variant | MODIFIER | c.2143-2664C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131775401 | ||||||
chr12:131775421
|
G | A | 6 | a0001c0001t0001g0113a0001c0001t0001g0124a0001c0001t0001g0127others(3): Show | 6 | HG01978.hp1 HG03831.hp2 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.2143-2644G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131775421 | ||||||
chr12:131775434
|
C | T | 1 | a0001c0001t0001g0202 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2143-2631C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131775434 | ||||||
chr12:131775435
|
G | A | 15 | a0001c0001t0002g0084a0001c0001t0002g0085a0001c0001t0002g0086others(12): Show | 15 | HG01106.hp2 HG01167.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.2143-2630G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131775435 | ||||||
chr12:131775757
|
T | C | 113 | a0000c0005t0001g0251a0001c0001t0001g0003a0001c0001t0001g0004others(110): Show | 118 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.2143-2308T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131775757 | ||||||
chr12:131775935
|
C | CA | 9 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0112others(6): Show | 9 | HG00597.hp1 HG01243.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.2143-2113dupA | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr12 | 131775935 | |||||
chr12:131775969
|
G | T | 1 | a0001c0001t0003g0018 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2143-2096G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131775969 | ||||||
chr12:131776008
|
A | G | 1 | a0001c0001t0002g0087 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2143-2057A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131776008 | ||||||
chr12:131776034
|
G | A | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2143-2031G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131776034 | ||||||
chr12:131776062
|
A | G | 1 | a0001c0001t0003g0021 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2143-2003A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131776062 | ||||||
chr12:131776076
|
C | T | 1 | a0001c0001t0001g0258 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2143-1989C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131776076 | ||||||
chr12:131776096
|
G | T | 2 | a0001c0001t0001g0141a0001c0001t0001g0149 | 2 | HG02129.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.2143-1969G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131776096 | ||||||
chr12:131776097
|
C | T | 2 | a0001c0001t0001g0141a0001c0001t0001g0149 | 2 | HG02129.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.2143-1968C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131776097 | ||||||
chr12:131776139
|
C | G | 111 | a0000c0005t0001g0251a0001c0001t0001g0003a0001c0001t0001g0004others(108): Show | 116 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.2143-1926C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131776139 | ||||||
chr12:131776327
|
G | A | 2 | a0001c0001t0001g0157a0002c0028t0004g0309 | 2 | HG03017.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.2143-1738G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131776327 | ||||||
chr12:131776554
|
C | T | 2 | a0001c0001t0001g0135a0001c0001t0001g0151 | 2 | HG00597.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.2143-1511C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131776554 | ||||||
chr12:131776556
|
G | A | 18 | a0000c0023t0001g0051a0001c0001t0001g0048a0001c0001t0001g0049others(15): Show | 18 | HG00323.hp1 HG00733.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.2143-1509G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131776556 | ||||||
chr12:131776625
|
T | C | 3 | a0001c0001t0001g0194a0001c0019t0001g0195a0012c0030t0001g0196 | 3 | HG02735.hp1 HG04228.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.2143-1440T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131776625 | ||||||
chr12:131776680
|
C | G | 1 | a0001c0001t0001g0179 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2143-1385C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131776680 | ||||||
chr12:131776730
|
C | T | 2 | a0001c0012t0001g0044a0001c0012t0001g0045 | 2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2143-1335C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131776730 | ||||||
chr12:131777145
|
AT | A | 5 | a0000c0005t0001g0251a0001c0001t0001g0006a0001c0001t0001g0250others(2): Show | 6 | HG02015.hp2 HG03490.hp2 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.2143-911delT | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr12 | 131777145 | |||||
chr12:131777388
|
C | G | 1 | a0001c0001t0001g0234 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2143-677C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131777388 | ||||||
chr12:131777441
|
G | T | 1 | a0001c0004t0001g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2143-624G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131777441 | ||||||
chr12:131777695
|
T | G | 1 | a0001c0001t0001g0110 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2143-370T>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131777695 | ||||||
chr12:131777715
|
C | T | 1 | a0001c0004t0001g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2143-350C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 13/17 | chr12 | 131777715 | ||||||
chr12:131778366
|
A | T | 21 | a0001c0001t0001g0265a0001c0002t0001g0283a0001c0002t0001g0285others(18): Show | 21 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.2408+36A>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131778366 | ||||||
chr12:131778478
|
T | A | 4 | a0001c0006t0001g0014a0001c0006t0001g0016a0001c0006t0001g0017others(1): Show | 4 | HG02922.hp1 HG03130.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2408+148T>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131778478 | ||||||
chr12:131778558
|
C | G | 1 | a0001c0001t0001g0234 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2408+228C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131778558 | ||||||
chr12:131778603
|
C | T | 1 | a0004c0014t0001g0272 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2408+273C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131778603 | ||||||
chr12:131778678
|
T | C | 1 | a0001c0001t0001g0241 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2408+348T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131778678 | ||||||
chr12:131778807
|
C | A | 2 | a0001c0012t0001g0044a0001c0012t0001g0045 | 2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2408+477C>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131778807 | ||||||
chr12:131778846
|
A | G | 1 | a0000c0005t0001g0251 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2408+516A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131778846 | ||||||
chr12:131778887
|
G | A | 1 | a0001c0001t0002g0019 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2408+557G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131778887 | ||||||
chr12:131779074
|
G | A | 80 | a0000c0005t0001g0120a0000c0005t0001g0121a0000c0005t0001g0199others(77): Show | 81 | HG00280.hp2 HG00597.hp1 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.2408+744G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131779074 | ||||||
chr12:131779076
|
A | G | 3 | a0001c0008t0001g0235a0001c0008t0001g0236a0001c0031t0001g0046 | 3 | HG00733.hp2 HG01175.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2408+746A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131779076 | ||||||
chr12:131779101
|
T | TA | 6 | a0001c0001t0001g0193a0001c0001t0001g0241a0001c0001t0001g0242others(3): Show | 6 | HG01358.hp2 HG01952.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.2408+772dupA | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131779101 | |||||
chr12:131779104
|
A | G | 1 | a0001c0002t0001g0301 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2408+774A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131779104 | ||||||
chr12:131779208
|
T | TGTGTATG others(50): Show |
1 | a0001c0001t0001g0247 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2408+882_2408+883i others(59): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131779208 | |||||
chr12:131779208
|
T | TGTGTATG others(49): Show |
109 | a0000c0005t0001g0251a0001c0001t0001g0003a0001c0001t0001g0004others(106): Show | 114 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.2408+882_2408+883i others(58): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131779208 | |||||
chr12:131779208
|
T | TGTGTATG others(77): Show |
27 | a0001c0001t0001g0265a0001c0002t0001g0283a0001c0002t0001g0285others(24): Show | 27 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.2408+882_2408+883i others(86): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131779208 | |||||
chr12:131779208
|
T | TGTGTGTG others(79): Show |
1 | a0001c0001t0001g0146 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2408+901_2408+902i others(88): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131779208 | |||||
chr12:131779208
|
T | TGTGTGTG others(78): Show |
2 | a0001c0001t0001g0117a0001c0001t0001g0170 | 2 | HG01496.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.2408+929_2408+930i others(87): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131779208 | |||||
chr12:131779208
|
T | TGTGTGTG others(49): Show |
17 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0114others(14): Show | 17 | HG01243.hp1 HG01891.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.2408+933_2408+934i others(58): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131779208 | |||||
chr12:131779208
|
T | TGTGTGTG others(78): Show |
1 | a0001c0001t0001g0124 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2408+933_2408+934i others(87): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131779208 | |||||
chr12:131779208
|
T | TGTGTGTG others(77): Show |
70 | a0000c0005t0001g0120a0000c0005t0001g0121a0000c0005t0001g0199others(67): Show | 71 | HG00280.hp2 HG00597.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.2408+933_2408+934i others(86): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131779208 | |||||
chr12:131779208
|
T | TGTGTGTG others(105): Show |
1 | a0001c0001t0001g0130 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.2408+933_2408+934i others(114): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131779208 | |||||
chr12:131779208
|
T | TGTGTGTG others(161): Show |
3 | a0001c0001t0001g0063a0001c0001t0001g0067a0001c0001t0001g0074 | 3 | HG01069.hp2 HG01071.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.2408+933_2408+934i others(170): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131779208 | |||||
chr12:131779208
|
T | TGTGTGTG others(189): Show |
2 | a0001c0001t0001g0047a0001c0001t0001g0070 | 2 | HG01517.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2408+933_2408+934i others(198): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131779208 | |||||
chr12:131779208
|
T | TGTGTGTG others(162): Show |
1 | a0001c0001t0001g0068 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2408+933_2408+934i others(171): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131779208 | |||||
chr12:131779208
|
T | TGTGTGTG others(161): Show |
12 | a0000c0023t0001g0051a0001c0001t0001g0048a0001c0001t0001g0049others(9): Show | 12 | HG00323.hp1 HG00733.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.2408+933_2408+934i others(170): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131779208 | |||||
chr12:131779208
|
T | TGTGTGTG others(161): Show |
1 | a0003c0009t0001g0052 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2408+933_2408+934i others(170): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131779208 | |||||
chr12:131779208
|
T | TGTGTGTG others(162): Show |
1 | a0001c0001t0001g0072 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2408+928_2408+929i others(171): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131779208 | |||||
chr12:131779230
|
G | GGTGAGCG others(78): Show |
1 | a0001c0001t0001g0156 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2408+933_2408+934i others(87): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131779230 | |||||
chr12:131779237
|
G | C | 57 | a0000c0005t0001g0251a0001c0001t0001g0003a0001c0001t0001g0004others(54): Show | 62 | HG00558.hp2 HG00597.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.2408+907G>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131779237 | ||||||
chr12:131779264
|
T | C | 1 | a0001c0001t0001g0159 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2408+934T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131779264 | ||||||
chr12:131779368
|
G | A | 1 | a0001c0001t0002g0057 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2408+1038G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131779368 | ||||||
chr12:131779508
|
C | T | 111 | a0000c0005t0001g0251a0001c0001t0001g0003a0001c0001t0001g0004others(108): Show | 116 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.2408+1178C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131779508 | ||||||
chr12:131779565
|
G | A | 111 | a0000c0005t0001g0251a0001c0001t0001g0003a0001c0001t0001g0004others(108): Show | 116 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.2408+1235G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131779565 | ||||||
chr12:131779607
|
G | A | 4 | a0001c0006t0001g0014a0001c0006t0001g0016a0001c0006t0001g0017others(1): Show | 4 | HG02922.hp1 HG03130.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2408+1277G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131779607 | ||||||
chr12:131779614
|
C | CT | 80 | a0000c0005t0001g0120a0000c0005t0001g0121a0000c0005t0001g0199others(77): Show | 81 | HG00280.hp2 HG00597.hp1 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.2408+1285dupT | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131779614 | |||||
chr12:131779880
|
A | G | 2 | a0001c0012t0001g0044a0001c0012t0001g0045 | 2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2408+1550A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131779880 | ||||||
chr12:131779953
|
A | T | 1 | a0001c0001t0001g0264 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2408+1623A>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131779953 | ||||||
chr12:131779995
|
A | T | 1 | a0001c0001t0001g0135 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2408+1665A>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131779995 | ||||||
chr12:131780079
|
C | T | 1 | a0001c0001t0001g0012 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2408+1749C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131780079 | ||||||
chr12:131780223
|
T | C | 7 | a0001c0001t0002g0019a0001c0004t0002g0009a0001c0004t0002g0010others(4): Show | 7 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.2408+1893T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131780223 | ||||||
chr12:131780342
|
G | A | 4 | a0001c0001t0001g0230a0001c0004t0002g0009a0001c0004t0002g0010others(1): Show | 4 | HG01891.hp2 HG02723.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.2408+2012G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131780342 | ||||||
chr12:131780506
|
T | C | 1 | a0001c0004t0001g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2408+2176T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131780506 | ||||||
chr12:131780551
|
G | A | 7 | a0001c0001t0002g0019a0001c0004t0002g0009a0001c0004t0002g0010others(4): Show | 7 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.2408+2221G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131780551 | ||||||
chr12:131780621
|
G | A | 23 | a0001c0001t0001g0265a0001c0002t0001g0283a0001c0002t0001g0285others(20): Show | 23 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.2408+2291G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131780621 | ||||||
chr12:131780687
|
T | TA | 7 | a0001c0001t0002g0019a0001c0004t0002g0009a0001c0004t0002g0010others(4): Show | 7 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.2408+2363dupA | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131780687 | |||||
chr12:131780719
|
G | A | 2 | a0001c0012t0001g0044a0001c0012t0001g0045 | 2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2408+2389G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131780719 | ||||||
chr12:131780890
|
G | A | 1 | a0000c0005t0001g0199 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.2408+2560G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131780890 | ||||||
chr12:131781155
|
G | A | 1 | a0002c0003t0003g0026 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2408+2825G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131781155 | ||||||
chr12:131781167
|
C | T | 1 | a0001c0006t0001g0016 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2408+2837C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131781167 | ||||||
chr12:131781171
|
T | A | 111 | a0000c0005t0001g0251a0001c0001t0001g0003a0001c0001t0001g0004others(108): Show | 116 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.2408+2841T>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131781171 | ||||||
chr12:131781234
|
AT | A | 34 | a0001c0001t0001g0061a0001c0001t0001g0160a0001c0001t0002g0054others(31): Show | 34 | HG00639.hp1 HG01106.hp2 HG01167.hp2 others(31): Show |
intron_variant | MODIFIER | c.2408+2927delT | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131781234 | |||||
chr12:131781235
|
T | TTA | 29 | a0000c0005t0001g0121a0001c0001t0001g0229a0001c0001t0001g0265others(26): Show | 29 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.2408+2906_2408+290 others(6): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131781235 | |||||
chr12:131781236
|
T | TA | 138 | a0000c0005t0001g0120a0000c0005t0001g0199a0001c0001t0001g0002others(135): Show | 139 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.2408+2906_2408+290 others(5): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131781236 | ||||||
chr12:131781236
|
T | TATTA | 3 | a0001c0004t0002g0306a0001c0004t0002g0307a0001c0015t0002g0008 | 3 | HG02451.hp1 HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2408+2906_2408+290 others(8): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131781236 | ||||||
chr12:131781237
|
T | A | 78 | a0000c0005t0001g0251a0000c0023t0001g0051a0001c0001t0001g0003others(75): Show | 83 | HG00323.hp1 HG00558.hp2 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.2408+2907T>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131781237 | ||||||
chr12:131781238
|
T | A | 8 | a0000c0005t0001g0121a0001c0001t0001g0160a0001c0001t0001g0229others(5): Show | 8 | HG00733.hp2 HG01175.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.2408+2908T>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131781238 | ||||||
chr12:131781239
|
T | A | 138 | a0000c0005t0001g0120a0000c0005t0001g0199a0001c0001t0001g0002others(135): Show | 139 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.2408+2909T>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131781239 | ||||||
chr12:131781240
|
T | A | 73 | a0000c0005t0001g0251a0001c0001t0001g0003a0001c0001t0001g0004others(70): Show | 78 | HG00323.hp1 HG00558.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.2408+2910T>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131781240 | ||||||
chr12:131781241
|
T | A | 5 | a0001c0001t0001g0229a0001c0004t0001g0099a0001c0008t0001g0235others(2): Show | 5 | HG00733.hp2 HG01175.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2408+2911T>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131781241 | ||||||
chr12:131781242
|
T | A | 60 | a0001c0001t0001g0107a0001c0001t0001g0110a0001c0001t0001g0124others(57): Show | 60 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(57): Show |
intron_variant | MODIFIER | c.2408+2912T>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131781242 | ||||||
chr12:131781243
|
T | A | 49 | a0000c0005t0001g0251a0001c0001t0001g0003a0001c0001t0001g0004others(46): Show | 54 | HG00558.hp2 HG00597.hp2 HG01261.hp1 others(51): Show |
intron_variant | MODIFIER | c.2408+2913T>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131781243 | ||||||
chr12:131781245
|
T | A | 4 | a0001c0006t0001g0014a0001c0006t0001g0016a0001c0006t0001g0017others(1): Show | 4 | HG02922.hp1 HG03130.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2408+2915T>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131781245 | ||||||
chr12:131781246
|
T | A | 1 | a0001c0001t0001g0260 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2408+2916T>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131781246 | ||||||
chr12:131781295
|
T | A | 1 | a0001c0001t0001g0013 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2408+2965T>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131781295 | ||||||
chr12:131781299
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2408+2969G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131781299 | ||||||
chr12:131781383
|
G | A | 1 | a0001c0001t0003g0021 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2408+3053G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131781383 | ||||||
chr12:131781456
|
C | T | 2 | a0001c0012t0001g0044a0001c0012t0001g0045 | 2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2408+3126C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131781456 | ||||||
chr12:131781478
|
C | A | 1 | a0001c0001t0001g0159 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2408+3148C>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131781478 | ||||||
chr12:131781480
|
A | G | 11 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0002g0019others(8): Show | 11 | HG01243.hp1 HG01891.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.2408+3150A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131781480 | ||||||
chr12:131781489
|
G | A | 36 | a0001c0001t0001g0061a0001c0001t0002g0050a0001c0001t0002g0054others(33): Show | 36 | HG00639.hp1 HG01106.hp2 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.2408+3159G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131781489 | ||||||
chr12:131781532
|
C | T | 1 | a0001c0004t0001g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2408+3202C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131781532 | ||||||
chr12:131781710
|
G | A | 5 | a0001c0001t0003g0018a0001c0001t0003g0025a0001c0001t0003g0031others(2): Show | 5 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.2408+3380G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131781710 | ||||||
chr12:131781789
|
C | T | 303 | a0000c0005t0001g0120a0000c0005t0001g0121a0000c0005t0001g0199others(300): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.2408+3459C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131781789 | ||||||
chr12:131781904
|
C | T | 1 | a0001c0001t0002g0062 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2408+3574C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131781904 | ||||||
chr12:131782004
|
C | T | 1 | a0001c0001t0001g0069 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2408+3674C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131782004 | ||||||
chr12:131782118
|
G | T | 1 | a0001c0001t0001g0116 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2408+3788G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131782118 | ||||||
chr12:131782153
|
G | C | 1 | a0001c0001t0001g0189 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2408+3823G>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131782153 | ||||||
chr12:131782218
|
T | C | 23 | a0001c0001t0001g0265a0001c0002t0001g0283a0001c0002t0001g0285others(20): Show | 23 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.2408+3888T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131782218 | ||||||
chr12:131782472
|
C | A | 1 | a0001c0001t0002g0057 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2409-3991C>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131782472 | ||||||
chr12:131782511
|
T | C | 6 | a0001c0001t0001g0003a0001c0001t0001g0185a0001c0001t0001g0186others(3): Show | 7 | HG02027.hp2 NA18939.hp2 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.2409-3952T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131782511 | ||||||
chr12:131782512
|
T | C | 2 | a0001c0001t0001g0194a0012c0030t0001g0196 | 2 | HG02735.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.2409-3951T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131782512 | ||||||
chr12:131782665
|
A | G | 1 | a0001c0001t0001g0069 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2409-3798A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131782665 | ||||||
chr12:131782699
|
C | T | 250 | a0000c0005t0001g0120a0000c0005t0001g0121a0000c0005t0001g0199others(247): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.2409-3764C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131782699 | ||||||
chr12:131782948
|
A | G | 1 | a0001c0001t0001g0230 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2409-3515A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131782948 | ||||||
chr12:131783016
|
A | T | 21 | a0000c0023t0001g0051a0001c0001t0001g0047a0001c0001t0001g0048others(18): Show | 21 | HG00323.hp1 HG00733.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.2409-3447A>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131783016 | ||||||
chr12:131783074
|
G | A | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2409-3389G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131783074 | ||||||
chr12:131783179
|
T | TA | 36 | a0001c0001t0001g0063a0001c0001t0001g0067a0001c0001t0001g0083others(33): Show | 36 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.2409-3265dupA | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783179 | |||||
chr12:131783179
|
TA | T | 9 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0127others(6): Show | 9 | HG01496.hp1 HG01975.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.2409-3265delA | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783179 | |||||
chr12:131783289
|
T | C | 1 | a0001c0001t0002g0057 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2409-3174T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131783289 | ||||||
chr12:131783476
|
A | T | 1 | a0001c0001t0001g0079 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2409-2987A>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131783476 | ||||||
chr12:131783518
|
G | A | 7 | a0001c0001t0002g0019a0001c0004t0002g0009a0001c0004t0002g0010others(4): Show | 7 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.2409-2945G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131783518 | ||||||
chr12:131783530
|
G | A | 1 | a0001c0001t0003g0021 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2409-2933G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131783530 | ||||||
chr12:131783696
|
G | A | 218 | a0000c0005t0001g0120a0000c0005t0001g0121a0000c0005t0001g0199others(215): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.2409-2767G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131783696 | ||||||
chr12:131783728
|
A | G | 303 | a0000c0005t0001g0120a0000c0005t0001g0121a0000c0005t0001g0199others(300): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.2409-2735A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131783728 | ||||||
chr12:131783734
|
G | A | 18 | a0000c0005t0001g0251a0001c0001t0001g0005a0001c0001t0001g0006others(15): Show | 21 | HG00558.hp2 HG02015.hp2 HG02040.hp1 others(18): Show |
intron_variant | MODIFIER | c.2409-2729G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131783734 | ||||||
chr12:131783774
|
G | A | 2 | a0001c0001t0001g0267a0001c0001t0001g0268 | 2 | HG01934.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2409-2689G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131783774 | ||||||
chr12:131783792
|
T | TATATATA others(24): Show |
1 | a0001c0001t0001g0166 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2409-2671_2409-267 others(35): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131783792 | ||||||
chr12:131783792
|
T | TATATATA others(28): Show |
1 | a0001c0001t0001g0118 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2409-2671_2409-267 others(39): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131783792 | ||||||
chr12:131783792
|
T | TTA | 6 | a0001c0001t0001g0012a0001c0001t0003g0036a0001c0001t0003g0037others(3): Show | 6 | HG02257.hp2 HG02630.hp2 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.2409-2642_2409-264 others(6): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783792 | |||||
chr12:131783792
|
T | TTATA | 5 | a0001c0001t0001g0105a0001c0001t0002g0019a0001c0004t0001g0099others(2): Show | 5 | HG01934.hp2 HG02109.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2409-2644_2409-264 others(8): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783792 | |||||
chr12:131783792
|
T | TTATATA | 4 | a0001c0001t0001g0013a0001c0001t0001g0145a0001c0001t0001g0158others(1): Show | 4 | HG01243.hp1 NA18941.hp2 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.2409-2646_2409-264 others(10): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783792 | |||||
chr12:131783792
|
T | TTATATAT others(3): Show |
5 | a0001c0001t0001g0203a0001c0001t0001g0205a0001c0001t0001g0227others(2): Show | 5 | HG00558.hp1 HG01978.hp2 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.2409-2650_2409-264 others(14): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783792 | |||||
chr12:131783792
|
T | TTATATAT others(5): Show |
7 | a0001c0001t0001g0202a0001c0001t0001g0204a0001c0001t0001g0215others(4): Show | 7 | HG00099.hp1 HG00609.hp2 HG00673.hp1 others(4): Show |
intron_variant | MODIFIER | c.2409-2652_2409-264 others(16): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783792 | |||||
chr12:131783792
|
T | TTATATAT others(7): Show |
9 | a0001c0001t0001g0047a0001c0001t0001g0107a0001c0001t0001g0208others(6): Show | 9 | HG00140.hp2 HG01952.hp2 HG02293.hp1 others(6): Show |
intron_variant | MODIFIER | c.2409-2654_2409-264 others(18): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783792 | |||||
chr12:131783792
|
T | TTATATAT others(9): Show |
8 | a0001c0001t0001g0207a0001c0001t0001g0220a0001c0001t0001g0271others(5): Show | 8 | HG00642.hp1 HG01074.hp1 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.2409-2656_2409-264 others(20): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783792 | |||||
chr12:131783792
|
T | TTATATAT others(11): Show |
7 | a0001c0001t0001g0176a0001c0001t0001g0200a0001c0002t0001g0294others(4): Show | 7 | HG00741.hp1 HG01099.hp2 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.2409-2658_2409-264 others(22): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783792 | |||||
chr12:131783792
|
T | TTATATAT others(13): Show |
6 | a0001c0001t0001g0073a0001c0001t0001g0179a0001c0001t0001g0212others(3): Show | 6 | HG00140.hp1 HG01243.hp2 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.2409-2660_2409-264 others(24): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783792 | |||||
chr12:131783792
|
T | TTATATAT others(15): Show |
5 | a0001c0001t0001g0140a0001c0002t0001g0283a0001c0002t0001g0288others(2): Show | 5 | HG00673.hp2 HG01071.hp2 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.2409-2662_2409-264 others(26): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783792 | |||||
chr12:131783792
|
T | TTATATAT others(17): Show |
5 | a0001c0001t0001g0110a0001c0001t0001g0230a0001c0001t0001g0281others(2): Show | 5 | HG00639.hp2 HG02040.hp2 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.2409-2664_2409-264 others(28): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783792 | |||||
chr12:131783792
|
T | TTATATAT others(19): Show |
5 | a0001c0001t0001g0113a0001c0001t0001g0143a0001c0001t0001g0228others(2): Show | 5 | HG01517.hp2 HG02148.hp2 NA18941.hp1 others(2): Show |
intron_variant | MODIFIER | c.2409-2666_2409-264 others(30): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783792 | |||||
chr12:131783792
|
T | TTATATAT others(21): Show |
5 | a0001c0001t0001g0112a0001c0001t0001g0133a0001c0001t0001g0134others(2): Show | 5 | HG00099.hp2 HG02071.hp1 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.2409-2668_2409-264 others(32): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783792 | |||||
chr12:131783792
|
T | TTATATAT others(23): Show |
8 | a0000c0005t0001g0199a0001c0001t0001g0130a0001c0001t0001g0147others(5): Show | 8 | HG02293.hp2 HG02698.hp1 NA18962.hp2 others(5): Show |
intron_variant | MODIFIER | c.2409-2670_2409-264 others(34): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783792 | |||||
chr12:131783792
|
T | TTATATAT others(25): Show |
14 | a0001c0001t0001g0002a0001c0001t0001g0114a0001c0001t0001g0116others(11): Show | 15 | HG00738.hp2 HG01069.hp1 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.2409-2641_2409-264 others(36): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783792 | |||||
chr12:131783792
|
T | TTATATAT others(27): Show |
13 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0106others(10): Show | 13 | HG00735.hp2 HG01168.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.2409-2641_2409-264 others(38): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783792 | |||||
chr12:131783792
|
T | TTATATAT others(29): Show |
15 | a0001c0001t0001g0066a0001c0001t0001g0069a0001c0001t0001g0072others(12): Show | 15 | HG01123.hp1 HG01975.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.2409-2641_2409-264 others(40): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783792 | |||||
chr12:131783792
|
T | TTATATAT others(31): Show |
5 | a0000c0005t0001g0120a0001c0001t0001g0070a0001c0001t0001g0079others(2): Show | 5 | HG01517.hp1 HG01884.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.2409-2641_2409-264 others(42): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783792 | |||||
chr12:131783792
|
T | TTATATAT others(33): Show |
4 | a0001c0001t0001g0109a0001c0001t0001g0141a0001c0001t0001g0144others(1): Show | 4 | HG02129.hp1 HG02132.hp2 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.2409-2641_2409-264 others(44): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783792 | |||||
chr12:131783792
|
T | TTATATAT others(35): Show |
1 | a0001c0001t0001g0129 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2409-2641_2409-264 others(46): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783792 | |||||
chr12:131783792
|
T | TTATATAT others(37): Show |
3 | a0001c0001t0001g0068a0001c0001t0001g0159a0001c0001t0001g0171 | 3 | HG00280.hp2 HG01261.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.2409-2641_2409-264 others(48): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783792 | |||||
chr12:131783792
|
T | TTATATAT others(41): Show |
1 | a0001c0001t0001g0152 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2409-2641_2409-264 others(52): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783792 | |||||
chr12:131783792
|
T | TTATATAT others(43): Show |
2 | a0001c0001t0001g0063a0001c0001t0001g0067 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.2409-2641_2409-264 others(54): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783792 | |||||
chr12:131783792
|
T | TTATATAT others(49): Show |
1 | a0000c0005t0001g0121 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2409-2641_2409-264 others(60): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783792 | |||||
chr12:131783792
|
T | TTATATAT others(17): Show |
1 | a0001c0002t0001g0301 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2409-2652_2409-265 others(28): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783792 | |||||
chr12:131783792
|
T | TTATTATA others(38): Show |
1 | a0001c0001t0001g0157 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2409-2668_2409-266 others(49): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783792 | |||||
chr12:131783792
|
T | TTTTATAT others(17): Show |
1 | a0001c0001t0001g0275 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2409-2670_2409-266 others(28): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783792 | |||||
chr12:131783792
|
T | TTTTATAT others(21): Show |
2 | a0001c0001t0001g0273a0001c0001t0001g0274 | 2 | HG01167.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.2409-2670_2409-266 others(32): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783792 | |||||
chr12:131783792
|
T | TTTTATAT others(25): Show |
1 | a0001c0001t0001g0277 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.2409-2670_2409-266 others(36): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783792 | |||||
chr12:131783792
|
T | TTTTATAT others(29): Show |
1 | a0001c0001t0001g0151 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2409-2670_2409-266 others(40): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783792 | |||||
chr12:131783792
|
T | TTTTATAT others(41): Show |
1 | a0001c0001t0001g0269 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2409-2670_2409-266 others(52): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783792 | |||||
chr12:131783792
|
T | TTTTTTAT others(25): Show |
1 | a0001c0001t0001g0278 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2409-2670_2409-266 others(36): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783792 | |||||
chr12:131783792
|
TTA | T | 94 | a0000c0005t0001g0251a0001c0001t0001g0003a0001c0001t0001g0004others(91): Show | 99 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(96): Show |
intron_variant | MODIFIER | c.2409-2642_2409-264 others(6): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783792 | |||||
chr12:131783792
|
TTATA | T | 19 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0175others(16): Show | 19 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(16): Show |
intron_variant | MODIFIER | c.2409-2644_2409-264 others(8): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783792 | |||||
chr12:131783792
|
TTATATA | T | 8 | a0000c0023t0001g0051a0001c0001t0001g0150a0001c0006t0001g0014others(5): Show | 8 | HG01891.hp1 HG02258.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.2409-2646_2409-264 others(10): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783792 | |||||
chr12:131783792
|
TTATATAT others(3): Show |
T | 1 | a0001c0001t0001g0083 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2409-2650_2409-264 others(14): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783792 | |||||
chr12:131783821
|
T | TATATATA others(5): Show |
2 | a0001c0008t0001g0235a0001c0008t0001g0236 | 2 | HG00733.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.2409-2641_2409-264 others(16): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783821 | |||||
chr12:131783821
|
T | TATATATA others(35): Show |
1 | a0001c0001t0001g0168 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2409-2641_2409-264 others(46): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783821 | |||||
chr12:131783821
|
T | TATATATA others(41): Show |
1 | a0001c0001t0001g0163 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2409-2641_2409-264 others(52): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783821 | |||||
chr12:131783821
|
T | TATATATA others(43): Show |
1 | a0001c0001t0001g0169 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.2409-2641_2409-264 others(54): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131783821 | |||||
chr12:131783849
|
A | G | 1 | a0001c0001t0001g0070 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.2409-2614A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131783849 | ||||||
chr12:131783967
|
T | A | 1 | a0001c0001t0001g0225 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2409-2496T>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131783967 | ||||||
chr12:131784011
|
G | A | 1 | a0001c0001t0001g0264 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2409-2452G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131784011 | ||||||
chr12:131784013
|
A | G | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2409-2450A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131784013 | ||||||
chr12:131784231
|
T | TG | 11 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0002g0019others(8): Show | 11 | HG01243.hp1 HG01891.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.2409-2229dupG | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131784231 | |||||
chr12:131784244
|
G | A | 2 | a0001c0001t0002g0055a0001c0001t0002g0056 | 2 | HG03654.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.2409-2219G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131784244 | ||||||
chr12:131784273
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2409-2190C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131784273 | ||||||
chr12:131784299
|
A | C | 50 | a0001c0001t0001g0107a0001c0001t0001g0175a0001c0001t0001g0176others(47): Show | 50 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(47): Show |
intron_variant | MODIFIER | c.2409-2164A>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131784299 | ||||||
chr12:131784377
|
C | T | 1 | a0001c0001t0002g0100 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2409-2086C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131784377 | ||||||
chr12:131784416
|
T | C | 80 | a0000c0005t0001g0120a0000c0005t0001g0121a0000c0005t0001g0199others(77): Show | 81 | HG00280.hp2 HG00597.hp1 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.2409-2047T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131784416 | ||||||
chr12:131784670
|
G | A | 1 | a0001c0001t0001g0273 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2409-1793G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131784670 | ||||||
chr12:131784954
|
C | T | 5 | a0001c0001t0003g0018a0001c0001t0003g0025a0001c0001t0003g0031others(2): Show | 5 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.2409-1509C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131784954 | ||||||
chr12:131785099
|
G | T | 2 | a0001c0012t0001g0044a0001c0012t0001g0045 | 2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2409-1364G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131785099 | ||||||
chr12:131785235
|
AACTG | A | 21 | a0000c0023t0001g0051a0001c0001t0001g0047a0001c0001t0001g0048others(18): Show | 21 | HG00323.hp1 HG00733.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.2409-1225_2409-122 others(8): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131785235 | |||||
chr12:131785285
|
G | GA | 227 | a0000c0005t0001g0251a0000c0023t0001g0051a0001c0001t0001g0003others(224): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.2409-1172dupA | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr12 | 131785285 | |||||
chr12:131785770
|
G | A | 1 | a0001c0001t0002g0064 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2409-693G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131785770 | ||||||
chr12:131785913
|
T | C | 50 | a0001c0001t0001g0107a0001c0001t0001g0175a0001c0001t0001g0176others(47): Show | 50 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(47): Show |
intron_variant | MODIFIER | c.2409-550T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131785913 | ||||||
chr12:131785941
|
C | A | 1 | a0001c0019t0001g0195 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2409-522C>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131785941 | ||||||
chr12:131786021
|
G | A | 2 | a0001c0012t0001g0044a0001c0012t0001g0045 | 2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2409-442G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131786021 | ||||||
chr12:131786199
|
G | A | 1 | a0001c0001t0002g0058 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2409-264G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131786199 | ||||||
chr12:131786221
|
G | A | 4 | a0001c0006t0001g0014a0001c0006t0001g0016a0001c0006t0001g0017others(1): Show | 4 | HG02922.hp1 HG03130.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2409-242G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131786221 | ||||||
chr12:131786238
|
G | A | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2409-225G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131786238 | ||||||
chr12:131786304
|
A | T | 3 | a0001c0004t0002g0009a0001c0004t0002g0010a0001c0004t0002g0011 | 3 | HG01891.hp2 HG02723.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2409-159A>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 14/17 | chr12 | 131786304 | ||||||
chr12:131786680
|
G | A | 2 | a0001c0001t0001g0248a0001c0001t0001g0260 | 2 | HG00558.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.2534+92G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131786680 | ||||||
chr12:131786718
|
A | C | 1 | a0001c0001t0001g0165 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2534+130A>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131786718 | ||||||
chr12:131786790
|
G | A | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2534+202G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131786790 | ||||||
chr12:131786819
|
C | T | 2 | a0001c0001t0001g0006a0001c0001t0003g0037 | 3 | HG03490.hp2 HG03492.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2534+231C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131786819 | ||||||
chr12:131787118
|
G | A | 7 | a0001c0001t0002g0019a0001c0004t0002g0009a0001c0004t0002g0010others(4): Show | 7 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.2534+530G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131787118 | ||||||
chr12:131787276
|
A | C | 1 | a0001c0001t0003g0311 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2534+688A>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131787276 | ||||||
chr12:131787300
|
AC | A | 60 | a0001c0001t0001g0061a0001c0001t0002g0050a0001c0001t0002g0054others(57): Show | 61 | HG00639.hp1 HG01106.hp2 HG01167.hp2 others(58): Show |
intron_variant | MODIFIER | c.2534+716delC | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 131787300 | |||||
chr12:131787312
|
A | G | 4 | a0001c0001t0001g0113a0001c0001t0001g0127a0001c0001t0001g0133others(1): Show | 4 | NA18979.hp2 NA18986.hp1 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.2534+724A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131787312 | ||||||
chr12:131787469
|
G | C | 2 | a0001c0012t0001g0044a0001c0012t0001g0045 | 2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2534+881G>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131787469 | ||||||
chr12:131787573
|
T | C | 1 | a0001c0001t0002g0087 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2534+985T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131787573 | ||||||
chr12:131787680
|
A | G | 307 | a0000c0005t0001g0120a0000c0005t0001g0121a0000c0005t0001g0199others(304): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.2534+1092A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131787680 | ||||||
chr12:131787871
|
C | T | 108 | a0000c0005t0001g0251a0001c0001t0001g0003a0001c0001t0001g0004others(105): Show | 113 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.2534+1283C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131787871 | ||||||
chr12:131787874
|
A | T | 1 | a0001c0001t0005g0222 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2534+1286A>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131787874 | ||||||
chr12:131788033
|
C | A | 306 | a0000c0005t0001g0120a0000c0005t0001g0121a0000c0005t0001g0199others(303): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.2534+1445C>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131788033 | ||||||
chr12:131788180
|
T | C | 55 | a0000c0005t0001g0251a0001c0001t0001g0003a0001c0001t0001g0004others(52): Show | 60 | HG00558.hp2 HG00597.hp2 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.2534+1592T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131788180 | ||||||
chr12:131788253
|
C | T | 1 | a0001c0001t0002g0019 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2534+1665C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131788253 | ||||||
chr12:131788277
|
C | T | 2 | a0001c0001t0001g0221a0001c0001t0005g0222 | 2 | HG00642.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.2534+1689C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131788277 | ||||||
chr12:131788282
|
A | G | 1 | a0001c0001t0001g0180 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2534+1694A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131788282 | ||||||
chr12:131788531
|
G | GT | 26 | a0000c0005t0001g0251a0001c0001t0001g0113a0001c0001t0001g0119others(23): Show | 26 | HG01074.hp2 HG01496.hp2 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.2534+1955dupT | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 131788531 | |||||
chr12:131788771
|
A | G | 202 | a0000c0005t0001g0251a0000c0023t0001g0051a0001c0001t0001g0003others(199): Show | 208 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.2534+2183A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131788771 | ||||||
chr12:131788819
|
C | T | 1 | a0001c0001t0001g0241 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2534+2231C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131788819 | ||||||
chr12:131788862
|
T | C | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2534+2274T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131788862 | ||||||
chr12:131788922
|
G | A | 7 | a0001c0001t0002g0019a0001c0004t0002g0009a0001c0004t0002g0010others(4): Show | 7 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.2534+2334G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131788922 | ||||||
chr12:131788988
|
A | C | 1 | a0001c0006t0001g0014 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2534+2400A>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131788988 | ||||||
chr12:131789156
|
A | G | 2 | a0001c0012t0001g0044a0001c0012t0001g0045 | 2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2534+2568A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131789156 | ||||||
chr12:131789236
|
C | T | 4 | a0001c0006t0001g0014a0001c0006t0001g0016a0001c0006t0001g0017others(1): Show | 4 | HG02922.hp1 HG03130.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2534+2648C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131789236 | ||||||
chr12:131789362
|
A | T | 1 | a0001c0001t0001g0126 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.2534+2774A>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131789362 | ||||||
chr12:131789373
|
A | G | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2534+2785A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131789373 | ||||||
chr12:131789403
|
A | G | 2 | a0001c0001t0001g0262a0001c0001t0001g0263 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.2534+2815A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131789403 | ||||||
chr12:131789590
|
C | T | 2 | a0001c0012t0001g0044a0001c0012t0001g0045 | 2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2534+3002C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131789590 | ||||||
chr12:131789723
|
A | C | 23 | a0001c0001t0001g0265a0001c0002t0001g0283a0001c0002t0001g0285others(20): Show | 23 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.2534+3135A>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131789723 | ||||||
chr12:131789811
|
G | A | 9 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0208others(6): Show | 9 | HG00558.hp1 HG00609.hp2 NA18948.hp2 others(6): Show |
intron_variant | MODIFIER | c.2534+3223G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131789811 | ||||||
chr12:131789969
|
G | A | 3 | a0001c0001t0003g0031a0001c0001t0003g0308a0008c0021t0003g0020 | 3 | HG02258.hp1 HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.2534+3381G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131789969 | ||||||
chr12:131790001
|
A | G | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2534+3413A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131790001 | ||||||
chr12:131790103
|
C | A | 1 | a0001c0001t0003g0311 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2534+3515C>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131790103 | ||||||
chr12:131790203
|
T | G | 1 | a0001c0004t0001g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2534+3615T>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131790203 | ||||||
chr12:131790417
|
G | A | 1 | a0001c0001t0001g0264 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2534+3829G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131790417 | ||||||
chr12:131790540
|
C | T | 1 | a0001c0001t0002g0078 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2534+3952C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131790540 | ||||||
chr12:131790738
|
G | A | 1 | a0002c0003t0003g0026 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2534+4150G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131790738 | ||||||
chr12:131790755
|
G | A | 112 | a0000c0023t0001g0051a0001c0001t0001g0012a0001c0001t0001g0013others(109): Show | 112 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(109): Show |
intron_variant | MODIFIER | c.2534+4167G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131790755 | ||||||
chr12:131790811
|
A | G | 2 | a0001c0004t0002g0306a0001c0004t0002g0307 | 2 | HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2534+4223A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131790811 | ||||||
chr12:131790845
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2534+4257G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131790845 | ||||||
chr12:131790916
|
T | C | 1 | a0002c0003t0003g0028 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2534+4328T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131790916 | ||||||
chr12:131790985
|
C | A | 23 | a0001c0001t0001g0265a0001c0002t0001g0283a0001c0002t0001g0285others(20): Show | 23 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.2534+4397C>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131790985 | ||||||
chr12:131791042
|
A | G | 87 | a0000c0023t0001g0051a0001c0001t0001g0047a0001c0001t0001g0048others(84): Show | 88 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(85): Show |
intron_variant | MODIFIER | c.2534+4454A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131791042 | ||||||
chr12:131791085
|
G | A | 1 | a0001c0001t0001g0166 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2534+4497G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131791085 | ||||||
chr12:131791120
|
C | T | 60 | a0001c0001t0001g0061a0001c0001t0002g0050a0001c0001t0002g0054others(57): Show | 61 | HG00639.hp1 HG01106.hp2 HG01167.hp2 others(58): Show |
intron_variant | MODIFIER | c.2534+4532C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131791120 | ||||||
chr12:131791159
|
A | G | 9 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0002g0019others(6): Show | 9 | HG01243.hp1 HG01891.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.2534+4571A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131791159 | ||||||
chr12:131791220
|
C | T | 65 | a0000c0005t0001g0251a0001c0001t0001g0003a0001c0001t0001g0004others(62): Show | 70 | HG00558.hp2 HG00597.hp2 HG00738.hp1 others(67): Show |
intron_variant | MODIFIER | c.2534+4632C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131791220 | ||||||
chr12:131791225
|
A | T | 66 | a0000c0005t0001g0251a0001c0001t0001g0003a0001c0001t0001g0004others(63): Show | 71 | HG00558.hp2 HG00597.hp2 HG00738.hp1 others(68): Show |
intron_variant | MODIFIER | c.2534+4637A>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131791225 | ||||||
chr12:131791273
|
C | T | 2 | a0001c0012t0001g0044a0001c0012t0001g0045 | 2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2534+4685C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131791273 | ||||||
chr12:131791593
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2534+5005G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131791593 | ||||||
chr12:131791625
|
G | A | 1 | a0001c0001t0001g0221 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2534+5037G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131791625 | ||||||
chr12:131791778
|
T | C | 2 | a0001c0001t0001g0194a0012c0030t0001g0196 | 2 | HG02735.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.2534+5190T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131791778 | ||||||
chr12:131791779
|
T | A | 21 | a0000c0023t0001g0051a0001c0001t0001g0047a0001c0001t0001g0048others(18): Show | 21 | HG00323.hp1 HG00733.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.2534+5191T>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131791779 | ||||||
chr12:131791952
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2535-5226G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131791952 | ||||||
chr12:131792026
|
T | C | 1 | a0001c0001t0002g0101 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2535-5152T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131792026 | ||||||
chr12:131792026
|
TCGTGTGT others(28): Show |
T | 2 | a0001c0004t0002g0306a0001c0004t0002g0307 | 2 | HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2535-5132_2535-509 others(39): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 131792026 | |||||
chr12:131792028
|
GTGTGTGT others(63): Show |
G | 1 | a0002c0003t0003g0026 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2535-5098_2535-502 others(74): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 131792028 | |||||
chr12:131792040
|
G | A | 5 | a0001c0001t0002g0019a0001c0004t0002g0009a0001c0004t0002g0010others(2): Show | 5 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.2535-5138G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131792040 | ||||||
chr12:131792094
|
G | A | 2 | a0001c0004t0001g0099a0003c0009t0001g0053 | 2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.2535-5084G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131792094 | ||||||
chr12:131792098
|
A | G | 2 | a0001c0004t0002g0306a0001c0004t0002g0307 | 2 | HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2535-5080A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131792098 | ||||||
chr12:131792116
|
GTACTGTG others(98): Show |
G | 4 | a0001c0006t0001g0014a0001c0006t0001g0016a0001c0006t0001g0017others(1): Show | 4 | HG02922.hp1 HG03130.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2535-5050_2535-494 others(4): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 131792116 | |||||
chr12:131792133
|
G | A | 1 | a0001c0001t0001g0242 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2535-5045G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131792133 | ||||||
chr12:131792144
|
C | T | 80 | a0000c0005t0001g0120a0000c0005t0001g0121a0000c0005t0001g0199others(77): Show | 81 | HG00280.hp2 HG00597.hp1 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.2535-5034C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131792144 | ||||||
chr12:131792154
|
C | G | 3 | a0001c0001t0003g0031a0001c0001t0003g0308a0008c0021t0003g0020 | 3 | HG02258.hp1 HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.2535-5024C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131792154 | ||||||
chr12:131792253
|
CCAGTACT others(28): Show |
C | 1 | a0001c0001t0001g0220 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2535-4908_2535-487 others(39): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 131792253 | |||||
chr12:131792279
|
A | ATTCACAG others(165): Show |
2 | a0001c0002t0001g0294a0001c0002t0001g0298 | 2 | HG01346.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.2535-4836_2535-466 others(176): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 131792279 | |||||
chr12:131792289
|
C | T | 3 | a0000c0023t0001g0051a0003c0009t0001g0052a0003c0009t0001g0053 | 3 | HG01891.hp1 HG02258.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.2535-4889C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131792289 | ||||||
chr12:131792342
|
TGTGTGTG others(28): Show |
T | 1 | a0001c0001t0001g0253 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2535-4811_2535-477 others(39): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 131792342 | |||||
chr12:131792417
|
C | T | 203 | a0000c0005t0001g0251a0000c0023t0001g0051a0001c0001t0001g0003others(200): Show | 209 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.2535-4761C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131792417 | ||||||
chr12:131792433
|
G | A | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2535-4745G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131792433 | ||||||
chr12:131792451
|
G | A | 1 | a0001c0001t0002g0019 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2535-4727G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131792451 | ||||||
chr12:131792514
|
C | T | 307 | a0000c0005t0001g0120a0000c0005t0001g0121a0000c0005t0001g0199others(304): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.2535-4664C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131792514 | ||||||
chr12:131792546
|
G | A | 21 | a0001c0001t0001g0175a0001c0001t0001g0177a0001c0001t0001g0178others(18): Show | 21 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.2535-4632G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131792546 | ||||||
chr12:131792584
|
G | A | 23 | a0001c0001t0003g0018a0001c0001t0003g0021a0001c0001t0003g0025others(20): Show | 24 | HG01934.hp2 HG02055.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.2535-4594G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131792584 | ||||||
chr12:131792611
|
ACATGTGT others(27): Show |
A | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2535-4550_2535-451 others(38): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 131792611 | |||||
chr12:131792658
|
C | T | 1 | a0001c0006t0001g0016 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2535-4520C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131792658 | ||||||
chr12:131792680
|
A | G | 80 | a0000c0005t0001g0120a0000c0005t0001g0121a0000c0005t0001g0199others(77): Show | 81 | HG00280.hp2 HG00597.hp1 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.2535-4498A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131792680 | ||||||
chr12:131792789
|
G | A | 1 | a0002c0003t0003g0041 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2535-4389G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131792789 | ||||||
chr12:131792889
|
C | G | 2 | a0001c0012t0001g0044a0001c0012t0001g0045 | 2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2535-4289C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131792889 | ||||||
chr12:131793057
|
A | G | 2 | a0001c0001t0001g0227a0001c0001t0001g0270 | 2 | HG02056.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.2535-4121A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131793057 | ||||||
chr12:131793092
|
C | A | 3 | a0001c0004t0002g0009a0001c0004t0002g0010a0001c0004t0002g0011 | 3 | HG01891.hp2 HG02723.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2535-4086C>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131793092 | ||||||
chr12:131793134
|
T | A | 1 | a0001c0001t0001g0126 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.2535-4044T>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131793134 | ||||||
chr12:131793165
|
G | T | 1 | a0001c0001t0003g0021 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2535-4013G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131793165 | ||||||
chr12:131793169
|
G | A | 1 | a0001c0001t0001g0130 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.2535-4009G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131793169 | ||||||
chr12:131793319
|
A | G | 32 | a0001c0001t0001g0061a0001c0001t0002g0050a0001c0001t0002g0054others(29): Show | 32 | HG00639.hp1 HG01106.hp2 HG01167.hp2 others(29): Show |
intron_variant | MODIFIER | c.2535-3859A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131793319 | ||||||
chr12:131793330
|
T | C | 3 | a0001c0001t0001g0005a0001c0001t0001g0180a0001c0001t0001g0255 | 4 | HG02040.hp1 HG02132.hp1 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.2535-3848T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131793330 | ||||||
chr12:131793644
|
G | A | 1 | a0002c0003t0004g0024 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2535-3534G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131793644 | ||||||
chr12:131793647
|
A | G | 62 | a0001c0001t0001g0061a0001c0001t0002g0050a0001c0001t0002g0054others(59): Show | 63 | HG00639.hp1 HG01106.hp2 HG01167.hp2 others(60): Show |
intron_variant | MODIFIER | c.2535-3531A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131793647 | ||||||
chr12:131793716
|
T | C | 1 | a0001c0001t0003g0021 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2535-3462T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131793716 | ||||||
chr12:131793852
|
C | A | 60 | a0001c0001t0001g0061a0001c0001t0002g0050a0001c0001t0002g0054others(57): Show | 61 | HG00639.hp1 HG01106.hp2 HG01167.hp2 others(58): Show |
intron_variant | MODIFIER | c.2535-3326C>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131793852 | ||||||
chr12:131793860
|
G | A | 23 | a0001c0001t0001g0265a0001c0002t0001g0283a0001c0002t0001g0285others(20): Show | 23 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.2535-3318G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131793860 | ||||||
chr12:131793910
|
G | T | 122 | a0000c0005t0001g0251a0001c0001t0001g0003a0001c0001t0001g0004others(119): Show | 127 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.2535-3268G>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131793910 | ||||||
chr12:131793940
|
C | T | 3 | a0001c0001t0001g0200a0001c0008t0001g0235a0001c0008t0001g0236 | 3 | HG00733.hp2 HG01175.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.2535-3238C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131793940 | ||||||
chr12:131793948
|
G | C | 21 | a0000c0023t0001g0051a0001c0001t0001g0047a0001c0001t0001g0048others(18): Show | 21 | HG00323.hp1 HG00733.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.2535-3230G>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131793948 | ||||||
chr12:131793981
|
T | G | 3 | a0001c0001t0003g0031a0001c0001t0003g0308a0008c0021t0003g0020 | 3 | HG02258.hp1 HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.2535-3197T>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131793981 | ||||||
chr12:131793985
|
G | A | 111 | a0000c0005t0001g0251a0001c0001t0001g0003a0001c0001t0001g0004others(108): Show | 116 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.2535-3193G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131793985 | ||||||
chr12:131794021
|
T | G | 21 | a0000c0023t0001g0051a0001c0001t0001g0047a0001c0001t0001g0048others(18): Show | 21 | HG00323.hp1 HG00733.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.2535-3157T>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131794021 | ||||||
chr12:131794164
|
A | G | 23 | a0001c0001t0001g0265a0001c0002t0001g0283a0001c0002t0001g0285others(20): Show | 23 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.2535-3014A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131794164 | ||||||
chr12:131794374
|
A | T | 1 | a0001c0001t0001g0141 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2535-2804A>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131794374 | ||||||
chr12:131794695
|
C | G | 2 | a0001c0012t0001g0044a0001c0012t0001g0045 | 2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2535-2483C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131794695 | ||||||
chr12:131794787
|
G | A | 61 | a0001c0001t0001g0061a0001c0001t0002g0050a0001c0001t0002g0054others(58): Show | 62 | HG00639.hp1 HG01106.hp2 HG01167.hp2 others(59): Show |
intron_variant | MODIFIER | c.2535-2391G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131794787 | ||||||
chr12:131794797
|
A | G | 62 | a0001c0001t0001g0061a0001c0001t0002g0050a0001c0001t0002g0054others(59): Show | 63 | HG00639.hp1 HG01106.hp2 HG01167.hp2 others(60): Show |
intron_variant | MODIFIER | c.2535-2381A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131794797 | ||||||
chr12:131795067
|
A | G | 2 | a0001c0008t0001g0235a0001c0008t0001g0236 | 2 | HG00733.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.2535-2111A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131795067 | ||||||
chr12:131795412
|
G | A | 2 | a0001c0012t0001g0044a0001c0012t0001g0045 | 2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2535-1766G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131795412 | ||||||
chr12:131795482
|
A | G | 111 | a0000c0005t0001g0251a0001c0001t0001g0003a0001c0001t0001g0004others(108): Show | 116 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.2535-1696A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131795482 | ||||||
chr12:131795539
|
C | G | 1 | a0001c0001t0001g0273 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2535-1639C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131795539 | ||||||
chr12:131795664
|
C | T | 2 | a0001c0012t0001g0044a0001c0012t0001g0045 | 2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2535-1514C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131795664 | ||||||
chr12:131795721
|
G | A | 1 | a0001c0006t0001g0014 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2535-1457G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131795721 | ||||||
chr12:131795885
|
C | T | 1 | a0002c0003t0003g0032 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2535-1293C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131795885 | ||||||
chr12:131795929
|
T | C | 1 | a0001c0001t0001g0167 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2535-1249T>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131795929 | ||||||
chr12:131795964
|
C | T | 113 | a0000c0005t0001g0251a0001c0001t0001g0003a0001c0001t0001g0004others(110): Show | 118 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.2535-1214C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131795964 | ||||||
chr12:131795964
|
CGGGAGGG others(9): Show |
C | 1 | a0001c0002t0001g0300 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2535-1201_2535-118 others(20): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 131795964 | |||||
chr12:131795964
|
CGGGAGGG others(32): Show |
C | 1 | a0001c0001t0003g0036 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2535-1201_2535-116 others(43): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 131795964 | |||||
chr12:131795971
|
G | A | 1 | a0001c0001t0001g0106 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2535-1207G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131795971 | ||||||
chr12:131795978
|
T | TAGGGGAG others(16): Show |
2 | a0001c0001t0001g0152a0001c0001t0001g0173 | 2 | HG01168.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.2535-1159_2535-113 others(27): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 131795978 | |||||
chr12:131795979
|
AGGGGAGG others(11): Show |
A | 1 | a0001c0001t0002g0077 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2535-1182_2535-116 others(22): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 131795979 | |||||
chr12:131795979
|
AGGGGAGG others(34): Show |
A | 2 | a0001c0001t0001g0221a0001c0001t0005g0222 | 2 | HG00642.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.2535-1182_2535-114 others(45): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 131795979 | |||||
chr12:131795991
|
GGGAGAGG others(44): Show |
G | 1 | a0001c0001t0002g0019 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2535-1162_2535-111 others(55): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 131795991 | |||||
chr12:131795995
|
G | A | 1 | a0001c0001t0003g0021 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2535-1183G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131795995 | ||||||
chr12:131795995
|
GAGGGGGA others(15): Show |
G | 2 | a0001c0012t0001g0044a0001c0012t0001g0045 | 2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2535-1182_2535-116 others(26): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131795995 | ||||||
chr12:131795997
|
G | GGGGGAGG others(39): Show |
2 | a0001c0001t0001g0279a0007c0020t0001g0280 | 2 | HG02071.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.2535-1165_2535-116 others(50): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 131795997 | |||||
chr12:131795997
|
G | GGGGGAGG others(21): Show |
60 | a0000c0005t0001g0120a0000c0005t0001g0121a0001c0001t0001g0002others(57): Show | 61 | HG00597.hp1 HG00609.hp1 HG00735.hp2 others(58): Show |
intron_variant | MODIFIER | c.2535-1164_2535-113 others(32): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 131795997 | |||||
chr12:131795997
|
G | GGGGGAGG others(22): Show |
1 | a0001c0001t0001g0144 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2535-1160_2535-115 others(33): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 131795997 | |||||
chr12:131795997
|
G | GGGGGGAG others(22): Show |
1 | a0006c0024t0001g0131 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2535-1177_2535-117 others(33): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 131795997 | |||||
chr12:131795997
|
GGGGGA | G | 20 | a0000c0023t0001g0051a0001c0001t0001g0048a0001c0001t0001g0049others(17): Show | 20 | HG00323.hp1 HG00733.hp1 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.2535-1164_2535-116 others(9): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 131795997 | |||||
chr12:131795997
|
GGGGGAGG others(15): Show |
G | 3 | a0001c0001t0001g0198a0001c0001t0001g0261a0001c0001t0002g0282 | 3 | HG01099.hp1 HG02071.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.2535-1176_2535-115 others(26): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 131795997 | |||||
chr12:131795998
|
G | A | 1 | a0000c0005t0001g0199 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.2535-1180G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131795998 | ||||||
chr12:131796014
|
G | A | 1 | a0001c0001t0001g0230 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2535-1164G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131796014 | ||||||
chr12:131796017
|
A | AGAGGGGG others(23): Show |
1 | a0001c0001t0001g0126 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.2535-1137_2535-113 others(34): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 131796017 | |||||
chr12:131796018
|
G | A | 1 | a0001c0001t0001g0181 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2535-1160G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131796018 | ||||||
chr12:131796019
|
A | AGGGGGAG others(22): Show |
3 | a0001c0001t0001g0123a0001c0001t0001g0140a0001c0001t0001g0165 | 3 | HG00673.hp2 HG02056.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.2535-1137_2535-113 others(33): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 131796019 | |||||
chr12:131796019
|
A | G | 2 | a0001c0012t0001g0044a0001c0012t0001g0045 | 2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2535-1159A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131796019 | ||||||
chr12:131796019
|
AGGGGGAG others(16): Show |
A | 171 | a0000c0005t0001g0251a0001c0001t0001g0003a0001c0001t0001g0004others(168): Show | 177 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.2535-1156_2535-113 others(27): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 131796019 | |||||
chr12:131796020
|
G | GGGGGAGG others(20): Show |
1 | a0001c0001t0001g0159 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2535-1137_2535-113 others(31): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 131796020 | |||||
chr12:131796020
|
GGGGGA | G | 23 | a0001c0001t0001g0265a0001c0002t0001g0283a0001c0002t0001g0285others(20): Show | 23 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.2535-1141_2535-113 others(9): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 131796020 | |||||
chr12:131796022
|
G | A | 1 | a0002c0003t0003g0030 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2535-1156G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131796022 | ||||||
chr12:131796024
|
G | A | 1 | a0002c0003t0003g0030 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2535-1154G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131796024 | ||||||
chr12:131796025
|
A | AGGGGAGG others(22): Show |
1 | a0000c0005t0001g0199 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.2535-1137_2535-113 others(33): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 131796025 | |||||
chr12:131796025
|
A | AGGGGAGG others(39): Show |
4 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0142others(1): Show | 4 | NA18995.hp1 NA19009.hp2 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.2535-1137_2535-113 others(50): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 131796025 | |||||
chr12:131796025
|
A | G | 1 | a0002c0003t0003g0030 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2535-1153A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131796025 | ||||||
chr12:131796027
|
G | A | 1 | a0001c0001t0003g0021 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2535-1151G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131796027 | ||||||
chr12:131796027
|
G | GGGAGGGG others(25): Show |
1 | a0001c0001t0001g0158 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2535-1144_2535-114 others(36): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 131796027 | |||||
chr12:131796042
|
C | A | 132 | a0000c0005t0001g0120a0000c0005t0001g0121a0000c0005t0001g0199others(129): Show | 133 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.2535-1136C>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131796042 | ||||||
chr12:131796042
|
C | G | 3 | a0001c0001t0001g0138a0001c0001t0001g0146a0001c0001t0001g0154 | 3 | HG03927.hp2 NA18993.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.2535-1136C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131796042 | ||||||
chr12:131796047
|
A | AGGGGGAG others(22): Show |
2 | a0001c0001t0001g0146a0001c0001t0001g0154 | 2 | HG03927.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.2535-1112_2535-111 others(33): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 131796047 | |||||
chr12:131796047
|
A | AGGGGGAG others(25): Show |
1 | a0001c0001t0001g0138 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.2535-1116_2535-111 others(36): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 131796047 | |||||
chr12:131796047
|
A | G | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2535-1131A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131796047 | ||||||
chr12:131796136
|
A | G | 1 | a0001c0001t0001g0183 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2535-1042A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131796136 | ||||||
chr12:131796160
|
G | A | 3 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0185 | 3 | HG01243.hp1 HG03098.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.2535-1018G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131796160 | ||||||
chr12:131796264
|
G | A | 1 | a0001c0001t0003g0021 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2535-914G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131796264 | ||||||
chr12:131796597
|
A | ACAACAGA others(7): Show |
1 | a0000c0005t0001g0199 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.2535-579_2535-566d others(16): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr12 | 131796597 | |||||
chr12:131796608
|
A | C | 2 | a0001c0012t0001g0044a0001c0012t0001g0045 | 2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2535-570A>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131796608 | ||||||
chr12:131796610
|
A | C | 2 | a0001c0012t0001g0044a0001c0012t0001g0045 | 2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2535-568A>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131796610 | ||||||
chr12:131796717
|
G | C | 3 | a0001c0001t0002g0050a0001c0001t0002g0054a0001c0001t0002g0058 | 3 | HG02027.hp1 NA18979.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.2535-461G>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131796717 | ||||||
chr12:131796778
|
C | T | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2535-400C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131796778 | ||||||
chr12:131796962
|
A | G | 307 | a0000c0005t0001g0120a0000c0005t0001g0121a0000c0005t0001g0199others(304): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.2535-216A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131796962 | ||||||
chr12:131797006
|
A | G | 7 | a0001c0001t0002g0019a0001c0004t0002g0009a0001c0004t0002g0010others(4): Show | 7 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.2535-172A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131797006 | ||||||
chr12:131797020
|
A | G | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2535-158A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 15/17 | chr12 | 131797020 | ||||||
chr12:131797511
|
G | A | 2 | a0001c0008t0001g0235a0001c0008t0001g0236 | 2 | HG00733.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.2717+151G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 16/17 | chr12 | 131797511 | ||||||
chr12:131797535
|
C | T | 59 | a0001c0001t0002g0050a0001c0001t0002g0054a0001c0001t0002g0055others(56): Show | 60 | HG00639.hp1 HG01106.hp2 HG01167.hp2 others(57): Show |
intron_variant | MODIFIER | c.2717+175C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 16/17 | chr12 | 131797535 | ||||||
chr12:131797537
|
C | A | 23 | a0001c0001t0001g0265a0001c0002t0001g0283a0001c0002t0001g0285others(20): Show | 23 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.2717+177C>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 16/17 | chr12 | 131797537 | ||||||
chr12:131797547
|
G | A | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2717+187G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 16/17 | chr12 | 131797547 | ||||||
chr12:131797571
|
C | G | 7 | a0001c0001t0002g0019a0001c0004t0002g0009a0001c0004t0002g0010others(4): Show | 7 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.2717+211C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 16/17 | chr12 | 131797571 | ||||||
chr12:131797957
|
G | A | 1 | a0001c0001t0001g0241 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2717+597G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 16/17 | chr12 | 131797957 | ||||||
chr12:131797967
|
G | A | 1 | a0001c0001t0001g0267 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.2717+607G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 16/17 | chr12 | 131797967 | ||||||
chr12:131798079
|
A | G | 7 | a0001c0001t0002g0019a0001c0004t0002g0009a0001c0004t0002g0010others(4): Show | 7 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.2717+719A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 16/17 | chr12 | 131798079 | ||||||
chr12:131798135
|
A | G | 1 | a0001c0018t0001g0015 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2717+775A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 16/17 | chr12 | 131798135 | ||||||
chr12:131798276
|
C | G | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2718-761C>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 16/17 | chr12 | 131798276 | ||||||
chr12:131798316
|
A | G | 21 | a0000c0023t0001g0051a0001c0001t0001g0047a0001c0001t0001g0048others(18): Show | 21 | HG00323.hp1 HG00733.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.2718-721A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 16/17 | chr12 | 131798316 | ||||||
chr12:131798406
|
G | A | 21 | a0000c0023t0001g0051a0001c0001t0001g0047a0001c0001t0001g0048others(18): Show | 21 | HG00323.hp1 HG00733.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.2718-631G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 16/17 | chr12 | 131798406 | ||||||
chr12:131798449
|
C | T | 2 | a0001c0012t0001g0044a0001c0012t0001g0045 | 2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2718-588C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 16/17 | chr12 | 131798449 | ||||||
chr12:131798460
|
G | A | 1 | a0001c0001t0002g0097 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2718-577G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 16/17 | chr12 | 131798460 | ||||||
chr12:131798616
|
G | A | 1 | a0001c0001t0001g0229 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2718-421G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 16/17 | chr12 | 131798616 | ||||||
chr12:131798696
|
C | T | 1 | a0001c0001t0002g0019 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2718-341C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 16/17 | chr12 | 131798696 | ||||||
chr12:131798746
|
C | T | 1 | a0001c0001t0001g0241 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2718-291C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 16/17 | chr12 | 131798746 | ||||||
chr12:131798845
|
G | A | 6 | a0001c0001t0002g0084a0001c0001t0002g0091a0001c0001t0002g0092others(3): Show | 6 | HG02145.hp1 HG02895.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.2718-192G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 16/17 | chr12 | 131798845 | ||||||
chr12:131798975
|
A | G | 7 | a0001c0001t0002g0019a0001c0004t0002g0009a0001c0004t0002g0010others(4): Show | 7 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.2718-62A>G | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 16/17 | chr12 | 131798975 | ||||||
chr12:131799246
|
G | A | 1 | a0001c0001t0003g0036 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2790+137G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 17/17 | chr12 | 131799246 | ||||||
chr12:131799256
|
G | C | 21 | a0000c0023t0001g0051a0001c0001t0001g0047a0001c0001t0001g0048others(18): Show | 21 | HG00323.hp1 HG00733.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.2790+147G>C | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 17/17 | chr12 | 131799256 | ||||||
chr12:131799313
|
G | A | 59 | a0001c0001t0002g0050a0001c0001t0002g0054a0001c0001t0002g0055others(56): Show | 60 | HG00639.hp1 HG01106.hp2 HG01167.hp2 others(57): Show |
intron_variant | MODIFIER | c.2791-110G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 17/17 | chr12 | 131799313 | ||||||
chr12:131799327
|
C | CTT | 9 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0002g0019others(6): Show | 9 | HG01243.hp1 HG01891.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.2791-95_2791-94ins others(2): Show |
SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr12 | 131799327 | |||||
chr12:131799346
|
C | T | 2 | a0001c0012t0001g0044a0001c0012t0001g0045 | 2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2791-77C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 17/17 | chr12 | 131799346 | ||||||
chr12:131799380
|
G | A | 1 | a0004c0014t0001g0272 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2791-43G>A | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 17/17 | chr12 | 131799380 | ||||||
chr12:131799413
|
C | T | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2791-10C>T | SFSWAP | ENSG00000061936.10 | transcript | ENST00000261674.9 | protein_coding | 17/17 | chr12 | 131799413 |